Seroatlas · Human Serome Atlas

GIMAP2

GTPase IMAP family member 2

Also known as: DKFZp586D0824, GIMA2_HUMAN, HIMAP2, IAN12, IMAP2

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q9UG22
Gene
GIMAP2
Ensembl
ENSG00000106560
Chromosome
7
Canonical length
337 aa
Protein class
Predicted intracellular proteins, Predicted membrane proteins
Subcellular location
Nucleoplasm,Lipid droplets
Quaternary structure
Homodimer

OverviewNCBI Gene

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 2008]

Canonical amino-acid sequenceUniProt

337 residues, UniProt reviewed canonical sequence.

>Q9UG22|GIMAP2
     1  MDQNEHSHWG PHAKGQCASR SELRIILVGK TGTGKSAAGN SILRKQAFES KLGSQTLTKT
    61  CSKSQGSWGN REIVIIDTPD MFSWKDHCEA LYKEVQRCYL LSAPGPHVLL LVTQLGRYTS
   121  QDQQAAQRVK EIFGEDAMGH TIVLFTHKED LNGGSLMDYM HDSDNKALSK LVAACGGRIC
   181  AFNNRAEGSN QDDQVKELMD CIEDLLMEKN GDHYTNGLYS LIQRSKCGPV GSDERVKEFK
   241  QSLIKYMETQ RSYTALAEAN CLKGALIKTQ LCVLFCIQLF LRLIILWLCI LHSMCNLFCC
   301  LLFSMCNLFC SLLFIIPKKL MIFLRTVIRL ERKTPRL

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against GIMAP2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.

Antibody reachability
Intracellular
Secreted
No
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.35
Highest tissue expression
73 nTPM

Expression across tissuesHPA

Tissue

  • lymph node: 73 nTPM
  • spleen: 59 nTPM
  • tonsil: 54 nTPM
  • thymus: 47 nTPM
  • appendix: 38 nTPM
  • lung: 21 nTPM

Single-cell type

  • kupffer cells: 203 nCPM
  • monocytes: 59 nCPM
  • hematopoietic stem cells: 56 nCPM
  • t-cells: 49 nCPM
  • thymocytes: 48 nCPM
  • hofbauer cells: 47 nCPM

Immune cell

  • naive CD4 T-cell: 167 nTPM
  • NK-cell: 137 nTPM
  • total PBMC: 130 nTPM
  • naive CD8 T-cell: 125 nTPM
  • memory CD4 T-cell: 122 nTPM
  • non-classical monocyte: 122 nTPM

Brain region

  • medulla oblongata: 11 nTPM
  • white matter: 9.5 nTPM
  • pons: 9 nTPM
  • spinal cord: 9 nTPM
  • midbrain: 7.1 nTPM
  • thalamus: 6.9 nTPM

Genetic constraint and essentialitygnomAD · DepMap

Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.

gnomAD LOEUF (loss-of-function intolerance)
1.69
gnomAD pLI
0.41
gnomAD missense Z
0.12
DepMap mean gene effect
0.11
DepMap dependency class
none

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads GIMAP2 as an antibody target. Whether an autoantibody or antibody against GIMAP2 could matter depends on whether native GIMAP2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

GIMAP2 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.

Annotation status

The present source text does not explicitly label GIMAP2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/GIMAP2. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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