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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- 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: TCERG1L ENSG00000176769

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Description

transcription elongation regulator 1-like [Source:HGNC Symbol;Acc:23533]

Gene Synonyms

FLJ38950

Location

Chromosome 10: 132,890,654-133,109,984 reverse strand.

GRCh37:CM000672.1

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
ENST00000368642.4	TCERG1L-002	2618	586aa	ENSP00000357631.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS7662	Q5VWI1	NM_174937.3	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,
ENST00000483040.1	TCERG1L-001	4394	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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