SLC35A5

gene
On this page

Also known as FLJ20730

Summary

SLC35A5 (solute carrier family 35 member A5, HGNC:20792) is a protein-coding gene on chromosome 3q13.2, encoding UDP-sugar transporter protein SLC35A5 (Q9BS91). Probable UDP-sugar:UMP transmembrane antiporter involved in UDP-alpha-D-glucuronate/UDP-GlcA, UDP-GlcNAc/UDP-N-acetyl-alpha-D-glucosamine and UDP-N-acetyl-alpha-D-galactosamine/UDP-GalNAc transport from the cytosol to the lumen of the Golgi.

This gene encodes a transmembrane protein which belongs to subfamily 35A of the solute carrier superfamily. The encoded protein is a nucleoside-sugar transporter. Alternative splicing results in multiple transcript variants.

Source: NCBI Gene 55032 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 60 total
  • MANE Select transcript: NM_017945

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:20792
Approved symbolSLC35A5
Namesolute carrier family 35 member A5
Location3q13.2
Locus typegene with protein product
StatusApproved
AliasesFLJ20730
Ensembl geneENSG00000138459
Ensembl biotypeprotein_coding
OMIM620298
Entrez55032

Gene structure

Transcript identifiers

Ensembl transcripts: 21 — 18 protein_coding, 2 protein_coding_CDS_not_defined, 1 retained_intron

ENST00000261034, ENST00000460615, ENST00000460713, ENST00000468642, ENST00000484995, ENST00000492406, ENST00000494706, ENST00000890627, ENST00000890628, ENST00000890629, ENST00000890630, ENST00000890631, ENST00000890632, ENST00000890633, ENST00000931385, ENST00000931386, ENST00000931387, ENST00000931388, ENST00000931389, ENST00000959802, ENST00000959803

RefSeq mRNA: 8 — MANE Select: NM_017945 NM_001348905, NM_001348906, NM_001348907, NM_001348908, NM_001348909, NM_001348910, NM_001348911, NM_017945

CCDS: CCDS2967, CCDS87121

Canonical transcript exons

ENST00000492406 — 7 exons

ExonStartEnd
ENSE00001845623112562045112562273
ENSE00001955168112582671112585579
ENSE00002348060112563385112563533
ENSE00003559311112573889112573956
ENSE00003589242112570540112570670
ENSE00003639745112580546112581326
ENSE00003651242112569171112569269

Expression profiles

Bgee: expression breadth ubiquitous, 280 present calls, max score 94.80.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 25.6977 / max 592.0902, expressed in 1790 samples.

FANTOM5 promoters (4 alternative TSS)

Promoter IDTPM avgSamples expressed
3793011.40161725
3792910.96781748
379313.06361312
379320.264892

Top tissues by expression

289 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099194.80gold quality
corpus callosumUBERON:000233694.46gold quality
C1 segment of cervical spinal cordUBERON:000646994.35gold quality
spinal cordUBERON:000224094.08gold quality
adrenal tissueUBERON:001830393.85gold quality
cortical plateUBERON:000534393.52gold quality
ponsUBERON:000098893.28gold quality
islet of LangerhansUBERON:000000692.42gold quality
gall bladderUBERON:000211092.37gold quality
monocyteCL:000057692.36gold quality
mononuclear cellCL:000084292.09gold quality
leukocyteCL:000073891.92gold quality
rectumUBERON:000105291.92gold quality
subthalamic nucleusUBERON:000190691.90gold quality
calcaneal tendonUBERON:000370191.90gold quality
prefrontal cortexUBERON:000045191.74gold quality
inferior vagus X ganglionUBERON:000536391.69gold quality
ganglionic eminenceUBERON:000402391.63gold quality
oocyteCL:000002391.60gold quality
pigmented layer of retinaUBERON:000178290.87gold quality
retinaUBERON:000096690.85gold quality
superior vestibular nucleusUBERON:000722790.85gold quality
secondary oocyteCL:000065590.55gold quality
medulla oblongataUBERON:000189690.39gold quality
jejunal mucosaUBERON:000039990.14gold quality
Brodmann (1909) area 9UBERON:001354090.01gold quality
stromal cell of endometriumCL:000225589.98gold quality
placentaUBERON:000198789.97gold quality
ventricular zoneUBERON:000305389.92gold quality
substantia nigra pars compactaUBERON:000196589.72gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 2.

