Gene Details



MAN2B1 and homologs in 1 species are found in 311 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 187 Genes GS171907: HP:0004299 Hernia of the abdominal wall
Expand Tier I Human 385 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human GO 72 Genes GS198454: GO:0048029 monosaccharide binding
Expand Tier I Human GO 333 Genes GS204027: GO:0044708 single-organism behavior
Expand Tier I Human 33 Genes GS172194: HP:0002970 Genu varum
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 CTD 391 Genes GS121370: Clofibrate interacting genes (MeSH:D002994) in CTD
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 8 Genes GS177044: HP:0001922 Vacuolated lymphocytes
Expand Tier I Human 220 Genes GS171791: HP:0000370 Abnormality of the middle ear
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 100 Genes GS175101: HP:0000280 Coarse facial features
Expand Tier I Human 141 Genes GS174721: HP:0000772 Abnormality of the ribs
Expand Tier I Human 17 Genes GS172814: HP:0000336 Prominent supraorbital ridges
Expand Tier I Human GO 588 Genes GS205780: GO:0044723 single-organism carbohydrate metabolic process
Expand Tier I Human 201 Genes GS175802: HP:0003272 Abnormality of the hip bone
Expand Tier I Human CTD 916 Genes GS121965: Amiodarone interacting genes (MeSH:D000638) in CTD
Expand Tier I Human 214 Genes GS176167: HP:0001257 Spasticity
Expand Tier I Human 407 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 122 Genes GS173384: HP:0002750 Delayed skeletal maturation
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Human GO 89 Genes GS196642: GO:0004553 hydrolase activity, hydrolyzing O-glycosyl compounds
Expand Tier I Human 12 Genes GS171241: HP:0002492 Abnormality of the corticospinal tract
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 123 Genes GS175665: HP:0006504 Abnormality involving the diaphyses of the limbs
Expand Tier I Human CTD 2422 Genes GS123265: Estradiol interacting genes (MeSH:D004958) in CTD
Expand Tier I Human 129 Genes GS173247: HP:0007957 Reduction of corneal clarity
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 68 Genes GS173148: HP:0003712 Muscle hypertrophy
Expand Tier I Human 189 Genes GS176004: HP:0100656 Thoracoabdominal wall defects
Expand Tier I Human 95 Genes GS171217: HP:0003487 Babinski sign
Expand Tier I Human 116 Genes GS173868: HP:0002143 Abnormality of the spinal cord
Expand Tier I Human CTD 377 Genes GS124417: Propylthiouracil interacting genes (MeSH:D011441) in CTD
Expand Tier I Human 105 Genes GS175571: HP:0011492 Abnormality of corneal stroma
Expand Tier I Human 375 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Human 129 Genes GS173792: HP:0002815 Abnormality of the knees
Expand Tier I Human 489 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 282 Genes GS171902: HP:0010987 Abnormality of cellular immune system
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 Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 51 Genes GS172891: HP:0100538 Abnormality of the supraorbital ridges
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human GO 13 Genes GS201821: GO:0015923 mannosidase activity
Expand Tier I Human 13 Genes GS172942: HP:0002942 Thoracic kyphosis
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human GO 341 Genes GS197314: GO:0000323 lytic vacuole
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human 63 Genes GS172617: HP:0004313 Hypogammaglobulinemia
Expand Tier I Human 27 Genes GS175193: HP:0002062 Abnormality of the pyramidal tracts
Expand Tier I Human 6 Genes GS170956: HP:0005619 Thoracolumbar kyphosis
Expand Tier I Human 510 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human CTD 306 Genes GS123351: Omeprazole interacting genes (MeSH:D009853) in CTD
Expand Tier I Human 122 Genes GS173563: HP:0000692 Misalignment of teeth
Expand Tier I Human 184 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Human 226 Genes GS172470: HP:0001743 Abnormality of the spleen
Expand Tier I Human 323 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human 32 Genes GS171849: HP:0000599 Abnormality of the frontal hairline
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 187 Genes GS172471: HP:0001744 Splenomegaly
Expand Tier I Human 134 Genes GS171627: HP:0000470 Short neck
Expand Tier I Human 468 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human CTD 2014 Genes GS126646: Carbon Tetrachloride interacting genes (MeSH:D002251) in CTD
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 146 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Human GO 2455 Genes GS196595: GO:0006464 cellular protein modification process
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier I Human 66 Genes GS176033: HP:0011039 Abnormality of the helix
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human 5 Genes GS176229: HP:0004570 Increased vertebral height
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human 138 Genes GS174847: HP:0000940 Abnormal diaphysis morphology
Expand Tier I Human 1 Genes GS171980: HP:0007232 Spinocerebellar tract disease in lower limbs
Expand Tier I Human 231 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Human CTD 5081 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human 6 Genes GS172728: HP:0008850 Severe postnatal growth retardation
Expand Tier I Human 284 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human CTD 284 Genes GS125104: Ethionine interacting genes (MeSH:D005001) in CTD
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 18 Genes GS173403: HP:0002684 Thickened calvaria
Expand Tier I Human 136 Genes GS173751: HP:0000998 Hypertrichosis
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human 64 Genes GS176627: HP:0000457 Flat nose
Expand Tier I Human 532 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human 8 Genes GS172680: HP:0003302 Spondylolisthesis
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 263 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human 69 Genes GS170981: HP:0011361 Congenital abnormal hair pattern
Expand Tier I Human 173 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier I Human 77 Genes GS172699: HP:0002652 Skeletal dysplasia
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 84 Genes GS176462: HP:0100240 Synostosis of joints
Expand Tier I Human 418 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 621 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Human 259 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human 32 Genes GS176916: HP:0004437 Cranial hyperostosis
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 309 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Human 20 Genes GS175409: HP:0002070 Limb ataxia
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human 46 Genes GS170961: HP:0000158 Macroglossia
Expand Tier I Human 16 Genes GS172250: HP:0000943 Dysostosis multiplex
Expand Tier I Human 238 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 307 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human 269 Genes GS174948: HP:0100763 Abnormality of the lymphatic system
Expand Tier I Human 413 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human 178 Genes GS175902: HP:0003468 Abnormality of the vertebrae
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 195 Genes GS174236: HP:0000534 Abnormality of the eyebrow
Expand Tier I Human 273 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human CTD 1291 Genes GS125402: Diethylnitrosamine interacting genes (MeSH:D004052) in CTD
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human GO 2 Genes GS195021: GO:0006517 protein deglycosylation
Expand Tier I Human CTD 1001 Genes GS124711: Genistein interacting genes (MeSH:D019833) in CTD
Expand Tier I Human 65 Genes GS171559: HP:0000388 Otitis media
Expand Tier I Human 160 Genes GS176803: HP:0001260 Dysarthria
Expand Tier I Human GO 2331 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human GO 3902 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 16 Genes GS174507: HP:0100711 Abnormality of the thoracic spine
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Human 78 Genes GS171959: HP:0000400 Macrotia
Expand Tier I Human 356 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human 104 Genes GS175835: HP:0007759 Opacification of the corneal stroma
Expand Tier I Human CTD 747 Genes GS125403: Diethylstilbestrol interacting genes (MeSH:D004054) in CTD
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 159 Genes GS175096: HP:0000286 Epicanthus
Expand Tier I Human 65 Genes GS175131: HP:0000023 Inguinal hernia
Expand Tier I Human GO 341 Genes GS207982: GO:0005764 lysosome
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human 394 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human 6 Genes GS171884: HP:0003133 Abnormality of the spinocerebellar tracts
Expand Tier I Human 2 Genes GS175466: HP:0007893 Progressive retinal degeneration
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human 450 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 316 Genes GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
Expand Tier I Human 63 Genes GS171802: HP:0009553 Abnormality of the hairline
Expand Tier I Human GO 1974 Genes GS203688: GO:0008270 zinc ion binding
Expand Tier I Human GO 6548 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 513 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human GO 9 Genes GS198550: GO:0006013 mannose metabolic process
Expand Tier I Human GO 404 Genes GS209163: GO:0005773 vacuole
Expand Tier I Human CTD 284 Genes GS121771: Benzbromarone interacting genes (MeSH:D001553) in CTD
Expand Tier I Human CTD 1523 Genes GS124579: Selenium interacting genes (MeSH:D012643) in CTD
Expand Tier I Human 156 Genes GS176612: HP:0000272 Malar flattening
Expand Tier I Human 80 Genes GS175456: HP:0100037 Abnormality of the scalp hair
Expand Tier I Human 86 Genes GS176008: HP:0010701 Abnormal immunoglobulin level
Expand Tier I Human 77 Genes GS174230: HP:0000303 Mandibular prognathia
Expand Tier I Human 49 Genes GS173812: HP:0000738 Hallucinations
Expand Tier I Human 41 Genes GS175113: HP:0000574 Thick eyebrow
Expand Tier I Human GO 2216 Genes GS209291: GO:0046914 transition metal ion binding
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 413 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human 233 Genes GS174257: HP:0000309 Abnormality of the midface
Expand Tier I Human 23 Genes GS175301: HP:0000294 Low anterior hairline
Expand Tier I Human 83 Genes GS172024: HP:0001369 Arthritis
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 1 Genes GS172910: HP:0007163 Corticospinal tract disease in lower limbs
Expand Tier I Human 94 Genes GS173327: HP:0005368 Abnormality of humoral immunity
Expand Tier I Human 186 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier I Human 346 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 175 Genes GS173048: HP:0005557 Abnormality of the zygomatic arch
Expand Tier I Human 61 Genes GS174926: HP:0000768 Pectus carinatum
Expand Tier I Human 88 Genes GS173557: HP:0005372 Abnormality of B cell physiology
Expand Tier I Human CTD 671 Genes GS121369: Clofibric Acid interacting genes (MeSH:D002995) in CTD
Expand Tier I Human 39 Genes GS172815: HP:0000337 Broad forehead
Expand Tier I Human 20 Genes GS171661: HP:0000617 Abnormality of ocular smooth pursuit
Expand Tier I Human 469 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human 317 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human 395 Genes GS173137: HP:0011821 Abnormality of facial skeleton
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 267 Genes GS196679: GO:0030246 carbohydrate binding
Expand Tier I Human 430 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 212 Genes GS176185: HP:0100790 Hernia
Expand Tier I Human GO 4003 Genes GS208978: GO:0043169 cation binding
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 218 Genes GS175994: HP:0000464 Abnormality of the neck
Expand Tier I Human 56 Genes GS173337: HP:0000689 Dental malocclusion
Expand Tier I Human GO 786 Genes GS199922: GO:0005975 carbohydrate metabolic process
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 GO 1235 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human 22 Genes GS172329: HP:0005469 Flat occiput
Expand Tier I Human 9 Genes GS174506: HP:0100712 Abnormality of the lumbar spine
Expand Tier I Human GO 18 Genes GS209597: GO:0005537 mannose binding
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 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 286 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier I Human 576 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 33 Genes GS176924: HP:0000212 Gingival overgrowth
Expand Tier I Human GO 3239 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Human CTD 1556 Genes GS125506: Valproic Acid interacting genes (MeSH:D014635) in CTD
Expand Tier I Human 123 Genes GS170894: HP:0006487 Bowing of the long bones
Expand Tier I Human 25 Genes GS175546: HP:0010885 Aseptic necrosis
Expand Tier I Human CTD 573 Genes GS124594: 3-(4'-hydroxy-3'-adamantylbiphenyl-4-yl)acrylic acid interacting genes (MeSH:C472791) in CTD
Expand Tier I Human 76 Genes GS171176: HP:0001547 Abnormality of the morphology of the rib cage
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier I Human 598 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 173 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Human 317 Genes GS176591: HP:0001276 Hypertonia
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 278 Genes GS171204: HP:0011314 Abnormality of long bone morphology
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 72 Genes GS176488: HP:0010720 Abnormal hair pattern
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 196 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier I Human 150 Genes GS174920: HP:0000766 Abnormality of the sternum
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 228 Genes GS171908: HP:0004298 Abnormality of the abdominal wall
Expand Tier I Human GO 3863 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human 41 Genes GS175197: HP:0002066 Gait ataxia
Expand Tier I Human 127 Genes GS172916: HP:0003312 Abnormal form of the vertebral bodies
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Human 676 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human GO 1691 Genes GS209960: GO:0003008 system process
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human 88 Genes GS171346: HP:0002846 Abnormality of B cells
Expand Tier I Human GO 250 Genes GS201922: GO:0019318 hexose metabolic process
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 154 Genes GS199951: GO:0007611 learning or memory
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 93 Genes GS174308: HP:0002979 Bowing of the legs
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 GO 113 Genes GS204516: GO:0016798 hydrolase activity, acting on glycosyl bonds
Expand Tier I Human 51 Genes GS171296: HP:0008897 Postnatal growth retardation
Expand Tier I Human 82 Genes GS171602: HP:0001965 Abnormality of the scalp
Expand Tier I Human 248 Genes GS171793: HP:0000377 Abnormality of the pinna
Expand Tier I Human 322 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 2455 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Human 262 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
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 282 Genes GS175119: HP:0001881 Abnormality of leukocytes
Expand Tier I Human 12 Genes GS170954: HP:0000885 Broad ribs
Expand Tier I Human 171 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier I Human GO 168 Genes GS209865: GO:0050890 cognition
Expand Tier I Human 34 Genes GS174909: HP:0000546 Retinal degeneration
Expand Tier I Human 18 Genes GS175558: HP:0002516 Increased intracranial pressure
Expand Tier I Human 6 Genes GS175783: HP:0002503 Spinocerebellar tract degeneration
Expand Tier I Human GO 2549 Genes GS194336: GO:0043412 macromolecule modification
Expand Tier I Human 85 Genes GS173666: HP:0005978 Type II diabetes mellitus
Expand Tier I Human GO 12 Genes GS208375: GO:0004559 alpha-mannosidase activity
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 CTD 478 Genes GS125040: Thioacetamide interacting genes (MeSH:D013853) in CTD
Expand Tier I Human 444 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 5764 Genes GS206742: GO:0043167 ion binding
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 53 Genes GS176964: HP:0011217 Abnormal shape of the occiput
Expand Tier I Human 22 Genes GS173334: HP:0000687 Widely spaced teeth
Expand Tier I Human 70 Genes GS171600: HP:0000168 Abnormality of the gingiva
Expand Tier I Human 27 Genes GS175974: HP:0004493 Craniofacial hyperostosis
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 57 Genes GS174337: HP:0002718 Recurrent bacterial infections
Expand Tier I Human 146 Genes GS172906: HP:0003319 Abnormality of the cervical spine
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 280 Genes GS207949: GO:0005996 monosaccharide metabolic process
Expand Tier I Human 87 Genes GS176588: HP:0001272 Cerebellar atrophy
Expand Tier I Human 104 Genes GS173512: HP:0000306 Abnormality of the chin
Expand Tier I Human CTD 238 Genes GS121381: fumonisin B1 interacting genes (MeSH:C056933) in CTD
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 108 Genes GS172118: HP:0004332 Abnormality of lymphocytes
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 16 Genes GS173187: HP:0007772 Impaired smooth pursuit
Expand Tier I Human 39 Genes GS174178: HP:0100774 Hyperostosis
Expand Tier I Human 469 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance