Gene Details



INPP5E and homologs in 1 species are found in 366 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 385 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human GO 3402 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human 11 Genes GS172496: HP:0000742 Self-mutilation
Expand Tier I Human 72 Genes GS176835: HP:0000426 Prominent nasal bridge
Expand Tier I Human 270 Genes GS176826: HP:0000202 Oral cleft
Expand Tier I Human GO 1454 Genes GS205144: GO:0048468 cell development
Expand Tier I Human 38 Genes GS173462: HP:0001651 Dextrocardia
Expand Tier I Human GO 3108 Genes GS198685: GO:0048522 positive regulation of cellular process
Expand Tier I Human 64 Genes GS174379: HP:0002084 Encephalocele
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 GO 249 Genes GS205884: GO:0016311 dephosphorylation
Expand Tier I Human 260 Genes GS172033: HP:0000369 Low-set ears
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Human 81 Genes GS171773: HP:0000532 Chorioretinal abnormality
Expand Tier I Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human GO 137 Genes GS201235: GO:0046488 phosphatidylinositol metabolic process
Expand Tier I Human 92 Genes GS171656: HP:0000610 Abnormality of the choroid
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 6 Genes GS174960: HP:0011932 Abnormality of the superior cerebellar peduncle
Expand Tier I Human 84 Genes GS173946: HP:0002438 Cerebellar malformation
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Human 99 Genes GS175130: HP:0000750 Delayed speech and language development
Expand Tier I Human 50 Genes GS176834: HP:0002793 Abnormal respiratory patterns
Expand Tier I Human 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human 407 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human GO 258 Genes GS197043: GO:0044282 small molecule catabolic process
Expand Tier I Human 50 Genes GS173113: HP:0002186 Apraxia
Expand Tier I Human GO 1066 Genes GS196002: GO:0048699 generation of neurons
Expand Tier I Human 267 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Human 5 Genes GS172633: HP:0002871 Central apnea
Expand Tier I Human 6 Genes GS175837: HP:0002419 Molar tooth sign on MRI
Expand Tier I Human GO 97 Genes GS194400: GO:0006661 phosphatidylinositol biosynthetic process
Expand Tier I Human GO 350 Genes GS198370: GO:0042578 phosphoric ester hydrolase activity
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Human 34 Genes GS173140: HP:0011534 Abnormal spatial orientation of the cardiac segments
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 288 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human 46 Genes GS173617: HP:0011220 Prominent forehead
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 CTD 200 Genes GS125369: Lamivudine interacting genes (MeSH:D019259) in CTD
Expand Tier I Human 13 Genes GS171055: HP:0002342 Intellectual disability, moderate
Expand Tier I Human 68 Genes GS173148: HP:0003712 Muscle hypertrophy
Expand Tier I Human GO 15 Genes GS202709: GO:0052745 inositol phosphate phosphatase activity
Expand Tier I Human CTD 377 Genes GS121976: Zidovudine interacting genes (MeSH:D015215) in CTD
Expand Tier I Human GO 2364 Genes GS207365: GO:0005829 cytosol
Expand Tier I Human 17 Genes GS172643: HP:0002365 Hypoplasia of the brainstem
Expand Tier I Human 116 Genes GS173868: HP:0002143 Abnormality of the spinal cord
Expand Tier I Human 375 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human 70 Genes GS175439: HP:0009136 Duplication involving bones of the feet
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human GO 70 Genes GS209967: GO:0005930 axoneme
Expand Tier I Human CTD 223 Genes GS125187: Sulindac interacting genes (MeSH:D013467) in CTD
Expand Tier I Human 80 Genes GS175635: HP:0002251 Aganglionic megacolon
Expand Tier I Human GO 65 Genes GS204325: GO:0019751 polyol metabolic process
Expand Tier I Human GO 2653 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Human GO 232 Genes GS202625: GO:0045017 glycerolipid biosynthetic process
Expand Tier I Human 69 Genes GS176657: HP:0000054 Micropenis
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human CTD 1151 Genes GS121437: Fluorouracil interacting genes (MeSH:D005472) in CTD
Expand Tier I Human 70 Genes GS171543: HP:0000276 Long face
Expand Tier I Human GO 12 Genes GS205241: GO:0034593 phosphatidylinositol bisphosphate phosphatase activity
Expand Tier I Human 209 Genes GS173206: HP:0003241 Genital hypoplasia
Expand Tier I Human 489 Genes GS176385: HP:0001249 Intellectual disability
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 156 Genes GS172363: HP:0004324 Increased body weight
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human 598 Genes GS176718: HP:0000078 Abnormality of the genital system
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 GO 731 Genes GS208043: GO:0016788 hydrolase activity, acting on ester bonds
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 530 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 38 Genes GS176220: HP:0011620 Abnormality of abdominal situs
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Human GO 237 Genes GS206874: GO:0006650 glycerophospholipid metabolic process
Expand Tier I Human GO 4250 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 2 Genes GS175455: HP:0002508 Malformation of brainstem structures
Expand Tier I Human 487 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 80 Genes GS172801: HP:0000752 Hyperactivity
Expand Tier I Human GO 5190 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Human 521 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human GO 441 Genes GS209602: GO:0051960 regulation of nervous system development
Expand Tier I Human 404 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 468 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 332 Genes GS206569: GO:0045664 regulation of neuron differentiation
Expand Tier I Human 69 Genes GS172825: HP:0001829 Polydactyly (feet)
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human GO 2816 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 136 Genes GS175674: HP:0007360 Aplasia/Hypoplasia of the cerebellum
Expand Human 195 Genes GS222320: Genes associated with high risk of intellectual disability.
Expand Tier I Human 62 Genes GS172992: HP:0001320 Cerebellar vermis hypoplasia
Expand Tier I Human 5 Genes GS173217: HP:0005957 Breathing dysregulation
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 407 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 209 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Human GO 1786 Genes GS208893: GO:0005856 cytoskeleton
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 72 Genes GS171658: HP:0000612 Iris coloboma
Expand Tier I Human GO 217 Genes GS196055: GO:0008654 phospholipid biosynthetic process
Expand Tier I Human 107 Genes GS172094: HP:0000589 Coloboma
Expand Tier I Human 61 Genes GS175264: HP:0001162 Postaxial polydactyly (hands)
Expand Tier I Human GO 3300 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier I Human GO 10 Genes GS205244: GO:0034595 phosphatidylinositol phosphate 5-phosphatase activity
Expand Tier I Human 5 Genes GS176393: HP:0011933 Elongated superior cerebellar peduncle
Expand Tier I Human 111 Genes GS173651: HP:0009142 Duplication of bones involving the upper extremities
Expand Tier I Human GO 473 Genes GS200117: GO:0051130 positive regulation of cellular component organization
Expand Tier I Human 259 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human 4 Genes GS175631: HP:0100951 Enlarged fossa interpeduncularis
Expand Tier I Human 300 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 66 Genes GS176263: HP:0100259 Postaxial polydactyly
Expand Tier I Human 6 Genes GS173139: HP:0002418 Abnormality of the midbrain
Expand Tier I Human 46 Genes GS170961: HP:0000158 Macroglossia
Expand Tier I Human GO 929 Genes GS200809: GO:0030030 cell projection organization
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 116 Genes GS172063: HP:0000107 Renal cysts
Expand Tier I Human 46 Genes GS172570: HP:0000341 Narrow forehead
Expand Tier I Human 484 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human GO 1006 Genes GS196988: GO:0045595 regulation of cell differentiation
Expand Tier I Human GO 209 Genes GS200626: GO:0044262 cellular carbohydrate metabolic process
Expand Tier I Human GO 253 Genes GS195576: GO:0016791 phosphatase activity
Expand Tier I Human GO 985 Genes GS204095: GO:0030182 neuron differentiation
Expand Tier I Human 296 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Human 413 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human GO 237 Genes GS196129: GO:0005929 cilium
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human GO 1179 Genes GS195151: GO:0019637 organophosphate metabolic process
Expand Tier I Human 195 Genes GS174236: HP:0000534 Abnormality of the eyebrow
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 35 Genes GS171655: HP:0000611 Choroid coloboma
Expand Tier I Human 442 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human GO 3116 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human 34 Genes GS172513: HP:0001696 Situs inversus totalis
Expand Tier I Human GO 2331 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human 113 Genes GS173262: HP:0000864 Abnormality of the hypothalamus-pituitary axis
Expand Tier I Human 4 Genes GS175402: HP:0002876 Tachypnea, episodic
Expand Tier I Human GO 13 Genes GS206950: GO:0046856 phosphatidylinositol dephosphorylation
Expand Tier I Human GO 2486 Genes GS209235: GO:0006793 phosphorus metabolic process
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human GO 22 Genes GS206952: GO:0046854 phosphatidylinositol phosphorylation
Expand Tier I Human 200 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human GO 316 Genes GS201237: GO:0046486 glycerolipid metabolic process
Expand Tier I Human GO 494 Genes GS200286: GO:0060284 regulation of cell development
Expand Tier I Human GO 636 Genes GS201839: GO:0044463 cell projection part
Expand Tier I Human 38 Genes GS174087: HP:0003363 Abdominal situs inversus
Expand Tier I Human GO 10 Genes GS198912: GO:0046838 phosphorylated carbohydrate dephosphorylation
Expand Tier I Human GO 4338 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human GO 665 Genes GS205609: GO:0044431 Golgi apparatus part
Expand Tier I Human 542 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 159 Genes GS175096: HP:0000286 Epicanthus
Expand Tier I Human GO 1994 Genes GS207862: GO:0009056 catabolic process
Expand Tier I Human 64 Genes GS172899: HP:0011815 Cephalocele
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Human GO 1135 Genes GS205691: GO:0022008 neurogenesis
Expand Tier I Human 214 Genes GS172139: HP:0010993 Abnormality of the cerebral subcortex
Expand Tier I Human GO 5014 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human 65 Genes GS170884: HP:0006919 Abnormal aggressive, impulsive or violent behavior
Expand Tier I Human 450 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Human 513 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 454 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human GO 214 Genes GS197927: GO:0010975 regulation of neuron projection development
Expand Tier I Human GO 322 Genes GS200827: GO:0006066 alcohol metabolic process
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 115 Genes GS172148: HP:0010442 Polydactyly
Expand Tier I Human 33 Genes GS172620: HP:0000657 Oculomotor apraxia
Expand Tier I Human 80 Genes GS173031: HP:0004362 Abnormality of the enteric ganglia
Expand Tier I Human GO 3432 Genes GS203057: GO:0048518 positive regulation of biological process
Expand Tier I Human GO 144 Genes GS209189: GO:0030258 lipid modification
Expand Tier I Human 199 Genes GS176660: HP:0000050 Hypoplastic genitalia
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 5 Genes GS172511: HP:0002335 Agenesis of cerebellar vermis
Expand Tier I Human 413 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human GO 519 Genes GS198012: GO:0046434 organophosphate catabolic process
Expand Tier I Human GO 53 Genes GS197482: GO:0046164 alcohol catabolic process
Expand Tier I Human GO 117 Genes GS201074: GO:0005795 Golgi stack
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect 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 GO 521 Genes GS194460: GO:0090407 organophosphate biosynthetic process
Expand Tier I Human 38 Genes GS172855: HP:0004307 Abnormal anatomic location of the heart
Expand Tier I Human GO 2361 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 219 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Human GO 17 Genes GS198911: GO:0046839 phospholipid dephosphorylation
Expand Tier I Human 122 Genes GS173242: HP:0001337 Tremor
Expand Tier I Human 42 Genes GS172670: HP:0002363 Abnormality of the brainstem
Expand Tier I Human 4 Genes GS176837: HP:0002790 Neonatal breathing dysregulation
Expand Tier I Human GO 59 Genes GS197926: GO:0010976 positive regulation of neuron projection development
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human GO 17 Genes GS210010: GO:0046174 polyol catabolic process
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human GO 1257 Genes GS197087: GO:0016310 phosphorylation
Expand Tier I Human GO 10 Genes GS206951: GO:0046855 inositol phosphate dephosphorylation
Expand Tier I Human 47 Genes GS174712: HP:0002553 Highly arched eyebrow
Expand Tier I Human 63 Genes GS174833: HP:0006817 Aplasia/Hypoplasia of the cerebellar vermis
Expand Tier I Human 13 Genes GS172095: HP:0000588 Optic nerve coloboma
Expand Tier I Human 313 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human 20 Genes GS171661: HP:0000617 Abnormality of ocular smooth pursuit
Expand Tier I Human 1 Genes GS171093: HP:0007271 Occipital myelomeningocele
Expand Tier I Human 469 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human GO 52 Genes GS207989: GO:0035085 cilium axoneme
Expand Tier I Human GO 135 Genes GS202025: GO:0031346 positive regulation of cell projection organization
Expand Tier I Human 23 Genes GS171937: HP:0004346 Increased respiratory rate or depth of breathing
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 430 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human GO 2423 Genes GS209232: GO:0006796 phosphate-containing compound metabolic process
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 170 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Human 34 Genes GS172418: HP:0000567 Chorioretinal coloboma
Expand Tier I Human 483 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human 28 Genes GS173311: HP:0010651 Abnormality of the meninges
Expand Tier I Human 101 Genes GS175263: HP:0001161 Polydactyly (hands)
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 68 Genes GS176437: HP:0002334 Abnormality of the cerebellar vermis
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier I Human 74 Genes GS171850: HP:0002414 Spina bifida
Expand Tier I Human 487 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 36 Genes GS172842: HP:0000480 Retinal coloboma
Expand Tier I Human 21 Genes GS171403: HP:0001956 Truncal obesity
Expand Tier I Human GO 541 Genes GS196667: GO:0008610 lipid biosynthetic process
Expand Tier I Human GO 786 Genes GS199922: GO:0005975 carbohydrate metabolic process
Expand Tier I Human GO 1223 Genes GS208482: GO:0042995 cell projection
Expand Tier I Human 386 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 3 Genes GS172749: HP:0002436 Occipital meningocele
Expand Tier I Human GO 793 Genes GS209568: GO:0048666 neuron development
Expand Tier I Human 564 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 1766 Genes GS194455: GO:0051239 regulation of multicellular organismal process
Expand Tier I Human GO 7650 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human GO 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 75 Genes GS172219: HP:0010301 Spinal dysraphism
Expand Tier I Human GO 71 Genes GS195616: GO:0032580 Golgi cisterna membrane
Expand Tier I Human GO 347 Genes GS202602: GO:0006644 phospholipid metabolic process
Expand Tier I Human 18 Genes GS175110: HP:0000570 Abnormality of saccadic eye movements
Expand Tier I Human GO 1166 Genes GS201075: GO:0005794 Golgi apparatus
Expand Tier I Human 22 Genes GS173165: HP:0002435 Meningocele
Expand Tier I Human GO 259 Genes GS202414: GO:0044712 single-organism catabolic process
Expand Tier I Human 51 Genes GS171787: HP:0001395 Hepatic fibrosis
Expand Tier I Human 435 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human GO 1430 Genes GS206618: GO:0050793 regulation of developmental process
Expand Tier I Human 178 Genes GS176589: HP:0001273 Abnormality of the corpus callosum
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 111 Genes GS171465: HP:0004275 Duplication of hand bones
Expand Tier I Human GO 86 Genes GS209547: GO:0031985 Golgi cisterna
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 1762 Genes GS196284: GO:0012505 endomembrane system
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 32 Genes GS199561: GO:0043647 inositol phosphate metabolic process
Expand Tier I Human GO 1212 Genes GS204438: GO:0051128 regulation of cellular component organization
Expand Tier I Human 94 Genes GS174879: HP:0002104 Apnea
Expand Tier I Human 532 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 36 Genes GS174701: HP:0000556 Retinal dystrophy
Expand Tier I Human GO 3116 Genes GS197892: GO:0043228 non-membrane-bounded organelle
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 I Human GO 5120 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Human GO 1095 Genes GS208716: GO:2000026 regulation of multicellular organismal development
Expand Tier I Human 20 Genes GS173102: HP:0010808 Protruding tongue
