MAP4K3-DT MAP4K3 divergent transcript [Homo sapiens (human)] - Gene

Summary

Official Symbol: MAP4K3-DTprovided by HGNC
Official Full Name: MAP4K3 divergent transcriptprovided by HGNC
Primary source: HGNC:HGNC:54056
See related: Ensembl:ENSG00000231312 AllianceGenome:HGNC:54056
Gene type: ncRNA
RefSeq status: VALIDATED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression: Ubiquitous expression in brain (RPKM 2.0), kidney (RPKM 1.5) and 24 other tissues See more
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Genomic context

Location:: 2p22.1

Exon count:: 6

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	2	NC_000002.12 (39437416..39601344)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	2	NC_060926.1 (39446299..39610354)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	2	NC_000002.11 (39664557..39828484)

Chromosome 2 - NC_000002.12 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Submit: New GeneRIF Correction

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

EBI GWAS Catalog

Description
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. EBI GWAS Catalog EBI GWAS CatalogPubMed

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Markers

G20271 (e-PCR)
- UniSTS:8482

A005C22 (e-PCR)
- UniSTS:8483

STS-AA037634 (e-PCR)
- UniSTS:29017

D11S3114 (e-PCR)
- UniSTS:152207

RH35860 (e-PCR)
- UniSTS:36018

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.