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Search references for FOXF1. Phrases containing FOXF1
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Search references for FOXF1. Phrases containing FOXF1
See searches and references containing FOXF1!FOXF1
Protein-coding gene in the species Homo sapiens
Forkhead box protein F1 (FOXF1) is a protein that in humans is encoded by the FOXF1 gene. This gene belongs to the forkhead family of transcription factors
FOXF1
Rare lung disease, present at birth and treatable by lung transplants
transplantation. Most cases of ACD are caused by mutations affecting the gene FOXF1 or its nearby enhancer region. Exactly how these mutations lead to abnormal
Alveolar_capillary_dysplasia
Non-coding RNA in the species Homo sapiens
FOXF1 adjacent non-coding developmental regulatory RNA is a long non-coding RNA that in humans is encoded by the FENDRR gene. This gene produces a spliced
FENDRR
Medical condition
Bamforth–Lazarus syndrome FOXE3 Anterior segment mesenchymal dysgenesis FOXF1 ACD/MPV FOXI1 Enlarged vestibular aqueduct FOXL2 Premature ovarian failure
Pitt–Hopkins_syndrome
Diseases of the space or tissue between the alveoli of the lungs
(mutations in CSFR2A and/or CSFR2B) Alveolar capillary dysplasia (mutations in FoxF1) Mutations in telomerase reverse transcriptase (TERT) Mutations in telomerase
Interstitial_lung_disease
motif from similar protein – High-throughput in vitro [256] BVYTAWRYAAACAD FOXF1 ENSG00000103241 Forkhead Known motif – In vivo/Misc source [257] YRHATAAACAHNB
List of human transcription factors
List_of_human_transcription_factors
Family of transcription factors involved in anatomical development
FOXD4L1, FOXD4L3, FOXD4L4, FOXD4L5, FOXD4L6 FOXE1 (thyroid), FOXE3 (lens) FOXF1 (lung), FOXF2 FOXG1 (brain) FOXH1 (widely expressed) FOXI1 (ear), FOXI2
FOX_proteins
Medical condition
Bamforth–Lazarus syndrome FOXE3 Anterior segment mesenchymal dysgenesis FOXF1 ACD/MPV FOXI1 Enlarged vestibular aqueduct FOXL2 Premature ovarian failure
Tricho-rhino-phalangeal syndrome Type 1
Tricho-rhino-phalangeal_syndrome_Type_1
Medical condition
Bamforth–Lazarus syndrome FOXE3 Anterior segment mesenchymal dysgenesis FOXF1 ACD/MPV FOXI1 Enlarged vestibular aqueduct FOXL2 Premature ovarian failure
Campomelic_dysplasia
Alveolar capillary dysplasia with misalignment of pulmonary veins; 265380; FOXF1 Alveolar soft part sarcoma; 606243; ASPSCR1 Alzheimer disease 1, familial;
List_of_OMIM_disorder_codes
HGNC:31986; Q3SYB3 5803 FOXE1 HGNC:3806; O00358 5804 FOXE3 HGNC:3808; Q13461 5805 FOXF1 HGNC:3809; Q12946 5806 FOXF2 HGNC:3810; Q12947 5807 FOXG1 HGNC:3811; P55316
List of human protein-coding genes 3
List_of_human_protein-coding_genes_3
Protein-coding gene in the species Homo sapiens
processes including recovering and stabilizing stalled replication forks. FoxF1 protein also interacts with the FA protein core and induces its binding
FANCF
FOXF1
FOXF1
FOXF1
FOXF1
Boy/Male
American, Australian, British, English, French, Teutonic
Keeper of the Garden; Gardener; Surname
Surname or Lastname
English
English : variant spelling of Gascoigne.
Boy/Male
Sikh
Of the God in heaven
Girl/Female
Tamil
Ray of light or Sun rays, Silken, Full of light
Boy/Male
Muslim/Islamic
Blessed
Boy/Male
Czechoslovakian
Strong.
Girl/Female
Indian
Dew
Surname or Lastname
English
English : metronymic from Mule 3.English : patronymic from Mule 1 or 2 (the Middle English word being moul until replaced by Old French mule), or a metronymic from Mould.
Girl/Female
French
Blackbird.
Girl/Female
Tamil
Padmamaladhara | பதà¯à®®à®¾à®‚மாஂலாதாராÂ
Wearer of lotus garland
FOXF1
FOXF1
FOXF1
FOXF1
FOXF1