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: 57475 | pleckstrin homology, MyTH4 and FERM domain containing H1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67533290..67589612) | | |
ID: 3915 | laminin subunit gamma 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (183023420..183145592) | LAMB2 | 150290 |
ID: 79739 | tubulin tyrosine ligase like 7 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (83865024..83999132, complement) | | 618813 |
ID: 51529 | anaphase promoting complex subunit 11 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (81890790..81900533) | APC11, Apc11p, HSPC214 | 614534 |
ID: 26064 | retinoic acid induced 14 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (34656328..34832612) | NORPEG, RAI13 | 606586 |
ID: 64423 | inverted formin 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (104689618..104722535) | C14orf151, C14orf173, CMTDIE, FSGS5, pp9484 | 610982 |
ID: 4430 | myosin IB [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (191245404..191425386) | MMI-alpha, MMIa, MYH-1c, myr1 | 606537 |
ID: 81567 | thioredoxin domain containing 5 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (7881517..7910788, complement) | ENDOPDI, ERP46, HCC-2, HCC2, PDIA15, STRF8, UNQ364 | 616412 |
ID: 9853 | RUN and SH3 domain containing 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35490111..35561895) | Iporin, MRT61 | 611053 |
ID: 26033 | attractin like 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (115093365..115948999) | ALP, bA338L11.1, bA454H24.1 | 612869 |
ID: 10951 | chromobox 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (48070059..48101478, complement) | CBX, HP1-BETA, HP1Hs-beta, HP1Hsbeta, Hp1beta, M31, MOD1, p25beta | 604511 |
ID: 396 | Rho GDP dissociation inhibitor alpha [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (81867721..81871337, complement) | GDIA1, HEL-S-47e, NPHS8, RHOGDI, RHOGDI-1 | 601925 |
ID: 23432 | G protein-coupled receptor 161 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (168079542..168137667, complement) | RE2 | 612250 |
ID: 64283 | Rho guanine nucleotide exchange factor 28 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (73626196..73941990) | RGNEF, RIP2, p190RHOGEF | 612790 |
ID: 23516 | solute carrier family 39 member 14 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22367278..22434129) | HCIN, HMNDYT2, LZT-Hs4, NET34, ZIP14, cig19 | 608736 |
ID: 54662 | TBC1 domain family member 13 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128787253..128810430) | | 616218 |
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: 26267 | F-box protein 10 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (37510892..37576380, complement) | FBX10, PRMT11 | 609092 |
ID: 4756 | neogenin 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (73051692..73305206) | IGDCC2, NGN, NTN1R2 | 601907 |