ICAM4
Intercellular adhesion molecule 4
Also known as: CD242, ICAM4_HUMAN, LW
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q14773
- Gene
- ICAM4
- Ensembl
- ENSG00000105371
- Chromosome
- 19
- Canonical length
- 271 aa
- Protein class
- Blood group antigen proteins, CD markers, Predicted intracellular proteins, Predicted membrane proteins
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
This gene encodes the Landsteiner-Wiener (LW) blood group antigen(s) that belongs to the immunoglobulin (Ig) superfamily, and that shares similarity with the intercellular adhesion molecule (ICAM) protein family. This ICAM protein contains 2 Ig-like C2-type domains and binds to the leukocyte adhesion LFA-1 protein. The molecular basis of the LW(A)/LW(B) blood group antigens is a single aa variation at position 100; Gln-100=LW(A) and Arg-100=LW(B). Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
271 residues, UniProt reviewed canonical sequence.
>Q14773|ICAM4
1 MGSLFPLSLL FFLAAAYPGV GSALGRRTKR AQSPKGSPLA PSGTSVPFWV RMSPEFVAVQ
61 PGKSVQLNCS NSCPQPQNSS LRTPLRQGKT LRGPGWVSYQ LLDVRAWSSL AHCLVTCAGK
121 TRWATSRITA YKPPHSVILE PPVLKGRKYT LRCHVTQVFP VGYLVVTLRH GSRVIYSESL
181 ERFTGLDLAN VTLTYEFAAG PRDFWQPVIC HARLNLDGLV VRNSSAPITL MLAWSPAPTA
241 LASGSIAALV GILLTVGAAY LCKCLAMKSQ ALocalizationUniProt · AlphaFold · HPA
Whether an antibody against ICAM4 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.4
- Highest tissue expression
- 13 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 13 nTPM
- lung: 8.7 nTPM
- placenta: 1.6 nTPM
- urinary bladder: 1.6 nTPM
- stomach: 1.4 nTPM
- tonsil: 1.3 nTPM
Single-cell type
- alveolar cells type 2: 76 nCPM
- transitional alveolar cells: 71 nCPM
- megakaryocyte-erythroid progenitors: 37 nCPM
- neutrophils: 33 nCPM
- megakaryocytes: 31 nCPM
- erythrocyte progenitors: 31 nCPM
Immune cell
- non-classical monocyte: 216 nTPM
- intermediate monocyte: 39 nTPM
- myeloid DC: 31 nTPM
- basophil: 24 nTPM
- eosinophil: 10 nTPM
- plasmacytoid DC: 10 nTPM
Brain region
- cerebral cortex: 9.1 nTPM
- basal ganglia: 7.5 nTPM
- white matter: 7.5 nTPM
- hippocampal formation: 7.4 nTPM
- cerebellum: 7.2 nTPM
- amygdala: 7.1 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
- gnomAD missense Z
- 0.4
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell adhesion
- cell-cell adhesion mediated by integrin
- heterotypic cell-cell adhesion
- leukocyte cell-cell adhesion
- phagocytosis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Intercellular adhesion molecule/vascular cell adhesion molecule, N-terminal
- Intercellular adhesion molecule, N-terminal
- Immunoglobulin-like fold
- Immunoglobulin-like domain superfamily
- Intercellular adhesion molecule/vascular cell adhesion molecule
- Intercellular adhesion molecule (ICAM), N-terminal domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ICAM4 as an antibody target. Whether an autoantibody or antibody against ICAM4 could matter depends on whether native ICAM4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ICAM4 is annotated at the cell surface, where native ICAM4 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label ICAM4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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