Gene Details



CRX and homologs in 5 species are found in 989 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - 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 Mouse GO 7747 Genes GS185131: GO:0044699 single-organism process
Expand Tier II Human 5314 Genes GS244604: [MeSH] Neoplasms : D009369
Expand Tier I Mouse MP 10 Genes GS170728: MP:0002565 delayed circadian phase
Expand Tier I Human GO 1049 Genes GS202082: GO:0051254 positive regulation of RNA metabolic process
Expand Tier II Human 18 Genes GS236059: [MeSH] Cyclic Nucleotide Phosphodiesterases, Type 6 : D054707
Expand Tier II Human 33 Genes GS242563: [MeSH] Fundus Oculi : D005654
Expand Tier II Human 76 Genes GS237263: [MeSH] Spinocerebellar Ataxias : D020754
Expand Tier II Human 3671 Genes GS238182: [MeSH] Oncogene Proteins : D015513
Expand Tier II Mouse 969 Genes GS136900: ventral midbrain iron content 4 (Vmbic4, Published QTL Chr 7)
Expand Tier II Human 619 Genes GS239009: [MeSH] Paired Box Transcription Factors : D051761
Expand Tier II Human 134 Genes GS239699: [MeSH] Otx Transcription Factors : D051857
Expand Tier I Mouse GO 1018 Genes GS185261: GO:0051254 positive regulation of RNA metabolic process
Expand Tier II Human 4818 Genes GS238504: [MeSH] Tissues : D014024
Expand Tier I Human 643 Genes GS227315: MSigDB Geneset - TGACATY_UNKNOWN
Expand Tier I Human 1177 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier II Human 3562 Genes GS237717: [MeSH] Tissue Distribution : D014018
Expand Tier II Human 5070 Genes GS243926: [MeSH] Exons : D005091
Expand Tier I Human GO 1169 Genes GS203018: GO:0045935 positive regulation of nucleobase-containing compound metabolic process
Expand Tier II Human 967 Genes GS242084: [MeSH] Neoplasms, Neuroepithelial : D018302
Expand Tier II Human 352 Genes GS245136: [MeSH] Frameshift Mutation : D016368
Expand Tier II Human 8948 Genes GS244882: [MeSH] Epithelial Cells : D004847
Expand Tier II Human 6611 Genes GS234210: [MeSH] HeLa Cells : D006367
Expand Tier II Mouse 1020 Genes GS136319: non-HDL QTL 6 (Nhdlq6, Published QTL Chr 7)
Expand Tier II Human 4210 Genes GS240575: [MeSH] RNA, Small Untranslated : D058727
Expand Tier II Human 6241 Genes GS236947: [MeSH] Brain : D001921
Expand Tier II Mouse 649 Genes GS135346: Avp transcript abundance QTL 1 (Avptaq1, Published QTL Chr 7)
Expand Tier I Mouse GO 453 Genes GS181012: GO:0007423 sensory organ development
Expand Tier I Mouse MP 105 Genes GS168338: MP:0001502 abnormal circadian rhythm
Expand Tier II Human 602 Genes GS245714: [MeSH] Face : D005145
Expand Tier I Mouse MP 72 Genes GS169907: MP:0002090 abnormal vision
Expand Tier I Mouse MP 151 Genes GS163581: MP:0001004 abnormal retinal photoreceptor morphology
Expand Tier I Human 2 Genes GS231327: OMIM Geneset - Genes with known associations to "Retinitis pigmentosa 3"
Expand Tier II Human 17829 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier II Human 14843 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier I Mouse MP 159 Genes GS166394: MP:0003728 abnormal retinal photoreceptor layer morphology
Expand Tier II Human 2757 Genes GS236717: [MeSH] Cell Survival : D002470
Expand Tier II Human 2992 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier I Mouse MP 35 Genes GS165142: MP:0003732 abnormal retinal outer plexiform layer morphology
Expand Tier II Human 81 Genes GS235593: [MeSH] Optic Nerve Diseases : D009901
Expand Tier II Human 6978 Genes GS245264: [MeSH] Nervous System : D009420
Expand Tier II Rat 1082 Genes GS223255: Bone structure and strength QTL 66 (Bss66 Published QTL Chr 1)
Expand Tier II Human 687 Genes GS237832: [MeSH] Response Elements : D020218
Expand Tier II Human 1628 Genes GS245413: [MeSH] TGF-beta Superfamily Proteins : D055411
Expand Tier I Human GO 2712 Genes GS199273: GO:0043233 organelle lumen
Expand Tier I Human 701 Genes GS227535: MSigDB Geneset - TGCCAAR_V$NF1_Q6
Expand Tier I Human 156 Genes GS172363: HP:0004324 Increased body weight
Expand Tier I Mouse GO 4618 Genes GS191019: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier II Rat 1082 Genes GS224178: Bone structure and strength QTL 69 (Bss69 Published QTL Chr 1)
Expand Tier II Human 115 Genes GS244494: [MeSH] Circadian Rhythm Signaling Peptides and Proteins : D056925
Expand Tier II Human 4278 Genes GS239955: [MeSH] Amino Acid Motifs : D020816
Expand Tier I Human 783 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Mouse GO 3776 Genes GS187887: GO:0080090 regulation of primary metabolic process
Expand Tier II Human 1749 Genes GS239907: [MeSH] Cell Surface Extensions : D022081
Expand Tier II Rat 1082 Genes GS224505: Bone structure and strength QTL 68 (Bss68 Published QTL Chr 1)
Expand Tier II Rat 766 Genes GS224576: Estrogen-induced pituitary tumorigenesis QTL 13 (Ept13 Published QTL Chr 1)
Expand Tier II Human 52 Genes GS236358: [MeSH] Retinal Neoplasms : D019572
Expand Tier II Human 7608 Genes GS241611: [MeSH] Organic Chemistry Processes : D055602
Expand Tier I Mouse MP 637 Genes GS168389: MP:0001186 pigmentation phenotype
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human 183 Genes GS230617: MSigDB Geneset - PIGF_UP.V1_DN
Expand Tier I Human 323 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Mouse GO 2763 Genes GS189669: GO:2000112 regulation of cellular macromolecule biosynthetic process
