ZMP
cfl1l
Ensembl ID:
ZFIN ID:
Description:
non-muscle cofilin 1 [Source:RefSeq peptide;Acc:NP_998804]
Human Orthologues:
CFL1, CFL2, DSTN
Human Descriptions:
cofilin 1 (non-muscle) [Source:HGNC Symbol;Acc:1874]
cofilin 2 (muscle) [Source:HGNC Symbol;Acc:1875]
destrin (actin depolymerizing factor) [Source:HGNC Symbol;Acc:15750]
cofilin 2 (muscle) [Source:HGNC Symbol;Acc:1875]
destrin (actin depolymerizing factor) [Source:HGNC Symbol;Acc:15750]
Mouse Orthologues:
Cfl1, Cfl2, Dstn, Gm6180
Mouse Descriptions:
cofilin 1, non-muscle Gene [Source:MGI Symbol;Acc:MGI:101757]
cofilin 2, muscle Gene [Source:MGI Symbol;Acc:MGI:101763]
destrin Gene [Source:MGI Symbol;Acc:MGI:1929270]
predicted pseudogene 6180 Pseudogene [Source:MGI Symbol;Acc:MGI:3643972]
cofilin 2, muscle Gene [Source:MGI Symbol;Acc:MGI:101763]
destrin Gene [Source:MGI Symbol;Acc:MGI:1929270]
predicted pseudogene 6180 Pseudogene [Source:MGI Symbol;Acc:MGI:3643972]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa5863 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa5863
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026464 | Essential Splice Site | 1 | 163 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 33831518)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 33497498 |
GRCz11 | 13 | 33607043 |
KASP Assay ID:
554-3944.1 (used for ordering genotyping assays)
KASP Sequence:
GGGCAACGACACACTNNTCTCTCTCTTCTCCAAACAAGCGACAGACATGG[T/A]AAGTGCTCAGATTTTGGTGTACGTTTTGTGGACTGTACTRTAGTGTCCAA
Long Flanking Sequence:
AATGAAGTTGCTGGTCTGTCGCTAAACATGAAACCACGTCACGCTCCGTGCATTTTTTACACCTGGATCCTCCCATCCGCGCAAATTTAGTATTTGAGCTCCTCTCACCAAATACGGGTTTTTGTCAGGCTTTCTATGCGTTTCTGTCTTCCTTATAAGGTCGTTTTGTTCAGTCTCCGCCTCCAAATCTGCGTCTGACTCACCTGAGCCATTTCACGTGCCATAAGCGCATAATTTTTATAACACCTTTTTTTATCACAAGCACAAAATATAAATAATTTTGCGGCAACGGGATATATTCCTACACAACCATCCAGTATTTAAAGTCGTTTGCAGTCGCGGACAGGCACAGCAGGTGGAAAGTCAGGTCGTTCAGGACTGATCTGTTTTGAGGAGGAGGAGGGAGTGTTCACATCCGCGCGCTGCTCGGAGTCGCTTTCTTGCAGTTCAGGGCAACGACACACTTCTCTCTCTCTTCTCCAAACAAGCGACAGACATGG[T/A]AAGTGCTCAGATTTTGGTGTACGTTTTGTGGACTGTACTATAGTGTCCAAATATGCTAATCAAGTGAAGGTAATTTGCATTAAAACGGTTTAGCGCCGTGCAGAGTAGCGTATGTTAAAAAAGCTATTACGCCAATTCATCCATGAGAGGCTTGTGGCTTCCTGTTCATTGGTAAACTTCTTTTATTTATTTAAATCCCTAATACTTTATATAAAAGGTTAAAACTAGCTTGTCAGTTTAAAATATAAAGCAATTAAAGTAATAAAAGCTCATTGACTTTGGTGAGACTTGGTGGAAAAGCCATATTTTAAGGTTTCTTATTTGTGTAATACTTTTCTAGATAATTGTTTGGACAGGACAGAATGTGTTGAGCCACACCTTACATCAGACATGTTCTCATGTCAAAAGCTCTGAGTAATGCTAATGAACTGCTGGTAGCTATAGTGTGTTAATACTTTTGAACTAGAGTAGCTCATTGCTTGTGTCAGAGTTGTATTCCA
Associated Phenotype:
Not determined