GIMAP2

gene
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Also known as DKFZp586D0824HIMAP2IMAP2IAN12

Summary

GIMAP2 (GTPase, IMAP family member 2, HGNC:21789) is a protein-coding gene on chromosome 7q36.1, encoding GTPase IMAP family member 2 (Q9UG22). The heterodimer formed by GIMAP2 and GIMAP7 has GTPase activity.

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.

Source: NCBI Gene 26157 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 53 total
  • MANE Select transcript: NM_015660

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:21789
Approved symbolGIMAP2
NameGTPase, IMAP family member 2
Location7q36.1
Locus typegene with protein product
StatusApproved
AliasesDKFZp586D0824, HIMAP2, IMAP2, IAN12
Ensembl geneENSG00000106560
Ensembl biotypeprotein_coding
OMIM608085
Entrez26157

Gene structure

Transcript identifiers

Ensembl transcripts: 3 — 2 protein_coding, 1 retained_intron

ENST00000223293, ENST00000474605, ENST00000487388

RefSeq mRNA: 1 — MANE Select: NM_015660 NM_015660

CCDS: CCDS5905

Canonical transcript exons

ENST00000223293 — 3 exons

ExonStartEnd
ENSE00000729852150687052150687087
ENSE00000872368150685706150685785
ENSE00000872369150692315150693641

Expression profiles

Bgee: expression breadth ubiquitous, 207 present calls, max score 97.54.

FANTOM5 (CAGE): breadth broad, TPM avg 14.8359 / max 602.9430, expressed in 803 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
8196114.6355802
819620.200398

Top tissues by expression

240 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
leukocyteCL:000073897.54gold quality
monocyteCL:000057697.52gold quality
granulocyteCL:000009496.59gold quality
vermiform appendixUBERON:000115494.54gold quality
bloodUBERON:000017893.78gold quality
lymph nodeUBERON:000002993.71gold quality
spleenUBERON:000210693.49gold quality
epithelium of nasopharynxUBERON:000195188.99gold quality
ileal mucosaUBERON:000033188.24gold quality
gall bladderUBERON:000211087.66gold quality
epithelial cell of pancreasCL:000008387.18silver quality
caecumUBERON:000115387.04gold quality
superficial temporal arteryUBERON:000161486.91gold quality
right lungUBERON:000216786.36gold quality
rectumUBERON:000105286.20gold quality
lower lobe of lungUBERON:000894985.95silver quality
calcaneal tendonUBERON:000370185.68gold quality
lungUBERON:000204884.97gold quality
bone marrowUBERON:000237184.69gold quality
upper lobe of lungUBERON:000894884.44gold quality
germinal epithelium of ovaryUBERON:000130484.32gold quality
upper lobe of left lungUBERON:000895284.32gold quality
smooth muscle tissueUBERON:000113583.97gold quality
small intestine Peyer’s patchUBERON:000345483.74gold quality
colonic epitheliumUBERON:000039783.41gold quality
jejunal mucosaUBERON:000039983.00gold quality
skin of hipUBERON:000155482.99gold quality
small intestineUBERON:000210882.77gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047382.65gold quality
omental fat padUBERON:001041482.33gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-ANND-3yes5.87
E-MTAB-5061no2.61

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

29 targeting GIMAP2, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-656-3P100.0072.152788
HSA-MIR-5692A100.0074.406850
HSA-MIR-4776-3P100.0068.731340
HSA-MIR-6508-5P99.9270.672465
HSA-MIR-380-3P99.8970.181978
HSA-MIR-806799.8669.592260
HSA-MIR-659-3P99.8570.691620
HSA-MIR-548AR-3P99.8571.263889
HSA-MIR-199A-3P99.7570.48929
HSA-MIR-199B-3P99.7570.48929
HSA-MIR-3129-5P99.7570.46914
HSA-MIR-1252-3P99.5567.712862
HSA-MIR-582-5P99.4770.792635
HSA-MIR-372-5P99.4169.112299
HSA-MIR-190B-3P99.3368.291382
HSA-MIR-452899.1869.771936
HSA-MIR-892C-5P99.1670.562116
HSA-MIR-376A-3P99.0669.171128
HSA-MIR-376B-3P99.0669.171128
HSA-MIR-607498.8969.642187
HSA-MIR-93698.8770.511124
HSA-MIR-3145-3P98.8569.072031
HSA-MIR-222-5P98.7569.171242
HSA-MIR-506-5P98.0267.411065
HSA-MIR-892B98.0067.11821
HSA-MIR-4693-5P97.3567.021234
HSA-MIR-92197.0966.45562
HSA-MIR-430195.0065.22554
HSA-MIR-317494.6363.64577

