Busch Lab

ZMP

pkhd1l1

Ensembl ID:
ENSDARG00000091116
ZFIN ID:
ZDB-GENE-060503-475
Description:
polycystic kidney and hepatic disease 1 (autosomal recessive)-like 1 [Source:RefSeq peptide;Acc:NP_
Human Orthologue:
PKHD1L1
Human Description:
polycystic kidney and hepatic disease 1 (autosomal recessive)-like 1 [Source:HGNC Symbol;Acc:20313]
Mouse Orthologue:
Pkhd1l1
Mouse Description:
polycystic kidney and hepatic disease 1-like 1 Gene [Source:MGI Symbol;Acc:MGI:2183153]

Alleles

There are 20 alleles of this gene:

Allele Name Consequence Status Availability
sa29197 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa18556 Essential Splice Site Available for shipment Available now
sa987 Nonsense Available for shipment Available now
sa29199 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa29200 Nonsense Mutation detected in F1 DNA Not yet available
sa23516 Nonsense Available for shipment Available now
sa15541 Nonsense Available for shipment Available now
sa39245 Nonsense Mutation detected in F1 DNA Not yet available
sa36833 Nonsense Mutation detected in F1 DNA Not yet available
sa43277 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa23517 Nonsense Available for shipment Available now
sa5923 Nonsense Mutation detected in F1 DNA Not yet available
sa17557 Nonsense Available for shipment Available now
sa32243 Essential Splice Site Available for shipment Available now
sa36834 Nonsense Mutation detected in F1 DNA Not yet available
sa6556 Nonsense Mutation detected in F1 DNA Not yet available
sa15346 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa29197
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127517 Essential Splice Site 451 4196 None 77
ENSDART00000130472 None None 3172 None 48

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 19 (position 23346766)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 23276181
GRCz11 19 22860504
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTACAGCACCCAGAGGTCCGCTGTCATGCGCTTAGAGAAGGGAAAACCG[T/G]AAGTTTTAAATGGTGCTTAAATGTGTGATGTGTGTCCAATTGGTGTGTAA
Long Flanking Sequence:
CCGAATGGACTGATTCAAAGGTTGCATAGGAAGGGCAATGGTCAACGCATAGCTTTAATAGAAAGAAAAAGCATAAAAATATAAAGCGAAAGCATAATTCTCTTCAACAGCTTTTGCAATTATATCACATTTAAGATTTCCCTGTTTGATGCTACTTTCACTTTTCATAGAACGATTAGAAATACTGAAAAAAAATTTAACAGGATAATAGCAGGATAGAATTGTAAAATACGGGAGAATCATAACATAACCGATATTTTTATGGTTTAGTTAAATTTGCTAATGCTAATGTCCCCTCTAAACATCACTTTTGGCCTCTTCGTTATGCTATATTTGTATAAAATGCTAATGATTTCAATTTTATCCAACTTCACCTTGTTTTTTTTTTCTTCATCATGTGCTTCCAGGTCAAGATTGCATATCAGCCTTATTATACAAACAGCTTCTTCACCTACAGCACCCAGAGGTCCGCTGTCATGCGCTTAGAGAAGGGAAAACCG[T/G]AAGTTTTAAATGGTGCTTAAATGTGTGATGTGTGTCCAATTGGTGTGTAAATAACTACACTGTAAAAAGTAAAGGTGCTTCAAATACCCTGTTGAGTACTCAACGTCTAAATGTACTTTAAATGCCTCAAAGCTCTTTCTCTCAAAAGGGTTTCTGTGAGGAAACACTGACAGTCTTTGCAGTACTTGTAGGACCATTTTGCTGTAATTAGGATCCTTCAAGCACTTTTTGTCAATACTGAGGGTCTGGAGTCACTGTTTCCTTACACTAAGACCCCAGAGCACTTTGAAAGATATTAGAGGAACTCATATTCCAATAAAGAGTATACTGGAAGATCTGTAAACTTATATAATGGTTCCTGGTGGATCTGTCTTCTAAAAACTAGCAGTTAGAGGAACCAATAGTTTTTATGACATTTAAATAGGACACTTGTAGAGACCAAAAAATGATATACATGTCTATTTAGTTATTTGTGAAATTAGAATGATATGAATTATTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18556
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127517 Essential Splice Site 504 4196 None 77
ENSDART00000130472 None None 3172 None 48

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 19 (position 23348269)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 23277684
GRCz11 19 22862007
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAGAAACAGCAGATCAACGCATACTACTCTATACTACCTGAAAAAYAGG[T/C]AAGTGAACTCACTTTAGGCAGAGTTCAAAGATTATCTAAAGATAAGATGG
Long Flanking Sequence:
GTTTAGGGGCGGGGTGTGGTGCCACGCCTCCTTTTTAAGATAATACATTTTCGTATGTTCAAATTTGTACAAATTAGCTACTAAATTGACAAAATGTAATATAGTTACATTTCCTTGTGAGATAAGACTGGCTATTCCGACGTGTGTTCTCAGAAAACAGTACAGTGTTTAAACCAAGACATTAACTGCAGTGCCATGTGATCGATAAAACAAATTGCAAATTTACAAACATACTGAAGACAATGGAGTTTTTCTTGTTAAAATAAACATAAAAGGTCTTGTTTTCTCCAATCTTGGATCTAAACATTTTCTCTGTATAATTCTTTCAATGTGCTGCAGGTACTACATCGAAGTTCTAATGCAGGAATATGCAGTAGTAGCATCAGTAGATGTGGGCTTTTTCAAAGAGGTCAGCCCTTTCACGGCCCAGCAGACAATAGAGTCTGTTAATGAGAAACAGCAGATCAACGCATACTACTCTATACTACCTGAAAAACAGG[T/C]AAGTGAACTCACTTTAGGCAGAGTTCAAAGATTATCTAAAGATAAGATGGAAGGAAGCCTTAGAAAAATCTGCAAACTTAATAGGAGAAAAGTTTTTCTGTCTGTACTGTATGTGTGTGTGTGTTTTAAACTCTATTAATACTGCTTTAGGTGATACGTTTTGATGGATGGACACCAGTAACTGCTGTGAATGAGGTTCAAACTTTAAGAATCAGCAGTGACTGTTTTTCTCAGGGCACATGTGAAAACACATACTACTCACTAGGATATGGAAATCTTACAACAGGTGTAATACAATACAATGGTTCTAAGAATGTGTTTAAAGGAGCCAAATATTCGTTTTTTAATTCACTTCTAAATTTTTACATGTTTGTGATACTTTTATTTGCATGTGTTGTAATGTTTACTGTAATTAATTACTGTGCGTGTTGTAGGACCGATCCCTGTCAGTGCTTCAGCAATGGATTTGCAGAATGCTCTGAATGACTTGTGGACGATTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa987
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127517 Nonsense 678 4196 19 77
ENSDART00000130472 None None 3172 None 48

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 19 (position 23349482)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 23278897
GRCz11 19 22863220
KASP Assay ID:
554-0891.1 (used for ordering genotyping assays)
KASP Sequence:
AATGTCCAGCAGAGATTCCAACCGCTGAGAACAGTAACGTGAAATTTTTC[A/T]GAGATTATGAGATGACCACCACAGGGGTAAGCTGCAAATGCACATGATCA
Long Flanking Sequence:
AAACATGTATAATAATATTTAAAGATGATATTTTTTATTTTGCGTATGAATTTAATTTTAAATTAAGTAAAAACTGAGTAATTTGCCAAATCAAAAAATATGTTTTATAACATTTTGAAAATGATCTCAGGTGACTTTGAGGATTTCGATTACATGATAATGGACTTAGATACGAACATCACAGTGACTGAAGCTGTGAAAGGGAAGGCCAGCATGGAGACATTTACGCTGCTGTGGGCAGAAGTTCCATCCCTCCCTCTGCCTTTCAATGCTTCTGAAACTGAGGTTCACCTTTGCTTTATATCTCTTAAAATTGACCATAGAATGTGTACCAAACTTTTACAACTTTTCTTTAAATGTTTCATACCTATATGATGGGTTTCATCTGTGTTTATTTTGTTTTTTATCAAATAAAGGTGCGTTCAGCACTAGATTTGATGATCACAGCTAAATGTCCAGCAGAGATTCCAACCGCTGAGAACAGTAACGTGAAATTTTTC[A/T]GAGATTATGAGATGACCACCACAGGGGTAAGCTGCAAATGCACATGATCATACGGTACATGTTTTACATGCTGAGCACTATTTAGTGAAGTTTATTCATAAACTAATTTCGAGAGGAGCACGTGATTATGATTGAACACGGCTGGTTCTGCATTAGCATGCTTGATCCACCAATCAGGCCATTCCTAACCACTATAAAGAGCCAGGGTTTTCTCACTACAGTTATCTTCGATTTGAAGAATCCCCCCTTCCACCCCTACCTTTTCACCTTTCCCTCCATAGGGCAGCACGGTGGCTCAGTGACTAGCACTGTCGCCTCACAGCAAGAACGTCACCGGTTCTAGTTCCTTAACAGGCCGGTGGTCGTTTCTGTGTGTAGTTTGCATGTTCTTCCCGTGCTTGCGTGGGTTTTCCCCGGGTTCTCCGGTTTCCTCCCACATTCCAAAAACATGTACAACAAGTTAATCGTTAAATCTAAATTTCAATACAGGTAATCTAATA
Associated Phenotype:
Normal
Stage Entity Quality Tag
Larval:Day 5
ZFS:0000037		 whole organism
ZFA:0001094		 quality
PATO:0000001		 normal
PATO:0000461

Mutation Details

Allele Name:
sa29199
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127517 Essential Splice Site 1433 4196 35 77
ENSDART00000130472 Essential Splice Site 374 3172 8 48
Genomic Location (Zv9):
Chromosome 19 (position 23371866)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 23301281
GRCz11 19 22885604
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTATGATGGCACGACTTTCAGCAGCGGAGACACACAAACTGCCAATGG[T/C]ACAAAACCACAACTTCTTGTCAGTAAACACACAGTTTATTCTAACGTACA
Long Flanking Sequence:
CTCTATCATGTGCTTTTGCTTTTAGTTAGAACATGATTTAAATCAGTCTTAAATCAGCCTTTGTGCCCGATAGTCAGGCACGTGTCTGTTTGTCCTCAATCTGGCAACCTGCACTTGTGTGTGTTTTGGTCCAGGAATGCAATTTACTGCATCTTTAAGTAATTATGATGTAATGGAAATTAAAATTTTAAAGGGTAAATGAAAAATTTAAAAGTCCTTAATTAAATGGTCATGAAAAAGAGACATTGATATTGTGCTATCTGTAAAACTGTTCCACTTGCATATAATTAATCACATTACATGTGTTCAGTGTATGGTCAGGGATATGCCTGGAGCCCTTCTGCATTAATAACCTCAGTGGGAGACACAGTGGTTTGGCGATGGAGCGCACCAGCTTTTGTGCCCGGTCTGGCCTACAGGGTCTTCAGTGTATCCAGTCCCAGCAGCACAAACTATGATGGCACGACTTTCAGCAGCGGAGACACACAAACTGCCAATGG[T/C]ACAAAACCACAACTTCTTGTCAGTAAACACACAGTTTATTCTAACGTACATGCATTAAGCAAACATTTAAACAGCATATAGTCTACTGAATAAGCAGCAAGAGTTAGTCCAATAGCCATGTCAAAAAAAAAAGAAGCTTTTTAATCATCTTTCCACATTTTTCGAGTGTCTTGGACTTACTTTTGCTGTTTATTCCAACAAATCCATTACCCAAAGAGCACCAACACATTATTTAGCTACACTGTCAAATAAATAAAATGTAAAATTACAGACATTTATCGTAAAATAACAAACAGTAAATTACAGAAATTTACTTCAATTTAAATTCCTGGTAAAGTTCTGTAATTTACTGTATGTTATTTTACAGTGTACAGTGTTTTTACAGTGTACCCTGAGCTCTTTTGATTTTGAATTTTTCAACATATTGTCAACATTTGACTGACTATTTTGAAAACCAGTCCTTAGTTAATGGACATTTTTTTTCTTATAAAGTCTTTCTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29200
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127517 Nonsense 1660 4196 38 77
ENSDART00000130472 Nonsense 601 3172 11 48
Genomic Location (Zv9):
Chromosome 19 (position 23375776)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 23305191
GRCz11 19 22889514
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGTTCTGGCTTCTTCAGTGGCTCAGTTATGGTAGCGAATGTTCCATGC[A/T]AAGTGGTTTCCTTTGATTATTCTCAAATGGTTTGCGATACTTCCCCGTCT
Long Flanking Sequence:
ATACAGTGAATACATTCTGCACTTTGATTGCCGGTAAATTTAATAATACTTTAATATAAGGAAGTTTGTTAAGTGTAATCACCCCACACAGATATTTTAAATGAGCTGAAAATTAATCAACTGAAGTATGTCTGAGAGTTGTGCAACTGAACACAACTGACTACTGAAACTGATTTTGTCTTATTTTTATGGGGCAACTAAAGGTCAAAGTTGGAGATCTTCCATGCAGCGTCATCAACAGCAGCTCCACTGAGATCAACTGCCAACTCAGTCCAGACAGCAGAGCACCAGTAGGCGTACCTTTACCCTTAACTGTCCAAGTCAACAATCTTGGCAATGCTCTCCTGACCATGCCAAAAGAAATCGACCGCAGATTTGTGGTTCTCCCAGTGGTCGATTCTATCTTTCCAGTAGTAGGCAGCACCACAGGCTCCACACGTCTGCTCATATCTGGTTCTGGCTTCTTCAGTGGCTCAGTTATGGTAGCGAATGTTCCATGC[A/T]AAGTGGTTTCCTTTGATTATTCTCAAATGGTTTGCGATACTTCCCCGTCTATAGCTCGCAGTGGAGATGTCACAGTTTACATCAACTCCATATCTTCTTCATGCAGTTCTGATTGCAAATTTGAATATTCAGACTCCATCACACCACAGGTCTCCACAGTGTCCCCTAGCTCAGTCAGTGGAAACTCCACCACTGTTACAGTCACTGGCAGTGGATTTGGGAACAATCCTGCTGATCTAATGATATTTGCTGACAACATCCTGCTAAAAGGGACACAAGTTAATGACAGCAGCATTGAGGTTTTAGCTGGTGCCCTTCCTGCTGGCACACACACTCTAAAGGTGGTGGTCATGAGCAAAGGTCTCGCCACAGGAAGTGCCACACTTACCAGCATAGCACAAGCCAGCATCAACCCAACATCAGGCAGCATTGCTGGAGGAACTCCGCTCTTGATCACAGGAAATGGATTTGTGGCAGGAAACACAACTGTGAAGCTTGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23516
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127517 Nonsense 2124 4196 42 77
ENSDART00000130472 Nonsense 1059 3172 15 48
Genomic Location (Zv9):
Chromosome 19 (position 23379411)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 23308826
GRCz11 19 22893149
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATCATCTGTGTGACCAATGCTGGGCCCAAATCTCAAGAAACTCAAGTG[C/T]GAGTTCAATTGGGGAACAGAGGAATTGCCAGAATGGTAATGTAAAATGTA
Long Flanking Sequence:
TGTGTTGTAGTCAATCAAGTAACCTGTCGAAGAAGGAGAAATGGATGTAAAACACCCTATCAAAAATTTTACATGTGGACTGTTATGTCAATCCTACATACTGCTCCTTTAATTGATAAACTATCTCATCAATAGCACCAAGAGTTGATCAAAATTTCAGAAACGCTATTAGCTAAAAGTGAACACTGGGCAGGTGATGTTAAGTTTTGAAAAAACAAAAAGTACCATCTAAATACTGTACAACCAAAAGTATTACAATTTGTACACTATGTCCCAAGTCTTTAAAGCCCAATTGGGGTAAACAAACATTAACCAAATGGTTTGAAACTAATCTGAATTTTTGAGTTTCCGGCATTTCTCTTTTCTGTTTTATTTATAGCTCAAATATCAGTGAAATTGCAGTCACAATCGCAGGCTCTATCTGTGATATCCAGTCTGCCAATGAAACTCAGATCATCTGTGTGACCAATGCTGGGCCCAAATCTCAAGAAACTCAAGTG[C/T]GAGTTCAATTGGGGAACAGAGGAATTGCCAGAATGGTAATGTAAAATGTAAATTCATTTATGTAAATGATATAATAATTGTCAATGTTTAGCTATTTCATTTATCTGTTCTCTTTTAACAACTTCTTACTGTTGGCCTGTTTTGATCAGCTAGATTAGTCTATTGCTGAACAGGGGTGCATTTCCGAATACCATCGCTAGCCAACTAAAGTCGCAAGTCCCTTCATTATAAAAAAATCTGTTGATTTGTCGTTTCCGAAATCCATCGTTCCAACGAACATTGCAACTACACTTCTGGAGTTGTAGTTTGAAACAAAGTGGCTGTGTTCTATTCCCAGTTATTCTCCCTATGCCCTATTCGTTTAGAACATTCTAACATTTAAACTTGGAATTATCCAAAGGAAAAAAAAAAGCATTAAAGTCATCACTCTTAGGTATAATTTGCTTTCAAAGTATTTTTACAGTTCAGTTTTAGCGATCTCCATGTTTACAATTATGCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15541
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127517 Nonsense 2146 4196 43 77
ENSDART00000130472 Nonsense 1081 3172 16 48
Genomic Location (Zv9):
Chromosome 19 (position 23381079)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 23310494
GRCz11 19 22894817
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCAATGTATGTCTCAGGATAATGCTTCCTTCTTCTACATTGACGTCTG[G/A]TCATCTCCCTACACATGGGGTGGTCTCTCTCCTCCTGAGGAGGGATCGTT
Long Flanking Sequence:
CACAAAGAAATGATGGGGTTCTTCTCTAAAGAAGTTGTTACTCCACCCCGTTTAGAACATCATTATGGTCATTTTACATTATAACTAACGTGGCAGAGAAACTACGAGTTTTAGGAAACACTCGTCACTACATCAATCTTTTCCCAAACAATGTATCGTACTATAGTTTAGCCCCAAGTTATGTCGATGTTTGAGGAATGCGCCTAGAGCATCTTCTTGATATGTCGACAGCATAAACTCTGCAATTAAGCAAATGTGTTATACATCATCAGGTTTGTGCAGGAAGTAAAACTGAAATGACTCTCTGACACTTACAGAGAGTTCAGAATTAGTTCTTTTTAATATGCACTTTGTTCCTTCTAATTCAGATCCTTTATACTACAGTAACACACAAATGTTTGTCTCAATATCTAAAAAAGAATAACAGAGGCATTTATTGTCTCTTCTTTTGCTCAATGTATGTCTCAGGATAATGCTTCCTTCTTCTACATTGACGTCTG[G/A]TCATCTCCCTACACATGGGGTGGTCTCTCTCCTCCTGAGGAGGGATCGTTTGCTGTAATCACTGCTGGTCAGACCATTCTTCTTGACACAAGCACTCCAATCCTTAAGATGCTGCTTATCCAAGGTATTCTTATTTAAACATGTGCAACTTTTATTAATTAAAGCCTTGGTGCACACATACAGTACTATACAGTACTCTAAATGTTTCTGTTTAGGTGGCCGACTGATATTTGATGAGGCAGACATTGAGCTGCAGGCGGAGAATATTCTGATCACAGATGGCGGAGCTCTGCAAATCGGAACAGAGCAGATGCCCTTCCAGCACAAGGCCATCATCACCCTGCATGGACACCTGCGCTCTCAAGAGCTTCCTGTCTATGGCACCAAAACACTGGGAGTCCGACAGGGCGTGTTGGATCTGCATGGTATGCAAATTAACATCATTTCTAAAGGGACTACTAGTTGACTCTCTAAAAAGTATTTGCTCGTTTTCAAAAAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39245
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127517 Nonsense 2251 4196 44 77
ENSDART00000130472 Nonsense 1186 3172 17 48
Genomic Location (Zv9):
Chromosome 19 (position 23381483)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 23310898
GRCz11 19 22895221
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGCTCTCAAGAGCTTCCTGTCTATGGCACCAAAACACTGGGAGTCCGA[C/T]AGGGCGTGTTGGATCTGCATGGTATGCAAATTAACATCATTTCTAAAGGG
Long Flanking Sequence:
CAATATCTAAAAAAGAATAACAGAGGCATTTATTGTCTCTTCTTTTGCTCAATGTATGTCTCAGGATAATGCTTCCTTCTTCTACATTGACGTCTGGTCATCTCCCTACACATGGGGTGGTCTCTCTCCTCCTGAGGAGGGATCGTTTGCTGTAATCACTGCTGGTCAGACCATTCTTCTTGACACAAGCACTCCAATCCTTAAGATGCTGCTTATCCAAGGTATTCTTATTTAAACATGTGCAACTTTTATTAATTAAAGCCTTGGTGCACACATACAGTACTATACAGTACTCTAAATGTTTCTGTTTAGGTGGCCGACTGATATTTGATGAGGCAGACATTGAGCTGCAGGCGGAGAATATTCTGATCACAGATGGCGGAGCTCTGCAAATCGGAACAGAGCAGATGCCCTTCCAGCACAAGGCCATCATCACCCTGCATGGACACCTGCGCTCTCAAGAGCTTCCTGTCTATGGCACCAAAACACTGGGAGTCCGA[C/T]AGGGCGTGTTGGATCTGCATGGTATGCAAATTAACATCATTTCTAAAGGGACTACTAGTTGACTCTCTAAAAAGTATTTGCTCGTTTTCAAAAAGTTTTAAAAGTATAAGAGTTTATTTTTGCTGTTTTTCAAAAGGTATTTTGAAGAATGTTGGTAACAAGACACAGTTGGCAGCAGCCATAAGTAGGAATAAATACAATGGAAGTCAAGAGCTGTTGGGTTACCTAAGTGTAAAAAATAAATAAATATATTTGTTCAACCAAAAAAAGAAAAGAAAAAAAAAAGACGACAGGAAAGACAGTGAATAACCAACAAATAGCATTATCATTGTTGTAGCATGGGTTTCCTCTGGGTTCTCCACAAACCAAAGAAATATATATAGAGTTTTTAGTCCTCTTCAATTTTTTTTATATATTTTCCAAATGATGTTTAACAGAGCAAGGAAATGTTTACAGTGTGTCAGTTAATATTTTTTTCTTCTGGAAAAAGTATTGTTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36833
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127517 Nonsense 2862 4196 50 77
ENSDART00000130472 Nonsense 1797 3172 23 48
Genomic Location (Zv9):
Chromosome 19 (position 23389662)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 23319077
GRCz11 19 22903400
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGACCCACACAATGGGCTGGTTGGTAATGTTGCCCACTGGTGAAACATA[C/A]AACTGGTACTTTAATGGTGCATCACAAATCACCAACATCTCATACAATGG
Long Flanking Sequence:
GCAGAGGTGTAGCTGCTTTACTGGGCCTACTACGCTATTGTATTTCAATACTGCTCATTTTGGTGGTACTTGGAGAGACATTTTTTTCTGAGGTAGTACTTGAGGAAAAAAGTTTGAGAACCACTGGTCTAGTGAATTGTTTCCCACCCCTGTAACAGGAGGCAGTACATATTTTTGATGTTATCTTATCTTACCTTGTTTGACTCATTAACTTAAGGTTGGTTTTGGAGTCTCATCTAATATTCTGATGAGCTGATTTAGGTGTGTTTGATTAGAAAGAGTTTAAAAAAAATGTTTAAAAAATTAAATTAAATGTGACTCAAGCTTCTGTGTTTGTTTGGTTCAAGTGAGCTGTGATACTTCGATGGCATTATGTTTAATGCATTAACTCTATGTGTCATATTTTTTTTATCTTTAGGTACATGCGTGCTTCCTTTTCTTAAAAAACTTGTGACCCACACAATGGGCTGGTTGGTAATGTTGCCCACTGGTGAAACATA[C/A]AACTGGTACTTTAATGGTGCATCACAAATCACCAACATCTCATACAATGGAATGGTCTACGGATTTCGGGTATAGTCTAAAAGTTTAATACAATTTTTATTTTTTTAAACATGCTATACAATATCGTCTTCTGCAGTACTATTTCATATTAATGCTAAAAGGGCAAAATAAAACTACTTCATACAACTACTGTGCTTATAGTGCACACACACACACACACACACACACACACACACACACACACATACATACACTATTGGTTTGGTATACTACACCCGACTAATAAATAATACATATGTTCGTGTGGAACAATGATGTTGTATGAATAGTATTAAAATGTTACCATTTAGTTATTTTAATTTCAACAGGTATTTTTTTTAAAACATCATACTTAGCTAAAGCAAAGGGATTTTATTTAATATGTATTATAAAAATTTACCCCCCACTATTTGAGATGTGTTACCTTTATTTTATAAACATATAACACATTTATATTTGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43277
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127517 Essential Splice Site 3076 4196 None 77
ENSDART00000130472 Essential Splice Site 2011 3172 None 48
Genomic Location (Zv9):
Chromosome 19 (position 23392176)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 23321591
GRCz11 19 22905914
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATGTTTAATTTTATCCGCAATAAAATCTTCTTATATTTTCACAAAATC[A/G]GGGTGGGCGTCTGATTGCCGGCTGGCCTGATGCACCCTTCAGAGGTCAAC
Long Flanking Sequence:
ACTCTTACTGCTGTTTTTCATTTAGCTTAGTTTTAGTTCTGTTTAAATGTCTCTTTTAGGTTTTATCATACCCAATCTATTAATTGTAGTTTTTTTTTTTTTTTTTTAATATTGGGAATATTTATTTTATTGATTCAGTTTTTGTTAATGGAATGAAACATTTGTTGAAATTCTAATAAACTTATTAATCAAATGATTTTACTCAAATTTATAAATGTGGTTACTGATCATGATGGTTCTTAATTTAATGTGGACAGTCATTTTGTGAGTTACCATATAGCGTGGATATATGGGTTTAAGATGGAGATTTCTGTGCTTTACATGCTGTGATAGTTGACGTTACATTCATTTGCACAACGTAATACTGCGCCTTACTATAGCAGGAATCCTAAGTTAATTAAACCAGCCTTTGATTAGCTGACCAAACAGTTAAATATTCCTCATACAAATACATGTTTAATTTTATCCGCAATAAAATCTTCTTATATTTTCACAAAATC[A/G]GGGTGGGCGTCTGATTGCCGGCTGGCCTGATGCACCCTTCAGAGGTCAACTTCAGATCATACTGAAAGGAAGCCATACCACTCCAGACTGGCTGTTACCATCTGGACCAAACCAAGGATCCAAAGTGCTGGGTAAATTACTTGAATTCAACCAAATTAAGCATTTGAGTTTGTCTTAAATGCTGTCATAAAGAAATCTTCATCAGTTTGAAAAAATAAAAATAAAAATTGGTTTCCATTTAAAACCCCTACAGCAGTCCATAATTGTATTCTCCCAAAAAAACATGTTTAAAAACAAATGTACATATTTAATTATTTAGCACACATACTAGGATATTTCTTAACATCTTGCATGATTTATTAAATGTATTAATGAAATTTCAAATAAGTGCAACCTCCACGTACTCATACTAGCTAGAAGAGAGCAATAAACACTACAAAATGACAAGTGGTAATATAGGATTAATTCAGCCATATACCCTTGAACCAGAACAATTTCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23517
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127517 Nonsense 3134 4196 56 77
ENSDART00000130472 Nonsense 2081 3172 29 48
Genomic Location (Zv9):
Chromosome 19 (position 23393534)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 23322949
