Gene Details



BSCL2 and homologs in 1 species are found in 295 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 GO 3402 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human 26 Genes GS175388: HP:0010514 Hyperpituitarism
Expand Tier I Human 98 Genes GS172242: HP:0004930 Abnormality of the pulmonary vasculature
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 231 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 5 Genes GS172576: HP:0000868 Decreased fertility in females
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 63 Genes GS175213: HP:0003693 Distal amyotrophy
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 49 Genes GS174071: HP:0009125 Lipodystrophy
Expand Tier I Human 17 Genes GS172814: HP:0000336 Prominent supraorbital ridges
Expand Tier I Human 55 Genes GS173418: HP:0000144 Decreased fertility
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Human 25 Genes GS175251: HP:0007340 Lower limb muscle weakness
Expand Tier I Human 214 Genes GS176167: HP:0001257 Spasticity
Expand Tier I Human 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 5359 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human 179 Genes GS175391: HP:0011004 Abnormality of the systemic arterial tree
Expand Tier I Human 318 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
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 GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 161 Genes GS171633: HP:0008373 Puberty and gonadal disorders
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 22 Genes GS171996: HP:0001765 Hammertoe
Expand Tier I Human 68 Genes GS173148: HP:0003712 Muscle hypertrophy
Expand Tier I Human 56 Genes GS173195: HP:0012091 Abnormality of pancreas physiology
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 GO 499 Genes GS201260: GO:0009894 regulation of catabolic process
Expand Tier I Human 2 Genes GS175105: HP:0003809 Nearly complete absence of metabolically active adipose tissue (subcutaneous, intraabdominal, intrathoracic)
Expand Tier I Human GO 228 Genes GS194306: GO:0031300 intrinsic to organelle membrane
Expand Tier I Human 139 Genes GS171000: HP:0000083 Renal insufficiency
Expand Tier I Human 72 Genes GS171187: HP:0000140 Abnormality of the menstrual cycle
Expand Tier I Human 158 Genes GS174814: HP:0001639 Hypertrophic cardiomyopathy
Expand Tier I Human 3 Genes GS176352: HP:0007181 Interosseus muscle atrophy
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human GO 104 Genes GS199148: GO:0030176 integral to endoplasmic reticulum membrane
Expand Tier I Human GO 2653 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Human 20 Genes GS173435: HP:0002155 Hypertriglyceridemia
Expand Tier I Human 120 Genes GS172358: HP:0003117 Abnormality of circulating hormone level
Expand Tier I Human GO 4 Genes GS193950: GO:0034389 lipid particle organization
Expand Tier I Human 66 Genes GS176153: HP:0100820 Glomerulopathy
Expand Tier I Human 489 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 86 Genes GS172908: HP:0002450 Abnormality of the motor neurons
Expand Tier I Human CTD 1696 Genes GS122142: Dietary Fats interacting genes (MeSH:D004041) in CTD
Expand Tier I Human 104 Genes GS171336: HP:0001732 Abnormality of the pancreas
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 58 Genes GS171822: HP:0000112 Nephropathy
Expand Tier I Human 45 Genes GS176166: HP:0001256 Intellectual disability, mild
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 51 Genes GS172891: HP:0100538 Abnormality of the supraorbital ridges
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 44 Genes GS171924: HP:0100578 Lipoatrophy
Expand Tier I Human 53 Genes GS171415: HP:0000138 Ovarian cysts
Expand Tier I Human 2 Genes GS175018: HP:0003392 First dorsal interossei muscle weakness
Expand Tier I Human 2 Genes GS173887: HP:0012062 Bone cyst
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 GO 1853 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human 65 Genes GS171788: HP:0001394 Cirrhosis
Expand Tier I Human 104 Genes GS173512: HP:0000306 Abnormality of the chin
Expand Tier I Human 390 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Human 88 Genes GS174323: HP:0004414 Abnormality of the pulmonary artery
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
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 487 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 401 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 344 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier I Human 469 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human 43 Genes GS175611: HP:0002092 Pulmonary hypertension
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 1137 Genes GS193812: GO:0006629 lipid metabolic process
Expand Tier I Human 2 Genes GS171668: HP:0002833 Cystic angiomatosis of bone
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
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 43 Genes GS174688: HP:0004890 Elevated pulmonary artery pressure
Expand Tier I Human 124 Genes GS174854: HP:0001410 Decreased liver function
Expand Tier I Human 213 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Human 2 Genes GS175256: HP:0003435 Cold-induced hand cramps
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
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 146 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Human CTD 307 Genes GS127028: Mifepristone interacting genes (MeSH:D015735) in CTD
Expand Tier I Human 52 Genes GS173419: HP:0000147 Polycystic ovaries
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human 45 Genes GS171785: HP:0001397 Hepatic steatosis
Expand Tier I Human 101 Genes GS172692: HP:0002659 Increased susceptibility to fractures
Expand Tier I Human GO 2816 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Human CTD 5081 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human 60 Genes GS171207: HP:0000098 Tall stature
Expand Tier I Human 72 Genes GS173062: HP:0003677 Slow progression
Expand Tier I Human GO 4201 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human 74 Genes GS174070: HP:0009124 Abnormality of adipose tissue
Expand Tier I Human 121 Genes GS172789: HP:0001537 Umbilical hernia
Expand Tier I Human 284 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 123 Genes GS171384: HP:0001551 Abnormality of the umbilicus
Expand Tier I Human 136 Genes GS173751: HP:0000998 Hypertrichosis
Expand Tier I Human GO 50 Genes GS194947: GO:0019915 lipid storage
Expand Tier I Human 127 Genes GS171035: HP:0002620 Systemic artery abnormality
Expand Tier I Human GO 218 Genes GS200311: GO:0019216 regulation of lipid metabolic process
Expand Tier I Human 25 Genes GS171234: HP:0002495 Impaired vibratory sensation
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
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 GO 3098 Genes GS203058: GO:0048519 negative regulation of biological process
Expand Tier I Human GO 4292 Genes GS204746: GO:0080090 regulation of primary metabolic process
Expand Tier I Human 263 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier I Human 19 Genes GS173950: HP:0000855 Insulin resistance
Expand Tier I Human 9 Genes GS174319: HP:0009130 Hand muscle atrophy
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 7 Genes GS172586: HP:0001833 Large feet
Expand Tier I Human 8 Genes GS174415: HP:0003484 Upper limb muscle weakness
Expand Tier I Human GO 3300 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Human 418 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human GO 768 Genes GS196729: GO:0005789 endoplasmic reticulum membrane
Expand Tier I Human GO 129 Genes GS202386: GO:0045444 fat cell differentiation
Expand Tier I Human GO 4787 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 42 Genes GS174226: HP:0001446 Abnormality of the musculature of the upper limbs
Expand Tier I Human 66 Genes GS171279: HP:0100545 Arterial stenosis
Expand Tier I Human 36 Genes GS173930: HP:0001677 Coronary artery disease
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 3 Genes GS171337: HP:0001735 Acute pancreatitis
Expand Tier I Human 15 Genes GS170826: HP:0002166 Impaired vibration sensation in the lower limbs
Expand Tier I Human 484 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 92 Genes GS172356: HP:0003119 Abnormality of lipid metabolism
Expand Tier I Human 307 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human GO 206 Genes GS205580: GO:0031301 integral to organelle membrane
Expand Tier I Human 269 Genes GS174948: HP:0100763 Abnormality of the lymphatic system
Expand Tier I Human 86 Genes GS172352: HP:0000137 Abnormality of the ovary
Expand Tier I Human 697 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 28 Genes GS172285: HP:0000826 Precocious puberty
Expand Tier I Human 72 Genes GS175158: HP:0011747 Abnormality of the anterior pituitary
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 915 Genes GS197025: GO:0044432 endoplasmic reticulum part
Expand Tier I Human CTD 1467 Genes GS125062: palm oil interacting genes (MeSH:C041786) in CTD
Expand Tier I Human 113 Genes GS173262: HP:0000864 Abnormality of the hypothalamus-pituitary axis
Expand Tier I Human 205 Genes GS176283: HP:0009830 Peripheral neuropathy
Expand Tier I Human 2 Genes GS171518: HP:0003427 Thenar muscle weakness
Expand Tier I Human 29 Genes GS170949: HP:0005616 Accelerated skeletal maturation
Expand Tier I Human GO 785 Genes GS204928: GO:0042175 nuclear outer membrane-endoplasmic reticulum membrane network
Expand Tier I Human 98 Genes GS176867: HP:0003577 Congenital onset
Expand Tier I Human GO 1428 Genes GS201262: GO:0009892 negative regulation of metabolic process
Expand Tier I Human 4 Genes GS172153: HP:0003449 Cold-induced muscle cramps
Expand Tier I Human 69 Genes GS175064: HP:0000975 Hyperhidrosis
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human 8 Genes GS175819: HP:0002591 Polyphagia
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Human 356 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human 2 Genes GS173333: HP:0004361 Abnormality of circulating leptin level
Expand Tier I Human 542 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human CTD 1454 Genes GS121893: Vitamin E interacting genes (MeSH:D014810) in CTD
Expand Tier I Human 66 Genes GS174437: HP:0005114 Abnormalities of the peripheral arteries
Expand Tier I Human GO 1994 Genes GS207862: GO:0009056 catabolic process
Expand Tier I Human GO 1690 Genes GS194905: GO:0008219 cell death
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 4 Genes GS171177: HP:0001544 Prominent umbilicus
Expand Tier I Human 13 Genes GS173706: HP:0000845 Growth hormone excess
Expand Tier I Human 382 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human 9 Genes GS172307: HP:0100696 Bone cysts
Expand Tier I Human 37 Genes GS174452: HP:0006704 Abnormality of the coronary arteries
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 35 Genes GS176655: HP:0000056 Abnormality of the clitoris
Expand Tier I Human GO 41 Genes GS208149: GO:0050994 regulation of lipid catabolic process
Expand Tier I Human GO 56 Genes GS205268: GO:0045833 negative regulation of lipid metabolic process
Expand Tier I Human 454 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human CTD 1523 Genes GS124579: Selenium interacting genes (MeSH:D012643) in CTD
Expand Tier I Human 270 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Human 77 Genes GS174230: HP:0000303 Mandibular prognathia
Expand Tier I Human 17 Genes GS174660: HP:0001421 Abnormality of the musculature of the hand
Expand Tier I Human 194 Genes GS173872: HP:0011368 Epidermal thickening
Expand Tier I Human 35 Genes GS174741: HP:0003394 Muscle cramps
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human CTD 4391 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Tier I Human CTD 5732 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human 77 Genes GS173703: HP:0000842 Hyperinsulinemia
Expand Tier I Human 198 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human GO 236 Genes GS198980: GO:0010876 lipid localization
Expand Tier I Human GO 2361 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 346 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human 45 Genes GS171036: HP:0002621 Atherosclerosis
Expand Tier I Human 72 Genes GS176656: HP:0000055 Abnormality of female external genitalia
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human 2 Genes GS172005: HP:0003292 Decreased serum leptin
Expand Tier I Human 48 Genes GS172577: HP:0003690 Limb muscle weakness
Expand Tier I Human 71 Genes GS174073: HP:0009127 Abnormality of the musculature of the limbs
Expand Tier I Human GO 1276 Genes GS196726: GO:0005783 endoplasmic reticulum
Expand Tier I Human 9 Genes GS172327: HP:0007149 Distal upper limb amyotrophy
Expand Tier I Human 395 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 6073 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human 5 Genes GS174740: HP:0003393 Thenar muscle atrophy
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 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 487 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 25 Genes GS174393: HP:0001733 Pancreatitis
Expand Tier I Human 21 Genes GS175469: HP:0001176 Large hands
Expand Tier I Human 47 Genes GS171267: HP:0002634 Arteriosclerosis
Expand Tier I Human 2 Genes GS176277: HP:0003426 First dorsal interossei muscle atrophy
Expand Tier I Human 62 Genes GS172355: HP:0002460 Distal muscle weakness
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 1820 Genes GS205820: GO:0033036 macromolecule localization
Expand Tier I Human 53 Genes GS176772: HP:0001007 Hirsutism
Expand Tier I Human 10 Genes GS174982: HP:0000831 Insulin-resistant diabetes mellitus
Expand Tier I Human 229 Genes GS175577: HP:0003202 Amyotrophy
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
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 41 Genes GS175192: HP:0002061 Lower limb spasticity
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 29 Genes GS171709: HP:0003077 Hyperlipidemia
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 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 554 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human 234 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Human GO 2104 Genes GS209928: GO:0006996 organelle organization
Expand Tier I Human 4 Genes GS175960: HP:0000065 Labial hypertrophy
Expand Tier I Human GO 17 Genes GS208148: GO:0050995 negative regulation of lipid catabolic process
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human 676 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human 20 Genes GS174647: HP:0000956 Acanthosis nigricans
Expand Tier I Human GO 252 Genes GS194309: GO:0016042 lipid catabolic process
Expand Tier I Human 2 Genes GS172565: HP:0003716 Generalized muscular appearance from birth
Expand Tier I Human 23 Genes GS173380: HP:0002064 Spastic gait
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism 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 78 Genes GS173387: HP:0002757 Recurrent fractures
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 31 Genes GS173433: HP:0001769 Broad foot
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 121 Genes GS199200: GO:0031227 intrinsic to endoplasmic reticulum membrane
Expand Tier I Human 80 Genes GS173498: HP:0001763 Pes planus
Expand Tier I Human GO 5243 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 9 Genes GS174069: HP:0009129 Upper limb amyotrophy
Expand Tier I Human 232 Genes GS170999: HP:0000082 Abnormality of renal physiology
Expand Tier I Human 11 Genes GS174057: HP:0100738 Abnormal eating behavior
Expand Tier I Human 23 Genes GS176653: HP:0000058 Abnormality of the labia
Expand Tier I Human 262 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier III Human 287 Genes GS213273: GenAge compiled genes related to human aging
Expand Tier I Human 38 Genes GS174374: HP:0005922 Abnormal hand morphology
Expand Tier I Human 110 Genes GS175068: HP:0000971 Abnormality of the sweat gland
Expand Tier I Human 171 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier I Human 193 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Human 262 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Human 2 Genes GS173483: HP:0000877 Insulin-resistant diabetes mellitus at puberty
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 GO 81 Genes GS201261: GO:0009895 negative regulation of catabolic process
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 25 Genes GS176654: HP:0000057 Clitoromegaly