Gene Gene information from NCBI Gene database.
Entrez ID 199745
Gene name THAP domain containing 8
Gene symbol THAP8
Synonyms (NCBI Gene)
-
Chromosome 19
Chromosome location 19q13.12
miRNA miRNA information provided by mirtarbase database.
59
miRTarBase ID miRNA Experiments Reference
MIRT518365 hsa-miR-590-3p PAR-CLIP 23446348
MIRT518364 hsa-miR-7845-5p PAR-CLIP 23446348
MIRT518363 hsa-miR-4735-5p PAR-CLIP 23446348
MIRT518362 hsa-miR-92b-5p PAR-CLIP 23446348
MIRT518361 hsa-miR-193b-5p PAR-CLIP 23446348
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
GO ID Ontology Definition Evidence Reference
GO:0003677 Function DNA binding IEA
GO:0005515 Function Protein binding IPI 25416956, 31515488, 32296183
GO:0008270 Function Zinc ion binding IEA
GO:0046872 Function Metal ion binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
612536 23191 ENSG00000161277
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8NA92
Protein name THAP domain-containing protein 8
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05485 THAP 5 85 THAP domain Domain
Sequence
MPKYCRAPNCSNTAGRLGADNRPVSFYKFPLKDGPRLQAWLQHMGCEHWVPSCHQHLCSE
HFTPSCFQWRWGVRYLRPDAVPSIF
SRGPPAKSQRRTRSTQKPVSPPPPLQKNTPLPQSP
AIPVSGPVRLVVLGPTSGSPKTVATMLLTPLAPAPTPERSQPEVPAQQAQTGLGPVLGAL
QRRVRRLQRCQERHQAQLQALERLAQQLHGESLLARARRGLQRLTTAQTLGPEESQTFTI
ICGGPDIAMVLAQDPAPATVDAKPELLDTRIPSA
Sequence length 274
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
SCHIZOPHRENIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations