Gene Gene information from NCBI Gene database.
Entrez ID 11342
Gene name Ring finger protein 13
Gene symbol RNF13
Synonyms (NCBI Gene)
DEE73EIEE73RZF
Chromosome 3
Chromosome location 3q25.1
Summary The protein encoded by this gene contains a RING zinc finger, a motif known to be involved in protein-protein interactions. The specific function of this gene has not yet been determined. Alternatively spliced transcript variants that encode the same prot
SNPs SNP information provided by dbSNP.
2
SNP ID Visualize variation Clinical significance Consequence
rs1559980771 T>C Pathogenic Non coding transcript variant, missense variant, coding sequence variant
rs1559980785 T>C Pathogenic Non coding transcript variant, missense variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
163
miRTarBase ID miRNA Experiments Reference
MIRT027479 hsa-miR-98-5p Microarray 19088304
MIRT449458 hsa-miR-4680-3p PAR-CLIP 22100165
MIRT449457 hsa-miR-219b-3p PAR-CLIP 22100165
MIRT449456 hsa-miR-219a-2-3p PAR-CLIP 22100165
MIRT449455 hsa-miR-3160-3p PAR-CLIP 22100165
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
33
GO ID Ontology Definition Evidence Reference
GO:0004842 Function Ubiquitin-protein transferase activity IEA
GO:0004842 Function Ubiquitin-protein transferase activity ISS
GO:0005515 Function Protein binding IPI 19690564, 25260751
GO:0005634 Component Nucleus IEA
GO:0005637 Component Nuclear inner membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
609247 10057 ENSG00000082996
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O43567
Protein name E3 ubiquitin-protein ligase RNF13 (EC 2.3.2.27) (RING finger protein 13)
Protein function E3 ubiquitin-protein ligase that regulates cell proliferation (PubMed:18794910, PubMed:23378536, PubMed:30595371). Involved in apoptosis regulation (PubMed:23378536, PubMed:30595371). Mediates ER stress-induced activation of JNK signaling pathwa
PDB 5ZBU , 5ZC4
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02225 PA 64 158 PA domain Family
PF13639 zf-RING_2 238 282 Ring finger domain Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed (at protein level). In normal pancreas, expressed in islets, but not in ducts, nor in acini (at protein level). {ECO:0000269|PubMed:18794910}.
Sequence
MLLSIGMLMLSATQVYTILTVQLFAFLNLLPVEADILAYNFENASQTFDDLPARFGYRLP
AEGLKGFLINSKPENACEPIVPPPVKDNSSGTFIVLIRRLDCNFDIKVLNAQRAGYKAAI
VHNVDSDDLISMGSNDIEVLKKIDIPSVFIGESSANSL
KDEFTYEKGGHLILVPEFSLPL
EYYLIPFLIIVGICLILIVIFMITKFVQDRHRARRNRLRKDQLKKLPVHKFKKGDEYDVC
AICLDEYEDGDKLRILPCSHAYHCKCVDPWLTKTKKTCPVCK
QKVVPSQGDSDSDTDSSQ
EENEVTEHTPLLRPLASVSAQSFGALSESRSHQNMTESSDYEEDDNEDTDSSDAENEINE
HDVVVQLQPNGERDYNIANTV
Sequence length 381
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Developmental and epileptic encephalopathy, 73 Likely pathogenic; Pathogenic rs2108622234, rs2473635400, rs2473635477, rs1559980771, rs1559980785 RCV003883179
RCV004798971
RCV002509894
RCV000766219
RCV000766220
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Uncertain significance rs1248927481 RCV005931576
Ovarian serous cystadenocarcinoma Uncertain significance rs552262347 RCV005926761
RNF13-related disorder Likely benign; Uncertain significance; Benign rs193248526, rs760365736, rs2473636530, rs2473204630, rs2473426711, rs150196894 RCV003933564
RCV004731301
RCV003399948
RCV003949476
RCV003914758
RCV003915901
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Blindness Associate 30595371
Brain Diseases Associate 30595371
Developmental Disabilities Associate 30595371
Epileptic Encephalopathy Early Infantile 3 Associate 34831286
Leukemia Myeloid Acute Associate 33083473
Microcephaly Associate 30595371
Neurodegenerative Diseases Associate 30595371
Uveal melanoma Associate 33387485