ZMP
si:ch211-15d5.2
Ensembl ID:
ZFIN ID:
Description:
COMM domain-containing protein 9 [Source:RefSeq peptide;Acc:NP_001082867]
Human Orthologue:
COMMD9
Human Description:
COMM domain containing 9 [Source:HGNC Symbol;Acc:25014]
Mouse Orthologue:
Commd9
Mouse Description:
COMM domain containing 9 Gene [Source:MGI Symbol;Acc:MGI:1923751]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa6477 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6477
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 |
|---|---|---|---|---|---|
| ENSDART00000092925 | Essential Splice Site | 17 | 197 | None | 6 |
The following transcripts of ENSDARG00000094258 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 24446891)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 24600333 |
| GRCz11 | 17 | 24618734 |
KASP Assay ID:
554-5028.1 (used for ordering genotyping assays)
KASP Sequence:
GGCTTTCATGACACAAGATCAGTTCACTGCTTTGCAACTGCTGTTAAAGG[T/C]AGTGTAATATCACATACTGTTTAGTATATYGCTGAATTACTTGGCTTGAT
Long Flanking Sequence:
AGGATGTTTTTTGTAATAATTAAACCAATTGTTCACCAAAAAAGGATGTTTTTGTTATCTAAGCAGCATTTTCTAAAACTGGTTGACCAATGGTTTATTGGAGAACTTTTGCATTTAATTTACCATGTTTATAAAATTGATGCTTTTTTAATTGCATCCTCTGTCAGACAAGAATTTGTTCTTCAGTTCAGCTAAATAGCTCAAGTAAATCTGGCCCTGTTCATTTTGATGGTTGACTAACATCTAAATTTTAGAACAGATTTGCTGAATATATTGCTTACGAGTTTTGTTTTTGTTAAGGCCTAGTAAAGTAAAGCTGTACGTTTTTTTTTTTAGAACTATACGCACTCGAAGCTAAATCTAAAATCTAGGCCCGAAGTCGCCTTCGTCGGACTTTTATTTTGACACCAGATCAAATCGTGAATTCACGTGACTTTCAGTATCAAACATGGCTTTCATGACACAAGATCAGTTCACTGCTTTGCAACTGCTGTTAAAGG[T/C]AGTGTAATATCACATACTGTTTAGTATATCGCTGAATTACTTGGCTTGATTGAGCTCGTGTATTCTGCCATCTTTTACTTTGATTCAGGCTCCGTCTAAAGATGCTGTTCGGCAGATCTGCACAGAGAGTTTCCCAGCCGGAGCCTTCAAGAGTCAGTCTGTAGTGGAGAAAACTGCCAATGCTCTCTCTGTCTCTCACAATGAAGCGGTCCAGGTGGGTTCAAGCGTTTTCATGCGTTAATTTTTCCGTCTAATGTGTTTCATGATGCTTACTAATGTAATTGGAAGAACACAGAAAATGCTCGTTTGGTCAATACAGTTGTAATAAAAGTTAACACCAATCATGATAAGTTGGTGTTTCATTTTTGTGAGAAAACTAAAAGATAATACGATAATAGTGTACATTTATTTTTAGTTAACGTACGCTGTTATTTCATAATAAACTTGTGAATGTGTATTGAAATTGTATTTGTTATTTATTTATGGTCACTAGTGTGATC
Associated Phenotype:
Not determined