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Medical condition
syndrome (MKS) is an autosomal recessive lethal malformation. Two MKS genes, MKS1 and MKS3, have been associated with the disorder. A study done recently has
Meckel–Gruber_syndrome
Protein-coding gene in the species Homo sapiens
Meckel syndrome, type 1 also known as MKS1 is a protein that in humans is encoded by the MKS1 gene. The MKS1 protein along with meckelin are part of the
MKS1
Group of autosomal recessive genetic disorders that affect Finns much more frequently
had been reported almost exclusively in Finland. Meckel syndrome type 1 (MKS1), a lethal condition, is known in 48 Finnish families. The European Organization
Finnish_heritage_disease
Theft of a vehicle for pleasure or thrill
Austin/MG/Rover Maestro (1983–1994) Austin/MG/Rover Montego (1984–1994) Ford Fiesta Mks1, 2 and 3 (1976–1995) The lack of security in older cars compared to modern
Joyride_(crime)
Genetic disease resulting in abnormal formation or function of cilia
PMID 16275743. Kyttälä M (May 2006). "Identification of the Meckel Syndrome Gene (MKS1) Exposes a Novel Ciliopathy" (PDF). National Public Health Institute. Archived
Ciliopathy
Ciliopathic recessive genetic disorder
BBS5, BBS7, TTC8/BBS8, BBS10, TRIM32/BBS11 BBS12, CCDC28B, CEP290, TMEM67, MKS1, MKKS chaperone: BBS6[citation needed] The diagnosis of BBS is established
Bardet–Biedl_syndrome
Autosomal recessive genetic disorder
Decker E, Mayr JA, Lunzer V, Koch J, Boltshauser E, et al. (August 2016). "MKS1 mutations cause Joubert syndrome with agenesis of the corpus callosum". European
Joubert_syndrome
Abnormal closure or absence of the vagina
BBS5, MKKS (BBS6), BBS7, TTC8 (BBS8), BBS9, BBS10, TRIM32 (BBS11), BBS12, MKS1 (BBS13), CEP290 (BBS14), WDPCP (BBS15), SDCCAG8 (BBS16), LZTFL1 (BBS17),
Vaginal_atresia
Organelle in eukaryotic cells
Lemley, Bethan; Pazour, Gregory J.; Lo, Cecilia W. (2011). "Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental
Centriole
Protein-coding gene in the species Homo sapiens
PMID 17160906. Khaddour R, Smith U, Baala L, et al. (2007). "Spectrum of MKS1 and MKS3 mutations in Meckel syndrome: a genotype-phenotype correlation.
TMEM67
Protein structure at the base of cilia or flagella
; Kohlschmidt, N.; Paavola-Sakki, P.; Peltonen, L.; Kestilä, M. (2006). "MKS1, encoding a component of the flagellar apparatus basal body proteome, is
Basal_body
Developmental disorder involving the eye
lethal microphthalmia FREM1 AR Manitoba oculotrichoanal syndrome (MOTA) MKS1, TMEM216, TMEM67, CEP290, RPGRIP1L AR Meckel–Gruber syndrome types 1-5 unknown
Syndromic_microphthalmia
signaling. Substrates of MPK4 are three proteins: WRKY33, WRKY25, and MKS1. Ternary MKS1-MPK4-WRKY33 complexes have been recognized by nuclear extracts. Recruitment
MAPK_networks
Q9H000 9613 MKRN2OS HGNC:40375; H3BPM6 9614 MKRN3 HGNC:7114; Q13064 9615 MKS1 HGNC:7121; Q9NXB0 9616 MKX HGNC:23729; Q8IYA7 9617 MLANA HGNC:7124; Q16655
List of human protein-coding genes 5
List_of_human_protein-coding_genes_5
Bardet–Biedl syndrome 12; 209900; BBS12 Bardet–Biedl syndrome 13; 209900; MKS1 Bardet–Biedl syndrome 14; 209900; CEP290 Bardet–Biedl syndrome 15; 209900;
List_of_OMIM_disorder_codes
MKS1
MKS1
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Surname or Lastname
English (of Norman origin)
English (of Norman origin) : habitational name from places in Eure and Seine-Maritime, France, called Cailly, from a Romano-Gallic personal name Callius + the locative suffix -acum.English : habitational name from a minor place called Caley in the parish of Winwick, Lancashire, named with Old English cÄ â€˜jackdaw’ + lÄ“ah ‘woodland clearing’.Irish : reduced and altered form of McCauley.Manx : variant of Callow.
Girl/Female
Indian
Goddess
Boy/Male
Hindu
Free, From france
Boy/Male
Hindu, Indian, Punjabi, Sikh, Traditional
Victorious; Famous; Rich
Boy/Male
Indian, Tamil
Success Forever; Victory Everywhere
Male
English
Anglicized form of Hebrew Yehowash, JEHOASH means "given by the Lord" or "whom Jehovah gave." In the bible, this is the name of a son of king Ahaziah and a son of king Jehoahaz.
Boy/Male
Muslim
Servant of the best-owner
Boy/Male
Tamil
Pranto | பà¯à®°à®¾à®‚தோ
Biblical
a valley; deepness
Boy/Male
Tamil
Ghananand | கநாநஂத
Happy like cloud
MKS1
MKS1
MKS1
MKS1
MKS1