ZMP
hsp90a.1
Ensembl ID:
ZFIN ID:
Description:
Heat shock protein HSP 90-alpha 1 [Source:UniProtKB/Swiss-Prot;Acc:Q90474]
Human Orthologues:
HSP90AB1, HSP90AB4P
Human Descriptions:
heat shock protein 90kDa alpha (cytosolic), class B member 1 [Source:HGNC Symbol;Acc:5258]
heat shock protein 90kDa alpha (cytosolic), class B member 4 (pseudogene) [Source:HGNC Symbol;Acc:32
heat shock protein 90kDa alpha (cytosolic), class B member 4 (pseudogene) [Source:HGNC Symbol;Acc:32
Mouse Orthologue:
Hsp90ab1
Mouse Description:
heat shock protein 90 alpha (cytosolic), class B member 1 Gene [Source:MGI Symbol;Acc:MGI:96247]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30722 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1396 | Nonsense | F2 line generated | Not yet available |
sa16631 | Nonsense | Available for shipment | Available now |
sa14009 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa30722
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 |
---|---|---|---|---|---|
ENSDART00000004756 | Nonsense | 398 | 725 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 54342824)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 54198227 |
GRCz11 | 20 | 53987673 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGGACTCTGAGGATCTGCCTCTGAACATCTCCAGAGAAATGCTTCAA[C/T]AGAGCAAAATCCTGAAGGTGATCCGCAAAAACCTGGTCAAGAAGTGTCTC
Long Flanking Sequence:
TAAGACAACTTTCAAAGGTTTTGAACCACTTCAAATGTTGACAACTGTATATCAATGTCAACCAATAGAATAAATGCTGACTTTCCTTGACTCTAGTCTGTTAAGTTATTAGACAATAATGCTCTACTTCAGGTGTGGATTATATAAGGCATAATTGCCATACTTAAAGGATATTAAATGCATGATGCAGAAGAAACTAAGCATCCATGTTTGATGAAAGCACATTTATTTTTTGTTAACTGTGATCAAAACTGACTGGAACTACCTGTGTGCATTAAAAATAATATTACACACTTTCCAGCCAATCAGAAACGAGTATTTCAACAGACCATTGTGTCATTTCTAACAATTCAATTGTTTGTTCTCAATTATTTCTTACTCATTCCAAAGTAATAATACACTATATAACATTCACAAAATCAACATTCCTTCCAGACTTTATTAAGGGTGTGGTGGACTCTGAGGATCTGCCTCTGAACATCTCCAGAGAAATGCTTCAA[C/T]AGAGCAAAATCCTGAAGGTGATCCGCAAAAACCTGGTCAAGAAGTGTCTCGATCTCTTCACCGAACTGGCAGAGGATAAAGACAACTATAAGAAATACTACGAGCAGTTCTCCAAAAACATCAAGGTGAATGTGCTACTCAAGTAACTAACGAACACAGAAATATAGAAAGTGCCCAAAATAACATGTTTCTTCTTCTTTTAGCTTGGCATCCACGAGGACTCTCAGAATCGCAAGAAACTTTCTGATCTTTTGCGCTACTACACTTCAGCTTCAGGAGATGAGATGGTGTCACTTAAAGACTATGTGTCTCGCATGAAGGACACACAGAAGCACATCTACTACATCACCGGTTAGTAGCGATTCAGTGAATTAACAGTCAGTGTTTTGAGTTATGGATTATAAGAAATGAGAGTTATGTAATCATTTACTTGAAAAAGTAATCTGATTACATAAGTTGGATTACCCTTAATAAATGAAAAAACTAATGAGTAATTTGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1396
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000004756 | Nonsense | 413 | 725 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 54342777)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 54198180 |
GRCz11 | 20 | 53987626 |
KASP Assay ID:
554-1308.1 (used for ordering genotyping assays)
KASP Sequence:
CAACAGAGYAAAATCCTGAAGGTGATCCGCAAAAACCTGGTCAAGAAGTG[T/A]CTCGATCTCTTCACCGAACTGGCAGAGGATAAAGACAACTAYAAGAAATA
Long Flanking Sequence:
TATATCAATGTCAACCAATAGAATAAATGCTGACTTTCCTTGACTCTAGTCTGTTAAGTTATTAGACAATAATGCTCTACTTCAGGTGTGGATTATATAAGGCATAATTGCCATACTTAAAGGATATTAAATGCATGATGCAGAAGAAACTAAGCATCCATGTTTGATGAAAGCACATTTATTTTTTGTTAACTGTGATCAAAACTGACTGGAACTACCTGTGTGCATTAAAAATAATATTACACACTTTCCAGCCAATCAGAAACGAGTATTTCAACAGACCATTGTGTCATTTCTAACAATTCAATTGTTTGTTCTCAATTATTTCTTACTCATTCCAAAGTAATAATACACTATATAACATTCACAAAATCAACATTCCTTCCAGACTTTATTAAGGGTGTGGTGGACTCTGAGGATCTGCCTCTGAACATCTCCAGAGAAATGCTTCAACAGAGCAAAATCCTGAAGGTGATCCGCAAAAACCTGGTCAAGAAGTG[T/A]CTCGATCTCTTCACCGAACTGGCAGAGGATAAAGACAACTATAAGAAATACTACGAGCAGTTCTCCAAAAACATCAAGGTGAATGTGCTACTCAAGTAACTAACGAACACAGAAATATAGAAAGTGCCCAAAATAACATGTTTCTTCTTCTTTTAGCTTGGCATCCACGAGGACTCTCAGAATCGCAAGAAACTTTCTGATCTTTTGCGCTACTACACTTCAGCTTCAGGAGATGAGATGGTGTCACTTAAAGACTATGTGTCTCGCATGAAGGACACACAGAAGCACATCTACTACATCACCGGTTAGTAGCGATTCAGTGAATTAACAGTCAGTGTTTTGAGTTATGGATTATAAGAAATGAGAGTTATGTAATCATTTACTTGAAAAAGTAATCTGATTACATAAGTTGGATTACCCTTAATAAATGAAAAAACTAATGAGTAATTTGCGAAACAACATTTTGGAAGAGGTTTTCTTTTAAGGTAAAAAGTAATCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16631
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004756 | Nonsense | 597 | 725 | 10 | 11 |
ENSDART00000004756 | Nonsense | 597 | 725 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 54338757)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 54194160 |
GRCz11 | 20 | 53983606 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCTCCAACCGTCTGGTGTCTTCGCCCTGCTGTATCGTCACCAGCAMATA[C/A]GGYTGGACGGCRAAMATGGAGAGGATCATGAAGTCTCAGGCTCTGAGGGA
Long Flanking Sequence:
TAGTTTCGGTTTCAATCAAGTCGTCCGCATAAGATCAACACATTCAGTTCGAGAAGAAAATTCACATTCACAATTCACAAATTGAAGCAAAAAACATCCTTTGAGTAATCGAGAGCGAGTGACGAGATGCTAATTTTCGTAAACAAAATTACGAATTTGAACTGGTAGATTACACACAAAGTCAATGAGTATGTGAAAAAATAGTAGTAATCCACGCAGAATTTCCAGAGGGTGTATTACTACTATTTGATCATGCATATAATTTGATTCTGAACAGGTCACAGTCTCCGACCATTTAATCTTTAACAACTAAAAAATCATGCGAGCTAATGACTCAAAGCAAATGCCCAAATAGAGGTGAAAATCCACTGGGTGGCACGAATGAGGCAAAATACACAGTGTATTACTATTACTTGCTCATGCATATAATTTGTGTCTGAATAGGTCACCGTCTCCAACCGTCTGGTGTCTTCGCCCTGCTGTATCGTCACCAGCACATA[C/A]GGCTGGACGGCGAACATGGAGAGGATCATGAAGTCTCAGGCTCTGAGGGATAACTCTACCATGGGCTACATGACCGCTAAAAAGCACCTAGAAATAAACCCAGCACACCCCATCGTGGAGACCCTCAGAGAGAAAGCGGAAGCCGACAAAAACGACAAGGCGGTGAAGGATCTGGTGATCCTGCTGTTCGAGACGGCGCTCTTATCCTCAGGCTTCACACTGGACGACCCACAGACTCATGCAAACCGCATCTACAGGATGATCAAACTCGGACTTGGTAAGTCTGATGGCTACAGAAGCTAGAGAACTTTATTATATAATATAGTCACAGTTGGATTTGTGTATTGCATGTATGGGGGGCCTAACTATGAGAAGAATACTTAATTATTATTTATTCATAATAATTATTATTATTATAAATATTATTAATACTTAATAATGAAGAATAATTACTATTAATATTAATAGTTTTATATAAAAATGGGCCTTTTGGATGGGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14009
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004756 | Nonsense | 597 | 725 | 10 | 11 |
ENSDART00000004756 | Nonsense | 597 | 725 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 54338757)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 54194160 |
GRCz11 | 20 | 53983606 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCTCCAACCGTCTGGTGTCTTCGCCCTGCTGTATCGTCACCAGCAMATA[C/A]GGYTGGACGGCRAAMATGGAGAGGATCATGAAGTCTCAGGCTCTGAGGGA
Long Flanking Sequence:
TAGTTTCGGTTTCAATCAAGTCGTCCGCATAAGATCAACACATTCAGTTCGAGAAGAAAATTCACATTCACAATTCACAAATTGAAGCAAAAAACATCCTTTGAGTAATCGAGAGCGAGTGACGAGATGCTAATTTTCGTAAACAAAATTACGAATTTGAACTGGTAGATTACACACAAAGTCAATGAGTATGTGAAAAAATAGTAGTAATCCACGCAGAATTTCCAGAGGGTGTATTACTACTATTTGATCATGCATATAATTTGATTCTGAACAGGTCACAGTCTCCGACCATTTAATCTTTAACAACTAAAAAATCATGCGAGCTAATGACTCAAAGCAAATGCCCAAATAGAGGTGAAAATCCACTGGGTGGCACGAATGAGGCAAAATACACAGTGTATTACTATTACTTGCTCATGCATATAATTTGTGTCTGAATAGGTCACCGTCTCCAACCGTCTGGTGTCTTCGCCCTGCTGTATCGTCACCAGCACATA[C/A]GGCTGGACGGCGAACATGGAGAGGATCATGAAGTCTCAGGCTCTGAGGGATAACTCTACCATGGGCTACATGACCGCTAAAAAGCACCTAGAAATAAACCCAGCACACCCCATCGTGGAGACCCTCAGAGAGAAAGCGGAAGCCGACAAAAACGACAAGGCGGTGAAGGATCTGGTGATCCTGCTGTTCGAGACGGCGCTCTTATCCTCAGGCTTCACACTGGACGACCCACAGACTCATGCAAACCGCATCTACAGGATGATCAAACTCGGACTTGGTAAGTCTGATGGCTACAGAAGCTAGAGAACTTTATTATATAATATAGTCACAGTTGGATTTGTGTATTGCATGTATGGGGGGCCTAACTATGAGAAGAATACTTAATTATTATTTATTCATAATAATTATTATTATTATAAATATTATTAATACTTAATAATGAAGAATAATTACTATTAATATTAATAGTTTTATATAAAAATGGGCCTTTTGGATGGGGG
Associated Phenotype:
Not determined