Gene Gene information from NCBI Gene database.
Entrez ID 51285
Gene name RAS like family 12
Gene symbol RASL12
Synonyms (NCBI Gene)
RIS
Chromosome 15
Chromosome location 15q22.31
miRNA miRNA information provided by mirtarbase database.
63
miRTarBase ID miRNA Experiments Reference
MIRT1292564 hsa-miR-106a CLIP-seq
MIRT1292565 hsa-miR-106b CLIP-seq
MIRT1292566 hsa-miR-138 CLIP-seq
MIRT1292567 hsa-miR-153 CLIP-seq
MIRT1292568 hsa-miR-17 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0003924 Function GTPase activity IBA
GO:0003924 Function GTPase activity IEA
GO:0003925 Function G protein activity IEA
GO:0005515 Function Protein binding IPI 28514442, 32296183, 33961781
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NYN1
Protein name Ras-like protein family member 12 (EC 3.6.5.2) (Ras-like protein Ris)
PDB 3C5C
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00071 Ras 22 185 Ras family Domain
Sequence
Sequence length 266
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
BILE ACID MALABSORPTION, PRIMARY, 2 Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CHOLESTASIS Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HYPERTENSION 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
Carcinoma Squamous Cell Squamous cell carcinoma Pubtator 38084139 Associate
★☆☆☆☆
Found in Text Mining only
Chronic Kidney Diseases Kidney Disease BEFREE 30523414
★☆☆☆☆
Found in Text Mining only
Demyelinating Diseases Demyelinating Diseases BEFREE 28831591
★☆☆☆☆
Found in Text Mining only
Gastroesophageal reflux disease Gastroesophageal Reflux Disease BEFREE 29687695
★☆☆☆☆
Found in Text Mining only
Multiple Sclerosis Multiple Sclerosis BEFREE 28831591
★☆☆☆☆
Found in Text Mining only
Neuromyelitis Optica Neuromyelitis Optica BEFREE 24524923
★☆☆☆☆
Found in Text Mining only
Optic Neuritis Optic Neuritis BEFREE 24524923
★☆☆☆☆
Found in Text Mining only
Refractory anemias Anemia BEFREE 29574518
★☆☆☆☆
Found in Text Mining only
Rheumatoid Arthritis Rheumatoid arthritis BEFREE 29574518
★☆☆☆☆
Found in Text Mining only
Schizophrenia Schizophrenia BEFREE 29568276
★☆☆☆☆
Found in Text Mining only