GRCz11 19 22907272
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGGTGTGTTTGGATCTCTTGACCTGTATGGCATGCCACACAACATCTA[T/A]CACACTAAGCTGGCAAGCACATCCCAGGCAGGAAACAACACTCTCTCTCT
Long Flanking Sequence:
AAATAAACGAACAAACAAACTGTAAATTGTTTTTTTTAAGCGTTAAACTTATTTTATTTGAGTAATTTGTTTCTATTTGCATTTAAATTTGAAAATGGATTTGTCTTCTCTTTTAATTTTGTTCTTTCATGTTATTATTGCACACTTTTTTTCTATTATTGCCCATGTATGTCGATCAGTAGTACCCTTTATAATCCTTCATTCTGAAAGGCGATTCGAAGTGGCCCTTCAGAGGGTGAAATCCCATTTTGAATGGACCATCAATGTCATAAAGAGTTAATAAAGATCATAATGCAAATAGAGTGAAAGTTTAGCTGCATTAGTGTTGACTGATGCATTTGAGCTTAGTTTATCTTTTAGTGCATTGAAGACACCAGACAGTCATGCAAACAATGGTAAAATACATTCTCCACAGTCTTTAAAGGTTCTAATTTTAACAGTCACTGTTTTCCAGGTGTGTTTGGATCTCTTGACCTGTATGGCATGCCACACAACATCTA[T/A]CACACTAAGCTGGCAAGCACATCCCAGGCAGGAAACAACACTCTCTCTCTACAGGAGTCTGTGGACTGGAAGGTCAGACGCTTTTTAATGGTGCTACCAAAAGGAGTTTAAAGAAGAATTTCATGATGTGTGATGCCATTAAGAGTCAAATCTCCTTTCATGAACTAAACTGCTTTTATTATCTTCAGGTTGGGGATAAGATCCTGCTGTCCACCACTAGCTATGACCCTTGGCAGACAGAAATACGCAACATTATTGCTGTTTCCAATTATGGTCGCACACTGACCCTGGACCAGCCTTTAACATATACACACATTGGTTAGTTTTCTACAGTAGTGTTTCCCAACTGAACGGTTTCACTTTCTCACAATTTTAGTTGTCAGAATCCAGTTTCTTTCTTCTGTTGAACACAAAATAAGTTATTTTGAAGATGGTAGTCATTGTCTTCCAAAATATTATTTTTTCCTACTATGGATGTCAGTGGTTGCTTTTCGAGTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5923
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127517 Nonsense 3170 4196 57 77
ENSDART00000130472 Nonsense 2117 3172 30 48
Genomic Location (Zv9):
Chromosome 19 (position 23393758)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 23323173
GRCz11 19 22907496
KASP Assay ID:
554-3836.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTATTATCWTCAGGTTGGGGATAAGATCCTGCTGTCCACCACTAGCTA[T/G]GACCCTTGGCAGACAGAAATMCGCAACATTATTGCTGTTTCCRATTATGG
Long Flanking Sequence:
CCCTTCAGAGGGTGAAATCCCATTTTGAATGGACCATCAATGTCATAAAGAGTTAATAAAGATCATAATGCAAATAGAGTGAAAGTTTAGCTGCATTAGTGTTGACTGATGCATTTGAGCTTAGTTTATCTTTTAGTGCATTGAAGACACCAGACAGTCATGCAAACAATGGTAAAATACATTCTCCACAGTCTTTAAAGGTTCTAATTTTAACAGTCACTGTTTTCCAGGTGTGTTTGGATCTCTTGACCTGTATGGCATGCCACACAACATCTATCACACTAAGCTGGCAAGCACATCCCAGGCAGGAAACAACACTCTCTCTCTACAGGAGTCTGTGGACTGGAAGGTCAGACGCTTTTTAATGGTGCTACCAAAAGGAGTTTAAAGAAGAATTTCATGATGTGTGATGCCATTAAGAGTCAAATCTCCTTTCATGAACTAAACTGCTTTTATTATCTTCAGGTTGGGGATAAGATCCTGCTGTCCACCACTAGCTA[T/G]GACCCTTGGCAGACAGAAATACGCAACATTATTGCTGTTTCCAATTATGGTCGCACACTGACCCTGGACCAGCCTTTAACATATACACACATTGGTTAGTTTTCTACAGTAGTGTTTCCCAACTGAACGGTTTCACTTTCTCACAATTTTAGTTGTCAGAATCCAGTTTCTTTCTTCTGTTGAACACAAAATAAGTTATTTTGAAGATGGTAGTCATTGTCTTCCAAAATATTATTTTTTCCTACTATGGATGTCAGTGGTTGCTTTTCGAGTATTTTCTTTTGTTTAAAAAATCTCATATTGTTTTGGAATTTTTAAAATCTAAAACATGTTGACATTTTGTTTAAACAACTACATTCTCAACTAAAAATAAAAAATGCATTTGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAAAGTGTTTTTTAAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17557
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127517 Nonsense 3356 4196 61 77
ENSDART00000130472 Nonsense 2303 3172 34 48
Genomic Location (Zv9):
Chromosome 19 (position 23396849)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 23326264
GRCz11 19 22910587
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGGGAGAYAGWAATGTGGTTCGKAGGAACTTGGTTACTTTGACACTGT[G/A]GCCYGGATCTTACAATGGCAGAGCAGAGGAATTTAACTTTCAATGGAATG
Long Flanking Sequence:
AGTGATAAAGCTTCACTCCCCATCTCTAAGGGTGCGCCCTTCAACCCTTTGAAAGAAGCTCATATTAGTAACTTGTGGTTGAGATCTTGCCCTTTTGGTAATGACCCAAAGTTCATGACCATTGGTGAGAATCGAGTGTTTTGCCTTTCATTCTTCCTCTATCTCCCTCTCCCATTGTGTTTAAATCTATGAAAGTAAATATCTTCCCAAGTTTGTTTTAGAGTTGTTTTATTATTTTAATTGTTCAGTTCCTCAGACATTGGCTACTAATTTATCCTCACTAGTAATACTACAGTTGTGTGAGTGCAGGAGGAATGTTCTGACAGGATGAACATGTGTGGAAATAGGCCTGCCACCACACCTAGAAAGAAAAACACTTTTACAGTATAAAACCACATGTAATCCCTCATCAAATTACTATTTTTATTTTAATTTCCAAGGAATCAGAGTCTGGGGAGATAGTAATGTGGTTCGGAGGAACTTGGTTACTTTGACACTGT[G/A]GCCTGGATCTTACAATGGCAGAGCAGAGGAATTTAACTTTCAATGGAATGCAGGAATTGAGGTACTACATACAGAATAAAGTCAGATGGGAATATCATGTTACTGTGCTTGAATGTGCTATTTAATGGCTACCATTTTCATATACTGTGTGTAATGGTACATGAAGCACTAATGCATGAATTACCATGTTACCATGTTGAAAATCATGGTAGACCCACTTTTAGAACTGCATATTTGCTTAAAAGATTAATACTATAAAAATATAATGTTGTGTGCCCTAGGTCAGTGAAGCAACCAATGTGATTCTTCAAGGAAATATTGTTGCTGGCTATGAACGAGTGGGATTCAGAATTGATGGAGAACCCTGCCCAGGTACAATATATGAAGCAAAAGTAATTTTAAAAAATAAACACAAACATACACACAAAATAAAGATTTCAACAATATGTCAAAAGGAGTTTCAAATCCAGTGGCCCAGTGGAGTCAGAATGAGGCGCATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32243
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127517 Essential Splice Site 3497 4196 64 77
ENSDART00000130472 Essential Splice Site 2444 3172 37 48
Genomic Location (Zv9):
Chromosome 19 (position 23397714)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 23327129
GRCz11 19 22911452
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTCCCGCGGTCAGTCACAGGTATTCTGACAAAACCGTTCGCGTGCAGG[T/C]GAGAATGCACTACAGTATAAACTGTGCACACTATACAGAAGTGGCCAAAA
Long Flanking Sequence:
CTGCCCAGGTACAATATATGAAGCAAAAGTAATTTTAAAAAATAAACACAAACATACACACAAAATAAAGATTTCAACAATATGTCAAAAGGAGTTTCAAATCCAGTGGCCCAGTGGAGTCAGAATGAGGCGCATGGTGGTCTTTTCGGGCTCTACATGAATAAAGATGGACTTCCTGGTTGCTCTCAGATCCAGGGCTTCACTGTCTGGAGAAGTTTTGATTTCGGCATTTATGTTCAAGTATGAAAAATGATTCATGCACATCCTGCTATTATATAATACCCATGTGTTCTCTTGGTCAAAATGTCCTAGTTCTACAAATGCATTGTGCCGATCGATCTAGCATTGTTTTAAATGACTGTTTTCTCACTTGCAGGTCTCCATGAGTGTGTTGATTTCTAATGTGAGCCTGATTGATAATGGAATGGGAATCATGTCTTTAATTTATGAACCTCCCGCGGTCAGTCACAGGTATTCTGACAAAACCGTTCGCGTGCAGG[T/C]GAGAATGCACTACAGTATAAACTGTGCACACTATACAGAAGTGGCCAAAATTAATAGAACGCTCGTTAGATCTGAAAACACTTGTTGCTCTGAGCACAACAACTATAAAATAAAGTGAGTCATATTGTTTAATTCACTTTTTACTTACCTACTATTTTGTATGTCCAGCAATTACAGGACATCTCTTTGGCACATTGTTATTTTTTTCCTCAGAACTTCAATAGTAATATGTTATTACTATTAAAGTTCTGATGTTATGTCTTATACTATAAGTCTCATAGTATATGTTAGTTATGCACCGGTTTTTAAAATAGCTCCTATGTCCACTGTTGTGTTTGTAGTCATGAATAATTTATGTAGCACTGCAACACGGTGGAACAGTTGGTAGTGCTGTCGCCTCACAGCAAAAGGTTGCTGGTTCGAGCCTCGGCTGGGTCAGTTGGCATTTCTTTGTGGAGTTTGCATGTTCTCCCCACGTTTGCGTGGGTTTCCTCCAGGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36834
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127517 Nonsense 3803 4196 70 77
ENSDART00000130472 Nonsense 2750 3172 43 48
Genomic Location (Zv9):
Chromosome 19 (position 23400594)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 23330009
GRCz11 19 22914332
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCAGTAAATCCTTTGACATCTATTTCACCAGCACAACACCACAGAACT[T/A]AAGACTTATGTTACTGAATGCTGGACCGACAGAGGTTAGTCTAGAAGAAG
Long Flanking Sequence:
CGCATACCTGTCAATCAGATCTCCCCTTACAAAGGTACAGTTTGTCTGAGAGCTGTTCATAATTCACAGTAATCTAAAAGAAATAGCATGACGTGTGTTACTTGTGCAGGTGTGATCAAGAAAAACTGTACCTACATGAGCACCTGGCAGAGCTACAAGTGCTTTGGGCTTAATTACAAGATGCTGGTCATCGAGAGTCTGGACGCTGACACTGAAACCAGGCGTCTTTCACCTGTAGCCATCCTGGGGGACAAATATGTGGATTTGATCAATGGTATGACTCTTAACTCCCTATTAAACCTATTGTCTTATGCATAATTTTGTGTGTGTTGTGCATTAATGCATTTTAAAATCCTACTTTGAATTTTTGATTACAGGCCCACAAGATCACGGCTGGTGCGCTGGCTACACGTGCCAGAAGCGTGTTTCTCTCTTTCATGCCATTGTTGCCACCAGTAAATCCTTTGACATCTATTTCACCAGCACAACACCACAGAACT[T/A]AAGACTTATGTTACTGAATGCTGGACCGACAGAGGTTAGTCTAGAAGAAGATTTATACTGACATTATACTGAAACAGCATGCCCAAGTTTAATTTTAATTATTTGGTTTTATTCTTAAGTATAATTTCAGTATGTGTCCATTGTGCCTTGCATTATTTCATCAAATACCTACACTGCAATAAATGTGGATGCAAACCTGCAATTATATATATATATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTATTTATTTTTATTTTTATTTTTTTTAATACATGATTTTAGTTTAAGCCTTCAAAGTATTAAACTAGATGTTTGACTCTACTTTAATGTTTTTTTTGTCCAGGCTGTCAGAGTGGCTGTATTTTACTCAAACCCTCAGCGGTTAGATGTATATGTTAACAATAGTTTGGTTGGTCCAACAAATGCTCAGTGGAATGCGGGAAACACTGATTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6556
