| ID: 29763 | protein kinase C and casein kinase substrate in neurons 3 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (47177522..47186434, complement) | SDPIII | 606513 |
| ID: 3229 | homeobox C13 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53938831..53946544) | ECTD9, HOX3, HOX3G | 142976 |
| ID: 3790 | potassium voltage-gated channel modifier subfamily S member 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (17877847..17932958) | KV9.3 | 603888 |
| ID: 55556 | enolase superfamily member 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (662986..712630, complement) | FUCD, RTS, TYMSAS | 607427 |
| ID: 81567 | thioredoxin domain containing 5 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (7881517..7910788, complement) | ENDOPDI, ERP46, HCC-2, HCC2, PDIA15, STRF8, UNQ364 | 616412 |
| ID: 84619 | zinc finger CCCH-type and G-patch domain containing [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63707442..63736142) | GPATC6, GPATCH6, KIAA1847, ZC3H9, ZC3HDC9, ZIP | 619577 |
| ID: 1981 | eukaryotic translation initiation factor 4 gamma 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (184314606..184335358) | EIF-4G1, EIF4F, EIF4G, EIF4GI, P220, PARK18 | 600495 |
| ID: 10951 | chromobox 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (48070059..48101478, complement) | CBX, HP1-BETA, HP1Hs-beta, HP1Hsbeta, Hp1beta, M31, MOD1, p25beta | 604511 |
| ID: 23176 | septin 8 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (132750819..132780083, complement) | SEP2, SEPT8, Septin-8 | 608418 |
| ID: 23516 | solute carrier family 39 member 14 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22367278..22434129) | HCIN, HMNDYT2, LZT-Hs4, NET34, ZIP14, cig19 | 608736 |
| ID: 389 | ras homolog family member C [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (112701131..112707408, complement) | ARH9, ARHC, H9, RHOH9 | 165380 |
| ID: 4862 | neuronal PAS domain protein 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (100818723..100996829) | MOP4, PASD4, bHLHe9 | 603347 |
| ID: 1294 | collagen type VII alpha 1 chain [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (48564073..48595329, complement) | EBD1, EBDCT, EBR1, NDNC8 | 120120 |
| ID: 22955 | Scm polycomb group protein homolog 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (41027202..41242306, complement) | Scml3 | 616396 |
| ID: 132671 | spermatogenesis associated 18 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (52051304..52097299) | Mieap, SPETEX1 | 612814 |
| ID: 26232 | F-box protein 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (11648387..11654429, complement) | FBG1, FBX2, Fbs1, NFB42, OCP1 | 607112 |
| ID: 928 | CD9 molecule [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (6199946..6238266) | BTCC-1, DRAP-27, MIC3, MRP-1, TSPAN-29, TSPAN29 | 143030 |
| ID: 51232 | cysteine rich transmembrane BMP regulator 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (36355778..36551135) | CRIM-1, S52 | 606189 |
| ID: 25829 | transmembrane protein 184B [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38216395..38273010, complement) | C22orf5, FM08, HS5O6A, HSPC256, SLC51C2 | |
| ID: 83959 | solute carrier family 4 member 11 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3227417..3239559, complement) | BTR1, CDPD1, CHED, CHED2, NABC1, dJ794I6.2 | 610206 |