complementation Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
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Genes

58 genes co-occuring with the biological term complementation in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
ANTXR1 anthrax toxin receptor 1
APOBEC1 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 1
APOBEC3A apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3A
APP amyloid beta (A4) precursor protein
ASL argininosuccinate lyase
ATR ATR serine/threonine kinase
BAK1 BCL2-antagonist/killer 1
BAX BCL2-associated X protein
BCL2 B-cell CLL/lymphoma 2
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CEBPD CCAAT/enhancer binding protein (C/EBP), delta
CETN2 centrin, EF-hand protein, 2
EEF1A1 eukaryotic translation elongation factor 1 alpha 1
EIF2AK2 eukaryotic translation initiation factor 2-alpha kinase 2
ERCC2 excision repair cross-complementation group 2
ERCC4 excision repair cross-complementation group 4
ERCC8 excision repair cross-complementation group 8
FANCA Fanconi anemia, complementation group A
FANCB Fanconi anemia, complementation group B
FANCD2 Fanconi anemia, complementation group D2
FANCL Fanconi anemia, complementation group L
FEN1 flap structure-specific endonuclease 1
ICAM1 intercellular adhesion molecule 1
IFNA1 interferon, alpha 1
IMMTP1 inner membrane protein, mitochondrial (mitofilin) pseudogene 1
JAK2 Janus kinase 2
LMNA lamin A/C
MAPT microtubule-associated protein tau
MBTPS1 membrane-bound transcription factor peptidase, site 1
MFN2 mitofusin 2
MIR503 microRNA 503
MKI67 marker of proliferation Ki-67
MMAA methylmalonic aciduria (cobalamin deficiency) cblA type
MMAB methylmalonic aciduria (cobalamin deficiency) cblB type
MMS19 MMS19 nucleotide excision repair homolog (S. cerevisiae)
MUT methylmalonyl CoA mutase
NAT1 N-acetyltransferase 1 (arylamine N-acetyltransferase)
NDUFA1 NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 1, 7.5kDa
ORC6 origin recognition complex, subunit 6
PEX1 peroxisomal biogenesis factor 1
PEX14 peroxisomal biogenesis factor 14
PEX6 peroxisomal biogenesis factor 6
POU5F1 POU class 5 homeobox 1
RAMP3 receptor (G protein-coupled) activity modifying protein 3
RFX5 regulatory factor X, 5 (influences HLA class II expression)
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)
SOX2 SRY (sex determining region Y)-box 2
TLR8 toll-like receptor 8
TMEM70 transmembrane protein 70
TNF tumor necrosis factor
TOPBP1 topoisomerase (DNA) II binding protein 1
USP6 ubiquitin specific peptidase 6
UXS1 UDP-glucuronate decarboxylase 1
VIM vimentin
WAS Wiskott-Aldrich syndrome
XPC xeroderma pigmentosum, complementation group C
XPO1 exportin 1