Gene Gene information from NCBI Gene database.
Entrez ID 6015
Gene name Ring finger protein 1
Gene symbol RING1
Synonyms (NCBI Gene)
RING1ARNF1
Chromosome 6
Chromosome location 6p21.32
Summary This gene belongs to the RING finger family, members of which encode proteins characterized by a RING domain, a zinc-binding motif related to the zinc finger domain. The gene product can bind DNA and can act as a transcriptional repressor. It is associate
miRNA miRNA information provided by mirtarbase database.
39
miRTarBase ID miRNA Experiments Reference
MIRT020727 hsa-miR-155-5p Proteomics 18668040
MIRT042052 hsa-miR-484 CLASH 23622248
MIRT2315812 hsa-miR-1197 CLIP-seq
MIRT2315813 hsa-miR-1275 CLIP-seq
MIRT2315814 hsa-miR-1587 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
35
GO ID Ontology Definition Evidence Reference
GO:0000151 Component Ubiquitin ligase complex IBA
GO:0000151 Component Ubiquitin ligase complex IEA
GO:0001739 Component Sex chromatin IEA
GO:0003682 Function Chromatin binding IBA
GO:0003682 Function Chromatin binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
602045 10018 ENSG00000204227
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q06587
Protein name E3 ubiquitin-protein ligase RING1 (EC 2.3.2.27) (Polycomb complex protein RING1) (RING finger protein 1) (RING-type E3 ubiquitin transferase RING1) (Really interesting new gene 1 protein)
Protein function Constitutes one of the E3 ubiquitin-protein ligases that mediate monoubiquitination of 'Lys-119' of histone H2A, thereby playing a central role in histone code and gene regulation. H2A 'Lys-119' ubiquitination gives a specific tag for epigenetic
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00097 zf-C3HC4 48 87 Zinc finger, C3HC4 type (RING finger) Domain
PF16207 RAWUL 282 400 RAWUL domain RING finger- and WD40-associated ubiquitin-like Domain
Sequence
MTTPANAQNASKTWELSLYELHRTPQEAIMDGTEIAVSPRSLHSELMCPICLDMLKNTMT
TKECLHRFCSDCIVTALRSGNKECPTC
RKKLVSKRSLRPDPNFDALISKIYPSREEYEAH
QDRVLIRLSRLHNQQALSSSIEEGLRMQAMHRAQRVRRPIPGSDQTTTMSGGEGEPGEGE
GDGEDVSSDSAPDSAPGPAPKRPRGGGAGGSSVGTGGGGTGGVGGGAGSEDSGDRGGTLG
GGTLGPPSPPGAPSPPEPGGEIELVFRPHPLLVEKGEYCQTRYVKTTGNATVDHLSKYLA
LRIALERRQQQEAGEPGGPGGGASDTGGPDGCGGEGGGAGGGDGPEEPALPSLEGVSEKQ
YTIYIAPGGGAFTTLNGSLTLELVNEKFWKVSRPLELCYA
PTKDPK
Sequence length 406
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Polycomb repressive complex   Oxidative Stress Induced Senescence
SUMOylation of DNA damage response and repair proteins
SUMOylation of transcription cofactors
SUMOylation of chromatin organization proteins
SUMOylation of RNA binding proteins
RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known
Regulation of PTEN gene transcription
Transcriptional Regulation by E2F6
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
COMPLEX NEURODEVELOPMENTAL DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INFLAMMATORY BOWEL DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
NON-SPECIFIC SYNDROMIC INTELLECTUAL DISABILITY Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Carcinoma Hepatocellular Associate 26141041
★☆☆☆☆
Found in Text Mining only
Carcinoma Non Small Cell Lung Stimulate 24414991
★☆☆☆☆
Found in Text Mining only
Carcinoma Non Small Cell Lung Associate 26141041
★☆☆☆☆
Found in Text Mining only
Carcinoma Renal Cell Inhibit 16528373
★☆☆☆☆
Found in Text Mining only
Colonic Neoplasms Associate 9199346
★☆☆☆☆
Found in Text Mining only
Endometrial Neoplasms Associate 38219048
★☆☆☆☆
Found in Text Mining only
Graft vs Host Disease Associate 33446692
★☆☆☆☆
Found in Text Mining only
Hereditary leiomyomatosis and renal cell cancer Associate 14982841
★☆☆☆☆
Found in Text Mining only
Leukemia Lymphoma Adult T Cell Associate 21228036
★☆☆☆☆
Found in Text Mining only
Lung Neoplasms Stimulate 24414991
★☆☆☆☆
Found in Text Mining only