Gene Details



CRX and homologs in 5 species are found in 917 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 Mouse GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier II Human 8052 Genes GS244604: [MeSH] Neoplasms : D009369
Expand Tier I Mouse MP 11 Genes GS170728: MP:0002565 delayed circadian phase
Expand Tier I Human GO 1050 Genes GS202082: GO:0051254 positive regulation of RNA metabolic process
Expand Tier II Human 32 Genes GS236059: [MeSH] Cyclic Nucleotide Phosphodiesterases, Type 6 : D054707
Expand Tier II Human 37 Genes GS242563: [MeSH] Fundus Oculi : D005654
Expand Tier II Human 136 Genes GS237263: [MeSH] Spinocerebellar Ataxias : D020754
Expand Tier II Human 6985 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 891 Genes GS239009: [MeSH] Paired Box Transcription Factors : D051761
Expand Tier III Human 49 Genes GS221924: Capture panel of retinitis pigmentosa (RP) genes used to diagnose Chinese probands
Expand Tier II Human 193 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 10505 Genes GS238504: [MeSH] Tissues : D014024
Expand Tier I Human 657 Genes GS227315: MSigDB Geneset - TGACATY_UNKNOWN
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier II Human 5416 Genes GS237717: [MeSH] Tissue Distribution : D014018
Expand Tier II Human 8606 Genes GS243926: [MeSH] Exons : D005091
Expand Tier I Human GO 1171 Genes GS203018: GO:0045935 positive regulation of nucleobase-containing compound metabolic process
Expand Tier II Human 1227 Genes GS242084: [MeSH] Neoplasms, Neuroepithelial : D018302
Expand Tier II Human 390 Genes GS245136: [MeSH] Frameshift Mutation : D016368
Expand Tier II Human 14353 Genes GS244882: [MeSH] Epithelial Cells : D004847
Expand Tier II Human 8563 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 8182 Genes GS240575: [MeSH] RNA, Small Untranslated : D058727
Expand Tier II Human 11812 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 454 Genes GS181012: GO:0007423 sensory organ development
Expand Tier I Mouse MP 119 Genes GS168338: MP:0001502 abnormal circadian rhythm
Expand Tier II Human 1599 Genes GS245714: [MeSH] Face : D005145
Expand Tier I Mouse 2 Genes GS231327: OMIM Geneset - Genes with known associations to "Retinitis pigmentosa 3"
Expand Tier I Mouse MP 182 Genes GS163581: MP:0001004 abnormal retinal photoreceptor morphology
Expand Tier II Human 70216 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier II Human 31959 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier I Mouse MP 190 Genes GS166394: MP:0003728 abnormal retinal photoreceptor layer morphology
Expand Tier II Human 4634 Genes GS236717: [MeSH] Cell Survival : D002470
Expand Tier II Human 4661 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier I Mouse MP 54 Genes GS165142: MP:0003732 abnormal retinal outer plexiform layer morphology
Expand Tier II Human 99 Genes GS235593: [MeSH] Optic Nerve Diseases : D009901
Expand Tier II Human 15702 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 1188 Genes GS237832: [MeSH] Response Elements : D020218
Expand Tier II Human 3056 Genes GS245413: [MeSH] TGF-beta Superfamily Proteins : D055411
Expand Tier I Human GO 2711 Genes GS199273: GO:0043233 organelle lumen
Expand Tier I Human 715 Genes GS227535: MSigDB Geneset - TGCCAAR_V$NF1_Q6
Expand Tier I Human 156 Genes GS172363: HP:0004324 Increased body weight
Expand Tier II Rat 1082 Genes GS224178: Bone structure and strength QTL 69 (Bss69 Published QTL Chr 1)
Expand Tier I Mouse GO 4619 Genes GS191019: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier II Human 274 Genes GS244494: [MeSH] Circadian Rhythm Signaling Peptides and Proteins : D056925
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier II Human 7591 Genes GS239955: [MeSH] Amino Acid Motifs : D020816
Expand Tier I Mouse GO 3776 Genes GS187887: GO:0080090 regulation of primary metabolic process
Expand Tier II Human 3455 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 63 Genes GS236358: [MeSH] Retinal Neoplasms : D019572
Expand Tier II Human 14581 Genes GS241611: [MeSH] Organic Chemistry Processes : D055602
Expand Tier I Mouse MP 632 Genes GS168389: MP:0001186 pigmentation phenotype
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human 189 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 172 Genes GS243778: [MeSH] S100 Calcium Binding Protein G : D064030
Expand Tier I Human GO 2878 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 1807 Genes GS238780: [MeSH] Head : D006257
Expand Tier II Human 4590 Genes GS241946: [MeSH] Gene Regulatory Networks : D053263
Expand Tier I Mouse GO 4353 Genes GS192017: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Mouse MP 22 Genes GS166388: MP:0006068 abnormal horizontal cell morphology
Expand Tier II Human 7025 Genes GS239838: [MeSH] Luminescent Proteins : D008164
Expand Human 195 Genes GS222320: Genes associated with high risk of intellectual disability.
