Gene Gene information from NCBI Gene database.
Entrez ID 283999
Gene name Transmembrane protein 235
Gene symbol TMEM235
Synonyms (NCBI Gene)
ARGM1
Chromosome 17
Chromosome location 17q25.3
miRNA miRNA information provided by mirtarbase database.
7
miRTarBase ID miRNA Experiments Reference
MIRT2351979 hsa-miR-3173-5p CLIP-seq
MIRT2645837 hsa-miR-324-5p CLIP-seq
MIRT2645838 hsa-miR-4733-5p CLIP-seq
MIRT2645839 hsa-miR-596 CLIP-seq
MIRT2645837 hsa-miR-324-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
5
GO ID Ontology Definition Evidence Reference
GO:0005737 Component Cytoplasm IEA
GO:0005783 Component Endoplasmic reticulum IEA
GO:0016020 Component Membrane IEA
GO:0016324 Component Apical plasma membrane IBA
GO:0016324 Component Apical plasma membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620272 27563 ENSG00000204278
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
A6NFC5
Protein name Transmembrane protein 235 (Claudin-27)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13903 Claudin_2 16 197 PMP-22/EMP/MP20/Claudin tight junction Family
Sequence
Sequence length 223
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
RHEUMATOID ARTHRITIS 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
Rheumatoid Arthritis Rheumatoid arthritis GWASCAT_DG 30891314
★★☆☆☆
Found in Text Mining + Unknown/Other Associations