Busch Lab

ZMP

GOLGA4

Ensembl ID:
ENSDARG00000075331
Description:
golgin A4 [Source:HGNC Symbol;Acc:4427]
Human Orthologue:
GOLGA4
Human Description:
golgin A4 [Source:HGNC Symbol;Acc:4427]
Mouse Orthologue:
Golga4
Mouse Description:
golgi autoantigen, golgin subfamily a, 4 Gene [Source:MGI Symbol;Acc:MGI:1859646]

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa13806 Essential Splice Site Available for shipment Available now
sa44796 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa24947 Nonsense Mutation detected in F1 DNA Not yet available
sa10793 Nonsense Available for shipment Available now
sa42302 Nonsense Mutation detected in F1 DNA Not yet available
sa38974 Nonsense Mutation detected in F1 DNA Not yet available
sa14408 Nonsense Available for shipment Available now
sa35592 Nonsense Mutation detected in F1 DNA Not yet available
sa22381 Nonsense Available for shipment Available now
sa15392 Nonsense Available for shipment Available now
sa13611 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa13806
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109469 Essential Splice Site 355 2037 9 18
Genomic Location (Zv9):
Chromosome 13 (position 49099762)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 47838144
GRCz11 13 48129174
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTACAGCAGCAGCTGCAGGAGAGACTGCAGGAGCTGGAGAAGATGAAGG[T/C]ACACAAACATCAACYATYACAAKACATGGAGAACAGTGCTGTRGAGCTTT
Long Flanking Sequence:
TGAGGATTAGCAGGCTAGTGCAGAAACTCTATTTAAAATACTGAGGTAAAATAAATTTTCATATTTTAAAGACATGGCTTGGAAAAATGGAGCTTATTGCAGTGCTTCTTGTCTAGTCTGAGACCCACTTTATATTGTATCTCAATCAGGCAGTGAAGGTCACTGATTTTTAAAGAAATCAGATCATGGAGATTTTGTAATGCTGGGAGTGCTTGACTAAAAATTAAACGTCTGTGTGAATATTCACCTTTGCAATTTCCCAACCCCTAGTTGACAGAAGTGCTGTGTGTGCATGTGTCCAACAGAGGGCAGTGTTGACTCGGGCAGCGCTGTGGATGTGGAGAGTCTCCAGAAGCGGGTCACAAGGCAGGAGTCTCTCCTCCAGAGGTGTAAAGAGATGATTCGCAGCAGTAAAGAGCGCTCCGCTCAGCTGAGCAGTGAGAGCGAGGTCTTACAGCAGCAGCTGCAGGAGAGACTGCAGGAGCTGGAGAAGATGAAGG[T/C]ACACAAACATCAACTATTACAAGACATGGAGAACAGTGCTGTGGAGCTTTCCTTTTATTTACATCTTACACATGCATATTTTATACATGATTTTTTATTTATACATGCACAGCTCTTTAGGTATTATGTACATTTTTTTAGTATTTTAATTTTTTTTTTAAAGTTTAAAACTCGCAGTGTGATTTTTACAGATTTTTATAACTTTTTAATTGTATTATTTTTTTCATTTGCAGTTTTTTTAATTATATACAAAAATTTTAAGCTAATTTATTTTAATGTATTTTTATTACATTTTTAGTATTTAGTTTAATTTTTTTCATGCATGGTATATTTTATTCTATATTTTATTTAACGTTTTTAAATTTTAACTTTTTATTTTTAATATCTACCTCTGTTTTGTGCTTAGCATTGTGCATGGCTTCAGCATCTGCTTTTCTGGGTGTGTGAACAGTCAGAGCAGAGGTTAACAGCTGACCTCAAATACACATTACTCCCCCTCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44796
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109469 Essential Splice Site 383 2037 10 18
Genomic Location (Zv9):
Chromosome 13 (position 49093424)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 47831806
GRCz11 13 48122836
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAGCTCGGAGACGCCAAAAACCTGATCGAGCAGCTGGAGCAGGACAAG[G/T]TGAGCGAGACGCTTCATTTCTCCTATCTGAAGGCTTCAGCTGTGCTCTGC
Long Flanking Sequence:
GACCCTAATATAAAAAAATGTCTGTTTTATGACCTCACCTGATGTAAATCTGCAGTAGGGGTCTCCAAAATAAATGTAGGACCTTTAAAATGTTACAACAAGGGAAGTTCTTGAGCACACCACAGCTTAAATACAATTTATGTGTTAACTTGTAGAGTAGTAGCTGATAAAAGTTTGTGTAGCCTGACTTATTGGATGCACAAAATTTCCCTTGACGTTCAAACAAACCATTTTTCCATATCCAGAGTTTCAGGTCAGTTCGTTTCCAGCTGGCCGGTGGGTTTTCATGCATCTCTAATCCTGCTCGTCTAGACCAGCTGACTCTGGAGTCTTCATGACAGACGCTCAATAAGTGTTGATTATTATTATACTAAGAATGATGTATTAAAATCCATGGTCATCTGTGTGTTTACCAGGAACTCCACACAACGGAGAAGACCAAGCTGATCACACAGCTCGGAGACGCCAAAAACCTGATCGAGCAGCTGGAGCAGGACAAG[G/T]TGAGCGAGACGCTTCATTTCTCCTATCTGAAGGCTTCAGCTGTGCTCTGCGGCGGCCACATGAATGCTTACGAGAGGAAAACAAATTCCTCTGGACAGAGATGAATTATAGCGGAAAGACTTTTTGAAAGCAATTGGAAAACAGGTTTTCTTTTGGGTCGCTCACTTTGACATGTTGGCTTATAAAAGTAAGCTTGTGGATATTGTCTTGCTTTTTTATTTTTGGAGATCAGGCAAGATCCAAAAAGAACTTTGTTTATGCTGTGAAATTTAAAGCATCGTAGTGTTCCACCAGAGACTATATACAGCCATATCGCGGTGCTACTCGTGTGATATGAACGTATGAGATGAAAGTGCGATTCAAAGACTTAATAAGGGTAATTAGGCAAGTCATTGTATAACAGTAGTTTCTTCTGCAGACAATCAAAAATATATTGCTAAAGGGGGCTAATAATATTGACCTTAAAATAGGTTTCAAAATATTTAAACCTGCTTTTATTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24947
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
ENSDART00000109469 Nonsense 791 2037 15 18
Genomic Location (Zv9):
Chromosome 13 (position 49079040)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 47817422
GRCz11 13 48108452
KASP Assay ID:
554-7353.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGGAAAAGTCTTTGCTGGAAGATGGAAGTGCGCAATTGGAGGAACTTT[G/A]GCTCAGGGCACAGTTAAATAAAGAGGCACTTGAGGAATCAAGATCACAGG
Long Flanking Sequence:
AGTGTCAGAGCAGATAACAGCTCTCAGACAGGAGCATGATGTCGCTATGGAAGAGCTCATTCACAAACATAAAGCAGAGATTGAATCCATTCTGAAAGACAAGGAGGAGCAGTTCCATTCTCATGTAGAAGACATGAACAAAAAGATACTTGATAAATTGAGTGATAAACAGACTGAGCTTGAGACTGTGTCTGCTGAACTCAGTGAGTTATTGAATAGTAAACAACAGTTAGAAGATAGATTGTCCTCTGTGGAGGCCACCAGTGAAACCTTAAGACAAGAGTTTGAGGAAAGGATCAAGAAAGAGCAAGCAAAACATCAGGCTGAGATTGAGGCTGCTAATAAAAATGAACAGTCATTTGCAGGAGTGGAGAAGATGCTGAAAGAAGAGATAAATCATCTGAAGATTGCGCTGGAGGAGAAGGAAAAAGTATTAGAGGAACATGTGCTCAGGGAAAAGTCTTTGCTGGAAGATGGAAGTGCGCAATTGGAGGAACTTT[G/A]GCTCAGGGCACAGTTAAATAAAGAGGCACTTGAGGAATCAAGATCACAGGTTAGCACACTTACAGATGAACTCCAACAAGCCAGGGATCAAGTAAAAAATCTTGAGGAAACCCTTGAGGCAGTGCGTAATGACTGTAAGGAGAAAGAAGTGTGTCTTGAAGAAAAGACAAATGAACTTCAGGAACTAGTTCAGAAGATTGAGCATATCAAGAAAGATCTATCTGAGAAAGAGAATTTGCATGCTGCAACTTGTAAAACATTGCAAGAGGAGCAAAACCGGTTGAGGAAGCAGCTAGATGACCAGAAGAGTTCTCAAGAGAAGAAACTTGAGAATATTAGAAAAGACATGGATTGCAAGCTGAAATCCCAGGAAAACAAACTGGAGAAATTCAAGCAGAAAGCCAAAGAAGCACAGGATAAGATGAAGAAGAAGCTTCAGGATCAGGAAGAGAGTGCAAAAGTGGAGTTATCAAAGAAGATTCAAGAGTTGGAACTGAAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10793
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109469 Nonsense 878 2037 15 18
Genomic Location (Zv9):
Chromosome 13 (position 49078779)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 47817161
GRCz11 13 48108191
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAAGATCTATCTGAGAAAGAGAATTTGCATGCTGCAACTTGTAAAACAT[T/A]GCAAGAGGAGCAAAACCGGTTGAGGAAGCAGCTAGATGACCAGAAGAGTT
Long Flanking Sequence:
CAGTGAAACCTTAAGACAAGAGTTTGAGGAAAGGATCAAGAAAGAGCAAGCAAAACATCAGGCTGAGATTGAGGCTGCTAATAAAAATGAACAGTCATTTGCAGGAGTGGAGAAGATGCTGAAAGAAGAGATAAATCATCTGAAGATTGCGCTGGAGGAGAAGGAAAAAGTATTAGAGGAACATGTGCTCAGGGAAAAGTCTTTGCTGGAAGATGGAAGTGCGCAATTGGAGGAACTTTGGCTCAGGGCACAGTTAAATAAAGAGGCACTTGAGGAATCAAGATCACAGGTTAGCACACTTACAGATGAACTCCAACAAGCCAGGGATCAAGTAAAAAATCTTGAGGAAACCCTTGAGGCAGTGCGTAATGACTGTAAGGAGAAAGAAGTGTGTCTTGAAGAAAAGACAAATGAACTTCAGGAACTAGTTCAGAAGATTGAGCATATCAAGAAAGATCTATCTGAGAAAGAGAATTTGCATGCTGCAACTTGTAAAACAT[T/A]GCAAGAGGAGCAAAACCGGTTGAGGAAGCAGCTAGATGACCAGAAGAGTTCTCAAGAGAAGAAACTTGAGAATATTAGAAAAGACATGGATTGCAAGCTGAAATCCCAGGAAAACAAACTGGAGAAATTCAAGCAGAAAGCCAAAGAAGCACAGGATAAGATGAAGAAGAAGCTTCAGGATCAGGAAGAGAGTGCAAAAGTGGAGTTATCAAAGAAGATTCAAGAGTTGGAACTGAAAGACCAGCAGCTAAAGGAGAAGATCCTTGAGATGGCACAAACAAGTTCTGAGGGCCTCAGCACTGCCATGTCTGATTTGGAGGCCAATCACAAGGAGCACTTAGACAAGCTTCAGGTGAACCATAAACAAGAGCTAGAAGACCTTGTTCGTCATTGGCAGGAGAAACTCAACCAGAATGAAGAGGAGATGCAAGAAAAGCATAGTCAAACTTTGCAAGATAAAGCCCAGGAGTTGGAGGAGATCTCACGTTTGCTTTCATCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42302
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
ENSDART00000109469 Nonsense 882 2037 15 18
Genomic Location (Zv9):
Chromosome 13 (position 49078768)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 47817150
GRCz11 13 48108180
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAGAAAGAGAATTTGCATGCTGCAACTTGTAAAACATTGCAAGAGGAG[C/T]AAAACCGGTTGAGGAAGCAGCTAGATGACCAGAAGAGTTCTCAAGAGAAG
Long Flanking Sequence:
TAAGACAAGAGTTTGAGGAAAGGATCAAGAAAGAGCAAGCAAAACATCAGGCTGAGATTGAGGCTGCTAATAAAAATGAACAGTCATTTGCAGGAGTGGAGAAGATGCTGAAAGAAGAGATAAATCATCTGAAGATTGCGCTGGAGGAGAAGGAAAAAGTATTAGAGGAACATGTGCTCAGGGAAAAGTCTTTGCTGGAAGATGGAAGTGCGCAATTGGAGGAACTTTGGCTCAGGGCACAGTTAAATAAAGAGGCACTTGAGGAATCAAGATCACAGGTTAGCACACTTACAGATGAACTCCAACAAGCCAGGGATCAAGTAAAAAATCTTGAGGAAACCCTTGAGGCAGTGCGTAATGACTGTAAGGAGAAAGAAGTGTGTCTTGAAGAAAAGACAAATGAACTTCAGGAACTAGTTCAGAAGATTGAGCATATCAAGAAAGATCTATCTGAGAAAGAGAATTTGCATGCTGCAACTTGTAAAACATTGCAAGAGGAG[C/T]AAAACCGGTTGAGGAAGCAGCTAGATGACCAGAAGAGTTCTCAAGAGAAGAAACTTGAGAATATTAGAAAAGACATGGATTGCAAGCTGAAATCCCAGGAAAACAAACTGGAGAAATTCAAGCAGAAAGCCAAAGAAGCACAGGATAAGATGAAGAAGAAGCTTCAGGATCAGGAAGAGAGTGCAAAAGTGGAGTTATCAAAGAAGATTCAAGAGTTGGAACTGAAAGACCAGCAGCTAAAGGAGAAGATCCTTGAGATGGCACAAACAAGTTCTGAGGGCCTCAGCACTGCCATGTCTGATTTGGAGGCCAATCACAAGGAGCACTTAGACAAGCTTCAGGTGAACCATAAACAAGAGCTAGAAGACCTTGTTCGTCATTGGCAGGAGAAACTCAACCAGAATGAAGAGGAGATGCAAGAAAAGCATAGTCAAACTTTGCAAGATAAAGCCCAGGAGTTGGAGGAGATCTCACGTTTGCTTTCATCCAGCAAAGAAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38974
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
ENSDART00000109469 Nonsense 1282 2037 15 18
Genomic Location (Zv9):
Chromosome 13 (position 49077568)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 47815950
