SLC35A1 - solute carrier family 35 member A1 Gene

Also Known as CST; hCST; CDG2F; CMPST

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 10559

About SLC35A1

Cytogenetic location: 6q15 Genomic coordinates (GRCh38): 6:87,472,974-87,512,336 (from NCBI)

This gene has 4 transcripts (splice variants), 200 orthologues, 4 paralogues and is associated with 3 phenotypes. Ubiquitous expression in colon (RPKM 23.8), lung (RPKM 21.7) and 25 other tissues.

Summary

The protein encoded by this gene is found in the membrane of the Golgi apparatus, where it transports nucleotide sugars into the Golgi. One such nucleotide sugar is CMP-sialic acid, which is imported into the Golgi by the encoded protein and subsequently glycosylated. Defects in this gene are a cause of congenital disorder of glycosylation type 2F (CDG2F). Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Dec 2009]

SLC35A1 Products (2)

mRNA Protein Name
NM_001168398.2 NP_001161870.1 CMP-sialic acid transporter isoform b
NM_006416.5 NP_006407.1 CMP-sialic acid transporter isoform a
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
Biological Process GO Annotation Evidence References Source
involved in CMP-N-acetylneuraminate transmembrane transport IDA
IDA: Inferred from direct assay
15576474 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

SLC35A1 Protein Structure

Nuc_sug_transp

Nuc_sug_transp: Nucleotide-sugar transporter (73 - 306)

