CD302

gene
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Also known as DCL-1KIAA0022BIMLECCLEC13A

Summary

CD302 (CD302 molecule, HGNC:30843) is a protein-coding gene on chromosome 2q24.2, encoding CD302 antigen (Q8IX05). Multifunctional C-type lectin receptor involved in endocytosis, phagocytosis and regulation of cell adhesion and migration.

CD302 is a C-type lectin receptor involved in cell adhesion and migration, as well as endocytosis and phagocytosis (Kato et al., 2007 [PubMed 17947679]).

Source: NCBI Gene 9936 — RefSeq curated summary.

At a glance

  • GWAS associations: 3
  • Clinical variants (ClinVar): 10 total
  • MANE Select transcript: NM_014880

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:30843
Approved symbolCD302
NameCD302 molecule
Location2q24.2
Locus typegene with protein product
StatusApproved
AliasesDCL-1, KIAA0022, BIMLEC, CLEC13A
Ensembl geneENSG00000241399
Ensembl biotypeprotein_coding
OMIM612246
Entrez9936

Gene structure

Transcript identifiers

Ensembl transcripts: 13 — 12 protein_coding, 1 protein_coding_CDS_not_defined

ENST00000259053, ENST00000429078, ENST00000480212, ENST00000553424, ENST00000856855, ENST00000856856, ENST00000856857, ENST00000856858, ENST00000856859, ENST00000856860, ENST00000856861, ENST00000966882, ENST00000966883

RefSeq mRNA: 3 — MANE Select: NM_014880 NM_001198763, NM_001198764, NM_014880

CCDS: CCDS33308, CCDS56139, CCDS74595

Canonical transcript exons

ENST00000259053 — 6 exons

ExonStartEnd
ENSE00003482872159783359159783469
ENSE00003560104159768628159772053
ENSE00003657339159798132159798208
ENSE00003730131159777938159777964
ENSE00003735029159780005159780178
ENSE00003743188159780882159780998

Expression profiles

Bgee: expression breadth ubiquitous, 279 present calls, max score 97.76.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 23.8494 / max 627.3352, expressed in 1477 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
3145418.72211411
314554.92531131
314560.202085

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
lower lobe of lungUBERON:000894997.76gold quality
monocyteCL:000057697.72gold quality
mononuclear cellCL:000084297.71gold quality
leukocyteCL:000073897.35gold quality
right lungUBERON:000216797.02gold quality
liverUBERON:000210796.54gold quality
synovial jointUBERON:000221796.24gold quality
trabecular bone tissueUBERON:000248396.21gold quality
layer of synovial tissueUBERON:000761695.57gold quality
right lobe of liverUBERON:000111495.37gold quality
calcaneal tendonUBERON:000370195.34gold quality
superficial temporal arteryUBERON:000161495.31gold quality
urethraUBERON:000005795.22gold quality
mammary ductUBERON:000176594.99gold quality
skin of hipUBERON:000155494.80gold quality
right coronary arteryUBERON:000162594.20gold quality
deciduaUBERON:000245093.98gold quality
pericardiumUBERON:000240793.95gold quality
epithelium of mammary glandUBERON:000324493.88gold quality
jejunal mucosaUBERON:000039993.65gold quality
lungUBERON:000204893.53gold quality
pigmented layer of retinaUBERON:000178293.52gold quality
blood vessel layerUBERON:000479793.46gold quality
thoracic mammary glandUBERON:000520093.44gold quality
pleuraUBERON:000097793.32gold quality
mammary glandUBERON:000191193.24gold quality
parietal pleuraUBERON:000240093.24gold quality
visceral pleuraUBERON:000240193.24gold quality
adipose tissueUBERON:000101393.08gold quality
gall bladderUBERON:000211093.06gold quality

Single-cell (SCXA)

Detected in 8 experiment(s), a significant marker in 8.