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 45 Genes GS174869: HP:0000551 Abnormality of color vision
Expand Tier I Mouse GO 3080 Genes GS177265: GO:0048731 system development
Expand Tier I Human GO 4138 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse GO 3865 Genes GS193238: GO:0031323 regulation of cellular metabolic process
Expand Tier I Human GO 3891 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 GO 3597 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 II Human 9980 Genes GS243345: [MeSH] Alternative Splicing : D017398
Expand Tier II Human 9719 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 1065 Genes GS237582: [MeSH] DEAD-box RNA Helicases : D053487
Expand Tier II Human 14842 Genes GS237183: [MeSH] Growth and Development : D048788
Expand Tier II Human 9858 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier II Human 208 Genes GS244365: [MeSH] Retinal Cone Photoreceptor Cells : D017949
Expand Tier I Human 389 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human GO 2092 Genes GS209551: GO:0031981 nuclear lumen
Expand Tier I Mouse MP 9 Genes GS168142: MP:0008583 absent photoreceptor inner segment
Expand Tier II Human 635 Genes GS237772: [MeSH] Feedback, Physiological : D025461
Expand Tier I Mouse GO 4114 Genes GS193414: GO:0044249 cellular biosynthetic process
Expand Tier I Human GO 818 Genes GS197472: GO:0044451 nucleoplasm part
Expand Tier II Human 4022 Genes GS234926: [MeSH] Epithelium : D004848
Expand Tier III Mouse 758 Genes GS225467: Differentially expressed in NAc cocaine-conditioned mice.
Expand Tier II Human 6705 Genes GS234738: [MeSH] Proto-Oncogene Proteins : D011518
Expand Tier I Human 563 Genes GS232301: PC Geneset - "GGATTA_V$PITX2_Q2" pathway genes
Expand Human 70 Genes GS221898: RetNet genes linked to retinitis pigmentosa (RP)
Expand Tier II Human 12291 Genes GS238872: [MeSH] Central Nervous System : D002490
Expand Tier II Human 2842 Genes GS237788: [MeSH] Acyltransferases : D000217
Expand Tier II Human 160 Genes GS234779: [MeSH] Mitochondrial Diseases : D028361
Expand Tier II Human 7543 Genes GS239550: [MeSH] Apoptosis : D017209
Expand Tier I Mouse MP 323 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 II Human 15855 Genes GS239444: [MeSH] Biological Evolution : D005075
Expand Tier II Human 56846 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier II Human 24839 Genes GS237194: [MeSH] Physiological Phenomena : D010829
Expand Tier II Human 8660 Genes GS239079: [MeSH] Cell Membrane : D002462
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier II Human 6533 Genes GS244610: [MeSH] Nervous System Diseases : D009422
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier II Mouse 980 Genes GS135458: bone mineral density 4 (Bomd4, Published QTL Chr 7)
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier II Human 8635 Genes GS239266: [MeSH] Morphogenesis : D009024
Expand Tier II Human 6240 Genes GS236309: [MeSH] Viral Regulatory and Accessory Proteins : D054334
Expand Tier I Human 124 Genes GS175492: HP:0000512 Abnormal electroretinogram
Expand Tier I Human GO 1391 Genes GS193937: GO:0006366 transcription from RNA polymerase II promoter
Expand Tier II Human 67553 Genes GS240572: [MeSH] DNA : D004247
Expand Tier II Human 670 Genes GS240521: [MeSH] p300-CBP Transcription Factors : D050880
Expand Tier II Human 5111 Genes GS242217: [MeSH] Muscle Proteins : D009124
Expand Tier II Human 2552 Genes GS243025: [MeSH] Neuroglia : D009457
Expand Human 24 Genes GS221927: Targeted exome capture and sequencing identifies novel PRPF31 mutations in autosomal dominant retinitis pigmentosa (RP) in Chinese families
Expand Tier I Human 36 Genes GS174701: HP:0000556 Retinal dystrophy
Expand Tier II Human 16067 Genes GS239024: [MeSH] Cytoplasmic Structures : D022083
Expand Tier II Human 43280 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier I Human GO 2310 Genes GS195643: GO:0003677 DNA binding
Expand Tier I Human GO 1839 Genes GS198572: GO:0010604 positive regulation of macromolecule metabolic process
