Organelle envelope
- AAAS: achalasia, adrenocortical insufficiency, alacrimia
- ABCB7: ATP-binding cassette, sub-family B (MDR/TAP), member 7
- ALAS2: aminolevulinate, delta-, synthase 2
- BRIP1: BRCA1 interacting protein C-terminal helicase 1
- CISD2: CDGSH iron sulfur domain 2
- CPOX: coproporphyrinogen oxidase
- CPT1A: carnitine palmitoyltransferase 1A (liver)
- CPT2: carnitine palmitoyltransferase 2
- CYP11B1: cytochrome P450, family 11, subfamily B, polypeptide 1
- CYP11B2: cytochrome P450, family 11, subfamily B, polypeptide 2
- DHCR7: 7-dehydrocholesterol reductase
- DHODH: dihydroorotate dehydrogenase (quinone)
- DMPK: dystrophia myotonica-protein kinase
- EMD: emerin
- ETFDH: electron-transferring-flavoprotein dehydrogenase
- GATA1: GATA binding protein 1 (globin transcription factor 1)
- GATM: glycine amidinotransferase (L-arginine:glycine amidinotransferase)
- GCH1: GTP cyclohydrolase 1
- GDAP1: ganglioside induced differentiation associated protein 1
- GHRHR: growth hormone releasing hormone receptor
- GUCY2D: guanylate cyclase 2D, membrane (retina-specific)
- HADHA: hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit
- HADHB: hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), beta subunit
- HAX1: HCLS1 associated protein X-1
- HSD3B2: hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2
- L2HGDH: L-2-hydroxyglutarate dehydrogenase
- LBR: lamin B receptor
- LETM1: leucine zipper-EF-hand containing transmembrane protein 1
- LMNA: lamin A/C
- LRRK2: leucine-rich repeat kinase 2
- MATR3: matrin 3
- MCCC1: methylcrotonoyl-CoA carboxylase 1 (alpha)
- MCCC2: methylcrotonoyl-CoA carboxylase 2 (beta)
- MFN2: mitofusin 2
- MPV17: MpV17 mitochondrial inner membrane protein
- MT-ATP6: mitochondrially encoded ATP synthase 6
- MT-ND1: mitochondrially encoded NADH dehydrogenase 1
- MT-ND4: mitochondrially encoded NADH dehydrogenase 4
- MT-ND4L: mitochondrially encoded NADH dehydrogenase 4L
- MT-ND5: mitochondrially encoded NADH dehydrogenase 5
- MT-ND6: mitochondrially encoded NADH dehydrogenase 6
- MYO6: myosin VI
- NPC1: Niemann-Pick disease, type C1
- OPA1: optic atrophy 1 (autosomal dominant)
- PAFAH1B1: platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
- PANK2: pantothenate kinase 2
- PML: promyelocytic leukemia
- PPOX: protoporphyrinogen oxidase
- PRICKLE1: prickle homolog 1 (Drosophila)
- PRODH: proline dehydrogenase (oxidase) 1
- PSEN1: presenilin 1
- PSEN2: presenilin 2 (Alzheimer disease 4)
- RAF1: v-raf-1 murine leukemia viral oncogene homolog 1
- SDHA: succinate dehydrogenase complex, subunit A, flavoprotein (Fp)
- SDHB: succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
- SDHC: succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa
- SDHD: succinate dehydrogenase complex, subunit D, integral membrane protein
- SLC25A13: solute carrier family 25 (aspartate/glutamate carrier), member 13
- SLC25A15: solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
- SLC25A19: solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
- SLC25A20: solute carrier family 25 (carnitine/acylcarnitine translocase), member 20
- SLC25A4: solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4
- SMAD3: SMAD family member 3
- SPG20: spastic paraplegia 20 (Troyer syndrome)
- SURF1: surfeit 1
- SYNE1: spectrin repeat containing, nuclear envelope 1
- TAZ: tafazzin
- TIMM8A: translocase of inner mitochondrial membrane 8 homolog A (yeast)
- TREX1: three prime repair exonuclease 1
- WHSC1: Wolf-Hirschhorn syndrome candidate 1
Source: Gene Ontology Consortium
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