Busch Lab

ZMP

cyp2j22

Ensembl ID:
ENSDARG00000022631
ZFIN ID:
ZDB-GENE-040120-2
Description:
cytochrome P450, family 2, subfamily J, polypeptide 22 [Source:RefSeq peptide;Acc:NP_956914]
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 5 alleles of this gene:

Allele Name Consequence Status Availability
sa23708 Nonsense Available for shipment Available now
sa9356 Nonsense Mutation detected in F1 DNA Not yet available
sa19234 Nonsense Mutation detected in F1 DNA Not yet available
sa45697 Nonsense Mutation detected in F1 DNA Not yet available
sa43441 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa23708
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000030229 Nonsense 23 496 1 9
ENSDART00000063128 Nonsense 23 497 1 9
Genomic Location (Zv9):
Chromosome 20 (position 25611369)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 25682672
GRCz11 20 25581762
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACGAGTGGATCGATATCAAAAGTATTTTGATATTTCTGTGTGTGTTTT[T/A]ATTGCTGGGTGATTATATAAAAAATAAAGCGCCCAAGAACTTTCCTCCTG
Long Flanking Sequence:
AGATGCCTTTTTACCTTTTTCTATAGGAAAACTGTTTCCAAATGATCCCAGTTCAGTTTAGTCCTCATATAAAGAAATGCATTATGATTATCTGTCGGTTTCTTTGATTTTCAGGAAAGAGAGTGTGTCTTGGGGAGCAGTTGACGAGGAGGCTTCCTCTTCATCTCCTCTCTGCTGCAGCGCTTCACTTTCTCTAAGTATTAAATTTTGAATCTTAATAAGGTTGTGGCTTTCTTTTTTTTTCTGTTTGGTGTGACTCGGTATTGCCACCATTTTTTGCAGTTAATGACCAAAAAAGTGGACTTTGGAACTTGATCATAGATAAGAGGGAATTACACACACACAGCCTATCTGGAGCCCAGCTCACTTGGATTACTGTACCGTTTATGCCAACCTCTGTTAAAACTGCTCAACAACACAGGAAAAGTTAGTCATGGACTTGTGGTACCTTTACGAGTGGATCGATATCAAAAGTATTTTGATATTTCTGTGTGTGTTTT[T/A]ATTGCTGGGTGATTATATAAAAAATAAAGCGCCCAAGAACTTTCCTCCTGGACCCTGGTCTTTGCCGATAATAGGAGATCTTCATCATATCGATAATAGCAAGATTCATCTTCAGTTCACAAAGGTAAAGTTCATCTCTATGTTCAAGCAAATCCTAATATAGTTTATGGCAAAAAACAAACGAGTCCAGTGTAATAAAAATGTAAAAAGTAATTGCTAAAAATTAAATATTCCTGTTCTTTGTAGATTACCTACTGTATGTTGATTGTACAATCATATTTTTCAGTTTGCAGAAAGATATGGCAATATTTTCAGCCTAAGACTTTTTGGACCAAGAATTGTGGTGTTGAACGGGTATAACTTGGTGAAAGAGGTGTATATAAAACAAGGAGACAACCTCGCTGATCGACCAGTGTTACCACTATTTTATGAAATTATTGGAGACAAAGGTCAGTCTAATGCCAGAATGTTCAAGTGGTGATTTAACAATTCAACAACAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9356
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000030229 Nonsense 126 496 3 9
ENSDART00000063128 Nonsense 127 497 3 9
ENSDART00000030229 Nonsense 126 496 3 9
ENSDART00000063128 Nonsense 127 497 3 9
Genomic Location (Zv9):
Chromosome 20 (position 25611937)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 25683240
GRCz11 20 25582330
KASP Assay ID:
2261-4338.1 (used for ordering genotyping assays)
KASP Sequence:
TAACTGTGAAGGTCTGCTTCATAAACAGGTATAGTTCTGTCCAGCGGATA[T/G]AAATGGAAGCATCAGAGGAGATTTGCACTYTCGACTCTTCGAAATTTCGG
Long Flanking Sequence:
ATAATAGGAGATCTTCATCATATCGATAATAGCAAGATTCATCTTCAGTTCACAAAGGTAAAGTTCATCTCTATGTTCAAGCAAATCCTAATATAGTTTATGGCAAAAAACAAACGAGTCCAGTGTAATAAAAATGTAAAAAGTAATTGCTAAAAATTAAATATTCCTGTTCTTTGTAGATTACCTACTGTATGTTGATTGTACAATCATATTTTTCAGTTTGCAGAAAGATATGGCAATATTTTCAGCCTAAGACTTTTTGGACCAAGAATTGTGGTGTTGAACGGGTATAACTTGGTGAAAGAGGTGTATATAAAACAAGGAGACAACCTCGCTGATCGACCAGTGTTACCACTATTTTATGAAATTATTGGAGACAAAGGTCAGTCTAATGCCAGAATGTTCAAGTGGTGATTTAACAATTCAACAACAAAAAAATTAATTATCAATTAACTGTGAAGGTCTGCTTCATAAACAGGTATAGTTCTGTCCAGCGGATA[T/G]AAATGGAAGCATCAGAGGAGATTTGCACTCTCGACTCTTCGAAATTTCGGATTGGGGAAGAAAAGCCTGGAGCCATCTATCAATCTCGAATGTGGCTTTCTGAATGAGGCCATCTCAAATGAACAAGGTTCAGTTTTAACTGAGTATTGTTAAATATATTTTAGGTGAAACCACAATGTTATTTACCACTTTCTGTTTAAGGTCGACCCTTTGACCCTCGCTTACTTCTGAACAACGCTGTCTCAAATGTGATCTGTGTGCTGGTGTTTGGTAATCGATTTGACTACAGTGACCATCACTTCCAGACTCTGTTAAAGCACATAAATGAAGCGATCTATCTGGAAGGAGGCATCTGTGCTCAAGTAAACATTTTCACTTTGTTTAACACTTGCTCTGCTCTTTTTGCTATTGTTGGAATTGGGCATATTTGAAATACATACTGCATGTTTGATGCTGATTTGAGCTCAGATTTCTGAGAATAAACAGAACTGTGTAAATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19234
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000030229 Nonsense 126 496 3 9
ENSDART00000063128 Nonsense 127 497 3 9
ENSDART00000030229 Nonsense 126 496 3 9
ENSDART00000063128 Nonsense 127 497 3 9
Genomic Location (Zv9):
Chromosome 20 (position 25611937)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 25683240
GRCz11 20 25582330
KASP Assay ID:
2261-4338.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACTGTGAAGGTCTGCTTCATAAACAGGTATAGTTCTGTCCAGCGGATA[T/G]AAATGGAAGCATCAGAGGAGATTTGCACTCTCGACTCTTCGAAATTTCGG
Long Flanking Sequence:
ATAATAGGAGATCTTCATCATATCGATAATAGCAAGATTCATCTTCAGTTCACAAAGGTAAAGTTCATCTCTATGTTCAAGCAAATCCTAATATAGTTTATGGCAAAAAACAAACGAGTCCAGTGTAATAAAAATGTAAAAAGTAATTGCTAAAAATTAAATATTCCTGTTCTTTGTAGATTACCTACTGTATGTTGATTGTACAATCATATTTTTCAGTTTGCAGAAAGATATGGCAATATTTTCAGCCTAAGACTTTTTGGACCAAGAATTGTGGTGTTGAACGGGTATAACTTGGTGAAAGAGGTGTATATAAAACAAGGAGACAACCTCGCTGATCGACCAGTGTTACCACTATTTTATGAAATTATTGGAGACAAAGGTCAGTCTAATGCCAGAATGTTCAAGTGGTGATTTAACAATTCAACAACAAAAAAATTAATTATCAATTAACTGTGAAGGTCTGCTTCATAAACAGGTATAGTTCTGTCCAGCGGATA[T/G]AAATGGAAGCATCAGAGGAGATTTGCACTCTCGACTCTTCGAAATTTCGGATTGGGGAAGAAAAGCCTGGAGCCATCTATCAATCTCGAATGTGGCTTTCTGAATGAGGCCATCTCAAATGAACAAGGTTCAGTTTTAACTGAGTATTGTTAAATATATTTTAGGTGAAACCACAATGTTATTTACCACTTTCTGTTTAAGGTCGACCCTTTGACCCTCGCTTACTTCTGAACAACGCTGTCTCAAATGTGATCTGTGTGCTGGTGTTTGGTAATCGATTTGACTACAGTGACCATCACTTCCAGACTCTGTTAAAGCACATAAATGAAGCGATCTATCTGGAAGGAGGCATCTGTGCTCAAGTAAACATTTTCACTTTGTTTAACACTTGCTCTGCTCTTTTTGCTATTGTTGGAATTGGGCATATTTGAAATACATACTGCATGTTTGATGCTGATTTGAGCTCAGATTTCTGAGAATAAACAGAACTGTGTAAATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45697
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000030229 Nonsense 214 496 4 9
ENSDART00000063128 Nonsense 215 497 4 9
Genomic Location (Zv9):
Chromosome 20 (position 25612275)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 25683578
GRCz11 20 25582668
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGACCATCACTTCCAGACTCTGTTAAAGCACATAAATGAAGCGATCTA[T/A]CTGGAAGGAGGCATCTGTGCTCAAGTAAACATTTTCACTTTGTTTAACAC
Long Flanking Sequence:
TCGACCAGTGTTACCACTATTTTATGAAATTATTGGAGACAAAGGTCAGTCTAATGCCAGAATGTTCAAGTGGTGATTTAACAATTCAACAACAAAAAAATTAATTATCAATTAACTGTGAAGGTCTGCTTCATAAACAGGTATAGTTCTGTCCAGCGGATATAAATGGAAGCATCAGAGGAGATTTGCACTCTCGACTCTTCGAAATTTCGGATTGGGGAAGAAAAGCCTGGAGCCATCTATCAATCTCGAATGTGGCTTTCTGAATGAGGCCATCTCAAATGAACAAGGTTCAGTTTTAACTGAGTATTGTTAAATATATTTTAGGTGAAACCACAATGTTATTTACCACTTTCTGTTTAAGGTCGACCCTTTGACCCTCGCTTACTTCTGAACAACGCTGTCTCAAATGTGATCTGTGTGCTGGTGTTTGGTAATCGATTTGACTACAGTGACCATCACTTCCAGACTCTGTTAAAGCACATAAATGAAGCGATCTA[T/A]CTGGAAGGAGGCATCTGTGCTCAAGTAAACATTTTCACTTTGTTTAACACTTGCTCTGCTCTTTTTGCTATTGTTGGAATTGGGCATATTTGAAATACATACTGCATGTTTGATGCTGATTTGAGCTCAGATTTCTGAGAATAAACAGAACTGTGTAAATAAAAGTATTTTGTAACCCTTTTTTTAGCTTTATAACATGTTCCCATGGCTCATGCAGCGACTGCCTGGATCACATAAGAAAGTTATTACTCTTTGGAAGAAGGTGATTGATTTTATCCGACAGAAGGTGAATGAACACAAAGTGGATCATGATCCATTGAATCCTCGAGACTACATTGACTGCTTTCTAGCTGAGATGGAGAAAGTAAGAATCTTCTCAAGTGTGCTGGTGCAGGAAAGTTCTTGTAATAATAATGTATGGCTTTTCATTTGAAAATATGTCAAATTTATGTTGTTCAGCTTAAAGATGACACAGCTGCAGGGTTTGATGTGGAGAACTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43441
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000030229 Nonsense 278 496 5 9
ENSDART00000063128 Nonsense 279 497 5 9
Genomic Location (Zv9):
Chromosome 20 (position 25612628)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 25683931
GRCz11 20 25583021
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGATCATGATCCATTGAATCCTCGAGACTACATTGACTGCTTTCTAGCT[G/T]AGATGGAGAAAGTAAGAATCTTCTCAAGTGTGCTGGTGCAGGAAAGTTCT
Long Flanking Sequence:
TTCTGTTTAAGGTCGACCCTTTGACCCTCGCTTACTTCTGAACAACGCTGTCTCAAATGTGATCTGTGTGCTGGTGTTTGGTAATCGATTTGACTACAGTGACCATCACTTCCAGACTCTGTTAAAGCACATAAATGAAGCGATCTATCTGGAAGGAGGCATCTGTGCTCAAGTAAACATTTTCACTTTGTTTAACACTTGCTCTGCTCTTTTTGCTATTGTTGGAATTGGGCATATTTGAAATACATACTGCATGTTTGATGCTGATTTGAGCTCAGATTTCTGAGAATAAACAGAACTGTGTAAATAAAAGTATTTTGTAACCCTTTTTTTAGCTTTATAACATGTTCCCATGGCTCATGCAGCGACTGCCTGGATCACATAAGAAAGTTATTACTCTTTGGAAGAAGGTGATTGATTTTATCCGACAGAAGGTGAATGAACACAAAGTGGATCATGATCCATTGAATCCTCGAGACTACATTGACTGCTTTCTAGCT[G/T]AGATGGAGAAAGTAAGAATCTTCTCAAGTGTGCTGGTGCAGGAAAGTTCTTGTAATAATAATGTATGGCTTTTCATTTGAAAATATGTCAAATTTATGTTGTTCAGCTTAAAGATGACACAGCTGCAGGGTTTGATGTGGAGAACTTGTGCATCTGTACCCTGGATCTATTTGTAGCAGGAACTGAGACCACCTCCACCACTCTGTACTGGGGTCTTCTCTACATGATGAAGTATCCTGTGATTCAAGGTATATAAAGATACAGCCATTAACATAAACAGTAGTTCACACTTTCAGTATTCTTATGGTCTTTCTGTATCCTCAGCTAAAGTTCAGGAGGAGATTGATCGTGTTGTTGGAGGCTCAAGGCATCCATCTGTATCAGACAGAGACAACATGCCCTACACTAATGCTGTCATTCATGAGATACAGAGGATGGGAAATATTATCCCAATAAATGTGACCAGGACTACTTCAGAGGATATTCGGATAGGAAAATAC
Associated Phenotype:
Not determined