Gene Details



SDHD and homologs in 5 species are found in 601 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 52 Genes GS210158: GO:0006084 acetyl-CoA metabolic process
Expand Tier I Mouse 641 Genes GS136290: morphine antinociception 2 (Morph2, Published QTL Chr 9)
Expand Tier I Mouse 610 Genes GS135298: alcohol preference QTL 1 (Alpq1, Published QTL Chr 9)
Expand Tier I Mouse 615 Genes GS136869: triglyceride QTL 1 (Trigq1, Published QTL Chr 9)
Expand Tier I Mouse 615 Genes GS135716: dermititis 1 (Derm1, Published QTL Chr 9)
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse MP 156 Genes GS168446: MP:0000631 abnormal neuroendocrine gland morphology
Expand Tier I Mouse MP 3631 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Mouse 642 Genes GS136709: susceptibility to lung cancer 10 (Sluc10, Published QTL Chr 9)
Expand Tier I Human GO 159 Genes GS208404: GO:0045333 cellular respiration
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Mouse GO 919 Genes GS178388: GO:0055114 oxidation-reduction process
Expand Tier I Mouse 522 Genes GS135548: CD4 T cell subset 4 (Cd4ts4, Published QTL Chr 9)
Expand Tier I Mouse 605 Genes GS135619: cholesterol 11 (Chol11, Published QTL Chr 9)
Expand Tier I Mouse 630 Genes GS136812: type 2 diabetes modifying QTL 1 (Tdmq1, Published QTL Chr 9)
Expand Tier I Human CTD 374 Genes GS124417: Propylthiouracil interacting genes (MeSH:D011441) in CTD
Expand Tier I Mouse 602 Genes GS136117: body length 4 (Lgth4, Published QTL Chr 9)
Expand Tier I Mouse 605 Genes GS135354: BALB/c autoimmunity 1 (Baa1, Published QTL Chr 9)
Expand Tier I Mouse 624 Genes GS136266: modifier of mammary tumor progression 3 (Mmtp3, Published QTL Chr 9)
Expand Tier I Human 3 Genes GS174664: HP:0006737 Extraadrenal pheochromocytoma
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Mouse GO 361 Genes GS179795: GO:0019866 organelle inner membrane
Expand Tier I Human 198 Genes GS175538: HP:0011276 Vascular skin abnormality
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human GO 4 Genes GS201556: GO:0000104 succinate dehydrogenase activity
Expand Tier I Human 135 Genes GS170969: HP:0000157 Abnormality of the tongue
Expand Tier I Human GO 2 Genes GS210660: GO:0006121 mitochondrial electron transport, succinate to ubiquinone
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Mouse MP 257 Genes GS165839: MP:0009701 abnormal birth body size
Expand Tier I Human 45 Genes GS170836: HP:0011772 Abnormality of thyroid morphology
Expand Tier I Human 141 Genes GS174906: HP:0000545 Myopia
Expand Tier I Human GO 157 Genes GS207864: GO:0009055 electron carrier activity
Expand Tier I Human 7 Genes GS174607: HP:0001605 Vocal cord paralysis
Expand Tier III Mouse 327 Genes GS216879: Co-expression cluster of haloperidol-induced catalepsy genes in striatum of HS mice short term selected lines. Blue Cluster
Expand Tier I Mouse MP 54 Genes GS166643: MP:0010055 abnormal sensory neuron physiology
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier I Mouse GO 32 Genes GS186213: GO:0022904 respiratory electron transport chain
Expand Tier I Mouse MP 471 Genes GS166225: MP:0009850 embryonic lethality between implantation and placentation
Expand Tier II Mouse 517 Genes GS84213: differences in cocaine responsiveness (Published QTL, Chr 9)
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 3 Genes GS172058: HP:0002331 Headache (with pheochromocytoma)
Expand Tier I Human GO 26 Genes GS199767: GO:0006099 tricarboxylic acid cycle
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse 1018 Genes GS128598: Ethanol Induced Ataxia Chr#9
Expand Tier I Human 11 Genes GS172137: HP:0002858 Meningioma
Expand Tier I Mouse 530 Genes GS135351: Alzheimer's disease modifier 3 (Azdm3, Published QTL Chr 9)
Expand Tier I Mouse GO 195 Genes GS182519: GO:0006732 coenzyme metabolic process
Expand Tier I Mouse GO 4001 Genes GS183543: GO:0051179 localization
Expand Tier I Mouse GO 43 Genes GS193215: GO:0006084 acetyl-CoA metabolic process
Expand Tier III Mouse 1048 Genes GS213200: Expression changes in the regulation of memory consolidation and synaptic function in FoxO6 vs. wild-type mice
Expand Tier I Mouse 677 Genes GS135647: cocaine induced activation 10 (Cocia10, Published QTL Chr 9)
Expand Tier I Mouse 522 Genes GS136500: proteoglycan induced arthritis 5 (Pgia5, Published QTL Chr 9)
Expand Tier I Mouse 642 Genes GS135527: castaneus 10 week body weight 2 (C10bw2, Published QTL Chr 9)
Expand Tier I Mouse 619 Genes GS136938: vertebral trabecular bone trait 6 (Vtbt6, Published QTL Chr 9)
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human 93 Genes GS174098: HP:0011792 Neoplasm by histology
Expand Tier I Mouse 638 Genes GS136556: protection against vaginal candidiasis 2 (Pvcan2, Published QTL Chr 9)
Expand Tier I Human 4 Genes GS176049: HP:0002377 Paraganglioma-related cranial nerve palsy
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 57 Genes GS176765: HP:0001009 Telangiectasia
Expand Tier I Mouse GO 1209 Genes GS178284: GO:0031090 organelle membrane
Expand Tier I Human 12 Genes GS172342: HP:0010615 Angiofibromas
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 147 Genes GS197469: GO:0044455 mitochondrial membrane part
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Mouse 641 Genes GS136507: prion incubation determinant 2 (Pid2, Published QTL Chr 9)
Expand Tier I Mouse 634 Genes GS135536: caffeine metabolism QTL 3 (Cafq3, Published QTL Chr 9)
Expand Tier I Human 29 Genes GS176913: HP:0002170 Intracranial hemorrhage
Expand Tier I Mouse GO 77 Genes GS181430: GO:0006637 acyl-CoA metabolic process
Expand Tier I Mouse GO 2565 Genes GS192299: GO:0006793 phosphorus metabolic process
Expand Tier I Human GO 93 Genes GS198220: GO:0006637 acyl-CoA metabolic process
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Mouse GO 714 Genes GS182173: GO:0031967 organelle envelope
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse MP 93 Genes GS164991: MP:0003674 oxidative stress
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier III Mouse 6105 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Human 6 Genes GS173145: HP:0011281 Abnormality of urine catecholamine concentration
Expand Tier I Human 89 Genes GS176988: HP:0008046 Abnormality of the retinal vasculature
Expand Tier II Mouse 476 Genes GS83993: cocaine related behavior 9 (Cocrb9, Published QTL, Chr 9)
Expand Tier I Human 3 Genes GS176561: HP:0001011 Diaphoresis (with pheochromocytoma)
Expand Tier I Human GO 93 Genes GS193942: GO:0035383 thioester metabolic process
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier II Mouse 468 Genes GS84217: differences in cocaine responsiveness (Published QTL, Chr 9)
Expand Tier I Mouse GO 6473 Genes GS184448: GO:0044425 membrane part
Expand Tier I Human 3 Genes GS176392: HP:0000740 Anxiety (with pheochromocytoma)
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Mouse GO 37 Genes GS177695: GO:0051187 cofactor catabolic process
Expand Tier I Mouse MP 1966 Genes GS166590: MP:0002873 normal phenotype
Expand Tier I Mouse GO 154 Genes GS180298: GO:0005506 iron ion binding
Expand Tier I Human 10 Genes GS174848: HP:0200008 Intestinal polyposis
Expand Tier I Human 33 Genes GS174605: HP:0001609 Hoarse voice
Expand Tier I Human GO 1852 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Mouse 602 Genes GS136644: serum IGFBP-5 level QTL 3 (Si5lq3, Published QTL Chr 9)
Expand Tier I Human 403 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse GO 5103 Genes GS192512: GO:0003824 catalytic activity
Expand Tier I Mouse GO 16 Genes GS179709: GO:0042775 mitochondrial ATP synthesis coupled electron transport
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 60 Genes GS173119: HP:0002315 Headache
Expand Tier II Mouse 26 Genes GS35611: Cerebellum Gene expression correlates of Morphine photocell counts minutes 15-30 in Females BXD
Expand Tier I Human 128 Genes GS171035: HP:0002620 Systemic artery abnormality
Expand Tier I Human GO 505 Genes GS198971: GO:0031966 mitochondrial membrane
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 709 Genes GS198755: GO:0016491 oxidoreductase activity
Expand Tier I Human 95 Genes GS176989: HP:0008047 Abnormality of the vasculature of the eye
Expand Tier II Mouse 329 Genes GS35276: Striatum Gene expression correlates of Maximum startle response to 85 db in Males BXD
Expand Tier I Human 3 Genes GS174610: HP:0001606 Vocal cord paralysis (caused by tumor impingement)
Expand Tier I Mouse 672 Genes GS136166: leishmaniasis resistance 2 (Lmr2, Published QTL Chr 9)
Expand Tier I Human GO 351 Genes GS198058: GO:0005743 mitochondrial inner membrane
Expand Tier I Mouse MP 4173 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Mouse MP 14 Genes GS169902: MP:0008504 abnormal adrenal chromaffin cell morphology
Expand Tier I Human 5 Genes GS171920: HP:0002668 Paraganglioma
Expand Tier I Human GO 1518 Genes GS194138: GO:0005739 mitochondrion