ExperimentMarker?Max mean expression
E-CURD-112yes7.29
E-ANND-3yes6.31

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

108 targeting SLC35A5, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-190A-3P100.0080.355520
HSA-MIR-30B-5P100.0076.293248
HSA-MIR-30C-5P100.0076.293248
HSA-MIR-30A-5P100.0076.313233
HSA-MIR-30D-5P100.0076.323233
HSA-MIR-30E-5P100.0076.323242
HSA-MIR-432-3P100.0067.86705
HSA-MIR-656-3P100.0072.152788
HSA-MIR-3646100.0073.565283
HSA-MIR-511-3P99.9968.851467
HSA-MIR-548AW99.9972.573559
HSA-MIR-485-3P99.9870.681585
HSA-MIR-539-3P99.9870.741616
HSA-MIR-4482-3P99.9872.503147
HSA-MIR-548N99.9871.944170
HSA-MIR-520D-5P99.9873.344883
HSA-MIR-524-5P99.9873.434882
HSA-MIR-1468-3P99.9672.743797
HSA-MIR-545-3P99.9570.742783
HSA-MIR-23A-3P99.9574.243163
HSA-MIR-23B-3P99.9574.243163
HSA-MIR-23C99.9573.923192
HSA-MIR-141-3P99.9472.792421
HSA-MIR-200A-3P99.9472.682420
HSA-MIR-144-3P99.9473.982698
HSA-MIR-381-3P99.9371.872854
HSA-MIR-515-5P99.9269.822343
HSA-MIR-519E-5P99.9269.622358
HSA-MIR-30099.9271.762856
HSA-MIR-205-3P99.9269.923165

Literature-anchored findings (GeneRIF, showing 1)

  • Study provide evidence suggesting that SLC35A5 might be the first mammalian nucleotide sugar transport (NST) engaged in the transport of three different UDP-sugars. It contains several diacidic motifs within its cytosolically exposed C-terminus, some of which might be capable of UDP-sugar binding. SLC35A5 protein might be a Golgi-resident multi-protein complex member engaged in NST. (PMID:30641943)

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
danio_rerioslc35a5ENSDARG00000000001
mus_musculusSlc35a5ENSMUSG00000022664
rattus_norvegicusSlc35a5ENSRNOG00000002069
drosophila_melanogastersenjuFBGN0031676

Paralogs (4): SLC35A2 (ENSG00000102100), SLC35A3 (ENSG00000117620), SLC35A1 (ENSG00000164414), SLC35A4 (ENSG00000176087)

Protein

Protein identifiers

UDP-sugar transporter protein SLC35A5Q9BS91 (reviewed: Q9BS91)

Alternative names: Solute carrier family 35 member A5

All UniProt accessions (4): C9J7U8, C9JXZ8, Q9BS91, H7BXF8

UniProt curated annotations — full annotation on UniProt →

Function. Probable UDP-sugar:UMP transmembrane antiporter involved in UDP-alpha-D-glucuronate/UDP-GlcA, UDP-GlcNAc/UDP-N-acetyl-alpha-D-glucosamine and UDP-N-acetyl-alpha-D-galactosamine/UDP-GalNAc transport from the cytosol to the lumen of the Golgi.

Subunit / interactions. Probably forms homooligomers and heterooligomers with SLC35A1, SLC35A2, SLC35A3 and SLC35A4.

Subcellular location. Golgi apparatus membrane.

Similarity. Belongs to the nucleotide-sugar transporter family. SLC35A subfamily.

RefSeq proteins (8): NP_001335834, NP_001335835, NP_001335836, NP_001335837, NP_001335838, NP_001335839, NP_001335840, NP_060415* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR007271Nuc_sug_transptFamily
IPR037185EmrE-likeHomologous_superfamily

Pfam: PF04142

Catalyzed reactions (Rhea), 3 shown:

  • UMP(out) + UDP-N-acetyl-alpha-D-glucosamine(in) = UMP(in) + UDP-N-acetyl-alpha-D-glucosamine(out) (RHEA:72695)
  • UMP(out) + UDP-alpha-D-glucuronate(in) = UMP(in) + UDP-alpha-D-glucuronate(out) (RHEA:72727)
  • UDP-N-acetyl-alpha-D-galactosamine(in) + UMP(out) = UDP-N-acetyl-alpha-D-galactosamine(out) + UMP(in) (RHEA:72735)

UniProt features (29 total): topological domain 11, transmembrane region 10, modified residue 3, chain 1, region of interest 1, compositionally biased region 1, glycosylation site 1, sequence variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9BS91-F176.540.38

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Post-translational modifications (3): 394, 416, 419

Glycosylation sites (1): 204

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 146 (showing top): GSE18804_BRAIN_VS_COLON_TUMORAL_MACROPHAGE_UP, TGCGCANK_UNKNOWN, GRAESSMANN_APOPTOSIS_BY_DOXORUBICIN_UP, GRAESSMANN_RESPONSE_TO_MC_AND_DOXORUBICIN_UP, GOBP_ORGANOPHOSPHATE_ESTER_TRANSPORT, GOMF_NUCLEOBASE_CONTAINING_COMPOUND_TRANSMEMBRANE_TRANSPORTER_ACTIVITY, GOBP_NUCLEOBASE_CONTAINING_COMPOUND_TRANSPORT, SCHAEFFER_PROSTATE_DEVELOPMENT_6HR_UP, CUI_TCF21_TARGETS_2_DN, MODULE_95, GOBP_CARBOHYDRATE_DERIVATIVE_TRANSPORT, GOBP_TRANSMEMBRANE_TRANSPORT, BALDWIN_PRKCI_TARGETS_UP, SCGGAAGY_ELK1_02, ARNT_01

GO Biological Process (2): transmembrane transport (GO:0055085), pyrimidine nucleotide-sugar transmembrane transport (GO:0090481)

GO Molecular Function (4): pyrimidine nucleotide-sugar transmembrane transporter activity (GO:0015165), antiporter activity (GO:0015297), transmembrane transporter activity (GO:0022857), protein binding (GO:0005515)

GO Cellular Component (3): Golgi membrane (GO:0000139), Golgi apparatus (GO:0005794), membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
transport1
cellular process1
nucleotide-sugar transmembrane transport1
nucleotide-sugar transmembrane transporter activity1
pyrimidine nucleotide-sugar transmembrane transport1
secondary active transmembrane transporter activity1
transporter activity1
transmembrane transport1
binding1
Golgi apparatus1
bounding membrane of organelle1
cytoplasm1
endomembrane system1
intracellular membrane-bounded organelle1
cellular anatomical structure1

Protein interactions and networks

STRING

974 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
SLC35A5SLC35B4Q969S0673
SLC35A5SLC35C1Q96A29605
SLC35A5SLC35D3Q5M8T2586
SLC35A5SLC35B1P78383583
SLC35A5SLC35B3Q9H1N7582
SLC35A5SLC35D2Q76EJ3576
SLC35A5SLC35H1Q9NQQ7570
SLC35A5SLC35D1Q9NTN3560
SLC35A5SLC35E1Q96K37548
SLC35A5SLC35F1Q5T1Q4543
SLC35A5ITM2CQ9NQX7525
SLC35A5SLC4A5Q9BY07508
SLC35A5SLC33A1O00400507
SLC35A5SLC30A3Q99726470
SLC35A5SYS1Q8N2H4451

IntAct

22 interactions, top by confidence:

ABTypeScore
SLC35A5TNKSpsi-mi:“MI:0914”(association)0.640
TMEM72SLC35A5psi-mi:“MI:0915”(physical association)0.560
SLC35A5TMEM100psi-mi:“MI:0915”(physical association)0.560
FKBP8SLC35A5psi-mi:“MI:0915”(physical association)0.560
SLC35A5SACM1Lpsi-mi:“MI:0915”(physical association)0.560
SLC35A5ACTL6Bpsi-mi:“MI:0914”(association)0.530
SLC35A5HNRNPUpsi-mi:“MI:0915”(physical association)0.400
SLC35A5psi-mi:“MI:0915”(physical association)0.370
LGALS8SLC22A23psi-mi:“MI:0914”(association)0.350
CANXHLA-Apsi-mi:“MI:0914”(association)0.350
SLC35A5CLGNpsi-mi:“MI:0914”(association)0.350
TMEM100SLC35A5psi-mi:“MI:0915”(physical association)0.000
FKBP8SLC35A5psi-mi:“MI:0915”(physical association)0.000
SACM1LSLC35A5psi-mi:“MI:0915”(physical association)0.000

BioGRID (68): SLC35A5 (Affinity Capture-MS), MBOAT7 (Affinity Capture-MS), TNKS2 (Affinity Capture-MS), TNKS (Affinity Capture-MS), CSGALNACT2 (Affinity Capture-MS), SLC41A1 (Affinity Capture-MS), RHOB (Affinity Capture-MS), TNKS2 (Affinity Capture-MS), TNKS (Affinity Capture-MS), CSGALNACT2 (Affinity Capture-MS), SLC35A5 (Affinity Capture-MS), MBOAT7 (Affinity Capture-MS), ACTL6B (Affinity Capture-MS), SLC35A5 (Two-hybrid), TMEM100 (Two-hybrid)

ESM2 similar proteins: A1L272, A2RV80, A4IF30, A6QL92, A6QPI1, O02777, O80605, P17200, P20272, P21554, P47746, P51810, P56971, P70259, Q1LZI2, Q2V4F9, Q3TDN0, Q3UGM2, Q4R794, Q5F383, Q5FVJ3, Q5IS73, Q5R4D7, Q5R6J3, Q5RD30, Q66H88, Q6P0E8, Q6P499, Q6R5J2, Q71SP5, Q8BGN5, Q8BZK4, Q8CBH5, Q8IY50, Q8NA31, Q8NBV4, Q8R314, Q8RWF4, Q8WV83, Q91WB2

Diamond homologs: A6QPI1, Q5R4D7, Q6DCG9, Q90X48, Q921R7, Q9BS91

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

60 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance50
Likely benign3
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1230 predictions. Top by Δscore:

VariantEffectΔscore
3:112561451:GCTTA:Gdonor_loss1.0000
3:112561452:CTTA:Cdonor_loss1.0000
3:112561453:TTA:Tdonor_loss1.0000
3:112561454:TACCT:Tdonor_loss1.0000
3:112561455:ACCT:Adonor_loss1.0000
3:112561456:C:Gdonor_loss1.0000
3:112569265:GAAAG:Gdonor_gain1.0000
3:112570538:A:Gacceptor_gain1.0000
3:112573883:TTCTA:Tacceptor_loss1.0000
3:112573884:TCTA:Tacceptor_loss1.0000
3:112573886:TAGGC:Tacceptor_loss1.0000
3:112573887:A:AGacceptor_gain1.0000
3:112573888:G:GGacceptor_gain1.0000
3:112573888:G:GTacceptor_loss1.0000
3:112573888:GGCC:Gacceptor_gain1.0000
3:112573954:GAA:Gdonor_gain1.0000
3:112573955:AAGTA:Adonor_loss1.0000
3:112573956:AGT:Adonor_loss1.0000
3:112573957:G:Cdonor_loss1.0000
3:112573957:G:GGdonor_gain1.0000
3:112573958:TA:Tdonor_loss1.0000
3:112573959:AA:Adonor_loss1.0000
3:112575216:G:GTdonor_gain1.0000
3:112562094:G:GTdonor_gain0.9900
3:112562271:G:GTdonor_gain0.9900
3:112562271:G:Tdonor_gain0.9900
3:112569164:ATTTC:Aacceptor_loss0.9900
3:112569165:TTTCA:Tacceptor_loss0.9900
3:112569166:TTCAG:Tacceptor_loss0.9900
3:112569167:TCAGA:Tacceptor_loss0.9900

