ZMP
zgc:195245
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC565483 [Source:RefSeq peptide;Acc:NP_001119894]
Human Orthologue:
FAM107A
Human Description:
family with sequence similarity 107, member A [Source:HGNC Symbol;Acc:30827]
Mouse Orthologue:
Fam107a
Mouse Description:
family with sequence similarity 107, member A Gene [Source:MGI Symbol;Acc:MGI:3041256]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa13586 | Essential Splice Site | Available for shipment | Available now |
| sa45322 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13586
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 |
|---|---|---|---|---|---|
| ENSDART00000112611 | Essential Splice Site | 47 | 187 | 1 | 5 |
| ENSDART00000145179 | Essential Splice Site | 16 | 145 | 1 | 5 |
| ENSDART00000145894 | Essential Splice Site | 16 | 156 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 24633213)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 23759031 |
| GRCz11 | 8 | 23780270 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAATGCTGGACCTGAGCACRACGAAGAAACAATCATCTGTGTGCATTGAG[G/A]TGAGTGTTATTATGATTAGAGAATGATCGTGTACTTAAAACATTAGTGCA
Long Flanking Sequence:
GTTAACTTGTAAAAACACCTCATATTAAGCTTTACTTCACTTGCAAAACTTATTTTTGTATTAAAATCGTATTTCTGTATTTACAGCTTACAAAAAAGACACAGACACAACTACAGTAGTCAACATTGAAGTAGTCCAAAACCATTCATCAAAAGCGTCTTAATCCTACTTTTTGTTTTAGGACCATTTTTGATCCACTTCAAATGTTGACTTGGCTACTATGAGTACTAGATCAAGAGTTGAGGCTGATGTTTCCAAAGGAAGGAAGAGAGTTAAAATCAGCTCTGATGTCTACGGTAATTAGTTAATCTGGCATCCTGCGTGCCTCGTATAGGTGCAGGTTAATCTGGAAGGGCGTAATGAGCTTGAACGCACTGTCTGCATCAAGCGTCACTGAACATAAACAGGGCAGCACACTGACTGAAGGCCACAGTCTCGACACCGGGCGCACAATGCTGGACCTGAGCACAACGAAGAAACAATCATCTGTGTGCATTGAG[G/A]TGAGTGTTATTATGATTAGAGAATGATCGTGTACTTAAAACATTAGTGCATGACTGTTGGTGTTTGATAGTTAAGCCCTTTCACATTATCAACGCTTTGTATTGACCTGTTTAGAATGGACAATCAAAATTCAAGCTCATTCTTGCAGACAGGATTAATTTTTTTAAAGCCTGATAATTCTAACAATTTATGAATAACTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTAGAAAAAAGAAGCTTACAAGTTGCAAGAGTATGCAAACACAGTTTGATGTTTTATTGCAATTCTGAAAAAAAAGAAGTTTGCAAAAAACAGTTTGATGTTTTATTGCAATTCTGAGCATGCCATGTAATGTTATACTCCTGATTTAGAGATAGCTCAAAAAAAAAGTAATGAACTTTGATTTCTGAGCTAAAGGTAGAATTCAGTTTTTTTTTTCTATTTTTATTTAATGTAATTGCAATTTTCTGACTCACTTTTTGGTTTTGTTGAGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45322
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112611 | Nonsense | 170 | 187 | 5 | 5 |
| ENSDART00000145179 | None | None | 145 | 5 | 5 |
| ENSDART00000145894 | Nonsense | 139 | 156 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 24629942)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 23755760 |
| GRCz11 | 8 | 23776999 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTATGAGATGGAGGAACAGAGGCGTCTTGAGGATGAGAAAAATGTCCCA[G/T]AATTTGTACGAGTGAAAGAGAATCTGCGCCGCATACAGTTGGCCGAAAGC
Long Flanking Sequence:
CAAGACAAGAATGGGTGTTCAATAGTCTTAGGAACCCTTCCATGAATACTTTTTGGTGTACTTCAGATGTTGACTACTCTATTCCAATGAAACCAGGTTTGCTAAAGAGAAGTTTTATAAATTTTAGAGGCCTATTGTTGGAGGAGAAACCAGAATTGCAGCGTGTGTTACAGCAGAGGAGACTTGACCTGCACAGAGAGCAGGAACTTGCCCTCCAACCTCCTTCAGACCTAGAACAGGAGCTTCGCAAGAGACAGCAGAAAATGCAGGAGGTACTGACTGTTCCCAATCCACTGTGTTCCTCAAATGAAGTGGAGATCAAGAGTTGGCCAGATGTCTGGTGATACAGTTTAATTGTAAAGTGACCAGTAGAATTTGCTCTTGATTTCTTGTGTTACAAAATAATCATTTTGTATGTTGTAGTTTATCATTTGTTCTCCATTTCTCTACAGTATGAGATGGAGGAACAGAGGCGTCTTGAGGATGAGAAAAATGTCCCA[G/T]AATTTGTACGAGTGAAAGAGAATCTGCGCCGCATACAGTTGGCCGAAAGCAACTGATGGATCTGTGGAGAGAAAAAAAAATGCCTTGGAATTTTTATGTATGTTTTCATATTAAAATAATAGGATGTTTTGATTGTTGGGAAGTGTCAAATGGCTGTGTTTAGTAATGAGGCACTGTATTTATTGTTACAATAAAATACTGTATATTTGAGTCAAATTAAAGCTTGTCTGAAATCTGAACCTTTTTTATTTTGCATTAGAATTGATAGATTTAACATTTTAACTAAACACATCCCTAGTATAGCCAAAGTACCTCATGTTTCTGTAGATCTCCTTTTTTGGCTTTGTAATGTTTGACTAACTGGATTTGTATAGAGGTTGCACCTACTTTAATATTGAAAACAGATTAATAAAAACACTTATCTTGGCACCGAACTATTATCGCAACAAAGGGGAAAAACACTTCTTCCCCCCCATCCCCCCCCCCCCCCCCTCATCTTA
Associated Phenotype:
Not determined