Gene Gene information from NCBI Gene database.
Entrez ID 219623
Gene name Transmembrane protein 26
Gene symbol TMEM26
Synonyms (NCBI Gene)
-
Chromosome 10
Chromosome location 10q21.2
Summary This gene encodes a protein containing multiple transmembrane helices. It is a selective surface protein marker of brite/beige adipocytes, which may coexist with classical brown adipocytes in brown adipose tissue. Alternative splicing of this gene results
miRNA miRNA information provided by mirtarbase database.
90
miRTarBase ID miRNA Experiments Reference
MIRT1436189 hsa-let-7a CLIP-seq
MIRT1436190 hsa-let-7b CLIP-seq
MIRT1436191 hsa-let-7c CLIP-seq
MIRT1436192 hsa-let-7d CLIP-seq
MIRT1436193 hsa-let-7e CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617803 28550 ENSG00000196932
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6ZUK4
Protein name Transmembrane protein 26
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF09772 Tmem26 3 303 Transmembrane protein 26 Family
Sequence
Sequence length 368
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
ASTHMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HODGKINS LYMPHOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SCHIZOPHRENIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Breast Neoplasms Associate 27224909
★☆☆☆☆
Found in Text Mining only
Endocrine System Diseases Inhibit 27224909
★☆☆☆☆
Found in Text Mining only
HIV Infections Associate 26756119, 31714428
★☆☆☆☆
Found in Text Mining only
Lung Injury Associate 22986903
★☆☆☆☆
Found in Text Mining only
Neoplasms Inhibit 27224909
★☆☆☆☆
Found in Text Mining only
Pulmonary Disease Chronic Obstructive Associate 22986903
★☆☆☆☆
Found in Text Mining only
Urinary Bladder Neoplasms Associate 22529986
★☆☆☆☆
Found in Text Mining only