AK8
Adenylate kinase 8
Also known as: C9orf98, FLJ32704, KAD8_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96MA6
- Gene
- AK8
- Ensembl
- ENSG00000165695
- Chromosome
- 9
- Canonical length
- 479 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Flagellar centriole,Mid piece,Principal piece,End piece
OverviewNCBI Gene
Enables AMP binding activity and nucleobase-containing compound kinase activity. Predicted to be involved in nucleoside monophosphate phosphorylation. Predicted to act upstream of or within ventricular system development. Located in 9+2 motile cilium. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
479 residues, UniProt reviewed canonical sequence.
>Q96MA6|AK8
1 MDATIAPHRI PPEMPQYGEE NHIFELMQNM LEQLLIHQPE DPIPFMIQHL HRDNDNVPRI
61 VILGPPASGK TTIAMWLCKH LNSSLLTLEN LILNEFSYTA TEARRLYLQR KTVPSALLVQ
121 LIQERLAEED CIKQGWILDG IPETREQALR IQTLGITPRH VIVLSAPDTV LIERNLGKRI
181 DPQTGEIYHT TFDWPPESEI QNRLMVPEDI SELETAQKLL EYHRNIVRVI PSYPKILKVI
241 SADQPCVDVF YQALTYVQSN HRTNAPFTPR VLLLGPVGSG KSLQAALLAQ KYRLVNVCCG
301 QLLKEAVADR TTFGELIQPF FEKEMAVPDS LLMKVLSQRL DQQDCIQKGW VLHGVPRDLD
361 QAHLLNRLGY NPNRVFFLNV PFDSIMERLT LRRIDPVTGE RYHLMYKPPP TMEIQARLLQ
421 NPKDAEEQVK LKMDLFYRNS ADLEQLYGSA ITLNGDQDPY TVFEYIESGI INPLPKKIPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against AK8 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)
- 0.3
- Highest tissue expression
- 24 nTPM
Expression across tissuesHPA
Tissue
- fallopian tube: 24 nTPM
- epididymis: 18 nTPM
- testis: 18 nTPM
- choroid plexus: 9.7 nTPM
- thyroid gland: 4.4 nTPM
- tonsil: 4 nTPM
Single-cell type
- respiratory ciliated cells: 324 nCPM
- ependymal cells: 250 nCPM
- late spermatids: 200 nCPM
- early spermatids: 159 nCPM
- fallopian tube ciliated cells: 125 nCPM
- endometrial ciliated cells: 101 nCPM
Immune cell
- memory B-cell: 6.2 nTPM
- naive B-cell: 5 nTPM
- NK-cell: 3.1 nTPM
- naive CD4 T-cell: 0.1 nTPM
- total PBMC: 0.1 nTPM
- basophil: 0 nTPM
Brain region
- midbrain: 13 nTPM
- choroid plexus: 11 nTPM
- medulla oblongata: 8.5 nTPM
- spinal cord: 6.4 nTPM
- pons: 6.1 nTPM
- hypothalamus: 5.5 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)
- 1.19
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.71
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- none
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 AK8 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 AK8 as an antibody target. Whether an autoantibody or antibody against AK8 could matter depends on whether native AK8 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
AK8 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 AK8 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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