| ID: 146664 | alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76868404..76950393) | GnT-IX, GnT-VB | 612441 |
| ID: 25932 | chloride intracellular channel 4 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (24745447..24844321) | CLIC4L, H1, MTCLIC, huH1, p64H1 | 606536 |
| ID: 9715 | family with sequence similarity 131 member B [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (143353400..143382304, complement) | | 619282 |
| ID: 22904 | strawberry notch homolog 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (1107638..1174268, complement) | KIAA0963, SNO, STNO | 615729 |
| ID: 2786 | G protein subunit gamma 4 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (235547685..235650608, complement) | HG3C | 604388 |
| ID: 92737 | delta/notch like EGF repeat containing [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (229357629..229714555, complement) | UNQ26, bet | 607299 |
| ID: 124930 | ankyrin repeat domain 13B [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (29593132..29614761) | | 615124 |
| ID: 65009 | NDRG family member 4 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (58463715..58515387) | BDM1, SMAP-8, SMAP8 | 614463 |
| ID: 84329 | hydrogen voltage gated channel 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (110648686..110704952, complement) | HV1, VSOP | 611227 |
| ID: 9478 | calcium binding protein 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (120640626..120680866) | CALBRAIN, HCALB_BR | 605563 |
| ID: 57540 | dispatched RND transporter family member 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (11479155..11537551) | PTCHD2 | 611251 |
| ID: 162494 | rhomboid like 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (32265832..32324661) | RHBDL4, VRHO | 619017 |
| ID: 4192 | midkine [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (46380784..46383837) | ARAP, MK, NEGF2 | 162096 |
| ID: 29956 | ceramide synthase 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (150965186..150974835, complement) | L3, LASS2, SP260, TMSG1 | 606920 |
| ID: 80757 | transmembrane protein 121 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (105526583..105530198) | TMEM121A, hhole, hole | |
| ID: 1788 | DNA methyltransferase 3 alpha [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (25227874..25342590, complement) | DNMT3A2, HESJAS, M.HsaIIIA, TBRS | 602769 |
| ID: 388677 | notch 2 N-terminal like A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (146148865..146229021, complement) | N2N, NOTCH2NL | 618023 |
| ID: 2775 | G protein subunit alpha o1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (56191489..56357444) | DEE17, EIEE17, G-ALPHA-o, GNAO, HG1G, HLA-DQB1, NEDIM | 139311 |
| ID: 135295 | serine and arginine rich splicing factor 12 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (89095959..89118071, complement) | SFRS13B, SFRS19, SRrp35 | |