ExperimentMarker?Max mean expression
E-CURD-46yes33.68
E-MTAB-9221yes28.53
E-GEOD-134144yes26.30
E-HCAD-10yes26.04
E-CURD-112yes24.96
E-CURD-88yes20.61
E-ANND-3yes14.37
E-MTAB-9467yes11.66

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

149 targeting CD302, 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-5011-5P100.0083.465820
HSA-MIR-3163100.0077.238605
HSA-MIR-4262100.0073.263931
HSA-MIR-1252-5P100.0069.802774
HSA-MIR-340-5P100.0072.504437
HSA-MIR-190A-3P100.0080.355520
HSA-MIR-5692B100.0071.322622
HSA-MIR-5692C100.0071.322622
HSA-MIR-6867-5P100.0082.213464
HSA-MIR-518D-5P100.0067.51979
HSA-MIR-518E-5P100.0067.66954
HSA-MIR-518F-5P100.0067.51979
HSA-MIR-519A-5P100.0067.66954
HSA-MIR-519B-5P100.0067.66954
HSA-MIR-519C-5P100.0067.66954
HSA-MIR-520C-5P100.0067.51979
HSA-MIR-522-5P100.0067.66954
HSA-MIR-523-5P100.0067.66954
HSA-MIR-526A-5P100.0067.51979
HSA-MIR-513A-5P100.0069.772465
HSA-MIR-1277-5P100.0073.955056
HSA-MIR-428299.9975.366408
HSA-MIR-181A-5P99.9972.962995
HSA-MIR-181B-5P99.9972.972996
HSA-MIR-181C-5P99.9972.952996
HSA-MIR-181D-5P99.9973.042997
HSA-MIR-520G-5P99.9966.76658
HSA-MIR-186-5P99.9970.833707
HSA-MIR-548P99.9872.253784
HSA-MIR-548N99.9871.944170

Literature-anchored findings (GeneRIF, showing 6)

  • Hodgkin’s lymphoma cell lines express a fusion protein encoded by intergenically spliced mRNA for the multilectin receptor DEC-205 (CD205) and a novel C-type lectin receptor DCL-1 (PMID:12824192)
  • hDCL-1 is an unconventional lectin receptor that plays roles not only in endocytosis/phagocytosis but also in cell adhesion and migration (PMID:17947679)
  • DLC1 equilibrium unfolding is characterized at the amino acid level. (PMID:19317456)
  • These studies confirm a functional role for CD302 in myeloid dendritic cells migration. (PMID:27316686)
  • Particle Morphology of Medusavirus Inside and Outside the Cells Reveals a New Maturation Process of Giant Viruses. (PMID:35297671)
  • The Human Liver-Expressed Lectin CD302 Restricts Hepatitis C Virus Infection. (PMID:35297672)

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
danio_reriocd302ENSDARG00000086100
mus_musculusCd302ENSMUSG00000060703
rattus_norvegicusCd302ENSRNOG00000006623
caenorhabditis_elegansWBGENE00010228

Paralogs (4): MRC2 (ENSG00000011028), LY75 (ENSG00000054219), PLA2R1 (ENSG00000153246), MRC1 (ENSG00000260314)

Protein

Protein identifiers

CD302 antigenQ8IX05 (reviewed: Q8IX05)

Alternative names: C-type lectin BIMLEC, C-type lectin domain family 13 member A, DEC205-associated C-type lectin 1, Type I transmembrane C-type lectin receptor DCL-1

All UniProt accessions (2): Q8IX05, A0A087WT00

UniProt curated annotations — full annotation on UniProt →

Function. Multifunctional C-type lectin receptor involved in endocytosis, phagocytosis and regulation of cell adhesion and migration. Plays a critical role in guiding dendritic cells to lymph nodes. Also functions as a restriction factor for Hepatitis C virus (HCV) at the liver cell surface, likely by inhibiting a viral cell entry step.

Subcellular location. Cell membrane. Cell projection. Filopodium. Cytoplasm. Cell cortex. Microvillus.

Tissue specificity. Expressed at moderate levels in monocytes, myeloid blood dendritic cells and granulocytes and at low levels in plasmacytoid blood dendritic cells, monocyte-derived macrophages and monocyte-derived dendritic cells, with no expression detected in T-lymphocytes, B-lymphocytes and natural killer cells (at protein level). Expressed widely in different tissues, with highest expression levels in liver, lung, peripheral blood leukocytes and spleen, and lowest levels in neuronal tissues, skeletal muscle and ovary. Isoform 2 and isoform 3 are expressed in malignant Hodgkin lymphoma cells called Hodgkin and Reed-Sternberg (HRS) cells.

Post-translational modifications. May be heterogeneously N-glycosylated in some cell types.

Miscellaneous. Isoform 2 and isoform 3 are produced in HRS cells by a transcriptional control mechanism which cotranscribe an mRNA containing LY75 and CD302 prior to generating the intergenically spliced mRNA to produce LY75/CD302 fusion proteins. Produced by intergenic splicing of LY75 and CD302.

Isoforms (5)

UniProt IDNamesCanonical?
Q8IX05-11yes
O60449-14
Q8IX05-25
O60449-22, Fusion protein variant V34-2
O60449-33, Fusion protein variant V33-2

RefSeq proteins (3): NP_001185692, NP_001185693, NP_055695* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001304C-type_lectin-likeDomain
IPR016186C-type_lectin-like/link_sfHomologous_superfamily
IPR016187CTDL_foldHomologous_superfamily
IPR050111C-type_lectin/snaclec_domainFamily

Pfam: PF00059

UniProt features (25 total): strand 8, turn 3, helix 2, topological domain 2, splice variant 2, signal peptide 1, chain 1, sequence variant 1, sequence conflict 1, transmembrane region 1, domain 1, glycosylation site 1, disulfide bond 1

Structure

Experimental structures (PDB)

1 structures.

PDBMethodResolution (Å)
2NANSOLUTION NMR

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8IX05-F180.530.50

Functional residue map

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

Disulfide bonds (1): 128–143

Glycosylation sites (1): 109

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 215 (showing top): BUYTAERT_PHOTODYNAMIC_THERAPY_STRESS_DN, MODULE_45, GOBP_VESICLE_MEDIATED_TRANSPORT, LINDGREN_BLADDER_CANCER_CLUSTER_2A_DN, GNF2_MCL1, GNF2_CD1D, KOYAMA_SEMA3B_TARGETS_UP, HOSHIDA_LIVER_CANCER_SUBCLASS_S3, chr2q24, SANSOM_APC_TARGETS_DN, GNF2_HCK, BASAKI_YBX1_TARGETS_DN, VECCHI_GASTRIC_CANCER_EARLY_DN, GOBP_IMPORT_INTO_CELL, RIGGINS_TAMOXIFEN_RESISTANCE_DN

GO Biological Process (1): phagocytosis (GO:0006909)

GO Molecular Function (3): carbohydrate binding (GO:0030246), signaling receptor activity (GO:0038023), protein binding (GO:0005515)

GO Cellular Component (6): microvillus (GO:0005902), cell cortex (GO:0005938), membrane (GO:0016020), filopodium (GO:0030175), cytoplasm (GO:0005737), cell projection (GO:0042995)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cellular anatomical structure3
binding2
actin-based cell projection2
endocytosis1
molecular transducer activity1
actin filament bundle1
cytoplasm1
cell periphery1
intracellular anatomical structure1

Protein interactions and networks

STRING

612 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
CD302AGO1Q9UL18785
CD302DICER1Q9UPY3723
CD302SRRTQ9BXP5670
CD302MILR1Q7Z6M3571
CD302DROSHAQ9NRR4546
CD302PIWIL4Q7Z3Z4512
CD302AGO4Q9HCK5510
CD302PIWIL1Q96J94507
CD302LY75O60449500
CD302SNRPD3P43331443
CD302AGO2Q9UKV8409
CD302CX3CL1P78423408
CD302HSPB8Q9UJY1392
CD302SLC27A3Q5K4L6384
CD302SEC14L2O76054379

IntAct

33 interactions, top by confidence:

ABTypeScore
CD302IL7Rpsi-mi:“MI:0915”(physical association)0.560
CD302IL10RApsi-mi:“MI:0915”(physical association)0.560
CD302FNDC9psi-mi:“MI:0915”(physical association)0.560
CD302ERGIC3psi-mi:“MI:0915”(physical association)0.560
IL7RCD302psi-mi:“MI:0915”(physical association)0.560
IL10RACD302psi-mi:“MI:0915”(physical association)0.560
CD53CD302psi-mi:“MI:0915”(physical association)0.560
OPRM1CD302psi-mi:“MI:0915”(physical association)0.560
IFNGR2CD302psi-mi:“MI:0915”(physical association)0.560
CD302GPX8psi-mi:“MI:0915”(physical association)0.560
GET1CD302psi-mi:“MI:0915”(physical association)0.560
ARL13BCD302psi-mi:“MI:0915”(physical association)0.560
METTL3TUBAL3psi-mi:“MI:0914”(association)0.350
FAM171A2psi-mi:“MI:0914”(association)0.350
CD302ERGIC3psi-mi:“MI:0915”(physical association)0.000
CD302CD53psi-mi:“MI:0915”(physical association)0.000
CD302OPRM1psi-mi:“MI:0915”(physical association)0.000
CD302IFNGR2psi-mi:“MI:0915”(physical association)0.000
CD302GPX8psi-mi:“MI:0915”(physical association)0.000
CD302ARL13Bpsi-mi:“MI:0915”(physical association)0.000
CD302GET1psi-mi:“MI:0915”(physical association)0.000

BioGRID (12): FATE1 (Two-hybrid), CD302 (Affinity Capture-MS), CD302 (Two-hybrid), CD302 (Two-hybrid), CD302 (Two-hybrid), CD302 (Two-hybrid), CD302 (Two-hybrid), CD302 (Two-hybrid), CD302 (Two-hybrid), CD302 (Affinity Capture-MS), CD302 (Affinity Capture-MS), CD302 (Affinity Capture-Western)

ESM2 similar proteins: A0A7H0DND3, A1XRN2, A8WH72, A8WH74, A8WH75, A8WUV1, B1A4M7, B1A4N2, B1A4N8, B1A4P2, B1A4P6, B1A4P7, B1A4P8, B1A4P9, B1A4Q0, B1A4Q2, B1A4Q3, B1A4Q5, B1A4Q6, B1A4Q8, B1A4Q9, B1A4R0, B1A4R4, B2D1Y0, O55159, P0DQP8, P10721, P16234, P21057, P21755, P21756, P24761, P24765, P26618, P26619, P33851, Q16YE7, Q1L867, Q3T0L5, Q5FVR3

Diamond homologs: A8WH72, A8WH74, A8WH75, Q02988, Q5FVR3, Q8IX05, Q9DCG2, O45824, P49260, Q60767, Q91ZX1, Q9PSM5

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance8
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

846 predictions. Top by Δscore:

VariantEffectΔscore
2:159777933:CTTA:Cdonor_loss1.0000
2:159777934:TTA:Tdonor_loss1.0000
2:159777935:TA:Tdonor_loss1.0000
2:159777936:A:Tdonor_loss1.0000
2:159777937:C:CGdonor_loss1.0000
2:159777961:GGGA:Gacceptor_gain1.0000
2:159777965:C:CCacceptor_gain1.0000
2:159779999:ACTT:Adonor_loss1.0000
2:159780001:TT:Tdonor_loss1.0000
2:159780001:TTA:Tdonor_loss1.0000
2:159780002:TA:Tdonor_loss1.0000
2:159780003:A:ACdonor_gain1.0000
2:159780003:A:Tdonor_loss1.0000
2:159780003:ACTAG:Adonor_gain1.0000
2:159780004:C:CAdonor_loss1.0000
2:159780004:C:CCdonor_gain1.0000
2:159780004:CT:Cdonor_gain1.0000
2:159780004:CTA:Cdonor_gain1.0000
2:159780004:CTAG:Cdonor_gain1.0000
2:159780004:CTAGC:Cdonor_gain1.0000
2:159780878:TTA:Tdonor_loss1.0000
2:159780879:TA:Tdonor_loss1.0000
2:159780880:A:ACdonor_gain1.0000
2:159780880:A:Tdonor_loss1.0000
2:159780880:AC:Adonor_gain1.0000
2:159780880:ACCAT:Adonor_gain1.0000
2:159780881:C:CCdonor_gain1.0000
2:159780881:C:CGdonor_loss1.0000
2:159780881:C:CTdonor_loss1.0000
2:159780881:CC:Cdonor_gain1.0000

AlphaMissense

1538 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
2:159780060:C:AW138C0.998
2:159780060:C:GW138C0.998
2:159780162:C:AW104C0.997
2:159780162:C:GW104C0.997
2:159780062:A:GW138R0.996
2:159780062:A:TW138R0.996
2:159780016:C:GC153S0.993
2:159780017:A:TC153S0.993
2:159780164:A:GW104R0.993
2:159780164:A:TW104R0.993
2:159783370:C:GC56S0.992
2:159783371:A:TC56S0.992
2:159783371:A:GC56R0.988
2:159780129:C:AW115C0.987
2:159780129:C:GW115C0.987
2:159780980:A:TI66K0.987
2:159783369:A:CC56W0.986
2:159780017:A:GC153R0.985
2:159780015:G:CC153W0.984
2:159780016:C:TC153Y0.982
2:159780061:C:GW138S0.982
2:159780092:A:GC128R0.982
2:159780046:C:GC143S0.981
2:159780047:A:TC143S0.981
2:159780091:C:GC128S0.979
2:159780092:A:TC128S0.979
2:159780980:A:CI66R0.979
2:159780982:G:CS65R0.979
2:159780982:G:TS65R0.979
2:159780984:T:GS65R0.979

dbSNP variants (sampled 300 via entrez): RS1000026673 (2:159789003 T>C), RS1000071193 (2:159777069 T>C,G), RS1000242066 (2:159775900 T>G), RS1000250223 (2:159782567 TACAA>T), RS1000352494 (2:159769754 C>T), RS1000403869 (2:159782440 G>A,C,T), RS1000549648 (2:159795222 CG>C,CGG), RS1000561141 (2:159784013 A>G), RS1000579684 (2:159777137 G>A,C), RS1000655401 (2:159787903 G>C), RS1000822467 (2:159771409 A>G), RS1000891579 (2:159769955 T>C,G), RS1000962225 (2:159775736 C>A), RS1001046313 (2:159795686 A>C), RS1001086571 (2:159771038 A>C)

Disease associations

OMIM: gene MIM:612246 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

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

GWAS associations

3 associations (top):

StudyTraitp-value
GCST007277_3Tourette syndrome2.000000e-07
GCST009391_1633Metabolite levels9.000000e-07
GCST012490_496Femur bone mineral density x serum urate levels interaction2.000000e-08

EFO canonical traits (2, from GWAS)

EFO IDTrait name
EFO:0007787plasma betaine measurement
EFO:0004531urate measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

45 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidaffects cotreatment, increases expression, affects expression9
bisphenol Aincreases expression, affects cotreatment2
Dexamethasoneincreases expression, affects cotreatment2
Cyclosporinedecreases expression2
aristolochic acid Idecreases expression1
bisphenol Faffects cotreatment, increases expression1
quercitrindecreases expression1
terbufosincreases methylation1
trichostatin Aincreases expression1
tris(1,3-dichloro-2-propyl)phosphatedecreases expression1
di-n-butylphosphoric acidaffects expression1
CGP 52608affects binding, increases reaction1
entinostatincreases expression1
monomethylarsonous acidincreases expression1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideincreases expression, affects cotreatment1
dorsomorphinaffects cotreatment, increases expression1
jinfukangaffects cotreatment, increases expression1
NSC 689534affects binding, decreases expression1
Dasatinibincreases expression1
Acetaminophendecreases expression1
Air Pollutantsaffects expression, increases abundance1
Benzo(a)pyrenedecreases expression1
Bilirubindecreases expression1
Cadmiumincreases expression1
Cisplatinaffects cotreatment, increases expression1
Copperaffects binding, decreases expression1
Doxorubicindecreases expression1
Fonofosincreases methylation1
Ethyl Methanesulfonatedecreases expression1
Formaldehydedecreases expression1

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.