MAP1B
Sign in to saveAlso known as FUTSCH, MAP5, PPP1R102, microtubule-associated protein 1B, microtubule associated protein 1B, PVNH9, DFNA83
gen van de soort Homo sapiens
In the Vinony graph
Vinony's link graph records 282 inbound references to MAP1B, and connects out to PubMed, human chromosome 5 and Ensembl genome database project.
It is catalogued under the topic Genes on human chromosome 5.
Vinony links it to 6 Wikipedia language editions.
Gene data
MAP1B- Name
- microtubule associated protein 1B
- Type
- protein-coding
- Position
- 72,107,234–72,209,565 (+)
- Aliases
- DFNA83, FUTSCH, MAP5, PPP1R102, PVNH9
- Ensembl
- ENSG00000131711
- RefSeq RNA
- NM_001324255.2, NM_005909.5, NM_032010.1
- RefSeq protein
- NP_001311184.1, NP_005900.2
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. [provided by RefSeq, Jul 2008].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
microtubule associated protein 1B
- Symbol
- MAP1B
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 5:72,107,234-72,209,565
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 9 more facts
- HomoloGene ID
- 38111
- exact match
- identifiers.org/ncbigene/4131
- genetic association
- attention deficit hyperactivity disorder
- found in taxon
- Homo sapiens
- chromosome
- human chromosome 5
- genomic start
- 71403061
- genomic end
- 72209565
- cytogenetic location
- 5q13.2
- expressed in
- postcentral gyrus
via Wikidata · CC0