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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Paralogues
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: TCTN2 ENSG00000168778

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Description

tectonic family member 2 [Source:HGNC Symbol;Acc:25774]

Gene Synonyms

C12orf38, FLJ12975, MKS8, TECT2

Location

Chromosome 12: 124,155,660-124,192,948 forward strand.

GRCh37:CM000674.1

About this gene

This gene has 4 transcripts (splice variants) and is associated with 5 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000303372.5	TCTN2-001	2910	697aa	ENSP00000304941.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS9253	Q96GX1	NM_024809.4	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,
ENST00000426174.2	TCTN2-002	2513	696aa	ENSP00000395171.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS45007	Q96GX1	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000541523.1	TCTN2-003	556	60aa	ENSP00000437644.1	Nonsense mediated decay		F5H6G0	-	-
ENST00000543998.1	TCTN2-004	2918	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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