Busch Lab

ZMP

si:ch211-270n8.2

Ensembl ID:
ENSDARG00000077188
ZFIN ID:
ZDB-GENE-081028-60
Description:
Novel protein similar to vertebrate attractin (ATRN) [Source:UniProtKB/TrEMBL;Acc:B7ZDE5]
Human Orthologue:
ATRNL1
Human Description:
attractin-like 1 [Source:HGNC Symbol;Acc:29063]
Mouse Orthologue:
Atrnl1
Mouse Description:
attractin like 1 Gene [Source:MGI Symbol;Acc:MGI:2147749]

Alleles

There are 12 alleles of this gene:

Allele Name Consequence Status Availability
sa14748 Essential Splice Site Available for shipment Available now
sa10964 Nonsense Available for shipment Available now
sa22271 Nonsense Available for shipment Available now
sa12259 Nonsense Available for shipment Available now
sa12330 Nonsense Available for shipment Available now
sa42177 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa22272 Nonsense Available for shipment Available now
sa17103 Essential Splice Site Available for shipment Available now
sa10875 Nonsense Available for shipment Available now
sa12385 Nonsense Available for shipment Available now
sa42178 Nonsense Mutation detected in F1 DNA Not yet available
sa14797 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa14748
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089533 Essential Splice Site 144 1400 4 30
ENSDART00000147217 None None 812 None 19
Genomic Location (Zv9):
Chromosome 13 (position 20092320)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 19832673
GRCz11 13 19963655
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTTACCACCGTATGTAAAAAGGGCCTGTGTGTTGTTTTCTTGCATGTCT[A/C]GTGGCCTGGTTGTCCCAGAAACGAAAGGAAATGAAACCATCCCAGAAGTT
Long Flanking Sequence:
ATTTTACTGTGTACTGGGATATAATGTTTATTTTACAATAAAAACTAAGTGTAGCATGTCTTGCTGGCATTTAAAACATAACACACCAGAGCTGTAGTGTATGCAGTTTGTAAACTTACTGGGAGGTGTTGGTCAATAGTCATACTGCGCACCACGTTATTGAACTGTATCAATTGGCAATTCCTGCAAAACTGAAAGCGAAAGTATTATACGCACACATTTATACGCTATTTAAAAGCAGAAAAAAGAGGAAAACAGGAACCCCCCACCCCCATGGTGATTCTGGTATTACTGGTGTTGTCACATGTCGATTAACCGGGAAATTTGCTCATCCCTAGCGTTAAGCTCTCTCAGCCACCGTACAAAATTGTACAAGCACATAATATTTCAGTCACATTTACAAGTGTATTAAGGGATTTCACATATAAACAACAGACTGACAAAACTGTATCTTACCACCGTATGTAAAAAGGGCCTGTGTGTTGTTTTCTTGCATGTCT[A/C]GTGGCCTGGTTGTCCCAGAAACGAAAGGAAATGAAACCATCCCAGAAGTTGTGACCACATCTGGGTACGCATTGTTGCACTTTTTCAGTGACGCTGCCTACAATCTCACAGGATTCAACATCTTTTATTCGTGAGTACTGCTAGATGGTATATGGTATTATTTGTGAGGATTGTACATGTGTATATGTGTAAATACATACAGTGCGGGAAATAAGTATTGAACATGTCATGTTTTTTTTCCTGGGAATATTATTTCTAAAGGAGCTGTTGACATGCAGTTCATCCAGATTTTGGTAAAAACCCAAACGATACAAATGTAAAAATAGAAGAAAACAAAAATCTGAAAAATGAGTTATATGTAATAACAATGGATTTACACAAGGAGAAAGTACTGATGCACTGCAATGTGTCATCATTACATCATTGTCTAGCTGAAATGTCCACCCTGGATTCATCTTAATCTTCCTGGAAATGTAGATGTTGGGCTGAAGCAGCTAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10964
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089533 Nonsense 260 1400 6 30
ENSDART00000147217 None None 812 None 19
Genomic Location (Zv9):
Chromosome 13 (position 20096573)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 19836926
GRCz11 13 19967908
KASP Assay ID:
2260-6276.1 (used for ordering genotyping assays)
KASP Sequence:
AAAGTTTAGTCTCTCATCTGACATTTCTTTYCCATCTCAGGTCCCGACTG[C/A]TCTTTAAAGGTTCCTTCGGCTGAGTCCTACTGGTTCCWGCCTAATGTRAA
Long Flanking Sequence:
TTTTTTGTTGCTCTGTTATAATATTTGCTTGCAATTTGTTTATTATTTTGTATACATAATTCACGTCCTTACAAAAGTCACCCTAATCGAGTTCTTTTCAAATAGATCTATTCAAGCTATCTGGTGAAATTGTATTCATATCACAATATATATCGCAGAGAAACAAACTATCGCAATATCAGATTTTTCCAACGTCGTGCAGGCCTAATTTAATGTGTTTATGACAATGTTTTTTTTTTTTTTAATCAAAATGTTAACATTGTGTTTACTACATATTTTAATTTTTAAAAATGTTTATTGGACAAAAGAGACAGATTAAGTGTGTGGAAATGTGTTTTCTTTTTTTTTGTGATCTAATAAACCAAAATCATGTGTATTATGTAAACAGGGCCACTTTGACTTATTAGTGAGTGTATCACTTTCATGCAGGTCCTGTGAACATACTTCTCTAAAGTTTAGTCTCTCATCTGACATTTCTTTTCCATCTCAGGTCCCGACTG[C/A]TCTTTAAAGGTTCCTTCGGCTGAGTCCTACTGGTTCCTGCCTAATGTGAAGCCTGATGGCCAGTCACTTGGTCGGGCTTCCCATAAAGCAGTGGTTCATGGGAAGCTGATGTGGGTTATTGGAGGCTTTACCTTCAATTACAGCTCCTTTCAGATGGTTATGAAGTAGGTTACACGCTGGTGATATCATAAGCAGTTTTTTGGTAATATGCAGATGTTATCTTCCACTGCTTATTTTTTCTGTGGTTTTGTAGTTATAATCTAGAGAGCAGCACATGGGATGTAGTGCCAATCAATGGTGGACCCCTACAGCGCTATGGACATTCTCTTGCTCTTCACAAAGTAAGCATGGTCTATTTGTATATCAATGCTGTGAGTGTTTCGACAGACTGTCTTGTGGCTGATATGCTAAATAAGGGATTTACAATTGAGAAGATGCCTCCCTGGTCAATTGTCCATAATGCTACAGGTTTAGCTTCTTATGCTGAGTTTTATATATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22271
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089533 Nonsense 268 1400 6 30
ENSDART00000147217 None None 812 None 19
Genomic Location (Zv9):
Chromosome 13 (position 20096595)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 19836948
GRCz11 13 19967930
KASP Assay ID:
2260-6277.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTCTTTTCCATCTCAGGTCCCGACTGCTCTTTAAAGGTTCCTTCGGCT[G/T]AGTCCTACTGGTTCCTGCCTAATGTGAAGCCTGATGGCCAGTCACTTGGT
Long Flanking Sequence:
ATTTGCTTGCAATTTGTTTATTATTTTGTATACATAATTCACGTCCTTACAAAAGTCACCCTAATCGAGTTCTTTTCAAATAGATCTATTCAAGCTATCTGGTGAAATTGTATTCATATCACAATATATATCGCAGAGAAACAAACTATCGCAATATCAGATTTTTCCAACGTCGTGCAGGCCTAATTTAATGTGTTTATGACAATGTTTTTTTTTTTTTTAATCAAAATGTTAACATTGTGTTTACTACATATTTTAATTTTTAAAAATGTTTATTGGACAAAAGAGACAGATTAAGTGTGTGGAAATGTGTTTTCTTTTTTTTTGTGATCTAATAAACCAAAATCATGTGTATTATGTAAACAGGGCCACTTTGACTTATTAGTGAGTGTATCACTTTCATGCAGGTCCTGTGAACATACTTCTCTAAAGTTTAGTCTCTCATCTGACATTTCTTTTCCATCTCAGGTCCCGACTGCTCTTTAAAGGTTCCTTCGGCT[G/T]AGTCCTACTGGTTCCTGCCTAATGTGAAGCCTGATGGCCAGTCACTTGGTCGGGCTTCCCATAAAGCAGTGGTTCATGGGAAGCTGATGTGGGTTATTGGAGGCTTTACCTTCAATTACAGCTCCTTTCAGATGGTTATGAAGTAGGTTACACGCTGGTGATATCATAAGCAGTTTTTTGGTAATATGCAGATGTTATCTTCCACTGCTTATTTTTTCTGTGGTTTTGTAGTTATAATCTAGAGAGCAGCACATGGGATGTAGTGCCAATCAATGGTGGACCCCTACAGCGCTATGGACATTCTCTTGCTCTTCACAAAGTAAGCATGGTCTATTTGTATATCAATGCTGTGAGTGTTTCGACAGACTGTCTTGTGGCTGATATGCTAAATAAGGGATTTACAATTGAGAAGATGCCTCCCTGGTCAATTGTCCATAATGCTACAGGTTTAGCTTCTTATGCTGAGTTTTATATATTTCATCATTGAATGTTTGTGTTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12259
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089533 Nonsense 540 1400 10 30
ENSDART00000147217 None None 812 None 19
Genomic Location (Zv9):
Chromosome 13 (position 20109435)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 19849788
GRCz11 13 19980770
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTCGCTCAGTAACGGGGCCAAATGTTTCTCCTCCGACTTCCTCTCCTA[T/G]GACATCGGTATGGACCACCTGTGACCTTCTTCTCTTATTACAGTAGCATT
Long Flanking Sequence:
AGGTTTAGTCACATTAACATCTGATTTTTTTTCAAGTACAGAATTAAAATGATTTAGTTGACATCACTTTACGGCTTGTGAAACTTAAATAAATGTGATATGACTGACTTATTTTTGTAACACAATAGAAGTTGAGGATTTTGTGTGCACGAGTGCTTCATACATACAGTGCATGGGTTTCTTCATGTGGATAAAAGTCTCTGTGGTGCCACATTACTGATGGCGTCCGTCTGCGTATCTGACCTAGCCTGTGGAGAGTGACCTTCAGACCAACTGTTCCATCCCATAAGCTAAACGCTCGCGCACACGCTGCATTACAATAGCCAATGAGATGTGTGTTTGCTTCTCCCCAGGTTTATTCTGAAGGAAAGTGGTCTGGCACGATACCTCCACTCCGCTGTGCTGATCAGTGGAGTTCTGCTGGTGTTTGGTGGAAACACTCATAACGACACCTCGCTCAGTAACGGGGCCAAATGTTTCTCCTCCGACTTCCTCTCCTA[T/G]GACATCGGTATGGACCACCTGTGACCTTCTTCTCTTATTACAGTAGCATTACTTTAAAGATGAAATGTGGAATAGCAATATCCAGTCTGAAATCAATAATAGTGCCTGTGTTTGGAAACATTTGGATTTAGCTCCTAATGAAGCTTTAAAATGTACACTTCCACCACACTTTGAATTAATTTGCCATATGATTTATGACTCTTGAATATGAATGGGTCCTGCGACGTATTGTGAGAAACAGAATGCATGCTCAGTCAGCGGTACAGTTACTGTAAATTGTTTCGTTGGAGCTGCTGCAGTGTGATGTTACTGACAGTTCATTACAGGAAGCTGATAAGCCAGTGGAGATCTACTGGAATGCATATATGAGTCATAATGGATTTTCCCAGAATATGCCGACATATGCAAGCGAGACACACACACAGGATGCGATACTGCATGTGTGGTGTCTGTAATCAGATCTTTGGTGCTCTCCCCGTGGAAGACCTCCCGGTGCACAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12330
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089533 Nonsense 745 1400 15 30
ENSDART00000147217 Nonsense 164 812 4 19
Genomic Location (Zv9):
Chromosome 13 (position 20151595)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 19891631
GRCz11 13 20022613
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCATTCGAAGTGAGCAGGTCTGTAGCAAACTGGTSAACTGCAGGAGTTG[T/A]TCGCTTAACATTAACTGCCAGTGGGAGCCACAACAGCAGGAATGTCATGC
Long Flanking Sequence:
ATGGCTAAGACTGCCTGCATTTAAAAATCATGAAATGTAGTGGGGACACAAAGAAATTTAAAAAGTCGAAGGGACGTGTTCCAGTGGAAGTGATGCCCCAAGCTGATGATCATAAGAATATATTAAATATATACAAATTTTCCTAATGCCTTCTTATGTTTTGTCTATATTCAGCTTACAGTTGAGCTTGCTCGCCACCCTCGTGGTCCGCTGTACCTCAATCCTCCCCCTGCTATGTTGTCTGAACACCAGCTCTCTATTTGGAAACCCGGTGTGCGCAAAAACGGCCAGGTATGAAGCTTATGAATTGACTAATTGGCTTAAACATGTTGCACCTGTAACCACTTAGTTCCACCTAAAACTTTCTTGTCCACATTCAAATTTGTAGACAGAGTACTGAAAGTTTTTCTTTATCTTGTTTTTCAGTCTATCAAGAACCATACCAAATGTAGCATTCGAAGTGAGCAGGTCTGTAGCAAACTGGTGAACTGCAGGAGTTG[T/A]TCGCTTAACATTAACTGCCAGTGGGAGCCACAACAGCAGGAATGTCATGCTTTACCTGGTGAGTTAAAGTATGGAGATTGCATTGCATTGTTTTGATTAAGCGTCATTGAATCTTTATTTTAAAAACAACAACATTTGTGCTATTGTTTGCCCTGTTCTACACTTAATTCTGGGGTCAGTATTTTTGTTTTGTTTGTTGTGTCTTTCACTGCATTTTTGGGAAGAATAAAGATTCAGCACTGACTTCATAACATAAATTTAATTAAAAAAATGCATACATATTAAGTTAGATTGCTATTTAAATGTATATTCCTCTATTTTTATTTTGTACTTTTGAAGCAGCCCTTTAAGCATAACAGATCGAACGCTGAAAATTAAATCTCACTGACATCAAACTTTTGAACAACAGTATAAATGCCATTAAAGTGTATAGTTGACTTTTTGATCATGCTGTGCTCTGGAAAGATCACAGGAAAGTTTCTATTTTTAGGGCTTCCTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42177
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089533 Essential Splice Site 827 1400 16 30
ENSDART00000147217 Essential Splice Site 246 812 5 19
Genomic Location (Zv9):
Chromosome 13 (position 20157250)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 19897286
GRCz11 13 20028268
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGGAGTTCATCCTGGAGGAGCTGCAGAAGTATCAGCTGCAGGAGCGG[G/A]TGAGTTCAGCTCAAATACTGACGTAGATTTGTCTTGATACGTGATTTGGT
Long Flanking Sequence:
AATTCATAAAAGGTTAAAGTGGGAGTAGGGTGGACAGTACAGCTTTAGTAAGCTGAAGTCATTCAATATAAAGTACTTTTTCAAAAAGGTGATATCTATACTATATCTTTGTAAAACTGTGTGTGTTTATAAGTAAGTATCTGGTGCAAACAGAAAGGAAAGAGTACCTTTCCTACAGGTGTTTTTCAAGCTGATTCACCTATGTGGAGCACACTCAGAATTTTCAGTGTTTTCAACATTTTCCAATATTTTGTGGGAGTAAGGCCTAGTTTGGACTGAAGCTTTATACTGAATTTCTCTGTTTCTTTTCAGCTCATTTGTGCGGTGAGGACTGGAGTCAGGTTGGAGATGTGTGTCTGAGGCTGAACGCCAGCAAGGAGAGTTATGATAACGCCCAGCACTACTGTAAGAACCTGGAGGGCAGCATCGCCTCTCTGACATCAGCCAGACAGGTGGAGTTCATCCTGGAGGAGCTGCAGAAGTATCAGCTGCAGGAGCGG[G/A]TGAGTTCAGCTCAAATACTGACGTAGATTTGTCTTGATACGTGATTTGGTGTATATCTAGAACACAACCAATGGTTAAGATTTTCTAGATTTGTTTCAAACTGGTCATAGCTGCTTCTATTGAGAACAGGCTGCATTTTGATATAAGCTATAGCAATCGTCATTGTTAAAAAAAAAATAATAATAATTTTTAGAATGCATGCATGGACAGGAAGTACAATGCATTTTAATTTTGTGTGCAGTTTGCCTAGACCAGGGATGGGCAAACTTGATCCTCGAGGGCCGGTGTCCCTGCAGAGTTTTTTTTTCCAACACTAGTCAAACACACCTGCACAAGTTAATCAGTGTCTTCAAGATCACTTGAACTCTATAGGGAGGTCTTTTTGAATAGGGTTGGAGCTAAACTATGCAGGACACTGGCCCTCCAGGATCAAGTTTGCCCACACCTGGCCTAGACTGAGGCCACAAAATAATATATTGAGCTCACAATATTTTTTAAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22272
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
ENSDART00000089533 Nonsense 909 1400 18 30
ENSDART00000147217 Nonsense 328 812 7 19
Genomic Location (Zv9):
Chromosome 13 (position 20167476)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 19907512
GRCz11 13 20038494
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCATTTTCCTCCCCCTAGTGAGTCCAAACCTTAGCGTGCGTCCATGT[A/T]AGATGCCCTGTGCCCTGCGAACCACCTGCGCCAACTGCACCAGCCAGGCC
Long Flanking Sequence:
TAAAACCAATAAACAAATAATAGTTTACATTGCCAACAAACTACACAAAATAAGATTTCAAATACCTAAATTGAAATCAAGATAGAAGTTATTAATAATACTCAAATAGATCAAAACTGAAAATAGAAATATAAAACCTTTAAAAATAAAATGTATGAAAAAACCTAAAGCACCTTAATAATATATTACACACAAATGTTTAAAATAAGCTAAAAATAACATAAAAGCTTTTTATACTAATTATATACACTTGTATGATTTAAATGTAGTGTTTATTTTGGCTGTTTAAGATTTTGAATAGTTTTTTATAATTTGCATTTGTAATTTTTATTTGTGGACTTTTCTGTGTATTATCAGGAACTTGTTGTGTATTTAGTTCACAGTTGTCTATATAACAGATTTAATGTTTCAAATGATGTAACTTGCTTTGGGGTCATTGCAATACTGACTACTGCATTTTCCTCCCCCTAGTGAGTCCAAACCTTAGCGTGCGTCCATGT[A/T]AGATGCCCTGTGCCCTGCGAACCACCTGCGCCAACTGCACCAGCCAGGCCATGGAGTGCATGTGGTGCAGCAGCACTAAACGCTGTGTGGATTCCAACGCGTATGTGATCTCCTTCCCCTACGGCCAGTGTCTGGAGTGGCAGACTGGAGACTGTGGAGGTGAGTCAACACTGGAACCATCAAGGACACTAGCACATTAAGATATATAGCAGACTAGAAGCTGGAGTTATGAGTGAACTGGTGAACACACACACTGGCACACATACACACAGAGCTTCTAACTCGTTTACTTTCCGCCTTCTCATTTTTCCCGTCTGTTGTGAGCCTAAGGGAGATTGAGTTCTGAGAGAGCAGATGCTGTGAGCGCTCAGCCTTCTGCACAGGCAGGTATCAAACTCACTATAAACTCCTGTCAACCCCTGACTGGCCTCCACCGGAAAATCTATAAACTATCGACGTCTTTCCGGCCTTGCACATGAGACTGCAAAGACAGAAAAAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17103
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089533 Essential Splice Site 1081 1400 20 30
ENSDART00000147217 Essential Splice Site 500 812 9 19
Genomic Location (Zv9):
Chromosome 13 (position 20184299)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 19924335
