ZMP
zgc:85676
Ensembl ID:
ZFIN ID:
Description:
chromosome 7 open reading frame 23 [Source:RefSeq peptide;Acc:NP_998084]
Human Orthologue:
C7orf23
Human Description:
chromosome 7 open reading frame 23 [Source:HGNC Symbol;Acc:21707]
Mouse Orthologue:
4930420K17Rik
Mouse Description:
RIKEN cDNA 4930420K17 gene Gene [Source:MGI Symbol;Acc:MGI:3606159]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa26224 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa26224
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041289 | Essential Splice Site | 79 | 125 | 6 | 6 |
The following transcripts of ENSDARG00000033179 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 8681081)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 9617929 |
GRCz11 | 4 | 9618845 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACCAAAATTAAAATCAATGCAAGTAAATGCAATCTCTCTCATTCTTTC[A/T]GATATACTGGTATAGGCAGGGAGATCTGGAGCCTAAGTTCCGCAACTTGA
Long Flanking Sequence:
TACAGCTTACACTGTACACTAATATAATGCTGTTGATCACCTCCAGGATAGAATCATCAATCTAGTAGTCGGTGGACTTGCATCTTTACTTGTTCTGGTAAGTGTTTACCTCTTATGAAAATTTCAGGGGCCATTTATGCAACACCACTTTCAATTAAAAATGGTTCTTGGTTCTTCATTTGCTTTTGAAACAGTGTAATCCATGTAATGTAGTTTTTTTTTTGGTGAAAACTGTGATTTTAGTACATCATCATATAAGCATATCATCAGTCAACCTGTTTATCATATTTGACTCAAACTCAGCCTCTCTTTCAGGTGACCATCATTAGCTCATTCGTCTTTCCTTCACTGCCTCCCAAACCACTCAATATATTCTTTGCCATCTGCATCATGCTAGTCTGCGGCTCAGTGTTGGTTCTGGTAAGTAAAAAAGCATTGATTATTTCAATCGTACCAAAATTAAAATCAATGCAAGTAAATGCAATCTCTCTCATTCTTTC[A/T]GATATACTGGTATAGGCAGGGAGATCTGGAGCCTAAGTTCCGCAACTTGATCTACTACATGCTCTGCTCCATCGTTCTGCTGTGTATCTGTGCCAACTTGTACTTTCACGATGTGGGACGTGATAAACAGAGCAATGCCTTATAAAAACCACAGGAAGCGCAGAATGTTCATCGTTATGTGGGAGCTTTGGAAACCCACATAAACCCCACCTGAATTCTTGAATCAGGAGAATTCATTTTCCTACAAGCCCCGTTTGTGTGGGCAGGCCAGTCTGCCTTTGGGAGCCATATTAATGCACATAAACATATTATAGATGCAAATATGTTAGCGATCAGTAGCACTCTGGGATGTCCGTGCACATGTTTGCACCCTCTATGCTGTACACAGCTTAACTTATATGCCAATGTAAAGACAAGAGCAGAGTTTTTGAGATAAGCCATCCACAATGCTTTTATATTTGTACATGATACATCTACGGTACACATTCCTAATGAAGAAA
Associated Phenotype:
Not determined