ZMP
hif1an
Ensembl ID:
ZFIN ID:
Description:
Hypoxia-inducible factor 1-alpha inhibitor [Source:UniProtKB/Swiss-Prot;Acc:P59723]
Human Orthologue:
HIF1AN
Human Description:
hypoxia inducible factor 1, alpha subunit inhibitor [Source:HGNC Symbol;Acc:17113]
Mouse Orthologue:
Hif1an
Mouse Description:
hypoxia-inducible factor 1, alpha subunit inhibitor Gene [Source:MGI Symbol;Acc:MGI:2442345]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38947 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31936 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38947
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000042049 | Nonsense | 252 | 344 | 5 | 8 |
The following transcripts of ENSDARG00000031915 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 30188435)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 29834383 |
| GRCz11 | 13 | 29964833 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAATCCTGACTATGACAAGTTTCCTAATTTCAAAAATGCTGTTGGGTA[T/A]GAGGCTGTCGTGGGACCCGGAGATGTGCTGTACATCCCCATGTATTGGTA
Long Flanking Sequence:
AGAAATTTATATTCTTTCCCAATACATGTAGAATGGGCTGTTTTTTATGTTGAATAATATGCATTTTTACTATGATTTACAGTAGTCACCCACTTAAATGTCAGGCAGATAGGACATGAATCATTAGATGAAATCAAAAGCATATTTAAAGATGAATGTGCAATGTCAAAATACTTAATAACAATAATTAATTGTAATTTAAAGTATTCAAGAAACACTTTAATTGCATTTAATAAGCTTTCTCTGTATACAAATTCAATTATTTTGACTCGAACATCAAAAATGGTACCTCAACTTTTTCCAATATATATAAGTGCTATTCCAAGAAGTACAGCAGGTTAAATGTTTTTGGCCTGAAAAGTTATATTCACAGGTTGATTAAAACTTTTTAATATTTTCATCTGCAAAATGTTCAATGCAAATTTGTTTTTGCACTCTTAGGTTGATTTTGAAAATCCTGACTATGACAAGTTTCCTAATTTCAAAAATGCTGTTGGGTA[T/A]GAGGCTGTCGTGGGACCCGGAGATGTGCTGTACATCCCCATGTATTGGTAAGTTTGTTTTCAAATACTCTGAGAAAGTGGATCACAATTATTACCTTAAGCTGAATCACGTAATTCAGTCAGACTGGCTTAACCCAATGTGGAGTATGGGGTGGAGCTAACTGTTAAATGTTAGGAATTATTTTTTAGGATATTACAAATTGAAGTTTTAAAGAGCCCCTATTATACATGAAATAGGGTCCTATTTTGGTTGTAAGGCTCTCCAACAATAGTCTAATATGCATGCAAGGTCAAAAAACACTTTTATGGTCTTATAATCTGCATTTATTTTTACCTAATTATCCCAGCGACTCCGATAAAAATCGTTCAGTGATTCATTTGTTACCAAACCCCTCCTTACCGCGAAGCTAATTTGTGCTGATTGGACCGATGACAGCCTGTTGCAATTGGTCGACACCGACAGCCTTCAGCGCAAGACAGAGTGAAATACCCAGCAGCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31936
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 |
|---|---|---|---|---|---|
| ENSDART00000042049 | Essential Splice Site | 268 | 344 | None | 8 |
The following transcripts of ENSDARG00000031915 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 30188386)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 29834334 |
| GRCz11 | 13 | 29964784 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAGGCTGTCGTGGGACCCGGAGATGTGCTGTACATCCCCATGTATTGG[T/G]AAGTTTGTTTTCAAATACTCTGAGAAAGTGGATCACAATTATTACCTTAA
Long Flanking Sequence:
TTGAATAATATGCATTTTTACTATGATTTACAGTAGTCACCCACTTAAATGTCAGGCAGATAGGACATGAATCATTAGATGAAATCAAAAGCATATTTAAAGATGAATGTGCAATGTCAAAATACTTAATAACAATAATTAATTGTAATTTAAAGTATTCAAGAAACACTTTAATTGCATTTAATAAGCTTTCTCTGTATACAAATTCAATTATTTTGACTCGAACATCAAAAATGGTACCTCAACTTTTTCCAATATATATAAGTGCTATTCCAAGAAGTACAGCAGGTTAAATGTTTTTGGCCTGAAAAGTTATATTCACAGGTTGATTAAAACTTTTTAATATTTTCATCTGCAAAATGTTCAATGCAAATTTGTTTTTGCACTCTTAGGTTGATTTTGAAAATCCTGACTATGACAAGTTTCCTAATTTCAAAAATGCTGTTGGGTATGAGGCTGTCGTGGGACCCGGAGATGTGCTGTACATCCCCATGTATTGG[T/G]AAGTTTGTTTTCAAATACTCTGAGAAAGTGGATCACAATTATTACCTTAAGCTGAATCACGTAATTCAGTCAGACTGGCTTAACCCAATGTGGAGTATGGGGTGGAGCTAACTGTTAAATGTTAGGAATTATTTTTTAGGATATTACAAATTGAAGTTTTAAAGAGCCCCTATTATACATGAAATAGGGTCCTATTTTGGTTGTAAGGCTCTCCAACAATAGTCTAATATGCATGCAAGGTCAAAAAACACTTTTATGGTCTTATAATCTGCATTTATTTTTACCTAATTATCCCAGCGACTCCGATAAAAATCGTTCAGTGATTCATTTGTTACCAAACCCCTCCTTACCGCGAAGCTAATTTGTGCTGATTGGACCGATGACAGCCTGTTGCAATTGGTCGACACCGACAGCCTTCAGCGCAAGACAGAGTGAAATACCCAGCAGCTAATCAACAATATAAAAGTAGTCACAGTGCATACACGCTCAATAGTGTAAGG
Associated Phenotype:
Not determined