ENG

GENERAL INFORMATION

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Gene name

ENG

Gene description

Endoglin

Protein class

Cancer-related genes
Candidate cardiovascular disease genes
CD markers
Disease related genes
Plasma proteins
Predicted membrane proteins

Predicted localization

Membrane

Number of transcripts

3
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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

Selective expression in endothelial cells and placental trophoblasts.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining consistent with RNA expression data. Antibody staining in cells/structures not annotated, view images.

Data reliability

Supportive based on 4 antibodies.
HPA011862 , HPA067440 , CAB000096 , CAB072873
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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

Spleen

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

ENG (HGNC Symbol)

Synonyms

CD105, END, HHT1, ORW, ORW1

Description

Endoglin (HGNC Symbol)

Entrez gene summary

This gene encodes a homodimeric transmembrane protein which is a major glycoprotein of the vascular endothelium. This protein is a component of the transforming growth factor beta receptor complex and it binds to the beta1 and beta3 peptides with high affinity. Mutations in this gene cause hereditary hemorrhagic telangiectasia, also known as Osler-Rendu-Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia. This gene may also be involved in preeclampsia and several types of cancer. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2013]

Chromosome

9

Cytoband

q34.11

Chromosome location (bp)

127815012 - 127854756

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000106991 (version 78.38)

Entrez gene

2022

UniProt

P17813 (UniProt - Evidence at protein level)

neXtProt

NX_P17813

Antibodypedia

ENG antibodies


PROTEIN BROWSER

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ENST00000344849
 
ENST00000373203
 
ENST00000480266
 
 
 
 


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)

ENG-001 ENSP00000341917
ENST00000344849
P17813
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Show » Show » 625 67.5 Yes 1
ENG-002 ENSP00000362299
ENST00000373203
P17813
Show all »
Show » Show » 658 70.6 Yes 1
ENG-201 ENSP00000479015
ENST00000480266
F5GX88
Show all »
Show » 476 51.1 No 1