2. Gene
  3. RAI14 - retinoic acid induced 14 Gene

RAI14 - retinoic acid induced 14 Gene

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

中文名称：视黄酸诱导 14

种属: Homo sapiens

同用名: RAI13; NORPEG

基因 ID: 26064 | 基因类型: protein coding

关于 RAI14

Cytogenetic location: 5p13.2 Genomic coordinates (GRCh38): 5:34,656,328-34,832,612 (from NCBI)

This gene has 28 transcripts (splice variants) and 203 orthologues. Broad expression in endometrium (RPKM 27.5), placenta (RPKM 14.1) and 23 other tissues.

功能概要

预测启用肌动蛋白结合活性。预计参与多个过程，包括凋亡信号通路； NIK/NF-kappaB 信号的调节；和精子发生。位于胞质溶胶中；纤维中心;和核质。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to enable actin binding activity. Predicted to be involved in several processes, including apoptotic signaling pathway; regulation of NIK/NF-kappaB signaling; and spermatogenesis. Located in cytosol; fibrillar center; and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

RAI14 基因产物(6)

mRNA Protein Name
NM_001145520.1 NP_001138992.1 ankycorbin isoform a
NM_001145521.2 NP_001138993.1 ankycorbin isoform a
NM_001145522.2 NP_001138994.1 ankycorbin isoform b
NM_001145523.2 NP_001138995.1 ankycorbin isoform c
NM_001145525.2 NP_001138997.1 ankycorbin isoform d
NM_015577.3 NP_056392.2 ankycorbin isoform a
基因本体论
  • 分子功能
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
15161933 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

RAI14 蛋白结构

Ank_2

Ank_2: Ankyrin repeats (3 copies) (23 - 110)

Ank_2

Ank_2: Ankyrin repeats (3 copies) (115 - 182)

Ank_2

Ank_2: Ankyrin repeats (3 copies) (185 - 242)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 980 a.a.
蛋白主名 其他名称

ankycorbin

ankyrin repeat and coiled-coil structure-containing protein

RAI14 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
RAI14 Q9P0K7 YWHAZ Homo sapiens P63104
Pull Down
15161933
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Cardiomyopathy, Infantile Histiocytoid

Histiocytoid Cardiomyopathy

Foamy Myocardial Transformation Of Infancy

Infantile Histiocytoid Cardiomyopathy

Infantile Xanthomatous Cardiomyopathy

Oncocytic Cardiomyopathy

Cardiomyopathy, Infantile Xanthomatous

Cardiomyopathy, Focal Lipid

Cardiomyopathy, Oncocytic

Focal Lipid Cardiomyopathy

Infantile Cardiomyopathy With Histiocytoid Change

CMIH

Cardiomyopathy Focal Lipid

Cardiomyopathy Infantile Xanthomatous

Cardiomyopathy Oncocytic
Twin-To-Twin Transfusion Syndrome

Twin To Twin Transfusion Syndrome

Twin Twin Transfusion Syndrome

Fetal Blood Loss From Fetal Hemorrhage Into Co-Twin

Fetal Hemorrhage Into Co-Twin

Twin To Twin Transfusion

Twin-To-Twin Blood Transfer

Fetal Transfusion Syndrome

Fetofetal Transfusion Syndrome

Ttts

Feto-Fetal Transfusion Syndrome

Fetofetal Transfusion

Fetus-To-Fetus Placental Transfusion Syndrome
Potocki-Lupski Syndrome

PTLS

Chromosome 17p11.2 Duplication Syndrome

17p11.2 Microduplication Syndrome

Duplication 17p11.2 Syndrome

Trisomy 17p11.2

Potocki-Lupski Syndrome (Dup(17)(P11.2p11.2))

17p11.2 Duplication Syndrome

Dup(17)(P11.2p11.2)

Pls

Chromosome 17, Trisomy 17p11 2
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-RS11625 RAI14 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 RAI14 VGNC VGNC:45329
Felis catus RAI14 VGNC VGNC:64482
Bos taurus RAI14 VGNC VGNC:33696
Rattus norvegicus RAI14 RGD RGD:1305942
Mus musculus RAI14 MGD MGI:1922896
Macaca mulatta RAI14 VGNC VGNC:76478
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