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Chromosomal Location search: -> chromosome X
Sort by: -> Chromosomal location
Found 375 genes. Show from 1 to 375.

Ensembl Gene ID (Gene Symbol) Chr Human Ortholog OMIM Description Unitraps
ENSMUSG00000068270 (Shroom4) X ENSG00000158352 300434 - STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME 2
ENSMUSG00000062393 (Dgkk) X ENSG00000204466 - 4
ENSMUSG00000051592 (Ccnb3) X ENSG00000147082 - 2
ENSMUSG00000004317 (Clcn5) X ENSG00000171365 310468 - NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE 4
ENSMUSG00000063018 (2010204K13Rik) X - - 1
ENSMUSG00000039556 (Ppp1r3f) X ENSG00000049769 - 1
ENSMUSG00000031143 (Ccdc22) X ENSG00000101997 - 2
ENSMUSG00000031144 (Syp) X ENSG00000102003 - 3
ENSMUSG00000031145 (Prickle3) X ENSG00000012211 - 3
ENSMUSG00000031146 (Plp2) X ENSG00000102007 - 3
ENSMUSG00000031147 (Magix) X ENSG00000017621 - 4
ENSMUSG00000039382 (Wdr45) X ENSG00000196998 - 7
ENSMUSG00000031149 (Praf2) X ENSG00000102050 - 2
ENSMUSG00000031150 (Ccdc120) X ENSG00000147144 - 3
ENSMUSG00000000134 (Tcfe3) X ENSG00000068323 606243 - ALVEOLAR SOFT-PART SARCOMA 7
ENSMUSG00000031153 (Gripap1) X ENSG00000068400 - 4
ENSMUSG00000031154 (Otud5) X ENSG00000068308 - 5
ENSMUSG00000031156 (Slc35a2) X ENSG00000102100 - 2
ENSMUSG00000031157 (Pqbp1) X ENSG00000102103 309500 - RENPENNING SYNDROME 1 8
ENSMUSG00000031158 (Timm17b) X - - 1
ENSMUSG00000039278 (Pcsk1n) X ENSG00000102109 - 2
ENSMUSG00000031160 (Eras) X ENSG00000187682 - 1
ENSMUSG00000031161 (Hdac6) X ENSG00000094631 - 1
ENSMUSG00000031162 (Gata1) X ENSG00000102145 314050 - THROMBOCYTOPENIA, PLATELET DYSFUNCTION, HEMOLYSIS, AND IMBALANCED 1
ENSMUSG00000031163 (Glod5) X ENSG00000171433 - 3
ENSMUSG00000039231 (Suv39h1) X - - 4
ENSMUSG00000031165 (Was) X ENSG00000015285 313900 - THROMBOCYTOPENIA 1 2
ENSMUSG00000031166 (Wdr13) X ENSG00000101940 - 4
ENSMUSG00000031167 (Rbm3) X ENSG00000102317 - 6
ENSMUSG00000055188 (2900002K06Rik) X - - 2
ENSMUSG00000039201 (Tbc1d25) X ENSG00000068354 - 3
ENSMUSG00000031168 (Ebp) X ENSG00000147155 302960 - CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT 4
ENSMUSG00000031169 (Porcn) X ENSG00000102312 305600 - FOCAL DERMAL HYPOPLASIA 4
ENSMUSG00000031171 (Ftsj1) X ENSG00000068438 309549 - MENTAL RETARDATION, X-LINKED 9 8
ENSMUSG00000031170 (Slc38a5) X ENSG00000017483 - 2
ENSMUSG00000068218 (Ssxb9) X - - 1
ENSMUSG00000079704 (OTTMUSG00000016698) X - - 1
ENSMUSG00000035371 (Ssx9) X ENSG00000185319 - 1
ENSMUSG00000015342 (Xk) X - - 1
ENSMUSG00000015340 (Cybb) X ENSG00000165168 306400 - GRANULOMATOUS DISEASE, CHRONIC, X-LINKED 1
ENSMUSG00000031174 (Rpgr) X ENSG00000156313 304020 - CONE-ROD DYSTROPHY, X-LINKED, 1 2
ENSMUSG00000058254 (Tspan7) X ENSG00000156298 300210 - MENTAL RETARDATION, X-LINKED 58 1
ENSMUSG00000073288 (AL671335.12) X - - 1
ENSMUSG00000040363 (Bcor) X ENSG00000183337 300166 - MICROPHTHALMIA, SYNDROMIC 2 4
ENSMUSG00000031007 (Atp6ap2) X ENSG00000182220 300423 - MENTAL RETARDATION, X-LINKED, WITH EPILEPSY 6
ENSMUSG00000064127 (Med14) X ENSG00000180182 - 2
ENSMUSG00000031010 (Usp9x) X ENSG00000124486 - 29
ENSMUSG00000000787 (Ddx3x) X ENSG00000215301 - 6
ENSMUSG00000031012 (Cask) X ENSG00000147044 - 6
ENSMUSG00000047678 (Gpr82) X ENSG00000171657 - 1
ENSMUSG00000025038 (Efhc2) X ENSG00000183690 - 1
ENSMUSG00000037369 (Utx) X ENSG00000147050 - 4
ENSMUSG00000037358 (4930578C19Rik) X - - 1
ENSMUSG00000037341 (Slc9a7) X ENSG00000065923 - 1
ENSMUSG00000060090 (Rp2h) X ENSG00000102218 312600 - RETINITIS PIGMENTOSA 2 3
ENSMUSG00000037315 (Phf16) X ENSG00000102221 - 5
ENSMUSG00000031059 (Ndufb11) X ENSG00000147123 - 1
ENSMUSG00000031060 (Rbm10) X ENSG00000182872 - 5
ENSMUSG00000001924 (Uba1) X - - 1
ENSMUSG00000031065 (Pctk1) X ENSG00000102225 - 1
ENSMUSG00000031066 (Usp11) X ENSG00000102226 - 1
ENSMUSG00000001127 (Araf) X ENSG00000078061 - 2
ENSMUSG00000037217 (Syn1) X ENSG00000008056 300491 - EPILEPSY, X-LINKED, WITH VARIABLE LEARNING DISABILITIES AND BEHAVIOR 5
ENSMUSG00000001131 (Timp1) X ENSG00000102265 - 4
ENSMUSG00000001128 (Cfp) X ENSG00000126759 312060 - PROPERDIN DEFICIENCY, X-LINKED 3
ENSMUSG00000001134 (Uxt) X ENSG00000126756 - 2
ENSMUSG00000054737 (Zfp182) X ENSG00000147118 - 1
ENSMUSG00000036782 (Klhl13) X ENSG00000003096 - 7
ENSMUSG00000036769 (Wdr44) X ENSG00000131725 - 4
ENSMUSG00000006373 (Pgrmc1) X ENSG00000101856 - 1
ENSMUSG00000059708 (Sfrs17b) X ENSG00000214992 - 2
ENSMUSG00000037636 (Slc25a43) X ENSG00000077713 - 3
ENSMUSG00000016319 (Slc25a5) X ENSG00000005022 - 2
ENSMUSG00000006423 (C330007P06Rik) X ENSG00000018610 - 4
ENSMUSG00000016308 (Ube2a) X ENSG00000077721 - 3
ENSMUSG00000044149 (Nkrf) X ENSG00000186416 - 1
ENSMUSG00000050379 (Sept6) X ENSG00000125354 - 2
ENSMUSG00000079641 (Rpl39) X ENSG00000198918 - 1
ENSMUSG00000036572 (Upf3b) X ENSG00000125351 300676 - MENTAL RETARDATION, X-LINKED, SYNDROMIC 14 5
ENSMUSG00000016409 (Nkap) X ENSG00000101882 - 1
ENSMUSG00000063709 (RP23-457N24.1) X - - 1
ENSMUSG00000006200 (Rhox6) X ENSG00000203989 - 2
ENSMUSG00000068048 (Rhox9) X ENSG00000203989 - 1
ENSMUSG00000071766 (Rhox12) X - - 1
ENSMUSG00000050197 (Rhox13) X - - 1
ENSMUSG00000048047 (Zbtb33) X ENSG00000177485 - 1
ENSMUSG00000016534 (Lamp2) X ENSG00000005893 300257 - DANON DISEASE 3
ENSMUSG00000031095 (Cul4b) X ENSG00000158290 300639 - MENTAL RETARDATION, X-LINKED, WITH BRACHYDACTYLY AND MACROGLOSSIA 9
