Gene Details



SDHAF2 and homologs in 1 species are found in 98 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Human GO 618 Genes GS196553: GO:0005730 nucleolus
Expand Tier I Human 4 Genes GS172446: HP:0003001 Glomus jugular tumor
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 2455 Genes GS196595: GO:0006464 cellular protein modification process
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 69 Genes GS198579: GO:0006119 oxidative phosphorylation
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 555 Genes GS195139: GO:0055114 oxidation-reduction process
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human GO 3116 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Human GO 58 Genes GS196470: GO:0042773 ATP synthesis coupled electron transport
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human GO 3863 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human GO 2479 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 11 Genes GS174608: HP:0001604 Vocal cord paresis
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human 120 Genes GS177000: HP:0001291 Abnormality of the cranial nerves
Expand Tier I Human 3 Genes GS174610: HP:0001606 Vocal cord paralysis (caused by tumor impingement)
Expand Tier I Human 39 Genes GS171701: HP:0100568 Neoplasm of the endocrine system
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 356 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 9 Genes GS194895: GO:0018065 protein-cofactor linkage
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 147 Genes GS203053: GO:0022900 electron transport chain
Expand Tier I Human 9 Genes GS170983: HP:0100634 Neuroendocrine neoplasm
Expand Tier I Human 2 Genes GS175572: HP:0002886 Vagal paraganglioma
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 3 Genes GS172763: HP:0001686 Loss of voice
Expand Tier I Human GO 6256 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 90 Genes GS171351: HP:0003581 Adult onset
Expand Tier I Human GO 449 Genes GS197593: GO:0006091 generation of precursor metabolites and energy
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 3116 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human GO 2092 Genes GS209551: GO:0031981 nuclear lumen
Expand Tier I Human 182 Genes GS174612: HP:0001600 Abnormality of the larynx
Expand Tier I Human GO 2486 Genes GS209235: GO:0006793 phosphorus metabolic process
Expand Tier I Human 5 Genes GS171920: HP:0002668 Paraganglioma
Expand Tier I Human 132 Genes GS174606: HP:0001608 Abnormality of the voice
Expand Tier I Human GO 1515 Genes GS194138: GO:0005739 mitochondrion
Expand Tier I Human GO 2756 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 159 Genes GS208404: GO:0045333 cellular respiration
Expand Tier I Human 4 Genes GS172376: HP:0002864 Paraganglioma of head and neck
Expand Tier I Human 2 Genes GS174235: HP:0006715 Glomus tympanicum paraganglioma
Expand Tier I Human 4 Genes GS175616: HP:0008629 Pulsatile tinnitus
Expand Tier I Human GO 2455 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 12 Genes GS171443: HP:0008777 Abnormality of the vocal cords
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human 11 Genes GS172027: HP:0000360 Tinnitus
Expand Tier I Human GO 328 Genes GS208795: GO:0015980 energy derivation by oxidation of organic compounds
Expand Tier I Human GO 2549 Genes GS194336: GO:0043412 macromolecule modification
Expand Tier I Human GO 5908 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human CTD 1192 Genes GS125069: Sodium Selenite interacting genes (MeSH:D018038) in CTD
Expand Tier I Human 4 Genes GS172026: HP:0000361 Pulsatile tinnitus (tympanic paraganglioma)
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 16 Genes GS176091: HP:0100007 Neoplasm of the peripheral nervous system
Expand Tier I Human 67 Genes GS173092: HP:0004375 Neoplasm of the nervous system
Expand Tier I Human 392 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Human GO 2711 Genes GS199273: GO:0043233 organelle lumen
Expand Tier I Human GO 1 Genes GS202632: GO:0018293 protein-FAD linkage
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human GO 1257 Genes GS197087: GO:0016310 phosphorylation
Expand Tier I Human GO 110 Genes GS203056: GO:0022904 respiratory electron transport chain
Expand Tier I Human GO 58 Genes GS196468: GO:0042775 mitochondrial ATP synthesis coupled electron transport
Expand Tier I Human 396 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Human 3 Genes GS174401: HP:0001613 Hoarse voice (caused by tumor impingement)
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 2 Genes GS210660: GO:0006121 mitochondrial electron transport, succinate to ubiquinone
Expand Tier I Human 106 Genes GS175048: HP:0006824 Cranial nerve paralysis
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 33 Genes GS174605: HP:0001609 Hoarse voice
Expand Tier I Human GO 2423 Genes GS209232: GO:0006796 phosphate-containing compound metabolic process
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 4 Genes GS176049: HP:0002377 Paraganglioma-related cranial nerve palsy
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 2665 Genes GS205543: GO:0070013 intracellular organelle lumen
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 256 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Human GO 3239 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Human 7 Genes GS174607: HP:0001605 Vocal cord paralysis
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding