Gene Details



SH3TC2 and homologs in 1 species are found in 170 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 19 Genes GS196464: GO:0014044 Schwann cell development
Expand Tier I Human 1 Genes GS172331: HP:0004466 Prolonged brainstem auditory evoked potentials
Expand Tier I Human GO 1185 Genes GS207015: GO:0042592 homeostatic process
Expand Tier I Human GO 96 Genes GS198898: GO:0007009 plasma membrane organization
Expand Human 123 Genes GS221330: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_FACTORS_INVOLVED_IN_MEGAKARYOCYTE_DEVELOPMENT_AND_PLATELET_PRODUCTION
Expand Tier I Human GO 406 Genes GS199582: GO:0016044 cellular membrane organization
Expand Tier I Human GO 1454 Genes GS205144: GO:0048468 cell development
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier III Human 2616 Genes GS218390: Alcoholism Susceptibility Chr 1
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
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 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human GO 1691 Genes GS209960: GO:0003008 system process
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 27 Genes GS172613: HP:0003477 Peripheral axonal neuropathy
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 752 Genes GS202715: GO:0035637 multicellular organismal signaling
Expand Tier I Human 56 Genes GS174922: HP:0000762 Decreased nerve conduction velocity
Expand Tier I Human 63 Genes GS175213: HP:0003693 Distal amyotrophy
Expand Tier I Human GO 9526 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 I Human 70 Genes GS177025: HP:0010628 Facial palsy
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 121 Genes GS175588: HP:0001311 Neurophysiological abnormality
Expand Tier I Human 27 Genes GS176587: HP:0001271 Polyneuropathy
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 596 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 Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Human GO 7 Genes GS196057: GO:0032287 peripheral nervous system myelin maintenance
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 395 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 Human GO 648 Genes GS198498: GO:0050801 ion homeostasis
Expand Tier I Human GO 410 Genes GS201052: GO:0061024 membrane organization
Expand Tier I Human GO 2499 Genes GS196934: GO:0065008 regulation of biological quality
Expand Tier I Human GO 4085 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 82 Genes GS172000: HP:0001761 Pes cavus
Expand Tier I Human 245 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Human 10 Genes GS172451: HP:0007210 Lower limb amyotrophy
Expand Tier I Human GO 2653 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 710 Genes GS200565: GO:0019725 cellular homeostasis
Expand Tier I Human GO 74 Genes GS206352: GO:0055037 recycling endosome
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 471 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 8 Genes GS175374: HP:0010546 Muscle fibrillation
Expand Tier I Human 86 Genes GS172908: HP:0002450 Abnormality of the motor neurons
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 135 Genes GS170969: HP:0000157 Abnormality of the tongue
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Human 123 Genes GS221081: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_FACTORS_INVOLVED_IN_MEGAKARYOCYTE_DEVELOPMENT_AND_PLATELET_PRODUCTION
Expand Human 123 Genes GS222118: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_FACTORS_INVOLVED_IN_MEGAKARYOCYTE_DEVELOPMENT_AND_PLATELET_PRODUCTION
Expand Tier I Human 135 Genes GS172857: HP:0004305 Involuntary movements
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 396 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Human GO 4014 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 27 Genes GS199684: GO:0014037 Schwann cell differentiation
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 18 Genes GS173678: HP:0003383 Onion bulb formation
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 Human GO 4250 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 344 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier I Human GO 70 Genes GS202683: GO:0021782 glial cell development
Expand Tier I Human 22 Genes GS171659: HP:0000615 Abnormality of the pupil
Expand Tier I Human GO 833 Genes GS196920: GO:0048878 chemical homeostasis
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 4575 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human 58 Genes GS171880: HP:0003134 Abnormality of peripheral nerve conduction
Expand Tier I Human GO 559 Genes GS208092: GO:0005768 endosome
Expand Tier I Human 1098 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 Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 24 Genes GS176061: HP:0002355 Difficulty walking
Expand Tier I Human 25 Genes GS173680: HP:0003380 Decreased number of peripheral myelinated nerve fibers
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 1722 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Human GO 2816 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Human GO 4201 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 143 Genes GS176586: HP:0001270 Motor delay
Expand Tier I Human 44 Genes GS174918: HP:0000764 Peripheral axonal degeneration
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human GO 166 Genes GS194334: GO:0042063 gliogenesis
Expand Tier I Human GO 83 Genes GS207579: GO:0007272 ensheathment of neurons
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 8 Genes GS174415: HP:0003484 Upper limb muscle weakness
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
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 Human GO 136 Genes GS201741: GO:0001508 regulation of action potential
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 79 Genes GS173516: HP:0000301 Abnormality of facial musculature
Expand Tier I Human 128 Genes GS174657: HP:0001425 Heterogeneous
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 4575 Genes GS206355: GO:0023052 signaling
Expand Tier I Human 7 Genes GS173467: HP:0001308 Tongue fasciculations
Expand Tier I Human GO 585 Genes GS201310: GO:0006873 cellular ion homeostasis
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 90 Genes GS171351: HP:0003581 Adult onset
Expand Tier I Human 90 Genes GS172611: HP:0003474 Sensory impairment
Expand Human 471 Genes GS222221: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_HEMOSTASIS
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Human 123 Genes GS220035: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_FACTORS_INVOLVED_IN_MEGAKARYOCYTE_DEVELOPMENT_AND_PLATELET_PRODUCTION
Expand Tier I Human 8 Genes GS174434: HP:0007107 Segmental peripheral demyelination
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 98 Genes GS204614: GO:0019228 regulation of action potential in neuron
Expand Tier I Human 205 Genes GS176283: HP:0009830 Peripheral neuropathy
Expand Human 123 Genes GS220904: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_FACTORS_INVOLVED_IN_MEGAKARYOCYTE_DEVELOPMENT_AND_PLATELET_PRODUCTION
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human GO 4701 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human GO 736 Genes GS204608: GO:0019226 transmission of nerve impulse
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 4338 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 1135 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 I Human 49 Genes GS171306: HP:0003130 Abnormal peripheral myelination
Expand Tier I Human 70 Genes GS173601: HP:0010827 Abnormality of the seventh cranial nerve
Expand Tier I Human 46 Genes GS171759: HP:0002936 Distal sensory impairment
Expand Tier I Human 17 Genes GS176929: HP:0003584 Late onset
Expand Tier I Human GO 80 Genes GS206464: GO:0042552 myelination
Expand Tier I Human GO 144 Genes GS204441: GO:0010001 glial cell differentiation
Expand Tier I Human GO 17 Genes GS208537: GO:0032292 peripheral nervous system axon ensheathment
Expand Tier I Human 48 Genes GS172577: HP:0003690 Limb muscle weakness
Expand Tier I Human 117 Genes GS174102: HP:0011799 Abnormality of facial soft tissue
Expand Human 123 Genes GS219579: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_FACTORS_INVOLVED_IN_MEGAKARYOCYTE_DEVELOPMENT_AND_PLATELET_PRODUCTION
Expand Tier I Human 397 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human 21 Genes GS174553: HP:0002380 Fasciculations
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 628 Genes GS209611: GO:0055082 cellular chemical homeostasis
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 7 Genes GS173684: HP:0003387 Decreased number of large peripheral myelinated nerve fibers
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 487 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 1235 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human 62 Genes GS172355: HP:0002460 Distal muscle weakness
Expand Tier I Human 576 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 96 Genes GS172854: HP:0004302 Functional motor problems.
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 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 1 Genes GS172705: HP:0007686 Abnormal pupillary function
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 9 Genes GS171322: HP:0008944 Distal lower limb amyotrophy
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology