PARM1

gene
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Also known as DKFZP564O0823Cipar1WSC4

Summary

PARM1 (prostate androgen-regulated mucin-like protein 1, HGNC:24536) is a protein-coding gene on chromosome 4q13.3, encoding Prostate androgen-regulated mucin-like protein 1 (Q6UWI2). May regulate TLP1 expression and telomerase activity, thus enabling certain prostatic cells to resist apoptosis.

Located in several cellular components, including Golgi apparatus; endosome; and nucleoplasm.

Source: NCBI Gene 25849 — RefSeq curated summary.

At a glance

  • GWAS associations: 3
  • Clinical variants (ClinVar): 47 total
  • MANE Select transcript: NM_015393

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:24536
Approved symbolPARM1
Nameprostate androgen-regulated mucin-like protein 1
Location4q13.3
Locus typegene with protein product
StatusApproved
AliasesDKFZP564O0823, Cipar1, WSC4
Ensembl geneENSG00000169116
Ensembl biotypeprotein_coding
OMIM617688
Entrez25849

Gene structure

Transcript identifiers

Ensembl transcripts: 8 — 8 protein_coding

ENST00000307428, ENST00000513238, ENST00000856900, ENST00000856901, ENST00000856902, ENST00000946485, ENST00000946486, ENST00000946487

RefSeq mRNA: 1 — MANE Select: NM_015393 NM_015393

CCDS: CCDS47077

Canonical transcript exons

ENST00000307428 — 4 exons

ExonStartEnd
ENSE000011274437501242575013150
ENSE000014865037504616375050113
ENSE000014865047503388375033961
ENSE000020230367493311674933370

Expression profiles

Bgee: expression breadth ubiquitous, 271 present calls, max score 98.43.

FANTOM5 (CAGE): breadth broad, TPM avg 14.0130 / max 683.4132, expressed in 810 samples.

FANTOM5 promoters (5 alternative TSS)

Promoter IDTPM avgSamples expressed
4829111.2470770
482891.1416359
482921.1268328
482900.2856147
2032440.2120112

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
urethraUBERON:000005798.43gold quality
saphenous veinUBERON:000731898.29gold quality
deciduaUBERON:000245098.27gold quality
rectumUBERON:000105297.97gold quality
mucosa of sigmoid colonUBERON:000499397.80gold quality
colonic mucosaUBERON:000031797.58gold quality
right lobe of thyroid glandUBERON:000111997.29gold quality
islet of LangerhansUBERON:000000697.16gold quality
left lobe of thyroid glandUBERON:000112097.15gold quality
thyroid glandUBERON:000204696.77gold quality
vena cavaUBERON:000408796.30gold quality
descending thoracic aortaUBERON:000234596.13gold quality
seminal vesicleUBERON:000099896.12gold quality
pigmented layer of retinaUBERON:000178295.67gold quality
hair follicleUBERON:000207395.65gold quality
retinaUBERON:000096695.64gold quality
popliteal arteryUBERON:000225095.49gold quality
tibial arteryUBERON:000761095.48gold quality
aortaUBERON:000094795.36gold quality
thoracic aortaUBERON:000151595.22gold quality
right coronary arteryUBERON:000162595.11gold quality
ascending aortaUBERON:000149695.08gold quality
right atrium auricular regionUBERON:000663194.81gold quality
cardiac atriumUBERON:000208194.57gold quality
cauda epididymisUBERON:000436094.46gold quality
mucosa of transverse colonUBERON:000499194.25gold quality
prostate glandUBERON:000236794.13gold quality
lower lobe of lungUBERON:000894993.72gold quality
transverse colonUBERON:000115793.53gold quality
coronary arteryUBERON:000162193.48gold quality

Single-cell (SCXA)

Detected in 9 experiment(s), a significant marker in 8.

