tsc Gene Set

Dataset	GeneRIF Biological Term Annotations
Category	structural or functional annotations
Type	biological term
Description	An autosomal dominant condition that often leads to seizure and other neurological symptoms and that may be linked to deregulations in the mTOR signaling pathway. (Pathway Ontology, PW_0000179)
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Genes

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

Symbol	Name
ADRB3	adrenoceptor beta 3
AKT1	v-akt murine thymoma viral oncogene homolog 1
CLCNKB	chloride channel, voltage-sensitive Kb
CRTC1	CREB regulated transcription coactivator 1
CUL4A	cullin 4A
DDB1	damage-specific DNA binding protein 1, 127kDa
EREG	epiregulin
FBXW5	F-box and WD repeat domain containing 5
FKBP8	FK506 binding protein 8, 38kDa
MTOR	mechanistic target of rapamycin (serine/threonine kinase)
PPP1R15A	protein phosphatase 1, regulatory subunit 15A
PTEN	phosphatase and tensin homolog
RBX1	ring-box 1, E3 ubiquitin protein ligase
SLC12A3	solute carrier family 12 (sodium/chloride transporter), member 3
SLC7A5	solute carrier family 7 (amino acid transporter light chain, L system), member 5
TBC1D7	TBC1 domain family, member 7
TSC1	tuberous sclerosis 1
TSC2	tuberous sclerosis 2
YWHAB	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, beta