2. Gene
  3. BMS1 - BMS1 ribosome biogenesis factor Gene

BMS1 - BMS1 ribosome biogenesis factor Gene

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

中文名称：BMS1 核糖体生物发生因子

种属: Homo sapiens

同用名: ACC; BMS1L

基因 ID: 9790 | 基因类型: protein coding

关于 BMS1

Cytogenetic location: 10q11.21 Genomic coordinates (GRCh38): 10:42,782,795-42,834,937 (from NCBI)

This gene has 1 transcript (splice variant), 227 orthologues, 1 paralogue and is associated with 2 phenotypes. Ubiquitous expression in testis (RPKM 6.4), appendix (RPKM 5.6) and 25 other tissues.

功能概要

该基因可能编码核糖体组装蛋白。酵母中的一种类似蛋白质在 35S-rRNA 加工中起作用，其中包括一系列对 40S 核糖体形成至关重要的切割步骤。相关假基因存在于染色体 2、9、10、15、16 和 22 上。[RefSeq 提供，2009 年 3 月]

This gene likely encodes a ribosome assembly protein. A similar protein in yeast functions in 35S-rRNA processing, which includes a series of cleavage steps critical for formation of 40S ribosomes. Related pseudogenes exist on chromosomes 2, 9, 10, 15, 16, and 22.[provided by RefSeq, Mar 2009]

BMS1 基因产物(1)

mRNA Protein Name
NM_014753.4 NP_055568.3 ribosome biogenesis protein BMS1 homolog

BMS1 蛋白结构

AARP2CN

AARP2CN: AARP2CN (NUC121) domain (231 - 317)

RIBIOP_C

RIBIOP_C: 40S ribosome biogenesis protein Tsr1 and BMS1 C-terminal (818 - 1104)

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  • 1282 a.a.
蛋白主名 其他名称

ribosome biogenesis protein BMS1 homolog

BMS1 homolog, ribosome assembly protein

关联疾病

疾病名称 别名
Aplasia Cutis Congenita, Nonsyndromic

ACC

Congenital Defect Of Skull And Scalp

Acces Syndrome

Nonsyndromic Aplasia Cutis Congenita

Scalp Defect, Congenital

ACCES

Aplasia Cutis Congenita With Ectrodactyly Skeletal Syndrome

Congenital Absence Of Skin On Scalp

Congenital Defect Of The Skull And Scalp

Congenital Ulcer Of The Newborn

Scalp Defect Congenital

Aplasia Cutis Congenita, Non-Syndromic

Congenital Scalp Defect

Aplasia Cutis Congenita
Aplasia Cutis Congenita

Aplasia Cutis Congenita Of Limbs Recessive

Congenital Absence Of Skin On The Upper Or Lower Limbs

Recessive Aplasia Cutis Congenita Of The Limbs

Aplasia Cutis Congenita Nonsyndromic

Congenital Defect Of Skull And Scalp

Scalp Defect Congenital
Adams-Oliver Syndrome

Adams Oliver Syndrome

Aos

Congenital Scalp Defects With Distal Limb Reduction Anomalies

Aplasia Cutis Congenita With Terminal Transverse Limb Defects

Congenital Scalp Defects With Distal Limb Anomalies

Limb, Scalp And Skull Defects

Limb Scalp And Skull Defects

Absence Defect Of Limbs, Scalp, And Skull
Tooth Erosion

Generalized Erosion

Localized Erosion

Generalized Erosions

Erosion, Localized
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 (2)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-19991 BMS-1 99.56% 否
HY-RS01555 BMS1 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 BMS1 VGNC VGNC:38487
Rattus norvegicus BMS1 RGD RGD:1308043
Mus musculus BMS1 MGD MGI:2446132
Felis catus BMS1 VGNC VGNC:97367
Bos taurus BMS1 VGNC VGNC:26527
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