ZMP
hspa8
Ensembl ID:
ZFIN ID:
Description:
Heat shock cognate 71 kDa protein [Source:UniProtKB/Swiss-Prot;Acc:Q90473]
Human Orthologue:
HSPA8
Human Description:
heat shock 70kDa protein 8 [Source:HGNC Symbol;Acc:5241]
Mouse Orthologue:
Hspa8
Mouse Description:
heat shock protein 8 Gene [Source:MGI Symbol;Acc:MGI:105384]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41685 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa45412 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41685
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 |
|---|---|---|---|---|---|
| ENSDART00000099994 | Nonsense | 574 | 649 | 8 | 9 |
| ENSDART00000132212 | None | None | 188 | None | 5 |
| ENSDART00000141549 | None | None | 127 | None | 3 |
Genomic Location (Zv9):
Chromosome 10 (position 30760833)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 29966736 |
| GRCz11 | 10 | 29853076 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAAGGGCAAGATCAGTGACGAGGACAAACAGAAGATTCTTGACAAGTG[T/A]AATGAAGTCATCGGCTGGCTTGACAAGAACCAGGTGAACTTGCTGTCATT
Long Flanking Sequence:
AATATTTTTATTTTTCCCTCTTTCAGGTCTATGAGGGTGAACGTGCAATGACGAAGGACAACAACTTGCTGGGCAAATTTGAGCTCACTGGAATCCCACCTGCACCTCGTGGTGTCCCTCAAATTGAGGTCACCTTTGACATTGATGCCAATGGCATCATGAATGTTTCAGCTGTTGACAAGAGCACTGGCAAGGAGAACAAAATCACTATCACTAATGATAAGGGTAAGCACGTCACTCCCTAAATATTTAAATGAATTTACATCAGTCATTTCAGAAGTTAACTTAAGATGCATTTCAGGTCGTCTCAGCAAGGAGGACATTGAGCGCATGGTGCAGGAAGCTGAGAAGTACAAGGCTGAGGATGATGTGCAGCGTGACAAGGTTTCTGCCAAGAACGGTCTGGAGTCTTATGCTTTCAACATGAAGTCCACTGTGGAAGATGAGAAGCTGAAGGGCAAGATCAGTGACGAGGACAAACAGAAGATTCTTGACAAGTG[T/A]AATGAAGTCATCGGCTGGCTTGACAAGAACCAGGTGAACTTGCTGTCATTTGAGATATTTGGACAGTCATGGCATGTAGATTTGCATTTGCTAACCTATTTTAGAAGTCTAAATTAACTTTTGCATTTTGTTTGAATAAATTCAGACTGCAGAGAGGGAGGAGTTTGAGCACCAGCAGAAGGAGCTGGAGAAGGTATGCAACCCCATCATCACTAAGCTGTACCAGAGTGCTGGAGGCATGCCTGGTGGAATGCCCGAAGGCATGCCCGGTGGATTCCCAGGTGCTGGTGCTGCTCCAGGTGGTGGATCCTCCGGCCCAACCATCGAGGAGGTCGACTAAGCCATTCCAAAGCCACTATGCTACCTCCATAGCAATGTTTACTGTTGCCCTCTGTTGTTGAACTCCTCTAAAATGTATTACTACTTGTAAAGGTTTTAGAGGACCTCAACTTGCAGAGAGATTGTTGCAATTATAAAAAGAAAAGGGGATTAAAGGATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45412
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 |
|---|---|---|---|---|---|
| ENSDART00000099994 | Nonsense | 596 | 649 | 9 | 9 |
| ENSDART00000132212 | None | None | 188 | None | 5 |
| ENSDART00000141549 | None | None | 127 | None | 3 |
Genomic Location (Zv9):
Chromosome 10 (position 30761009)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 29966912 |
| GRCz11 | 10 | 29853252 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGTTTGAATAAATTCAGACTGCAGAGAGGGAGGAGTTTGAGCACCAG[C/T]AGAAGGAGCTGGAGAAGGTATGCAACCCCATCATCACTAAGCTGTACCAG
Long Flanking Sequence:
GACAAGAGCACTGGCAAGGAGAACAAAATCACTATCACTAATGATAAGGGTAAGCACGTCACTCCCTAAATATTTAAATGAATTTACATCAGTCATTTCAGAAGTTAACTTAAGATGCATTTCAGGTCGTCTCAGCAAGGAGGACATTGAGCGCATGGTGCAGGAAGCTGAGAAGTACAAGGCTGAGGATGATGTGCAGCGTGACAAGGTTTCTGCCAAGAACGGTCTGGAGTCTTATGCTTTCAACATGAAGTCCACTGTGGAAGATGAGAAGCTGAAGGGCAAGATCAGTGACGAGGACAAACAGAAGATTCTTGACAAGTGTAATGAAGTCATCGGCTGGCTTGACAAGAACCAGGTGAACTTGCTGTCATTTGAGATATTTGGACAGTCATGGCATGTAGATTTGCATTTGCTAACCTATTTTAGAAGTCTAAATTAACTTTTGCATTTTGTTTGAATAAATTCAGACTGCAGAGAGGGAGGAGTTTGAGCACCAG[C/T]AGAAGGAGCTGGAGAAGGTATGCAACCCCATCATCACTAAGCTGTACCAGAGTGCTGGAGGCATGCCTGGTGGAATGCCCGAAGGCATGCCCGGTGGATTCCCAGGTGCTGGTGCTGCTCCAGGTGGTGGATCCTCCGGCCCAACCATCGAGGAGGTCGACTAAGCCATTCCAAAGCCACTATGCTACCTCCATAGCAATGTTTACTGTTGCCCTCTGTTGTTGAACTCCTCTAAAATGTATTACTACTTGTAAAGGTTTTAGAGGACCTCAACTTGCAGAGAGATTGTTGCAATTATAAAAAGAAAAGGGGATTAAAGGATCACACTTCCAGATCACAGGGAACAGACTTTCTACCTAGATTGCACAGTTTAAACTTGTGACGTTTCACAAGCCTTTTTTTTTTCCAACTGCCTTGATGCTTTGAAGGACAAGAATAAAATGGTGACTTATTCCCAATTATATTTGTTGTCTTTTTACCTTTACATCTCAATGTGTTAG
Associated Phenotype:
Not determined