Search Results for: TMEM97

75 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
KIR2DL3 killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 3
  • Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell
LEUTX leucine twenty homeobox
  • Zygotic genome activation (ZGA)
LHFPL5 LHFPL tetraspan subfamily member 5
  • Sensory processing of sound by inner hair cells of the cochlea
  • Sensory processing of sound by outer hair cells of the cochlea
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 HFTC
  • Defective C1GALT1C1 causes TNPS
  • Defective GALNT12 causes CRCS1
  • Dectin-2 family
  • Interleukin-4 and Interleukin-13 signaling
  • O-linked glycosylation of mucins
  • Termination of O-glycan biosynthesis
  • Developmental Lineage of Mammary Gland Luminal Epithelial Cells
  • Developmental Lineage of Mammary Gland Alveolar Cells
  • 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
  • Co-inhibition by PD-1
  • PD-L1(CD274) glycosylation and translocation to plasma membrane
PDZK1IP1 PDZK1 interacting protein 1
PLP1 proteolipid protein 1
  • Hypomyelinating leukodystrophy (HLD); Pelizaeus-Merzbacher disease (PMD)
  • Hereditary spastic paraplegia (SPG)
PSCA prostate stem cell antigen
  • Post-translational modification: synthesis of GPI-anchored proteins
REEP1 receptor accessory protein 1
  • Expression and translocation of olfactory receptors
  • 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

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