Busch Lab

ZMP

hspa13

Ensembl ID:
ENSDARG00000040984
ZFIN ID:
ZDB-GENE-070410-58
Description:
heat shock 70 kDa protein 13 [Source:RefSeq peptide;Acc:NP_001082948]
Human Orthologue:
HSPA13
Human Description:
heat shock protein 70kDa family, member 13 [Source:HGNC Symbol;Acc:11375]
Mouse Orthologue:
Hspa13
Mouse Description:
heat shock protein 70 family, member 13 Gene [Source:MGI Symbol;Acc:MGI:1309463]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa15986 Nonsense Available for shipment Available now
sa28474 Nonsense Mutation detected in F1 DNA Not yet available
sa35914 Nonsense Mutation detected in F1 DNA Not yet available
sa16121 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa15986
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
ENSDART00000060049 Nonsense 23 438 2 5

The following transcripts of ENSDARG00000040984 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 15 (position 28905042)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 29623072
GRCz11 15 29555948
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCTCCAGGTTCTGTCATCCTGGCTCTACTTCTRGCTGGGTATCTGGGA[C/T]AGCAGTATCTACCGCCTCCAAAGCCCAGGGTCATTGGGCTGGATCTTGGG
Long Flanking Sequence:
TAAATAGTTTTCTTGTTTGGCATAACACAAAGCCGCCAGCCTGTAAAATAAGCTGTTATATGCCAGTCGACTTTCGTTCTTTATGGTAAGTTACAGATGTTACAGCAGTTGGGTCTAAACACCATGTTAACTACCTGTCTAGCTATTTGGTCATCATCAGGAACATTGTCTAGACACCGTACCAAACCATATAAGTGTTTTTTATGTTTTAGTTTTTCTACGTGACATTTATATGTATACCATACAGGCACATGCTAGAAACCTTTATATTTAAATGGAATGTTCATGATTGCTATTATATGGTAACCACTAGTTAAGTGGTGAACTAAAGTATCGTGGTATTACCATCTGACACTGTATCCTATGTGCGTGTTGTAGTGGATTTCAAGCGATAGCAACTTCACATTGCTTATTAGTCAACATTATTTTTTAGCCATACATAATTGTGTGTTTCTCCAGGTTCTGTCATCCTGGCTCTACTTCTGGCTGGGTATCTGGGA[C/T]AGCAGTATCTACCGCCTCCAAAGCCCAGGGTCATTGGGCTGGATCTTGGGACCACGTTCTGCTCTGTGGGAGTGCTTCAGCCTGGCACTGGCGAGATTGAAATTATCGAAGATGACAAAGGTCGCAAAAGCATCCCGAGTGTGGTGTCATTCACTCTGACCGGTGTGTTTGCTGGACATGAGGGCCAGGAACTGTCTGACGTAAATCCTCAAAATACAATCTATGATGCTAAGAGATTTATTGGAAAGATTTTCGATGAAGAGACTTTAGAAAAAGAGAGTGCAAGATACCCATTTAAGGTAAAAAAATTTTCTTGTTACACTCTATCATTTCTTATCGTGTCTCTGACATTATCATTGCTATTTTGCAGGTGATATTCAACAATGGCAGTGCAGATTTTTTAGTCAATACAAACAGCACTTTCACGGTTACTCCTGAATTTATCGGATCCCGTCTCCTGCTGAAAATGAGGAAGATGGCTGAGAAGCAGCTGGGAGTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28474
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000060049 Nonsense 133 438 3 5

The following transcripts of ENSDARG00000040984 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 15 (position 28904640)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 29622670
GRCz11 15 29555546
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCATTGCTATTTTGCAGGTGATATTCAACAATGGCAGTGCAGATTTTT[T/A]AGTCAATACAAACAGCACTTTCACGGTTACTCCTGAATTTATCGGATCCC
Long Flanking Sequence:
ACATTGCTTATTAGTCAACATTATTTTTTAGCCATACATAATTGTGTGTTTCTCCAGGTTCTGTCATCCTGGCTCTACTTCTGGCTGGGTATCTGGGACAGCAGTATCTACCGCCTCCAAAGCCCAGGGTCATTGGGCTGGATCTTGGGACCACGTTCTGCTCTGTGGGAGTGCTTCAGCCTGGCACTGGCGAGATTGAAATTATCGAAGATGACAAAGGTCGCAAAAGCATCCCGAGTGTGGTGTCATTCACTCTGACCGGTGTGTTTGCTGGACATGAGGGCCAGGAACTGTCTGACGTAAATCCTCAAAATACAATCTATGATGCTAAGAGATTTATTGGAAAGATTTTCGATGAAGAGACTTTAGAAAAAGAGAGTGCAAGATACCCATTTAAGGTAAAAAAATTTTCTTGTTACACTCTATCATTTCTTATCGTGTCTCTGACATTATCATTGCTATTTTGCAGGTGATATTCAACAATGGCAGTGCAGATTTTT[T/A]AGTCAATACAAACAGCACTTTCACGGTTACTCCTGAATTTATCGGATCCCGTCTCCTGCTGAAAATGAGGAAGATGGCTGAGAAGCAGCTGGGAGTTCCTGTCGAGAAAGCGGTCATATCAGTGCCAGCAGAGTTTGATGAGAGGCAGAGAAACTACACCATAAGAGCTGCTAACCTAGCTGGTCAGTTTTAGGATTCAGTTTTTAAGCTTGCATTTCATTTCAACAGGAATCCAATTATTCCAGTCTCATGCTACAGCAAAATATATTGCAACAGTTTCTGACTAAATTCATCGCAGTGATCAACAGAAATCCAATATTTGCCTGTCAAAACTCTGTCTGATATTAGGTCTGCATGGGGAAATATTTCATCTCATATGAGATTCAACTCAAGATGTGTATATAATTGAGAGATTACTGTGTTTGGGTGCAGCCTTATACCTTGTGCTGCTGTATACAATTCTACAACATCTATTGTAAAATCTGGAGAAGAAAAGCAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35914
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
ENSDART00000060049 Nonsense 270 438 5 5

The following transcripts of ENSDARG00000040984 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 15 (position 28899287)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 29617317
GRCz11 15 29550193
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTCGGAGGGCAGGACTTCACCCAGCGTTTGCTCCAGTACACCACAGAG[C/T]GAGTTCGGCAGCAATATGGCGTTCCCCCTACTCTTAAAGAAGACATCCAT
Long Flanking Sequence:
GGTTTCGGATGCAGCCCAGGACTTTTAATTGATGGATACAACAAACACAAAACAGTCCTTCATAGAAAATTAAAATAAATAGAAATACAAATTAATAGAAAATACAAACCGAAAAAAACTAGAAAATACAAACTGAAAAAAATGTGAGATTTGGGAAGATATGACAGCTGTGAGTAGAGAGAGATCATTCTGCATTATGATCGTGAGCTCCTCAATGGAAACTAGTCATCTCTTTTCTGCCGTAAAAATATTTAGTTGGATCGTTGCGTTACATTCAATCTAAGTTAGGTGGTGCAACATATTTAGTAATGTGTAAGTTGTAACTTAGTGTCACTTTAAGCCACAACTAAGCTACGTTTTAACTTGCACACTGCTGGTGCAACTGGCCCCATGAGCACAACCCACCTGTTTGGCCCCATAATTAACACTTAATCTCCACAGGTAATAACCAGCTCGGAGGGCAGGACTTCACCCAGCGTTTGCTCCAGTACACCACAGAG[C/T]GAGTTCGGCAGCAATATGGCGTTCCCCCTACTCTTAAAGAAGACATCCATCTCCTCCGACAGGCTGTAGAGGCCGCCAAACTTAACCTCACCCAAGAACCTCACGTTCACCTCCGAGTTCCTCTGTACCTCCAGATGACAGGAGCCAGCGGAGCGCAAGAGGAGAAAGTCCTGTTTGAGGAGAAGCTGACCAGGGAGACATTTGAGGAGCTCAATGCCGACCTCTTCCAGAAGATCCTGGCTCCCATCGAGACCGTCCTCGTCGAGGGCCATCTGGACAAGCAGGAGGTGGATGAGATTGTCCTGGTTGGAGGGTCTACGCGGATCCCTCGGATCCGGCAGCTCATCAGTCAATATTTCGGAAAGGAGCCGAACACGTCAGTGGACCCGGACTTGGCAGTGGTGACCGGTGTGGCCATTCAGGCAGGCATTATGGGTGGTTCTTGGCCTCTTCAAGTCAGTGCAATTGAAATTCCCAATAGACATCTTCGCAAGACTAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16121
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
ENSDART00000060049 Nonsense 421 438 5 5

The following transcripts of ENSDARG00000040984 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 15 (position 28898834)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 29616864
GRCz11 15 29549740
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGACCGGTGTGGCCATTCAGGCAGGCATTATGGGTGGTTCTTGGCCTCTT[C/T]AAGTCAGTGCAATTGAAATTCCCAATAGACATCTTCGCAAGACTAACTTT
Long Flanking Sequence:
TCGGAGGGCAGGACTTCACCCAGCGTTTGCTCCAGTACACCACAGAGCGAGTTCGGCAGCAATATGGCGTTCCCCCTACTCTTAAAGAAGACATCCATCTCCTCCGACAGGCTGTAGAGGCCGCCAAACTTAACCTCACCCAAGAACCTCACGTTCACCTCCGAGTTCCTCTGTACCTCCAGATGACAGGAGCCAGCGGAGCGCAAGAGGAGAAAGTCCTGTTTGAGGAGAAGCTGACCAGGGAGACATTTGAGGAGCTCAATGCCGACCTCTTCCAGAAGATCCTGGCTCCCATCGAGACCGTCCTCGTCGAGGGCCATCTGGACAAGCAGGAGGTGGATGAGATTGTCCTGGTTGGAGGGTCTACGCGGATCCCTCGGATCCGGCAGCTCATCAGTCAATATTTCGGAAAGGAGCCGAACACGTCAGTGGACCCGGACTTGGCAGTGGTGACCGGTGTGGCCATTCAGGCAGGCATTATGGGTGGTTCTTGGCCTCTT[C/T]AAGTCAGTGCAATTGAAATTCCCAATAGACATCTTCGCAAGACTAACTTTAGTTGATCTTTTATTTGTCATATGACTGCTTTGTGCCAGCAAACCAAAAGATGGTTGAGTGACATTGCTTCCTCATGTCTTTGCTTCCTCAAATGCATTAGTTTCAGAGTTAATCAAGACCAACGCAGCAGTTATGTGAAGATGTGGTCTTCAGAACAGACGCAGAGTATTTATTTAGTTCTTCATTATATCAATAGCATCAAGGAGATGCTTTTCTACTGTATCCAGAGCAAGTGTCTGTTTTGGGGTGTGCGATATTTATTATATTATATTATATAATATAATATCAAAACTGAGGTTTTGATAATGTGCAAGCATTATTGTGATTGTGCATTATCATGTCAGTCACTTTGAGGAAGAAAAAAAGTAAACAAACACACTGGATTTGTTATGTATAAGTAATCATATGATTAACTGATATCACTAAAGCAAGGGTGCAGTTTGTTTTTG
Associated Phenotype:
Not determined