GRCz11 13 20055317
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTACCTGGTTATTATGGAGRCCCCACTAATGGAGGGAAATGCCAAGG[T/A]AAGATRTTTGTCTTTGTATGTKCAAGGGTTTGTCCCYTTGTCTGTRTGTG
Long Flanking Sequence:
GACACCAAACATGACAAAGTTATATGAAAGAACATCACGAGCAGATGAATCGTGTATGGGGAAAAGCACATGGTTACTGTAAGCAAATGGCAGAGATGTGTATTGGATCTGTGATAAACTCTGCCATGCCAGTAGGACCCATCCCATGCTTAGAATGTCCCCATAGTCCTTCATTACCATTAAAGGAATAGAATATACAACTTTCTCAGCTTACAAAAGTTTTTGTTCAGTGCTTTGGTTATTTAATTAAACTGTCTACTATCATGGTATATTAATTACCTCATTTCTAAAATGATTCAATCACTGATCAAAACCTTTACAAATTATTAATAGTCTAATCTCCTCACATTCTATTTTTCAGCATGCCAGTGTAATGGACACAGTACGTGTGTTAATGGCAGCGTATGTGAGCAGTGCAAGAATCTTACAGCTGGGCTGCATTGCCAGTTCTGTTTACCTGGTTATTATGGAGACCCCACTAATGGAGGGAAATGCCAAGG[T/A]AAGATGTTTGTCTTTGTATGTTCAAGGGTTTGTCCCTTTGTCTGTGTGTGCTTGCTTGAATCAGCATTTTAAAAAATCAGTGAGTAGGTTTCTTGAAAGATTGGTTTGTGTACACAAGATTTTGTCCTCATCTGCTCATTCTTCCAAGCATGCATGATTTTGTCCCTCTGTGGAACACAACAGATATGTTTATCAGATAATCCTGATGTCACTTCACATACATTGGAAGTGGATGGTAAACAGGGATCCTGCAGAGCATTCTAAGCAATATATGAGAGAATAGTGTGAAGATAAAAAAAAAAAAGATTACTGGACTTCGTTACATGACTCAACATGAGGAGTAAAGTGATTTGATCTGATTTTGTTAAAGTGTATAACATATTAAACATATAAACATATGTAAACACAAATATATTGGTTATGGTTATCTGGCACTGAGACATGCAAACAAATTATATTGGTCTAATATAAAATAGTAATATAAAAATGTATTAAATTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10875
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089533 Nonsense 1091 1400 21 30
ENSDART00000147217 Nonsense 510 812 10 19
Genomic Location (Zv9):
Chromosome 13 (position 20208670)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 19948706
GRCz11 13 20079688
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTMTGTCTTYTCCTCAGCCTGCAGATGTAACAACCATGCCAAYGTCTG[C/A]CACTCCAGCTCAGGGAAATGCTACTGTACCACTAAAGGGGTCAAAGGAGA
Long Flanking Sequence:
AGTTGCCTACTCAGACTTTCGCTGCACCAGCAGTGTTTATTTCTGCCTCATAAATGCATTATATTTCTGTAAATGTTATCTCTTAATCTTCAACAGGGAAATGAATTGCTGGCTGTCTCACATGTGCATGTGTCACACTTTCAAGTGCATATGATCCAGAGTTAAACACAAACTTTGTGATAAACTCTGAGCTAACAGAGACAGTTTCTAGCAAGCTTTGTGAAACCCTGTAACCTGGTTTTAACCAGTTTGGAGATGCTGGTTTTGTAAACCCAGAGTTTGTTTAGCTCATTTTGTGGAACAGGCCTCAGTTGGGAATCAAAAGTTTATATTAATGAGTTTACATTAACAGTGATGACAATAGCATTTCAGTTTTGAAACAACATGCGTTTGAATAATTGTCTACAGAATTTATTTTGGAGTGAACTATTTTTTTAACACACTTCTTCCCTTTCTGTCTTTTCCTCAGCCTGCAGATGTAACAACCATGCCAACGTCTG[C/A]CACTCCAGCTCAGGGAAATGCTACTGTACCACTAAAGGGGTCAAAGGAGACCAGTGCCAGCTGTGAGTATCTCTGCATAACCTATCATCTTCCCTGCATTCTGTCATTCAGAGAGTGAGTGACACACACACACACACACACACACACACAGACACACACACACACACACACACACACACACGCACACACACACACACACACACACACAAACCCTTCAACTAAACACAACGGTGCTCTCATTAGCATCATAGCACATGTTTAACCCTCTCATAATGTTCTCTGGTATTAATTCCCACCTAAGTGTCTTTCTAATCCCAGGACATTAATTTTAATGGCAACCTCTGCTGTGCTGTGTCAGCAAGCCCCCTGTTCATAGTGGCTAAGGGAACTTATCAGTGGCTTAAATAGCACTTTTGGGGCTGACACTGTGCCCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12385
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089533 Nonsense 1137 1400 23 30
ENSDART00000147217 Nonsense 556 812 12 19
Genomic Location (Zv9):
Chromosome 13 (position 20247009)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 19987045
GRCz11 13 20118027
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAATCTGTGTTTTTCCTTTCACTTCACTAGATAATCTACTGATAGACTAC[C/T]AGTTCACCTTCAGTCTGCTTCWGGAAGACGATCAGCACTACACTGGTAKT
Long Flanking Sequence:
CTAAAAGGTCATAAATGATAACTAGAATCCAGCAAACGCCTCTTTTTTTTACTTTTTTTTGTCCAATATTGTCAATGACAGTTCAGTGTTTTCTTTCTTCGGCAGAGTTGATATTAATTTTGACCTGCTGGACAATCAAATCAATCCTCTGCCTTCCTCTGTCTGTTGCTATTTAATCATATGCCGTCTTCACAATTGAATTGGACAAGGTGACCTTTAGTTGCTCGTGCAGATGTGAGCTGTCAAAAAGTCCTTCATATCATATCAAATGCTTCTCTCTAAACCAGACTTTGTGTTTGACTTTGAGGGAAAGCTGTGATTGCCATGATATTTTGATTTAAGCAAGATGTGAACATGAAGACTTGTTCCAAGCAGTCACCTTAACATGTTAGCTAAACTCAAGATGTTTATGCTGAAATTGTTTGACTTACAAATTCTAAATACTTTTTAAAATCTGTGTTTTTCCTTTCACTTCACTAGATAATCTACTGATAGACTAC[C/T]AGTTCACCTTCAGTCTGCTTCAGGAAGACGATCAGCACTACACTGGTATTAACTTCATGGCAAATCCAGAAGAGGTCAGTGCCTTTACAGAGAATTAAGAAACAAGCTTTTTAACTATTTGTATTTTATTTTGAAGTGTACTCCAAATAACATCTTTGTAACAACAGCATTTGTGTCCTAAAAAGACACAATGACAAGATGTTTTTTTTTTTTTTTTTTGAGCACAATGGATGCTAAAGTAATATGTGACAACATAATTACAGCCATTCATTTGATAGTTACTGCACTTTACCTTTTAATTAGGAAACTAAAATGTGTTAAGCTTGTAATCAAAATTGACGTCGGATGAATGGACATACAGATTGATGGATGTATGTATTGATGGACTGATGCACAGATGGACGGATGATGGATGAATGGATGGATGGATGGTTGGAAAGACAGATTGTTGAATGGTTGGACTAATGCACAGATGGATGGATGAATGGACTGATGCACAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42178
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
ENSDART00000089533 Nonsense 1277 1400 27 30
ENSDART00000147217 Nonsense 689 812 16 19
Genomic Location (Zv9):
Chromosome 13 (position 20307386)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 20047422
GRCz11 13 20178404
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGCTGTTTCCTGTCCCTGCTGTTGGTTGCGGCTGTGGTTTGGAAAGTC[A/T]AACAGACGTGCTGGGCATCACGCAGGAGAGAGGTAACATCTGCACAACAT
Long Flanking Sequence:
TGTCATCATGTTGTGTGAATTCTGCCAATGGTAAAAAAAAAAAAAAAAAAAAAAAACACAAAGAGGAATGCTGCTTTTTATTTGTGCATTTAAAATTACTAGCCCTTCTCAAGGCCAGCATTTTTTTTTAATATGATCAAACATCTCCCGTCTTTCCAAAAATAGACGTTGTGCAGTCTATGGCTTTAGAGAGAAAATCAGCCCTGTTCACTGCACCGGCTGGCATTGCGTATAGAGTATGATTGACACAACTGTCAGTTCCATAAGGCATTGATTCTTTCATGCTGGATGAACTTGTTTATTATTGATTGTGGGATTTGAAATACAAATATGAAACAGCTGTCCTCAGTCTAGCCTCTGAGGTTAGTGGAATGTTTTCCACGATTGCGATTACAGACTCATGAATTTGATTTGATTGACTGATCTATTGATTTTCTGTGCGTTTTGTCTCCAGCTGTTTCCTGTCCCTGCTGTTGGTTGCGGCTGTGGTTTGGAAAGTC[A/T]AACAGACGTGCTGGGCATCACGCAGGAGAGAGGTAACATCTGCACAACATTGATGGGTCCAAACCTAAGTGCCAATTACATGTGGGTTCTTGTTAAAGTTGAAACGTTTAACACCAGAACCATCAGGGATCATTATACACCGAAAATTGTCAGCAAATAAAATTTACACATGCACTACTGTTTATGCCCAAAACATGTATTACATTGCTGCATTACACTGTGTCCTAACAACACATCACAAGATTCCCGTGACATGCAATTTGTCTTTCTGCACCAGACACGACATGACAGAAACATTTCAAGGTCTCGTGAAGTGCTTTGAAATGTGCATTTTTATTCTAAATTTGATGTACTGTAATCTCAATTGAAACATGAAGACAGGGTGAGAAATACAGTATCATAGCTTCTCTTTTTAATAAATATATAAAAAAACAGCCAATAGCGTTTTGTTTTTGAGAGTTTAAGTGCATCACATCAAAAGCAAATGAAAAGCGTCTTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14797
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089533 Essential Splice Site 1324 1400 29 30
ENSDART00000147217 Essential Splice Site 736 812 18 19
Genomic Location (Zv9):
Chromosome 13 (position 20456951)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 20196987
GRCz11 13 20327969
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGCAAGAAYCCCCTSTCTCACAGTGAGTTATTTGCTCTTCTTTTCTCTC[A/T]GGCTGGTCCCATAGCCGTGGAGCCATGTTCTGGGAATAGTGCTGCCGTGC
Long Flanking Sequence:
TTTGTATGTTGTCATCTACAGTACATATAAAACACTTCAATTCAAAAGATGTTATGCTTTCAAAAGAAGCATCTTACTAAGGCAAATTTTCTTTGATCAATATTATAAAATATGTTTACAGTTTGTAAATCAAAATGGCTTTATTTATTTGTTTTATTTATTATTATTATTATTATTATTATTTATTTATTTATATTTTATTTTTTTTTGTAATGGCAAAGGTGAATTTTGAACAACTTTAACTGTTCAACTTTTCAACAATTCCCCAAATGTTCTTTTTTGTCTGCCATGGATACCTGTAGGGCTTGTCTTGAACATCATAGATTCTGTGCTGATGAACACTTTTTATGTCTGATACTTTTTTTTTTTTTTCATTTTTATCATCATTAAGAAAAATTGTGCAGCTAAGAAATGTTTGCATTATTCACACACTTGTGTTAGTGTCGTGCATAGCAAGAATCCCCTGTCTCACAGTGAGTTATTTGCTCTTCTTTTCTCTC[A/T]GGCTGGTCCCATAGCCGTGGAGCCATGTTCTGGGAATAGTGCTGCCGTGCAAACATTGCTGATGAGTCTTCCACGAGCATCTTCTGGAGTGTCTCCCCCTGGCCAATGTGGTGAGATTTTAACATTCACTCTTAGCTTTGCTGTAGATTAAGATCATACACGTGCATCTTTAACATGTAGCTGTGTACTTGTTAATAATTTAGATTTATTTGGTTTATTTACATACCCACATGCTTATTTTCACTAAAGCATGAATCTCTAAAGTACAATTTTAAAACACATGTGCATTGAAGGTAATCACGTGCTGAGGAATTTGGCTTAATAAGTATGATTACTTATTAAATATAGATTTGGTAAGATCATTTTTAGATTTGGTATGTTTATTTATATGCTTAGATATTATTTATTTATTTTTTTACTTATGAAACAATCGTTTAAAATATTTTTTTGCAAAATCACTTGTACATTGGCTGGTATCAAAATCAAAAAAAATCTAATTG
Associated Phenotype:
Not determined