Seroatlas · Human Serome Atlas

KRTAP16-1

Keratin-associated protein 16-1

Also known as: KAP16.1, KR161_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
A8MUX0
Gene
KRTAP16-1
Ensembl
ENSG00000212657
Chromosome
17
Canonical length
517 aa
Protein class
Predicted intracellular proteins

OverviewNCBI Gene

Predicted to enable structural molecule activity. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

517 residues, UniProt reviewed canonical sequence.

>A8MUX0|KRTAP16-1
     1  MSGSCSSRKC FSVPATSLCS TEVSCGGPIC LPSSCQSQTW QLVTCQDSCG SSSCGPQCRQ
    61  PSCPVSSCAQ PLCCDPVICE PSCSVSSGCQ PVCCEATTCE PSCSVSNCYQ PVCFEATICE
   121  PSCSVSNCCQ PVCFEATVCE PSCSVSSCAQ PVCCEPAICE PSCSVSSCCQ PVGSEATSCQ
   181  PVLCVPTSCQ PVLCKSSCCQ PVVCEPSCCS AVCTLPSSCQ PVVCEPSCCQ PVCPTPTCSV
   241  TSSCQAVCCD PSPCEPSCSE SSICQPATCV ALVCEPVCLR PVCCVQSSCE PPSVPSTCQE
   301  PSCCVSSICQ PICSEPSPCS PAVCVSSPCQ PTCYVVKRCP SVCPEPVSCP STSCRPLSCS
   361  PGSSASAICR PTCPRTFYIP SSSKRPCSAT ISYRPVSRPI CRPICSGLLT YRQPYMTSIS
   421  YRPACYRPCY SILRRPACVT SYSCRPVYFR PSCTESDSCK RDCKKSTSSQ LDCVDTTPCK
   481  VDVSEEAPCQ PTEAKPISPT TREAAAAQPA ASKPANC

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against KRTAP16-1 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)
0.62
Highest tissue expression
15 nTPM

Expression across tissuesHPA

Tissue

  • skin: 15 nTPM
  • bone marrow: 0.9 nTPM
  • adipose tissue: 0.3 nTPM
  • adrenal gland: 0 nTPM
  • amygdala: 0 nTPM
  • appendix: 0 nTPM

Single-cell type

  • adipocytes: 0 nCPM
  • adrenal cortex cells: 0 nCPM
  • adrenal medulla cells: 0 nCPM
  • alveolar cells type 1: 0 nCPM
  • alveolar cells type 2: 0 nCPM
  • astrocytes: 0 nCPM

Immune cell

  • memory CD4 T-cell: 0.2 nTPM
  • memory CD8 T-cell: 0.2 nTPM
  • naive B-cell: 0.2 nTPM
  • neutrophil: 0.2 nTPM
  • naive CD4 T-cell: 0.1 nTPM
  • basophil: 0 nTPM

Brain region

  • amygdala: 0 nTPM
  • basal ganglia: 0 nTPM
  • cerebellum: 0 nTPM
  • cerebral cortex: 0 nTPM
  • choroid plexus: 0 nTPM
  • hippocampal formation: 0 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)
1.13
gnomAD pLI
0
gnomAD missense Z
0.74
DepMap mean gene effect
-0.06
DepMap dependency class
selective

OntologyGO

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads KRTAP16-1 as an antibody target. Whether an autoantibody or antibody against KRTAP16-1 could matter depends on whether native KRTAP16-1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

KRTAP16-1 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 KRTAP16-1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/KRTAP16-1. 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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