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Chromosomal Location search: -> chromosome 18
Sort by: -> Chromosomal location
Found 313 genes. Show from 1 to 313.

Ensembl Gene ID (Gene Symbol) Chr Human Ortholog OMIM Description Unitraps
ENSMUSG00000063889 (Crem) 18 ENSG00000095794 - 3
ENSMUSG00000024231 (Cul2) 18 ENSG00000108094 - 5
ENSMUSG00000073647 (AC123048.4) 18 - - 1
ENSMUSG00000024234 (Papd1) 18 ENSG00000107951 - 2
ENSMUSG00000033960 (9430020K01Rik) 18 ENSG00000165757 - 1
ENSMUSG00000024236 (Svil) 18 ENSG00000197321 - 6
ENSMUSG00000050945 (Zfp438) 18 ENSG00000183621 - 2
ENSMUSG00000063087 (AC121576.2) 18 - - 1
ENSMUSG00000024238 (Zeb1) 18 ENSG00000148516 609141 - CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3 5
ENSMUSG00000041225 (Arhgap12) 18 ENSG00000165322 - 4
ENSMUSG00000006740 (Kif5b) 18 ENSG00000170759 - 7
ENSMUSG00000024240 (Epc1) 18 ENSG00000120616 - 6
ENSMUSG00000039540 (4921524L21Rik) 18 - - 2
ENSMUSG00000073639 (Rab18) 18 ENSG00000099246 - 3
ENSMUSG00000061802 (Armc4) 18 ENSG00000169126 - 2
ENSMUSG00000057440 (Mpp7) 18 ENSG00000150054 - 6
ENSMUSG00000024283 (Wac) 18 ENSG00000095787 - 5
ENSMUSG00000024286 (Ccny) 18 ENSG00000108100 - 1
ENSMUSG00000036103 (Colec12) 18 ENSG00000158270 - 2
ENSMUSG00000024287 (Thoc1) 18 ENSG00000079134 - 3
ENSMUSG00000047879 (Usp14) 18 ENSG00000101557 - 8
ENSMUSG00000024290 (Rock1) 18 ENSG00000067900 - 6
ENSMUSG00000042942 (AK220484) 18 ENSG00000141449 - 3
ENSMUSG00000024293 (Esco1) 18 ENSG00000141446 - 5
ENSMUSG00000002477 (Snrpd1) 18 ENSG00000167088 - 2
ENSMUSG00000024294 (Mib1) 18 ENSG00000101752 - 3
ENSMUSG00000005836 (Gata6) 18 ENSG00000141448 - 1
ENSMUSG00000041238 (Rbbp8) 18 ENSG00000101773 - 3
ENSMUSG00000040957 (Cables1) 18 ENSG00000134508 - 3
ENSMUSG00000049411 (6030446N20Rik) 18 ENSG00000134490 - 4
ENSMUSG00000024404 (Riok3) 18 ENSG00000101782 - 6
ENSMUSG00000024413 (Npc1) 18 ENSG00000141458 257220 - NIEMANN-PICK DISEASE, TYPE C1 4
ENSMUSG00000024421 (Lama3) 18 ENSG00000053747 245660 - LARYNGOONYCHOCUTANEOUS SYNDROME 4
ENSMUSG00000044252 (Osbpl1a) 18 ENSG00000141447 - 17
ENSMUSG00000024423 (Impact) 18 ENSG00000214890 - 3
ENSMUSG00000024420 (Zfp521) 18 ENSG00000198795 - 2
ENSMUSG00000037013 (Ss18) 18 ENSG00000141380 - 8
ENSMUSG00000036743 (Psma8) 18 ENSG00000154611 - 2
ENSMUSG00000054321 (Taf4b) 18 ENSG00000141384 - 2
ENSMUSG00000047161 (Chst9) 18 ENSG00000154080 - 3
ENSMUSG00000024304 (Cdh2) 18 ENSG00000170558 - 1
ENSMUSG00000001804 (Dsg4) 18 ENSG00000175065 607903 - HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE 1
ENSMUSG00000056632 (Dsg3) 18 - - 1
ENSMUSG00000044393 (Dsg2) 18 ENSG00000046604 610193 - ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10 2
ENSMUSG00000061808 (Ttr) 18 ENSG00000118271 176300 - TRANSTHYRETIN 1
ENSMUSG00000056124 (B4galt6) 18 ENSG00000118276 - 4
ENSMUSG00000033382 (D030074E01Rik) 18 ENSG00000153339 - 5
ENSMUSG00000033107 (Rnf125) 18 ENSG00000101695 - 6
ENSMUSG00000024317 (Rnf138) 18 ENSG00000134758 - 5
ENSMUSG00000024313 (Mep1b) 18 ENSG00000141434 - 2
ENSMUSG00000042680 (Gm944) 18 ENSG00000141441 - 2
ENSMUSG00000042514 (Klhl14) 18 - - 1
ENSMUSG00000024306 (4921528I01Rik) 18 ENSG00000166960 - 3
ENSMUSG00000045215 (Asxl3) 18 ENSG00000141431 - 2
ENSMUSG00000041923 (Nol4) 18 ENSG00000101746 - 2
ENSMUSG00000073620 (AC131338.4) 18 - - 1
ENSMUSG00000024302 (Dtna) 18 ENSG00000134769 606617 - NONCOMPACTION OF LEFT VENTRICULAR MYOCARDIUM WITH CONGENITAL HEART 1
ENSMUSG00000024277 (Mapre2) 18 ENSG00000166974 - 2
ENSMUSG00000024276 (Zfp397) 18 ENSG00000186812 - 2
ENSMUSG00000063281 (Zfp35) 18 - - 2
ENSMUSG00000051469 (Zfp191) 18 ENSG00000172466 - 1
ENSMUSG00000047989 (Ino80c) 18 ENSG00000153391 - 3
ENSMUSG00000066708 (AC134856.3) 18 - - 1
ENSMUSG00000000420 (Galnt1) 18 ENSG00000141429 - 4
ENSMUSG00000024273 (2700062C07Rik) 18 ENSG00000141428 - 1
ENSMUSG00000040446 (Rprd1a) 18 ENSG00000141425 - 4
ENSMUSG00000024270 (Slc39a6) 18 ENSG00000141424 - 1
ENSMUSG00000024271 (Elp2) 18 ENSG00000134759 - 2
ENSMUSG00000039616 (Mocos) 18 ENSG00000075643 603592 - XANTHINURIA, TYPE II 3
ENSMUSG00000034295 (Fhod3) 18 ENSG00000134775 - 4
ENSMUSG00000024269 (5730494M16Rik) 18 ENSG00000134779 - 2
ENSMUSG00000033632 (AW554918) 18 ENSG00000150477 - 3
ENSMUSG00000024268 (Brunol4) 18 ENSG00000101489 - 3
ENSMUSG00000046636 (AC102562.13) 18 - - 1
ENSMUSG00000033628 (Pik3c3) 18 ENSG00000078142 - 5
ENSMUSG00000057455 (Rit2) 18 ENSG00000152214 - 3
ENSMUSG00000024259 (Slc25a46) 18 ENSG00000164209 - 3
ENSMUSG00000024260 (Sap130) 18 ENSG00000136715 - 7
ENSMUSG00000041915 (Ammecr1l) 18 ENSG00000144233 - 2
ENSMUSG00000024258 (Polr2d) 18 ENSG00000144231 - 2
ENSMUSG00000024400 (Wdr33) 18 ENSG00000136709 - 11
ENSMUSG00000024395 (Lims2) 18 ENSG00000072163 - 2
ENSMUSG00000024388 (Myo7b) 18 ENSG00000169994 - 2
ENSMUSG00000024384 (Iws1) 18 ENSG00000163166 - 3
ENSMUSG00000024386 (Proc) 18 ENSG00000115718 612304 - THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL 2
ENSMUSG00000024383 (Map3k2) 18 ENSG00000169967 - 5
ENSMUSG00000024382 (Ercc3) 18 ENSG00000163161 610651 - XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B 1
ENSMUSG00000024381 (Bin1) 18 ENSG00000136717 255200 - MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE 1
ENSMUSG00000038299 (Wdr36) 18 ENSG00000134987 609887 - GLAUCOMA 1, OPEN ANGLE, G 2
ENSMUSG00000038128 (Camk4) 18 ENSG00000152495 - 2
ENSMUSG00000042834 (D0H4S114) 18 ENSG00000134986 - 1
ENSMUSG00000024376 (Epb4.1l4a) 18 ENSG00000129595 - 17
ENSMUSG00000005871 (Apc) 18 ENSG00000134982 276300 - MISMATCH REPAIR CANCER SYNDROME 7
ENSMUSG00000014504 (Srp19) 18 ENSG00000153037 - 1
ENSMUSG00000005873 (Reep5) 18 ENSG00000129625 - 3
ENSMUSG00000014503 (Pkd2l2) 18 ENSG00000078795 - 1
ENSMUSG00000036501 (2610024E20Rik) 18 ENSG00000031003 - 5
ENSMUSG00000035984 (Nme5) 18 ENSG00000112981 - 1
ENSMUSG00000003778 (Brd8) 18 ENSG00000112983 - 6
ENSMUSG00000003779 (Kif20a) 18 ENSG00000112984 - 4
ENSMUSG00000024370 (Cdc23) 18 ENSG00000094880 - 7
ENSMUSG00000024366 (Gfra3) 18 ENSG00000146013 - 1
ENSMUSG00000044201 (Cdc25c) 18 ENSG00000158402 - 4
ENSMUSG00000034300 (2810012G03Rik) 18 ENSG00000120709 - 1
ENSMUSG00000038773 (Jmjd1b) 18 ENSG00000120733 - 15
ENSMUSG00000038555 (Reep2) 18 ENSG00000132563 - 1
ENSMUSG00000024360 (Etf1) 18 ENSG00000120705 - 7
ENSMUSG00000024359 (Hspa9) 18 ENSG00000113013 - 13
ENSMUSG00000037815 (Ctnna1) 18 ENSG00000044115 - 10
ENSMUSG00000024357 (Sil1) 18 ENSG00000120725 248800 - MARINESCO-SJOGREN SYNDROME 3
ENSMUSG00000037236 (Matr3) 18 ENSG00000015479 - 9
ENSMUSG00000037058 (Paip2) 18 ENSG00000120727 - 10
ENSMUSG00000024354 (Slc23a1) 18 ENSG00000170482 - 1
ENSMUSG00000024353 (2010001M09Rik) 18 ENSG00000170476 - 2
ENSMUSG00000024352 (5133400G04Rik) 18 ENSG00000170469 - 1
ENSMUSG00000024350 (Dnajc18) 18 ENSG00000170464 - 3
ENSMUSG00000073599 (1110006O17Rik) 18 - - 3
ENSMUSG00000073598 (1700066B19Rik) 18 - - 1
ENSMUSG00000046668 (Cxxc5) 18 ENSG00000171604 - 2
ENSMUSG00000060275 (Nrg2) 18 ENSG00000158458 - 1
ENSMUSG00000043991 (Pura) 18 ENSG00000185129 - 1
ENSMUSG00000046727 (0610010O12Rik) 18 ENSG00000120306 - 3
ENSMUSG00000024346 (Pfdn1) 18 ENSG00000113068 - 3
ENSMUSG00000024486 (Hbegf) 18 ENSG00000113070 - 2
ENSMUSG00000024485 (Slc4a9) 18 ENSG00000113073 - 1
ENSMUSG00000024483 (Ankhd1) 18 ENSG00000131503 - 12
ENSMUSG00000006050 (Sra1) 18 ENSG00000213523 - 1
ENSMUSG00000033272 (Slc35a4) 18 ENSG00000176087 - 2
ENSMUSG00000044719 (E230025N22Rik) 18 - - 2
ENSMUSG00000051439 (Cd14) 18 ENSG00000170458 - 1
ENSMUSG00000006850 (Tmco6) 18 ENSG00000113119 - 4
ENSMUSG00000014294 (Ndufa2) 18 ENSG00000131495 - 2
ENSMUSG00000024474 (Ik) 18 ENSG00000113141 - 3
ENSMUSG00000042660 (Wdr55) 18 ENSG00000120314 - 1
ENSMUSG00000001380 (Hars) 18 ENSG00000170445 - 4
ENSMUSG00000001383 (Zmat2) 18 ENSG00000146007 - 3
ENSMUSG00000079714 (Pcdha6) 18 ENSG00000204962 - 1
ENSMUSG00000007440 (Pcdha10) 18 ENSG00000081842 - 1
ENSMUSG00000051316 (Taf7) 18 ENSG00000178913 - 1
ENSMUSG00000023036 (Pcdhgc4) 18 ENSG00000081853 - 7
ENSMUSG00000024456 (Diap1) 18 ENSG00000131504 124900 - DEAFNESS, AUTOSOMAL DOMINANT 1 13
ENSMUSG00000024454 (Hdac3) 18 ENSG00000171720 - 1
ENSMUSG00000038524 (Fchsd1) 18 ENSG00000197948 - 1
ENSMUSG00000024442 (0610009O20Rik) 18 ENSG00000081791 - 1
ENSMUSG00000024440 (Pcdh12) 18 ENSG00000113555 - 1
ENSMUSG00000060450 (Rnf14) 18 ENSG00000013561 - 2
ENSMUSG00000052102 (Gnpda1) 18 ENSG00000113552 - 2
ENSMUSG00000024425 (Ndfip1) 18 ENSG00000131507 - 5
ENSMUSG00000024427 (Spry4) 18 ENSG00000187678 - 1
ENSMUSG00000073576 (9630014M24Rik) 18 - - 2
ENSMUSG00000036585 (Fgf1) 18 ENSG00000113578 - 4
ENSMUSG00000073575 (EG545253) 18 - - 1
ENSMUSG00000036452 (Arhgap26) 18 ENSG00000145819 607785 - JUVENILE MYELOMONOCYTIC LEUKEMIA 2
ENSMUSG00000024487 (Yipf5) 18 ENSG00000145817 - 2
ENSMUSG00000056671 (Prelid2) 18 ENSG00000186314 - 3
ENSMUSG00000057719 (Sh3rf2) 18 ENSG00000156463 - 1
ENSMUSG00000024493 (Lars) 18 ENSG00000133706 - 7
ENSMUSG00000024491 (Rbm27) 18 ENSG00000091009 - 7
ENSMUSG00000024498 (Tcerg1) 18 ENSG00000113649 - 11
ENSMUSG00000024500 (Ppp2r2b) 18 ENSG00000156475 604326 - SPINOCEREBELLAR ATAXIA 12 1
ENSMUSG00000039954 (Stk32a) 18 ENSG00000169302 - 1
ENSMUSG00000024501 (Dpysl3) 18 ENSG00000113657 - 3
ENSMUSG00000071858 (Gm94) 18 - - 1
ENSMUSG00000024471 (Myot) 18 - - 1
ENSMUSG00000024472 (Dcp2) 18 ENSG00000172795 - 2
ENSMUSG00000071856 (Mcc) 18 ENSG00000171444 - 2
ENSMUSG00000034653 (Ythdc2) 18 ENSG00000047188 - 3
ENSMUSG00000033949 (Trim36) 18 ENSG00000152503 - 4
ENSMUSG00000024477 (Pggt1b) 18 ENSG00000164219 - 3
ENSMUSG00000033319 (Fem1c) 18 ENSG00000145780 - 2
ENSMUSG00000033184 (AC127342.3) 18 - - 2
ENSMUSG00000057561 (Eif1a) 18 ENSG00000198692 - 2
ENSMUSG00000033022 (Cdo1) 18 ENSG00000129596 - 1
ENSMUSG00000032905 (Atg12) 18 ENSG00000145782 - 1
ENSMUSG00000024480 (Ap3s1) 18 ENSG00000177879 - 2
ENSMUSG00000024481 (4833403I15Rik) 18 ENSG00000172901 - 1
ENSMUSG00000073568 (Gm949) 18 - - 1
ENSMUSG00000042705 (Commd10) 18 ENSG00000145781 - 3
