Intrinsic to organelle membrane
- ABCD1: ATP-binding cassette, sub-family D (ALD), member 1
- BSCL2: Berardinelli-Seip congenital lipodystrophy 2 (seipin)
- CLN3: ceroid-lipofuscinosis, neuronal 3
- CPT1A: carnitine palmitoyltransferase 1A (liver)
- DMPK: dystrophia myotonica-protein kinase
- ELOVL4: ELOVL fatty acid elongase 4
- ETFDH: electron-transferring-flavoprotein dehydrogenase
- EXT1: exostosin glycosyltransferase 1
- G6PC: glucose-6-phosphatase, catalytic subunit
- GDAP1: ganglioside induced differentiation associated protein 1
- HLA-B: major histocompatibility complex, class I, B
- HLA-DQA1: major histocompatibility complex, class II, DQ alpha 1
- HLA-DQB1: major histocompatibility complex, class II, DQ beta 1
- HLA-DRB1: major histocompatibility complex, class II, DR beta 1
- ITM2B: integral membrane protein 2B
- L2HGDH: L-2-hydroxyglutarate dehydrogenase
- LBR: lamin B receptor
- MFN2: mitofusin 2
- PKD2: polycystic kidney disease 2 (autosomal dominant)
- PPOX: protoporphyrinogen oxidase
- SLC37A4: solute carrier family 37 (glucose-6-phosphate transporter), member 4
- WFS1: Wolfram syndrome 1 (wolframin)
Source: Gene Ontology Consortium
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