SLC3A2 - solute carrier family 3 member 2 Gene

Also Known as 4F2; CD98; MDU1; 4F2HC; 4T2HC; NACAE; CD98HC

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 6520

About SLC3A2

Cytogenetic location: 11q12.3 Genomic coordinates (GRCh38): 11:62,856,109-62,888,860 (from NCBI)

This gene has 41 transcripts (splice variants), 275 orthologues and 7 paralogues. Ubiquitous expression in kidney (RPKM 68.6), bone marrow (RPKM 41.5) and 25 other tissues.

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, Nov 2010]

SLC3A2 Products (4)

mRNA Protein Name
NM_001012662.3 NP_001012680.1 4F2 cell-surface antigen heavy chain isoform b
NM_001012664.3 NP_001012682.1 4F2 cell-surface antigen heavy chain isoform e
NM_001013251.3 NP_001013269.1 4F2 cell-surface antigen heavy chain isoform f
NM_002394.6 NP_002385.3 4F2 cell-surface antigen heavy chain isoform c
Molecular Function GO Annotation Evidence Verweise Source
enables L-alanine transmembrane transporter activity IGI
IGI: Inferred from genetic interaction
10391915 GOA
enables L-leucine transmembrane transporter activity IGI
IGI: Inferred from genetic interaction
10391915 GOA
enables aromatic amino acid transmembrane transporter activity IGI
IGI: Inferred from genetic interaction
15589117 GOA
enables double-stranded RNA binding IDA
IDA: Inferred from direct assay
21266579 GOA
enables exogenous protein binding IDA
IDA: Inferred from direct assay
30341327 GOA
enables neutral L-amino acid secondary active transmembrane transporter activity IDA
IDA: Inferred from direct assay
33298890 GOA
enables neutral L-amino acid transmembrane transporter activity IGI
IGI: Inferred from genetic interaction
17197568 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
9878049 GOA
enables protein heterodimerization activity IDA
IDA: Inferred from direct assay
33298890 GOA
Biological Process GO Annotation Evidence Verweise Source
involved in L-alanine import across plasma membrane IGI
IGI: Inferred from genetic interaction
10391915 GOA
involved in L-histidine transport IDA
IDA: Inferred from direct assay
9751058 GOA
involved in L-leucine import across plasma membrane IGI
IGI: Inferred from genetic interaction
10391915 GOA
involved in L-leucine transport IDA
IDA: Inferred from direct assay
9751058 GOA
involved in L-leucine transport IMP
IMP: Inferred from mutant phenotype
30341327 GOA
involved in isoleucine transport IDA
IDA: Inferred from direct assay
11311135 GOA
involved in methionine transport IDA
IDA: Inferred from direct assay
11557028 GOA
involved in phenylalanine transport IDA
IDA: Inferred from direct assay
9751058 GOA
involved in phenylalanine transport IGI
IGI: Inferred from genetic interaction
15589117 GOA
involved in proline transport IDA
IDA: Inferred from direct assay
10574970 GOA
acts upstream of or within response to exogenous dsRNA IMP
IMP: Inferred from mutant phenotype
21266579 GOA
involved in symbiont entry into host cell IMP
IMP: Inferred from mutant phenotype
30341327 GOA
involved in thyroid hormone transport IDA
IDA: Inferred from direct assay
11564694 GOA
involved in tryptophan transport IDA
IDA: Inferred from direct assay
10574970 GOA
involved in tyrosine transport IDA
IDA: Inferred from direct assay
11557028 GOA
involved in valine transport IDA
IDA: Inferred from direct assay
11557028 GOA
Cellular Component GO Annotation Evidence Verweise Source
part of amino acid transport complex IDA
IDA: Inferred from direct assay
30867591 GOA
located in apical plasma membrane IDA
IDA: Inferred from direct assay
31791063 GOA
located in basolateral plasma membrane IDA
IDA: Inferred from direct assay
31791063 GOA
located in cell surface IDA
IDA: Inferred from direct assay
25063885 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
11311135 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SLC3A2 Protein Structure

Alpha-amylase

Alpha-amylase: Alpha amylase, catalytic domain (239 - 320)

Alpha-amylase

Alpha-amylase: Alpha amylase, catalytic domain (321 - 475)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 600
  • 630 a.a.
Protein Preferred Names Protein Names

4F2 cell-surface antigen heavy chain

  • CD98 heavy chain

SLC3A2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Verweise
Cross
SLC3A2 P08195 sepZ Escherichia coli O52302
Y2H
20374249
Cross
SLC3A2 P08195 sepZ Escherichia coli O52302 20374249
Cross
SLC3A2 P08195 sepZ Escherichia coli O52302 20374249
Intra
SLC3A2 P08195 GPR37 Homo sapiens O15354 28298427
Intra
SLC3A2 P08195 SLC7A11 Homo sapiens Q9UPY5 34880232
Intra
SLC3A2 P08195 SLC7A5 Homo sapiens Q01650 30867591
Intra
SLC3A2 P08195 SLC7A5 Homo sapiens Q01650
GMS
30867591
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant SLC3A2 Proteins

Art. -Nr. Produktname Accession Reinheit
HY-P75368 CD98 Protein, Human (HEK293, His) P08195-1 (R206-A630) ≥ 95%, as determined by reducing SDS-PAGE.

