Gene Gene information from NCBI Gene database.
Entrez ID 389158
Gene name Phospholipid scramblase family member 5
Gene symbol PLSCR5
Synonyms (NCBI Gene)
-
Chromosome 3
Chromosome location 3q24
miRNA miRNA information provided by mirtarbase database.
10
miRTarBase ID miRNA Experiments Reference
MIRT1243313 hsa-miR-181a CLIP-seq
MIRT1243314 hsa-miR-181b CLIP-seq
MIRT1243315 hsa-miR-181c CLIP-seq
MIRT1243316 hsa-miR-181d CLIP-seq
MIRT1243317 hsa-miR-3613-3p CLIP-seq
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:0005886 Component Plasma membrane IBA
GO:0017121 Process Plasma membrane phospholipid scrambling IBA
GO:0017121 Process Plasma membrane phospholipid scrambling IEA
GO:0017128 Function Phospholipid scramblase activity IBA
GO:0017128 Function Phospholipid scramblase activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
A0PG75
Protein name Phospholipid scramblase family member 5
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03803 Scramblase 44 266 Scramblase Domain
Sequence
Sequence length 271
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
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
ATTENTION DEFICIT HYPERACTIVITY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BARRETT'S ESOPHAGUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
STROKE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SUBSTANCE ABUSE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations