KIAA1328
Protein hinderin
Also known as: K1328_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q86T90
- Gene
- KIAA1328
- Ensembl
- ENSG00000150477
- Chromosome
- 18
- Canonical length
- 577 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nuclear speckles,Vesicles,Lipid droplets,Plasma membrane
OverviewNCBI Gene
No narrative summary is available for KIAA1328 in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
577 residues, UniProt reviewed canonical sequence.
>Q86T90|KIAA1328
1 MADVAGPSRP SAAAFWSRDF SDEEQSVVYV PGISAEGNVR SRHKLMSPKA DVKLKTSRVT
61 DASISMESLK GTGDSVDEQN SCRGEIKSAS LKDLCLEDKR RIANLIKELA RVSEEKEVTE
121 ERLKAEQESF EKKIRQLEEQ NELIIKEREA LQLQYRECQE LLSLYQKYLS EQQEKLTMSL
181 SELGAARMQE QQVSSRKSTL QCSSVELDGS YLSIARPQTY YQTKQRPKSA VQDSASESLI
241 AFRNNSLKPV TLHHPKDDLD KIPSETTTCN CESPGRKPAV PTEKMPQEEL HMKECPHLKP
301 TPSQCCGHRL AADRVHDSHP TNMTPQHPKT HPESCSYCRL SWASLVHGGG ALQPIETLKK
361 QISEDRKQQL MLQKMELEIE KERLQHLLAQ QETKLLLKQQ QLHQSRLDYN CLLKSNCDGW
421 LLGTSSSIKK HQDPPNSGEN RKERKTVGFH SHMKDDAQWS CQKKDTCRPQ RGTVTGVRKD
481 ASTSPMPTGS LKDFVTTASP SLQHTTSRYE TSLLDLVQSL SPNSAPKPQR YPSREAGAWN
541 HGTFRLSPLK STRKKMGMHR TPEELEENQI LEDIFFILocalizationUniProt · AlphaFold · HPA
Whether an antibody against KIAA1328 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.64
- Highest tissue expression
- 20 nTPM
Expression across tissuesHPA
Tissue
- retina: 20 nTPM
- bone marrow: 14 nTPM
- testis: 12 nTPM
- skin: 8.1 nTPM
- ovary: 7.1 nTPM
- skeletal muscle: 6.8 nTPM
Single-cell type
- choroid plexus epithelial cells: 630 nCPM
- renal collecting duct intercalated cells: 351 nCPM
- fibro-adipogenic progenitors: 283 nCPM
- lactotrophs: 269 nCPM
- adrenal medulla cells: 255 nCPM
- thyrotrophs: 255 nCPM
Immune cell
- basophil: 20 nTPM
- naive B-cell: 9.6 nTPM
- eosinophil: 8.5 nTPM
- neutrophil: 8.5 nTPM
- MAIT T-cell: 8.3 nTPM
- T-reg: 8.3 nTPM
Brain region
- white matter: 225 nTPM
- cerebral cortex: 210 nTPM
- cerebellum: 201 nTPM
- amygdala: 179 nTPM
- choroid plexus: 174 nTPM
- basal ganglia: 173 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)
- 0.93
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.67
- DepMap mean gene effect
- -0.11
- DepMap dependency class
- selective
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).
Protein domainsUniProt · Pfam · InterPro
- Protein hinderin
- Uncharacterised protein KIAA1328
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of KIAA1328 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 KIAA1328 as an antibody target. Whether an autoantibody or antibody against KIAA1328 could matter depends on whether native KIAA1328 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KIAA1328 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 KIAA1328 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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