ENSMUSG00000000355 (Mcts1) X ENSG00000101898 - 5
ENSMUSG00000048970 (C1galt1c1) X ENSG00000171155 300622 - TN SYNDROME 1
ENSMUSG00000051361 (6030498E09Rik) X - - 1
ENSMUSG00000001986 (Gria3) X - - 1
ENSMUSG00000037475 (Thoc2) X ENSG00000125676 - 2
ENSMUSG00000025860 (Xiap) X ENSG00000180152 - 6
ENSMUSG00000025862 (Stag2) X ENSG00000101972 - 2
ENSMUSG00000016150 (Odz1) X ENSG00000009694 - 2
ENSMUSG00000079616 (AL773587.11) X - - 2
ENSMUSG00000045284 (Wdr40b) X ENSG00000198354 - 1
ENSMUSG00000031099 (Smarca1) X - - 1
ENSMUSG00000001173 (Ocrl) X ENSG00000122126 309000 - LOWE OCULOCEREBRORENAL SYNDROME 2
ENSMUSG00000037005 (Xpnpep2) X ENSG00000122121 - 1
ENSMUSG00000031101 (Sash3) X ENSG00000122122 - 1
ENSMUSG00000036985 (Zdhhc9) X ENSG00000188706 - 2
ENSMUSG00000063785 (Utp14a) X ENSG00000214320 - 6
ENSMUSG00000036959 (Bcorl1) X - - 1
ENSMUSG00000031103 (Elf4) X ENSG00000102034 - 1
ENSMUSG00000031104 (Rab33a) X ENSG00000134594 - 1
ENSMUSG00000036916 (Zfp280c) X ENSG00000056277 - 3
ENSMUSG00000031105 (Slc25a14) X ENSG00000102078 - 1
ENSMUSG00000031109 (Enox2) X ENSG00000165675 - 4
ENSMUSG00000062184 (Hs6st2) X ENSG00000171004 - 1
ENSMUSG00000031119 (Gpc4) X ENSG00000076716 - 2
ENSMUSG00000055653 (Gpc3) X ENSG00000147257 312870 - SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1 4
ENSMUSG00000055110 (A630012P03Rik) X - - 1
ENSMUSG00000073207 (6330534C20Rik) X ENSG00000203952 - 1
ENSMUSG00000067946 (BX649621.5) X - - 1
ENSMUSG00000025626 (Phf6) X ENSG00000156531 301900 - BORJESON-FORSSMAN-LEHMANN SYNDROME 2
ENSMUSG00000025630 (Hprt1) X ENSG00000165704 300322 - LESCH-NYHAN SYNDROME 5
ENSMUSG00000061082 (Plac1) X ENSG00000170965 - 2
ENSMUSG00000036022 (4632404H22Rik) X ENSG00000156504 - 2
ENSMUSG00000036013 (4930432H15Rik) X ENSG00000156500 - 2
ENSMUSG00000023074 (Mospd1) X - - 1
ENSMUSG00000054727 (1700013H16Rik) X - - 1
ENSMUSG00000061273 (Tmem32) X ENSG00000169446 - 2
ENSMUSG00000023092 (Fhl1) X ENSG00000022267 300718 - MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET 2
ENSMUSG00000053852 (Gpr112) X ENSG00000156920 - 2
ENSMUSG00000031133 (Arhgef6) X ENSG00000129675 300436 - MENTAL RETARDATION, X-LINKED 46 1
ENSMUSG00000031134 (Rbmx) X ENSG00000147274 - 1
ENSMUSG00000079584 (Gm364) X - - 1
ENSMUSG00000067860 (Zic3) X ENSG00000156925 306955 - HETEROTAXY, VISCERAL, 1, X-LINKED 3
ENSMUSG00000031139 (Mcf2) X ENSG00000101977 - 2
ENSMUSG00000062949 (Atp11c) X ENSG00000101974 - 3
ENSMUSG00000050900 (AL928886.7) X - - 1
ENSMUSG00000079577 (RP23-45N17.3) X ENSG00000139351 270960 - AZOOSPERMIA DUE TO PERTURBATIONS OF MEIOSIS 1
ENSMUSG00000000838 (Fmr1) X ENSG00000102081 300623 - FRAGILE X TREMOR/ATAXIA SYNDROME 3
ENSMUSG00000062170 (Fmr1nb) X ENSG00000176988 - 2
