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2024-04-20 10:48:57, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001256691 2256 bp mRNA linear PRI 18-APR-2013
DEFINITION Homo sapiens maternal embryonic leucine zipper kinase (MELK),
transcript variant 7, mRNA.
ACCESSION NM_001256691
VERSION NM_001256691.1 GI:375493541
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 2256)
AUTHORS Choi,S. and Ku,J.L.
TITLE Resistance of colorectal cancer cells to radiation and 5-FU is
associated with MELK expression
JOURNAL Biochem. Biophys. Res. Commun. 412 (2), 207-213 (2011)
PUBMED 21806965
REMARK GeneRIF: MELK could be associated with increased resistance of
colorectal cancer cells against radiation and 5-FU.
REFERENCE 2 (bases 1 to 2256)
AUTHORS Nakano,I., Joshi,K., Visnyei,K., Hu,B., Watanabe,M., Lam,D.,
Wexler,E., Saigusa,K., Nakamura,Y., Laks,D.R., Mischel,P.S.,
Viapiano,M. and Kornblum,H.I.
TITLE Siomycin A targets brain tumor stem cells partially through a
MELK-mediated pathway
JOURNAL Neuro-oncology 13 (6), 622-634 (2011)
PUBMED 21558073
REMARK GeneRIF: High MELK is associated with brain tumor.
REFERENCE 3 (bases 1 to 2256)
AUTHORS Pickard,M.R., Green,A.R., Ellis,I.O., Caldas,C., Hedge,V.L.,
Mourtada-Maarabouni,M. and Williams,G.T.
TITLE Dysregulated expression of Fau and MELK is associated with poor
prognosis in breast cancer
JOURNAL Breast Cancer Res. 11 (4), R60 (2009)
PUBMED 19671159
REMARK GeneRIF: MELK expression is increased in breast cancer tissue and
this is associated with poor survival. The most important factors
controlling Bcl-G activity are post-translational modification by
Fau & MELK.
REFERENCE 4 (bases 1 to 2256)
AUTHORS Marie,S.K., Okamoto,O.K., Uno,M., Hasegawa,A.P., Oba-Shinjo,S.M.,
Cohen,T., Camargo,A.A., Kosoy,A., Carlotti,C.G. Jr., Toledo,S.,
Moreira-Filho,C.A., Zago,M.A., Simpson,A.J. and Caballero,O.L.
TITLE Maternal embryonic leucine zipper kinase transcript abundance
correlates with malignancy grade in human astrocytomas
JOURNAL Int. J. Cancer 122 (4), 807-815 (2008)
PUBMED 17960622
REMARK GeneRIF: Maternal embryonic leucine zipper kinase transcript
abundance correlates with malignancy grade in astrocytomas
REFERENCE 5 (bases 1 to 2256)
AUTHORS Nakano,I., Masterman-Smith,M., Saigusa,K., Paucar,A.A., Horvath,S.,
Shoemaker,L., Watanabe,M., Negro,A., Bajpai,R., Howes,A.,
Lelievre,V., Waschek,J.A., Lazareff,J.A., Freije,W.A., Liau,L.M.,
Gilbertson,R.J., Cloughesy,T.F., Geschwind,D.H., Nelson,S.F.,
Mischel,P.S., Terskikh,A.V. and Kornblum,H.I.
TITLE Maternal embryonic leucine zipper kinase is a key regulator of the
proliferation of malignant brain tumors, including brain tumor stem
cells
JOURNAL J. Neurosci. Res. 86 (1), 48-60 (2008)
PUBMED 17722061
REMARK GeneRIF: a critical role for MELK in the proliferation of brain
tumors, including their stem cells, and suggest that MELK may be a
compelling molecular target for treatment of high-grade brain
tumors.
REFERENCE 6 (bases 1 to 2256)
AUTHORS Vulsteke,V., Beullens,M., Boudrez,A., Keppens,S., Van Eynde,A.,
Rider,M.H., Stalmans,W. and Bollen,M.
TITLE Inhibition of spliceosome assembly by the cell cycle-regulated
protein kinase MELK and involvement of splicing factor NIPP1
JOURNAL J. Biol. Chem. 279 (10), 8642-8647 (2004)
PUBMED 14699119
REFERENCE 7 (bases 1 to 2256)
AUTHORS Davezac,N., Baldin,V., Blot,J., Ducommun,B. and Tassan,J.P.
