You are using an outdated browser. Please upgrade your browser to improve your experience.

Tbio
KERA
Keratocan

Protein Summary
Description
May be important in developing and maintaining corneal transparency and for the structure of the stromal matrix. The protein encoded by this gene is a keratan sulfate proteoglycan that is involved in corneal transparency. Defects in this gene are a cause of autosomal recessive cornea plana 2 (CNA2).[provided by RefSeq, May 2010]
Uniprot Accession IDs
Gene Name
Ensembl ID
  • ENST00000266719
  • ENSP00000266719
  • ENSG00000139330

Symbol
  • SLRR2B
  • KTN
  • CNA2
  • SLRR2B
Illumination Graph
Knowledge Table
Most Knowledge About
Knowledge Value (0 to 1 scale)
pathway
0.93
cell type or tissue
0.82
gene perturbation
0.61
cell line
0.59
cellular component
0.53


IDG Development Level Summary
Tdark

These are targets about which virtually nothing is known. They do not have known drug or small molecule activities
- AND - satisfy two or more of the following criteria:

Pubmed score: 133.69   (req: < 5)
Gene RIFs: 15   (req: <= 3)
Antibodies: 131   (req: <= 50)
Tbio

These targets do not have known drug or small molecule activities
- AND - satisfy two or more of the following criteria:

Pubmed score: 133.69   (req: >= 5)
Gene RIFs: 15   (req: > 3)
Antibodies: 131   (req: > 50)

- OR - satisfy the following criterion:

Gene Ontology Terms: 5
Tchem

Target has at least one ChEMBL compound with an activity cutoff of < 30 nM - AND - satisfies the preceding conditions

Active Ligand: 0
Tclin

Target has at least one approved drug - AND - satisfies the preceding conditions

Active Drug: 0
Pathways (13)
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) (R-HSA-3656244)

Click on a row in the table to change the structure displayed.

Items per page:
1 – 5 of 12
Data Source
Name
Explore in Pharos
Explore in Source
Reactome
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
Reactome
Defective CHST6 causes MCDC1
Reactome
Defective ST3GAL3 causes MCT12 and EIEE15
Reactome
Disease
Reactome
Diseases associated with glycosaminoglycan metabolism
Name
Explore in Pharos
Explore in Source
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
Defective CHST6 causes MCDC1
Defective ST3GAL3 causes MCT12 and EIEE15
Disease
Diseases associated with glycosaminoglycan metabolism
Gene Ontology Terms (9)
Items per page:
10
1 – 4 of 4
GO Term
Evidence
Assigned by
Traceable Author Statement (TAS)
Reactome
Traceable Author Statement (TAS)
Reactome
Traceable Author Statement (TAS)
Reactome
Non-traceable Author Statement (NAS)
UniProtKB
Protein-Protein Interactions (78)
1 – 10 of 78
NUDT12
Tbio
Family: Enzyme
Novelty: 0.18740719
p_int: 0.999999988
p_ni: 1.1e-8
p_wrong: 1e-9
Score: 0.76
Data Source: BioPlex,STRINGDB
CNPY4
Tdark
Novelty: 0.59578334
p_int: 0.999997001
p_ni: 8.42e-7
p_wrong: 0.000002157
Score: 0.195
Data Source: BioPlex,STRINGDB
VWA8
Tdark
Novelty: 0.17546432
p_int: 0.999536841
p_ni: 0.000463159
Score: 0.537
Data Source: BioPlex,STRINGDB
EID2
Tbio
Novelty: 0.02022264
p_int: 0.998633831
p_ni: 0.000005253
p_wrong: 0.001360915
Score: 0.319
Data Source: BioPlex,STRINGDB
FBXO21
Tbio
Novelty: 0.2186203
p_int: 0.996756472
p_ni: 0.003243528
Score: 0.188
Data Source: BioPlex,STRINGDB
BLMH
Tbio
Family: Enzyme
Novelty: 0.00855614
p_int: 0.990459728
p_ni: 0.009540272
Score: 0.874
Data Source: BioPlex,STRINGDB
SQSTM1
Tbio
Novelty: 0.00100555
p_int: 0.979900907
p_ni: 0.020099093
Score: 0.202
Data Source: BioPlex,STRINGDB
MAP3K7
Tchem
Family: Kinase
Novelty: 0.00540177
p_int: 0.957008177
p_ni: 0.042989198
p_wrong: 0.000002625
Score: 0.255
Data Source: BioPlex,STRINGDB
B4GALT5
Tbio
Family: Enzyme
Novelty: 0.04538678
p_int: 0.942658562
p_ni: 0.053523639
p_wrong: 0.0038178
Score: 0.91
Data Source: BioPlex,STRINGDB
PRKCI
Tchem
Family: Kinase
Novelty: 0.0076377
p_int: 0.849991603
p_ni: 0.150007984
p_wrong: 4.13e-7
Score: 0.265
Data Source: BioPlex,STRINGDB
Publication Statistics
PubMed Score  133.69

PubMed score by year
PubTator Score  43.68

PubTator score by year
Amino Acid Sequence
Residue Counts
Protein Sequence
ProtVista Viewer