Gene Details



ABCC9 and homologs in 5 species are found in 569 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 112 Genes GS174327: HP:0003198 Myopathy
Expand Tier I Human GO 203 Genes GS198194: GO:0034702 ion channel complex
Expand Tier I Mouse GO 782 Genes GS192507: GO:0006812 cation transport
Expand Tier I Mouse GO 641 Genes GS185985: GO:0016818 hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides
Expand Tier I Human GO 1839 Genes GS205510: GO:0001883 purine nucleoside binding
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human CTD 419 Genes GS121514: Paraquat interacting genes (MeSH:D010269) in CTD
Expand Tier I Human 100 Genes GS175101: HP:0000280 Coarse facial features
Expand Tier I Mouse GO 2260 Genes GS189855: GO:0043168 anion binding
Expand Tier I Mouse 394 Genes GS135957: HDL QTL 24 (Hdlq24, Published QTL Chr 6)
Expand Tier I Human 99 Genes GS173687: HP:0001643 Patent ductus arteriosus
Expand Tier I Mouse MP 398 Genes GS166257: MP:0005291 abnormal glucose tolerance
Expand Tier I Human GO 70 Genes GS204008: GO:0008076 voltage-gated potassium channel complex
Expand Tier I Human 61 Genes GS175897: HP:0000939 Osteoporosis
Expand Tier I Mouse GO 95 Genes GS183655: GO:0015405 P-P-bond-hydrolysis-driven transmembrane transporter activity
Expand Tier I Human 322 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Mouse MP 140 Genes GS170204: MP:0005595 abnormal vascular smooth muscle physiology
Expand Tier I Mouse GO 1774 Genes GS184984: GO:0032553 ribonucleotide binding
Expand Tier I Mouse MP 33 Genes GS170590: MP:0006135 artery stenosis
Expand Tier I Mouse GO 550 Genes GS191193: GO:0009607 response to biotic stimulus
Expand Tier II Mouse 244 Genes GS35266: Striatum Gene expression correlates of Maximum startle response to 80 db in Males BXD
Expand Tier I Mouse GO 1765 Genes GS183645: GO:0017076 purine nucleotide binding
Expand Tier I Mouse GO 1 Genes GS192550: GO:0008281 sulfonylurea receptor activity
Expand Tier I Human 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human 20 Genes GS175507: HP:0010055 Broad hallux
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Human GO 1099 Genes GS195083: GO:0007267 cell-cell signaling
Expand Tier I Human 104 Genes GS176638: HP:0011603 Congenital malformation of the great arteries
Expand Tier I Human 491 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 157 Genes GS172363: HP:0004324 Increased body weight
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Mouse GO 774 Genes GS181423: GO:0022891 substrate-specific transmembrane transporter activity
Expand Tier I Mouse 363 Genes GS136587: renal cystic disease severity (Rencd, Published QTL Chr 6)
Expand Tier I Human CTD 2013 Genes GS126646: Carbon Tetrachloride interacting genes (MeSH:D002251) in CTD
Expand Tier I Human 149 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Human 121 Genes GS172789: HP:0001537 Umbilical hernia
Expand Tier I Human GO 2625 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 136 Genes GS173751: HP:0000998 Hypertrichosis
Expand Tier I Human GO 273 Genes GS196857: GO:0034220 ion transmembrane transport
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Mouse GO 417 Genes GS184917: GO:0002252 immune effector process
Expand Tier I Human GO 790 Genes GS210137: GO:0016462 pyrophosphatase activity
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 278 Genes GS195770: GO:0015672 monovalent inorganic cation transport
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 20 Genes GS172151: HP:0002673 Coxa valga
Expand Tier I Mouse GO 1106 Genes GS192508: GO:0006811 ion transport
Expand Tier I Human 114 Genes GS176840: HP:0001911 Abnormality of granulocytes
Expand Tier I Mouse GO 209 Genes GS190368: GO:0042623 ATPase activity, coupled
Expand Tier I Mouse GO 4001 Genes GS183543: GO:0051179 localization
Expand Tier I Mouse GO 602 Genes GS178909: GO:0017111 nucleoside-triphosphatase activity
Expand Tier III Mouse 1048 Genes GS213200: Expression changes in the regulation of memory consolidation and synaptic function in FoxO6 vs. wild-type mice
Expand Tier I Human 7 Genes GS172525: HP:0001698 Pericardial effusion
Expand Tier I Mouse 350 Genes GS135469: blood pressure QTL 5 (Bpq5, Published QTL Chr 6)
Expand Tier I Human 184 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Mouse MP 1082 Genes GS166660: MP:0001731 abnormal postnatal growth
Expand Tier I Mouse MP 72 Genes GS163843: MP:0000231 hypertension
Expand Tier I Human 202 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Mouse MP 80 Genes GS166979: MP:0004130 abnormal muscle cell glucose uptake
Expand Tier I Human GO 2 Genes GS209491: GO:0008281 sulfonylurea receptor activity
Expand Tier I Human GO 2432 Genes GS209108: GO:0000166 nucleotide binding
