ZMP
zgc:110692
Ensembl ID:
ZFIN ID:
Description:
cytochrome P450 [Source:RefSeq peptide;Acc:NP_001018658]
Human Orthologues:
CYP2F1, CYP2S1
Human Descriptions:
cytochrome P450, family 2, subfamily F, polypeptide 1 [Source:HGNC Symbol;Acc:2632]
cytochrome P450, family 2, subfamily S, polypeptide 1 [Source:HGNC Symbol;Acc:15654]
cytochrome P450, family 2, subfamily S, polypeptide 1 [Source:HGNC Symbol;Acc:15654]
Mouse Orthologues:
Cyp2f2, Cyp2s1, Cyp2t4
Mouse Descriptions:
cytochrome P450, family 2, subfamily f, polypeptide 2 Gene [Source:MGI Symbol;Acc:MGI:88608]
cytochrome P450, family 2, subfamily s, polypeptide 1 Gene [Source:MGI Symbol;Acc:MGI:1921384]
cytochrome P450, family 2, subfamily t, polypeptide 4 Gene [Source:MGI Symbol;Acc:MGI:2686296]
cytochrome P450, family 2, subfamily s, polypeptide 1 Gene [Source:MGI Symbol;Acc:MGI:1921384]
cytochrome P450, family 2, subfamily t, polypeptide 4 Gene [Source:MGI Symbol;Acc:MGI:2686296]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa815 | Nonsense | Available for shipment | Available now |
| sa2784 | Nonsense | F2 line generated | Not yet available |
| sa42457 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa815
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000002842 | Nonsense | 141 | 491 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 69311)
KASP Assay ID:
554-0719.1 (used for ordering genotyping assays)
KASP Sequence:
TGAGGCGGTTCACGCTCACCACACTGAGGGATTTTGGAATGGGACGCAAA[C/T]AAATGGAGCAATGGATTCAAGAAGAGAGCAGATACTTGCTCAAGAGTTTT
Long Flanking Sequence:
TTGTTTTTTAAACATGAGATTTTTTTAAGCAATCTTCAAATATCAAATATTTTGAGTTGCCACATAATTTTTTATCAAATGAAAAAATGTTTCTGAGATCAATGTCATTGTTTTACAACCAGTTTAAATTCTCATTAGTGTTTGATAATGATGTCTGTTCTTTTAATCAGTGGAGAAAAACCTATGGGTCTGTGATGACGGTGCACCTCGGGCCTCAGAGAATGGTGGTTCTGGTGGGTTACGAAACAGTGAAGGAAGCTCTGGTGGACCAGGCTGAAGACTTTGCACCCAGGGCTCCCATTGCCTTTATGAACAGAATTGTGAAGGGCTACGGTGAGGGATTTGTTTATTTACTTTGTTTAAAAAACATAAACTATCAATTTAATGTGTCCTAGCTAAAGTATTTGTTTGTAGGTCTGGCCATCAGCAATGGTGAACGCTGGCGTCAACTGAGGCGGTTCACGCTCACCACACTGAGGGATTTTGGAATGGGACGCAAA[C/T]AAATGGAGCAATGGATTCAAGAAGAGAGCAGATACTTGCTCAAGAGTTTTGAAGAAACCAAATGTGAGGAAACAGAGTACATGACATTTACATGAGTTTCATATTCGAGCTGTGTTCTGCACTCACAGCTGTCAGAGATGTGTAATAACATTAAGGCTTTTCTTCTTCAGCCAAACCAGTTGATCCAACATTCTTCTTTAGTCGGACTGTGTCCAACGTCATCTGCTCTCTGGTGTTTGGGCAGCGCTTTGATTATGAAGACAAAAACTTCCTGCAGTTGCTCCAGATCATCTCCAAACTACTGCGATTTTTAAGCAGCCCTTGGGGACAGGTGAGACCGTGTAACTGCTTGTAACTATGTTTGTATGCTTTCAACACCTTAGCCTTCAGTATTAAACAATATAGACAGAGAATTGGCAAATGTGTTTCTCTAACATCTCCATCACTGTAATTTTCACTCCCTTATTTAACAAGCCTGATTGAACTCTAAACAAAGAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2784
Status:
F2 line generated
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:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000002842 | Nonsense | 215 | 491 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 68982)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 101900 |
| GRCz11 | 15 | 29709 |
KASP Assay ID:
554-2482.1 (used for ordering genotyping assays)
KASP Sequence:
TGCTCCAGATCATCTCCAAACTACTGCGATTTTTAAGCAGCCCTTGGGGA[C/T]AGGTGAGACCGTGTAACTGYTTGTAACTATGTTTGTRTGCTTTCAACACC
Long Flanking Sequence:
TACGGTGAGGGATTTGTTTATTTACTTTGTTTAAAAAACATAAACTATCAATTTAATGTGTCCTAGCTAAAGTATTTGTTTGTAGGTCTGGCCATCAGCAATGGTGAACGCTGGCGTCAACTGAGGCGGTTCACGCTCACCACACTGAGGGATTTTGGAATGGGACGCAAACAAATGGAGCAATGGATTCAAGAAGAGAGCAGATACTTGCTCAAGAGTTTTGAAGAAACCAAATGTGAGGAAACAGAGTACATGACATTTACATGAGTTTCATATTCGAGCTGTGTTCTGCACTCACAGCTGTCAGAGATGTGTAATAACATTAAGGCTTTTCTTCTTCAGCCAAACCAGTTGATCCAACATTCTTCTTTAGTCGGACTGTGTCCAACGTCATCTGCTCTCTGGTGTTTGGGCAGCGCTTTGATTATGAAGACAAAAACTTCCTGCAGTTGCTCCAGATCATCTCCAAACTACTGCGATTTTTAAGCAGCCCTTGGGGA[C/T]AGGTGAGACCGTGTAACTGCTTGTAACTATGTTTGTATGCTTTCAACACCTTAGCCTTCAGTATTAAACAATATAGACAGAGAATTGGCAAATGTGTTTCTCTAACATCTCCATCACTGTAATTTTCACTCCCTTATTTAACAAGCCTGATTGAACTCTAAACAAAGAGAGTCACAGAAGAGAGCTACAGCCTAGAGTGTAAATAAAGGTCCAGAAATGTCTTTACCTTACCTGTGATCTGATTCCCAACAGCTCTACAACATCTTCCCCCAAGTAATGGAACGCTTTTCTAGTAGACATCACGCCATCTTAAAAGACGTAGAAAACATCCGGACCTTCATTAGGAACAAAGTTAAGGAACATGAACAGAGATTAGACTTCAGTGACCCAAGTGATTTTATTGACTGCTTCCTTATCAGACTCACTCAGGTATCTAATTGTCTTATTGCTGTGCTTTCTTATCTTCTGCAGCATATAACACATGTTTAAACCTATTGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42457
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000002842 | Nonsense | 370 | 491 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 66804)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 99939 |
| GRCz11 | 15 | 27748 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGAAGTGCAGCGCTATATGGACATTGTGCCTCTAAGTCTTCCCCACTA[T/A]GCCATGAAAGACATCACTTTCAGAGGCTATAAAATCCCCAAGGTAACGAT
Long Flanking Sequence:
AAATGTACAGTTGTGTTCTCATGAAAGTTACTCTTGCATTAGTTGAGGATAAATTGCAACCTAGCATCCCGTTATGTCACATGTTTGTTCATGATTGGTGCTACTGACCCTTATTCACAGCTTATTGGAGGTCTATCAAACTGACATTTATACTAACCAAGCGCAGTCCACAGACCACTCCTCTATCCTGTGAGCTAAAGGTCTCATTATGCAATAAAATCTCAAAAAAGATTCTTGAAAATATGCTCAGATGTAATAGTTTGTGTAGATAGAGCCAACAATGCAATCTAATGCAATATGTAGGGTCTTTGCTTTCTTTACAATTATTCAATTTTTTCAAATGTTTTTGTTTAAGAGCAAATGCAGAGGGAGATAGATCGCGTTATTGGACAGAACAGAATTCCTACAATGGAGGACAGAAAGTCTCTTCCCTTCACTGATGCTGTGATTCATGAAGTGCAGCGCTATATGGACATTGTGCCTCTAAGTCTTCCCCACTA[T/A]GCCATGAAAGACATCACTTTCAGAGGCTATAAAATCCCCAAGGTAACGATGGACATTTACTGTCTTTGAGTTTTATTAATGAACAGTAAATGCATGGTTGGAGGAGATATATTATTGAAAAAATAATAATAATATCCCGCAGTAATCCTCAGTTGATTTGTTGTGTGCATCTGGATATTGTGAGTAATTGTAAATCTATTTCGCCAGGACACAGTAATTATTCCTATGCTGCACTCTGTCTTAAGGGATGAGGGGCAGTGGGAAACCCCTTGGACGTTTAACCCGGAACATTTTCTGGACTCCAATGGCAACTTTAAGAAGAATCCAGCCTTTATGCCCTTTTCTGCAGGTAAACCCTTGTCCAAAGGTAGCTATTCATTAATGACGGAACAGTATATGACTAGCAGATTGTCTTCACTACATTTTTATTATCAGACCATAGCTTTTAGGTATAAATAATCAATAGCCCAGTGGTTAGTGGGTTGACGCATGGTGCAGCA
Associated Phenotype:
Not determined