FLVCR2 (FLVCR heme transporter 2)

2007-07-01  

Identity

HGNC
LOCATION
14q24.3
LOCUSID
ALIAS
C14orf58,CCT,EPV,FLVCRL14q,MFSD7C,PVHH,SLC49A2
FUSION GENES

Other Information

Locus ID:

NCBI: 55640
MIM: 610865
HGNC: 20105
Ensembl: ENSG00000119686

Variants:

dbSNP: 55640
ClinVar: 55640
TCGA: ENSG00000119686
COSMIC: FLVCR2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000119686ENST00000238667Q9UPI3
ENSG00000119686ENST00000539311Q9UPI3
ENSG00000119686ENST00000553341G3V5Y3
ENSG00000119686ENST00000553587G3V458
ENSG00000119686ENST00000554580G3V4G2
ENSG00000119686ENST00000555027G3V5P5
ENSG00000119686ENST00000555058G3V391
ENSG00000119686ENST00000556856G3V5Q8

Expression (GTEx)

0
5
10
15
20
25
30
35
40
45

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
208232652010The Fowler syndrome-associated protein FLVCR2 is an importer of heme.39
202063342010Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome).18
206901162010High-throughput sequencing of a 4.1 Mb linkage interval reveals FLVCR2 deletions and mutations in lethal cerebral vasculopathy.7
259069272015Genetics and molecular biology of brain calcification.6
256777352016Mutations in FLVCR2 associated with Fowler syndrome and survival beyond infancy.5
251318042015Hydranencephaly in a newborn with a FLVCR2 mutation and prenatal exposure to cocaine.0

Citation

Dessen P

FLVCR2 (FLVCR heme transporter 2)

Atlas Genet Cytogenet Oncol Haematol. 2007-07-01

Online version: http://atlasgeneticsoncology.org/gene/47618/flvcr2