ZMP
si:ch211-195c22.1
Ensembl ID:
ZFIN IDs:
Description:
FCH domain only protein 2 [Source:UniProtKB/Swiss-Prot;Acc:Q502I9]
Human Orthologue:
FCHO2
Human Description:
FCH domain only 2 [Source:HGNC Symbol;Acc:25180]
Mouse Orthologue:
Fcho2
Mouse Description:
FCH domain only 2 Gene [Source:MGI Symbol;Acc:MGI:3505790]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33648 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33648
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 |
---|---|---|---|---|---|
ENSDART00000051271 | Nonsense | 200 | 848 | 6 | 27 |
ENSDART00000139673 | None | None | 569 | None | 18 |
ENSDART00000141218 | None | None | 299 | None | 8 |
The following transcripts of ENSDARG00000035389 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 36796161)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 34578110 |
GRCz11 | 5 | 35178263 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATACGCCACTGCCAAGACTGAATTTGAGCAAAGAATGACAGAAACCGCA[C/T]AAGTAAGATGTGGTGGAGTGTGTTTGTTGGGGTCTGCGTTATGGGTGCAC
Long Flanking Sequence:
TTACTGAATTTTTTTGTGCCTCTCTTGCTTATAGACAAAGGAGGAAGTTGCGTCAACTCTAGAGGCAGTGCATAACATTCAGAGCGTCTCACAGGCTTTGCTAAAAAGCAAAGAAAACTACATCAACAAGACACTCGAGCAAGAGCGCATGCGCAAAGAGGGAGCCAAACAGGGAGACCTGGACAAGGTACAAACACACACGCACACACACTCTTACATCAACTACTGAGCAATACTGGAAAGTTTGCTGGATCAGTTCCTGTAGGTAACTCCCAACTTAAGCTCCTGGAAGGATTATTTTCTGTGCTAAATGCTAGAGGCAGGAAATTTTAAAGCGCATCCTCAAAAACAAACGTGTCTAATCTGGCCTCTGTCTGTTTTGTGTTCTTTGTTTGTAGGCTGGATTGAAGGTCAAGAAAGCCACTGAGTCTTATAAGTCATATGTGGAGAAATACGCCACTGCCAAGACTGAATTTGAGCAAAGAATGACAGAAACCGCA[C/T]AAGTAAGATGTGGTGGAGTGTGTTTGTTGGGGTCTGCGTTATGGGTGCACTTTTTCGAGGAGAATTTAAAAATTTGATGATTTTATTTAAAAGCTATTGTGATTCTTGGTCTGGATTAACAATATTAAAACCAGACACATTTACTTGTATACATCCTATAGCTGTGTCCAAATAATGTATTTTTTTAATTAGTATTATACCAGACCATACATTGTAGTATATTATACAGAATTAATAAGGATACAGACGGTCTAAGTTTTTTTTTGTCACTATCCACTCAAAATAAAATAAATAAAGATAAAATTACATTTATTAACTAGTGTGTGCATGCATGTAAATCAATATAATAAAGTAAAACAGAATTTTTTCAACTCTGACTATACCATATCTTCTGGATAATAAGTCATTATTAGTCACATTCTAGGTTGCACTTTGCCTTAATTGTTTTGTTGCAAGAAATAACACACTGGTGTAGAAGTCACATTTAAGGATTAAAATAA
Associated Phenotype:
Not determined