ZMP
zgc:194733
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100170784 [Source:RefSeq peptide;Acc:NP_001124095]
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 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa45134 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa12197 | Nonsense | Available for shipment | Available now |
| sa33102 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa40007 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa13788 | Essential Splice Site | Available for shipment | Available now |
| sa14880 | Essential Splice Site | Available for shipment | Available now |
| sa19954 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45134
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000059182 | Essential Splice Site | 66 | 507 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 12482332)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 12633317 |
| GRCz11 | 3 | 12784766 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAACTTGCACACATTGGACCTAAAAAACCTGCACGTGAGCCTTTGGGAA[G/A]TGAGTTAAATATAGTTTATTTCCTTGCCTTGTTTTAAAAAGTTAGTTCAG
Long Flanking Sequence:
GATGTATTCATTTCTCATAAAGCTGATAAATCATACCGAATGAGTTTTTTTTTTTCAGAAAGTGAACCTGCTAACAGTTTCCTGTGAGGGCTAGTTGGCTTTAGGGATATTGTAGGGGTATAGTGCAATACAGTTCAGTATAGAAACAATGGAAATGTCCCCACAATTCATGAACACAAACCCGTGTTCGTGTTCAGCTCCTCCCTTCATTCAGTAGAGCGTGTGTTTCACAATGTCGAAACCTGAGTTACAACAGCAGTCTCGTGTGAAGACTCGCTGTCGTAGTGGAGATCTCTGTTATTATGGCTGTGATGGAGACTCTGCTCATGCCTGTGTCCATTACAGGAGTTTTACTTTCTGCTGTGCTGTTGTTTCTGGTTGTTTATCTAATCTCTATCAGCTCCAGCTCTCCTGAAGATCCTCCAGGACCCAAACCACTGCCACTTTTGGGGAACTTGCACACATTGGACCTAAAAAACCTGCACGTGAGCCTTTGGGAA[G/A]TGAGTTAAATATAGTTTATTTCCTTGCCTTGTTTTAAAAAGTTAGTTCAGGACTGTAATTGTTTCTAAAAGAATTGGCATTTCCAATTAGACTAGCATTTTAAAAGGATTTCCTAATAATGGAATTGCAGCAAAAAAAAAAAAAAAAAAAAAAGGCTAAACATTTACAGGTTTTTGCCATGTATTAAGGCAAAGGTCCTTGGTGCTTGCTTTTTCTTTCTTGAATGTGATGTATTTCAAAAAAGGAATTTAATATGTCGTTTAACAAGAAATATAGAATAATTTATTTCATATTTTTCTTATTTCAAACCTGATGTTTAAGTGTGAGAGAATTCAACTCCTGAAAAGGGTAGACAATTGCTAAATGTCAGCTACAGCCTTATATATACAGTGAAACTTGGCTACTTTATTTCAATTTGCTAACACAAATACCAAACAACACATTGTAACACATCAAAATCAGCATGACATTTCAAAGTAGAAAGATATGGATTTCATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12197
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 |
|---|---|---|---|---|---|
| ENSDART00000059182 | Nonsense | 120 | 507 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 12480117)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 12635532 |
| GRCz11 | 3 | 12786981 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATTTGGAGAAAGGGACATTACACMGATATTCCAGGACTGTAATCAGGGA[C/T]AAGGTAAAACAKCAACTATAAGATTAATATGAYACTGCAYGTTTGTGGST
Long Flanking Sequence:
GCTTTAAGCTCAACAGAGTGAGTTTTTTGGAATGGCCATCACAAAGCCCTGACCCTCAATCCTATAGAAAATTTGTGGGCAGATTTGAAAAAGCGAGAAAATAAGTCAATGACTGCTTCTTTCCAACCTTCTTCAGTATATATTTCTCTGTGTTCAACAGAAGAAAGAAACTCAAACAGGTTTGAGATAGGTGAAGAAAGTATATGATGACAGAATTGTCATATTTGGGTGAAATATGCCTTTAAGATCCACTTAAAAGCTTTGCTTGTTCATGAGTTGTAGCTAATAACAGCTAATAAAATCAAAGTATATCTTGCAATAATCGGTTTTGTGTTTCACAGTTGTCTAAGAAGTATGGGCCTGTGTTCAAAGTGCATTTAGGACGCAAGAAGGTTGTGGTTCTGGCCGGGTACAAAACAGTTAAACAAGCACTTGTGAACCAGGCCGAGGAATTTGGAGAAAGGGACATTACACCGATATTCCAGGACTGTAATCAGGGA[C/T]AAGGTAAAACATCAACTATAAGATTAATATGACACTGCATGTTTGTGGCTCTTGAGCTTAATCATTGGCAGCAACCAATCTATCCTATATAAAAAGTAACATAATATAGGATTAAAAATCAGGCAAAAGTTATAATGTGGTGGCAATTTATGAATACGGATAGATGGGCACAACTGTGTAGGATAAACTTTTTAAATGATAAGAAAAATGTACATAAACTATGATGGATACACATTTACTGAATAAATATAAAAAAGTAAGGTGATGTTGCTTTAAAAGATCATGTTGTGGTAAAAACAGCTGCAATGGGATGGCATTATTGGACAAACCAGTGAGCTGACCAAATGTTTTCATGATTTTGAGATAATTTAAGTGAAATATACTTCAAGTGTGTTCAAAAGCTCATTGTTTCACTTTGTTGGATGCTCCCTAATAAGCTTGTTGCTCATGACCTCTGGACTGCTTTGCTCATTCTGCTCCCTTAATTGCTGCTTGTAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33102
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000059182 | Essential Splice Site | 170 | 507 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 12477953)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 12637696 |
| GRCz11 | 3 | 12789145 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCGTGGATGAAACACGTTATCTGCGGGAAGTGTTTATGAAGTTTGAAG[G/T]TACCGTAGAGCGATCGCCGATGCGAATGCTTTTCTTTTCTACATATCAAT
Long Flanking Sequence:
AAAGTCCATCATCAAAGTGGTTCAGTATTATTATGTTTCTCTTCTCCAGAACTGTTTTGAGTGTCTGCTAAACCCCTAGATCGCCTTACACCTCCAAAAGCCACCATAATTTTCGTCATCATCTGAGGCACAAGTGATATGTTATATAGTAAAAAAGCTCCCTCGGTGGTTTCTCCTGCCACCAATTTCTCTTTTTCAGTTTTGATATTTGGCACCAGGAAGTGATGATTTTGTTCTTTTTGACTCATTAGTTGGAAATTGCTTTATTTGCAAATGTTTTATGTGATAATCTAGTTTTGTGCAAATAATTAGCATCTTTGATTGGAAACATGTCTAATGTTTTTCTTCAGGAATCGTCTTTGCAAATGGTGAAAGATGGAGGACGATGAGAAGATTCGCTCTCTCAACTCTTCGAGACTTTGGAATGGGCAAAAAACTGAGTGAAGAAAAAATCGTGGATGAAACACGTTATCTGCGGGAAGTGTTTATGAAGTTTGAAG[G/T]TACCGTAGAGCGATCGCCGATGCGAATGCTTTTCTTTTCTACATATCAATTTACAATAAATCTCCTCTCTGTATTTGCCTTGCAGGACAACCATTTGATACAACCCAACCGGTAAACTATGCCGTCTCCAACATCATCTCAGCTATTGTTTATGGGAAACGGTTTGAATATGAGGACCCAGCGTTTCAGGATATGGTGAACAAAGCAAACATGAACATCCGTATGATTGGTTCTGCTGTGATACAGGTACTCACCACTGGTTTTTCTTGTGCAAAACTTATTTTAGTATCATGAATATTTAAAACAAAATAAAGGTTGCCAATGACATCTTTCGCAGACAATCCTGCAAGCTATCTGCACATTACAGCCCCTTTAAACTAAATGAAAATGGGAAAATATTAACCTTGGTTCCTCATGCTGGTGTGGACCAGTCGTGGATCTAGCTTTAGGTGTTCCTTATATGGTAACCTGAAACCGCTCCATACAGATGGAATTTAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40007
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 |
|---|---|---|---|---|---|
| ENSDART00000059182 | Nonsense | 229 | 507 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 12474495)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 12641154 |
| GRCz11 | 3 | 12792603 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGCCTTTTAAAGCTGTTTGTGTCTCTTCTTGCAGATCTACAACATGTG[T/A]CCATTTTTGGGTCCCTGGATTAAGACCTGGAGACAGCTAATGAAAAATAT
