ID: 7410 | vav guanine nucleotide exchange factor 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133761894..133992324, complement) | VAV-2 | 600428 |
ID: 144811 | laccase domain containing 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (43879178..43893932) | C13orf31, FAMIN, JUVAR | 613409 |
ID: 283638 | centrosomal protein 170B [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (104864513..104896747) | CEP170R, FAM68C, KIAA0284 | 620251 |
ID: 10979 | FERM domain containing kindlin 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (52857273..52951050, complement) | KIND2, MIG2, PLEKHC1, UNC112, UNC112B, mig-2 | 607746 |
ID: 5774 | protein tyrosine phosphatase non-receptor type 3 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (109375694..109538420, complement) | PTP-H1, PTPH1 | 176877 |
ID: 59277 | netrin 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95657807..95791155, complement) | PRO3091 | 610401 |
ID: 5727 | patched 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95442980..95516971, complement) | BCNS, BCNS1, NBCCS, PTC, PTC1, PTCH | 601309 |
ID: 64423 | inverted formin 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (104681133..104722535) | C14orf151, C14orf173, CMTDIE, FSGS5, pp9484 | 610982 |
ID: 84706 | glutamic--pyruvic transaminase 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (46884362..46931289) | ALT2, GPT 2, MRT49, NEDSPM | 138210 |
ID: 4756 | neogenin 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (73051692..73305206) | IGDCC2, NGN, NTN1R2 | 601907 |
ID: 2260 | fibroblast growth factor receptor 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (38411143..38468635, complement) | BFGFR, CD331, CEK, ECCL, FGFBR, FGFR-1, FLG, FLT-2, FLT2, HBGFR, HH2, HRTFDS, KAL2, N-SAM, OGD, bFGF-R-1 | 136350 |
ID: 1978 | eukaryotic translation initiation factor 4E binding protein 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (38030534..38060365) | 4E-BP1, 4EBP1, BP-1, PHAS-I | 602223 |
ID: 5527 | protein phosphatase 2 regulatory subunit B'gamma [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (101760573..101927992) | B56G, B56gamma, PR61G | 601645 |
ID: 10131 | TNF receptor associated protein 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (3658037..3717524, complement) | HSP 75, HSP75, HSP90L, TRAP-1 | 606219 |