SLC3A2 Antibodies

Art. -Nr. Produktname Anwendung Reactivity
HY-P89798 CD98 Antibody (YA9142) WB, ICC/IF, IF-Tissue, FC, IP human

Related Diseases

Diseases Alias
Lysinuric Protein Intolerance
  • LPI

  • Dibasic Amino Aciduria Ii

  • Hyperdibasic Aminoaciduria

  • Dibasic Aminoaciduria 2

  • Dibasicamino Aciduria Ii

  • Congenital Lysinuria

  • Lpi - Lysinuric Protein Intolerance

Cystinuria
  • CSNU

  • Cystinuria Type B

  • Cystinuria Type A

  • Cystinuria, Type I, Formerly

  • Csnu1, Formerly

  • Cystinuria, Type Ii, Formerly

  • Cystinuria, Type Iii, Formerly

  • Csnu3, Formerly

  • Cystinuria, Type Non-I, Formerly

  • Cystinuria-Lysinuria

  • Cystinuria-Lysinuria Syndrome

  • Csnu1

  • Csnu3

  • Cystinuria 1

  • Cystinuria Type A/B

  • Cystinuria Type I

  • Cystinuria Type Ii

  • Cystinuria Type Iii

  • Cystinuria Type Non-I

  • Cystinuria, Type A/B

  • Cystinuria Type 1

  • Cystinuria - Lysinuria

  • Csnu - [Cystinuria]

  • Cystine Disease

Hepatitis C Virus
  • Hepatitis C Virus, Susceptibility To

  • Hepatitis C Virus Infection, Response To Therapy Of

  • Hcv

  • Hcv, Susceptibility To

  • Hepatitis C Virus, Resistance To

  • Hepatitis C Virus, Response To Therapy Of

  • Resistance To Hepatitis C Virus

Choriocarcinoma
  • Chorioepithelioma

Hepatitis
  • Chronic Hepatitis

  • Chronic Persistent Hepatitis

  • Acute Hepatitis

  • Hepatitis, Chronic

  • Acute And Subacute Liver Necrosis

  • Acute/Subac. Necrosis Of Liver

  • Animal Hepatitis

  • Hepatitis Chronic

  • Hepatitis A

  • Hepatitis, Animal

  • Hepatitis Due To Toxoplasmosis

  • Hepatitis In Toxoplasmosis

  • Toxoplasmal Hepatitis

  • Chronic Hepatitis, Unspecified

  • Chronic Active Hepatitis Nec

  • Other Specified Chronic Hepatitis

  • Chronic Persistent Hepatitis Nec

  • Chronic Lobular Hepatitis Nec

Null-Cell Leukemia
  • Null Cell Acute Lymphoblastic Leukemia

  • Null Cell Acute Lymphoblastic Leukaemia

  • Null-Cell Leukaemia

Colon Carcinoma In Situ
  • Carcinoma In Situ Of Colon

  • Stage 0 Colonic Carcinoma

  • Stage 0 Carcinoma Of Colon

  • Intraepithelial Neoplasia Of Colon, High Grade

  • Carcinoma In Situ Of Cecum

  • Carcinoma In Situ Of Hepatic Flexure

  • Carcinoma In Situ Of Ileocecal Valve

  • Carcinoma In Situ Of Hepatic Flexure Of Colon

Intestine Carcinoma In Situ
Lung Pleomorphic Carcinoma
Hartnup Disorder
  • Hartnup Disease

  • HND

  • Neutral 1 Amino Acid Transport Defect

  • Neutral Amino Acid Transport Defect

  • Deficiency Of Tryptophan Oxygenase

  • Hartnup'S Disease

  • Aminoaciduria, Hartnup Type

  • Disorder Of Neutral Amino Acid Transport

Akinetopsia
Autism Spectrum Disorder
  • Asd

  • Autism Spectrum Disorders

  • Autistic Continuum

  • Pervasive Developmental Disorder

  • Pervasive Development Disorder

  • Autistic Behavior

  • Autistic Disorder

  • Autistic

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Childhood Autism

  • Kanner Syndrome

  • Pervasive Developmental Delay Nos

  • Pervasive Developmental Disorder, Not Otherwise Specified

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus SLC3A2 RGD RGD:3073
Mus musculus SLC3A2 MGD MGI:96955
Macaca mulatta SLC3A2 VGNC VGNC:77463
Bos taurus SLC3A2 VGNC VGNC:34871
Canis familiaris SLC3A2 VGNC VGNC:46410
Felis catus SLC3A2 VGNC VGNC:65366
Others SLC3A2 NCBI