SCNN1A (sodium channel, nonvoltage-gated 1 alpha)

Identity

Other names	ENaCa
	ENaCalpha
	FLJ21883
	SCNEA
	SCNN1
HGNC	SCNN1A
Location	12p13
Location_base_pair	Starts at 6326274 and ends at 6354976 bp from pter ( according to hg18-March_2006).
Note	Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

External links

	Nomenclature
HGNC	SCNN1A   10599
Entrez_Gene	SCNN1A  6337  sodium channel, nonvoltage-gated 1 alpha
	Cards
GeneCards	SCNN1A
Ensembl	SCNN1A [Search_View]   ENSG00000111319 [Gene_View]
Genatlas	SCNN1A
GeneLynx	SCNN1A
eGenome	SCNN1A
euGene	6337
	Genomic and cartography
GoldenPath	SCNN1A  -  12p13   chr12:6326274-6354976 -  12p13.31   [Description]    (hg18-March_2006)
Ensembl	SCNN1A - 12p13.31 [CytoView]
NCBI	Mapview
OMIM	Disease map [OMIM]
HomoloGene	SCNN1A
	Gene and transcription
Genbank	AK025536 [ ENTREZ ]
Genbank	AK172792 [ ENTREZ ]
Genbank	AK304379 [ ENTREZ ]
Genbank	AY365119 [ ENTREZ ]
Genbank	BC006526 [ ENTREZ ]
RefSeq	NM_001038 [ SRS ]    NM_001038 [ ENTREZ ]
RefSeq	AC_000055 [ SRS ]    AC_000055 [ ENTREZ ]
RefSeq	AC_000144 [ SRS ]    AC_000144 [ ENTREZ ]
RefSeq	NC_000012 [ SRS ]    NC_000012 [ ENTREZ ]
RefSeq	NG_007506 [ SRS ]    NG_007506 [ ENTREZ ]
RefSeq	NT_009759 [ SRS ]    NT_009759 [ ENTREZ ]
RefSeq	NW_001838050 [ SRS ]    NW_001838050 [ ENTREZ ]
RefSeq	NW_925295 [ SRS ]    NW_925295 [ ENTREZ ]
AceView	SCNN1A AceView - NCBI
Unigene	Hs.591047 [ SRS ]    Hs.591047 [ NCBI ]     HS591047 [ spliceNest ]
Fast-db	955 (alternative variants)
	Protein : pattern, domain, 3D structure
SwissProt	P37088 [ SRS]    P37088 [ EXPASY ]     P37088 [ INTERPRO ]     P37088 [ UNIPROT ]
Prosite	PS01206 ASC [ SRS ]    PS01206 ASC [ Expasy ]
Interpro	IPR004724 EnaC [ SRS ]    IPR004724 EnaC [ EBI ]
Interpro	IPR001873 Na+channel_ASC [ SRS ]    IPR001873 Na+channel_ASC [ EBI ]
CluSTr	P37088
Pfam	PF00858 ASC [ SRS ]    PF00858 ASC [ Sanger ]    pfam00858 [ NCBI-CDD ]
Blocks	P37088
HPRD	02575
	Protein Interaction databases
DIP	P37088
IntAct	P37088
	Polymorphism : SNP, mutations, diseases
OMIM	264350;600228    [ map ]
GENECLINICS	264350;600228
SNP	SCNN1A [dbSNP-NCBI]
SNP	NM_001038 [SNP-NCI]
SNP	SCNN1A [GeneSNPs - Utah]  SCNN1A] [HGBASE - SRS]
HAPMAP	SCNN1A [HAPMAP]
HGMD	SCNN1A
	General knowledge
Family Browser	SCNN1A [UCSC Family Browser]
SOURCE	NM_001038
SMD	Hs.591047
SAGE	Hs.591047
GO	ion channel activity [Amigo]  ion channel activity
GO	protein binding [Amigo]  protein binding
GO	ion transport [Amigo]  ion transport
GO	sodium ion transport [Amigo]  sodium ion transport
GO	excretion [Amigo]  excretion
GO	amiloride-sensitive sodium channel activity [Amigo]  amiloride-sensitive sodium channel activity
GO	membrane [Amigo]  membrane
GO	integral to membrane [Amigo]  integral to membrane
GO	apical plasma membrane [Amigo]  apical plasma membrane
GO	sodium ion binding [Amigo]  sodium ion binding
GO	response to stimulus [Amigo]  response to stimulus
GO	sensory perception of taste [Amigo]  sensory perception of taste
KEGG	Taste transduction
PubGene	SCNN1A
TreeFam	SCNN1A
CTD	6337 [Comparative ToxicoGenomics Database]
	Other databases
	Probes
Probe	SCNN1A Related clones (RZPD - Berlin)
	PubMed
PubMed	56 Pubmed reference(s) in Entrez

Genes in title	automatic search in PubMed
REVIEW articles	automatic search in PubMed
Last year publications	automatic search in PubMed

Search in all EBI   NCBI

Contributor(s)

Written	09-2002	Dessen P, Le Minor S
Updated	03-2008	Dessen P

© Atlas of Genetics and Cytogenetics in Oncology and Haematology

indexed on : Tue Oct 14 20:53:56 2008