Busch Lab

ZMP

hecw2a

Ensembl ID:
ENSDARG00000062447
ZFIN ID:
ZDB-GENE-090311-22
Human Orthologue:
HECW2
Human Description:
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 [Source:HGNC Symbol;Acc:29853]
Mouse Orthologue:
Hecw2
Mouse Description:
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 Gene [Source:MGI Symbol;Acc:MGI:2685

Alleles

There are 14 alleles of this gene:

Allele Name Consequence Status Availability
sa614 Nonsense Available for shipment Available now
sa12065 Essential Splice Site Available for shipment Available now
sa34642 Nonsense Mutation detected in F1 DNA Not yet available
sa7184 Nonsense Mutation detected in F1 DNA Not yet available
sa38741 Essential Splice Site, Missense Mutation detected in F1 DNA Not yet available
sa41420 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa21490 Nonsense Available for shipment Available now
sa7630 Missense Mutation detected in F1 DNA Not yet available
sa21491 Nonsense Available for shipment Available now
sa34643 Nonsense Mutation detected in F1 DNA Not yet available
sa15103 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa614
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
ENSDART00000092240 None None 1263 None 25
ENSDART00000137756 Nonsense 106 1411 2 29
Genomic Location (Zv9):
Chromosome 9 (position 25196267)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 24352053
GRCz11 9 24162922
KASP Assay ID:
554-0524.1 (used for ordering genotyping assays)
KASP Sequence:
CAGATTTCTAASAGTGTTAATGCAATGTGCTTTTTATCAGATGAAACCTG[T/A]CCATCAAATGTGTGGGACTGTAAGAACCGTGGGGTAAACGGCACACAGTG
Long Flanking Sequence:
CGATGTTATTTGCAGAGCCACTGCAGATTTGTTATACATACTGTTGTAAAATTTGTCACTGTTATGTGGTGGTGCAATTTTTTATTCAGTCTTTTCAACTTGATTCTTGTGCTGCAGATTAACCACCAAAGTTCCATTAATCTTTATGATGAAAAAAATAATTTCATTACATTTTACAGTAAAATACTTGTAAATGTGCAGTTTTGGAAGTAAAAAAAGCAAGCAGATTTATAGTTTATAGTTACATCATTTCAGTTTCACATGTTGCTATGTTGATGTTCTGTATGACTCTGTGCACTTTATATTGTACAGTACTTAAGTCAGATAGGTTACTTGTGGTTATTTTTATTAACAGTGTTTTTTTTTTAAATTTTCCACCTGTTATAAAAAGGTTTTGCCCCATTGTAAAGTGTACTGGCAACAACAGTTGATGTGTTACTATACATTTGACAGATTTCTAAGAGTGTTAATGCAATGTGCTTTTTATCAGATGAAACCTG[T/A]CCATCAAATGTGTGGGACTGTAAGAACCGTGGGGTAAACGGCACACAGTGTGGTCAGATCGTCTGGAGATTAGAGGTCGGGCCATACTTTCTTGAATGTGAGTAACTGCAGCCTTCCAGTTTTATGTTATGAAATACTTAATGGAGCAGAAGGTTAGACAACAGTAGAGATCCTGACTTATGCTATAACATTCAGTTGTTTTATAATCTTGGCGCTAAGATTCATTGTGAAAGTTGAAGATTCTAAAAATGCTTATTTTTTTTAATGTTACAGTATATTCAATATAGTGCTGACTATACAGATATGCTGAGCAGATGAGTAATGCTGACACTTATCTGGTTCTCTCTTCTAGCTGAGACAAGGATCTGCTTTAAATACTACCATGGAGTAAGTGGAGCATTGAGAGCCACGACTCCCTGCATCACAGTCAAGAACCCCAGAGCCTCGGTCAGTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTGTGTGTGTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12065
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092240 Essential Splice Site 47 1263 1 25
ENSDART00000137756 Essential Splice Site 250 1411 5 29
Genomic Location (Zv9):
Chromosome 9 (position 25199030)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 24354816
GRCz11 9 24165685
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCGATCCGGCATTACAACTAACACCACTAATCCTGTTTGGCATGGAGAG[G/A]TGACACACACATAATGACACTTACAGCATACACTTACTCTCTTATTCAGA
Long Flanking Sequence:
ATATGCTGGAAAAGTTGGCGGCTTATTCTACTGTGGGGACCGCTGATGAATGAAGGGACTTAGCTGCAGGAAAATGATTGCATGAATGAATACATATAAATTACCACTCACAAAAATAAATGTTCTAGGTTGATGGCCAAGGAGAAGGACAACAAGCTTCAGACAGTAGTCGAAAACTGGTTAGCTTTACGCTATCAGGTAAATTTTACATGTGTAAGAGATAAAAATGATTTATGCTCTTCAAATAACTCTCAATGACTTCTACTAATATTATCCTACTCCACCGATTTATTTGAGCTGTTTTTATTACTAGATTGTTGTTTGTTTTAGATATCCGAGCTGTTGGCCTGAAGAAGGGGATGTTTTTTAACCCAGACCCTTATCTGAAGATGAGCATTCATCCAGGCAAAAGAAGCTGCTTTCCGACCTTTTCCCATCACGGCCAAGAGAGGCGATCCGGCATTACAACTAACACCACTAATCCTGTTTGGCATGGAGAG[G/A]TGACACACACATAATGACACTTACAGCATACACTTACTCTCTTATTCAGATAGTACAAATTGACTGAACTGATGAGATAAAAATGCTTCTCTCATTATTTTTCCTTGCAGAAACATACTTTTGTGGCTCTTATGACAGATGTATTAGTGATTGAGGTTAAAGACAAGTTTGCTAAAAGTCGACCCATTATTAAACGCTTCTTGGGTCAGCTGAATATTCCTGTGCAGCTGCTGCTGGAGAGACATTCGACAGGGTAAGCATGACACAAAACATACGATTTATGCAAACAGACATGATCCTTATCCTTCTTTCATGATTCATTTTCCATGCAACATAAACACAGATATTAGAAGATCAGTAATATACTACCCTTAAGACGTTACGGGTTAGCAAGCTATTTTTTGAAGGAATTATTCATTTTATTCTGTAAGACTGCATAAAACGCATTAAAGTAAATGTAAAATCATTGAATCATGAAAGATATACAAGTTTTTCAGATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34642
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092240 Nonsense 217 1263 4 25
ENSDART00000137756 Nonsense 420 1411 8 29
Genomic Location (Zv9):
Chromosome 9 (position 25200297)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 24356083
GRCz11 9 24166952
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCTCCAGACCTGCTCCAGGGGTCTTTCAGCGAGCAGCTTGATGCCATC[G/T]AGGCTCCTAAGGGCCCAGGTGACAGACCTCTAGGAGCAGCTTCTCCAAAA
Long Flanking Sequence:
TGAACAGTGTTATGTGTGTAACTGTGTGTGTTTTAATGGCTACAGGAACCAGTCACTCAGCTTCTCCCTATGTCGTCGTTTGCCCACTGATCATGTGAGTGGTCAAATGCACTTTAAAGTGGATGTCACGTCTATGGGCCCAGATGGTAAGCTCACATACATTTGTGCGCTTACTCAATGGCACTAATAACCACTGTTTTCCATTTATTTTAAGTTAACTCACCTCACCTCTCATAGATGTGTCTCCCGAGACAATTCTGGGGGCAGCAGCCCTCAATGGAGCTCCTGGAACCCCTTCAGATGACGAAGAGCTGCCTCATCCTCTACCCATCTCATCAGCAGGCCCTTCCCCAACAGCCTCCCTGGGGTCCAATAGAAATGGGGAGGGGAGCAGCATTCCCTCCCCCGACACAGAAATCTATGGTGGCACCCTGGACGACGAGGCCCCTTCTTCTCCAGACCTGCTCCAGGGGTCTTTCAGCGAGCAGCTTGATGCCATC[G/T]AGGCTCCTAAGGGCCCAGGTGACAGACCTCTAGGAGCAGCTTCTCCAAAACTCCGCTCCAGCTTTCCCACACATACGCGACTCAGTGCCATGCTGCACATCGACTCAGATGAAGATGAGGACAGATCTGCTGCTACAGAGGCCACGTTGTCAACATTTAACGGCATTCCAAGGTCTTATCAAACACCCCCAAAAGCAGCAGCAAGAGGAGCTGTGTTTGATGGAGGCATAGAGGAACCTTCAGAAGAGGCTGGGCTGGAGTCTGAAGTAGAAACTCTGAATGCAGGAGAAGAGGTGCCTCCTGAGCCAGAGGTCGTGCCCAGTTCAGTCGCTCCCGAGGTGGAAACCGCCAGTCTGATGGAGAGGCAGGAGGAACAGGGCCGGGAGGTGGAGGTAGAGGAGGAGGAGGAAGAGGGCCTGGCGCGCAGTGAAGAGTTGGCAACCGAAGTTGATATCTCCTCAATGGCATCTGACTGCTGCCCGGGGCCTGCATCAGCATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7184
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
ENSDART00000092240 Nonsense 276 1263 4 25
ENSDART00000137756 Nonsense 479 1411 8 29
Genomic Location (Zv9):
Chromosome 9 (position 25200476)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 24356262
GRCz11 9 24167131
KASP Assay ID:
554-5042.1 (used for ordering genotyping assays)
KASP Sequence:
GCTGCTACAGAGGCCACGTTGTCAACATTTAACGGCATTCCAAGGTCTTA[T/A]CAAACACCCCCAAAAGCAGCAGCAAGAGGAGCTGTGTTTGATGGAGGCRT
Long Flanking Sequence:
GGCACTAATAACCACTGTTTTCCATTTATTTTAAGTTAACTCACCTCACCTCTCATAGATGTGTCTCCCGAGACAATTCTGGGGGCAGCAGCCCTCAATGGAGCTCCTGGAACCCCTTCAGATGACGAAGAGCTGCCTCATCCTCTACCCATCTCATCAGCAGGCCCTTCCCCAACAGCCTCCCTGGGGTCCAATAGAAATGGGGAGGGGAGCAGCATTCCCTCCCCCGACACAGAAATCTATGGTGGCACCCTGGACGACGAGGCCCCTTCTTCTCCAGACCTGCTCCAGGGGTCTTTCAGCGAGCAGCTTGATGCCATCGAGGCTCCTAAGGGCCCAGGTGACAGACCTCTAGGAGCAGCTTCTCCAAAACTCCGCTCCAGCTTTCCCACACATACGCGACTCAGTGCCATGCTGCACATCGACTCAGATGAAGATGAGGACAGATCTGCTGCTACAGAGGCCACGTTGTCAACATTTAACGGCATTCCAAGGTCTTA[T/A]CAAACACCCCCAAAAGCAGCAGCAAGAGGAGCTGTGTTTGATGGAGGCATAGAGGAACCTTCAGAAGAGGCTGGGCTGGAGTCTGAAGTAGAAACTCTGAATGCAGGAGAAGAGGTGCCTCCTGAGCCAGAGGTCGTGCCCAGTTCAGTCGCTCCCGAGGTGGAAACCGCCAGTCTGATGGAGAGGCAGGAGGAACAGGGCCGGGAGGTGGAGGTAGAGGAGGAGGAGGAAGAGGGCCTGGCGCGCAGTGAAGAGTTGGCAACCGAAGTTGATATCTCCTCAATGGCATCTGACTGCTGCCCGGGGCCTGCATCAGCATCTCAGGTCAGAAGCAGATTTACTGAAGGGAAAATGTTTAATTCAAGGGACTTTTTAATTCGAAATATAAGAGTTTTCAAAGCCTTCTGCAAATGCATCCACTTCAAATGTTATCACTTGATTAAATGACCATTATCAGTGGTTATTAGCTGATAGATATGGGCCAATAGAGGCCTTTTGCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38741
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, Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092240 Missense 330 1263 4 25
ENSDART00000137756 Essential Splice Site 532 1411 8 29
Genomic Location (Zv9):
Chromosome 9 (position 25200636)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 24356422
GRCz11 9 24167291
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAGGTGCCTCCTGAGCCAGAGGTCGTGCCCAGTTCAGTCGCTCCCGAG[G/A]TGGAAACCGCCAGTCTGATGGAGAGGCAGGAGGAACAGGGCCGGGAGGTG
Long Flanking Sequence:
CAGGCCCTTCCCCAACAGCCTCCCTGGGGTCCAATAGAAATGGGGAGGGGAGCAGCATTCCCTCCCCCGACACAGAAATCTATGGTGGCACCCTGGACGACGAGGCCCCTTCTTCTCCAGACCTGCTCCAGGGGTCTTTCAGCGAGCAGCTTGATGCCATCGAGGCTCCTAAGGGCCCAGGTGACAGACCTCTAGGAGCAGCTTCTCCAAAACTCCGCTCCAGCTTTCCCACACATACGCGACTCAGTGCCATGCTGCACATCGACTCAGATGAAGATGAGGACAGATCTGCTGCTACAGAGGCCACGTTGTCAACATTTAACGGCATTCCAAGGTCTTATCAAACACCCCCAAAAGCAGCAGCAAGAGGAGCTGTGTTTGATGGAGGCATAGAGGAACCTTCAGAAGAGGCTGGGCTGGAGTCTGAAGTAGAAACTCTGAATGCAGGAGAAGAGGTGCCTCCTGAGCCAGAGGTCGTGCCCAGTTCAGTCGCTCCCGAG[G/A]TGGAAACCGCCAGTCTGATGGAGAGGCAGGAGGAACAGGGCCGGGAGGTGGAGGTAGAGGAGGAGGAGGAAGAGGGCCTGGCGCGCAGTGAAGAGTTGGCAACCGAAGTTGATATCTCCTCAATGGCATCTGACTGCTGCCCGGGGCCTGCATCAGCATCTCAGGTCAGAAGCAGATTTACTGAAGGGAAAATGTTTAATTCAAGGGACTTTTTAATTCGAAATATAAGAGTTTTCAAAGCCTTCTGCAAATGCATCCACTTCAAATGTTATCACTTGATTAAATGACCATTATCAGTGGTTATTAGCTGATAGATATGGGCCAATAGAGGCCTTTTGCGCTTACTGGTTGGCTCAGAGGGCTGTTATCATACATCCACATAGTTAATCAGCTATACTAATAGAGAAGACTCCAGATCTGTTTTTACATTACTGTGGCTGTTGGGTTTAGGATTGGGGACGTTAGGATTGGTAGACGTTATTAAAATGCTATTAATGGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41420
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
ENSDART00000092240 Essential Splice Site 491 1263 5 25
ENSDART00000137756 Essential Splice Site 639 1411 9 29
Genomic Location (Zv9):
