2. Gene
  3. ASIC5 - acid sensing ion channel subunit family member 5 Gene

ASIC5 - acid sensing ion channel subunit family member 5 Gene

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

中文名称：酸感应离子通道亚基家族成员 5

种属: Homo sapiens

同用名: INAC; ACCN5; HINAC

基因 ID: 51802 | 基因类型: protein coding

关于 ASIC5

Cytogenetic location: 4q32.1 Genomic coordinates (GRCh38): 4:155,829,729-155,866,277 (from NCBI)

This gene has 1 transcript (splice variant), 120 orthologues and 8 paralogues. Low expression observed in reference dataset.

功能概要

该基因属于阿米洛利敏感的 Na+ 通道和退化蛋白 (NaC/DEG) 家族，其成员已在从线虫到人类的许多动物物种中被发现。由该基因编码的阿米洛利敏感 Na (+) 通道主要在小肠中表达，但其确切功能尚不清楚。[RefSeq 提供，2008 年 7 月]

This gene belongs to the amiloride-sensitive Na+ channel and degenerin (NaC/DEG) family, members of which have been identified in many animal species ranging from the nematode to human. The amiloride-sensitive Na(+) channel encoded by this gene is primarily expressed in the small intestine, however, its exact function is not known. [provided by RefSeq, Jul 2008]

ASIC5 基因产物(1)

mRNA Protein Name
NM_017419.3 NP_059115.1 acid-sensing ion channel 5

ASIC5 蛋白结构

ASC

ASC: Amiloride-sensitive sodium channel (41 - 467)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 505 a.a.
蛋白主名 其他名称

acid-sensing ion channel 5

acid sensing (proton gated) ion channel family member 5

关联疾病

疾病名称 别名
Pregnancy Loss, Recurrent 3

Pregnancy Loss, Recurrent, Susceptibility To, 3

RPRGL3

Pregnancy Loss, Recurrent, 3

Pregnancy Loss, Recurrent, Susceptibility To, Type 3
Pseudohypoaldosteronism
Liddle Syndrome 1

Liddle Syndrome

Pseudoaldosteronism

Liddle'S Syndrome

LIDLS1

Lidls

Pseudohyperaldosteronism

Pseudoprimary Hyperaldosteronism

Pseudohyperaldosteronism Type 1

Liddles Syndrome
Hyperpigmentation With Or Without Hypopigmentation, Familial Progressive

FPHH

Melanosis Universalis Hereditaria

Muh

Familial Progressive Hyperpigmentation With Or Without Hypopigmentation

Hyperpigmentation, Familial Progressive, 2, Formerly

Fph2, Formerly

Hyperpigmentation With Or Without Hypopigmentation

Familial Progressive Hyper- And Hypopigmentation

Hyperpigmentation, Familial Progressive
Ocular Albinism

Albinism, Ocular

Oa

Xloa

Albinism Ocular
Pseudohypoaldosteronism, Type I, Autosomal Recessive

Autosomal Recessive Pseudohypoaldosteronism Type 1

PHA1B

Pseudohypoaldosteronism Type 1

Pseudohypoaldosteronism, Type I

Generalized Pha1

Generalized Pseudohypoaldosteronism Type 1

Pseudohypoaldosteronism Type 1 Autosomal Recessive

Pha1

Pseudohypoaldosteronism

Pha I, Autosomal Recessive

Autosomal Recessive Pha 1

Pseudohypoaldosteronism Type 1, Recessive

Pseudohypoaldosteronism Type I

Autosomal Recessive Pha1

Pha Type 1

Pseudohypoaldosteronism 1, Autosomal Recessive

Multisystem Pseudohypoaldosteronism

Pha Type I, Autosomal Recessive

Pseudohypoaldosteronism Type I, Autosomal Recessive
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-RS01093 ASIC5 Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Mus musculus ASIC5 MGD MGI:1929259
Bos taurus ASIC5 VGNC VGNC:26213
Rattus norvegicus ASIC5 RGD RGD:69295
Canis familiaris ASIC5 VGNC VGNC:38181
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