cyp2j26

Ensembl ID:
ENSDARG00000018485
ZFIN ID:
ZDB-GENE-040912-139
Description:
cytochrome P450, family 2, subfamily V, polypeptide 2 [Source:RefSeq peptide;Acc:NP_001009890]
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 are 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa29363 Essential Splice Site Mutation detected in F1 DNA During 2015
sa16671 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa29363
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2015.
Mutation:
T > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016501 Essential Splice Site 72 505 None 9
ENSDART00000102913 Essential Splice Site 72 504 None 9
ENSDART00000128897   None 479 None 11
Genomic Location:
Chromosome 20 (position 25582114)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GAATGTTTTCAACCTGGATACTTCACAACCTCATATTGACTTAACTAAGG[T/A]AATTCTTATTTGTTATTACATGTTGTGATTTGATTTCTTAAATATTCGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16671
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000016501 Nonsense 88 505 2 9
ENSDART00000102913 Nonsense 88 504 2 9
ENSDART00000128897 Nonsense 64 479 3 11
Genomic Location:
Chromosome 20 (position 25584321)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GCAGATGTCRGACCACTATGGCAACATAWTCAGCTTGCGTCTGGGAAGCY[T/G]AAACACAGTTGTTGTGAACACCTACAGTATGGTGAAGAAAGTTCTTAATG
Associated Phenotype:
Not determined

Register

If you would like to be informed when the status of this gene changes (for example, a new allele is generated or an allele is made available for distribution) then please enter your details below:

* quick link - http://q.sanger.ac.uk/7ymm2i8p