ZMP
chchd4
Ensembl ID:
ZFIN ID:
Description:
Mitochondrial intermembrane space import and assembly protein 40 [Source:UniProtKB/Swiss-Prot;Acc:Q6
Human Orthologue:
CHCHD4
Human Description:
coiled-coil-helix-coiled-coil-helix domain containing 4 [Source:HGNC Symbol;Acc:26467]
Mouse Orthologues:
AU015836, Chchd4
Mouse Descriptions:
coiled-coil-helix-coiled-coil-helix domain containing 4 Gene [Source:MGI Symbol;Acc:MGI:1919420]
expressed sequence AU015836 Gene [Source:MGI Symbol;Acc:MGI:2147954]
expressed sequence AU015836 Gene [Source:MGI Symbol;Acc:MGI:2147954]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35133 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35133
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039847 | Nonsense | 66 | 146 | 3 | 3 |
ENSDART00000135725 | None | None | 44 | None | 3 |
Genomic Location (Zv9):
Chromosome 11 (position 35896976)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 34518285 |
GRCz11 | 11 | 34780278 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAACTGGAACTGCCCGTGTTTGGGCGGCATGGCCAGTGGCCCTTGTGGA[C/T]AGCAGTTCAAGGATGCGTTTTCATGTTTCCACTATAGCAAAGAGGAGATA
Long Flanking Sequence:
TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCATGTGTGCATGCGTGCGCGCGCATGTATGCGTGCATGCCAAGCCCAAGAAAATTCTTACCCCTGGGGTAGGAGTCATTTTGGCCTTGAAAGTAATTTAAACACACATTATGCCAAAACAAACTTTTTTTTTTGGATGCAGTTAATCACTACAACTCTGCGCAGCACTAGATAAATTACATTTATTTATATACCAATTTTTTTGTGTAATAGGTTGATTATCTATACAATCAAACATGGGGTTTTTCTATCTTTATATACAGTTATCAAAAATTCGTAATACTCAACAACATGGGATCTTTTCCCAGTATCGTGCAGCCATATCAGCTAGCATCATTTAAATCTCTTCTATAATTGATCTCCACAATACCCGTTTGCTATGATCCCACAGGTCTTATTCTACCTAATGGCGACATAAACTGGAACTGCCCGTGTTTGGGCGGCATGGCCAGTGGCCCTTGTGGA[C/T]AGCAGTTCAAGGATGCGTTTTCATGTTTCCACTATAGCAAAGAGGAGATAAAGGGCTCCGATTGTGTGGAAAACTTCCGGGGTATGCAGGAGTGTATGCAGAAATACCCTGAGCTTTACCCTCAGGAAGACGACAACGACAGTGCCCCCTCTGGTGAAGCAAATACTGCACCCACTGACTCTCTCCCAGCATCCTCTACTGATTCCACAGCAGCAGCAGCCACAGAAAACCCAGCGACTAGCTAATGTTATCCTCACTTCACCCCCTCACAGCAAAGACAGCTCCACTTTTGACTATGAAGAGATCATATGTAACAATGCCCCAGAATCTGTGAAGCAAACAGATGCAGGAAGCTCTTAAACGTCAGGTTTTGTGATTAAAATGTGACATTAACGTGCACTTGAGAGACCTAAAAATGAGGTTCGGGATCTAAATGAGTGGCAGGTGAGTCTGCGCTTGGCTCTGTGAAACATTAGACTTCATTTGAATCATCCTGGTTT
Associated Phenotype:
Not determined