Expand Tier II Human 65203 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier II Human 1950 Genes GS235382: [MeSH] Transgenes : D019076
Expand Tier II Human 774 Genes GS239663: [MeSH] Deoxyuridine : D003857
Expand Tier II Human 4671 Genes GS236527: [MeSH] Species Specificity : D013045
Expand Tier II Human 1975 Genes GS243180: [MeSH] Pigments, Biological : D010860
Expand Tier II Human 14624 Genes GS236362: [MeSH] Organic Chemistry Phenomena : D055601
Expand Tier I Human GO 999 Genes GS195340: GO:0045893 positive regulation of transcription, DNA-dependent
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Human 528 Genes GS231724: PC Geneset - "TGAYRTCA_V$ATF3_Q6" pathway genes
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier II Human 629 Genes GS235117: [MeSH] Interneurons : D007395
Expand Tier II Human 627 Genes GS236902: [MeSH] Orphan Nuclear Receptors : D057093
Expand Tier I Mouse MP 3159 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Human 177 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier II Human 15724 Genes GS239132: [MeSH] Gene Expression Regulation, Developmental : D018507
Expand Tier II Human 565 Genes GS241436: [MeSH] Spinal Cord Diseases : D013118
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier II Human 480 Genes GS235824: [MeSH] 5' Untranslated Regions : D020121
Expand Tier II Human 18300 Genes GS238771: [MeSH] Transferases : D014166
Expand Tier II Human 61 Genes GS238726: [MeSH] Blindness : D001766
Expand Tier II Human 79329 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier II Human 67130 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier I Human 169 Genes GS173988: HP:0000501 Glaucoma
Expand Tier I Human GO 3099 Genes GS206544: GO:2000112 regulation of cellular macromolecule biosynthetic process
Expand Tier I Mouse GO 3021 Genes GS182703: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Human GO 1255 Genes GS210178: GO:0031328 positive regulation of cellular biosynthetic process
Expand Tier I Human 248 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Human 578 Genes GS228870: MSigDB Geneset - GGATTA_V$PITX2_Q2
Expand Tier I Mouse MP 959 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier II Human 7601 Genes GS234579: [MeSH] Phylogeny : D010802
Expand Tier I Human 280 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human GO 1214 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 4098 Genes GS235532: [MeSH] Central Nervous System Diseases : D002493
Expand Tier I Human 89 Genes GS176988: HP:0008046 Abnormality of the retinal vasculature
Expand Tier I Mouse GO 4500 Genes GS186790: GO:0006725 cellular aromatic compound metabolic process
Expand Tier II Human 5833 Genes GS242178: [MeSH] Neoplasms by Site : D009371
Expand Tier II Human 59585 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier II Human 62071 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier I Human GO 5400 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 1197 Genes GS199501: GO:0051173 positive regulation of nitrogen compound metabolic process
Expand Tier II Human 16797 Genes GS241667: [MeSH] Cytoplasm : D003593
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier II Human 7284 Genes GS236354: [MeSH] Gene Deletion : D017353
Expand Tier II Human 89 Genes GS244027: [MeSH] Eye Neoplasms : D005134
Expand Tier II Human 3405 Genes GS235775: [MeSH] Basic Helix-Loop-Helix Transcription Factors : D051792
Expand Tier I Human GO 4129 Genes GS206329: GO:0060255 regulation of macromolecule metabolic process
Expand Tier II Human 10296 Genes GS240252: [MeSH] Intercellular Signaling Peptides and Proteins : D036341
Expand Tier I Mouse MP 125 Genes GS163943: MP:0005201 abnormal retinal pigment epithelium morphology
Expand Tier II Human 8099 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier I Human 171 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier II Human 22 Genes GS241472: [MeSH] Optic Atrophy, Hereditary, Leber : D029242
Expand Tier II Human 23706 Genes GS235056: [MeSH] Peptides : D010455
Expand Tier II Human 47536 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier I Human GO 5908 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 3522 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Mouse 2 Genes GS231286: OMIM Geneset - Genes with known associations to "Cone-rod dystrophy, X-linked, 1"
Expand Tier I Human 122 Genes GS171946: HP:0002269 Abnormality of neuronal migration
Expand Tier II Human 9754 Genes GS243806: [MeSH] Time : D013995
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 36279 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier II Human 764 Genes GS241397: [MeSH] Bromodeoxyuridine : D001973
Expand Tier I Mouse GO 8386 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier I Mouse 1026 Genes GS128580: BECs at LORR Recovery Chr# 7
Expand Tier I Mouse GO 1149 Genes GS186178: GO:0045935 positive regulation of nucleobase-containing compound metabolic process
Expand Tier II Human 38809 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Human 19302 Genes GS236470: [MeSH] DNA-Binding Proteins : D004268
Expand Tier II Human 3004 Genes GS240265: [MeSH] Neurons, Afferent : D009475
Expand Tier I Mouse GO 2588 Genes GS187343: GO:0006351 transcription, DNA-dependent
Expand Tier II Human 21260 Genes GS238232: [MeSH] Nucleoproteins : D009698
Expand Tier II Human 9078 Genes GS239596: [MeSH] Expressed Sequence Tags : D020224
Expand Tier II Human 15356 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 361 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 1476 Genes GS203369: GO:0005654 nucleoplasm
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Mouse GO 8942 Genes GS185492: GO:0050789 regulation of biological process
Expand Tier II Human 314 Genes GS236508: [MeSH] Leucine Zippers : D016350
Expand Tier II Human 3936 Genes GS245455: [MeSH] Metabolic Diseases : D008659
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 167 Genes GS232340: PC Geneset - "V$MSX1_01" pathway genes
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier II Human 3784 Genes GS235626: [MeSH] Brain Diseases : D001927
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse GO 1777 Genes GS184445: GO:0044428 nuclear part
Expand Tier I Human 510 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Mouse GO 5892 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 264 Genes GS240358: [MeSH] Opsins : D055355
Expand Tier II Human 13521 Genes GS245544: [MeSH] Conserved Sequence : D017124
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 Mouse GO 1147 Genes GS191150: GO:0010557 positive regulation of macromolecule biosynthetic process
Expand Tier I Mouse GO 713 Genes GS177859: GO:0045944 positive regulation of transcription from RNA polymerase II promoter
Expand Tier II Human 8754 Genes GS241960: [MeSH] Protein Structure, Secondary : D017433
Expand Tier II Human 2379 Genes GS243535: [MeSH] Neurodegenerative Diseases : D019636
Expand Tier I Mouse 195 Genes GS227702: MSigDB Geneset - GSE32423_CTRL_VS_IL7_MEMORY_CD8_TCELL_DN
Expand Tier I Human 532 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier II Human 50108 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier I Human 513 Genes GS229037: MSigDB Geneset - WTTGKCTG_UNKNOWN
Expand Tier II Human 58105 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier I Human GO 4292 Genes GS204746: GO:0080090 regulation of primary metabolic process
Expand Tier II Human 32929 Genes GS243578: [MeSH] Reading Frames : D016364
Expand Tier II Human 14459 Genes GS239072: [MeSH] Recombinant Proteins : D011994
Expand Tier I Human GO 2479 Genes GS201249: GO:0044428 nuclear part
Expand Tier II Human 246 Genes GS236744: [MeSH] Ataxia : D001259
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human 95 Genes GS176989: HP:0008047 Abnormality of the vasculature of the eye
Expand Tier II Human 1220 Genes GS236872: [MeSH] Pyrimidine Nucleosides : D011741
Expand Tier II Human 4761 Genes GS236987: [MeSH] Tumor Suppressor Proteins : D025521
Expand Tier II Human 29996 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier II Human 4413 Genes GS239859: [MeSH] Prosencephalon : D016548
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier II Human 2477 Genes GS237394: [MeSH] Point Mutation : D017354
Expand Tier I Human GO 3603 Genes GS198456: GO:0019438 aromatic compound biosynthetic process
Expand Tier II Human 1084 Genes GS244978: [MeSH] LIM Domain Proteins : D060588
Expand Tier II Rat 713 Genes GS224075: Bone structure and strength QTL 86 (Bss86 Published QTL Chr 1)
Expand Tier II Human 72 Genes GS237259: [MeSH] Transcription Factor Brn-3B : D050820
Expand Tier II Human 12085 Genes GS240544: [MeSH] Pregnancy : D011247
Expand Tier II Human 649 Genes GS241346: [MeSH] Genome, Bacterial : D016680
Expand Tier I Mouse GO 2907 Genes GS181667: GO:0019438 aromatic compound biosynthetic process
Expand Tier II Human 102 Genes GS238692: [MeSH] Parvalbumins : D010320
Expand Tier I Human GO 3277 Genes GS194088: GO:0003676 nucleic acid binding
Expand Tier II Human 20421 Genes GS237820: [MeSH] DNA Primers : D017931
Expand Tier II Human 5853 Genes GS241597: [MeSH] Disease Models, Animal : D004195
Expand Tier II Rat 1129 Genes GS224484: Heart rate QTL 1 (Hrtrt1 Published QTL Chr 1)
Expand Tier I Mouse GO 3090 Genes GS188511: GO:0010468 regulation of gene expression
Expand Tier II Human 23569 Genes GS235276: [MeSH] Signal Transduction : D015398
Expand Tier II Human 14819 Genes GS244426: [MeSH] Tumor Cells, Cultured : D014407
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Mouse MP 459 Genes GS163138: MP:0005253 abnormal eye physiology
Expand Tier II Human 13237 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 8331 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 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier II Human 12343 Genes GS236576: [MeSH] Promoter Regions, Genetic : D011401
Expand Tier II Human 11815 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 3795 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 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 II Rat 707 Genes GS224774: Food consumption QTL 2 (Foco2 Published QTL Chr 1)
Expand Tier II Human 572 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 18755 Genes GS242691: [MeSH] Embryonic Structures : D004628
Expand Tier I Human 199 Genes GS228538: MSigDB Geneset - GSE3982_CTRL_VS_PMA_STIM_EOSINOPHIL_DN
Expand Tier I Mouse GO 3382 Genes GS191021: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human GO 3468 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 899 Genes GS84191: alcohol preference 7 QTL (Ap7q, Published QTL, Chr 7)
Expand Tier I Human GO 2539 Genes GS203335: GO:0048513 organ development
Expand Tier II Human 2796 Genes GS239355: [MeSH] Body Patterning : D019521
Expand Tier II Human 58261 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
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 9717 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 30111 Genes GS244835: [MeSH] Chromosomes : D002875
Expand Tier I Human 381 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Mouse MP 223 Genes GS169032: MP:0005551 abnormal eye electrophysiology
Expand Tier I Human GO 676 Genes GS196540: GO:0043565 sequence-specific DNA binding
Expand Tier II Human 161 Genes GS238585: [MeSH] Retinitis Pigmentosa : D012174
Expand Tier I Mouse MP 23 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 73996 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 5 Genes GS164848: MP:0006075 abnormal retinal cone bipolar cell morphology
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier II Human 9876 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 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 2857 Genes GS195291: GO:0006355 regulation of transcription, DNA-dependent
Expand Tier I Human GO 5337 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier II Human 58105 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 29719 Genes GS237296: [MeSH] RNA, Antisense : D016372
