Gene Details



SH3TC2 and homologs in 4 species are found in 297 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 Mouse GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Human 1 Genes GS172331: HP:0004466 Prolonged brainstem auditory evoked potentials
Expand Tier I Mouse MP 331 Genes GS165366: MP:0002272 abnormal nervous system electrophysiology
Expand Tier I Mouse 239 Genes GS136725: susceptibility to lung cancer 28 (Sluc28, Published QTL Chr 18)
Expand Tier I Human GO 408 Genes GS199582: GO:0016044 cellular membrane organization
Expand Tier I Mouse MP 1724 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier III Human 2187 Genes GS218390: Alcoholism Susceptibility Chr 1
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Mouse GO 3706 Genes GS188641: GO:0071944 cell periphery
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 63 Genes GS175213: HP:0003693 Distal amyotrophy
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier II Mouse 238 Genes GS84311: high-dose ethanol actions (Published QTL, Chr 18)
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 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse 267 Genes GS135266: age-related hearing loss 6 (Ahl6, Published QTL Chr 18)
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Human GO 649 Genes GS198498: GO:0050801 ion homeostasis
Expand Tier I Mouse 405 Genes GS135307: angle of entrainment 3 (Angle3, Published QTL Chr 18)
Expand Tier I Human GO 412 Genes GS201052: GO:0061024 membrane organization
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human GO 2507 Genes GS196934: GO:0065008 regulation of biological quality
Expand Tier I Mouse GO 9 Genes GS190433: GO:0043217 myelin maintenance
Expand Tier I Human GO 2661 Genes GS207797: GO:0030154 cell differentiation
Expand Tier III Mouse 8107 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier I Mouse GO 5111 Genes GS187146: GO:0044700 single organism signaling
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 86 Genes GS172908: HP:0002450 Abnormality of the motor neurons
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 135 Genes GS170969: HP:0000157 Abnormality of the tongue
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Mouse GO 123 Genes GS187753: GO:0019228 regulation of action potential in neuron
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Mouse 201 Genes GS135963: HDL QTL 31 (Hdlq31, Published QTL Chr 18)
Expand Tier I Human GO 27 Genes GS199684: GO:0014037 Schwann cell differentiation
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human 18 Genes GS173678: HP:0003383 Onion bulb formation
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Human 106 Genes GS175048: HP:0006824 Cranial nerve paralysis
Expand Tier I Human 2 Genes GS176173: HP:0003400 Basal lamina 'onion bulb' formation
Expand Tier I Mouse GO 2538 Genes GS190893: GO:0030154 cell differentiation
Expand Tier I Mouse 289 Genes GS136387: ocular degeneration with sex reversal modifier 1 (Odsm1, Published QTL Chr 18)
Expand Tier I Human GO 4283 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human GO 70 Genes GS202683: GO:0021782 glial cell development
Expand Tier I Mouse 268 Genes GS135982: wound healing/regeneration 9 (Heal9, Published QTL Chr 18)
Expand Tier I Human GO 837 Genes GS196920: GO:0048878 chemical homeostasis
Expand Tier I Human GO 4593 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Mouse 165 Genes GS129162: proteoglycan induced spondylitis 1 (Pgis1 Published QTL Chr 18)
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Human 58 Genes GS171880: HP:0003134 Abnormality of peripheral nerve conduction
Expand Tier I Human GO 564 Genes GS208092: GO:0005768 endosome
Expand Tier I Mouse GO 296 Genes GS177347: GO:0042391 regulation of membrane potential
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human GO 79 Genes GS197803: GO:0007422 peripheral nervous system development
Expand Tier I Mouse GO 24 Genes GS182883: GO:0014037 Schwann cell differentiation
Expand Tier I Mouse 208 Genes GS136409: organ weight QTL 9 (Orgwq9, Published QTL Chr 18)
Expand Tier I Mouse GO 606 Genes GS184506: GO:0006873 cellular ion homeostasis
Expand Tier I Human 25 Genes GS173680: HP:0003380 Decreased number of peripheral myelinated nerve fibers
Expand Tier I Human GO 2824 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Mouse 241 Genes GS135726: duration of locomotor activity 2 (Dloc2, Published QTL Chr 18)
Expand Tier I Human 44 Genes GS174918: HP:0000764 Peripheral axonal degeneration
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Mouse 239 Genes GS136491: proteoglycan induced arthritis 11 (Pgia11, Published QTL Chr 18)
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse GO 3493 Genes GS177570: GO:0016043 cellular component organization
Expand Tier I Mouse GO 3080 Genes GS177265: GO:0048731 system development
Expand Tier I Mouse GO 58 Genes GS189481: GO:0055037 recycling endosome
Expand Tier I Human GO 166 Genes GS194334: GO:0042063 gliogenesis
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse 442 Genes GS136565: radiation pulmonary fibrosis 4 (Radpf4, Published QTL Chr 18)
Expand Tier I Mouse MP 221 Genes GS169362: MP:0000920 abnormal myelination
Expand Tier I Human 8 Genes GS174415: HP:0003484 Upper limb muscle weakness
Expand Tier I Mouse MP 245 Genes GS170569: MP:0005404 abnormal axon morphology
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Mouse GO 3615 Genes GS178359: GO:0071840 cellular component organization or biogenesis
Expand Tier I Mouse GO 658 Genes GS192669: GO:0055082 cellular chemical homeostasis
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 129 Genes GS174657: HP:0001425 Heterogeneous
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Mouse GO 100 Genes GS189593: GO:0042552 myelination
Expand Tier I Mouse 439 Genes GS135602: circulating hormone level QTL 10 (Chlq10, Published QTL Chr 18)
Expand Tier I Human 7 Genes GS173467: HP:0001308 Tongue fasciculations
Expand Tier I Mouse GO 980 Genes GS188826: GO:0022008 neurogenesis
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 90 Genes GS172611: HP:0003474 Sensory impairment
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 8 Genes GS174434: HP:0007107 Segmental peripheral demyelination
Expand Tier I Human GO 98 Genes GS204614: GO:0019228 regulation of action potential in neuron
Expand Tier I Mouse GO 18 Genes GS179705: GO:0014044 Schwann cell development
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human GO 735 Genes GS204608: GO:0019226 transmission of nerve impulse
Expand Tier I Mouse 248 Genes GS135403: body growth late QTL 12 (Bglq12, Published QTL Chr 18)
Expand Tier I Mouse 251 Genes GS135651: cocaine induced activation 14 (Cocia14, Published QTL Chr 18)
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Mouse MP 80 Genes GS167104: MP:0005403 abnormal nerve conduction
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Mouse 391 Genes GS135521: body weight at necropsy 5 (Bwtn5, Published QTL Chr 18)
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Mouse MP 48 Genes GS167939: MP:0008814 reduced nerve conduction velocity
Expand Tier I Mouse 289 Genes GS136821: triglyceride QTL 1 (Tgq1, Published QTL Chr 18)
Expand Tier I Human 46 Genes GS171759: HP:0002936 Distal sensory impairment
Expand Tier I Mouse 391 Genes GS136713: susceptibility to lung cancer 14 (Sluc14, Published QTL Chr 18)
Expand Tier I Human GO 80 Genes GS206464: GO:0042552 myelination
Expand Tier I Mouse GO 5221 Genes GS179211: GO:0007154 cell communication
Expand Tier I Mouse 249 Genes GS136435: pulmonary adenoma susceptibility 7 (Pas7, Published QTL Chr 18)
Expand Tier I Mouse GO 160 Genes GS177596: GO:0042063 gliogenesis
Expand Tier I Mouse GO 9323 Genes GS180152: GO:0065007 biological regulation
Expand Tier I Human GO 17 Genes GS208537: GO:0032292 peripheral nervous system axon ensheathment
Expand Tier I Human 117 Genes GS174102: HP:0011799 Abnormality of facial soft tissue
Expand Tier I Mouse MP 574 Genes GS166743: MP:0002229 neurodegeneration
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human 7 Genes GS173684: HP:0003387 Decreased number of large peripheral myelinated nerve fibers
Expand Tier II Mouse 107 Genes GS35318: Neocortex Gene expression correlates of Acoustic Startle Response Percentage of maximum response at 85 db in Males BXD
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier I Human 27 Genes GS171008: HP:0011096 Peripheral demyelination
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Mouse 400 Genes GS136156: limb length QTL 6 (Lmblgq6, Published QTL Chr 18)
Expand Tier I Mouse MP 3543 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 1236 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 96 Genes GS172854: HP:0004302 Functional motor problems.
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 1 Genes GS172705: HP:0007686 Abnormal pupillary function
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Mouse GO 1398 Genes GS181215: GO:0007399 nervous system development
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 9 Genes GS171322: HP:0008944 Distal lower limb amyotrophy
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 97 Genes GS198898: GO:0007009 plasma membrane organization
Expand Tier I Mouse GO 2172 Genes GS180156: GO:0065008 regulation of biological quality
Expand Tier I Mouse 248 Genes GS136102: lupus NZB x NZW 6 (Lbw6, Published QTL Chr 18)
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 Mouse GO 5111 Genes GS189484: GO:0023052 signaling
Expand Tier I Mouse 420 Genes GS136017: heart failure modifier 4 (Hrtfm4, Published QTL Chr 18)
Expand Tier I Mouse GO 16 Genes GS191605: GO:0032292 peripheral nervous system axon ensheathment
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Human GO 1693 Genes GS209960: GO:0003008 system process
Expand Tier I Human GO 751 Genes GS202715: GO:0035637 multicellular organismal signaling
Expand Tier I Mouse MP 3543 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Mouse MP 875 Genes GS168958: MP:0003492 abnormal involuntary movement
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human 25 Genes GS171767: HP:0003431 Decreased motor nerve conduction velocity
Expand Tier I Human GO 17 Genes GS210069: GO:0022011 myelination in peripheral nervous system
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 123 Genes GS175588: HP:0001311 Neurophysiological abnormality
Expand Tier I Human 27 Genes GS176587: HP:0001271 Polyneuropathy
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 8 Genes GS173506: HP:0009053 Distal lower limb muscle weakness
Expand Tier I Human GO 248 Genes GS194078: GO:0042391 regulation of membrane potential
Expand Tier I Mouse 456 Genes GS136197: lung squamous cell carcinoma 3 (Lscc3, Published QTL Chr 18)
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 7 Genes GS196057: GO:0032287 peripheral nervous system myelin maintenance
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Mouse GO 851 Genes GS180142: GO:0048878 chemical homeostasis
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 255 Genes GS176610: HP:0003593 Infantile onset
Expand Tier I Mouse MP 441 Genes GS170131: MP:0008415 abnormal neurite morphology
Expand Tier I Mouse 421 Genes GS136615: colon tumor susceptibility 5 (Scc5, Published QTL Chr 18)
Expand Tier I Mouse 391 Genes GS136199: lung tumor shape-determining 1 (Ltsd1, Published QTL Chr 18)
Expand Tier I Mouse 441 Genes GS135940: HDL level 40 (Hdl40, Published QTL Chr 18)
Expand Tier I Mouse GO 2710 Genes GS192471: GO:0048869 cellular developmental process
Expand Tier I Mouse GO 563 Genes GS187747: GO:0019226 transmission of nerve impulse
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 82 Genes GS172000: HP:0001761 Pes cavus
Expand Tier I Human 246 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Human 10 Genes GS172451: HP:0007210 Lower limb amyotrophy
Expand Tier I Mouse MP 3716 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 715 Genes GS200565: GO:0019725 cellular homeostasis
Expand Tier I Human GO 75 Genes GS206352: GO:0055037 recycling endosome
Expand Tier I Mouse 99 Genes GS129141: insulin dependent diabetes susceptibility 21.2 (Idd21.2 Published QTL Chr 18)
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 8 Genes GS175374: HP:0010546 Muscle fibrillation
Expand Tier I Mouse GO 737 Genes GS183767: GO:0019725 cellular homeostasis
