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 387 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human GO 381 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 271 Genes GS176826: HP:0000202 Oral cleft
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human GO 732 Genes GS194703: GO:0051726 regulation of cell cycle
Expand Tier I Human GO 1439 Genes GS205623: GO:0009888 tissue development
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 101 Genes GS176684: HP:0008678 Renal hypoplasia/aplasia
Expand Tier I Human 232 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human 40 Genes GS174330: HP:0002714 Downturned corners of mouth
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 275 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Human 96 Genes GS176759: HP:0000982 Palmoplantar keratoderma
Expand Tier I Human 414 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 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 537 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 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 282 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 3324 Genes GS210180: GO:0031326 regulation of cellular biosynthetic process
Expand Tier I Human 85 Genes GS173946: HP:0002438 Cerebellar malformation
Expand Tier I Human 174 Genes GS172015: HP:0000969 Edema
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human GO 3354 Genes GS205622: GO:0009889 regulation of biosynthetic process
Expand Tier I Human 181 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 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 322 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 845 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 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier III Human 3178 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human 150 Genes GS174586: HP:0005930 Abnormality of the epiphyses
Expand Tier I Human 489 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 5400 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human GO 230 Genes GS194306: GO:0031300 intrinsic to organelle membrane
Expand Tier I Human 117 Genes GS173868: HP:0002143 Abnormality of the spinal cord
Expand Tier III Human 38 Genes GS26324: Differential expression of genes in hippocampus of human cocaine abusers
Expand Tier I Human GO 3199 Genes GS208061: GO:0010556 regulation of macromolecule biosynthetic process
Expand Tier I Human 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human GO 2317 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 2661 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Human 374 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human 121 Genes GS170890: HP:0006483 Abnormal number of teeth
Expand Tier I Human 46 Genes GS173611: HP:0002219 Facial hypertrichosis
Expand Tier I Human 106 Genes GS175048: HP:0006824 Cranial nerve paralysis
Expand Tier I Human GO 681 Genes GS204029: GO:0010648 negative regulation of cell communication
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human 33 Genes GS174605: HP:0001609 Hoarse voice
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human 177 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human GO 819 Genes GS198970: GO:0031967 organelle envelope
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
Expand Tier I Human 111 Genes GS176907: HP:0009804 Reduced number of teeth
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 155 Genes GS172040: HP:0000962 Hyperkeratosis
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human GO 1379 Genes GS209190: GO:0007049 cell cycle
Expand Tier I Human 39 Genes GS174178: HP:0100774 Hyperostosis
Expand Tier I Human 95 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 98 Genes GS174851: HP:0000944 Abnormality of the metaphyses
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human GO 4593 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 4377 Genes GS210182: GO:0031323 regulation of cellular metabolic process
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 3401 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 150 Genes GS176233: HP:0004209 Clinodactyly of the 5th finger
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 39 Genes GS172454: HP:0100335 Non-midline cleft lip
Expand Tier I Human 228 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 405 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human GO 444 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 470 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 215 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Human 221 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier I Human 588 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 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 435 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human GO 2896 Genes GS206108: GO:2001141 regulation of RNA biosynthetic process
Expand Tier I Human GO 2335 Genes GS206192: GO:0048583 regulation of response to stimulus
Expand Tier I Human 35 Genes GS176775: HP:0001004 Lymphedema
Expand Tier I Human 76 Genes GS171608: HP:0011338 Abnormality of mouth shape
Expand Tier I Human 416 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human 141 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 102 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 2033 Genes GS201132: GO:0010646 regulation of cell communication
Expand Tier I Human GO 2824 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 4983 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human 287 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Human GO 2625 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 136 Genes GS173751: HP:0000998 Hypertrichosis
Expand Tier I Human 543 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 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human 92 Genes GS173061: HP:0003676 Progressive disorder
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 409 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Human 316 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human GO 3104 Genes GS203058: GO:0048519 negative regulation of biological process
Expand Tier I Human GO 4314 Genes GS204746: GO:0080090 regulation of primary metabolic process
Expand Tier I Human GO 2486 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human 174 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier I Human 79 Genes GS172699: HP:0002652 Skeletal dysplasia
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 302 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 4811 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Human 303 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human 67 Genes GS174328: HP:0002716 Lymphadenopathy
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 360 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier I Human 311 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 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 2957 Genes GS202080: GO:0051252 regulation of RNA metabolic process
Expand Tier I Human 346 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 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 213 Genes GS176040: HP:0011032 Abnormality of fluid regulation
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 189 Genes GS172253: HP:0001376 Limitation of joint mobility
Expand Tier I Human GO 3310 Genes GS194088: GO:0003676 nucleic acid binding
Expand Tier I Human GO 208 Genes GS205580: GO:0031301 integral to organelle membrane
Expand Tier I Human GO 4593 Genes GS206355: GO:0023052 signaling
Expand Tier I Human 271 Genes GS174948: HP:0100763 Abnormality of the lymphatic system
Expand Tier I Human 416 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 43 Genes GS171179: HP:0003764 Nevus
Expand Tier I Human 198 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 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 4084 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 88 Genes GS173938: HP:0001679 Abnormality of the aorta
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human GO 4719 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human 132 Genes GS174606: HP:0001608 Abnormality of the voice
Expand Tier I Human 202 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 8 Genes GS171699: HP:0100561 Spinal cord lesions
Expand Tier I Human 224 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier I Human 913 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 358 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 2432 Genes GS209108: GO:0000166 nucleotide binding
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 320 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 384 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 202 Genes GS171413: HP:0004097 Deviation of finger
Expand Tier I Human 50 Genes GS173052: HP:0000325 Triangular face
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 150 Genes GS175149: HP:0009179 Deviation of the 5th finger
Expand Tier I Human 456 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 2027 Genes GS206356: GO:0023051 regulation of signaling
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 3487 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 196 Genes GS173872: HP:0011368 Epidermal thickening
Expand Tier I Human GO 2545 Genes GS203335: GO:0048513 organ development
Expand Tier III Human 2430 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 1051 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 416 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human 83 Genes GS172024: HP:0001369 Arthritis
Expand Tier I Human 246 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 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human GO 781 Genes GS206190: GO:0048585 negative regulation of response to stimulus
Expand Tier I Human 607 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 397 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Human GO 2373 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 6 Genes GS175970: HP:0100784 Peripheral arteriovenous fistula
Expand Tier I Human 348 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human GO 1776 Genes GS205147: GO:0009966 regulation of signal transduction
Expand Tier I Human 123 Genes GS173242: HP:0001337 Tremor
Expand Tier I Human 990 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 2403 Genes GS137413: Supplementary Table 2. CNA Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human 315 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human 397 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human 250 Genes GS172246: HP:0001371 Flexion contracture
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 334 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 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 2875 Genes GS195291: GO:0006355 regulation of transcription, DNA-dependent
Expand Tier I Human 741 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 3344 Genes GS205369: GO:0010468 regulation of gene expression
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 7689 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human 117 Genes GS170989: HP:0010766 Ectopic calcification
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 258 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Human GO 678 Genes GS206354: GO:0023057 negative regulation of signaling
Expand Tier I Human 229 Genes GS175577: HP:0003202 Amyotrophy
Expand Tier I Human 27 Genes GS176003: HP:0100651 Type I diabetes mellitus
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier I Human 601 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 174 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 281 Genes GS171204: HP:0011314 Abnormality of long bone morphology
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 1771 Genes GS196284: GO:0012505 endomembrane system
Expand Tier I Human 530 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 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 179 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 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 44 Genes GS173157: HP:0003326 Myalgia
Expand Tier I Human GO 2332 Genes GS195643: GO:0003677 DNA binding
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 680 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 9585 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 186 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Tier I Human GO 3118 Genes GS206544: GO:2000112 regulation of cellular macromolecule biosynthetic process
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 123 Genes GS176672: HP:0000980 Pallor
Expand Tier I Human GO 31 Genes GS195377: GO:0032924 activin receptor signaling pathway
Expand Tier I Human 79 Genes GS173387: HP:0002757 Recurrent fractures
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 2833 Genes GS198684: GO:0048523 negative regulation of cellular process
Expand Tier I Human GO 8137 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 599 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 324 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Human GO 5320 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 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 5452 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 55 Genes GS171298: HP:0002829 Arthralgia
Expand Tier I Human 266 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 313 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Human 37 Genes GS173744: HP:0000995 Pigmented nevi
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human GO 4151 Genes GS206329: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Human 174 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier I Human GO 832 Genes GS194556: GO:0031975 envelope
Expand Tier I Human 52 Genes GS175933: HP:0000245 Abnormality of the sinuses
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human 17 Genes GS172883: HP:0002308 Arnold-Chiari malformation
Expand Tier I Human GO 638 Genes GS205146: GO:0009968 negative regulation of signal transduction
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 13 Genes GS173823: HP:0100721 Mediastinal lymphadenopathy
Expand Tier I Human 282 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Human 446 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 2433 Genes GS203886: GO:1901265 nucleoside phosphate binding
Expand Tier III Human 40 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 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 337 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton