KNDC1
Kinase non-catalytic C-lobe domain-containing protein 1
Also known as: bB439H18.3, C10orf23, FLJ25027, KIAA1768, KNDC1_HUMAN, RASGEF2, v-KIND, Very-KIND
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q76NI1
- Gene
- KNDC1
- Ensembl
- ENSG00000171798
- Chromosome
- 10
- Canonical length
- 1749 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles,Plasma membrane,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is a Ras guanine nucleotide exchange factor that appears to negatively regulate dendritic growth in the brain. Knockdown of this gene in senescent umbilical vein endothelial cells partially reversed the senescence, showing that this gene could potentially be targeted by anti-aging therapies. [provided by RefSeq, Dec 2016]
Canonical amino-acid sequenceUniProt
1749 residues, UniProt reviewed canonical sequence.
>Q76NI1|KNDC1
1 MQAMDPAAAD LYEEDGKDLD FYDFEPLPTL PEDEENVSLA DILSLRDRGL SEQEAWAVCL
61 ECSLSMRSVA HAAIFQSLCI TPDTLAFNTS GNVCFMEQLS DDPEGAFVPP EFDVTGNTFE
121 AHIYSLGATL KAALEYVAEP TLEPRLSQDL EALLSRMQAE DPGDRPDLES IIALCEEKLQ
181 LTSSCRVCRS LSAVGRRVLS IESFGALQDV SESSWRERPA PGNAGPRRPP GDPSTDPEVL
241 PTPEGPESET SRGPRASPTK ALLSTPVRNG ESHSREGLAG LVLDAERTLG ELDRDALRRS
301 RLRKVQTFPR LLSDSPEATL CLPLTRGKSQ LPISELFSPD PRKAFLDRKN GLSSFQAQPK
361 CRLWPEQEPE HQLGRVPCAG RSTDRGPGVP GSPGQPETSH PSQGPAEAPA DPRDASGEAQ
421 TPRDDERIPE GARQLESAAA EQWVSLQDLL SQLGRPFREY ELWALCLACL RALQTRPEHP
481 AYLCLDSVLV AEDGAVLFQP PPANGSYDSF FLAPELAEER LVTEKASVYC VAAVLWTAAK
541 FSVPRNHKLA LPRRLKTLLL DMARRSAPER PSAAEAIKVC GSYLLQRGMD SRKILAHLRA
601 SICQVYQEEE TISLQNAFSV VELKPSVAPA PEPSPGFLPV NSDTGLVAVP GPVPGQHPCG
661 EEATQLPAAF TSEATHFKPI VLAQNASVAR DQPALAQEES EERGGQREGE GEEKLSLEAH
721 AGSPSLKTPD GPVPGPGPQG AAPEPLGASV QRDSAQGRPC PPPQAPANQP EGASSAAPGS
781 PVPAPPTKAS ALPVEQGPAE PIPPGVASGG LRPDALGPTT AHHGPRHPPK PPRSKATERP
841 GQEPEGPGAT PAGERDDQSP DSVPERPRPA DRRLCLPCVD ASPLPGRTAC PSLQEATRLI
901 QEEFAFDGYL DNGLEALIMG EYIFALKDLT FATFCGAISE KFCDLYWDEK LLQNLFKVVN
961 GQASPSPSTA EEAGSQLEGS QSPRSPSSKR PSLHRLGKEK PAMARTSSRA PCSPTSVSDV
1021 DSDALSRGNF EVGFRPQRSV KAERAQQPEA GEDRRPAGGA SDVEAVTRLA RSKGVGPALS
1081 PGPAGFQSCS PGWCSAFYEA DCFGADVHNY VKDLGRQQAD GALPDAQSPE LEQQLMMEKR
1141 NYRKTLKFYQ KLLQKEKRNK GSDVKTMLSK LKGQLEEMKS RVQFLSLVKK YLQVMYAERW
1201 GLEPCTLPVI VNIAAAPCDT LDFSPLDESS SLIFYNVNKH PGGRQKARIL QAGTPLGLMA
1261 YLYSSDAFLE GYVQQFLYTF RYFCTPHDFL HFLLDRINST LTRAHQDPTS TFTKIYRRSL
1321 CVLQAWVEDC YAVDFPRNSG LLGKLEDFIS SKILPLDGSA KHLLGLLEVG MDRRAEGNPR
1381 GTDLENPREA EEDARPFNAL CKRLSEDGIS RKSFPWRLPR GNGLVLPPHK ERPYTIAAAL
1441 PKPCFLEDFY GPCAKTSEKG PYFLTEYSTH QLFSQLTLLQ QELFQKCHPV HFLNSRALGV
1501 MDKSTAIPKA SSSESLSAKT CSLFLPNYVQ DKYLLQLLRN ADDVSTWVAA EIVTSHTSKL
1561 QVNLLSKFLL IAKSCYEQRN FATAMQILSG LEHLAVRQSP AWRILPAKIA EVMEELKAVE
1621 VFLKSDSLCL MEGRRFRAQP TLPSAHLLAM HIQQLETGGF TMTNGAHRWS KLRNIAKVVS
1681 QVHAFQENPY TFSPDPKLQS YLKQRIARFS GADISTLAAD SRANFHQVSS EKHSRKIQDK
1741 LRRMKATFQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KNDC1 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)
- 0.47
- Highest tissue expression
- 42 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 42 nTPM
- cerebral cortex: 39 nTPM
- amygdala: 28 nTPM
- pituitary gland: 24 nTPM
- hippocampal formation: 23 nTPM
- hypothalamus: 22 nTPM
Single-cell type
- ependymal cells: 188 nCPM
- astrocytes: 162 nCPM
- somatotrophs: 148 nCPM
- gonadotrophs: 135 nCPM
- corticotrophs: 125 nCPM
- respiratory ciliated cells: 109 nCPM
Immune cell
- non-classical monocyte: 1.1 nTPM
- basophil: 0.6 nTPM
- intermediate monocyte: 0.6 nTPM
- neutrophil: 0.4 nTPM
- classical monocyte: 0.1 nTPM
- naive B-cell: 0.1 nTPM
Brain region
- cerebral cortex: 167 nTPM
- amygdala: 134 nTPM
- thalamus: 113 nTPM
- hippocampal formation: 101 nTPM
- cerebellum: 100 nTPM
- white matter: 94 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)
- 0.4
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.89
- DepMap mean gene effect
- 0.08
- 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
- cerebellar granule cell differentiation
- regulation of dendrite development
- regulation of dendrite morphogenesis
- small GTPase-mediated signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Ras-like guanine nucleotide exchange factor, N-terminal
- Ras guanine-nucleotide exchange factors catalytic domain
- Protein kinase-like domain superfamily
- KIND domain
- Ras guanine nucleotide exchange factor domain superfamily
- Ras guanine-nucleotide exchange factor, catalytic domain superfamily
- RasGEF domain
- RasGEF N-terminal motif
- Kinase non-catalytic C-lobe domain
- Kinase non-catalytic C-lobe domain-containing protein 1
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of KNDC1 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 KNDC1 as an antibody target. Whether an autoantibody or antibody against KNDC1 could matter depends on whether native KNDC1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KNDC1 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 KNDC1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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