RIT2 - Ras like without CAAX 2 Gene

Homo sapiens

Also known as RIN; RIBA; ROC2

Gene ID: 6014 | Gene type: protein coding

About RIT2

Cytogenetic location: 18q12.3 Genomic coordinates (GRCh38): 18:42,743,227-43,115,685 (from NCBI)

This gene has 5 transcripts (splice variants), 102 orthologues and 35 paralogues. Biased expression in brain (RPKM 5.4) and adrenal (RPKM 0.9).

RIN belongs to the Ras (HRAS; MIM 190020) superfamily of small GTPases (Shao et al., 1999 [PubMed 10545207]).[supplied by OMIM, Mar 2008]

mRNA	Protein	Name
NM_001272077.2	NP_001259006.1	GTP-binding protein Rit2 isoform 2
NM_002930.4	NP_002921.1	GTP-binding protein Rit2 isoform 1

Ras

Protein Preferred Names

Protein Names

GTP-binding protein Rit2

GTP-binding protein Roc2

Diseases

Alias

Amyotrophic Lateral Sclerosis, Juvenile, With Dementia

Juvenile Amyotrophic Lateral Sclerosis With Dementia

Als-Dementia Complex

Immunodeficiency 18

IMD18	Cd3-Epsilon Deficiency
Immunodeficiency 18, Scid Variant	Cd3epsilon Deficiency
Immunodeficiency 18, Severe Combined Immunodeficiency Variant	Immunodeficiency, Type 18

Ehrlichiosis

Human Ehrlichiosis	He
Hey

Balo Concentric Sclerosis

Balo'S Concentric Sclerosis	Balo Disease
Diffuse Cerebral Sclerosis Of Schilder	Tumefactive Multiple Sclerosis
Concentric Demyelination	Balo'S Disease
Baló Concentric Sclerosis	Encephalitis Periaxialis Concentrica
Marburg Variant

Autism Spectrum Disorder

Asd	Autism Spectrum Disorders
Autistic Continuum	Pervasive Developmental Disorder
Pervasive Development Disorder	Autistic Behavior
Autistic Disorder	Autistic
Autistic Disorder Of Childhood Onset	Infantile Autism
Childhood Autism	Kanner Syndrome
Pervasive Developmental Delay Nos	Pervasive Developmental Disorder, Not Otherwise Specified

Parkinson Disease, Late-Onset

Parkinson Disease	Parkinson'S Disease
PD	PARK
Parkinson Disease, Susceptibility To	Late Onset Parkinson'S Disease
Late Onset Parkinson Disease	Paralysis Agitans
Primary Parkinsonism	Idiopathic Parkinson Disease
Parkinson'S	Parkinson Disease, Late-Onset, Susceptibility To
Parkinson Disease, Age Of Onset, Modifier	Lewy Body Parkinson Disease
Idiopathic Parkinson'S Disease	Pd - [Parkinson Disease]
Parkinson Disease Nos	Parkinson, Nos
Primary Parkinson Disease

Autism

Autistic Disorder	Autism Susceptibility 1
Childhood Autism	Autistic Disorder Of Childhood Onset
Infantile Autism	Kanner'S Syndrome
Autistic

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS12004	RIT2 Human Pre-designed siRNA Set A		/	Unkown

Species	Symbol	Source	ID
Canis familiaris	RIT2	VGNC	VGNC:45601
Macaca mulatta	RIT2	VGNC	VGNC:104243
Felis catus	RIT2	VGNC	VGNC:64645
Rattus norvegicus	RIT2	RGD	RGD:1307654
Mus musculus	RIT2	MGD	MGI:108054

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