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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: NUTM2A ENSG00000184923

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Description

NUT family member 2A [Source:HGNC Symbol;Acc:23438]

Gene Synonyms

FAM22A, KIAA2020

Location

Chromosome 10: 88,985,205-88,996,665 forward strand.

GRCh37:CM000672.1

About this gene

This gene has 2 transcripts (splice variants), 6 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000381707.2	NUTM2A-001	3290	878aa	ENSP00000371126.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS44452	Q8IVF1	NM_001099338.1	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000381689.4	NUTM2A-002	3974	629aa	ENSP00000371107.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding		Q8IVF1	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Summary

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