FGF17

GENERAL INFORMATION

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Gene name

FGF17

Gene description

Fibroblast growth factor 17

Protein class

Cancer-related genes
Disease related genes
Predicted secreted proteins
RAS pathway related proteins

Predicted localization

Secreted

Number of transcripts

2
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Mixed
GTEx:Tissue enhanced (cerebellum)

Protein evidence

Evidence at protein level

Protein localization

Leydig cells and subsets of germinal center cells in lymphoid tissues displayed strong cytoplasmic positivity. Respiratory epithelia, hepatocytes and adrenal gland showed weak to moderate staining. Strong staining was observed in subsets of vessels. Remaining normal cells were negative.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA052600
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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:  Mixed

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (cerebellum)

Organ

Expression



GENE INFORMATION

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Gene name

FGF17 (HGNC Symbol)

Synonyms

FGF-13

Description

Fibroblast growth factor 17 (HGNC Symbol)

Entrez gene summary

The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes including embryonic development cell growth, morphogenesis, tissue repair, tumor growth and invasion. This gene was shown to be prominently expressed in the cerebellum and cortex. The mouse homolog of this gene was localized to specific sites in the midline structures of the forebrain, the midbrain-hindbrain junction, developing skeleton and developing arteries, which suggests a role in central nervous system, bone and vascular development. This gene was referred to as FGF-13 in reference 2, however, its amino acid sequence and chromosomal localization are identical to FGF17. [provided by RefSeq, Jul 2008]

Chromosome

8

Cytoband

p21.3

Chromosome location (bp)

22042398 - 22048809

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000158815 (version 78.38)

Entrez gene

8822

UniProt

O60258 (UniProt - Evidence at protein level)

neXtProt

NX_O60258

Antibodypedia

FGF17 antibodies


PROTEIN BROWSER

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ENST00000359441
 
ENST00000518533
 
 
 
 


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)

FGF17-001 ENSP00000352414
ENST00000359441
O60258
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Show » Show » 216 24.9 Yes 0
FGF17-002 ENSP00000431041
ENST00000518533
O60258
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Show » Show » 205 23.7 Yes 0