ZMP
cyp11b2
Ensembl ID:
ZFIN ID:
Description:
cytochrome P450, family 11, subfamily B, polypeptide 2 [Source:RefSeq peptide;Acc:NP_001073673]
Human Orthologues:
CYP11B1, CYP11B2
Human Descriptions:
cytochrome P450, family 11, subfamily B, polypeptide 1 [Source:HGNC Symbol;Acc:2591]
cytochrome P450, family 11, subfamily B, polypeptide 2 [Source:HGNC Symbol;Acc:2592]
cytochrome P450, family 11, subfamily B, polypeptide 2 [Source:HGNC Symbol;Acc:2592]
Mouse Orthologues:
Cyp11b1, Cyp11b2
Mouse Descriptions:
cytochrome P450, family 11, subfamily b, polypeptide 1 Gene [Source:MGI Symbol;Acc:MGI:88583]
cytochrome P450, family 11, subfamily b, polypeptide 2 Gene [Source:MGI Symbol;Acc:MGI:88584]
cytochrome P450, family 11, subfamily b, polypeptide 2 Gene [Source:MGI Symbol;Acc:MGI:88584]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44863 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44863
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061572 | Essential Splice Site | 315 | 628 | None | 13 |
ENSDART00000131093 | Essential Splice Site | 310 | 623 | None | 13 |
Genomic Location (Zv9):
Chromosome 16 (position 57908979)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 54643617 |
GRCz11 | 16 | 54463019 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACTGACCCTTGACCCCAGTCCTGACCTCTTCCGCTTCGCATTGGAAGG[T/G]CAGCCTCTTCTAATTCCTCGTTAATAGAGAAGGGCTGTTACTGAAACTGC
Long Flanking Sequence:
GTGTGTGGGTTTGAGTGTGTGCGTAAATATGTGGATGTAGTGCTTTTAATGCGCACACCTAACCCCGCCCCTCACAGTGACATCACTCGCTCCCTTGAGTGTGTGTGTGTGACGCTGCATCTCTGAGACATGCAGTGTCAGCTCACATATGCTAGTCTGCATCCGGATACTGCTGTGTGTGTAAGTGTAGATGTATGTCAGTTTGTGTGTACATTTTTGTGTGTTATATGGCTCAAATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAGGAACGGGACGGAGTGGCGTGCTGACCGTCTGCTGCTGAACCGTGAGGTGATGGTGTCCTCGTCTGTCCACCGCTTTCTCCCGCTGCTGGATGAAGTGGCGCAGGATTTCTGCCGTTCGCTGCGGCGCCGCGTTCAGGCGGACGGGTTCGAGAAGGCGGGGCAGCACACACTGACCCTTGACCCCAGTCCTGACCTCTTCCGCTTCGCATTGGAAGG[T/G]CAGCCTCTTCTAATTCCTCGTTAATAGAGAAGGGCTGTTACTGAAACTGCAGGGCGGGACTTTGTCAGTTGCTGATTGGATGTTGAGATGTGGGCGTGGCTCTACATATCAGAGGCGGAGCTGAATGTAATGCAGTGGATTGTAACAGAGGCGGGGCCAGAGAAGACTGATGACTGTCATATATTTAAATAATGTTTGCCGTGTGATCGTCAGATAATTAAATCAATTAAATTAAATATTAGGAGTGTTTCCCTCCGCTGATGATGCGATCAGTAAGAGCAGCTGTGATTGGTCTGTGCAGCGAGCTGTCACGTTCTGTACGGCGAGCGGATTGGCCTGTTCTCCTCGTGCCCGTCTGACGAATCAGAGCGCTTCATTTCGGCTGTGGAGCGAATGCTGGCCACGACCCCCCCGCTGCTGTACCTGCCCCCCCGCCTGCTGCTGCGGCTGCGCGCCTCCCTGTGGACAACACACGCCACTGCATGGGACGACATCTTCAG
Associated Phenotype:
Not determined