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
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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