RAI1: Difference between revisions

RAI1
Identifiers
Aliases	RAI1, SMCR, SMS, retinoic acid induced 1
External IDs	OMIM: 607642; MGI: 103291; HomoloGene: 7508; GeneCards: RAI1; OMA:RAI1 - orthologs
Gene location (Human)
Chr.	Chromosome 17 (human)
End	17,811,453 bp
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	60,199,197 bp
RNA expression pattern
	Top expressed in
	retinal pigment epithelium; ; nipple; ; palpebral conjunctiva; ; urethra; ; pylorus; ; tibia; ; Brodmann area 23; ; cardia; ; human penis; ; parietal lobe;
	Top expressed in
	lateral septal nucleus; ; habenula; ; anterior amygdaloid area; ; olfactory tubercle; ; ventromedial nucleus; ; subiculum; ; dorsomedial hypothalamic nucleus; ; Rostral migratory stream; ; lateral hypothalamus; ; mammillary body;
	More reference expression data
	n/a
Gene ontology
Molecular function	protein binding; metal ion binding; DNA-binding transcription factor activity;
Cellular component	cytoplasm; mitochondrion; nucleoplasm; nucleus;
Biological process	positive regulation of transcription, DNA-templated; skeletal system development; negative regulation of multicellular organism growth; regulation of transcription by RNA polymerase II; circadian regulation of gene expression; rhythmic process; positive regulation of transcription by RNA polymerase II;
	Sources:Amigo / QuickGO
Orthologs
	10743
	19377
	ENSG00000108557
	ENSMUSG00000062115
	Q7Z5J4
	Q61818
	NM_030665; NM_017574; NM_152256
	NM_001037764; NM_009021
	NP_109590
	NP_001032853; NP_033047
	Wikidata
View/Edit Human	View/Edit Mouse

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Latest revision as of 00:01, 19 March 2023

RAI1 is a transcription factor associated with Smith–Magenis syndrome when individuals have deletions of the gene and Potocki–Lupski syndrome when individuals have a duplication. It is known as retinoic acid induced 1.

This biochemistry article is a stub. You can help Wikipedia by expanding it.

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000108557 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000062115 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

@@ Line 1: / Line 1: @@
+{{Short description|Mammalian protein found in Homo sapiens}}
-{{protein
+{{about|the protein|the Italian television channel|Rai 1}}
-|Name=[[retinoic acid]] induced 1
+{{infobox gene}}
-|caption=
+'''RAI1''' is a [[transcription factor]] associated with [[Smith–Magenis syndrome]] when individuals have deletions of the gene and [[Potocki–Lupski syndrome]] when individuals have a duplication. It is known as ''retinoic acid induced 1''.
-|image=
-|width=
+==See also==
-|HGNCid=9834
+* [[Retinoic acid]]
-|Symbol=RAI1
-|AltSymbols=
+==External links==
-|EntrezGene=10743
+* [https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms  GeneReviews/NIH/NCBI/UW entry on Smith-Magenis Syndrome]
-|OMIM=607642
+* {{MeSH name|RAI1+protein,+human}}
-|RefSeq=NM_030665
-|UniProt=Q7Z5J4
-|PDB=
-|ECnumber=
-|Chromosome=17
-|Arm=p
-|Band=11.2
-|LocusSupplementaryData=
-}}
-'''RAI1''' is a [[transcription factor]] associated with [[Smith-Magenis syndrome]]. It is known as ''retinoic acid inducible 1''.
-==External Links==
-* [http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms  GeneReviews/NIH/NCBI/UW entry on Smith-Magenis Syndrome]
-* {{MeshName|RAI1+protein,+human}}
 {{biochem-stub}}