Human Gene MAP2 (uc002vdh.1)
  Description: Homo sapiens microtubule-associated protein 2 (MAP2), transcript variant 5, mRNA.
RefSeq Summary (NM_031845): 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 (Including UTRs)
   Position: hg19 chr2:210,476,049-210,598,834 Size: 122,786 Total Exon Count: 12 Strand: +
Coding Region
   Position: hg19 chr2:210,517,895-210,595,121 Size: 77,227 Coding Exon Count: 10 

Page IndexSequence and LinksPrimersGenetic AssociationsMalaCardsCTD
Gene AllelesRNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther Species
mRNA DescriptionsPathwaysOther NamesModel InformationMethods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr2:210,476,049-210,598,834)mRNA (may differ from genome)Protein (528 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
GeneNetworkH-INVHGNCLynxMalacardsMGI
OMIMPubMedTreefamUniProtKBWikipediaBioGrid CRISPR DB

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  Genetic Association Studies of Complex Diseases and Disorders
  Genetic Association Database (archive): MAP2
CDC HuGE Published Literature: MAP2
Positive Disease Associations: Heart Rate , Insulin , Macular Degeneration , Platelet Aggregation
Related Studies:
  1. Heart Rate
    , , . [PubMed 0]
  2. Insulin
    James B Meigs et al. BMC medical genetics 2007, Genome-wide association with diabetes-related traits in the Framingham Heart Study., BMC medical genetics. [PubMed 17903298]
    Framingham 100K SNP data is a resource for association tests of known and novel genes with diabetes and related traits posted at http://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?id=phs000007 webcite. Framingham 100K data replicate the TCF7L2 association with diabetes.
  3. Macular Degeneration
    , , . [PubMed 0]
           more ... click here to view the complete list

-  MalaCards Disease Associations
  MalaCards Gene Search: MAP2
Diseases sorted by gene-association score: central neurocytoma (20), pituicytoma (12), human monocytic ehrlichiosis (11), ganglioglioma (11), chiari malformation (10), brain ischemia (9), papillary tumor of the pineal region (9), olivopontocerebellar atrophy (9), dysembryoplastic neuroepithelial tumor (8), striatonigral degeneration (8), merkel cell carcinoma (7), mucopolysaccharidosis type iiia (7), prion disease (7), occlusion precerebral artery (7), hemimegalencephaly (7), neuronal migration disorders (6), chondroid chordoma (6), pleomorphic xanthoastrocytoma (6), scrapie (6), optic nerve neoplasm (6), transient cerebral ischemia (6), mixed germ cell cancer (5), carotid artery occlusion (5), cerebellar liponeurocytoma (5), brain glioma (5), clear cell ependymoma (5), ischemia (4), optic nerve glioma (4), medulloblastoma (2), schizophrenia (1), stroke, ischemic (1), parkinson disease, late-onset (1), amyotrophic lateral sclerosis 1 (0)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           more ... click here to view the complete list

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 93.45 RPKM in Brain - Anterior cingulate cortex (BA24)
Total median expression: 764.96 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -19.95147-0.136 Picture PostScript Text
3' UTR -949.303713-0.256 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  Pfam Domains:
PF00418 - Tau and MAP protein, tubulin-binding repeat
PF10522 - RII binding domain

ModBase Predicted Comparative 3D Structure on P11137-2
FrontTopSide
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologGenome BrowserNo orthologNo orthologNo orthologNo ortholog
Gene DetailsGene Details    
Gene SorterGene Sorter    
 RGD    
 Protein Sequence    
 Alignment    

-  Descriptions from all associated GenBank mRNAs
  BC038857 - Homo sapiens microtubule-associated protein 2, mRNA (cDNA clone IMAGE:5223046), complete cds.
BC066648 - Homo sapiens microtubule-associated protein 2, mRNA (cDNA clone IMAGE:6012668), partial cds.
BC110423 - Homo sapiens microtubule-associated protein 2, mRNA (cDNA clone IMAGE:5242955), complete cds.
U01828 - Human microtubule-associated protein 2 (MAP2) mRNA, complete cds.
AK307603 - Homo sapiens cDNA, FLJ97551.
AB209330 - Homo sapiens mRNA for microtubule-associated protein 2 isoform 2 variant protein.
BC027583 - Homo sapiens microtubule-associated protein 2, mRNA (cDNA clone IMAGE:4837202).
BC143245 - Homo sapiens microtubule-associated protein 2, mRNA (cDNA clone IMAGE:9051746), complete cds.
BC117123 - Homo sapiens microtubule-associated protein 2, mRNA (cDNA clone IMAGE:40125674), complete cds.
JD301986 - Sequence 283010 from Patent EP1572962.
AK291446 - Homo sapiens cDNA FLJ77141 complete cds, highly similar to Homo sapiens microtubule-associated protein 2 (MAP2), transcript variant 2, mRNA.
JD530091 - Sequence 511115 from Patent EP1572962.
CU691614 - Synthetic construct Homo sapiens gateway clone IMAGE:100020908 5' read MAP2 mRNA.
AB529090 - Synthetic construct DNA, clone: pF1KB4240, Homo sapiens MAP2 gene for microtubule-associated protein 2, without stop codon, in Flexi system.
BC172263 - Synthetic construct Homo sapiens clone IMAGE:100068957, MGC:198968 microtubule-associated protein 2 (MAP2) mRNA, encodes complete protein.
BC172568 - Synthetic construct Homo sapiens clone IMAGE:100069262, MGC:199273 microtubule-associated protein 2 (MAP2) mRNA, encodes complete protein.
JF432335 - Synthetic construct Homo sapiens clone IMAGE:100073523 microtubule-associated protein 2 (MAP2) gene, encodes complete protein.
KJ897165 - Synthetic construct Homo sapiens clone ccsbBroadEn_06559 MAP2 gene, encodes complete protein.
U89329 - Human alternatively spliced microtubule-associated protein 2C (MAP2) mRNA, complete cds.
U89330 - Human alternatively spliced microtubule-associated protein 2 (MAP2) mRNA, complete cds.
M25668 - Human microtubule associated protein 2 (MAP2) mRNA, partial sequence.
AL833567 - Homo sapiens mRNA; cDNA DKFZp686I2148 (from clone DKFZp686I2148).
S76756 - 4R-MAP2=microtubule-associated protein 2 4R isoform [human, brain, mRNA Partial, 1012 nt].
CQ873794 - Sequence 213 from Patent WO2004076622.
DD413631 - Regulation of Mammalian Cells.
JD338412 - Sequence 319436 from Patent EP1572962.
JD073691 - Sequence 54715 from Patent EP1572962.
JD315289 - Sequence 296313 from Patent EP1572962.
JD166751 - Sequence 147775 from Patent EP1572962.
JD090410 - Sequence 71434 from Patent EP1572962.
JD291334 - Sequence 272358 from Patent EP1572962.
AF088065 - Homo sapiens full length insert cDNA clone ZD86B04.
AK055674 - Homo sapiens cDNA FLJ31112 fis, clone IMR322000316.
AK056148 - Homo sapiens cDNA FLJ31586 fis, clone NT2RI2002211.

-  Biochemical and Signaling Pathways
  BioCarta from NCI Cancer Genome Anatomy Project
h_akapCentrosomePathway - Protein Kinase A at the Centrosome

-  Other Names for This Gene
  Alternate Gene Symbols: BC027583, NM_031845, NP_114033, P11137-2
UCSC ID: uc002vdh.1
RefSeq Accession: NM_031845
Protein: P11137-2, splice isoform of P11137

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: BC027583.1
exon count: 12CDS single in 3' UTR: no RNA size: 1870
ORF size: 1587CDS single in intron: no Alignment % ID: 99.95
txCdsPredict score: 3315.00frame shift in genome: no % Coverage: 98.98
has start codon: yes stop codon in genome: no # of Alignments: 1
has end codon: yes retained intron: no # AT/AC introns 0
selenocysteine: no end bleed into intron: 0# strange splices: 0
Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.