ZMP
vac14
Ensembl ID:
ZFIN ID:
Description:
Protein VAC14 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q66L58]
Human Orthologue:
VAC14
Human Description:
Vac14 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:25507]
Mouse Orthologue:
Vac14
Mouse Description:
Vac14 homolog (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:2157980]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38043 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa8773 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38043
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000009767 | Essential Splice Site | 198 | 771 | 5 | 19 |
The following transcripts of ENSDARG00000014303 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 25 (position 17955298)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 17499162 |
| GRCz11 | 25 | 17595562 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGGATTTACTCCAATAACCAATATGCTCGTCAATTCATTATCTCCTGG[G/A]TGAGTTGAGCACTTTCACCTGTCTGCAACATTCAAAGTCAGTATGGCATT
Long Flanking Sequence:
AAATAAACATTTAAAATGAAATGATAAAATAAAGGCCATTAATAAAATATTAAATACTATTACATACATTTTAAAAGAACAGATAAAATGTTTTATGTGTTCATTTTTAAGACAATTGTACATTAGTAAAATGATGCAGAAAAACAGCAGGCAACATTATTAATGTGTTATTGATAATTAAAATTTCATACATTCCAATGGAGGTCCACATTTATCCCTATTATAACTTATTATGACCCAATCTGCTCTTTATAGCTTGCAGCAGATCCTGATCCCAATGTAAAGAGTGGCTCTGAGCTCCTTGACCGCCTGCTTAAGGTGAGTTTGACTAAAAACAAGAATGTACTAAATGACATAATGGCATCCTTTGACTTTGATTCGTGTTTTTTAAGGACATCGTAACAGAGAGCAACAAGTTTGACCTGGTGGCTTTTGTCCCCCTGTTGCGTGAGAGGATTTACTCCAATAACCAATATGCTCGTCAATTCATTATCTCCTGG[G/A]TGAGTTGAGCACTTTCACCTGTCTGCAACATTCAAAGTCAGTATGGCATTAAAGTTGTGAGACACTTTTCTTCACAGTGTGAAGTAAATGGCTTCTTAAGTAAGAATAAAATATGCCCCATTCACGAGGGGCTTCAGCGTCAACACTTGTCTCAAGTTGAGGCTGACGTGATCGTCATAGCAGTGTTAGCCAATGAAATTAGTCAGCAATAGGCCACAGTCTGAGCTGGTGTATTTGCATACAGCGATCTGATTGGCTGATGCTTCCGTCGCCGCTTGAAAAGTTGAGCAAGTCCCAACTTTTGCAGCGAGCAATGCCTCTGAAGCGGCGCCGACGGATCCACAATGCAGTTCGGCAACGCCTGACGTCACCCATTTAAAGTGAATGGGCAGCGTTGACTCTGACGCCCCTTGTGAAAAAGGCTTTATGGGTCAGTGATGCTAACATTTGGCACAAATCTATGAGTTTCGCCTTTTTGGCTGTCCTTTCTATGAATGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8773
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000009767 | Essential Splice Site | 322 | 771 | 8 | 19 |
The following transcripts of ENSDARG00000014303 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 25 (position 17957764)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 17501628 |
| GRCz11 | 25 | 17598028 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATTGACAGCAGTGCTGCCTTGCCTGTCCTACGATGACCGCAAAAAGAG[T/A]ATCCTACACTGCCGTACACTCTCAATGATGCATTTMMAAGTGTTTAAGAA
Long Flanking Sequence:
AATTCTTTTCCAGTTGGCTAAATATTAATTTAATAGTCCTTCAAACATCTTTACCGAAGCCTCTCAATTTGACAGTTACTCTCGCACATCCACCACGTTTCTAGTTACACTCTTTACTCTTTACGTTTCTACATTACACTTTTTACTTGAGATTGTAGTTCTAATCGAATTAATTTCCAACATGCAAAGTATTACAATTTTACACAAATTTTTACTATAAATAGTAGACCATCCAGGAACCTTTGGCATACCCTTTTCAACATACTACAGTTTGGGACATGCTAATTCTATTTTCGAATATTTAGGACAGGTAATATGTGAATTAGGATGCAGTAATTGTCTTGTGTTTGTCTTTCTACAGCTAACGATCTTATCCAGCTGACGTCTATGACATGGATGAGAGAGTTTATTCAGCTTGCTGGGAGAGTTGTGCTGCCATATTCTTCTGGCATATTGACAGCAGTGCTGCCTTGCCTGTCCTACGATGACCGCAAAAAGAG[T/A]ATCCTACACTGCCGTACACTCTCAATGATGCATTTCAAAGTGTTTAAGAACATGACATTTTTATCAGTTAAGCCCTGCTTACTATGTGCAATTTTTATTTTCAGCTGTTCTTTTAAATTGAGAAAGATTTTGGTCGCACTTTACAATAAGAATATTCATTAGAATATCTTGGTTACTATATAATGAACAACAAATTGTACAGCATTTAATAAATAGTTATTGACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATCCACATGTTTATATCTTTGGCAGTTTTGGGGCTCTTGTTGTGGTTCTGTTGTCACCATTTAAATCAATTTCCTTAATAAATCACCTTCAGGTACTAAAGAAGCAGCCAGTGCGTGTAACCACAGCCTGATGAAGCTTGTGACTCCAGAGGATGATGAAGATGATGAAGAATCACAGACAAAATCTTC
Associated Phenotype:
Not determined