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2024-04-26 04:51:17, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001256269 2208 bp mRNA linear PRI 16-JUN-2013
DEFINITION Homo sapiens kinesin family member 22 (KIF22), transcript variant
2, mRNA.
ACCESSION NM_001256269
VERSION NM_001256269.1 GI:372266145
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 2208)
AUTHORS van der Harst,P., Zhang,W., Mateo Leach,I., Rendon,A., Verweij,N.,
Sehmi,J., Paul,D.S., Elling,U., Allayee,H., Li,X.,
Radhakrishnan,A., Tan,S.T., Voss,K., Weichenberger,C.X.,
Albers,C.A., Al-Hussani,A., Asselbergs,F.W., Ciullo,M., Danjou,F.,
Dina,C., Esko,T., Evans,D.M., Franke,L., Gogele,M., Hartiala,J.,
Hersch,M., Holm,H., Hottenga,J.J., Kanoni,S., Kleber,M.E.,
Lagou,V., Langenberg,C., Lopez,L.M., Lyytikainen,L.P., Melander,O.,
Murgia,F., Nolte,I.M., O'Reilly,P.F., Padmanabhan,S., Parsa,A.,
Pirastu,N., Porcu,E., Portas,L., Prokopenko,I., Ried,J.S.,
Shin,S.Y., Tang,C.S., Teumer,A., Traglia,M., Ulivi,S., Westra,H.J.,
Yang,J., Zhao,J.H., Anni,F., Abdellaoui,A., Attwood,A., Balkau,B.,
Bandinelli,S., Bastardot,F., Benyamin,B., Boehm,B.O., Cookson,W.O.,
Das,D., de Bakker,P.I., de Boer,R.A., de Geus,E.J., de Moor,M.H.,
Dimitriou,M., Domingues,F.S., Doring,A., Engstrom,G.,
Eyjolfsson,G.I., Ferrucci,L., Fischer,K., Galanello,R.,
Garner,S.F., Genser,B., Gibson,Q.D., Girotto,G., Gudbjartsson,D.F.,
Harris,S.E., Hartikainen,A.L., Hastie,C.E., Hedblad,B., Illig,T.,
Jolley,J., Kahonen,M., Kema,I.P., Kemp,J.P., Liang,L.,
Lloyd-Jones,H., Loos,R.J., Meacham,S., Medland,S.E., Meisinger,C.,
Memari,Y., Mihailov,E., Miller,K., Moffatt,M.F., Nauck,M.,
Novatchkova,M., Nutile,T., Olafsson,I., Onundarson,P.T.,
Parracciani,D., Penninx,B.W., Perseu,L., Piga,A., Pistis,G.,
Pouta,A., Puc,U., Raitakari,O., Ring,S.M., Robino,A., Ruggiero,D.,
Ruokonen,A., Saint-Pierre,A., Sala,C., Salumets,A., Sambrook,J.,
Schepers,H., Schmidt,C.O., Sillje,H.H., Sladek,R., Smit,J.H.,
Starr,J.M., Stephens,J., Sulem,P., Tanaka,T., Thorsteinsdottir,U.,
Tragante,V., van Gilst,W.H., van Pelt,L.J., van Veldhuisen,D.J.,
Volker,U., Whitfield,J.B., Willemsen,G., Winkelmann,B.R.,
Wirnsberger,G., Algra,A., Cucca,F., d'Adamo,A.P., Danesh,J.,
Deary,I.J., Dominiczak,A.F., Elliott,P., Fortina,P., Froguel,P.,
Gasparini,P., Greinacher,A., Hazen,S.L., Jarvelin,M.R., Khaw,K.T.,
Lehtimaki,T., Maerz,W., Martin,N.G., Metspalu,A., Mitchell,B.D.,
Montgomery,G.W., Moore,C., Navis,G., Pirastu,M., Pramstaller,P.P.,
Ramirez-Solis,R., Schadt,E., Scott,J., Shuldiner,A.R., Smith,G.D.,
Smith,J.G., Snieder,H., Sorice,R., Spector,T.D., Stefansson,K.,
Stumvoll,M., Tang,W.H., Toniolo,D., Tonjes,A., Visscher,P.M.,
Vollenweider,P., Wareham,N.J., Wolffenbuttel,B.H., Boomsma,D.I.,
Beckmann,J.S., Dedoussis,G.V., Deloukas,P., Ferreira,M.A.,
Sanna,S., Uda,M., Hicks,A.A., Penninger,J.M., Gieger,C.,
Kooner,J.S., Ouwehand,W.H., Soranzo,N. and Chambers,J.C.
TITLE Seventy-five genetic loci influencing the human red blood cell
JOURNAL Nature 492 (7429), 369-375 (2012)
PUBMED 23222517
REFERENCE 2 (bases 1 to 2208)
AUTHORS Boyden,E.D., Campos-Xavier,A.B., Kalamajski,S., Cameron,T.L.,
Suarez,P., Tanackovic,G., Andria,G., Ballhausen,D., Briggs,M.D.,
Hartley,C., Cohn,D.H., Davidson,H.R., Hall,C., Ikegawa,S.,
Jouk,P.S., Konig,R., Megarbane,A., Nishimura,G., Lachman,R.S.,
Mortier,G., Rimoin,D.L., Rogers,R.C., Rossi,M., Sawada,H.,
Scott,R., Unger,S., Valadares,E.R., Bateman,J.F., Warman,M.L.,
Superti-Furga,A. and Bonafe,L.
TITLE Recurrent dominant mutations affecting two adjacent residues in the
motor domain of the monomeric kinesin KIF22 result in skeletal
dysplasia and joint laxity
JOURNAL Am. J. Hum. Genet. 89 (6), 767-772 (2011)
PUBMED 22152678
REMARK GeneRIF: Recurrent dominant mutations affecting two adjacent
residues in the motor domain of the monomeric kinesin KIF22 result
in skeletal dysplasia and joint laxity
Erratum:[Am J Hum Genet. 2012 Jan 13;90(1):170. Tanackovich,
Goranka [corrected to Tanackovic, Goranka]]
REFERENCE 3 (bases 1 to 2208)
AUTHORS Min,B.J., Kim,N., Chung,T., Kim,O.H., Nishimura,G., Chung,C.Y.,
Song,H.R., Kim,H.W., Lee,H.R., Kim,J., Kang,T.H., Seo,M.E.,
Yang,S.D., Kim,D.H., Lee,S.B., Kim,J.I., Seo,J.S., Choi,J.Y.,
Kang,D., Kim,D., Park,W.Y. and Cho,T.J.
TITLE Whole-exome sequencing identifies mutations of KIF22 in
spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic
type
JOURNAL Am. J. Hum. Genet. 89 (6), 760-766 (2011)
PUBMED 22152677
REMARK GeneRIF: Whole-exome sequencing identifies mutations of KIF22 in
spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic
type
REFERENCE 4 (bases 1 to 2208)
AUTHORS Bruzzoni-Giovanelli,H., Fernandez,P., Veiga,L., Podgorniak,M.P.,
Powell,D.J., Candeias,M.M., Mourah,S., Calvo,F. and Marin,M.
TITLE Distinct expression patterns of the E3 ligase SIAH-1 and its
partner Kid/KIF22 in normal tissues and in the breast tumoral
processes
JOURNAL J. Exp. Clin. Cancer Res. 29, 10 (2010)
PUBMED 20144232
REMARK GeneRIF: in all breast tumor tissues analyzed, variations in the
Kid/KIF22 mRNA levels mirrored those seen with SIAH-1 mRNAs.
Publication Status: Online-Only
REFERENCE 5 (bases 1 to 2208)
AUTHORS Ohsugi,M., Adachi,K., Horai,R., Kakuta,S., Sudo,K., Kotaki,H.,
Tokai-Nishizumi,N., Sagara,H., Iwakura,Y. and Yamamoto,T.
TITLE Kid-mediated chromosome compaction ensures proper nuclear envelope
formation
JOURNAL Cell 132 (5), 771-782 (2008)
PUBMED 18329364
REMARK GeneRIF: These data suggest that Kid-mediated anaphase/telophase
chromosome compaction prevents formation of multinucleated cells.
REFERENCE 6 (bases 1 to 2208)
AUTHORS Loftus,B.J., Kim,U.J., Sneddon,V.P., Kalush,F., Brandon,R.,
Fuhrmann,J., Mason,T., Crosby,M.L., Barnstead,M., Cronin,L.,
Deslattes Mays,A., Cao,Y., Xu,R.X., Kang,H.L., Mitchell,S.,
Eichler,E.E., Harris,P.C., Venter,J.C. and Adams,M.D.
