Busch Lab

ZMP

hsp90ab1

Ensembl ID:
ENSDARG00000029150
ZFIN ID:
ZDB-GENE-990415-95
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
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
sa10 Essential Splice Site Confirmed mutation in F2 line Not yet available
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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:
sa10
Status:
Confirmed mutation in F2 line
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000020084 Essential Splice Site 318 725 6 12
ENSDART00000129014 Essential Splice Site 303 710 6 12

The following transcripts of ENSDARG00000029150 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 51537521)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 51389590
GRCz11 20 51202810
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTACAAGAGCCTGACCAACGACTGGGAAGACCACCTGGCTGTCAAGG[T/C]AATAGGAGCTCTACTAAGTGGGATGTAATGTATTAGGGATGTAATGAACT
Long Flanking Sequence:
TGTGACCATTTGAGGGCAAGTAAATAGATTTTTGGGTGAACTCTATTTATAAATTTGCATCCTCTATGATTTGATAATTGCACTAAGCCATATATTGATTTAGGTTATATTTGGAATAATTGTGCAGGCCTGTGTTCCTCAAGTTAATTGAGCTTTGCAATGACAACGCACAATCAAAACTGTCCCACAGGTGGAGAAGGAACGTGACAAGGAGATCAGCGACGACGAGGCAGAAGAGGAGAAGGCAGAGAAAGAGGAGAAGGAGGAGGAAGGAGAAGACAAGCCCAAGATTGAAGATGTCGGCTCGGATGATGAGGAAGACACCAAAGACAAGGACAAGAAGAAAAAGAAGAAGATCAAGGAGAAGTACATCGACCAGGAGGAGCTGAACAAAACCAAGCCCATCTGGACCCGCAACCCTGACGACATCTCCAATGAAGAGTACGGAGAGTTTTACAAGAGCCTGACCAACGACTGGGAAGACCACCTGGCTGTCAAGG[T/C]AATAGGAGCTCTACTAAGTGGGATGTAATGTATTAGGGATGTAATGAACTCATGATTCAATTTAATTTCACAATTCAAACTTTATTTTTTTAATAAAAGGAGATTCAAGATTAAATTATAACGTCTTTTTAATTTAAGGGTATTGCTGCACGTTTCAATAAGGAGTGTAAGAACTAAAATCGAAAAACATCAAATAAGTTGCTTAAATACAAAGTCTCTTCATAAAAACTGAGGCTCTTTTTTTAATGCTGTTTCCCTTTTAAAATTAGAAGCAGATTCTGCATCTTATTCAATATCCAAAAAATATGCATCATACATTCAACAAGAGCCTTTTTAATCTAAGTGGAAGCTTAAAAGTCTGGCTTTAGTATAGTCAAACTATTGGTTTACTACATAAAACAGTGGAATGAAATCGCAGTCGAGCTGAACAAGCCAGAGTTTTACTCTAACAGCAGGTGGCACTTATGAATGATGATGCTGCATTTCCTGGCTTACTACTG
Associated Phenotype:
Normal
Stage Entity Quality Tag
Larval:Day 5
ZFS:0000037		 whole organism
ZFA:0001094		 quality
PATO:0000001		 normal
PATO:0000461

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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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