CTNNA3 (Entrez ID: 29119)

Entrez Gene ID	29119
Official Gene Symbol	CTNNA3 (GeneCards)
Full name	catenin alpha 3
Location	10q21.3
Other ids	Vega : OTTHUMG00000018334 MIM : 607667 HGNC : HGNC:2511 Ensembl : ENSG00000183230
Other names	VR22, ARVD13
Summary	This gene encodes a protein that belongs to the vinculin/alpha-catenin family. The encoded protein plays a role in cell-cell adhesion in muscle cells. Mutations in this gene are associated with arrhythmogenic right ventricular dysplasia, familial 13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]

Variants

Found 26 variants in this database.

Variant ID	Entrez Gene ID	Gene	Chromsome	Start	End	Disease	Method
1242	29119	CTNNA3	10	69366755	69366755	Autism Spectrum Disorders	NextSeq500 v2
13844	29119	CTNNA3	10	68370081	68370081	Asymptomatic	NextSeq500 v2 HiSeq X Ten
13857	29119	CTNNA3	10	67787472	67787472	Asymptomatic	NextSeq500 v2 HiSeq X Ten
13896	29119	CTNNA3	10	67974126	67974126	Asymptomatic	NextSeq500 v2 HiSeq X Ten
13941	29119	CTNNA3	10	69246729	69246729	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
13973	29119	CTNNA3	10	68853113	68853113	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
14034	29119	CTNNA3	10	68980229	68980229	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
14271	29119	CTNNA3	10	67721202	67721202	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
14374	29119	CTNNA3	10	68952483	68952483	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
14450	29119	CTNNA3	10	69498476	69498476	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
14469	29119	CTNNA3	10	69008524	69008524	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
14540	29119	CTNNA3	10	68525609	68525609	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
14557	29119	CTNNA3	10	68280473	68280473	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
14558	29119	CTNNA3	10	68954018	68954018	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
14688	29119	CTNNA3	10	68292849	68292849	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000
14742	29119	CTNNA3	10	68356406	68356406	Cockayne syndrome	NextSeq500 v2 HiSeq X Ten HiSeq 2000
14809	29119	CTNNA3	10	68962443	68962443	Cockayne syndrome	NextSeq500 v2 HiSeq X Ten HiSeq 2000
14851	29119	CTNNA3	10	68452444	68452444	Xeroderma Pigmentosum	NextSeq500 v2 HiSeq X Ten HiSeq 2000
14852	29119	CTNNA3	10	68452445	68452445	Xeroderma Pigmentosum	NextSeq500 v2 HiSeq X Ten HiSeq 2000
14951	29119	CTNNA3	10	68781918	68781918	Xeroderma Pigmentosum	NextSeq500 v2 HiSeq X Ten HiSeq 2000
23499	29119	CTNNA3	10	69425741	69425741	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000 Single cell Sequencing Cell cloning
26973	29119	CTNNA3	10	68293980	68293980	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000 Single cell Sequencing Cell cloning
27057	29119	CTNNA3	10	69527473	69527473	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000 Single cell Sequencing Cell cloning
29832	29119	CTNNA3	10	69366755	69366755	Autism Spectrum Disorders	NextSeq500 v2 HiSeq X Ten HiSeq 2000 Single cell Sequencing Cell cloning NextSeq500
34480	29119	CTNNA3	10	68752418	68752418	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000 Single cell Sequencing Cell cloning NextSeq500 Whole Genome Sequencing Ion Torrent PGM Sequencing
34481	29119	CTNNA3	10	69069626	69069626	Asymptomatic	NextSeq500 v2 HiSeq X Ten HiSeq 2000 Single cell Sequencing Cell cloning NextSeq500 Whole Genome Sequencing Ion Torrent PGM Sequencing