Gene Gene information from NCBI Gene database.
Entrez ID 4858
Gene name NOVA alternative splicing regulator 2
Gene symbol NOVA2
Synonyms (NCBI Gene)
ANOVANEDASBNOVA-2NOVA3
Chromosome 19
Chromosome location 19q13.32
SNPs SNP information provided by dbSNP.
1
SNP ID Visualize variation Clinical significance Consequence
rs1600596180 A>- Pathogenic Frameshift variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
88
miRTarBase ID miRNA Experiments Reference
MIRT655803 hsa-miR-7114-5p HITS-CLIP 23824327
MIRT655804 hsa-miR-134-3p HITS-CLIP 23824327
MIRT655802 hsa-miR-627-3p HITS-CLIP 23824327
MIRT655801 hsa-miR-3119 HITS-CLIP 23824327
MIRT655800 hsa-miR-4474-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
30
GO ID Ontology Definition Evidence Reference
GO:0000381 Process Regulation of alternative mRNA splicing, via spliceosome IBA
GO:0000381 Process Regulation of alternative mRNA splicing, via spliceosome IEA
GO:0000381 Process Regulation of alternative mRNA splicing, via spliceosome IMP 32197073
GO:0000381 Process Regulation of alternative mRNA splicing, via spliceosome ISS
GO:0000398 Process MRNA splicing, via spliceosome IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601991 7887 ENSG00000104967
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9UNW9
Protein name RNA-binding protein Nova-2 (Astrocytic NOVA1-like RNA-binding protein) (Neuro-oncological ventral antigen 2)
Protein function Functions to regulate alternative splicing in neurons by binding pre-mRNA in a sequence-specific manner to activate exon inclusion or exclusion (PubMed:32197073). It binds specifically to the sequences 5'-YCAY-3' and regulates splicing in only a
PDB 1DTJ , 1EC6
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00013 KH_1 35 101 KH domain Domain
PF00013 KH_1 132 198 KH domain Domain
PF00013 KH_1 408 475 KH domain Domain
Tissue specificity TISSUE SPECIFICITY: Brain. Expression restricted to astrocytes.
Sequence
MEPEAPDSRKRPLETPPEVVCTKRSNTGEEGEYFLKVLIPSYAAGSIIGKGGQTIVQLQK
ETGATIKLSKSKDFYPGTTERVCLVQGTAEALNAVHSFIAE
KVREIPQAMTKPEVVNILQ
PQTTMNPDRAKQAKLIVPNSTAGLIIGKGGATVKAVMEQSGAWVQLSQKPEGINLQERVV
TVSGEPEQVHKAVSAIVQ
KVQEDPQSSSCLNISYANVAGPVANSNPTGSPYASPADVLPA
AAAASAAAASGLLGPAGLAGVGAFPAALPAFSGTDLLAISTALNTLASYGYNTNSLGLGL
NSAAASGVLAAVAAGANPAAAAAANLLASYAGEAGAGPAGGAAPPPPPPPGALGSFALAA
AANGYLGAGAGGGAGGGGGPLVAAAAAAGAAGGFLTAEKLAAESAKELVEIAVPENLVGA
ILGKGGKTLVEYQELTGARIQISKKGEFLPGTRNRRVTITGSPAATQAAQYLISQ
RVTYE
QGVRASNPQKVG
Sequence length 492
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
8
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)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Intellectual disability Pathogenic rs2146406775 RCV002273906
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities Likely pathogenic; Pathogenic rs2146406554, rs2513852929, rs2513852016, rs1600596180, rs1967742137, rs1967741450, rs1967739365, rs1967737959, rs1967741386 RCV001786534
RCV002465435
RCV003992061
RCV001090014
RCV001090015
RCV001090016
RCV001090017
RCV001090018
RCV001090019
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
NOVA2-related disorder Likely pathogenic rs2513851808 RCV003412461
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Severe intellectual disability Pathogenic rs1600596180 RCV001002674
★★★★☆
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
COMPLEX NEURODEVELOPMENTAL DISORDER ClinGen, Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
NEUROTIC DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
NON-SPECIFIC SYNDROMIC INTELLECTUAL DISABILITY Disgenet, Orphanet
Disgenet, Orphanet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Adenocarcinoma of Lung Associate 37920146
★☆☆☆☆
Found in Text Mining only
Apraxias Associate 35607920
★☆☆☆☆
Found in Text Mining only
Arthropathy progressive pseudorheumatoid of childhood Associate 40549212
★☆☆☆☆
Found in Text Mining only
Attention Deficit Disorder with Hyperactivity Associate 35607920
★☆☆☆☆
Found in Text Mining only
Autoimmune Diseases of the Nervous System Associate 10368286
★☆☆☆☆
Found in Text Mining only
Brain Diseases Associate 35607920
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Associate 32101070
★☆☆☆☆
Found in Text Mining only
Carcinoma Non Small Cell Lung Associate 37864285
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Associate 28276498
★☆☆☆☆
Found in Text Mining only
Developmental Disabilities Associate 35607920
★☆☆☆☆
Found in Text Mining only