Entity Details

Primary name FLVC1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9Y5Y0
EntryNameFLVC1_HUMAN
FullNameFeline leukemia virus subgroup C receptor-related protein 1
TaxID9606
Evidenceevidence at protein level
Length555
SequenceStatuscomplete
DateCreated2004-04-13
DateModified2021-06-02

Ontological Relatives

GenesFLVCR1

GO terms

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GOName
GO:0001568 blood vessel development
GO:0001701 in utero embryonic development
GO:0005739 mitochondrion
GO:0005743 mitochondrial inner membrane
GO:0005886 plasma membrane
GO:0006783 heme biosynthetic process
GO:0006839 mitochondrial transport
GO:0006879 cellular iron ion homeostasis
GO:0015232 heme transmembrane transporter activity
GO:0015886 heme transport
GO:0016021 integral component of membrane
GO:0020037 heme binding
GO:0030218 erythrocyte differentiation
GO:0035264 multicellular organism growth
GO:0042733 embryonic digit morphogenesis
GO:0043249 erythrocyte maturation
GO:0046620 regulation of organ growth
GO:0048536 spleen development
GO:0048704 embryonic skeletal system morphogenesis
GO:0060323 head morphogenesis
GO:0097037 heme export

Subcellular Location

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Subcellular Location
Cell membrane
Mitochondrion membrane

Domains

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DomainNameCategoryType
IPR011701 Major facilitator superfamilyFamilyFamily
IPR020846 Major facilitator superfamily domainDomainDomain
IPR036259 MFS transporter superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
609033 OMIMPosterior column ataxia with retinitis pigmentosa (PCARP)A neurodegenerative syndrome beginning in infancy with areflexia and retinitis pigmentosa. Nyctalopia (night blindness) and peripheral visual field loss are usually evident during late childhood or teenage years, with subsequent progressive constriction of the visual fields and loss of central retinal function over time. A sensory ataxia caused by degeneration of the posterior columns of the spinal cord results in a loss of proprioceptive sensation that is clinically evident in the second decade of life and gradually progresses. Scoliosis, camptodactyly, achalasia, gastrointestinal dysmotility, and a sensory peripheral neuropathy are variable features of the disease. Affected individuals have no clinical or radiological evidence of cerebral or cerebellar involvement. The disease is caused by variants affecting the gene represented in this entry. Defective neuronal heme transmembrane export due to FLVCR1 mutations may abrogate the neuroprotective effects of neuroglobin and initiate an apoptotic cascade that results in the selective degeneration of photoreceptors in the neurosensory retina and sensory neurons in the posterior spinal cord.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
FLVC1_HUMANAP2C_HUMANIntAct24835590 details