FLVCR1

GENERAL INFORMATION

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Gene name

FLVCR1

Gene description

Feline leukemia virus subgroup C cellular receptor 1

Protein class

Disease related genes
Potential drug targets
Predicted membrane proteins
Transporters

Predicted localization

Membrane

Number of transcripts

2
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (small intestine)
GTEx:Mixed

Protein evidence

Evidence at protein level

Protein localization

Most normal tissues showed weak to moderate cytoplasmic positivity. Glandular cells in prostate, small intestine, epididymis and skin displayed additional membranous positivity. Stomach, small intestine, exocrine pancreas, adrenal gland and renal tubules exhibited strong immunoreactivity. Lung, liver, cells of CNS, spleen, adipocytes and smooth muscle were negative.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA046646
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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

Pancreas

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 (small intestine)

Organ

Expression

GTEx dataset
RNA tissue category:  Mixed

Organ

Expression



GENE INFORMATION

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Gene name

FLVCR1 (HGNC Symbol)

Synonyms

AXPC1, FLVCR, MFSD7B, PCA

Description

Feline leukemia virus subgroup C cellular receptor 1 (HGNC Symbol)

Entrez gene summary

This gene encodes a member of the major facilitator superfamily of transporter proteins. The encoded protein is a heme transporter that may play a critical role in erythropoiesis by protecting developing erythroid cells from heme toxicity. This gene may play a role in posterior column ataxia with retinitis pigmentosa and the hematological disorder Diamond-Blackfan syndrome. [provided by RefSeq, Jan 2011]

Chromosome

1

Cytoband

q32.3

Chromosome location (bp)

212858255 - 212899363

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000162769 (version 78.38)

Entrez gene

28982

UniProt

Q9Y5Y0 (UniProt - Evidence at protein level)

neXtProt

NX_Q9Y5Y0

Antibodypedia

FLVCR1 antibodies


PROTEIN BROWSER

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ENST00000366971
 
ENST00000419102
 
 
 
 


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)

FLVCR1-001 ENSP00000355938
ENST00000366971
Q9Y5Y0
Show all »
Show » Show » 555 59.9 No >9
FLVCR1-004 ENSP00000414680
ENST00000419102
Show » Show » 354 38.1 No 7