ZMP
vps13a
Ensembl ID:
ZFIN ID:
Description:
vacuolar protein sorting 13 homolog A [Source:RefSeq peptide;Acc:NP_001112365]
Human Orthologue:
VPS13A
Human Description:
vacuolar protein sorting 13 homolog A (S. cerevisiae) [Source:HGNC Symbol;Acc:1908]
Mouse Orthologue:
Vps13a
Mouse Description:
vacuolar protein sorting 13A (yeast) Gene [Source:MGI Symbol;Acc:MGI:2444304]
Alleles
There are 17 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21398 | Nonsense | Available for shipment | Available now |
sa16081 | Essential Splice Site | Available for shipment | Available now |
sa731 | Essential Splice Site | Available for shipment | Available now |
sa21397 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21398
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009383 | None | None | 318 | None | 11 |
ENSDART00000108923 | Nonsense | 551 | 3217 | 18 | 71 |
ENSDART00000110359 | Nonsense | 551 | 3236 | 18 | 72 |
ENSDART00000111204 | Nonsense | 551 | 3194 | 18 | 73 |
Genomic Location (Zv9):
Chromosome 8 (position 54349177)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 52084536 |
GRCz11 | 8 | 52071065 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCGCTCAGCTGTCGTCGTTTGAAGTGTCCGGTCTCCCGCGGGAAAAGT[C/A]GGCCCCGATCCTGCTTTCTCCACGTCATGTGGACGGCATGAAGGATAAAA
Long Flanking Sequence:
ATTACAATTAATAAAATGACGGTAGATTATGTTTACTTTATGTACAATATATTACAGTTTAATATATTATTATATAATAAACTTGGCATTTCTCTGTGAAAACTGCACCGCCCCCAATTATTTTGATTACAATAATAAAAAAAAATGCTAAAATAATGAAATCTAAAAGCTTAAATAATAAACAGAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGGTATAATTAAAAGCTAATGGAATTTAAATTGGAAAAATTGAAAATTAAATTAGTAAACCTTTTTATGATGGTAAAGTAACCCTGTCGTAGAGAAAATTAACTTAATAGTGTTTTATGATTTTGATTATATGATTTAATGTTATTTATGTAATTGAAATATATTTTATTAAAGCAGTATTAATTTTGCTATTGTCCTGTCAGGATCTCCGCTCAGCTGTCGTCGTTTGAAGTGTCCGGTCTCCCGCGGGAAAAGT[C/A]GGCCCCGATCCTGCTTTCTCCACGTCATGTGGACGGCATGAAGGATAAAAGTCTGCTGAACCTCATGTTCGAGACCAACCCGCTGGACGCTCGTGCTGACCAGAGACTGCGCATCGAGTCCCAGCCGCTGGAGATCATCTATGATGCAGTGAGGCTCTGTGACAGTTAATATATTCTTCATATATTCCCAAAGGCCCGTTTACACCAAACATGATAACTCTAAGGCTCACGATAATGACGTAGTTGCTACTGATAATGACGTAGTTCTTAAAACAATATGATTGGGATCACTGTCAGATTTTATTCTAGGTTATAAACAATAAAAACCAGTCAGAATCCCTTTAAATCTTTATTTAAAGTTAAAATTTGAATGTAAAGTTAAAAAAGTCACAGTTTTTAAATAATAATTCCAGTGTTTATTAGAGTTAATGTGTTCTTTTAACCTTTAATCAAAATATCTTCCCCTCTCTCATCTATCTTTTCTCCTCCCTGATTGGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16081
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009383 | None | None | 318 | None | 11 |
