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Gene Gene information from NCBI Gene database.
Entrez ID 7499
Gene name Xg glycoprotein (Xg blood group)
Gene symbol XG
Synonyms (NCBI Gene)
PBDX
Chromosome X
Chromosome location Xp22.33
Summary This gene encodes the XG blood group antigen, and is located at the pseudoautosomal boundary on the short (p) arm of chromosome X. The three 5` exons reside in the pseudoautosomal region and the remaining exons within the X-specific end. A truncated copy
miRNA miRNA information provided by mirtarbase database.
69 Show/Hide all (69)
miRTarBase ID miRNA Experiments Reference
MIRT1495325 hsa-miR-197 CLIP-seq
MIRT1495326 hsa-miR-3140-5p CLIP-seq
MIRT1495327 hsa-miR-3611 CLIP-seq
MIRT1495328 hsa-miR-3913-3p CLIP-seq
MIRT1495329 hsa-miR-483-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7 Show/Hide all (7)
GO ID Ontology Definition Evidence Reference
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IDA 7533029
GO:0005886 Component Plasma membrane IEA
GO:0016020 Component Membrane IEA
GO:0034109 Process Homotypic cell-cell adhesion IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
300879 12806 ENSG00000124343
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P55808
Protein name Glycoprotein Xg (Protein PBDX)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12301 CD99L2 25 → 180 CD99 antigen like protein 2 Family
Tissue specificity TISSUE SPECIFICITY: Expressed in erythroid tissues, including thymus, bone marrow and fetal liver, and in several nonerythroid tissues, such as heart, placenta, skeletal muscle, thyroid and trachea, as well as in skin fibroblasts. Expression is low or und
Sequence
Sequence length 180
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
6
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.
Show/Hide Unknown Diseases (6)
Phenotype Name Clinical Significance Source Reference Evidence Score
Cervical cancer Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Clear cell carcinoma of kidney Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Familial cancer of breast Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Melanoma Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Ovarian cancer Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Albinism Ocular Ocular albinism Pubtator 8301646 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Colorectal neoplasm Pubtator 24349560 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Oculocerebrorenal Syndrome Oculocerebrorenal syndrome Pubtator 7180850 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only