Chromosome 9 (position 25202789)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 24358575
GRCz11 9 24169444
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAATCTGTGGACTCTGAGACTTTTGTTACGGAGACAGAGTCAGAATTAG[G/A]TATTCACACAGCCATTTATGTGTTAATCAAGTAGATTATGAAAATACACC
Long Flanking Sequence:
GCAGACAGATAGACTGAATGACAGATAGATAGATAGATAGATAGATAGATAGATAGATAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACGATGATAGATATAAAGAAAGAAAGAAAAAAAAGAAAGAAAAAAAGAAGGTAATCTGTCTTTGTGAACTTGGTCTTCACAGGAGGCGGAGCAGGGGGCAGAGGCAGCCATTGACCCAGGGGGAGAAGATCTCTCAGATGATCCACCTACCACTTACGAGGTTGCAGAGACTGCTGAAGAAACACATCTAACTAATGAGCCGGAGAGAGAGGCTCCAAAACCAGAGCCCCCCACCAACGAGGAAGAGGAATGTGAAGATGTGACTGAGGATACCATGTCCAGAAGATGGAGCCTGGAGGCCACAGCAGGAGTGTCACAGGAGGATGAAGATGAGTTGATACCATCCGGAGATGGGGAATCTGTGGACTCTGAGACTTTTGTTACGGAGACAGAGTCAGAATTAG[G/A]TATTCACACAGCCATTTATGTGTTAATCAAGTAGATTATGAAAATACACCCTGATGTATTGTATCTAAATGTTTTGCAGGCGTTCCTCAGGTAAACGGAGATCAGCGTGTTAATTCTCTGCCATCTGTAAGACAAGACATCCACCGATACCAGCGTGTGGACGAGCCCTTACCTCCCAGTGAGTGTGTGTATGTGTTTCTGTAAGTCTGCATGCGCTTCAGTGTGGTTTAAGGTGTCCTCAGTAATATTGGCACCTCTGGAAAATATAAGCAAAAAGGCTAGTTTAACATAAAAAAACAGTATGTTTCAGTTTATTATTAGATGTGAGAGTAGCTTACCTTTTTCTTAAAACCCTTTCGAAACTTTTGTACTTTTTGACAGTTTCATTTGTGAATTTTGGAGATTTTTTTACCAGGCTTAGTCACAACACAACATCAAATTTGACTATCACTGCTTTTGTAAACGAGTCTGCAAGAGCCTACTGGAGTCTGGAGTTTTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21490
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
ENSDART00000092240 Nonsense 654 1263 10 25
ENSDART00000137756 Nonsense 802 1411 14 29
Genomic Location (Zv9):
Chromosome 9 (position 25209605)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 24365391
GRCz11 9 24176260
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTTTAACAGCTTCTTGTCATGATTTCTTGTTCACCTTCAGAGTGCCTA[T/A]CGGATGTTCACAAGTAACACGTGTCTGAAGCACATGATCAGTAAAGTTCG
Long Flanking Sequence:
GCCATTTTATAATAGTTTAACATTATAATTTAATTATTTAATGGTTAATGATCGATCACAAATTGATTAAGAACAGAAGAGTTGCATTGAATCTTGCATTAGCGCTGTTCACACTATCAAATGTTTTCAAGATGCTTTCATTGGTTTCAAGAACCAGATGCATTTAGACCTGTATCTGTTTACTCTGGAATGCGTCCCAGACCCCCTCCTGAAGTAGTTTGAGCGATTGAATCGGAATGCATTTCGGAGGGCATTAACAACTCTTCATGATGGAATGGCAATACAATCAGAAAAAACACAAGAAGTGACTAGGTGTAAACAGCCACAGGGAACCACCTGCTCTTTTGACTGACCTACTTCTCAAACATTGCAGGACGTGTTGTTACAGTGCACTGTCCAGAGAGCAGAGGCGTAGTTACAGCATGTGGTGTCCATCTGTGGCATGTTGCGTATTTTAACAGCTTCTTGTCATGATTTCTTGTTCACCTTCAGAGTGCCTA[T/A]CGGATGTTCACAAGTAACACGTGTCTGAAGCACATGATCAGTAAAGTTCGACGGGATGCCCAACACTTTGAGCGGTACCAGCACAACCGAGACCTGGTCAACTTCCTCAATCTGTTCTCCAACAAGCAGCTGGAGCTTCCCCGGGGCTGGGAGATGAAACATGACCATACTGGGAAGGTGTGTGTGTGCGTGCGTGCGTCCATGCGTGTGTGTGTGTGTGTTTTCAGTTTTCTGTGCACCTGTTTAAAGGAATAGTTGACACAAAAATATTATGGAAGTCGTGACCAGTTTTCAGTTTTCTTCAAAATATCTTCTTTTGTGATCAAACTCAAACAGAAACTCAAACAAGTGAAGAGTGAGCAAATTATGACAGAGTTTTTAGTTTTGGGTGAACAATCCCTTTAATCTTAGACCTGCATGTGACAAACTGTACAGATGAAATCTGAGTTAAATGTGTTTACGGAGGCCCATCTGCTTTAAACCGTAAACAGATTTCTGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7630
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:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092240 Missense 690 1263 10 25
ENSDART00000137756 Missense 838 1411 14 29
Genomic Location (Zv9):
Chromosome 9 (position 25209712)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 24365498
GRCz11 9 24176367
KASP Assay ID:
554-4260.1 (used for ordering genotyping assays)
KASP Sequence:
TGCCCAACACTTTGAGCGGTACCAGCACAACCGAGACCTGGTCAACTTCC[T/G]CAATCTGTTCTCCAAYAAGCAGCTGGAGCTTCCCCGGGGCTGGGAGATGA
Long Flanking Sequence:
TTCACACTATCAAATGTTTTCAAGATGCTTTCATTGGTTTCAAGAACCAGATGCATTTAGACCTGTATCTGTTTACTCTGGAATGCGTCCCAGACCCCCTCCTGAAGTAGTTTGAGCGATTGAATCGGAATGCATTTCGGAGGGCATTAACAACTCTTCATGATGGAATGGCAATACAATCAGAAAAAACACAAGAAGTGACTAGGTGTAAACAGCCACAGGGAACCACCTGCTCTTTTGACTGACCTACTTCTCAAACATTGCAGGACGTGTTGTTACAGTGCACTGTCCAGAGAGCAGAGGCGTAGTTACAGCATGTGGTGTCCATCTGTGGCATGTTGCGTATTTTAACAGCTTCTTGTCATGATTTCTTGTTCACCTTCAGAGTGCCTATCGGATGTTCACAAGTAACACGTGTCTGAAGCACATGATCAGTAAAGTTCGACGGGATGCCCAACACTTTGAGCGGTACCAGCACAACCGAGACCTGGTCAACTTCC[T/G]CAATCTGTTCTCCAACAAGCAGCTGGAGCTTCCCCGGGGCTGGGAGATGAAACATGACCATACTGGGAAGGTGTGTGTGTGCGTGCGTGCGTCCATGCGTGTGTGTGTGTGTGTTTTCAGTTTTCTGTGCACCTGTTTAAAGGAATAGTTGACACAAAAATATTATGGAAGTCGTGACCAGTTTTCAGTTTTCTTCAAAATATCTTCTTTTGTGATCAAACTCAAACAGAAACTCAAACAAGTGAAGAGTGAGCAAATTATGACAGAGTTTTTAGTTTTGGGTGAACAATCCCTTTAATCTTAGACCTGCATGTGACAAACTGTACAGATGAAATCTGAGTTAAATGTGTTTACGGAGGCCCATCTGCTTTAAACCGTAAACAGATTTCTGTTTACAAATTTACTGCTCAAACTTCTTGTCTATGTGTTCATGCGTCACAGGCCTTCTTTGTAGACCACAACTGTCGTGCCACAACATTTATTGACCCGCGGCTGCCCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21491
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
