2. Gene
  3. MAP9 - microtubule associated protein 9 Gene

MAP9 - microtubule associated protein 9 Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：微管相关蛋白 9

种属: Homo sapiens

同用名: ASAP

基因 ID: 79884 | 基因类型: protein coding

关于 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.

功能概要

ASAP 是纺锤体功能、有丝分裂进展和胞质分裂所需的微管相关蛋白 (Saffin 等人，2005 [PubMed 16049101]) 。[OMIM 提供，2008 年 3 月]

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 基因产物(1)

mRNA Protein Name
NM_001039580.2 NP_001034669.1 microtubule-associated protein 9
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables microtubule binding IMP
IMP: 通过突变表型推断
16049101 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in mitotic spindle assembly IDA
IDA: 通过直接分析推断
16049101 GOA
involved in regulation of mitotic centrosome separation IMP
IMP: 通过突变表型推断
16049101 GOA
involved in regulation of mitotic cytokinesis IMP
IMP: 通过突变表型推断
16049101 GOA
involved in regulation of mitotic spindle organization IMP
IMP: 通过突变表型推断
16049101 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in astral microtubule IDA
IDA: 通过直接分析推断
16049101 GOA
located in cytoplasm IDA
IDA: 通过直接分析推断
16049101 GOA
located in mitotic spindle IDA
IDA: 通过直接分析推断
16049101 GOA
located in spindle midzone IDA
IDA: 通过直接分析推断
16049101 GOA
EXP：通过实验结果推断 IDA：通过直接分析推断 IPI：通过物理相互作用推断 IMP：通过突变表型推断 IGI：通过遗传相互作用推断 IEP：通过表达模式推断
蛋白主名 其他名称

microtubule-associated protein 9

aster-associated protein

关联疾病

疾病名称 别名
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
疾病名称 别名
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS08091 MAP9 Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 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
嗨！很高兴为您提供帮助！

尊敬的 MCE 客户您好，
请您选择所在区域，我们将转接对应客服为您服务！

热门区域

A

B

C

F

G

H

J

L

N

Q

S

T

X

Y

Z

热 A B C F G H J L N Q S T X Y Z