RIN2

GENERAL INFORMATION

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Gene name

RIN2

Gene description

Ras and Rab interactor 2

Protein class

Disease related genes
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

2
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Most of the normal cells showed moderate cytoplasmic immunoreactivity. Strong staining was observed in megakaryocytes. The thyroid, pancreatic islets, bile duct cells, alveolar cells, breast and lymphoid tissues were weakly stained or negative.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA034641
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

RIN2 (HGNC Symbol)

Synonyms

RASSF4

Description

Ras and Rab interactor 2 (HGNC Symbol)

Entrez gene summary

The RAB5 protein is a small GTPase involved in membrane trafficking in the early endocytic pathway. The protein encoded by this gene binds the GTP-bound form of the RAB5 protein preferentially over the GDP-bound form, and functions as a guanine nucleotide exchange factor for RAB5. The encoded protein is found primarily as a tetramer in the cytoplasm and does not bind other members of the RAB family. Mutations in this gene cause macrocephaly alopecia cutis laxa and scoliosis (MACS) syndrome, an elastic tissue disorder, as well as the related connective tissue disorder, RIN2 syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2011]

Chromosome

20

Cytoband

p11.23

Chromosome location (bp)

19886521 - 20002457

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000132669 (version 78.38)

Entrez gene

54453

UniProt

Q8WYP3 (UniProt - Evidence at protein level)

neXtProt

NX_Q8WYP3

Antibodypedia

RIN2 antibodies


PROTEIN BROWSER

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ENST00000255006
 
ENST00000440354
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

RIN2-003 ENSP00000255006
ENST00000255006
Q8WYP3
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Show » Show » 944 105.6 No 0
RIN2-201 ENSP00000391239
ENST00000440354
E7EPJ1
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Show » Show » 462 53.1 No 0