ZMP
hsp90ab1
Ensembl ID:
ZFIN ID:
Description:
Heat shock protein HSP 90-beta [Source:UniProtKB/Swiss-Prot;Acc:O57521]
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 |
---|---|---|---|
sa12875 | Essential Splice Site | Available for shipment | Available now |
sa15412 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12875
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020084 | Essential Splice Site | 49 | 725 | None | 12 |
ENSDART00000129014 | Essential Splice Site | 49 | 710 | None | 12 |
The following transcripts of ENSDARG00000029150 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 51534611)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 51386680 |
GRCz11 | 20 | 51199900 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAKGRTTAATTGATRCATCDGCAAAATRTTCCCATTKCTCNNTTTTAAT[A/T]GGCTCTTGACAAAATCAGATATGAAAGYTTGACAGATCCCACCAAACTGG
Long Flanking Sequence:
ATAAAAATACATTTACTTATAAAAGTATTTTCCTGCCATTTCTGTTTTGTAGAGTTGTTATGGAATCACTTTTTTGTTTTAATTTATCAAAAATAGGGCCAAAATATTATGAATGTAGCGTTATGCGCATCAGTTTGTTTTACGAAAAATTTTATTTTTGGGGGAAAAAAATAATCTATAATTTGTAGATTTTTTTTACCATTGTGTTATAACAGCTGTGTTAATGGAAATATAACACATTTAAACTATTTCTTTGCTTTCTTAAGATGCCTGAAGAAATGCGCCAAGAAGAAGAGGCTGAGACCTTTGCCTTCCAGGCAGAGATCGCCCAGCTGATGTCTCTCATTATCAACACCTTCTACTCCAACAAAGAGATTTTCCTCAGGGAGCTTGTTTCCAACGCCTCTGACGTAAGACTAGTGATGCTTTTAATATTTGTCTGCCTTTTTAAAATGGTTAATTGATGCATCGGCAAAATGTTCCCATTTCTCTTTTTTAAT[A/T]GGCTCTTGACAAAATCAGATATGAAAGTTTGACAGATCCCACCAAACTGGACAGCGGCAAAGACCTGAAGATCGACATTATCCCTAATGTTCAAGAACGCACCCTCACCCTCATCGACACAGGGATTGGGATGACCAAAGCCGATCTAATCAACAACTTGGGTACCATTGCAAAGTCCGGGACAAAGGCTTTCATGGAGGCTCTGCAGGTGATTGAATGGGGTTATAAGAGAATTTACATGGGTCCTTGAATGTTTAAAATCTGAAAATGAATATTTCAATTTTATGAATATAAAATTGTGGGTTTATGAATATTTCAACATTAATAAATGACATCCTTTGAAAGCAGTTGAATTTTTGTACAAGAAGTTTACTGGAGGAAATCCCTCAAGCACAAACCAGCCTTATGTTGCCAGGGTGTATTTGGCAGTAGACAAAAATACATTGTCTGGCTCAATTATAGATTTCTTTAATGTAAGAAATCATTGTAATATTAGGCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15412
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 |
---|---|---|---|---|---|
ENSDART00000020084 | Nonsense | 471 | 725 | 9 | 12 |
ENSDART00000129014 | Nonsense | 456 | 710 | 9 | 12 |
The following transcripts of ENSDARG00000029150 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 51540752)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 51392821 |
GRCz11 | 20 | 51206041 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTTACCAGAGCTCRCAGTCCGGCGACGAGATGASCTCCCTCACAGAATA[C/A]GTCAGCCGTATGAAGGAGAACCAAAAGTCCATCTATTACATCACTGGTAA
Long Flanking Sequence:
AATGACCAATTCTGATGGAATTTGTCTTGCTGCACATTTAGTGTTGATTTTGTGCTTTTTTTAAATTTTTCATTTGCACTACAGTTTTTAAGTAGCACCACTAACCTCTCTGAAACATTGGTCTTCCTCAGACTTCATCCGTGGTGTGGTTGACTCTGAAGATCTGCCCCTCAACATCTCCAGAGAGATGCTGCAGCAGAGCAAGATCCTCAAAGTCATCCGCAAGAACATCGTCAAGAAGTGCCTGGAGCTGTTTGCTGAGCTCGCCGAGGACAAGGACAACTACAAGAAGTTCTACGATGCCTTCTCCAAGAATCTGAAAGTACGTTTCCACCTTAGATTTGCGTCTAAACGGGTGTATAATAAAAACTGGTATTAACAGATGTTCGCTTCCTCCAGCTTGGCATCCACGAGGACTCTCAGAACCGCAAGAAGCTGTCAGAACTGCTGCGTTACCAGAGCTCACAGTCCGGCGACGAGATGACCTCCCTCACAGAATA[C/A]GTCAGCCGTATGAAGGAGAACCAAAAGTCCATCTATTACATCACTGGTAAGATTTCAACCGCATTAACCTGGATTAGTCAGATGTGCAACCATCTTCCTACTTGTGATTAAATGTGCTTCTTAAACTTTTGAACCAAAAGCCCTTAATGTAGTTCATTTATTTTGAAAGTATATTCAAAAACAGCCACAAGACTGTACATAAAGTGCTCTACGTAAAACTACAAAAACAATAATAATATTAAACCATTATAATTAACAGTGTCAGTTGGTTTTAATAGCCTGAATTTGTGATTTGAAATACATTAAGTCCTAAGTTTACTGAAATATTGCATTTTAGATCTTAAATCCTTTTTTTAAATAGACAAACAAGAATAAAGACATGTAAATCTACCCAAAAAAACATCCAATCACCAACAAACCATCTCAAATTGACCAGTTACATTTTTTTTCTCTATTTACCAATATGAGTAGCAAGTAAATTACCAGTTTCTACTTGTAAA
Associated Phenotype:
Not determined