ZMP
hif1aa
Ensembl ID:
ZFIN ID:
Human Orthologue:
HIF1A
Human Description:
hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) [Source:HGNC
Mouse Orthologue:
Hif1a
Mouse Description:
hypoxia inducible factor 1, alpha subunit Gene [Source:MGI Symbol;Acc:MGI:106918]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6314 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16875 | Nonsense | Available for shipment | Available now |
sa13792 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6314
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044282 | Essential Splice Site | 75 | 760 | None | 16 |
ENSDART00000144328 | Essential Splice Site | 61 | 189 | None | 10 |
ENSDART00000147222 | Essential Splice Site | 65 | 708 | None | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 31993605)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31639553 |
GRCz11 | 13 | 31770003 |
KASP Assay ID:
554-5251.1 (used for ordering genotyping assays)
KASP Sequence:
ATGAGACTGGCTCTCAGTTACCTGCGCCTGCGTAAACTGCTGAACAGCGG[T/A]GAGAGAGGATGAATGTGYGGTGAGATCATGAACTCTCMTGTGTTTGATGC
Long Flanking Sequence:
AAGCCTCCATTTTCATCTTTATTTGTTAATATATCAAGGCAAATATCAAAAGGTTAAACAATAAAGACCTTTTTCCCTCAGCCTTCTTTGCTAATATTTACCAATATGATTGAAGGGCACTGTCTCCTCTCAGCATGTGCTGTAGCTTCCTCAATAACATTGCATTCTGCTGGTTTATATGCTGTGAAATACATGTGTGTGTTTTACAGCTCTATGATGTATGTTTTAGACAGTTTGACAGATTTCTGACAGCACAGGCCCCTGAGCATGGTTTATATATGTCTGTGTTTGTGGTGTGTTTTTGATAGGGTGAGTTCAGAGCGAAGGAAGGAGAAATCCAGAGACGCAGCACGTTGTCGGAGAGGAAAAGAGTCTGAGGTGTTTTATGAGCTGTCCAGAGAACTCCCTCTCCCCCACAGCGTCACCTCTAACCTGGATAAAGCATCGGTCATGAGACTGGCTCTCAGTTACCTGCGCCTGCGTAAACTGCTGAACAGCGG[T/A]GAGAGAGGATGAATGTGCGGTGAGATCATGAACTCTCATGTGTTTGATGCTGACAGCCTGTGTTCATCTCTGTCTGTCTCTCTAGATGTGCTGGAGAAGGAGACTGCATTAGACACTCAGTGGAACGGTTCATTTCTGAAAGCTCTGGACGGGTTTCTTTTGGTTCTTTCAGCTGATGGTGATATTGTCTACCTTTCAGAGAATGTCAGCAAGTGCTTGGGCCTTCCTCAGGTGATTTTAAGCACACTTCCGATTCAGAATGTGTAGGTTCATGTGAATGTGGGTCTTTTATTTCTTTCTTCTGTCAAAATCAAAGGTAAATAATTTGAATAAAGATGAAAACCTGTAAGCATTGACTTTCATTGTAAGAAAAAGATACTATGGAAGTCAATGGTTATCTATATTCACCCAAAAATGAAGAATTACTCGCTTTTTATTAATCCTCAAGTGGTTATAAATCTTAAAAGGTTTCTTTCTTCTGTTGAAATCAAAGGAAGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16875
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044282 | Nonsense | 278 | 760 | 7 | 16 |
ENSDART00000144328 | None | None | 189 | 7 | 10 |
ENSDART00000147222 | Nonsense | 267 | 708 | 6 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 31998291)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31644239 |
GRCz11 | 13 | 31774689 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGGGTTTTGATCCAGWGGATGTGTTACAGCATTCWGTGTATGAATACTA[T/A]CATGCGTTGGATTCAGACCACATGACCAAAACACACCACAGCCGTAAGAT
