Gene Gene information from NCBI Gene database.
Entrez ID 153768
Gene name PRELI domain containing 2
Gene symbol PRELID2
Synonyms (NCBI Gene)
-
Chromosome 5
Chromosome location 5q32
miRNA miRNA information provided by mirtarbase database.
215
miRTarBase ID miRNA Experiments Reference
MIRT498346 hsa-miR-141-3p PAR-CLIP 22291592
MIRT498345 hsa-miR-200a-3p PAR-CLIP 22291592
MIRT498344 hsa-miR-22-3p PAR-CLIP 22291592
MIRT498343 hsa-miR-6515-3p PAR-CLIP 22291592
MIRT498342 hsa-miR-1236-3p PAR-CLIP 22291592
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
5
GO ID Ontology Definition Evidence Reference
GO:0005758 Component Mitochondrial intermembrane space IBA
GO:0005758 Component Mitochondrial intermembrane space IEA
GO:0015914 Process Phospholipid transport IBA
GO:0120009 Process Intermembrane lipid transfer IEA
GO:1990050 Function Phosphatidic acid transfer activity IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620750 28306 ENSG00000186314
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N945
Protein name PRELI domain-containing protein 2
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04707 PRELI 16 185 PRELI-like family Family
Sequence
Sequence length 189
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DYSHIDROSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
RHEUMATIC FEVER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Carcinoma Pancreatic Ductal Associate 37973221
★☆☆☆☆
Found in Text Mining only
Carcinoma Renal Cell Associate 35529267
★☆☆☆☆
Found in Text Mining only
Coronary Artery Disease Associate 22369142
★☆☆☆☆
Found in Text Mining only
Hypoxia Associate 37973221
★☆☆☆☆
Found in Text Mining only
Pancreatic Neoplasms Associate 37973221
★☆☆☆☆
Found in Text Mining only
Squamous Cell Carcinoma of Head and Neck Associate 31698994
★☆☆☆☆
Found in Text Mining only