ENSMUSG00000031189 (Aff2) X ENSG00000155966 309548 - FRAGILE SITE, FOLIC ACID TYPE, RARE, FRA(X)(q28) 1
ENSMUSG00000031337 (Mtm1) X ENSG00000171100 310400 - MYOTUBULAR MYOPATHY 1 5
ENSMUSG00000035776 (Cd99l2) X ENSG00000102181 - 1
ENSMUSG00000031343 (Gabra3) X - - 2
ENSMUSG00000031347 (Cetn2) X ENSG00000147400 - 1
ENSMUSG00000031349 (Nsdhl) X ENSG00000147383 308050 - CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB 2
ENSMUSG00000031351 (Zfp185) X ENSG00000147394 - 2
ENSMUSG00000031383 (Dusp9) X ENSG00000130829 - 1
ENSMUSG00000002015 (Bcap31) X ENSG00000185825 300475 - CONTIGUOUS ABCD1/DXS1375E DELETION SYNDROME 5
ENSMUSG00000031378 (Abcd1) X ENSG00000214330 - 4
ENSMUSG00000031385 (Plxnb3) X ENSG00000198753 - 1
ENSMUSG00000002010 (Idh3g) X ENSG00000067829 - 5
ENSMUSG00000002014 (Ssr4) X ENSG00000180879 - 3
ENSMUSG00000002006 (Pdzd4) X ENSG00000067840 - 5
ENSMUSG00000031391 (L1cam) X - - 1
ENSMUSG00000031388 (Ard1) X ENSG00000102030 - 3
ENSMUSG00000031386 (Hcfc1) X ENSG00000172534 - 3
ENSMUSG00000031392 (Irak1) X ENSG00000184216 - 3
ENSMUSG00000031393 (Mecp2) X ENSG00000169057 312750 - RETT SYNDROME 3
ENSMUSG00000031328 (Flna) X ENSG00000196924 608578 - CEREBROFRONTOFACIAL SYNDROME 9
ENSMUSG00000001964 (Emd) X ENSG00000102119 310300 - EMERY-DREIFUSS MUSCULAR DYSTROPHY, X-LINKED 1
ENSMUSG00000008682 (Rpl10) X ENSG00000178464 - 2
ENSMUSG00000019087 (Atp6ap1) X ENSG00000071553 - 2
ENSMUSG00000001962 (D0HXS9928E) X ENSG00000071859 - 1
ENSMUSG00000015289 (Lage3) X ENSG00000196976 - 2
ENSMUSG00000015290 (Ubl4) X ENSG00000102178 - 2
ENSMUSG00000032806 (Slc10a3) X - - 1
ENSMUSG00000031399 (1810037C20Rik) X ENSG00000071889 - 2
ENSMUSG00000004221 (Ikbkg) X - - 1
ENSMUSG00000032750 (Gab3) X ENSG00000160219 - 1
ENSMUSG00000031403 (Dkc1) X ENSG00000130826 305000 - DYSKERATOSIS CONGENITA, X-LINKED 3
ENSMUSG00000031402 (Mpp1) X ENSG00000130830 - 1
ENSMUSG00000073094 (4930428E23Rik) X - - 1
ENSMUSG00000031196 (F8) X ENSG00000185010 306700 - HEMOPHILIA A 2
ENSMUSG00000031198 (Fundc2) X ENSG00000182814 - 2
ENSMUSG00000079529 (Mtcp1) X ENSG00000182712 - 1
ENSMUSG00000031201 (Brcc3) X ENSG00000185515 - 3
ENSMUSG00000031197 (Vbp1) X ENSG00000155959 - 3
ENSMUSG00000016382 (Pls3) X ENSG00000102024 - 2
ENSMUSG00000025246 (Tbl1x) X ENSG00000092377 - 3
ENSMUSG00000079518 (BX284111.7) X ENSG00000219186 - 1
ENSMUSG00000046942 (2410003J06Rik) X ENSG00000189023 - 1
ENSMUSG00000067669 (AL844863.7) X - - 1
ENSMUSG00000045103 (Dmd) X ENSG00000198947 310200 - MUSCULAR DYSTROPHY, DUCHENNE TYPE 14
ENSMUSG00000035476 (Map3k7ip3) X ENSG00000157625 - 4
ENSMUSG00000025059 (Gyk) X ENSG00000198814 307030 - HYPERGLYCEROLEMIA 2
ENSMUSG00000035427 (CN716893) X - - 1
ENSMUSG00000052372 (Il1rapl1) X ENSG00000169306 300143 - MENTAL RETARDATION, X-LINKED 21 4
ENSMUSG00000067649 (Mageb18) X ENSG00000176774 - 1
ENSMUSG00000006678 (Pola1) X ENSG00000101868 - 11
ENSMUSG00000035246 (Pcyt1b) X ENSG00000102230 - 7
ENSMUSG00000081044 (RP23-158M12.2) X - - 1
ENSMUSG00000079509 (Zfx) X ENSG00000067646 - 5
ENSMUSG00000035150 (Eif2s3x) X ENSG00000180574 - 3
ENSMUSG00000079508 (Apoo) X ENSG00000184831 - 1
ENSMUSG00000025656 (Arhgef9) X - - 1
ENSMUSG00000035045 (Zc3h12b) X - - 1
ENSMUSG00000031207 (Msn) X ENSG00000147065 - 2
ENSMUSG00000034457 (Eda2r) X ENSG00000131080 - 4
ENSMUSG00000046532 (Ar) X - - 1
ENSMUSG00000031214 (Ophn1) X ENSG00000079482 300486 - MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE 1
ENSMUSG00000031216 (Stard8) X ENSG00000130052 - 2
ENSMUSG00000071719 (Tmem28) X - - 1
ENSMUSG00000059327 (Eda) X ENSG00000158813 305100 - ECTODERMAL DYSPLASIA, HYPOHIDROTIC, X-LINKED 1
ENSMUSG00000015668 (Pdzd11) X ENSG00000120509 - 2
ENSMUSG00000034311 (Kif4) X ENSG00000090889 - 4
ENSMUSG00000000881 (Dlg3) X ENSG00000082458 300189 - DISCS LARGE, DROSOPHILA, HOMOLOG OF, 3 3
ENSMUSG00000009670 (Tex11) X ENSG00000120498 - 3
ENSMUSG00000031297 (Slc7a3) X ENSG00000165349 - 3
ENSMUSG00000046032 (Snx12) X ENSG00000147164 - 2
ENSMUSG00000042903 (Mllt7) X ENSG00000184481 - 3
ENSMUSG00000031304 (Il2rg) X ENSG00000147168 312863 - COMBINED IMMUNODEFICIENCY, X-LINKED 2
ENSMUSG00000031302 (Nlgn3) X ENSG00000196338 300494 - ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 4
ENSMUSG00000047797 (Gjb1) X ENSG00000169562 302800 - CHARCOT-MARIE-TOOTH DISEASE, X-LINKED, 1 3
ENSMUSG00000031310 (Zmym3) X ENSG00000147130 - 5
ENSMUSG00000031311 (Nono) X ENSG00000147140 - 6
ENSMUSG00000031314 (Taf1) X ENSG00000122728 - 3
ENSMUSG00000034160 (Ogt) X ENSG00000147162 - 6
ENSMUSG00000045010 (AL805980.28) X ENSG00000215113 - 2
ENSMUSG00000079483 (AL807784.11-203) X - - 2
ENSMUSG00000079480 (Pin4) X ENSG00000102309 - 1
ENSMUSG00000051220 (Ercc6l) X ENSG00000186871 - 1
ENSMUSG00000084142 (AL807784.11-206) X - - 1
ENSMUSG00000031320 (Rps4x) X - - 1
ENSMUSG00000067567 (Hdac8) X ENSG00000147099 - 1
ENSMUSG00000034055 (Phka1) X - - 1
ENSMUSG00000031325 (4930519F16Rik) X - - 2
ENSMUSG00000031326 (Cdx4) X ENSG00000131264 - 1
ENSMUSG00000031327 (Chic1) X ENSG00000204116 - 3
ENSMUSG00000031329 (Tsx) X - - 4
ENSMUSG00000056537 (Rnf12) X ENSG00000131263 - 4
ENSMUSG00000046449 (C77370) X ENSG00000050030 - 1
ENSMUSG00000031333 (Abcb7) X ENSG00000131269 301310 - ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA 1
ENSMUSG00000073016 (Uprt) X ENSG00000094841 - 1
ENSMUSG00000033906 (Zdhhc15) X ENSG00000102383 300577 - MENTAL RETARDATION, X-LINKED 91 2
