ZMP
si:ch211-237a6.7
Ensembl ID:
ZFIN ID:
Human Orthologue:
HSF2BP
Human Description:
heat shock transcription factor 2 binding protein [Source:HGNC Symbol;Acc:5226]
Mouse Orthologue:
Hsf2bp
Mouse Description:
heat shock transcription factor 2 binding protein Gene [Source:MGI Symbol;Acc:MGI:1921627]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14014 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14014
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000075546 | Essential Splice Site | 96 | 347 | 3 | 8 |
| ENSDART00000133246 | Essential Splice Site | 99 | 365 | 3 | 9 |
The following transcripts of ENSDARG00000035080 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 28068353)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 28333911 |
| GRCz11 | 1 | 29137743 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAAACCAGAMTAGATGCTGCCCTGAATGAGTGTCAGAATGAGAAACAGG[T/C]ACTATAACAGAAAGGATGAGAGACTGCAGAGACCACACTGAAGTGAAACA
Long Flanking Sequence:
ACAAACATAGACAGTAACAATAGTTATTGGTAACAATAGCTGACATCAAACACAGACATGGAAAGGAAAAAAGAGGAAAACACACACAAACACGTATACCAAAAACACATTAAACAGCCTAGAAAAATATAAATAATTATATAAATAATAATTAAAAACAGTAAATTAATTATATAACTAAATGGGAAACAATGCCTACATGTGTACAACCTCAAAACTGAAATTCAAGATAATTTAAATTTGAAAGTGGTTCCAGCAAACTCAGAAAATTAACTTTTAAAAGGACAATTTAAAGTTGATAAAGTGCTGTATTATACTAAATGGCAAAAAAAGATGTAGTCATCTGATAATTTTGACTGGTGACTTACTGTTTTAAATTGTTTTTGACTTTTATATAGTTCAAGAACTCTGTGATCGTGAGCAGCAAGAAAGAGAGAATTGTCTACATATTCAAACCAGACTAGATGCTGCCCTGAATGAGTGTCAGAATGAGAAACAGG[T/C]ACTATAACAGAAAGGATGAGAGACTGCAGAGACCACACTGAAGTGAAACATAATTTAGTTTAAGATTCTAGAAAAGCATATACACAAATAACATTTTTACATACTATTTAAATTTTTCTATAAACTACTTTTAATTATCACACAGAAGGTGTCTATATAGAGCATCTTAAATTAGATCATGCAAGACTTTAAATATAAGTAAATAGTATCCATTATTTGAACTCATTTTTTATTTGTACTGTATTATAGCGTTGTCATGCTCTTAGAAAAGCTGTGTATGTTTATGTCTTCTCATATACATTTGTAGGAGAAGCTGGTTCTTAAGCAGCAGTTATGGGAATGCAGAGGACAGCTTCAGCAGCAGAAAGACTTTTGTACTGAGCTGGGTGCTTCATGTTGCACGTTGCTGTGGAGTGCATCTCAGAAGGAGGAAGCCATCAGAGACATATTGGCTAATGTGAGTTTAAGTTTGAGTTTGATTGAACACAATTAAAAGTTGT
Associated Phenotype:
Not determined