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Mouse 363 Genes GS136146: lithogenic gene 6 (Lith6, Published QTL Chr 6)
Expand Tier I Mouse MP 2357 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier I Human GO 1374 Genes GS203494: GO:0051704 multi-organism process
Expand Tier I Human 246 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human 49 Genes GS174245: HP:0001844 Abnormality of the hallux
Expand Tier I Mouse GO 1745 Genes GS188652: GO:0001882 nucleoside binding
Expand Tier I Human GO 1639 Genes GS204106: GO:0060089 molecular transducer activity
Expand Tier I Mouse GO 160 Genes GS192506: GO:0006813 potassium ion transport
Expand Tier I Mouse GO 37 Genes GS191171: GO:0030315 T-tubule
Expand Tier I Mouse 484 Genes GS135881: femur geometry 5 (Fmgty5, Published QTL Chr 6)
Expand Tier I Mouse 491 Genes GS136206: lung tumor shape-determining 8 (Ltsd8, Published QTL Chr 6)
Expand Tier I Mouse 395 Genes GS136960: weight adult 2 (Wta2, Published QTL Chr 6)
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human GO 1836 Genes GS201799: GO:0032550 purine ribonucleoside binding
Expand Tier I Human GO 1877 Genes GS201800: GO:0032553 ribonucleotide binding
Expand Tier I Mouse 469 Genes GS135505: bulb size 2 (Bulb2, Published QTL Chr 6)
Expand Tier I Mouse GO 888 Genes GS192671: GO:0055085 transmembrane transport
Expand Tier I Mouse GO 1736 Genes GS188651: GO:0001883 purine nucleoside binding
Expand Tier I Mouse MP 632 Genes GS170733: MP:0000188 abnormal circulating glucose level
Expand Tier III Rat 28 Genes GS137837: Genes differentially expressed in the CA1 field of the hippocampi of aged-superior learners (SL) vs. age learning-impaired (AI) vs. young rats
Expand Tier I Human 534 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 179 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier I Mouse GO 96 Genes GS192203: GO:0015399 primary active transmembrane transporter activity
Expand Tier I Human GO 3125 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Human 3 Genes GS174998: HP:0007665 Curly eyelashes
Expand Tier I Mouse GO 1064 Genes GS179401: GO:0005215 transporter activity
Expand Tier I Human 129 Genes GS172916: HP:0003312 Abnormal form of the vertebral bodies
Expand Tier I Mouse GO 142 Genes GS189443: GO:0044449 contractile fiber part
Expand Tier I Human GO 5637 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 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Human GO 1914 Genes GS198782: GO:0044459 plasma membrane part
Expand Tier I Human GO 145 Genes GS206312: GO:0044449 contractile fiber part
Expand Tier I Human GO 751 Genes GS202715: GO:0035637 multicellular organismal signaling
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier II Mouse 119 Genes GS36775: Hippocampus Gene expression correlates of Zero Maze - Percentage open time in Males BXD
Expand Tier III Mouse 6105 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier I Human 186 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Tier I Mouse GO 649 Genes GS180228: GO:0005887 integral to plasma membrane
Expand Tier I Human 249 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Mouse GO 89 Genes GS177749: GO:0071804 cellular potassium ion transport
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 281 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Mouse MP 990 Genes GS169075: MP:0002078 abnormal glucose homeostasis
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Mouse GO 5225 Genes GS189860: GO:0043167 ion binding
Expand Tier I Mouse GO 366 Genes GS179009: GO:0015672 monovalent inorganic cation transport
Expand Tier I Human 266 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Mouse GO 2190 Genes GS191129: GO:0016787 hydrolase activity
Expand Tier I Human GO 4 Genes GS194001: GO:0010107 potassium ion import
Expand Tier I Mouse GO 6473 Genes GS184448: GO:0044425 membrane part
Expand Tier I Mouse 363 Genes GS136630: small effect CIA locus 3 (Secia3, Published QTL Chr 6)
Expand Tier I Human GO 1262 Genes GS199199: GO:0031226 intrinsic to plasma membrane
Expand Tier I Human 169 Genes GS171752: HP:0001713 Abnormality of cardiac ventricle
Expand Tier I Human GO 4144 Genes GS200341: GO:0051179 localization
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human 16 Genes GS174486: HP:0000527 Long eyelashes
Expand Tier I Mouse MP 1856 Genes GS165386: MP:0001262 decreased body weight
Expand Tier I Human GO 798 Genes GS202828: GO:0016817 hydrolase activity, acting on acid anhydrides
Expand Tier I Mouse MP 169 Genes GS163929: MP:0002891 increased insulin sensitivity
Expand Tier I Mouse GO 48 Genes GS182594: GO:0019905 syntaxin binding
Expand Tier I Human 71 Genes GS171600: HP:0000168 Abnormality of the gingiva
Expand Tier I Human GO 260 Genes GS204130: GO:0009615 response to virus
Expand Tier I Human GO 39 Genes GS208574: GO:0044325 ion channel binding
Expand Tier I Mouse GO 281 Genes GS192646: GO:0022804 active transmembrane transporter activity
Expand Tier I Human GO 651 Genes GS195082: GO:0007268 synaptic transmission
Expand Tier I Human 44 Genes GS171924: HP:0100578 Lipoatrophy
Expand Tier I Human CTD 71 Genes GS126830: Potassium interacting genes (MeSH:D011188) in CTD
Expand Tier I Human 121 Genes GS170890: HP:0006483 Abnormal number of teeth
Expand Tier I Human 148 Genes GS172906: HP:0003319 Abnormality of the cervical spine
Expand Tier I Mouse MP 185 Genes GS165208: MP:0002842 increased systemic arterial blood pressure
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 53 Genes GS174719: HP:0000774 Narrow chest
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 98 Genes GS174851: HP:0000944 Abnormality of the metaphyses
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 14 Genes GS174014: HP:0010109 Small hallux
Expand Tier I Mouse GO 5103 Genes GS192512: GO:0003824 catalytic activity
Expand Tier I Mouse GO 1736 Genes GS180644: GO:0032549 ribonucleoside binding
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier III Mouse 5726 Genes GS213077: Genes with suggestive difference in (PWD) vs (PB6F1 + B6PF1 + B6) comparison
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 14 Genes GS171862: HP:0008362 Aplasia/Hypoplasia of the hallux
Expand Tier I Human 435 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human 35 Genes GS176775: HP:0001004 Lymphedema
Expand Tier I Mouse GO 256 Genes GS182559: GO:0005261 cation channel activity
Expand Tier I Mouse GO 777 Genes GS186645: GO:0051704 multi-organism process
Expand Tier I Human 141 Genes GS174847: HP:0000940 Abnormal diaphysis morphology
Expand Tier I Mouse GO 3614 Genes GS180229: GO:0005886 plasma membrane
Expand Tier I Human GO 102 Genes GS199048: GO:0016820 hydrolase activity, acting on acid anhydrides, catalyzing transmembrane movement of substances
Expand Tier I Mouse 347 Genes GS135769: experimental autoimmune myocarditis 2 (Eamcd2, Published QTL Chr 6)
Expand Tier I Human 266 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier I Mouse MP 3437 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Mouse GO 55 Genes GS184146: GO:0000149 SNARE binding
Expand Tier I Mouse MP 56 Genes GS166661: MP:0000250 abnormal vasoconstriction
Expand Tier I Mouse GO 3 Genes GS191726: GO:0008282 ATP-sensitive potassium channel complex
Expand Tier I Mouse GO 2126 Genes GS192680: GO:0038023 signaling receptor activity
Expand Tier II Mouse 329 Genes GS35276: Striatum Gene expression correlates of Maximum startle response to 85 db in Males BXD
Expand Tier I Mouse 395 Genes GS135447: bone length and organs 3 (Bod3, Published QTL Chr 6)
Expand Tier I Mouse GO 1603 Genes GS177409: GO:0005739 mitochondrion
Expand Tier I Mouse GO 46 Genes GS191639: GO:0044325 ion channel binding
Expand Tier III Rat 3441 Genes GS135132: bHR vs bLR genes different in Nucleus Acumbens
Expand Tier I Human 240 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Human 104 Genes GS173535: HP:0001874 Abnormality of neutrophils
Expand Tier I Human 56 Genes GS176099: HP:0000926 Platyspondyly
Expand Tier I Mouse MP 4173 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Mouse GO 153 Genes GS191982: GO:0030016 myofibril
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human CTD 999 Genes GS124711: Genistein interacting genes (MeSH:D019833) in CTD
Expand Tier III Rat 3441 Genes GS135133: bHR vs bLR genes different in Hippocampus
Expand Tier I Human 224 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Mouse 350 Genes GS136655: skeletal muscle weight 14 (Skmw14, Published QTL Chr 6)
Expand Tier I Mouse GO 101 Genes GS181685: GO:0042383 sarcolemma
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human GO 2392 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human 13 Genes GS176189: HP:0009103 Aplasia/Hypoplasia involving the pelvis
Expand Tier I Mouse GO 397 Genes GS178812: GO:0015267 channel activity
Expand Tier I Mouse GO 130 Genes GS191983: GO:0030017 sarcomere
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 24 Genes GS172590: HP:0001837 Broad toe
Expand Tier I Mouse GO 88 Genes GS190365: GO:0042626 ATPase activity, coupled to transmembrane movement of substances
Expand Tier I Mouse 350 Genes GS136124: lipoprotein QTL 1 (Lipq1, Published QTL Chr 6)
Expand Tier I Mouse GO 2038 Genes GS187881: GO:0004888 transmembrane signaling receptor activity
Expand Tier I Human 196 Genes GS173872: HP:0011368 Epidermal thickening
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier III Human 2430 Genes GS216491: Genes that are binding sites for CREB and zif268,transcription factors mediating nieuronal activity and plasticity, in Homo sapiens.
