Mus musculus Protein: Alx4
Summary
InnateDB Protein IDBP-192633.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Alx4
Protein Name aristaless-like homeobox 4
Synonyms lst;
Species Mus musculus
Ensembl Protein ENSMUSP00000047962
InnateDB Gene IDBG-192631 (Alx4)
Protein Structure
UniProt Annotation
Function Transcription factor involved in skull and limb development.
Subcellular Localization Nucleus.
Disease Associations Note=Defects in Alx4 are the cause of Strong luxoid (lst) phenotype. At heterozygosity lst is characterized by preaxial abnormalities of the hindfeet and, very rarely, of the forefeet. Homozygotes show preaxial polydactyly of all four limbs, reductions and duplications of the radius, absence of the tibia, craniofacial defects, reduction of the pubis, and dorsal alopecia.
Tissue Specificity Expressed in osteoblasts. Not expressed in brain, heart, intestine, kidney, liver, muscle, spleen and testis.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 35 experimentally validated interaction(s) in this database.
They are also associated with 9 interaction(s) predicted by orthology.
Experimentally validated
Total 35 [view]
Protein-Protein 34 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 9 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0003700 sequence-specific DNA binding transcription factor activity
GO:0005515 protein binding
GO:0043565 sequence-specific DNA binding
GO:0046982 protein heterodimerization activity
GO:0071837 HMG box domain binding
Biological Process
GO:0001942 hair follicle development
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0006357 regulation of transcription from RNA polymerase II promoter
GO:0007389 pattern specification process
GO:0007517 muscle organ development
GO:0009791 post-embryonic development
GO:0009952 anterior/posterior pattern specification
GO:0035108 limb morphogenesis
GO:0035115 embryonic forelimb morphogenesis
GO:0035116 embryonic hindlimb morphogenesis
GO:0042733 embryonic digit morphogenesis
GO:0042981 regulation of apoptotic process
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:0048565 digestive tract development
GO:0048704 embryonic skeletal system morphogenesis
GO:0048705 skeletal system morphogenesis
GO:0060021 palate development
Cellular Component
GO:0005634 nucleus
GO:0005667 transcription factor complex
Protein Structure and Domains
PDB ID MGI:108359
InterPro IPR001356 Homeobox domain
IPR003654 OAR domain
IPR009057 Homeodomain-like
PFAM PF00046
PF03826
PRINTS
PIRSF
SMART SM00389
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt O35137
PhosphoSite PhosphoSite-
TrEMBL
UniProt Splice Variant
Entrez Gene 11695
UniGene Mm.389389
RefSeq NP_031468
MGI ID
MGI Symbol Alx4
OMIM
CCDS CCDS16455
HPRD
IMGT
EMBL AF001465
GenPept AAC39943