VGLL1 - vestigial like family member 1 Gene

Also Known as TDU; VGL1

生物種: Homo sapiens

遺伝子タイプ: protein coding
遺伝子ID: 51442

About 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).

Summary

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 Products (1)

mRNA Protein Name
NM_016267.4 NP_057351.1 transcription cofactor vestigial-like protein 1
Molecular Function GO Annotation Evidence 参考文献 由来
enables protein binding IPI
IPI: Inferred from physical interaction
20211142 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

VGLL1 Protein Structure

Vg_Tdu

Vg_Tdu: Vestigial/Tondu family (21 - 52)

  • 0
  • 100
  • 200
  • 258 a.a.
Protein Preferred Names Protein Names

transcription cofactor vestigial-like protein 1

  • TONDU

VGLL1 Protein-protein interaction Information

Type
タンパク質名 Protein ID Interactor Interactor Species Interactor ID Detection Method 参考文献
Intra
VGLL1 Q99990 TEAD3 Homo sapiens Q99594 32296183
Intra
VGLL1 Q99990 TEAD3 Homo sapiens Q99594 32296183
Intra
VGLL1 Q99990 AIRIM Homo sapiens Q9NX04 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

VGLL1 抗体

製品番号 製品名 アプリケーション 反応性
HY-P89740 Vgl-1 Antibody (YA9084) WB, IP, ELISA human

関連疾患

Diseases Alias
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

Diseases Alias
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

Orthologs Information

生物種 Symbol 由来 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
Others VGLL1 NCBI