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2025-05-09 18:28:58, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_002374 9445 bp mRNA linear PRI 05-MAY-2013
DEFINITION Homo sapiens microtubule-associated protein 2 (MAP2), transcript
variant 1, mRNA.
ACCESSION NM_002374
VERSION NM_002374.3 GI:87578395
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 9445)
AUTHORS Zhang,J. and Dong,X.P.
TITLE Dysfunction of microtubule-associated proteins of MAP2/tau family
in Prion disease
JOURNAL Prion 6 (4), 334-338 (2012)
PUBMED 22874672
REMARK GeneRIF: Dysfunction of MAP2/tau family leads to disruption of
microtubule structure and impairment of axonal transport, and
eventually triggers apoptosis in neurons, which becomes an
essential pathway for prion to induce the neuropathology.
REFERENCE 2 (bases 1 to 9445)
AUTHORS Sontag,J.M., Nunbhakdi-Craig,V., White,C.L. III, Halpain,S. and
Sontag,E.
TITLE The protein phosphatase PP2A/Balpha binds to the
microtubule-associated proteins Tau and MAP2 at a motif also
recognized by the kinase Fyn: implications for tauopathies
JOURNAL J. Biol. Chem. 287 (18), 14984-14993 (2012)
PUBMED 22403409
REMARK GeneRIF: The protein phosphatase PP2A/Balpha binds to the
microtubule-associated proteins Tau and MAP2 at a motif also
recognized by the kinase Fyn.
REFERENCE 3 (bases 1 to 9445)
AUTHORS Guo,Y., Gong,H.S., Zhang,J., Xie,W.L., Tian,C., Chen,C., Shi,Q.,
Wang,S.B., Xu,Y., Zhang,B.Y. and Dong,X.P.
TITLE Remarkable reduction of MAP2 in the brains of scrapie-infected
rodents and human prion disease possibly correlated with the
increase of calpain
JOURNAL PLoS ONE 7 (1), E30163 (2012)
PUBMED 22272295
REMARK GeneRIF: Data indicate that the decline of MAP2 is a common
phenomenon in transmissible spongiform encephalopathies (TSEs),
which seems to occur at an early stage of incubation period.
REFERENCE 4 (bases 1 to 9445)
AUTHORS Song,Z., He,C.D., Sun,C., Xu,Y., Jin,X., Zhang,Y., Xiao,T.,
Wang,Y., Lu,P., Jiang,Y., Wei,H. and Chen,H.D.
TITLE Increased expression of MAP2 inhibits melanoma cell proliferation,
invasion and tumor growth in vitro and in vivo
JOURNAL Exp. Dermatol. 19 (11), 958-964 (2010)
PUBMED 20100193
REMARK GeneRIF: Increased MAP2 expression in malignant melanoma cells
significantly inhibits tumor cell growth and neoplasm invasiveness,
and induces apoptosis and cell cycle arrest.
REFERENCE 5 (bases 1 to 9445)
AUTHORS Bailey,S.D., Xie,C., Do,R., Montpetit,A., Diaz,R., Mohan,V.,
Keavney,B., Yusuf,S., Gerstein,H.C., Engert,J.C. and Anand,S.
CONSRTM DREAM investigators
TITLE Variation at the NFATC2 locus increases the risk of
thiazolidinedione-induced edema in the Diabetes REduction
Assessment with ramipril and rosiglitazone Medication (DREAM) study
JOURNAL Diabetes Care 33 (10), 2250-2253 (2010)
PUBMED 20628086
REMARK GeneRIF: Observational study of gene-disease association,
gene-environment interaction, and pharmacogenomic / toxicogenomic.
(HuGE Navigator)
REFERENCE 6 (bases 1 to 9445)
AUTHORS Alberts,M.J., Kandt,R.S., Pericak-Vance,M.A., Bebout,J.,
Speer,M.C., Siddique,T.S., Yamaoka,L., Hung,W.Y., Gaskell,P.C. and
Roses,A.D.
TITLE MspI RFLP for microtubule associated protein-2 (MAP2)
JOURNAL Nucleic Acids Res. 19 (4), 960 (1991)
PUBMED 1708129
REFERENCE 7 (bases 1 to 9445)
AUTHORS Dammerman,M., Yen,S.H. and Shafit-Zagardo,B.
TITLE Sequence of a human MAP-2 region sharing epitopes with Alzheimer
neurofibrillary tangles
JOURNAL J. Neurosci. Res. 24 (4), 487-495 (1989)
PUBMED 2481044
REFERENCE 8 (bases 1 to 9445)
AUTHORS Rubino,H.M., Dammerman,M., Shafit-Zagardo,B. and Erlichman,J.
TITLE Localization and characterization of the binding site for the
regulatory subunit of type II cAMP-dependent protein kinase on MAP2
JOURNAL Neuron 3 (5), 631-638 (1989)
PUBMED 2701845
REFERENCE 9 (bases 1 to 9445)
AUTHORS Obar,R.A., Dingus,J., Bayley,H. and Vallee,R.B.
TITLE The RII subunit of cAMP-dependent protein kinase binds to a common
amino-terminal domain in microtubule-associated proteins 2A, 2B,
and 2C
JOURNAL Neuron 3 (5), 639-645 (1989)
PUBMED 2561973
REFERENCE 10 (bases 1 to 9445)
AUTHORS Kosik,K.S., Orecchio,L.D., Bakalis,S., Duffy,L. and Neve,R.L.
