2. Gene
  3. EPYC - epiphycan Gene

EPYC - epiphycan Gene

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

中文名称：附生素

种属: Homo sapiens

同用名: PGLB; DSPG3; Pg-Lb; SLRR3B

基因 ID: 1833 | 基因类型: protein coding

关于 EPYC

Cytogenetic location: 12q21.33 Genomic coordinates (GRCh38): 12:90,963,682-91,004,972 (from NCBI)

This gene has 3 transcripts (splice variants), 203 orthologues and 10 paralogues. Biased expression in placenta (RPKM 4.1), endometrium (RPKM 0.8) and 1 other tissue.

功能概要

硫酸皮肤素蛋白多糖 3 是富含亮氨酸的小重复蛋白多糖家族的成员。该基因由七个外显子组成。它通过与胶原原纤维和其他细胞外基质蛋白相互作用来调节原纤维形成。[RefSeq 提供，2008 年 7 月]

Dermatan sulfate proteoglycan 3 is a member of the small leucine-rich repeat proteoglycan family. This gene is composed of seven exons. It regulates fibrillogenesis by interacting with collagen fibrils and other extracellular matrix proteins. [provided by RefSeq, Jul 2008]

EPYC 基因产物(1)

mRNA Protein Name
NM_004950.5 NP_004941.2 epiphycan precursor

EPYC 蛋白结构

LRRNT

LRRNT: Leucine rich repeat N-terminal domain (121 - 142)

LRR_8

LRR_8: Leucine rich repeat (152 - 203)

LRR_6

LRR_6: Leucine Rich repeat (211 - 229)

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

epiphycan

dermatan sulfate proteoglycan 3

重组 EPYC 蛋白

目录号 产品名 蛋白编号 纯度
HY-P76323 DSPG3/Epiphycan Protein, Human (HEK293, His) Q99645 (A20-V322) ≥95%

关联疾病

疾病名称 别名
Corneal Dystrophy, Posterior Amorphous

Posterior Amorphous Corneal Dystrophy

PACD

Chromosome 12q21.33 Deletion Syndrome

Posterior Amorphous Stromal Dystrophy
Cornea Plana

Flat Cornea
Breast Apocrine Carcinoma

Apocrine Carcinoma Of Breast

Apocrine Breast Carcinoma
Stromal Dystrophy
Myopia

Near-Sightedness

Short-Sightedness

Nearsightedness

Nearsighted

Near Vision

Close Sighted

Myopic

Short-Sighted

Near Sighted
Corneal Dystrophy, Congenital Stromal

Congenital Stromal Corneal Dystrophy

CSCD

Congenital Hereditary Stromal Dystrophy

Congenital Hereditary Stromal Dystrophy Of The Cornea

Congenital Stromal Dystrophy Of The Cornea

Dacs

Decorin-Associated Congenital Stromal Corneal Dystrophy

Dystrophia Corneae Parenchymatosa Congenita

Witschel Dystrophy

Dystrophy, Corneal, Stromal, Congenital
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-RS04460 EPYC 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 EPYC RGD RGD:1305904
Canis familiaris EPYC VGNC VGNC:40431
Bos taurus EPYC VGNC VGNC:28558
Felis catus EPYC VGNC VGNC:61924
Mus musculus EPYC MGD MGI:107942
Macaca mulatta EPYC VGNC VGNC:72145
Others EPYC NCBI
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