Ecm1 Gene Search Result

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4 records found for search term Ecm1

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RGD ID	Symbol	Name	Description	Chr	Start	Stop	Species	Annotations	Match	Type
1605731	ECM1	extracellular matrix protein 1	This gene encodes a soluble protein that is involved in endochondral bone formation, angiogenesis, and tumor biology. It also interacts with a variety of extracellular and structural proteins, contributing to the maintenance of skin integrity and homeostasis. Mutations in this gene are associated wi ... (more) th lipoid proteinosis disorder (also known as hyalinosis cutis et mucosae or Urbach-Wiethe disease) that is characterized by generalized thickening of skin, mucosae and certain viscera. Alternatively spliced transcript variants encoding distinct isoforms have been described for this gene. [provided by RefSeq, Feb 2011]	1	150508109	150513789	Human	252	symbol , COSMIC , Human Proteome Map	gene, protein-coding, REVIEWED [RefSeq]
6480815	FALEC	focally amplified lncRNA regulator of ECM1	INTERACTS WITH 2-hydroxypropanoic acid; lipopolysaccharide; propofol	1	150515752	150536788	Human	5	name	gene, ncrna, VALIDATED [RefSeq]
8548277	ECM1P1	extracellular matrix protein 1 pseudogene 1		9	4768630	4769895	Human		symbol , COSMIC , Human Proteome Map	gene, pseudo, INFERRED [RefSeq]
10400028	ECM1P2	extracellular matrix protein 1 pseudogene 2		4	12639086	12641009	Human		symbol , COSMIC , Human Proteome Map	gene, pseudo, INFERRED [RefSeq]