Gene Gene information from NCBI Gene database.
Entrez ID 256472
Gene name Transmembrane protein 151A
Gene symbol TMEM151A
Synonyms (NCBI Gene)
DYT36EKD3TMEM151
Chromosome 11
Chromosome location 11q13.2
miRNA miRNA information provided by mirtarbase database.
130
miRTarBase ID miRNA Experiments Reference
MIRT718487 hsa-miR-4722-3p HITS-CLIP 19536157
MIRT718486 hsa-miR-6727-3p HITS-CLIP 19536157
MIRT718485 hsa-miR-6747-3p HITS-CLIP 19536157
MIRT718484 hsa-miR-3653-5p HITS-CLIP 19536157
MIRT718483 hsa-miR-1976 HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
GO ID Ontology Definition Evidence Reference
GO:0005783 Component Endoplasmic reticulum IBA
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005783 Component Endoplasmic reticulum IMP 34518509
GO:0005789 Component Endoplasmic reticulum membrane IEA
GO:0016020 Component Membrane IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620108 28497 ENSG00000179292
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N4L1
Protein name Transmembrane protein 151A
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14857 TMEM151 26 373 TMEM151 family Family
Sequence
Sequence length 468
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
11
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Episodic kinesigenic dyskinesia 3 Pathogenic rs1229777829, rs2495260968, rs138482881, rs2495261927, rs2495261382, rs1857487337, rs1857505875, rs2495260613, rs916841534 RCV003152480
RCV003152481
RCV003152482
RCV003152483
RCV003152484
RCV003152485
RCV003152486
RCV003333701
RCV003333702
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
TMEM151A-related disorder Uncertain significance; Likely benign rs774742558, rs552250699 RCV003153086
RCV004539438
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Asthma Associate 37259023
Familial paroxysmal dystonia Associate 39454747