ZMP
hyou1
Ensembl ID:
ZFIN ID:
Description:
Hypoxia up-regulated protein 1 [Source:UniProtKB/Swiss-Prot;Acc:Q7ZUW2]
Human Orthologue:
HYOU1
Human Description:
hypoxia up-regulated 1 [Source:HGNC Symbol;Acc:16931]
Mouse Orthologue:
Hyou1
Mouse Description:
hypoxia up-regulated 1 Gene [Source:MGI Symbol;Acc:MGI:108030]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41684 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa30941 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41684
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 |
|---|---|---|---|---|---|
| ENSDART00000100032 | Essential Splice Site | 157 | 980 | 6 | 24 |
| ENSDART00000100032 | Essential Splice Site | 157 | 980 | 6 | 24 |
Genomic Location (Zv9):
Chromosome 10 (position 30664742)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 29887146 |
| GRCz11 | 10 | 29773486 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGGGCATGATTTTGAACTACTCTCGCACTCTGGCTCAAGACTTTGCAG[G/A]TTTGATTATAAGAAGCTCTTTTTTATTTTATATAAGTTGCGAATTGGGAT
Long Flanking Sequence:
TTTGAACTTTTGAACAGTAGTGTAAATTATTTCAACATAAGACCCTACTCCTGGCATGCCAAAGTAAATGGTCCATTTTGTTTTCATGTTTACTTAAAAATAAAATAGAGACATGACAAACACATCTTCACTTTTTCTGGTGATCTGACTCTATCGTGACAGGCTGTGAAGAATCCTAAAGTGGTTTACAGATTCCTCCAGAGCATTTTGGGAAAGACGGCAGACAACCCACAGGTGGCAGAATATCAGAAACACTTCCCTGAGCACCAGCTGCAGAAAGATGAGAAAAGGGGCACCGTGTATTTCAAGTTCTCTGAGTAAGTAATGCAGCTTTTGCAGGTGCGTTAGTTGTAACCATTGTGCTTCATATTACTATGAAAAATGACTCTGAATATTATTTTTATACATATCATCATCAACTAGAGAGATGCAGTATACTCCAGAGGAACTTTTGGGCATGATTTTGAACTACTCTCGCACTCTGGCTCAAGACTTTGCAG[G/A]TTTGATTATAAGAAGCTCTTTTTTATTTTATATAAGTTGCGAATTGGGATTTAAACACTAATATTCTTATTGGTTTTCCTCCAAACAGAACAGCCCATAAAAGATGCAGTGATTACAGTCCCAGCCTATTTTAATCAGGCAGAACGCAGGGCAGTTTTGCAGGCTGCTCATATTGCAGGTCTAAAGGTCCTTCAGCTAATCAATGATAACACTGCTGTGGCTTTGAACTATGGAGTCTTCAGGAGAAAGGACATCAACTCGACTGCACAGGTACTTTAAAGCACAGTTTACACTTGCTTTTTGTCAAGCCAGTCACAAGTAGATGATGCCAAATACAGGATTTAAAATGTCCACTTTTGACTACTACTACTAGGTAGTGAAAAATGCATCGGTTCACATTTGATTTGCGTTCATTGTTTAAAAAGTCATGTGGTTAAATGTATTTGAACAAGTATTGTCCCAGTACTACCTAATATTAATCTAGATACTGAACTGATACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30941
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 |
|---|---|---|---|---|---|
| ENSDART00000100032 | Essential Splice Site | 157 | 980 | 6 | 24 |
| ENSDART00000100032 | Essential Splice Site | 157 | 980 | 6 | 24 |
Genomic Location (Zv9):
Chromosome 10 (position 30664742)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 29887146 |
| GRCz11 | 10 | 29773486 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGGGCATGATTTTGAACTACTCTCGCACTCTGGCTCAAGACTTTGCAG[G/A]TTTGATTATAAGAAGCTCTTTTTTATTTTATATAAGTTGCGAATTGGGAT
Long Flanking Sequence:
TTTGAACTTTTGAACAGTAGTGTAAATTATTTCAACATAAGACCCTACTCCTGGCATGCCAAAGTAAATGGTCCATTTTGTTTTCATGTTTACTTAAAAATAAAATAGAGACATGACAAACACATCTTCACTTTTTCTGGTGATCTGACTCTATCGTGACAGGCTGTGAAGAATCCTAAAGTGGTTTACAGATTCCTCCAGAGCATTTTGGGAAAGACGGCAGACAACCCACAGGTGGCAGAATATCAGAAACACTTCCCTGAGCACCAGCTGCAGAAAGATGAGAAAAGGGGCACCGTGTATTTCAAGTTCTCTGAGTAAGTAATGCAGCTTTTGCAGGTGCGTTAGTTGTAACCATTGTGCTTCATATTACTATGAAAAATGACTCTGAATATTATTTTTATACATATCATCATCAACTAGAGAGATGCAGTATACTCCAGAGGAACTTTTGGGCATGATTTTGAACTACTCTCGCACTCTGGCTCAAGACTTTGCAG[G/A]TTTGATTATAAGAAGCTCTTTTTTATTTTATATAAGTTGCGAATTGGGATTTAAACACTAATATTCTTATTGGTTTTCCTCCAAACAGAACAGCCCATAAAAGATGCAGTGATTACAGTCCCAGCCTATTTTAATCAGGCAGAACGCAGGGCAGTTTTGCAGGCTGCTCATATTGCAGGTCTAAAGGTCCTTCAGCTAATCAATGATAACACTGCTGTGGCTTTGAACTATGGAGTCTTCAGGAGAAAGGACATCAACTCGACTGCACAGGTACTTTAAAGCACAGTTTACACTTGCTTTTTGTCAAGCCAGTCACAAGTAGATGATGCCAAATACAGGATTTAAAATGTCCACTTTTGACTACTACTACTAGGTAGTGAAAAATGCATCGGTTCACATTTGATTTGCGTTCATTGTTTAAAAAGTCATGTGGTTAAATGTATTTGAACAAGTATTGTCCCAGTACTACCTAATATTAATCTAGATACTGAACTGATACC
Associated Phenotype:
Not determined