Emx1 | ENSMUSG00000033726 | NCBI 13796

Details for: Emx1

Gene ID: 13796

Symbol: Emx1

Ensembl ID: ENSMUSG00000033726

Description: empty spiracles homeobox 1

Associated with

Brain development
(GO:0007420)
Brain morphogenesis
(GO:0048854)
Central nervous system development
(GO:0007417)
Cerebral cortex development
(GO:0021987)
Cerebral cortex neuron differentiation
(GO:0021895)
Cerebral cortex regionalization
(GO:0021796)
Chromosome
(GO:0005694)
Dna-binding transcription factor activity, rna polymerase ii-specific
(GO:0000981)
Dna binding
(GO:0003677)
Homeostasis of number of cells
(GO:0048872)
In utero embryonic development
(GO:0001701)
Multicellular organism development
(GO:0007275)
Neuroepithelial cell differentiation
(GO:0060563)
Neuron differentiation
(GO:0030182)
Neuron projection extension
(GO:1990138)
Nucleolus
(GO:0005730)
Nucleus
(GO:0005634)
Post-embryonic development
(GO:0009791)
Protein binding
(GO:0005515)
Radial glial cell differentiation
(GO:0060019)
Regulation of dna-templated transcription
(GO:0006355)
Regulation of oligodendrocyte progenitor proliferation
(GO:0070445)
Regulation of transcription by rna polymerase ii
(GO:0006357)
Response to xenobiotic stimulus
(GO:0009410)
Rna polymerase ii cis-regulatory region sequence-specific dna binding
(GO:0000978)
Sequence-specific double-stranded dna binding
(GO:1990837)
Telencephalon development
(GO:0021537)

Other Information

Proteins

Homeobox protein EMX1

Genular Protein ID: 1250616686

Symbol: EMX1_MOUSE

Name: Homeobox protein EMX1

UniProtKB Accession Codes:

Q04742 Q3SXG0

Database IDs:

Citations:

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 1352754

Title: Two vertebrate homeobox genes related to the Drosophila empty spiracles gene are expressed in the embryonic cerebral cortex.

PubMed ID: 1352754

DOI: 10.1002/j.1460-2075.1992.tb05319.x

PubMed ID: 1353865

Title: Nested expression domains of four homeobox genes in developing rostral brain.

PubMed ID: 1353865

DOI: 10.1038/358687a0

PubMed ID: 15147765

Title: Emx1 and Emx2 cooperate in initial phase of archipallium development.

PubMed ID: 15147765

DOI: 10.1016/j.mod.2004.03.013

PubMed ID: 20887964

Title: WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

PubMed ID: 20887964

DOI: 10.1016/j.ajhg.2010.08.018

PubMed ID: 29263200

Title: WDR11-mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome.

PubMed ID: 29263200

DOI: 10.15252/embr.201744632

Sequence Information:

Length: 257
Mass: 28173
Checksum: EC0051BC674430DF
Sequence:

MFQPAAKRGF TIESLVAKDG GTGGSPGSGG AGSHPLAVAA SEEPLRPTAL NYPHPSAAET 
AFVSGFPAAA AAGAGRSLYG GPELVFPEAM NHPALTVHPA HQLGSSSLQP PHSFFSAQHR 
DPLHFYPWVL RNRFFGHRFQ ASDVPQDGLL LHGPFARKPK RIRTAFSPSQ LLRLERAFEK 
NHYVVGAERK QLAGSLSLSE TQVKVWFQNR RTKYKRQKLE EEGPESEQKK KGSHHINRWR 
IATKQANGED IDVTSND

The gene details are incomplete or unavailable at the moment.

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.

Details for: Emx1

Associated with

Other Information

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). PubMed ID: 15489334

Two vertebrate homeobox genes related to the Drosophila empty spiracles gene are expressed in the embryonic cerebral cortex. PubMed ID: 1352754

Nested expression domains of four homeobox genes in developing rostral brain. PubMed ID: 1353865

Emx1 and Emx2 cooperate in initial phase of archipallium development. PubMed ID: 15147765

WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. PubMed ID: 20887964