ID: 284654 | R-spondin 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37611350..37634892, complement) | CRISTIN3, RSPO | 609595 |
ID: 170302 | aristaless related homeobox [Homo sapiens (human)] | Chromosome X, NC_000023.11 (25003694..25015965, complement) | CT121, EIEE1, ISSX, MRX29, MRX32, MRX33, MRX36, MRX38, MRX43, MRX54, MRX76, MRX87, MRXS1, PRTS | 300382 |
ID: 166379 | Bardet-Biedl syndrome 12 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (122700442..122744939) | C4orf24 | 610683 |
ID: 129880 | Bardet-Biedl syndrome 5 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (169479494..169506655) | | 603650 |
ID: 128674 | prokineticin receptor 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (5299218..5316954, complement) | GPR73L1, GPR73b, GPRg2, HH3, KAL3, PKR2, dJ680N4.3 | 607123 |
ID: 123016 | tetratricopeptide repeat domain 8 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88824153..88881079) | BBS8, RP51 | 608132 |
ID: 84733 | chromobox 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (79777311..79787983) | CDCA6, M33, SRXY5 | 602770 |
ID: 84634 | KISS1 receptor [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (917333..921005) | AXOR12, CPPB1, GPR54, HH8, HOT7T175, KISS-1R | 604161 |
ID: 84100 | ARF like GTPase 6 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (97764521..97801242) | BBS3, RP55 | 608845 |
ID: 79738 | Bardet-Biedl syndrome 10 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (76344474..76348415, complement) | C12orf58 | 610148 |
ID: 60675 | prokineticin 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (71771655..71785148, complement) | BV8, HH4, KAL4, MIT1, PK2 | 607002 |
ID: 55733 | hedgehog acyltransferase [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (210327328..210676290) | MART2, NNMS, SKI1, Skn | 605743 |
ID: 55636 | chromodomain helicase DNA binding protein 7 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (60678740..60868028) | CRG, HH5, IS3, KAL5 | 608892 |
ID: 55212 | Bardet-Biedl syndrome 7 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (121824329..121870474, complement) | BBS2L1 | 607590 |
ID: 54361 | Wnt family member 4 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (22117313..22143097, complement) | SERKAL, WNT-4 | 603490 |
ID: 51741 | WW domain containing oxidoreductase [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (78099654..79212667) | D16S432E, DEE28, EIEE28, FOR, FRA16D, HHCMA56, PRO0128, SCAR12, SDR41C1, WOX1 | 605131 |
ID: 50846 | desert hedgehog signaling molecule [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (49086656..49094801, complement) | GDMN, GDXYM, HHG-3, SRXY7 | 605423 |
ID: 27241 | Bardet-Biedl syndrome 9 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (33129285..33635767) | B1, C18, D1, PTHB1 | 607968 |
ID: 23414 | zinc finger protein, FOG family member 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (105318438..105804539) | DIH3, FOG2, SRXY9, ZC2HC11B, ZNF89B, hFOG-2 | 603693 |
ID: 22954 | tripartite motif containing 32 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (116687305..116701299) | BBS11, HT2A, LGMD2H, LGMDR8, TATIP | 602290 |