1. Gene
  2. VGLL1 - vestigial like family member 1 Gene

VGLL1 - vestigial like family member 1 Gene

中文名称:遗迹样家族成员 1

种属: Homo sapiens

同用名: TDU; VGL1

基因 ID: 51442 | 基因类型: protein coding

关于 VGLL1

Cytogenetic location: Xq26.3 Genomic coordinates (GRCh38): X:136,532,215-136,556,799 (from NCBI)

This gene has 4 transcripts (splice variants), 104 orthologues and 2 paralogues. Restricted expression toward placenta (RPKM 103.1).

功能概要

由该基因编码的蛋白质通过在其 N 末端发现的 Vg (残留) 同源区域结合转录因子 (TEF) 的 TEA 域家族的蛋白质。因此,它可以作为哺乳动物 TEF 的特异性共激活剂。[RefSeq 提供,2009 年 9 月]

The protein encoded by this gene binds proteins of the TEA domain family of transcription factors (TEFs) through the Vg (vestigial) homology region found in its N-terminus. It may thus function as a specific coactivator for the mammalian TEFs. [provided by RefSeq, Sep 2009]

VGLL1 基因产物(1)

mRNA Protein Name
NM_016267.4 NP_057351.1 transcription cofactor vestigial-like protein 1
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 protein binding IPI
IPI: 通过物理相互作用推断
20211142 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

VGLL1 蛋白结构

Vg_Tdu

Vg_Tdu: Vestigial/Tondu family (21 - 52)

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

transcription cofactor vestigial-like protein 1

TONDU

VGLL1 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
VGLL1 Q99990 TEAD3 Homo sapiens Q99594
Y2H Prey Pooling
32296183
种属内
VGLL1 Q99990 TEAD3 Homo sapiens Q99594
Y2H Array
32296183
种属内
VGLL1 Q99990 AIRIM Homo sapiens Q9NX04
Validated Y2H
32296183
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
46,Xy Sex Reversal 8

SRXY8

Male Pseudohermaphroditism Due To Deficiency Of Testicular 17,20-Desmolase

Tdd

46,Xy Disorder Of Sex Development Due To Testicular 17,20-Desmolase Deficiency

46xy Sex Reversal 8

46xy Sex Reversal 8, Modifier Of

Male Pseudohermaphroditism: Deficiency Of Testicular 17,20-Desmolase

Sveinsson Chorioretinal Atrophy

SCRA

Atrophia Areata

Helicoid Peripapillary Chorioretinal Degeneration

Hpcd

Aa

Peripapillary Chorioretinal Degeneration, Icelandic Type

Helicoidal Peripapillary Chorioretinal Degeneration

Atrophy, Chorioretinal, Sveinsson

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
Bos taurus VGLL1 VGNC VGNC:56958
Felis catus VGLL1 VGNC VGNC:82514
Mus musculus VGLL1 MGD MGI:2655768
Canis familiaris VGLL1 VGNC VGNC:48257
Rattus norvegicus VGLL1 RGD RGD:1564038