SIGLECL1

gene
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Also known as FLJ40235

Summary

SIGLECL1 (SIGLEC family like 1, HGNC:26856) is a protein-coding gene on chromosome 19q13.41, encoding SIGLEC family-like protein 1 (Q8N7X8).

Predicted to be located in membrane.

Source: NCBI Gene 284369 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 27 total
  • MANE Select transcript: NM_001385465

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:26856
Approved symbolSIGLECL1
NameSIGLEC family like 1
Location19q13.41
Locus typegene with protein product
StatusApproved
AliasesFLJ40235
Ensembl geneENSG00000179213
Ensembl biotypeprotein_coding
Entrez284369

Gene structure

Transcript identifiers

Ensembl transcripts: 8 — 6 protein_coding, 2 protein_coding_CDS_not_defined

ENST00000316401, ENST00000593968, ENST00000596117, ENST00000597610, ENST00000597824, ENST00000599553, ENST00000601727, ENST00000614422

RefSeq mRNA: 5 — MANE Select: NM_001385465 NM_001308437, NM_001385465, NM_001385466, NM_001385467, NM_173635

CCDS: CCDS12827, CCDS77341

Canonical transcript exons

ENST00000601727 — 6 exons

ExonStartEnd
ENSE000012555235126536851265649
ENSE000013646865126857151269330
ENSE000014173155126388351264094
ENSE000034779755126577751265882
ENSE000036765595126737351267529
ENSE000039307895125108051251545

Expression profiles

Bgee: expression breadth broad, 53 present calls, max score 93.93.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.0601 / max 36.0868, expressed in 10 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
1772070.03494
1772080.01678
1772090.00863

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
spermCL:000001993.93gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099189.91gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047386.17gold quality
left testisUBERON:000453384.65gold quality
right testisUBERON:000453482.91gold quality
testisUBERON:000047382.61gold quality
adult organismUBERON:000702380.24gold quality
monocyteCL:000057651.39gold quality
leukocyteCL:000073850.03gold quality
sural nerveUBERON:001548848.62silver quality
upper leg skinUBERON:000426243.50silver quality
skeletal muscle tissue of rectus abdominisUBERON:000451143.37gold quality
granulocyteCL:000009442.98silver quality
secondary oocyteCL:000065542.57gold quality
cortical plateUBERON:000534341.77gold quality
epithelium of nasopharynxUBERON:000195141.70gold quality
spleenUBERON:000210641.56silver quality
vastus lateralisUBERON:000137941.41gold quality
quadriceps femorisUBERON:000137741.37gold quality
bloodUBERON:000017841.34gold quality
superficial temporal arteryUBERON:000161441.33gold quality
palpebral conjunctivaUBERON:000181241.10gold quality
mucosa of stomachUBERON:000119941.04silver quality
mucosa of paranasal sinusUBERON:000503040.98gold quality
amniotic fluidUBERON:000017340.69gold quality
jejunal mucosaUBERON:000039940.59gold quality
biceps brachiiUBERON:000150740.57gold quality
myocardiumUBERON:000234940.45gold quality
gingival epitheliumUBERON:000194940.43gold quality
germinal epithelium of ovaryUBERON:000130440.33gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-ANND-3yes3.28

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

29 targeting SIGLECL1, 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-453199.9969.703181
HSA-MIR-196A-1-3P99.9972.152772
HSA-MIR-548N99.9871.944170
HSA-MIR-520D-5P99.9873.344883
HSA-MIR-524-5P99.9873.434882
HSA-MIR-3065-5P99.9771.563281
HSA-MIR-3529-3P99.9073.553045
HSA-MIR-465899.7764.94514
HSA-MIR-6790-5P99.7765.24505
HSA-MIR-467999.7669.191229
HSA-MIR-365999.7067.97694
HSA-MIR-451699.6167.783390
HSA-MIR-4677-3P99.4967.911246
HSA-MIR-488-5P99.2868.12821
HSA-MIR-4685-5P99.2565.991563
HSA-MIR-6837-5P99.2565.471632
HSA-MIR-806599.1970.381289
HSA-MIR-155-3P99.0367.99924
HSA-MIR-570198.9769.541502
HSA-MIR-6868-3P98.6369.642259
HSA-MIR-6776-5P98.5467.431304
HSA-MIR-4662A-5P98.4867.181007
HSA-MIR-138-5P98.4370.491292
HSA-MIR-7113-5P97.8867.331735
HSA-MIR-127997.8367.501898
HSA-MIR-447597.3666.95761
HSA-MIR-6892-5P97.2768.60847
HSA-MIR-7161-3P96.7968.79798
HSA-MIR-365586.1161.77117

Literature-anchored findings (GeneRIF, showing 1)

