ZMP
si:dkeyp-68f9.9
Ensembl ID:
ZFIN ID:
Description:
LOC402831 protein [Source:UniProtKB/TrEMBL;Acc:Q7SXE6]
Human Orthologue:
CYP27A1
Human Description:
cytochrome P450, family 27, subfamily A, polypeptide 1 [Source:HGNC Symbol;Acc:2605]
Mouse Orthologue:
Cyp27a1
Mouse Description:
cytochrome P450, family 27, subfamily a, polypeptide 1 Gene [Source:MGI Symbol;Acc:MGI:88594]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9857 | Nonsense | Available for shipment | Available now |
| sa18959 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9857
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 |
|---|---|---|---|---|---|
| ENSDART00000045588 | Nonsense | 263 | 531 | 4 | 9 |
| ENSDART00000100483 | Nonsense | 172 | 248 | 3 | 8 |
| ENSDART00000045588 | Nonsense | 263 | 531 | 4 | 9 |
| ENSDART00000100483 | Nonsense | 172 | 248 | 3 | 8 |
The following transcripts of ENSDARG00000033802 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 39465294)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 38603190 |
| GRCz11 | 9 | 38412985 |
KASP Assay ID:
2260-2203.1 (used for ordering genotyping assays)
KASP Sequence:
TATTGCACAGATGCTCACCTACAGCATGCCCGTGGTGTTTATGCCCAACT[G/A]GACCCGCAATTACTTGCCATTCYGGCAAAGGTACATTGGCGGCTGGGATG
Long Flanking Sequence:
AACTTAAACATTTCATCAACCAATCAGATCAGATTTGAACAATAAATACAAGTTATAAGATCTCAAAAAAACAATGATCTTCTATTGATATTGCAGTATATATTGTCTAAGCAATTTATGGTGTTTGTAATAAAATGTATTGCATCCACTGATCTATATAGAACAATGGACAATTATTAATATTATTGTTATTATTATACTATTCTATTCTGTTATTTTATTCTCTATTATAAATCAGTGACTTTATCATAGATTTTAACATGGCTGAATTCATGTATGTGTTTTGTTTTTGTCATGACAGTTATTGCGCATACTAATTCATCACCAATATTTAACATGTACTCCATTTGCAACCATTTCCTCCACAGGAATCTCCTCCATTCTGTTTGAGACACGCATTGGCTGCCTGGAGAAAGAGATTCCTGCTGAGACGCAACATTTCATTAATTCTATTGCACAGATGCTCACCTACAGCATGCCCGTGGTGTTTATGCCCAACT[G/A]GACCCGCAATTACTTGCCATTCTGGCAAAGGTACATTGGCGGCTGGGATGGCATATTCAAGTTCGGTTAGTGTGTTAGTTCCCACATTGTGTTCTTGCAGACTACAAGAGATACATGCATGATGTTTTCTATAATGTTGTTGATTACATTTATATATTATGCATAGCTGGAAAAATGATTGACATGAAGATGGAGGCCCTTCAGAAGCGTGTAGATGCAAATCAGGAGGTTGCTGGAGAATATCTCACATATCTGCTTTCTAATGGCAAGATGAGCAGCAAAGATGTTTATGGAAGTGTATCTGAGCTGCTGCTGGCTGGCGTCGACACAGTAAGACATCTTTTTTTGTAGTTTACAGAAGTTTACAAAATTAGACATCTTCATTAACGTCTGTGTGAACCAGAAATGGCTGAGACTTTTATCGCAGTATGTTGATGTGTTTCCAACTGAAGCAGAATAATGAGTAGGGGGTGGGGTTAGTAATGGCCATTAGTTTGCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18959
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000045588 | Nonsense | 263 | 531 | 4 | 9 |
| ENSDART00000100483 | Nonsense | 172 | 248 | 3 | 8 |
| ENSDART00000045588 | Nonsense | 263 | 531 | 4 | 9 |
| ENSDART00000100483 | Nonsense | 172 | 248 | 3 | 8 |
The following transcripts of ENSDARG00000033802 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 39465294)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 38603190 |
| GRCz11 | 9 | 38412985 |
KASP Assay ID:
2260-2203.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTGCACAGATGCTCACCTACAGCATGCCCGTGGTGTTTATGCCCAACT[G/A]GACCCGCAATTACTTGCCATTCTGGCAAAGGTACATTGGCGGCTGGGATG
Long Flanking Sequence:
AACTTAAACATTTCATCAACCAATCAGATCAGATTTGAACAATAAATACAAGTTATAAGATCTCAAAAAAACAATGATCTTCTATTGATATTGCAGTATATATTGTCTAAGCAATTTATGGTGTTTGTAATAAAATGTATTGCATCCACTGATCTATATAGAACAATGGACAATTATTAATATTATTGTTATTATTATACTATTCTATTCTGTTATTTTATTCTCTATTATAAATCAGTGACTTTATCATAGATTTTAACATGGCTGAATTCATGTATGTGTTTTGTTTTTGTCATGACAGTTATTGCGCATACTAATTCATCACCAATATTTAACATGTACTCCATTTGCAACCATTTCCTCCACAGGAATCTCCTCCATTCTGTTTGAGACACGCATTGGCTGCCTGGAGAAAGAGATTCCTGCTGAGACGCAACATTTCATTAATTCTATTGCACAGATGCTCACCTACAGCATGCCCGTGGTGTTTATGCCCAACT[G/A]GACCCGCAATTACTTGCCATTCTGGCAAAGGTACATTGGCGGCTGGGATGGCATATTCAAGTTCGGTTAGTGTGTTAGTTCCCACATTGTGTTCTTGCAGACTACAAGAGATACATGCATGATGTTTTCTATAATGTTGTTGATTACATTTATATATTATGCATAGCTGGAAAAATGATTGACATGAAGATGGAGGCCCTTCAGAAGCGTGTAGATGCAAATCAGGAGGTTGCTGGAGAATATCTCACATATCTGCTTTCTAATGGCAAGATGAGCAGCAAAGATGTTTATGGAAGTGTATCTGAGCTGCTGCTGGCTGGCGTCGACACAGTAAGACATCTTTTTTTGTAGTTTACAGAAGTTTACAAAATTAGACATCTTCATTAACGTCTGTGTGAACCAGAAATGGCTGAGACTTTTATCGCAGTATGTTGATGTGTTTCCAACTGAAGCAGAATAATGAGTAGGGGGTGGGGTTAGTAATGGCCATTAGTTTGCCA
Associated Phenotype:
Not determined