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127517 Nonsense 3807 4196 70 77
ENSDART00000130472 Nonsense 2754 3172 43 48
Genomic Location (Zv9):
Chromosome 19 (position 23400606)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 23330021
GRCz11 19 22914344
KASP Assay ID:
554-4436.1 (used for ordering genotyping assays)
KASP Sequence:
CTTTGACATCTATTTCACCAGCACAACACCACAGAACTTAAGACTTATGT[T/A]ACTGAATGCTGGACCGACAGAGGTTAGTCTAGAAGAAGATTTATACTGAC
Long Flanking Sequence:
AATCAGATCTCCCCTTACAAAGGTACAGTTTGTCTGAGAGCTGTTCATAATTCACAGTAATCTAAAAGAAATAGCATGACGTGTGTTACTTGTGCAGGTGTGATCAAGAAAAACTGTACCTACATGAGCACCTGGCAGAGCTACAAGTGCTTTGGGCTTAATTACAAGATGCTGGTCATCGAGAGTCTGGACGCTGACACTGAAACCAGGCGTCTTTCACCTGTAGCCATCCTGGGGGACAAATATGTGGATTTGATCAATGGTATGACTCTTAACTCCCTATTAAACCTATTGTCTTATGCATAATTTTGTGTGTGTTGTGCATTAATGCATTTTAAAATCCTACTTTGAATTTTTGATTACAGGCCCACAAGATCACGGCTGGTGCGCTGGCTACACGTGCCAGAAGCGTGTTTCTCTCTTTCATGCCATTGTTGCCACCAGTAAATCCTTTGACATCTATTTCACCAGCACAACACCACAGAACTTAAGACTTATGT[T/A]ACTGAATGCTGGACCGACAGAGGTTAGTCTAGAAGAAGATTTATACTGACATTATACTGAAACAGCATGCCCAAGTTTAATTTTAATTATTTGGTTTTATTCTTAAGTATAATTTCAGTATGTGTCCATTGTGCCTTGCATTATTTCATCAAATACCTACACTGCAATAAATGTGGATGCAAACCTGCAATTATATATATATATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTATTTATTTTTATTTTTATTTTTTTTAATACATGATTTTAGTTTAAGCCTTCAAAGTATTAAACTAGATGTTTGACTCTACTTTAATGTTTTTTTTGTCCAGGCTGTCAGAGTGGCTGTATTTTACTCAAACCCTCAGCGGTTAGATGTATATGTTAACAATAGTTTGGTTGGTCCAACAAATGCTCAGTGGAATGCGGGAAACACTGATTACACGCTGCTCGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15346
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127517 Nonsense 4023 4196 73 77
ENSDART00000130472 Nonsense 2970 3172 46 48
Genomic Location (Zv9):
Chromosome 19 (position 23401807)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 23331222
GRCz11 19 22915545
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCATCCATGGGTATCATTCCTCCTCCACCCTCATCCASTGACCCAGCCT[G/A]GAATAATGTAAGAYGTTAATCYACTTGTTTTATTTGAACAATATATAKCC
Long Flanking Sequence:
TACAAATCCGCACCTCCCCAGTTCTGTTTGTGGCCTTCAACCTCCCGGCTATGACTGAGGCGGAATTCTTTGGCGCAAATTTAATCAACAATCTTGCTGCATTCCTAAAAATTCCTTCGTACAAAATCCGAATCACCAACATAATCCGTGAAGGAACTAATGCTAGACGACGGCGCTCGACAGGACTGACAGTGGAGGTGGAGATCAGGGAGCCGCCGACTCAGACGACCACCAACAGCACCACAGGTGACAACAGACAGCTATATTGCATTTAAACAAAAAATGATTAATACACAACAGCATTTAAATCACATCATATTGACCGAAATTGTATATTAATATTCTTTCTTTAGATAACACCCAACAGTTTGATGTCCTGAAGAACATTGCTGATGATCTGGGCCGTGCTGCTGTATCCGGAAATCTGAGTCAGTCCATCGGCTTCAATGTGTCATCCATGGGTATCATTCCTCCTCCACCCTCATCCAGTGACCCAGCCT[G/A]GAATAATGTAAGACGTTAATCTACTTGTTTTATTTGAACAATATATATCCTTAGGGTATCTTAGTGTTTTATATACATGTACACTTCAAATAAGAGTCAAATATGTAGAAATGCAATAGTTTGGATAAAAGAATGAAACATTTAAAATGTAATTTGTAAAATGAACCCAATGGTTTGGTTTGTCCATATATCTTCAGTAATATACCTCATATAGACATCTGTGTTTAATATGTTATATATAAATAAAAGCAAAATAAAAATAAATAAAAATAAAAGCAAAAGCTTGTAAACATAATTTAATGCAGAAACTACAAACATTAAGCACGGGTCACATTATCAAAGAAGGTGAGATGAATCAGGGAACAATCATAACACAACATAACTGATACACTCTAAAAATACTGGGTTGTTGTTACCCAGCGTTGGATCGAATATGGACACATGCATCCACTGGGTTAAAAAGTTTAATTTATATGTTATTGAAAAAAAGTTAACTCAAT
Associated Phenotype:
Not determined