TITLE Partial sequence of MAP2 in the region of a shared epitope with
Alzheimer neurofibrillary tangles
JOURNAL J. Neurochem. 51 (2), 587-598 (1988)
PUBMED 2455776
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from U01828.1, BX490896.1,
BC066648.1, M25668.1, BX431335.2, U89330.1, BC027583.1, BC038857.1,
AL833567.1, AK055674.1, CK903071.1 and AK056148.1.
On Feb 16, 2006 this sequence version replaced gi:14195623.
Summary: This gene encodes a protein that belongs to the
microtubule-associated protein family. The proteins of this family
are thought to be involved in microtubule assembly, which is an
essential step in neurogenesis. The products of similar genes in
rat and mouse are neuron-specific cytoskeletal proteins that are
enriched in dentrites, implicating a role in determining and
stabilizing dentritic shape during neuron development. A number of
alternatively spliced variants encoding distinct isoforms have been
described. [provided by RefSeq, Jan 2010].
Transcript Variant: This longest variant (1) includes three
alternate in-frame exons, compared to variant 2, resulting in the
longest 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 :: U01828.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025082, ERS025084 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-15 U01828.1 1-15
16-298 BX490896.1 279-561
299-3218 BC066648.1 440-3359
3219-3313 M25668.1 1492-1586
3314-3430 BC066648.1 3455-3571
3431-3581 M25668.1 1704-1854
3582-4052 BX431335.2 338-808
4053-5211 U89330.1 3793-4951
5212-5509 BC027583.1 1216-1513
5510-5853 BC038857.1 1898-2241
5854-6971 AL833567.1 1271-2388
6972-8295 AK055674.1 295-1618
8296-8824 AL833567.1 3712-4240
8825-9161 CK903071.1 233-569
9162-9445 AK056148.1 1841-2124
FEATURES Location/Qualifiers
source 1..9445
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="2"
/map="2q34-q35"
gene 1..9445
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/note="microtubule-associated protein 2"
/db_xref="GeneID:4133"
/db_xref="HGNC:6839"
/db_xref="MIM:157130"
exon 1..77
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/inference="alignment:Splign:1.39.8"
exon 78..142
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/inference="alignment:Splign:1.39.8"
exon 143..219
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/inference="alignment:Splign:1.39.8"
variation 149
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:186333656"
variation 181
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:189850574"
exon 220..510
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/inference="alignment:Splign:1.39.8"
misc_feature 243..245
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/note="upstream in-frame stop codon"
CDS 249..5732
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/note="isoform 1 is encoded by transcript variant 1;
MAP-2"
/codon_start=1
/product="microtubule-associated protein 2 isoform 1"
/protein_id="NP_002365.3"
/db_xref="GI:87578396"
/db_xref="CCDS:CCDS2384.1"
/db_xref="GeneID:4133"
/db_xref="HGNC:6839"
/db_xref="MIM:157130"
/translation="
MADERKDEAKAPHWTSAPLTEASAHSHPPEIKDQGGAGEGLVRSANGFPYREDEEGAFGEHGSQGTYSNTKENGINGELTSADRETAEEVSARIVQVVTAEAVAVLKGEQEKEAQHKDQTAALPLAAEETANLPPSPPPSPASEQTVTVEEDLLTASKMEFHDQQELTPSTAEPSDQKEKESEKQSKPGEDLKHAALVSQPETTKTYPDKKDMQGTEEEKAPLALFGHTLVASLEDMKQKTEPSLVVPGIDLPKEPPTPKEQKDWFIEMPTEAKKDEWGLVAPISPGPLTPMREKDVFDDIPKWEGKQFDSPMPSPFQGGSFTLPLDVMKNEIVTETSPFAPAFLQPDDKKSLQQTSGPATAKDSFKIEEPHEAKPDKMAEAPPSEAMTLPKDAHIPVVEEHVMGKVLEEEKEAINQETVQQRDTFTPSGQEPILTEKETELKLEEKTTISDKEAVPKESKPPKPADEEIGIIQTSTEHTFSEQKDQEPTTDMLKQDSFPVSLEQAVTDSAMTSKTLEKAMTEPSALIEKSSIQELFEMRVDDKDKIEGVGAATSAELDMPFYEDKSGMSKYFETSALKEEATKSIEPGSDYYELSDTRESVHESIDTMSPMHKNGDKEFQTGKESQPSPPAQEAGYSTLAQSYPSDLPEEPSSPQERMFTIDPKVYGEKRDLHSKNKDDLTLSRSLGLGGRSAIEQRSMSINLPMSCLDSIALGFNFGRGHDLSPLASDILTNTSGSMDEGDDYLPATTPALEKAPCFPVESKEEEQIEKVKATGEESTQAEISCESPFLAKDFYKNGTVMAPDLPEMLDLAGTRSRLASVSADAEVARRKSVPSETVVEDSRTGLPPVTDENHVIVKTDSQLEDLGYCVFNKYTVPLPSPVQDSENLSGESGTFYEGTDDKVRRDLATDLSLIEVKLAAAGRVKDEFSVDKEASAHISGDKSGLSKEFDQEKKANDRLDTVLEKSEEHADSKEHAKKTEEAGDEIETFGLGVTYEQALAKDLSIPTDASSEKAEKGLSSVPEIAEVEPSKKVEQGLDFAVQGQLDVKISDFGQMASGLNIDDRRATELKLEATQDMTPSSKAPQEADAFMGVESGHMKEGTKVSETEVKEKVAKPDLVHQEAVDKEESYESSGEHESLTMESLKADEGKKETSPESSLIQDEIAVKLSVEIPCPPAVSEADLATDERADVQMEFIQGPKEESKETPDISITPSDVAEPLHETIVSEPAEIQSEEEEIEAQGEYDKLLFRSDTLQITDLGVSGAREEFVETCPSEHKGVIESVVTIEDDFITVVQTTTDEGESGSHSVRFAALEQPEVERRPSPHDEEEFEVEEAAEAQAEPKDGSPEAPASPEREEVALSEYKTETYDDYKDETTIDDSIMDADSLWVDTQDDDRSIMTEQLETIPKEEKAEKEARRSSLEKHRKEKPFKTGRGRISTPERKVAKKEPSTVSRDEVRRKKAVYKKAELAKKTEVQAHSPSRKFILKPAIKYTRPTHLSCVKRKTTAAGGESALAPSVFKQAKDKVSDGVTKSPEKRSSLPRPSSILPPRRGVSGDRDENSFSLNSSISSSARRTTRSEPIRRAGKSGTSTPTTPGSTAITPGTPPSYSSRTPGTPGTPSYPRTPHTPGTPKSAILVPSEKKVAIIRTPPKSPATPKQLRLINQPLPDLKNVKSKIGSTDNIKYQPKGGQVQIVTKKIDLSHVTSKCGSLKNIRHRPGGGRVKIESVKLDFKEKAQAKVGSLDNAHHVPGGGNVKIDSQKLNFREHAKARVDHGAEIITQSPGRSSVASPRRLSNVSSSGSINLLESPQLATLAEDVTAALAKQGL
"
misc_feature 435..437
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 1377..4763
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/note="MAP2/Tau projection domain; Region: MAP2_projctn;
pfam08377"
/db_xref="CDD:203922"
misc_feature 2076..2078
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 2208..2210
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 2433..2435
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 2709..2711
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 4287..4289
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P11137.4); phosphorylation site"
misc_feature 4287..4289
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 4305..4307
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
(P11137.4); phosphorylation site"
misc_feature 4587..4649
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/inference="non-experimental evidence, no additional
details recorded"
/note="propagated from UniProtKB/Swiss-Prot (P11137.4);
Region: Calmodulin-binding (Potential)"
misc_feature 4866..4868
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
/db_xref="HPRD:07353"
misc_feature 5028..5030
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 5052..5054
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 5061..5063
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 5070..5072
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 5226..5321
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/note="Tau and MAP protein, tubulin-binding repeat;
Region: Tubulin-binding; pfam00418"
/db_xref="CDD:144129"
misc_feature 5229..5321
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P11137.4);
Region: Tau/MAP 1"
misc_feature 5271..5273
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
/db_xref="HPRD:03382"
misc_feature 5283..5285
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
/db_xref="HPRD:07353"
misc_feature 5322..5414
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P11137.4);
Region: Tau/MAP 2"
misc_feature 5322..5414
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/note="Tau and MAP protein, tubulin-binding repeat;
Region: Tubulin-binding; pfam00418"
/db_xref="CDD:144129"
misc_feature 5376..5378
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
/db_xref="HPRD:07353"
misc_feature 5415..5510
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="propagated from UniProtKB/Swiss-Prot (P11137.4);
Region: Tau/MAP 3"
misc_feature 5415..5510
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/note="Tau and MAP protein, tubulin-binding repeat;
Region: Tubulin-binding; pfam00418"
/db_xref="CDD:144129"
misc_feature 5631..5633
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
/db_xref="HPRD:07353"
misc_feature 5640..5642
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 5643..5645
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
/db_xref="HPRD:07353"
misc_feature 5646..5648
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
misc_feature 5652..5654
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/experiment="experimental evidence, no additional details
recorded"
/note="phosphorylation site"
/db_xref="HPRD:07353"
variation 261
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:138782038"
variation 262
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:148723167"
variation 267
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:201525773"
variation 269
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:2271252"
variation 301
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:145598155"
variation 353
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:149857613"
variation 361
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:188840497"
variation 365
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:148825736"
variation 380
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:143419670"
variation 381
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:181207847"
variation 411
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:139310749"
variation 418
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace=""
/replace="c"
/db_xref="dbSNP:35935403"
variation 430
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:370545736"
variation 442
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:138654038"
variation 461
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:201204279"
variation 493
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:2271251"
exon 511..624
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/inference="alignment:Splign:1.39.8"
variation 576
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:138065981"
variation 606
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:370307941"
variation 609
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:147456890"
exon 625..702
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/inference="alignment:Splign:1.39.8"
variation 656
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:201319995"
exon 703..4428
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/inference="alignment:Splign:1.39.8"
variation 712
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:374954491"
variation 719
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:369308118"
variation 734
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:6720659"
variation 749
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:148774557"
variation 750
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:374208822"
variation 760
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:377700467"
variation 767
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:371129624"
variation 774
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:375849922"
variation 782
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:201765886"
variation 784
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:6749066"
variation 896
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:741007"
variation 919
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:144699107"
variation 929
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:139978953"
variation 985
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:373380585"
variation 997
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:374108590"
variation 1030
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:148073159"
variation 1050
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:147043359"
variation 1059
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:200313728"
variation 1061
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:147274334"
variation 1075
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:370541070"
variation 1113
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:202130770"
variation 1127
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:373965031"
variation 1166
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:367976518"
variation 1195
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:149416048"
variation 1225
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:75373148"
variation 1233
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:144780312"
variation 1261
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:144486691"
variation 1263
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:368108274"
variation 1272
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:143122612"
variation 1305
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:371836048"
variation 1363
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:375194510"
variation 1385
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:140194857"
variation 1412
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:376544152"
variation 1467
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:755708"
variation 1484
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:201958756"
variation 1488
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:41265969"
variation 1516
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:741006"
variation 1586
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:371770931"
variation 1590
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:193121376"
variation 1605
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:374131363"
variation 1608
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:376769791"
variation 1612
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:369176617"
variation 1646
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:377651062"
variation 1653
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:141459532"
variation 1689
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:199575901"
variation 1723
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:185552042"
variation 1745
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:138285352"
variation 1749
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:200834782"
variation 1753
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:201025312"
variation 1763
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:199806559"
variation 1797
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace=""
/replace="c"
/db_xref="dbSNP:5838179"
variation 1798
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:369903670"
variation 1805
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:200288911"
variation 1812
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:373541213"
variation 1834
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:373786563"
variation 2046
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:111865603"
variation 2063
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:143216392"
variation 2064
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:191979907"
variation 2095
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:375864756"
variation 2129
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:148468330"
variation 2213
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:113862755"
variation 2255
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:148436232"
variation 2265
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:370470543"
variation 2269
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:111505040"
variation 2285
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:35994200"
variation 2289
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:368345253"
variation 2327
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:371506846"
variation 2346
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:147861980"
variation 2362
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:146432517"
variation 2363
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:376603789"
variation 2404
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:148922251"
variation 2435
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:369033681"
variation 2436
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:201346969"
variation 2495
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:376263721"
variation 2502
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:142338628"
variation 2528
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:34693874"
variation 2541
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:151284006"
variation 2546
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:139047749"
variation 2593
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:184529696"
variation 2609
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:373702192"
variation 2621
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:141522729"
variation 2667
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:140395814"
variation 2674
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:141466442"
variation 2679
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:201819060"
variation 2711
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:142716142"
variation 2721
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:370579546"
variation 2751
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:370133321"
variation 2771
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:150391168"
variation 2779
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:372993675"
variation 2795
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:138369259"
variation 2841
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:188844755"
variation 2887
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:200147409"
variation 2983
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:375700439"
variation 2993
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:145128145"
variation 3014
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:370274933"
variation 3015
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:142105837"
variation 3059
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:181175771"
variation 3066
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:141654180"
variation 3071
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:140435275"
variation 3080
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:147042067"
variation 3082
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:147371599"
variation 3105
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:373966847"
variation 3137
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:149920552"
variation 3147
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:377222605"
variation 3173
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:200567427"
variation 3175
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:13425372"
variation 3195
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:200573921"
variation 3196
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:375248306"
variation 3202
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:377375608"
variation 3208
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:147736799"
variation 3213
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:368543818"
variation 3219
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:35927101"
variation 3251
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:184423634"
variation 3256
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:146804096"
variation 3267
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:200048191"
variation 3300
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:150454433"
variation 3306
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:149636178"
variation 3312
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:187200977"
variation 3314
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:2239672"
variation 3328
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:147381270"
variation 3348
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:202024964"
variation 3376
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:201382010"
variation 3425
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:202114371"
variation 3434
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:201420432"
variation 3454
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:200163105"
variation 3457
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:376509566"
variation 3468
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:199753872"
variation 3503
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:141758882"
variation 3526
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:139654422"
variation 3543
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:17745550"
variation 3558
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:143781991"
variation 3569
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:146908968"
variation 3578
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:113287686"
variation 3635
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:36091461"
variation 3648
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:200010488"
variation 3688
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:144069172"
variation 3689
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:181666710"
variation 3709
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:200843201"
variation 3746
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:376049781"
variation 3767
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:201672675"
STS 3819..4760
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/standard_name="GDB:197515"
/db_xref="UniSTS:155933"
variation 3829
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:202122082"
variation 3832
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:141235153"
variation 3844
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:370180460"
variation 3852
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:143629615"
variation 3859
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:200150779"
variation 3880
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:139321161"
variation 3916
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:145228580"
variation 3919
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:149194467"
variation 3924
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:374394903"
variation 3964
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:200437236"
variation 3972
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:367929783"
variation 3973
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:200382253"
variation 3990
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:374935033"
variation 3999
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:141848998"
variation 4000
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:142649637"
variation 4004
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:185809016"
variation 4083
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:150116230"
variation 4106
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:141793873"
variation 4142
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:372111314"
variation 4172
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:368301391"
variation 4193
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:138157736"
variation 4249
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:142643213"
variation 4253
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:190220894"
variation 4279
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:35915945"
variation 4325
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:139772651"
variation 4349
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:113557467"
variation 4358
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:147926728"
variation 4372
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:201499809"
variation 4411..4412
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace=""
/replace="c"
/db_xref="dbSNP:35581436"
exon 4429..4635
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/inference="alignment:Splign:1.39.8"
variation 4460
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:372011116"
variation 4500
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:200795471"
variation 4549
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:145390170"
variation 4620
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:368819881"
variation 4628
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:372071871"
exon 4636..4770
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/inference="alignment:Splign:1.39.8"
variation 4697
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:201357901"
variation 4703
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:148758170"
variation 4758
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:369892280"
variation 4759
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:149033530"
variation 4765..4766
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace=""
/replace="t"
/db_xref="dbSNP:11460425"
exon 4771..4832
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/inference="alignment:Splign:1.39.8"
variation 4828
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:377593461"
exon 4833..4980
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/inference="alignment:Splign:1.39.8"
variation 4835
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:143089892"
variation 4836
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:145501967"
variation 4861
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:200474600"
variation 4862
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:151128639"
variation 4925
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:371482707"
variation 4954
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:199728294"
variation 4969
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:376761772"
exon 4981..5321
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/inference="alignment:Splign:1.39.8"
variation 5004
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:373881033"
variation 5018
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:377028684"
variation 5046
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:149674945"
variation 5107
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:370309886"
variation 5180
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:140691086"
variation 5314
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:199628162"
exon 5322..5403
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/inference="alignment:Splign:1.39.8"
variation 5399
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:151301293"
exon 5404..5516
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/inference="alignment:Splign:1.39.8"
variation 5429
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:376936549"
exon 5517..9445
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/inference="alignment:Splign:1.39.8"
variation 5528
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:144328342"
variation 5532
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:148804064"
variation 5536
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:146867931"
variation 5568
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:377443387"
variation 5569
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:369928322"
variation 5570
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:146470554"
variation 5663
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:372398391"
variation 5685
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:375692292"
variation 5696
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:374130088"
STS 5769..5961
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/standard_name="STS-U01828"
/db_xref="UniSTS:47976"
variation 5775
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:377596861"
variation 5841
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:370387493"
variation 5935
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:16843614"
variation 5993..5994
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace=""
/replace="g"
/db_xref="dbSNP:35306148"
variation 6364
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:116515304"
variation 6390
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:185373390"
variation 6431
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:16843618"
variation 6484
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:16843621"
variation 6616
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:189690356"
variation 6639
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:116288447"
variation 6691
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:183379883"
variation 6766
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:186592423"
variation 6786
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:144149734"
variation 6839
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:147770023"
variation 6946..6947
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace=""
/replace="t"
/db_xref="dbSNP:369294009"
STS 6971..7120
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/standard_name="WI-14008"
/db_xref="UniSTS:82070"
variation 7040
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:192256255"
variation 7081
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:141166524"
variation 7156
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:79583267"
variation 7182
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:75843462"
variation 7188..7189
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace=""
/replace="c"
/db_xref="dbSNP:35418396"
variation 7426
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:183583631"
variation 7436
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:76792277"
variation 7480
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:188580062"
variation 7497
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:192754387"
variation 7550..7551
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace=""
/replace="g"
/db_xref="dbSNP:34608863"
variation 7550
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:147006373"
variation 7556
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:113505378"
variation 7561
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:114531804"
variation 7605
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:145124407"
variation 7709
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:183144733"
variation 7789
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:186657740"
variation 7842
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:191454639"
variation 7892
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:149078889"
variation 8079
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:183588119"
variation 8104
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="c"
/db_xref="dbSNP:143141412"
variation 8136
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:187882319"
variation 8232
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace=""
/replace="a"
/db_xref="dbSNP:140319670"
variation 8283
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:148102787"
variation 8294
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:373722340"
variation 8301
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:367832102"
variation 8335
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="t"
/db_xref="dbSNP:372258315"
variation 8339
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:12613838"
variation 8340
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:112627538"
variation 8410
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:78101873"
variation 8411
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:55677311"
variation 8418
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:141300266"
variation 8441
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:185252440"
variation 8483
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:11678041"
variation 8544
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:145081211"
variation 8595
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:73074730"
variation 8756
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="t"
/db_xref="dbSNP:113589742"
variation 8796..8799
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace=""
/replace="caca"
/db_xref="dbSNP:112861196"
variation 8797
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace=""
/replace="ac"
/replace="acac"
/db_xref="dbSNP:10578247"
variation 8805..8808
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace=""
/replace="ac"
/replace="acac"
/db_xref="dbSNP:71395565"
variation 8829..8830
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace=""
/replace="acct"
/db_xref="dbSNP:372175517"
variation 8875..8876
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace=""
/replace="c"
/db_xref="dbSNP:35320310"
variation 8878
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="a"
/replace="g"
/db_xref="dbSNP:190103484"
variation 8955
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="g"
/replace="t"
/db_xref="dbSNP:199952940"
variation 9083
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:13392748"
STS 9133..9292
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/standard_name="RH66399"
/db_xref="UniSTS:31584"
variation 9152
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:138809066"
variation 9216..9217
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace=""
/replace="a"
/db_xref="dbSNP:137944482"
variation 9217
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace=""
/replace="a"
/db_xref="dbSNP:370182851"
variation 9230
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/replace="c"
/replace="g"
/db_xref="dbSNP:45548435"
STS 9244..9393
/gene="MAP2"
/gene_synonym="MAP2A; MAP2B; MAP2C"
/standard_name="MAP2"
/db_xref="UniSTS:503898"
ORIGIN
gggataatgctcccggagaaggattctgcagcagttctcaaaggctagacttgagtggtattgctgcatatgcgctgattcttcagcttgtctctaaccgaggaagcattgattgggagctactcattcagaaaattaaaagaaagaagccagaaaatattatcaaccctttgagaacacgacacaacgaactttatattttaccacttccttgaatagttgcaggagaaataacaaggcattgaagaatggcagatgaacggaaagatgaagcaaaggcacctcactggacctcagcaccgctaacagaggcatctgcacactcacatccacctgagattaaggatcaaggcggagcaggggaaggacttgtccgaagcgccaatggattcccatacagggaggatgaagagggtgcctttggagagcatgggtcacagggcacctattcaaataccaaagagaatgggatcaacggagagctgacctcagctgacagagaaacagcagaggaggtgtctgcaaggatagttcaagtagtcactgctgaggctgtagcagtcctgaaaggtgaacaagagaaagaagctcaacataaagaccagactgcagctctgcctttagcagctgaagaaacagctaatctgcctccttctccacccccatcacctgcctcagaacagactgtcacagtggaggaagatttacttacagcctcgaagatggagttccacgatcaacaggaattgactccctctacagctgagccttcagaccagaaggaaaaggagtcagagaagcaaagtaagcctggtgaagaccttaaacatgctgccttagtttctcagccagagacaactaaaacttaccctgataaaaaggacatgcaaggcacggaagaagaaaaagcacccctagctttgtttgggcacactcttgttgccagcctggaagacatgaaacagaagacagaaccaagccttgtagtacctggcattgacctccctaaagagcctccaactccaaaagaacaaaaggactggttcatcgaaatgccaacggaagcaaaaaaggatgagtggggtttagttgcccccatatctcctggccctctgactcccatgagggaaaaagatgtatttgatgatatcccaaaatgggaagggaaacagtttgattctcccatgccaagtccctttcaagggggaagcttcactcttcctttagatgtcatgaagaatgaaatagttacagaaacatcgccctttgcccctgcctttttacagccagatgacaaaaaatctctgcaacaaaccagtggcccagctactgccaaagatagttttaaaattgaagagccccatgaggctaaacctgacaaaatggcagaagcaccaccctcagaggcaatgaccttacccaaagatgctcacattccagttgtagaagaacatgttatggggaaagttttagaggaagaaaaggaggccataaatcaagagactgtgcagcaaagggatactttcacccccagtggacaggaacctatacttactgaaaaggaaactgagctgaagcttgaagaaaaaaccaccatttctgacaaagaagctgtgccaaaagagagtaaacccccaaaacctgcagatgaagaaataggcataattcagacctccacagagcacactttctcagaacagaaagaccaagagcctaccacagatatgttgaaacaggactcgttccctgtaagtttggagcaagcagttacagattcagccatgacctctaaaacactggagaaagccatgaccgaaccatctgcattaattgaaaagagctcaattcaggaactttttgaaatgagagttgatgacaaagataagattgaaggagttggagctgcaacatcagctgagcttgatatgccattttatgaagataaatcaggaatgtccaagtactttgaaacatctgccttgaaagaagaagcaacaaaaagcattgagccaggcagtgattactatgaactgagtgacactagagaaagtgtccatgagtctattgataccatgtctcccatgcataaaaatggtgacaaggagtttcaaacaggaaaagaatcccagcccagtcctccagcacaagaagcagggtacagcactctcgcacagagttatccatcagatttacctgaagaacccagttctcctcaagaaagaatgttcactattgatccaaaagtgtatggagagaaaagggacctccacagtaagaataaggatgatttgacccttagcaggagtttaggacttggtggtaggtctgcaatagaacaaagaagcatgtcaatcaatttgccgatgtcttgcctagattccatagcccttggatttaactttggtcggggacatgatctttctcctctggcttccgatattctaaccaacactagtggaagtatggatgaaggggatgattaccttccagccaccacacctgcactggagaaagccccttgcttccctgtagaaagcaaagaggaagaacagatagagaaagtaaaagctactggagaagaaagtactcaagcggagatatcatgtgagtctcctttcctagccaaagatttttacaaaaatggtactgtcatggcacctgaccttcctgaaatgctagatctggcaggcacaaggtcaagattggcttctgtgagtgcagatgctgaggttgccaggaggaaatcagtcccatcagagactgtggttgaggatagtcgtactggcttgcccccggtaactgatgaaaaccatgtcattgtaaaaacggacagtcagctcgaagacctgggctactgtgtgttcaataagtacacagtcccattgccatcacctgttcaagacagtgagaatttatcaggggagagtggtaccttttacgaaggcactgatgataaagttcgaagagatttggccacagacctttcactgattgaagtgaaactggcagcagccggaagagtcaaagatgagttcagtgttgacaaagaagcatccgcgcatatctctggtgacaaatcaggactgagtaaggagtttgaccaagagaagaaagctaatgataggttggatactgtactagaaaagagtgaagaacatgctgattcaaaagaacatgccaagaaaactgaagaggctggtgatgaaatagaaacattcggattaggagtaacctatgagcaagctttggccaaagatttgtcaataccaacagatgcatcctctgagaaagcagagaagggtcttagttcagtgccagagatagctgaggtagaaccatccaaaaaggtggaacaaggtctggattttgctgtccagggtcaactagatgttaaaattagtgactttggacagatggcttcagggctaaacatagatgatagaagggcaacagagctaaaacttgaggctacacaggacatgaccccctcatccaaagcaccgcaggaggcagatgcatttatgggtgttgagtctggccacatgaaagaaggcactaaagttagtgagacagaagtcaaagagaaggtggccaagcctgacttggtgcaccaggaggctgtagacaaggaggagtcctatgaatctagtggtgagcatgaaagtctcaccatggagtccttgaaagctgatgagggcaagaaggaaacatctccagaatcatctctaattcaagatgagattgccgtcaaattgtcagtggaaataccttgcccacctgctgtttcagaggctgatttagccacagatgagagagctgatgtccagatggaatttattcaggggccaaaagaagaaagcaaagagaccccagatatatccatcacgccttctgatgttgcagagccattgcatgaaacgatcgtatctgaaccagcagagattcagagtgaggaagaagagatagaagcccagggagaatatgataaactgctcttccgctcagacacccttcagataactgacctgggtgtctcaggtgccagggaggaatttgtggagacctgcccaagtgaacacaaaggagtgattgagtctgttgtgaccatcgaggatgatttcatcactgtagtgcaaaccacaactgatgaaggggagtcagggtcccacagcgtgcgttttgcagccctagagcagcctgaggtggaaaggagaccatctcctcatgatgaagaagagtttgaagtagaagaggcagctgaagcccaggcagaacccaaagatggttccccagaggctccagcttcccctgagagagaagaggttgcactttctgaatataagacagaaacctatgacgattacaaagatgagaccaccattgacgactccatcatggacgctgacagcctctgggtggacactcaagatgatgataggagcatcatgacagaacagttagaaactattcctaaagaggagaaagctgaaaaggaagctcggagatcatctcttgagaaacatagaaaagaaaagccttttaaaaccgggagaggcagaatttccactcctgaaagaaaagtagctaaaaaggaacctagcacagtctccagagatgaagtgagaaggaaaaaagcagtttataagaaggctgaacttgctaaaaaaacagaagttcaggcccactctccctccaggaaattcattttaaaacctgctatcaaatatactagaccaactcatctctcctgtgttaagcggaaaaccacagcagcaggtggggaatcagctctggctcccagtgtatttaaacaggcaaaggacaaagtctctgacggagtaaccaagagcccagaaaagcgctcttctctcccaagaccttcctccattctccctcctcggcgaggtgtgtcaggagacagagatgagaattccttctctctcaacagttctatctcttcttcagcacggcggaccaccaggtcagagccaattcgcagagcagggaagagtggtacctcaacacccactacccctgggtctactgccatcactcctggcaccccaccaagttattcttcacgcacaccaggcactcctggaacccctagctatcccaggacccctcacacaccaggaacccccaagtctgccatcttggtgccgagtgagaagaaggtcgccatcatacgtactcctccaaaatctcctgcgactcccaagcagcttcggcttattaaccaaccactgccagacctgaagaatgtcaaatccaaaatcggatcaacagacaacatcaaataccagcctaaaggggggcaggtacaaattgttaccaagaaaatagacctaagccatgtgacatccaaatgtggctctctgaagaacatccgccacaggccaggtggcggacgtgtgaaaattgagagtgtaaaactagatttcaaagaaaaggcccaagctaaagttggttctcttgataatgctcatcatgtacctggaggtggtaatgtcaagattgacagccaaaagttgaacttcagagagcatgctaaagcccgtgtggaccatggggctgagatcattacacagtccccaggcagatccagcgtggcatcaccccgacgactcagcaatgtctcctcgtctggaagcatcaacctgctcgaatctcctcagcttgccactttggctgaggatgtcactgctgcactcgctaagcagggcttgtgaatatttctcatttagcattgaaataataatatttaggcatgagctcttggcaggagtgggctctgagcagttgttatattcattctttataaaccataaaataaataatctcatccccaaactgtagtaattgttacaattttctatttaaaaaatgaatagtacatgcagaaattgacctgatttccatttgcaacaggaagacactggctttacatgggttcaattggacaattatttttgctctgctctgttttgcatggagtattattattttaaaaattgcatttttacctttcatgtgcctgaaggctatccactacattctgaaggccttgttaaaatccaagctgctcatttcactattctgtttctgagtgagaagataaaaactgcccattgtaacttatttcaggttaaattaaaccaaggagtctgattgcaggaagggaagagcatgtaagaaataagtttttttaaagtgttattttgtataaatgggaagaaagattcaattaagttattaacatttgggacctggataattatatcagagtatgtcagtccaataaattatttaactaattaaaaaatagttgcaaagcatttgagctgtggttgaggaagtggtgtaaaagtgcatccattaggaatgatgcactttcattaggatggactcgtgtctgattagaatgtcagttgatcagctagatttgtgtccacactaccagtttcacaccccctttccatctgtttgatacagtattatagatataaatatatatatatttctctgtggccatttgtgatacttcctcatatacttgaatattatacttctttattcacagtatctgtgtctcctgcaccctttggtgttgcaattttagatatgtgaaagtagatgttagcagggttctctccctatttaaaaaaaatacattaaaaaagacaaaaaattttagcatgaagttgctttctgtaacaactcaaagccgtaaccctgttttagtgccagatacaagtctctcccgtgatgctagacaaaaaattatttttctttgctttcaccaacatggagtttgtgggggtgggtccagttatacatgaaagggtttacagattgttggtttaagattatggatttatctcatttttaatcacaggatagtttggggtttattcctattattattcatgaaaccgacttaagattttttctttatttttctttttttttccatttgctaaagttgaaagttgaaactaactataatagtttgaaacatgttttctcatttttccaaatagtatctgtttattaaattctctaatagaagatgtttgtctttcttacccaaagtaaagatcccctgatcagaaagaaaaaatacaatactttgggaagctatagctataaaacacttgagacacagatatctaaatcagtttttttccaagactccaacattgcactctgtaaagtaacacactgtgatctagtattatttatcagtagataatactgttctgactgtatatacagtctagaactcacaaatcaattagttcctctcacaaatcattcatcttagacttacaaataaggaatgaaatagtcaatggcctgattaaggcaaagagctaccaggctagatggacactttttaaaaattttatctgttctttttcttgctcagggctggtaggttggatctgaaccattaaaatcaaatggtccactaggcgtatgatctctttgagccaaatcagttcctgaatataaaggaggaaatgatgaggatgtactgaggcaacggggaagtatagaaacatccaagacaaaagccaagggatgcaaaggcagagacacaggtgctttttggtgacccagtggatatggcaaccagtgtaactgccatacaagaaaccctaggagcaaacccacaccactcattctcagctaagagattttacacaggcaaacgtgtcttaaaccatctataaatcagttattttatatgacagtcaaaaccttagaaaccttaggatcattatatctattttctgcctattaattgctgtgaggtttgatttgaccaatctgggcaatttattcatcagcttcccttgaagtgcaccagaaaatagaagaaaggtgtgtggagacttagggtattttattacatgttttcatagtcttaaatagtgattaaatttctctagaaagaagttaacagctcattagaaaagttttaacctgtgaaataagtatttttctcaacattctttaaagtttttatataagttaacactaggtaaacattctgcatactagaagtcagtttattacaaatacatgtcaaaaataaagattatacaaggcaccaaactactagatttggcattaaaacaaatgtttatttctaatcacaacaaaattataatgaataaatgttcttgctttgtatggaaatacaattctttattaaagttaacagaaaggaactgatcgtttgtaccagtaaaagagagaaacacacaggttaaatatcttcttgtggggttaaggggtagaacctatcttgccttcactctcaagataacgactcaaattaagctttttgagcaccactcttgtggggacacacatacgctgatctaggaatgaaatcttcgtggtctcaattctagatctactatgccagtttctctctggctttagcctttgagaacctgtataagaatacgtaagtaatccagagctgtgaagagtttaaaggccaacttctccagtgaactcaacctctgggtcacttgcaaccagaaattggatacctcataatgatgcaggaaagacccgagttcatgatgagtttcaaaggccacgttcatttaggaaccaactctctctggatttacctgctgagttccagcagcgtgatgggctgacatcccacctacaagtatgacacctgtgtaacaccagctaggtacggctggagaaggctgaagagagaatgccattaaatggaagaatgtactgattgtagtgaccttctccacacacacacacacacacacacacacacacacctacagtaatacagcaagcgtggaataatcagccaatatataacattccatcagtattttattaaggaaataacctgaatgtggttgattttgacatagctgcaattacagttttcttctatttttcaagccacaataaggaaaataaactactcatggtctaaatactagagataaagtagattcatggcttggtaaggaaattttaagcattccttcaaagattgacgtgctaaaataagcattgatgttttgagtttttttacacctaggatttttagcttgggtgtgtaggtgaaggccaagactctctgcaggaaaaagcttattttcaaactcagaaaataaaatgtcaatcataaaaatctacttcaactttagcaaaaagaaaaaaaaatcaacaaaaagtatactctgtatgctgggattccgaggttccaacacactgttacaaatctgtggggggtttctttcttctgataattctagagcctgttaccatagaaaggcatttcttcaatggctggttgtagttagttcatgtttttcaatcaaatttgcaaatgtatttgttgctgtatagtgattgttttgcaaaataaaattgcttgtcacct
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:4133 -> Molecular function: GO:0002162 [dystroglycan binding] evidence: IPI
GeneID:4133 -> Molecular function: GO:0005198 [structural molecule activity] evidence: NAS
GeneID:4133 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:4133 -> Molecular function: GO:0005516 [calmodulin binding] evidence: IEA
GeneID:4133 -> Molecular function: GO:0008017 [microtubule binding] evidence: IEA
GeneID:4133 -> Biological process: GO:0001578 [microtubule bundle formation] evidence: IEA
GeneID:4133 -> Biological process: GO:0007409 [axonogenesis] evidence: IEA
GeneID:4133 -> Biological process: GO:0018107 [peptidyl-threonine phosphorylation] evidence: IEA
GeneID:4133 -> Biological process: GO:0021954 [central nervous system neuron development] evidence: IEP
GeneID:4133 -> Biological process: GO:0031175 [neuron projection development] evidence: IEP
GeneID:4133 -> Biological process: GO:0048813 [dendrite morphogenesis] evidence: IEP
GeneID:4133 -> Biological process: GO:0071310 [cellular response to organic substance] evidence: IEA
GeneID:4133 -> Cellular component: GO:0005737 [cytoplasm] evidence: IEA
GeneID:4133 -> Cellular component: GO:0005874 [microtubule] evidence: IEA
GeneID:4133 -> Cellular component: GO:0005875 [microtubule associated complex] evidence: TAS
GeneID:4133 -> Cellular component: GO:0034399 [nuclear periphery] evidence: IEA
GeneID:4133 -> Cellular component: GO:0043025 [neuronal cell body] evidence: IEA
GeneID:4133 -> Cellular component: GO:0043198 [dendritic shaft] evidence: IEA
by
@meso_cacase at
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