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MAP1B

MAP1B
Identifiers
Aliases MAP1B, FUTSCH, MAP5, PPP1R102, microtubule-associated protein 1B, microtubule associated protein 1B
External IDs MGI: 1306778 HomoloGene: 38111 GeneCards: MAP1B
Genetically Related Diseases
attention deficit hyperactivity disorder
RNA expression pattern
PBB GE MAP1B 214577 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005909
NM_032010
NM_001324255

NM_008634

RefSeq (protein)

NP_001311184
NP_005900

NP_001311184
NP_005900
NP_032660.2
NP_032660

Location (UCSC) Chr 5: 72.11 – 72.21 Mb Chr 13: 99.42 – 99.52 Mb
PubMed search

NM_005909
NM_032010
NM_001324255

NM_008634

NP_001311184
NP_005900

NP_001311184
NP_005900
NP_032660.2
NP_032660

Microtubule-associated protein 1B is a protein that in humans is encoded by the MAP1B gene.

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 product of this gene is a precursor polypeptide that presumably undergoes proteolytic processing to generate the final MAP1B heavy chain and LC1 light chain. Gene knockout studies of the mouse microtubule-associated protein 1B gene suggested an important role in development and function of the nervous system. Two alternatively spliced transcript variants have been described.


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