Expand Tier II Human 4977 Genes GS239472: [MeSH] Homeodomain Proteins : D018398
Expand Tier I Human GO 3325 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 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Human 386 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier II Human 41481 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier II Human 109 Genes GS237886: [MeSH] Vision Disorders : D014786
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 7650 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier II Human 52588 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Human GO 1179 Genes GS208060: GO:0010557 positive regulation of macromolecule biosynthetic process
Expand Tier II Human 2465 Genes GS234230: [MeSH] Glutathione Transferase : D005982
Expand Tier I Mouse GO 4478 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 I Mouse GO 765 Genes GS187370: GO:0001071 nucleic acid binding transcription factor activity
Expand Tier II Human 20860 Genes GS239302: [MeSH] Oligonucleotides : D009841
Expand Tier II Human 3607 Genes GS240531: [MeSH] Neoplasms, Glandular and Epithelial : D009375
Expand Tier II Human 1917 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 I Mouse 200 Genes GS230015: MSigDB Geneset - GSE1448_CTRL_VS_ANTI_VALPHA2_DP_THYMOCYTE_UP
Expand Tier II Rat 1027 Genes GS224721: Serum cholesterol QTL 36 (Scl36 Published QTL Chr 1)
Expand Tier I Human GO 14 Genes GS200472: GO:0030275 LRR domain binding
Expand Tier II Human 816 Genes GS239537: [MeSH] Uridine : D014529
Expand Tier II Human 1521 Genes GS241000: [MeSH] Ribonucleases : D012260
Expand Tier II Human 1485 Genes GS242199: [MeSH] Diencephalon : D004027
Expand Tier I Mouse GO 3293 Genes GS186214: GO:0048518 positive regulation of biological process
Expand Tier II Human 771 Genes GS241594: [MeSH] Neurosecretory Systems : D009490
Expand Tier I Human GO 3714 Genes GS194038: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier II Human 3263 Genes GS237180: [MeSH] Genetic Markers : D005819
Expand Tier I Rat DRG 3886 Genes provisional GS86769: Table S2: HIPPOCAMPUS MGC MICROARRAY [DRG]
Expand Tier II Human 19354 Genes GS242551: [MeSH] Physiological Processes : D055705
Expand Tier II Human 10034 Genes GS243396: [MeSH] Neoplasm Proteins : D009363
Expand Tier I Human 64 Genes GS174379: HP:0002084 Encephalocele
Expand Tier I Mouse MP 34 Genes GS170724: MP:0002561 abnormal circadian phase
Expand Tier II Human 54 Genes GS241434: [MeSH] Retinal Bipolar Cells : D051245
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier II Human 13987 Genes GS237817: [MeSH] Cell Line, Tumor : D045744
Expand Tier II Human 5073 Genes GS238252: [MeSH] Neoplasms by Histologic Type : D009370
Expand Tier I Human 231 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human 42 Genes GS174449: HP:0001123 Visual field defect
Expand Tier II Human 28877 Genes GS238592: [MeSH] Cells, Cultured : D002478
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 136 Genes GS232407: PC Geneset - "V$MEIS1BHOXA9_01" pathway genes
Expand Tier I Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier II Mouse 897 Genes GS135415: bronchial hyperresponsiveness 6 (Bhr6, Published QTL Chr 7)
Expand Tier I Human 92 Genes GS171656: HP:0000610 Abnormality of the choroid
Expand Tier II Human 1389 Genes GS245899: [MeSH] Genes, Developmental : D050437
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse GO 4651 Genes GS177310: GO:1901360 organic cyclic compound metabolic process
Expand Tier II Human 2690 Genes GS239924: [MeSH] Intercellular Junctions : D007365
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier II Human 1979 Genes GS237451: [MeSH] Neuroectodermal Tumors : D017599
Expand Tier I Human GO 3304 Genes GS210180: GO:0031326 regulation of cellular biosynthetic process
Expand Tier II Human 406 Genes GS239087: [MeSH] S100 Proteins : D009418
Expand Tier II Rat 734 Genes GS224623: Serum cholesterol level QTL 6 (Scl6 Published QTL Chr 1)
Expand Tier I Human 141 Genes GS230584: MSigDB Geneset - V$MEIS1BHOXA9_01
Expand Tier II Human 4400 Genes GS240538: [MeSH] Embryonic Development : D047108
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human GO 3334 Genes GS205622: GO:0009889 regulation of biosynthetic process
Expand Tier II Human 1364 Genes GS243263: [MeSH] Genes, Homeobox : D005801
Expand Tier I Mouse GO 2835 Genes GS191151: GO:0010556 regulation of macromolecule biosynthetic process
Expand Tier I Mouse MP 135 Genes GS163942: MP:0005200 abnormal eye pigment epithelium morphology
Expand Tier II Human 3012 Genes GS234181: [MeSH] Retina : D012160
Expand Tier I Human GO 1079 Genes GS209282: GO:0010628 positive regulation of gene expression
Expand Tier I Mouse GO 3757 Genes GS189460: GO:0060255 regulation of macromolecule metabolic process
Expand Tier II Human 20775 Genes GS245804: [MeSH] Transcription Factors : D014157
Expand Tier I Human GO 3853 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Mouse GO 5247 Genes GS178448: GO:0005634 nucleus
Expand Tier II Human 23211 Genes GS235538: [MeSH] Protein Binding : D011485
Expand Tier II Human 2111 Genes GS242842: [MeSH] Neoplasms, Germ Cell and Embryonal : D009373
Expand Tier I Human 288 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier II Human 5185 Genes GS234976: [MeSH] Acylation : D000215
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 691 Genes GS232110: PC Geneset - "TGCCAAR_V$NF1_Q6" pathway genes
Expand Tier I Mouse MP 702 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier II Human 2555 Genes GS242366: [MeSH] Inheritance Patterns : D040582
Expand Tier II Rat 1482 Genes GS224476: Bone structure and strength QTL 55 (Bss55 Published QTL Chr 1)
Expand Tier I Human GO 3180 Genes GS208061: GO:0010556 regulation of macromolecule biosynthetic process
Expand Tier II Human 2276 Genes GS235071: [MeSH] Acetyltransferases : D000123
Expand Tier I Mouse GO 2536 Genes GS178537: GO:0006355 regulation of transcription, DNA-dependent
Expand Tier II Human 9707 Genes GS235744: [MeSH] Neurons : D009474
Expand Tier I Mouse MP 433 Genes GS165390: MP:0003224 neuron degeneration
Expand Tier II Human 6187 Genes GS243844: [MeSH] Receptors, G-Protein-Coupled : D043562
Expand Tier II Human 640 Genes GS241148: [MeSH] Multipotent Stem Cells : D039902
Expand Tier II Human 650 Genes GS243363: [MeSH] Polymorphism, Single-Stranded Conformational : D018807
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier II Human 13218 Genes GS245439: [MeSH] Protein Kinases : D011494
Expand Tier II Human 1090 Genes GS238326: [MeSH] Galactosidases : D005696
Expand Tier II Human 554 Genes GS241350: [MeSH] Afferent Pathways : D000344
Expand Tier I Mouse GO 327 Genes GS187984: GO:0003682 chromatin binding
Expand Tier II Human 278 Genes GS241278: [MeSH] Cerebellar Diseases : D002526
Expand Tier II Rat 1641 Genes GS223264: Neuroinflammation QTL 8 (Neuinf8 Published QTL Chr 1)
Expand Tier II Human 58766 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier I Human 209 Genes GS173206: HP:0003241 Genital hypoplasia
Expand Tier I Human 157 Genes GS171968: HP:0000405 Conductive hearing impairment
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 II Human 977 Genes GS242523: [MeSH] Oligonucleotides, Antisense : D016376
Expand Tier I Mouse 199 Genes GS227534: MSigDB Geneset - GSE17721_POLYIC_VS_GARDIQUIMOD_0.5H_BMDM_DN
Expand Tier II Mouse 649 Genes GS135679: Crhr1 transcript abundance QTL 1 (Crhr1taq1, Published QTL Chr 7)
Expand Tier II Human 152 Genes GS238549: [MeSH] Choline O-Acetyltransferase : D002795
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier II Human 1062 Genes GS236204: [MeSH] beta-Galactosidase : D001616
Expand Tier I Human 158 Genes GS171900: HP:0011452 Functional abnormality of the middle ear
Expand Tier I Mouse MP 11449 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier II Human 23476 Genes GS237836: [MeSH] Carrier Proteins : D002352