ExperimentMarker?Max mean expression
E-GEOD-86618yes431.38
E-GEOD-135922yes30.50
E-GEOD-125970yes28.80
E-CURD-112yes14.85
E-MTAB-6678yes13.02
E-CURD-119yes11.66
E-GEOD-83139yes9.60
E-ENAD-27no3.70
E-ANND-3no0.00

Regulation

Is transcription factor: no

Upstream regulators (CollecTRI, top): ESR1

miRNA regulators (miRDB)

151 targeting PARM1, 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-6867-5P100.0082.213464
HSA-MIR-6873-3P100.0071.422626
HSA-MIR-4262100.0073.263931
HSA-MIR-4776-3P100.0068.731340
HSA-MIR-6833-3P100.0070.633197
HSA-MIR-7110-3P100.0073.182486
HSA-MIR-340-5P100.0072.504437
HSA-MIR-4768-5P100.0069.492861
HSA-MIR-190A-3P100.0080.355520
HSA-MIR-5692A100.0074.406850
HSA-MIR-5193100.0067.261744
HSA-MIR-10401-5P99.9965.79948
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-450099.9972.722367
HSA-MIR-186-5P99.9970.833707
HSA-MIR-371B-5P99.9975.344759
HSA-LET-7A-5P99.9872.291790
HSA-LET-7B-5P99.9872.311790
HSA-LET-7C-5P99.9872.291790
HSA-LET-7E-5P99.9872.291790
HSA-LET-7F-5P99.9872.561784
HSA-LET-7G-5P99.9872.371784
HSA-LET-7I-5P99.9872.371788
HSA-MIR-98-5P99.9872.331787
HSA-MIR-569699.9872.364487
HSA-MIR-373-5P99.9875.364753
HSA-MIR-616-5P99.9875.584775

Literature-anchored findings (GeneRIF, showing 4)

  • Ectopic expression of hPARM-1 in PC3 prostate cancer cells increased colony formation, suggesting a probable role in cell proliferation. (PMID:18027867)
  • PARM1 does not play a major role in the development of epispadias (PMID:22766399)
  • Our results strongly suggest the oncogenic potential of PARM-1. (PMID:23902727)
  • Neurexophilin and PC-esterase domain family member 4 (NXPE4) and prostate androgen-regulated mucin-like protein 1 (PARM1) as prognostic biomarkers for colorectal cancer. (PMID:31297877)

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusParm1ENSMUSG00000034981
rattus_norvegicusParm1ENSRNOG00000002579

Protein

Protein identifiers

Prostate androgen-regulated mucin-like protein 1Q6UWI2 (reviewed: Q6UWI2)

All UniProt accessions (2): Q6UWI2, D6RBB6

UniProt curated annotations — full annotation on UniProt →

Function. May regulate TLP1 expression and telomerase activity, thus enabling certain prostatic cells to resist apoptosis.

Subcellular location. Cell membrane. Golgi apparatus membrane. Endosome membrane.

Tissue specificity. Widely expressed with highest levels in heart, kidney and placenta.

Post-translational modifications. Highly N-glycosylated and O-glycosylated.

Induction. By androgens.

Similarity. Belongs to the PARM family.

RefSeq proteins (1): NP_056208* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR031431PARM1Family

Pfam: PF17061

UniProt features (18 total): glycosylation site 4, compositionally biased region 4, sequence conflict 2, topological domain 2, signal peptide 1, chain 1, modified residue 1, sequence variant 1, transmembrane region 1, region of interest 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q6UWI2-F152.350.04

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 (1): 298

Glycosylation sites (4): 58, 62, 80, 176

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 190 (showing top): BENPORATH_ES_WITH_H3K27ME3, KAAB_HEART_ATRIUM_VS_VENTRICLE_UP, GAUSSMANN_MLL_AF4_FUSION_TARGETS_A_DN, BROWNE_HCMV_INFECTION_16HR_UP, YAO_TEMPORAL_RESPONSE_TO_PROGESTERONE_CLUSTER_1, CHANDRAN_METASTASIS_DN, chr4q13, MODULE_66, SHEDDEN_LUNG_CANCER_GOOD_SURVIVAL_A4, WONG_ENDMETRIUM_CANCER_DN, SCHAEFFER_PROSTATE_DEVELOPMENT_48HR_DN, CREIGHTON_ENDOCRINE_THERAPY_RESISTANCE_5, RICKMAN_HEAD_AND_NECK_CANCER_A, DOUGLAS_BMI1_TARGETS_DN, FLECHNER_BIOPSY_KIDNEY_TRANSPLANT_REJECTED_VS_OK_DN

GO Biological Process (0):

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

GO Cellular Component (10): Golgi membrane (GO:0000139), nucleoplasm (GO:0005654), early endosome (GO:0005769), late endosome (GO:0005770), Golgi apparatus (GO:0005794), cytosol (GO:0005829), plasma membrane (GO:0005886), endosome membrane (GO:0010008), endosome (GO:0005768), membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cellular anatomical structure3
endosome3
bounding membrane of organelle2
cytoplasm2
endomembrane system2
binding1
Golgi apparatus1
nuclear lumen1
intracellular membrane-bounded organelle1
membrane1
cell periphery1
cytoplasmic vesicle membrane1
cytoplasmic vesicle1

Protein interactions and networks

STRING

1136 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
PARM1AKNAD1Q5T1N1489
PARM1SUSD1Q6UWL2456
PARM1MON1BQ7L1V2438
PARM1KIF26AQ9ULI4419
PARM1NDNFQ8TB73402
PARM1GPKOWQ92917382
PARM1ATP6AP1LQ52LC2380
PARM1CSDC2Q9Y534372
PARM1SLC35A5Q9BS91354
PARM1TMEM184AQ6ZMB5346
PARM1MYBPC1Q00872343
PARM1SPATS2LQ9NUQ6322
PARM1RPS25P25111321
PARM1UBAP1LF5GYI3311
PARM1TBC1D24Q9ULP9311

IntAct

5 interactions, top by confidence:

ABTypeScore
PARM1UBQLN2psi-mi:“MI:0915”(physical association)0.560
PARM1ORC4psi-mi:“MI:0914”(association)0.350
PARM1UBQLN2psi-mi:“MI:0915”(physical association)0.000

BioGRID (14): UBQLN2 (Two-hybrid), CENPH (Affinity Capture-MS), STEAP2 (Affinity Capture-MS), ERGIC2 (Affinity Capture-MS), ORC4 (Affinity Capture-MS), SCCPDH (Affinity Capture-MS), SORBS3 (Affinity Capture-MS), SNX17 (Affinity Capture-MS), GALNT16 (Affinity Capture-MS), LRRC16A (Affinity Capture-MS), LGALS1 (Affinity Capture-MS), IL6ST (Affinity Capture-MS), ULBP3 (Affinity Capture-MS), STEAP3 (Affinity Capture-MS)

ESM2 similar proteins: A0A2R8Y7Y5, A1KXC4, A6QLF8, J3KML8, O00592, O35188, O55145, O57604, P06484, P07141, P13838, P14220, P15702, P16150, P18827, P20934, P26260, P34740, P47951, P59647, P78423, P97808, Q08DZ5, Q1ECS6, Q28270, Q28645, Q29RT9, Q3MIW9, Q3TNW5, Q52S86, Q58Y74, Q5RAF8, Q62170, Q64314, Q6MG22, Q6P9X9, Q6UWI2, Q6UXF1, Q86YL7, Q8BHE4

Diamond homologs: Q5RAF8, Q6P9X9, Q6UWI2, Q923D3

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance33
Likely benign4
Benign1

Top pathogenic / likely-pathogenic (0)

SpliceAI

1073 predictions. Top by Δscore:

VariantEffectΔscore
4:74933366:TGCAG:Tdonor_loss1.0000
4:74933368:CAGGT:Cdonor_loss1.0000
4:74933369:AGG:Adonor_loss1.0000
4:74933370:GGTA:Gdonor_loss1.0000
4:74933371:G:GAdonor_loss1.0000
4:74933372:T:Gdonor_loss1.0000
4:75033959:CAGG:Cdonor_loss1.0000
4:75033960:AGG:Adonor_loss1.0000
4:75033961:GGTGA:Gdonor_loss1.0000
4:75033962:G:Cdonor_loss1.0000
4:75033963:T:Gdonor_loss1.0000
4:75046272:GAT:Gdonor_gain1.0000
4:74933332:TCTAC:Tdonor_gain0.9900
4:74933778:G:Tdonor_gain0.9900
4:75012419:CCACA:Cacceptor_loss0.9900
4:75012420:CACAG:Cacceptor_loss0.9900
4:75012421:ACAGG:Aacceptor_loss0.9900
4:75012422:CAG:Cacceptor_loss0.9900
4:75012423:A:Cacceptor_loss0.9900
4:75012424:G:Aacceptor_loss0.9900
4:75013126:G:GTdonor_gain0.9900
4:75013147:TCAGG:Tdonor_loss0.9900
4:75013148:CAGGT:Cdonor_loss0.9900
4:75013149:AGG:Adonor_loss0.9900
4:75013150:GGT:Gdonor_loss0.9900
4:75013151:G:GCdonor_loss0.9900
4:75013152:T:Adonor_loss0.9900
4:75019313:A:AGdonor_gain0.9900
4:75025705:TGC:Tdonor_gain0.9900
4:75033881:A:AGacceptor_gain0.9900

