ZMP
hmha1
Ensembl ID:
ZFIN ID:
Description:
Hmha1 protein [Source:UniProtKB/TrEMBL;Acc:A4FVN1]
Human Orthologue:
HMHA1
Human Description:
histocompatibility (minor) HA-1 [Source:HGNC Symbol;Acc:17102]
Mouse Orthologue:
Hmha1
Mouse Description:
histocompatibility (minor) HA-1 Gene [Source:MGI Symbol;Acc:MGI:1917969]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa45767 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa24143 | Nonsense | Available for shipment | Available now |
| sa37489 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45767
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089171 | Essential Splice Site | 214 | 1126 | None | 23 |
| ENSDART00000132565 | None | None | 861 | None | 17 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 17865688)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 17616623 |
| GRCz11 | 22 | 17641601 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGTGGAGACGCTCACCGCTGCTGGAAAACTCATCTCACAGGTCAAAGG[T/G]CAGAGCAAGGCACTTCTGGGTCTCGAAATTAAACACATTCTCAAACTCTG
Long Flanking Sequence:
TGTGAAACAGTATGGGTGTTTCTCAGAACTGGGTTGCAGTTGTTGGAGCATAAGTTGTATATATGCTGGATAAGTTGGCAGGTCATTTCGCTGTGGCGACCTCAACTGAATAAAGGGCCTAAGCTGAAGAAAAATGAATGACTCAGTTATTTTATCAAACATTTTTTCCAGCTTGTCCATTCTGCCCTTTGTTTGTGGTGAAACATGACCCAGACGTTTTTACAGTGTTGCTCTGTTATCAAAGTGTGAAAAGTGAAGGCGTTGGTCATTTAGCTGACAGAAAACGCTAAAGTGACAAGTGAGTGTCGTCTGTAGAGCAGCCCTTACTCTGGTTTTTCTGTATTTTGTGTGTCAGATAAGCAGGAGAACCGACGTCCGCTGGCTCACGAGTGTCTGGGTGAAGTGCTGCGGGTCCTGCGGCAGGTCATCAGCATGTACCCACTGCTCAACACCGTGGAGACGCTCACCGCTGCTGGAAAACTCATCTCACAGGTCAAAGG[T/G]CAGAGCAAGGCACTTCTGGGTCTCGAAATTAAACACATTCTCAAACTCTGTGTTTAGAATTATGCATCTCTGCAGATATTTTAAATGCTTCAAGGTCCCATGAAATTAAAATAAATTTATATTAATAATATGTTGTTGTTATTATTAGTATTGTTTGTTTTTAAGCTATCTTTAAGCTAGTGTGCTCCGGAACAGTGACCAAATTTGTGTTTATAAGATATAAAACTGATATAAACATGTAAAGCTTGTAATTTGTCACTTCCATCTAAATGGATCAACGGTTTTATTCACGTCAACCTGTATTACAATTTCTCATAACATCACAACCAATCAAATGCTCTCTAGTATCTGGCATGCCCCGCCCCCTTCAAGATGCTTCTTGTTTGCTTTTCATTTGATGCACTTGAGCTCAAACACCCACTAGCTGTGTCTCATTACAGAGGCTGCATCCTTCGAAGGATGCATTTGAAGTGTGCTACATCATCGCGGTGCGACGAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24143
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089171 | Nonsense | 604 | 1126 | 14 | 23 |
| ENSDART00000132565 | Nonsense | 339 | 861 | 8 | 17 |
Genomic Location (Zv9):
Chromosome 22 (position 17846512)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 17597447 |
| GRCz11 | 22 | 17622425 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCGCACCGACAGCGCTAATGCTGAAGCTCAGAGCAGTGCTGAGGTGCCA[C/T]AAACTGCAGGAGAGACTGGAGACACGAGCAGCTCACAGAAAGATGATCAG
Long Flanking Sequence:
CTTTAAACTCTGATCAGAATATCTGTGCTTGTTTACATGCTTAAGCAATGGCCCAGTCTTGCATTTCTTGGACTTAATAGAAACAAATAAATGCTGAAACACAGCCAGAAAATCTAAATCCAGCTTGAGCGGGTTTTAACTGTGAGCTCTGAAAAAAAAAACTTTTTCCAGGCCACCATCTCCTACTACCAGATCATGCACATGCAGACGGTCGCGCTGCCGGTCCACTACCAGACTCTGTGCGAGAGCAGTAAACAGTACGACCCGGGACAGCAGTACGGCACGCACGTCAAAGACCTTCAGATGAGCGAAGAACCTGAAACGCATTATGAGTTTGAGGCCTACTCTGCCTCCTCTGTCCAGTAAGACACGCATACTAAAACATGTATTCTGAAAGTTGCTGTGAATGTTACTTTTAATGTGGTGTTTATTTCAGGCAGTCGGTTAGGCCGCGCACCGACAGCGCTAATGCTGAAGCTCAGAGCAGTGCTGAGGTGCCA[C/T]AAACTGCAGGAGAGACTGGAGACACGAGCAGCTCACAGAAAGATGATCAGAAGAGGGGTATGTGCGAATTATCTTTGTTTACTTCAATAATAATTTAAAATGTTTTGTTTTATACAGCGCCTTTTAAAACCTTTTTAAATATACATAAACAACATAGAGTTAAACATTTAAAAACTATACAAAAACACAGCAGAATAAGGTCAACATAGAACATGCTTTTCTAATGGTCATGAAGTAAATTCAAATGTAGAACCTACTGAAGAAGTATGCGATTTCGGACATAGCACTATCCAAAGGCAAATTTGGATAGAGCCCTGCATTAGCCTTAAATGTAAGCCCGAGCCTGGCCCTGGCCCAAGATGCACAGGCTGTATCCCTGCCTTTGTCCAAAATCTTTTTTCCGCCAAACAGTTACAACCATTAAAATAGACCATATTTGTATTTAATAGAAAGTTGATGTTTTTTCGCTTCTTATTTTTGTTTTTTTGTTTTATCATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37489
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089171 | Nonsense | 895 | 1126 | 20 | 23 |
| ENSDART00000132565 | Nonsense | 630 | 861 | 14 | 17 |
Genomic Location (Zv9):
Chromosome 22 (position 17841901)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 17592836 |
| GRCz11 | 22 | 17617814 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGTCCAGAGGGAGCTGACAGTGGTAAAGGACCAGACCTGATGGACCTT[G/T]GACCTGAGACGGATCCTGAACTCTTGGTCCTCGTGGACAGACTTAAAAAT
Long Flanking Sequence:
TGGGATCCCCTTCATAATCAAGAAGTGCATCGCTGAGATAGAGAGACGAGCTTTAAGGATGAAGGTATGCAAACTACCGGTCAGATCTTGCACGTCTTCACCGATTAAAAAGCGATAACGAATTCTCTCCTATTTCTGTCAGGGCATTTATCGAGTGAATGGAGTAAAGACGCGGGTGGAGAAACTCTGCCAGGCATTTGAGAACGGCAAAGAGCTGGTCGAACTATCACAGTCATCTCCACATGACATCAGTAATGTCCTGAAGCTTTACCTGCGACAGGTGAACAAAACATCCATGAAAAACATTGAAGACATCTAGCAAAAACATTCAAAGTCAAATCCACTTAACTCTGTTTGTGTGTGTGTGTTTTCTTCAGCTTCCGGAGCCCATCATGCCCTTCCGCCTCTACAACAGTCTCATGGGTCTGGCCAAGGAAAGTCTGGCTGTTGTGGGTCCAGAGGGAGCTGACAGTGGTAAAGGACCAGACCTGATGGACCTT[G/T]GACCTGAGACGGATCCTGAACTCTTGGTCCTCGTGGACAGACTTAAAAATCTCCTGAAAGAGCTGCCCAAACCAAACACCGCCACGCTCCGCTACCTAGCGCGTCATCTGAGGAGGTAAACTGGTCACACTTTACAATATGGTTTCATTAGTTTATGTTAATGCATCAATTAACATTAGTAAATGCATCAAACAACATTAACTAATACAAGATTTACTAATTTTCTCAATACAAACTTTTCTAAATGCTTTAAGCATATCATTTTTGCTAAATCTCTAATTGAGGTTTTGAATAATAATTTTAAAAATCTATAATAAAAGAAATGAATTAATAATAAATTGTTGAATAAAATAAACGCAAAGCAACTTAAGTGTTTGTCAAAGTATGTAAAAAATGTATCAAATTTTAATTAAAAATAATAAATTTGTCATAAATTCTTACTTTTAGGAAATGTACACTTTTAATACATTTTATATACACTCACTGGCCACTTTATTAGG
Associated Phenotype:
Not determined