full name
Smad nuclear interacting protein 1

synonyms
PMRED, SNIP1, ENSG00000163877

HGNC
HGNC:30587

Entrez Gene
Gene:79753

ENSEMBL
ENSG00000163877

location
chr: 1
start: 38000050
stop: 38019945
strand: -

OMIM
OMIM:608241: SNIP1 (Autosomal recessive inheritance)
OMIM:614501: Psychomotor retardation, epilepsy, and craniofacial dysmorphism

transcripts
NM_024700.3

pathways
Regulation of nuclear SMAD2/3 signaling [NCBI:137963] [Pathway Interaction Database:smad2_3nuclearpathway] [PUBMED:15009097] [PUBMED:11114293] [PUBMED:10973944] [PUBMED:10995736] [PUBMED:10022869] [PUBMED:15363409] [PUBMED:11790301] [PUBMED:11836524] [PUBMED:14993291] [PUBMED:12904571] [PUBMED:11058129] [PUBMED:9707553] [PUBMED:9702197] [PUBMED:12718878] [PUBMED:9722503] [PUBMED:11013220] [PUBMED:14729983] [PUBMED:10878024] [PUBMED:10887155] [PUBMED:9679060] [PUBMED:11331591] [PUBMED:9606191] [PUBMED:12167862] [PUBMED:12374795] [PUBMED:10037600] [PUBMED:12150994] [PUBMED:11555647] [PUBMED:12631740] [PUBMED:10748032] [PUBMED:10518526] [PUBMED:15688032] [PUBMED:14691252] [PUBMED:10575014] [PUBMED:15241418] [PUBMED:10485843] [PUBMED:14671321] [PUBMED:10964912] [PUBMED:11283614] [PUBMED:11711431] [PUBMED:11427533] [PUBMED:11571228] [PUBMED:11707452] [PUBMED:10531362] [PUBMED:12551947] [PUBMED:15044954] [PUBMED:17074756] [PUBMED:11801598] [PUBMED:10085140] [PUBMED:9618481] [PUBMED:10843994] [PUBMED:15084259] [PUBMED:12226080] [PUBMED:10531062] [PUBMED:9732876] [PUBMED:10652350] [PUBMED:10557285] [PUBMED:11927558] [PUBMED:16959612] [PUBMED:10199400] [PUBMED:9702198] [PUBMED:10722728] [PUBMED:17478422] [PUBMED:9679056]
TGF-beta Receptor Signaling Pathway [NCBI:198774] [WikiPathways:WP366]