ID: 57213 | SPRY domain containing 7 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (49912702..49936340, complement) | C13orf1, CLLD6 | 607866 |
ID: 6934 | transcription factor 7 like 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (112950247..113167678) | TCF-4, TCF4 | 602228 |
ID: 7316 | ubiquitin C [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (124911646..124914650, complement) | HMG20 | 191340 |
ID: 328 | apurinic/apyrimidinic endodeoxyribonuclease 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20455226..20457767) | APE, APE1, APEN, APEX, APX, HAP1, REF1 | 107748 |
ID: 558 | AXL receptor tyrosine kinase [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (41219223..41261766) | ARK3, JTK11, Tyro7, UFO, AXL | 109135 |
ID: 358 | aquaporin 1 (Colton blood group) [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (30911853..30925516) | AQP-CHIP, CHIP28, CO | 107776 |
ID: 8452 | cullin 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (224470150..224585363, complement) | CUL-3, NEDAUS, PHA2E | 603136 |
ID: 2318 | filamin C [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128830406..128859272) | ABP-280, ABP280A, ABPA, ABPL, ARVC15, CMH26, FLN2, MFM5, MPD4, RCM5 | 102565 |
ID: 189 | alanine--glyoxylate aminotransferase [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (240868824..240880500) | AGT, AGT11, PH1, SPAT, SPT, Ser-PyrAT, TLH6, AGXT | 604285 |
ID: 291 | solute carrier family 25 member 4 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (185143266..185150382) | AAC1, ANT, ANT 1, ANT1, MTDPS12, MTDPS12A, PEO2, PEO3, PEOA2, T1 | 103220 |
ID: 23064 | senataxin [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (132261356..132356744, complement) | ALS4, AOA2, SCAN2, SCAR1, STEX, Sen1, bA479K20.2 | 608465 |
ID: 9319 | thyroid hormone receptor interactor 13 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (892884..919348) | 16E1BP, MVA3, OOMD9, OZEMA9 | 604507 |
ID: 9070 | ASH2 like, histone lysine methyltransferase complex subunit [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (38105493..38140080) | ASH21, ASH2L2, Bre2, ASH2L | 604782 |
ID: 816 | calcium/calmodulin dependent protein kinase II beta [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (44217154..44326013, complement) | CAM2, CAMK2, CAMKB, CaMKIIbeta, MRD54 | 607707 |
ID: 8604 | solute carrier family 25 member 12 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171783405..171894244, complement) | AGC1, ARALAR, DEE39, EIEE39 | 603667 |
ID: 84676 | tripartite motif containing 63 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (26051301..26067630, complement) | IRF, MURF1, MURF2, RNF28, SMRZ | 606131 |
ID: 23545 | ATPase H+ transporting V0 subunit a2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123712353..123761755) | A2, ARCL, ARCL2A, ATP6A2, ATP6N1D, J6B7, RTF, STV1, TJ6, TJ6M, TJ6S, VPH1, WSS, a2V | 611716 |
ID: 5528 | protein phosphatase 2 regulatory subunit B'delta [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (42984570..43012342) | B56D, B56delta, HJS1, MRD35 | 601646 |
ID: 23126 | pogo transposable element derived with ZNF domain [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151402724..151459494, complement) | MRD37, WHSUS, ZNF280E, ZNF635, ZNF635m | 614787 |
ID: 5013 | orthodenticle homeobox 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (63049735..63057831) | | 600036 |