GRCz11 13 48106980
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACTCTGCAGTTTGGGGAAAGTTCAGAGACTCTTAAAGCCTTACAAACT[G/T]AACGGGAATCTCTGCAAACTGATGCAGAGAGTCGCTTCCAGGTACTTTCT
Long Flanking Sequence:
TGCAGGATGAACTGAGAAAGGTTGAGGAAACTAGTAAAGAGAAACTGCAGGCCATATCTGAAGAGTTAGTAAACACTCAGCAAAAAATAAGCTTGCTTGAAACTTCCAAGTGTAAAGAGGGTGAACATCTCCAGAGGACACTTGCAGAAAAAACTGCTGAGCTCCAAAATAAAGAAAAAGAGTTCCAGGCACAATTGTGTTCCCTCACAATGGAGTTTAAGCAGTGTTGTCAGGAAGCCCAAGCTAAGATAGATGGTTTTTCTGTTGAGCTGTGTAAGAAAGTTGATGAACGAGTTGGGGCGTTACAACTCCGGGTAATAGATCACCAAAATAAGGTTGCATATCTAAGAAATATTATCAAGACGAAGGACAACAGAATCAGCACTTTAGAGAAAGAACTTCAGCACACTTTGGATGTGAATCATAATCTAAAGAGCTCTCTTGATGAGATTACTCTGCAGTTTGGGGAAAGTTCAGAGACTCTTAAAGCCTTACAAACT[G/T]AACGGGAATCTCTGCAAACTGATGCAGAGAGTCGCTTCCAGGTACTTTCTGAGAAAGACCTTCACATTAAGCAGCTATGTGAAGAAAAACAAAACGTATCAGAAAATCTCAAAGCAAATATTTTGCAAATCAGCGATCTAGAATCTGCAATAAATGACTTGAAGACCCAGTTAGCAAGTAGCATAACTGAGAAAGAGGAAGCCATATCTCTGCTGAATCAGCAACACAGTAAGGACAAAGAGAGGGTGACGTCCCAAATGGGGGAAACTGTAGAAAAGCTAGAAAAAGAGAAGACCTTGCTTCAAGAGCAGGTAGACTCACTCAGGAATAAGTTCTCTGAGCTGAAAAAGAAGTTCAGTCAGAGTCACAGCACTGTTAAATCTCTTCAAGATAAACTTGCAGACATGGAGAGGCAAATTGCAGAGAAGGATGGACAGCTTCAGACGCTCACTGCCAGCGTTGACAATCACTCCATTAGTAAGTCCGAGATGGACCAGGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14408
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
ENSDART00000109469 Nonsense 1427 2037 15 18
Genomic Location (Zv9):
Chromosome 13 (position 49077133)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 47815515
GRCz11 13 48106545
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAAGATAAACTTGCAGACATGGAGAGGCAAATTGCWGAGAAGGATGRA[C/T]AGCTTCAGAYGCTCACTGCCAGCGTTGACAATCACTCCATTAGTAAGTCC
Long Flanking Sequence:
GCTCTCTTGATGAGATTACTCTGCAGTTTGGGGAAAGTTCAGAGACTCTTAAAGCCTTACAAACTGAACGGGAATCTCTGCAAACTGATGCAGAGAGTCGCTTCCAGGTACTTTCTGAGAAAGACCTTCACATTAAGCAGCTATGTGAAGAAAAACAAAACGTATCAGAAAATCTCAAAGCAAATATTTTGCAAATCAGCGATCTAGAATCTGCAATAAATGACTTGAAGACCCAGTTAGCAAGTAGCATAACTGAGAAAGAGGAAGCCATATCTCTGCTGAATCAGCAACACAGTAAGGACAAAGAGAGGGTGACGTCCCAAATGGGGGAAACTGTAGAAAAGCTAGAAAAAGAGAAGACCTTGCTTCAAGAGCAGGTAGACTCACTCAGGAATAAGTTCTCTGAGCTGAAAAAGAAGTTCAGTCAGAGTCACAGCACTGTTAAATCTCTTCAAGATAAACTTGCAGACATGGAGAGGCAAATTGCAGAGAAGGATGGA[C/T]AGCTTCAGACGCTCACTGCCAGCGTTGACAATCACTCCATTAGTAAGTCCGAGATGGACCAGGCTCTTAGTGAGAAAGATCAGAGAGTTCATGCCTTGACCTCAGAGCTGGAAAGTTGCTCAAAGAAAGTTTGTGATTTGGAGGAGCAGTTACAGTTAAGGGTAAAAGAACGGGATCAGCTTGCAGCTGATTTGCAGCAGCATCATAACATAAGGGAGAGTGAAAAGACAGAGTTGATGAAACAGGTGCAGGAAGCTCAGGACCAAAGCTCTCAAAACGGTGCCCTAATGCAAAAAACTGAGGAAAGTCTTCAGTCTTTGAGGAAAGATATTGAATCAGCCAAGCAGGAGCTGGAATCCCAGAGGAAGGATTTCGAGAGGGAGAAGGCTGAGATTCTTAAAGAGAAAAAGGAGGCTGTAAAAGCTGCCCAGGTAAAGGCATCCTCTGAGACTGGTGTTAAAGTGGCTGAGTTGAAGAAAAAGGCAGAGCAGAAGATTGGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35592
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
ENSDART00000109469 Nonsense 1515 2037 15 18
Genomic Location (Zv9):
Chromosome 13 (position 49076869)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 47815251
GRCz11 13 48106281
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAGAGTGAAAAGACAGAGTTGATGAAACAGGTGCAGGAAGCTCAGGAC[C/T]AAAGCTCTCAAAACGGTGCCCTAATGCAAAAAACTGAGGAAAGTCTTCAG
Long Flanking Sequence:
AAGCCATATCTCTGCTGAATCAGCAACACAGTAAGGACAAAGAGAGGGTGACGTCCCAAATGGGGGAAACTGTAGAAAAGCTAGAAAAAGAGAAGACCTTGCTTCAAGAGCAGGTAGACTCACTCAGGAATAAGTTCTCTGAGCTGAAAAAGAAGTTCAGTCAGAGTCACAGCACTGTTAAATCTCTTCAAGATAAACTTGCAGACATGGAGAGGCAAATTGCAGAGAAGGATGGACAGCTTCAGACGCTCACTGCCAGCGTTGACAATCACTCCATTAGTAAGTCCGAGATGGACCAGGCTCTTAGTGAGAAAGATCAGAGAGTTCATGCCTTGACCTCAGAGCTGGAAAGTTGCTCAAAGAAAGTTTGTGATTTGGAGGAGCAGTTACAGTTAAGGGTAAAAGAACGGGATCAGCTTGCAGCTGATTTGCAGCAGCATCATAACATAAGGGAGAGTGAAAAGACAGAGTTGATGAAACAGGTGCAGGAAGCTCAGGAC[C/T]AAAGCTCTCAAAACGGTGCCCTAATGCAAAAAACTGAGGAAAGTCTTCAGTCTTTGAGGAAAGATATTGAATCAGCCAAGCAGGAGCTGGAATCCCAGAGGAAGGATTTCGAGAGGGAGAAGGCTGAGATTCTTAAAGAGAAAAAGGAGGCTGTAAAAGCTGCCCAGGTAAAGGCATCCTCTGAGACTGGTGTTAAAGTGGCTGAGTTGAAGAAAAAGGCAGAGCAGAAGATTGGCATGATTCGTAAACAATTGACTTCACAAATTGAGGAGAAGGAGCAGGTCATCAAAGACCTGCATGTGCAGTTGGAAACTATCAAGCAATCCCAGATTGAAAAAGAAGAACATATAAAATCACTCGAGAAAACGATGCAAGAAACCACTGCGAAATTAAATGAGGACCACGCAAAGCATCTACAAGAATTGCAGGAGAAGGAGAAAGATGAAAGACTGACCTCTTTGCAAAATTTACAAGAAATGTACGAGGAGAAGCTTGCTTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22381
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
ENSDART00000109469 Nonsense 1735 2037 15 18
Genomic Location (Zv9):
Chromosome 13 (position 49076209)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 47814591
GRCz11 13 48105621
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGCCAACTACCAAAATGAGGTGAGTCGCCTTAAAGAAGATCTGATTGAA[C/T]AGACATCTAGAGTGCAAGAGCTTCAACAGACATGCTCTGATCTTCGAGAA
Long Flanking Sequence:
CTGCCCAGGTAAAGGCATCCTCTGAGACTGGTGTTAAAGTGGCTGAGTTGAAGAAAAAGGCAGAGCAGAAGATTGGCATGATTCGTAAACAATTGACTTCACAAATTGAGGAGAAGGAGCAGGTCATCAAAGACCTGCATGTGCAGTTGGAAACTATCAAGCAATCCCAGATTGAAAAAGAAGAACATATAAAATCACTCGAGAAAACGATGCAAGAAACCACTGCGAAATTAAATGAGGACCACGCAAAGCATCTACAAGAATTGCAGGAGAAGGAGAAAGATGAAAGACTGACCTCTTTGCAAAATTTACAAGAAATGTACGAGGAGAAGCTTGCTTGTCTTCATAAAGACATATCTGCGAAGGAGGAGCACTCTGCTGCTGCTGCTAGAGAAACGTCTTCAAGACTTGTAGATCTTGAGACCAAACTCTCAGAATCTAATGAGCAGATCGCCAACTACCAAAATGAGGTGAGTCGCCTTAAAGAAGATCTGATTGAA[C/T]AGACATCTAGAGTGCAAGAGCTTCAACAGACATGCTCTGATCTTCGAGAACAGATTAAGCAGAAACAGATTGATGAAGTTGAGAGGGAACAGGTTTGTGAGGTGCAAATAAACAGTAATAGGTTAGGAATGGAGCCTGCAATGTTAGTAGCAAAGGAAAACATGGACACTGTTGGGAACCAGGATGACTGGTTGAGTCAAAAGAATTTATTGGTGAAAGAATACGAAGAGAAGCTGCTAGATTTACAGCAGAGGCTAGAAGATAAAGAAAACGAGTTAAAAGCACAACAAAGTTCGCCTCAAAGAAACGGGGAGAGTGATGGGGAGTGCCTAATCAACAATACAAACACCTCAGAGAATGATCTTCAGAGAAAGCTGGTGGAAGCCGAGAATGAAAAGCAGAAGATCCACAAAGATTATAGCAGACTGCAAAAAGATCTCCGTTCTCTAAGGAAAGAGCATGAGAAGGAGTTGGAGTTCCTGAAAAAAGAGATGGCTGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15392
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
ENSDART00000109469 Nonsense 1757 2037 15 18
Genomic Location (Zv9):
Chromosome 13 (position 49076143)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 47814525
GRCz11 13 48105555
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AARAGCTTCAACAGACATGCTCTGAKCTTSGAGAACAGATTAAGCAGAAA[C/T]AGATTGATGAARTTGAGAGGGAACAGGTTTGTGARGTGCAAATAAACAGT
Long Flanking Sequence:
AGAAGATTGGCATGATTCGTAAACAATTGACTTCACAAATTGAGGAGAAGGAGCAGGTCATCAAAGACCTGCATGTGCAGTTGGAAACTATCAAGCAATCCCAGATTGAAAAAGAAGAACATATAAAATCACTCGAGAAAACGATGCAAGAAACCACTGCGAAATTAAATGAGGACCACGCAAAGCATCTACAAGAATTGCAGGAGAAGGAGAAAGATGAAAGACTGACCTCTTTGCAAAATTTACAAGAAATGTACGAGGAGAAGCTTGCTTGTCTTCATAAAGACATATCTGCGAAGGAGGAGCACTCTGCTGCTGCTGCTAGAGAAACGTCTTCAAGACTTGTAGATCTTGAGACCAAACTCTCAGAATCTAATGAGCAGATCGCCAACTACCAAAATGAGGTGAGTCGCCTTAAAGAAGATCTGATTGAACAGACATCTAGAGTGCAAGAGCTTCAACAGACATGCTCTGATCTTCGAGAACAGATTAAGCAGAAA[C/T]AGATTGATGAAGTTGAGAGGGAACAGGTTTGTGAGGTGCAAATAAACAGTAATAGGTTAGGAATGGAGCCTGCAATGTTAGTAGCAAAGGAAAACATGGACACTGTTGGGAACCAGGATGACTGGTTGAGTCAAAAGAATTTATTGGTGAAAGAATACGAAGAGAAGCTGCTAGATTTACAGCAGAGGCTAGAAGATAAAGAAAACGAGTTAAAAGCACAACAAAGTTCGCCTCAAAGAAACGGGGAGAGTGATGGGGAGTGCCTAATCAACAATACAAACACCTCAGAGAATGATCTTCAGAGAAAGCTGGTGGAAGCCGAGAATGAAAAGCAGAAGATCCACAAAGATTATAGCAGACTGCAAAAAGATCTCCGTTCTCTAAGGAAAGAGCATGAGAAGGAGTTGGAGTTCCTGAAAAAAGAGATGGCTGAGGAAAATGAGAAGAAGCTCAAGTAAGATTTATGTGACTTTTTTTTCTCTTTCATTTTAGAAACAGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13611
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
ENSDART00000109469 Nonsense 1963 2037 17 18
Genomic Location (Zv9):
Chromosome 13 (position 49071758)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 47810140
GRCz11 13 48101170
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCACGCAGAGAAAGCTCAGTGTGTTGAAACGGAGCTTATAGAAAGCCAT[C/T]GAGATGAAGTCAGTCAGCTTCAGAAAATAATCTCTCAGAAGGAAGAAGAC
Long Flanking Sequence:
TGCTTTGACACAGTCTACATTGTAAAAGCGCTATACAAATAAAGCTGAATTAAATTGAATTGAATATTAAAATGAGCATTATGAACACTCTGCTTGTCTTCTTTTGTGTTTCACACATTAATAACCGTATGAATTTCTTTCGTTTGTGGAAGTACAAGAGTTTACAATCTTGAATGAAGTATTCCTTTGAGTAAAATTTAAAAAAAATCTTGTTAAAGATACCGAATAAAATCTTGGAAAGCATTGTTGACATGAACAAAAAACGTTTTCATAGTTGGTCTCATTTTCTGATTTACTGACCTTCAGGAAATGTGAGAGATGGAATTCATAACTGATTCACCATGTGTTTTCAATCCTGCCATGTTTTCCTTTCAGTCTGGAAATGAGTGTTGTACACTCACTTTATGGTGACCTTCATGTCTTCTTACTGTACTTTTTTTGTTTGTTATATCCACGCAGAGAAAGCTCAGTGTGTTGAAACGGAGCTTATAGAAAGCCAT[C/T]GAGATGAAGTCAGTCAGCTTCAGAAAATAATCTCTCAGAAGGAAGAAGACCTAAACAGAACGGTTCAACGCTACGAGCAGGTCCTTCAGGTACAGCCAAATAAAGTGAAACCGTAGCTTTGTGTTTAACTGTGAGATACCTGATAAATGGCTAGCAGATGCTTCAGATAATACAACTTTATAGAAAGACATTGGCACTAGAGGAATTCTCTGAGGAGTTTATTGCCTTTTGCTTAATTCCAGCACATAGTCTGTAAGTTCAAGTTTCAGCTAATAGTTTGTTTATCATCAGGAAACACTTACCTCAGTCACCTAGCACCTCAAACCCCTCCGAGAGCTGTAGTGAATGATACAGACCGTATGCTGATGCTTACATCCAGCCTGATAGAGAAGCACACTAACTATTTGTCATAGGATTATTTCCGCATTCTCTAGATCTAATTGTTTACCTGTGCATTTTATGACCCAAGTTTATTAGCTGAAAATGAACTAGTATGGCAG
Associated Phenotype:
Not determined