ZMP
zgc:162815
Ensembl ID:
ZFIN ID:
Description:
cytochrome P450-like [Source:RefSeq peptide;Acc:NP_001036243]
Human Orthologue:
CYP2W1
Human Description:
cytochrome P450, family 2, subfamily W, polypeptide 1 [Source:HGNC Symbol;Acc:20243]
Mouse Orthologue:
Cyp2w1
Mouse Description:
cytochrome P450, family 2, subfamily w, polypeptide 1 Gene [Source:MGI Symbol;Acc:MGI:3616076]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13143 | Nonsense | Available for shipment | Available now |
sa7539 | Missense | Mutation detected in F1 DNA | Not yet available |
sa16722 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13143
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 |
---|---|---|---|---|---|
ENSDART00000055971 | Nonsense | 155 | 503 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 12507786)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 12607863 |
GRCz11 | 3 | 12759312 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTWTWAGCAACCTGCGAGACTTTGGGATGGGCAAAAGAGGGAGCGAAGMG[A/T]AAATCATTGAAGAAATTCWTCATCTCAAAGGAGAATTTGATAAGTTTGAA
Long Flanking Sequence:
AAATCTTTTTTTGTAAATGCTTTTTATTTATTTATTTTTTTTTTGTCCTCCAGCTGTCCAAAACCTATGGGAATGTGTACCAAGTGTTTTTGGGTCCCAAAAAAGTCGTCGTACTTATTGGACACAAAACTGTTAAAGAAGCTCTTGTGAATTATGCAGATGAGTTTGGCGAGCGAGATATTACACCTATTTTCAGGATACTTGCTAATGATCATGGTAAGAATAACCCAGTGCTTTGTTTTTTATCATTCAAGTGTAATAGAGGCCCATTGATCCAACTGTTGCATTTTTTTATGGTTGCACCTTTGCCATTGGAGTTTATTGCAGTCCCATTATTACGTTAAGAACATTTTTAAATAGTATCAAAGATGTTTGTTGTATTTGACTGATTTTATTGGTTAGGGATCCTCTTTTCTAATGGAGAAAGCTGGAAAGAGATGCGACGCTTCGCTATTAGCAACCTGCGAGACTTTGGGATGGGCAAAAGAGGGAGCGAAGAG[A/T]AAATCATTGAAGAAATTCATCATCTCAAAGGAGAATTTGATAAGTTTGAAGGTACGAGATGAGCAAGACACATAAATGGACATCTTCACTCATCCTCTTAGTTTATAAGATCCAATGAGAGACGTTTGTTGCTGTTTTTATTAACAGGGAAACCCTTTGACACAACACAGCCTGTGAACTACGCTGTGTCAAACATCATCTCGTCTATTGTGTACGGCAGCAGATTTGAATACACAGACCCTCGATTCACAGAAATGGTTGATAGAGCAAATGAAAATATTCGAGTTAGCGGATCAGTTTCAATGATGGTATGGAAATATGATTTTTGAGAAATTTAGTTTGCAAATGACATTAACGTATTGATGCATATCTTCCTCTGTATGTATTTCAGCTTTACAATATCTTTCCATGGCTGGGTCTATTCCTCAACAGCAAAAGGACTGTCGTGAGAAACATGTTAAAAAACAGAGCAGAATTTATGAAGTTGATCACTGGCCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7539
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:
A > G
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055971 | Missense | 311 | 503 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 12504958)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 12610691 |
GRCz11 | 3 | 12762140 |
KASP Assay ID:
554-4341.1 (used for ordering genotyping assays)
KASP Sequence:
TTCATGCAGAGAATCTTCTCATGACRGTGGGAAATCTGTTTGCTGCTGGT[A/G]CTGATACYACAGGAACAACTCTGCGCTGGGGTCTGATGCTCATGGCCAAA