TITLE Human pEg3 kinase associates with and phosphorylates CDC25B
phosphatase: a potential role for pEg3 in cell cycle regulation
JOURNAL Oncogene 21 (50), 7630-7641 (2002)
PUBMED 12400006
REMARK GeneRIF: pEg3 is a potential regulator of the G2/M progression and
may act antagonistically to the CDC25B phosphatase,pEg3 kinase is
able to specifically phosphorylate CDC25B in vitro. One
phosphorylation site was identified and corresponded to serine 323
REFERENCE 8 (bases 1 to 2256)
AUTHORS Seong,H.A., Gil,M., Kim,K.T., Kim,S.J. and Ha,H.
TITLE Phosphorylation of a novel zinc-finger-like protein, ZPR9, by
murine protein serine/threonine kinase 38 (MPK38)
JOURNAL Biochem. J. 361 (PT 3), 597-604 (2002)
PUBMED 11802789
REFERENCE 9 (bases 1 to 2256)
AUTHORS Gil,M., Yang,Y., Lee,Y., Choi,I. and Ha,H.
TITLE Cloning and expression of a cDNA encoding a novel protein
serine/threonine kinase predominantly expressed in hematopoietic
cells
JOURNAL Gene 195 (2), 295-301 (1997)
PUBMED 9305775
REFERENCE 10 (bases 1 to 2256)
AUTHORS Heyer,B.S., Warsowe,J., Solter,D., Knowles,B.B. and Ackerman,S.L.
TITLE New member of the Snf1/AMPK kinase family, Melk, is expressed in
the mouse egg and preimplantation embryo
JOURNAL Mol. Reprod. Dev. 47 (2), 148-156 (1997)
PUBMED 9136115
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
BP365611.1, AK293423.1, AI590871.1, W01871.1 and DB368226.1.
Transcript Variant: This variant (7) initiates translation at an
alternate start codon and lacks two exons in the 5' coding region,
but maintains the reading frame, compared to variant 1. The encoded
isoform (7) is shorter and has a distinct N-terminus, compared to
isoform 1.
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 :: AK293423.1 [ECO:0000332]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-35 BP365611.1 3-37
36-1639 AK293423.1 1-1604
1640-1640 AI590871.1 619-619 c
1641-1987 AK293423.1 1606-1952
1988-2255 W01871.1 16-283 c
2256-2256 DB368226.1 1-1 c
FEATURES Location/Qualifiers
source 1..2256
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="9"
/map="9p13.2"
gene 1..2256
/gene="MELK"
/gene_synonym="HPK38"
/note="maternal embryonic leucine zipper kinase"
/db_xref="GeneID:9833"
/db_xref="HGNC:16870"
/db_xref="MIM:607025"
exon 1..146
/gene="MELK"
/gene_synonym="HPK38"
/inference="alignment:Splign:1.39.8"
variation 30
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:368403180"
variation 35
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:188647479"
variation 63
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:73436949"
variation 68
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:139108274"
variation 84
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="g"
/db_xref="dbSNP:192249789"
variation 106..108
/gene="MELK"
/gene_synonym="HPK38"
/replace=""
/replace="ctt"
/db_xref="dbSNP:143350018"
variation 108..110
/gene="MELK"
/gene_synonym="HPK38"
/replace=""
/replace="tct"
/db_xref="dbSNP:371278776"
exon 147..242
/gene="MELK"
/gene_synonym="HPK38"
/inference="alignment:Splign:1.39.8"
variation 172
/gene="MELK"
/gene_synonym="HPK38"
/replace="g"
/replace="t"
/db_xref="dbSNP:182440001"
misc_feature 186..188
/gene="MELK"
/gene_synonym="HPK38"
/note="upstream in-frame stop codon"
CDS 195..1910
/gene="MELK"
/gene_synonym="HPK38"
/EC_number="2.7.11.1"
/EC_number="2.7.10.2"
/note="isoform 7 is encoded by transcript variant 7; pEg3
kinase; protein kinase PK38; protein kinase Eg3;
tyrosine-protein kinase MELK"
/codon_start=1
/product="maternal embryonic leucine zipper kinase isoform
7"
/protein_id="NP_001243620.1"
/db_xref="GI:375493542"
/db_xref="GeneID:9833"
/db_xref="HGNC:16870"
/db_xref="MIM:607025"
/translation="
MMNFSNIMNYMKLLGQSDLPRIKTEIEALKNLRHQHICQLYHVLETANKIFMVLEENLLFDEYHKLKLIDFGLCAKPKGNKDYHLQTCCGSLAYAAPELIQGKSYLGSEADVWSMGILLYVLMCGFLPFDDDNVMALYKKIMRGKYDVPKWLSPSSILLLQQMLQVDPKKRISMKNLLNHPWIMQDYNYPVEWQSKNPFIHLDDDCVTELSVHHRNNRQTMEDLISLWQYDHLTATYLLLLAKKARGKPVRLRLSSFSCGQASATPFTDIKSNNWSLEDVTASDKNYVAGLIDYDWCEDDLSTGAATPRTSQFTKYWTESNGVESKSLTPALCRTPANKLKNKENVYTPKSAVKNEEYFMFPEPKTPVNKNQHKREILTTPNRYTTPSKARNQCLKETPIKIPVNSTGTDKLMTGVISPERRCRSVELDLNQAHMEETPKRKGAKVFGSLERGLDKVITVLTRSKRKGSARDGPRRLKLHYNVTTTRLVNPDQLLNEIMSILPKKHVDFVQKGYTLKCQTQSDFGKVTMQFELEVCQLQKPDVVGIRRQRLKGDAWVYKRLVEDILSSCKV
"
misc_feature 243..743
/gene="MELK"
/gene_synonym="HPK38"
/note="Serine/Threonine protein kinases, catalytic domain;
Region: S_TKc; smart00220"
/db_xref="CDD:197582"
misc_feature <360..740
/gene="MELK"
/gene_synonym="HPK38"
/note="Protein Kinases, catalytic domain; Region:
PKc_like; cl09925"
/db_xref="CDD:213116"
misc_feature order(360..362,411..413,462..473)
/gene="MELK"
/gene_synonym="HPK38"
/note="substrate binding site [chemical binding]; other
site"
/db_xref="CDD:173623"
misc_feature order(399..416,420..422,462..473)
/gene="MELK"
/gene_synonym="HPK38"
/note="activation loop (A-loop); other site"
/db_xref="CDD:173623"
misc_feature 1770..1907
/gene="MELK"
/gene_synonym="HPK38"
/note="Kinase associated domain 1; Region: KA1; pfam02149"
/db_xref="CDD:190228"
variation 220
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="c"
/db_xref="dbSNP:371313222"
variation 235
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:202138204"
exon 243..359
/gene="MELK"
/gene_synonym="HPK38"
/inference="alignment:Splign:1.39.8"
variation 265
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:35233455"
variation 287
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:200697039"
variation 322
/gene="MELK"
/gene_synonym="HPK38"
/replace="g"
/replace="t"
/db_xref="dbSNP:147513197"
variation 326
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:148574125"
variation 331
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:115531852"
exon 360..428
/gene="MELK"
/gene_synonym="HPK38"
/inference="alignment:Splign:1.39.8"
variation 395
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:146379072"
variation 401
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:374766454"
variation 425
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="g"
/db_xref="dbSNP:139481227"
exon 429..521
/gene="MELK"
/gene_synonym="HPK38"
/inference="alignment:Splign:1.39.8"
variation 431
/gene="MELK"
/gene_synonym="HPK38"
/replace="g"
/replace="t"
/db_xref="dbSNP:374077047"
variation 432
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:199834356"
variation 486
/gene="MELK"
/gene_synonym="HPK38"
/replace="g"
/replace="t"
/db_xref="dbSNP:149686898"
variation 495
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="c"
/db_xref="dbSNP:115586289"
exon 522..620
/gene="MELK"
/gene_synonym="HPK38"
/inference="alignment:Splign:1.39.8"
variation 525
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="g"
/db_xref="dbSNP:199880240"
variation 533
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="g"
/db_xref="dbSNP:374075415"
variation 539
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:146709588"
variation 562
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:369063583"
variation 610
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:35142210"
variation 611
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:144075335"
exon 621..689
/gene="MELK"
/gene_synonym="HPK38"
/inference="alignment:Splign:1.39.8"
variation 653
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:111341110"
variation 661
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:376164595"
variation 682
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:112003774"
exon 690..788
/gene="MELK"
/gene_synonym="HPK38"
/inference="alignment:Splign:1.39.8"
variation 712
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:201211316"
variation 714
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:146486300"
exon 789..875
/gene="MELK"
/gene_synonym="HPK38"
/inference="alignment:Splign:1.39.8"
variation 800
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:56115025"
variation 812
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:374946247"
variation 813
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:374744271"
variation 821
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:190200350"
exon 876..1007
/gene="MELK"
/gene_synonym="HPK38"
/inference="alignment:Splign:1.39.8"
variation 895
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:116620621"
variation 902
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="g"
/db_xref="dbSNP:368444354"
variation 930
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="g"
/db_xref="dbSNP:148081976"
variation 931
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:146185715"
variation 945
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="g"
/db_xref="dbSNP:140963190"
variation 946
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:146537035"
variation 952
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:34655121"
variation 953
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:372595506"
variation 962
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:1137377"
variation 997
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:55845414"
variation 1006
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:369940373"
exon 1008..1130
/gene="MELK"
/gene_synonym="HPK38"
/inference="alignment:Splign:1.39.8"
variation 1015
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="t"
/db_xref="dbSNP:147502395"
variation 1016
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:138281295"
variation 1037
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:55637735"
variation 1038
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:377133091"
variation 1060
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:370552987"
variation 1063
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:144405877"
variation 1073
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:148610937"
variation 1120
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:147684393"
variation 1124
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="t"
/db_xref="dbSNP:200203253"
exon 1131..1362
/gene="MELK"
/gene_synonym="HPK38"
/inference="alignment:Splign:1.39.8"
variation 1172
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:56223064"
variation 1211
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:369328430"
variation 1220
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:371627417"
variation 1232
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:201838679"
variation 1260
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:374730094"
variation 1264
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:139147189"
variation 1333
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:144052967"
variation 1334
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:369059064"
exon 1363..1459
/gene="MELK"
/gene_synonym="HPK38"
/inference="alignment:Splign:1.39.8"
variation 1364
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:377540320"
variation 1375
/gene="MELK"
/gene_synonym="HPK38"
/replace="g"
/replace="t"
/db_xref="dbSNP:150974354"
variation 1397
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:56176668"
variation 1412
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:149745317"
variation 1430
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:145670187"
variation 1442
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:200256801"
variation 1458
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:148905986"
exon 1460..1628
/gene="MELK"
/gene_synonym="HPK38"
/inference="alignment:Splign:1.39.8"
variation 1464
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:200746617"
variation 1473
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="c"
/db_xref="dbSNP:2068826"
variation 1487
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:376763778"
variation 1498
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:375073240"
variation 1502
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:370585219"
variation 1522
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="g"
/db_xref="dbSNP:202227041"
variation 1532
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:375455193"
variation 1573
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:62637654"
variation 1588
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="t"
/db_xref="dbSNP:147882939"
variation 1602
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:141614983"
variation 1610
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:115242044"
variation 1611
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:370307671"
exon 1629..1732
/gene="MELK"
/gene_synonym="HPK38"
/inference="alignment:Splign:1.39.8"
variation 1640
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:2274473"
variation 1649
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:375021615"
variation 1673
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:372375679"
variation 1695
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:117713820"
variation 1702
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="g"
/db_xref="dbSNP:141986091"
variation 1726
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:199547857"
variation 1730
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:150268458"
exon 1733..2256
/gene="MELK"
/gene_synonym="HPK38"
/inference="alignment:Splign:1.39.8"
variation 1802
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="g"
/db_xref="dbSNP:200440363"
variation 1899
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:113044021"
variation 1905
/gene="MELK"
/gene_synonym="HPK38"
/replace="g"
/replace="t"
/db_xref="dbSNP:138922465"
variation 1911
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:142248586"
variation 1924
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:201409152"
variation 1933
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:201509530"
STS 1934..2106
/gene="MELK"
/gene_synonym="HPK38"
/standard_name="RH25391"
/db_xref="UniSTS:52302"
variation 1934
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:374341087"
variation 1956
/gene="MELK"
/gene_synonym="HPK38"
/replace="g"
/replace="t"
/db_xref="dbSNP:368962453"
variation 1997
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="c"
/db_xref="dbSNP:12685407"
variation 2038
/gene="MELK"
/gene_synonym="HPK38"
/replace="c"
/replace="t"
/db_xref="dbSNP:375359642"
variation 2065
/gene="MELK"
/gene_synonym="HPK38"
/replace="g"
/replace="t"
/db_xref="dbSNP:138890476"
variation 2184
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:12347708"
variation 2221
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:189562435"
variation 2251
/gene="MELK"
/gene_synonym="HPK38"
/replace="a"
/replace="g"
/db_xref="dbSNP:141466859"
ORIGIN
gagatttgattcccttggcgggcggaagcggccacaacccggcgatcgaaaagattcttaggaacgccgtaccagccgcgtctctcaggacagcaggcccctgtccttctgtcgggcgccgctcagccgtgccctccgcccctcaggttctttttctaattccaaataaacttgcaagaggactatgaaagattatgatgaacttctcaaatattatgaattacatgaaactattgggacagagtgatttgccccggatcaaaacggagattgaggccttgaagaacctgagacatcagcatatatgtcaactctaccatgtgctagagacagccaacaaaatattcatggttcttgaggaaaatttgctgtttgatgaatatcataaattaaagctgattgactttggtctctgtgcaaaacccaagggtaacaaggattaccatctacagacatgctgtgggagtctggcttatgcagcacctgagttaatacaaggcaaatcatatcttggatcagaggcagatgtttggagcatgggcatactgttatatgttcttatgtgtggatttctaccatttgatgatgataatgtaatggctttatacaagaagattatgagaggaaaatatgatgttcccaagtggctctctcccagtagcattctgcttcttcaacaaatgctgcaggtggacccaaagaaacggatttctatgaaaaatctattgaaccatccctggatcatgcaagattacaactatcctgttgagtggcaaagcaagaatccttttattcacctcgatgatgattgcgtaacagaactttctgtacatcacagaaacaacaggcaaacaatggaggatttaatttcactgtggcagtatgatcacctcacggctacctatcttctgcttctagccaagaaggctcggggaaaaccagttcgtttaaggctttcttctttctcctgtggacaagccagtgctaccccattcacagacatcaagtcaaataattggagtctggaagatgtgaccgcaagtgataaaaattatgtggcgggattaatagactatgattggtgtgaagatgatttatcaacaggtgctgctactccccgaacatcacagtttaccaagtactggacagaatcaaatggggtggaatctaaatcattaactccagccttatgcagaacacctgcaaataaattaaagaacaaagaaaatgtatatactcctaagtctgctgtaaagaatgaagagtactttatgtttcctgagccaaagactccagttaataagaaccagcataagagagaaatactcactacgccaaatcgttacactacaccctcaaaagctagaaaccagtgcctgaaagaaactccaattaaaataccagtaaattcaacaggaacagacaagttaatgacaggtgtcattagccctgagaggcggtgccgctcagtggaattggatctcaaccaagcacatatggaggagactccaaaaagaaagggagccaaagtgtttgggagccttgaaagggggttggataaggttatcactgtgctcaccaggagcaaaaggaagggttctgccagagacgggcccagaagactaaagcttcactataacgtgactacaactagattagtgaatccagatcaactgttgaatgaaataatgtctattcttccaaagaagcatgttgactttgtacaaaagggttatacactgaagtgtcaaacacagtcagattttgggaaagtgacaatgcaatttgaattagaagtgtgccagcttcaaaaacccgatgtggtgggtatcaggaggcagcggcttaagggcgatgcctgggtttacaaaagattagtggaagacatcctatctagctgcaaggtataattgatggattcttccatcctgccggatgagtgtgggtgtgatacagcctacataaagactgttatgatcgctttgattttaaagttcattggaactaccaacttgtttctaaagagctatcttaagaccaatatctctttgtttttaaacaaaagatattattttgtgtatgaatctaaatcaagcccatctgtcattatgttactgtcttttttaatcatgtggttttgtatattaataattgttgactttcttagattcacttccatatgtgaatgtaagctcttaactatgtctctttgtaatgtgtaatttctttctgaaataaaaccatttgtgaatatag
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:9833 -> Molecular function: GO:0004674 [protein serine/threonine kinase activity] evidence: IDA
GeneID:9833 -> Molecular function: GO:0004715 [non-membrane spanning protein tyrosine kinase activity] evidence: IDA
GeneID:9833 -> Molecular function: GO:0005509 [calcium ion binding] evidence: IDA
GeneID:9833 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:9833 -> Molecular function: GO:0005524 [ATP binding] evidence: IEA
GeneID:9833 -> Molecular function: GO:0008289 [lipid binding] evidence: IEA
GeneID:9833 -> Biological process: GO:0000086 [G2/M transition of mitotic cell cycle] evidence: TAS
GeneID:9833 -> Biological process: GO:0006915 [apoptotic process] evidence: IDA
GeneID:9833 -> Biological process: GO:0008283 [cell proliferation] evidence: IDA
GeneID:9833 -> Biological process: GO:0030097 [hemopoiesis] evidence: ISS
GeneID:9833 -> Biological process: GO:0043065 [positive regulation of apoptotic process] evidence: ISS
GeneID:9833 -> Biological process: GO:0046777 [protein autophosphorylation] evidence: IDA
GeneID:9833 -> Biological process: GO:0061351 [neural precursor cell proliferation] evidence: ISS
GeneID:9833 -> Cellular component: GO:0005886 [plasma membrane] evidence: IDA
GeneID:9833 -> Cellular component: GO:0005938 [cell cortex] evidence: IDA
ANNOTATIONS from NCBI Entrez Gene (20130726):
NP_001243620 -> EC 2.7.10.2
NP_001243620 -> EC 2.7.11.1
by
@meso_cacase at
DBCLS
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