Gene Gene information from NCBI Gene database.
Entrez ID 114791
Gene name Tubulin gamma complex component 5
Gene symbol TUBGCP5
Synonyms (NCBI Gene)
GCP5
Chromosome 15
Chromosome location 15q11.2
miRNA miRNA information provided by mirtarbase database.
214
miRTarBase ID miRNA Experiments Reference
MIRT030812 hsa-miR-21-5p Microarray 18591254
MIRT648893 hsa-miR-500a-5p HITS-CLIP 23824327
MIRT648892 hsa-miR-5697 HITS-CLIP 23824327
MIRT648891 hsa-miR-2116-3p HITS-CLIP 23824327
MIRT648890 hsa-miR-6778-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
26
GO ID Ontology Definition Evidence Reference
GO:0000226 Process Microtubule cytoskeleton organization IEA
GO:0000278 Process Mitotic cell cycle IBA
GO:0000922 Component Spindle pole IEA
GO:0000930 Component Gamma-tubulin complex IBA
GO:0000931 Component Gamma-tubulin ring complex IDA 11694571
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608147 18600 ENSG00000275835
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96RT8
Protein name Gamma-tubulin complex component 5 (GCP-5)
Protein function Component of the gamma-tubulin ring complex (gTuRC) which mediates microtubule nucleation (PubMed:38305685, PubMed:38609661, PubMed:39321809). The gTuRC regulates the minus-end nucleation of alpha-beta tubulin heterodimers that grow into microtu
PDB 6L81 , 6V69 , 6V6S , 7AS4 , 7QJ0 , 7QJ1 , 7QJ2 , 7QJ3 , 7QJ4 , 7QJ5 , 7QJ6 , 7QJ7 , 7QJ8 , 7QJ9 , 7QJA , 7QJB , 7QJC , 7QJD , 7QJE , 8Q62 , 8RX1 , 8VRD , 8VRJ , 8VRK
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17681 GCP_N_terminal 271 713 Gamma tubulin complex component N-terminal Domain
PF04130 GCP_C_terminal 716 1018 Gamma tubulin complex component C-terminal Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed, with highest levels in heart and skeletal muscle and moderate levels in brain. {ECO:0000269|PubMed:14508708}.
Sequence
MARHGPPWSRLDAQQERDVRELVRGVAGLQDEADPNFQLALNFAWSNFRFHRFLDVNSHK
IEKTIEGIYEKFVIHSDLSKAASWKRLTEEFLNAPLPSIKEIKTDAHYSILSLLLCLSDS
PSNSSYVETPRNKEVEKKDDFDWGKYLMEDEEMDIGPYMDTPNWSEESEEENDQQPLSRE
DSGIQVDRTPLEEQDQNRKLDPCISWKDEPDDRSWLEHHVVHQYWTARPSQFPHSLHLHS
NLAAVWDQHLYSSDPLYVPDDRVLVTETQVIRETLWLLSGVKKLFIFQLIDGKVTVRNNI
IVTHLTHSCLRSVLEQIAAYGQVVFRLQEFIDEVMGHSSESMLPGSGSVPKKSTEAPFRT
YQAFMWALYKYFISFKEELAEIEKCIINNDTTITLAIVVDKLAPRLSQLKVLHKVFSTGV
AEVPPDTRNVVRASHLLNTLYKAILEYDNVGEASEQTVSLLFSLWVETVRPYLQTVDEWI
VHGHLWDGAREFIIQRNKNVPVNHRDFWYATYTLYSVSEKTENEEKMSDNASASSGSDQG
PSSRQHTMVSFLKPVLKQIIMAGKSMQLLKNLQCAESTTCQAGARDAERKSLYTLFLESV
QSRLRHGEDSTPQVLTEQQATKENLMKMQSIAESHLELDDVHDPLLAINFARMYLEQSDF
HEKFAGGDVCVDRSSESVTCQTFELTLRSCLYPHIDKQYLDCCGNLMQTLKKD
YRLVEYL
QAMRNFFLMEGGDTMYDFYTSIFDKIREKETWQNVSFLNVQLQEAVGQRYPEDSSRLSIS
FENVDTAKKKLPVHILDGLTLSYKVPWPVDIVISLECQKIYNQVFLLLLQIKWAKYSLDV
LLFGELVSTAEKPRLKEGLIHEQDTVAQFGPQKEPVRQQIHRMFLLRVKLMHFVNSLHNY
IMTRILHSTGLEFQHQVEEAKDLDQLIKIHYRYLSTIHDRCLLREKVSFVKEAIMKVLNL
ALMFADGWQAGLGTWRMESIEKMESDFKNCHMFLVTILNKAVCRGSFPHLESLALSLM
AG
MEQS
Sequence length 1024
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Recruitment of mitotic centrosome proteins and complexes
Recruitment of NuMA to mitotic centrosomes
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
12
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
Acute myeloid leukemia Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Adrenocortical carcinoma, hereditary Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BIPOLAR DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Colorectal cancer 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
Angelman Syndrome Angelman Syndrome BEFREE 28387067
★☆☆☆☆
Found in Text Mining only
Autism Spectrum Disorder Autism Pubtator 33562221 Associate
★☆☆☆☆
Found in Text Mining only
Autistic Disorder Autism BEFREE 16183798
★☆☆☆☆
Found in Text Mining only
Autistic Disorder Autism Pubtator 16183798 Associate
★☆☆☆☆
Found in Text Mining only
Clumsiness - motor delay Motor delay BEFREE 28254235
★☆☆☆☆
Found in Text Mining only
Developmental Disabilities Developmental disability Pubtator 34680874 Associate
★☆☆☆☆
Found in Text Mining only
Global developmental delay Developmental Delay BEFREE 30543990
★☆☆☆☆
Found in Text Mining only
Hydrocephalus Hydrocephalus Pubtator 30342661 Associate
★☆☆☆☆
Found in Text Mining only
Language Development Disorders Language development disorders Pubtator 28254235 Associate
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of stomach Stomach Neoplasms BEFREE 30557546
★☆☆☆☆
Found in Text Mining only