(Q21498386)

Homeobox domain, protein family

1 reference

based on heuristic

inferred from protein domain or family

Homeobox domain, metazoa, protein family

1 reference

based on heuristic

inferred from protein domain or family

Homeobox, conserved site, protein family

1 reference

based on heuristic

inferred from protein domain or family

1 reference

25 May 2022

1 reference

25 May 2022

2 references

sequence-specific DNA binding

1 reference

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

1 reference

14 February 2019

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

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

3 references

27 March 2018

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

http://www.ebi.ac.uk/QuickGO/annotations?protein=Q04742&geneProductId=UniProtKB:Q04742

27 March 2018

http://www.ebi.ac.uk/QuickGO/annotations?protein=Q04742&geneProductId=UniProtKB:Q04742

27 March 2018

Ensembl genome database project

http://www.ebi.ac.uk/QuickGO/annotations?protein=Q04742&geneProductId=UniProtKB:Q04742

2 references

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

14 February 2019

Ensembl genome database project

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

4 references

14 February 2019

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

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

14 February 2019

Ensembl genome database project

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

14 February 2019

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

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

radial glial cell differentiation

IDA

biological process

1 reference

14 February 2019

Proliferative defects and formation of a double cortex in mice lacking Mltt4 and Cdh2 in the dorsal telencephalon

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

multicellular organism development

1 reference

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

cerebral cortex neuron differentiation

IEA

1 reference

14 February 2019

Microcephaly gene links trithorax and REST/NRSF to control neural stem cell proliferation and differentiation

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

regulation of oligodendrocyte progenitor proliferation

1 reference

14 February 2019

Proliferative defects and formation of a double cortex in mice lacking Mltt4 and Cdh2 in the dorsal telencephalon

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

telencephalon development

1 reference

14 February 2019

Proliferative defects and formation of a double cortex in mice lacking Mltt4 and Cdh2 in the dorsal telencephalon

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

2 references

14 February 2019

Emx1 and Emx2 cooperate to regulate cortical size, lamination, neuronal differentiation, development of cortical efferents, and thalamocortical pathfinding

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

14 February 2019

Absence of Cajal-Retzius cells and subplate neurons associated with defects of tangential cell migration from ganglionic eminence in Emx1/2 double mutant cerebral cortex

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

in utero embryonic development

IMP

1 reference

14 February 2019

Loss of Usp9x disrupts cortical architecture, hippocampal development and TGFβ-mediated axonogenesis

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

regulation of transcription, DNA-templated

1 reference

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

post-embryonic development

IEA

1 reference

14 February 2019

The Rho-GTPase cdc42 regulates neural progenitor fate at the apical surface

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

homeostasis of number of cells

IMP

1 reference

14 February 2019

Proliferative defects and formation of a double cortex in mice lacking Mltt4 and Cdh2 in the dorsal telencephalon

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

cerebral cortex regionalization

1 reference

14 February 2019

Emx1 and Emx2 cooperate in initial phase of archipallium development

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

Emx1 and Emx2 cooperate to regulate cortical size, lamination, neuronal differentiation, development of cortical efferents, and thalamocortical pathfinding

neuron differentiation

1 reference

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

neuron projection extension

IMP

1 reference

14 February 2019

Loss of Usp9x disrupts cortical architecture, hippocampal development and TGFβ-mediated axonogenesis

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

neuroepithelial cell differentiation

1 reference

14 February 2019

Proliferative defects and formation of a double cortex in mice lacking Mltt4 and Cdh2 in the dorsal telencephalon

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

cerebral cortex development

3 references

14 February 2019

The Rho-GTPase cdc42 regulates neural progenitor fate at the apical surface

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

14 February 2019

Emx1, emx2 and pax6 in specification, regionalization and arealization of the cerebral cortex

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

14 February 2019

Proliferative defects and formation of a double cortex in mice lacking Mltt4 and Cdh2 in the dorsal telencephalon

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q04742

1 reference

Homeobox, conserved site

1 reference

stated in

Homeobox domain, metazoa

1 reference

stated in