Gene Gene information from NCBI Gene database.
Entrez ID 5672
Gene name Pregnancy specific beta-1-glycoprotein 4
Gene symbol PSG4
Synonyms (NCBI Gene)
PSBG-4PSBG-9PSG9
Chromosome 19
Chromosome location 19q13.31
Summary The protein encoded by this gene is a pregnancy-specific glycoprotein (PSG), one of several encoded by a cluster of similar genes on chromosome 19. This gene is a member of the carcinoembryonic antigen (CEA) gene family and may play a role in regulation o
miRNA miRNA information provided by mirtarbase database.
105
miRTarBase ID miRNA Experiments Reference
MIRT437515 hsa-miR-19b-3p Immunoprecipitaion 22382630
MIRT724778 hsa-miR-7109-3p HITS-CLIP 19536157
MIRT724777 hsa-miR-6819-3p HITS-CLIP 19536157
MIRT724776 hsa-miR-6877-3p HITS-CLIP 19536157
MIRT724775 hsa-miR-6892-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
2
GO ID Ontology Definition Evidence Reference
GO:0005576 Component Extracellular region IEA
GO:0007565 Process Female pregnancy TAS 1690992, 7794280
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
176393 9521 ENSG00000243137
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q00888
Protein name Pregnancy-specific beta-1-glycoprotein 4 (PS-beta-G-4) (PSBG-4) (Pregnancy-specific glycoprotein 4) (Pregnancy-specific beta-1-glycoprotein 9) (PS-beta-G-9) (PSBG-9) (Pregnancy-specific glycoprotein 9)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07686 V-set 38 143 Immunoglobulin V-set domain Domain
PF13927 Ig_3 148 221 Domain
PF13895 Ig_2 238 328 Immunoglobulin domain Domain
PF13895 Ig_2 334 413 Immunoglobulin domain Domain
Sequence
Sequence length 419
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Cell surface interactions at the vascular wall
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
AUTISM SPECTRUM DISORDER CTD
★★☆☆☆
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 33824285
★☆☆☆☆
Found in Text Mining only
Exocrine Pancreatic Insufficiency Associate 33857242
★☆☆☆☆
Found in Text Mining only
Lymphatic Metastasis Associate 33824285
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 33824285
★☆☆☆☆
Found in Text Mining only