Gene Details



RPGRIP1 and homologs in 3 species are found in 426 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Mouse GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Mouse 573 Genes GS136327: non-insulin-dependent diabetes mellitus 2 in NSY (Nidd2n, Published QTL Chr 14)
Expand Tier I Mouse 576 Genes GS135493: behavioral response to methamphetamines 9 (Brmth9, Published QTL Chr 14)
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse 561 Genes GS136598: resistance to thymic deletion 4 (Rthyd4, Published QTL Chr 14)
Expand Tier I Human 269 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Mouse GO 454 Genes GS181012: GO:0007423 sensory organ development
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Mouse MP 184 Genes GS163581: MP:0001004 abnormal retinal photoreceptor morphology
Expand Tier I Mouse MP 192 Genes GS166394: MP:0003728 abnormal retinal photoreceptor layer morphology
Expand Tier II Mouse 378 Genes GS36049: Neocortex Gene expression correlates of Light- Dark Box Total seconds spent in light compartment in Females & Males BXD
Expand Tier I Mouse 572 Genes GS136342: nicotine induced locomotor activity 8 (Nilac8, Published QTL Chr 14)
Expand Tier I Human 70 Genes GS175439: HP:0009136 Duplication involving bones of the feet
Expand Tier I Mouse 468 Genes GS136307: myocardial infarction 2 (Myci2, Published QTL Chr 14)
Expand Tier I Human 49 Genes GS173605: HP:0004426 Abnormality of the cheeks
Expand Tier I Human 135 Genes GS170969: HP:0000157 Abnormality of the tongue
Expand Tier I Human 168 Genes GS170916: HP:0008056 Aplasia/Hypoplasia affecting the eye
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 38 Genes GS176220: HP:0011620 Abnormality of abdominal situs
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human 324 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human 13 Genes GS174063: HP:0100732 Pancreatic fibrosis
Expand Tier I Human 69 Genes GS172825: HP:0001829 Polydactyly (feet)
Expand Tier I Human 46 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 12234 Genes GS201251: GO:0044424 intracellular part
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 I Human 66 Genes GS176263: HP:0100259 Postaxial polydactyly
Expand Tier I Human 117 Genes GS172063: HP:0000107 Renal cysts
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Mouse 573 Genes GS136682: skull morphology 21 (Skull21, Published QTL Chr 14)
Expand Tier I Human 30 Genes GS174729: HP:0010322 Abnormality of the 5th toe
Expand Tier I Human 202 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Mouse GO 912 Genes GS179236: GO:0048699 generation of neurons
Expand Tier I Human 348 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Mouse MP 331 Genes GS163432: MP:0006069 abnormal retinal neuronal layer morphology
Expand Tier I Human 101 Genes GS175263: HP:0001161 Polydactyly (hands)
Expand Tier I Human 69 Genes GS176437: HP:0002334 Abnormality of the cerebellar vermis
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Mouse 3319 Genes GS127931: Olfactory bulb - Allen Mouse Brain Atlas
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Mouse GO 758 Genes GS188757: GO:0009887 organ morphogenesis
Expand Tier I Human 46 Genes GS173882: HP:0001305 Dandy-Walker malformation
Expand Tier I Mouse MP 63 Genes GS170695: MP:0002699 abnormal vitreous body morphology
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 179 Genes GS176589: HP:0001273 Abnormality of the corpus callosum
Expand Tier I Human 124 Genes GS175492: HP:0000512 Abnormal electroretinogram
Expand Tier I Mouse GO 244 Genes GS179362: GO:0005929 cilium
Expand Tier II Mouse 155 Genes GS36608: Cerebellum Gene expression correlates of Morphine vertical activity counts minutes 105-120 in Females BXD
Expand Tier I Human 30 Genes GS172587: HP:0001830 Postaxial polydactyly of foot
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Human GO 2050 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Mouse 2963 Genes GS127934: Retrohippocampal region - Allen Mouse Brain Atlas
Expand Tier I Human 65 Genes GS174481: HP:0010576 Intracranial cystic lesion
