ZMP
cyp17a1
Ensembl ID:
ZFIN ID:
Description:
cytochrome P450, family 17, subfamily A, polypeptide 1 [Source:RefSeq peptide;Acc:NP_997971]
Human Orthologue:
CYP17A1
Human Description:
cytochrome P450, family 17, subfamily A, polypeptide 1 [Source:HGNC Symbol;Acc:2593]
Mouse Orthologue:
Cyp17a1
Mouse Description:
cytochrome P450, family 17, subfamily a, polypeptide 1 Gene [Source:MGI Symbol;Acc:MGI:88586]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7373 | Missense | Mutation detected in F1 DNA | Not yet available |
sa35505 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22316 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7373
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 > C
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000043156 | Missense | 37 | 519 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 28834118)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 28480066 |
GRCz11 | 13 | 28610516 |
KASP Assay ID:
554-4320.1 (used for ordering genotyping assays)
KASP Sequence:
CTCTGGCAGCTCTGTATCTCAAACARAAGATGAATGGATTTGTGCCAGCA[G/C]GAAAYAGATSTCCTCCAAGTCTCCCTTCACTGCCCATCATCGGSAGTCTG
Long Flanking Sequence:
GTGCAATTTAATTAGTATTTTGATAGCTTTGTGCTATCAAAAGACTAATTTGTGGCAGTGTGCTGATTTTTTTAAAATTTTATTTAGCCATATATAGACCCACCACAGACCTTTACAAGGATTTAAAGCAAAACATTGATGATATCATTCTAATACAGGGTCTGCAGAGTTTAAGTGGCCGATTGTGCTCACACAAGCATCTCTGAATATGAGGAAACGATCAACAGCTCTGTTGAAAACAGCCTCCCTGACACTTAGATAGTTGAAGCTGAACTGTTTCAGGGTCAAGGAGGTGGCATTGAAGGATCTGCATAAAAGTCTCCTGTCGGCTCGCTAACACAGGCAGTGCTGTTCAGAAGAGCTGGAGGACACTCAGTTGAATATAGCTGACAATGGCTGAAGCACTCATCCTGCCCTGGCTGCTCTGTTTAAGCCTGTTCTCCGCAGTGACTCTGGCAGCTCTGTATCTCAAACAGAAGATGAATGGATTTGTGCCAGCA[G/C]GAAATAGATCTCCTCCAAGTCTCCCTTCACTGCCCATCATCGGGAGTCTGATGAGCCTGGTGAGCGACAGTCCTCCGCACATCTTCTTTCAGGACCTGCAGAAGAAATACGGAGATCTGTATTCCCTCATGATGGGCTCCCACAAACTGCTCATTGTGAACAACCACCATCATGCGAAGGAGATCCTGATCAAAAAAGGAAAAATATTTGCAGGGAGGCCACGGACTGTAAGTACATACAATCACATTCAGTTTAATTAGCCATTTTTAGCTGTTTAAATTTTGTTAATTTAAATATGGCCCATCTGCATATGGTTAAACTAAATTTACATATTCATTCATTCATTCATTTCTTTTTGGCTTAGTCCCTTTATTAATCAGAGGTCGTCAGAGCAGAATGAACTGCCTAAATCTGTATATTAAATACCATTAAACATATCATTCAATTGTAAGAATATTTCACATTAATGTGATTTGTTTTTTTTACTAAATATGAACTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35505
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 |
---|---|---|---|---|---|
ENSDART00000043156 | Essential Splice Site | 264 | 519 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 28830358)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 28476306 |
GRCz11 | 13 | 28606756 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATTTCCATCAGAGATAAACTGCTTCAGAAGAAATATGAGGAACACAAG[G/A]TAAATGTGCAATTTCATATTACAAAAAAATGTAGCCTATGAAATGAATAC
Long Flanking Sequence:
TACAGTTGCAAAGGACAGCTTGGTGGATATTTTCCCATGGCTGCAGGTGAGATTTGAGTTCATGTGTTAAGGTAAATGTTTGGGGTTATTAAAAGTTGACACTGATTTTGATGATTTCTTTCATATTTAATAAAATCAAATTATATTATTGTGAAATATTCTTACAATTAAATGAACTTTTAATTTTACCATGATTTTTAATGTGTTTTAAGGTTTATAGAAATATTTCTAAATTTAGTTTTTAACTATATGCACATGGGCCATATTTAGTTAAATTCAAATAGCCCAAAACAGCTATTCCTACTTTTTACTTATGTTTATTAATATTATAATATTATAGTTTTGTTGCAACCAGATTGAAGAAATATTTTAATTCTATTCCATAACTACACTAATTTAATTTTTCCTTTCAGATTTTCCCAAATAAAGACCTCAGAATCCTAAGACAATGCATTTCCATCAGAGATAAACTGCTTCAGAAGAAATATGAGGAACACAAG[G/A]TAAATGTGCAATTTCATATTACAAAAAAATGTAGCCTATGAAATGAATACAAGTAAAAGATAATCTTTATATAGCCTACTTTTTGAGTAATCTAAATAATCCTTTTCTACTGCACTCTCAGAAGAAAAGTTCCAAAAGTCTTTTAGAACATTTGAGGAGTTCAGATGCGAAAATCTGGAATTTTCTTCTACAACGAGCATTTTTCTCAGCCCCTTATGTTAATGTTCGGTTATTTCACCAATTATTTATTATTTATTATATGACCAATTCTTTGCCATAAAAGTGAAATTACTGAACATAGACATAGGAGCCTGAGAAAAATGCTAATTTTAGAAGAATTTCAGATGGCACGTAGAGGTTTTTGCATCTGAACTCCTCATTCGATTAATTTGAACAGTACAGAATCTTTTGTGGAATGGAGAGGTTCTAAGAATATTAAAGGGACATTTCACCCCAAAATTTACTCATTATTTGATCACCTTTTACTTTTTCCAAACCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22316
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000043156 | Nonsense | 469 | 519 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 28825849)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 28471797 |
GRCz11 | 13 | 28602247 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTCTCGGCGAGGCCCTGGCAAAGATGGAGCTCTTTCTCTTCCTGGCGT[G/A]GATTTTGCAAAGGTTTACTCTGGAGATGCCCACTGGCCAGCCTCTGCCTG
Long Flanking Sequence:
TCATATAAACTTCTGTTACACTTCTTACATTTCTGTCAATCCTCTTAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTAAATAGAGTGAAAACCCTTATCGTCTTAGACTCATGCTAATATTGAAATGGTTCACTCTTATTTGTACAGTGTTGGTGAATACACAGTGCAGAAAGGGACGCGGGTCGTTATTAACCTCTGGTCTTTACATCATGATGAGAAGGAATGGAAGAACCCTGAGCTCTTTGACCCAGGTGAGGATCTGCTATGATGAAAGCCGGTTGTCTCTCGCTGTCTCTCGCTTTGAACATTATCAGTAACAGTGAATCCTCTAATCTGACAGGACGCTTTCTGAATGAGGAGGGTGATGGTTTGTGCTGCCCGTCGGGCAGTTATCTGCCATTCGGCGCAGGGGTGCGTGTTTGTCTCGGCGAGGCCCTGGCAAAGATGGAGCTCTTTCTCTTCCTGGCGT[G/A]GATTTTGCAAAGGTTTACTCTGGAGATGCCCACTGGCCAGCCTCTGCCTGACCTCCAGGGCAAGTTTGGCGTGGTTCTTCAACCCAAGAAATTCAAGGTTGTTGCTAAAGTAAGAGCAGACTGGGAGAAATCCCCACTCATGCAGCACTGCTGAGCTTAATGTCAGATGCTGAAATCTTAATCTAATGAGAATCTTTTTCTCAGCTTCCTCTGTGTAGATTGTGTATTTTCACTTTTATGGCAGAACGTTGGTTCTTTTTATCAAATTTAGAGTGAAATAAACATAATGCTGAGGAAATATTCTCTTTTAGAAGATCATTTCAGACGGCGCTCAGTCAAATAGCACACATCAAACATAAATTCAAAGAAGGATTTTGAACAGTCAGAATATGGAGGGAACACATTTATTCATATAAGCTGATTATTAATGATGGTTTATTGACTGTTAAAGAGCAACAAGGGTGTTATTGATGGCATGTGTTTTTGTTGAAGCCACCAGG
Associated Phenotype:
Not determined