celf4

Ensembl ID:
ENSDARG00000070045
ZFIN ID:
ZDB-GENE-040718-300
Description:
CUGBP Elav-like family member 4 [Source:UniProtKB/Swiss-Prot;Acc:Q6DGV1]
Human Orthologue:
CELF4
Human Description:
CUGBP, Elav-like family member 4 [Source:HGNC Symbol;Acc:14015]
Mouse Orthologue:
Celf4
Mouse Description:
CUGBP, Elav-like family member 4 Gene [Source:MGI Symbol;Acc:MGI:1932407]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa37252 Essential Splice Site Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa37252
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
G > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000081510 Essential Splice Site 59 404 2 11
ENSDART00000131538 Essential Splice Site 59 404 2 12
Genomic Location (Zv9):
Chromosome 21 (position 10534356)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 12017719
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CAGCATTGAGGAGTGCACCATCCTCAGAGGACCTGACGGAAACAGCAAAG[G/A]TTTCACTGCATTCACTCTCACTTTATACACTCAGTGGAATGAACACTGAT
Associated Phenotype:
Not determined

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