ZMP
strumpellin
Ensembl ID:
ZFIN ID:
Description:
WASH complex subunit strumpellin [Source:UniProtKB/Swiss-Prot;Acc:Q7ZVM1]
Human Orthologue:
KIAA0196
Human Description:
KIAA0196 [Source:HGNC Symbol;Acc:28984]
Mouse Orthologue:
E430025E21Rik
Mouse Description:
RIKEN cDNA E430025E21 gene Gene [Source:MGI Symbol;Acc:MGI:2146110]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22932 | Nonsense | Available for shipment | Available now |
| sa28731 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22932
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 |
|---|---|---|---|---|---|
| ENSDART00000005653 | Nonsense | 134 | 1021 | 3 | 25 |
Genomic Location (Zv9):
Chromosome 16 (position 46159945)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 43412956 |
| GRCz11 | 16 | 43316714 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATGCTTTATGTCTGCTTATATTTCACTCCCTCCATCCTGCACACACAA[C/T]AGGCCAAGATGAGAGAGATCGTGGACAAATACTTCCCTGACAACTGGGTG
Long Flanking Sequence:
GTAAATACAAACTTAATTGAAAAAAATACTTCAACATTTTTAAAATGCTTTTATGTAAACATTATTAATTCTATTGATAGATAAAATGCAAAACAATTATAGAAATTTTCATATAAAGTATAATGAAATCATTTTTCCACATTTGTTTTAAATCTGCTGACGATTAAAATGCAAAAAATAAAATAAAAAATAAATGTAATAATATTTACTGTGGTAATAATAATAATAATAATAATAATAATAATATATTTATTACTTTTGTGTTTTCCTACACCCAGCTTTATATCAGAAAATGCTTCCTCATATTTATATTTTAAGAACAGTTTGAAAACCTCTCATTCAGCTGGATATCTCATGTTTATTCCTGCTTTGTGCAAATGTATGCTCTGTTGTAGGTCTCTGCGTATCCTCTGCCGGAGCACCGCAGCACAGCTCTGGCGACTCAGGCCGCTATGCTTTATGTCTGCTTATATTTCACTCCCTCCATCCTGCACACACAA[C/T]AGGCCAAGATGAGAGAGATCGTGGACAAATACTTCCCTGACAACTGGGTGAGAAGACTTTAATCATCATGTCTTTTCAGAAAATGTGACCCACTTGATATTTTAACTACAACATCGACCTTGCATCTTCAGGTTATAAGCATATACATGGGCATCACAGTGAACTTGGTGGAGGCGTGGGAACCATATAAAGCTGCTAAAATAGCCCTGAACTACACGCTGGACACAGCTAACATCAGAGAACAGGTACAGTCATCTGTGCTCTTTCTGTTCACACATGTTCAGAGTAATCCAGAGTCACTCTGGATTAGTGTTGGGCAAGTTATTTTTAAATAAATTTTTCATGATGTAGGTAATAATAAATGACTTTTTATTGCTTATGTCTGAAAAAAAATGCCATTACCCCTAAGGAATTTAATTTCTTGAGTTAATAGTGCTGTAATTTCAACTATTTTTTATTCTTTAAGTTTGAGTCATATACTGCATGATCTTTGTAGCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28731
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000005653 | Essential Splice Site | 287 | 1021 | 6 | 25 |
Genomic Location (Zv9):
Chromosome 16 (position 46156358)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 43409369 |
| GRCz11 | 16 | 43313127 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTCAGCTGCTGCTGGACACGGCTCAGTTTGAGTTCATACTCAAAGAG[G/A]TAAATATAAAAAATTGAATTATTTTGAAATTATATTTCTCAATGTTAAAT
Long Flanking Sequence:
AAACTGCATAGTGCGGACTTATAACAGAATCTTAAAATGTATTTAGAATGATAAAACAGCACTACTTCTTTTCTATATGATCACAAGTGGAAAGACCGGAAGGAATGACAAAATTAAAGCTCCTTATTCTGCTACATGCTGCCCTGATGCTGCTTTTAGTTAACAACTTTAGCTCATCCATGAACATGATATCTGCAGGAGTCCCATAGGATGAAATGAAGACTACAACCCCCATGATTCACACAATTTGAAAATTACATACTGTGCCTTTAAGAAAACCTTTAGATTCTGTTTGAGTTTTGATTAATTATTGATTTTTATGGAATTAGAAAAATGCTTTTCTAAGTTTTGTTGTTGTTGTTGCTCTTGAAGCTTATGATCCAAACAACAAGAGGCTTCGTCAGATCAAAGACCAAGTCATCAACGACTCCAAATACAACCCCAAAATTCTGTTTCAGCTGCTGCTGGACACGGCTCAGTTTGAGTTCATACTCAAAGAG[G/A]TAAATATAAAAAATTGAATTATTTTGAAATTATATTTCTCAATGTTAAATTGAAGCTTTTTTTGGACAAGAATGTAATGAATTCTAATGCAGTCCACTAATCTTGGTTCAGGTCTTCAGTCTGTCTGAGAAATACACCTTTTAAATTCAAATATTTCGTTCAACCAAAATGGAAAATTCTGTATTTATTTACTTATCGTTTCCTTGTTACAAAGCTGTTTCTTGTTTCTATAGAACAGGAAAAAAAGATAATTTGAAAAATGTTGGAAATCTGTAACCATTGACTTCCTTAAATTTAGTTTTTTCTACTATGAAAGTCAATGGTAACTCATTCTTCAAAATATCTTCTTTAGTGATCAGTGGAATAAAGAAACTCACACAGGTTCGGATAAATAGTGAGTAAATTATAGTTTTGGGGTAAACTATCTCTTTTTCCTTCAGGAAAGCTATCTTATTTAGTAATTTAAATAAATGAACATGTAAACAAATCTTGTATTATGT
Associated Phenotype:
Not determined