Long Flanking Sequence:
GGATACTTCACTTCACTTAGAGCTGTGTTACACACTACATGGAGGGGAATTTTCAAAAACCCATAATATGGGCTCTTTAATGAGTTATGGGTGTGTTTTGAGCATAACGTGCATTAAACCAATCAGAGACTCATCTCTCATTACCTTTAAGAGTCAGTTGCATCGTGCCATGATGCATTTGCTGTTTAGGATGCTCCAGGAGCTAGGGGTAAAATATAACATGTTATCTGTGGTCAAAAAACCTGTGATATATTTTGGATGTAAATTTTAAATTTGGTTGATTTGACACAATGGTGCTGTTGTTGTTGTTTTTTACAAGCATTATACATTTGCCTAAGCATATTAAATTTATTATAACCAACAAAAATAGTTTACATTAACTTTTTAAAAAATGCTTCAATGATGTGTGGATTTCTATTTATTAGCAATTAGGCAAGAAGGACTCATACTTTCATGCAGAGAATCTTCTCATGACGGTGGGAAATCTGTTTGCTGCTGGT[A/G]CTGATACTACAGGAACAACTCTGCGCTGGGGTCTGATGCTCATGGCCAAATACCCTCAAATACAAGGTAAAAATAGTCATATGAAGAATTTTCCTTCAGTGTTGAATACATTGTAGGTCAAAGCACCAAATATGTTGCATTTGTGGGCAGATCGAGTTCAAGAGGAGATTGACAGAGTGATTGGTGGACGTCAGCCGGTGGTGGAAGACAGGAAGAAATTACCATATACAGATGCTGTCATTCATGAAATTCAGAGACTGGCCAACATAGTTCCCATGAATCTCCCTCATGTGACCAGCTGTGATGTTACCTTCAATGGATACTTCATCAAGAAGGTCTATCAGAAGAATGTGTATTAAAATAAGTAAAATATATTGAAGTCCACATTTTAATTTAGTCTTTTTATTTGTTCTATAGGGGACCACTGTTATTCCTCTGCTGACGTCTGTTCTGAAGGATGAAAGTGAATGGGAGAAACCAAACAGCTTTTACCCAGAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16722
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 |
---|---|---|---|---|---|
ENSDART00000055971 | Essential Splice Site | 333 | 503 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 12504809)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 12610840 |
GRCz11 | 3 | 12762289 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTTGAAYACATTGTAGGWCAAAGCACCAAATATGTNNTGCATTTGTGGGC[A/T]GATCGAGTTCAAGAGGWGATTGAYRGAGTGATTGGTGGACGWCAGCCGGY
Long Flanking Sequence:
AGAGTCAGTTGCATCGTGCCATGATGCATTTGCTGTTTAGGATGCTCCAGGAGCTAGGGGTAAAATATAACATGTTATCTGTGGTCAAAAAACCTGTGATATATTTTGGATGTAAATTTTAAATTTGGTTGATTTGACACAATGGTGCTGTTGTTGTTGTTTTTTACAAGCATTATACATTTGCCTAAGCATATTAAATTTATTATAACCAACAAAAATAGTTTACATTAACTTTTTAAAAAATGCTTCAATGATGTGTGGATTTCTATTTATTAGCAATTAGGCAAGAAGGACTCATACTTTCATGCAGAGAATCTTCTCATGACGGTGGGAAATCTGTTTGCTGCTGGTACTGATACTACAGGAACAACTCTGCGCTGGGGTCTGATGCTCATGGCCAAATACCCTCAAATACAAGGTAAAAATAGTCATATGAAGAATTTTCCTTCAGTGTTGAATACATTGTAGGTCAAAGCACCAAATATGTTGCATTTGTGGGC[A/T]GATCGAGTTCAAGAGGAGATTGACAGAGTGATTGGTGGACGTCAGCCGGTGGTGGAAGACAGGAAGAAATTACCATATACAGATGCTGTCATTCATGAAATTCAGAGACTGGCCAACATAGTTCCCATGAATCTCCCTCATGTGACCAGCTGTGATGTTACCTTCAATGGATACTTCATCAAGAAGGTCTATCAGAAGAATGTGTATTAAAATAAGTAAAATATATTGAAGTCCACATTTTAATTTAGTCTTTTTATTTGTTCTATAGGGGACCACTGTTATTCCTCTGCTGACGTCTGTTCTGAAGGATGAAAGTGAATGGGAGAAACCAAACAGCTTTTACCCAGAACACTTCCTTGATGAGAAGGGCCAGTTCGTCAAGAGAGATGCTTTCATGCCCTTTTCTGCAGGTATGATCAATATAAACACACAGTTTTGAAGAAACGAGCATGTGAATTGGAATAAAATATATTTGCTGTTTGGTCAGGGCGCAGGGTTTG
Associated Phenotype:
Not determined