ID: 100188862 | chromosome 3q29 microduplication syndrome [Homo sapiens (human)] | | MICRODUP3Q29 | 611936 |
ID: 100188788 | Chromosome 3q29 microdeletion syndrome [Homo sapiens (human)] | | MICRODEL3Q29 | 609425 |
ID: 1739 | discs large MAGUK scaffold protein 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (197042560..197299321, complement) | DLGH1, SAP-97, SAP97, hdlg | 601014 |
ID: 5062 | p21 (RAC1) activated kinase 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (196739857..196832647) | KNO2, PAK65, PAKgamma | 605022 |
ID: 200933 | F-box protein 45 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (196568660..196589059) | Fbx45 | 609112 |
ID: 375387 | negative regulator of reactive oxygen species [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (196639694..196662004) | ELLP3030, GARPL1, LRRC33, SENEBAC, UNQ3030 | 615322 |
ID: 7037 | transferrin receptor [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (196049284..196082090, complement) | CD71, IMD46, T9, TFR, TFR1, TR, TRFR, p90 | 190010 |
ID: 6165 | ribosomal protein L35a [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (197950190..197956610) | DBA5, L35A, eL33 | 180468 |
ID: 4976 | OPA1 mitochondrial dynamin like GTPase [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (193593208..193697811) | BERHS, MGM1, MTDPS14, NPG, NTG, largeG | 605290 |
ID: 4585 | mucin 4, cell surface associated [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (195746771..195811929, complement) | ASGP, HSA276359, MUC-4 | 158372 |
ID: 3280 | hes family bHLH transcription factor 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (194136148..194138732) | HES-1, HHL, HRY, bHLHb39 | 139605 |
ID: 347 | apolipoprotein D [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (195568705..195583940, complement) | | 107740 |
ID: 10188 | tyrosine kinase non receptor 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (195863364..195908551, complement) | ACK, ACK-1, ACK1, p21cdc42Hs | 606994 |
ID: 165918 | ring finger protein 168 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (196468783..196503768, complement) | RIDL, hRNF168 | 612688 |
ID: 4241 | melanotransferrin [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (197001740..197029817, complement) | CD228, MAP97, MFI2, MTF1, MTf | 155750 |
ID: 5130 | phosphate cytidylyltransferase 1A, choline [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (196234368..196287726, complement) | CCTA, CCTalpha, CT, CTA, CTPCT, PCYT1, SMDCRD | 123695 |
ID: 22916 | nuclear cap binding protein subunit 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (196935406..196942528, complement) | CBC2, CBP20, NIP1, PIG55 | 605133 |
ID: 9711 | rubicon autophagy regulator [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (197668867..197749820, complement) | KIAA0226, RUBICON, SCAR15 | 613516 |
ID: 5504 | protein phosphatase 1 regulatory inhibitor subunit 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (195514428..195543325, complement) | IPP-2, IPP2A, PPP1R2 | 601792 |
ID: 2814 | glycoprotein V platelet [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (194394821..194399266, complement) | CD42d, GPV | 173511 |