| 1 | KANK1, KANK2, KIF21A
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| Structural basis for the recognition of kinesin family member 21A (KIF21A) by the ankyrin domains of KANK1 and KANK2 proteins.
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| Guo Q, Liao S, Zhu Z, Li Y, Li F, Xu C.
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| J Biol Chem Biol Chem. 2017 Nov 28. pii: jbc.M117.817494. doi: 10.1074/jbc.M117.817494. [Epub ahead of print]
2017
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| 2 | FEOM1, KANK1, KIF21A, KIF21B
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| A major mutation of KIF21A associated with congenital fibrosis of the extraocular muscles type 1 (CFEOM1) enhances translocation of Kank1 to the membrane.
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| Kakinuma N, Kiyama R.
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| Biochem Biophys Res Commun 386(4):639-44. Epub 2009 Jun 24.PMID: 19559006 2009
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| 3 | ARFGEF1, KIF21A
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| Interaction of brefeldin A-inhibited guanine nucleotide-exchange protein (BIG) 1 and kinesin motor protein KIF21A.
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| Shen X, Meza-Carmen V, Puxeddu E, Wang G, Moss J, Vaughan M.
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| Proc Natl Acad Sci U S A 105(48):18788-93. Epub 2008 Nov 19.
2008
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| 4 | FEOM1, KIF21A
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| Novel and recurrent KIF21A mutations in congenital fibrosis of the extraocular muscles type 1 and 3.
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| Lu S, Zhao C, Zhao K, Li N, Larsson C.
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| Arch Ophthalmol 126(3):388-94.PMID: 18332320 2008
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| 5 | FEOM1, KIF21A
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| Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1.
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| Chan WM, Andrews C, Dragan L, Fredrick D, Armstrong L, Lyons C, Geraghty MT, Hunter DG, Yazdani A, Traboulsi EI, Pott JW, Gutowski NJ, Ellard S, Young E, Hanisch F, Koc F, Schnall B, Engle EC.
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| BMC Genet 8:26.PMID: 17511870 2007
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| 6 | KIF21A, FEOM1
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| KIF21A gene c.2860C>T mutation in congenital fibrosis of extraocular muscles type 1 and 3.
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| Lin LK, Chien YH, Wu JY, Wang AH, Chiang SC, Hwu WL.
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| Mol Vis 11:245-8. 2005
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| 7 | KIF21A, FEOM1
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| A novel KIF21A mutation in a patient with congenital fibrosis of the extraocular muscles and Marcus Gunn jaw-winking phenomenon.
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| Yamada K, Hunter DG, Andrews C, Engle EC.
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| Arch Ophthalmol 123(9):1254-9. Review. 2005
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| 8 | KIF21A, FEOM1
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| Mutation analysis of KIF21A in congenital fibrosis of the extraocular muscles (CFEOM) patients.
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| Tiab L, Manzi V, Borruat FX, Munier F, Schorderet D.
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| Ophthalmic Genet 25(4):241-6. 2004
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| 9 | KIF21A, FEOM1
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| Mutation analysis of the KIF21A gene in an Indian family with CFEOM1: implication of CpG methylation for most frequent mutations.
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| Ali M, Venkatesh C, Ragunath A, Kumar A.
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| Ophthalmic Genet 25(4):247-55. 2004
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| 10 | FEOM1, FEOM3, KIF21A
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| Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).
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| Yamada K, Chan WM, Andrews C, Bosley TM, Sener EC, Zwaan JT, Mullaney PB, Ozturk BT, Akarsu AN, Sabol LJ, Demer JL, Sullivan TJ, Gottlob I, Roggenkaemper P, Mackey DA, De Uzcategui CE, Uzcategui N, Ben-Zeev B, Traboulsi EI, Magli A, de Berardinis T, Gagliardi V, Awasthi-Patney S, Vogel MC, Rizzo JF 3rd, Engle EC.
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| Invest Ophthalmol Vis Sci 45(7):2218-23. 2004
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| 11 | KIF21A, FEOM1
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| Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).
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| Yamada K, Andrews C, Chan WM, McKeown CA, Magli A, de Berardinis T, Loewenstein A, Lazar M, O'Keefe M, Letson R, London A, Ruttum M, Matsumoto N, Saito N, Morris L, Del Monte M, Johnson RH, Uyama E, Houtman WA, de Vries B, Carlow TJ, Hart BL, Krawiecki N, Shoffner J, Vogel MC, Katowitz J, Goldstein SM, Levin AV, Sener EC, Ozturk BT, Akarsu AN, Brodsky MC, Hanisch F, Cruse RP, Zubcov AA, Robb RM, Roggenkaemper P, Gottlob I, Kowal L, Battu R, Traboulsi EI, Franceschini P, Newlin A, Demer JL, Engle EC.
