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: 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: 23176 | septin 8 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (132750819..132780083, complement) | SEP2, SEPT8, Septin-8 | 608418 |
ID: 2181 | acyl-CoA synthetase long chain family member 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (222861036..222944639) | ACS3, FACL3, LACS 3, LACS3, PRO2194 | 602371 |
ID: 4040 | LDL receptor related protein 6 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (12116025..12267044, complement) | ADCAD2, STHAG7 | 603507 |
ID: 26064 | retinoic acid induced 14 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (34656328..34832612) | NORPEG, RAI13 | 606586 |
ID: 396 | Rho GDP dissociation inhibitor alpha [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (81867721..81871337, complement) | GDIA1, HEL-S-47e, NPHS8, RHOGDI, RHOGDI-1 | 601925 |
ID: 664 | BCL2 interacting protein 3 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (131967684..131981923, complement) | HABON, NIP3 | 603293 |
ID: 23432 | G protein-coupled receptor 161 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (168079542..168137667, complement) | RE2 | 612250 |
ID: 3915 | laminin subunit gamma 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (183023420..183145592) | LAMB2 | 150290 |
ID: 7280 | tubulin beta 2A class IIa [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (3153666..3157544, complement) | CDCBM5, TUBB, TUBB2 | 615101 |
ID: 80741 | lymphocyte antigen 6 family member G5C [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31676684..31681067, complement) | C6orf20, G5CA, LY6G5CB, NG33, LY6G5C | 610434 |
ID: 5621 | prion protein (Kanno blood group) [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (4686456..4701588) | ASCR, AltPrP, CD230, CJD, GSS, KURU, PRIP, PrP, PrP27-30, PrP33-35C, PrPc, p27-30 | 176640 |
ID: 322 | amyloid beta precursor protein binding family B member 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (6395124..6419453, complement) | FE65, MGC:9072, RIR | 602709 |
ID: 7936 | negative elongation factor complex member E [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31952087..31958971, complement) | D6S45, NELF-E, RD, RDBP, RDP | 154040 |
ID: 79155 | TNFAIP3 interacting protein 2 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (2741648..2756336, complement) | ABIN2, FLIP1, KLIP | 610669 |
ID: 25829 | transmembrane protein 184B [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38216395..38273010, complement) | C22orf5, FM08, HS5O6A, HSPC256, SLC51C2 | |
ID: 26033 | attractin like 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (115093365..115948999) | ALP, bA338L11.1, bA454H24.1 | 612869 |
ID: 821 | calnexin [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (179678656..179731641) | CNX, IP90, P90 | 114217 |
ID: 254428 | solute carrier family 41 member 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (205789095..205813198, complement) | MgtE, NPHPL2 | 610801 |