Gene Gene information from NCBI Gene database.
Entrez ID 65983
Gene name GRAM domain containing 2B
Gene symbol GRAMD2B
Synonyms (NCBI Gene)
GRAMD3NS3TP2
Chromosome 5
Chromosome location 5q23.2
miRNA miRNA information provided by mirtarbase database.
31
miRTarBase ID miRNA Experiments Reference
MIRT165172 hsa-miR-15a-5p HITS-CLIP 19536157
MIRT165173 hsa-miR-16-5p HITS-CLIP 19536157
MIRT165177 hsa-miR-15b-5p HITS-CLIP 19536157
MIRT165180 hsa-miR-195-5p HITS-CLIP 19536157
MIRT165183 hsa-miR-424-5p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
5
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 25910212, 26871637, 29892012, 31515488, 32296183
GO:0005737 Component Cytoplasm IEA
GO:0005881 Component Cytoplasmic microtubule IBA
GO:0005881 Component Cytoplasmic microtubule IDA 23264731
GO:0042802 Function Identical protein binding IPI 25416956, 32296183
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620182 24911 ENSG00000155324
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96HH9
Protein name GRAM domain-containing protein 2B (HCV NS3-transactivated protein 2)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02893 GRAM 110 218 GRAM domain Domain
Sequence
MTELQQDVEDTKPAKVLGKRESKLGSAHSEAENGVEEKKKACRSPTAQSPTPSVEADSPD
QKKIISLWSKSSFDGASLASDKNDCKTESKNDPKTERKKSSSSSQYKANMHFHKLFLSVP
TEEPLKQSFTCALQKEILYQGKLFVSENWICFHSKVFGKDTKISIPAFSVTLIKKTKTAL
LVPNALIIATVTDRYIFVSLLSRDSTYKLLKSVCGHLE
NTSVGNSPNPSSAENSFRADRP
SSLPLDFNDEFSDLDGVVQQRRQDMEGYSSSGSQTPESENSRDFHATESQTVLNVSKGEA
KPTRADAHVNRVPEGKAKSLPVQGLSETVGILHKVKSQKCPMLHHILIFYAIVVCALIIS
TFYMRYRINTLEEQLGLLTSIVDTHNTEQAAPSGLRSQVQFNVEVLCQELTANIVKLEKI
QNNLQKLLENGD
Sequence length 432
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
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
ASTHMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARDIOVASCULAR DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Cervical cancer Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DIABETIC NEPHROPATHY GWAS catalog
★★☆☆☆
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
Chronic kidney disease stage 5 Kidney Disease BEFREE 31092297
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus, Non-Insulin-Dependent Diabetes Mellitus BEFREE 31092297
★☆☆☆☆
Found in Text Mining only
Glycogen Storage Disease Type II Glycogen storage disease Pubtator 20360305 Associate
★☆☆☆☆
Found in Text Mining only
Kidney Failure, Chronic Kidney Failure BEFREE 31092297
★☆☆☆☆
Found in Text Mining only