ZMP
zgc:63546
Ensembl ID:
ZFIN ID:
Description:
cytochrome P450 CYP2AA3v1 [Source:RefSeq peptide;Acc:NP_001073321]
Human Orthologues:
AC008537.2, CYP2A7P1
Human Description:
cytochrome P450, family 2, subfamily A, polypeptide 7 pseudogene 1 [Source:HGNC Symbol;Acc:2612]
Mouse Orthologues:
Cyp2ab1, Cyp2j13
Mouse Descriptions:
cytochrome P450, family 2, subfamily ab, polypeptide 1 Gene [Source:MGI Symbol;Acc:MGI:3644957]
cytochrome P450, family 2, subfamily j, polypeptide 13 Gene [Source:MGI Symbol;Acc:MGI:2385197]
cytochrome P450, family 2, subfamily j, polypeptide 13 Gene [Source:MGI Symbol;Acc:MGI:2385197]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44050 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31096 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44050
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 |
---|---|---|---|---|---|
ENSDART00000012284 | Nonsense | 111 | 496 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 23 (position 42833817)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 42517142 |
GRCz11 | 23 | 42482638 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGGTTCAGGATACTTTTTCTGGGAAGCCATATCTGCCTGTTATAGAGT[G/A]GATATCTAAAGGATTCGGTCAGTAACACTTTACTTATTAAAGCTTCCAAT
Long Flanking Sequence:
TCTGGCTCCTCCCTCTTCTGCTGTTATAAAGCACATGACCTTCTGCTGCTGTTGTGTTTGTCCCGAACTCAATCTGTCATCATGTTTACGGCTCTCCTGAAGTTAGACCTGGCCTCTGTGGGCTTGACTCTGTTTCTAGGCTTAATTATTCTGGTTCTGTTTGAGATCTTCAGGATTCATTCCTACAAACGTCGAACTCCACCTGGTCCAACACCTCTGCCTTTTGTGGGAACCATACCTCATTTCTTGAAGAATCCATTGGGCTTCATAAGATCGGTAAGTCTTTGCCGTTTTCTCTCATTGTGAAGCTCTGCTGCTATATTCTGAAAAACATATACATGCATTGTTTATGTCCTTCAAACAGATGTCTCAATATGGAGACATGTCCACTATGTATCTCGGGAGAAAGCCAGCAATTTTCCTTAATACAATCCAGCTTGCTAAGGAAACCCTGGTTCAGGATACTTTTTCTGGGAAGCCATATCTGCCTGTTATAGAGT[G/A]GATATCTAAAGGATTCGGTCAGTAACACTTTACTTATTAAAGCTTCCAATTGAAAGATTTCACAGACATGCAATAGACGAACCATTTTGTTTCCCTAAGGTCAGTTTATAAATCCCAGGATACATTTTGTAAGAGTGTACAATTGAGCAAAATTAAACCATGTCACTATGCAAAAGATGTGTAAGCTAGATTTGTTTCTCTCCTTCTTAGGTATAGCAATGGTCACATTTAACCACTCCTGGAGGCAGCAGAGACGGTTCGCTCTGCACACACTCAAGAATTTTGGCCTGGGGAAGAAATCAGTTGAAGACCGTGTGTTAGAGGAAAGCCGATATCTGATTGCTGAAATGCTCAAAGATGAAGGTATGACATGTTTATGTTCTACTTGAGCACATCCCCCACTGTGTCAGGCTCCAAACAAGCTCACCGGTGCTTTTTAAATGTCAAACTATTCATTCATTTTCTTTTCGGCTTAGGGCACACTCACACTATGCTATCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31096
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012284 | Essential Splice Site | 117 | 496 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 23 (position 42833798)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 42517161 |
GRCz11 | 23 | 42482657 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGGGAAGCCATATCTGCCTGTTATAGAGTGGATATCTAAAGGATTCGG[T/A]CAGTAACACTTTACTTATTAAAGCTTCCAATTGAAAGATTTCACAGACAT
Long Flanking Sequence:
GCTGTTATAAAGCACATGACCTTCTGCTGCTGTTGTGTTTGTCCCGAACTCAATCTGTCATCATGTTTACGGCTCTCCTGAAGTTAGACCTGGCCTCTGTGGGCTTGACTCTGTTTCTAGGCTTAATTATTCTGGTTCTGTTTGAGATCTTCAGGATTCATTCCTACAAACGTCGAACTCCACCTGGTCCAACACCTCTGCCTTTTGTGGGAACCATACCTCATTTCTTGAAGAATCCATTGGGCTTCATAAGATCGGTAAGTCTTTGCCGTTTTCTCTCATTGTGAAGCTCTGCTGCTATATTCTGAAAAACATATACATGCATTGTTTATGTCCTTCAAACAGATGTCTCAATATGGAGACATGTCCACTATGTATCTCGGGAGAAAGCCAGCAATTTTCCTTAATACAATCCAGCTTGCTAAGGAAACCCTGGTTCAGGATACTTTTTCTGGGAAGCCATATCTGCCTGTTATAGAGTGGATATCTAAAGGATTCGG[T/A]CAGTAACACTTTACTTATTAAAGCTTCCAATTGAAAGATTTCACAGACATGCAATAGACGAACCATTTTGTTTCCCTAAGGTCAGTTTATAAATCCCAGGATACATTTTGTAAGAGTGTACAATTGAGCAAAATTAAACCATGTCACTATGCAAAAGATGTGTAAGCTAGATTTGTTTCTCTCCTTCTTAGGTATAGCAATGGTCACATTTAACCACTCCTGGAGGCAGCAGAGACGGTTCGCTCTGCACACACTCAAGAATTTTGGCCTGGGGAAGAAATCAGTTGAAGACCGTGTGTTAGAGGAAAGCCGATATCTGATTGCTGAAATGCTCAAAGATGAAGGTATGACATGTTTATGTTCTACTTGAGCACATCCCCCACTGTGTCAGGCTCCAAACAAGCTCACCGGTGCTTTTTAAATGTCAAACTATTCATTCATTTTCTTTTCGGCTTAGGGCACACTCACACTATGCTATCCAAACCGTGTCCCGGATTGTT
Associated Phenotype:
Not determined