ADAMTSL2

GENERAL INFORMATION

? »

Gene name

ADAMTSL2

Gene description

ADAMTS-like 2

Protein class

Disease related genes
Plasma proteins
Predicted intracellular proteins
Predicted secreted proteins

Predicted localization

Intracellular,Secreted

Number of transcripts

3
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Tissue enhanced (adrenal gland, kidney)
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic expression in a subset of tissues.

ANTIBODY RELIABILITY

? »

Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 2 antibodies.
HPA045634 , HPA053812
SHOW MORE

RNA AND PROTEIN EXPRESSION SUMMARY

? »
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

Bone marrow

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Tissue enhanced (adrenal gland, kidney)

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

? »

Gene name

ADAMTSL2 (HGNC Symbol)

Synonyms

KIAA0605

Description

ADAMTS-like 2 (HGNC Symbol)

Entrez gene summary

This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) and ADAMTS-like 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 protein encoded by this gene lacks the protease domain, and is therefore of a member of the the ADAMTS-like protein subfamily. It is a secreted glycoprotein that binds the cell surface and extracellular matrix; it also interacts with latent transforming growth factor beta binding protein 1. Mutations in this gene have been associated with geleophysic dysplasia. [provided by RefSeq, Feb 2009]

Chromosome

9

Cytoband

q34.2

Chromosome location (bp)

133532164 - 133575519

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000197859 (version 78.38)

Entrez gene

9719

UniProt

Q86TH1 (UniProt - Evidence at protein level)

neXtProt

NX_Q86TH1

Antibodypedia

ADAMTSL2 antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000354484
 
ENST00000393060
 
ENST00000393061
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

ADAMTSL2-001 ENSP00000346478
ENST00000354484
Q86TH1
Show all »
Show » Show » 951 104.6 Yes 0
ADAMTSL2-002 ENSP00000376781
ENST00000393061
B1B0D4
Show all »
Show » Show » 1060 116.3 No 0
ADAMTSL2-201 ENSP00000376780
ENST00000393060
Q86TH1
Show all »
Show » Show » 951 104.6 Yes 0