TCF4 (1 of 2)

Ensembl ID:
ENSDARG00000075546
Description:
transcription factor 4 [Source:HGNC Symbol;Acc:11634]
Human Orthologue:
TCF4
Human Description:
transcription factor 4 [Source:HGNC Symbol;Acc:11634]
Mouse Orthologue:
Tcf4
Mouse Description:
transcription factor 4 Gene [Source:MGI Symbol;Acc:MGI:98506]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa23834 Nonsense Mutation detected in F1 DNA During 2014

Mutation Details

Allele Name:
sa23834
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 2014.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098728 Nonsense 100 116 2 3
Genomic Location:
Chromosome 21 (position 1799683)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CATTGGCCGCCGCTCACCATGCAATGGGCGAGGCGTCCAATCCCATGGGA[C/T]AAATGTAAAGAGCCACACCCCCGTAAATGGTCAGAAGATTTCACTCTACA
Associated Phenotype:
Not determined

GWAS

This gene's human homologue has been identified in the following GWAS studies:

(GWAS data comes from http://www.genome.gov/gwastudies/.)

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* quick link - http://q.sanger.ac.uk/3t5vxaa8