2. Gene
  3. CNGA2 - cyclic nucleotide gated channel subunit alpha 2 Gene

CNGA2 - cyclic nucleotide gated channel subunit alpha 2 Gene

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

中文名称：环核苷酸门控通道亚基 alpha 2

种属: Homo sapiens

同用名: CNCA; CNG2; CNCA1; OCNC1; OCNCa; OCNCALPHA

基因 ID: 1260 | 基因类型: protein coding

关于 CNGA2

Cytogenetic location: Xq28 Genomic coordinates (GRCh38): X:151,734,746-151,745,564 (from NCBI)

This gene has 1 transcript (splice variant), 268 orthologues, 17 paralogues and is associated with 1 phenotype. Low expression observed in reference dataset.

功能概要

该基因编码的蛋白质代表环状核苷酸门控嗅觉通道的α亚基。编码的蛋白质包含介导通道形成的羧基末端亮氨酸拉链。[RefSeq 提供，2010 年 1 月]

The protein encoded by this gene represents the alpha subunit of a cyclic nucleotide-gated olfactory channel. The encoded protein contains a carboxy-terminal leucine zipper that mediates channel formation. [provided by RefSeq, Jan 2010]

CNGA2 基因产物(1)

mRNA Protein Name
NM_005140.3 NP_005131.1 cyclic nucleotide-gated olfactory channel

CNGA2 蛋白结构

Ion_trans

Ion_trans: Ion transport protein (177 - 371)

cNMP_binding

cNMP_binding: Cyclic nucleotide-binding domain (473 - 564)

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

cyclic nucleotide-gated olfactory channel

CNG channel alpha-2

关联疾病

疾病名称 别名
Anosmia, Isolated Congenital

ANIC

Isolated Congenital Anosmia

Anosmia, Congenital

Congenital Anosmia
Retinitis Pigmentosa 45

RP45

Retinitis Pigmentosa, Type 45
Achromatopsia 2

ACHM2

Rod Monochromatism 2

Rod Monochromacy 2

Rmch2

Colorblindness, Total

Complete Achromatopsia

Total Colorblindness

Achromatopsia-2

Achromatopsia, Type 2

Color Blindness

Achromatopsia
Seckel Syndrome 7

SCKL7

Microcephalic Primordial Dwarfism, Dauber Type

Seckel Syndrome, Type 7
Orofaciodigital Syndrome Ix

OFD9

Orofaciodigital Syndrome With Retinal Abnormalities

Oral-Facial-Digital Syndrome With Retinal Abnormalities

Orofaciodigital Syndrome 9

Oral-Facial-Digital Syndrome Type 9

Ofds Ix

Oral-Facial-Digital Syndrome, Type Ix

Ofd Syndrome 9

Ofds 9

Oral Facial Digital Syndrome 9

Oral Facial Digital Syndrome Type 9

Orofaciodigital Syndrome Type 9

Orofaciodigital Syndrome, Type Ix
Retinitis Pigmentosa 83

RP83

Retinitis Pigmentosa, Type 83
Cone-Rod Dystrophy 2

Cone-Rod Dystrophy

CORD2

Cone-Rod Retinal Dystrophy

Rcrd2

Cone-Rod Retinal Dystrophy 2

Crd2

Cord

Crd

Retinal Cone-Rod Dystrophy

Cone-Rod Retinal Dystrophy-2

Retinal Cone-Rod Dystrophy 2

Tapetoretinal Degeneration

Cone-Rod Degeneration

Cone Rod Dystrophy

Dystrophy, Cone-Rod

Dystrophy, Cone-Rod, Type 2

Retinitis Pigmentosa

Retinitis Pigmentosa 2

Progressive Cone-Rod Dystrophy
Retinitis Pigmentosa

RP

Rod-Cone Dystrophy

Autosomal Recessive Retinitis Pigmentosa

Non-Syndromic Retinitis Pigmentosa

Pericentral Pigmentary Retinopathy

Pigmentary Retinopathy

Tapetoretinal Degeneration

Rcd

Retinitis Pigmentosa Autosomal Recessive

ARRP

Retinitis Pigmentosa, Autosomal Recessive

Retinitis Pigmentosa 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-RS02880 CNGA2 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 CNGA2 RGD RGD:2367
Canis familiaris CNGA2 VGNC VGNC:39396
Bos taurus CNGA2 VGNC VGNC:27498
Felis catus CNGA2 VGNC VGNC:61012
Mus musculus CNGA2 MGD MGI:108040
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