Gene Details



LEMD3 and homologs in 1 species are found in 331 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 380 Genes GS196559: GO:0019866 organelle inner membrane
Expand Tier I Human 17 Genes GS173032: HP:0007513 Generalized hypopigmentation
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 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human GO 731 Genes GS194703: GO:0051726 regulation of cell cycle
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 100 Genes GS176684: HP:0008678 Renal hypoplasia/aplasia
Expand Tier I Human 231 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human 39 Genes GS174330: HP:0002714 Downturned corners of mouth
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 274 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Human 95 Genes GS176759: HP:0000982 Palmoplantar keratoderma
Expand Tier I Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human GO 871 Genes GS198861: GO:0007167 enzyme linked receptor protein signaling pathway
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 39 Genes GS175930: HP:0000246 Sinusitis
Expand Tier I Human 54 Genes GS176464: HP:0100242 Sarcoma
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 280 Genes GS175900: HP:0009118 Aplasia/Hypoplasia of the mandible
Expand Tier I Human 51 Genes GS173085: HP:0000490 Deeply set eye
Expand Tier I Human GO 65 Genes GS204254: GO:0030512 negative regulation of transforming growth factor beta receptor signaling pathway
Expand Tier I Human GO 3304 Genes GS210180: GO:0031326 regulation of cellular biosynthetic process
Expand Tier I Human 84 Genes GS173946: HP:0002438 Cerebellar malformation
Expand Tier I Human 174 Genes GS172015: HP:0000969 Edema
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 GO 3334 Genes GS205622: GO:0009889 regulation of biosynthetic process
Expand Tier I Human 179 Genes GS175391: HP:0011004 Abnormality of the systemic arterial tree
Expand Tier I Human 182 Genes GS174612: HP:0001600 Abnormality of the larynx
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 318 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 20 Genes GS175073: HP:0200013 Neoplasm of fatty tissue
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 III Human 3028 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human 148 Genes GS174586: HP:0005930 Abnormality of the epiphyses
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human GO 190 Genes GS198969: GO:0031965 nuclear membrane
Expand Tier I Human GO 5348 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human GO 228 Genes GS194306: GO:0031300 intrinsic to organelle membrane
Expand Tier I Human 116 Genes GS173868: HP:0002143 Abnormality of the spinal cord
Expand Tier III Human 48 Genes GS26324: Differential expression of genes in hippocampus of human cocaine abusers
Expand Tier I Human GO 3180 Genes GS208061: GO:0010556 regulation of macromolecule biosynthetic process
Expand Tier I Human 375 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human GO 2308 Genes GS209215: GO:0007166 cell surface receptor signaling pathway
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 372 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
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 GO 4014 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 106 Genes GS175048: HP:0006824 Cranial nerve paralysis
Expand Tier I Human GO 679 Genes GS204029: GO:0010648 negative regulation of cell communication
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 174 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human GO 817 Genes GS198970: GO:0031967 organelle envelope
Expand Tier I Human 110 Genes GS176907: HP:0009804 Reduced number of teeth
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 153 Genes GS172040: HP:0000962 Hyperkeratosis
Expand Tier I Human 487 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 423 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human GO 1378 Genes GS209190: GO:0007049 cell cycle
Expand Tier I Human 39 Genes GS174178: HP:0100774 Hyperostosis
Expand Tier I Human 94 Genes GS176560: HP:0001010 Hypopigmentation of the skin
Expand Tier I Human 25 Genes GS172554: HP:0100685 Abnormality of Sharpey fibers
Expand Tier I Human 96 Genes GS174851: HP:0000944 Abnormality of the metaphyses
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 4575 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human GO 300 Genes GS195200: GO:0005635 nuclear envelope
Expand Tier I Human GO 33 Genes GS204252: GO:0030514 negative regulation of BMP signaling pathway
Expand Tier I Human GO 4354 Genes GS210182: GO:0031323 regulation of cellular metabolic process
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 3383 Genes GS200312: GO:0019219 regulation of nucleobase-containing compound metabolic process
Expand Tier I Human GO 67 Genes GS204256: GO:0030510 regulation of BMP signaling pathway
Expand Tier I Human 148 Genes GS176233: HP:0004209 Clinodactyly of the 5th finger
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 39 Genes GS172454: HP:0100335 Non-midline cleft lip
Expand Tier I Human 226 Genes GS172470: HP:0001743 Abnormality of the spleen
Expand Tier I Human GO 202 Genes GS195060: GO:0051146 striated muscle cell differentiation
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 GO 445 Genes GS200490: GO:0061061 muscle structure development
Expand Tier I Human 32 Genes GS172698: HP:0002653 Bone pain
Expand Tier I Human 81 Genes GS172821: HP:0000213 Thin lips
Expand Tier I Human 468 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 213 Genes GS176973: HP:0001072 Thickened skin
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 5 Genes GS198767: GO:0044453 nuclear membrane part
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 433 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human GO 2878 Genes GS206108: GO:2001141 regulation of RNA biosynthetic process
Expand Tier I Human GO 2321 Genes GS206192: GO:0048583 regulation of response to stimulus
Expand Tier I Human 35 Genes GS176775: HP:0001004 Lymphedema
Expand Tier I Human 75 Genes GS171608: HP:0011338 Abnormality of mouth shape
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
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 GO 180 Genes GS200705: GO:0060538 skeletal muscle organ development
Expand Tier I Human 20 Genes GS171556: HP:0001387 Joint stiffness
Expand Tier I Human 101 Genes GS172692: HP:0002659 Increased susceptibility to fractures
Expand Tier I Human GO 30 Genes GS195198: GO:0005637 nuclear inner membrane
Expand Tier I Human GO 2026 Genes GS201132: GO:0010646 regulation of cell communication
Expand Tier I Human GO 2816 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Human GO 4 Genes GS195197: GO:0005639 integral to nuclear inner membrane
Expand Tier I Human GO 4960 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human 284 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Human GO 2603 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
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 GO 4 Genes GS199197: GO:0031229 intrinsic to nuclear inner membrane
Expand Tier I Human 532 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human 92 Genes GS173061: HP:0003676 Progressive disorder
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 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 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 GO 2479 Genes GS201249: GO:0044428 nuclear part
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 GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 300 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human 120 Genes GS177000: HP:0001291 Abnormality of the cranial nerves
Expand Tier I Human GO 4787 Genes GS204612: GO:0019222 regulation of metabolic process
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 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 356 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier I Human 309 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Human GO 93 Genes GS206245: GO:0090101 negative regulation of transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 2939 Genes GS202080: GO:0051252 regulation of RNA metabolic process
Expand Tier I Human 344 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Human GO 21 Genes GS202522: GO:0032925 regulation of activin receptor signaling pathway
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 213 Genes GS176040: HP:0011032 Abnormality of fluid regulation
Expand Tier I Human 484 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 187 Genes GS172253: HP:0001376 Limitation of joint mobility
Expand Tier I Human GO 3277 Genes GS194088: GO:0003676 nucleic acid binding
Expand Tier I Human GO 206 Genes GS205580: GO:0031301 integral to organelle membrane
Expand Tier I Human GO 4575 Genes GS206355: GO:0023052 signaling
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 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 43 Genes GS171179: HP:0003764 Nevus
Expand Tier I Human 195 Genes GS174236: HP:0000534 Abnormality of the eyebrow
Expand Tier I Human GO 304 Genes GS206182: GO:0060537 muscle tissue development
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 165 Genes GS210361: GO:0090092 regulation of transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Human GO 9 Genes GS202523: GO:0032926 negative regulation of activin receptor signaling pathway
Expand Tier I Human 61 Genes GS175740: HP:0010747 Medial flaring of the eyebrow
Expand Tier I Human 87 Genes GS173938: HP:0001679 Abnormality of the aorta
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human GO 4701 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human 132 Genes GS174606: HP:0001608 Abnormality of the voice
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 8 Genes GS171699: HP:0100561 Spinal cord lesions
Expand Tier I Human 222 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human GO 167 Genes GS204627: GO:0007179 transforming growth factor beta receptor signaling pathway
Expand Tier I Human 356 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 2410 Genes GS209108: GO:0000166 nucleotide binding
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 GO 292 Genes GS194519: GO:0014706 striated muscle tissue development
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 200 Genes GS171413: HP:0004097 Deviation of finger
Expand Tier I Human 50 Genes GS173052: HP:0000325 Triangular face
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 148 Genes GS175149: HP:0009179 Deviation of the 5th finger
Expand Tier I Human 454 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human 93 Genes GS174098: HP:0011792 Neoplasm by histology
Expand Tier I Human GO 2020 Genes GS206356: GO:0023051 regulation of signaling
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 3468 Genes GS199499: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Human 41 Genes GS175113: HP:0000574 Thick eyebrow
Expand Tier I Human 194 Genes GS173872: HP:0011368 Epidermal thickening
Expand Tier I Human GO 2539 Genes GS203335: GO:0048513 organ development
Expand Tier III Human 2161 Genes GS216491: Genes that are binding sites for CREB and zif268,transcription factors mediating nieuronal activity and plasticity, in Homo sapiens.