Expand Tier I Human 191 Genes GS229536: MSigDB Geneset - GSE10325_BCELL_VS_LUPUS_BCELL_UP
Expand Tier I Mouse 2 Genes GS230945: OMIM Geneset - Genes with known associations to "Macular degeneration, X-linked atrophic"
Expand Tier I Human 176 Genes GS230657: MSigDB Geneset - GSE26928_EFF_MEM_VS_CENTR_MEM_CD4_TCELL_DN
Expand Tier II Human 5087 Genes GS234776: [MeSH] Endocrine System : D004703
Expand Tier II Rat 1758 Genes GS223048: Hepatocarcinoma susceptibility QTL 2 (Hcas2 Published QTL Chr 1)
Expand Tier I Human GO 539 Genes GS199393: GO:0019904 protein domain specific binding
Expand Tier I Mouse MP 27 Genes GS166481: MP:0008518 retinal outer nuclear layer degeneration
Expand Tier II Human 6867 Genes GS243608: [MeSH] Viral Proteins : D014764
Expand Tier II Human 16221 Genes GS239275: [MeSH] Intracellular Signaling Peptides and Proteins : D047908
Expand Tier II Human 58901 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Mouse MP 18 Genes GS163167: MP:0006074 abnormal retinal rod bipolar cell morphology
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Mouse GO 3136 Genes GS187045: GO:0016070 RNA metabolic process
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human GO 792 Genes GS205616: GO:0009887 organ morphogenesis
Expand Tier II Human 134 Genes GS245568: [MeSH] Microphthalmia-Associated Transcription Factor : D051739
Expand Tier I Human GO 4354 Genes GS210182: GO:0031323 regulation of cellular metabolic process
Expand Tier II Human 61 Genes GS236134: [MeSH] Retinoblastoma : D012175
Expand Tier II Rat 710 Genes GS223509: Serum renin concentration QTL 4 (Srn4 Published QTL Chr 1)
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier II Human 482 Genes GS235047: [MeSH] Retinal Degeneration : D012162
Expand Tier II Human 2569 Genes GS235802: [MeSH] Homeostasis : D006706
Expand Tier II Human 3539 Genes GS246002: [MeSH] Receptors, Cytoplasmic and Nuclear : D018160
Expand Tier II Human 231 Genes GS238686: [MeSH] Retinal Rod Photoreceptor Cells : D017948
Expand Tier II Human 15607 Genes GS241444: [MeSH] Reproductive Physiological Phenomena : D055703
Expand Tier II Human 499 Genes GS235763: [MeSH] Chromosomes, Human, Pair 19 : D002888
Expand Tier II Human 641 Genes GS241711: [MeSH] Operon : D009876
Expand Tier II Human 17 Genes GS244912: [MeSH] Nuclear Receptor Subfamily 1, Group F, Member 2 : D057095
Expand Tier II Human 1026 Genes GS245475: [MeSH] Chromosomes, Human, 19-20 : D002903
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Human 62 Genes GS221933: Mutations of 60 known causative genes in 157 families with retinitis pigmentosa (RP) based on exome sequencing
Expand Tier II Human 2732 Genes GS239261: [MeSH] Calcium-Binding Proteins : D002135
Expand Tier II Human 971 Genes GS244545: [MeSH] Communication : D003142
Expand Tier II Rat 2769 Genes GS223189: Non-insulin dependent diabetes mellitus QTL 44 (Niddm44 Published QTL Chr 1)
Expand Tier II Human 36882 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
Expand Tier II Rat 1272 Genes GS223302: Bone mineral density QTL 1 (Bmd1 Published QTL Chr 1)
Expand Tier I Human 8 Genes GS171975: HP:0000533 Chorioretinal atrophy
Expand Tier II Human 6413 Genes GS235807: [MeSH] Cytokines : D016207
Expand Tier I Human 284 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Mouse 2105 Genes GS128573: Ethanol Induced Hypothermia Chr# 7
Expand Tier I Mouse GO 2981 Genes GS177761: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier II Mouse 581 Genes GS136298: maternal performance (Mprf, Published QTL Chr 7)
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 209 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Human GO 3271 Genes GS199267: GO:0043234 protein complex
Expand Tier II Human 172 Genes GS239403: [MeSH] Calbindins : D064026
Expand Tier II Human 898 Genes GS239468: [MeSH] Periodicity : D010507
Expand Tier II Human 1528 Genes GS242356: [MeSH] Photoreceptor Cells : D010786
Expand Tier II Mouse 971 Genes GS136602: sperm beat cross frequency (Sbcf, Published QTL Chr 7)