KXD1
KxDL motif-containing protein 1
Also known as: BORCS4, C19orf50, FLJ25480, KXDL, KXDL1_HUMAN, MGC2749
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BQD3
- Gene
- KXD1
- Ensembl
- ENSG00000105700
- Chromosome
- 19
- Canonical length
- 176 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoli fibrillar center,Centrosome,Cytosol
OverviewNCBI Gene
Involved in lysosome localization. Part of BORC complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
176 residues, UniProt reviewed canonical sequence.
>Q9BQD3|KXD1
1 MDLPDSASRV FCGRILSMVN TDDVNAIILA QKNMLDRFEK TNEMLLNFNN LSSARLQQMS
61 ERFLHHTRTL VEMKRDLDSI FRRIRTLKGK LARQHPEAFS HIPEASFLEE EDEDPIPPST
121 TTTIATSEQS TGSCDTSPDT VSPSLSPGFE DLSHVQPGSP AINGRSQTDD EEMTGELocalizationUniProt · AlphaFold · HPA
Whether an antibody against KXD1 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.58
- Highest tissue expression
- 110 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 110 nTPM
- spinal cord: 108 nTPM
- liver: 100 nTPM
- skeletal muscle: 95 nTPM
- pancreas: 91 nTPM
- spleen: 89 nTPM
Single-cell type
- early spermatids: 236 nCPM
- hofbauer cells: 146 nCPM
- extravillous trophoblasts: 144 nCPM
- esophageal suprabasal cells: 135 nCPM
- esophageal basal cells: 129 nCPM
- syncytiotrophoblasts: 127 nCPM
Immune cell
- non-classical monocyte: 126 nTPM
- intermediate monocyte: 125 nTPM
- classical monocyte: 110 nTPM
- neutrophil: 108 nTPM
- T-reg: 104 nTPM
- myeloid DC: 100 nTPM
Brain region
- white matter: 110 nTPM
- medulla oblongata: 110 nTPM
- cerebral cortex: 106 nTPM
- midbrain: 98 nTPM
- pons: 95 nTPM
- thalamus: 95 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)
- 1.23
- gnomAD pLI
- 0.03
- gnomAD missense Z
- 0.9
- DepMap mean gene effect
- -0.18
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- lysosome localization
- organelle transport along microtubule
- regulation of endosome size
- regulation of lysosome size
- vesicle-mediated transport
Cellular components
Protein domainsUniProt · Pfam · InterPro
- KxDL domain
- KxDL motif-containing protein 1-like
- Uncharacterized conserved protein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of KXD1 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 KXD1 as an antibody target. Whether an autoantibody or antibody against KXD1 could matter depends on whether native KXD1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KXD1 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 KXD1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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