Gene Gene information from NCBI Gene database.
Entrez ID 25849
Gene name Prostate androgen-regulated mucin-like protein 1
Gene symbol PARM1
Synonyms (NCBI Gene)
Cipar1DKFZP564O0823PARM-1WSC4
Chromosome 4
Chromosome location 4q13.3
miRNA miRNA information provided by mirtarbase database.
334
miRTarBase ID miRNA Experiments Reference
MIRT024754 hsa-miR-215-5p Microarray 19074876
MIRT026677 hsa-miR-192-5p Microarray 19074876
MIRT043100 hsa-miR-324-5p CLASH 23622248
MIRT526220 hsa-miR-6835-3p PAR-CLIP 22012620
MIRT526219 hsa-miR-4422 PAR-CLIP 22012620
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005654 Component Nucleoplasm IDA
GO:0005768 Component Endosome IEA
GO:0005769 Component Early endosome IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617688 24536 ENSG00000169116
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6UWI2
Protein name Prostate androgen-regulated mucin-like protein 1 (PARM-1)
Protein function May regulate TLP1 expression and telomerase activity, thus enabling certain prostatic cells to resist apoptosis.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17061 PARM 15 310 PARM Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed with highest levels in heart, kidney and placenta. {ECO:0000269|PubMed:18027867}.
Sequence
Sequence length 310
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
NEPHROTIC SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SCOLIOSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Colorectal Carcinoma Colorectal Cancer BEFREE 31297877
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Colorectal neoplasm Pubtator 32749190, 34552157 Associate
★☆☆☆☆
Found in Text Mining only
Crohn Disease Crohn Disease BEFREE 21752155
★☆☆☆☆
Found in Text Mining only
Epispadias Epispadias BEFREE 22766399
★☆☆☆☆
Found in Text Mining only
Functional Gastrointestinal Disorders Functional Gastrointestinal Disorders BEFREE 21752155
★☆☆☆☆
Found in Text Mining only
Insulin Resistance Diabetes mellitus, type 2 Pubtator 30678306 Associate
★☆☆☆☆
Found in Text Mining only
Irritable Bowel Syndrome Irritable bowel syndrome Pubtator 18237869 Associate
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of prostate Prostate cancer BEFREE 18027867
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 31297877
★☆☆☆☆
Found in Text Mining only
Nephrotic Syndrome Nephrotic Syndrome GWASCAT_DG 31263063
★★☆☆☆
Found in Text Mining + Unknown/Other Associations