ZMP
zgc:55292
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC321491 [Source:RefSeq peptide;Acc:NP_955840]
Human Orthologue:
C1orf77
Human Description:
chromosome 1 open reading frame 77 [Source:HGNC Symbol;Acc:24511]
Mouse Orthologue:
2500003M10Rik
Mouse Description:
RIKEN cDNA 2500003M10 gene Gene [Source:MGI Symbol;Acc:MGI:1913761]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa6123 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6123
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000079842 | Essential Splice Site | 72 | 231 | None | 6 |
| ENSDART00000126079 | Essential Splice Site | 72 | 241 | None | 7 |
| ENSDART00000139856 | Essential Splice Site | 47 | 206 | None | 4 |
The following transcripts of ENSDARG00000057234 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 24400028)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 24330140 |
| GRCz11 | 19 | 23914363 |
KASP Assay ID:
554-3822.1 (used for ordering genotyping assays)
KASP Sequence:
GCAGATGGAGAACAGGCCCTCTGWGCAGGCTGCACTTCATCACAAACAGG[T/C]AAGAGGACAAAAAGTGCAAACCACMGGAAATGGTAGAGATGTCAATGTCA
Long Flanking Sequence:
TTTCAGTGTTTAGGATCTTTAAAAGGGTTCTATTCCGGACTAATGTGGATGTAGCCTCTATCGCTCTTCTGTCATCCCTCTTTGCTTAAAACCATATTCCAAGCATTCAGTTTAACCCAAACTGCTGATTTGTTGGGGTGTCTCTACATGTAACAGAGAGAGAGAGTAAATGACAGCACATGTGGTCTATTCAGGCCATTACTAGATTGCTACAGGATCCACTGTAGCTGCGTCCATGCTGTGCGAAATGATTTGATTTGGAACCATCCTTTCCTCGTATCCCCCTTTCCCTCTTCCTTCTTTCTGTCTCTCTCTGTCTACCCTCCTCCTCCTGTTGTGTCCTAAAAGCTTTACAAACATGCTGAAGAACAAGCAGCCGACAGTGAGTAGCATCCGGGCGACCATGCAGCAACAGCACATGGCCAGTGCACACAACCGCCTCCTTGCTCAGCAGATGGAGAACAGGCCCTCTGTGCAGGCTGCACTTCATCACAAACAGG[T/C]AAGAGGACAAAAAGTGCAAACCACCGGAAATGGTAGAGATGTCAATGTCATGGTACACAAAGAAAAGTGTTGAATTTACAGAAATGTTATGATAGTTGTATTTATTCTGTTCTTGGTTTTGGTTTAATATAAAGGTTTGTGTACATTTTTGCTTTTGCTTACCATCAGTATTTTGACACCAATGAAACCAGCAGCTCTACATTTCTCTTGCTCTGTGTATCATTCTTCGTTATTAGCAAGGTGTAGCTGCCTAGACCATTTTATGCCAACAAGTCATGTTTTACTGTTTATTCAGCAGTTCCACTAGTGTGAAAAAAAGCAACAAACTCATTGGTTGACCTATTTTTAATGCTGCGCATCAAAAAGAAAGAAAAAAAAACGTTCATGCATATGTGTAGTCATTATAAGTTTTCCTGAATTATTAGCTCGTTTGTATGTTTTTTTGCCACATACAACGACGACAAGCTGAAAAAAAAAACGTTGCTGTCACTAAGTTTTAT
Associated Phenotype:
Not determined