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solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 OKDB#: 4512
 Symbols: SLC3A2 Species: human
 Synonyms: 4F2, CD98, MDU1, 4F2HC, 4T2HC, NACAE, CD98HC,  Locus: 11q13 in Homo sapiens


For retrieval of Nucleotide and Amino Acid sequences please go to: OMIM Entrez Gene
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General Comment NCBI Summary: This gene is a member of the solute carrier family and encodes a cell surface, transmembrane protein. The protein exists as the heavy chain of a heterodimer, covalently bound through di-sulfide bonds to one of several possible light chains. The encoded transporter plays a role in regulation of intracellular calcium levels and transports L-type amino acids. Alternatively spliced transcript variants, encoding different isoforms, have been characterized. [provided by RefSeq]
General function Channel/transport protein
Comment
Cellular localization Plasma membrane
Comment
Ovarian function Early embryo development
Comment
Expression regulated by
Comment
Ovarian localization
Comment
Follicle stages
Comment
Phenotypes
Mutations 1 mutations

Species: mouse
Mutation name: None
type: null mutation
fertility: embryonic lethal
Comment: Extracellular domain of CD98hc is required for early murine development. Sato Y et al. ABSTRACT:

Genomic Region show genomic region
Phenotypes and GWAS show phenotypes and GWAS
Links
OMIM (Online Mendelian Inheritance in Man: an excellent source of general gene description and genetic information.)
OMIM \ Animal Model
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created: July 4, 2011, 10:28 a.m. by: hsueh   email:
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last update: July 4, 2011, 10:29 a.m. by: hsueh    email:



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