PRELID3B (PRELI domain containing 3B)

Gene Gene information from NCBI Gene database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID 51012
Gene name PRELI domain containing 3B
Gene symbol PRELID3B
Synonyms (NCBI Gene)
C20orf45SLMO2UPS2dJ543J19.5
Chromosome 20
Chromosome location 20q13.32
miRNA miRNA information provided by mirtarbase database.
27
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (27)
miRTarBase ID miRNA Experiments Reference
MIRT561556 hsa-miR-548aa PAR-CLIP 20371350
MIRT561555 hsa-miR-548ap-3p PAR-CLIP 20371350
MIRT561554 hsa-miR-548t-3p PAR-CLIP 20371350
MIRT561553 hsa-miR-548as-3p PAR-CLIP 20371350
MIRT561552 hsa-miR-548at-3p PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (7)
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 27499296, 28514442, 33961781
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005758 Component Mitochondrial intermembrane space IBA
GO:0005758 Component Mitochondrial intermembrane space IEA
GO:0015914 Process Phospholipid transport IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
620754 15892 ENSG00000101166
Protein Protein information from UniProt database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9Y3B1
Protein name PRELI domain containing protein 3B (Protein slowmo homolog 2)
PDB 6I4Y
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04707 PRELI 15 → 170 PRELI-like family Family
Sequence
Sequence length 194
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
Gene miRNA Gene ontology Other IDs Protein Associated diseases
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)
Show/Hide Unknown Diseases (3)
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
CORONARY ARTERY DISEASE — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HYPERTENSION — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Show/Hide Text Mining Associations (4)
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Breast Neoplasms Breast neoplasm Pubtator 25148458, 38212657 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Critical Illness Critical illness Pubtator 25254322 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Lung Neoplasms Lung neoplasms Pubtator 38212657 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Osteoporosis Osteoporosis Pubtator 25148458 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only