AlphaMissense

1962 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
4:75033895:C:AA261D0.998
4:75046226:C:AN304K0.998
4:75046226:C:GN304K0.998
4:75033916:C:AA268D0.997
4:75033937:G:AG275E0.997
4:75033885:A:CS258R0.996
4:75033887:C:AS258R0.996
4:75033887:C:GS258R0.996
4:75033892:C:AA260D0.996
4:75033910:T:AV266D0.996
4:75033936:G:AG275R0.995
4:75033936:G:CG275R0.995
4:75046217:C:AN301K0.995
4:75046217:C:GN301K0.995
4:75033898:T:AI262N0.994
4:75033946:C:AA278D0.994
4:75013144:A:CS255R0.993
4:75013146:T:AS255R0.993
4:75013146:T:GS255R0.993
4:75033913:T:AI267N0.993
4:75033925:T:GL271R0.993
4:75033928:T:GL272R0.993
4:75033931:T:AV273E0.993
4:75033952:T:CL280P0.993
4:75033961:G:TR283M0.993
4:75046211:G:CW299C0.993
4:75046211:G:TW299C0.993
4:75033943:C:AA277E0.992
4:75046231:T:CL306P0.992
4:75046237:A:TD308V0.992

dbSNP variants (sampled 300 via entrez): RS1000099771 (4:75016616 A>T), RS1000121137 (4:75039906 C>T), RS1000126788 (4:74972253 T>C), RS1000179559 (4:74973677 C>A), RS1000182357 (4:74996403 C>G,T), RS1000198529 (4:74988825 G>T), RS1000311512 (4:74940964 TCACTGC>T), RS10003137 (4:74942554 T>A,C,G), RS1000324736 (4:74945549 A>G), RS1000326793 (4:74958681 G>A), RS1000335747 (4:75002511 G>A), RS1000350461 (4:75028808 T>C), RS1000357596 (4:74985423 A>T), RS1000395033 (4:75036502 A>G), RS1000412974 (4:74951686 G>A)

Disease associations

OMIM: gene MIM:617688 | disease phenotypes: MIM:192350

GenCC curated gene-disease

Mondo (1): VACTERL/vater association (MONDO:0008642)

Orphanet (1): VACTERL/VATER association (Orphanet:887)

HPO phenotypes

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

GWAS associations

3 associations (top):

StudyTraitp-value
GCST004744_34Lung adenocarcinoma3.000000e-06
GCST005784_2Bone mineral density (femoral neck) in inflammatory bowel disease2.000000e-07
GCST008456_8Childhood steroid-sensitive nephrotic syndrome3.000000e-08

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0007785femoral neck bone mineral density

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

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

ChemicalActions (top 5)PubMed papers
Valproic Acidaffects cotreatment, increases expression6
sodium arseniteaffects methylation, decreases expression2
Benzo(a)pyreneaffects methylation, increases methylation2
Estradioldecreases expression2
Phenylmercuric Acetateaffects cotreatment, increases expression2
aristolochic acid Idecreases expression1
triphenyl phosphateaffects expression1
butyraldehydedecreases expression1
zinc chromateincreases abundance, increases expression1
S-(1,2-dichlorovinyl)cysteinedecreases expression1
chromium hexavalent ionincreases abundance, increases expression1
2-palmitoylglycerolincreases expression1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, increases expression1
abrinedecreases expression1
dorsomorphinaffects cotreatment, increases expression1
Resveratrolaffects cotreatment, increases expression1
Temozolomideincreases expression1
Sunitinibincreases expression1
Zoledronic Acidincreases expression1
Acetaminophenincreases expression1
Cadmiumdecreases expression, increases abundance1
Cytarabinedecreases expression1
Doxorubicindecreases expression1
Lipopolysaccharidesincreases expression, affects cotreatment1
Silicon Dioxidedecreases expression1
Tobacco Smoke Pollutionincreases expression1
Zincincreases expression1
Cyclosporineincreases expression1
Asbestos, Serpentinedecreases expression1
Cadmium Chloridedecreases expression, increases abundance1

Clinical trials (associated diseases)

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

TrialPhaseStatusTitle
NCT03799705Not specifiedCOMPLETEDGenetic Variants in Nicotinamide Adenine Dinucleotide (NAD) Synthesis Pathway