FAM174C

gene
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Also known as FLJ20640

Summary

FAM174C (family with sequence similarity 174 member C, HGNC:26073) is a protein-coding gene on chromosome 19p13.3, encoding Protein FAM174C (Q9BVV8).

Located in cytoplasm and extracellular region.

Source: NCBI Gene 55009 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 3 total

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:26073
Approved symbolFAM174C
Namefamily with sequence similarity 174 member C
Location19p13.3
Locus typegene with protein product
StatusApproved
AliasesFLJ20640
Ensembl geneENSG00000228300
Ensembl biotypeprotein_coding
Entrez55009

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000469144

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

ENST00000469144 — 3 exons

ExonStartEnd
ENSE0000190665512760211276103
ENSE0000447392412771831277299
ENSE0000447439512787771279244

Expression profiles

Bgee: expression breadth ubiquitous, 238 present calls, max score 96.39.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
mucosa of transverse colonUBERON:000499196.39gold quality
right lobe of liverUBERON:000111496.37gold quality
right adrenal glandUBERON:000123395.65gold quality
lower esophagus mucosaUBERON:003583495.29gold quality
right adrenal gland cortexUBERON:003582795.15gold quality
left adrenal glandUBERON:000123495.13gold quality
left adrenal gland cortexUBERON:003582594.97gold quality
apex of heartUBERON:000209894.94gold quality
granulocyteCL:000009494.11gold quality
adrenal cortexUBERON:000123593.74gold quality
adenohypophysisUBERON:000219693.71gold quality
right lobe of thyroid glandUBERON:000111993.50gold quality
body of pancreasUBERON:000115093.05gold quality
body of stomachUBERON:000116192.93gold quality
right testisUBERON:000453492.74gold quality
left lobe of thyroid glandUBERON:000112092.70gold quality
left testisUBERON:000453392.64gold quality
adrenal glandUBERON:000236992.41gold quality
metanephros cortexUBERON:001053392.33gold quality
skin of abdomenUBERON:000141692.26gold quality
stromal cell of endometriumCL:000225592.20gold quality
skin of legUBERON:000151192.10gold quality
left coronary arteryUBERON:000162691.91gold quality
spleenUBERON:000210691.88gold quality
minor salivary glandUBERON:000183091.83gold quality
esophagus mucosaUBERON:000246991.78gold quality
omental fat padUBERON:001041491.77gold quality
peritoneumUBERON:000235891.72gold quality
pituitary glandUBERON:000000791.71gold quality
transverse colonUBERON:000115791.62gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes9.27

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

9 targeting FAM174C, 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-6798-5P100.0065.77699
HSA-MIR-6762-3P99.6666.941188
HSA-MIR-1212299.5669.331672
HSA-MIR-6722-3P99.4567.621919
HSA-MIR-6734-3P99.1566.271627
HSA-MIR-1909-3P99.0366.561662
HSA-MIR-797798.6566.182590
HSA-MIR-64797.7367.79927
HSA-MIR-448696.9660.61931

Literature-anchored findings (GeneRIF, showing 1)

  • The isolation and characterization of a novel human non-classical secreted protein which is encoded by the hypothetical gene C19orf24 (chromosome 19 open reading frame 24), is reported. (PMID:16847563)

Cross-species orthologs

0 orthologs

Protein

Protein identifiers

Protein FAM174CQ9BVV8 (reviewed: Q9BVV8)

All UniProt accessions (1): D6W5Y7

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

Similarity. Belongs to the FAM174 family.

RefSeq proteins (0): (*=MANE)

Domains & families (InterPro)

IDNameType
IPR009565FAM174-likeFamily

Pfam: PF06679

UniProt features (10 total): modified residue 3, region of interest 2, signal peptide 1, chain 1, transmembrane region 1, compositionally biased region 1, glycosylation site 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9BVV8-F164.020.09

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): 113, 117, 120

Glycosylation sites (1): 47

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 65 (showing top): DOUGLAS_BMI1_TARGETS_UP, chr19p13, GAZDA_DIAMOND_BLACKFAN_ANEMIA_ERYTHROID_DN, NAKAMURA_ADIPOGENESIS_EARLY_UP, NAKAMURA_ADIPOGENESIS_LATE_UP, BANP_TARGET_GENES, DLX6_TARGET_GENES, FEV_TARGET_GENES, FOXD2_TARGET_GENES, FOXN3_TARGET_GENES, NAB2_TARGET_GENES, RBM34_TARGET_GENES, SETD7_TARGET_GENES, ZBTB12_TARGET_GENES, ZNF184_TARGET_GENES

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (3): extracellular region (GO:0005576), cytoplasm (GO:0005737), membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cellular anatomical structure3
intracellular anatomical structure1

Protein interactions and networks

STRING

418 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
FAM174CRBISQ8N0T1576
FAM174CCBARPQ8N350544
FAM174CTMEM259Q4ZIN3537
FAM174CSBNO2Q9Y2G9511
FAM174CCCDC160A6NGH7495
FAM174CCIRBPQ14011484
FAM174CLRRCC1Q9C099482
FAM174CARHGAP45Q92619482
FAM174CC19orf25Q9UFG5477
FAM174CR3HDM4Q96D70476
FAM174CWDR18Q9BV38459
FAM174CSLC25A53Q5H9E4449
FAM174CDAZAP1Q96EP5441
FAM174CCFAP73A6NFT4419
FAM174CPOLR2EP19388415