Expand Tier I Human 70 Genes GS175064: HP:0000975 Hyperhidrosis
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human 30 Genes GS175081: HP:0006753 Neoplasm of the stomach
Expand Tier I Human 66 Genes GS174437: HP:0005114 Abnormalities of the peripheral arteries
Expand Tier I Human 34 Genes GS174723: HP:0000771 Gynecomastia
Expand Tier I Human 384 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human 60 Genes GS176021: HP:0010927 Abnormality of divalent inorganic cation homeostasis
Expand Tier I Human 4 Genes GS172026: HP:0000361 Pulsatile tinnitus (tympanic paraganglioma)
Expand Tier I Human 196 Genes GS173872: HP:0011368 Epidermal thickening
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Mouse 602 Genes GS135675: cholesterol QTL 4 (Cq4, Published QTL Chr 9)
Expand Tier I Human GO 4 Genes GS204477: GO:0045281 succinate dehydrogenase complex
Expand Tier I Human GO 1263 Genes GS197087: GO:0016310 phosphorylation
Expand Tier I Human 162 Genes GS175556: HP:0011675 Arrhythmia
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Mouse 470 Genes GS136453: postnatal body weight growth 15 (Pbwg15, Published QTL Chr 9)
Expand Tier I Mouse 602 Genes GS136643: serum IGFBP-5 level QTL 2 (Si5lq2, Published QTL Chr 9)
Expand Tier I Mouse 659 Genes GS135267: alopecia areata 2 (Alaa2, Published QTL Chr 9)
Expand Tier III Mouse 1964 Genes GS865: Sey_Pax6_Age_Reduced_Linear_Incr
Expand Tier I Human 211 Genes GS175164: HP:0011927 Short digit
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier I Human GO 741 Genes GS201250: GO:0044429 mitochondrial part
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 232 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human CTD 4423 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
Expand Tier I Human 12 Genes GS171599: HP:0001962 Palpitations
Expand Tier I Human 220 Genes GS171791: HP:0000370 Abnormality of the middle ear
Expand Tier I Mouse MP 57 Genes GS168809: MP:0003243 abnormal dopaminergic neuron morphology
Expand Tier III Mouse 603 Genes GS1778: Tabakoff et al 2003: Differential Gene Expression of acute functional tolerance to an incoordinating effect of ethanol (HAFT2 vs LAFT2)
Expand Tier I Human 51 Genes GS176092: HP:0100006 Neoplasm of the central nervous system
Expand Tier I Mouse MP 42 Genes GS167560: MP:0001001 abnormal chemoreceptor morphology
Expand Tier I Mouse MP 1692 Genes GS169833: MP:0005380 embryogenesis phenotype
Expand Tier I Mouse GO 22 Genes GS182966: GO:0006099 tricarboxylic acid cycle
Expand Tier I Human CTD 917 Genes GS121965: Amiodarone interacting genes (MeSH:D000638) in CTD
Expand Tier I Human GO 27 Genes GS209846: GO:0046356 acetyl-CoA catabolic process
Expand Tier I Human GO 3861 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human CTD 377 Genes GS121976: Zidovudine interacting genes (MeSH:D015215) in CTD
Expand Tier I Human GO 328 Genes GS208795: GO:0015980 energy derivation by oxidation of organic compounds
Expand Tier I Mouse MP 28 Genes GS168810: MP:0003244 loss of dopaminergic neurons
Expand Tier I Human 16 Genes GS176091: HP:0100007 Neoplasm of the peripheral nervous system
Expand Tier I Human 20 Genes GS173952: HP:0000853 Goiter
Expand Tier I Human 157 Genes GS171968: HP:0000405 Conductive hearing impairment
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Mouse MP 325 Genes GS170368: MP:0000249 abnormal blood vessel physiology
Expand Tier I Human 12 Genes GS174198: HP:0009720 Adenoma sebaceum
Expand Tier I Mouse 662 Genes GS135322: APP associated premature death 1 (Appd1, Published QTL Chr 9)
Expand Tier I Mouse MP 29 Genes GS164909: MP:0008289 abnormal adrenal medulla morphology
Expand Tier I Mouse 530 Genes GS136547: periosteal circumference 6 (Pstc6, Published QTL Chr 9)
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human 3 Genes GS173929: HP:0001676 Palpitations (with pheochromocytoma)
Expand Tier I Mouse 687 Genes GS135300: alcohol preference QTL 3 (Alpq3, Published QTL Chr 9)
Expand Tier II Mouse 481 Genes GS84216: alcohol consumption (Published QTL, Chr 9)
Expand Tier I Mouse 1353 Genes GS128581: BECs at LORR Recovery Chr# 9
Expand Tier I Human 103 Genes GS176735: HP:0010929 Abnormality of cation homeostasis
Expand Tier I Human CTD 5075 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human GO 33 Genes GS202498: GO:0009109 coenzyme catabolic process
Expand Tier I Human 41 Genes GS171157: HP:0100742 Vascular neoplasm
Expand Tier I Human 114 Genes GS172283: HP:0000820 Abnormality of the thyroid gland
