SIM2

GENERAL INFORMATION

? »

Gene name

SIM2

Gene description

Single-minded family bHLH transcription factor 2

Protein class

Predicted intracellular proteins
Transcription factors

Predicted localization

Intracellular

Number of transcripts

3
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Tissue enhanced (esophagus, kidney)
GTEx:Tissue enhanced (esophagus, kidney)

Protein evidence

Evidence at protein level

Protein localization

General nuclear expression.

ANTIBODY RELIABILITY

? »

Data reliability
description

Antibody staining not consistent with RNA expression data. External characterization data supports antibody staining.

Data reliability

Uncertain based on 1 antibody.
HPA029295
SHOW MORE

RNA AND PROTEIN EXPRESSION SUMMARY

? »
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

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Tissue enhanced (esophagus, kidney)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (esophagus, kidney)

Organ

Expression



GENE INFORMATION

? »

Gene name

SIM2 (HGNC Symbol)

Synonyms

bHLHe15, MGC119447, SIM

Description

Single-minded family bHLH transcription factor 2 (HGNC Symbol)

Entrez gene summary

This gene represents a homolog of the Drosophila single-minded (sim) gene, which encodes a transcription factor that is a master regulator of neurogenesis. The encoded protein is ubiquitinated by RING-IBR-RING-type E3 ubiquitin ligases, including the parkin RBR E3 ubiquitin protein ligase. This gene maps within the so-called Down syndrome chromosomal region, and is thus thought to contribute to some specific Down syndrome phenotypes. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Sep 2014]

Chromosome

21

Cytoband

q22.13

Chromosome location (bp)

36699133 - 36749917

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000159263 (version 78.38)

Entrez gene

6493

UniProt

Q14190 (UniProt - Evidence at protein level)

neXtProt

NX_Q14190

Antibodypedia

SIM2 antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000290399
 
ENST00000431229
 
ENST00000483178
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

SIM2-001 ENSP00000290399
ENST00000290399
Q14190
Show all »
Show » Show » 667 73.2 No 0
SIM2-004 ENSP00000392003
ENST00000431229
Show » Show » 480 53.7 No 0
SIM2-005 ENSP00000476273
ENST00000483178
V9GY04
Show all »
Show » Show » 73 8.3 No 0