Expand Tier I Human 63 Genes GS173367: HP:0005257 Thoracic hypoplasia
Expand Tier I Human 94 Genes GS171105: HP:0006494 Aplasia/Hypoplasia involving bones of the feet
Expand Tier I Human 61 Genes GS171609: HP:0011339 Abnormality of upper lip vermillion
Expand Tier I Mouse GO 122 Genes GS193288: GO:0015079 potassium ion transmembrane transporter activity
Expand Tier I Human 19 Genes GS172514: HP:0001697 Abnormality of the pericardium
Expand Tier I Human 41 Genes GS171758: HP:0001714 Ventricular hypertrophy
Expand Tier I Mouse GO 600 Genes GS179671: GO:0030001 metal ion transport
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Mouse GO 384 Genes GS188954: GO:0022838 substrate-specific channel activity
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse GO 415 Genes GS181424: GO:0022890 inorganic cation transmembrane transporter activity
Expand Tier I Mouse DRG 2693 Genes GS87380: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). (Whole Table) [DRG]
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 5 Genes GS171235: HP:0010184 Abnormality of the proximal phalanges of the toes
Expand Tier I Human 9 Genes GS173361: HP:0004540 Congenital, generalized hypertrichosis
Expand Tier I Mouse GO 65 Genes GS178899: GO:0016247 channel regulator activity
Expand Tier I Mouse 395 Genes GS136232: mandible length 6 (Manln6, Published QTL Chr 6)
Expand Tier I Mouse GO 549 Genes GS180083: GO:0034220 ion transmembrane transport
Expand Tier I Human GO 964 Genes GS209451: GO:0006811 ion transport
Expand Tier III Mouse 1964 Genes GS865: Sey_Pax6_Age_Reduced_Linear_Incr
Expand Tier I Human 211 Genes GS175164: HP:0011927 Short digit
Expand Tier I Mouse MP 205 Genes GS169557: MP:0008489 slow postnatal weight gain
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier I Mouse GO 339 Genes GS181532: GO:0046873 metal ion transmembrane transporter activity
Expand Tier I Mouse GO 277 Genes GS178478: GO:0015077 monovalent inorganic cation transmembrane transporter activity
Expand Tier I Mouse GO 2439 Genes GS179580: GO:0036094 small molecule binding
Expand Tier I Human GO 108 Genes GS209137: GO:0015399 primary active transmembrane transporter activity
Expand Tier I Human 140 Genes GS175471: HP:0001172 Abnormality of the thumb
Expand Tier I Human GO 1510 Genes GS201792: GO:0032559 adenyl ribonucleotide binding
Expand Tier I Human 1 Genes GS172552: HP:0004634 Cuboid-shaped vertebral bodies
Expand Tier I Mouse GO 509 Genes GS192789: GO:0008324 cation transmembrane transporter activity
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human GO 497 Genes GS196432: GO:0030001 metal ion transport
Expand Tier I Human 14 Genes GS172154: HP:0002679 Abnormality of the sella turcica
Expand Tier I Human 12 Genes GS173691: HP:0001647 Bicuspid aortic valve
Expand Tier I Human CTD 4423 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
Expand Tier I Human 45 Genes GS174915: HP:0003016 Metaphyseal widening
Expand Tier I Human 96 Genes GS176759: HP:0000982 Palmoplantar keratoderma
Expand Tier I Human 26 Genes GS173686: HP:0001640 Cardiomegaly
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 354 Genes GS208384: GO:0016887 ATPase activity
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 77 Genes GS172300: HP:0001991 Aplasia/Hypoplasia of the toes
Expand Tier I Human GO 583 Genes GS203491: GO:0051707 response to other organism
Expand Tier I Human 143 Genes GS174721: HP:0000772 Abnormality of the ribs
Expand Tier I Mouse GO 166 Genes GS189317: GO:0043292 contractile fiber
Expand Tier I Mouse MP 3110 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Human GO 70 Genes GS198193: GO:0034705 potassium channel complex
Expand Tier I Mouse MP 1777 Genes GS164263: MP:0002083 premature death
Expand Tier I Mouse MP 2099 Genes GS165616: MP:0002127 abnormal cardiovascular system morphology
Expand Tier I Mouse MP 1615 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier I Human 49 Genes GS174071: HP:0009125 Lipodystrophy
Expand Tier I Mouse GO 263 Genes GS191457: GO:0016887 ATPase activity
Expand Tier I Mouse GO 886 Genes GS181425: GO:0022892 substrate-specific transporter activity
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human 411 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 2 Genes GS173630: HP:0002690 Large sella turcica
Expand Tier I Human GO 1850 Genes GS205511: GO:0001882 nucleoside binding
Expand Tier I Human GO 25 Genes GS194489: GO:0071805 potassium ion transmembrane transport
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Human GO 3861 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human 46 Genes GS173617: HP:0011220 Prominent forehead
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Mouse GO 2876 Genes GS182474: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Mouse 434 Genes GS135367: B.burgdorferi-associated arthritis 5 (Bbaa5, Published QTL Chr 6)
Expand Tier I Human 112 Genes GS172569: HP:0000343 Long philtrum
Expand Tier I Human 160 Genes GS174814: HP:0001639 Hypertrophic cardiomyopathy
Expand Tier I Human GO 29 Genes GS204171: GO:0015459 potassium channel regulator activity
Expand Tier I Mouse GO 5 Genes GS177274: GO:0010107 potassium ion import
Expand Tier I Mouse GO 101 Genes GS181406: GO:0034703 cation channel complex
Expand Tier I Mouse 350 Genes GS136075: insulin QTL 8 (Insq8, Published QTL Chr 6)
Expand Tier I Human 139 Genes GS171397: HP:0000177 Abnormality of upper lip
Expand Tier I Mouse MP 167 Genes GS166675: MP:0005292 improved glucose tolerance
Expand Tier I Human GO 74 Genes GS195655: GO:0016247 channel regulator activity
Expand Tier I Human 108 Genes GS171228: HP:0002823 Abnormality of the femur
Expand Tier I Mouse 346 Genes GS136425: pulmonary adenoma susceptibility 1 (Pas1, Published QTL Chr 6)
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Mouse MP 77 Genes GS169706: MP:0006144 increased systemic arterial systolic blood pressure
Expand Tier I Mouse MP 325 Genes GS170368: MP:0000249 abnormal blood vessel physiology
Expand Tier I Human 45 Genes GS176166: HP:0001256 Intellectual disability, mild
Expand Tier I Human GO 118 Genes GS209449: GO:0006813 potassium ion transport
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 128 Genes GS208922: GO:0030017 sarcomere
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Human GO 4283 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 111 Genes GS176907: HP:0009804 Reduced number of teeth
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human GO 4593 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human 150 Genes GS176233: HP:0004209 Clinodactyly of the 5th finger
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human GO 613 Genes GS208107: GO:0009607 response to biotic stimulus
Expand Tier I Human 405 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 470 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 215 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Human GO 1514 Genes GS203649: GO:0030554 adenyl nucleotide binding
Expand Tier I Human 2 Genes GS176154: HP:0010068 Broad first metatarsal
Expand Tier I Mouse GO 2350 Genes GS187247: GO:0060089 molecular transducer activity
Expand Tier I Human CTD 5075 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human 60 Genes GS171207: HP:0000098 Tall stature
Expand Tier I Mouse GO 802 Genes GS190027: GO:0006952 defense response
Expand Tier I Human 3 Genes GS173234: HP:0004975 Erlenmeyer flask deformity of the femurs
Expand Tier I Human 74 Genes GS174070: HP:0009124 Abnormality of adipose tissue
Expand Tier I Human GO 761 Genes GS209613: GO:0055085 transmembrane transport
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 210 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Human GO 100 Genes GS210132: GO:0043492 ATPase activity, coupled to movement of substances