ENSMUSG00000059040 (AC150274.2) 18 - - 1
ENSMUSG00000024505 (Dtwd2) 18 ENSG00000169570 - 2
ENSMUSG00000037416 (Dmxl1) 18 ENSG00000172869 - 10
ENSMUSG00000062210 (Tnfaip8) 18 ENSG00000145779 - 2
ENSMUSG00000024507 (Hsd17b4) 18 ENSG00000133835 261515 - D-BIFUNCTIONAL PROTEIN DEFICIENCY 5
ENSMUSG00000073565 (Prr16) 18 - - 1
ENSMUSG00000024528 (Srfbp1) 18 ENSG00000151304 - 3
ENSMUSG00000034484 (Snx2) 18 ENSG00000205302 - 7
ENSMUSG00000024535 (Snx24) 18 ENSG00000064652 - 2
ENSMUSG00000024538 (Ppic) 18 ENSG00000168938 - 1
ENSMUSG00000073563 (Csnk1g3) 18 ENSG00000151292 - 4
ENSMUSG00000001700 (Gramd3) 18 ENSG00000155324 - 1
ENSMUSG00000053644 (Aldh7a1) 18 ENSG00000164904 266100 - EPILEPSY, PYRIDOXINE-DEPENDENT 5
ENSMUSG00000008301 (Rnuxa) 18 ENSG00000164902 - 3
ENSMUSG00000024590 (Lmnb1) 18 ENSG00000113368 169500 - LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT 5
ENSMUSG00000032656 (March3) 18 - - 1
ENSMUSG00000024592 (C330018D20Rik) 18 ENSG00000164241 - 1
ENSMUSG00000024593 (Megf10) 18 ENSG00000145794 - 1
ENSMUSG00000024594 (Prrc1) 18 ENSG00000164244 - 4
ENSMUSG00000058925 (1700011I03Rik) 18 - - 2
ENSMUSG00000024597 (Slc12a2) 18 ENSG00000064651 - 2
ENSMUSG00000024598 (Fbn2) 18 ENSG00000138829 121050 - CONTRACTURAL ARACHNODACTYLY, CONGENITAL 1
ENSMUSG00000024600 (Slc27a6) 18 - - 1
ENSMUSG00000024601 (Isoc1) 18 ENSG00000066583 - 1
ENSMUSG00000053441 (Adamts19) 18 ENSG00000145808 - 1
ENSMUSG00000058152 (Chsy3) 18 - - 1
ENSMUSG00000073554 (AC151990.6) 18 - - 1
ENSMUSG00000038059 (2010002N04Rik) 18 - - 1
ENSMUSG00000024603 (Dctn4) 18 ENSG00000132912 - 3
ENSMUSG00000049173 (Myoz3) 18 ENSG00000164591 - 1
ENSMUSG00000043079 (Synpo) 18 ENSG00000171992 - 1
ENSMUSG00000054008 (Ndst1) 18 ENSG00000070614 - 4
ENSMUSG00000024608 (Rps14) 18 - - 7
ENSMUSG00000024613 (Tcof1) 18 ENSG00000070814 154500 - TREACHER COLLINS-FRANCESCHETTI SYNDROME 12
ENSMUSG00000024617 (Camk2a) 18 ENSG00000070808 - 6
ENSMUSG00000052026 (Slc6a7) 18 ENSG00000011083 - 1
ENSMUSG00000024619 (Cdx1) 18 ENSG00000113722 - 1
ENSMUSG00000024622 (A630042L21Rik) 18 ENSG00000113716 - 3
ENSMUSG00000024575 (Pde6a) 18 ENSG00000132915 268000 - RETINITIS PIGMENTOSA 2
ENSMUSG00000069367 (AC121903.2) 18 - - 1
ENSMUSG00000024576 (Csnk1a1) 18 ENSG00000113712 - 6
ENSMUSG00000024578 (Il17b) 18 ENSG00000127743 - 2
ENSMUSG00000033032 (Afap1l1) 18 ENSG00000157510 - 2
ENSMUSG00000045629 (Sh3tc2) 18 ENSG00000169247 601596 - CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C 2
