KIF4A
Chromosome-associated kinesin KIF4A
Also known as: FLJ12530, FLJ12655, FLJ14204, FLJ20631, HSA271784, KIF4, KIF4-G1, KIF4A_HUMAN, MRX100
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O95239
- Gene
- KIF4A
- Ensembl
- ENSG00000090889
- Chromosome
- X
- Canonical length
- 1232 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Midbody,Acrosome,Equatorial segment,Mid piece,Principal piece
OverviewNCBI Gene
This gene encodes a member of the kinesin 4 subfamily of kinesin related proteins. The encoded protein is an ATP dependent microtubule-based motor protein that is involved in the intracellular transport of membranous organelles. This protein also associates with condensed chromosome arms and may be involved in maintaining chromosome integrity during mitosis. This protein may also be involved in the organization of the central spindle prior to cytokinesis. A pseudogene of this gene is found on chromosome X.[provided by RefSeq, Mar 2010]
Canonical amino-acid sequenceUniProt
1232 residues, UniProt reviewed canonical sequence.
>O95239|KIF4A
1 MKEEVKGIPV RVALRCRPLV PKEISEGCQM CLSFVPGEPQ VVVGTDKSFT YDFVFDPSTE
61 QEEVFNTAVA PLIKGVFKGY NATVLAYGQT GSGKTYSMGG AYTAEQENEP TVGVIPRVIQ
121 LLFKEIDKKS DFEFTLKVSY LEIYNEEILD LLCPSREKAQ INIREDPKEG IKIVGLTEKT
181 VLVALDTVSC LEQGNNSRTV ASTAMNSQSS RSHAIFTISL EQRKKSDKNS SFRSKLHLVD
241 LAGSERQKKT KAEGDRLKEG ININRGLLCL GNVISALGDD KKGGFVPYRD SKLTRLLQDS
301 LGGNSHTLMI ACVSPADSNL EETLNTLRYA DRARKIKNKP IVNIDPQTAE LNHLKQQVQQ
361 LQVLLLQAHG GTLPGSITVE PSENLQSLME KNQSLVEENE KLSRGLSEAA GQTAQMLERI
421 ILTEQANEKM NAKLEELRQH AACKLDLQKL VETLEDQELK ENVEIICNLQ QLITQLSDET
481 VACMAAAIDT AVEQEAQVET SPETSRSSDA FTTQHALRQA QMSKELVELN KALALKEALA
541 RKMTQNDSQL QPIQYQYQDN IKELELEVIN LQKEKEELVL ELQTAKKDAN QAKLSERRRK
601 RLQELEGQIA DLKKKLNEQS KLLKLKESTE RTVSKLNQEI RMMKNQRVQL MRQMKEDAEK
661 FRQWKQKKDK EVIQLKERDR KRQYELLKLE RNFQKQSNVL RRKTEEAAAA NKRLKDALQK
721 QREVADKRKE TQSRGMEGTA ARVKNWLGNE IEVMVSTEEA KRHLNDLLED RKILAQDVAQ
781 LKEKKESGEN PPPKLRRRTF SLTEVRGQVS ESEDSITKQI ESLETEMEFR SAQIADLQQK
841 LLDAESEDRP KQRWENIATI LEAKCALKYL IGELVSSKIQ VSKLESSLKQ SKTSCADMQK
901 MLFEERNHFA EIETELQAEL VRMEQQHQEK VLYLLSQLQQ SQMAEKQLEE SVSEKEQQLL
961 STLKCQDEEL EKMREVCEQN QQLLRENEII KQKLTLLQVA SRQKHLPKDT LLSPDSSFEY
1021 VPPKPKPSRV KEKFLEQSMD IEDLKYCSEH SVNEHEDGDG DDDEGDDEEW KPTKLVKVSR
1081 KNIQGCSCKG WCGNKQCGCR KQKSDCGVDC CCDPTKCRNR QQGKDSLGTV ERTQDSEGSF
1141 KLEDPTEVTP GLSFFNPVCA TPNSKILKEM CDVEQVLSKK TPPAPSPFDL PELKHVATEY
1201 QENKAPGKKK KRALASNTSF FSGCSPIEEE AHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KIF4A 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)
- 0.44
- Highest tissue expression
- 12 nTPM
Expression across tissuesHPA
Tissue
- thymus: 12 nTPM
- bone marrow: 11 nTPM
- tonsil: 6.1 nTPM
- lymph node: 5.1 nTPM
- rectum: 4.2 nTPM
- colon: 3.5 nTPM
Single-cell type
- monocyte progenitors: 108 nCPM
- erythrocyte progenitors: 89 nCPM
- megakaryocyte progenitors: 62 nCPM
- neutrophil progenitors: 54 nCPM
- ependymal cells: 43 nCPM
- enteric transient amplifying cells: 33 nCPM
Immune cell
- T-reg: 0.7 nTPM
- memory CD8 T-cell: 0.3 nTPM
- memory B-cell: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- medulla oblongata: 1.9 nTPM
- midbrain: 1.6 nTPM
- spinal cord: 1.5 nTPM
- hypothalamus: 1.3 nTPM
- pons: 1.3 nTPM
- thalamus: 0.9 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about KIF4A.
Disease | AllUniProt
Conditions KIF4A is implicated in, by any mechanism.
- Intellectual developmental disorder, X-linked 100 (XLID100) MIM:300923
- Taurodontism, microdontia, and dens invaginatus (TMDI) MIM:313490
Disease | GeneticClinVar
8 pathogenic / likely-pathogenic of 338 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Intellectual disability, X-linked 100
- Taurodontism, microdontia, and dens invaginatus
- Ventriculomegaly
- Multicystic kidney dysplasia
- Hydrocephalus
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)
- 0.2
- gnomAD pLI
- 1
- gnomAD missense Z
- 2.56
- DepMap mean gene effect
- -0.63
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- anterograde axonal transport
- mitotic cytokinesis
- mitotic spindle midzone assembly
- mitotic spindle organization
- organelle organization
- spindle elongation
Molecular functions
- ATP binding
- DNA binding
- iron-sulfur cluster binding
- metal ion binding
- microtubule binding
- microtubule motor activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of KIF4A 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 KIF4A as an antibody target. Whether an autoantibody or antibody against KIF4A could matter depends on whether native KIF4A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KIF4A 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 KIF4A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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