Expand Tier I Mouse 593 Genes GS135239: activity response to ethanol 6 (Actre6, Published QTL Chr 9)
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human GO 3275 Genes GS199267: GO:0043234 protein complex
Expand Tier I Mouse 595 Genes GS136939: vertebral trabecular bone trait 7 (Vtbt7, Published QTL Chr 9)
Expand Tier I Mouse GO 4224 Genes GS193059: GO:0044446 intracellular organelle part
Expand Tier I Mouse 462 Genes GS135371: B.burgdorferi-associated arthritis 9 (Bbaa9, Published QTL Chr 9)
Expand Tier I Human 28 Genes GS176196: HP:0004796 Gastrointestinal obstruction
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse MP 256 Genes GS165811: MP:0009703 decreased birth body size
Expand Tier I Mouse MP 56 Genes GS166331: MP:0005156 bradykinesia
Expand Tier I Human 189 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human 66 Genes GS171279: HP:0100545 Arterial stenosis
Expand Tier I Mouse GO 33 Genes GS185666: GO:0009109 coenzyme catabolic process
Expand Tier I Human 9 Genes GS170983: HP:0100634 Neuroendocrine neoplasm
Expand Tier I Mouse MP 103 Genes GS166559: MP:0001905 abnormal dopamine level
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 5 Genes GS173569: HP:0003574 Positive regitine blocking test
Expand Tier I Mouse MP 1307 Genes GS170198: MP:0001614 abnormal blood vessel morphology
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 100 Genes GS176774: HP:0001005 Dermatological manifestations of systemic disorders
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 132 Genes GS174606: HP:0001608 Abnormality of the voice
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 4 Genes GS175616: HP:0008629 Pulsatile tinnitus
Expand Tier I Mouse MP 1672 Genes GS165260: MP:0001392 abnormal locomotor behavior
Expand Tier I Mouse MP 1692 Genes GS169603: MP:0001672 abnormal embryogenesis/ development
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human CTD 281 Genes GS121771: Benzbromarone interacting genes (MeSH:D001553) in CTD
Expand Tier I Human 87 Genes GS172544: HP:0000834 Abnormality of the adrenal glands
Expand Tier I Human 28 Genes GS173761: HP:0000519 Congenital cataract
Expand Tier I Human CTD 363 Genes GS125936: Tunicamycin interacting genes (MeSH:D014415) in CTD
Expand Tier I Human GO 2241 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier I Human 14 Genes GS171923: HP:0100579 Mucosal telangiectasiae
Expand Tier I Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Mouse MP 553 Genes GS165385: MP:0008946 abnormal neuron number
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Human 15 Genes GS171345: HP:0001048 Cavernous hemangioma
Expand Tier I Human 397 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Mouse GO 26 Genes GS181790: GO:0006119 oxidative phosphorylation
Expand Tier I Human CTD 670 Genes GS121369: Clofibric Acid interacting genes (MeSH:D002995) in CTD
Expand Tier I Human 117 Genes GS174102: HP:0011799 Abnormality of facial soft tissue
Expand Tier I Mouse MP 639 Genes GS164032: MP:0004811 abnormal neuron physiology
Expand Tier I Mouse MP 3494 Genes GS170601: MP:0005621 abnormal cell physiology
Expand Tier I Mouse GO 1395 Genes GS185366: GO:0044248 cellular catabolic process
Expand Tier I Mouse GO 32 Genes GS187277: GO:0009060 aerobic respiration
Expand Tier I Mouse GO 1572 Genes GS192354: GO:0046914 transition metal ion binding
Expand Tier I Mouse MP 3543 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Human 6 Genes GS172429: HP:0002640 Hypertension associated with pheochromocytoma
Expand Tier I Mouse 632 Genes GS136038: inflammatory bowel disease QTL 1 (Ibdq1, Published QTL Chr 9)
Expand Tier I Mouse 602 Genes GS135618: cholesterol 10 (Chol10, Published QTL Chr 9)
Expand Tier I Mouse MP 1963 Genes GS166718: MP:0002169 no abnormal phenotype detected
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 258 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Mouse MP 349 Genes GS166160: MP:0011092 complete embryonic lethality
Expand Tier I Human 77 Genes GS175999: HP:0100659 Abnormality of the cerebral vasculature
Expand Tier I Human 27 Genes GS175512: HP:0005214 Intestinal obstruction
Expand Tier I Human GO 262 Genes GS202364: GO:0048037 cofactor binding
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 2 Genes GS173894: HP:0003334 Elevated circulating catecholamine level
Expand Tier II Mouse 517 Genes GS84214: differences in cocaine responsiveness (Published QTL, CHr 9)
