Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
7224
Gene name Gene Name - the full gene name approved by the HGNC.
Transient receptor potential cation channel subfamily C member 5
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TRPC5
Synonyms (NCBI Gene) Gene synonyms aliases
PPP1R159, TRP5
Chromosome Chromosome number
X
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Xq23
Summary Summary of gene provided in NCBI Entrez Gene.
This gene belongs to the transient receptor family. It encodes one of the seven mammalian TRPC (transient receptor potential channel) proteins. The encoded protein is a multi-pass membrane protein and is thought to form a receptor-activated non-selective
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT038711 hsa-miR-29b-2-5p CLASH 23622248
MIRT438273 hsa-miR-320a Luciferase reporter assay, qRT-PCR, Western blot 25159093
MIRT438273 hsa-miR-320a Luciferase reporter assay, qRT-PCR, Western blot 25159093
MIRT533448 hsa-miR-32-3p PAR-CLIP 22012620
MIRT533446 hsa-miR-4789-3p PAR-CLIP 22012620
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003779 Function Actin binding IEA
GO:0005262 Function Calcium channel activity IDA 20164195
GO:0005515 Function Protein binding IPI 20164195, 32110987
GO:0005737 Component Cytoplasm IEA
GO:0005886 Component Plasma membrane TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
300334 12337 ENSG00000072315
Protein
UniProt ID Q9UL62
Protein name Short transient receptor potential channel 5 (TrpC5) (Transient receptor protein 5) (TRP-5) (hTRP-5) (hTRP5)
Protein function Forms a receptor-activated non-selective calcium permeant cation channel (PubMed:16284075, PubMed:38959890, PubMed:37137991). Mediates calcium-dependent phosphatidylserine externalization and apoptosis in neurons via its association with PLSCR1
PDB 6YSN , 7D4P , 7D4Q , 7E4T , 7WDB , 7X6C , 7X6I , 8GVW , 8GVX
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12796 Ank_2 36 126 Ankyrin repeats (3 copies) Repeat
PF08344 TRP_2 176 238 Transient receptor ion channel II Family
PF00520 Ion_trans 363 636 Ion transport protein Family
Tissue specificity TISSUE SPECIFICITY: Expressed in brain with higher levels in fetal brain. Found in cerebellum and occipital pole. {ECO:0000269|PubMed:9687496}.
Sequence
MAQLYYKKVNYSPYRDRIPLQIVRAETELSAEEKAFLNAVEKGDYATVKQALQEAEIYYN
VNINCMDPLGRSALLIAIENENLEIMELLLNHSVYVGDALLYAIRKEVVGAVELLLSYRR
PSGEKQ
VPTLMMDTQFSEFTPDITPIMLAAHTNNYEIIKLLVQKRVTIPRPHQIRCNCVE
CVSSSEVDSLRHSRSRLNIYKALASPSLIALSSEDPILTAFRLGWELKELSKVENEFK
AE
YEELSQQCKLFAKDLLDQARSSRELEIILNHRDDHSEELDPQKYHDLAKLKVAIKYHQKE
FVAQPNCQQLLATLWYDGFPGWRRKHWVVKLLTCMTIGFLFPMLSIAYLISPRSNLGLFI
KKPFIKFICHTASYLTFLFMLLLASQHIVRTDLHVQGPPPTVVEWMILPWVLGFIWGEIK
EMWDGGFTEYIHDWWNLMDFAMNSLYLATISLKIVAYVKYNGSRPREEWEMWHPTLIAEA
LFAISNILSSLRLISLFTANSHLGPLQISLGRMLLDILKFLFIYCLVLLAFANGLNQLYF
YYETRAIDEPNNCKGIRCEKQNNAFSTLFETLQSLFWSVFGLLNLYVTNVKARHEFTEFV
GATMFGTYNVISLVVLLNMLIAMMNNSYQLIADHAD
IEWKFARTKLWMSYFDEGGTLPPP
FNIIPSPKSFLYLGNWFNNTFCPKRDPDGRRRRRNLRSFTERNADSLIQNQHYQEVIRNL
VKRYVAAMIRNSKTHEGLTEENFKELKQDISSFRYEVLDLLGNRKHPRSFSTSSTELSQR
DDNNDGSGGARAKSKSVSFNLGCKKKTCHGPPLIRTMPRSSGAQGKSKAESSSKRSFMGP
SLKKLGLLFSKFNGHMSEPSSEPMYTISDGIVQQHCMWQDIRYSQMEKGKAEACSQSEIN
LSEVELGEVQGAAQSSECPLACSSSLHCASSICSSNSKLLDSSEDVFETWGEACDLLMHK
WGDGQEEQVTTRL
Sequence length 973
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Axon guidance
GnRH secretion
  TRP channels
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Hypertension Hypertensive disease rs13306026 17351372
Unknown
Disease term Disease name Evidence References Source
Neurodevelopmental Disorders neurodevelopmental disorder GenCC
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Associate 32205467
Atrial Fibrillation Associate 28839241
Autism Spectrum Disorder Associate 36323681
Breast Neoplasms Associate 28032400, 37174704
Colorectal Neoplasms Associate 29463225
Congenital Hyperinsulinism Associate 23869231
Glioma Associate 18211288, 39189437
Intellectual Disability Associate 15254149, 36323681
Intracranial Hemorrhage Hypertensive Inhibit 21957871
Neoplasms Associate 28032400