ID: 10549 | peroxiredoxin 4 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (23667493..23686397) | AOE37-2, AOE372, HEL-S-97n, PRX-4 | 300927 |
ID: 90550 | mitochondrial calcium uniporter [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (72692143..72887694) | C10orf42, CCDC109A, HsMCU | 614197 |
ID: 3985 | LIM domain kinase 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (31212298..31280080) | | 601988 |
ID: 9519 | TATA-box binding protein like 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (133952174..133990432) | MGC:8389, MGC:9620, STUD, TLF, TLP, TRF2 | 605521 |
ID: 84306 | programmed cell death 2 like [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34404399..34426168) | | 615661 |
ID: 7917 | BAG cochaperone 6 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31639028..31652661, complement) | BAG-6, BAT3, D6S52E, G3 | 142590 |
ID: 29998 | BRD4 interacting chromatin remodeling complex associated protein [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47608196..47703277) | CSS12, GLTSCR1, SMARCK1 | 605690 |
ID: 51114 | zinc finger DHHC-type palmitoyltransferase 9 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129803288..129843886, complement) | CGI89, CXorf11, DHHC9, MMSA1, MRXSR, MRXSZ, ZDHHC10, ZNF379, ZNF380 | 300646 |
ID: 9991 | polypyrimidine tract binding protein 3 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (112217715..112379882, complement) | ROD1 | 607527 |
ID: 38 | acetyl-CoA acetyltransferase 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (108116705..108147603) | ACAT, MAT, T2, THIL | 607809 |
ID: 126295 | zinc finger protein 57 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2900928..2918473) | ZNF424 | |
ID: 338657 | centrosomal AT-AC splicing factor [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (118998138..119015793) | CCDC84, DLNB14, MVA4 | 620142 |
ID: 30850 | cerebellar degeneration related protein 2 like [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (74987632..75005800) | HUMPPA | |
ID: 373156 | glutathione S-transferase kappa 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (143263441..143269115) | GST, GST 13-13, GST13, GST13-13-1, hGSTK1, GSTK1 | 602321 |
ID: 10054 | ubiquitin like modifier activating enzyme 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34428381..34471251) | ACCES, ARX, HRIHFB2115, SAE2 | 613295 |
ID: 51011 | fumarylacetoacetate hydrolase domain containing 2A [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (95402708..95421656) | CGI-105 | |
ID: 51148 | cerebral endothelial cell adhesion molecule [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128419160..128437351) | CEECAM1, GLT25D3 | 616626 |
ID: 1911 | polyhomeotic homolog 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (8913843..8941467) | EDR1, HPH1, MCPH11, RAE28 | 602978 |
ID: 2230 | ferredoxin 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (110429331..110464884) | ADX, FDX, LOH11CR1D | 103260 |
ID: 653308 | N-acylsphingosine amidohydrolase 2B [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (50739936..50759255) | ASAH2C, ASAH2L, bA449O16.3, bA98I6.3 | 610987 |