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| Nat Genet 35(4):318-21. Epub 2003 Nov 02. 2003
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| 12 | KIF21A, FEOM1
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| A Japanese family with FEOM1-linked congenital fibrosis of the extraocular muscles type 1 associated with spinal canal stenosis and refinement of the FEOM1 critical region.
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| Uyama E, Yamada K, Kawano H, Chan WM, Andrews C, Yoshioka M, Uchino M, Engle EC.
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| Neuromuscul Disord 13(6):472-8. 2003
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| 13 | ACAP3, AMBRA1, CMIP, CNTNAP3, CNTNAP4, CPEB4, DAB2IP, DDHD1, DISP2, EEPD1, EXOC4, FAM40A, HELZ2, ITPRIP, KIAA1683, KIAA1712, KIAA1715, KIAA1737, KIAA1751, KIAA1755, KIF21A, MTMR12, PHACTR1, PHF21A, PRDM16, RAPH1, RHOXF1, SEMA4B, SEMA4C, SET7, SH3BP5L, SPHKAP, SSH2, TET1, TEX2, TNKS1BP1, UBE2O, UNC13A, UNK, WNK2, ZCCHC2, ZFHX2, ZNF407, ZNF436
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| Prediction of the coding sequences of unidentified human genes. XIX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
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| Nagase T, Kikuno R, Hattori A, Kondo Y, Okumura K, Ohara O.
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| DNA Res 7(6):347-55. 2000
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| 14 | ANKRD13A, C14orf131, CACTIN, CCDC34, CEP83, KCTD3, KIF21A, MED6, NEK1, PHF11, PPP2R3B, PPP2R3BY, QTLIGES1, RBM5, RNF12, USP32, YTHDF2, YTHDF2P, ZC3H14, ZKSCAN1, ZNF608
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| Antigens recognized by autologous antibody in patients with renal-cell carcinoma.
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| Scanlan MJ, Gordan JD, Williamson B, Stockert E, Bander NH, Jongeneel V, Gure AO, Jager D, Jager E, Knuth A, Chen YT, Old LJ.
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| Int J Cancer 83(4):456-64. 1999
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| 15 | KIF21A
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| Novel dendritic kinesin sorting identified by different process targeting of two related kinesins: KIF21A and KIF21B.
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| Marszalek JR, Weiner JA, Farlow SJ, Chun J, Goldstein LS.
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| J Cell Biol 145(3):469-79. 1999
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| 16 | KIF21A, KIF21B
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| Novel dendritic kinesin sorting identified by different process targeting of two related kinesins: KIF21A and KIF21B.
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| Marszalek JR, Weiner JA, Farlow SJ, Chun J, Goldstein LS.
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| J Cell Biol 145(3):469-79.PMID: 10225949 1999
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| 17 | AATK, ACIN1, ACOT11, ACSBG1, ADAMTS4, ADGRV1, AKAP11, ANKLE2, ARHGAP26, ARHGEF2, ASTN2, ATP2C2, ATP9A, BICD2, BZRAP1, C12orf51, CAND2, CEP135, CLASP1, CLASP2, CLUAP1, CLUH, CNOT3, COBL, CPNE3, CRTC1, CRY2, CSTF2T, CUL3, CUL4B, DAAM1, DAGLA, DEPDC5, DNAJC13, DOCK10, DZIP3, FBXW11, FKBP15, G3BP2, HEPH, HIP1R, HIPK1, ICOSLG, KIAA0649, KIAA0652, KIF13B, KIF1C, KIF21A, L3MBTL1, LDB3, MAGI2, MAP4K4, MFAP3L, MGEA5, MRC2, MTMR4, N4BP1, NPHP4, OBSL1, PAN2, PHACTR2, PHF2, PHLDB1, PLXND1, PPFIA3, PTCD1, RAB11FIP3, RBM19, RICH2, RNF40, RNF8, ROCK2, RRP12, SAPS2, SETX, SIN3B, SLC24A1, SMCHD1, SNAP91, SOCS5, SS18L1, SWAP70, TBC1D9B, TELO2, TNRC15, TSC22D2, UBE4B, UHRF1BP1L, ULK2, ZBED4, ZC3H11A, ZNF623
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| Prediction of the coding sequences of unidentified human genes. X. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro.
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| Ishikawa K, Nagase T, Suyama M, Miyajima N, Tanaka A, Kotani H, Nomura N,Ohara O.
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| DNA Res 5(3):169-76. 1998
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