Gene Details



SIX1 and homologs in 1 species are found in 424 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 Human GO 91 Genes GS197114: GO:0043524 negative regulation of neuron apoptotic process
Expand Tier I Human GO 1050 Genes GS202082: GO:0051254 positive regulation of RNA metabolic process
Expand Tier I Human GO 279 Genes GS206188: GO:0048589 developmental growth
Expand Tier I Human 270 Genes GS176826: HP:0000202 Oral cleft
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human GO 195 Genes GS206380: GO:0001763 morphogenesis of a branching structure
Expand Tier I Human GO 14 Genes GS194513: GO:0061323 cell proliferation involved in heart morphogenesis
Expand Tier I Human GO 348 Genes GS197668: GO:0051241 negative regulation of multicellular organismal process
Expand Tier I Human GO 3108 Genes GS198685: GO:0048522 positive regulation of cellular process
Expand Tier I Human GO 248 Genes GS206757: GO:0072001 renal system development
Expand Tier I Human GO 43 Genes GS201786: GO:0021545 cranial nerve development
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human GO 5184 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 274 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Human GO 11 Genes GS198010: GO:0072164 mesonephric tubule development
Expand Tier I Human CTD 62 Genes GS124975: Lithium Chloride interacting genes (MeSH:D018021) in CTD
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 280 Genes GS175900: HP:0009118 Aplasia/Hypoplasia of the mandible
Expand Tier I Human GO 1171 Genes GS203018: GO:0045935 positive regulation of nucleobase-containing compound metabolic process
Expand Tier I Human GO 688 Genes GS210376: GO:0007417 central nervous system development
Expand Tier I Human GO 3304 Genes GS210180: GO:0031326 regulation of cellular biosynthetic process
Expand Tier I Human GO 429 Genes GS210555: GO:0007389 pattern specification process
Expand Tier I Human GO 31 Genes GS206242: GO:0090102 cochlea development
Expand Tier I Human GO 222 Genes GS205296: GO:0045165 cell fate commitment
Expand Tier I Human 70 Genes GS177025: HP:0010628 Facial palsy
Expand Tier I Human CTD 916 Genes GS121965: Amiodarone interacting genes (MeSH:D000638) in CTD
Expand Tier I Human GO 3334 Genes GS205622: GO:0009889 regulation of biosynthetic process
Expand Tier I Human GO 652 Genes GS208657: GO:0008284 positive regulation of cell proliferation
Expand Tier I Human GO 7 Genes GS202535: GO:0003266 regulation of secondary heart field cardioblast proliferation
Expand Tier I Human GO 161 Genes GS207039: GO:0060485 mesenchyme development
Expand Tier I Human GO 1066 Genes GS196002: GO:0048699 generation of neurons
Expand Tier I Human GO 35 Genes GS202574: GO:0048701 embryonic cranial skeleton morphogenesis
Expand Tier I Human GO 329 Genes GS198056: GO:0048568 embryonic organ development
Expand Tier I Human GO 1079 Genes GS209282: GO:0010628 positive regulation of gene expression
Expand Tier I Human GO 1334 Genes GS200555: GO:0010605 negative regulation of macromolecule metabolic process
Expand Tier I Human GO 3853 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human 84 Genes GS175531: HP:0000003 Multicystic kidney dysplasia
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 I Human GO 559 Genes GS195206: GO:0002520 immune system development
Expand Tier I Human GO 133 Genes GS197707: GO:0016331 morphogenesis of embryonic epithelium
Expand Tier I Human GO 5348 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human 139 Genes GS171000: HP:0000083 Renal insufficiency
Expand Tier I Human GO 3180 Genes GS208061: GO:0010556 regulation of macromolecule biosynthetic process
Expand Tier I Human GO 908 Genes GS202930: GO:2000113 negative regulation of cellular macromolecule biosynthetic process
Expand Tier I Human GO 132 Genes GS209984: GO:0050954 sensory perception of mechanical stimulus
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human GO 580 Genes GS199789: GO:0043069 negative regulation of programmed cell death
Expand Tier I Human GO 2653 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Human GO 8 Genes GS202533: GO:0003263 cardioblast proliferation
Expand Tier I Human GO 124 Genes GS210482: GO:0007605 sensory perception of sound
Expand Tier I Human GO 1098 Genes GS195083: GO:0007267 cell-cell signaling
Expand Tier I Human GO 490 Genes GS202261: GO:0001568 blood vessel development
Expand Tier I Human GO 1174 Genes GS207161: GO:0006928 cellular component movement
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human GO 91 Genes GS208230: GO:1901215 negative regulation of neuron death
Expand Tier I Human 24 Genes GS175426: HP:0010767 Sacrococcygeal pilonidal abnormality
Expand Tier I Human GO 598 Genes GS201231: GO:0060548 negative regulation of cell death
Expand Tier I Human GO 2711 Genes GS199273: GO:0043233 organelle lumen
Expand Tier I Human 157 Genes GS171968: HP:0000405 Conductive hearing impairment
Expand Tier I Human GO 4 Genes GS201298: GO:0072095 regulation of branch elongation involved in ureteric bud branching
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 49 Genes GS205637: GO:0060688 regulation of morphogenesis of a branching structure
Expand Tier I Human GO 4 Genes GS199688: GO:0072198 mesenchymal cell proliferation involved in ureter development
Expand Tier I Human GO 4014 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 158 Genes GS171900: HP:0011452 Functional abnormality of the middle ear
Expand Tier I Human GO 811 Genes GS195339: GO:0045892 negative regulation of transcription, DNA-dependent
Expand Tier I Human GO 145 Genes GS208229: GO:1901214 regulation of neuron death
Expand Tier I Human 106 Genes GS175048: HP:0006824 Cranial nerve paralysis
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 263 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Human GO 1555 Genes GS201869: GO:0008104 protein localization
Expand Tier I Human GO 82 Genes GS210615: GO:0045995 regulation of embryonic development
Expand Tier I Human GO 48 Genes GS197126: GO:0060993 kidney morphogenesis
Expand Tier I Human CTD 178 Genes GS124922: vanadyl sulfate interacting genes (MeSH:C034028) in CTD
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 44 Genes GS174484: HP:0000521 Abnormality of tear glands or tear production
Expand Tier I Human GO 792 Genes GS205616: GO:0009887 organ morphogenesis
Expand Tier I Human GO 5190 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Human GO 4575 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human GO 433 Genes GS203054: GO:0048514 blood vessel morphogenesis
Expand Tier I Human GO 169 Genes GS209954: GO:0003007 heart morphogenesis
Expand Tier I Human GO 4354 Genes GS210182: GO:0031323 regulation of cellular metabolic process
Expand Tier I Human GO 1533 Genes GS196282: GO:0012501 programmed cell death
Expand Tier I Human GO 4 Genes GS196476: GO:0072106 regulation of ureteric bud formation
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human GO 441 Genes GS209602: GO:0051960 regulation of nervous system development
Expand Tier I Human 404 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human GO 445 Genes GS200490: GO:0061061 muscle structure development
Expand Tier I Human GO 3 Genes GS206032: GO:0072513 positive regulation of secondary heart field cardioblast proliferation
Expand Tier I Human GO 4 Genes GS199687: GO:0072199 regulation of mesenchymal cell proliferation involved in ureter development
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 332 Genes GS206569: GO:0045664 regulation of neuron differentiation
Expand Tier I Human GO 2878 Genes GS206108: GO:2001141 regulation of RNA biosynthetic process
Expand Tier I Human GO 22 Genes GS207368: GO:0090189 regulation of branching involved in ureteric bud morphogenesis
Expand Tier I Human GO 782 Genes GS208559: GO:0040007 growth
Expand Tier I Human GO 180 Genes GS200705: GO:0060538 skeletal muscle organ development
Expand Tier I Human GO 2816 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Human CTD 5081 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human 2 Genes GS176509: HP:0009795 Branchial fistula
Expand Tier I Human GO 204 Genes GS196231: GO:0001822 kidney development
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 3 Genes GS176510: HP:0009794 Branchial anomaly
Expand Tier I Human GO 516 Genes GS194493: GO:0001944 vasculature development
Expand Tier I Human GO 931 Genes GS195273: GO:0070727 cellular macromolecule localization
Expand Tier I Human GO 37 Genes GS203325: GO:0003156 regulation of organ formation
Expand Tier I Human GO 40 Genes GS205363: GO:0010464 regulation of mesenchymal cell proliferation
Expand Tier I Human GO 3271 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human GO 52 Genes GS196771: GO:0048645 organ formation
Expand Tier I Human GO 156 Genes GS195919: GO:0051402 neuron apoptotic process
Expand Tier I Human GO 95 Genes GS197513: GO:0042472 inner ear morphogenesis
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 Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human GO 3891 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Human GO 36 Genes GS209419: GO:0002053 positive regulation of mesenchymal cell proliferation
Expand Tier I Human GO 1876 Genes GS210181: GO:0031325 positive regulation of cellular metabolic process
Expand Tier I Human GO 142 Genes GS196756: GO:0043523 regulation of neuron apoptotic process
Expand Tier I Human GO 4787 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human GO 2939 Genes GS202080: GO:0051252 regulation of RNA metabolic process
Expand Tier I Human 116 Genes GS172063: HP:0000107 Renal cysts
Expand Tier I Human GO 986 Genes GS210179: GO:0031327 negative regulation of cellular biosynthetic process
Expand Tier I Human 484 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human GO 1006 Genes GS196988: GO:0045595 regulation of cell differentiation
Expand Tier I Human GO 985 Genes GS204095: GO:0030182 neuron differentiation
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human GO 35 Genes GS197539: GO:0014812 muscle cell migration
Expand Tier I Human GO 1977 Genes GS204568: GO:0009893 positive regulation of metabolic process
Expand Tier I Human GO 3116 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human GO 2092 Genes GS209551: GO:0031981 nuclear lumen
Expand Tier I Human GO 48 Genes GS205367: GO:0010463 mesenchymal cell proliferation
Expand Tier I Human 44 Genes GS176179: HP:0000076 Vesicoureteral reflux
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human GO 7 Genes GS210543: GO:0021561 facial nerve development
Expand Tier I Human GO 2756 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 236 Genes GS171395: HP:0000175 Cleft palate
Expand Tier I Human GO 8 Genes GS202536: GO:0003264 regulation of cardioblast proliferation
Expand Tier I Human GO 14 Genes GS195249: GO:0072189 ureter development
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 5928 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human GO 818 Genes GS197472: GO:0044451 nucleoplasm part
Expand Tier I Human 238 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier I Human GO 493 Genes GS209225: GO:0007600 sensory perception
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 454 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human GO 3550 Genes GS203607: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Human GO 4 Genes GS210073: GO:0072107 positive regulation of ureteric bud formation
Expand Tier I Human GO 591 Genes GS195737: GO:0022603 regulation of anatomical structure morphogenesis
Expand Tier I Human GO 435 Genes GS197802: GO:0007423 sensory organ development
Expand Tier I Human GO 931 Genes GS199500: GO:0051172 negative regulation of nitrogen compound metabolic process
Expand Tier I Human GO 19 Genes GS197566: GO:0035909 aorta morphogenesis
Expand Tier I Human GO 20 Genes GS199029: GO:0048745 smooth muscle tissue development
Expand Tier I Human GO 298 Genes GS199757: GO:0035239 tube morphogenesis
Expand Tier I Human 346 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human GO 216 Genes GS198051: GO:0048562 embryonic organ morphogenesis
Expand Tier I Human GO 898 Genes GS201125: GO:0009790 embryo development
Expand Tier I Human 117 Genes GS174102: HP:0011799 Abnormality of facial soft tissue
Expand Tier I Human GO 1001 Genes GS204232: GO:0001071 nucleic acid binding transcription factor activity
Expand Tier I Human GO 288 Genes GS206898: GO:0001655 urogenital system development
Expand Tier I Human 395 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human GO 21 Genes GS206243: GO:0090103 cochlea morphogenesis
Expand Tier I Human GO 335 Genes GS194775: GO:0007517 muscle organ development
Expand Tier I Human GO 4 Genes GS210187: GO:0072172 mesonephric tubule formation
Expand Tier I Human GO 28 Genes GS202155: GO:0003401 axis elongation
Expand Tier I Human GO 15 Genes GS194202: GO:0060914 heart formation
Expand Tier I Human GO 919 Genes GS203019: GO:0045934 negative regulation of nucleobase-containing compound metabolic process
Expand Tier I Human 47 Genes GS171564: HP:0000383 Abnormality of periauricular region
Expand Tier I Human GO 48 Genes GS203320: GO:0003151 outflow tract morphogenesis
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 1235 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human GO 136 Genes GS202180: GO:0035270 endocrine system development
Expand Tier I Human GO 1766 Genes GS194455: GO:0051239 regulation of multicellular organismal process
Expand Tier I Human GO 529 Genes GS194284: GO:0048534 hematopoietic or lymphoid organ development
Expand Tier I Human 576 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human GO 1820 Genes GS205820: GO:0033036 macromolecule localization
Expand Tier I Human 78 Genes GS175969: HP:0000069 Abnormality of the ureter
Expand Tier I Human GO 27 Genes GS198886: GO:0010092 specification of organ identity
Expand Tier I Human GO 680 Genes GS205338: GO:0051094 positive regulation of developmental process
Expand Tier I Human 30 Genes GS171190: HP:0000413 Atresia of the external auditory canal
Expand Tier I Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human GO 315 Genes GS204842: GO:0003682 chromatin binding
Expand Tier I Human GO 1430 Genes GS206618: GO:0050793 regulation of developmental process
Expand Tier I Human GO 6 Genes GS207454: GO:0021610 facial nerve morphogenesis
Expand Tier I Human GO 1241 Genes GS196080: GO:0040011 locomotion
Expand Tier I Human GO 618 Genes GS196553: GO:0005730 nucleolus
Expand Tier I Human GO 1322 Genes GS207282: GO:0031324 negative regulation of cellular metabolic process
Expand Tier I Human GO 1533 Genes GS208664: GO:0008283 cell proliferation
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 1391 Genes GS193937: GO:0006366 transcription from RNA polymerase II promoter
Expand Tier I Human 8 Genes GS176880: HP:0100267 Lip pit
Expand Tier I Human GO 62 Genes GS198778: GO:0021675 nerve development
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 1155 Genes GS206237: GO:0042981 regulation of apoptotic process
Expand Tier I Human GO 13 Genes GS198425: GO:2000136 regulation of cell proliferation involved in heart morphogenesis
Expand Tier I Human GO 172 Genes GS200488: GO:0007519 skeletal muscle tissue development
Expand Tier I Human GO 4682 Genes GS205364: GO:0010467 gene expression
Expand Tier I Human GO 904 Genes GS206715: GO:0051674 localization of cell
Expand Tier I Human GO 386 Genes GS207498: GO:0001501 skeletal system development
Expand Tier I Human GO 595 Genes GS199620: GO:0060429 epithelium development
Expand Tier I Human GO 1516 Genes GS194172: GO:0006915 apoptotic process
Expand Tier I Human GO 3116 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 1197 Genes GS201696: GO:0010941 regulation of cell death
Expand Tier I Human GO 2310 Genes GS195643: GO:0003677 DNA binding
Expand Tier I Human GO 12 Genes GS205801: GO:0072163 mesonephric epithelium development
Expand Tier I Human GO 1775 Genes GS194586: GO:0002376 immune system process
Expand Tier I Human GO 1839 Genes GS198572: GO:0010604 positive regulation of macromolecule metabolic process
Expand Tier I Human GO 489 Genes GS197667: GO:0051240 positive regulation of multicellular organismal process
Expand Tier I Human GO 51 Genes GS204715: GO:0060840 artery development
Expand Tier I Human GO 5120 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Human GO 1095 Genes GS208716: GO:2000026 regulation of multicellular organismal development
Expand Tier I Human GO 306 Genes GS209956: GO:0003002 regionalization
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 GO 333 Genes GS196532: GO:0000975 regulatory region DNA binding
Expand Tier I Human GO 1691 Genes GS209960: GO:0003008 system process
Expand Tier I Human GO 25 Genes GS202816: GO:0001759 organ induction
Expand Tier I Human GO 49 Genes GS195896: GO:0048483 autonomic nervous system development
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 1278 Genes GS201265: GO:0009891 positive regulation of biosynthetic process
Expand Tier I Human GO 466 Genes GS204511: GO:0048729 tissue morphogenesis
Expand Tier I Human GO 398 Genes GS209887: GO:0050767 regulation of neurogenesis
Expand Tier I Human GO 273 Genes GS201756: GO:0042692 muscle cell differentiation
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 3099 Genes GS206544: GO:2000112 regulation of cellular macromolecule biosynthetic process
Expand Tier I Human GO 1255 Genes GS210178: GO:0031328 positive regulation of cellular biosynthetic process
Expand Tier I Human GO 6256 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human GO 753 Genes GS204108: GO:0072358 cardiovascular system development
Expand Tier I Human GO 239 Genes GS209714: GO:0034504 protein localization to nucleus
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 2828 Genes GS198684: GO:0048523 negative regulation of cellular process
Expand Tier I Human GO 8094 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 258 Genes GS206111: GO:0097285 cell-type specific apoptotic process
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 I Human GO 182 Genes GS204087: GO:0043583 ear development
Expand Tier I Human GO 535 Genes GS205331: GO:0051093 negative regulation of developmental process
Expand Tier I Human GO 31 Genes GS205669: GO:0072088 nephron epithelium morphogenesis
Expand Tier I Human GO 13 Genes GS194271: GO:0072079 nephron tubule formation
Expand Tier I Human GO 145 Genes GS208717: GO:2000027 regulation of organ morphogenesis
Expand Tier I Human GO 1965 Genes GS210586: GO:0051641 cellular localization
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 5400 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 3 Genes GS195283: GO:2000729 positive regulation of mesenchymal cell proliferation involved in ureter development
Expand Tier I Human GO 1197 Genes GS199501: GO:0051173 positive regulation of nitrogen compound metabolic process
Expand Tier I Human 232 Genes GS170999: HP:0000082 Abnormality of renal physiology
Expand Tier I Human GO 38 Genes GS194514: GO:0061326 renal tubule development
Expand Tier I Human 310 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Human GO 18 Genes GS194270: GO:0072078 nephron tubule morphogenesis
Expand Tier I Human GO 162 Genes GS196633: GO:0070997 neuron death
Expand Tier I Human GO 4129 Genes GS206329: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Human GO 21 Genes GS194095: GO:0030878 thyroid gland development
Expand Tier I Human GO 432 Genes GS207210: GO:0035295 tube development
Expand Tier I Human GO 14 Genes GS194275: GO:0072075 metanephric mesenchyme development
Expand Tier I Human GO 305 Genes GS202276: GO:0030855 epithelial cell differentiation
Expand Tier I Human GO 5908 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human GO 33 Genes GS194280: GO:0048538 thymus development
Expand Tier I Human GO 520 Genes GS201126: GO:0009792 embryo development ending in birth or egg hatching
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 290 Genes GS198991: GO:0005667 transcription factor complex
Expand Tier I Human GO 157 Genes GS201548: GO:0048754 branching morphogenesis of a tube
Expand Tier I Human 280 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Human GO 4134 Genes GS200341: GO:0051179 localization
Expand Tier I Human GO 178 Genes GS202566: GO:0048705 skeletal system morphogenesis
Expand Tier I Human GO 86 Genes GS206759: GO:0072006 nephron development
Expand Tier I Human 36 Genes GS171790: HP:0000372 Abnormality of the auditory canal
Expand Tier I Human GO 4415 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Human GO 570 Genes GS199782: GO:0043066 negative regulation of apoptotic process
Expand Tier I Human 56 Genes GS173053: HP:0000324 Facial asymmetry
Expand Tier I Human GO 4 Genes GS199689: GO:0072191 ureter smooth muscle development
Expand Tier I Human 58 Genes GS174923: HP:0008572 External ear malformation
Expand Tier I Human GO 15 Genes GS194274: GO:0072074 kidney mesenchyme development
Expand Tier I Human GO 108 Genes GS198765: GO:0001838 embryonic epithelial tube formation
Expand Tier I Human GO 325 Genes GS202371: GO:0044212 transcription regulatory region DNA binding
Expand Tier I Human GO 999 Genes GS195678: GO:0003700 sequence-specific DNA binding transcription factor activity
Expand Tier I Human GO 21 Genes GS201103: GO:0035904 aorta development
Expand Tier I Human GO 116 Genes GS194241: GO:0035148 tube formation
Expand Tier I Human GO 108 Genes GS202572: GO:0048706 embryonic skeletal system development
Expand Tier I Human GO 131 Genes GS210018: GO:0060560 developmental growth involved in morphogenesis
Expand Tier I Human 335 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier I Human GO 22 Genes GS197888: GO:2000826 regulation of heart morphogenesis
Expand Tier I Human GO 333 Genes GS208604: GO:0001067 regulatory region nucleic acid binding
Expand Tier I Human GO 1170 Genes GS209951: GO:0042127 regulation of cell proliferation
Expand Tier I Human GO 44 Genes GS200692: GO:0048844 artery morphogenesis
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 136 Genes GS175524: HP:0000009 Functional abnormality of the bladder
Expand Tier I Human GO 16 Genes GS204414: GO:0060602 branch elongation of an epithelium
Expand Tier I Human 390 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 344 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier I Human GO 34 Genes GS198083: GO:0072028 nephron morphogenesis
Expand Tier I Human GO 68 Genes GS200104: GO:0060675 ureteric bud morphogenesis
Expand Tier I Human GO 2665 Genes GS205543: GO:0070013 intracellular organelle lumen
Expand Tier I Human 32 Genes GS172593: HP:0010609 Skin tags
Expand Tier I Human 144 Genes GS175754: HP:0000014 Abnormality of the bladder
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 3383 Genes GS200312: GO:0019219 regulation of nucleobase-containing compound metabolic process
Expand Tier I Human GO 4 Genes GS199691: GO:0072193 ureter smooth muscle cell differentiation
Expand Tier I Human GO 20 Genes GS196394: GO:0071599 otic vesicle development
Expand Tier I Human GO 835 Genes GS205758: GO:0016477 cell migration
Expand Tier I Human 433 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human GO 108 Genes GS208640: GO:0048638 regulation of developmental growth
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 168 Genes GS195660: GO:0061138 morphogenesis of a branching epithelium
Expand Tier I Human GO 39 Genes GS210446: GO:0031128 developmental induction
Expand Tier I Human GO 1722 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Human GO 3178 Genes GS204204: GO:0006351 transcription, DNA-dependent
Expand Tier I Human 48 Genes GS171726: HP:0005107 Abnormality of the sacrum
Expand Tier I Human GO 22 Genes GS197515: GO:0042474 middle ear morphogenesis
Expand Tier I Human GO 41 Genes GS195058: GO:0051145 smooth muscle cell differentiation
Expand Tier I Human GO 103 Genes GS206905: GO:0001657 ureteric bud development
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 29 Genes GS171563: HP:0000384 Preauricular skin tag
Expand Tier I Human GO 113 Genes GS197510: GO:0042471 ear morphogenesis
Expand Tier I Human GO 688 Genes GS194602: GO:0045944 positive regulation of transcription from RNA polymerase II promoter
Expand Tier I Human GO 3098 Genes GS203058: GO:0048519 negative regulation of biological process
Expand Tier I Human GO 4292 Genes GS204746: GO:0080090 regulation of primary metabolic process
Expand Tier I Human GO 15 Genes GS195893: GO:0048486 parasympathetic nervous system development
Expand Tier I Human GO 2479 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 22 Genes GS207636: GO:0061333 renal tubule morphogenesis
Expand Tier I Human GO 1001 Genes GS201264: GO:0009890 negative regulation of biosynthetic process
Expand Tier I Human GO 5347 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Human 300 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human GO 3603 Genes GS198456: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Human 120 Genes GS177000: HP:0001291 Abnormality of the cranial nerves
Expand Tier I Human GO 5567 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human GO 525 Genes GS208562: GO:0040008 regulation of growth
Expand Tier I Human GO 4 Genes GS210188: GO:0072171 mesonephric tubule morphogenesis
Expand Tier I Human GO 156 Genes GS196324: GO:0048839 inner ear development
Expand Tier I Human 79 Genes GS173516: HP:0000301 Abnormality of facial musculature
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 753 Genes GS204107: GO:0072359 circulatory system development
Expand Tier I Human GO 5526 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human GO 277 Genes GS193992: GO:0048732 gland development
Expand Tier I Human GO 238 Genes GS210016: GO:0060562 epithelial tube morphogenesis
Expand Tier I Human GO 3277 Genes GS194088: GO:0003676 nucleic acid binding
Expand Tier I Human GO 5 Genes GS194238: GO:0060681 branch elongation involved in ureteric bud branching
Expand Tier I Human GO 4575 Genes GS206355: GO:0023052 signaling
Expand Tier I Human GO 499 Genes GS204077: GO:0033365 protein localization to organelle
Expand Tier I Human GO 304 Genes GS206182: GO:0060537 muscle tissue development
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human GO 4 Genes GS196007: GO:0090191 negative regulation of branching involved in ureteric bud morphogenesis
Expand Tier I Human GO 1169 Genes GS199781: GO:0043067 regulation of programmed cell death
Expand Tier I Human GO 3264 Genes GS205266: GO:0032774 RNA biosynthetic process
Expand Tier I Human GO 4701 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human GO 841 Genes GS202079: GO:0051253 negative regulation of RNA metabolic process
Expand Tier I Human GO 1428 Genes GS201262: GO:0009892 negative regulation of metabolic process
Expand Tier I Human GO 12 Genes GS202684: GO:0021783 preganglionic parasympathetic nervous system development
Expand Tier I Human GO 494 Genes GS200286: GO:0060284 regulation of cell development
Expand Tier I Human GO 375 Genes GS207935: GO:0007507 heart development
Expand Tier I Human CTD 747 Genes GS125403: Diethylstilbestrol interacting genes (MeSH:D004054) in CTD
Expand Tier I Human GO 64 Genes GS206907: GO:0001658 branching involved in ureteric bud morphogenesis
Expand Tier I Human GO 1690 Genes GS194905: GO:0008219 cell death
Expand Tier I Human GO 1135 Genes GS205691: GO:0022008 neurogenesis
Expand Tier I Human 394 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 5014 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human GO 292 Genes GS194519: GO:0014706 striated muscle tissue development
Expand Tier I Human GO 484 Genes GS209725: GO:0000122 negative regulation of transcription from RNA polymerase II promoter
Expand Tier I Human GO 19 Genes GS200939: GO:0021602 cranial nerve morphogenesis
Expand Tier I Human GO 3617 Genes GS206953: GO:0018130 heterocycle biosynthetic process
Expand Tier I Human 70 Genes GS173601: HP:0010827 Abnormality of the seventh cranial nerve
Expand Tier I Human GO 3468 Genes GS199499: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Human GO 3432 Genes GS203057: GO:0048518 positive regulation of biological process
Expand Tier I Human GO 2539 Genes GS203335: GO:0048513 organ development
Expand Tier I Human GO 40 Genes GS205301: GO:0045168 cell-cell signaling involved in cell fate commitment
Expand Tier I Human GO 927 Genes GS208787: GO:0034613 cellular protein localization
Expand Tier I Human GO 109 Genes GS207298: GO:0072175 epithelial tube formation
Expand Tier I Human GO 3697 Genes GS194499: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Human GO 6 Genes GS200103: GO:0060676 ureteric bud formation
Expand Tier I Human GO 63 Genes GS194277: GO:0072073 kidney epithelium development
Expand Tier I Human GO 364 Genes GS200690: GO:0002009 morphogenesis of an epithelium
Expand Tier I Human GO 948 Genes GS208067: GO:0010558 negative regulation of macromolecule biosynthetic process
Expand Tier I Human GO 492 Genes GS201848: GO:0048598 embryonic morphogenesis
Expand Tier I Human GO 676 Genes GS196540: GO:0043565 sequence-specific DNA binding
Expand Tier I Human GO 20 Genes GS194855: GO:0090190 positive regulation of branching involved in ureteric bud morphogenesis
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human GO 1587 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Human GO 84 Genes GS206901: GO:0001656 metanephros development
Expand Tier I Human GO 899 Genes GS209281: GO:0010629 negative regulation of gene expression
Expand Tier I Human GO 37 Genes GS205665: GO:0072080 nephron tubule development
Expand Tier I Human GO 4245 Genes GS207858: GO:0009059 macromolecule biosynthetic process
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 430 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 21 Genes GS176680: HP:0100276 Skin pits
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 I Human 218 Genes GS175994: HP:0000464 Abnormality of the neck
Expand Tier I Human GO 3325 Genes GS205369: GO:0010468 regulation of gene expression
Expand Tier I Human GO 53 Genes GS207373: GO:0090183 regulation of kidney development
Expand Tier I Human GO 3 Genes GS200779: GO:0051451 myoblast migration
Expand Tier I Human GO 7650 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human GO 1179 Genes GS208060: GO:0010557 positive regulation of macromolecule biosynthetic process
Expand Tier I Human CTD 1556 Genes GS125506: Valproic Acid interacting genes (MeSH:D014635) in CTD
Expand Tier I Human GO 904 Genes GS196918: GO:0048870 cell motility
Expand Tier I Human GO 46 Genes GS204353: GO:0072009 nephron epithelium development
Expand Tier I Human GO 3714 Genes GS194038: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier I Human GO 1454 Genes GS205144: GO:0048468 cell development
Expand Tier I Human GO 1435 Genes GS205623: GO:0009888 tissue development
Expand Tier I Human GO 21 Genes GS196230: GO:0001823 mesonephros development
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human GO 15 Genes GS200913: GO:0060037 pharyngeal system development
Expand Tier I Human 100 Genes GS176684: HP:0008678 Renal hypoplasia/aplasia
Expand Tier I Human 220 Genes GS171791: HP:0000370 Abnormality of the middle ear
Expand Tier I Human GO 80 Genes GS202567: GO:0048704 embryonic skeletal system morphogenesis
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 514 Genes GS207807: GO:0043009 chordate embryonic development
Expand Tier I Human GO 7 Genes GS200102: GO:0060677 ureteric bud elongation
Expand Tier I Human GO 1692 Genes GS203755: GO:0016265 death