ZMP
zgc:109719
Ensembl ID:
ZFIN IDs:
Description:
UPF0704 protein C6orf165 homolog [Source:UniProtKB/Swiss-Prot;Acc:A2RV06]
Human Orthologue:
C6orf165
Human Description:
chromosome 6 open reading frame 165 [Source:HGNC Symbol;Acc:21405]
Mouse Orthologue:
1700003M02Rik
Mouse Description:
RIKEN cDNA 1700003M02 gene Gene [Source:MGI Symbol;Acc:MGI:1916579]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa29293 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa29293
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000036373 | Essential Splice Site | 37 | 624 | 2 | 12 |
ENSDART00000081549 | Essential Splice Site | 37 | 245 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 2696403)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 2650587 |
GRCz11 | 20 | 2667563 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTATTGTGTCCAGGTAAAAGACACACAACACTGAATTATTATTGTGTCC[A/G]GGTGAAAGCTGTAGTTCTGGACCCCACCAATCATTTCAACGTGGACAGAA
Long Flanking Sequence:
ATTTTAAAAAAACTTTATAAACTCATACCGGCCACAACCTGCACACCTGCAGAGCCAGTCAGATCAGGCATTCAGCAGCTCGTGTTTGTGTTTGGTGCAGAAGCCCATGCGCACACGGTCCATCTCCATGACAACGATACAACGCGAGAGGACAGACACACCGCCGCCGGACACTAATGAGTGTAAAAACACGGTAAACGCGGTAAATACAGTAGCTGGTCATCATGTCGAGTTCACAGGCTGAAGGAGTGATAAGAAACATAATCCGAGAAATCTCGCAGACGTGTTTGAGCAGAGGACAAACTCTGAGTGAGACTCTCATCGCGTTCATGGTGAGTCTGAAGTAACGTTACACAAACACACAACACTAACTTACATGACTGAACAACTGTACAACTCTTCAGGTCAGTGGTTGATTGTGTGCAGGTGACAAACACACAACACTAAATTATTATTGTGTCCAGGTAAAAGACACACAACACTGAATTATTATTGTGTCC[A/G]GGTGAAAGCTGTAGTTCTGGACCCCACCAATCATTTCAACGTGGACAGAACTCTTACAAAGCAAGATGTGCAGAAACTTATTGAGGTAAACATTCTATCAATCAATCAATCAATCAATCAATCAATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCCATCCATCCAGGGGCGCAACTACACATATACTGAGAGGTATGCGGGTTCAAGTTTTGTAACTAAAATAAAATAGTTTTGAACAAAAAAAAAGTTACCAAAAGGCCTGATGTATCAATATGACACATAATAAATTTATAAAAACATGTATATTGTATAAAATGGACCTTGATAGAAGGATTAAAAACATTTCAGTTCCAAAAAATGTGAATATTCGGACAATTTGTTCATGTGTCAACTTTAACAGGGTTAAAAATCATTATAATC
Associated Phenotype:
Not determined