ZMP
zgc:103558
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC494057 [Source:RefSeq peptide;Acc:NP_001008600]
Human Orthologues:
FAM113A, FAM113B
Human Descriptions:
family with sequence similarity 113, member A [Source:HGNC Symbol;Acc:16212]
family with sequence similarity 113, member B [Source:HGNC Symbol;Acc:28255]
family with sequence similarity 113, member B [Source:HGNC Symbol;Acc:28255]
Mouse Orthologues:
Fam113a, Fam113b
Mouse Descriptions:
family with sequence similarity 113, member A Gene [Source:MGI Symbol;Acc:MGI:2442177]
family with sequence similarity 113, member B Gene [Source:MGI Symbol;Acc:MGI:2446270]
family with sequence similarity 113, member B Gene [Source:MGI Symbol;Acc:MGI:2446270]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11694 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11694
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012483 | Nonsense | 266 | 415 | 7 | 10 |
ENSDART00000131530 | Nonsense | 266 | 295 | 7 | 8 |
ENSDART00000139455 | None | None | 196 | None | 5 |
Genomic Location (Zv9):
Chromosome 7 (position 26001964)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 24563716 |
GRCz11 | 7 | 24834873 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCTTCATGCAGATCAGCAGGATTCTAAACCAGCAACCCAGCAGAACCGA[C/T]AAAGCGGGCTTTCAACTCCTCCTGTGCGCTATAGAGGTAYACTGTCAATG
Long Flanking Sequence:
CCCAATCTCAGATAGAGCACATGGGCCCATCGTTAAGATTTGATGTCATTGAAGCGAATTACTTTGGAGCCACACTTGCCAATGAGTCTGGCTTTGATGTGCTGGACCTCCATTACCAGTTTCGTTTCAGCCTGCAGCATCGAACTCGTGATGGTGTCCACTGGAATGCTGTGGCTCACCGGAAACTATCATCCCTTCTGCTGCAACACGTCGCAGAAGCATGGGGTGTTGAACTGCCGAAGCTAGGTGAGAAATGCAGGTTGAGTTGGTGCTTCTGGTTGGCAAAATAAAGTAATTTTGTTATAGATTGTTTGCTGGGGTCCCAGAATGATGATGAGAATGTTATTGTTTTCTCTCTCTTTATACTAACTGAATATTACAGATAATCACATTTGCAAAAAAATGACTTGGTTAAGGATGCATGGAACATAGTCACAGATCTGTTTTGTTGTCTTCATGCAGATCAGCAGGATTCTAAACCAGCAACCCAGCAGAACCGA[C/T]AAAGCGGGCTTTCAACTCCTCCTGTGCGCTATAGAGGTACACTGTCAATGGGCTGAGAAGTTTCTTTTTGTTCAATTATGTGAACACAGTGTATAATTGATATGCACATATGAATACACATGTATTTAATGAAATAGATGATGTTTACATGTGTGTGCTTAGATAATGTAATGTTTTATTAATATATTTGTATATAAAGAGTTCAGATGCAAAAGCTGCTAAACGTCAGTCACTTCAGCCAAAAATGAACTAATGACATTGAGTGAATGCTTTAGGCACGTACTACACCATCAACAAACAGTTTTGCTTCAAATCATTTAAATCTCAGCGTTAGCACATTCAGAAATGTTTGTTTGCAAAAGCCTCTAAACACCACGCCGGCTTTTATGAGGAGACTGTTTTATTCTGATTTAGATTTTAAAAGCTGGAGTTTGATGAATTGAATGAGCCTGTCTGACTGTCAGTGAATGGCAAATGAAAACGTCTCTTACCTCAAAACT
Associated Phenotype:
Not determined