Expand Tier I Mouse GO 102 Genes GS190680: GO:0007272 ensheathment of neurons
Expand Tier I Human 135 Genes GS172857: HP:0004305 Involuntary movements
Expand Tier I Human 399 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Mouse GO 102 Genes GS192188: GO:0008366 axon ensheathment
Expand Tier I Mouse 239 Genes GS135306: angiogenesis due to FGF2 QTL 4 (Angfq4, Published QTL Chr 18)
Expand Tier I Mouse GO 323 Genes GS184244: GO:0061024 membrane organization
Expand Tier I Mouse MP 2406 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Mouse MP 898 Genes GS169390: MP:0002067 abnormal sensory capabilities/reflexes/nociception
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 346 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier I Human 22 Genes GS171659: HP:0000615 Abnormality of the pupil
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse 430 Genes GS136484: plasmacytoma susceptibility 6 (Pcyts6, Published QTL Chr 18)
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Mouse GO 134 Genes GS187579: GO:0010001 glial cell differentiation
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 24 Genes GS176061: HP:0002355 Difficulty walking
Expand Tier I Mouse 437 Genes GS136268: "macronutrient intake, fat 2" (Mnif2, Published QTL Chr 18)
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse GO 3614 Genes GS180229: GO:0005886 plasma membrane
Expand Tier I Human GO 1724 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Mouse GO 4073 Genes GS180034: GO:0032502 developmental process
Expand Tier I Human GO 4213 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human 143 Genes GS176586: HP:0001270 Motor delay
Expand Tier I Mouse GO 587 Genes GS185880: GO:0035637 multicellular organismal signaling
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human GO 83 Genes GS207579: GO:0007272 ensheathment of neurons
Expand Tier II Mouse 246 Genes GS83969: cocaine induced activation 14 (Cocia14, Published QTL, Chr 18)
Expand Tier I Mouse 267 Genes GS136423: pulmonary adenoma resistance 2 (Par2, Published QTL Chr 18)
Expand Tier I Mouse 458 Genes GS135810: experimental severe malaria resistance (Esmr, Published QTL Chr 18)
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Human 1 Genes GS176284: HP:0009831 Mononeuropathy
Expand Tier I Human 120 Genes GS177000: HP:0001291 Abnormality of the cranial nerves
Expand Tier I Mouse GO 16 Genes GS193125: GO:0022011 myelination in peripheral nervous system
Expand Tier I Human GO 136 Genes GS201741: GO:0001508 regulation of action potential
Expand Tier I Mouse MP 648 Genes GS164023: MP:0001961 abnormal reflex
Expand Tier I Human 79 Genes GS173516: HP:0000301 Abnormality of facial musculature
Expand Tier I Mouse MP 3 Genes GS164279: MP:0010732 abnormal node of Ranvier morphology
Expand Tier I Mouse GO 7 Genes GS179287: GO:0032287 peripheral nervous system myelin maintenance
Expand Tier I Human GO 4593 Genes GS206355: GO:0023052 signaling
Expand Tier I Human GO 586 Genes GS201310: GO:0006873 cellular ion homeostasis
Expand Tier I Human 90 Genes GS171351: HP:0003581 Adult onset
Expand Tier I Mouse GO 2138 Genes GS186067: GO:0050877 neurological system process
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Mouse 208 Genes GS135922: growth traits 7 (Gwth7, Published QTL Chr 18)
Expand Tier I Human 207 Genes GS176283: HP:0009830 Peripheral neuropathy
Expand Tier I Mouse GO 2498 Genes GS193018: GO:0003008 system process
Expand Tier I Human GO 4719 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Mouse GO 52 Genes GS181013: GO:0007422 peripheral nervous system development
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Mouse GO 487 Genes GS191180: GO:0005768 endosome
Expand Tier I Human GO 1136 Genes GS205691: GO:0022008 neurogenesis
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Human GO 83 Genes GS209121: GO:0008366 axon ensheathment
Expand Tier I Human GO 10 Genes GS207330: GO:0043217 myelin maintenance
Expand Tier II Mouse 107 Genes GS35298: Neocortex Gene expression correlates of Prepulse inhibition at 85db in Males BXD
Expand Tier I Human 49 Genes GS171306: HP:0003130 Abnormal peripheral myelination
Expand Tier I Mouse 201 Genes GS136375: obesity QTL 21 (Obq21, Published QTL Chr 18)
Expand Tier I Mouse 429 Genes GS136159: leishmaniasis resistance 13 (Lmr13, Published QTL Chr 18)
Expand Tier I Human 70 Genes GS173601: HP:0010827 Abnormality of the seventh cranial nerve
Expand Tier I Human 17 Genes GS176929: HP:0003584 Late onset
Expand Tier I Mouse GO 95 Genes GS182106: GO:0007009 plasma membrane organization
Expand Tier I Mouse GO 1195 Genes GS190124: GO:0042592 homeostatic process
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Mouse GO 1378 Genes GS188287: GO:0048468 cell development
Expand Tier I Human GO 144 Genes GS204441: GO:0010001 glial cell differentiation
Expand Tier I Mouse 433 Genes GS136622: Stem cell proliferation 10 (Scpro10, Published QTL Chr 18)
Expand Tier I Mouse 391 Genes GS135255: adiposity 8 (Adip8, Published QTL Chr 18)
Expand Tier I Human 48 Genes GS172577: HP:0003690 Limb muscle weakness
Expand Tier I Mouse MP 255 Genes GS166583: MP:0001513 limb grasping
Expand Tier I Human 21 Genes GS174553: HP:0002380 Fasciculations
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 631 Genes GS209611: GO:0055082 cellular chemical homeostasis
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Mouse MP 2200 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier I Human 62 Genes GS172355: HP:0002460 Distal muscle weakness
Expand Tier I Mouse GO 317 Genes GS182784: GO:0016044 cellular membrane organization
Expand Tier I Mouse GO 669 Genes GS181708: GO:0050801 ion homeostasis
Expand Tier I Mouse 416 Genes GS136934: vertebral trabecular bone trait 19 (Vtbt19, Published QTL Chr 18)
Expand Tier I Human 229 Genes GS175577: HP:0003202 Amyotrophy
Expand Tier I Human 11 Genes GS176314: HP:0006958 Abnormal auditory evoked potentials
Expand Tier I Human GO 19 Genes GS196464: GO:0014044 Schwann cell development
Expand Tier I Mouse GO 57 Genes GS185847: GO:0021782 glial cell development
Expand Tier I Human GO 1191 Genes GS207015: GO:0042592 homeostatic process
Expand Tier I Human GO 1456 Genes GS205144: GO:0048468 cell development
Expand Tier I Mouse 427 Genes GS136541: psoriasis susceptibility 7 (Psrs7, Published QTL Chr 18)
Expand Tier I Mouse 301 Genes GS135424: bleomycin-induced pulmonary fibrosis 5 (Blmpf5, Published QTL Chr 18)
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 1 Genes GS176888: HP:0007695 Abnormal pupillary light reflex
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Human 27 Genes GS172613: HP:0003477 Peripheral axonal neuropathy
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 56 Genes GS174922: HP:0000762 Decreased nerve conduction velocity
Expand Tier I Human 70 Genes GS177025: HP:0010628 Facial palsy
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Mouse 221 Genes GS135757: experimental allergic encephalomyelitis susceptibility 25 (Eae25, Published QTL Chr 18)
Expand Tier I Mouse 399 Genes GS136281: modifier of engrailed QTL 1 (Moen1, Published QTL Chr 18)
Expand Tier I Mouse GO 167 Genes GS184927: GO:0001508 regulation of action potential
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular