Gene Gene information from NCBI Gene database.
Entrez ID 8834
Gene name Transmembrane protein 11
Gene symbol TMEM11
Synonyms (NCBI Gene)
C17orf35PM1PMI
Chromosome 17
Chromosome location 17p11.2
miRNA miRNA information provided by mirtarbase database.
122
miRTarBase ID miRNA Experiments Reference
MIRT045019 hsa-miR-186-5p CLASH 23622248
MIRT712121 hsa-miR-544b HITS-CLIP 19536157
MIRT712120 hsa-miR-20a-3p HITS-CLIP 19536157
MIRT712119 hsa-miR-3184-5p HITS-CLIP 19536157
MIRT712118 hsa-miR-423-5p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16189514, 21516116, 25416956, 27107012, 28514442, 32296183, 33961781
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005739 Component Mitochondrion IDA
GO:0005739 Component Mitochondrion IEA
GO:0005743 Component Mitochondrial inner membrane IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
618817 16823 ENSG00000178307
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P17152
Protein name Transmembrane protein 11, mitochondrial (Protein PM1) (Protein PMI)
Protein function Plays a role in mitochondrial morphogenesis.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14972 Mito_morph_reg 28 190 Mitochondrial morphogenesis regulator Family
Sequence
Sequence length 192
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
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Anxiety Anxiety Disorder BEFREE 29861834
★☆☆☆☆
Found in Text Mining only
Anxiety Disorders Anxiety Disorder BEFREE 29861834
★☆☆☆☆
Found in Text Mining only
Cardiovascular Diseases Cardiovascular Diseases BEFREE 20705404
★☆☆☆☆
Found in Text Mining only
Complete atrioventricular block Complete Atrioventricular Block BEFREE 31060956
★☆☆☆☆
Found in Text Mining only
Congenital disorder of glycosylation type 1B Congenital disorder of glycosylation BEFREE 11134235, 21949237
★☆☆☆☆
Found in Text Mining only
Congenital disorder of glycosylation type 1B Congenital disorder of glycosylation Pubtator 11567948 Associate
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus, Non-Insulin-Dependent Diabetes Mellitus BEFREE 18555856
★☆☆☆☆
Found in Text Mining only
Dysarthria Dysarthria BEFREE 30987467
★☆☆☆☆
Found in Text Mining only
Hyperinsulinism Hyperinsulinism BEFREE 24521217
★☆☆☆☆
Found in Text Mining only
Hypertensive disease Hypertension BEFREE 28528304
★☆☆☆☆
Found in Text Mining only