ZMP

zgc:63546

Ensembl ID:

ENSDARG00000034070

ZFIN ID:

ZDB-GENE-031030-8

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]

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.

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.

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