ZMP
obfc2ab
Ensembl ID:
ZFIN ID:
Description:
oligonucleotide/oligosaccharide-binding fold containing 2Ab [Source:RefSeq peptide;Acc:NP_001025423
Human Orthologues:
OBFC2A, OBFC2B
Human Descriptions:
oligonucleotide/oligosaccharide-binding fold containing 2A [Source:HGNC Symbol;Acc:26232]
oligonucleotide/oligosaccharide-binding fold containing 2B [Source:HGNC Symbol;Acc:28412]
oligonucleotide/oligosaccharide-binding fold containing 2B [Source:HGNC Symbol;Acc:28412]
Mouse Orthologues:
Obfc2a, Obfc2b
Mouse Descriptions:
oligonucleotide/oligosaccharide-binding fold containing 2A Gene [Source:MGI Symbol;Acc:MGI:1923258]
oligonucleotide/oligosaccharide-binding fold containing 2B Gene [Source:MGI Symbol;Acc:MGI:1917167]
oligonucleotide/oligosaccharide-binding fold containing 2B Gene [Source:MGI Symbol;Acc:MGI:1917167]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2323 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa2323
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000064149 | Essential Splice Site | 153 | 216 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 6 (position 9093697)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 8466963 |
GRCz11 | 6 | 8702502 |
KASP Assay ID:
554-3328.1 (used for ordering genotyping assays)
KASP Sequence:
CGGCAGCAATCCTYCTCTAGTGAATCCCGTGCCACCTGCTGKACCTACAG[G/A]TTTACATTTTTAAAGCTTATTGTTTGACATTGGCCATTTTTAWTCMAAAT
Long Flanking Sequence:
GAGATAATTGACACCATAATACATTTGAATACATGTTTTGATCGTTATTATAAGGCTCCAATTTGGTAAAAGTAAATGTATAAAACACAAGAAAATAATCCTGTGTATATATTTTTCAGATATGCGTCTCTCTTTAAAGGCTGTCTTACGCTGTATATTGGAAGAACAGGAGACCTCCAGAAGATCGGAGAGTAGGTCATCTCAGCTGACTTATTTAATGCAAGGGGAAATGACAGCAGTAACCGTTCCTTTTTGCGTCTATTAAAGGTTCTGCATGATTTTCTCTGAGACTCCAAATTTCAGTGAGCCCAACCCAGAGGTGCTGGCTAAAATAAACCAAATAAACAACACCCATGTGAGTGCAAAAATACTGCTCAAATTGCACCAACAGTAAGAGGAACACAGAATGAGTGTGTGTTTTATCTCCTAACAGGTAAAAACAGAGGCTCACGGCAGCAATCCTTCTCTAGTGAATCCCGTGCCACCTGCTGGACCTACAG[G/A]TTTACATTTTTAAAGCTTATTGTTTGACATTGGCCATTTTTAATCAAAATCGTGTGTTGTGGACTTACATGTTGCTATCACTGATTAAGTCAGGGGCCACCAAACTTATTCCTGGAGGGCCGGTGTCCTGCAGATATTAGCTCCAACCCTAAACAAACACACCTGAACAAGCTAATCAAGATCTTACTAGCTATACTTGAAACATCCAGGTGTGTTGAGGCAAGTTGGAACTAAACCCTGCAGGGACACCAGCCCTCAAGGACTGAGATTAGTGACCCCTGGATTAAGTGGATAGCTTGAAATAATTTAAAATAAGACAAAAGATTTAAAATACTTGCCTACATTCTACCATTGGTTCCTTATTAATGTATAGAACATGAATTATTTCCAGACTGTCTCTATAAACACCCCATGCCCTGTTGTGTAAAGATACATGTTTTTAAGATTCTTGTCCTTGCAATATTTTGCACTTTTATATGTGGCTTGACAGTAAAGAGCTA
Associated Phenotype:
Not determined