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  • 11.0 [archived version]
STRINGSTRING
NKX2-8 NKX2-8 CABIN1 CABIN1 CEP162 CEP162 NLRP13 NLRP13 C11orf57 C11orf57 C1orf21 C1orf21 C5orf51 C5orf51 CD97 CD97 SEMA3C SEMA3C ZNF19 ZNF19 ELMSAN1 ELMSAN1
"C1orf21" - Uncharacterized protein C1orf21 in Homo sapiens
Nodes:
Network nodes represent proteins
splice isoforms or post-translational modifications are collapsed, i.e. each node represents all the proteins produced by a single, protein-coding gene locus.
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colored nodes:
query proteins and first shell of interactors
white nodes:
second shell of interactors
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empty nodes:
proteins of unknown 3D structure
filled nodes:
some 3D structure is known or predicted
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Edges represent protein-protein associations
associations are meant to be specific and meaningful, i.e. proteins jointly contribute to a shared function; this does not necessarily mean they are physically binding each other.
Known Interactions
from curated databases
experimentally determined
Predicted Interactions
gene neighborhood
gene fusions
gene co-occurrence
Others
textmining
co-expression
protein homology
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[Homology]
Score
C1orf21Uncharacterized protein C1orf21; Chromosome 1 open reading frame 21 (121 aa)    
Predicted Functional Partners:
C5orf51
UPF0600 protein C5orf51; Chromosome 5 open reading frame 51; Belongs to the UPF0600 family (294 aa)
           
  0.669
CEP162
Centrosomal protein of 162 kDa; Required to promote assembly of the transition zone in primary cilia. Acts by specifically recognizing and binding the axonemal microtubule. Localizes to the distal ends of centrioles before ciliogenesis and directly binds to axonemal microtubule, thereby promoting and restricting transition zone formation specifically at the cilia base. Required to mediate CEP290 association with microtubules; Belongs to the CEP162 family (1403 aa)
           
  0.598
C11orf57
Uncharacterized protein NKAPD1; Chromosome 11 open reading frame 57 (293 aa)
           
  0.556
ZNF19
Zinc finger protein 19; May be involved in transcriptional regulation; Zinc fingers C2H2-type (458 aa)
           
  0.543
SEMA3C
Semaphorin-3C; Binds to plexin family members and plays an important role in the regulation of developmental processes. Required for normal cardiovascular development during embryogenesis. Functions as attractant for growing axons, and thereby plays an important role in axon growth and axon guidance (By similarity); I-set domain containing (751 aa)
           
  0.530
ELMSAN1
ELM2 and Myb/SANT domain containing 1 (1045 aa)
           
  0.476
NKX2-8
Homeobox protein Nkx-2.8; NKL subclass homeoboxes and pseudogenes (239 aa)
           
  0.475
CABIN1
Calcineurin-binding protein cabin-1; May be required for replication-independent chromatin assembly. May serve as a negative regulator of T-cell receptor (TCR) signaling via inhibition of calcineurin. Inhibition of activated calcineurin is dependent on both PKC and calcium signals. Acts as a negative regulator of p53/TP53 by keeping p53 in an inactive state on chromatin at promoters of a subset of it’s target genes (2220 aa)
           
  0.435
NLRP13
NACHT, LRR and PYD domains-containing protein 13; Involved in inflammation; NLR family (1043 aa)
           
  0.426
CD97
CD97 antigen; Receptor potentially involved in both adhesion and signaling processes early after leukocyte activation. Plays an essential role in leukocyte migration (By similarity); Belongs to the G-protein coupled receptor 2 family. LN-TM7 subfamily (835 aa)
           
  0.404
Your Current Organism:
Homo sapiens
NCBI taxonomy Id: 9606
Other names: H. sapiens, Homo sapiens, human, man
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