Gene Gene information from NCBI Gene database.
Entrez ID 5676
Gene name Pregnancy specific beta-1-glycoprotein 7
Gene symbol PSG7
Synonyms (NCBI Gene)
PS-beta-G-7PSBG-7PSG1PSGGA
Chromosome 19
Chromosome location 19q13.31
Summary This gene is a member of the pregnancy-specific glycoprotein (PSG) gene family. The PSG genes are a subgroup of the carcinoembryonic antigen (CEA) family of immunoglobulin-like genes, and are found in a gene cluster at 19q13.1-q13.2 telomeric to another c
miRNA miRNA information provided by mirtarbase database.
39
miRTarBase ID miRNA Experiments Reference
MIRT1269739 hsa-miR-24 CLIP-seq
MIRT1269740 hsa-miR-4269 CLIP-seq
MIRT1269741 hsa-miR-4284 CLIP-seq
MIRT1269742 hsa-miR-4303 CLIP-seq
MIRT1269743 hsa-miR-4468 CLIP-seq
Transcription factors Transcription factors information provided by TRRUST V2 database.
1
Transcription factor Regulation Reference
FOXF2 Repression 19562724
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
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
176396 9524 ENSG00000221878
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q13046
Protein name Pregnancy-specific beta-1-glycoprotein 7 (PS-beta-G-7) (PSBG-7) (Pregnancy-specific glycoprotein 7)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07686 V-set 38 141 Immunoglobulin V-set domain Domain
PF13927 Ig_3 148 221 Domain
PF13895 Ig_2 239 328 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.).
2
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
AUTISM SPECTRUM DISORDERS Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Pre Eclampsia Stimulate 35322669
★☆☆☆☆
Found in Text Mining only
Preeclamptic toxemia Stimulate 35322669
★☆☆☆☆
Found in Text Mining only