1. Gene
  2. ARGFX - arginine-fifty homeobox Gene

ARGFX - arginine-fifty homeobox Gene

中文名称:精氨酸 50 同源框

种属: Homo sapiens

基因 ID: 503582 | 基因类型: protein coding

关于 ARGFX

Cytogenetic location: 3q13.33 Genomic coordinates (GRCh38): 3:121,567,949-121,590,622 (from NCBI)

This gene has 2 transcripts (splice variants), 25 orthologues and 50 paralogues. Low expression observed in reference dataset.

功能概要

同源框基因编码 DNA 结合蛋白,其中许多被认为与早期胚胎发育有关。同源框基因编码 60 至 63 个氨基酸的 DNA 结合域,称为同源域。该基因是 ARGFX 同源盒基因家族的成员。[RefSeq 提供,2008 年 7 月]

Homeobox genes encode DNA-binding proteins, many of which are thought to be involved in early embryonic development. Homeobox genes encode a DNA-binding domain of 60 to 63 Amino acids referred to as the homeodomain. This gene is a member of the ARGFX homeobox gene family. [provided by RefSeq, Jul 2008]

ARGFX 基因产物(1)

mRNA Protein Name
NM_001012659.2 NP_001012677.1 arginine-fifty homeobox
基因本体论
  • 分子功能
分子功能 GO 注释 逻辑证据 参考文献 来源
enables sequence-specific double-stranded DNA binding IDA
IDA: 通过直接分析推断
28473536 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

ARGFX 蛋白结构

Homeobox

Homeobox: Homeobox domain (80 - 135)

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

arginine-fifty homeobox

关联疾病

疾病名称 别名
Senior-Loken Syndrome 1

Senior-Loken Syndrome

Renal Dysplasia And Retinal Aplasia

Renal-Retinal Syndrome

Loken-Senior Syndrome

Juvenile Nephronophthisis With Leber Amaurosis

SLSN1

Senior-Loken Syndrome-1

Loken Senior Syndrome

Senior Loken Syndrome

Renal Dysplasia Retinal Aplasia

Nephronophthisis With Retinal Dystrophy

Renal Dysplasia-Retinal Aplasia Syndrome

Slsn

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