ZMP

hsp90b1

Ensembl ID:

ENSDARG00000003570

ZFIN ID:

ZDB-GENE-031002-1

Description:

endoplasmin [Source:RefSeq peptide;Acc:NP_937853]

Human Orthologues:

HSP90B1, HSP90B2P

Human Descriptions:

heat shock protein 90kDa beta (Grp94), member 1 [Source:HGNC Symbol;Acc:12028]
heat shock protein 90kDa beta (Grp94), member 2 (pseudogene) [Source:HGNC Symbol;Acc:12099]

Mouse Orthologue:

Hsp90b1

Mouse Description:

heat shock protein 90, beta (Grp94), member 1 Gene [Source:MGI Symbol;Acc:MGI:98817]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa12898	Nonsense	Available for shipment	Available now
sa40227	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa12898

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:

T > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000004879	Nonsense	359	793	8	18

The following transcripts of ENSDARG00000003570 do not overlap with this mutation:

ENSDART00000139949

Genomic Location (Zv9):

Chromosome 4 (position 8902366)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	9839214
GRCz11	4	9840130

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGGCAGAGACCTGCAAAGGAAGTGGAGGAAGATGAATATACAGCCTTCTA[T/G]AAAACTTTCTCCAGGGTKAGTAAAACYGGTGTGTGGCACAAATGGTTAGC

Long Flanking Sequence:

TGGTGATGAAAGAGGAAGCTTCTGACTACCTTGAGCTGGAGACCATTAAGAACCTGGTGAAGAAATACTCCCAATTCATCAACTTCCCCATCTACGTATGGAGCAGCAAGGTCTGTTCACAAAAGACCCCAGACACTATAACATAACCAGATGTTGGACTTCTTAAACTCACTGATTTGTGTCATTTCCCAGACCGAGACCGTAGAAGAGCCTATTGAGGATGAGGCTGAGGCAGAGAAGGAAGAAGCCACTGAAGATGAAGCTGAAGTTGAGGAAGAGGAGGAAGACAAGGACAAACCAAAGACTAAGAAGGTTTTTAGATGGAGATATTCAACCCAACATTAGAAGTTATCCTATACTTTTTTTCCAGTGAATTTTAATTAATATTTGTTGTTTTAGGTGGAGAAGACTGTGTGGGATTGGGAGCTGATGAATGACATTAAACCCATCTGGCAGAGACCTGCAAAGGAAGTGGAGGAAGATGAATATACAGCCTTCTA[T/G]AAAACTTTCTCCAGGGTGAGTAAAACCGGTGTGTGGCACAAATGGTTAGCTTTTTATGGTCCACTGCGACCTCTGGATCAGTTCAATTGGATCGTTGTCATTTCAGGACACTGATGAGCCACTGTCACACATTCACTTCACCGCTGAAGGCGAAGTCACTTTCAAGTCCATCCTCTTTGTTCCTGCATCTGCACCCAGAGGTCTTTTTGACGAGTATGGCACCAAGAAGAATGACTTCATTAAGGTAATTTGTGAACATTAAGTGAGAAATGGGAACTTGTTTTTGGTACGAGTTGCTAATTAGACTTGTTTGTTTCATTTAGCTGTTCGTGCGTAGAGTCTTCATCACTGATGACTTCCATGACATGATGCCCAAGTACCTCAACTTCATCAAGGGTGTTGTAAGTGCCTGTCTTTCAGTTTAGCATTTCATTGGGCAATGCATAATGCTAAATGTTCCATTTAGCCTGTGTATTGGCTTAAAAGTTGGCCCACATGGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40227

Status:

Mutation detected in F1 DNA
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
ENSDART00000004879	Essential Splice Site	785	793	None	18

The following transcripts of ENSDARG00000003570 do not overlap with this mutation:

ENSDART00000139949

Genomic Location (Zv9):

Chromosome 4 (position 8905706)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	9842554
GRCz11	4	9843470

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGCTGAGGATGAGGAGGAGGTCCAGGCAGATGAAGCAGAAGAGGAATCAG[T/C]GAGTGCCCTTCCAAACAAAAGTCTCTTTAGGAGCTGGAATTCTGGTCTTC

Long Flanking Sequence:

GTCAAGCGTTCTCATTTAGCCTAGCAAATTGTGCCTTCAATCTTATTTCAAATGAATATATTGTGCATTTTGTGTTGTAGGAAGACGCTGAGGATAAGACGGCCGCAGATTTAGCCGTAGTGCTGTTTGAGACCGCCACACTGCGATCAGGATACCAGCTCCAAGACACCAAAGCCTACGGAGAAAGAATAGAGCGCATGCTGCGGCTCAGCATGAATGTAGACCTTGACGCTCAGGTATGGATGTTCAAATCAAGCATCAGATTATTCTGAAGGTCTGCTTGTGAAGATCTCTGCTTTATGTAATAAGTCTATCTCCTGGTATCGGAAACATTCAGACTGAGCTTGATTTTATTAATGGAACTCCCAGAACCAGGACACTTAGAATCCTGTTGTTGCATCTACAGGTAGAGGAAGAGCCAGAGGAGGAACCAGAAGAACAGACAGAGGAAGCTGAGGATGAGGAGGAGGTCCAGGCAGATGAAGCAGAAGAGGAATCAG[T/C]GAGTGCCCTTCCAAACAAAAGTCTCTTTAGGAGCTGGAATTCTGGTCTTCATATATCTGAATATGTATGTTCTCTGCGTTTCAGGAGGCCACATCCAAAGATGAGCTGTAATGTGTAAATTTGGAAGGGATGGGAAGGGGTGTCTGACTGTGATGCAGAGTGAAGATGGCGACGTCAACGCGGTTGTCTTTTCTCTGTGCGGGTGGGCTTGGGGGATAGGAGCTGTTTTTTTTAAAGCGCTGCTTTTGTGTTTGCAATTTCTTTTTTTACATTCCTCCATGATTGTAAATTTGTTAATATTTAACTGACCCAGTTGTGGAGTGCTGACTCCTGTCCACAGAACGATTAAATGTTTCCGGAAAAGGATTTTTGTGTGCAATTTCTTAATTTGCGTCATGTTAACCAGTTCTATTAAATAACATTTTAGGATATTTTAGCAGCATCAATAGTGCTTTGATTAAAGTCCAGTTTGAATTTAAAGGGATAGTTCACACAGTTTA

Associated Phenotype:

Not determined