2. Gene
  3. RBM27 - RNA binding motif protein 27 Gene

RBM27 - RNA binding motif protein 27 Gene

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

中文名称：RNA 结合基序蛋白 27

种属: Homo sapiens

同用名: Psc1; ARRS1; ZC3H18; ZC3H20

基因 ID: 54439 | 基因类型: protein coding

关于 RBM27

Cytogenetic location: 5q32 Genomic coordinates (GRCh38): 5:146,203,605-146,289,223 (from NCBI)

This gene has 2 transcripts (splice variants), 206 orthologues and 1 paralogue. Ubiquitous expression in testis (RPKM 10.3), bone marrow (RPKM 8.5) and 25 other tissues.

功能概要

启用 RNA 结合活性。预计参与 mRNA 加工。预计位于细胞质和核斑点。预计活跃于核心。 [由基因组资源联盟提供，2022 年 4 月]

Enables RNA binding activity. Predicted to be involved in mRNA processing. Predicted to be located in cytoplasm and nuclear speck. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

RBM27 基因产物(1)

mRNA Protein Name
NM_018989.2 NP_061862.1 RNA-binding protein 27

RBM27 蛋白结构

PWI

PWI: PWI domain (7 - 73)

zf-CCCH

zf-CCCH: Zinc finger C-x8-C-x5-C-x3-H type (and similar) (277 - 299)

RRM_5

RRM_5: RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) (617 - 672)

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  • 1060 a.a.
蛋白主名 其他名称

RNA-binding protein 27

acidic rich RS domain containing 1

关联疾病

疾病名称 别名
Osteogenesis Imperfecta, Type Xv

Osteogenesis Imperfecta Type 15

OI15

Osteogenesis Imperfecta Type Xv

Oi, Type Xv

Osteogenesis Imperfecta 15

Oi Type Xv

Oi-Xv
Brachydactyly, Type B1

Brachydactyly Type B1

Brachydactyly Type B

BDB1

Brachydactyly, Type B

Bdb

Brachydactyly B1
Osteopetrosis, Autosomal Dominant 1

OPTA1

Autosomal Dominant Osteopetrosis 1

Autosomal Dominant Osteopetrosis Type 1

Osteopetrosis Autosomal Dominant Type 1

Osteopetrosis, Autosomal Dominant, Type I

Osteopetrosis, Autosomal Dominant, Type 1
Robinow Syndrome, Autosomal Recessive 1

Robinow Syndrome, Autosomal Recessive

Autosomal Recessive Robinow Syndrome

Covesdem Syndrome

RRS1

Costovertebral Segmentation Defect-Mesomelia Syndrome

Rrs

Costovertebral Segmentation Defect With Mesomelia, Formerly

Covesdem Syndrome, Formerly

Costovertebral Segmentation Defect With Mesomelia

Robinow Syndrome Autosomal Recessive With Aplasia/Hypoplasia Of Phalanges And Metacarpals/Metatarsals

Robinow Syndrome Autosomal Recessive With Brachy-Syn-Polydactyly

Robinow Syndrome, Autosomal Recessive, With Aplasia/Hypoplasia Of Phalanges And Metacarpals/Metatarsals

Robinow Syndrome, Autosomal Recessive, With Brachy-Syn-Polydactyly

Robinow, Autosomal Recessive Syndrome, Type 1
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-RS11745 RBM27 Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Rattus norvegicus RBM27 RGD RGD:1311966
Mus musculus RBM27 MGD MGI:2147194
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