Busch Lab

ZMP

col14a1

Ensembl ID:
ENSDARG00000005762
ZFIN ID:
ZDB-GENE-030131-9889
Description:
Col14a1 protein [Source:UniProtKB/TrEMBL;Acc:Q6NW57]
Human Orthologue:
COL14A1
Human Description:
collagen, type XIV, alpha 1 [Source:HGNC Symbol;Acc:2191]
Mouse Orthologue:
Col14a1
Mouse Description:
collagen, type XIV, alpha 1 Gene [Source:MGI Symbol;Acc:MGI:1341272]

Alleles

There are 14 alleles of this gene:

Allele Name Consequence Status Availability
sa11768 Splice Site, Nonsense Available for shipment Available now
sa44843 Nonsense Mutation detected in F1 DNA Not yet available
sa7420 Missense Mutation detected in F1 DNA Not yet available
sa11818 Essential Splice Site Available for shipment Available now
sa12938 Nonsense Available for shipment Available now
sa45568 Nonsense Mutation detected in F1 DNA Not yet available
sa42688 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa36074 Nonsense Mutation detected in F1 DNA Not yet available
sa28616 Nonsense Mutation detected in F1 DNA Not yet available
sa12349 Nonsense Available for shipment Available now
sa22787 Nonsense Available for shipment Available now
sa10929 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa11768
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000027982 Splice Site, Nonsense 347 1864 8 47
ENSDART00000134087 None None 1382 None 37
ENSDART00000137912 None None 253 None 8
ENSDART00000138611 None None 96 None 5
Genomic Location (Zv9):
Chromosome 16 (position 17096689)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 14911550
GRCz11 16 14801670
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGACYAGGACGGTGTGTGATGGAGYGGAGCAACAGGACAAAGAAATTAAA[C/T]GTGAGTRCTTATACCTAATGTAGATGTGTCATATGTGRAAAGGGATCAAA
Long Flanking Sequence:
TAACTATTAATCAAAACATATTTTAATCATAAGCATATTATATTGGGACTTGTGTGAACTAAGAGAAAAACAGAAACATGTCAAAGTTACAAACAGTGGAAAATTACACGCTTTGTTAATGTTGTTGCATTCTGTTTGTTTACCTTCAAATTGAATATTTTTTTTACATTTTAAATGATTTTCAAATCAATTAAAAATTATTTTAAATAAGTCTGTGATAATTAGATTTTATTATGATTTTTTATGTATAGTATTAGAAAGAAAATCGTAATTGTCAAAAATGTATATATTTCAGAAATGTGAAATATGACCTGGTGTGTGTATACCGCATGTGTGTAGGTGTGAAGAATGCTGATGAAAATGAGCTGAAGGCCATTGCGTCTGAACCAGAGGACACACATGTTTATAATGTGGCTGACTTCAGTATTATGGGCACCATAGTGGAAGGTTTGACCAGGACGGTGTGTGATGGAGTGGAGCAACAGGACAAAGAAATTAAA[C/T]GTGAGTACTTATACCTAATGTAGATGTGTCATATGTGGAAAGGGATCAAAAACCTCATGATTTCCTCGCAATTAACAGAAGATTCTGTCCCCGAGGAGACTGTGTCAACTCCTCTGAACCTGCTCATTTCTGAGGTGACGGCACACAGTTTCCGAGTGTCCTGGACTCATTCGGCTGGCAAGGTGGAAAAGTATCGTGTGGTTTACCATCCGACCGATGCAGACATTCCAGAAGAGGTGACTTGATGTTCATTTTAAGGTTATCTACAATATAAGCTAGTGTGCTACAGTTAAACAAAAACAGTTACACAGTTCACATTTAAAAGATTAAGAGCCCTATAACCCCGGCACAAGACACATTTGGCGCAGTTTGTTGCTATTTTCATACCAACACAACACAAATTTTCACGTTTTGCACCATGTTATTTAAATGGTAAATCTATTTGCGCCACTTTGTGGATTCATGGGTGTTCTGATCTAGAAAGGAGGAGTGTTTGAGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44843
