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Gene : MFSD2A Homo sapiens

Name  ? major facilitator superfamily domain containing 2A Cytological Location  1p34.2
Brief Description  major facilitator superfamily domain containing 2A
description  The protein encoded by this gene is a transmembrane protein and sodium-dependent lysophosphatidylcholine transporter. The encoded protein is involved in the establishment of the blood-brain barrier and is required for brain growth and function. Defects in this gene are a cause of a progressive microcephaly syndrome. [provided by RefSeq, Mar 2017]
  • synonyms:
  • HGNC:25897,
  • MFSD2A,
  • sodium-dependent lysophosphatidylcholine symporter 1,
  • AK093223,
  • OTTHUMG00000009293,
  • uc001ceu.5,
  • NM_032793,
  • major facilitator superfamily domain containing 2,
  • FLJ14490,
  • NLS1,
  • MFSD2,
  • MCPH15,
  • MFSD2
  • identifiers:
  • 84879,
  • ENSG00000168389,
  • MFSD2A

Genome feature

Region: gene ? Length: 14857  
Location: 1:39955112-39969968 Cyto location: 1p34.2

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Orthologues


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



140 SN Ps

4 Cross References

17 Data Sets

6 Homologues

0 Located Features

90 Rna Seq Results