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human 49 Genes GS175394: HP:0011001 Increased bone mineral density
Expand Tier I Human 413 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human 83 Genes GS172024: HP:0001369 Arthritis
Expand Tier I Human 242 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human 20 Genes GS176562: HP:0001012 Multiple lipomas
Expand Tier I Human GO 109 Genes GS199937: GO:0030509 BMP signaling pathway
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human GO 777 Genes GS206190: GO:0048585 negative regulation of response to stimulus
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 24 Genes GS175894: HP:0000934 Chondrocalcinosis
Expand Tier I Human 20 Genes GS174565: HP:0012031 Lipomatous tumor
Expand Tier I Human 89 Genes GS176824: HP:0000204 Cleft upper lip
Expand Tier I Human 392 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Human GO 2361 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 6 Genes GS175970: HP:0100784 Peripheral arteriovenous fistula
Expand Tier I Human 346 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human GO 1770 Genes GS205147: GO:0009966 regulation of signal transduction
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 103 Genes GS173741: HP:0100699 Scarring
Expand Tier I Human 7 Genes GS174743: HP:0003396 Syringomyelia
Expand Tier III Human 2273 Genes GS137413: Supplementary Table 2. CNA Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human 313 Genes GS176568: HP:0000486 Strabismus
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 249 Genes GS172246: HP:0001371 Flexion contracture
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 335 Genes GS194775: GO:0007517 muscle organ development
Expand Tier I Human 64 Genes GS171273: HP:0100542 Abnormal localization of kidneys
Expand Tier I Human GO 6073 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 514 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 2857 Genes GS195291: GO:0006355 regulation of transcription, DNA-dependent
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 30 Genes GS172669: HP:0003103 Abnormal cortical bone morphology
Expand Tier I Human GO 3325 Genes GS205369: GO:0010468 regulation of gene expression
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
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 7650 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human 116 Genes GS170989: HP:0010766 Ectopic calcification
Expand Tier I Human 576 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 256 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Human GO 676 Genes GS206354: GO:0023057 negative regulation of signaling
Expand Tier I Human 229 Genes GS175577: HP:0003202 Amyotrophy
Expand Tier I Human 26 Genes GS176003: HP:0100651 Type I diabetes mellitus
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 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 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 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 172 Genes GS200488: GO:0007519 skeletal muscle tissue development
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 177 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier I Human GO 267 Genes GS204628: GO:0007178 transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 44 Genes GS173157: HP:0003326 Myalgia
Expand Tier I Human GO 2310 Genes GS195643: GO:0003677 DNA binding
Expand Tier I Human 554 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 676 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human GO 89 Genes GS193946: GO:0017015 regulation of transforming growth factor beta receptor signaling pathway
Expand Tier I Human 43 Genes GS172862: HP:0000664 Synophrys
Expand Tier I Human 1 Genes GS174717: HP:0010739 Osteopoikilosis
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 53 Genes GS210117: GO:0035914 skeletal muscle cell differentiation
Expand Tier I Human GO 273 Genes GS201756: GO:0042692 muscle cell differentiation
Expand Tier I Human 184 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Tier I Human GO 3099 Genes GS206544: GO:2000112 regulation of cellular macromolecule biosynthetic 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 121 Genes GS176672: HP:0000980 Pallor
Expand Tier I Human GO 31 Genes GS195377: GO:0032924 activin receptor signaling pathway
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 2828 Genes GS198684: GO:0048523 negative regulation of cellular process
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 596 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human GO 1214 Genes GS198360: GO:0006357 regulation of transcription from RNA polymerase II promoter
Expand Tier I Human 37 Genes GS172691: HP:0100026 Arteriovenous malformation
Expand Tier I Human 100 Genes GS176744: HP:0000987 Atypical scarring of skin
Expand Tier I Human 322 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Human GO 5243 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human 19 Genes GS171480: HP:0100555 Asymmetric growth
Expand Tier I Human 40 Genes GS174495: HP:0002566 Intestinal malrotation
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 5400 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human 74 Genes GS175265: HP:0002733 Abnormality of the lymph nodes
Expand Tier I Human 54 Genes GS171298: HP:0002829 Arthralgia
Expand Tier I Human 262 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 310 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Human 37 Genes GS173744: HP:0000995 Pigmented nevi
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 395 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human GO 4129 Genes GS206329: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Human 171 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier I Human GO 830 Genes GS194556: GO:0031975 envelope
Expand Tier I Human 52 Genes GS175933: HP:0000245 Abnormality of the sinuses
Expand Tier I Human GO 5908 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human 17 Genes GS172883: HP:0002308 Arnold-Chiari malformation
Expand Tier I Human GO 635 Genes GS205146: GO:0009968 negative regulation of signal transduction
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 13 Genes GS173823: HP:0100721 Mediastinal lymphadenopathy
Expand Tier I Human 280 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Human 444 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 2411 Genes GS203886: GO:1901265 nucleoside phosphate binding
Expand Tier III Human 48 Genes GS1256: Gene Expression in Human Hippocampus from Cocaine Addicts
Expand Tier I Human 185 Genes GS173065: HP:0003679 Pace of progression
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 335 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier I Human 120 Genes GS170890: HP:0006483 Abnormal number of teeth
Expand Tier I Human 46 Genes GS173611: HP:0002219 Facial hypertrichosis
Expand Tier I Human 361 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human 33 Genes GS174605: HP:0001609 Hoarse voice
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human 6 Genes GS171483: HP:0100559 Lower limb asymmetry
Expand Tier I Human 6 Genes GS172985: HP:0004947 Arteriovenous fistula
Expand Tier I Human 141 Genes GS172281: HP:0000822 Hypertension