ZMP
FCHSD2 (6 of 6)
Ensembl ID:
Description:
FCH and double SH3 domains 2 [Source:HGNC Symbol;Acc:29114]
Human Orthologue:
FCHSD2
Human Description:
FCH and double SH3 domains 2 [Source:HGNC Symbol;Acc:29114]
Mouse Orthologue:
Fchsd2
Mouse Description:
FCH and double SH3 domains 2 Gene [Source:MGI Symbol;Acc:MGI:2448475]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34955 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34955
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000130633 | Nonsense | 307 | 743 | 10 | 24 |
Genomic Location (Zv9):
Chromosome 10 (position 38093476)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 36816414 |
| GRCz11 | 10 | 36760172 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTATTCAGGACAACGCTGTGTTTCAAAAAGCCGCCCCCTTTCAGTAT[C/T]AGCCCGGTGAAAATGATTCGGTAGGTGTCTATTACATATTTTCATATATT
Long Flanking Sequence:
TACGGTACTCAGGTTTAATGTCTCCAGTCCAGCATCAAGTTACACACACACACGCACGTACAGTGATCTGTATAGGGACTTCCCATAGACTTTTTATACTGTACAAACTGTATGTTCTATCCACCAACTCCAACCCTGCCACTAAAACCAAAGAAAAAATCTGCATTCTGCCTTATTTATGATCTGTTTTCCTCATGGAGACCAAAACAATGTGCCCACTAGGTCAAAACGTTTTGTTATTGCCATACCTTTGGTCTCCACCATGTAAGCAATACCAGATGCACAGACACACACGCACAAACACATATTCTGTTCATGAATTTCCTACTCTGGGGATCTGTTGTTGTTTTACGGAGGATAATGTATTGGCTGTGCTACTGTTCTAGTCATCGTCACATTAATAGTTTGCATTTTTGTGTTTGTAGGTGACACAGGAGACACACCAACAGATCTTTATTCAGGACAACGCTGTGTTTCAAAAAGCCGCCCCCTTTCAGTAT[C/T]AGCCCGGTGAAAATGATTCGGTAGGTGTCTATTACATATTTTCATATATTTTAACATTACTAATAAACAATCATATGAGAAAAAAAATGCTAAACTTCTTTCCTCCATCCACCAACATGATTTTACCAGACATGTTTGACATTCATTGTGGGTTAAAAGTGGCTTAAATGAAAGTTCACCACATAATTTGAAGTTTGTTAAATGCAGCTTTGGGGAAAGTTACTTTAGAAAATAATGCATTACAATATTGAGTCACTCTCCAAAAAAGTAACTAGTTGCATTACTTAGTTACTTTTTATGGTAAGTAATGCATTACGTTACTTTTGCATTACTTTTTATTACCTGGCTGAGGCTTGATCTCTTTCAGAGCTTGTTATTTTTTTTGCTTCTTTCTTCTTGTTGCATTTAGCACTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA
Associated Phenotype:
Not determined