FBN3

GENERAL INFORMATION

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Gene name

FBN3

Gene description

Fibrillin 3

Protein class

Predicted intracellular proteins
Predicted secreted proteins

Predicted localization

Intracellular,Secreted

Number of transcripts

5
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (lung)
GTEx:Tissue enhanced (salivary gland, thyroid gland)

Protein evidence

Evidence at protein level

Protein localization

RNA-based expert annotation could not be performed.

ANTIBODY RELIABILITY

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Data reliability
description

Presumed off target binding observed and disregarded. Pending external verification.

Data reliability

Uncertain based on 1 antibody.
HPA049482
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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:  Tissue enhanced (lung)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (salivary gland, thyroid gland)

Organ

Expression



GENE INFORMATION

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Gene name

FBN3

Synonyms

Description

Fibrillin 3 (HGNC Symbol)

Entrez gene summary

This gene encodes a protein that belongs to the fibrillin gene family. Fibrillins are extracellular matrix molecules that assemble into microfibrils in many connective tissues. This gene is most highly expressed in fetal tissues and its protein product is localized to extracellular microfibrils of developing skeletal elements, skin, lung, kidney, and skeletal muscle. This gene is potentially involved in Weill-Marchesani syndrome. While several transcript variants may exist for this gene, their full-length natures have not been described to date. [provided by RefSeq, Jul 2008]

Chromosome

19

Cytoband

p13.2

Chromosome location (bp)

8065402 - 8149846

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000142449 (version 78.38)

Entrez gene

84467

UniProt

Q75N90 (UniProt - Evidence at transcript level)

neXtProt

NX_Q75N90

Antibodypedia

FBN3 antibodies


PROTEIN BROWSER

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ENST00000270509
 
ENST00000600128
 
ENST00000601281
 
ENST00000601739
 
ENST00000602121
 
 
 
 


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)

FBN3-001 ENSP00000470498
ENST00000600128
Q75N90
Show all »
Show » Show » 2809 300.4 Yes 0
FBN3-002 ENSP00000472324
ENST00000601739
Q75N90
Show all »
Show » Show » 2809 300.4 Yes 0
FBN3-003 ENSP00000270509
ENST00000270509
Q75N90
Show all »
Show » Show » 2809 300.4 Yes 0
FBN3-006 ENSP00000469256
ENST00000602121
Show » Show » 188 20.2 No 0
FBN3-007 ENSP00000472729
ENST00000601281
Show » Show » 171 18.2 No 0