GLI2

GENERAL INFORMATION

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Gene name

GLI2

Gene description

GLI family zinc finger 2

Protein class

Disease related genes
Predicted intracellular proteins
Transcription factors

Predicted localization

Intracellular

Number of transcripts

5
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (ovary)
GTEx:Tissue enhanced (ovary)

Protein evidence

Evidence at protein level

Protein localization

Ubiquitous nuclear expression.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly not consistent with RNA expression data.

Data reliability

Uncertain based on 1 antibody.
CAB008558
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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
Nasopharynx
N/A
N/A
Bronchus
N/A
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis

Ovary



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (ovary)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (ovary)

Organ

Expression



GENE INFORMATION

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Gene name

GLI2 (HGNC Symbol)

Synonyms

HPE9, THP1, THP2

Description

GLI family zinc finger 2 (HGNC Symbol)

Entrez gene summary

This gene encodes a protein which belongs to the C2H2-type zinc finger protein subclass of the Gli family. Members of this subclass are characterized as transcription factors which bind DNA through zinc finger motifs. These motifs contain conserved H-C links. Gli family zinc finger proteins are mediators of Sonic hedgehog (Shh) signaling and they are implicated as potent oncogenes in the embryonal carcinoma cell. The protein encoded by this gene localizes to the cytoplasm and activates patched Drosophila homolog (PTCH) gene expression. It is also thought to play a role during embryogenesis. The encoded protein is associated with several phenotypes- Greig cephalopolysyndactyly syndrome, Pallister-Hall syndrome, preaxial polydactyly type IV, postaxial polydactyly types A1 and B. [provided by RefSeq, Jul 2008]

Chromosome

2

Cytoband

q14.2

Chromosome location (bp)

120735623 - 120992653

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000074047 (version 78.38)

Entrez gene

2736

UniProt

P10070 (UniProt - Evidence at protein level)

neXtProt

NX_P10070

Antibodypedia

GLI2 antibodies


PROTEIN BROWSER

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ENST00000314490
 
ENST00000360874
 
ENST00000361492
 
ENST00000418323
 
ENST00000452319
 
 
 
 


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)

GLI2-007 ENSP00000398992
ENST00000418323
Q1PSW9
Show all »
Show » 82 8.5 No 0
GLI2-009 ENSP00000390436
ENST00000452319
P10070
Show all »
Show » Show » 1586 167.8 No 0
GLI2-012 ENSP00000441454
ENST00000360874
H0YG23
Show all »
Show » 176 18.4 No 0
GLI2-201 ENSP00000312694
ENST00000314490
Show » Show » 522 57.2 No 0
GLI2-202 ENSP00000354586
ENST00000361492
P10070
Show all »
Show » Show » 1586 167.8 No 0