Gene Details



VPS13A and homologs in 1 species are found in 222 GeneSets:


- Entrez   - GeneNetwork   - 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 3 Genes GS174667: HP:0002339 Abnormality of the caudate nucleus
Expand Tier I Human 112 Genes GS174327: HP:0003198 Myopathy
Expand Tier I Human 11 Genes GS172496: HP:0000742 Self-mutilation
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human GO 333 Genes GS204027: GO:0044708 single-organism behavior
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 71 Genes GS170917: HP:0100852 Abnormal fear/anxiety-related behavior
Expand Tier I Human 41 Genes GS171926: HP:0007018 Attention deficit hyperactivity disorder
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 10 Genes GS173117: HP:0100660 Dyskinesia
Expand Tier I Human 541 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 535 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 1692 Genes GS203755: GO:0016265 death
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Human 7 Genes GS177041: HP:0001927 Acanthocytosis
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 49 Genes GS173815: HP:0000736 Short attention span
Expand Tier I Human 100 Genes GS174372: HP:0002024 Malabsorption
Expand Tier I Human 11 Genes GS173817: HP:0000734 Disinhibition
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 110 Genes GS171784: HP:0001399 Hepatic failure
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human 30 Genes GS176897: HP:0002354 Memory impairment
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 107 Genes GS173786: HP:0003457 EMG abnormality
Expand Tier I Human 1 Genes GS175493: HP:0008767 Self-mutilation of tongue and lips due to involuntary movements
Expand Tier I Human 158 Genes GS174814: HP:0001639 Hypertrophic cardiomyopathy
Expand Tier I Human 3 Genes GS172145: HP:0010994 Abnormality of the striatum
Expand Tier III Human 728 Genes GS1229: Differential gene expression among Heroin Abusers
Expand Tier I Human GO 1123 Genes GS196794: GO:0046907 intracellular transport
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 3 Genes GS171052: HP:0002340 Caudate atrophy
Expand Tier I Human 4 Genes GS171814: HP:0001575 Mood changes
Expand Tier I Human CTD 2787 Genes GS123332: 7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide interacting genes (MeSH:D015123) in CTD
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 4014 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human 93 Genes GS176289: HP:0002120 Cerebral cortical atrophy
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier III Human 14 Genes GS26287: Positional candidates from genome-wide association study for nicotine dependence
Expand Tier I Human 530 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human GO 1555 Genes GS201869: GO:0008104 protein localization
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 401 Genes GS170791: HP:0010978 Abnormality of immune system physiology
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 80 Genes GS172801: HP:0000752 Hyperactivity
Expand Tier I Human 469 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 521 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human GO 938 Genes GS194065: GO:0016192 vesicle-mediated transport
Expand Tier I Human 67 Genes GS175906: HP:0002910 Elevated hepatic transaminases
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 226 Genes GS172470: HP:0001743 Abnormality of the spleen
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 187 Genes GS172471: HP:0001744 Splenomegaly
Expand Tier I Human 124 Genes GS174854: HP:0001410 Decreased liver function
Expand Tier I Human 106 Genes GS173246: HP:0001332 Dystonia
Expand Tier I Human 77 Genes GS171254: HP:0002360 Sleep disturbance
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human GO 1228 Genes GS199113: GO:0015031 protein transport
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 130 Genes GS174137: HP:0002017 Nausea and vomiting
Expand Tier I Human 20 Genes GS176236: HP:0002307 Drooling
Expand Tier I Human 614 Genes GS176171: HP:0001250 Seizures
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 472 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 1 Genes GS173730: HP:0007326 Progressive choreoathetosis
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human GO 1266 Genes GS197769: GO:0045184 establishment of protein localization
Expand Tier I Human 532 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human 113 Genes GS172283: HP:0000820 Abnormality of the thyroid gland
Expand Tier I Human 92 Genes GS173061: HP:0003676 Progressive disorder
Expand Tier I Human 61 Genes GS174375: HP:0002027 Abdominal pain
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 315 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 36 Genes GS171175: HP:0001541 Ascites
Expand Tier I Human 263 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier I Human 189 Genes GS174579: HP:0002031 Abnormality of the esophagus
Expand Tier III Human 34 Genes GS26305: Nicotine dependence Candidate Genes combined from GWAS and SNP association methods
Expand Tier I Human GO 1925 Genes GS201025: GO:0071702 organic substance transport
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier I Human 621 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human GO 73 Genes GS196048: GO:0006892 post-Golgi vesicle-mediated transport
Expand Tier I Human GO 181 Genes GS196459: GO:0048193 Golgi vesicle transport
Expand Tier I Human 84 Genes GS174760: HP:0002376 Developmental regression
Expand Tier I Human 300 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human 67 Genes GS174328: HP:0002716 Lymphadenopathy
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 123 Genes GS176799: HP:0001265 Hyporeflexia
Expand Tier I Human 307 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human GO 136 Genes GS202323: GO:0007626 locomotory behavior
Expand Tier I Human 269 Genes GS174948: HP:0100763 Abnormality of the lymphatic system
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 273 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 95 Genes GS174135: HP:0002015 Dysphagia
Expand Tier I Human 160 Genes GS176803: HP:0001260 Dysarthria
Expand Tier I Human 205 Genes GS176283: HP:0009830 Peripheral neuropathy
Expand Tier I Human 27 Genes GS175840: HP:0000739 Anxiety
Expand Tier I Human GO 3310 Genes GS209452: GO:0006810 transport
Expand Tier I Human 267 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier I Human GO 9 Genes GS196054: GO:0006895 Golgi to endosome transport
Expand Tier I Human 35 Genes GS176798: HP:0001266 Choreoathetosis
Expand Tier I Human 542 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 26 Genes GS176059: HP:0002134 Abnormality of the basal ganglia
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human CTD 158 Genes GS125949: Clorgyline interacting genes (MeSH:D003010) in CTD
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 1690 Genes GS194905: GO:0008219 cell death
Expand Tier I Human 214 Genes GS172139: HP:0010993 Abnormality of the cerebral subcortex
Expand Tier I Human 65 Genes GS170884: HP:0006919 Abnormal aggressive, impulsive or violent behavior
Expand Tier I Human 393 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Human 382 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human GO 6548 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human GO 36 Genes GS198040: GO:0035176 social behavior
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 33 Genes GS174504: HP:0000709 Psychosis
Expand Tier I Human 19 Genes GS174934: HP:0004447 Poikilocytosis
Expand Tier I Human GO 140 Genes GS195505: GO:0016197 endosomal transport
Expand Tier I Human GO 1362 Genes GS203494: GO:0051704 multi-organism process
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human CTD 5732 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human 15 Genes GS171130: HP:0000751 Personality changes
Expand Tier I Human 2 Genes GS173420: HP:0100033 Tics
Expand Tier I Human 83 Genes GS175811: HP:0011021 Abnormality of circulating enzyme level
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Human 58 Genes GS172829: HP:0001824 Weight loss
Expand Tier I Human 198 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier I Human GO 3364 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Human 16 Genes GS174301: HP:0000719 Inappropriate behavior
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 38 Genes GS173459: HP:0001300 Parkinsonism
Expand Tier I Human 186 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier I Human GO 58 Genes GS203493: GO:0051705 multi-organism behavior
Expand Tier I Human 122 Genes GS173242: HP:0001337 Tremor
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human 19 Genes GS171265: HP:0002633 Vasculitis
Expand Tier I Human 48 Genes GS172577: HP:0003690 Limb muscle weakness
Expand Tier I Human 107 Genes GS176797: HP:0001268 Mental deterioration
Expand Tier I Human 397 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 170 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Human 73 Genes GS175408: HP:0002071 Abnormality of extrapyramidal motor function
Expand Tier I Human 514 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human 53 Genes GS175407: HP:0002072 Chorea
Expand Tier I Human 483 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
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 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 10 Genes GS176326: HP:0006554 Acute hepatic failure
Expand Tier I Human GO 1820 Genes GS205820: GO:0033036 macromolecule localization
Expand Tier I Human 3 Genes GS175884: HP:0007374 Atrophy/Degeneration involving the caudate nucleus
Expand Tier I Human 62 Genes GS174055: HP:0000726 Dementia
Expand Tier I Human 229 Genes GS175577: HP:0003202 Amyotrophy
Expand Tier I Human 95 Genes GS170930: HP:0001284 Areflexia
Expand Tier I Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human 532 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 6 Genes GS173047: HP:0002310 Orofacial dyskinesia
Expand Tier I Human 196 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 554 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human DRG 868 Genes provisional GS86977: Table S1: All transcripts significantly different in abundance between the majority of heroin subjects and their matched controls [DRG]
Expand Tier I Human 201 Genes GS175171: HP:0001315 Reduced tendon reflexes
Expand Tier I Human 101 Genes GS177035: HP:0001928 Abnormality of coagulation
Expand Tier I Human 46 Genes GS174921: HP:0000763 Sensory neuropathy
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human GO 1745 Genes GS210579: GO:0051649 establishment of localization in cell
Expand Tier I Human 676 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human 21 Genes GS176207: HP:0003781 Excessive salivation
Expand Tier I Human 168 Genes GS175668: HP:0007369 Atrophy/Degeneration affecting the cerebrum
Expand Tier I Human CTD 3168 Genes GS127127: Benzo(a)pyrene interacting genes (MeSH:D001564) in CTD
Expand Tier I Human 83 Genes GS174968: HP:0003236 Elevated serum creatine phosphokinase
Expand Tier I Human 121 Genes GS176672: HP:0000980 Pallor
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 596 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 24 Genes GS174509: HP:0100716 Autoagression
Expand Tier I Human 60 Genes GS174300: HP:0000718 Aggressive behavior
Expand Tier I Human GO 1965 Genes GS210586: GO:0051641 cellular localization
Expand Tier I Human 74 Genes GS175265: HP:0002733 Abnormality of the lymph nodes
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 341 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Human 193 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier I Human 82 Genes GS172000: HP:0001761 Pes cavus
Expand Tier I Human GO 507 Genes GS206091: GO:0007610 behavior
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 4134 Genes GS200341: GO:0051179 localization
Expand Tier I Human 185 Genes GS173065: HP:0003679 Pace of progression
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 471 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier I Human 111 Genes GS177023: HP:0010876 Abnormality of circulating protein level
Expand Tier I Human 135 Genes GS172857: HP:0004305 Involuntary movements
Expand Tier I Human 396 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Human 243 Genes GS173534: HP:0001877 Abnormality of erythrocytes
Expand Tier I Human 31 Genes GS175341: HP:0100755 Abnormality of salivation
Expand Tier I Human 390 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Human CTD 768 Genes GS123769: 2-(1'H-indolo-3'-carbonyl)thiazole-4-carboxylic acid methyl ester interacting genes (MeSH:C548651) in CTD