Busch Lab

ZMP

hspa4b

Ensembl ID:
ENSDARG00000018989
ZFIN ID:
ZDB-GENE-030131-6018
Description:
heat shock protein 4b [Source:RefSeq peptide;Acc:NP_956151]
Human Orthologue:
HSPA4
Human Description:
heat shock 70kDa protein 4 [Source:HGNC Symbol;Acc:5237]
Mouse Orthologue:
Hspa4
Mouse Description:
heat shock protein 4 Gene [Source:MGI Symbol;Acc:MGI:1342292]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa18551 Nonsense Available for shipment Available now
sa9130 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa18551
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002469 Nonsense 483 840 12 19
Genomic Location (Zv9):
Chromosome 14 (position 24604326)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 23402850
GRCz11 14 23700095
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGTGGTTCCCCAGGCCTCCGGTGAGAGTTCAAAGGTTAAAGTGAAGGTG[C/T]GAGTGAACATTCATGGCATCTTTAGYGTTTCCAGTGCTTCACTAGTKGAG
Long Flanking Sequence:
AGATCAGTCAGAGACTTCAAAAAAGTTGAAATTAATTTAACGAATCAAATGGATAAAACATACAGGGCCCTGGGTAGCAGAGAACAGCAGCACAGGCCGTTGTCAGCTGCGCACCCCCCCACCCCCCAGTTGTCACAAATGATCTGCACAGAAAAAGTTTTACACACACAGAACACACAAGACAGAGCCTAAAAGAAAGAATTATAACATTTTTCTGATAACAAGTTCTCTGAATTTAATTTTTTGGTTATCAGTCACAAAACCACAGCTGTTATGGAGCAAGGTTTTATGAGGTGAAGCACACAAACATGAGTTCATATACTTTATTAAAACAGGATTCAATTATTAATGCATAAAACAAAGTTAGAAAACATCATAACTACTTCAATACTGTCAGTATGTAAAAAATAAATAAACTAAATTTCTCTGCAGGCCAGTATGTTGTCCAGAAAGTGGTTCCCCAGGCCTCCGGTGAGAGTTCAAAGGTTAAAGTGAAGGTG[C/T]GAGTGAACATTCATGGCATCTTTAGTGTTTCCAGTGCTTCACTAGTGGAGGTGCAGAAATCTGAGGAGGAAGAGGAGAGCATGGAAACCGAGCAGAGCACAGAAAAAGAAAATGAGGTACTGAGTGCTTTTTCTTAAACACTAGCTGAAGTACTCATGAAATGCCGTTTCATCACAGTTCTAAAATGATGCAGAAGTGGGTGTCTTGAAAAATTAGGCAAAGCTTGTTTTCATATGATGTGGACACGCCTCATCATAAATATTTAAGACATTAACACAGATTTTCAGTAATGCAATACACTCACCTGCCACTTCATTAGGTACACCTGTATAACTGTTTTTTTACGCAAAGTTCTAATCAGCCAATAACATGGCAGCAACTCGATGCATTTAGGCATGTAGACATGGTCAAGATGATTGCTGCAGTTCAAACCGAGCATCAGAATGGGGAAGAAAGGTGATTTAAGTGACTGAACATGGCATGTTTTTTTTGTGCCAGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9130
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002469 Nonsense 810 840 19 19
Genomic Location (Zv9):
Chromosome 14 (position 24611991)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 23410515
GRCz11 14 23707760
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTTGCCAAAAGAAGAGAACCCATCAGAACCCAACGGGCCCGTCAACACA[C/T]AGGAAAACCCTGAAGCTCAGCCCGGCGGCACAGAACCAGCTGCTGCAGAC
Long Flanking Sequence:
TTTACTGACCAAGGTTGTCGACGCCACTATAACGACACAGATCACTCTGCCTATTCATGCCAAAACCTCTGAAAAAGTGATTGACAGGTGGTAATTTGTGTTTAACTTATCTGTATTTATTTAGGATTTGTTTATGGGTAAAACAAAGATCATGCAGGTCAGGTAGTTGAAACGGTAGGCTACAAATAATTAATTTGTTTTGAATAATTAATTATTCATAATTAATTTGCCTCCGCCTGTGCTGACGATGCCTTCATCCATCAGGATGTGTCACATTAGACATTGTACGATGCCAGATTGTTCGACATCGCCCAACCCTAGTTTCCACACATTGTTATTGGCTGATTAGATAGCAGTGTGCATTTTGCTACATAAATTTATTTCAACATTTTCCACAGGAGCTGTTTTCTACTTGCAATCCAGTCGTGACCAAACCCAAGCCCAAAGTGGACTTGCCAAAAGAAGAGAACCCATCAGAACCCAACGGGCCCGTCAACACA[C/T]AGGAAAACCCTGAAGCTCAGCCCGGCGGCACAGAACCAGCTGCTGCAGACAGTGCAGGAAACACAGAAAACAAGCCTGACATGGACCTTGATTAAACACGCTGTGTAATGTTATGTTAACGTTACACGTTATGTTATGTAACATAATGTTTTGTTAATGTTAACTTATGTTTCCAGTGACTAGAATGCTAAATCATCATCATCATCCTCCTCAAAACAGGGAGACTCTAACAGTGAGCGATTCAGTGGCTACATTTGCATGTCGTTTTATATTAAGAAAATCATAAGTCATAATGCTGTAAGACTTCTGATTGAGAACAATTCTGTCTGCCTACAATTGAGTTTCTGTCATATGCCGGTTCTGTCAGCTGTTGTTTCAATAAATATGGATTGAAACGTGTGCAAATTTATGTTGAGGTTATTTAGTGTAATGCAAAGGAGTCTATATTTGTTTTGTTCAGGTTGCTTTACCGTTTGGTTTAAGGATGAATTTACATGTGA
Associated Phenotype:
Not determined