Gene Gene information from NCBI Gene database.
Entrez ID 59353
Gene name Transmembrane protein 35A
Gene symbol TMEM35A
Synonyms (NCBI Gene)
NACHOTMEM35TUF-1
Chromosome X
Chromosome location Xq22.1
miRNA miRNA information provided by mirtarbase database.
21
miRTarBase ID miRNA Experiments Reference
MIRT625851 hsa-miR-8485 HITS-CLIP 23313552
MIRT625850 hsa-miR-4797-5p HITS-CLIP 23313552
MIRT625849 hsa-miR-1244 HITS-CLIP 23313552
MIRT625851 hsa-miR-8485 HITS-CLIP 23824327
MIRT625850 hsa-miR-4797-5p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
19
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005777 Component Peroxisome IEA
GO:0005778 Component Peroxisomal membrane IEA
GO:0005783 Component Endoplasmic reticulum IBA
GO:0005783 Component Endoplasmic reticulum IDA 26875622
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q53FP2
Protein name Novel acetylcholine receptor chaperone
Protein function Molecular chaperone which mediates the proper assembly and functional expression of the nicotinic acetylcholine receptors (nAChRs) throughout the brain (PubMed:26875622, PubMed:27789755, PubMed:28445721, PubMed:32204458, PubMed:32783947). Essent
PDB 9H9E
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13564 DoxX_2 11 127 DoxX-like family Family
Sequence
Sequence length 167
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
GOUT GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations