ZMP

cyp2j28

Ensembl ID:

ENSDARG00000021172

ZFIN ID:

ZDB-GENE-020812-2

Description:

cytochrome P450, family 2, subfamily J, polypeptide 28 [Source:RefSeq peptide;Acc:NP_694486]

Human Orthologue:

CYP2J2

Human Description:

cytochrome P450, family 2, subfamily J, polypeptide 2 [Source:HGNC Symbol;Acc:2634]

Mouse Orthologues:

Cyp2j11-ps, Cyp2j5, Cyp2j6, Cyp2j9

Mouse Descriptions:

cytochrome P450, family 2, subfamily j, polypeptide 11, pseudogene Pseudogene [Source:MGI Symbol;Acc
cytochrome P450, family 2, subfamily j, polypeptide 5 Gene [Source:MGI Symbol;Acc:MGI:1270149]
cytochrome P450, family 2, subfamily j, polypeptide 6 Gene [Source:MGI Symbol;Acc:MGI:1270148]
cytochrome P450, family 2, subfamily j, polypeptide 9 Gene [Source:MGI Symbol;Acc:MGI:1921769]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa6633	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa6633

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024350	Nonsense	346	492	7	9
ENSDART00000122431	Nonsense	335	481	9	11

The following transcripts of ENSDARG00000021172 do not overlap with this mutation:

ENSDART00000130500

Genomic Location (Zv9):

Chromosome 20 (position 25567599)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	25638902
GRCz11	20	25537992

KASP Assay ID:

554-5030.1 (used for ordering genotyping assays)

KASP Sequence:

CAGAGATAGACAGARTGATTGGACAGTCACGTMAACCCTGCTTGGATGAC[A/T]GAGTTAATATGCCCTATACTGAAGCTGTTTTACATGAGATTCAAAGATTT

Long Flanking Sequence:

GGCCCTCACCAAAAAGTATTTTCTAACTATAAGAAGATTACACAGTCCTTGAAAGACGAGATTATTAAGCACAGAGAGGACTGGGACCCTGCAAACCCACGTGACTTTATCGACAACTACCTGACTGAGATGGAAAAGGTAACTAATTGAATTTCAAAGACTTGAATTTGAATGATTTAATATTAAGCATTTGTTATATTTTTCCCCCAGAAAAAGAGTGACCCTCAAGCTGGCTTTAACATAGAAAGTTTAATCATTTCTTGCCTAGACATAGTTGAGGCTGGGACAGAGACGGGTGCGACTACATTACGCTGGGGTCTGCTTTTTATGATCAAGTTCCCAGAAATACAGAGTAAGTGTGGTTTTATTTTAAGGTTAAAGAATACTCATATTGTCCAAATGTCCATACTTTGGTTCAAACTTGTATTTGTCTGTCAGAAAAAGTCCAGGCAGAGATAGACAGAGTGATTGGACAGTCACGTCAACCCTGCTTGGATGAC[A/T]GAGTTAATATGCCCTATACTGAAGCTGTTTTACATGAGATTCAAAGATTTGGGGATGTTGTTCCACTTGGATTCCCCAAACAAGCAGCTGTAGACACAAAAATTGGGAACTACTTCATTCCAAAGGTTCTATTAATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTCTATTTCTGCCAAGTCTGAACAAATCCAGTAGATTTCATTCTCTCTTTATTAGGGGACTTCTATTACAACAAACCTGTCTTCGGTCCTGCATGATCCAAACGAATGGGAAACCCCAGACACTTTCAACCCTGGACACTTCCTAGATAAAAATGGCCAGTTCCGGAAAAGAGATGCCTTCCTGCCTTTTTCCGCAGGTAATATTAGTTTT

Associated Phenotype:

Not determined