Gene Gene information from NCBI Gene database.
Entrez ID 55266
Gene name Transmembrane protein 19
Gene symbol TMEM19
Synonyms (NCBI Gene)
-
Chromosome 12
Chromosome location 12q21.1
miRNA miRNA information provided by mirtarbase database.
648
miRTarBase ID miRNA Experiments Reference
MIRT050994 hsa-miR-17-5p CLASH 23622248
MIRT046235 hsa-miR-27b-3p CLASH 23622248
MIRT036879 hsa-miR-877-3p CLASH 23622248
MIRT649391 hsa-miR-6890-3p HITS-CLIP 23824327
MIRT649390 hsa-miR-6840-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16189514, 25416956, 31515488, 32296183
GO:0016020 Component Membrane IBA
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
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.
Q96HH6
Protein name Transmembrane protein 19
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01940 DUF92 59 322 Integral membrane protein DUF92 Family
Sequence
Sequence length 336
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
CARCINOMA, BASAL CELL CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Lung cancer Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Malignant tumor of esophagus Benign ClinVar
★★☆☆☆
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
Orofacial Cleft 1 Orofacial cleft Pubtator 28232668 Associate
★☆☆☆☆
Found in Text Mining only