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
ENSDART00000027982 Nonsense 412 1864 10 47
ENSDART00000134087 None None 1382 None 37
ENSDART00000137912 None None 253 None 8
ENSDART00000138611 None None 95 None 5
Genomic Location (Zv9):
Chromosome 16 (position 17104371)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 14919232
GRCz11 16 14809352
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTTGCTGTACAGATTGTGGTGGGCGGTTTGGAGAATTCTGTGGTCCTG[C/T]AGAACTTGAACTCTCTGACTGAATACGAGATTGCAGTGTTCGCTGTGTAT
Long Flanking Sequence:
ATGTTTATATACACTAGTGACCCGTATCAGATTGGGGACACAAATAGCTTGATTGGGAAAATCTTTCTAGATATATATATTTTTTATATTCCATTGAGTAAGTAAATGAATAGAGGTTTGGAACACTGTGAGGGTGAAATAAAATGATCTGGCAGACAATAATGTGTTTTAAAAGTAATTTCCATATATATTTTAAAAAATAAGTCTGGCTTTTTTTTATAAAGCAATGACATTTTTTAACTGTCAGTAGTGTCAAAATACTTTTTAAGACTAGCTTACTGTCTCTGTTTGATCTCATTTATTCTTTTTTTGATTTCTTTCTTTATATTTTGTTATGGGTGACATCACAGTGCTATAAATATTATGTGCCGCAGTTTGGCACGTTATTTAATTCTGTTTTGGTTTTATTTTTCCTAATGGCTCTCTGAACTGCTGTCACAAACCACTGTTGTCTTGCTGTACAGATTGTGGTGGGCGGTTTGGAGAATTCTGTGGTCCTG[C/T]AGAACTTGAACTCTCTGACTGAATACGAGATTGCAGTGTTCGCTGTGTATCGCAGCGCAGCGAGTGATGCTCTCAGAGGCAGCGAGATCACACGTGAGTCATCTCTAAACTCAACATAGCATCTGTAAACACATGAGCTTCACGACAGCATCATTCCACATTTGTATATGTCAAAATATATCTTTGTTTAATTTAAATATTTAAAAAATTATATTTTACAAAATATATCTTATTCATAATGTATAATATATTTTGGGCATTTCAAATACGATATTCTTTCTAAAATATAATGAAATATATTTTTATAAAAATATAATTTCTACAAAAAAATTTGGGGGCTTTTATATATTTTTTAAAATATGTAATAAATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATATATATACATATATATAATATATTTCATTTCAATATTTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7420
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:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000027982 Missense 822 1864 20 47
ENSDART00000134087 Missense 340 1382 10 37
ENSDART00000137912 None None 253 None 8
ENSDART00000138611 None None 96 None 5
Genomic Location (Zv9):
Chromosome 16 (position 17166137)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 14980998
GRCz11 16 14871118
KASP Assay ID:
554-4323.1 (used for ordering genotyping assays)
KASP Sequence:
CCTYATTGCTAATGCTAATAWTGGYTTTCTCTTTTCTGATTGGTTAGTGC[C/A]ACTTTCTGGCCCCAGYAACCTCAGGGTGTCTGATGAATGGTACAATCGCT
Long Flanking Sequence:
AATTAAGTGAAAAATATAGACTATTATTAGAGAATGTTATTTTCAATGTAATGTAATGTGTATTAAAAATATAATTCTTCTAAGCTGTTGAATCATCAACAAACATTGAAGTAACAGTTGCTGAAAATGTAGCTTTACAGTCGCAGGAATAACTGCATTTTGTTTTTTTTACTGACATTACTTTAATATTCTAATAATATTTAAAATTTTACTATTAATTACACTACTTTTGATCAAATTAGTGCAATCTTGGTGAGTCTTTCAAATAATTACTGGTGGACTTTTTAAATATTTAAATAGTTAAATATAATAATTTACCTTTCAGTCATTTTTTTTTATTTTATTTTACAACTTTAAAGGTGTCAATGTTACAGTATATTTTTTTATGATTCCACTTGCAAGTGCTAAATTATTTTGAGATTTGGCTGACCAGTAATTGGCAAGAAATGACCTTATTGCTAATGCTAATAATGGTTTTCTCTTTTCTGATTGGTTAGTGC[C/A]ACTTTCTGGCCCCAGCAACCTCAGGGTGTCTGATGAATGGTACAATCGCTTCCGCATTAGCTGGGACAGTCCTCAATTCCCCACCATGGGTTACAGAGTCATCTATCAGCCCATCTCTGGTATGTACACTCACACACAAACAGAGAGACACACAAGTACACATTTTAAAAGGCTCCTTGTTTATTAGTACATTTATTATTTTTTTTTATTATAGTTGGTGTGCAATGTTACTTGGCATAAGCTATATATGAAATTAAACTGTTCAAAGCTCAATGGAGAGGGAGATACTATCATTTTACAGAAGTCACTTTTAAAGTCCTATAACAAGTCGGCTGCAATAGCCTAGAGGTTATGTGTGCCTATATAAAACACTGAGCTGTTCATGGTGACCTGTCTGTAATCTTAATTGTTCCATCCTAATATATACATCAAACAGCAAACAGCTTTTGGGGAGTACATGAGCTTTTTCTTGGTTTTTGTATAAACCCTGGCCCCAGGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11818
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
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Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000027982 Essential Splice Site 1000 1864 23 47
ENSDART00000134087 Essential Splice Site 518 1382 13 37
ENSDART00000137912 None None 253 None 8
ENSDART00000138611 None None 96 None 5
Genomic Location (Zv9):
Chromosome 16 (position 17196940)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 15011801
GRCz11 16 14901921
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
KTTTTWCAGGACACAGAGGGCCCTGCTGTCAYCACCATGGTCACCACTGG[T/A]AAATACACTCAGAAAAATTAAYACTATACTATTTACTTGAGWGRAAGAAA
Long Flanking Sequence:
TACATCAGGCTAACATGTCAAAACAGTTAAAGAGCATAGTGTAAAACTCAGAGAGTAAAATGCTGGTCCTTTTTTTAGCAGTGGAAAAATCATAGATGACAATTAGCTGAATTAGTGTTGAATTTTCCTTCATTTGCAGACAAATTTGTAAGCAGCAACTCATGCCTGTTAAAAAATAACAACACTTTGACGACTGCTGTGGTGCCACTTCTGTCATTTTGAGTCTTTGTTTGTTGGCTGAGGACTCTAATGACTCTCATTAATTAGGATGATTGTTTGCTTGAGGAAGCTGATGTGATTTTGTATTATACTTTTATTTGTTGTTTGAATGCCATTTGTCTTTATTTTGCAGACGGGCAGAAACAGGAGGTGAGGGTCGGTGGTGGTGCGTCCAGAGAGTGTTTCTTCAGACTTTCCCCCAACACCCAGTACAAGATAAGTGTATACACCGTTTTACAGGACACAGAGGGCCCTGCTGTCACCACCATGGTCACCACTGG[T/A]AAATACACTCAGAAAAATTAATACTATACTATTTACTTGAGTGGAAGAAAAATGCCTCAATAAATGTGAAATAAATTTGACAGGTGTGTGAGGATATTTTAAATACCAGTAATAGATGTGTTTTGTGGTAATGCAATTTCAGGGGTAAAAATAATAGACTAGAGACAATATTTAAATTTGGAACACTGCTTACATCTTGTGGGACCTGTGTCAAACTCTCAACTTTGGAGCTGTCTTACACACAAACATAAAAATAGAAAAGAAAAGTTAGAGGCTATTAAAAATAAAAAAATGCAGTTAGGGGCCATTCACACAGAGCAGAGTGCATGTTTTGCATTGAAAATTATGAGACACTGGCAGTGGAATGAGGAAAATGCAGGCTTCAAGATGTGTTTTGTGAAGTTGAACTTCTTTAAACTTGAAAACAACATTTGTGTTGTGGTCAGACACATCTGTCTAATATGTTTACTTTAAAAAACAATGGTTAAGTATTGGAGTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12938
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000027982 Nonsense 1376 1864 33 47
ENSDART00000134087 Nonsense 894 1382 23 37
ENSDART00000137912 None None 253 None 8
ENSDART00000138611 None None 96 None 5
Genomic Location (Zv9):
Chromosome 16 (position 17268904)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 15083765
GRCz11 16 14973885
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTTCATGTGGCCATCAGCAAAACTGCTGCTAAAGTGGTGATCGACTGC[A/T]AGACRGTTGGAGAGAAATCCATCAATGCCGCAGGGAAYATCAGCATTGAT
Long Flanking Sequence:
TATTGTGTGACTGTACAATAGTAGTTATTGTTAAGCCACATTATTATTAACCTTTTTATTTGTTGGTATGTATTTGTTTTTTTTTCTCATTGTATGTGCTTAAGTTGATACTATTTCTTGATATACTATATATATATATATATATATATATATATGTATATATATATATATATATATATATATATATATACATACATACATACATACATACATACACATACATATATAAATATAAAAACATCTTTATAATTGATGAATGAAGAATAGTAATTAGGAAAGCAGGGGGTTTGTCTTTTTAACACAACAATTCTCAGTTTTTATTTTTAGTTATTTTTTAATCTTCTTTAACACTTAACTATATTTACTATGTCTCTCAAATAGTTATCCTCCATAAACATCAGAACATCCCTATTTGCCATTAAACCTTATTTGTCTCTTCTTGTCCCACACAGCTTCATGTGGCCATCAGCAAAACTGCTGCTAAAGTGGTGATCGACTGC[A/T]AGACGGTTGGAGAGAAATCCATCAATGCCGCAGGGAACATCAGCATTGATGGAGTGGAGGTTCTAGGGCGAATGGTCCGATCACGGGGACGGAAAGACAATTCAGCACCGGTAAGACTTTCAGTACACAAATCAAGCGGACTAAAAATAACAGATATCATAATAACACATAACTCCAGTAGGTAAGCTTACAAGGCCATCTTTTTAATTCCATAGTGCAAAGTAATAACCCTTCTGTTGACTTAAAATGACTCATGACCATTTTAAAAACTTGTTAATAAAAATGACCCTTAATGATGAAAATTTAATCGTCAATAATAATAAATGTACAAAAATATTGTCATAAACTGATAACCCTACTGATGATTAATGATTATTCAAACAAGTGTAAATGATAAAACATTGAAAATATAATTATAATAATTTATTTTTGCCAAAAAAAATGAATAAATGTGTGTAAAAACATGTATCACTGCAACATGTGTTAGCATTTTAATAGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45568
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000027982 Nonsense 1426 1864 34 47
ENSDART00000134087 Nonsense 944 1382 24 37
ENSDART00000137912 None None 253 None 8
ENSDART00000138611 None None 95 None 5
Genomic Location (Zv9):
Chromosome 16 (position 17290602)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 15105463
GRCz11 16 14995583
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTCTACAGTTTCAGCTCCAGATGTTTGACATAGTCTGCAGTACATCAT[G/A]GGCCAGTCGGGATAAGTGCTGTGAACTCCCGGGATTGGTAAGAACCCATC
Long Flanking Sequence:
TAATTTAATACTAACAATCATTTAATTATTCAATCAGCACTAGAATAAACCCCTATAAATAATCAGGTATGTCCTACCCTGTTATCCTTAGTATCCCTCAACCACCCCATCTCCAGACTTTCAAATTCATTTACGTGCACTTCGACCCCTCTCACTCTCTCTTCTAGCAAAGAGAATAACATGAGTTAGAGTGTCCTTCTGAGCTCCCGGACAGCTCCCCAAATATGCCTAAATTATTATGTCAATTATCTGTAAGTGTGAACTCTTGAATCAAACATACCTGATCAAACTAATTGAGTCCTTCAGGCTTGTTTGAAATCCACATATGTTTGATATGCTATAGGTTTAGATTATTTCATAATATTTGTGTTGATAAGATTTATAAAAACATGTACATATCTTGGAAATGAATGACTGCAATTCAACAGATTTACATGTGATTATATGGTCTTGTCTACAGTTTCAGCTCCAGATGTTTGACATAGTCTGCAGTACATCAT[G/A]GGCCAGTCGGGATAAGTGCTGTGAACTCCCGGGATTGGTAAGAACCCATCAATTGGTATTTTGTATTAATATATGCTTCATCAAATCATATAAGCCACATGGTAATCAGCTTACATTAATACTCTTTTTCTGTCTCTGGTAAGGCCCAGATATTTAAATCCAATCCTGACCACAATGTGAAACTCAAATACGACTAGCACATTAGGTAATCATTATGATATGCTGAGAGTCAATCAGAAACATGTACCAATGCCTCGGTCAAGTAGTTTGCTGCCTGTTGTTTGTTTTTCGCATGCACATATACAACTGTCATCAGCATATGTTTGCATACTAATAGAAGGACAGACTTGTGGCAGGTCATTTATGTATAAACTAAACAGGATGGGGCCCAAAATTGACTCTTGAGGAACTTCAGTTACAGATTCTTTACACTGATTGTCTATTTCCAAGATGCACACATTGTCCCCTGTTTGTCAAATATGAAGTCATCTATTTAATAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42688
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
ENSDART00000027982 Essential Splice Site 1630 1864 43 47
ENSDART00000134087 Essential Splice Site 1148 1382 33 37
ENSDART00000137912 None None 253 None 8
ENSDART00000138611 None None 96 None 5
Genomic Location (Zv9):
Chromosome 16 (position 17329641)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 15144502
GRCz11 16 15034622
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCGCTGTTCGTGCAATAGCTCGACAAGTTTGTGAACAGCTTATTCAGAG[T/C]GAGTTGACCATGTATTTTGTCTAACATTGTTCCTCATTTACTTAATGATT
Long Flanking Sequence:
TAGCACTGTTGCCTCACAGCAAGAAAGTCGCTGGTTCGAGTCCCAGCTGTGTCAGTTGGTATTTCTGTGTGGAGTTTGCCTGTTCTCCCCGTGTCGGCCTGGGTTTCCTTCGGCTGCTCCAGTTCCCCCACAGTCCAAACACATGTGGTAAAGGTGAATTGAATAAACTATGAGTGTGTCTTAGTGCATATGGGTGTTTCCCAGTACTGGGTAGCAGCTGGAAAGACATCCGCTGTGTAATACATATGCTGGATAAGTTGGCGGTTTATTCCACTGTGGTGACCCATGATGAACAAAAGGAATAAGACAAAAAGCAAATGAATGATTGAATGAATGTTTTCATTTTTTTGCTCACCCATGTGTCAATGGCTTAAAATGATTGTGAGTTTAACCTAAATTAAAACTTTAATTCCATGCTGTTTGTTTCTGAAGGGTGACATGCAGTCTCATGCCGCTGTTCGTGCAATAGCTCGACAAGTTTGTGAACAGCTTATTCAGAG[T/C]GAGTTGACCATGTATTTTGTCTAACATTGTTCCTCATTTACTTAATGATTCACAGGAAATCATTCAACCCCTGTTGACAAACCAAGTGATTTCTCTTTTCGTTGTCATGCGTAGGTCACTTGTCTCGCTACAACTCGATCCTGAACCAGATTCCCAGTCAGTCAGTTTCAGTACGAACAGTACCAGGTCCGCCAGGTGAGCCCGGTCGGCCAGGACTTCAGGGGCCACAGGGAGAGCAGGGTCCTCCTGGCAGACCAGGATTCCCTGGAGCCAGTGGGCAAAACGGCCGCCCAGGAGAGAGAGGTAAAGATTTTTTTTTTAAAGTTACCATGCACACAACTGTTTTAAAAATGAAGTAAATAGTTGAAAGTTTTGAGGAAGTAATTATGGACAATAGTAGATGAATTATTGAACCCTTGGAAATGGAGCGAAATTGTCTTGTCAAGGAGGAATTAGATGCATAAGCAAACTGCACAGGGGTTTACTGGAATATTTTTAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36074
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
ENSDART00000027982 Nonsense 1671 1864 44 47
ENSDART00000134087 Nonsense 1189 1382 34 37
ENSDART00000137912 None None 253 None 8
ENSDART00000138611 None None 96 None 5
Genomic Location (Zv9):
Chromosome 16 (position 17329878)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 15144739
GRCz11 16 15034859
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCGCCAGGTGAGCCCGGTCGGCCAGGACTTCAGGGGCCACAGGGAGAG[C/T]AGGGTCCTCCTGGCAGACCAGGATTCCCTGGAGCCAGTGGGCAAAACGGC
Long Flanking Sequence:
TAATACATATGCTGGATAAGTTGGCGGTTTATTCCACTGTGGTGACCCATGATGAACAAAAGGAATAAGACAAAAAGCAAATGAATGATTGAATGAATGTTTTCATTTTTTTGCTCACCCATGTGTCAATGGCTTAAAATGATTGTGAGTTTAACCTAAATTAAAACTTTAATTCCATGCTGTTTGTTTCTGAAGGGTGACATGCAGTCTCATGCCGCTGTTCGTGCAATAGCTCGACAAGTTTGTGAACAGCTTATTCAGAGTGAGTTGACCATGTATTTTGTCTAACATTGTTCCTCATTTACTTAATGATTCACAGGAAATCATTCAACCCCTGTTGACAAACCAAGTGATTTCTCTTTTCGTTGTCATGCGTAGGTCACTTGTCTCGCTACAACTCGATCCTGAACCAGATTCCCAGTCAGTCAGTTTCAGTACGAACAGTACCAGGTCCGCCAGGTGAGCCCGGTCGGCCAGGACTTCAGGGGCCACAGGGAGAG[C/T]AGGGTCCTCCTGGCAGACCAGGATTCCCTGGAGCCAGTGGGCAAAACGGCCGCCCAGGAGAGAGAGGTAAAGATTTTTTTTTTAAAGTTACCATGCACACAACTGTTTTAAAAATGAAGTAAATAGTTGAAAGTTTTGAGGAAGTAATTATGGACAATAGTAGATGAATTATTGAACCCTTGGAAATGGAGCGAAATTGTCTTGTCAAGGAGGAATTAGATGCATAAGCAAACTGCACAGGGGTTTACTGGAATATTTTTAAATCTAGTAGGAGTAGTATGGAGGATGATTAGTCGACGGTCCTCAAGAGTAATGTTGCCCTGCAGCTTAAGGTTAAACCGTGGTTCTGAGTCTATAATTATACGGAGCATTAACATGACCTCTGTCACCCAGTCTATTGCAGATTAAGTCCCATTTCTCAGAGGGCCAGTGATTAATTTTGTCAACATCTTGGCTGACAGCCCTGGCTAACCCTTACAGCCATCATCATAAACAATATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28616
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
ENSDART00000027982 Nonsense 1709 1864 45 47
ENSDART00000134087 Nonsense 1227 1382 35 37
ENSDART00000137912 None None 253 None 8
ENSDART00000138611 None None 96 None 5
Genomic Location (Zv9):
Chromosome 16 (position 17332068)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 15146929
GRCz11 16 15037049
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGTCTTCCAGGAGAAAGGGGAGAGAAGGGCAGCCCAGGTGTGGGGACA[C/T]AAGGCCCTCGTGGTCCTCCAGGATCTCCAGGTGAAAGACTGTTAAAAAGT
Long Flanking Sequence:
CTAAATATCAACATAATTTGACATCGTTATTGCACGTCAAAATAATGTTGTTCTTTAGATGCTGGCTAAAAGTTGAATTTTGGTCACCTGACATAATGACGTAAATCTTACTTAATATTACCATCTTATGATGTTGTGTGCCTGCTGGGTAGACAGATGGATAAATACACACTGACAGATGCCATGAATAGATGGCAAGATACTATATATTGCAGACATGTAAACTGATTCTATGAATGGATATATATTGCTGGTGGATAAATGCATTGAATGGATATGCAGATAAATGCATAGTACTATAGATGGAAGATTTATTAATGCAAATTAGTTGGTTTGATAGTCTGATCTTCTATTTCTATTCCAGTGGTCTGAAACAGGTTAAATCACATGGACTGAAGGTTACAGCTTCTTCAGAAGGTTTTGGATGTTCTAAGAGATCTCTGTTTTTTCCAGGTCTTCCAGGAGAAAGGGGAGAGAAGGGCAGCCCAGGTGTGGGGACA[C/T]AAGGCCCTCGTGGTCCTCCAGGATCTCCAGGTGAAAGACTGTTAAAAAGTGACACTTAAGTTCAAATAAATAATTTCTTTGTCCTCAAGTTAGTAGTAAAAAAAAATAATTTCAGTCCGAATTGAAAAATAAAGCTCTGTATCTTCATATTGCTCAGACTGCGGGAGTTCCCGATATTAAATGTACCCTGTCAAAGAAAACACAAGCTTGCAAACTTTTTTTAATAACCTCTGCACACATCTTGATCTGTTTTGGGTTCCTTTGATTCCTCTCTAGAATATCAAGCAGATATTGAAACAATATTTGGGTCTGGGAGAAATGTTTTCCTATCGATTTTTAGCTGTGCAGCTTGTCGGTAGATTTTGAAAAATGTCAGCGTCGCTCGCTGTTAATTGCGCTTTGATCAATACTCTTCACAAATGAGATTCATTGAAGCAACACAGCTATATGAGCTAGCGACATGTGAGAAGGATGTGGACTGGCATTAGCTGAAACTTGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12349
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
ENSDART00000027982 Nonsense 1767 1864 46 47
ENSDART00000134087 Nonsense 1285 1382 36 37
ENSDART00000137912 None None 253 None 8
ENSDART00000138611 None None 96 None 5
Genomic Location (Zv9):
Chromosome 16 (position 17332812)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 15147673
GRCz11 16 15037793
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTCCTGCTGGACCGCCCGGCTACTGCGACCARAAYTCCTGCCTCGGRTA[C/A]AATGTTGGAGGTAATAATCTCATTCTCTACATCTGTTTCTCAAACTNTCT
Long Flanking Sequence:
GATCTGTTTTGGGTTCCTTTGATTCCTCTCTAGAATATCAAGCAGATATTGAAACAATATTTGGGTCTGGGAGAAATGTTTTCCTATCGATTTTTAGCTGTGCAGCTTGTCGGTAGATTTTGAAAAATGTCAGCGTCGCTCGCTGTTAATTGCGCTTTGATCAATACTCTTCACAAATGAGATTCATTGAAGCAACACAGCTATATGAGCTAGCGACATGTGAGAAGGATGTGGACTGGCATTAGCTGAAACTTGTATTTTGTGAGGAAGAGATCCAGACCCGCTGTGGGTGTGGAGTTTAGCTGCTTTCATTGTGTAGATACAGTATTAATGGCCAACATTATATCCCATTCAGGGCCTGCTGGAGAAGGGCGAACAGGAAGCCAGGGTCCACCAGGGAGACCTGGAATTCAAGGCACCCAAGGACGTCCAGGTACCCCAGGCAGTCCTGGTCCTGCTGGACCGCCCGGCTACTGCGACCAGAACTCCTGCCTCGGGTA[C/A]AATGTTGGAGGTAATAATCTCATTCTCTACATCTGTTTCTCAAACTCTCTCAGTGCGTCTGAAATCGCATACTTCGATTAATATATAGTACATGAAAAAGTAGTGAGCCAAGTAATGTTTAGTGTATGGTACTTGACAATAACACTCAATTGAACATATAAAGAATTTGTAACGTATTCCTATTCATTTCAAACACATTGGATTTATTGACCAGTTTACATAAATCTTATTCTTACTTATTTAATCGAGATTTAACTAACAAATGCATATTACATACAATTTATTGTAAAATTTGTATGTAATTTGAATACATAAATTCTTTTTCTTTGGCCTAATTATTTTTATTTTTTTGAGTGCATGTTCAAATTCATAGTATATGATAAACAGTGGGTAAAAATTCTTGGATTACCTACTACTTTCAGCAAGATGTGCACATCCATTGGAGAGACACATGGGACAATTTACAAATGCAAGTAAATCAATGCAAGTGAAGCATGAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22787
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
ENSDART00000027982 Nonsense 1791 1864 47 47
ENSDART00000134087 Nonsense 1309 1382 37 37
ENSDART00000137912 None None 253 None 8
ENSDART00000138611 None None 96 None 5
Genomic Location (Zv9):
Chromosome 16 (position 17343320)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 15158181
GRCz11 16 15048301
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCCTCCAATCCCTACCAAAACTACGGCCCCGCCACCAACTACAACCCT[G/T]AGGATGAGGAGGAGGATGACCCTTATGGCGGCTACCGGGCCTACCCTCCT
Long Flanking Sequence:
TGTTACAAATTTTTGGTTTAACATAGGTTACTATTCACATGACGAAATTAGCATCATAAACACTATGCACTGACCTTCAAATATGCATACAAAAATGAAAGATACCTGGGGCTTGGAAACCCTCCAAAATCAATAAGTCACTGTATAGTATTAGAGCCACACTCATTCGTTATTAAAAAAAATGGCTGCCAGTAACAATTATTTCAGCCAGGTTCAACACTTAACAAGCAAGGGCTAAATAAGTCATGCTAACAATTAACTGTTGATCCATCAGTCCGAACTAATCTAATGACAATAACAACTCTCTTCTTCCTTTCTGCACTGACTTTGTTCCTTCATTCTTTGTCGTTTCCTTCACTCTTTCTAACTCGACACCTGCTCCCCTGGTGGTGGTGACTGAAAAAAGAAGGCAATCGATCTAATTCCCCCGTGTTCCCATAGTACAACAGTTGTCCTCCAATCCCTACCAAAACTACGGCCCCGCCACCAACTACAACCCT[G/T]AGGATGAGGAGGAGGATGACCCTTATGGCGGCTACCGGGCCTACCCTCCTCAATACTACCAACCCAGCTACCCCGACCCCCGTGGCGCCAGGCCTGGCCCCGTACACCCTGGTGACACGGCGGGCATGAGGGCACCCGGCGCACGCCGCTTCACCCGCAGCACAGCTGAAGAGGGCATCGTCCATCAGCCGCAGGAGCATGTGAAGGAAGAAGAGCTGTGGTGACCGACAGATCGTCCACATACAAACACTTTTCAGCAGAATGTCCTGCAGGATTGGACCGAGGGAAATCCGAAAAGTGCCTGCTATATGCATCCTTATTGGGGCGGGTGAGTGAAGATTAGGAAAAAAAAAAAAAAAAAAACTGTGCCGAAATTCATTCAGTGACTTTTCTGTCTTTTGTGAGGCTGCATGTAGCCAATGAAACGAAAAGCTGAAGGAGGAACTCTGCAAATACGTTTTCTTAATGAGTGTTTTTGAATTGTTGTCTAGGTAAAATAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10929
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
ENSDART00000027982 Nonsense 1864 1864 47 47
ENSDART00000134087 Nonsense 1382 1382 37 37
ENSDART00000137912 None None 253 None 8
ENSDART00000138611 None None 96 None 5
Genomic Location (Zv9):
Chromosome 16 (position 17343541)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 15158402
GRCz11 16 15048522
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGGCATCGTCCATCAGCCGCAGGAGCATGTGAAGGAAGAAGAGCTGTG[G/A]TGACCGACAGAYCGTCCACATACAAACACTTTTCAGCAKAAYGTYCTGCA
Long Flanking Sequence:
TAACAAGCAAGGGCTAAATAAGTCATGCTAACAATTAACTGTTGATCCATCAGTCCGAACTAATCTAATGACAATAACAACTCTCTTCTTCCTTTCTGCACTGACTTTGTTCCTTCATTCTTTGTCGTTTCCTTCACTCTTTCTAACTCGACACCTGCTCCCCTGGTGGTGGTGACTGAAAAAAGAAGGCAATCGATCTAATTCCCCCGTGTTCCCATAGTACAACAGTTGTCCTCCAATCCCTACCAAAACTACGGCCCCGCCACCAACTACAACCCTGAGGATGAGGAGGAGGATGACCCTTATGGCGGCTACCGGGCCTACCCTCCTCAATACTACCAACCCAGCTACCCCGACCCCCGTGGCGCCAGGCCTGGCCCCGTACACCCTGGTGACACGGCGGGCATGAGGGCACCCGGCGCACGCCGCTTCACCCGCAGCACAGCTGAAGAGGGCATCGTCCATCAGCCGCAGGAGCATGTGAAGGAAGAAGAGCTGTG[G/A]TGACCGACAGATCGTCCACATACAAACACTTTTCAGCAGAATGTCCTGCAGGATTGGACCGAGGGAAATCCGAAAAGTGCCTGCTATATGCATCCTTATTGGGGCGGGTGAGTGAAGATTAGGAAAAAAAAAAAAAAAAAAACTGTGCCGAAATTCATTCAGTGACTTTTCTGTCTTTTGTGAGGCTGCATGTAGCCAATGAAACGAAAAGCTGAAGGAGGAACTCTGCAAATACGTTTTCTTAATGAGTGTTTTTGAATTGTTGTCTAGGTAAAATACACACAACATTCTGAAGATAAAGACAGACATTTTACAGCATAAATATGTATTATAATTGACAATCATTGGCAGATTAAATTTTTTTTTTCAGTGTAGCTTTACAATAATGATAATAATGAAATTTAAATGATAAATATTTAATATTATTGTTGTTGACGACAATGATAAAAAGAAATGACATCATAATGTTATTTAATTAAATCTTAATTAAATTTAATTTA
Associated Phenotype:
Not determined