Expand Tier I Human 3 Genes GS171680: HP:0100642 Neoplasm of the adrenal medulla
Expand Tier I Mouse GO 4 Genes GS184750: GO:0000104 succinate dehydrogenase activity
Expand Tier I Human 20 Genes GS172391: HP:0000221 Furrowed tongue
Expand Tier I Mouse GO 232 Genes GS177696: GO:0051186 cofactor metabolic process
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 4 Genes GS198078: GO:0005749 mitochondrial respiratory chain complex II
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Mouse 531 Genes GS135343: atherosclerosis 29 (Ath29, Published QTL Chr 9)
Expand Tier I Mouse 642 Genes GS136407: organ weight QTL 7 (Orgwq7, Published QTL Chr 9)
Expand Tier I Mouse MP 102 Genes GS166502: MP:0003186 abnormal redox activity
Expand Tier I Mouse MP 4592 Genes GS165537: MP:0005376 homeostasis/metabolism phenotype
Expand Tier I Mouse 467 Genes GS135911: G protein deficiency-induced colitis 3 (Gpdc3, Published QTL Chr 9)
Expand Tier II Mouse 610 Genes GS84211: cocaine related behavior (Published QTL, Chr 9)
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human 39 Genes GS171701: HP:0100568 Neoplasm of the endocrine system
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human 67 Genes GS171115: HP:0001053 Hypopigmented skin patches
Expand Tier II Mouse 321 Genes GS35261: Striatum Gene expression correlates of Maximum startle response to 80 db in Females BXD
Expand Tier I Human 3 Genes GS172763: HP:0001686 Loss of voice
Expand Tier I Mouse GO 5859 Genes GS182404: GO:0031224 intrinsic to membrane
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier II Mouse 668 Genes GS83965: cocaine induced activation 10 (Cocia10, Published QTL, Chr 9, MGI:3040201)
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Mouse MP 576 Genes GS168750: MP:0002191 abnormal artery morphology
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 5320 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human 40 Genes GS172679: HP:0001028 Hemangioma
Expand Tier I Mouse MP 1130 Genes GS163227: MP:0003313 abnormal locomotor activation
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 1 Genes GS174861: HP:0006723 Intestinal carcinoid
Expand Tier I Mouse 610 Genes GS136801: "body temperature response to dietary restriction, QTL 1" (Tbdr1, Published QTL Chr 9)
Expand Tier I Human 12 Genes GS171443: HP:0008777 Abnormality of the vocal cords
Expand Tier I Human 344 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Mouse GO 4588 Genes GS177309: GO:1901363 heterocyclic compound binding
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 111 Genes GS175068: HP:0000971 Abnormality of the sweat gland
Expand Tier I Mouse GO 342 Genes GS181270: GO:0005743 mitochondrial inner membrane
Expand Tier I Mouse MP 585 Genes GS165985: MP:0000965 abnormal sensory neuron morphology
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Mouse GO 23 Genes GS192900: GO:0046356 acetyl-CoA catabolic process
Expand Tier I Mouse MP 487 Genes GS167105: MP:0008948 decreased neuron number
Expand Tier I Human 15 Genes GS177048: HP:0011371 Recurrent viral skin infections
Expand Tier I Human 16 Genes GS171687: HP:0003072 Hypercalcemia
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier II Mouse 70 Genes GS36193: Cerebellum Gene expression correlates of Locomotor activity after second saline treatment. in Males BXD
Expand Tier I Mouse 475 Genes GS136084: keratinocyte stem cell locus 1 (Ksc1, Published QTL Chr 9)
Expand Tier I Mouse MP 114 Genes GS164970: MP:0000639 abnormal adrenal gland morphology
Expand Tier I Mouse GO 4637 Genes GS177382: GO:0097159 organic cyclic compound binding
Expand Tier I Mouse MP 5 Genes GS167245: MP:0003437 abnormal carotid body morphology
Expand Tier I Human 399 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 150 Genes GS175074: HP:0001156 Brachydactyly syndrome
Expand Tier I Mouse GO 55 Genes GS177317: GO:0016627 oxidoreductase activity, acting on the CH-CH group of donors
Expand Tier I Mouse GO 3211 Genes GS192509: GO:0006810 transport
Expand Tier I Human 391 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Human 141 Genes GS172281: HP:0000822 Hypertension
Expand Tier I Mouse 602 Genes GS135579: cystic fibrosis modifier QTL 2 (Cfmq2, Published QTL Chr 9)
Expand Tier I Human 155 Genes GS172040: HP:0000962 Hyperkeratosis
Expand Tier I Mouse 624 Genes GS136764: soft tissue heal 8 (Stheal8, Published QTL Chr 9)
Expand Tier I Human 157 Genes GS174877: HP:0001892 Abnormal bleeding
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human 95 Genes GS176560: HP:0001010 Hypopigmentation of the skin
Expand Tier I Mouse 604 Genes GS136024: hypothermia sensitivity (Hts, Published QTL Chr 9)
Expand Tier I Mouse MP 1825 Genes GS168956: MP:0003491 abnormal voluntary movement
Expand Tier I Human 4 Genes GS172376: HP:0002864 Paraganglioma of head and neck
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human 6 Genes GS174837: HP:0001095 Hypertensive retinopathy
Expand Tier I Human 4 Genes GS172446: HP:0003001 Glomus jugular tumor
Expand Tier I Human 138 Genes GS174289: HP:0002577 Abnormality of the stomach
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Mouse MP 461 Genes GS169957: MP:0001402 hypoactivity
Expand Tier I Human 616 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse MP 3924 Genes GS163934: MP:0001764 abnormal homeostasis
Expand Tier I Mouse GO 4333 Genes GS184452: GO:0044422 organelle part
Expand Tier I Mouse 605 Genes GS135595: mean cell hemoglobin concentration QTL 2 (Chcmq2, Published QTL Chr 9)
Expand Tier I Human 144 Genes GS175128: HP:0011123 Inflammatory abnormality of the skin
Expand Tier I Human 39 Genes GS175738: HP:0011732 Abnormality of adrenal morphology
Expand Tier I Mouse MP 5057 Genes GS165525: MP:0010768 mortality/aging
Expand Tier I Human 3 Genes GS175283: HP:0006748 Adrenal pheochromocytoma
Expand Tier I Human GO 58 Genes GS196470: GO:0042773 ATP synthesis coupled electron transport
Expand Tier I Mouse MP 24 Genes GS170673: MP:0010913 abnormal neuroendocrine cell morphology
Expand Tier I Human 11 Genes GS174608: HP:0001604 Vocal cord paresis
Expand Tier I Human 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 626 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 120 Genes GS177000: HP:0001291 Abnormality of the cranial nerves
Expand Tier I Mouse 677 Genes GS136379: obesity QTL 5 (Obq5, Published QTL Chr 9)
Expand Tier I Human 360 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier I Mouse GO 2507 Genes GS192296: GO:0006796 phosphate-containing compound metabolic process
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 148 Genes GS203053: GO:0022900 electron transport chain
Expand Tier I Human GO 13 Genes GS202368: GO:0048038 quinone binding
Expand Tier I Rat DRG 4920 Genes GS86932: Table S3: CORTEX 17K MICROARRAY [DRG]
Expand Tier II Mouse 427 Genes GS35271: Striatum Gene expression correlates of Maximum startle response to 85 db in Females BXD
Expand Tier I Human 86 Genes GS172352: HP:0000137 Abnormality of the ovary
Expand Tier I Human 90 Genes GS171351: HP:0003581 Adult onset
Expand Tier I Human 177 Genes GS175431: HP:0011122 Abnormality of skin physiology
Expand Tier I Human CTD 1291 Genes GS125402: Diethylnitrosamine interacting genes (MeSH:D004052) in CTD
Expand Tier I Mouse MP 156 Genes GS166015: MP:0006036 abnormal mitochondrial physiology
Expand Tier I Mouse MP 154 Genes GS163896: MP:0011479 abnormal catecholamine level
Expand Tier I Mouse MP 4772 Genes GS165524: MP:0010769 abnormal survival
Expand Tier I Human GO 76 Genes GS204180: GO:0070469 respiratory chain
Expand Tier I Human 27 Genes GS175840: HP:0000739 Anxiety
Expand Tier I Human GO 2494 Genes GS209235: GO:0006793 phosphorus metabolic process
Expand Tier I Human 268 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier I Human 129 Genes GS174925: HP:0000769 Abnormality of the breast
Expand Tier I Mouse 642 Genes GS136673: skull morphology 12 (Skull12, Published QTL Chr 9)
Expand Tier I Mouse MP 3815 Genes GS165243: MP:0010770 preweaning lethality
Expand Tier I Human GO 4 Genes GS207058: GO:0045283 fumarate reductase complex
Expand Tier I Human 13 Genes GS171993: HP:0100631 Neoplasm of the adrenal gland
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Mouse GO 78 Genes GS191477: GO:0045333 cellular respiration
Expand Tier I Human 9 Genes GS172307: HP:0100696 Bone cysts
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human CTD 18 Genes GS123977: 2,6-dichloro-4-nitrophenol interacting genes (MeSH:C015802) in CTD
Expand Tier I Human 199 Genes GS171637: HP:0008872 Feeding difficulties in infancy
Expand Tier I Human 271 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Mouse 137 Genes GS129137: fecundity QTL 4 (Fecq4 Published QTL Chr 9)
Expand Tier I Mouse GO 482 Genes GS181271: GO:0005740 mitochondrial envelope
Expand Tier I Human 8 Genes GS171438: HP:0008776 Abnormality of the renal artery
Expand Tier I Mouse 605 Genes GS135233: activity-distance traveled 4 (Actd4, Published QTL Chr 9)
Expand Tier II Mouse 29 Genes GS35566: Cerebellum Gene expression correlates of Morphine photocell counts minutes 0-15 in Females BXD
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human CTD 4389 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Mouse MP 36 Genes GS170213: MP:0004181 abnormal carotid artery morphology
Expand Tier I Human 12 Genes GS171550: HP:0001064 Diaphoresis
Expand Tier I Human 67 Genes GS173092: HP:0004375 Neoplasm of the nervous system
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 34 Genes GS173962: HP:0001581 Recurrent skin infections
Expand Tier I Mouse MP 1628 Genes GS167505: MP:0008762 embryonic lethality
Expand Tier I Mouse MP 2644 Genes GS169829: MP:0005385 cardiovascular system phenotype
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human GO 4 Genes GS208854: GO:0045273 respiratory chain complex II
Expand Tier I Human 8 Genes GS171915: HP:0002666 Pheochromocytoma
Expand Tier I Mouse 517 Genes GS135374: body length 4 (Bdln4, Published QTL Chr 9)
Expand Tier I Human GO 257 Genes GS194434: GO:0051186 cofactor metabolic process
Expand Tier I Human 5 Genes GS173584: HP:0003345 Elevated urinary norepinephrine
Expand Tier I Human GO 2431 Genes GS209232: GO:0006796 phosphate-containing compound metabolic process
Expand Tier I Mouse 3329 Genes GS127933: Pons - Allen Mouse Brain Atlas
Expand Tier I Human 172 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Mouse GO 3268 Genes GS177721: GO:0051234 establishment of localization
Expand Tier I Mouse MP 2263 Genes GS164262: MP:0002080 prenatal lethality
Expand Tier I Mouse MP 68 Genes GS168762: MP:0005423 abnormal somatic nervous system physiology
Expand Tier I Mouse MP 2200 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier I Mouse GO 1648 Genes GS190954: GO:0009056 catabolic process
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Mouse GO 8072 Genes GS184218: GO:0071704 organic substance metabolic process
Expand Tier I Mouse GO 18 Genes GS179711: GO:0042773 ATP synthesis coupled electron transport
Expand Tier I Mouse MP 305 Genes GS166156: MP:0011096 complete embryonic lethality between implantation and somite formation
Expand Tier I Human 2 Genes GS174235: HP:0006715 Glomus tympanicum paraganglioma
Expand Tier I Human GO 381 Genes GS196559: GO:0019866 organelle inner membrane
Expand Tier I Mouse GO 77 Genes GS177219: GO:0035383 thioester metabolic process
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Mouse MP 1724 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier I Human 71 Genes GS170917: HP:0100852 Abnormal fear/anxiety-related behavior
Expand Tier I Human 54 Genes GS176464: HP:0100242 Sarcoma
Expand Tier I Human GO 139 Genes GS194657: GO:0046906 tetrapyrrole binding
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse GO 5588 Genes GS193061: GO:0044444 cytoplasmic part
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 114 Genes GS186210: GO:0022900 electron transport chain
Expand Tier I Human 2 Genes GS171927: HP:0100570 Carcinoid
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse GO 3537 Genes GS192041: GO:0043169 cation binding
Expand Tier I Human 181 Genes GS175391: HP:0011004 Abnormality of the systemic arterial tree
Expand Tier I Human 182 Genes GS174612: HP:0001600 Abnormality of the larynx
Expand Tier I Mouse GO 292 Genes GS180799: GO:0006091 generation of precursor metabolites and energy
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human GO 5400 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human 11 Genes GS172027: HP:0000360 Tinnitus
Expand Tier I Human 138 Genes GS174644: HP:0000953 Hyperpigmentation of the skin
Expand Tier I Human GO 55 Genes GS194047: GO:0016627 oxidoreductase activity, acting on the CH-CH group of donors
Expand Tier I Human 374 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human 120 Genes GS172358: HP:0003117 Abnormality of circulating hormone level
Expand Tier I Human GO 44 Genes GS204135: GO:0009060 aerobic respiration
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Mouse GO 735 Genes GS181962: GO:0016491 oxidoreductase activity
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 3 Genes GS202367: GO:0048039 ubiquinone binding
Expand Tier I Mouse MP 1628 Genes GS163852: MP:0001544 abnormal cardiovascular system physiology
Expand Tier I Human GO 1668 Genes GS202188: GO:0044248 cellular catabolic process
Expand Tier I Human 58 Genes GS173335: HP:0004363 Abnormality of calcium homeostasis