Expand Tier II Human 150 Genes GS243778: [MeSH] S100 Calcium Binding Protein G : D064030
Expand Tier I Human GO 2879 Genes GS206108: GO:2001141 regulation of RNA biosynthetic process
Expand Tier II Rat 710 Genes GS223738: Renal function QTL 29 (Rf29 Published QTL Chr 1)
Expand Tier II Human 701 Genes GS238780: [MeSH] Head : D006257
Expand Tier II Human 1338 Genes GS241946: [MeSH] Gene Regulatory Networks : D053263
Expand Tier I Mouse MP 14 Genes GS166388: MP:0006068 abnormal horizontal cell morphology
Expand Tier I Mouse GO 4352 Genes GS192017: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier II Human 3757 Genes GS239838: [MeSH] Luminescent Proteins : D008164
Expand Tier II Human 1303 Genes GS244119: [MeSH] Genome, Microbial : D064349
Expand Tier II Human 813 Genes GS245250: [MeSH] Optical Phenomena : D055620
Expand Tier I Human 1219 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 136 Genes GS175674: HP:0007360 Aplasia/Hypoplasia of the cerebellum
Expand Human 188 Genes GS222320: Genes associated with high risk of intellectual disability.
Expand Tier I Mouse GO 13184 Genes GS191106: GO:0044464 cell part
Expand Tier I Human 951 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 45 Genes GS174869: HP:0000551 Abnormality of color vision
Expand Tier II Human 497 Genes GS234908: [MeSH] POU Domain Factors : D050809
Expand Tier I Mouse GO 3076 Genes GS177265: GO:0048731 system development
Expand Tier I Human GO 4137 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Mouse GO 3599 Genes GS186227: GO:0090304 nucleic acid metabolic process
Expand Tier II Human 3187 Genes GS239559: [MeSH] Oxidoreductases : D010088
Expand Tier I Human GO 12166 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse GO 3865 Genes GS193238: GO:0031323 regulation of cellular metabolic process
Expand Tier II Human 574 Genes GS239294: [MeSH] Heredodegenerative Disorders, Nervous System : D020271
Expand Tier II Human 4976 Genes GS243100: [MeSH] Protein-Serine-Threonine Kinases : D017346
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human GO 3892 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Mouse GO 2955 Genes GS181893: GO:0048522 positive regulation of cellular process
Expand Tier I Human GO 204 Genes GS210485: GO:0007601 visual perception
Expand Tier I Mouse MP 146 Genes GS168193: MP:0000966 decreased sensory neuron number
Expand Tier I Human GO 4787 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Mouse GO 3592 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier II Rat 1482 Genes GS224475: Bone structure and strength QTL 54 (Bss54 Published QTL Chr 1)
Expand Tier I Mouse 193 Genes GS228537: MSigDB Geneset - GSE15930_STIM_VS_STIM_AND_IFNAB_24H_CD8_T_CELL_DN
Expand Tier II Rat 1082 Genes GS223254: Bone structure and strength QTL 67 (Bss67 Published QTL Chr 1)
Expand Tier II Human 1576 Genes GS235073: [MeSH] Pyrimidines : D011743
Expand Tier II Human 7063 Genes GS243345: [MeSH] Alternative Splicing : D017398
Expand Tier II Human 4598 Genes GS244871: [MeSH] Time Factors : D013997
Expand Tier II Mouse 969 Genes GS136531: prion resistance 2 (Prnr2, Published QTL Chr 7)
Expand Tier II Human 473 Genes GS237582: [MeSH] DEAD-box RNA Helicases : D053487
Expand Tier II Human 1650 Genes GS243730: [MeSH] Cytoplasmic Vesicles : D022162
Expand Tier II Human 6064 Genes GS237183: [MeSH] Growth and Development : D048788
Expand Tier II Human 7832 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier II Human 126 Genes GS244365: [MeSH] Retinal Cone Photoreceptor Cells : D017949
Expand Tier II Rat 1192 Genes GS223341: Experimental allergic encephalomyelitis QTL 29 (Eae29 Published QTL Chr 1)
Expand Tier I Mouse MP 18 Genes GS167528: MP:0008519 thin retinal outer plexiform layer
Expand Tier II Human 4862 Genes GS244627: [MeSH] Biological Processes : D055694
Expand Tier I Human 389 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Mouse MP 74 Genes GS166313: MP:0008450 retinal photoreceptor degeneration
Expand Tier I Human GO 2093 Genes GS209551: GO:0031981 nuclear lumen
Expand Tier II Human 14167 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Tier II Human 1252 Genes GS242884: [MeSH] 3' Untranslated Regions : D020413
Expand Tier II Mouse 827 Genes GS136728: susceptibility to lung cancer 30 (Sluc30, Published QTL Chr 7)
Expand Tier II Human 9588 Genes GS240239: [MeSH] Sequence Homology : D017385
Expand Tier I Mouse MP 4 Genes GS168142: MP:0008583 absent photoreceptor inner segment
Expand Tier II Human 381 Genes GS237772: [MeSH] Feedback, Physiological : D025461
Expand Tier I Human GO 2757 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier I Human 170 Genes GS230530: MSigDB Geneset - V$MSX1_01
Expand Tier II Human 14336 Genes GS238002: [MeSH] Antisense Elements (Genetics) : D016375
Expand Tier I Mouse GO 4114 Genes GS193414: GO:0044249 cellular biosynthetic process
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human GO 817 Genes GS197472: GO:0044451 nucleoplasm part
Expand Tier II Human 2173 Genes GS234926: [MeSH] Epithelium : D004848
Expand Tier III Mouse 757 Genes GS225467: Differentially expressed in NAc cocaine-conditioned mice.
Expand Tier II Human 13572 Genes GS242639: [MeSH] Metabolic Phenomena : D055754
Expand Tier I Human GO 493 Genes GS209225: GO:0007600 sensory perception
Expand Tier II Human 3512 Genes GS234738: [MeSH] Proto-Oncogene Proteins : D011518
Expand Tier II Human 3848 Genes GS238044: [MeSH] Acid Anhydride Hydrolases : D017766
Expand Tier I Human 553 Genes GS232301: PC Geneset - "GGATTA_V$PITX2_Q2" pathway genes
Expand Tier I Human GO 3551 Genes GS203607: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier II Human 6336 Genes GS238872: [MeSH] Central Nervous System : D002490
Expand Tier II Human 2369 Genes GS243385: [MeSH] Dose-Response Relationship, Drug : D004305
Expand Tier II Human 369 Genes GS244605: [MeSH] Basic Helix-Loop-Helix Leucine Zipper Transcription Factors : D051778
Expand Tier I Human GO 434 Genes GS197802: GO:0007423 sensory organ development
Expand Tier I Human 413 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier II Human 1372 Genes GS237788: [MeSH] Acyltransferases : D000217
Expand Tier II Human 119 Genes GS234779: [MeSH] Mitochondrial Diseases : D028361
Expand Tier II Human 3726 Genes GS244254: [MeSH] Antigens, Surface : D000954
Expand Tier II Human 3604 Genes GS240446: [MeSH] Pharmacokinetics : D010599
Expand Tier II Human 142 Genes GS239635: [MeSH] Cranial Nerve Diseases : D003389
Expand Tier I Mouse GO 8412 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier II Human 3976 Genes GS239550: [MeSH] Apoptosis : D017209
Expand Tier I Mouse MP 273 Genes GS163432: MP:0006069 abnormal retinal neuronal layer morphology
Expand Tier I Mouse GO 763 Genes GS178922: GO:0003700 sequence-specific DNA binding transcription factor activity
Expand Tier I Human 103 Genes GS173741: HP:0100699 Scarring
Expand Tier I Mouse GO 1832 Genes GS187708: GO:0009893 positive regulation of metabolic process
Expand Tier II Human 16597 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier II Human 4189 Genes GS239444: [MeSH] Biological Evolution : D005075
Expand Tier II Mouse 581 Genes GS136233: mandible length 7 (Manln7, Published QTL Chr 7)
Expand Tier I Human GO 1002 Genes GS204232: GO:0001071 nucleic acid binding transcription factor activity
Expand Tier I Human 397 Genes GS172134: HP:0000639 Nystagmus
Expand Tier II Human 16030 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier II Human 17816 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier II Human 6916 Genes GS237481: [MeSH] Recombination, Genetic : D011995
Expand Tier II Human 10126 Genes GS237194: [MeSH] Physiological Phenomena : D010829
Expand Tier II Human 3993 Genes GS239079: [MeSH] Cell Membrane : D002462
Expand Tier II Human 3924 Genes GS244610: [MeSH] Nervous System Diseases : D009422
Expand Tier I Human 1163 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier II Human 1704 Genes GS241605: [MeSH] Embryo, Nonmammalian : D004625
Expand Tier II Rat 1656 Genes GS223864: Stress Responsive Adrenal Weight QTL 1 (Sradr1 Published QTL Chr 1)
Expand Tier II Human 296 Genes GS239560: [MeSH] Retinal Ganglion Cells : D012165
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier II Human 2605 Genes GS236040: [MeSH] Nutritional and Metabolic Diseases : D009750
Expand Tier II Mouse 980 Genes GS135458: bone mineral density 4 (Bomd4, Published QTL Chr 7)
Expand Tier II Human 306 Genes GS242559: [MeSH] Circadian Rhythm : D002940
Expand Tier II Rat 1704 Genes GS223785: Anxiety related response QTL 24 (Anxrr24 Published QTL Chr 1)
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier II Human 3665 Genes GS239266: [MeSH] Morphogenesis : D009024
Expand Tier II Human 3143 Genes GS236309: [MeSH] Viral Regulatory and Accessory Proteins : D054334
Expand Tier II Human 11962 Genes GS245976: [MeSH] Cellular Structures : D022082
Expand Tier I Human 124 Genes GS175492: HP:0000512 Abnormal electroretinogram
Expand Tier I Mouse GO 591 Genes GS182595: GO:0019904 protein domain specific binding
Expand Tier II Human 18212 Genes GS240572: [MeSH] DNA : D004247
Expand Tier I Human GO 1390 Genes GS193937: GO:0006366 transcription from RNA polymerase II promoter
Expand Tier II Human 11733 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier II Human 730 Genes GS240502: [MeSH] Deoxyribonucleosides : D003853
Expand Tier II Human 502 Genes GS240521: [MeSH] p300-CBP Transcription Factors : D050880
Expand Tier II Human 4523 Genes GS241137: [MeSH] Cell Growth Processes : D048708
Expand Tier II Human 2330 Genes GS242217: [MeSH] Muscle Proteins : D009124
Expand Tier II Human 1358 Genes GS243025: [MeSH] Neuroglia : D009457
Expand Tier I Human 532 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier II Human 11248 Genes GS237794: [MeSH] Oligodeoxyribonucleotides : D009838
Expand Tier I Human 36 Genes GS174701: HP:0000556 Retinal dystrophy
Expand Tier II Human 6703 Genes GS239024: [MeSH] Cytoplasmic Structures : D022083
Expand Tier II Human 15234 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier I Human GO 2313 Genes GS195643: GO:0003677 DNA binding
Expand Tier II Human 16814 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier I Human GO 1838 Genes GS198572: GO:0010604 positive regulation of macromolecule metabolic process
Expand Tier II Human 943 Genes GS235382: [MeSH] Transgenes : D019076
Expand Tier II Human 600 Genes GS239663: [MeSH] Deoxyuridine : D003857
Expand Tier II Human 2125 Genes GS236527: [MeSH] Species Specificity : D013045
Expand Tier II Human 1120 Genes GS243180: [MeSH] Pigments, Biological : D010860
Expand Tier II Human 7632 Genes GS236362: [MeSH] Organic Chemistry Phenomena : D055601
Expand Tier I Human GO 998 Genes GS195340: GO:0045893 positive regulation of transcription, DNA-dependent
Expand Tier I Human GO 5627 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Mouse GO 9739 Genes GS186744: GO:0043226 organelle
Expand Tier I Human 523 Genes GS231724: PC Geneset - "TGAYRTCA_V$ATF3_Q6" pathway genes
Expand Tier II Human 3849 Genes GS235980: [MeSH] Mechanical Phenomena : D055595
Expand Tier II Human 466 Genes GS235117: [MeSH] Interneurons : D007395
Expand Tier II Human 410 Genes GS236902: [MeSH] Orphan Nuclear Receptors : D057093
Expand Tier II Human 850 Genes GS243717: [MeSH] Electromagnetic Radiation : D060733
Expand Tier I Mouse MP 3256 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier II Human 7529 Genes GS239132: [MeSH] Gene Expression Regulation, Developmental : D018507
Expand Tier II Human 369 Genes GS241436: [MeSH] Spinal Cord Diseases : D013118
Expand Tier I Human 177 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier I Mouse GO 11363 Genes GS182835: GO:0005622 intracellular
Expand Tier II Human 386 Genes GS235824: [MeSH] 5' Untranslated Regions : D020121
Expand Tier II Human 7336 Genes GS238771: [MeSH] Transferases : D014166
Expand Tier II Human 34 Genes GS238726: [MeSH] Blindness : D001766
Expand Tier II Human 19180 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier I Human GO 9158 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier II Human 17454 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier I Human 169 Genes GS173988: HP:0000501 Glaucoma
Expand Tier I Human GO 3099 Genes GS206544: GO:2000112 regulation of cellular macromolecule biosynthetic process
Expand Tier I Mouse GO 3021 Genes GS182703: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Human GO 1253 Genes GS210178: GO:0031328 positive regulation of cellular biosynthetic process
Expand Tier I Human 249 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Human 560 Genes GS228870: MSigDB Geneset - GGATTA_V$PITX2_Q2
Expand Tier I Mouse MP 786 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier II Human 2285 Genes GS234579: [MeSH] Phylogeny : D010802
Expand Tier I Human 281 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human GO 1213 Genes GS198360: GO:0006357 regulation of transcription from RNA polymerase II promoter
Expand Tier I Human GO 2047 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier II Human 2544 Genes GS235532: [MeSH] Central Nervous System Diseases : D002493
Expand Tier I Mouse GO 4499 Genes GS186790: GO:0006725 cellular aromatic compound metabolic process
Expand Tier II Human 4234 Genes GS242178: [MeSH] Neoplasms by Site : D009371
Expand Tier I Human 89 Genes GS176988: HP:0008046 Abnormality of the retinal vasculature
Expand Tier II Human 17923 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier II Human 16633 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier II Human 161 Genes GS238473: [MeSH] DNA-Cytosine Methylases : D015257
Expand Tier I Human GO 5411 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 1195 Genes GS199501: GO:0051173 positive regulation of nitrogen compound metabolic process
Expand Tier II Human 7025 Genes GS241667: [MeSH] Cytoplasm : D003593
Expand Tier II Human 3643 Genes GS236354: [MeSH] Gene Deletion : D017353
Expand Tier II Human 74 Genes GS244027: [MeSH] Eye Neoplasms : D005134
Expand Tier I Human 402 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier II Human 4897 Genes GS236231: [MeSH] Antigens : D000941
Expand Tier II Human 1726 Genes GS235775: [MeSH] Basic Helix-Loop-Helix Transcription Factors : D051792
Expand Tier II Human 450 Genes GS236541: [MeSH] Cytoplasmic Granules : D003594
Expand Tier II Human 4880 Genes GS240252: [MeSH] Intercellular Signaling Peptides and Proteins : D036341
Expand Tier I Human GO 4130 Genes GS206329: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Mouse MP 163 Genes GS163943: MP:0005201 abnormal retinal pigment epithelium morphology
Expand Tier II Human 7440 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier II Human 18 Genes GS241472: [MeSH] Optic Atrophy, Hereditary, Leber : D029242
Expand Tier I Human 171 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier II Human 10170 Genes GS235056: [MeSH] Peptides : D010455
Expand Tier II Human 15712 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier II Human 1992 Genes GS234965: [MeSH] Cell Adhesion Molecules : D015815
Expand Tier II Human 1213 Genes GS238938: [MeSH] Nervous System Physiological Processes : D052778
Expand Tier I Human GO 5911 Genes GS195199: GO:0005634 nucleus
Expand Tier I Mouse GO 1232 Genes GS193234: GO:0031328 positive regulation of cellular biosynthetic process
Expand Tier I Human 136 Genes GS171855: HP:0000597 Ophthalmoparesis
Expand Tier I Mouse MP 2915 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human CTD 148 Genes GS122300: Camptothecin interacting with Homo sapiens associated genes (MeSH:D002166) in CTD
Expand Tier I Human 2 Genes GS231286: OMIM Geneset - Genes with known associations to "Cone-rod dystrophy, X-linked, 1"
Expand Tier II Human 4608 Genes GS243806: [MeSH] Time : D013995
Expand Tier I Human 122 Genes GS171946: HP:0002269 Abnormality of neuronal migration
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Mouse GO 2540 Genes GS189240: GO:2001141 regulation of RNA biosynthetic process
Expand Tier I Human 471 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier II Human 13540 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier II Human 595 Genes GS241397: [MeSH] Bromodeoxyuridine : D001973
Expand Tier I Mouse 986 Genes GS128580: BECs at LORR Recovery Chr# 7
Expand Tier I Mouse MP 50 Genes GS167572: MP:0001006 abnormal retinal cone cell morphology
Expand Tier I Mouse GO 1149 Genes GS186178: GO:0045935 positive regulation of nucleobase-containing compound metabolic process
Expand Tier I Mouse GO 8384 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier II Human 15098 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Human 7493 Genes GS236470: [MeSH] DNA-Binding Proteins : D004268
Expand Tier II Human 1136 Genes GS240265: [MeSH] Neurons, Afferent : D009475
Expand Tier I Mouse GO 2588 Genes GS187343: GO:0006351 transcription, DNA-dependent
Expand Tier II Human 311 Genes GS234692: [MeSH] Melanocytes : D008544
Expand Tier II Human 4260 Genes GS238232: [MeSH] Nucleoproteins : D009698
Expand Tier II Human 5292 Genes GS239596: [MeSH] Expressed Sequence Tags : D020224
Expand Tier II Human 120 Genes GS243344: [MeSH] Melanosomes : D020460
Expand Tier II Human 9339 Genes GS234761: [MeSH] Reproductive Physiological Processes : D055704
Expand Tier II Mouse 969 Genes GS135988: Hfe modifier 1 (Hfem1, Published QTL Chr 7)
Expand Tier I Human 362 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human GO 1475 Genes GS203369: GO:0005654 nucleoplasm
Expand Tier I Human 1069 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Mouse GO 8939 Genes GS185492: GO:0050789 regulation of biological process
Expand Tier II Human 202 Genes GS236508: [MeSH] Leucine Zippers : D016350
Expand Tier II Human 2389 Genes GS245455: [MeSH] Metabolic Diseases : D008659
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 166 Genes GS232340: PC Geneset - "V$MSX1_01" pathway genes
Expand Tier I Mouse GO 10875 Genes GS181473: GO:0005488 binding
Expand Tier II Human 2362 Genes GS235626: [MeSH] Brain Diseases : D001927
Expand Tier I Mouse GO 1777 Genes GS184445: GO:0044428 nuclear part
Expand Tier I Human 2115 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 511 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Mouse GO 5884 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 1087 Genes GS192345: GO:0010628 positive regulation of gene expression
Expand Tier II Human 124 Genes GS240358: [MeSH] Opsins : D055355
Expand Tier II Human 6093 Genes GS245544: [MeSH] Conserved Sequence : D017124
Expand Tier I Human GO 8581 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 3381 Genes GS200312: GO:0019219 regulation of nucleobase-containing compound metabolic process
Expand Tier I Mouse GO 713 Genes GS177859: GO:0045944 positive regulation of transcription from RNA polymerase II promoter
Expand Tier I Mouse GO 1147 Genes GS191150: GO:0010557 positive regulation of macromolecule biosynthetic process
Expand Tier II Human 4886 Genes GS241960: [MeSH] Protein Structure, Secondary : D017433
Expand Tier II Human 1555 Genes GS243535: [MeSH] Neurodegenerative Diseases : D019636
Expand Tier I Mouse 182 Genes GS227702: MSigDB Geneset - GSE32423_CTRL_VS_IL7_MEMORY_CD8_TCELL_DN
Expand Tier II Human 17259 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier I Human 533 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human 504 Genes GS229037: MSigDB Geneset - WTTGKCTG_UNKNOWN
Expand Tier II Human 16451 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier II Human 15903 Genes GS243578: [MeSH] Reading Frames : D016364
Expand Tier I Human GO 4291 Genes GS204746: GO:0080090 regulation of primary metabolic process
Expand Tier II Human 7201 Genes GS239072: [MeSH] Recombinant Proteins : D011994
Expand Tier II Human 167 Genes GS236744: [MeSH] Ataxia : D001259
Expand Tier I Human GO 2480 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human GO 8546 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier II Human 900 Genes GS236872: [MeSH] Pyrimidine Nucleosides : D011741
Expand Tier II Human 2865 Genes GS236987: [MeSH] Tumor Suppressor Proteins : D025521
Expand Tier II Human 11159 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier II Human 2461 Genes GS239859: [MeSH] Prosencephalon : D016548
Expand Tier I Human 95 Genes GS176989: HP:0008047 Abnormality of the vasculature of the eye
Expand Tier II Human 1669 Genes GS237394: [MeSH] Point Mutation : D017354
Expand Tier I Human GO 3507 Genes GS193991: GO:0048731 system development
Expand Tier II Human 679 Genes GS244978: [MeSH] LIM Domain Proteins : D060588
Expand Tier I Human GO 3604 Genes GS198456: GO:0019438 aromatic compound biosynthetic process
Expand Tier II Rat 713 Genes GS224075: Bone structure and strength QTL 86 (Bss86 Published QTL Chr 1)
Expand Tier II Human 67 Genes GS237259: [MeSH] Transcription Factor Brn-3B : D050820
Expand Tier II Human 8835 Genes GS240544: [MeSH] Pregnancy : D011247
Expand Tier II Human 387 Genes GS241346: [MeSH] Genome, Bacterial : D016680
Expand Tier I Mouse GO 2907 Genes GS181667: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Mouse CTD 10652 Genes GS256287: Tetrachlorodibenzodioxin interacting with Mus musculus associated genes (MeSH:D013749) in CTD
Expand Tier II Human 82 Genes GS238692: [MeSH] Parvalbumins : D010320
Expand Tier II Human 11230 Genes GS237820: [MeSH] DNA Primers : D017931
Expand Tier I Human GO 3282 Genes GS194088: GO:0003676 nucleic acid binding
Expand Tier II Human 3173 Genes GS241597: [MeSH] Disease Models, Animal : D004195
Expand Tier I Mouse GO 3090 Genes GS188511: GO:0010468 regulation of gene expression
Expand Tier II Rat 1129 Genes GS224484: Heart rate QTL 1 (Hrtrt1 Published QTL Chr 1)
Expand Tier II Human 9485 Genes GS235276: [MeSH] Signal Transduction : D015398
Expand Tier II Human 9704 Genes GS244426: [MeSH] Tumor Cells, Cultured : D014407
Expand Tier I Human 2365 Genes GS175529: HP:0000001 All
Expand Tier I Mouse MP 427 Genes GS163138: MP:0005253 abnormal eye physiology
Expand Tier II Human 6676 Genes GS241118: [MeSH] Binding Sites : D001665
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Mouse GO 994 Genes GS178589: GO:0045893 positive regulation of transcription, DNA-dependent
Expand Tier III Mouse 8264 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier II Mouse 589 Genes GS136894: ventricular size 3 (Vent3, Published QTL Chr 7)
Expand Tier I Mouse GO 11123 Genes GS184447: GO:0044424 intracellular part
Expand Tier II Human 6493 Genes GS236576: [MeSH] Promoter Regions, Genetic : D011401
Expand Tier II Human 5577 Genes GS238961: [MeSH] Nerve Tissue Proteins : D009419
Expand Tier I Mouse GO 2947 Genes GS193236: GO:0031326 regulation of cellular biosynthetic process
Expand Tier II Human 2461 Genes GS235248: [MeSH] Algorithms : D000465
Expand Tier II Rat 713 Genes GS224074: Bone structure and strength QTL 87 (Bss87 Published QTL Chr 1)
Expand Tier II Human 894 Genes GS236279: [MeSH] Radiation : D011827
Expand Tier I Human 382 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human GO 6547 Genes GS209863: GO:0050896 response to stimulus
Expand Tier II Rat 707 Genes GS224774: Food consumption QTL 2 (Foco2 Published QTL Chr 1)
Expand Tier II Human 390 Genes GS243728: [MeSH] LIM-Homeodomain Proteins : D060850
Expand Tier II Mouse 581 Genes GS136096: long bones 6 (Lbn6, Published QTL Chr 7)
Expand Tier II Human 10961 Genes GS242691: [MeSH] Embryonic Structures : D004628
Expand Tier I Mouse GO 3382 Genes GS191021: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human 198 Genes GS228538: MSigDB Geneset - GSE3982_CTRL_VS_PMA_STIM_EOSINOPHIL_DN
Expand Tier I Human GO 3466 Genes GS199499: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Mouse GO 106 Genes GS187835: GO:0060041 retina development in camera-type eye
Expand Tier II Mouse 895 Genes GS84191: alcohol preference 7 QTL (Ap7q, Published QTL, Chr 7)
Expand Tier II Human 1149 Genes GS239355: [MeSH] Body Patterning : D019521
Expand Tier II Human 17884 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier I Human GO 2540 Genes GS203335: GO:0048513 organ development
Expand Tier I Mouse GO 1582 Genes GS188684: GO:0070013 intracellular organelle lumen
Expand Tier I Human 199 Genes GS176660: HP:0000050 Hypoplastic genitalia
Expand Tier I Mouse GO 9716 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier II Rat 1532 Genes GS224632: Blood pressure QTL 96 (Bp96 Published QTL Chr 1)
Expand Tier II Human 8777 Genes GS244835: [MeSH] Chromosomes : D002875
Expand Tier II Human 2091 Genes GS237069: [MeSH] Congenital Abnormalities : D000013
Expand Tier I Human 381 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Mouse MP 203 Genes GS169032: MP:0005551 abnormal eye electrophysiology
Expand Tier I Human GO 675 Genes GS196540: GO:0043565 sequence-specific DNA binding
Expand Tier II Human 102 Genes GS238585: [MeSH] Retinitis Pigmentosa : D012174
Expand Tier I Mouse MP 17 Genes GS168576: MP:0008585 absent photoreceptor outer segment
Expand Tier II Rat 775 Genes GS223131: Insulin/glucose ratio QTL 3 (Insglur3 Published QTL Chr 1)
Expand Tier II Rat 743 Genes GS224213: Bone structure and strength QTL 94 (Bss94 Published QTL Chr 1)
Expand Tier II Human 18365 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier I Mouse GO 1587 Genes GS182475: GO:0043233 organelle lumen
Expand Tier I Mouse GO 3978 Genes GS188506: GO:0010467 gene expression
Expand Tier I Mouse MP 7 Genes GS164848: MP:0006075 abnormal retinal cone bipolar cell morphology
Expand Tier I Human GO 14550 Genes GS208012: GO:0044464 cell part
Expand Tier II Human 4823 Genes GS239522: [MeSH] Growth : D006128
Expand Tier II Mouse 581 Genes GS136238: mandible size 5 (Manz5, Published QTL Chr 7)
Expand Tier I Human GO 16873 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 2858 Genes GS195291: GO:0006355 regulation of transcription, DNA-dependent
Expand Tier I Human GO 5335 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier II Human 17873 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 14315 Genes GS237296: [MeSH] RNA, Antisense : D016372
Expand Tier II Human 2419 Genes GS239472: [MeSH] Homeodomain Proteins : D018398
Expand Tier I Human GO 3326 Genes GS205369: GO:0010468 regulation of gene expression
Expand Tier I Mouse GO 4218 Genes GS192073: GO:1901576 organic substance biosynthetic process
Expand Tier I Mouse GO 7642 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Human 387 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier II Human 13809 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier II Human 68 Genes GS237886: [MeSH] Vision Disorders : D014786
Expand Tier I Mouse MP 25 Genes GS169166: MP:0008456 abnormal retinal rod cell outer segment morphology
Expand Tier I Mouse GO 2984 Genes GS188762: GO:0009889 regulation of biosynthetic process
Expand Tier I Human 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 7653 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier II Human 16145 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Human GO 1177 Genes GS208060: GO:0010557 positive regulation of macromolecule biosynthetic process
Expand Tier II Human 1705 Genes GS234230: [MeSH] Glutathione Transferase : D005982
Expand Tier I Mouse GO 4477 Genes GS184435: GO:0046483 heterocycle metabolic process
Expand Tier II Rat 707 Genes GS224383: Body weight QTL 29 (Bw29 Published QTL Chr 1)
Expand Tier II Human 2582 Genes GS235747: [MeSH] Musculoskeletal and Neural Physiological Phenomena : D055687
Expand Tier I Mouse GO 765 Genes GS187370: GO:0001071 nucleic acid binding transcription factor activity
Expand Tier II Human 11279 Genes GS239302: [MeSH] Oligonucleotides : D009841
Expand Tier II Human 2711 Genes GS240531: [MeSH] Neoplasms, Glandular and Epithelial : D009375
Expand Tier II Human 1110 Genes GS244158: [MeSH] Protein Kinase C : D011493
Expand Tier II Rat 1482 Genes GS224478: Bone structure and strength QTL 53 (Bss53 Published QTL Chr 1)
Expand Tier II Rat 1027 Genes GS224721: Serum cholesterol QTL 36 (Scl36 Published QTL Chr 1)
Expand Tier I Mouse 196 Genes GS230015: MSigDB Geneset - GSE1448_CTRL_VS_ANTI_VALPHA2_DP_THYMOCYTE_UP
Expand Tier II Human 628 Genes GS239537: [MeSH] Uridine : D014529
Expand Tier II Human 542 Genes GS241000: [MeSH] Ribonucleases : D012260
Expand Tier I Human GO 14 Genes GS200472: GO:0030275 LRR domain binding
Expand Tier I Mouse MP 130 Genes GS167461: MP:0002792 abnormal retinal vasculature morphology
