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

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Gene: INMT-FAM188B ENSG00000254959

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Description

INMT-FAM188B readthrough (NMD candidate) [Source:HGNC Symbol;Acc:41995]

Gene Synonyms

TEMT

Location

Chromosome 7: 30,791,753-30,931,696 forward strand.

GRCh37:CM000669.1

About this gene

This gene has 2 transcripts (splice variants) and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000458257.1	INMT-FAM188B-001	2877	141aa	ENSP00000456039.1	Nonsense mediated decay		F8WBC2	-	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,
ENST00000451002.2	INMT-FAM188B-002	975	122aa	ENSP00000456833.2	Nonsense mediated decay		-	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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