Seroatlas · Human Serome Atlas

CALML4

Calmodulin-like protein 4

Also known as: CALL4_HUMAN, MGC4809, NY-BR-20

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

Protein identityUniProt · HPA

UniProt accession
Q96GE6
Gene
CALML4
Ensembl
ENSG00000129007
Chromosome
15
Canonical length
196 aa
Protein class
Predicted intracellular proteins, RAS pathway related proteins
Subcellular location
Nucleoplasm,Golgi apparatus,Cytosol

OverviewNCBI Gene

Enables myosin head/neck binding activity. Involved in brush border assembly. Located in microvillus. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

196 residues, UniProt reviewed canonical sequence.

>Q96GE6|CALML4
     1  MAAEHLLPGP PPSLADFRLE AGGKGTERGS GSSKPTGSSR GPRMAKFLSQ DQINEYKECF
    61  SLYDKQQRGK IKATDLMVAM RCLGASPTPG EVQRHLQTHG IDGNGELDFS TFLTIMHMQI
   121  KQEDPKKEIL LAMLMVDKEK KGYVMASDLR SKLTSLGEKL THKEVDDLFR EADIEPNGKV
   181  KYDEFIHKIT LPGRDY

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against CALML4 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)
0.42
Highest tissue expression
36 nTPM

Expression across tissuesHPA

Tissue

  • duodenum: 36 nTPM
  • small intestine: 29 nTPM
  • rectum: 29 nTPM
  • choroid plexus: 27 nTPM
  • colon: 27 nTPM
  • kidney: 12 nTPM

Single-cell type

  • colonocytes: 21 nCPM
  • fallopian tube ciliated cells: 18 nCPM
  • enterocytes: 18 nCPM
  • choroid plexus epithelial cells: 16 nCPM
  • epididymal efferent duct ciliated cells: 15 nCPM
  • endometrial ciliated cells: 14 nCPM

Immune cell

  • non-classical monocyte: 66 nTPM
  • intermediate monocyte: 57 nTPM
  • classical monocyte: 31 nTPM
  • myeloid DC: 18 nTPM
  • neutrophil: 18 nTPM
  • total PBMC: 9.1 nTPM

Brain region

  • choroid plexus: 14 nTPM
  • cerebellum: 3.2 nTPM
  • cerebral cortex: 2.6 nTPM
  • white matter: 2.1 nTPM
  • hippocampal formation: 1.9 nTPM
  • thalamus: 1.9 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)
1.55
gnomAD pLI
0
gnomAD missense Z
-0.7
DepMap mean gene effect
-0.1
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

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of CALML4 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads CALML4 as an antibody target. Whether an autoantibody or antibody against CALML4 could matter depends on whether native CALML4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

CALML4 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 CALML4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/CALML4. 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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