Human Gene GNAI3 (ENST00000369851.7) Description and Page Index
  Description: Homo sapiens G protein subunit alpha i3 (GNAI3), mRNA. (from RefSeq NM_006496)
Gencode Transcript: ENST00000369851.7
Gencode Gene: ENSG00000065135.12
Transcript (Including UTRs)
   Position: hg38 chr1:109,548,615-109,600,195 Size: 51,581 Total Exon Count: 9 Strand: +
Coding Region
   Position: hg38 chr1:109,548,721-109,592,233 Size: 43,513 Coding Exon Count: 8 

Page IndexSequence and LinksUniProtKB CommentsProtein StructureOther NamesMethods
Data last updated at UCSC: 2021-06-20 19:51:40

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr1:109,548,615-109,600,195)mRNA (may differ from genome)Protein (354 aa)
Gene SorterGenome BrowserOther Species FASTATable SchemaExonPrimerGeneCards
HGNCMGIPubMedUniProtKB

-  Comments and Description Text from UniProtKB
  ID: GNAI3_HUMAN
DESCRIPTION: RecName: Full=Guanine nucleotide-binding protein G(k) subunit alpha; AltName: Full=G(i) alpha-3;
FUNCTION: Guanine nucleotide-binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling systems. G(k) is the stimulatory G protein of receptor- regulated K(+) channels. The active GTP-bound form prevents the association of RGS14 with centrosomes and is required for the translocation of RGS14 from the cytoplasm to the plasma membrane. May play a role in cell division.
SUBUNIT: G proteins are composed of 3 units; alpha, beta and gamma. The alpha chain contains the guanine nucleotide binding site. Interacts with GPSM1. Interacts (via active GTP- or inactive GDP-bound form) with RGS14 (By similarity).
SUBCELLULAR LOCATION: Cytoplasm. Cell membrane. Cytoplasm, cytoskeleton, centrosome. Note=Localizes in the centrosomes of interphase and mitotic cells. Detected at the cleavage furrow and/or the midbody.
DISEASE: Defects in GNAI3 are the cause of auriculocondylar syndrome 1 (ARCND1) [MIM:602483]. ARCND1 is an autosomal dominant craniofacial malformation syndrome characterized by variable mandibular anomalies, including mild to severe micrognathia, temporomandibular joint ankylosis, cleft palate, and a characteristic ear malformation that consists of separation of the lobule from the external ear, giving the appearance of a question mark (question-mark ear). Other frequently described features include prominent cheeks, cupped and posteriorly rotated ears, preauricular tags, and microstomia.
SIMILARITY: Belongs to the G-alpha family. G(i/o/t/z) subfamily.

+  Protein Domain and Structure Information
  Press "+" in the title bar above to open this section.

-  Other Names for This Gene
  UCSC ID: ENST00000369851.7
Representative RNA: NM_006496
Protein: P08754 (aka GNAI3_HUMAN or GBAK_HUMAN)

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.