Gene Gene information from NCBI Gene database.
Entrez ID 26157
Gene name GTPase, IMAP family member 2
Gene symbol GIMAP2
Synonyms (NCBI Gene)
HIMAP2IAN12IMAP2
Chromosome 7
Chromosome location 7q36.1
Summary This gene encodes a protein belonging to the GTP-binding superfamily and to the immuno-associated nucleotide (IAN) subfamily of nucleotide-binding proteins. In humans, the IAN subfamily genes are located in a cluster at 7q36.1. [provided by RefSeq, Jul 20
miRNA miRNA information provided by mirtarbase database.
6
miRTarBase ID miRNA Experiments Reference
MIRT016593 hsa-miR-193b-3p Microarray 20304954
MIRT019166 hsa-miR-335-5p Microarray 18185580
MIRT1018960 hsa-miR-140-3p CLIP-seq
MIRT1018961 hsa-miR-4693-5p CLIP-seq
MIRT1018962 hsa-miR-5095 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0003924 Function GTPase activity IBA
GO:0005515 Function Protein binding IPI 23454188, 32814053
GO:0005525 Function GTP binding IEA
GO:0005654 Component Nucleoplasm IDA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608085 21789 ENSG00000106560
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9UG22
Protein name GTPase IMAP family member 2 (Immunity-associated protein 2) (hIMAP2)
Protein function The heterodimer formed by GIMAP2 and GIMAP7 has GTPase activity. In contrast, GIMAP2 has no GTPase activity by itself.
PDB 2XTM , 2XTN , 2XTO , 2XTP , 3P1J
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04548 AIG1 23 234 AIG1 family Domain
Tissue specificity TISSUE SPECIFICITY: Detected in T-cells. {ECO:0000269|PubMed:23454188}.
Sequence
Sequence length 337
Interactions View interactions
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
MULTIPLE SCLEROSIS GWAS catalog
★★☆☆☆
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
Leukemia Leukemia Pubtator 36129940 Associate
★☆☆☆☆
Found in Text Mining only
Sarcoma Sarcoma Pubtator 33316779 Associate
★☆☆☆☆
Found in Text Mining only