Literature-anchored findings (GeneRIF, showing 1)

  • GDP-bound GIMAP2(21-260) and GDP-bound GIMAP2(1-234) crystallized in space group P2(1)2(1)2(1) and the crystals diffracted X-rays to 2.9 and 1.7 A resolution, respectively. (PMID:20516611)

Cross-species orthologs

0 orthologs

Paralogs (7): GIMAP6 (ENSG00000133561), GIMAP4 (ENSG00000133574), GIMAP8 (ENSG00000171115), GIMAP7 (ENSG00000179144), GIMAP5 (ENSG00000196329), GIMAP1 (ENSG00000213203), GIMD1 (ENSG00000250298)

Protein

Protein identifiers

GTPase IMAP family member 2Q9UG22 (reviewed: Q9UG22)

Alternative names: Immunity-associated protein 2

All UniProt accessions (3): Q9UG22, A0A090N8H4, C9JND7

UniProt curated annotations — full annotation on UniProt →

Function. The heterodimer formed by GIMAP2 and GIMAP7 has GTPase activity. In contrast, GIMAP2 has no GTPase activity by itself.

Subunit / interactions. Monomer in the presence of bound GDP and in the absence of bound nucleotide. Homodimer in the presence of bound GTP. Can form linear oligomers. Heterodimer with GIMAP7.

Subcellular location. Lipid droplet.

Tissue specificity. Detected in T-cells.

Similarity. Belongs to the TRAFAC class TrmE-Era-EngA-EngB-Septin-like GTPase superfamily. AIG1/Toc34/Toc159-like paraseptin GTPase family. IAN subfamily.

RefSeq proteins (1): NP_056475* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR006703G_AIG1Domain
IPR027417P-loop_NTPaseHomologous_superfamily
IPR045058GIMA/IAN/TocFamily

Pfam: PF04548

UniProt features (37 total): helix 11, binding site 6, strand 6, region of interest 5, sequence variant 3, mutagenesis site 2, turn 2, chain 1, domain 1

Structure

Experimental structures (PDB)

5 structures.

PDBMethodResolution (Å)
2XTPX-RAY DIFFRACTION1.5
2XTMX-RAY DIFFRACTION1.7
2XTNX-RAY DIFFRACTION1.9
3P1JX-RAY DIFFRACTION2.58
2XTOX-RAY DIFFRACTION2.8

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9UG22-F189.040.71

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Ligand- & substrate-binding residues (6): 147–149; 184; 318–320; 31–37; 50; 57–58

Mutagenesis-validated functional residues (2):

PositionPhenotype
54abolishes gtp-induced dimerization.
117abolishes gtp-induced dimerization.

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 76 (showing top): FUJII_YBX1_TARGETS_UP, RIGGI_EWING_SARCOMA_PROGENITOR_UP, GOMF_GTPASE_ACTIVITY, GOMF_HYDROLASE_ACTIVITY_ACTING_ON_ACID_ANHYDRIDES, WANG_RESPONSE_TO_GSK3_INHIBITOR_SB216763_UP, LEE_DIFFERENTIATING_T_LYMPHOCYTE, GENTLES_LEUKEMIC_STEM_CELL_UP, GOCC_LIPID_DROPLET, GARGALOVIC_RESPONSE_TO_OXIDIZED_PHOSPHOLIPIDS_PINK_DN, MIR582_5P, MIR1252_3P, MIR380_3P, MIR4528, MIR659_3P, MIR222_5P

GO Biological Process (0):

GO Molecular Function (5): GTPase activity (GO:0003924), GTP binding (GO:0005525), identical protein binding (GO:0042802), nucleotide binding (GO:0000166), protein binding (GO:0005515)