  • 0
  • 100
  • 200
  • 300
  • 337 a.a.
Protein Preferred Names Protein Names

CMP-sialic acid transporter

  • CMP-SA-Tr

SLC35A1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
SLC35A1 P78382 SDC3 Homo sapiens A0A0S2Z4U3 32296183
Intra
SLC35A1 P78382 SDC3 Homo sapiens A0A0S2Z4U3 32296183
Intra
SLC35A1 P78382 RELL2 Homo sapiens Q8NC24 32296183
Intra
SLC35A1 P78382 RELL2 Homo sapiens Q8NC24 32296183
Intra
SLC35A1 P78382 RELL2 Homo sapiens Q8NC24 32296183
Intra
SLC35A1 P78382 PIK3IP1 Homo sapiens Q96FE7 32296183
Intra
SLC35A1 P78382 PIK3IP1 Homo sapiens Q96FE7 32296183
Intra
SLC35A1 P78382 PIK3IP1 Homo sapiens Q96FE7 32296183
Intra
SLC35A1 P78382 PLPP4 Homo sapiens Q5VZY2 32296183
Intra
SLC35A1 P78382 PLPP4 Homo sapiens Q5VZY2 32296183
Intra
SLC35A1 P78382 PLPP4 Homo sapiens Q5VZY2 32296183
Intra
SLC35A1 P78382 ARL13B Homo sapiens Q3SXY8 32296183
Intra
SLC35A1 P78382 ARL13B Homo sapiens Q3SXY8 32296183
Intra
SLC35A1 P78382 ARL13B Homo sapiens Q3SXY8 32296183
Intra
SLC35A1 P78382 GPX8 Homo sapiens Q8TED1 32296183
Intra
SLC35A1 P78382 GPX8 Homo sapiens Q8TED1 32296183
Intra
SLC35A1 P78382 GPX8 Homo sapiens Q8TED1 32296183
Intra
SLC35A1 P78382 FNDC9 Homo sapiens Q8TBE3 32296183
Intra
SLC35A1 P78382 FNDC9 Homo sapiens Q8TBE3 32296183
Intra
SLC35A1 P78382 FNDC9 Homo sapiens Q8TBE3 32296183
Intra
SLC35A1 P78382 FXYD3 Homo sapiens Q14802-3 32296183
Intra
SLC35A1 P78382 FXYD3 Homo sapiens Q14802-3 32296183
Intra
SLC35A1 P78382 FXYD3 Homo sapiens Q14802-3 32296183
Intra
SLC35A1 P78382 ASZ1 Homo sapiens Q8WWH4 32296183
Intra
SLC35A1 P78382 ASZ1 Homo sapiens Q8WWH4 32296183
Intra
SLC35A1 P78382 ASZ1 Homo sapiens Q8WWH4 32296183
Intra
SLC35A1 P78382 TMPRSS2 Homo sapiens O15393-2 32296183
Intra
SLC35A1 P78382 TMPRSS2 Homo sapiens O15393-2 32296183
Intra
SLC35A1 P78382 ASGR2 Homo sapiens P07307-3 32296183
Intra
SLC35A1 P78382 ASGR2 Homo sapiens P07307-3 32296183
Intra
SLC35A1 P78382 SLC34A2 Homo sapiens O95436-2 32296183
Intra
SLC35A1 P78382 SLC34A2 Homo sapiens O95436-2 32296183
Intra
SLC35A1 P78382 AQP6 Homo sapiens Q13520 32296183
Intra
SLC35A1 P78382 AQP6 Homo sapiens Q13520 32296183
Intra
SLC35A1 P78382 AQP6 Homo sapiens Q13520 32296183
Intra
SLC35A1 P78382 KIR3DL3 Homo sapiens Q8N743 32296183
Intra
SLC35A1 P78382 KIR3DL3 Homo sapiens Q8N743 32296183
Intra
SLC35A1 P78382 KIR3DL3 Homo sapiens Q8N743 32296183
Intra
SLC35A1 P78382 SSMEM1 Homo sapiens Q8WWF3 32296183
Intra
SLC35A1 P78382 SSMEM1 Homo sapiens Q8WWF3 32296183
Intra
SLC35A1 P78382 SSMEM1 Homo sapiens Q8WWF3 32296183
Intra
SLC35A1 P78382 CPLX4 Homo sapiens Q7Z7G2 32296183
Intra
SLC35A1 P78382 CPLX4 Homo sapiens Q7Z7G2 32296183
Intra
SLC35A1 P78382 CPLX4 Homo sapiens Q7Z7G2 32296183
Intra
SLC35A1 P78382 FAM209A Homo sapiens Q5JX71 32296183
Intra
SLC35A1 P78382 FAM209A Homo sapiens Q5JX71 32296183
Intra
SLC35A1 P78382 FAM209A Homo sapiens Q5JX71 32296183
Intra
SLC35A1 P78382 CERS4 Homo sapiens Q9HA82 32296183
Intra
SLC35A1 P78382 CERS4 Homo sapiens Q9HA82 32296183
Intra
SLC35A1 P78382 MCFD2 Homo sapiens Q8NI22 32296183
Intra
SLC35A1 P78382 MCFD2 Homo sapiens Q8NI22 32296183
Intra
SLC35A1 P78382 MCFD2 Homo sapiens Q8NI22 32296183
Intra
SLC35A1 P78382 LHFPL5 Homo sapiens Q8TAF8 32296183
Intra
SLC35A1 P78382 LHFPL5 Homo sapiens Q8TAF8 32296183
Intra
SLC35A1 P78382 LHFPL5 Homo sapiens Q8TAF8 32296183
Intra
SLC35A1 P78382 SAR1A Homo sapiens Q9NR31 32296183
Intra
SLC35A1 P78382 SAR1A Homo sapiens Q9NR31 32296183
Intra
SLC35A1 P78382 SAR1A Homo sapiens Q9NR31 32296183
Intra
SLC35A1 P78382 TCTA Homo sapiens P57738 32296183
Intra
SLC35A1 P78382 TCTA Homo sapiens P57738 32296183
Intra
SLC35A1 P78382 TMX2 Homo sapiens Q9Y320 32296183
Intra
SLC35A1 P78382 TMX2 Homo sapiens Q9Y320 32296183
Intra
SLC35A1 P78382 TMX2 Homo sapiens Q9Y320 32296183
Intra
SLC35A1 P78382 CD53 Homo sapiens P19397 32296183
Intra
SLC35A1 P78382 CD53 Homo sapiens P19397 32296183
Intra
SLC35A1 P78382 TMEM139 Homo sapiens Q8IV31 32296183
Intra
SLC35A1 P78382 TMEM139 Homo sapiens Q8IV31 32296183
Intra
SLC35A1 P78382 TMEM139 Homo sapiens Q8IV31 32296183
Intra
SLC35A1 P78382 MGST3 Homo sapiens O14880 32296183
Intra
SLC35A1 P78382 MGST3 Homo sapiens O14880 32296183
Intra
SLC35A1 P78382 F11R Homo sapiens Q9Y624 32296183
Intra
SLC35A1 P78382 F11R Homo sapiens Q9Y624 32296183
Intra
SLC35A1 P78382 F11R Homo sapiens Q9Y624 32296183
Intra
SLC35A1 P78382 SLC1A1 Homo sapiens P43005 32296183
Intra
SLC35A1 P78382 SLC1A1 Homo sapiens P43005 32296183
Intra
SLC35A1 P78382 BCL2L13 Homo sapiens Q9BXK5 32296183
Intra
SLC35A1 P78382 BCL2L13 Homo sapiens Q9BXK5 32296183
Intra
SLC35A1 P78382 BCL2L13 Homo sapiens Q9BXK5 32296183
Intra
SLC35A1 P78382 MRPS18B Homo sapiens Q9Y676 32296183
Intra
SLC35A1 P78382 MRPS18B Homo sapiens Q9Y676 32296183
Intra
SLC35A1 P78382 MRPS18B Homo sapiens Q9Y676 32296183
Intra
SLC35A1 P78382 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
SLC35A1 P78382 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
SLC35A1 P78382 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
SLC35A1 P78382 SYT2 Homo sapiens Q8N9I0 32296183
Intra
SLC35A1 P78382 SYT2 Homo sapiens Q8N9I0 32296183
Intra
SLC35A1 P78382 SYT2 Homo sapiens Q8N9I0 32296183
Intra
SLC35A1 P78382 EBAG9 Homo sapiens O00559 32296183
Intra
SLC35A1 P78382 EBAG9 Homo sapiens O00559 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Congenital Disorder Of Glycosylation, Type Iif
  • CDG2F

