FAM151A

gene
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Also known as MGC27169

Summary

FAM151A (family with sequence similarity 151 member A, HGNC:25032) is a protein-coding gene on chromosome 1p32.3, encoding Protein FAM151A (Q8WW52).

Located in extracellular exosome. Implicated in colorectal adenocarcinoma.

Source: NCBI Gene 338094 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 8 total
  • MANE Select transcript: NM_176782

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:25032
Approved symbolFAM151A
Namefamily with sequence similarity 151 member A
Location1p32.3
Locus typegene with protein product
StatusApproved
AliasesMGC27169
Ensembl geneENSG00000162391
Ensembl biotypeprotein_coding
Entrez338094

Gene structure

Transcript identifiers

Ensembl transcripts: 5 — 5 protein_coding

ENST00000302250, ENST00000371304, ENST00000877511, ENST00000877512, ENST00000877513

RefSeq mRNA: 1 — MANE Select: NM_176782 NM_176782

CCDS: CCDS594

Canonical transcript exons

ENST00000302250 — 8 exons

ExonStartEnd
ENSE000010646985461602054616172
ENSE000010646995461248654612710
ENSE000010647025461470054614859
ENSE000010647045461986454620007
ENSE000011399725461041254610555
ENSE000011399805461160654611745
ENSE000011568055460918154609941
ENSE000038486325462327854623525

Expression profiles

Bgee: expression breadth ubiquitous, 141 present calls, max score 91.85.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.2653 / max 69.1575, expressed in 66 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
124720.187459
124710.077917

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
adult mammalian kidneyUBERON:000008291.85gold quality
adult organismUBERON:000702390.75gold quality
kidneyUBERON:000211384.78gold quality
small intestine Peyer’s patchUBERON:000345484.56gold quality
small intestineUBERON:000210880.00gold quality
right lobe of liverUBERON:000111478.08gold quality
cortex of kidneyUBERON:000122577.45gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047377.42gold quality
mucosa of transverse colonUBERON:000499176.44gold quality
apex of heartUBERON:000209874.91gold quality
liverUBERON:000210774.38gold quality
metanephros cortexUBERON:001053373.09gold quality
heart left ventricleUBERON:000208471.28gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099170.78gold quality
cardiac ventricleUBERON:000208270.24gold quality
lymph nodeUBERON:000002969.16gold quality
rectumUBERON:000105267.89gold quality
transverse colonUBERON:000115767.46gold quality
lower esophagus mucosaUBERON:003583466.72gold quality
renal medullaUBERON:000036265.06gold quality
metanephrosUBERON:000008164.63gold quality
heartUBERON:000094864.27gold quality
intestineUBERON:000016063.07gold quality
right atrium auricular regionUBERON:000663162.48gold quality
hindlimb stylopod muscleUBERON:000425262.45gold quality
cardiac atriumUBERON:000208161.92gold quality
colonic epitheliumUBERON:000039761.00gold quality
right lobe of thyroid glandUBERON:000111959.72gold quality
colonUBERON:000115558.08gold quality
large intestineUBERON:000005957.69gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no1.63

Regulation

Is transcription factor: no

Cross-species orthologs

5 orthologs

OrganismSymbolGene ID
danio_reriofam151aENSDARG00000058218
mus_musculusFam151aENSMUSG00000034871
rattus_norvegicusFam151aENSRNOG00000007799
drosophila_melanogasterCG7231FBGN0031968
caenorhabditis_elegansWBGENE00012184

Paralogs (1): FAM151B (ENSG00000152380)

Protein

Protein identifiers

Protein FAM151AQ8WW52 (reviewed: Q8WW52)

All UniProt accessions (1): Q8WW52

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

Similarity. Belongs to the menorin family.

Isoforms (2)

UniProt IDNamesCanonical?
Q8WW52-11yes
Q8WW52-22

RefSeq proteins (1): NP_788954* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR019356Menorin_domDomain

Pfam: PF10223

UniProt features (10 total): sequence variant 6, chain 1, transmembrane region 1, splice variant 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8WW52-F192.080.77

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 27 (showing top): ZWANG_TRANSIENTLY_UP_BY_2ND_EGF_PULSE_ONLY, SUPT16H_TARGET_GENES, ZNF7_TARGET_GENES, GSE15324_ELF4_KO_VS_WT_NAIVE_CD8_TCELL_DN, GSE15930_STIM_VS_STIM_AND_IL12_24H_CD8_T_CELL_DN, GSE15930_STIM_VS_STIM_AND_IL12_72H_CD8_T_CELL_DN, GSE15930_STIM_VS_STIM_AND_IFNAB_72H_CD8_T_CELL_UP, GSE17721_PAM3CSK4_VS_CPG_16H_BMDC_UP, DESCARTES_FETAL_LIVER_HEPATOBLASTS, CARRILLOREIXACH_HEPATOBLASTOMA_VS_NORMAL_DN, GSE2826_WT_VS_XID_BCELL_DN, GSE29615_CTRL_VS_DAY7_LAIV_FLU_VACCINE_PBMC_DN, ZHANG_FH_DEFICIENT_RCC_TUMOR_VS_NORMAL_DN, KONIGORSKI_INCREASED_SUBCUTANEOUS_ADIPOSE_TISSUE_MASS_UP, GSE32423_CTRL_VS_IL7_MEMORY_CD8_TCELL_UP

GO Biological Process (1): biological_process (GO:0008150)

GO Molecular Function (1): molecular_function (GO:0003674)

GO Cellular Component (3): obsolete extracellular space (GO:0005615), membrane (GO:0016020), extracellular exosome (GO:0070062)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cellular anatomical structure1
extracellular vesicle1

Protein interactions and networks

STRING

288 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
FAM151ACRB2Q5IJ48456
FAM151APLEKHH3Q7Z736454
FAM151AFETUBQ9UGM5421
FAM151ADCAF8L2P0C7V8399
FAM151AFAM174CQ9BVV8393
FAM151ATMEM213A2RRL7367
FAM151AADA2Q9NZK5367
FAM151AARL14Q8N4G2364
FAM151ASTOX2Q9P2F5364
FAM151ACASZ1Q86V15347
FAM151AKCNH4Q9UQ05342
FAM151ASHFQ7M4L6314
FAM151AKRT24Q2M2I5310
FAM151ACDH16O75309296
FAM151ASLC6A12P48065292

IntAct

5 interactions, top by confidence:

ABTypeScore
CD81STX3psi-mi:“MI:0914”(association)0.350
CD81PVRpsi-mi:“MI:0914”(association)0.350
CD81CD276psi-mi:“MI:0914”(association)0.350

BioGRID (1): APP (Reconstituted Complex)

ESM2 similar proteins: A0A5F8AH41, A0AVI4, A7S641, O75843, P10937, P25235, P40935, P70345, Q06AU9, Q08DJ7, Q08DK0, Q0IJ33, Q14AI0, Q28647, Q28CM7, Q3V3N7, Q4R7D0, Q503C8, Q5FVF4, Q5R5N9, Q5RDY9, Q5XIL6, Q5ZI25, Q68F70, Q6IR55, Q6NWH5, Q6PD82, Q74ZJ1, Q7KNA0, Q7QIL2, Q80YU0, Q8CHY3, Q8CIM8, Q8IV36, Q8K304, Q8MRQ4, Q8NFJ9, Q8R1F6, Q8R307, Q8WW52

Diamond homologs: A5PN38, D3YUE4, Q5RDY9, Q642A7, Q6UXP7, Q8QZW3, Q8WW52, O45879

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance5
Likely benign1
Benign2

Top pathogenic / likely-pathogenic (0)

SpliceAI

1550 predictions. Top by Δscore:

VariantEffectΔscore
1:54609942:C:CCacceptor_gain1.0000
1:54609953:G:Tacceptor_gain1.0000
1:54610556:C:CCacceptor_gain1.0000
1:54611599:T:Adonor_gain1.0000
1:54611600:CCTTA:Cdonor_loss1.0000
1:54611602:TTAC:Tdonor_loss1.0000
1:54611603:TACA:Tdonor_loss1.0000
1:54611604:A:ACdonor_gain1.0000
1:54611604:A:ATdonor_loss1.0000
1:54611604:ACAGG:Adonor_gain1.0000
1:54611605:C:CAdonor_gain1.0000
1:54611605:CAGG:Cdonor_gain1.0000
1:54611605:CAGGC:Cdonor_gain1.0000
1:54611618:TGA:Tdonor_gain1.0000
1:54611743:TAC:Tacceptor_gain1.0000
1:54611746:CT:Cacceptor_loss1.0000
1:54612622:T:TAdonor_gain1.0000
1:54612708:AACC:Aacceptor_loss1.0000
1:54612711:C:CCacceptor_gain1.0000
1:54612711:CT:Cacceptor_loss1.0000
1:54614693:CACTC:Cdonor_loss1.0000
1:54614694:ACTCA:Adonor_loss1.0000
1:54614695:CTCAC:Cdonor_loss1.0000
1:54614696:TCACT:Tdonor_loss1.0000
1:54614697:CA:Cdonor_loss1.0000
1:54614698:A:ACdonor_gain1.0000
1:54614699:C:CAdonor_gain1.0000
1:54614699:CT:Cdonor_gain1.0000
1:54614699:CTG:Cdonor_gain1.0000
1:54614699:CTGT:Cdonor_gain1.0000

AlphaMissense

3765 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
1:54614852:T:AK141N0.983
1:54614852:T:GK141N0.983
1:54612658:A:GW210R0.982
1:54612658:A:TW210R0.982
1:54616053:A:GW128R0.982
1:54616053:A:TW128R0.982
1:54614846:G:CD143E0.981
1:54614846:G:TD143E0.981
1:54614843:G:CF144L0.979
1:54614843:G:TF144L0.979
1:54614845:A:GF144L0.979
1:54612554:G:CF244L0.978
1:54612554:G:TF244L0.978
1:54612556:A:GF244L0.978
1:54612555:A:GF244S0.977
1:54612707:G:CF193L0.977
1:54612707:G:TF193L0.977
1:54612709:A:GF193L0.977
1:54614764:A:GW171R0.975
1:54614764:A:TW171R0.975
1:54614840:C:AK145N0.974
1:54614840:C:GK145N0.974
1:54619912:A:GW72R0.973
1:54619912:A:TW72R0.973
1:54614844:A:GF144S0.972
1:54611739:G:CS269R0.970
1:54611739:G:TS269R0.970
1:54611741:T:GS269R0.970
1:54612708:A:GF193S0.970
1:54616152:C:GA95P0.970

dbSNP variants (sampled 300 via entrez): RS1000138150 (1:54623836 G>A), RS1000157062 (1:54623509 C>G,T), RS1000687442 (1:54616687 T>C), RS1000731408 (1:54608690 C>G,T), RS1000753654 (1:54614242 G>A), RS1000767734 (1:54617946 C>A,T), RS1001036633 (1:54616546 G>A,C), RS1001101500 (1:54622475 G>C), RS1001282266 (1:54610005 C>T), RS1001438080 (1:54620739 C>A,T), RS1001551040 (1:54621099 G>T), RS1001761573 (1:54615262 TAG>T), RS1001851491 (1:54610079 G>A), RS1002159479 (1:54621318 G>A), RS1002212572 (1:54615523 G>C)

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
GCST006585_805Blood protein levels2.000000e-22

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

19 total (human), top 19 by PubMed support.

ChemicalActions (top 5)PubMed papers
Benzo(a)pyrenedecreases expression3
Aflatoxin B1decreases expression, increases methylation3
lasiocarpinedecreases expression1
methyleugenoldecreases expression1
pirinixic acidaffects binding, increases activity, increases expression1
terbufosincreases methylation1
sodium arsenitedecreases expression1
S-(1,2-dichlorovinyl)cysteineaffects cotreatment, increases expression1
Fonofosincreases methylation1
Estradioldecreases expression1
Hydrogen Peroxideaffects expression1
Lipopolysaccharidesaffects cotreatment, increases expression1
N-Nitrosopyrrolidinedecreases expression1
Parathionincreases methylation1
Tetrachlorodibenzodioxindecreases expression1
Tobacco Smoke Pollutiondecreases expression1
Urethanedecreases expression1
Okadaic Aciddecreases expression1
Copper Sulfatedecreases 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.