ZMP
hira
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate HIR histone cell cycle regulation defective homolog A (S. cerevi
Human Orthologue:
HIRA
Human Description:
HIR histone cell cycle regulation defective homolog A (S. cerevisiae) [Source:HGNC Symbol;Acc:4916]
Mouse Orthologue:
Hira
Mouse Description:
histone cell cycle regulation defective homolog A (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:99
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa40382 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa33557 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40382
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 |
|---|---|---|---|---|---|
| ENSDART00000006215 | Essential Splice Site | 371 | 993 | 11 | 26 |
| ENSDART00000132164 | Essential Splice Site | 371 | 1010 | 11 | 25 |
The following transcripts of ENSDARG00000013434 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 19652146)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 17552119 |
| GRCz11 | 5 | 18056115 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGACTTCTCGCAGGATGAACTGGGAGACCCCTTGAATGAAGAGGAAAAG[G/A]TGGAGAAAAAGCACACAAACCAGAGTTGAACACTTAGAGTTAGTGTAATT
Long Flanking Sequence:
ATTAAGCAGTGAGTTTTCTCATTTAATATTTTATTTCTCTAGAAACTGTGTCACAATATGAAAAAAAAACAAACAGTTGTAGCCTTTGGTTCATGTAAACTTTAAGAGCTAAGACTCATGACCAAAGAAATTTTTCATTTCTGAATGCCTAAATAAAATCACACAATTAGGGTATGATGTTTCTGTATGTTGACATGATGCACCTTTAATCAGATGTCCTGTTTTTTCAGCTCACCTCACTCAAGCGTCCTTTGGTGGTCATCCATGACCTATTTGACAAATCCATAATGGATATTACATGGTAGGGAAAGGCTTTATGTTTCAAGCTTTGTAAAGAGTCACAGAGATCTTATTGGGGTAAATCCTTACATGCATGTTGTGAATTGACTCTTAGGACACTGAATGGACTGGGACTCCTGGTGTGCTCCATGGATGGAACTGTGGCCTTCCTGGACTTCTCGCAGGATGAACTGGGAGACCCCTTGAATGAAGAGGAAAAG[G/A]TGGAGAAAAAGCACACAAACCAGAGTTGAACACTTAGAGTTAGTGTAATTTCAAAGCAAAATCAACTTTATTTTGCTTGCACCATTGGCTTGTTTTAAAGAAAAACTCACTGAGTGTTGAATAATTATTTTTGAAAACAAGACAATATTTTTTGCTTGTCTAGAAAGTCCTTCTTGATTTTTAAGAATTTTTAGGTATTTGGAGTAGAAACAAGACAAAAAAGTATATATATATTTTTTTTTTTGCAGTGTAGCTAACATTTAACAGTGTTTATAGACAGCAAAAACTCATTATTATATAATTATGAGGGGGGGTGTTATGATTTTATTTAGTATTAAGTATTTTTAAGTATATAAGTATTTGTATATCACAAAAGTGAAATCTAATTTAAGAGTACACCCATTAATTTAACTGATAAATTCATAATTAAGAAAGTAAATGTCTTGTTTTTTGAGCAATTGGTTGAATCGTTTTTTCCAGATACAGACAATCTAGAGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33557
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006215 | Nonsense | 562 | 993 | 15 | 26 |
| ENSDART00000132164 | Nonsense | 562 | 1010 | 15 | 25 |
The following transcripts of ENSDARG00000013434 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 19645313)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 17558952 |
| GRCz11 | 5 | 18062948 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGCTGACTTCTGCCTCCAAAATCGAGCCCATGAAAGCACTAGATTCA[C/T]GATTTACTGAAAGGTCAAAAGCCACACCAGGGGTCACTAGCGTACCCATC
Long Flanking Sequence:
CTAATCAAGGACTAAGGCTGTTAAATTAGCTATTGGCTGCTTTGAAAGTTATCCTGCATTGTCCCTGTTATTAAAATCCACTGATAAAGAGGTAGTATTACTTTGCTGTAGGGAACAGCAAAGAAAATAATTGTTACAAAAAAAAGAAAAGTAATCTATAGGAACCAAACCACAGGGGATTCAAAGAAGCGCTTGCTATTGGTTGTAATCACTTTAAAATACTAACAGTTATTTCCGTTGGATGGGTAAAAATAAAGCACTATTGTTAGCAGAGTCTTATTATTTATAGCTGTTGGTTTCAATTCTTAATGGAAGTTTCCCAAACTGTAATTGCAACCCATAATATGGCAGTAGGAACAAGGTGGATACTTGATCTTATTTCATGTATTATCTCTGCTCTCTCTTTTAGTGCAACAGCACCTGTAAACTCCATTGGTATGAAATCAACTCTGCTGCTGACTTCTGCCTCCAAAATCGAGCCCATGAAAGCACTAGATTCA[C/T]GATTTACTGAAAGGTCAAAAGCCACACCAGGGGTCACTAGCGTACCCATCACCATAGGCATCACGCCACTTGACAGGTAATAAAGTTATTGTGGTTATTAGTGCATTTTTTTTCTTTTAACTAAACTAAAAACCAAGCTGAAGATGTTTTGCGTGTCTGTCTCAGGGCAAAAGACAGCAGCTCTGTGAAGGAGCCGAAAGGAAAAGATGAAACCAGCAGCGACAGCGAGGACAAGATCATGAACAAAACACTGTCTATGGCCAAGAGGAAGGGAGAGATTGAGGGAGGAGAGGTGGTGGAGAAGAGGAAGAAGGGAAGGCCGAGGAAAGATGCCAAAATGATGATGCCCATATCACAGCCTTTCCCGCAGGTGACATAACTTCTTGAGACATGTTTTGAAAACACCAATTTCAAAATCGACTGCCTTTTTGTTTATTTTTTTTACTGGATTGGGTATCGGCCAGATGGGACAGATTGAAATCTGATGTTGTGCATGTACT
Associated Phenotype:
Not determined