Search Results for: TMEM97

70 interactions involving TMEM97 - transmembrane protein 97 found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
LHFPL5 LHFPL tetraspan subfamily member 5
LIME1 Lck interacting transmembrane adaptor 1
LRRC59 leucine rich repeat containing 59
MFF mitochondrial fission factor
MRM1 mitochondrial rRNA methyltransferase 1
  • rRNA modification in the mitochondrion
MTIF3 mitochondrial translational initiation factor 3
  • Mitochondrial translation initiation
MUC1 mucin 1, cell surface associated
  • Defective GALNT3 causes familial hyperphosphatemic tumoral calcinosis (HFTC)
  • Defective C1GALT1C1 causes Tn polyagglutination syndrome (TNPS)
  • Defective GALNT12 causes colorectal cancer 1 (CRCS1)
  • Dectin-2 family
  • Interleukin-4 and Interleukin-13 signaling
  • O-linked glycosylation of mucins
  • Termination of O-glycan biosynthesis
  • TG4010
NDUFAF1 NADH:ubiquinone oxidoreductase complex assembly factor 1
  • Complex I biogenesis
NDUFAF2 NADH:ubiquinone oxidoreductase complex assembly factor 2
  • Complex I biogenesis
  • Mitochondrial respiratory chain deficiencies (MRCD), including: Mitochondrial complex I deficiency (MT-C1D); Complex II deficiency (MT-C2D); Complex III deficiency (MT-C3D); Complex IV deficiency (MT-C4D); Complex V deficiency (MT-ATPSD); Leigh syndrome (LS); Kearns-Sayre Syndrome (KSS); LCHD deficiency (LCHD); Leber Hereditary Optic Neuropathy (LHON); Myoclonic Epilepsy and Ragged-Red Fiber Disease (MERRF); NARP; MELAS; ACAD9 deficiency; HADH deficiency; HIBCH deficiency; GRACILE syndrome
NEMP1 nuclear envelope integral membrane protein 1
PDCD1LG2 programmed cell death 1 ligand 2
  • PD-1 signaling
PDZK1IP1 PDZK1 interacting protein 1
PLP1 proteolipid protein 1
  • Hereditary spastic paraplegia (SPG)
  • Hypomyelinating leukodystrophy (HLD); Pelizaeus-Merzbacher disease (PMD)
PSCA prostate stem cell antigen
  • Post-translational modification: synthesis of GPI-anchored proteins
REEP1 receptor accessory protein 1
  • Olfactory Signaling Pathway
  • Hereditary spastic paraplegia (SPG)
RHCG Rh family C glycoprotein
  • Rhesus glycoproteins mediate ammonium transport.
RNF170 ring finger protein 170
SAR1A secretion associated Ras related GTPase 1A
SGPL1 sphingosine-1-phosphate lyase 1
  • Sphingolipid de novo biosynthesis
  • Pyridoxal phosphate
SLC14A1 solute carrier family 14 member 1 (Kidd blood group)
  • Transport of bile salts and organic acids, metal ions and amine compounds

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