ENSDART00000092240 Nonsense 787 1263 13 25
ENSDART00000137756 Nonsense 935 1411 17 29
Genomic Location (Zv9):
Chromosome 9 (position 25211774)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 24367560
GRCz11 9 24178429
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTACGCATCTGTGTTTTTCAGCCTATAATGATAAGATTGTTGCCTTTT[T/A]GCGACAACCCAACATTTTTGAGATCCTGCAAGAGAGACAGCCAGAACTTG
Long Flanking Sequence:
ATTACAATTTTCAGTAATTTAAATGAACACAATTCCAATTCAGATTGTTTTGGTTTTCTCAGTGATGTCATCGAGGAACAATTTTAAGCTCCTCAAAGCATGTGTCTTAAAAGGAGACCATTTTAATAAAAAGATCATTTGAATATTTTCATAAGGAAAATACAGTATGATTCCTGCTCTGATGTTTCAGGTTGGAGATGACTCTCGTTCCCCGAGTCCTCCAGTCCAGGGCCGGTCATCTAGAAACAGTCAGTATCAGGACCTGGTGCCTGTGGGTGAGTGTGTGTTTGTGTCTGTGAGTGTATGTGTATGCGTGCGTGTGTGTGTTTGTGTGCGCGTGTGAGTGTGTGTGTGTGTGTGTGTGCGCGCATGTGTGTGTGTGTGCGCATGTGTGCGTGCATGTGATCTCATGTGTTTACAGACAGACGTATCGAAACATGTGCACTGACATGTTACGCATCTGTGTTTTTCAGCCTATAATGATAAGATTGTTGCCTTTT[T/A]GCGACAACCCAACATTTTTGAGATCCTGCAAGAGAGACAGCCAGAACTTGTGAGAAACCATTCCCTTAGGTACTTTTATCTGCAGTTTTATGATTCAACAACAGATGTGAACAGAGAGTCACTCATTTCGCTCTGCACTTGAGGAGTTTGTGCTGTCATTGCTCAATGCTTAAAGTCTTGTTTCATATTGTTATTTTCAGGGAGAAGGTTCAGTTTATCCGCAATGAGGGGGCAACAGGGTTAACTCGTCTGTCCAGTGATGCAGACCTGGTTATGTTGCTCAGGTAAGTGTGTGCAGATTTTGCATTATATTTAAATACAGCTTATGGTGTGCCTGCCTCTTTCCCTTTGTCCCAGACATGCATGCATTAGTTGAGTTTGTATTTACTCTATTGTACTGTTCAAAACATTGGGGTCAGTATGATTACATTTTTCATTTTATTATTATTTTTTGGCCAATGTTTTATTTAGCAATGATGCATCGCATATGTTAAAATAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34643
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
ENSDART00000092240 Nonsense 1186 1263 23 25
ENSDART00000137756 Nonsense 1334 1411 27 29
Genomic Location (Zv9):
Chromosome 9 (position 25219666)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 24375452
GRCz11 9 24186321
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCGATGGTTCTGGGCTGCTGTGGAGAGATTCAACAATGAACAGAGACTA[C/T]GACTCCTTCAGGTACTCTCACATCTCAATTGGGATATGGGGTCAGGAAGA
Long Flanking Sequence:
GGATCTGGCATCGCTGTGTCAGACAAGAACAAGAAAGAGTACATTGAGCGCATGGTGAAGTGGCGGATTGAGAGAGGTGTGGCTCAGCAGACAGAGAGTCTTGTGCGAGGATTTTATGAGGTACAGTCTGAATCTGTGAATAATAATGACTAATAAAGATATTAACTAATCAAAATTACAATAATAACTTATAACAGGATGTTGATCTGAGAACATGTACCTGTGCAGGTGGTGGATGTGCGGCTCGTCTCAGTGTTTGATGCCCGAGAGCTGGAGCTGGTCATTGCTGGAACAGCAGAGATAGACCTGTCCGACTGGAGAAACAACACAGAATACAGGGGAGGTATTACTGAAACTGATCCAGGTGTTTTTTTTACTGAAATATCACTGAATGTCTGAAAATGTTTATTATCACTGTTCTTGAAGGTTATCATGACAACCACATAGTGATTCGATGGTTCTGGGCTGCTGTGGAGAGATTCAACAATGAACAGAGACTA[C/T]GACTCCTTCAGGTACTCTCACATCTCAATTGGGATATGGGGTCAGGAAGATATTTTTTTAATCTAAAAGAGTATGTTTAATTCATCAAAAGTGTCAATAAAGGCTTTATTTGTACTGGTTTTGGTGGTTTACAAGGACAGAAATTTGTATAATGACAAAAATGAGTATTCTATTAGGGTGGTTTACGAGGACATGCCTTGTGTCTTTATTAATCAAAATTCTTAAAATACATACTTAATACATACATTCAATTTTCGTGATGGTTTGGTTCAGGAGTAGTGGTGGGGTTTTTACCAGACTGAATACATCATGCCTATATACAGTACCTATGTCCTTCCCTATAAATCACCATTACCAACGTGTGTGGTTTTGATCAAATAATTATAGCGTTTCTGATAGGAAAATTTGAAAAAGAAACTTTAAATAAAATTAAAAATATTAAAACTAATTAAAAATGTGTACTTCATTTTAGATCAAAGATTTAGCTTCACATAGTGAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15103
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
ENSDART00000092240 Nonsense 1234 1263 25 25
ENSDART00000137756 Nonsense 1382 1411 29 29
Genomic Location (Zv9):
Chromosome 9 (position 25220485)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 24376271
GRCz11 9 24187140
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACTGTCATGTTTCTTTATATRTTTGTGTAGGGCTCACACCTGCTTTAAC[C/T]GACTGGATCTCCCTCCCTACCCCTCGTTCTCCATGCTCTATGAGAAGATG
Long Flanking Sequence:
TACAGTACCTATGTCCTTCCCTATAAATCACCATTACCAACGTGTGTGGTTTTGATCAAATAATTATAGCGTTTCTGATAGGAAAATTTGAAAAAGAAACTTTAAATAAAATTAAAAATATTAAAACTAATTAAAAATGTGTACTTCATTTTAGATCAAAGATTTAGCTTCACATAGTGAGCTTGTACTGTATAGATGAACACTATTCAAAACTTCGAAAGTCTTCTCTGCATAGATTAAATTAGCCAATTCAACATGTGTCTCTGTCTTCCTTAAGTTTGTAACAGGAACTTCCAGCATTCCCTATGAGGGCTTTGCCTCTCTGCGGGGCAGTAATGGTCCACGCCGATTCTGTGTGGAGAAATGGGGCAAAGTGACCTCCCTCCCACGGTACAGCTAGCATTTTTAGAGTGGGCTTTACATGTTAACCAGCACTGATAATCAATCAGCTACTGTCATGTTTCTTTATATGTTTGTGTAGGGCTCACACCTGCTTTAAC[C/T]GACTGGATCTCCCTCCCTACCCCTCGTTCTCCATGCTCTATGAGAAGATGGTCACGGCTGTGGAGGAAACCAGCACCTTTGGTCTGGAATGAGCTCCAGTCACAGCAAAAGTGCTATTCATTTGTTTTTCTTAGTTCTGGAAACCTGACTTGGCGTGCAGGCTTAATTATCATTCCTCACTCTTTATTACAGCCTTTGTCACCAGACACTTACATAATCATTTTATCAGAGTCTATGGAACTGAAATATACAGTATGTCATCTAGTGACTCTCTGAGCGAGTGCCAACTCTTGTTCTATACCGTATGGAGTCGACAGCCTGCTGTGAAAACTGCATTTCATTCTTCATCCAAACAGACTTTCACATTCACAGAAATCAGAGCCAGGGTCTTGATCACTTGGGTTTGGTCTTTGCTTTAGACTGAGTGTGCCTCATGTGTCCTGATAAGTGAAGCCAAAACATTGTTTGCCCCCTGTTGACTGGATGTAGAACAGATCATA
Associated Phenotype:
Not determined