Long Flanking Sequence:
CAGTCATATGATTTTTATAGGGTCCAGGGAGGTCAGTGTTGTTTCAGAGGTGTTTCCCATAGCAATTAGATTTGAAGGTGGAGTCAACCCTCAATCTCGACCAGAGGAATTCTGCTAACTCATAGGATGTCACAGTGAATAATGCAGTTTTTTTCTCAAATGGAAAGAATATACAACAAAACTAAAAACATGTTACAAATTGAATACTTTCTTATAGTCAGTGAAGAAACTGCCTAACTGAAAAGTTGGTCATCTAGAGTATTTCTACCTGCAATTTCAGATCTAATGGATATTCAAACATTGTTTAGTAGGAAACGATGGATGTTTTTTATACACAGGATAGGTCAGGATTTATGGCCTGGATTTCTTCGCCATCTGGTGGCGAATTGCAAAATGTGCGGCATCACAGAGCAGCATGTGTTTGTTGATGTTTGCAGGATCACAGAGCTCTTGGGTTTTGATCCAGAGGATGTGTTACAGCATTCTGTGTATGAATACTA[T/A]CATGCGTTGGATTCAGACCACATGACCAAAACACACCACAGCCGTAAGATCAGATAAATGAAAGTTTACTTATGCAAATCTAAATTAAGATATTTCATAATACTTTATTGGTCTCTCTCTGCAGTTTTTGTGAAGGGGCAAGTGTGTACCGGACAGTACCGTCTGCTGGCTAAAGCCGGAGGGTTTGTTTGGGCAGAGACTCAGGCCACTGTGATCTATAACAGTAAAAACTCTCAGGCACAGTGTGTGGTTTGTGTCAACTACATCCTCAGGTGGGACTTTATACTCTATGTTTGACCTGAATACTAGTATTTGTGTGTGTTTGTGATGGTATGAATGCACCATTTAATCTATTTGTACTTTCTTATTCTGCAGTGGCATTGAACAACCCAAACAAATCCTGTCGCTTCAGCAAACCAACAGCACAAAAATAAAACAGGAAGAACACCAGGAGGAGGTTGAGGTGACCATGGCAGAGTTGAAAGAGGAGGAAAAGGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13792
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044282 | Nonsense | 683 | 760 | 15 | 16 |
ENSDART00000144328 | None | None | 189 | None | 10 |
ENSDART00000147222 | Nonsense | 631 | 708 | 13 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 32006864)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31652812 |
GRCz11 | 13 | 31783262 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGCTTTCTCCCAGGGGTCTGTGCTGCAGGTTGTTACCGATTTTCCAGAG[A/T]AAAAGGTCCGCAAAACAGATGCTCCATCATCAGAAGGAATTCGTCATGCT
Long Flanking Sequence:
CTGTAAATAATGTTCATTTTCTTGCACAGATACTTTATAAGACTTTAGTATGAATAAAATTTTTTCCTGTTTTCGTTTTTTGACTGTCCAAATCTGGTAGTCATTGGTTTGCATTTTATGAATCACCAAAAGTTTAAGATAAAAAAAATCTTCTAACATGTTCTGTTGAAGAGAAAAAAGTAGCCTAAAACCTGGATGTCCTGATGTTAAGTAAATTATCAGCATTTTATTTTTTTTGATGAACTATCCCTTCAAGAAGTTGAGAAATACACCGATTAATGTGCATTCAGCTGAGCATTATAGCATATTAAAAAATATAATGTGTTTAAACCAAACATTTATATAGGCCTACCATTCACTGTAAATGTATAGTATTTATAAATGTCTCTGTGAAGGGTAGTAAAATTGTTACAACTTGTGCAAAAAGTGTTTATTATTGACTGTTAATGTGTGCTTTCTCCCAGGGGTCTGTGCTGCAGGTTGTTACCGATTTTCCAGAG[A/T]AAAAGGTCCGCAAAACAGATGCTCCATCATCAGAAGGAATTCGTCATGCTACGATACTGTTGCTGCCATCCAGTACGTCACCCTCAGTCTGTTGAATCCTTGCGAATGTTGTGAGGCCAGTTGTTTTCCATTTAAACAGTAAGTAACTGCTCTTTTTCAGATGTTGCAAGTCGGTTATTGAGCAGATCGTCAGAGGGCGGAGCCATAGCTATGCCCCTCCCCCAAATCACCCATCACGACTGTGAGGTAAATGCACCTGTGATTGGACGACAGCACCTGCTGCAGGGGGAGGAGCTTCTTTGTGCCTTGGATTTAGTTATTTAAAAAAAGCCATACTCATGTTAATTTAACAATTATCAGTGGCATTATGGATGGACTTCCATTCTAAAGAAACAGGGGTGAGCAATCAGAACAGCTGGGTTGCTTCTGCTTCTCATAAGCAGTTGGTAAATACATGCTGGACATTAAAGAAACAATAATTAATGACAAGGGAAATGTAA
Associated Phenotype:
Not determined