Gene Details



EDARADD and homologs in 1 species are found in 130 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 173 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 385 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 12 Genes GS174503: HP:0000704 Periodontitis
Expand Tier I Human 130 Genes GS175744: HP:0001231 Abnormality of the fingernails
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 1435 Genes GS205623: GO:0009888 tissue development
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 22 Genes GS170891: HP:0006480 Premature loss of teeth
Expand Tier I Human 231 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human GO 177 Genes GS201227: GO:0060541 respiratory system development
Expand Tier I Human 22 Genes GS174676: HP:0002217 Slow-growing hair
Expand Tier I Human 58 Genes GS172176: HP:0000232 Everted lower lip vermilion
Expand Tier I Human 274 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human GO 261 Genes GS194762: GO:0042633 hair cycle
Expand Tier I Human 48 Genes GS174713: HP:0002213 Fine hair
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 211 Genes GS174189: HP:0001597 Abnormality of the nail
Expand Tier I Human 28 Genes GS174237: HP:0000535 Sparse eyebrow
Expand Tier I Human 14 Genes GS173874: HP:0006323 Premature loss of primary teeth
Expand Tier I Human 12 Genes GS174782: HP:0002047 Malignant hyperthermia
Expand Tier I Human GO 8094 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human GO 2047 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human 407 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 90 Genes GS170889: HP:0006482 Abnormality of dental morphology
Expand Tier I Human 322 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Human 24 Genes GS172624: HP:0000653 Sparse eyelashes
Expand Tier I Human 3 Genes GS173979: HP:0001106 Periorbital hyperpigmentation
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human 310 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Human 122 Genes GS171390: HP:0000178 Abnormality of lower lip
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human 69 Genes GS171136: HP:0100840 Aplasia/Hypoplasia of the eyebrow
Expand Tier I Human 450 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 113 Genes GS176227: HP:0010719 Abnormality of hair texture
Expand Tier I Human 51 Genes GS176598: HP:0000668 Hypodontia
Expand Tier I Human 110 Genes GS175068: HP:0000971 Abnormality of the sweat gland
Expand Tier I Human GO 6548 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 174 Genes GS173540: HP:0002115 Sparse or absent hair
Expand Tier I Human 93 Genes GS174190: HP:0001596 Alopecia
Expand Tier I Human 375 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human GO 2539 Genes GS203335: GO:0048513 organ development
Expand Tier I Human GO 13 Genes GS203953: GO:0060438 trachea development
Expand Tier I Human 139 Genes GS171397: HP:0000177 Abnormality of upper lip
Expand Tier I Human GO 2653 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 61 Genes GS171609: HP:0011339 Abnormality of upper lip vermillion
Expand Tier I Human 55 Genes GS174818: HP:0007495 Prematurely aged appearance
Expand Tier I Human GO 261 Genes GS197298: GO:0042303 molting cycle
Expand Tier I Human 70 Genes GS171600: HP:0000168 Abnormality of the gingiva
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 5 Genes GS174822: HP:0010803 Everted upper lip vermilion
Expand Tier I Human GO 255 Genes GS208672: GO:0022404 molting cycle process
Expand Tier I Human GO 4014 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 3 Genes GS203212: GO:0061152 trachea submucosa development
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
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 120 Genes GS170890: HP:0006483 Abnormal number of teeth
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 30 Genes GS170892: HP:0006481 Abnormality of primary teeth
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human GO 103 Genes GS197516: GO:0042476 odontogenesis
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 4 Genes GS173100: HP:0000674 Anodontia
Expand Tier I Human 80 Genes GS174550: HP:0000958 Dry skin
Expand Tier I Human 50 Genes GS173561: HP:0000691 Microdontia
Expand Tier I Human 110 Genes GS176907: HP:0009804 Reduced number of teeth
Expand Tier I Human GO 453 Genes GS194627: GO:0008544 epidermis development
Expand Tier I Human 59 Genes GS175262: HP:0000964 Eczema
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 88 Genes GS173087: HP:0000499 Abnormality of the eyelashes
Expand Tier I Human GO 792 Genes GS205616: GO:0009887 organ morphogenesis
Expand Tier I Human 564 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 7650 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 17 Genes GS176773: HP:0001006 Hypotrichosis
Expand Tier I Human GO 4575 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human GO 255 Genes GS208673: GO:0022405 hair cycle process
Expand Tier I Human 94 Genes GS176573: HP:0008065 Aplasia/Hypoplasia of the skin
Expand Tier I Human 9 Genes GS176415: HP:0100678 Premature skin wrinkling
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human 184 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier I Human 22 Genes GS171992: HP:0011363 Abnormality of hair growth rate
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 72 Genes GS170824: HP:0002164 Nail dysplasia
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human GO 255 Genes GS194492: GO:0001942 hair follicle development
Expand Tier I Human 34 Genes GS172053: HP:0000966 Hypohidrosis
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human 44 Genes GS172038: HP:0000963 Thin skin
Expand Tier I Human GO 2816 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Human 144 Genes GS175128: HP:0011123 Inflammatory abnormality of the skin
Expand Tier I Human GO 4960 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 64 Genes GS176627: HP:0000457 Flat nose
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 74 Genes GS171391: HP:0000179 Thick lower lip vermilion
Expand Tier I Human 173 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier I Human GO 68 Genes GS197514: GO:0042475 odontogenesis of dentin-containing tooth
Expand Tier I Human 6 Genes GS175309: HP:0002046 Heat intolerance
Expand Tier I Human GO 277 Genes GS193992: GO:0048732 gland development
Expand Tier I Human GO 4575 Genes GS206355: GO:0023052 signaling
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 3 Genes GS171449: HP:0000607 Periorbital wrinkles
Expand Tier I Human 195 Genes GS174236: HP:0000534 Abnormality of the eyebrow
Expand Tier I Human 177 Genes GS175431: HP:0011122 Abnormality of skin physiology
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 4065 Genes GS209199: GO:0007165 signal transduction
Expand Tier I Human GO 4701 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human 85 Genes GS175086: HP:0008388 Abnormality of the toenails
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human GO 3 Genes GS203211: GO:0061153 trachea gland development
Expand Tier I Human 122 Genes GS176258: HP:0004370 Abnormality of temperature regulation