ZMP
zgc:172246
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC796447 [Source:RefSeq peptide;Acc:NP_001093526]
Human Orthologue:
C6orf58
Human Description:
chromosome 6 open reading frame 58 [Source:HGNC Symbol;Acc:20960]
Mouse Orthologue:
2310057J18Rik
Mouse Description:
RIKEN cDNA 2310057J18 gene Gene [Source:MGI Symbol;Acc:MGI:1914969]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1814 | Missense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa1814
Status:
F2 line generated
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064419 | None | None | 364 | None | 6 |
ENSDART00000126408 | Missense | 67 | 364 | 1 | 6 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 1422243)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 1378108 |
GRCz11 | 20 | 1398934 |
KASP Assay ID:
554-1806.1 (used for ordering genotyping assays)
KASP Sequence:
GTCCAGGTAAACCCGTGGGTCTACTCCCAGAGGATGACCATGTTGAAAAT[G/T]GTGATCAACGCTACTAATGCCTACATGAGCTCCATGGGCCCCGGGGAGCA
Long Flanking Sequence:
CCGGATGTGAGGCACATGAATTTTGCTAGCTGGGATTGATGAAGGCTCATAACTGAATCGATTGGTTTTTCTTTTCTCCCGTGATTCGTTTAATGAGTTATTGAGTGTGACCTTCTTTGGTATTTGCCATTTGTCGATATTTGGCATGGAAACGAGACTAAAGTATGTTTTTGTGCCGTGGGTGTGTTTTTCTCCACCCACACTGGTTTGGTTTTGTCTCCATGTGGGATCAAAGTCCATGTGCTGCCCATTGATTAAAGCTCCTCTCTGCTGGACTCAGTGTTTCAGCAGTCCTGCTAGATGTCTGAGATGGGTTTCCTGCGATCAGTGGCCGCTGTGCTCTTGTTGGCTGTGTTTAGCCACGCAGCAGTAGTGACTGAGAATGGACTGCCGATTCAATGGAGAAAAGCTCCCAGCGATCTCTCCCACCTGCCCATATCGAACACGGGGGTCCAGGTAAACCCGTGGGTCTACTCCCAGAGGATGACCATGTTGAAAAT[G/T]GTGATCAACGCTACTAATGCCTACATGAGCTCCATGGGCCCCGGGGAGCAGGAGAATCCGCTCTGGAGTCTTCCTCTGCAGCTCGGCTGGAAACTCAAATCAGGTGCCCTTTATTTTGCACTGTAGGAAACAACACCCTAGCTAATTGGCTGTGATTTCAATGCCTGGTTAACAGGAAGTTTCATTAATATATAGTTAAATTCTGAATTATTCTGCCCCCATTTATTTTCCCCCCAATTTCTGTTTACCAGCACATTTCTAAACATAGTTTTAATAACTCATCTCTAATAACTGATTTATTTAGTCTTTGACATGATGACAGTAAATAATAAATAACTAGATATTTTTAAAGATGTTTTGGATTCTTGTTGTGGTCATTATTATTATGGTGGCTTGAGAAAGCCACCATTTTGATATTCTACATAACCTTATAATTATTCTTCCGTCTTCTGAGACTAATTTTAAAGTGTATCTCCTCCTAAGCCTTTCTAGCTACATAC
Associated Phenotype:
Not determined