ENSMUSG00000042211 (Fbxo38) 18 ENSG00000145868 - 6
ENSMUSG00000044176 (Spink10) 18 - - 1
ENSMUSG00000041482 (9430028L06Rik) 18 - - 1
ENSMUSG00000024583 (Txnl1) 18 ENSG00000091164 - 4
ENSMUSG00000040560 (Wdr7) 18 ENSG00000091157 - 10
ENSMUSG00000024588 (Fech) 18 ENSG00000066926 177000 - PROTOPORPHYRIA, ERYTHROPOIETIC 2
ENSMUSG00000024587 (Nars) 18 ENSG00000134440 - 1
ENSMUSG00000039529 (Atp8b1) 18 ENSG00000081923 243300 - CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 1 1
ENSMUSG00000024589 (Nedd4l) 18 ENSG00000049759 - 7
ENSMUSG00000032688 (Malt1) 18 ENSG00000172175 - 2
ENSMUSG00000042439 (Zfp532) 18 ENSG00000074657 - 5
ENSMUSG00000046610 (5330437I02Rik) 18 - - 1
ENSMUSG00000024517 (Grp) 18 ENSG00000134443 - 1
ENSMUSG00000041891 (Lman1) 18 ENSG00000074695 227300 - FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF 5
ENSMUSG00000046318 (Ccbe1) 18 - - 1
ENSMUSG00000024524 (Gnal) 18 - - 1
ENSMUSG00000062526 (Mppe1) 18 ENSG00000154889 - 1
ENSMUSG00000024525 (Impa2) 18 ENSG00000141401 - 6
ENSMUSG00000046415 (B430212C06Rik) 18 - - 1
ENSMUSG00000024526 (Cidea) 18 ENSG00000176194 - 3
ENSMUSG00000024527 (Afg3l2) 18 ENSG00000141385 - 3
ENSMUSG00000024530 (Slmo1) 18 ENSG00000141391 - 3
ENSMUSG00000024533 (Spire1) 18 ENSG00000134278 - 7
ENSMUSG00000073542 (Cep76) 18 ENSG00000101624 - 3
ENSMUSG00000024537 (Psmg2) 18 ENSG00000128789 - 2
ENSMUSG00000024539 (Ptpn2) 18 ENSG00000175354 - 6
ENSMUSG00000079614 (Seh1l) 18 ENSG00000085415 - 5
ENSMUSG00000079613 (Cep192) 18 - - 7
ENSMUSG00000024542 (AC127236.3) 18 ENSG00000101639 - 4
ENSMUSG00000024544 (D18Ertd653e) 18 ENSG00000168675 - 3
ENSMUSG00000038121 (4933403F05Rik) 18 ENSG00000177150 - 2
ENSMUSG00000009535 (Rnmt) 18 ENSG00000101654 - 4
ENSMUSG00000024546 (4930546C10Rik) 18 - - 1
ENSMUSG00000053477 (Tcf4) 18 ENSG00000196628 610954 - PITT-HOPKINS SYNDROME 7
ENSMUSG00000038903 (Ccdc68) 18 - - 1
ENSMUSG00000024511 (Rab27b) 18 ENSG00000041353 - 1
ENSMUSG00000044906 (4930503L19Rik) 18 ENSG00000166845 - 3
ENSMUSG00000038425 (Poli) 18 ENSG00000101751 - 2
ENSMUSG00000024513 (Mbd2) 18 ENSG00000134046 - 3
ENSMUSG00000037253 (Mex3c) 18 ENSG00000176624 611014 - HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 8 1
ENSMUSG00000024515 (Smad4) 18 ENSG00000141646 260350 - PANCREATIC CARCINOMA 3
ENSMUSG00000024556 (Me2) 18 ENSG00000082212 - 2
ENSMUSG00000024558 (Mapk4) 18 ENSG00000141639 - 1
ENSMUSG00000036223 (2810433K01Rik) 18 ENSG00000154839 - 2
ENSMUSG00000024560 (Cxxc1) 18 ENSG00000154832 - 1