Expand Tier II Human 933 Genes GS242199: [MeSH] Diencephalon : D004027
Expand Tier I Mouse GO 3292 Genes GS186214: GO:0048518 positive regulation of biological process
Expand Tier II Human 454 Genes GS241594: [MeSH] Neurosecretory Systems : D009490
Expand Tier I Human GO 3715 Genes GS194038: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier I Mouse MP 582 Genes GS165612: MP:0002128 abnormal blood circulation
Expand Tier II Human 2198 Genes GS237180: [MeSH] Genetic Markers : D005819
Expand Tier I Rat DRG 3865 Genes provisional GS86769: Table S2: HIPPOCAMPUS MGC MICROARRAY [DRG]
Expand Tier II Human 7589 Genes GS242551: [MeSH] Physiological Processes : D055705
Expand Tier II Human 5393 Genes GS243396: [MeSH] Neoplasm Proteins : D009363
Expand Tier I Human 64 Genes GS174379: HP:0002084 Encephalocele
Expand Tier I Mouse MP 30 Genes GS170724: MP:0002561 abnormal circadian phase
Expand Tier II Human 50 Genes GS241434: [MeSH] Retinal Bipolar Cells : D051245
Expand Tier II Human 9375 Genes GS237817: [MeSH] Cell Line, Tumor : D045744
Expand Tier I Human 1206 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier II Human 3532 Genes GS238252: [MeSH] Neoplasms by Histologic Type : D009370
Expand Tier I Human 231 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier II Human 13275 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier I Human 42 Genes GS174449: HP:0001123 Visual field defect
Expand Tier I Human 81 Genes GS171773: HP:0000532 Chorioretinal abnormality
Expand Tier I Human 220 Genes GS171791: HP:0000370 Abnormality of the middle ear
Expand Tier I Human 135 Genes GS232407: PC Geneset - "V$MEIS1BHOXA9_01" pathway genes
Expand Tier I Human 412 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier II Mouse 897 Genes GS135415: bronchial hyperresponsiveness 6 (Bhr6, Published QTL Chr 7)
Expand Tier II Human 569 Genes GS245899: [MeSH] Genes, Developmental : D050437
Expand Tier I Human 92 Genes GS171656: HP:0000610 Abnormality of the choroid
Expand Tier I Human 1563 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse GO 4650 Genes GS177310: GO:1901360 organic cyclic compound metabolic process
Expand Tier II Human 1268 Genes GS239924: [MeSH] Intercellular Junctions : D007365
Expand Tier I Human 1223 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier II Human 1455 Genes GS237451: [MeSH] Neuroectodermal Tumors : D017599
Expand Tier I Mouse CTD 10652 Genes GS256288: Tetracaine interacting with Mus musculus associated genes (MeSH:D013748) in CTD
Expand Tier I Mouse MP 1731 Genes GS165616: MP:0002127 abnormal cardiovascular system morphology
Expand Tier II Human 299 Genes GS239087: [MeSH] S100 Proteins : D009418
Expand Tier I Human GO 3304 Genes GS210180: GO:0031326 regulation of cellular biosynthetic process
Expand Tier II Rat 734 Genes GS224623: Serum cholesterol level QTL 6 (Scl6 Published QTL Chr 1)
Expand Tier I Human 139 Genes GS230584: MSigDB Geneset - V$MEIS1BHOXA9_01
Expand Tier II Human 2422 Genes GS240538: [MeSH] Embryonic Development : D047108
Expand Tier I Mouse GO 13185 Genes GS182834: GO:0005623 cell
Expand Tier II Human 548 Genes GS243263: [MeSH] Genes, Homeobox : D005801
Expand Tier I Human GO 3334 Genes GS205622: GO:0009889 regulation of biosynthetic process
Expand Tier I Mouse GO 2835 Genes GS191151: GO:0010556 regulation of macromolecule biosynthetic process
Expand Tier II Human 1285 Genes GS234181: [MeSH] Retina : D012160
Expand Tier I Human GO 1078 Genes GS209282: GO:0010628 positive regulation of gene expression
Expand Tier I Mouse MP 36 Genes GS164351: MP:0010097 abnormal retinal blood vessel morphology
Expand Tier I Mouse GO 3757 Genes GS189460: GO:0060255 regulation of macromolecule metabolic process
Expand Tier II Human 7908 Genes GS245804: [MeSH] Transcription Factors : D014157
Expand Tier I Human GO 3851 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Mouse GO 5246 Genes GS178448: GO:0005634 nucleus
Expand Tier II Human 9890 Genes GS235538: [MeSH] Protein Binding : D011485
Expand Tier II Human 1545 Genes GS242842: [MeSH] Neoplasms, Germ Cell and Embryonal : D009373
Expand Tier I Human 288 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human 1003 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12490 Genes GS199635: GO:0005622 intracellular
Expand Tier II Human 4645 Genes GS238960: [MeSH] Membrane Glycoproteins : D008562
Expand Tier II Human 3882 Genes GS234976: [MeSH] Acylation : D000215
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 682 Genes GS232110: PC Geneset - "TGCCAAR_V$NF1_Q6" pathway genes
Expand Tier I Mouse MP 579 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier II Human 1449 Genes GS242366: [MeSH] Inheritance Patterns : D040582