ZMP
hspa13
Ensembl ID:
ZFIN ID:
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 |
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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:
sa16121
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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