2. Gene
  3. POP7 - POP7 homolog, ribonuclease P/MRP subunit Gene

POP7 - POP7 homolog, ribonuclease P/MRP subunit Gene

  • 基因
  • 蛋白
  • 疾病
  • 直系同源

中文名称：POP7 同系物，核糖核酸酶 P/MRP 亚基

种属: Homo sapiens

同用名: RPP2; RPP20; 0610037N12Rik

基因 ID: 10248 | 基因类型: protein coding

关于 POP7

Cytogenetic location: 7q22.1 Genomic coordinates (GRCh38): 7:100,706,121-100,707,486 (from NCBI)

This gene has 2 transcripts (splice variants) and 182 orthologues. Ubiquitous expression in prostate (RPKM 11.3), brain (RPKM 11.1) and 25 other tissues.

功能概要

启用核糖核酸酶 P RNA 结合活性。有助于核糖核酸酶 P 活性。参与 tRNA 5'-前导去除。位于核仁。多聚核糖核酸酶 P 复合物和核糖核酸酶 MRP 复合物的一部分。 [由基因组资源联盟提供，2022 年 4 月]

Enables ribonuclease P RNA binding activity. Contributes to ribonuclease P activity. Involved in tRNA 5'-leader removal. Located in nucleolus. Part of multimeric ribonuclease P complex and ribonuclease MRP complex. [provided by Alliance of Genome Resources, Apr 2022]

POP7 基因产物(1)

mRNA Protein Name
NM_005837.3 NP_005828.2 ribonuclease P protein subunit p20

POP7 蛋白结构

Rpp20

Rpp20: Rpp20 subunit of nuclear RNase MRP and P (33 - 133)

  • 0
  • 100
  • 140 a.a.
蛋白主名 其他名称

ribonuclease P protein subunit p20

POP7 (processing of precursor, S. cerevisiae) homolog

关联疾病

疾病名称 别名
Anauxetic Dysplasia 2

ANXD2
Loiasis

Loa Loa Filariasis

Mansonelliasis

African Eye Worm

Mansonella Perstans Infections

Mansonellosis

Eye Worm Disease Of Africa

Loa Loa Infestation

African Eyeworm Disease

Calabar Swelling
Anauxetic Dysplasia 1

Anauxetic Dysplasia

Spondylometaepiphyseal Dysplasia, Menger Type

Spondylometaepiphyseal Dysplasia, Anauxetic Type

Spondyloepimetaphyseal Dysplasia, Anauxetic Type

ANXD1

Anxd

Spondylometaepiphyseal Dysplasia Anauxetic Type

Spondylometaepiphyseal Dysplasia Menger Type

Ad

Spondyloepimetaphyseal Dysplasia, Menger Type

Dysplasia, Anauxetic, Type 1
Peroxisome Biogenesis Disorder 1b

Peroxisome Biogenesis Disorder

Infantile Refsum Disease

Infantile Phytanic Acid Storage Disease

PBD1B

Refsum Disease, Infantile

Adrenoleukodystrophy, Autosomal Neonatal

Ird

Mild Pbd-Zsd

Mild Peroxisome Biogenesis Disorder-Zellweger Spectrum Disorder

Pbd-Zsd

Peroxisome Biogenesis Disorder Spectrum

Peroxisome Biogenesis Disorder-Zellweger Spectrum Disorder

Autosomal Neonatal Adrenoleukodystrophy

Refsum Disease Infantile

Peroxisome Biogenesis Disorders

Peroxisome Biogenesis Disorder, Type 1b
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
Bos taurus POP7 VGNC VGNC:33166
Felis catus POP7 VGNC VGNC:64299
Macaca mulatta POP7 VGNC VGNC:76079
Rattus norvegicus POP7 RGD RGD:1306413
Mus musculus POP7 MGD MGI:1921347
Canis familiaris POP7 VGNC VGNC:44818