1. Gene
  2. Alx1 - ALX homeobox 1 Gene

Alx1 - ALX homeobox 1 Gene

Rattus norvegicus

Also known as Cart1; CART1X

Gene ID: 25401 | Gene type: protein coding

About Alx1

Summary

Enables DNA-binding transcription factor activity and protein homodimerization activity. Involved in negative regulation of transcription, DNA-templated and positive regulation of transcription, DNA-templated. Located in nucleus. Orthologous to human ALX1 (ALX homeobox 1). [provided by Alliance of Genome Resources, Apr 2022]

Alx1 Products(1)

mRNA Protein Name
NM_012921.1 NP_037053.1 ALX homeobox protein 1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
NOT enables DNA binding IMP
IMP: Inferred from mutant phenotype
12390248 RGD
enables DNA-binding transcription factor activity IDA
IDA: Inferred from direct assay
12390248 RGD
enables DNA-binding transcription factor activity IMP
IMP: Inferred from mutant phenotype
12929931 RGD
enables protein homodimerization activity IDA
IDA: Inferred from direct assay
12390248 RGD
Biological Process GO Annotation Evidence Reference Source
involved in negative regulation of DNA-templated transcription IMP
IMP: Inferred from mutant phenotype
12390248 RGD
involved in positive regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
12929931 RGD
involved in positive regulation of DNA-templated transcription IMP
IMP: Inferred from mutant phenotype
12390248 RGD
Cellular Component GO Annotation Evidence Reference Source
located in nucleus IDA
IDA: Inferred from direct assay
12390248 RGD
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
Protein Preferred Names Protein Names

ALX homeobox protein 1

CART-1

cartilage homeo protein 1

cartilage homeoprotein 1

Orthologs Information

Species Symbol Source ID
Homo sapiens Alx1 NCBI NCBI:8092