1. Gene
  2. BANK1 - B cell scaffold protein with ankyrin repeats 1 Gene

BANK1 - B cell scaffold protein with ankyrin repeats 1 Gene

中文名称:具有锚蛋白重复 1 的 B 细胞支架蛋白

种属: Homo sapiens

同用名: BANK

基因 ID: 55024 | 基因类型: protein coding

关于 BANK1

Cytogenetic location: 4q24 Genomic coordinates (GRCh38): 4:101,790,730-102,074,812 (from NCBI)

This gene has 8 transcripts (splice variants), 175 orthologues, 1 paralogue and is associated with 1 phenotype. Biased expression in lymph node (RPKM 39.0), spleen (RPKM 27.4) and 8 other tissues.

功能概要

由该基因编码的蛋白质是一种 B 细胞特异性支架蛋白,在 B 细胞受体诱导的细胞内钙动员中发挥作用。这种蛋白质还可以促进 Lyn 介导的肌醇 1,4,5-三磷酸受体的酪氨酸磷酸化。该基因的多态性与系统性红斑狼疮的易感性有关。可变剪接导致多个转录本变体。[RefSeq 提供,2009 年 10 月]

The protein encoded by this gene is a B-cell-specific scaffold protein that functions in B-cell receptor-induced calcium mobilization from intracellular stores. This protein can also promote Lyn-mediated tyrosine phosphorylation of inositol 1,4,5-trisphosphate receptors. Polymorphisms in this gene are associated with susceptibility to systemic lupus erythematosus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]

BANK1 基因产物(3)

mRNA Protein Name
NM_001083907.3 NP_001077376.3 B-cell scaffold protein with ankyrin repeats isoform 2
NM_001127507.3 NP_001120979.3 B-cell scaffold protein with ankyrin repeats isoform 3
NM_017935.5 NP_060405.5 B-cell scaffold protein with ankyrin repeats isoform 1
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 phospholipase binding IPI
IPI: 通过物理相互作用推断
23555801 GOA
enables protease binding IPI
IPI: 通过物理相互作用推断
23555801 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
11782428 GOA
enables protein tyrosine kinase binding IPI
IPI: 通过物理相互作用推断
11782428 GOA
enables signaling adaptor activity IDA
IDA: 通过直接分析推断
23555801 GOA
enables signaling receptor binding IPI
IPI: 通过物理相互作用推断
11782428 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in B cell activation IDA
IDA: 通过直接分析推断
11782428 GOA
involved in positive regulation of peptidyl-tyrosine phosphorylation IMP
IMP: 通过突变表型推断
11782428 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in perinuclear region of cytoplasm IDA
IDA: 通过直接分析推断
23555801 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

BANK1 蛋白结构

DBB

DBB: Dof, BCAP, and BANK (DBB) motif, (199 - 326)

  • 0
  • 200
  • 400
  • 600
  • 785 a.a.
蛋白主名 其他名称

B-cell scaffold protein with ankyrin repeats

BANK1 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
BANK1 Q8NDB2 BLK Homo sapiens P51451 21978998
种属内
BANK1 Q8NDB2 BLK Homo sapiens P51451 21978998
种属内
BANK1 Q8NDB2 BLK Homo sapiens P51451 21978998
种属内
BANK1 Q8NDB2 LYN Homo sapiens P07948 11782428
种属内
BANK1 Q8NDB2 LYN Homo sapiens P07948 11782428
种属内
BANK1 Q8NDB2 LYN Homo sapiens P07948 11782428
种属间: 跨种属相互作用 种属内: 同种属相互作用

BANK1 抗体

目录号 产品名 应用 反应物种
HY-P81434 BANK1 Antibody (YA1179) IHC-P Human

关联疾病

疾病名称 别名
Systemic Lupus Erythematosus

Lupus Nephritis

SLE

Disseminated Lupus Erythematosus

Systemic Lupus Erythematosus, Susceptibility To

Lupus Erythematosus, Systemic

Lupus Nephritis, Susceptibility To

Libman-Sacks Disease

Systemic Lupus Erythematosus Susceptibility To

Sle - Lupus Erythematosus, Systemic

Le Syndrome

Lupus

Lupus Erythematosus Systemic

Lupus Erythematosus, Systemic, Susceptibility To

Lupus Vulgaris

Lupus Erythematosus, Discoid

Lupus Erythematosus

Systemic Lupus Erythematosus Nos

Sle - [Systemic Lupus Erythematosus]

Lupus Erythematosus

Lupus

Lupus Vulgaris

Lupus Erythematosus, Discoid

Lupus Erythematosus, Systemic

Subacute Cutaneous Lupus

Le - [Lupus Erythematosus]

Facial Hemiatrophy

Parry-Romberg Syndrome

Diffuse Scleroderma

Diffuse Systemic Sclerosis

Systemic Sclerosis, Diffuse

Scleroderma, Diffuse

Systemic Scleroderma

Progressive System Sclerosis

Limited Scleroderma

Limited Cutaneous Systemic Sclerosis

Limited Systemic Sclerosis

Systemic Sclerosis Sine Scleroderma

Crest Syndrome

Limited Cutaneous Systemic Scleroderma

Scleroderma, Limited

Systemic Sclerosis, Limited

Progressive Systemic Sclerosis Sine Scleroderma

Scleroderma, Sine

Crest - [Calcinosis, Raynaud Phenomenon, Oesophageal Dysmotility, Sclerodactyly, And Telangiectasia] Syndrome

Crst - [Calcinosis, Raynaud Phenomenon, Sclerodactyly And Telangiectasia] Syndrome

Potocki-Shaffer Syndrome

Proximal 11p Deletion Syndrome

Chromosome 11p11.2 Deletion Syndrome

Pss

11p11.2 Deletion

P11pds

Defect11 Syndrome

Deletion Of Chromosome 11p11.2

POSHS

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

直系同源

种属 基因名 来源 基因 ID
Canis familiaris BANK1 VGNC VGNC:38377
Mus musculus BANK1 MGD MGI:2442120
Bos taurus BANK1 VGNC VGNC:106648
Macaca mulatta BANK1 VGNC VGNC:70090
Rattus norvegicus BANK1 RGD RGD:1564639
Felis catus BANK1 VGNC VGNC:78456