GRTP1 (growth hormone regulated TBC protein 1)

Gene
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
79774
Gene name Gene Name - the full gene name approved by the HGNC.
Growth hormone regulated TBC protein 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
GRTP1
Synonyms (NCBI Gene) Gene synonyms aliases
TBC1D6
Chromosome Chromosome number
13
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
13q34
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(11)
miRTarBase ID miRNA Experiments Reference
MIRT029761 hsa-miR-26b-5p Microarray 19088304
MIRT050409 hsa-miR-23a-3p CLASH 23622248
MIRT1035582 hsa-miR-1297 CLIP-seq
MIRT1035583 hsa-miR-26a CLIP-seq
MIRT1035584 hsa-miR-26b CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all(4)
GO ID Ontology Definition Evidence Reference
GO:0005096 Function GTPase activator activity IBA
GO:0005096 Function GTPase activator activity IEA
GO:0005737 Component Cytoplasm IBA
GO:0005886 Component Plasma membrane IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
620890 20310 ENSG00000139835
Protein
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Q5TC63
Protein name Growth hormone-regulated TBC protein 1 (TBC1 domain family member 6)
Protein function May act as a GTPase-activating protein for Rab family protein(s).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00566 RabGAP-TBC 71 → 278 Rab-GTPase-TBC domain Family
Sequence
Sequence length 336
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide Unknown Diseases (1)
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
Astrocytoma Pilocytic astrocytoma N/A N/A GWAS
Show/Hide Text Mining Associations (3)
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Autism Spectrum Disorder Stimulate 26290361
Pain Associate 33573686
Sciatica Associate 33573686