THSD7A

GENERAL INFORMATION

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Gene name

THSD7A

Gene description

Thrombospondin, type I, domain containing 7A

Protein class

Predicted membrane proteins

Predicted localization

Membrane

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

Membranous expression in renal glomeruli and Leydig cells. RNA-based expert annotation could not be performed.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly consistent with RNA expression data. Pending external verification.

Data reliability

Supportive based on 1 antibody.
HPA000923
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
N/A
Endocrine tissues
N/A
Bone marrow & immune system
N/A
Muscle tissues
N/A
Lung
N/A
Nasopharynx
N/A
N/A
Bronchus
N/A
N/A
Lung
N/A
Liver & gallbladder
N/A
Liver
N/A
Pancreas
N/A
Pancreas
N/A
Gastrointestinal tract
N/A
Kidney & urinary bladder
N/A
Male tissues
N/A
Testis
N/A
Epididymis
N/A
N/A
Prostate
N/A
Seminal vesicle
N/A
N/A
Female tissues
N/A
Breast
N/A
N/A
Vagina
N/A
N/A
Cervix, uterine
N/A
N/A
Ovary
N/A
Placenta
N/A
Adipose & soft tissue
N/A
Skin
N/A
Skin
N/A
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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RNA-based expert annotation could not be performed, due to inconclusive results. View immunohistochemistry primary data.


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

THSD7A (HGNC Symbol)

Synonyms

KIAA0960

Description

Thrombospondin, type I, domain containing 7A (HGNC Symbol)

Entrez gene summary

The protein encoded by this gene is found almost exclusively in endothelial cells from placenta and umbilical cord. The encoded protein appears to interact with alpha(V)beta(3) integrin and paxillin to inhibit endothelial cell migration and tube formation. This protein may be involved in cytoskeletal organization. Variations in this gene may be associated with low bone mineral density in osteoporosis. [provided by RefSeq, Aug 2010]

Chromosome

7

Cytoband

p21.3

Chromosome location (bp)

11370357 - 11832198

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000005108 (version 78.38)

Entrez gene

221981

UniProt

Q9UPZ6 (UniProt - Evidence at protein level)

neXtProt

NX_Q9UPZ6

Antibodypedia

THSD7A antibodies


PROTEIN BROWSER

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ENST00000423059
 
ENST00000617773
 
 
 
 


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)

THSD7A-001 ENSP00000406482
ENST00000423059
Q9UPZ6
Show all »
Show » Show » 1657 185.4 Yes 1
THSD7A-201 ENSP00000481440
ENST00000617773
Show » 1657 185.4 Yes 1