  • CD33 and SIGLECL1 Immunoglobulin Superfamily Involved in Dementia. (PMID:32647856)

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusSiglecl1ENSMUSG00000108695
rattus_norvegicusSiglecl1ENSRNOG00000059992

Paralogs (16): CD22 (ENSG00000012124), SIGLEC1 (ENSG00000088827), SIGLEC8 (ENSG00000105366), CD33 (ENSG00000105383), SIGLEC6 (ENSG00000105492), MAG (ENSG00000105695), SIGLEC9 (ENSG00000129450), SIGLEC10 (ENSG00000142512), TMEM25 (ENSG00000149582), SIGLEC11 (ENSG00000161640), SIGLEC16 (ENSG00000161643), SIGLEC7 (ENSG00000168995), SIGLEC15 (ENSG00000197046), SIGLEC14 (ENSG00000254415), SIGLEC12 (ENSG00000254521), SIGLEC5 (ENSG00000268500)

Protein

Protein identifiers

SIGLEC family-like protein 1Q8N7X8 (reviewed: Q8N7X8)

All UniProt accessions (5): B7ZLS6, Q8N7X8, M0QY48, M0QY54, M0R2N8

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

RefSeq proteins (5): NP_001295366, NP_001372394, NP_001372395, NP_001372396, NP_775906 (=MANE)

Domains & families (InterPro)

IDNameType
IPR013783Ig-like_foldHomologous_superfamily
IPR036179Ig-like_dom_sfHomologous_superfamily
IPR051036SIGLECFamily

UniProt features (4 total): chain 1, transmembrane region 1, region of interest 1, compositionally biased region 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8N7X8-F182.980.61

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 15 (showing top): E2F5_TARGET_GENES, MAFG_TARGET_GENES, ZNF274_TARGET_GENES, MIR8065, MIR138_5P, MIR7113_5P, MIR3659, GSE13485_DAY1_VS_DAY3_YF17D_VACCINE_PBMC_UP, GSE13485_DAY1_VS_DAY7_YF17D_VACCINE_PBMC_UP, GSE15659_NAIVE_CD4_TCELL_VS_NONSUPPRESSIVE_TCELL_UP, GSE15659_CD45RA_NEG_CD4_TCELL_VS_NONSUPPRESSIVE_TCELL_UP, GSE15659_RESTING_TREG_VS_NONSUPPRESSIVE_TCELL_UP, GSE17974_IL4_AND_ANTI_IL12_VS_UNTREATED_48H_ACT_CD4_TCELL_DN, GSE2706_R848_VS_R848_AND_LPS_8H_STIM_DC_DN, chr19q13

GO Biological Process (0):

GO Molecular Function (1): protein binding (GO:0005515)

GO Cellular Component (1): membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
binding1
cellular anatomical structure1

Protein interactions and networks

STRING

732 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
SIGLECL1NTMT2Q5VVY1332
SIGLECL1KLHL11Q9NVR0286
SIGLECL1AK5Q9Y6K8242
SIGLECL1CACNG3O60359229
SIGLECL1ZNF16P17020203
SIGLECL1KCNF1Q9H3M0203
SIGLECL1SCARA3Q6AZY7186
SIGLECL1GPC5P78333185
SIGLECL1FAT3Q8TDW7176
SIGLECL1ARHGAP26Q9UNA1171
SIGLECL1AK1P00568166
SIGLECL1TTRP02766166
SIGLECL1GSX1Q9H4S2166
SIGLECL1BIN1O00499166
SIGLECL1MRLNP0DMT0166
SIGLECL1PRCPP42785166
SIGLECL1ADAM8P78325166

IntAct

14 interactions, top by confidence:

ABTypeScore
TTMPSIGLECL1psi-mi:“MI:0915”(physical association)0.670
APODSIGLECL1psi-mi:“MI:0915”(physical association)0.560
EMP3SIGLECL1psi-mi:“MI:0915”(physical association)0.560
SIGLECL1KIAA1324Lpsi-mi:“MI:0914”(association)0.350
SIGLECL1RBFOX3psi-mi:“MI:0914”(association)0.350
SIGLECL1ELAPOR2psi-mi:“MI:0914”(association)0.350
SIGLECL1IPO5psi-mi:“MI:0914”(association)0.350
APODSIGLECL1psi-mi:“MI:0915”(physical association)0.000
TTMPSIGLECL1psi-mi:“MI:0915”(physical association)0.000
EMP3SIGLECL1psi-mi:“MI:0915”(physical association)0.000

BioGRID (202): FAM73B (Affinity Capture-MS), TNPO2 (Affinity Capture-MS), VPS8 (Affinity Capture-MS), FAM73A (Affinity Capture-MS), TBC1D22B (Affinity Capture-MS), DFNA5 (Affinity Capture-MS), BTAF1 (Affinity Capture-MS), IPO9 (Affinity Capture-MS), STAG1 (Affinity Capture-MS), MPZL1 (Affinity Capture-MS), RADIL (Affinity Capture-MS), XPO4 (Affinity Capture-MS), KIF14 (Affinity Capture-MS), CWC22 (Affinity Capture-MS), SDK2 (Affinity Capture-MS)

ESM2 similar proteins: A0JNM1, A1L1A6, A6QNY1, A6QQC6, B0CLX4, B2RTN2, B8JI67, D3YX43, O02733, O88324, P01881, P01883, P12342, P21995, P26898, P86176, Q01151, Q0VCB1, Q0VFL4, Q2YDG7, Q3U0X8, Q5RCS3, Q5UKY4, Q6AXW8, Q6PCB8, Q7TMJ8, Q7TQM3, Q7TSN7, Q8BJN4, Q8IW00, Q8N7X8, Q8R526, Q8TBE3, Q8TDX9, Q8VCP9, Q8VD31, Q91V87, Q91ZV2, Q91ZV3, Q96FE7

Diamond homologs: A6NMB1, O15389, O43699, P20138, Q08ET2, Q460M5, Q63994, Q64JA4, Q6ZMC9, Q80TG9, Q80ZE3, Q8N7X8, Q91Y57, Q920G3, Q95LH0, Q96LC7, Q96PQ1, Q96RL6, Q9BE71, Q9NYZ4, Q9ULH4, Q9Y286, Q9Y336, D4ABX8, F1NY98, Q3URE9, Q6AZB0, Q7L985, Q80XU8, Q8K099, Q8VHZ8, Q9ERC8, Q9JMH2, Q9P2V4, P06731, Q9UQ72, D3YXG0, P35329, Q8NDA2, Q96LA5

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance22
Likely benign4
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

0 predictions. Top by Δscore:

AlphaMissense

537 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:51265462:G:CW39C0.980
19:51265462:G:TW39C0.980
19:51265430:T:CF29L0.973
19:51265432:C:AF29L0.973
19:51265432:C:GF29L0.973
19:51265460:T:AW39R0.965
19:51265460:T:CW39R0.965
19:51265547:A:CS68R0.964
19:51265549:C:AS68R0.964
19:51265549:C:GS68R0.964
19:51265431:T:GF29C0.948
19:51265436:G:TG31W0.937
19:51265418:T:AC25S0.935
19:51265419:G:CC25S0.935
19:51265418:T:CC25R0.928
19:51265437:G:AG31E0.921
19:51265554:T:AI70N0.916
19:51265424:T:CC27R0.915
19:51265540:G:CW65C0.911
19:51265540:G:TW65C0.911
19:51265437:G:TG31V0.909
19:51265431:T:CF29S0.904
19:51265394:T:CC17R0.902
19:51265461:G:CW39S0.902
19:51265394:T:AC17S0.901
19:51265395:G:CC17S0.901
19:51265554:T:GI70S0.900
19:51265426:T:GC27W0.895
19:51265554:T:CI70T0.894
19:51265541:G:CA66P0.892

dbSNP variants (sampled 300 via entrez): RS1000156516 (19:51261764 T>C), RS1000278422 (19:51267716 T>G), RS1000588998 (19:51251341 A>C), RS1000792906 (19:51256325 G>A), RS1000813251 (19:51257295 A>G), RS1001170279 (19:51249910 A>G,T), RS1001261878 (19:51250282 G>A), RS1001526912 (19:51263109 C>G,T), RS1001542339 (19:51252305 AAAAAGAAAAG>A,AAAAAG,AAAAAGAAAAGAAAAG), RS1001565545 (19:51268683 C>A,G), RS1001841106 (19:51255568 A>G), RS1001945125 (19:51264592 A>G), RS1002171263 (19:51251136 G>A,T), RS1002205721 (19:51268366 C>T), RS1002266056 (19:51251324 G>A)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

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

GWAS associations

1 associations (top):

StudyTraitp-value
GCST001838_9Palmitic acid (16:0) levels9.000000e-07

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

6 total (human), top 6 by PubMed support.

ChemicalActions (top 5)PubMed papers
Benzo(a)pyreneaffects methylation, increases mutagenesis2
S-(1,2-dichlorovinyl)cysteineaffects response to substance, increases expression, affects cotreatment1
Lipopolysaccharidesaffects response to substance, increases expression, affects cotreatment1
Silicon Dioxidedecreases expression1
Valproic Aciddecreases methylation1
Asbestos, Serpentinedecreases methylation1

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.