MAP9 - microtubule associated protein 9 Gene

Also Known as ASAP

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 79884

About MAP9

Cytogenetic location: 4q32.1 Genomic coordinates (GRCh38): 4:155,342,658-155,376,965 (from NCBI)

This gene has 9 transcripts (splice variants) and 188 orthologues. Broad expression in brain (RPKM 7.7), thyroid (RPKM 7.3) and 23 other tissues.

Summary

ASAP is a microtubule-associated protein required for spindle function, mitotic progression, and cytokinesis (Saffin et al., 2005 [PubMed 16049101]).[supplied by OMIM, Mar 2008]

MAP9 Products (1)

mRNA Protein Name
NM_001039580.2 NP_001034669.1 microtubule-associated protein 9

Gene Ontology

  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence References Source
enables microtubule binding IMP
IMP: Inferred from mutant phenotype
16049101 GOA
Biological Process GO Annotation Evidence References Source
involved in mitotic spindle assembly IDA
IDA: Inferred from direct assay
16049101 GOA
involved in regulation of mitotic centrosome separation IMP
IMP: Inferred from mutant phenotype
16049101 GOA
involved in regulation of mitotic cytokinesis IMP
IMP: Inferred from mutant phenotype
16049101 GOA
involved in regulation of mitotic spindle organization IMP
IMP: Inferred from mutant phenotype
16049101 GOA
Cellular Component GO Annotation Evidence References Source
located in astral microtubule IDA
IDA: Inferred from direct assay
16049101 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
16049101 GOA
located in mitotic spindle IDA
IDA: Inferred from direct assay
16049101 GOA
located in spindle midzone IDA
IDA: Inferred from direct assay
16049101 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

microtubule-associated protein 9

  • aster-associated protein

Related Diseases

Diseases Alias
Joubert Syndrome 7

  • JBTS7

  • Cerebello-Oculo-Renal Syndrome 3

  • Cors3

  • Joubert Syndrome, Type 7
Cone-Rod Dystrophy 6

  • CORD6

  • Retinal Cone Dystrophy 2

  • Rcd2

  • Dystrophy, Cone-Rod, Type 6

  • Retinitis Pigmentosa 6

  • Progressive Cone Degeneration

  • Cone Dystrophy
Cone-Rod Dystrophy 2

  • Cone-Rod Dystrophy

  • CORD2

  • Cone-Rod Retinal Dystrophy

  • Rcrd2

  • Cone-Rod Retinal Dystrophy 2

  • Crd2

  • Cord

  • Crd

  • Retinal Cone-Rod Dystrophy

  • Cone-Rod Retinal Dystrophy-2

  • Retinal Cone-Rod Dystrophy 2

  • Tapetoretinal Degeneration

  • Cone-Rod Degeneration

  • Cone Rod Dystrophy

  • Dystrophy, Cone-Rod

  • Dystrophy, Cone-Rod, Type 2

  • Retinitis Pigmentosa

  • Retinitis Pigmentosa 2

  • Progressive Cone-Rod Dystrophy
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS08091 MAP9 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Canis familiaris MAP9 VGNC VGNC:103691
Macaca mulatta MAP9 VGNC VGNC:100244
Mus musculus MAP9 MGD MGI:2442208
Bos taurus MAP9 VGNC VGNC:31211
Felis catus MAP9 VGNC VGNC:107344
Rattus norvegicus MAP9 RGD RGD:1560368
Others MAP9 NCBI