ADAMTS10

GENERAL INFORMATION

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Gene name

ADAMTS10

Gene description

ADAM metallopeptidase with thrombospondin type 1 motif, 10

Protein class

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

Predicted localization

Intracellular,Secreted

Number of transcripts

3
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Mixed
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Most normal tissues showed moderate to strong cytoplasmic positivity. Lymphoid tissues, renal glomeruli, bile ducts and most cells in cerebellum were negative.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA040223
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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

Skin



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:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

ADAMTS10 (HGNC Symbol)

Synonyms

ADAM-TS10

Description

ADAM metallopeptidase with thrombospondin type 1 motif, 10 (HGNC Symbol)

Entrez gene summary

This gene belongs to the ADAMTS (a disintegrin and metalloproteinase domain with thrombospondin type-1 motifs) family of zinc-dependent proteases. ADAMTS proteases are complex secreted enzymes containing a prometalloprotease domain of the reprolysin type attached to an ancillary domain with a highly conserved structure that includes at least one thrombospondin type 1 repeat. They have been demonstrated to have important roles in connective tissue organization, coagulation, inflammation, arthritis, angiogenesis and cell migration. The product of this gene plays a major role in growth and in skin, lens, and heart development. It is also a candidate gene for autosomal recessive Weill-Marchesani syndrome. [provided by RefSeq, Jul 2008]

Chromosome

19

Cytoband

p13.2

Chromosome location (bp)

8580242 - 8610735

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000142303 (version 78.38)

Entrez gene

81794

UniProt

Q9H324 (UniProt - Evidence at protein level)

neXtProt

NX_Q9H324

Antibodypedia

ADAMTS10 antibodies


PROTEIN BROWSER

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ENST00000270328
 
ENST00000595838
 
ENST00000597188
 
 
 
 


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)

ADAMTS10-001 ENSP00000471851
ENST00000597188
Show » Show » 1103 120.9 Yes 0
ADAMTS10-003 ENSP00000470501
ENST00000595838
Q9H324
Show all »
Show » Show » 590 62.5 No 0
ADAMTS10-201 ENSP00000270328
ENST00000270328
Show » Show » 1103 120.9 Yes 0