Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23731
Gene name Gene Name - the full gene name approved by the HGNC.
Transmembrane protein 245
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TMEM245
Synonyms (NCBI Gene) Gene synonyms aliases
C9orf5, CG-2, CG2
Chromosome Chromosome number
9
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9q31.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT016078 hsa-miR-374b-5p Sequencing 20371350
MIRT019650 hsa-miR-340-5p Sequencing 20371350
MIRT020473 hsa-miR-106b-5p Microarray 17242205
MIRT021185 hsa-miR-186-5p Sequencing 20371350
MIRT024168 hsa-miR-221-3p Sequencing 20371350
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003674 Function Molecular_function ND
GO:0008150 Process Biological_process ND
GO:0016021 Component Integral component of membrane NAS 10564813
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
620252 1363 ENSG00000106771
Protein
UniProt ID Q9H330
Protein name Transmembrane protein 245 (Protein CG-2)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01594 AI-2E_transport 590 841 AI-2E family transporter Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed. {ECO:0000269|PubMed:10564813}.
Sequence
MADGGGPKDAPSLRSSPGPAPRVPRAVGPSGGGGETPRTAALALRFDKPIKQAFYNTGAV
LFVCLCCGAAVLVYFILEAFLRPLLWAVLCGTFLHPFKSSLTRLGRHWLQRLHRAHTPIV
LAALLLPLCFVDYGVEALGEQALRRRRLLLLLGAGGPLLYGLYCLGSYLGVQVLLVHAAT
LICRGLDYFSSLWIWTLVVGYVLTVSFKWNASTERYLRAVSIPVWIILLFHLASLAGSWR
IPVFLVIVFLMSVGTLYEKQNGKESSGAELPGQVISMAASTLANLAISITGYESSSEDQP
STQPAEAVDRGESAPTLSTSPSPSSPSPTSPSPTLGRRRPEIGTFLRKKKTSDIYFVSLV
WAIVVMQIWLNLWIVQLLPVPIAVWILKKLVIHFGVVDFLEKRYHVWWGIIESFLKERQG
ALAPWPIVGLGKFLLKVDSKLWHWLNKKMIIWLEKMLDKIISIFIIFLLVIGTLLLALLL
TAKVHQESVHMIEVTSNLINETLANHPEWANWLPEAQVVQRALNSAANNVYQYGREWITH
KLHKILGDKVNNTAVIEKQVLELWDRLYHSWFVKNVTHSGRHKGQKLHVSRQNSWLGDIL
DWQDIVSFVHENIETFLSILESLWIVMSRNVSLLFTTVTTLLTILFYSGTALLNFVLSLI
IFLTTLFYLLSSSDEYYKPVKWVISLTPLSQPGPSSNIIGQSVEEAIRGVFDASLKMAGF
YGLYTWLTHTMFGINIVFIPSALAAILGAVPFLGTYWAAVPAVLDLWLTQGLGCKAILLL
IFHLLPTYFVDTAIYSDISGGGHPYLTGLAVAGGAYYLGLEGAIIGPILLCILVVASNIY
S
AMLVSPTNSVPTPNQTPWPAQPQRTFRDISEDLKSSVG
Sequence length 879
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
23382809
Unknown
Disease term Disease name Evidence References Source
Heart Failure Heart Failure GWAS
Associations from Text Mining
Disease Name Relationship Type References
Prostatic Neoplasms Associate 18676839
Prostatitis Stimulate 18676839