Expand Tier I Mouse GO 639 Genes GS192628: GO:0048666 neuron development
Expand Tier I Human 123 Genes GS171946: HP:0002269 Abnormality of neuronal migration
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Mouse 572 Genes GS135363: B.burgdorferi-associated arthritis 21 (Bbaa21, Published QTL Chr 14)
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human 31 Genes GS172499: HP:0000037 Male pseudohermaphroditism
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 825 Genes GS187237: GO:0030182 neuron differentiation
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 435 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human 141 Genes GS174847: HP:0000940 Abnormal diaphysis morphology
Expand Tier I Human 232 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Human GO 1724 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Human 61 Genes GS175264: HP:0001162 Postaxial polydactyly (hands)
Expand Tier I Human 298 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Human 21 Genes GS172367: HP:0000647 Sclerocornea
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Mouse MP 466 Genes GS163138: MP:0005253 abnormal eye physiology
Expand Tier I Mouse 462 Genes GS136025: heart weight quantitative locus 1 (Hwq1, Published QTL Chr 14)
Expand Tier I Mouse 3267 Genes GS127938: Striatum - Allen Mouse Brain Atlas
Expand Tier III Mouse 8392 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier II Mouse 97 Genes GS35150: Cerebellum Gene expression correlates of Cocaine Sensitization - SEN_CHCL_ADIST_4 minus LOC_CHCL_ADIST_3 in Females BXD
Expand Tier III Mouse 62 Genes GS637: Differential Expression in Amygdala and Hippocampus of High vs. Low Anxiety Selected Lines
Expand Tier I Mouse GO 106 Genes GS187835: GO:0060041 retina development in camera-type eye
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human 236 Genes GS174257: HP:0000309 Abnormality of the midface
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Mouse MP 226 Genes GS169032: MP:0005551 abnormal eye electrophysiology
Expand Tier I Human 221 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Mouse MP 23 Genes GS168576: MP:0008585 absent photoreceptor outer segment
Expand Tier II Mouse 94 Genes GS36713: Cerebellum Gene expression correlates of Morphine vertical activity counts minutes 45-60 in Females BXD
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
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 1456 Genes GS205144: GO:0048468 cell development
Expand Tier I Human 64 Genes GS174379: HP:0002084 Encephalocele
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human CTD 4423 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
Expand Tier I Human 81 Genes GS171773: HP:0000532 Chorioretinal abnormality
Expand Tier I Human 92 Genes GS171656: HP:0000610 Abnormality of the choroid
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 1067 Genes GS196002: GO:0048699 generation of neurons
Expand Tier I Mouse 3096 Genes GS127928: Lateral septal complex - Allen Mouse Brain Atlas
Expand Tier I Human 126 Genes GS175665: HP:0006504 Abnormality involving the diaphyses of the limbs
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 145 Genes GS171586: HP:0001560 Abnormality of the amniotic fluid
Expand Tier I Human 285 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Mouse 2918 Genes GS127935: Striatum dorsal region - Allen Mouse Brain Atlas
Expand Tier I Mouse MP 438 Genes GS165390: MP:0003224 neuron degeneration
Expand Tier III Mouse 8107 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
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 GO 2538 Genes GS190893: GO:0030154 cell differentiation
Expand Tier I Human 498 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human GO 126 Genes GS201851: GO:0048592 eye morphogenesis
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Mouse GO 38 Genes GS185982: GO:0001754 eye photoreceptor cell differentiation
Expand Tier I Human 416 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human GO 2824 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 173 Genes GS175117: HP:0001883 Talipes
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 986 Genes GS204095: GO:0030182 neuron differentiation
Expand Tier I Human 15 Genes GS171339: HP:0001737 Pancreatic cysts
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
Expand Tier I Human 78 Genes GS172553: HP:0100689 Decreased corneal thickness
Expand Tier II Mouse 378 Genes GS36019: Neocortex Gene expression correlates of Light-Dark Box Total seconds spent in dark compartment in Females & Males BXD
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human GO 236 Genes GS203525: GO:0043010 camera-type eye development
Expand Tier I Mouse MP 1385 Genes GS163971: MP:0002092 abnormal eye morphology
Expand Tier II Mouse 559 Genes GS84274: METH responses for home cage activity (Published QTL, Chr 14)
Expand Tier I Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier II Mouse 137 Genes GS36593: Cerebellum Gene expression correlates of Morphine vertical activity counts minutes 90-105 in Females BXD
Expand Tier I Human 97 Genes GS173091: HP:0004374 Hemiplegia/hemiparesis
Expand Tier I Mouse MP 574 Genes GS166743: MP:0002229 neurodegeneration
Expand Tier I Mouse GO 2279 Genes GS186488: GO:0048513 organ development
Expand Tier II Mouse 661 Genes GS84275: cocaine seizure (Published QTL, Chr 14)
Expand Tier I Human 39 Genes GS175468: HP:0001177 Preaxial polydactyly (hands)
Expand Tier I Human 487 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier II Mouse 107 Genes GS35318: Neocortex Gene expression correlates of Acoustic Startle Response Percentage of maximum response at 85 db in Males BXD
Expand Tier I Human GO 1236 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human 79 Genes GS175373: HP:0011486 Abnormality of corneal thickness
Expand Tier I Human GO 794 Genes GS209568: GO:0048666 neuron development
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 44 Genes GS175961: HP:0000062 Ambiguous genitalia
Expand Tier I Mouse MP 90 Genes GS170245: MP:0004022 abnormal cone electrophysiology
Expand Tier I Human 51 Genes GS171628: HP:0008053 Aplasia/Hypoplasia of the iris
Expand Tier I Human 438 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Mouse 3375 Genes GS127927: Hypothalamus - Allen Mouse Brain Atlas
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 111 Genes GS171465: HP:0004275 Duplication of hand bones
Expand Tier I Mouse GO 1398 Genes GS181215: GO:0007399 nervous system development
Expand Tier I Human 281 Genes GS171204: HP:0011314 Abnormality of long bone morphology
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 47 Genes GS172604: HP:0005445 Widened posterior fossa
Expand Tier I Human 20 Genes GS172391: HP:0000221 Furrowed tongue
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Mouse MP 574 Genes GS167217: MP:0001325 abnormal retina morphology
Expand Tier I Human 67 Genes GS172844: HP:0000482 Microcornea
Expand Tier I Human GO 1693 Genes GS209960: GO:0003008 system process
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse GO 123 Genes GS193540: GO:0007601 visual perception
Expand Tier I Mouse 557 Genes GS135791: epilepsy 5 (El5, Published QTL Chr 14)
Expand Tier I Human 50 Genes GS174418: HP:0010950 Abnormality of the fourth ventricle
Expand Tier I Mouse GO 286 Genes GS190016: GO:0001654 eye development
Expand Tier I Human 142 Genes GS171178: HP:0000238 Hydrocephalus
Expand Tier I Mouse 3289 Genes GS127924: Cerebral cortex - Allen Mouse Brain Atlas
Expand Tier I Human GO 275 Genes GS206897: GO:0001654 eye development
Expand Tier I Mouse MP 140 Genes GS169804: MP:0003731 abnormal retinal outer nuclear layer morphology
Expand Tier I Mouse 3384 Genes GS127925: Hippocampal formation - Allen Mouse Brain Atlas
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 324 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human 28 Genes GS171678: HP:0002612 Congenital hepatic fibrosis
Expand Tier I Mouse MP 17 Genes GS163030: MP:0008582 short photoreceptor inner segment
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 75 Genes GS174446: HP:0001120 Abnormality of corneal size
Expand Tier I Human 41 Genes GS172019: HP:0001360 Holoprosencephaly
Expand Tier I Human 20 Genes GS173717: HP:0002323 Anencephaly
Expand Tier I Mouse GO 1466 Genes GS180001: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Human 202 Genes GS171631: HP:0008051 Abnormality of the retinal pigment epithelium
Expand Tier I Human 196 Genes GS172034: HP:0000368 Low-set, posteriorly rotated ears
Expand Tier I Human 197 Genes GS175785: HP:0002500 Abnormality of the cerebral white matter
Expand Tier I Human 258 Genes GS172272: HP:0001197 Abnormality of prenatal development or birth
Expand Tier I Human 263 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Mouse GO 2710 Genes GS192471: GO:0048869 cellular developmental process
Expand Tier I Mouse MP 92 Genes GS170195: MP:0008515 thin retinal outer nuclear layer
Expand Tier I Mouse 583 Genes GS136712: susceptibility to lung cancer 13 (Sluc13, Published QTL Chr 14)
Expand Tier I Mouse MP 585 Genes GS165985: MP:0000965 abnormal sensory neuron morphology
Expand Tier I Mouse MP 647 Genes GS164446: MP:0005195 abnormal posterior eye segment morphology
Expand Tier I Mouse DRG 1187 Genes provisional GS87137: Table S2: List of probe-sets of genes differentially expressed among the four inbred strains of mice. Gene Ranks [DRG]
Expand Tier I Mouse MP 48 Genes GS169803: MP:0003730 abnormal photoreceptor inner segment morphology
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 106 Genes GS171336: HP:0001732 Abnormality of the pancreas
Expand Tier I Mouse MP 106 Genes GS166716: MP:0003729 abnormal photoreceptor outer segment morphology
Expand Tier I Human 337 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier I Mouse 2944 Genes GS127937: Striatum-like amygdalar nuclei - Allen Mouse Brain Atlas
Expand Tier I Mouse MP 1476 Genes GS169531: MP:0005391 vision/eye phenotype
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Mouse 2962 Genes GS127936: Striatum ventral region - Allen Mouse Brain Atlas
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human GO 25 Genes GS206549: GO:0042462 eye photoreceptor cell development
Expand Tier I Mouse MP 592 Genes GS165809: MP:0002864 abnormal ocular fundus morphology
Expand Tier I Human 228 Genes GS172470: HP:0001743 Abnormality of the spleen
Expand Tier I Mouse GO 29 Genes GS189672: GO:0042462 eye photoreceptor cell development
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human 162 Genes GS175958: HP:0000795 Abnormality of the urethra
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 Human 59 Genes GS171588: HP:0001562 Oligohydramnios
Expand Tier I Mouse GO 1394 Genes GS191552: GO:0042995 cell projection
Expand Tier I Mouse DRG 267 Genes provisional GS86830: Table S2: List of probe-sets of genes differentially expressed among the four inbred strains of mice. C57BL/6J [DRG]
Expand Tier I Human 616 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse GO 4333 Genes GS184452: GO:0044422 organelle part
Expand Tier I Mouse GO 4073 Genes GS180034: GO:0032502 developmental process
Expand Tier I Human 65 Genes GS176627: HP:0000457 Flat nose
Expand Tier I Human 111 Genes GS173651: HP:0009142 Duplication of bones involving the upper extremities
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 Human GO 105 Genes GS204694: GO:0060041 retina development in camera-type eye
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human 346 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Mouse GO 49 Genes GS183545: GO:0046530 photoreceptor cell differentiation
Expand Tier I Human 188 Genes GS171512: HP:0007703 Abnormal retinal pigmentation
Expand Tier I Rat DRG 4920 Genes GS86932: Table S3: CORTEX 17K MICROARRAY [DRG]
Expand Tier I Mouse GO 126 Genes GS185036: GO:0048592 eye morphogenesis
Expand Tier I Human 416 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Mouse GO 6947 Genes GS192918: GO:0050896 response to stimulus
Expand Tier I Mouse DRG 228 Genes provisional GS86553: Table S2: List of probe-sets of genes differentially expressed among the four inbred strains of mice. 129P3/J [DRG]
Expand Tier I Human 445 Genes GS175423: HP:0010461 Abnormality of the male genitalia
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 34 Genes GS172513: HP:0001696 Situs inversus totalis
Expand Tier I Mouse 484 Genes GS136088: lean body mass 10 (Lbm10, Published QTL Chr 14)
Expand Tier I Human 120 Genes GS171657: HP:0000613 Photophobia
Expand Tier I Human 38 Genes GS174087: HP:0003363 Abdominal situs inversus
Expand Tier I Human 358 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier II Mouse 511 Genes GS84277: METH responses for home cage activity (Published QTL, Chr 14)
Expand Tier I Human 64 Genes GS172899: HP:0011815 Cephalocele
Expand Tier I Mouse MP 96 Genes GS164692: MP:0004021 abnormal rod electrophysiology
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Human GO 1136 Genes GS205691: GO:0022008 neurogenesis
Expand Tier I Mouse 3315 Genes GS127939: Thalamus - Allen Mouse Brain Atlas
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier II Mouse 191 Genes GS35839: Neocortex Gene expression correlates of Cocaine CPP - Proportion of time spent in conditioned side prior to conditioning in Males BXD
Expand Tier I Human 115 Genes GS172148: HP:0010442 Polydactyly
Expand Tier II Mouse 51 Genes GS36117: Striatum Gene expression correlates of Contextual activity in fear conditioning apparatus in Males BXD
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Mouse GO 1378 Genes GS188287: GO:0048468 cell development
Expand Tier I Human 38 Genes GS172855: HP:0004307 Abnormal anatomic location of the heart
Expand Tier I Human 49 Genes GS175305: HP:0000293 Full cheeks
Expand Tier I Mouse GO 245 Genes GS186677: GO:0043010 camera-type eye development
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human GO 1588 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Human GO 30 Genes GS206550: GO:0042461 photoreceptor cell development
Expand Tier I Human 63 Genes GS174833: HP:0006817 Aplasia/Hypoplasia of the cerebellar vermis
Expand Tier I Mouse GO 1850 Genes GS186562: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human 433 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Mouse 3343 Genes GS127930: Midbrain - Allen Mouse Brain Atlas
Expand Tier I Mouse 3329 Genes GS127933: Pons - Allen Mouse Brain Atlas
Expand Tier I Human GO 1224 Genes GS208482: GO:0042995 cell projection
Expand Tier I Mouse MP 2200 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier I Human 56 Genes GS176885: HP:0002693 Abnormality of the skull base
Expand Tier I Human GO 205 Genes GS209987: GO:0050953 sensory perception of light stimulus
Expand Tier I Human 271 Genes GS176826: HP:0000202 Oral cleft
Expand Tier I Mouse MP 1724 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier I Mouse 576 Genes GS136852: Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 3 (Tmevd3, Published QTL Chr 14)
Expand Tier I Human 38 Genes GS173462: HP:0001651 Dextrocardia
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human 282 Genes GS175900: HP:0009118 Aplasia/Hypoplasia of the mandible
Expand Tier I Mouse MP 6 Genes GS165589: MP:0003381 vitreal fibroplasia
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Human 85 Genes GS173946: HP:0002438 Cerebellar malformation
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse 573 Genes GS135405: body growth late QTL 15 (Bglq15, Published QTL Chr 14)
Expand Tier I Mouse MP 396 Genes GS170108: MP:0003727 abnormal retinal layer morphology
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Human 84 Genes GS175531: HP:0000003 Multicystic kidney dysplasia
Expand Tier I Human 129 Genes GS173247: HP:0007957 Reduction of corneal clarity
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Mouse GO 123 Genes GS193046: GO:0050953 sensory perception of light stimulus
Expand Tier I Mouse 3109 Genes GS127923: Cerebellum - Allen Mouse Brain Atlas
Expand Tier I Human GO 70 Genes GS209967: GO:0005930 axoneme
Expand Tier I Human GO 2661 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 52 Genes GS171623: HP:0008055 Aplasia/Hypoplasia affecting the uvea
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human 51 Genes GS175893: HP:0000932 Abnormality of the posterior cranial fossa
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier II Mouse 500 Genes GS84278: chronic alcohol withdrawal severity (Published QTL, Chr 14)
Expand Tier I Human 533 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 264 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Rat DRG 4920 Genes GS86494: Table S1: Hippocampus 17 K microarray data. [DRG]
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 13 Genes GS175255: HP:0010459 True hermaphroditism
Expand Tier I Mouse MP 3019 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Human GO 34 Genes GS202819: GO:0001754 eye photoreceptor cell differentiation
Expand Tier I Mouse 569 Genes GS136040: insulin dependent diabetes susceptibility 12 (Idd12, Published QTL Chr 14)
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 137 Genes GS175674: HP:0007360 Aplasia/Hypoplasia of the cerebellum
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Human CTD 2047 Genes GS127205: Tamoxifen interacting genes (MeSH:D013629) in CTD
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Mouse GO 41 Genes GS193026: GO:0005930 axoneme
Expand Tier I Mouse 572 Genes GS136293: modifier of obesity related sterility 3 (Mors3, Published QTL Chr 14)
Expand Tier III Mouse 56 Genes GS640: Hippocampus vs. Amygdala main effect Contextual fear conditioning Selected Lines -Differential Expression
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Mouse 498 Genes GS129081: atherosclerosis 13 (Ath13 Published QTL Chr 14)
Expand Tier I Mouse MP 96 Genes GS166313: MP:0008450 retinal photoreceptor degeneration
Expand Tier I Human 174 Genes GS171806: HP:0005656 Positional foot deformities
Expand Tier I Mouse 354 Genes GS129167: plasma plant sterol 1a (Plast1a Published QTL Chr 14)
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 239 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier I Human GO 495 Genes GS209225: GO:0007600 sensory perception
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 435 Genes GS197802: GO:0007423 sensory organ development
Expand Tier I Human 416 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human 397 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Mouse 503 Genes GS136456: postnatal body weight growth 18 (Pbwg18, Published QTL Chr 14)
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 51 Genes GS171787: HP:0001395 Hepatic fibrosis
Expand Tier I Human 33 Genes GS173194: HP:0012090 Abnormality of pancreas morphology
Expand Tier I Mouse 3136 Genes GS127926: Hippocampal region - Allen Mouse Brain Atlas
Expand Tier I Human 154 Genes GS175880: HP:0007370 Aplasia/Hypoplasia of the corpus callosum
Expand Tier II Mouse 122 Genes GS36743: Cerebellum Gene expression correlates of Morphine vertical activity counts minutes 75-90 in Females BXD
Expand Tier I Mouse 3289 Genes GS127932: Pallidum - Allen Mouse Brain Atlas
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Mouse MP 983 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier II Mouse 15 Genes GS26242: Neocortex Gene expression correlates of Mechanical Nociception - Tail Clip Test in Females BXD
Expand Tier I Mouse GO 37 Genes GS189673: GO:0042461 photoreceptor cell development
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human 110 Genes GS172484: HP:0009997 Duplication of phalanx of hand
Expand Tier I Mouse DRG 321 Genes provisional GS86920: Table S3: Detailed description of Gene Ontology analysis presented in Table 1 and Table 2. Inter strain GO [DRG]
Expand Tier I Mouse MP 3716 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human 282 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Mouse 583 Genes GS135777: epistatic circling SWR/J (ecs, Published QTL Chr 14)
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier II Mouse 115 Genes GS36728: Cerebellum Gene expression correlates of Morphine vertical activity counts minutes 60-75 in Females BXD
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Mouse 461 Genes GS129121: cocaine seizure 2 (Cosz2 Published QTL Chr 14)
Expand Tier II Mouse 718 Genes GS84276: nicotine sensitivity (Published QTL, Chr 14)
Expand Tier I Human GO 41 Genes GS200343: GO:0046530 photoreceptor cell differentiation
Expand Tier I Mouse GO 609 Genes GS185024: GO:0044463 cell projection part
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Human 302 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human 19 Genes GS172315: HP:0010295 Aplasia/Hypoplasia of the tongue
Expand Tier I Human 311 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Mouse 3395 Genes GS127929: Medulla - Allen Mouse Brain Atlas
Expand Tier I Human 271 Genes GS174948: HP:0100763 Abnormality of the lymphatic system
Expand Tier I Human GO 238 Genes GS196129: GO:0005929 cilium
Expand Tier I Mouse GO 2138 Genes GS186067: GO:0050877 neurological system process
Expand Tier I Mouse GO 2498 Genes GS193018: GO:0003008 system process
Expand Tier I Human GO 637 Genes GS201839: GO:0044463 cell projection part
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier II Mouse 107 Genes GS35298: Neocortex Gene expression correlates of Prepulse inhibition at 85db in Males BXD
Expand Tier I Human GO 2545 Genes GS203335: GO:0048513 organ development
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier II Mouse 515 Genes GS83995: cocaine seizure 2 (Cosz2, Published QTL, Chr 14)
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier II Mouse 83 Genes GS36340: Hippocampus Gene expression correlates of Naloxone induced Morphine Withdrawal TOTAL vertical activity counts in 15 minutes in Males BXD
Expand Tier I Human 126 Genes GS170894: HP:0006487 Bowing of the long bones
Expand Tier I Human 140 Genes GS175471: HP:0001172 Abnormality of the thumb
Expand Tier I Human 262 Genes GS172033: HP:0000369 Low-set ears
Expand Tier I Mouse 504 Genes GS135743: dystrophic cardiac calcinosis 4 (Dyscalc4, Published QTL Chr 14)
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 19 Genes GS173221: HP:0006706 Cystic liver disease
Expand Tier I Human 49 Genes GS176262: HP:0100258 Preaxial polydactyly
Expand Tier I Human 68 Genes GS176574: HP:0008062 Aplasia/Hypoplasia affecting the anterior segment of the eye
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier II Mouse 404 Genes GS36411: Neocortex Gene expression correlates of Open Field - Total rears 5-10 minutes in Females BXD
Expand Tier I Mouse 459 Genes GS136280: modifier of ocular retardation 3 (Modor3, Published QTL Chr 14)
Expand Tier I Human 50 Genes GS171919: HP:0002198 Dilated fourth ventricle
Expand Tier I Human 34 Genes GS173140: HP:0011534 Abnormal spatial orientation of the cardiac segments
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Mouse MP 710 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier I Mouse DRG 439 Genes provisional GS86502: Table S3: List of Cocaine-Treated HDAC5 KO vs. Saline-Treated HDAC5 KO Significantly Regulated Genes. [DRG]
Expand Tier I Human 47 Genes GS176066: HP:0002350 Cerebellar cyst
Expand Tier I Mouse 569 Genes GS136627: Stem cell proliferation 9 (Scpro9, Published QTL Chr 14)
Expand Tier I Human 54 Genes GS172571: HP:0000340 Sloping forehead
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse 573 Genes GS135518: body weight 1 (Bwt1, Published QTL Chr 14)
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Human GO 792 Genes GS205616: GO:0009887 organ morphogenesis
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 II Mouse 64 Genes GS36698: Cerebellum Gene expression correlates of Morphine Vertical Activity 30-45 min in Females BXD
Expand Tier I Human 62 Genes GS172992: HP:0001320 Cerebellar vermis hypoplasia
Expand Tier I Human 409 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Human 96 Genes GS176616: HP:0000662 Night blindness
Expand Tier I Mouse 809 Genes GS129166: plasma plant sterol 1 (Plast1 Published QTL Chr 14)
Expand Tier I Mouse GO 980 Genes GS188826: GO:0022008 neurogenesis
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 237 Genes GS171395: HP:0000175 Cleft palate
Expand Tier I Mouse GO 1550 Genes GS192290: GO:0007600 sensory perception
Expand Tier III Mouse 3192 Genes GS213073: Genes with suggestive difference in (PB6F1) vs (B6PF1 + B6 + PWD) comparison
Expand Tier I Human 215 Genes GS172139: HP:0010993 Abnormality of the cerebral subcortex
Expand Tier I Mouse 573 Genes GS135391: body growth early QTL 13 (Bgeq13, Published QTL Chr 14)