The related to receptor tyrosine kinase (RYK)
gene encodes the
protein Ryk.
The protein encoded by this gene is an atypical member of the family of growth factor receptor protein tyrosine kinases, differing from other members at a number of conserved residues in the activation and nucleotide binding domains. This gene product belongs to a subfamily whose members do not appear to be regulated by phosphorylation in the activation segment. It has been suggested that mediation of biological activity by recruitment of a signaling-competent auxiliary protein may occur through an as yet uncharacterized mechanism. Two alternative splice variants have been identified, encoding distinct isoforms.[5]
History
The gene
encoding mouse RYK was first identified in 1992.[6]
Subsequently,
cDNAencoding the RYK protein have been isolated from the following species.[7]
Gough NM, Rakar S, Hovens CM, Wilks A (1995). "Localization of two mouse genes encoding the protein tyrosine kinase receptor-related protein RYK". Mamm. Genome. 6 (4): 255–6.
doi:
10.1007/BF00352411.
PMID7613029.
S2CID2577241.
Lee ST, Strunk KM, Spritz RA (1993). "A survey of protein tyrosine kinase mRNAs expressed in normal human melanocytes". Oncogene. 8 (12): 3403–3410.
PMID8247543.
Stacker SA, Hovens CM, Vitali A, et al. (1993). "Molecular cloning and chromosomal localisation of the human homologue of a receptor related to tyrosine kinases (RYK)". Oncogene. 8 (5): 1347–1356.
PMID8386829.
Tamagnone L, Partanen J, Armstrong E, et al. (1993). "The human ryk cDNA sequence predicts a protein containing two putative transmembrane segments and a tyrosine kinase catalytic domain". Oncogene. 8 (7): 2009–2014.
PMID8390040.
Watanabe A, Akita S, Tin NT, et al. (2006). "A mutation in RYK is a genetic factor for nonsyndromic cleft lip and palate". Cleft Palate Craniofac. J. 43 (3): 310–6.
doi:
10.1597/04-145.1.
PMID16681403.
S2CID23152169.
The related to receptor tyrosine kinase (RYK)
gene encodes the
protein Ryk.
The protein encoded by this gene is an atypical member of the family of growth factor receptor protein tyrosine kinases, differing from other members at a number of conserved residues in the activation and nucleotide binding domains. This gene product belongs to a subfamily whose members do not appear to be regulated by phosphorylation in the activation segment. It has been suggested that mediation of biological activity by recruitment of a signaling-competent auxiliary protein may occur through an as yet uncharacterized mechanism. Two alternative splice variants have been identified, encoding distinct isoforms.[5]
History
The gene
encoding mouse RYK was first identified in 1992.[6]
Subsequently,
cDNAencoding the RYK protein have been isolated from the following species.[7]
Gough NM, Rakar S, Hovens CM, Wilks A (1995). "Localization of two mouse genes encoding the protein tyrosine kinase receptor-related protein RYK". Mamm. Genome. 6 (4): 255–6.
doi:
10.1007/BF00352411.
PMID7613029.
S2CID2577241.
Lee ST, Strunk KM, Spritz RA (1993). "A survey of protein tyrosine kinase mRNAs expressed in normal human melanocytes". Oncogene. 8 (12): 3403–3410.
PMID8247543.
Stacker SA, Hovens CM, Vitali A, et al. (1993). "Molecular cloning and chromosomal localisation of the human homologue of a receptor related to tyrosine kinases (RYK)". Oncogene. 8 (5): 1347–1356.
PMID8386829.
Tamagnone L, Partanen J, Armstrong E, et al. (1993). "The human ryk cDNA sequence predicts a protein containing two putative transmembrane segments and a tyrosine kinase catalytic domain". Oncogene. 8 (7): 2009–2014.
PMID8390040.
Watanabe A, Akita S, Tin NT, et al. (2006). "A mutation in RYK is a genetic factor for nonsyndromic cleft lip and palate". Cleft Palate Craniofac. J. 43 (3): 310–6.
doi:
10.1597/04-145.1.
PMID16681403.
S2CID23152169.