ZMP
si:dkey-165a24.3
Ensembl ID:
ZFIN ID:
Human Orthologues:
CNFN, PLAC8L1
Human Descriptions:
PLAC8-like 1 [Source:HGNC Symbol;Acc:31746]
cornifelin [Source:HGNC Symbol;Acc:30183]
cornifelin [Source:HGNC Symbol;Acc:30183]
Mouse Orthologues:
Cnfn, Plac8l1
Mouse Descriptions:
PLAC8-like 1 Gene [Source:MGI Symbol;Acc:MGI:1916651]
cornifelin Gene [Source:MGI Symbol;Acc:MGI:1919633]
cornifelin Gene [Source:MGI Symbol;Acc:MGI:1919633]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa26942 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa26942
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077352 | Essential Splice Site | 35 | 127 | 1 | 3 |
ENSDART00000141048 | Essential Splice Site | 31 | 123 | 2 | 4 |
The following transcripts of ENSDARG00000055046 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 23826520)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 22388272 |
GRCz11 | 7 | 22659429 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACCAGTGGAGCTCTGGAATCTGCGACTGCTGTGACAATGTGCCCGAGT[G/A]TGAGTCTCTCTCACTCATTCTTTCAGTCTTGTTGATTTTGGTGTGTCTCT
Long Flanking Sequence:
GCTTACCCAACTCACCTATATCGCTTGTCTTTGGACTTGTGGGGGAAACCGGAGCACCCAGAGGAAACCCACGTGAACGCGGGAGAACATATAATCAAATCATCAAAAAATAAAAAAATAAATAGTTTTCCAATTCTTTTTGCAATTTTTACATTTTCAATAAACATCATGGTCTAAGTGTGTCAGTGTTACAAACTTTATCATTGCAGTTTATTGCAGTCTGTCATAGTTATGTTTGCATTTAATTATACTTGATTTAGTTATGATAAGCTAGTTTGATTTAATGTCGAAACACACACATAACATCTGATCTGTGGCCAGTGAACTGCTAAATTAACCATTCATCATTCCATATTTGTATGTACTGAAATGTTTGTGTCTGTTGCAGGATTACGCAATAAACAGAATGACCACTCAGCAGCCCGGGCAGTTTATGATAGCACAGACCAATGACCAGTGGAGCTCTGGAATCTGCGACTGCTGTGACAATGTGCCCGAGT[G/A]TGAGTCTCTCTCACTCATTCTTTCAGTCTTGTTGATTTTGGTGTGTCTCTGTGGGTGTATTTTCTTAAAGAATGTCACTTTTGATGCAGCGCACAATAGCATTGTTAAAACTAGTCTTGCATTGCTGGGATGTGTGTATAAAGGGAACACCAGAGGAGTGCCAGTGCATTTCTGAGAAAGAGAAAAGGCCACTTTATTTTGTGATCATTAATGGTTTACTGTACATTATTACTGTAATAATGCTTTTCTGTTGCTATTAACACTTTAAGGTGAACTACACTATTGGACTGAACATTGCTGGCATTAGTTCACAAATCTGATTCAGTAGTTTCTAGTAGGAGGCAGCAGAGTTGTATCCATACATGCTGCTAAAACTTGAGAGAGTTTGTATTTTATTTAAAGGGATAGTTCACCCAAAAAAGGAAAATTATGTCATTATTTACTCATCCCTTACTTGTCACACATCTGTTTGAGTTTCTATCTTCTGTTTAATACAAAAG
Associated Phenotype:
Not determined