AlphaMissense

2815 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
3:112569226:G:CK62N0.994
3:112569226:G:TK62N0.994
3:112581066:G:CG317R0.994
3:112581088:T:CL324P0.993
3:112570599:T:AW97R0.991
3:112570599:T:CW97R0.991
3:112580921:C:AN268K0.991
3:112580921:C:GN268K0.991
3:112581058:C:AA314E0.990
3:112563501:G:CR33P0.989
3:112570612:C:AA101D0.989
3:112570634:C:AN108K0.988
3:112570634:C:GN108K0.988
3:112581079:C:AA321D0.988
3:112569236:T:CC66R0.987
3:112581093:T:CF326L0.987
3:112581095:C:AF326L0.987
3:112581095:C:GF326L0.987
3:112569224:A:GK62E0.986
3:112570609:C:AP100H0.985
3:112581067:G:AG317D0.985
3:112581070:T:CL318P0.985
3:112580835:T:CC240R0.984
3:112580854:C:AA246D0.984
3:112580878:T:CL254P0.984
3:112570644:T:CF112L0.983
3:112570646:C:AF112L0.983
3:112570646:C:GF112L0.983
3:112580922:A:CS269R0.983
3:112580924:C:AS269R0.983

dbSNP variants (sampled 300 via entrez): RS1000096201 (3:112575513 T>G), RS1000101588 (3:112569400 G>A,T), RS1000164128 (3:112580079 G>A), RS1000365234 (3:112570430 C>A,T), RS1000470889 (3:112567576 A>T), RS1000598261 (3:112560717 A>G), RS1000697268 (3:112574080 T>A,C), RS1000796935 (3:112580370 CATTAA>C), RS1000829358 (3:112565115 T>C), RS1001361266 (3:112567013 T>C,G), RS1001484058 (3:112566499 A>G), RS1001487115 (3:112570026 G>C), RS1001762727 (3:112581784 G>A), RS1001847857 (3:112560140 A>G), RS1001877641 (3:112559967 T>C)

Disease associations

OMIM: gene MIM:620298 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

GtoPdb / IUPHAR curated pharmacology

(IUPHAR/BPS Guide to Pharmacology — expert-curated)

Target class: transporter — SLC35 family of nucleotide sugar transporters

CTD chemical–gene interactions

26 total (human), top 26 by PubMed support.

ChemicalActions (top 5)PubMed papers
Cadmium Chloridedecreases expression, increases abundance, increases expression2
FR900359affects phosphorylation1
dicrotophosdecreases expression1
arseniteaffects binding, increases reaction1
potassium chromate(VI)affects cotreatment, decreases expression1
epigallocatechin gallateaffects cotreatment, decreases expression1
polyhexamethyleneguanidineaffects expression1
deguelindecreases expression1
K 7174increases expression1
fenpyroximatedecreases expression1
4-chloro-N-((4-(1,1-dimethylethyl)phenyl)methyl)-3-ethyl-1-methyl-1H-pyrazole-5-carboxamidedecreases expression1
abrinedecreases expression1
Air Pollutantsdecreases expression, increases abundance1
Air Pollutants, Occupationaldecreases expression1
Antimycin Adecreases expression1
Cadmiumincreases abundance, increases expression1
Caffeinedecreases phosphorylation1
Doxorubicindecreases expression1
Nickeldecreases expression1
Tetrachlorodibenzodioxindecreases expression1
Tobacco Smoke Pollutiondecreases expression1
Urethaneincreases expression1
Zincincreases expression1
Aflatoxin B1decreases methylation1
Copper Sulfatedecreases expression1
Particulate Matterdecreases expression, increases abundance1

Cellosaurus cell lines

5 cell lines: 5 cancer cell line

First 10 cell lines (id-ordered, not curated):

CellosaurusNameCategorySex
CVCL_B2FZAbcam HeLa SLC35A5 KOCancer cell lineFemale
CVCL_D4LZHCT116-SLC35A5-KO-c1Cancer cell lineMale
CVCL_D4M0HCT116-SLC35A5-KO-c9Cancer cell lineMale
CVCL_TN08HAP1 SLC35A5 (-) 1Cancer cell lineMale
CVCL_TN09HAP1 SLC35A5 (-) 2Cancer cell lineMale

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.