Gene: TCF25

Alternate names for this Gene: FKSG26|Hulp1|NULP1|PRO2620|hKIAA1049

Gene Summary: TCF25 is a member of the basic helix-loop-helix (bHLH) family of transcription factors that are important in embryonic development (Steen and Lindholm, 2008 [PubMed 18068114]).[supplied by OMIM, Sep 2008]. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: SRR3476690.1091791.1, SRR1660809.32437.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1966682 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000263346.13/ ENSP00000263346.8 RefSeq Select criteria :: based on conservation, expression ##RefSeq-Attributes-END##

Gene is located in Chromosome: 16

Location in Chromosome : 16q24.3

Description of this Gene: transcription factor 25

Type of Gene: protein-coding

Gene: LOC112268179

Alternate names for this Gene:

Gene Summary:

Gene is located in Chromosome:

Location in Chromosome :

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rs182948919 in TCF25;LOC112268179 gene and Hair Color PMID 30531825 2018 Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability.

rs9939914 in TCF25;LOC112268179 gene and Reticulocyte count (procedure) PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.