2. Gene
  3. CKAP4 - cytoskeleton associated protein 4 Gene

CKAP4 - cytoskeleton associated protein 4 Gene

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

中文名称：细胞骨架相关蛋白 4

种属: Homo sapiens

同用名: p63; CLIMP63; CLIMP-63; ERGIC-63

基因 ID: 10970 | 基因类型: protein coding

关于 CKAP4

Cytogenetic location: 12q23.3 Genomic coordinates (GRCh38): 12:106,237,881-106,248,020 (from NCBI)

This gene has 3 transcripts (splice variants), 192 orthologues and 7 paralogues. Ubiquitous expression in bone marrow (RPKM 41.9), placenta (RPKM 30.9) and 25 other tissues.

功能概要

启用 RNA 结合活性。位于几种细胞成分中，包括脂滴；核斑点；和粗面内质网。 [由基因组资源联盟提供，2022 年 4 月]

Enables RNA binding activity. Located in several cellular components, including lipid droplet; nuclear speck; and rough endoplasmic reticulum. [provided by Alliance of Genome Resources, Apr 2022]

CKAP4 基因产物(1)

mRNA Protein Name
NM_006825.4 NP_006816.2 cytoskeleton-associated protein 4
蛋白主名 其他名称

cytoskeleton-associated protein 4

63 kDa membrane protein

重组 CKAP4 蛋白

目录号 产品名 蛋白编号 纯度
HY-P700976 CKAP4 Protein, Human (282a.a, His) Q07065 (H128-V602) ≥95%

关联疾病

疾病名称 别名
Cystitis

Infective Cystitis

Urocystitis

Pyocystitis
Bladder Exstrophy

Exstrophy Of The Bladder

Classic Exstrophy Of The Bladder
Axenfeld-Rieger Syndrome, Type 1

Axenfeld-Rieger Syndrome Type 1

RIEG1

Rieg

Rgs

Rieger Syndrome Type 1

Rieger Syndrome, Type 1

Axenfeld-Rieger Syndrome 1

Iridogoniodysgenesis With Somatic Anomalies
Retinitis Pigmentosa 20

RP20

Retinitis Pigmentosa, Type 20
Spastic Paraplegia 36, Autosomal Dominant

SPG36

Hereditary Spastic Paraplegia 36

Autosomal Dominant Spastic Paraplegia Type 36

Autosomal Dominant Spastic Paraplegia 36
Interstitial Cystitis

Bladder Pain Syndrome

Painful Bladder Syndrome

Ulcerative Cystitis

Ic/Bps

Ic/Pbs

Interstitial Cystitis/Bladder Pain Syndrome

Interstitial Cystitis/Painful Bladder Syndrome

Cystitis, Interstitial

Chronic Interstitial Cystitis

Pelvic Congestion Syndrome

Trigonitis
Amelogenesis Imperfecta

Ai

Congenital Enamel Hypoplasia

Al - [Amelogenesis Imperfecta]
Hereditary Spastic Paraplegia

Familial Spastic Paraplegia

Hereditary Spastic Paraparesis

Strumpell-Lorrain Disease

Familial Spastic Paraparesis

Hsp

Spg

Strümpell-Lorrain Disease

Spastic Paraplegia, Hereditary

French Settlement Disease

Strumpell-Lorrain Syndrome

Fsp

Spastic Paraplegia, Familial

Spastic Paraplegia Hereditary

Spastic Paraplegia 3, Autosomal Dominant

Spastic Paraparesis

Hereditary Spastic Paralysis

Familial Spastic Paralysis

Hereditary Spastic Ataxia
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-RS02734 CKAP4 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 CKAP4 VGNC VGNC:39288
Felis catus CKAP4 VGNC VGNC:83533
Mus musculus CKAP4 MGD MGI:2444926
Bos taurus CKAP4 VGNC VGNC:27382
Rattus norvegicus CKAP4 RGD RGD:1311989
Macaca mulatta CKAP4 VGNC VGNC:71190
Others CKAP4 NCBI
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