ceh-10 homeo domain containing homolog (C. elegans), isoform CRA_a [Ra - Protein

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Absence of chx10 causes neural progenitors to persist in the adult retina. [Invest Ophthalmol Vis Sci. 2006]
Absence of chx10 causes neural progenitors to persist in the adult retina.
Dhomen NS, Balaggan KS, Pearson RA, Bainbridge JW, Levine EM, Ali RR, Sowden JC. Invest Ophthalmol Vis Sci. 2006 Jan; 47(1):386-96.
Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. [Nat Genet. 2000]
Human microphthalmia associated with mutations in the retinal homeobox gene CHX10.
Ferda Percin E, Ploder LA, Yu JJ, Arici K, Horsford DJ, Rutherford A, Bapat B, Cox DW, Duncan AM, Kalnins VI, et al. Nat Genet. 2000 Aug; 25(4):397-401.
Chx10 is required to block photoreceptor differentiation but is dispensable for progenitor proliferation in the postnatal retina. [Proc Natl Acad Sci U S A. 2006]
Chx10 is required to block photoreceptor differentiation but is dispensable for progenitor proliferation in the postnatal retina.
Livne-Bar I, Pacal M, Cheung MC, Hankin M, Trogadis J, Chen D, Dorval KM, Bremner R. Proc Natl Acad Sci U S A. 2006 Mar 28; 103(13):4988-93. Epub 2006 Mar 17.

RefSeq protein isoforms
See 2 reference sequence protein isoforms for the Vsx2 gene.

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Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
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reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome

ceh-10 homeo domain containing homolog (C. elegans), isoform CRA_a [Rattus norve...
ceh-10 homeo domain containing homolog (C. elegans), isoform CRA_a [Rattus norvegicus]
gi|149025150|gb|EDL81517.1||gnl|WGS |rCP14662

Protein
PREDICTED: Piliocolobus tephrosceles alpha 1,3-galactosyltransferase 2 (A3GALT2)...
PREDICTED: Piliocolobus tephrosceles alpha 1,3-galactosyltransferase 2 (A3GALT2), mRNA
gi|1482605561|ref|XM_026457187.1|

Nucleotide
Mus musculus Casitas B-lineage lymphoma c, mRNA (cDNA clone MGC:117886 IMAGE:535...
Mus musculus Casitas B-lineage lymphoma c, mRNA (cDNA clone MGC:117886 IMAGE:5353413), complete cds
gi|84040242|gb|BC111037.1|

Nucleotide
Ullrich congenital muscular dystrophy 2
Ullrich congenital muscular dystrophy 2

MedGen
Charcot-Marie-Tooth disease dominant intermediate D
Charcot-Marie-Tooth disease dominant intermediate D

MedGen

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Protein