BICRA - BRD4 interacting chromatin remodeling complex associated protein Gene

Also Known as CSS12; GLTSCR1; SMARCK1

生物種: Homo sapiens

遺伝子タイプ: protein coding
遺伝子ID: 29998

About BICRA

Cytogenetic location: 19q13.33 Genomic coordinates (GRCh38): 19:47,608,196-47,703,277 (from NCBI)

This gene has 4 transcripts (splice variants), 183 orthologues, 1 paralogue and is associated with 2 phenotypes. Ubiquitous expression in spleen (RPKM 1.9), prostate (RPKM 1.7) and 25 other tissues.

Summary

Enables transcription regulator activator activity. Involved in positive regulation of transcription, DNA-templated. Located in nucleus. Part of SWI/SNF complex. Implicated in Coffin-Siris syndrome. [provided by Alliance of Genome Resources, Apr 2022]

BICRA Products (2)

mRNA Protein Name
NM_001394372.1 NP_001381301.1 BRD4-interacting chromatin-remodeling complex-associated protein
NM_015711.3 NP_056526.3 BRD4-interacting chromatin-remodeling complex-associated protein

BICRA Protein Structure

GLTSCR1

GLTSCR1: Conserved region of unknown function on GLTSCR protein (1084 - 1188)

  • 0
  • 300
  • 600
  • 900
  • 1200
  • 1560 a.a.
Protein Preferred Names Protein Names

BRD4-interacting chromatin-remodeling complex-associated protein

  • BRD4 interacting chromatin remodelling complex associated protein

BICRA 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
BICRA Q9NZM4 NCK1 Homo sapiens P16333 17474147
Intra
BICRA Q9NZM4 CRK Homo sapiens P46108 17474147
Cross: Cross-species interaction Intra: Intraspecies interaction

BICRA 抗体

製品番号 製品名 アプリケーション 反応性
HY-P810026 GLTSCR1 Antibody (YA9370) WB, ICC/IF, IF-Tissue, IP, ELISA human, mouse, rat

関連疾患

Diseases Alias
Coffin-Siris Syndrome 12
  • CSS12

Neuroma
Coffin-Siris Syndrome 1
  • Coffin-Siris Syndrome

  • Fifth Digit Syndrome

  • Css

  • CSS1

  • Mrd12

  • Mental Retardation, Autosomal Dominant 12

  • Hhid

  • Dwarfism-Onychodysplasia

  • Hypertrichosis, Hyperkeratosis, Mental Retardation, And Distinctive Facial Features

  • Autosomal Dominant Mental Retardation 12

  • Short Stature-Onychodysplasia.

  • Intellectual Disability With Absent Fifth Fingernail And Terminal Phalanx

  • Mental Retardation With Hypoplastic Fifth Fingernails And Toenails

  • Short Stature-Onychodysplasia

  • Coffin-Siris Syndrome, Type 1

  • Mental Retardation, Autosomal Dominant, Type 12

Hypertrichosis
Clark-Baraitser Syndrome
  • CLABARS

  • Baraitser Syndrome

  • Autosomal Dominant Intellectual Disability 49

  • Mental Retardation, Autosomal Dominant 49, Formerly

  • Mrd49, Formerly

  • Intellectual Developmental Disorder, Autosomal Dominant 49

  • Autosomal Dominant Mental Retardation 49

  • Intellectual Disability, Tall Stature, Obesity, Macrocephaly And Typical Facial Features

  • Mrd49

  • Progeria Short Stature Pigmented Nevi

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
Canis familiaris BICRA VGNC VGNC:38454
Felis catus BICRA VGNC VGNC:82434
Mus musculus BICRA MGD MGI:2154263
Bos taurus BICRA VGNC VGNC:26494
Macaca mulatta BICRA VGNC VGNC:70466
Rattus norvegicus BICRA RGD RGD:1306385
Others BICRA NCBI