ID: 353131 | late cornified envelope 1A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (152827473..152828097) | LEP1 | 612603 |
ID: 7040 | transforming growth factor beta 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (41330323..41353922, complement) | CED, DPD1, IBDIMDE, LAP, TGF-beta1, TGFB, TGFbeta | 190180 |
ID: 2896 | granulin precursor [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44345302..44353106) | CLN11, FTD2, GEP, GP88, PCDGF, PEPI, PGRN | 138945 |
ID: 358 | aquaporin 1 (Colton blood group) [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (30911853..30925516) | AQP-CHIP, CHIP28, CO | 107776 |
ID: 10253 | sprouty RTK signaling antagonist 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (80335976..80341126, complement) | IGAN3, hSPRY2 | 602466 |
ID: 4856 | cellular communication network factor 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (119416446..119424434) | IBP-9, IGFBP-9, IGFBP9, NOV, NOVh | 164958 |
ID: 2192 | fibulin 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45502883..45601135) | FBLN, FIBL1 | 135820 |
ID: 3198 | homeobox A1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (27092993..27096000, complement) | BSAS, HOX1, HOX1F | 142955 |
ID: 5199 | complement factor properdin [Homo sapiens (human)] | Chromosome X, NC_000023.11 (47623282..47630305, complement) | BFD, PFC, PFD, PROPERDIN | 300383 |
ID: 10252 | sprouty RTK signaling antagonist 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (123396795..123403760) | hSPRY1 | 602465 |
ID: 30008 | EGF containing fibulin extracellular matrix protein 2 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65866441..65872800, complement) | ARCL1B, FBLN4, MBP1, UPH1 | 604633 |
ID: 8399 | phospholipase A2 group X [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (14672548..14701850, complement) | GXPLA2, GXSPLA2, SPLA2, sPLA2-X | 603603 |
ID: 51316 | placenta associated 8 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (83090048..83114729, complement) | C15, DGIC, PNAS-144, onzin | 607515 |
ID: 7922 | solute carrier family 39 member 7 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (33200867..33204437) | AGM9, D6S115E, D6S2244E, H2-KE4, HKE4, KE4, RING5, ZIP7 | 601416 |
ID: 22795 | nidogen 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (52004809..52069059, complement) | NID-2 | 605399 |
ID: 54507 | ADAMTS like 4 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (150549408..150560937) | ADAMTSL-4, ECTOL2, TSRC1 | 610113 |
ID: 26575 | regulator of G protein signaling 17 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (153004459..153131282, complement) | RGS-17, RGSZ2, hRGS17 | 607191 |
ID: 353144 | late cornified envelope 3C [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (152600234..152601086) | LEP15, SPRL3A | 612615 |
ID: 8601 | regulator of G protein signaling 20 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (53851795..53959303) | RGSZ1, ZGAP1, g(z)GAP, gz-GAP | 607193 |
ID: 2519 | alpha-L-fucosidase 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (143494812..143511720, complement) | dJ20N2.5 | 136820 |