ENSDART00000108923 | Essential Splice Site | 1142 | 3217 | 31 | 71 |
ENSDART00000110359 | Essential Splice Site | 1142 | 3236 | 31 | 72 |
ENSDART00000111204 | Essential Splice Site | 1131 | 3194 | 31 | 73 |
Genomic Location (Zv9):
Chromosome 8 (position 54333164)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 52068523 |
GRCz11 | 8 | 52055052 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAGAACATCATCATTCTGGATTGTGACAAAGAGGYACTTTATAAAAAG[G/A]TAGAAAATGCTATTTAGYATMTTAAATATAAATTAATCAACTGGTACACT
Long Flanking Sequence:
TTGTGTTTTTTCGGTCTAATTTTAAATCAAGTTATTGATTATTACAAAATTACTTTATTTTATTCAATAAAATCATAAATAATTATTACAAACCATTTTCAGTTTCGCTTTTTTGGCCAAGTGCATGCAGAATTTTCTGCCCAGAATGTTAATTTCACCGCATGCCTGATTCTCATATTATTGTTTTTTTTCTGCTCCAGCCTACAAGAAGTCAAAGTTTGAGGATGTGGTGAATTTGCACATCCGCGCAGACCTCAACTGTCTGAAGGTGTTCATACGAGGAGAGAAAGCCAGGATCTCTGAGATCAGCATAGAGGGTAATAGACACATCTGTAGATGCACTCAAACACAAAAAACCAGGGAGAGCTTCTAACACAGCATGTTAACTCCCATCAGGACTGGTTTCTGAAGTTCAGATGAAGAAGAAGTCTGTGGAGATTCTGGCTAACTTGAAGAACATCATCATTCTGGATTGTGACAAAGAGGCACTTTATAAAAAG[G/A]TAGAAAATGCTATTTAGCATATTAAATATAAATTAATCAACTGGTACACTTTTATAAACAGTTTTATAGAACACTTTTACAGTGTTTTGAAGATAATCAAAACCTTTTATCAAAGAAATGTTAAAACAACTGAACAGCACCCAGTATTATTACCCATTTTAGTGTAAATTATGTAAAGAAGTTTAATGTGCTTAAAACTCAGGGGTGCAATTATTATTAATAAAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATCAAAAAAGTACACTTGATTTATAAATATTTCTGCTCCCAACTTTATTTAATAATTATGGAATTATACATGCTTTCCAAATATCAATGTAAAGTCCAGATACACTTTATTTTGTACCCAAAATACAGATAATAACCAAAAAGAAATATGAATAAAAAAATCTATTTAATGTTAGACTTTTAATTTTAAACAAACTTGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa731
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009383 | None | None | 318 | None | 11 |
ENSDART00000108923 | None | 1576 | 3217 | 39 | 71 |
ENSDART00000110359 | None | 1576 | 3236 | 39 | 72 |
ENSDART00000111204 | Essential Splice Site | 1562 | 3194 | 41 | 73 |
Genomic Location (Zv9):
Chromosome 8 (position 54321231)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 52056590 |
GRCz11 | 8 | 52043119 |
KASP Assay ID:
554-0638.1 (used for ordering genotyping assays)
KASP Sequence:
ARTAGCTGTATGATTTGTGTTATTCCTCTTCTAGCGGCTCCTGCTCCACC[A/T]GTGGTTGCTAAAACCGAGATGAATGTGGTGGTGAAGAACCCAGAGATCGT
Long Flanking Sequence:
ACACATTCACACACACACTCATACACTACGGACAATTTAGCCTACCCAATTCACCTGTACCGCATGTCTTTGGACTGTGGGGGAAACGGAGCACCCGGAGGAAACCCACGCGAAGGCAGAGAGAACATGCAAACTCCACACAGAAACGCCAACTGAGCCGAGGTTTGAACCAGCGACCTTCTTGCTGTGAGGCGACAGCACTACCTTCTGCGCCACTGCTTCACCTTGCTATATTTATTATTATTATTATTATTTTATTATTATTATTATTATTATTATTATTATTATTATATTAAGGTAGGAGAATAAAATGAGTTTGTTATTTAAATAATAAAAAATTAAGTAAAAAGTCAAACCAGTTATTAATTATGAATTATATTACTTCACTATTATACAGTACTAGTGTTGTTTTTGTATTTATAGTAATGTTTAAATAACGTTGATAGCAATAATAGCTGTATGATTTGTGTTATTCCTCTTCTAGCGGCTCCTGCTCCACC[A/T]GTGGTTGCTAAAACCGAGATGAATGTGGTGGTGAAGAACCCAGAGATCGTGTTTGTGGCGGATCTGACGCGTGCTGAAGCTCCGGCTCTGGTCATGACCACTCAGTGTGAGCTGGTGATGAAGAGCGAGCCCAGCGGTCAGTGCATGACGGCCGCCATTTCAGACCTGAAGATTGTGGCCTGTCCGTTCCTGCGGGAGAAGAGGGAGAACAACGTGACGACGGTCCTACAGCCCTGCGAGGTTTTCTTCCAGAGCCGACAGTCAAACACTGAGCCGCAGTGCATCGAGCTGTCCATCAGCGCACTCACGCTCAAGGTGAAATCACCACTAACATAATCCTGCAGTTATGTAGTATACAGCTGATGCTTGTGTACATGTTCAATCAAGTGTATTAAGTGTATATAATACTGCTGTCCTCTTCAGATCTTAACCCTTGTGTACTGTTCAAATTGACTCCCCTTTCATTATGTTGCGGTCTGTTTTCGCCCTATTGACTGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21397
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009383 | None | None | 318 | None | 11 |
ENSDART00000108923 | Nonsense | 2268 | 3217 | 47 | 71 |
ENSDART00000110359 | Nonsense | 2260 | 3236 | 47 | 72 |
ENSDART00000111204 | Nonsense | 2246 | 3194 | 49 | 73 |
Genomic Location (Zv9):
Chromosome 8 (position 54307985)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 52043344 |
GRCz11 | 8 | 52029873 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACACTCGCCGTACTGGATGGTGAATAAAACAAGCCGACTGCTGCAGTA[C/A]AAGGCGGATGATATTCATCGCAAACACCCCAAGGATTACGACATGCCGCT
Long Flanking Sequence:
AATTGTCACCACTCACCAATCAGAATCTAATATCTCAGACATCTGTGAAATAATCTGCAGTAACAACAACCCTCTGGATGTGCTTTATTTATCCTTTACATACGTTTTTAATATTTGATTGTCATGAAATATTGTTAACTTCTGCATGTAACAGTCATTAACAGTATCTTGTTTTGTTGACAGGGCATCGGAGATTCCCCCTCGGTGTCGCTGAAGGAGGGCCACTCATCCCAGATCCACACCGCCATCATGGACTTCTCCGTGTTGGATCTGAGGCTGCTGGGATACTTGCAGCAGGACTGGGAGTCTCAGTACAGCCTCAGCAGTGAACAAGACGAGATCAGCTTCATTAAGTTTCGCTCGCTCGCACGTGAGGAGGAGACTGAGAGCCGGCCGGAGCTGGACATCGCTATGCATGTGAAGAAGGAGGAGGGTCAGGTTGTGCTGGCCGTACACTCGCCGTACTGGATGGTGAATAAAACAAGCCGACTGCTGCAGTA[C/A]AAGGCGGATGATATTCATCGCAAACACCCCAAGGATTACGACATGCCGCTGCTCTTCTCCTTCAAGCCACGCAACTTCCTGCAAAACAACAAGGTTTGGAAGAAAGTTTTGTTTTTTCTGTCTGGCTGACATTAGTGAGGGTTTTTTCTGGTTAACTTTTTTTTTGTTTGTTTATTAAACATTCAAATAATAGTAATAATAATAGTACAAATAATAAATTAAAATAAATTGTTTAATTGTTAAATTCCGGCTGACAGGTTCTTCCTGATTTATCGCTTTTTTTATTTTTTTAAACCTTCAAATAATAGCCAGACATTATCATATTGCATTGTTAAACATATTTAACACTATATCCAACCGGAATATTACAAACAAAATAAACAAATAATAAAGTTAAATAAAACTTTTATTATTATATATAAACAAAGTAGTAAAATAATTATTTAAAATAAATAAAAGAAACATTTTCAAGCAGAATATTCAAAACAATTTAGTGAATA
Associated Phenotype:
Not determined