Long Flanking Sequence:
CGGGACAGCATGCCAAACGCTCTTTATAATCAATCATCAGCTAAGTTAATTTTAATTCAATTCATCTTTATTACTATAGCACTTTTACAATGTAGATTGTGTCAAAGCAGCTTAACATAGAAGTTCTAGTAAATTGAAATGTGTCAGTTCAGTTTTCAGAGCTGAAGTTCCGTTTAGTTCAGTTCAGTGTGGTTTAATTTTCACTGCTGAAAGTCCAAACACTGAAGAGCAAATCCATTGATGCGCAGCTGCACAAGTCCCAAACCAAGCAAGCCAGCGGCGACAGTGGAGGAACAAACTTCATCAATTGACCAAAGTGAAGGAAAAAAAGTCCTAGAGAGAAACCAGGCTCGGTTTAACTGAGGGTTGGGTTATTTTTAACAGTGAACTGACTCACATGCATAAGTGCTGTTAAAATGATTGTCTAAAACTCGTTTTGTCAGTCAAACAGGTGCCTTTTAAAGCTGTTTGTGTCTCTTCTTGCAGATCTACAACATGTG[T/A]CCATTTTTGGGTCCCTGGATTAAGACCTGGAGACAGCTAATGAAAAATATGGAAAGCACCAGGAGGCAAATACAGACCCTGGCAGATGTCTTACAGGAGACTTTGAACCCGCTTGACTGCAGAGGACTCATTGACTCTTTCCTCATCCGAAAACAGAACATACAAGTAAAGAATTACCTGGATTTAGACTTCACTTTTGACCAGTAAACTTTTAACTTAAAAGATTGTTTTTTCAGTACTGAATGACATGGTTTTTCAAGGGTCATAAAATATAATGGTATTTTGGAGTCAGGGAGTTTTATATACATTTGCACATCATAGAATATGAAGGACTTTTGTATTTTTGCTGTACCATGTTTTTTAAACACATTGTTTCACATGTTTTGCCTGTTGTTATATTTAGGCAATTTTTTTTACTTCCATTTAATTCCTTTAATTTTCAAAATGCATACTTGTCAACCGGCAATCAAATGCATTAATAGGGCTTTTTTAGGGTAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13788
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000059182 | Essential Splice Site | 331 | 507 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 12471952)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 12643697 |
| GRCz11 | 3 | 12795146 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACGCTGCGCTGGGGTCTGATGCTCATGGCCAAATACCCTCAAATACAAG[G/A]TCAGACGTACAAACTGAGGAGAAAAKATGCTGTTTTCNCTAGTRCCTTCMC
Long Flanking Sequence:
AGAAAATAGTCAAACTACTTGCTCTAAACAAGCAGGTGTGTTCATGACAATAAAGAGTAGAATAACATAATAAGCTGTTTTTAATGACTAAAAAAACCAATGAAAATGAATAAGACCGGTCTCAAATCTGGAGCCAAAAAGATTCCAATGGCTGCGGCTGCTCATATATCAAGAATAAAGCCAATAGGTCATGGAAATTCAGCTATTTTAGTCAGTGAATGTCAGAGCAAAATCAAGGATTTTGAGTGGGAGGGCTTAGAGTGGGAACCCTGGAATTGATATAAATACTGTATAATTGATTCATTGTACTGTATTTTAGTCTCATCGTAAGAATAAAAATCTTTTTTATTTCATGCAGGAAACTGGAGAAAAAGATTCATCTTTCAATGATCAGAATCTGCTCATTACTGTGTCAAATTTGTTTGCTGCTGGCACTGACACGACTGGCACGACGCTGCGCTGGGGTCTGATGCTCATGGCCAAATACCCTCAAATACAAG[G/A]TCAGACGTACAAACTGAGGAGAAAATATGCTGTTTTCCTAGTACCTTCCCATTTGTCTCTTATAAGCATCATAATGAAAGATCTCACTGCTGTTAAACACCTTCATGTGTTTTTTTTGTGATCTTGTTGGCCATAGATCGAGTTCAGGAGGAGATTGACCAGGTTCTGGGTGGCCGTGAACCAGTTGCAGAAGACAGAAAGAACTTACCGTATACAGATGCTGTGATTCATGAAACACAGAGACTGGCTAATATTCTACCACTGAATCTCCCTCATAAGACGAGCTGTGATGTTACCTTCAATGGATATTTCATCAAGAAGGTTGTGTAAATGCAGTGTAAAGATATTAACTTTGTGCCATGGTGAATTTTGAATTATTCAGAATTATAGATACCTGCCGAAATTCGGATCATAAAATACGGGAGAATTTCTATGGGGGGTGCGCGCAAAGTGAAGAGCGGGGGGGAAGGAGGTGGGGGTGTGCACGAACTGAAGAGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14880
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000059182 | Essential Splice Site | 441 | 507 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 12465244)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 12650405 |
| GRCz11 | 3 | 12801854 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACTSKGGTGTCTTAAAATAGYCATTCCTTACATGATTTGTTTTTCTMTC[A/C]GGGCGCAGGGCTTGTCTTGGARAGRGTTTGGCCAGRAWGGAGCTCTTCCT
Long Flanking Sequence:
CACCTACATGTCTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACACCAACACGGGGAGAACATGCAAACTCCACATGGAAATGCCACCTGACCCAGCCGAGACTCGAACCAGTAACCTTCTTGCTGTAAGTTGATAGCACTACCCACTGCGCCACTGTCGCCGATCTTTATTATTATGCGCAATTTTCCTTAACTTGGATCTTTAAAAATGGGTGTTAAAGATTTAATACACGAGACATGTGTATTACACTGATCTGAACTTTAACAGTGATATTTCTACCAAACTAAACTAAAACAGTTGCAGCTTATCTAGAACTACACCAAGATTCCACACTACTGCATTAATTTAAAATATTATGGCTTTTACTAACCCCATCTATGTTAAACTTTGACACAGTCTACATTGTAAAAGATGTATATAGAAATAAAGAGGAGTTGAAAACTGGGGTGTCTTAAAATAGCCATTCCTTACATGATTTGTTTTTCTCTC[A/C]GGGCGCAGGGCTTGTCTTGGAGAGAGTTTGGCCAGAATGGAGCTCTTCCTCTTCTTCACGTCTCTCCTTCAGTATTTCCGCTTCAGTCCTCCTCCTGGAGCGTCTGAAGATGAGCTGGATCTCACACCGGTGGTGGGCCTGACTTTGAACCCTTCACCCCACAAACTGTGTGCAGTCATCAGAGCGGAAAGACAACTAAACTGATCCCTTGTGAAAAGTTCAGTTCTTTATACAGTATATTACACATATGTATTATCTGATAGAGAATTATATTTAATGTGCTTTTCTGTGCATAGCATAAAGCGGTAAATGGTGCATATACCCACAGATTTTATTTCAGCCTGCCAACCTCGCTAACGGTAAACTCTTTCCATCATAAAATGAATAAATAAATCAGTGATCAAATAGATATACCATGGGCGTTGCTAGGGTTGAAAGGGATGAGGGGCTTAGCTGCAAAGAAGAAAATAAGATTTAAATAAAGATAAAAAGGCTTTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19954
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 |
|---|---|---|---|---|---|
| ENSDART00000059182 | Nonsense | 495 | 507 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 12465081)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 12650568 |
| GRCz11 | 3 | 12802017 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTGGATCTCACACCGGTGGTGGGCCTGACTTTGAACCCTTCACCCCAC[A/T]AACTGTGTGCAGTCATCAGAGCGGAAAGACAACTAAACTGATCCCTTGTG
Long Flanking Sequence:
ACTGTCGCCGATCTTTATTATTATGCGCAATTTTCCTTAACTTGGATCTTTAAAAATGGGTGTTAAAGATTTAATACACGAGACATGTGTATTACACTGATCTGAACTTTAACAGTGATATTTCTACCAAACTAAACTAAAACAGTTGCAGCTTATCTAGAACTACACCAAGATTCCACACTACTGCATTAATTTAAAATATTATGGCTTTTACTAACCCCATCTATGTTAAACTTTGACACAGTCTACATTGTAAAAGATGTATATAGAAATAAAGAGGAGTTGAAAACTGGGGTGTCTTAAAATAGCCATTCCTTACATGATTTGTTTTTCTCTCAGGGCGCAGGGCTTGTCTTGGAGAGAGTTTGGCCAGAATGGAGCTCTTCCTCTTCTTCACGTCTCTCCTTCAGTATTTCCGCTTCAGTCCTCCTCCTGGAGCGTCTGAAGATGAGCTGGATCTCACACCGGTGGTGGGCCTGACTTTGAACCCTTCACCCCAC[A/T]AACTGTGTGCAGTCATCAGAGCGGAAAGACAACTAAACTGATCCCTTGTGAAAAGTTCAGTTCTTTATACAGTATATTACACATATGTATTATCTGATAGAGAATTATATTTAATGTGCTTTTCTGTGCATAGCATAAAGCGGTAAATGGTGCATATACCCACAGATTTTATTTCAGCCTGCCAACCTCGCTAACGGTAAACTCTTTCCATCATAAAATGAATAAATAAATCAGTGATCAAATAGATATACCATGGGCGTTGCTAGGGTTGAAAGGGATGAGGGGCTTAGCTGCAAAGAAGAAAATAAGATTTAAATAAAGATAAAAAGGCTTTAACTGTGACAATAAATGGTTTATATGTCTTCCTCCAGCCATCTTAGGTATTTTTATAAGAATAAACTGCTTTAAAAATCTGATGCTAACTGACATGTTACAGTAGAATATCCGCTTGTTAAGTGATGACGTATTGGTGACGTATGTAATACTGTTTCCGGGTCCAA
Associated Phenotype:
Not determined