|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
27229
|
|
Gene name
Gene Name - the full gene name approved by the HGNC.
|
Tubulin gamma complex component 4 |
|
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
|
TUBGCP4 |
|
Synonyms (NCBI Gene)
Gene synonyms aliases
|
76P, GCP-4, GCP4, Grip76, MCCRP3 |
|
Chromosome
Chromosome number
|
15 |
|
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
15q15.3 |
|
Summary
Summary of gene provided in NCBI Entrez Gene.
|
This gene encodes a component of the gamma-tubulin ring complex, which is required for microtubule nucleation. In mammalian cells, the protein localizes to centrosomes in association with gamma-tubulin. Crystal structure analysis revealed a structure comp |
| UniProt ID |
Q9UGJ1
|
| Protein name |
Gamma-tubulin complex component 4 (GCP-4) (hGCP4) (Gamma-ring complex protein 76 kDa) (h76p) (hGrip76) |
| 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 |
3RIP
,
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 |
2 → 347 |
Gamma tubulin complex component N-terminal |
Domain |
|
PF04130
|
GCP_C_terminal |
350 → 655 |
Gamma tubulin complex component C-terminal |
Domain |
|
| Tissue specificity |
TISSUE SPECIFICITY: Ubiquitously expressed. |
| Sequence |
|
| Sequence length |
667 |
| Interactions |
View interactions
|
|
Causal
Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
|
| Disease merge term |
Disease name |
dbSNP ID |
References |
| Microcephaly with Chorioretinopathy |
Microcephaly and chorioretinopathy 3 |
rs200092283, rs794726855, rs794726856, rs1595496969 |
N/A |
|
|
Unknown
Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
|
| Disease merge term |
Disease name |
Evidence |
References |
Source |
| Optic Atrophy |
optic atrophy |
N/A |
N/A |
ClinVar |
| retinal dystrophy |
Retinal dystrophy |
N/A |
N/A |
ClinVar |
|
|
Associations from Text Mining
Disease associations identified through Pubtator
|
| Disease Name |
Relationship Type |
References |
| Amyotrophic Lateral Sclerosis |
Associate
|
30886340 |
| Aneuploidy |
Associate
|
25817018 |
| Autosomal Recessive Primary Microcephaly |
Associate
|
25817018 |
| Carcinoma Hepatocellular |
Associate
|
36530949 |
| Chorioretinitis |
Associate
|
25817018 |
| Congenital Abnormalities |
Associate
|
25817018 |
| Familial Exudative Vitreoretinopathies |
Associate
|
33137195 |
| Microcephaly |
Associate
|
25817018, 33137195 |
| Microcephaly with Chorioretinopathy Autosomal Dominant |
Associate
|
25817018, 33137195 |
| Microphthalmia Syndromic 6 |
Associate
|
25817018 |
| Retinal Diseases |
Associate
|
33137195 |
| Sveinsson Chorioretinal Atrophy |
Associate
|
33137195 |
|