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 177 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier I Human 153 Genes GS175880: HP:0007370 Aplasia/Hypoplasia of the corpus callosum
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 699 Genes GS205439: GO:0031175 neuron projection development
Expand Tier I Human GO 398 Genes GS209887: GO:0050767 regulation of neurogenesis
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 142 Genes GS171178: HP:0000238 Hydrocephalus
Expand Tier I Human 248 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Human GO 2509 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human GO 6256 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 576 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 8094 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 596 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 2 Genes GS171724: HP:0008915 Childhood-onset truncal obesity
Expand Tier I Human 24 Genes GS174509: HP:0100716 Autoagression
Expand Tier I Human 280 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human GO 547 Genes GS205302: GO:0000139 Golgi membrane
Expand Tier I Human 322 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Human 60 Genes GS174300: HP:0000718 Aggressive behavior
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 11 Genes GS201341: GO:0071545 inositol phosphate catabolic process
Expand Tier I Human 17 Genes GS175676: HP:0007362 Aplasia/Hypoplasia of the brainstem
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
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 395 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 110 Genes GS172484: HP:0009997 Duplication of phalanx of hand
Expand Tier I Human 5 Genes GS172725: HP:0007973 Retinal dysplasia
Expand Tier I Human GO 809 Genes GS195897: GO:0044255 cellular lipid metabolic process
Expand Tier I Human 194 Genes GS172034: HP:0000368 Low-set, posteriorly rotated ears
Expand Tier I Human 196 Genes GS175785: HP:0002500 Abnormality of the cerebral white matter
Expand Tier I Human GO 6 Genes GS209265: GO:0004439 phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity
Expand Tier I Human 262 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Human GO 257 Genes GS195002: GO:0031344 regulation of cell projection organization
Expand Tier I Human 16 Genes GS176249: HP:0002789 Tachypnea
Expand Tier I Human GO 4085 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 245 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Human 6 Genes GS173033: HP:0011931 Abnormality of the cerebellar peduncle
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 122 Genes GS171946: HP:0002269 Abnormality of neuronal migration
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 GO 23 Genes GS198906: GO:0046834 lipid phosphorylation
Expand Tier I Human 1 Genes GS172215: HP:0007910 Retinal dystrophy, congenital, nonprogressive
Expand Tier I Human 361 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human GO 1853 Genes GS209010: GO:1901575 organic substance catabolic process
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 423 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 16 Genes GS173187: HP:0007772 Impaired smooth pursuit
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 2 Genes GS172232: HP:0002195 Dysgenesis of the cerebellar vermis
Expand Tier I Human 510 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human GO 1137 Genes GS193812: GO:0006629 lipid metabolic process
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 8 Genes GS194970: GO:0046030 inositol trisphosphate phosphatase activity
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human GO 19 Genes GS194874: GO:0052866 phosphatidylinositol phosphate phosphatase activity
Expand Tier I Human GO 89 Genes GS209548: GO:0031984 organelle subcompartment
Expand Tier I Human 220 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
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 614 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 110 Genes GS210006: GO:0044441 cilium part
Expand Tier I Human GO 1722 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Human 148 Genes GS172295: HP:0001513 Obesity
Expand Tier I Human GO 4201 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human 532 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human GO 194 Genes GS198636: GO:0046474 glycerophospholipid biosynthetic process
Expand Tier I Human GO 7 Genes GS194250: GO:0004445 inositol-polyphosphate 5-phosphatase activity