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Protein-coding gene in the species Homo sapiens
Growth differentiation factor 6 (GDF6) is a protein that in humans is encoded by the GDF6 gene. GDF6 belongs to the transforming growth factor beta superfamily
GDF6
Congenital condition characterised by fusion of two or more vertebrae in the neck
GDF6 and GDF3 provide the body with instructions for making proteins involved in regulating the growth and maturation of bone and cartilage. GDF6 specifically
Klippel–Feil_syndrome
survival of neurones that respond to a neurotransmitter called dopamine. GDF6 interacts with bone morphogenetic proteins to regulate ectoderm patterning
Growth_differentiation_factor
Birth defect of the eye
DHX38 DPYD ERCC1 ERCC5 FADD FAM111A FNBP4 FOXL2 FRAS1 FREM1 FREM2 FZD5 GDF3 GDF6 GJA1 GRIP1 HCCS HMGB3 HMX1 IGBP1 KAT6B KMT2D LRP2 MAB21L2 MAF MFRP NAA10
Microphthalmia
Developmental disorder involving the eye
22 unknown AR Kapur–Toriello syndrome KMT2D AD Kabuki syndrome KDM6A XLD GDF6 AD Klippel–Feil syndrome types 1, 3 GDF3 XLD unknown XLD Macrosomia with
Syndromic_microphthalmia
Protein family
BMP4; BMP5; BMP6; BMP7; BMP8A; BMP8B; BMP10; BMP15; GDF1; GDF2; GDF3; GDF5; GDF6; GDF7; GDF9; GDF10; GDF11; GDF15; GDNF; INHA; INHBA; INHBB; INHBC; INHBE;
Transforming growth factor beta superfamily
Transforming_growth_factor_beta_superfamily
Rare inherited eye disease
eye:[citation needed] OTX2 is involved in the development of the retina; CRB1, CRX, GDF6, and PRPH2 in the formation of retinal photoreceptor cells; AIPL1 and GUCY2D
Leber_congenital_amaurosis
Human chromosome
protein 1 GDAP1: ganglioside-induced differentiation-associated protein 1 GDF6: growth differentiation factor 6 GLI4: encoding protein Gli family zinc finger
Chromosome_8
Signaling pathway involving transforming growth factor beta proteins
which can form disulfide bridges. It is believed that DAN antagonizes GDF5, GDF6 and GDF7. Follistatin inhibits Activin, which it binds. It directly affects
TGF_beta_signaling_pathway
Medical condition
syndrome. The genes GDF6, GDF3, MEOX1 used as examples, encode for making proteins that help with development. For example GDF6 gene plays an important
Cervicocranial_syndrome
Medical condition
pathogenesis of this condition appears to be due to over expression of two genes: GDF6 and SDC2. These genes are located on the long arm of chromosome 8(8q22.1)
Leri_pleonosteosis
Bone morphogenetic protein receptor
differing roles they play in osteogenesis. Agonists: BMP2, BMP4, BMP6, BMP7, GDF6 Antagonists: Noggin, Chordin BMPR1A, SMAD4 and PTEN are responsible for juvenile
BMPR1A
HGNC:4217; Q9UK05 6153 GDF3 HGNC:4218; Q9NR23 6154 GDF5 HGNC:4220; P43026 6155 GDF6 HGNC:4221; Q6KF10 6156 GDF7 HGNC:4222; Q7Z4P5 6157 GDF9 HGNC:4224; O60383
List of human protein-coding genes 3
List_of_human_protein-coding_genes_3
syndrome; 610253; EHMT1 Klippel–Feil syndrome, autosomal dominant; 118100; GDF6 Kniest dysplasia; 156550; COL2A1 Knobloch syndrome, type 1; 267750; COL18A1
List_of_OMIM_disorder_codes
GDF6
GDF6
GDF6
GDF6
Girl/Female
Indian, Sikh
Gods Beloved
Male
Finnish
Finnish form of Greek Ioannes (Latin Johannes), JONI means "God is gracious."
Girl/Female
Scottish
From the Gaelic 'dubhglas' meaning dark water, dark stream, or from the dark river.
Boy/Male
American, Australian, British, Christian, English, Jamaican, Scottish
From Scotland; A Gael; Diminutive of Scott; A Scotsman
Girl/Female
Hebrew
Strong as an oak.
Girl/Female
Hindu
Contentment, Complete satisfaction
Boy/Male
Arabic, Muslim
Ways; Pieces; Parts
Girl/Female
French, German, Indian, Telugu
Brightness
Girl/Female
Indian, Tamil
River in India
Surname or Lastname
English (Wiltshire and Gloucestershire)
English (Wiltshire and Gloucestershire) : nickname for someone thought to resemble a bird, from Old French oisel ‘bird’.
GDF6
GDF6
GDF6
GDF6
GDF6