Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
11321
Gene name Gene Name - the full gene name approved by the HGNC.
GPN-loop GTPase 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
GPN1
Synonyms (NCBI Gene) Gene synonyms aliases
ATPBD1A, MBDIN, NTPBP, RPAP4, XAB1
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p23.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a guanosine triphosphatase enzyme. The encoded protein may play a role in DNA repair and may function in activation of transcription. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT019517 hsa-miR-151a-5p Sequencing 20371350
MIRT027807 hsa-miR-98-5p Microarray 19088304
MIRT052371 hsa-let-7a-5p CLASH 23622248
MIRT044449 hsa-miR-320a CLASH 23622248
MIRT1029613 hsa-miR-1225-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003924 Function GTPase activity IBA 21873635
GO:0005515 Function Protein binding IPI 24981860, 25241168, 28514442, 32296183
GO:0005525 Function GTP binding IEA
GO:0005654 Component Nucleoplasm IDA
GO:0005739 Component Mitochondrion IDA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
611479 17030 ENSG00000198522
Protein
UniProt ID Q9HCN4
Protein name GPN-loop GTPase 1 (EC 3.6.5.-) (MBD2-interacting protein) (MBDin) (RNAPII-associated protein 4) (XPA-binding protein 1)
Protein function Small GTPase required for proper nuclear import of RNA polymerase II (RNAPII) (PubMed:20855544, PubMed:21768307). May act at an RNAP assembly step prior to nuclear import (PubMed:21768307). Forms an interface between the RNA polymerase II enzyme
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03029 ATP_bind_1 24 264 Conserved hypothetical ATP binding protein Domain
Tissue specificity TISSUE SPECIFICITY: Expressed ubiquitously.
Sequence
Sequence length 374
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Metabolic syndrome Metabolic Syndrome X rs367643250, rs587777380, rs777736953 21386085
Unknown
Disease term Disease name Evidence References Source
Psoriasis Psoriasis GWAS
Associations from Text Mining
Disease Name Relationship Type References
Diabetes Mellitus Type 2 Associate 21411509
Melanoma Associate 33046735
Mouth Neoplasms Associate 27749845
Neoplasms Associate 28940195