ZMP
zgc:101715
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC447894 [Source:RefSeq peptide;Acc:NP_001004633]
Human Orthologue:
C19orf12
Human Description:
chromosome 19 open reading frame 12 [Source:HGNC Symbol;Acc:25443]
Mouse Orthologue:
1600014C10Rik
Mouse Description:
RIKEN cDNA 1600014C10 gene Gene [Source:MGI Symbol;Acc:MGI:1919494]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40986 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40986
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005087 | Nonsense | 64 | 141 | 3 | 3 |
The following transcripts of ENSDARG00000092703 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 47602389)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 45720500 |
GRCz11 | 7 | 45992866 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATATTGATTTATCGAAGGTGCTGCAGTGGGAGGTGCGCTGGGAGCATG[G/A]ATGACCAGTGGCCAGTTCAGACCTCTTCCTGAAATCCTCATGGAACTGAC
Long Flanking Sequence:
ATTGGCAAGTGACTTTTAAAGTTACAGTTTGTAGTAAATTGACATGAAAAATCAAGAGCTACGAAATGGTTAAAATGATTTTTTTTATATTAGCTACCTACTTACAGCGTTAATACCGCTTATATTTTTGAGTTTGAACTCATTTATCGTTGTTTATCGCCCGGTTTAGGCAATAACACCTCAAATGGCGAATCGAAAAGATGATATTATAAAGTTTTGCTGTGAAATCTCCGCCGATAAGAAGATACAAGCCGCATTTAAAGGCTCGGCGAAAGGAGCAGCAGTTGCCGGTGGAGGTGCTTTTGTCGGAGGACTGATTGGAGGTCCAGCTGGCATTGCACTCGGTGCGTTTTCAGATGTTTATTTTGCATGCGCAAAGCCGCAAACTCTCTGTTTGACCACATGATGGTGCTGTATCATCATTGCATGTCATTATCATGTCATTTGATACCATATTGATTTATCGAAGGTGCTGCAGTGGGAGGTGCGCTGGGAGCATG[G/A]ATGACCAGTGGCCAGTTCAGACCTCTTCCTGAAATCCTCATGGAACTGACTCCTTCACAGCAGGACAAACTGTACTCCGATGTCATGGCCATAGTGGGTTCACTCAAATGGACTGACGTTCCTCAGCTGATGGCTCAGGTTCATGGGAATTCTTCTCTACAAGAGCAAGTGCTGGGTGCTATACTCAGTTATACTAAAAACCAGCTTAAAGCTGAGGTCAAGTTTGAGGATTGACCACTAGAGTTAATGTTACAGGTCAGCTTTCTAAGACATTTAGGACATTTATTCATTTGGCAACTTAAAGTAATGATAAAAGAAACACTTCAGAAAACTGGCAGTAAAGTAATTATAAACAAATATTGATTTAAAAATGCTCTATTTAGCTATGTATCATCGTGCATCTGTTGCATGTGTTTATTGGTTATTTTAAGAAGTTCTGACATGACATCCAAACAGAAGTGAACCATTTTAAAATGTATTTTTTATTCTTGTTATAAGAG
Associated Phenotype:
Not determined