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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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PSG7
pregnancy specific beta-1-glycoprotein 7
Chromosome 19 · 19q13.31
NCBI Gene: 5676Ensembl: ENSG00000221878.13HGNC: HGNC:9524UniProt: A0A096LNM5
19PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
protein bindingfemale pregnancyextracellular regionplacenta praeviapreeclampsiaobesity due to melanocortin 4 receptor deficiencypapillary thyroid carcinoma
✦AI Summary

PSG7 (pregnancy-specific beta-1-glycoprotein 7) is a member of the carcinoembryonic antigen gene family located on chromosome 19.2 1. The gene encodes a glycoprotein that functions as a biomarker and potentially pathogenic factor in pregnancy complications. PSG7 expression is minimal in undifferentiated trophoblast cells but significantly increases during cytotrophoblast differentiation, serving as an early marker of trophoblast syncytialization 2. The protein contains an RGD sequence in its N-domain and has a unique unblocked N-terminal structure with a cysteine residue that may allow dimerization 3. Clinically, PSG7 demonstrates significant biomarker potential for preeclampsia, with elevated circulating levels observed weeks before disease onset and in established severe cases 4. The protein's expression and secretion are induced by inflammatory cytokines TNF-α and IL-6, suggesting placental inflammation drives its production 4. Recent Mendelian randomization studies indicate increased fetal PSG7 levels may causally contribute to increased birthweight 5. Additionally, PSG7 expression shows sex-specific associations with poor survival outcomes in female lung adenocarcinoma patients, potentially through KRAS signaling pathway modulation 6.

Sources cited
1
PSG7 is located on chromosome 19q13.2 as part of the CEA gene family
PMID: 7851895
2
PSG7 expression increases during trophoblast differentiation and serves as an early marker
PMID: 20116096
3
PSG7 has unique structural features including RGD sequence and unblocked N-terminal
PMID: 2328001
4
PSG7 is elevated before preeclampsia onset and its expression is induced by inflammatory cytokines
PMID: 35322669
5
Increased fetal PSG7 levels are potentially causal for increased birthweight
PMID: 40991151
6
PSG7 shows sex-specific associations with survival in female lung adenocarcinoma patients
PMID: 40257008
Disease Associationsⓘ20
placenta praeviaOpen Targets
0.23Weak
preeclampsiaOpen Targets
0.08Suggestive
obesity due to melanocortin 4 receptor deficiencyOpen Targets
0.06Suggestive
papillary thyroid carcinomaOpen Targets
0.05Suggestive
LIPE-related familial partial lipodystrophyOpen Targets
0.04Suggestive
obesity due to leptin receptor gene deficiencyOpen Targets
0.04Suggestive
PLIN1-related familial partial lipodystrophyOpen Targets
0.04Suggestive
AXIN2-related attenuated familial adenomatous polyposisOpen Targets
0.04Suggestive
obesity due to pro-opiomelanocortin deficiencyOpen Targets
0.04Suggestive
obesity due to prohormone convertase I deficiencyOpen Targets
0.04Suggestive
lipodystrophy, congenital generalized, type 5Open Targets
0.04Suggestive
Muir-Torre syndromeOpen Targets
0.04Suggestive
obesity due to congenital leptin deficiencyOpen Targets
0.04Suggestive
short stature due to primary acid-labile subunit deficiencyOpen Targets
0.04Suggestive
AKT2-related familial partial lipodystrophyOpen Targets
0.03Suggestive
Familial partial lipodystrophy due to AKT2 mutationsOpen Targets
0.03Suggestive
familial partial lipodystrophy, Kobberling typeOpen Targets
0.03Suggestive
Familial partial lipodystrophy, Köbberling typeOpen Targets
0.03Suggestive
CIDEC-related familial partial lipodystrophyOpen Targets
0.03Suggestive
MODYOpen Targets
0.03Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
RLN1Shared pathway100%PZPShared pathway100%PSG6Protein interaction85%PSG1Protein interaction85%CSH1Protein interaction76%CSH2Protein interaction76%
Tissue Expression6 tissues
Brain
100%
Heart
0%
Bone Marrow
0%
Lung
0%
Liver
0%
Ovary
0%
Gene Interaction Network
Click a node to explore
PSG7RLN1PZPPSG6PSG1CSH1CSH2
PROTEIN STRUCTURE
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AlphaFoldAI-predicted · UniProt Q13046
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.58LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF1.27 [1.02–1.58]
RankingsWhere PSG7 stands among ~20K protein-coding genes
  • #14,507of 20,598
    Most Researched19
  • #15,602of 17,882
    Most Constrained (LOEUF)1.58
Genes detectedPSG7
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
PSG7 and 9 (Pregnancy-Specific β-1 Glycoproteins 7 and 9): Novel Biomarkers for Preeclampsia.
PMID: 35322669
J Am Heart Assoc · 2022
1.00
2
Identification of a new carcinoembryonic antigen (CEA) family member in human fetal liver--cloning and sequence determination of pregnancy-specific glycoprotein 7.
PMID: 2328001
Biochem Biophys Res Commun · 1990
0.90
3
Expression and transcriptional regulation of individual pregnancy-specific glycoprotein genes in differentiating trophoblast cells.
PMID: 20116096
Placenta · 2010
0.80
4
Gene organization of the pregnancy-specific glycoprotein region on human chromosome 19: assembly and analysis of a 700-kb cosmid contig spanning the region.
PMID: 7851895
Genomics · 1994
0.70
5
Proteome-Wide Mendelian Randomisation Study of Adverse Perinatal Outcomes.
PMID: 40991151
Behav Genet · 2025
0.60