ZMP
si:dkeyp-68f9.10
Ensembl ID:
ZFIN ID:
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 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14111 | Nonsense | Available for shipment | Available now |
sa21546 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14111
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100487 | None | None | 438 | None | 8 |
ENSDART00000135748 | Nonsense | 133 | 522 | 2 | 9 |
The following transcripts of ENSDARG00000069186 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 39472894)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 38610790 |
GRCz11 | 9 | 38420585 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAATATCCRTGCAGAGGAWMCATGACTCTGTGGACAGAGCAYCGGGACT[T/G]AAGAGGCATTAGCTATGGCCCTTTCACAGAGTAAAAACAAAKGATTTGTA
Long Flanking Sequence:
GATGGTGTTTTCTGAGACCCACGGCAGCGGCCACAGGCTTCAGGAGTGCAGCAGGAAATGCTGCGGCTGCTTCTGTCAGTGTCCAGGACGGCCACAGAAAGCTGAAGACTGAGGCTGACCTTCCAGAGATCAAAATCTTTACCATGTTGTATCAAATGCTCTTCAAAGGTTACCTCAACAGCGTACATGAGCTACAGGTATAAAGAAATAACGCAGCTGTATTTGTTTGTCATGTGATTTTATCTGCAGGACTCTTGACATTATTGTTATTGTTTATGTCCTGATGCTGTCAGGTGTTTTAATGAATTGAAAAGAAACGGCTGTCATTTTATCTCTCCAGTTATATCAAAAACAGGTTTATGGCCCCTTGTGGAAAATTAATGCTGGAAACCTCCAAGGCATTTCAATAAGCAGTGTGGAGCTGCTGGAAGAACTCCTTCGAAAAGATGAGAAATATCCATGCAGAGGATACATGACTCTGTGGACAGAGCACCGGGACT[T/G]AAGAGGCATTAGCTATGGCCCTTTCACAGAGTAAAAACAAAGGATTTGTATAAATAACACTCGTTTTACAGCCCATTTAAAAAGCAAGTTGGCAAAGTTGGCTAATGTAGCTGTTTCGTGTTATACAAAATCATGAACTCGGTAACACTTTACAATAGGTTCATTAGTTAATGCATTTGCTAACATGAACTAATCATGAACAACACTTGTACAGCATTTATTAACCATAATTGAACATTTACTAATGCATTATTAACATCCAAACTCACAATGAACTACTGTATTTTCATTAACTAACGTTAACTAACATGAACAAGAACTGTAGTAAATGTATTGTTCATTGTTTGTTCATGTTAGTAAATGCATTAAGTAACATTAACTAATGAACCTTATTGTAAAGTGTGACCATGAACTCTTATCAATTTCCGCTGTTCAGTTTCTCATATGAAAAAAGACTGTGTTGTTCAACAGAGAAGGAGAGAAATGGTACAAACTGCGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21546
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100487 | Nonsense | 217 | 438 | 4 | 8 |
ENSDART00000135748 | Nonsense | 301 | 522 | 5 | 9 |
The following transcripts of ENSDARG00000069186 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 39475782)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 38613678 |
GRCz11 | 9 | 38423473 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGCCATTCAGAAGCGTGTAGATACCAATCAGGATGTTGCTGGAGAGTA[T/G]CTCACATACCTGCTTTCTAATGGCAAGATAAGCAGGAAAGACGTTTATGG
Long Flanking Sequence:
TTTATTTTATAAGACATAAATGGTGTTAAATTGGTATGCAAATGACCATAATAATGTTAGTCATTTGAATACCAATTTATCACCATTTTAAACATGCTTTCAATTTGCCCACAATAATTGAGATACCTTTCTTCACAGGGATTGCGTCCATTCTCTTCGAGACGCGCATTGGCTGTCTGGAGAAAGAAATTCCTGCTGAGACACAAAAGTTTATTAATTTCATTGCTCAAATGTTCACCTACAGCATGCACGTGGCCCTTCTGCCCAACTGGACCCGCAAATATTTCCCATTCTGGCAGAAGTACATTGATGGCTGGGATGGCATATTCAAGTTCGGTAAGCTTCACACATCTGCTTCAGACTGACTTTAAGAGATTTGTTGTGGAGTTTAATAATGTTTATTGTACTAATGGATTACTCATAGGCACAAAAATGATTGACATGAAGATGGAGGCCATTCAGAAGCGTGTAGATACCAATCAGGATGTTGCTGGAGAGTA[T/G]CTCACATACCTGCTTTCTAATGGCAAGATAAGCAGGAAAGACGTTTATGGAAGTGTATCTGAGCTGCTGCTGGCTGGAGTCGACTCAGTAAGACGCTCCTTCTATAGATTTGACTGTGTAAACAACATTTGTAGGAGTTTTAAAAATTTGTAATTGTCAAGGTTTGGGTTAGGGAAGGACAAGTACTCATATGTAGGACTAAAAGATGGGTTTTTTAAATAAAAAATATAATAAAATGCGGAAAAAAAAAAACAATTGGGGAAAACATTAGCAAAAACAAACTTGGCTTTGCTGGCAGGGAAGAGCAGATCTGAACACGACAGGACAAAACTGGACACTAGAAGAATGACGTACAAACTGGCACAGGACAGTAGACATGAGGGAGCTATAAAGGAGAAAAATTAGCAAACAAATAGGTCAACAGAATTAACTAATAATATATATACTTATAATACATTATATTTTCATACCATATCAAAGACAAAATATATACTGATACA
Associated Phenotype:
Not determined