ZMP
zgc:91876
Ensembl ID:
ZFIN IDs:
Description:
cytochrome P450 like [Source:RefSeq peptide;Acc:NP_001002187]
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 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa13071 | Nonsense | Available for shipment | Available now |
| sa13766 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13071
Status:
Available for shipment
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:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064596 | Nonsense | 248 | 495 | 5 | 9 |
| ENSDART00000104197 | Nonsense | 244 | 428 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 25 (position 17746471)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 17293312 |
| GRCz11 | 25 | 17389712 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTTAAAAAAGGATTTGATCATGTGAAGGTATTAAAAGGTATGAATTTG[A/T]AGCTGATTGACGAACACAAGAGCACAAGAKTCCCWGGAAAGCCGAGAGAC
Long Flanking Sequence:
GTTTGGCCTGTCCTGACCCATATTTAAAATCAATTTCTATTTTAAATAAAGAAAAAAAAATTCTACTAATCAAGTCGCTTTGACAAAAAGCACACCCATAGCATGCCTAAAGTGCAATGATTCATGGGTTTATCAATTTCATTGCAGTCATGACACACCAACATATTTGGCCCAGTTCAGGATCAGATAGGGTTATTAACTTGGCTGAGACTTGGCCCAGATATGGTCCATGTTTGGCTCTTGTCTGAAAGCCAGACTTGGTGCAGTCATGTAATGTAATTCACTGCGGCATGTGGGCCAAGTACAAGCTGATTGTCTGGGCCAGAGATATTTTGTGGGGTGTATTTTGTTGATATTTAAAGGTATCTCTAAGCTACGTGTACTTAAATTTGGATGTTCTTTTATAACAGATATATGACACACTTCCCTTTTTGAGAATCCTGCCCCTGCCTTTTAAAAAAGGATTTGATCATGTGAAGGTATTAAAAGGTATGAATTTG[A/T]AGCTGATTGACGAACACAAGAGCACAAGAGTCCCTGGAAAGCCGAGAGACTTCATTGACTGCTATCTGGATGAGCTTGATAAGGTGCATCATTTTTCTGTAATGCAATGGTCTGGATGGTTTTGAAATGTTCATAACTGAAATCTGTAAATACTGTTTATGCACCACTGCTTGAGACTCAAATGAGAGATATCTTACAATCCTCAGAGAAAAAATGAGGTTTCCACCTTTTCCGAAGACCAGCTCCTCATGTACATTCTGGATCTGTACTTTGCCGGGACCGACACCACTTCTAACACCCTCCTCACTGCTTTCCTCTACCTCATGAACCACCCAGAGGTGCAAGGTTTGAGTTTGAAAAGCACACATTCATTTGTCTTCATTTAATCCAGGTTTAAACCAGAGAAAGTAGAGGAGTATCAACAGGAATGGAAACCTTTGTTATATTGTTAAGCCACATTAAAATAAGAAATTATAAATACAGTTTTGAAGTGTAATTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13766
Status:
Available for shipment
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:
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064596 | Essential Splice Site | 432 | 495 | 9 | 9 |
| ENSDART00000104197 | None | None | 428 | None | 9 |
Genomic Location (Zv9):
Chromosome 25 (position 17743797)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 17290638 |
| GRCz11 | 25 | 17387038 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTAGCTAWATATTTTAWWTTCATTTMTCCTGCATTTACTGTGTTTCTCC[A/T]GGYCCWCGTGTGTGTCTGGGTGAAGGTCTGGCCCGTATGGAGCTCTTCTT
Long Flanking Sequence:
ACATTACATATATGTAGTTTATAGGTATAATTTATTTTTCTAATTATACTTCTAGATTTATTGGGGACCCCCAGATTTCCTGGGGCCCTAACAGCCTCTTACCTCACTTATTGGTTAAATCTGTCTCTGGTCATCAGACAGATCGCCTATCAAATTTTTGACATTCTTTGAGAAACCTACATTTTTTAGTCCTAGACTTTTTTAATCAGTCTAAATGAAACCACTATAGTGCAATTGTCTAGGTCAACATTTATATTTAGGGTCATTTACAAAAGAGGTATGGTCAAATATACCAAAAATGCTTATATTCCTAAACAAAAATGAGTCTTAAATTGAAAACTGCTGTATTTCTTTTGCAAATGACTAGAAATGGCCAAAAAATCTTTTCATCCCTGATTTTAGCGATTGCTAAATTAGTTATTTTATATGAGCCCTTTAAGCACTTGAACTTGTAGCTATATATTTTATATTCATTTATCCTGCATTTACTGTGTTTCTCC[A/T]GGTCCACGTGTGTGTCTGGGTGAAGGTCTGGCCCGTATGGAGCTCTTCTTGGTTTTTGTCACTCTGTTGCGGCGTTATAAGTTTGTGTGGCCCAGAGATGCTGGGAAACCAGATTACACCCCTGTTTTCGGGATCACCATGACACCAAAACCCTACAGAATGCACATCAGATGGAGAAACACAGTTAAACAGTGAATCTTAATGCTGACAGTGCTGCTGTATTTAAAGTTGCAGGTAATCAATGATGACAGTAAGGTACTGGAGGTAAAAATTCAGTGAATTATTTTTCAGTACACAGTAACAATAACATTGTAATCTTTCAACATGAATAAACTTCAAGAGGATGAATGACACATCTTTCAAACATACTTTTGTGGATTTGATTTTTCAGCCTACACAATAAAGGTCTAATCAATCTTCATTTCTTTGAGTCATTCCTATAACATCACATATTTGTGAAGCAAATCTTCTCTTTGCACAGCCTCGATGTTCACTTTGAA
Associated Phenotype:
Not determined