ZMP
zgc:63667
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC393451 [Source:RefSeq peptide;Acc:NP_956773]
Human Orthologue:
CYP46A1
Human Description:
cytochrome P450, family 46, subfamily A, polypeptide 1 [Source:HGNC Symbol;Acc:2641]
Mouse Orthologue:
Cyp46a1
Mouse Description:
cytochrome P450, family 46, subfamily a, polypeptide 1 Gene [Source:MGI Symbol;Acc:MGI:1341877]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa29302 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa36958 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa29302
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 |
|---|---|---|---|---|---|
| ENSDART00000099258 | Essential Splice Site | 142 | 444 | 6 | 15 |
Genomic Location (Zv9):
Chromosome 20 (position 5301871)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 5217464 |
| GRCz11 | 20 | 5261871 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGTCATGCACGACCTGGTCAACTGTGTTACACTTGATGTCATTTGCAAG[G/A]TTTCTCCATCCTTCTTATTGATCCAAGGGAAAGTCTAATGTGTCAAATCA
Long Flanking Sequence:
TCATATGATTCACTATGTGCTACGTCTGTGGGCTGAAGCAGATAGGCTACGCACTCTTCATGTGACATTAAAAGACTTCATTCACCTCTTAGGAAATCATATTTGCACTGTCTCCATTCCTACATAGTACTATTACCCAAATAAACACATAATGTGTGTAACCGTTGAATCTCCTAGTTCCTTATGCTGACTGTGTATGCGTATGGCCAATGTATACCTCTCCGCCCCCTACACATTTTAAAAAGACTAATAAGGAGTTTTAAAATCCATTGGGCTCATGCTGGTCTGCTGATTTTTTGCCTGATCCTTCTTGCCACAGTGATATAACTTTTAATGTAACTGTTTCTGGCTTATTTATCAGATACTTACGAAGCTTGATAAGCACTTTTGACGAGATGTCAGAACGCCTGATGGACAAGCTGGAGGAAATGGCCAACAACAAAACCCCTGCCGTCATGCACGACCTGGTCAACTGTGTTACACTTGATGTCATTTGCAAG[G/A]TTTCTCCATCCTTCTTATTGATCCAAGGGAAAGTCTAATGTGTCAAATCAGCTGTTTATCAGTACTCAGTTGTAATATTTGCATTCGCAGGTGGCTTTTGGTGTTGATTTAAACTTCTTGGCGCAAAAGGATAGTCCCTTCCAGAACGCAGTAGAGCTTTGTTTAAATGGCATGACCGTAGATCTCAGGGACCCATTTTTTAGGGTAAGTAAATGTATCCAAAAACACGTCACTGTAATGTAGTAGGGTTAACTCTATATGATTGGTTTTTTTATTTTCTTATGTTGTTTGGGTTCTCAGCTTTTTCCCAAAAATTGGAAGCTTATACACCAAATCAGAGATGCAGCTGAACTCTTGCGTAAAACGGGAGAGAAATGGATACAAAACAGGAAGACAGCAGTGAAAAATGGAGAGGACGTCCCCAAAGACATTCTCACACAAATCCTCAAATCAGCAGGTATGTTGATCTCAAGTGAAGGAGAAATTCAGTGGTTAAAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36958
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099258 | Nonsense | 244 | 444 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 20 (position 5299581)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 5215174 |
| GRCz11 | 20 | 5259581 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCATCTTTTGTTGCAGAGGAAGAAAATGTTAATAACACAGATGATCTT[G/T]AGCAGATGTTGGACAATTTTGTGACTTTCTTTATAGCTGGTGAGTTACTC
Long Flanking Sequence:
AGATGTGCTATTAAAACTATTTTGATTAGAAATGTGTTGAAAATTTTTTTTCTCTCCGTTAAACAGAAATTGGGAAAAAAATAAACAGGGGGGCTAATAATTCTGACTTCAACTGTATATTTATCTCCTGTTTCTGAGATATCTCCAAAAATGCCCAATTTTGACTCTGGTGACAGATCAACCCTGTATACTTCAGATATAAAATATACTTCAGCCAAAATTGATTTTATTTCGTGCTAACAAAAGACTAGATATTTAAATGATACCACACTCACAGGCTCATGTTCAATGACATGGAAATAAAATAACTTCTGGAGTCACTTTTCAAAATGTCTCTTCAATATTCAATGTCTTTGAATGATATATTTTTGACAAATGCCATGATCCAACATTAGATTAATATTTAGATTATTTTATTATTCAGATTATTTTAACAGGTAGCGTAACACTCTTCATCTTTTGTTGCAGAGGAAGAAAATGTTAATAACACAGATGATCTT[G/T]AGCAGATGTTGGACAATTTTGTGACTTTCTTTATAGCTGGTGAGTTACTCCTCACTTTTGTTTTAGTTCATAAACTGTTGTGGATATGTACTGACTGCATGCAGGGTTTTTGTTGCATACACCAAACCCTGCCCCTGACACCACCATTAACAGTGATGTCACTAGCTCTATTGATTGCATGTGTCTGAGACTGCTTGTCTCAGCTTGCATGTCTTGCAGCCAGATACTATTGCTTTATTCCTCTGCAGGCCAAGAGACAACAGCCAATCAGCTCTCATTTGCAATCATGGCATTAGGGAGAAATCCAGAGATATACAAGCGGTAAAACACTTGTTAGAAATGTGTCCCTGTTCTGTCAGACTTTTATTATAATACTATAGTTCAATATTCCTTTCATTTCCAGAGCTAAAGCAGAGGTGGATGAAGTCCTCGGAACCAAAAGAGAAATTTCAAATGAAGACCTTGGAAAGTTTACTTACTTGTCTCAGGTTGGTTCATAG
Associated Phenotype:
Not determined