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  2. GDPD1 - glycerophosphodiester phosphodiesterase domain containing 1 Gene

GDPD1 - glycerophosphodiester phosphodiesterase domain containing 1 Gene

中文名称:含甘油磷酸二酯磷酸二酯酶结构域 1

种属: Homo sapiens

同用名: GDE4

基因 ID: 284161 | 基因类型: protein coding

关于 GDPD1

Cytogenetic location: 17q22 Genomic coordinates (GRCh38): 17:59,220,511-59,275,970 (from NCBI)

This gene has 7 transcripts (splice variants), 198 orthologues and 5 paralogues. Broad expression in brain (RPKM 4.9), testis (RPKM 3.0) and 22 other tissues.

功能概要

该基因编码甘油磷酸二酯磷酸二酯酶家族的一个成员,该酶催化脱酰甘油磷脂水解为磷酸甘油和醇。编码的蛋白质定位于细胞质并集中在核周区域附近。可变剪接导致多个转录本变体。[RefSeq 提供,2009 年 10 月]

This gene encodes a member of the glycerophosphodiester phosphodiesterase family of Enzymes that catalyze the hydrolysis of deacylated glycerophospholipids to glycerol phosphate and alcohol. The encoded protein is localized to the cytoplasm and concentrates near the perinuclear region. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]

GDPD1 基因产物(3)

mRNA Protein Name
NM_001165993.2 NP_001159465.1 lysophospholipase D GDPD1 isoform 3
NM_001165994.2 NP_001159466.1 lysophospholipase D GDPD1 isoform 2
NM_182569.4 NP_872375.2 lysophospholipase D GDPD1 isoform 1

GDPD1 蛋白结构

GDPD

GDPD: Glycerophosphoryl diester phosphodiesterase family (45 - 176)

  • 0
  • 100
  • 200
  • 314 a.a.
蛋白主名 其他名称

lysophospholipase D GDPD1

glycerophosphodiester phosphodiesterase 4

关联疾病

疾病名称 别名
Retinitis Pigmentosa 17

RP17

Retinitis Pigmentosa-17

Retinitis Pigmentosa, Type 17

Branchiooculofacial Syndrome

Branchio-Oculo-Facial Syndrome

BOFS

Bof Syndrome

Hemangiomatous Branchial Clefts-Lip Pseudocleft Syndrome

Lip Pseudocleft-Hemangiomatous Branchial Cyst Syndrome

Branchial Clefts With Characteristic Facies, Growth Retardation, Imperforate Nasolacrimal Duct, And Premature Aging

Branchial Clefts With Characteristic Facies Growth Retardation Imperforate Nasolacrimal Duct And Premature Aging

Bofs Syndrome

Lip Pseudocleft-Hemagiomatous Branchial Cyst Syndrome

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

直系同源

种属 基因名 来源 基因 ID
Canis familiaris GDPD1 VGNC VGNC:49766
Felis catus GDPD1 VGNC VGNC:99062
Bos taurus GDPD1 VGNC VGNC:29310
Macaca mulatta GDPD1 VGNC VGNC:99154
Mus musculus GDPD1 MGD MGI:1913819
Rattus norvegicus GDPD1 RGD RGD:1311813