From Wikipedia, the free encyclopedia
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 .
[5]
The MKS1 protein along with
meckelin are part of the
flagellar apparatus basal body proteome and are required for
cilium formation.
[6]
Mutations in the MKS1 are associated with
Meckel syndrome
[5]
[7] or
Bardet–Biedl syndrome .
[8]
^
a
b
c
GRCh38: Ensembl release 89: ENSG00000011143 –
Ensembl , May 2017
^
a
b
c
GRCm38: Ensembl release 89: ENSMUSG00000034121 –
Ensembl , May 2017
^
"Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^
"Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^
a
b Kyttälä M, Tallila J, Salonen R, Kopra O, Kohlschmidt N, Paavola-Sakki P, Peltonen L, Kestilä M (February 2006). "MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome". Nat. Genet . 38 (2): 155–7.
doi :
10.1038/ng1714 .
PMID
16415886 .
S2CID
10676530 .
^ Dawe HR, Smith UM, Cullinane AR, Gerrelli D, Cox P, Badano JL, Blair-Reid S, Sriram N, Katsanis N, Attie-Bitach T, Afford SC, Copp AJ, Kelly DA, Gull K, Johnson CA (January 2007).
"The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation" . Hum. Mol. Genet . 16 (2): 173–86.
doi :
10.1093/hmg/ddl459 .
PMID
17185389 .
^ Consugar MB, Kubly VJ, Lager DJ, Hommerding CJ, Wong WC, Bakker E, Gattone VH, Torres VE, Breuning MH, Harris PC (June 2007). "Molecular diagnostics of Meckel-Gruber syndrome highlights phenotypic differences between MKS1 and MKS3". Hum. Genet . 121 (5): 591–9.
doi :
10.1007/s00439-007-0341-3 .
PMID
17377820 .
S2CID
11815792 .
^ Leitch CC, Zaghloul NA, Davis EE, Stoetzel C, Diaz-Font A, Rix S, Alfadhel M, Al-Fadhel M, Lewis RA, Eyaid W, Banin E, Dollfus H, Beales PL, Badano JL, Katsanis N (April 2008). "Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome". Nat. Genet . 40 (4): 443–8.
doi :
10.1038/ng.97 .
PMID
18327255 .
S2CID
5282929 .
Stelzl U, Worm U, Lalowski M, et al. (2005). "A human protein-protein interaction network: a resource for annotating the proteome". Cell . 122 (6): 957–68.
doi :
10.1016/j.cell.2005.08.029 .
hdl :
11858/00-001M-0000-0010-8592-0 .
PMID
16169070 .
S2CID
8235923 .
Bialas NJ, Inglis PN, Li C, et al. (2009).
"Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins" . J. Cell Sci . 122 (Pt 5): 611–24.
doi :
10.1242/jcs.028621 .
PMC
2720918 .
PMID
19208769 .
Tammachote R, Hommerding CJ, Sinders RM, et al. (2009).
"Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3" . Hum. Mol. Genet . 18 (17): 3311–23.
doi :
10.1093/hmg/ddp272 .
PMC
2733821 .
PMID
19515853 .
Gerhard DS, Wagner L, Feingold EA, et al. (2004).
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)" . Genome Res . 14 (10B): 2121–7.
doi :
10.1101/gr.2596504 .
PMC
528928 .
PMID
15489334 .
Ota T, Suzuki Y, Nishikawa T, et al. (2004).
"Complete sequencing and characterization of 21,243 full-length human cDNAs" . Nat. Genet . 36 (1): 40–5.
doi :
10.1038/ng1285 .
PMID
14702039 .
Khaddour R, Smith U, Baala L, et al. (2007).
"Spectrum of MKS1 and MKS3 mutations in Meckel syndrome: a genotype-phenotype correlation. Mutation in brief #960. Online" . Hum. Mutat . 28 (5): 523–4.
doi :
10.1002/humu.9489 .
PMID
17397051 .
S2CID
6528744 .
Paavola P, Salonen R, Weissenbach J, Peltonen L (1995). "The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24". Nat. Genet . 11 (2): 213–5.
doi :
10.1038/ng1095-213 .
PMID
7550354 .
S2CID
20167521 .
Auber B, Burfeind P, Herold S, et al. (2007).
"A disease causing deletion of 29 base pairs in intron 15 in the MKS1 gene is highly associated with the campomelic variant of the Meckel-Gruber syndrome" . Clin. Genet . 72 (5): 454–9.
doi :
10.1111/j.1399-0004.2007.00880.x .
PMID
17935508 .
S2CID
22385403 .
Strausberg RL, Feingold EA, Grouse LH, et al. (2002).
"Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences" . Proc. Natl. Acad. Sci. U.S.A . 99 (26): 16899–903.
Bibcode :
2002PNAS...9916899M .
doi :
10.1073/pnas.242603899 .
PMC
139241 .
PMID
12477932 .
Frank V, Ortiz Brüchle N, Mager S, et al. (2007).
"Aberrant splicing is a common mutational mechanism in MKS1, a key player in Meckel-Gruber syndrome" . Hum. Mutat . 28 (6): 638–9.
doi :
10.1002/humu.9496 .
PMID
17437276 .
S2CID
27589823 .