ZMP
hif1al
Ensembl ID:
ZFIN ID:
Description:
hypoxia-inducible factor 3-alpha [Source:RefSeq peptide;Acc:NP_956699]
Human Orthologue:
HIF3A
Human Description:
hypoxia inducible factor 3, alpha subunit [Source:HGNC Symbol;Acc:15825]
Mouse Orthologue:
Hif3a
Mouse Description:
hypoxia inducible factor 3, alpha subunit Gene [Source:MGI Symbol;Acc:MGI:1859778]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45539 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18426 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45539
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 |
---|---|---|---|---|---|
ENSDART00000023421 | Essential Splice Site | 283 | 626 | 8 | 15 |
ENSDART00000060343 | Essential Splice Site | 283 | 626 | 8 | 15 |
ENSDART00000114884 | None | None | 237 | None | 6 |
ENSDART00000124696 | None | None | 170 | None | 7 |
Genomic Location (Zv9):
Chromosome 15 (position 24841881)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 25575214 |
GRCz11 | 15 | 25510479 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATAGAATTATAAAAGTGGCCAATTATAGTTTTTTTTCTGTGTACTTCCA[G/A]TGTTCTCCAAGGGTCAGGTGTGTACCGGCCAGTACCGTTTTCTTGCTAAG
Long Flanking Sequence:
TACTTCTGCATACTGTTTGTGTTGCTCTGCAATAACGCCTCCGATACACTAGCTGGCAGTAGGTTTTTCTGTTTTTCTGTTTCGAGTTTCTTCATGGGTCTTTAATTTTTTCTGAACGCTACCTTAATGTACAAGTAGCTGTAAACACAAAAAAAGTTTTCATCTGGAGCTCCTTCATGAGACTCAACACTTAAACAGCCGCACCAACGGGTTCGAGTGGCTCTCAGTCCTGCCACACTGGTCACAGCTACCAAGCCAACCAATCACCTTGCGCTACGCATCGTTGCGATATGTAGTTAAATTTATTATGAGGTGCACGTCAGCATTGGCATCAGCCACGTCGAGGGCTATTCAACCGCACGAAAACTGTGCTGGAGCATACACGTGCGCTTGACTCAAATATAAATCAGCCTTAAGTAATTTAATGTTGTTTTAATTCTTTGTATTTTTTATAGAATTATAAAAGTGGCCAATTATAGTTTTTTTTCTGTGTACTTCCA[G/A]TGTTCTCCAAGGGTCAGGTGTGTACCGGCCAGTACCGTTTTCTTGCTAAGAATGGAGGATTTGTGTGGACTGAGACTCAAGCCACTGTCCTCTACAACAGCAGGACCTCTCAGCCTGAGGCGGTGGTCTGCCTCAACTTCATTCTCAGGTAGCTCAAACATCTTTGTCTTCTGCCCTATTTTTGCTGGATCTGATGTTGTTTTATTAGCATTGACATACTGCTGTAGTTTTTATTCATCAATTTTATTTTCTGTAATTTTTTTTATAGTTTTTTTTATATTTAGTTGGAAATCACAATTATTAGATTTTTTTATTTATTTATTTATTTTTAAATATTTCCCAATTTTTACTGTATTTGCTATTATATTATTGATTATATATTTTGTCCTGCAGAAAGTCTTTGTTTGTTTTATTTCAGCTAGAATAAAAGCAGTTTTTATTTTTTTGAAAAATATTTAAGGTCAATATAAAAATATCTAGTAAAATATTATGTGCTGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18426
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023421 | Essential Splice Site | 562 | 626 | 13 | 15 |
ENSDART00000060343 | Essential Splice Site | 562 | 626 | 13 | 15 |
ENSDART00000114884 | None | None | 237 | None | 6 |
ENSDART00000124696 | Essential Splice Site | 106 | 170 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 15 (position 24838811)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 25572597 |
GRCz11 | 15 | 25507862 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATGAGCGGCTCGGTAGAGGACCAGCTTCTGCTCAGCCAYACATTRCTGG[T/G]AAATTCAGMTTATTTTTTNAAATGTGCAGAAGTAGGCTGTTAGTAAATCTG
Long Flanking Sequence:
GTGAGTGAGTGAGTGAGTGAGTGAGTGAGTGACTGACTGACTGACTGAGTGAGAGAGATATTATCCAGAAAATTTAAACACATCTATTGTATACCAAGGCTATGTTTATTTAATTAAAACACTACTAAAAAGTGATATTAATATGATTTTAAATACCTCTTTTCTATTTTAATATAGATCATTATATTATTTTATTGTTAATATTTCTATACTGTATTGTCATCAGCTAGTTTTTAGTCTGACATGAACCTTGTCAGAAATCATTGTATTATATATGAATTAAATGTTTTATGTTTAAATGTTTTAATAATCTTTTCAAAATGAAGATCTGTGTTTGATTGTACGATGTGTCTTTAATGTCCCGTTATGTGCTGTTCTTCACATCAGGTGTTTGGAAGATGATGATGATGATGACATTCCTGTTTTGGCTGCTAGATGGGACAAGAAACAGATGAGCGGCTCGGTAGAGGACCAGCTTCTGCTCAGCCACACATTACTGG[T/G]AAATTCAGCTTATTTTTTAAATGTGCAGAAGTAGGCTGTTAGTAAATCTGAACTAGGGCTGCACAATACTGAGAAAATATGCAATATATGATGTTGCTGTGATCATGTTTTTTGCTAGACTTCCTGACAATCAAAAAGCATTGTGTATTTTATTTTATTTGTACTCTGCACTGTATTGGTCTCAATTCCTGGAGGGTCACAGCTCTGCATAGTTTTCCTTCAGGAATCCAATTTGAGACTCAATATTTATCGTAGAAAAATACAAAATTGCAATGTCAATTTTCCCATATCAAACAGCCCTTATTTATGTCATGATCATATTAAAATAAACAGATACTAGATATAGTGTAATTACATCTAATTTGGGCTAATCAAAACGATGTGAAGGTGCAAACATTTAGACCAGGAGTTCTCAATCTCGGTTCTGGAGGTCTGGTGTCTTGCAGATTTTAGCTGCGCTGGTTGTGGAAATTCAAAATTGACCCAAAACATCATTAGGA
Associated Phenotype:
Not determined