ENSMUSG00000031226 (2610029G23Rik) X ENSG00000102390 - 2
ENSMUSG00000031229 (Atrx) X ENSG00000215766 - 17
ENSMUSG00000031232 (Magt1) X ENSG00000102158 300716 - MENTAL RETARDATION, X-LINKED 95 3
ENSMUSG00000031231 (Cox7b) X ENSG00000131174 - 2
ENSMUSG00000033792 (Atp7a) X ENSG00000215763 - 3
ENSMUSG00000062070 (Pgk1) X ENSG00000102144 300653 - PHOSPHOGLYCERATE KINASE 1 DEFICIENCY 2
ENSMUSG00000047242 (Taf9b) X ENSG00000215760 - 1
ENSMUSG00000052821 (Cysltr1) X - - 1
ENSMUSG00000049929 (Lpar4) X - - 1
ENSMUSG00000063663 (Brwd3) X ENSG00000165288 300659 - MENTAL RETARDATION, X-LINKED 93 7
ENSMUSG00000031245 (Nsbp1) X ENSG00000198157 - 2
ENSMUSG00000025665 (Rps6ka6) X ENSG00000072133 - 6
ENSMUSG00000034551 (Hdx) X ENSG00000165259 - 3
ENSMUSG00000079461 (L1Md-Gf21) X - - 1
ENSMUSG00000034555 (Tex16) X - - 1
ENSMUSG00000025525 (Apool) X ENSG00000155008 - 1
ENSMUSG00000025529 (Zfp711) X ENSG00000147180 - 1
ENSMUSG00000025531 (Chm) X ENSG00000188419 303100 - CHOROIDEREMIA 3
ENSMUSG00000025592 (Dach2) X - - 1
ENSMUSG00000034755 (Pcdh11x) X ENSG00000099715 - 2
ENSMUSG00000083294 (BX119993.9) X - - 1
ENSMUSG00000034480 (Diap2) X ENSG00000147202 300511 - PREMATURE OVARIAN FAILURE 2A 19
ENSMUSG00000031256 (Cstf2) X ENSG00000101811 - 3
ENSMUSG00000031258 (Xkrx) X ENSG00000182489 - 1
ENSMUSG00000067369 (4732479N06Rik) X ENSG00000188917 - 3
ENSMUSG00000033578 (Tmem35) X ENSG00000126950 - 1
ENSMUSG00000048007 (Timm8a1) X ENSG00000126953 311150 - OPTICOACOUSTIC NERVE ATROPHY WITH DEMENTIA 1
ENSMUSG00000031264 (Btk) X ENSG00000010671 307200 - HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED 8
ENSMUSG00000031266 (Gla) X ENSG00000102393 301500 - FABRY DISEASE 3
ENSMUSG00000045427 (Hnrph2) X ENSG00000126945 - 2
ENSMUSG00000033460 (Armcx1) X ENSG00000126947 - 2
ENSMUSG00000050394 (Armcx6) X - - 1
ENSMUSG00000033436 (Armcx2) X ENSG00000184867 - 1
ENSMUSG00000052676 (Zmat1) X - - 1
ENSMUSG00000058252 (1700008I05Rik) X ENSG00000215046 - 1
ENSMUSG00000060726 (1700129I15Rik) X - - 1
ENSMUSG00000072969 (Armcx5) X ENSG00000125962 - 1
ENSMUSG00000043384 (Gprasp1) X ENSG00000198932 - 1
ENSMUSG00000072964 (Bhlhb9) X ENSG00000198908 - 1
ENSMUSG00000047844 (Bex4) X ENSG00000102409 - 1
ENSMUSG00000051579 (Tceal8) X ENSG00000180964 - 2
ENSMUSG00000054034 (Tceal5) X ENSG00000204071 - 1
ENSMUSG00000050071 (Bex1) X ENSG00000133134 - 1
ENSMUSG00000079428 (Tceal7) X ENSG00000182916 - 1
ENSMUSG00000042712 (Wbp5) X ENSG00000185222 - 2
ENSMUSG00000046432 (Ngfrap1) X ENSG00000166681 - 2
ENSMUSG00000049536 (Tceal1) X ENSG00000172465 - 1
ENSMUSG00000031422 (Morf4l2) X ENSG00000123562 - 5
ENSMUSG00000018595 (Glra4) X - - 1
ENSMUSG00000031425 (Plp1) X ENSG00000123560 312920 - SPASTIC PARAPLEGIA 2, X-LINKED 1
ENSMUSG00000072955 (4930488E11Rik) X - - 1
ENSMUSG00000044348 (Mcart6) X ENSG00000176274 - 4
ENSMUSG00000042595 (BC031748) X ENSG00000123575 - 2
ENSMUSG00000059203 (Il1rapl2) X ENSG00000189108 - 4
ENSMUSG00000051257 (Trap1a) X - - 2
ENSMUSG00000084205 (AL714027.8) X - - 1
ENSMUSG00000042498 (D330045A20Rik) X - - 2
ENSMUSG00000031438 (Rnf128) X - - 1
ENSMUSG00000072945 (Ripply1) X ENSG00000147223 - 1
ENSMUSG00000031433 (Rbm41) X ENSG00000089682 - 5
ENSMUSG00000072944 (Nup62cl) X ENSG00000198088 - 2
ENSMUSG00000042433 (E230019M04Rik) X ENSG00000080572 - 1
ENSMUSG00000031432 (Prps1) X - - 2
ENSMUSG00000000266 (Mid2) X - - 1
ENSMUSG00000031429 (Psmd10) X ENSG00000101843 - 1
ENSMUSG00000079418 (Atg4a) X ENSG00000101844 - 1
ENSMUSG00000031274 (Col4a5) X ENSG00000188153 308940 - LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY 3
ENSMUSG00000054667 (Irs4) X ENSG00000133124 - 1
ENSMUSG00000042282 (Gucy2f) X ENSG00000101890 - 1
ENSMUSG00000031278 (Acsl4) X ENSG00000068366 300387 - MENTAL RETARDATION, X-LINKED 63 3
ENSMUSG00000047045 (Tmem164) X ENSG00000157600 - 5
ENSMUSG00000042225 (Ammecr1) X ENSG00000101935 300194 - AMME COMPLEX 2
ENSMUSG00000031284 (Pak3) X ENSG00000077264 300558 - MENTAL RETARDATION, X-LINKED 30 1
ENSMUSG00000079411 (Alg13) X - - 3
ENSMUSG00000041718 (OTTMUSG00000018917) X ENSG00000101901 - 16
ENSMUSG00000041710 (Trpc5) X ENSG00000072315 - 2
ENSMUSG00000071679 (Zcchc16) X ENSG00000187823 - 1
ENSMUSG00000041380 (Htr2c) X - - 1
ENSMUSG00000031290 (Lrch2) X ENSG00000130224 - 4
ENSMUSG00000041353 (Tmem29) X ENSG00000182646 - 1
ENSMUSG00000079367 (AL808140.5) X - - 1
ENSMUSG00000025269 (Apex2) X ENSG00000169188 - 4
ENSMUSG00000025271 (Pfkfb1) X ENSG00000158571 - 2
ENSMUSG00000025268 (Maged2) X ENSG00000102316 - 1
ENSMUSG00000025266 (Gnl3l) X ENSG00000215032 - 5
ENSMUSG00000025265 (Fgd1) X ENSG00000102302 305400 - FACIOGENITAL DYSPLASIA 5
ENSMUSG00000025264 (Tsr2) X ENSG00000158526 - 1
ENSMUSG00000041245 (Wnk3) X ENSG00000196632 - 4
ENSMUSG00000025262 (ORF34) X ENSG00000184083 - 1
ENSMUSG00000041229 (Phf8) X - - 3
ENSMUSG00000025261 (Huwe1) X ENSG00000086758 300706 - MENTAL RETARDATION, X-LINKED, SYNDROMIC, TURNER TYPE 27
ENSMUSG00000025257 (Ribc1) X ENSG00000158423 - 2
ENSMUSG00000041133 (Smc1a) X - - 1
ENSMUSG00000025332 (Jarid1c) X - - 8
ENSMUSG00000045180 (Shroom2) X ENSG00000146950 - 4
ENSMUSG00000071665 (Foxr2) X ENSG00000189299 - 2
ENSMUSG00000041658 (Rragb) X ENSG00000083750 - 2
ENSMUSG00000041649 (Klf8) X ENSG00000102349 - 6
ENSMUSG00000081702 (BX005465.14) X - - 1
ENSMUSG00000072100 (RP23-257P3.2) X - - 1
ENSMUSG00000025287 (Acot9) X ENSG00000123130 - 3
ENSMUSG00000025289 (Prdx4) X ENSG00000123131 - 2
ENSMUSG00000055109 (OTTMUSG00000019350) X - - 2
ENSMUSG00000057457 (Phex) X ENSG00000102174 307800 - HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT 2
ENSMUSG00000071708 (Sms) X ENSG00000102172 309583 - MENTAL RETARDATION, X-LINKED, SNYDER-ROBINSON TYPE 1
ENSMUSG00000046873 (Mbtps2) X ENSG00000012174 - 5
ENSMUSG00000041476 (Smpx) X ENSG00000091482 - 1
ENSMUSG00000031309 (Rps6ka3) X ENSG00000177189 303600 - COFFIN-LOWRY SYNDROME 6
ENSMUSG00000067194 (Eif1ay) X ENSG00000173674 - 4
ENSMUSG00000041020 (Mtap7d2) X ENSG00000184368 - 3
ENSMUSG00000044150 (A830080D01Rik) X ENSG00000173681 - 6
ENSMUSG00000040990 (Sh3kbp1) X ENSG00000147010 - 3
ENSMUSG00000031299 (Pdha1) X ENSG00000131828 312170 - PYRUVATE DECARBOXYLASE DEFICIENCY 6
ENSMUSG00000031295 (Phka2) X ENSG00000044446 306000 - GLYCOGEN STORAGE DISEASE IXa 2
ENSMUSG00000062168 (Ppef1) X ENSG00000086717 - 2
ENSMUSG00000031292 (Cdkl5) X ENSG00000008086 308350 - EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1 2
ENSMUSG00000000037 (Scml2) X ENSG00000102098 - 1
ENSMUSG00000059493 (Nhs) X ENSG00000188158 302350 - NANCE-HORAN SYNDROME 1
ENSMUSG00000040855 (Reps2) X ENSG00000169891 - 2
ENSMUSG00000031353 (Rbbp7) X ENSG00000102054 - 5
ENSMUSG00000038344 (4932441K18Rik) X ENSG00000131002 - 8
ENSMUSG00000031357 (Syap1) X ENSG00000169895 - 4
ENSMUSG00000031360 (Ctps2) X ENSG00000047230 - 4
ENSMUSG00000031364 (Grpr) X ENSG00000126010 - 1
ENSMUSG00000031367 (Ap1s2) X ENSG00000182287 300630 - MENTAL RETARDATION, X-LINKED 59 1
ENSMUSG00000031370 (Zrsr2) X - - 4
ENSMUSG00000031373 (Car5b) X ENSG00000169239 - 1
ENSMUSG00000040749 (Siah1b) X - - 3
ENSMUSG00000015401 (Tmem27) X ENSG00000147003 - 3
ENSMUSG00000031377 (Bmx) X ENSG00000102010 - 2
ENSMUSG00000031379 (Pir) X ENSG00000087842 - 7
ENSMUSG00000031380 (Figf) X ENSG00000165197 - 2
ENSMUSG00000061778 (Mospd2) X ENSG00000130150 - 2
ENSMUSG00000047757 (Fancb) X ENSG00000181544 314390 - VACTERL ASSOCIATION WITH HYDROCEPHALUS, X-LINKED 1
ENSMUSG00000040586 (Ofd1) X ENSG00000046651 311200 - OROFACIODIGITAL SYNDROME I 1
ENSMUSG00000079317 (Trappc2) X ENSG00000196459 313400 - SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED 1
ENSMUSG00000079316 (Rab9) X ENSG00000123595 - 3
ENSMUSG00000051224 (A630018P17Rik) X ENSG00000176896 - 4
ENSMUSG00000000402 (Egfl6) X ENSG00000198759 - 4
ENSMUSG00000049775 (Tmsb4x) X ENSG00000187653 - 2
ENSMUSG00000031355 (Arhgap6) X ENSG00000047648 - 2
ENSMUSG00000031352 (Hccs) X ENSG00000004961 309801 - MICROPHTHALMIA, SYNDROMIC 7 2
ENSMUSG00000035299 (Mid1) X ENSG00000101871 300000 - OPITZ GBBB SYNDROME, X-LINKED 10
ENSMUSG00000072844 (G530011O06Rik) X - - 1

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