ZMP
WSCD1 (1 of 3)
Ensembl ID:
Description:
WSC domain containing 1 [Source:HGNC Symbol;Acc:29060]
Human Orthologue:
WSCD1
Human Description:
WSC domain containing 1 [Source:HGNC Symbol;Acc:29060]
Mouse Orthologue:
Wscd1
Mouse Description:
WSC domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:2448493]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32116 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22980 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32116
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106061 | Essential Splice Site | 259 | 375 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 3057634)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 29965607 |
GRCz11 | 17 | 3284851 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGCTGGGCATCTGGGCTACGCTTCTGATCAGCACTGGAAGGGCAAAGG[T/C]ATTATGGGCATCTCTTTGTTCAGTTGAGCTCCGCAGGCACTGGGACTTGG
Long Flanking Sequence:
CTTTGATAATGCACATTTGGGCACAGCTGACCTTCTGTTCTCTATCAAATGCCAAACTTTATTGAGCAATTCTTTTTCTTTTTTCTCTCTACCATTAAAGAACTCGACCTGCTTGAAAGTCACTGTGCCTTTTCAAATCCATCACAGAAACCTGACGCACATTGGCTGGAGGGGGTCTGCGGTGCCCATGCCTGGATTAGAACAGCCTTTTTCTTATGGCGTTTTTGGAGTGTATGTGTTTGGATGGAGAGGCATGCAGTTGGCTGTATTCTAATCCGCTTCTCCTCCTACTGTGCAGGCTTCAAGGGTGAGAAAGATTACTGGAAGAGCGGACGAACCATCTGCGTGAAGACACATGAGAGCGGCCAGCGGGATATAGAGATGTATGACTCAGCAATACTGTTGATAAGAAACCCCTACCGATCGCTCATGGCCGAGTTCAACCGCAAGTGTGCTGGGCATCTGGGCTACGCTTCTGATCAGCACTGGAAGGGCAAAGG[T/C]ATTATGGGCATCTCTTTGTTCAGTTGAGCTCCGCAGGCACTGGGACTTGGATATATCATAATGAGACACTATTTCTGTCAGGGTGATTTTTGGTAATATTATGTACAGTTGAAGTCAAAACTATTAGCCCTTCTGTGAATTTCTTTTTCAAAGTTTTCCCAAATTATGCTTTATGGAGCAATGAATTTTTCACAGTATTTCCTATAATATGTTTTTTCTTCTGGAGAAAGTTGTATTTAATGTTTTAATGTTTTTTTTTTTTCAAAAACATAAGGGTCAAAATTATTCGCCCACTTAATTTATACTTTTTTTCCATTGTCAACTAAACAAACCATCCTTATACCATGACTTGCTTAATTACCCTAACTTGCTTAGTTAACCTAATTAACCTAGTCAAGCCTTTAAATGGTATTTTAAGCTGAAACCTCGTATCTTGAAAAATATCTAAAATAGATAAAAGAAAGATAAAAGGCAAAGATTAAAGAAATCAGTTAGAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22980
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106061 | Nonsense | 270 | 375 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 3056078)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 29964051 |
GRCz11 | 17 | 3283295 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTCTTCTTTCCAGAGTGGCCAGAGTTTGTGGGTAGTTATGCCTCCTG[G/A]TGGGCCTCTCATGTGCTGGATTGGCTGCGCTTTGGAAAGCAGCTTCTGGT
Long Flanking Sequence:
AGCCGAAATAAAACAAATAAGTGTGTGTGAATGTGTGTGTGTGTGGATGTTTCCCAGAGACGGGTTGCAGCTGGAAGTGGATCCGCTGCGTAAAAACTTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGACCCCGGATTAATAAAGGGACTAAGCCGACGAGAAAATGAATGAATGAAATGAAAATTTAATTGGTTCTCTTGGTTTTTAAATGACCTTTTGAACAATATAAAGTTAATGTATTTATTATTATTCAATATTAATATAAAACACACAATAACACATTTATATTAGTTAATACGTTCAAATATAAATATTTCTTACCAACCCAGAAACAGCATTTTCCATAATTCTAACTTAAAACAATATTCAGTATTTGACCATTACTTAGCCAGTAGTACTGTACTACAAGACAAATCCTTAATGTCATGTTTTTCACTGTCCTGCTTTCTCTTCTTTCCAGAGTGGCCAGAGTTTGTGGGTAGTTATGCCTCCTG[G/A]TGGGCCTCTCATGTGCTGGATTGGCTGCGCTTTGGAAAGCAGCTTCTGGTGGTGCATTATGAGGATCTGCAGCAATCGCTGGTGCCAACATTACGATCCATCACCTCTTTCCTCAACACCAGCGTCAGTGAAGAGCATCTCCTCTGTGCCGAATGCAACAAGGATGGTCACTTCAAGCGCTCAGGTGCGCGACGACCCGCCTTCGACCCCTTCACCGCAGATATGAAGCGGCTGATAGATGGCTATATCAACACTGTGGACCAGGCTCTCAGAGCCAGCAACCATTCTGGATTACCACAAGAATACCTTCCTAGATGATAAGTCCTCAAGTAGAGCATTCATTGATAAACTCACACACTGAGGCTGAAAATAACAGCATGCGGTGCTGTTCTCCACTGGTGCGCTTTGAGACCGTCATGTTTTAACGGCGGTCTGTAGATCAGAGACTGTTAATTATAAAAATAGAGCCTGACAAAAACATCTCTAGTCAGAGGCTAAAT
Associated Phenotype:
Not determined