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Gene Gene information from NCBI Gene database.
Entrez ID 645369
Gene name Transmembrane protein 200C
Gene symbol TMEM200C
Synonyms (NCBI Gene)
TTMA
Chromosome 18
Chromosome location 18p11.31
miRNA miRNA information provided by mirtarbase database.
114 Show/Hide all (114)
miRTarBase ID miRNA Experiments Reference
MIRT546303 hsa-miR-526b-3p PAR-CLIP 20371350
MIRT546302 hsa-miR-93-5p PAR-CLIP 20371350
MIRT546301 hsa-miR-519d-3p PAR-CLIP 20371350
MIRT546300 hsa-miR-106a-5p PAR-CLIP 20371350
MIRT546299 hsa-miR-20a-5p PAR-CLIP 20371350
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
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.
A6NKL6
Protein name Transmembrane protein 200C (Transmembrane protein TTMA) (Two transmembrane domain-containing family member A)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10177 DUF2371 14 → 201 Uncharacterised conserved protein (DUF2371) Family
Sequence
MIATGGLLRISARKQDPLRPPSQIPKRKRKAKKRRKNDVVVVKGKLKLCSISGLIALCGI
LVLLVGIAMAVVGYWPKATGTNREGGKQLPPAGSSHRVPTTANSSSSGSKNRSRSHPRAP
GGVNSSSAGAPRSTPPARAASPSSSSTSVGFFFRIFSGYLHSDKLKVFGPLIMGIGIFLF
ICANAVLHENRDKKTKIINLR
DLYSTVIDVHSLRAKDLAAAAAAAAAAAASSSSSAPAAA
PPGAIPLNGFLSYVQSRGLELKPGGCGGSGDAFGAAAMLAKGSWPPHPAAPSGGRPRGAA
SPPDLASSPRCPREPPSLAEAVYSVYRERSGVAGSRRAAAATAAAAASSCSSPAPCSPPE
SWGRQSTASSFVDSSLSAFALLPLQGGRDRGGDAEGASCSWQRPPGERGSQEIPRGELDL
SMTNLRGAEGSMRGARREPEEPEGAVAARAARGQGGRLPRTGRYAALRRRSTSGLPDYRA
PPSPEPPPSPGSADPDSSPLAKAASPSPPLRLEGSPPTRRDSGSSQSDDPSSSNKGYTPL
REAGTSTESVLDAVAGQTRDSAVAAPVLGAEQSSPEGASQEPPTAEQPQPVQRQFTNKEK
LIMISRSHAIGVEEELESTGI
Sequence length 621
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 Reference Evidence Score
EBV-positive nodal T- and NK-cell lymphoma Likely 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
Mental disorders Mental Disorders BEFREE 15722956
★★★★★
★☆☆☆☆
Found in Text Mining only