ADAMTS13

GENERAL INFORMATION

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Gene name

ADAMTS13

Gene description

ADAM metallopeptidase with thrombospondin type 1 motif, 13

Protein class

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

Predicted localization

Intracellular,Secreted

Number of transcripts

6
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (liver)
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Selective cytoplasmic expression in a few tissues, most abundant in hepatocytes, adrenal glands, renal tubules and Leydig cells in testis.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 2 antibodies.
HPA042014 , HPA042844
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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:  Tissue enhanced (liver)

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

ADAMTS13 (HGNC Symbol)

Synonyms

C9orf8, DKFZp434C2322, FLJ42993, MGC118899, MGC118900, TTP, vWF-CP, VWFCP

Description

ADAM metallopeptidase with thrombospondin type 1 motif, 13 (HGNC Symbol)

Entrez gene summary

This gene encodes a member of a family of proteins containing several distinct regions, including a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. The enzyme encoded by this gene specifically cleaves von Willebrand Factor (vWF). Defects in this gene are associated with thrombotic thrombocytopenic purpura. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]

Chromosome

9

Cytoband

q34.2

Chromosome location (bp)

133414358 - 133459402

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000160323 (version 78.38)

Entrez gene

11093

UniProt

Q76LX8 (UniProt - Evidence at protein level)

neXtProt

NX_Q76LX8

Antibodypedia

ADAMTS13 antibodies


PROTEIN BROWSER

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ENST00000355699
 
ENST00000356589
 
ENST00000371910
 
ENST00000371911
 
ENST00000371916
 
ENST00000371929
 
 
 
 


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)

ADAMTS13-001 ENSP00000360997
ENST00000371929
Q76LX8
Show all »
Show » Show » 1427 153.6 Yes 0
ADAMTS13-002 ENSP00000347927
ENST00000355699
Q76LX8
Show all »
Show » Show » 1371 147.8 Yes 0
ADAMTS13-003 ENSP00000348997
ENST00000356589
Q76LX8
Show all »
Show » Show » 1340 144.5 Yes 0
ADAMTS13-006 ENSP00000360978
ENST00000371910
Q76LX8
Show all »
Show » Show » 223 24.5 No 0
ADAMTS13-201 ENSP00000360979
ENST00000371911
Show » Show » 344 36.7 Yes 0
ADAMTS13-202 ENSP00000360984
ENST00000371916
Q6QNA4
Show all »
Show » Show » 444 48.3 No 0