IntAct

3 interactions, top by confidence:

ABTypeScore
FAM174CMAP2K7psi-mi:“MI:0914”(association)0.350
FAM174CfliMpsi-mi:“MI:0915”(physical association)0.000

BioGRID (5): MAP2K7 (Affinity Capture-MS), NSF (Affinity Capture-MS), RAB11FIP2 (Affinity Capture-MS), SLC41A1 (Affinity Capture-MS), VAMP3 (Affinity Capture-MS)

ESM2 similar proteins: A0A5F4BST2, A5PJC7, A8MWV9, D3ZZP4, O14836, P0CAN6, P11911, P11912, P14753, Q01114, Q07303, Q13113, Q2KI80, Q2KL21, Q3TS39, Q3URD2, Q4V9L6, Q5F267, Q5FVJ4, Q5FVQ7, Q5RA41, Q5T1S8, Q6P9G4, Q6UWJ8, Q6UX34, Q80VJ8, Q810F0, Q86XR5, Q8BRJ3, Q8BX43, Q8K064, Q8K5A9, Q8N112, Q8N4K4, Q8N6L0, Q8NBR0, Q8NC24, Q8QZT4, Q8R138, Q923S2

Diamond homologs: Q9BVV8, Q9DAZ5

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

501 predictions. Top by Δscore:

VariantEffectΔscore
19:1275823:GCGTT:Gdonor_gain1.0000
19:1275827:TTAGG:Tdonor_loss1.0000
19:1275829:AGG:Adonor_loss1.0000
19:1275831:GT:Gdonor_loss1.0000
19:1275832:T:Adonor_loss1.0000
19:1277176:C:Gacceptor_gain1.0000
19:1277178:TCCA:Tacceptor_loss1.0000
19:1277179:CCA:Cacceptor_loss1.0000
19:1277180:CAGG:Cacceptor_loss1.0000
19:1277181:A:AGacceptor_gain1.0000
19:1277182:G:Aacceptor_loss1.0000
19:1277182:G:GGacceptor_gain1.0000
19:1277296:GATG:Gdonor_gain1.0000
19:1277175:A:AGacceptor_gain0.9900
19:1277181:AG:Aacceptor_gain0.9900
19:1277181:AGGTT:Aacceptor_gain0.9900
19:1277182:GG:Gacceptor_gain0.9900
19:1277182:GGT:Gacceptor_gain0.9900
19:1277182:GGTT:Gacceptor_gain0.9900
19:1277182:GGTTG:Gacceptor_gain0.9900
19:1277288:G:GTdonor_gain0.9900
19:1275822:G:GTdonor_gain0.9800
19:1277179:CCAGG:Cacceptor_gain0.9800
19:1277278:T:TGdonor_gain0.9800
19:1277296:GATGG:Gdonor_loss0.9800
19:1277300:G:GGdonor_gain0.9800
19:1276370:GCT:Gdonor_gain0.9700
19:1277180:CAGGT:Cacceptor_gain0.9700
19:1277181:AGG:Aacceptor_gain0.9700
19:1277297:A:Gdonor_gain0.9700

AlphaMissense

833 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000091381 (19:1277843 C>G,T), RS1000099801 (19:1275515 TA>T), RS1000401424 (19:1275592 C>G,T), RS1000465668 (19:1279332 G>T), RS1000754597 (19:1279525 C>T), RS1001539687 (19:1277183 G>A,T), RS1001649380 (19:1274980 A>C), RS1001765224 (19:1275107 T>C), RS1001810716 (19:1276024 C>A,G,T), RS1001921135 (19:1277836 A>G), RS1001986180 (19:1274273 G>A), RS1002094510 (19:1276174 T>A), RS1002143295 (19:1278840 C>G,T), RS1002151238 (19:1274458 G>A), RS1002377493 (19:1277028 G>A,C,T)

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

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

23 total (human), top 23 by PubMed support.

ChemicalActions (top 5)PubMed papers
sodium arsenitedecreases expression, affects cotreatment, increases abundance, increases expression3
FR900359decreases phosphorylation1
bisphenol Aincreases methylation1
manganese chlorideaffects cotreatment, increases abundance, increases expression1
perfluorooctane sulfonic acidincreases expression1
K 7174decreases expression1
4-(4-((5-(4,5-dimethyl-2-nitrophenyl)-2-furanyl)methylene)-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-1-yl)benzoic aciddecreases expression1
Resveratrolaffects cotreatment, decreases expression1
Acetaminophendecreases expression1
Arsenicaffects cotreatment, increases abundance, increases expression1
Benzo(a)pyreneincreases expression1
Cannabidiolincreases expression1
Manganeseincreases expression, affects cotreatment, increases abundance1
Plant Extractsaffects cotreatment, decreases expression1
Smokedecreases expression1
Tetrachlorodibenzodioxinincreases expression1
Thiramdecreases expression1
Tobacco Smoke Pollutionincreases expression1
Valproic Acidincreases methylation1
Vitamin Edecreases expression1
Aflatoxin B1increases methylation1
Antirheumatic Agentsdecreases expression1
Okadaic Acidincreases expression1

Cellosaurus cell lines

1 cell lines: 1 transformed cell line

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

CellosaurusNameCategorySex
CVCL_B2WWAbcam HEK293T FAM174C KOTransformed cell lineFemale

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.