ENSMUSG00000024561 (Mbd1) 18 ENSG00000141644 - 1
ENSMUSG00000035394 (Ccdc11) 18 ENSG00000172361 - 1
ENSMUSG00000025885 (Myo5b) 18 - - 1
ENSMUSG00000036880 (Acaa2) 18 ENSG00000167315 - 3
ENSMUSG00000062328 (Rpl17) 18 - - 1
ENSMUSG00000036299 (BC031181) 18 ENSG00000177576 - 2
ENSMUSG00000035765 (Dym) 18 ENSG00000141627 607326 - SMITH-MCCORT DYSPLASIA 7
ENSMUSG00000025880 (Smad7) 18 ENSG00000101665 - 3
ENSMUSG00000052928 (Gm672) 18 ENSG00000134030 - 6
ENSMUSG00000044646 (Zbtb7c) 18 ENSG00000184828 - 3
ENSMUSG00000024563 (Smad2) 18 ENSG00000175387 - 3
ENSMUSG00000025421 (Hdhd2) 18 ENSG00000167220 - 4
ENSMUSG00000025420 (Katnal2) 18 ENSG00000167216 - 5
ENSMUSG00000025423 (Pias2) 18 ENSG00000078043 - 12
ENSMUSG00000025425 (St8sia5) 18 ENSG00000101638 - 2
ENSMUSG00000032818 (Loxhd1) 18 ENSG00000167210 - 1
ENSMUSG00000047466 (8030462N17Rik) 18 ENSG00000152242 - 9
ENSMUSG00000056682 (AC102195.14) 18 - - 1
ENSMUSG00000041840 (Ccdc5) 18 ENSG00000152240 - 7
ENSMUSG00000025428 (Atp5a1) 18 ENSG00000152234 - 6
ENSMUSG00000025429 (Pstpip2) 18 ENSG00000152229 - 1
ENSMUSG00000024552 (Slc14a2) 18 ENSG00000132874 - 1
ENSMUSG00000056214 (Pard6g) 18 ENSG00000178184 - 2
ENSMUSG00000053950 (Adnp2) 18 ENSG00000101544 - 2
ENSMUSG00000024570 (1110032A13Rik) 18 ENSG00000101546 - 2
ENSMUSG00000057130 (AC131065.16) 18 ENSG00000141759 - 3
ENSMUSG00000024571 (Txnl4a) 18 ENSG00000156269 - 1
ENSMUSG00000034006 (Pqlc1) 18 ENSG00000122490 - 1
ENSMUSG00000033323 (Ctdp1) 18 ENSG00000060069 604168 - CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY 5
ENSMUSG00000024566 (Atp9b) 18 ENSG00000166377 - 3
ENSMUSG00000024565 (Sall3) 18 ENSG00000151514 - 1
ENSMUSG00000041607 (Mbp) 18 ENSG00000197971 - 2
ENSMUSG00000041258 (Zfp236) 18 ENSG00000130856 - 3
ENSMUSG00000058881 (Zfp516) 18 ENSG00000101493 - 3
ENSMUSG00000046982 (Tshz1) 18 ENSG00000179981 - 1
ENSMUSG00000048410 (Zfp407) 18 ENSG00000215421 - 5
ENSMUSG00000044356 (AC124187.3) 18 - - 1
ENSMUSG00000056162 (Cndp1) 18 - - 1
ENSMUSG00000024644 (Cndp2) 18 ENSG00000133313 - 4
ENSMUSG00000024646 (Cyb5) 18 ENSG00000166347 250790 - METHEMOGLOBINEMIA DUE TO DEFICIENCY OF CYTOCHROME b5 4
ENSMUSG00000024645 (1700034H14Rik) 18 ENSG00000075336 - 1
ENSMUSG00000034391 (Fbxo15) 18 ENSG00000141665 - 8
ENSMUSG00000056153 (AC122398.2) 18 ENSG00000170677 - 3
ENSMUSG00000023066 (Rttn) 18 ENSG00000176225 - 10
ENSMUSG00000073514 (Dok6) 18 - - 1
ENSMUSG00000024614 (Txndc10) 18 ENSG00000166479 - 1

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