ZMP
zgc:66268
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC393484 [Source:RefSeq peptide;Acc:NP_956806]
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 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9457 | Nonsense | Available for shipment | Available now |
| sa26005 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9457
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 |
|---|---|---|---|---|---|
| ENSDART00000055972 | Nonsense | 335 | 455 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 12553526)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 12562123 |
| GRCz11 | 3 | 12713572 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAYAYATTGTAGATCAAAGCACCAAATATGTGTTGCATTTGTGTGCAGAT[C/T]GAGTTCAAGMGGAGATTGACAGAGTGATTGGTGGACGTCAGCCRGYGGTG
Long Flanking Sequence:
TATTATCCAAAGCAGAGCACAGATGACAAAGTTGATCACTGCTCTTCTGGAGACTCTGAATCCAAATGACCCCAGAGGCTTTGTTGACTCCTTTCTCATCCACAAACTGAGCGATGAGGTATGAACATTTGCAACAGTAGCTTTCACTGAAATAATCAGAAATTTAGGTTTGCAGTTTAACCAAGATCTGAATGGGACGATTATATGTTATTTTGATTATTTTACCGTTAAGGTTTACAATTTAAAAAAAAAATATGCATTGCATTCGACAGAAATCTGGAAAAAAGAACTCATACTTTCACAATGAGAATCTGATGATGAATGTGGCAAATCTGTTTGTCGCTGGTACTGACACCACAGGAACGACTCTGCGCTGGGGTCTGATGCTCATGGCCAAATACCCTCAGATACAGGGTAAAAAAAAGTTGTGAGAAGTATTTCTCAATGTTGAATACATTGTAGATCAAAGCACCAAATATGTGTTGCATTTGTGTGCAGAT[C/T]GAGTTCAAGAGGAGATTGACAGAGTGATTGGTGGACGTCAGCCGGCGGTGGAAGACAGGAAGAAATTACCATATACAGATGCTGTCATTCACGAAATTCAGAGATTTGCCAACATTGTACCACTGAATCTTCCACACACAACTAGCTGCGACATTACCTTCAATGGGTACTTCATCAAGAAGGTCAGCCAGAAGAATAAATGCACATTATTTTTATACATTTGTGAGAAAAAGTTATGAATTAAGGCAACTTTGGAATTAGGCTGTAACATAGGAAAAAGTGAATTACTGTGAATACTTTCTGTACGCACTGTACTGTACATATCGGTCCTAGAGAAGATAAATCATGTTCAGGACGTCAAGGTTTTGCTTTTTTTTTTCCTCCAATTTTATAGGGGACCACTGTTATTCCTCTGCTGACGTCTGTTCTGAAGGATGAAAGTGAATGGGAGAAACCAAACAGCTTTTACCCAGAACACTTCCTTGATGAGAAGGGCCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26005
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000055972 | Nonsense | 412 | 455 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 12553083)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 12562566 |
| GRCz11 | 3 | 12714015 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGGACCACTGTTATTCCTCTGCTGACGTCTGTTCTGAAGGATGAAAGT[G/T]AATGGGAGAAACCAAACAGCTTTTACCCAGAACACTTCCTTGATGAGAAG
Long Flanking Sequence:
AATGTTGAATACATTGTAGATCAAAGCACCAAATATGTGTTGCATTTGTGTGCAGATCGAGTTCAAGAGGAGATTGACAGAGTGATTGGTGGACGTCAGCCGGCGGTGGAAGACAGGAAGAAATTACCATATACAGATGCTGTCATTCACGAAATTCAGAGATTTGCCAACATTGTACCACTGAATCTTCCACACACAACTAGCTGCGACATTACCTTCAATGGGTACTTCATCAAGAAGGTCAGCCAGAAGAATAAATGCACATTATTTTTATACATTTGTGAGAAAAAGTTATGAATTAAGGCAACTTTGGAATTAGGCTGTAACATAGGAAAAAGTGAATTACTGTGAATACTTTCTGTACGCACTGTACTGTACATATCGGTCCTAGAGAAGATAAATCATGTTCAGGACGTCAAGGTTTTGCTTTTTTTTTTCCTCCAATTTTATAGGGGACCACTGTTATTCCTCTGCTGACGTCTGTTCTGAAGGATGAAAGT[G/T]AATGGGAGAAACCAAACAGCTTTTACCCAGAACACTTCCTTGATGAGAAGGGCCAGTTCGTCAAGAGAGATGCTTTCATGCCCTTTTCTGCAGGTACAGTTAAACATAAATATGAAAACAATGTGATCTAAAAATCTGCAGCCTGTTAAAAAGGCTCCATTAATGTCGCTTCACTTCATATGATTCTAATGAATGAAATGACTCACGTGAACTATTTACAATTCAGTAGTGTACTATTAAGACTTTACTGTTGTTTGCTTCTGCATGATCACTGCCTGTCTTTTTACTTCTATAGCAAAATGAACATCTAGAATGAAATGTTTAGCTACTTATTTCCTATTAAGTGTTAAAACTAAATCGTCAGGTATAGTTTTACTAATACCCCTCCACATTCTTTGAGTTGATTGGCTTCTTCAGTCATTCTGACATTGATGAGCGATGCTAGAGCCATCGAATAAAGCAGCAGTGACTATGGTTTCAAATCCACATGGAGCCTACCT
Associated Phenotype:
Not determined