TITLE Genome duplications and other features in 12 Mb of DNA sequence
from human chromosome 16p and 16q
JOURNAL Genomics 60 (3), 295-308 (1999)
PUBMED 10493829
REFERENCE 7 (bases 1 to 2208)
AUTHORS Song,J., Murakami,H., Yang,Z.Q., Koga,C., Adati,N., Murata,T.,
Geltinger,C., Saito-Ohara,F., Ikeuchi,T., Matsumura,M., Itakura,K.,
Kanazawa,I., Sun,K. and Yokoyama,K.K.
TITLE Human genes for KNSL4 and MAZ are located close to one another on
chromosome 16p11.2
JOURNAL Genomics 52 (3), 374-377 (1998)
PUBMED 9790757
REFERENCE 8 (bases 1 to 2208)
AUTHORS Song,J., Murakami,H., Tsutsui,H., Tang,X., Matsumura,M.,
Itakura,K., Kanazawa,I., Sun,K. and Yokoyama,K.K.
TITLE Genomic organization and expression of a human gene for
Myc-associated zinc finger protein (MAZ)
JOURNAL J. Biol. Chem. 273 (32), 20603-20614 (1998)
PUBMED 9685418
REFERENCE 9 (bases 1 to 2208)
AUTHORS Tokai,N., Fujimoto-Nishiyama,A., Toyoshima,Y., Yonemura,S.,
Tsukita,S., Inoue,J. and Yamamota,T.
TITLE Kid, a novel kinesin-like DNA binding protein, is localized to
chromosomes and the mitotic spindle
JOURNAL EMBO J. 15 (3), 457-467 (1996)
PUBMED 8599929
REFERENCE 10 (bases 1 to 2208)
AUTHORS Zhang,S. and Nonoyama,M.
TITLE The cellular proteins that bind specifically to the Epstein-Barr
virus origin of plasmid DNA replication belong to a gene family
JOURNAL Proc. Natl. Acad. Sci. U.S.A. 91 (7), 2843-2847 (1994)
PUBMED 8146198
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DC370294.1, AK316389.1,
AK223431.1 and BC028155.1.
Summary: The protein encoded by this gene is a member of the
kinesin-like protein family. The family members are
microtubule-dependent molecular motors that transport organelles
within cells and move chromosomes during cell division. The
C-terminal half of this protein has been shown to bind DNA. Studies
with the Xenopus homolog suggests its essential role in metaphase
chromosome alignment and maintenance. Alternatively spliced
transcript variants encoding different isoforms have been found for
this gene. [provided by RefSeq, Jan 2012].
Transcript Variant: This variant (2) has an additional exon in the
5' region, which results in a downstream AUG start codon, compared
to variant 1. The resulting isoform (2) is shorter at the
N-terminus than isoform 1. Variants 2 and 3 encode the same
isoform.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: AK316389.1 [ECO:0000332]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-41 DC370294.1 1-41
42-1325 AK316389.1 1-1284
1326-2167 AK223431.1 1263-2104
2168-2208 BC028155.1 2077-2117
FEATURES Location/Qualifiers
source 1..2208
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="16"
/map="16p11.2"
gene 1..2208
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/note="kinesin family member 22"
/db_xref="GeneID:3835"
/db_xref="HGNC:6391"
/db_xref="MIM:603213"
exon 1..117
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/inference="alignment:Splign:1.39.8"
variation 30
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:377474423"
variation 31
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="c"
/db_xref="dbSNP:373134041"
variation 39
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376028234"
variation 45
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144408025"
variation 46..47
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace=""
/replace="t"
/db_xref="dbSNP:34003197"
variation 51
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:373981964"
variation 53
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370681348"
variation 59
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374699250"
variation 64
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368873294"
variation 106
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201707911"
exon 118..166
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/inference="alignment:Splign:1.39.8"
misc_feature 160..162
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/note="upstream in-frame stop codon"
exon 167..362
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/inference="alignment:Splign:1.39.8"
variation 181
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:187362041"
variation 194
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:113256823"
variation 247
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:142818922"
variation 269
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:150774671"
variation 272
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:138031306"
variation 287
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201726114"
CDS 301..2094
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/note="isoform 2 is encoded by transcript variant 2; oriP
binding protein; origin of plasmid DNA replication-binding
protein; kinesin-like DNA-binding protein pseudogene;
kinesin-like protein 4"
/codon_start=1
/product="kinesin-like protein KIF22 isoform 2"
/protein_id="NP_001243198.1"
/db_xref="GI:372266146"
/db_xref="CCDS:CCDS58444.1"
/db_xref="GeneID:3835"
/db_xref="HGNC:6391"
/db_xref="MIM:603213"
/translation="