  • Congenital Disorder Of Glycosylation Type Iif

  • Cdg Iif

  • Cdgiif

  • Carbohydrate Deficient Glycoprotein Syndrome Type Iif

  • Cmp-Sialic Acid Transporter Deficiency

  • Slc35a1-Cdg

  • Cdg-Iif

  • Cdgiidf

  • Cdg Syndrome Type Iif

  • Congenital Disorder Of Glycosylation Type 2f

  • Congenital Disorder Of Glycosylation 2f

  • Glycosylation, Congenital Disorder Of, Type Iif

Immunodeficiency 47
  • Congenital Disorder Of Glycosylation Type Ii

  • CDG2E

  • Congenital Disorder Of Glycosylation Type Iie

  • IMD47

  • Cdg2s

  • Cdg Iis

  • Cdgiis

  • Immunodeficiency And Hepatopathy With Or Without Neurologic Features

  • Congenital Disorder Of Glycosylation, Type Ii

  • CDG1I

  • Congenital Disorder Of Glycosylation, Type Iie

  • Cdg Iie

  • Congenital Disorder Of Glycosylation Type 2e

  • Congenital Disorder Of Glycosylation, Type Iis

  • Cdg Ii

  • Cdgii

  • Cdgiie

  • Carbohydrate Deficient Glycoprotein Syndrome Type Iie

  • Cdg Syndrome Type Iie

  • Congenital Disorder Of Glycosylation Ii

  • Congenital Disorder Of Glycosylation 1i

  • Cdg-Iie

  • Alg2-Cdg

  • Cdg-Ii

  • Glycosylation, Congenital Disorder Of, Type Ii

  • Cdgiide

  • Congenital Disorder Of Glycosylation Type Iis

  • Cog7-Cdg

  • Cdg Syndrome Type Ii

  • Carbohydrate Deficient Glycoprotein Syndrome Type Ii

  • Congenital Disorder Of Glycosylation Type 1i

  • Mannosyltransferase 2 Deficiency

  • Congenital Disorder Of Glycosylation 2e

  • Congenital Disorder Of Glycosylation 2s

  • Congenital Disorders Of Glycosylation Type Ii

  • Glycosylation, Congenital Disorder Of, Type Iie

  • Immunodeficiency, Type 47

  • Congenital Disorder Of Glycosylation Type 2a

Sialuria
  • Sialuria, French Type

  • French Type Sialuria

  • Sialuria French Type

  • Sialic Acid Storage Disease

  • Sialic Acid Storage Disease, Finnish Type

  • Infantile Sialic Acid Storage Disease

Developmental And Epileptic Encephalopathy 36
  • Congenital Disorder Of Glycosylation Type I

  • Epileptic Encephalopathy, Early Infantile, 36

  • Congenital Disorder Of Glycosylation, Type Is

  • Cdg1s

  • Congenital Disorder Of Glycosylation, Type Ie

  • CDG1E

  • Congenital Disorder Of Glycosylation Type 1e

  • DEE36

  • Eiee36

  • Cdg Is

  • Cdgis

  • Congenital Disorder Of Glycosylation Ie

  • Congenital Disorder Of Glycosylation 1e

  • Cdg-Is

  • Congenital Disorder Of Glycosylation Type Is

  • Developmental And Epileptic Encephalopathy, 36

  • Cdg Ie

  • Cdgie

  • Early Infantile Epileptic Encephalopathy 36

  • Alg13-Cdg

  • Cdg Syndrome Type Is

  • Congenital Disorder Of Glycosylation Type 1s

  • Dpm1-Cdg

  • Cdg Syndrome Type Ie

  • Cdg-Ie

  • Carbohydrate Deficient Glycoprotein Syndrome Type Ie

  • Congenital Disorder Of Glycosylation Type Ie

  • Dol-P-Mannosyltransferase Deficiency

  • Congenital Disorder Of Glycosylation 1s

  • Glycosylation, Congenital Disorder Of, Type I

  • Glycosylation, Congenital Disorder Of, Type Ie

  • Congenital Disorder Of Glycosylation Type 1a

  • Congenital Disorder Of Glycosylation, Type Iu

Congenital Disorder Of Glycosylation, Type Iid
  • CDG2D

  • Congenital Disorder Of Glycosylation Type Iid

  • Cdg Iid

  • Cdgiid

  • B4galt1-Cdg

  • Cdg-Iid

  • Congenital Disorder Of Glycosylation Type 2d

  • Beta-1,4-Galactosyltransferase Deficiency

  • Cdg Syndrome Type Iid

  • Carbohydrate Deficient Glycoprotein Syndrome Type Iid

  • Congenital Disorder Of Glycosylation 2d

  • Glycosylation, Congenital Disorder Of, Type Iid

  • Congenital Disorder Of Glycosylation, Type Iiid

Congenital Disorder Of Glycosylation, Type Iib
  • CDG2B

  • CDGIIB

  • Glucosidase I Deficiency

  • Congenital Disorder Of Glycosylation Type Iib

  • Cdg Iib

  • Mogs-Cdg

  • Cdg Syndrome Type Iib

  • Cdg-Iib

  • Carbohydrate Deficient Glycoprotein Syndrome Type Iib

  • Congenital Disorder Of Glycosylation Type 2b

  • Glucosidase 1 Deficiency

  • Type Iib Congenital Disorder Of Glycosylation

  • Glycosylation, Congenital Disorder Of, Type Iib

Congenital Disorder Of Glycosylation, Type Iia
  • CDG2A

  • Congenital Disorder Of Glycosylation Type Iia

  • Cdg Iia

  • Cdgiia

  • Congenital Disorder Of Glycosylation Type 2a

  • Alkuraya Syndrome

  • Mental Retardation, Growth Retardation, Prominent Columella, And Open Mouth

  • Carbohydrate-Deficient Glycoprotein Syndrome, Type Ii

  • Mgat2-Cdg

  • Cdg-Iia

  • Carbohydrate-Deficient Glycoprotein Syndrome, Type Ii, Formerly

  • Cdgs2, Formerly

  • Cdgs2

  • Cdg Syndrome Type Iia

  • Carbohydrate Deficient Glycoprotein Syndrome Type Iia

  • N-Acetylglucosaminyltransferase 2 Deficiency

  • Congenital Disorder Of Glycosylation 2a

  • Carbohydrate-Deficient Glycoprotein Syndrome Type Ii

  • Cdgs Type Ii

  • Carbohydrate-Deficient Glycoprotein Syndrome Type 2

  • Glycosylation, Congenital Disorder Of, Type Iia

Congenital Disorder Of Glycosylation, Type In
  • Congenital Disorder Of Glycosylation

  • CDG1N

  • Congenital Disorders Of Glycosylation

  • Cdg In

  • Cdgin

  • Congenital Disorder Of Glycosylation 1n

  • Carbohydrate-Deficient Glycoprotein Syndrome

  • Cdg

  • Rft1-Cdg

  • Cdg-In

  • Congenital Disorder Of Glycosylation Type In

  • Carbohydrate Deficient Glycoprotein Syndrome

  • Cdg Syndrome

  • Congenital Disorder Of Glycosylation In

  • Carbohydrate-Deficient Glycoprotein Syndromes

  • Cdg Syndrome Type In

  • Carbohydrate Deficient Glycoprotein Syndrome Type In

  • Congenital Disorder Of Glycosylation Type 1n

  • Man5glcnac2-Pp-Dol Flippase Deficiency

  • Glycosylation, Congenital Disorder Of

  • Glycosylation, Congenital Disorder Of, Type In

Schneckenbecken Dysplasia
  • SHNKND

  • Chondrodysplasia, Lethal Neonatal, With Snail-Like Pelvis

  • Chondrodysplasia Lethal Neonatal With Snail Like Pelvis

  • Chondrodysplasia With Snail-Like Pelvis

  • Slc35d1-Cdg

  • Dysplasia, Schneckenbecken

Thrombocytopenia
  • Low Platelet Count

  • Low Platelets

  • Decreased Platelets

  • Platelet Dysfunction Nos

Walker-Warburg Syndrome
  • Hard Syndrome

  • Walker-Warburg Congenital Muscular Dystrophy

  • Cerebroocular Dysplasia-Muscular Dystrophy Syndrome

  • Cod-Md Syndrome

  • Chemke Syndrome

  • Hydrocephalus, Agyria And Retinal Dysplasia

  • Cerebroocular Dysgenesis

  • Cerebroocular Dysplasia Muscular Dystrophy Syndrome

  • Hard +/- E Syndrome

  • Pagon Syndrome

  • Warburg Syndrome

  • Hydrocephalus, Agyria, And Retinal Dysplasia

  • Mddga

  • Muscular Dystrophy-Dystroglycanopathy , Type A

  • Muscular Dystrophy-Dystroglycanopathy [With Brain And Eye Anomalies], Type A

  • Hydrocephalus-Agyria-Retinal Dysplasia Syndrome

  • Wws

  • Dystrophy, Muscular, Dystroglycanopathy, Type A

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
Felis catus SLC35A1 VGNC VGNC:65319
Canis familiaris SLC35A1 VGNC VGNC:46360
Rattus norvegicus SLC35A1 RGD RGD:1311359
Macaca mulatta SLC35A1 VGNC VGNC:83468
Mus musculus SLC35A1 MGD MGI:1345622
Bos taurus SLC35A1 VGNC VGNC:34819
Others SLC35A1 NCBI