GO Cellular Component (4): nucleoplasm (GO:0005654), endoplasmic reticulum (GO:0005783), lipid droplet (GO:0005811), membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cellular anatomical structure2
ribonucleoside triphosphate phosphatase activity1
guanyl ribonucleotide binding1
purine ribonucleoside triphosphate binding1
protein binding1
nucleoside phosphate binding1
heterocyclic compound binding1
binding1
nuclear lumen1
cytoplasm1
endomembrane system1
intracellular membrane-bounded organelle1
intracellular membraneless organelle1

Protein interactions and networks

STRING

1086 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
GIMAP2AIG1Q9NVV5589
GIMAP2C2orf78A6NCI8573
GIMAP2ZNF775Q96BV0500
GIMAP2GIMAP7Q8NHV1439
GIMAP2UBAC2Q8NBM4434
GIMAP2KLRC4O43908397
GIMAP2C7orf33Q8WU49370
GIMAP2TMEM176BQ3YBM2363
GIMAP2DRC11LA6NCM1360
GIMAP2SSC5DA1L4H1354
GIMAP2MELTFP08582354
GIMAP2GPR37O15354339
GIMAP2SETXQ7Z333333
GIMAP2ZBED11P0CF97325
GIMAP2C1orf50Q9BV19321

IntAct

17 interactions, top by confidence:

ABTypeScore
GIMAP2GIMAP2psi-mi:“MI:0407”(direct interaction)0.620
HTTGIMAP2psi-mi:“MI:0915”(physical association)0.560
GIMAP2TOR1Bpsi-mi:“MI:0914”(association)0.530
GIMAP2STOMpsi-mi:“MI:0914”(association)0.530
GIMAP7GIMAP2psi-mi:“MI:0407”(direct interaction)0.440
TRIM54GIMAP2psi-mi:“MI:0915”(physical association)0.000

BioGRID (13): TOR1B (Affinity Capture-MS), STOM (Affinity Capture-MS), TOR1B (Affinity Capture-MS), STOM (Affinity Capture-MS), FBP1 (Affinity Capture-MS), PRMT8 (Affinity Capture-MS), GIMAP2 (Two-hybrid), TOR1B (Affinity Capture-MS), PRMT8 (Affinity Capture-MS), STOM (Affinity Capture-MS), ARFIP1 (Affinity Capture-MS), TMEM159 (Affinity Capture-MS), PNPLA2 (Affinity Capture-MS)

ESM2 similar proteins: A4D126, A5PK43, A5PKB7, A6H603, C3VPR6, D2GU20, E9PW74, G1T469, G3MZQ6, O60294, O75578, O75616, P38570, P56201, P70224, Q149M9, Q17QI8, Q17QJ3, Q1JPJ9, Q2HJ51, Q53B87, Q53B88, Q5EBA0, Q5FVI9, Q5FVN6, Q5R6H6, Q5RJG7, Q5S6T3, Q5W0U4, Q643R3, Q6AYF9, Q6E804, Q6P5Z2, Q6P9H5, Q8BWF2, Q8BYR1, Q8K045, Q8K2J0, Q8K349, Q8K3L6

Diamond homologs: A5PKB7, F4HT21, G3X987, O23680, O81025, P54120, P70224, Q41009, Q4KLG2, Q5FVN6, Q6P9H5, Q75N62, Q8BWF2, Q8K349, Q8K3K9, Q8K3L6, Q8ND71, Q8NHV1, Q8WWP7, Q96F15, Q99JY3, Q99MI6, Q9C8U2, Q9C8V0, Q9C8V2, Q9NUV9, Q9T0F2, Q9T0F3, Q9T0F4, Q9UG22, E9PW74, Q9C8U5, Q9C8U6, Q9C8U7, Q9C8U8, Q9LVT3, O81283, Q6S5G3, D2GU20, O75616

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

53 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance43
Likely benign6
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

511 predictions. Top by Δscore:

VariantEffectΔscore
7:150685784:AGGT:Adonor_loss0.9900
7:150685785:GGTAA:Gdonor_loss0.9900
7:150685786:GTAA:Gdonor_loss0.9900
7:150685787:T:Adonor_loss0.9900
7:150689592:AT:Adonor_gain0.9800
7:150687046:TCTCA:Tacceptor_loss0.9600
7:150687047:CTCA:Cacceptor_loss0.9600
7:150687048:TCA:Tacceptor_loss0.9600
7:150687049:CAGG:Cacceptor_loss0.9600
7:150687085:GGG:Gdonor_gain0.9600
7:150687086:GGG:Gdonor_gain0.9600
7:150685754:G:GTdonor_gain0.9500
7:150687086:GG:Gdonor_gain0.9500
7:150687087:GG:Gdonor_gain0.9500
7:150687089:T:TCdonor_loss0.9500
7:150685786:G:GGdonor_gain0.9400
7:150689588:TGTA:Tdonor_gain0.9300
7:150689597:A:AGdonor_gain0.9200
7:150689587:GT:Gdonor_gain0.9100
7:150689593:T:Gdonor_gain0.9100
7:150690220:G:GAdonor_gain0.9000
7:150690345:C:Tdonor_gain0.9000
7:150685782:TCAG:Tdonor_gain0.8900
7:150687048:TCAGG:Tdonor_loss0.8900
7:150687050:AGG:Adonor_loss0.8900
7:150687050:A:AGacceptor_gain0.8800
7:150687051:G:GGacceptor_gain0.8800
7:150687088:G:GGdonor_gain0.8800
7:150687100:C:Gdonor_gain0.8700
7:150690319:TGG:Tdonor_gain0.8700

AlphaMissense

2242 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
7:150692428:T:CF48L0.961
7:150692430:T:AF48L0.961
7:150692430:T:GF48L0.961
7:150692683:T:CF133L0.937
7:150692685:T:AF133L0.937
7:150692685:T:GF133L0.937
7:150692714:T:AV143D0.912
7:150692719:T:CF145L0.912
7:150692721:T:AF145L0.912
7:150692721:T:GF145L0.912
7:150692530:T:CF82L0.911
7:150692532:T:AF82L0.911
7:150692532:T:GF82L0.911
7:150692830:T:CF182L0.895
7:150692832:T:AF182L0.895
7:150692832:T:GF182L0.895
7:150692392:A:CS36R0.894
7:150692394:T:AS36R0.894
7:150692394:T:GS36R0.894
7:150692720:T:CF145S0.865
7:150692360:T:CI25T0.848
7:150692391:A:CK35N0.848
7:150692391:A:TK35N0.848
7:150692372:G:TG29V0.843
7:150692411:T:CI42T0.838
7:150692517:C:AD77E0.832
7:150692517:C:GD77E0.832
7:150692390:A:TK35I0.822
7:150692411:T:GI42S0.820
7:150692819:G:CR178P0.817

dbSNP variants (sampled 300 via entrez): RS1000242562 (7:150689255 T>C), RS1000485732 (7:150689099 C>T), RS1000574537 (7:150688114 T>C), RS1000642566 (7:150689595 T>C), RS1001082075 (7:150688837 A>C), RS1001416847 (7:150687735 G>C), RS1002159761 (7:150687969 C>T), RS1002579753 (7:150685361 G>A), RS1002993817 (7:150692082 G>A), RS1003040165 (7:150685051 A>G), RS1003063998 (7:150691470 T>C), RS1003421492 (7:150685034 C>G,T), RS1004164599 (7:150685291 C>A,G), RS1004652349 (7:150685721 G>T), RS1004975999 (7:150689143 A>G)

Disease associations

OMIM: gene MIM:608085 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

1 associations (top):

StudyTraitp-value
GCST001113_18Age at smoking initiation in chronic obstructive pulmonary disease5.000000e-06

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0005670smoking initiation

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

16 total (human), top 16 by PubMed support.

ChemicalActions (top 5)PubMed papers
di-n-butylphosphoric acidaffects expression1
CGP 52608affects binding, increases reaction1
abrinedecreases expression1
bisphenol Sdecreases methylation1
Acetaminophendecreases expression1
Air Pollutantsaffects expression, increases abundance1
Atrazineincreases expression1
Calcitriolincreases expression1
Cisplatinincreases expression1
Ethyl Methanesulfonateincreases expression1
Methotrexatedecreases expression1
Ozoneaffects expression, increases abundance1
Tobacco Smoke Pollutiondecreases expression1
Valproic Aciddecreases methylation, decreases expression1
Cyclosporinedecreases expression1
Okadaic Aciddecreases expression1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.