ADAMTS2

GENERAL INFORMATION

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Gene name

ADAMTS2

Gene description

ADAM metallopeptidase with thrombospondin type 1 motif, 2

Protein class

Disease related genes
Enzymes
Plasma proteins
Potential drug targets
Predicted secreted proteins

Predicted localization

Secreted

Number of transcripts

2
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Mixed
GTEx:Mixed

Protein evidence

Evidence at protein level

Protein localization

Most of the normal tissues displayed moderate cytoplasmic positivity. Additional nuclear staining was observed in squamous epithelia. Hepatocytes, renal tubules and Purkinje cells showed strong staining. The bile ducts, alveolar cells, glial cells and reaction center cells 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.
HPA028444
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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:  Mixed

Organ

Expression

GTEx dataset
RNA tissue category:  Mixed

Organ

Expression



GENE INFORMATION

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Gene name

ADAMTS2 (HGNC Symbol)

Synonyms

ADAM-TS2, ADAMTS-3, hPCPNI, NPI, PCINP

Description

ADAM metallopeptidase with thrombospondin type 1 motif, 2 (HGNC Symbol)

Entrez gene summary

This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The enzyme encoded by this gene excises the N-propeptide of type I, type II and type V procollagens. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2010]

Chromosome

5

Cytoband

q35.3

Chromosome location (bp)

179110851 - 179345430

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000087116 (version 78.38)

Entrez gene

9509

UniProt

O95450 (UniProt - Evidence at transcript level)

neXtProt

NX_O95450

Antibodypedia

ADAMTS2 antibodies


PROTEIN BROWSER

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ENST00000251582
 
ENST00000274609
 
 
 
 


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)

ADAMTS2-001 ENSP00000251582
ENST00000251582
O95450
Show all »
Show » Show » 1211 134.8 Yes 0
ADAMTS2-002 ENSP00000274609
ENST00000274609
O95450
Show all »
Show » Show » 566 61.8 Yes 0