MDSCSLEIANWRNHQETLKYQFDAFYGERSTQQDIYAGSVQPILRHLLEGQNASVLAYGPTGAGKTHTMLGSPEQPGVIPRALMDLLQLTREEGAEGRPWALSVTMSYLEIYQEKVLDLLDPASGDLVIREDCRGNILIPGLSQKPISSFADFERHFLPASRNRTVGATRLNQRSSRSHAVLLVKVDQRERLAPFRQREGKLYLIDLAGSEDNRRTGNKGLRLKESGAINTSLFVLGKVVDALNQGLPRVPYRDSKLTRLLQDSLGGSAHSILIANIAPERRFYLDTVSALNFAARSKEVINRPFTNESLQPHALGPVKLSQKELLGPPEAKRARGPEEEEIGSPEPMAAPASASQKLSPLQKLSSMDPAMLERLLSLDRLLASQGSQGAPLLSTPKRERMVLMKTVEEKDLEIERLKTKQKELEAKMLAQKAEEKENHCPTMLRPLSHRTVTGAKPLKKAVVMPLQLIQEQAASPNAEIHILKNKGRKRKLESLDALEPEEKAEDCWELQISPELLAHGRQKILDLLNEGSARDLRSLQRIGPKKAQLIVGWRELHGPFSQVEDLERVEGITGKQMESFLKANILGLAAGQRCGAS
"
misc_feature 304..1221
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/note="Kinesin motor, catalytic domain. ATPase; Region:
KISc; smart00129"
/db_xref="CDD:197527"
misc_feature 310..1194
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/note="Kinesin motor domain, KIF22/Kid-like subgroup.
Members of this group might play a role in regulating
chromosomal movement along microtubules in mitosis. This
catalytic (head) domain has ATPase activity and belongs to
the larger group of P-loop NTPases; Region: KISc_KID_like;
cd01376"
/db_xref="CDD:30098"
misc_feature order(475..477,484..486,490..501,916..918)
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/note="ATP binding site [chemical binding]; other site"
/db_xref="CDD:30098"
misc_feature order(1057..1059,1066..1068,1075..1077)
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/note="microtubule interaction site [polypeptide binding];
other site"
/db_xref="CDD:30098"
misc_feature 1882..2046
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/note="Helix-hairpin-helix motif; Region: HHH_3;
pfam12836"
/db_xref="CDD:205097"
exon 363..490
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/inference="alignment:Splign:1.39.8"
variation 392
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:11545430"
variation 409
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200000231"
variation 419
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="g"
/replace="t"
/db_xref="dbSNP:201644402"
variation 480
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:144520063"
exon 491..645
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/inference="alignment:Splign:1.39.8"
variation 530
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:368750627"
variation 538
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:193922920"
variation 539
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:193922921"
variation 541
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:149549504"
variation 542
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:193922922"
variation 576
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371843824"
variation 586
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200923972"
variation 625
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:11545429"
exon 646..855
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/inference="alignment:Splign:1.39.8"
variation 658
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:202226507"
variation 671
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:377204303"
variation 672
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:11545431"
variation 675
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:11545428"
variation 701
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201572301"
variation 719
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:190757548"
variation 728
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:140332579"
variation 753
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369995078"
variation 760
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:1054392"
variation 791
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201659270"
variation 808
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374024953"
exon 856..1086
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/inference="alignment:Splign:1.39.8"
variation 871
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373330722"
variation 872
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:143337481"
variation 886
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:147345328"
variation 897
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:139563547"
variation 914
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370334885"
variation 975
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:193118115"
variation 996
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:372672551"
variation 1045
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:141032049"
variation 1056
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:184292991"
exon 1087..1240
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/inference="alignment:Splign:1.39.8"
variation 1125
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374670218"
variation 1144
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:149860938"
variation 1145
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368145244"
variation 1152
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:145872674"
variation 1165
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="t"
/db_xref="dbSNP:142042059"
variation 1167
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:372752891"
variation 1194
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:377306516"
variation 1202
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="t"
/db_xref="dbSNP:200544709"
variation 1205
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369734266"
variation 1226
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="g"
/replace="t"
/db_xref="dbSNP:145638867"
exon 1241..1376
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/inference="alignment:Splign:1.39.8"
variation 1253
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="t"
/db_xref="dbSNP:146534600"
variation 1298
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:142674782"
variation 1303
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:372409920"
variation 1320
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:375706074"
variation 1326
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:235648"
variation 1336
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:143289478"
variation 1360
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:367677680"
variation 1362
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:148042228"
variation 1365
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:371356040"
exon 1377..1545
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/inference="alignment:Splign:1.39.8"
variation 1396
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376040090"
variation 1399
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="t"
/db_xref="dbSNP:199715417"
variation 1406
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:372337472"
variation 1421
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201631186"
variation 1435
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:141728416"
variation 1467
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="g"
/replace="t"
/db_xref="dbSNP:150131602"
variation 1493
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:145879411"
variation 1499
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200809627"
variation 1521
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2450399"
exon 1546..1705
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/inference="alignment:Splign:1.39.8"
variation 1585
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373506513"
variation 1602
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:111981375"
variation 1625
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:375205158"
variation 1646
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:377591624"
variation 1648
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:139450040"
variation 1655
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:149491117"
variation 1660
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:235650"
variation 1692
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:143943794"
exon 1706..1773
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/inference="alignment:Splign:1.39.8"
variation 1715
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="t"
/db_xref="dbSNP:148628152"
variation 1743
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:142414573"
variation 1748
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:146832611"
variation 1752
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="g"
/replace="t"
/db_xref="dbSNP:372310662"
variation 1772
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="c"
/db_xref="dbSNP:375693479"
exon 1774..1986
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/inference="alignment:Splign:1.39.8"
variation 1801..1803
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace=""
/replace="gag"
/db_xref="dbSNP:370392084"
variation 1801
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369297142"
variation 1809
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:371212098"
variation 1825
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:374960997"
variation 1829
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370133905"
variation 1833
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144222256"
variation 1859
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:373411892"
variation 1860
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144499092"
variation 1873
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:377560147"
variation 1876
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:146561986"
STS 1877..2064
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/standard_name="STS-L29096"
/db_xref="UniSTS:18896"
variation 1882
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369514794"
variation 1887
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:374212297"
variation 1914
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="g"
/replace="t"
/db_xref="dbSNP:141198653"
variation 1935
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:377505621"
variation 1944
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2229347"
variation 1950
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:1054453"
variation 1958
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201146585"
variation 1966
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:372344655"
exon 1987..2046
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/inference="alignment:Splign:1.39.8"
variation 1990
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="g"
/db_xref="dbSNP:370766632"
variation 2014
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="t"
/db_xref="dbSNP:200193862"
variation 2022
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:148947920"
variation 2026
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="g"
/replace="t"
/db_xref="dbSNP:11545427"
exon 2047..2169
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/inference="alignment:Splign:1.39.8"
variation 2075
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="a"
/replace="g"
/db_xref="dbSNP:367899016"
variation 2102
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:183566608"
variation 2140
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:113809977"
variation 2156
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="g"
/replace="t"
/db_xref="dbSNP:368685286"
variation 2160
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
/replace="c"
/replace="t"
/db_xref="dbSNP:188427805"
polyA_site 2169
/gene="KIF22"
/gene_synonym="A-328A3.2; KID; KNSL4; OBP; OBP-1; OBP-2;
SEMDJL2"
ORIGIN
gcaccggggaattcgaatgggagaggcgggcccaaggagggagtggaatggccgcgggcggctcgacgcagcagaggcgacgcgagatggcggcagcttcagcggcggcgatctcagcaaatacttcttgagggcctactctgcgccaggtgttggggttagaaaggagctggtcgctgtcggctaagcaagattggagctactcgtcgtccacctccagctcgcgtaagggtggctgtgcgactgcggccatttgtggatggaacagcgggagcaagtgatcccccctgtgtgcggggcatggacagctgctctctagagattgctaactggaggaaccaccaggagactctcaaataccagtttgatgccttctatggggagaggagtactcagcaggacatctatgcaggttcagtgcagcccatcctaaggcacttgctggaagggcagaatgccagtgtgcttgcctatggacccacaggagctgggaagacgcacacaatgctgggcagcccagagcaacctggggtgatcccgcgggctctcatggacctcctgcagctcacaagggaggagggtgccgagggccggccatgggccctttctgtcaccatgtcttacctagagatctaccaggagaaggtattagacctcctggaccctgcttcgggagacctggtaatccgagaagactgccgggggaatatcctgattccgggtctctcccagaagcccatcagtagctttgctgattttgagcggcacttcctgccagccagtcgaaatcggactgtaggagccacccggctcaaccagcgctcctcccgcagtcatgctgtgctcctggtcaaggtggaccagcgggaacgtttggccccatttcgccagcgagagggaaaactctacctgattgacttggctgggtcagaggacaaccggcgcacaggcaacaagggccttcggctaaaagagagtggagccatcaacacctccctgtttgtcctgggcaaagtggtagatgcgctgaatcagggcctccctcgtgtaccttatcgggacagcaagctcactcgcctattgcaggactctctgggtggctcagcccacagtatccttattgccaacattgcccctgagagacgcttctacctagacacagtctccgcactcaactttgctgccaggtccaaggaggtgatcaatcggccttttaccaatgagagcctgcagcctcatgccttgggacctgttaagctgtctcagaaagaattgcttggtccaccagaggcaaagagagcccgaggccctgaggaagaggagatcgggagccctgagcccatggcagctccagcctctgcctcccagaaactcagccccctacagaagctaagcagcatggacccggccatgctggagcgcctcctcagcttggaccgtctgcttgcctcccaggggagccagggggcccctctgttgagtaccccaaagcgagagcggatggtgctaatgaagacagtggaagagaaggacctagagattgagaggcttaagacgaagcaaaaagaactggaggccaagatgttggcccagaaggctgaggaaaaggagaaccattgtcccacaatgctccggcccctttcacatcgcacagtcacaggggcaaagcccctgaaaaaggctgtggtgatgcccctacagctaattcaggagcaggcagcatccccaaatgccgagatccacatcctgaagaataaaggccggaagagaaagctggagtccctggatgccctagagcctgaggagaaggctgaggactgctgggagctacagatcagcccggagctactggctcatgggcgccaaaaaatactggatctgctgaacgaaggctcagcccgagatctccgcagtcttcagcgcattggcccgaagaaggcccagctaatcgtgggctggcgggagctccacggccccttcagccaggtggaggacctggaacgcgtggagggcataacggggaaacagatggagtccttcctgaaggcaaacatcctgggtctcgccgccggccagcgctgtggcgcctcctgaccgtcgtctcctcactccgccttttcaaatttttgtataaccccgtgttgtgtaaatacagtttttgctccggtgaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:3835 -> Molecular function: GO:0003677 [DNA binding] evidence: IEA
GeneID:3835 -> Molecular function: GO:0003777 [microtubule motor activity] evidence: IEA
GeneID:3835 -> Molecular function: GO:0005524 [ATP binding] evidence: IEA
GeneID:3835 -> Molecular function: GO:0008017 [microtubule binding] evidence: IEA
GeneID:3835 -> Biological process: GO:0006281 [DNA repair] evidence: IEA
GeneID:3835 -> Biological process: GO:0007018 [microtubule-based movement] evidence: TAS
GeneID:3835 -> Biological process: GO:0007067 [mitosis] evidence: TAS
GeneID:3835 -> Biological process: GO:0007596 [blood coagulation] evidence: TAS
GeneID:3835 -> Biological process: GO:0019886 [antigen processing and presentation of exogenous peptide antigen via MHC class II] evidence: TAS
GeneID:3835 -> Cellular component: GO:0000776 [kinetochore] evidence: TAS
GeneID:3835 -> Cellular component: GO:0000785 [chromatin] evidence: IEA
GeneID:3835 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
GeneID:3835 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
GeneID:3835 -> Cellular component: GO:0005819 [spindle] evidence: IEA
GeneID:3835 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
GeneID:3835 -> Cellular component: GO:0005871 [kinesin complex] evidence: IEA
GeneID:3835 -> Cellular component: GO:0005874 [microtubule] evidence: IEA
GeneID:3835 -> Cellular component: GO:0005925 [focal adhesion] evidence: IDA
by
@meso_cacase at
DBCLS
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