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Search references for FOXE3. Phrases containing FOXE3
See searches and references containing FOXE3!FOXE3
Protein-coding gene in the species Homo sapiens
box protein E3 (FOXE3) also known as forkhead-related transcription factor 8 (FREAC-8) is a protein that in humans is encoded by the FOXE3 gene located on
FOXE3
Codon that marks the end of a protein-coding sequence
PMID 12050213. Doucette, L.; et al. (2011). "A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis
Stop_codon
Medical condition
FOXC2 Lymphedema–distichiasis syndrome FOXE1 Bamforth–Lazarus syndrome FOXE3 Anterior segment mesenchymal dysgenesis FOXF1 ACD/MPV FOXI1 Enlarged vestibular
Pitt–Hopkins_syndrome
ENSG00000178919 Forkhead Known motif – High-throughput in vitro [255] BVYTAWRYAAACAD FOXE3 ENSG00000186790 Forkhead Inferred motif from similar protein – High-throughput
List of human transcription factors
List_of_human_transcription_factors
SCN11A dominant Familial thoracic aortic aneurysm and aortic dissection FOXE3, SMAD2, LOX, MAT2A, ELN, HEY2, TGFB3, TGFBR1, TGFBR2, FBN1, ACTA2, MYLK
List_of_genetic_disorders
Family of transcription factors involved in anatomical development
(vitiligo), FOXD4, FOXD4L1, FOXD4L3, FOXD4L4, FOXD4L5, FOXD4L6 FOXE1 (thyroid), FOXE3 (lens) FOXF1 (lung), FOXF2 FOXG1 (brain) FOXH1 (widely expressed) FOXI1
FOX_proteins
Medical condition
FOXC2 Lymphedema–distichiasis syndrome FOXE1 Bamforth–Lazarus syndrome FOXE3 Anterior segment mesenchymal dysgenesis FOXF1 ACD/MPV FOXI1 Enlarged vestibular
Tricho-rhino-phalangeal syndrome Type 1
Tricho-rhino-phalangeal_syndrome_Type_1
Medical condition
disorder is caused by mutations in one or more of the following genes: FOXE3 (located on 1p33) SMAD2 (located on 18q21.1) LOX (located on 5q23.3-31.2)
Familial thoracic aortic aneurysm and aortic dissection
Familial_thoracic_aortic_aneurysm_and_aortic_dissection
Medical condition
FOXC2 Lymphedema–distichiasis syndrome FOXE1 Bamforth–Lazarus syndrome FOXE3 Anterior segment mesenchymal dysgenesis FOXF1 ACD/MPV FOXI1 Enlarged vestibular
Campomelic_dysplasia
congenita; 206800; RSPO4 Anterior segment mesenchymal dysgenesis; 107250; FOXE3 Anterior segment mesenchymal dysgenesis; 107250; PITX3 Antithrombin III
List_of_OMIM_disorder_codes
Q5VV16 5802 FOXD4L6 HGNC:31986; Q3SYB3 5803 FOXE1 HGNC:3806; O00358 5804 FOXE3 HGNC:3808; Q13461 5805 FOXF1 HGNC:3809; Q12946 5806 FOXF2 HGNC:3810; Q12947
List of human protein-coding genes 3
List_of_human_protein-coding_genes_3
FOXE3
FOXE3
FOXE3
FOXE3
Male
French
French form of Latin Aristides, ARISTIDE means "best physique."
Surname or Lastname
English
English : variant of Terry.Scottish : probably a habitational name from Torry near Aberdeen.
Female
French
Medieval French form of Latin Agatha, AGACE means "good."
Female
Hindi/Indian
Hindi name RITSIKA means "tradition."
Girl/Female
Arabic, Muslim
Truthful; Righteous
Biblical
flowing (inhabitants)
Girl/Female
Indian
Morning Sun Ray's
Girl/Female
Arabic, Australian, French, Muslim
Tranquility; Devout; Allah-inspired Peace of Mind
Male
Hebrew
(יַחְלְ×ֵל) Hebrew name YACHLEEL means "God waits" or "whom God has made sick." In the bible, this is the name of a member of the tribe of Zebulun. The English form is Jahleel.
Girl/Female
Hindu, Indian
Victory
FOXE3
FOXE3
FOXE3
FOXE3
FOXE3