2. Gene
  3. CPXM1 - carboxypeptidase X, M14 family member 1 Gene

CPXM1 - carboxypeptidase X, M14 family member 1 Gene

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

中文名称：羧肽酶 X，M14 家族成员 1

种属: Homo sapiens

同用名: CPX1; CPXM

基因 ID: 56265 | 基因类型: protein coding

关于 CPXM1

Cytogenetic location: 20p13 Genomic coordinates (GRCh38): 20:2,794,074-2,800,627 (from NCBI)

This gene has 1 transcript (splice variant), 263 orthologues and 7 paralogues. Biased expression in endometrium (RPKM 64.0), gall bladder (RPKM 53.3) and 10 other tissues.

功能概要

该基因可能编码羧肽酶蛋白质家族的成员。在小鼠中克隆一个类似的基因座表明编码的蛋白质包含一个盘基蛋白结构域和一个羧肽酶结构域，但该蛋白质似乎缺乏羧肽酶活性所必需的残基。[RefSeq 提供，2010 年 5 月]

This gene likely encodes a member of the Carboxypeptidase family of proteins. Cloning of a comparable locus in mouse indicates that the encoded protein contains a discoidin domain and a Carboxypeptidase domain, but the protein appears to lack residues necessary for Carboxypeptidase activity.[provided by RefSeq, May 2010]

CPXM1 基因产物(2)

mRNA Protein Name
NM_001184699.2 NP_001171628.1 probable carboxypeptidase X1 isoform 2 precursor
NM_019609.5 NP_062555.1 probable carboxypeptidase X1 isoform 1 precursor

CPXM1 蛋白结构

F5_F8_type_C

F5_F8_type_C: F5/8 type C domain (150 - 271)

Peptidase_M14

Peptidase_M14: Zinc carboxypeptidase (305 - 612)

CarboxypepD_reg

CarboxypepD_reg: Carboxypeptidase regulatory-like domain (625 - 688)

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

probable carboxypeptidase X1

carboxypeptidase X (M14 family), member 1

关联疾病

疾病名称 别名
Mirror Movements 1

Congenital Mirror Movement Disorder

Bimanual Synergia

Congenital Mirror Movements

Familial Congenital Controlateral Synkinesia

Familial Congenital Mirror Movements

Hereditary Congenital Controlateral Synkinesia

Hereditary Congenital Mirror Movements

Isolated Congenital Controlateral Synkinesia

Isolated Congenital Mirror Movements

Mirror Movements

MRMV1

Mirror Movements 1 And/Or Agenesis Of The Corpus Callosum

Mirror Movements, Congenital

Bimanual Synkinesis

Cmm

Mirror Movements, 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-RS03128 CPXM1 Human Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 ID
Bos taurus CPXM1 VGNC VGNC:27681
Felis catus CPXM1 VGNC VGNC:61151
Macaca mulatta CPXM1 VGNC VGNC:71413
Canis familiaris CPXM1 VGNC VGNC:39585
Rattus norvegicus CPXM1 RGD RGD:1306937
Mus musculus CPXM1 MGD MGI:1934569
嗨！很高兴为您提供帮助！

尊敬的 MCE 客户您好，
请您选择所在区域，我们将转接对应客服为您服务！

热门区域

A

B

C

F

G

H

J

L

N

Q

S

T

X

Y

Z

热 A B C F G H J L N Q S T X Y Z