KANK4
KN motif and ankyrin repeat domain-containing protein 4
Also known as: ANKRD38, KANK4_HUMAN, KIAA0172
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5T7N3
- Gene
- KANK4
- Ensembl
- ENSG00000132854
- Chromosome
- 1
- Canonical length
- 995 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Microtubules,Cytosol
OverviewNCBI Gene
Predicted to be involved in negative regulation of actin filament polymerization. Located in cytosol and microtubule cytoskeleton. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
995 residues, UniProt reviewed canonical sequence.
>Q5T7N3|KANK4
1 MEKTDAKDQS SQGDEEKDPP KSHPYSVETP YGFHLDLDFL KYVDDIEKGN TIKRIPIHRR
61 AKQAKFSTLP RNFSLPDSGA RPPAAPPLQN WSPVVPREAS LGTQEQNQSP PLGNAPQAST
121 SRSEVSYHRK ALLAEATRQL EAAEPEDAEL TFGSGRPQLL RASSMPATLL HSRASEEPGL
181 SLGPPAPPAL PPLQGEGSVC DGTFEPAEGL AGFHSSSPRA STRIPELVQE GAEPPEGVVK
241 VPNHLPLPGP PFSFQNVLVV LEDKEDEHNA REAEVLFTPG SPTPSPPPLP SPIPENELLL
301 EEIELNISEI PPPPPVEVDM RSIGIRVTEE SLGLARVDPG SISSLKQQVS ALEGELSGRT
361 EELAQVRTAL QQQEEEIKAR EQRIRELEFT VAQLEGQFHQ ENAKDTQGQT DVMVNTDPVH
421 GLLTRESCDK GIEVNLLGSM ESESWGHRGE ENGLLWGPDG HKQGNQSPAE RVLLPQLSLP
481 QGPEQVLTSS VHSFLSTELR IEEAGTEQEG GPQGGTRGAG GFLWGSDRKT PPAGREETSS
541 NLPGKEHPGR PPSSPTDATI GQYVKKIQEL LQEQWNCLEH GYPELASAIK QPASKLSSIQ
601 SQLLSSLNLL LSAYSAQAHP PKEPPASSSS PPVEISPSTS LKSIMKKKDY GFRAGGNGTK
661 KNLQFVGVNG GYETTSSEET SGEDSTPEDL SDSEAEKKCD GPDHKHVKDA HLTCEAGQGI
721 PEGTCHAAQE SGPGEEVPHS KAERYKPSEE FLNACRALSQ HLPETGTTTD QLLRQSLNTI
781 SQEWFRVSSR KSSSPAVVAS YLHEVQPHSP HFLKLLVNLA DHNGNTALHY SVSHSNFSIV
841 KLLLETGVCN VDHQNKAGYT AVMITPLASA ETNEDMAVVW KLLREGNVNI QATQGGQTAL
901 MLGVSHDRED MVQALLSCQA DVNLQDHDGS SALMVACHHG NVDLVRLLLA HPACDSSLTD
961 KAGRTALSIA LKSPTHMEIA GLLRAHAEQG RSLGLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KANK4 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)
- 0.57
- Highest tissue expression
- 13 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 13 nTPM
- adipose tissue: 10 nTPM
- placenta: 10 nTPM
- spinal cord: 9.2 nTPM
- salivary gland: 8 nTPM
- midbrain: 7.4 nTPM
Single-cell type
- cytotrophoblasts: 198 nCPM
- adipocytes: 109 nCPM
- lacrimal acinar cells: 107 nCPM
- extravillous trophoblasts: 104 nCPM
- migrating cytotrophoblasts: 92 nCPM
- schwann cells: 67 nCPM
Immune cell
- basophil: 0.2 nTPM
- neutrophil: 0.2 nTPM
- eosinophil: 0.1 nTPM
- naive B-cell: 0.1 nTPM
- classical monocyte: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- pons: 48 nTPM
- midbrain: 31 nTPM
- medulla oblongata: 28 nTPM
- cerebellum: 22 nTPM
- white matter: 19 nTPM
- thalamus: 17 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)
- 0.8
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.2
- DepMap mean gene effect
- -0.02
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads KANK4 as an antibody target. Whether an autoantibody or antibody against KANK4 could matter depends on whether native KANK4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KANK4 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 KANK4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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