Expand Tier I Mouse 350 Genes GS135410: body growth late QTL 5 (Bglq5, Published QTL Chr 6)
Expand Tier I Human GO 3275 Genes GS199267: GO:0043234 protein complex
Expand Tier I Mouse 485 Genes GS135380: bone density traits 3 (Bdt3, Published QTL Chr 6)
Expand Tier I Human 32 Genes GS171753: HP:0001712 Left ventricular hypertrophy
Expand Tier I Mouse MP 314 Genes GS169915: MP:0005560 decreased circulating glucose level
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Mouse GO 92 Genes GS184485: GO:0008144 drug binding
Expand Tier II Mouse 83 Genes GS35256: Striatum Gene expression correlates of Maximum startle response to 70 db in Males BXD
Expand Tier I Human 310 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human GO 311 Genes GS209586: GO:0022804 active transmembrane transporter activity
Expand Tier I Mouse MP 1307 Genes GS170198: MP:0001614 abnormal blood vessel morphology
Expand Tier I Human 180 Genes GS175902: HP:0003468 Abnormality of the vertebrae
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Mouse GO 1444 Genes GS184976: GO:0032559 adenyl ribonucleotide binding
Expand Tier I Human GO 3125 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human 28 Genes GS171409: HP:0011306 Aplasia of the toes
Expand Tier I Human GO 278 Genes GS207263: GO:0042623 ATPase activity, coupled
Expand Tier I Human GO 3318 Genes GS209452: GO:0006810 transport
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human GO 735 Genes GS204608: GO:0019226 transmission of nerve impulse
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 17 Genes GS173343: HP:0001548 Overgrowth
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Mouse MP 36 Genes GS169711: MP:0006143 increased systemic arterial diastolic blood pressure
Expand Tier I Human 160 Genes GS175096: HP:0000286 Epicanthus
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Mouse 318 Genes GS135532: cadmium-induced forelimb autopod reduction defect (Cadfar, Published QTL Chr 6)
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
Expand Tier I Human 150 Genes GS175149: HP:0009179 Deviation of the 5th finger
Expand Tier I Mouse MP 115 Genes GS164586: MP:0010508 abnormal heart electrocardiography waveform feature
Expand Tier I Mouse GO 1350 Genes GS177843: GO:0002376 immune system process
Expand Tier I Human 41 Genes GS175113: HP:0000574 Thick eyebrow
Expand Tier I Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human GO 3372 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Mouse GO 2283 Genes GS185920: GO:0004872 receptor activity
Expand Tier I Mouse GO 1724 Genes GS185881: GO:0035639 purine ribonucleoside triphosphate binding
Expand Tier I Human 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Mouse GO 643 Genes GS185991: GO:0016817 hydrolase activity, acting on acid anhydrides
Expand Tier I Human GO 1639 Genes GS202760: GO:0004871 signal transducer activity
Expand Tier I Mouse MP 2606 Genes GS165397: MP:0001265 decreased body size
Expand Tier I Mouse MP 439 Genes GS170600: MP:0005620 abnormal muscle contractility
Expand Tier I Human 8 Genes GS176246: HP:0001783 Broad metatarsal
Expand Tier I Human 212 Genes GS176185: HP:0100790 Hernia
Expand Tier I Mouse 394 Genes GS135522: body weight QTL 10 (Bwtq10, Published QTL Chr 6)
Expand Tier I Human 487 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human 8 Genes GS176251: HP:0009104 Aplasia/Hypoplasia of the pubic bone
Expand Tier I Human GO 1236 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Mouse 363 Genes GS135946: HDL QTL 12 (Hdlq12, Published QTL Chr 6)
Expand Tier I Human 90 Genes GS173087: HP:0000499 Abnormality of the eyelashes
Expand Tier I Human 4 Genes GS175509: HP:0010059 Broad phalanges of the hallux
Expand Tier I Mouse GO 397 Genes GS186078: GO:0022803 passive transmembrane transporter activity
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Mouse 1153 Genes GS216490: Differential expression of the liver after chronic ethanol exposure in mice.
Expand Tier I Human GO 1827 Genes GS202716: GO:0035639 purine ribonucleoside triphosphate binding
Expand Tier I Human GO 1539 Genes GS202759: GO:0004872 receptor activity
Expand Tier I Human 601 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 174 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 281 Genes GS171204: HP:0011314 Abnormality of long bone morphology
Expand Tier I Mouse GO 516 Genes GS186642: GO:0051707 response to other organism
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 758 Genes GS195665: GO:0017111 nucleoside-triphosphatase activity
Expand Tier I Human 6 Genes GS171018: HP:0003173 Hypoplastic pubic bones
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Mouse 350 Genes GS136662: skin tumor susceptibility 12 (Skts12, Published QTL Chr 6)
Expand Tier I Human 47 Genes GS172604: HP:0005445 Widened posterior fossa
Expand Tier I Human 60 Genes GS174088: HP:0003366 Abnormality of the femoral neck and head region
Expand Tier I Human GO 1869 Genes GS200446: GO:0017076 purine nucleotide binding
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 229 Genes GS171908: HP:0004298 Abnormality of the abdominal wall
Expand Tier I Mouse 475 Genes GS136656: skeletal muscle weight 15 (Skmw15, Published QTL Chr 6)
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human GO 1790 Genes GS194586: GO:0002376 immune system process
Expand Tier I Human GO 1336 Genes GS209622: GO:0038023 signaling receptor activity
Expand Tier I Mouse GO 1733 Genes GS184983: GO:0032550 purine ribonucleoside binding
Expand Tier I Mouse MP 4592 Genes GS165537: MP:0005376 homeostasis/metabolism phenotype
Expand Tier I Mouse MP 140 Genes GS167984: MP:0003137 abnormal impulse conducting system conduction
Expand Tier I Mouse MP 10 Genes GS167347: MP:0003897 abnormal ST segment
Expand Tier I Mouse GO 1440 Genes GS181988: GO:0044459 plasma membrane part
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human GO 1693 Genes GS209960: GO:0003008 system process
Expand Tier I Mouse GO 2263 Genes GS192174: GO:0000166 nucleotide binding
Expand Tier I Mouse GO 2876 Genes GS181102: GO:0043228 non-membrane-bounded organelle
Expand Tier I Mouse MP 1007 Genes GS164742: MP:0001732 postnatal growth retardation
Expand Tier I Human 124 Genes GS171102: HP:0006493 Aplasia/Hypoplasia involving bones of the lower limbs
Expand Tier I Mouse 350 Genes GS136871: T cell ratio modifier QTL 1 (Trmq1, Published QTL Chr 6)
Expand Tier I Human GO 162 Genes GS206183: GO:0043292 contractile fiber
Expand Tier I Human 12 Genes GS171019: HP:0003172 Abnormality of the pubic bones
Expand Tier I Mouse GO 5859 Genes GS182404: GO:0031224 intrinsic to membrane
Expand Tier I Human CTD 1122 Genes GS127166: bisphenol A interacting genes (MeSH:C006780) in CTD
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 112 Genes GS173465: HP:0001654 Abnormality of the heart valves
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Mouse MP 576 Genes GS168750: MP:0002191 abnormal artery morphology
Expand Tier I Human 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Mouse GO 105 Genes GS185176: GO:0005267 potassium channel activity
Expand Tier I Human 324 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Mouse 500 Genes GS136278: modifier of ocular retardation 1 (Modor1, Published QTL Chr 6)
Expand Tier I Human 67 Genes GS172588: HP:0001831 Short toe
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 5320 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 3 Genes GS208663: GO:0008282 ATP-sensitive potassium channel complex
Expand Tier I Human 123 Genes GS171390: HP:0000178 Abnormality of lower lip
Expand Tier I Mouse GO 4588 Genes GS177309: GO:1901363 heterocyclic compound binding
Expand Tier I Mouse GO 684 Genes GS182402: GO:0031226 intrinsic to plasma membrane
Expand Tier I Human 285 Genes GS175119: HP:0001881 Abnormality of leukocytes
Expand Tier I Mouse 497 Genes GS136564: radiation pulmonary fibrosis 3 (Radpf3, Published QTL Chr 6)
Expand Tier I Human GO 99 Genes GS207260: GO:0042626 ATPase activity, coupled to transmembrane movement of substances
Expand Tier I Human 195 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Human 263 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Mouse GO 725 Genes GS178474: GO:0015075 ion transmembrane transporter activity
Expand Tier I Human GO 2433 Genes GS203886: GO:1901265 nucleoside phosphate binding
Expand Tier I Human GO 925 Genes GS197610: GO:0022857 transmembrane transporter activity
Expand Tier I Human 7 Genes GS176082: HP:0003175 Hypoplastic ischia
Expand Tier I Human GO 1242 Genes GS204740: GO:0004888 transmembrane signaling receptor activity
Expand Tier I Mouse GO 4637 Genes GS177382: GO:0097159 organic cyclic compound binding
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 150 Genes GS175074: HP:0001156 Brachydactyly syndrome
Expand Tier I Human CTD 18 Genes GS123803: Glyburide interacting genes (MeSH:D005905) in CTD
Expand Tier I Mouse GO 3211 Genes GS192509: GO:0006810 transport
Expand Tier I Human GO 132 Genes GS198195: GO:0034703 cation channel complex
Expand Tier I Human 263 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier I Human 27 Genes GS176727: HP:0003043 Abnormality of the shoulder
Expand Tier I Human GO 1100 Genes GS206909: GO:0006952 defense response
Expand Tier I Mouse GO 1759 Genes GS184978: GO:0032555 purine ribonucleotide binding
Expand Tier II Mouse 505 Genes GS84189: ethanol conditioned taste aversion (Published QTL, Chr 6)
Expand Tier I Human 155 Genes GS172040: HP:0000962 Hyperkeratosis
Expand Tier I Human 69 Genes GS172585: HP:0001832 Abnormality of the metatarsal bones
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human GO 1218 Genes GS197008: GO:0005887 integral to plasma membrane
Expand Tier I Human 186 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier I Human GO 152 Genes GS208921: GO:0030016 myofibril
Expand Tier I Human 48 Genes GS174251: HP:0010161 Abnormality of the phalanges of the toes
Expand Tier I Human GO 632 Genes GS209450: GO:0006812 cation transport
Expand Tier I Human 136 Genes GS171627: HP:0000470 Short neck
Expand Tier I Human 221 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier I Human 588 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Mouse GO 1418 Genes GS188322: GO:0005524 ATP binding
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse MP 3924 Genes GS163934: MP:0001764 abnormal homeostasis
Expand Tier I Mouse GO 4333 Genes GS184452: GO:0044422 organelle part
Expand Tier I Mouse GO 638 Genes GS193193: GO:0016462 pyrophosphatase activity
Expand Tier I Human 123 Genes GS171384: HP:0001551 Abnormality of the umbilicus
Expand Tier I Human 19 Genes GS172681: HP:0003300 Ovoid vertebral bodies
Expand Tier I Mouse MP 5057 Genes GS165525: MP:0010768 mortality/aging
Expand Tier I Mouse GO 132 Genes GS193052: GO:0051607 defense response to virus
Expand Tier I Human GO 1862 Genes GS201794: GO:0032555 purine ribonucleotide binding
Expand Tier I Human GO 1195 Genes GS196168: GO:0005215 transporter activity
Expand Mouse 1153 Genes GS216461: Differential expression of the liver after chronic ethanol exposure in mice.
Expand Tier I Human 75 Genes GS171391: HP:0000179 Thick lower lip vermilion
Expand Tier I Mouse GO 89 Genes GS177750: GO:0071805 potassium ion transmembrane transport
Expand Tier I Human 174 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier I Mouse GO 852 Genes GS180817: GO:0022857 transmembrane transporter activity
Expand Tier I Human 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 626 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Mouse GO 2263 Genes GS187023: GO:1901265 nucleoside phosphate binding
Expand Tier I Mouse DRG 2537 Genes provisional GS86906: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). Lists of probe sets and gene names altered by strain (3457). [DRG]
Expand Tier I Mouse MP 39 Genes GS164290: MP:0005412 vascular stenosis
Expand Tier I Human 1 Genes GS174549: HP:0005129 Congenital hypertrophy of left ventricle
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human 213 Genes GS176040: HP:0011032 Abnormality of fluid regulation
Expand Tier I Human GO 4593 Genes GS206355: GO:0023052 signaling
Expand Tier I Mouse GO 6947 Genes GS192918: GO:0050896 response to stimulus
Expand Tier II Mouse 44 Genes GS35246: Striatum Gene expression correlates of Maximum startle to 120 db in Males BXD
Expand Tier I Human 7 Genes GS172547: HP:0001520 Large for gestational age
Expand Tier II Mouse 494 Genes GS84190: METH responses for body temperature (Published QTL, Chr 6)
Expand Tier I Human 198 Genes GS174236: HP:0000534 Abnormality of the eyebrow
Expand Tier I Human CTD 453 Genes GS125669: Phenylephrine interacting genes (MeSH:D010656) in CTD
Expand Tier I Human 183 Genes GS176955: HP:0000431 Wide nasal bridge
Expand Tier I Mouse GO 166 Genes GS181405: GO:0034702 ion channel complex
Expand Tier I Mouse GO 1449 Genes GS186798: GO:0030554 adenyl nucleotide binding
Expand Tier I Mouse MP 4772 Genes GS165524: MP:0010769 abnormal survival
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier II Mouse 342 Genes GS35779: Neocortex Gene expression correlates of CPP - Time (s) in drug-paired compartment a in Males BXD
Expand Tier I Human GO 2353 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human GO 108 Genes GS200456: GO:0015405 P-P-bond-hydrolysis-driven transmembrane transporter activity
Expand Tier I Mouse GO 49 Genes GS187147: GO:0008076 voltage-gated potassium channel complex
Expand Tier I Mouse GO 89 Genes GS182249: GO:0016820 hydrolase activity, acting on acid anhydrides, catalyzing transmembrane movement of substances
Expand Tier I Human GO 4719 Genes GS195977: GO:0007154 cell communication