Expand Tier I Human 106 Genes GS175048: HP:0006824 Cranial nerve paralysis
Expand Tier I Mouse GO 5734 Genes GS190713: GO:0016021 integral to membrane
Expand Tier I Human 43 Genes GS173159: HP:0002239 Gastrointestinal hemorrhage
Expand Tier I Rat DRG 4920 Genes GS86494: Table S1: Hippocampus 17 K microarray data. [DRG]
Expand Tier I Human 88 Genes GS176142: HP:0001034 Hypermelanotic macule
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Mouse 610 Genes GS135660: cocaine related behavior 8 (Cocrb8, Published QTL Chr 9)
Expand Tier I Mouse 603 Genes GS136550: proteinuria 3 (Ptnu3, Published QTL Chr 9)
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Mouse MP 1941 Genes GS165528: MP:0005379 endocrine/exocrine gland phenotype
Expand Tier III Mouse 603 Genes GS1777: Tabakoff et al 2003: Differential Gene Expression of acute functional tolerance to an incoordinating effect of ethanol (HAFT1 vs LAFT1)
Expand Tier I Mouse MP 295 Genes GS164744: MP:0001730 embryonic growth arrest
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 69 Genes GS198579: GO:0006119 oxidative phosphorylation
Expand Tier I Human 73 Genes GS171209: HP:0000093 Proteinuria
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human CTD 281 Genes GS125104: Ethionine interacting genes (MeSH:D005001) in CTD
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 136 Genes GS173751: HP:0000998 Hypertrichosis
Expand Tier I Human 72 Genes GS175808: HP:0011028 Abnormality of blood circulation
Expand Tier I Human 104 Genes GS171211: HP:0000091 Abnormality of the renal tubule
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Mouse GO 459 Genes GS182174: GO:0031966 mitochondrial membrane
Expand Tier I Mouse 642 Genes GS135485: bone response to mechanical loading 5 (Brml5, Published QTL Chr 9)
Expand Tier I Human 13 Genes GS172519: HP:0001342 Cerebral hemorrhage
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Mouse 585 Genes GS136009: haloperidol-induced catelepsy 5 (Hpic5, Published QTL Chr 9)
Expand Tier I Human 303 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Mouse GO 3442 Genes GS181533: GO:0046872 metal ion binding
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier II Mouse 44 Genes GS35656: Cerebellum Gene expression correlates of Morphine photocell counts minutes 60-75 in Females BXD
Expand Tier II Mouse 773 Genes GS84210: alcohol preference QTL 1 (Alpq1 Published QTL, Chr 9)
Expand Tier I Human 3 Genes GS173934: HP:0001673 Tachycardia (with pheochromocytoma)
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier II Mouse 580 Genes GS84208: METH responses for home cage activity (Published QTL, Chr 9)
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 237 Genes GS174292: HP:0011968 Feeding difficulties
Expand Tier I Human GO 168 Genes GS197078: GO:0005506 iron ion binding
Expand Tier I Human CTD 480 Genes GS122634: Ketone Bodies interacting genes (MeSH:D007657) in CTD
Expand Tier I Mouse GO 1518 Genes GS192074: GO:1901575 organic substance catabolic process
Expand Tier I Human 2 Genes GS173191: HP:0012099 Abnormality of circulating catecholamine level
Expand Tier II Mouse 610 Genes GS83992: cocaine related behavior 8 (Cocrb8, Published QTL, Chr 9)
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 110 Genes GS203056: GO:0022904 respiratory electron transport chain
Expand Tier I Human GO 4034 Genes GS208978: GO:0043169 cation binding
Expand Tier I Mouse 522 Genes GS135768: experimental allergic encephalomyelitis susceptibility 9 (Eae9, Published QTL Chr 9)
Expand Tier I Mouse MP 60 Genes GS163205: MP:0005643 decreased dopamine level
Expand Tier I Human 49 Genes GS173990: HP:0000502 Abnormality of the conjunctiva
Expand Tier I Mouse MP 262 Genes GS164126: MP:0001388 abnormal stationary movement
Expand Tier I Human 72 Genes GS175809: HP:0011029 Internal hemorrhage
Expand Tier I Human 5 Genes GS173482: HP:0000875 Episodic hypertension
Expand Tier I Mouse MP 3 Genes GS167251: MP:0003438 abnormal carotid body physiology
Expand Tier I Human 151 Genes GS174920: HP:0000766 Abnormality of the sternum
Expand Tier I Human 22 Genes GS175941: HP:0100835 Benign neoplasm of the central nervous system
Expand Tier I Mouse 632 Genes GS135474: brachyury modifier 1 (Brm1, Published QTL Chr 9)
Expand Tier II Mouse 471 Genes GS84218: differences in cocaine responsiveness (Published QTL, Chr 9)
Expand Tier I Human 235 Genes GS175523: HP:0000008 Abnormality of female internal genitalia