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OFD1 is located on the X chromosome and encodes a centrosomal protein. Additionally we are shipping OFD1 Proteins (3) and many more products for this protein.
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Human Polyclonal OFD1 Primary Antibody for ICC, IF - ABIN4341360
Jerman, Ward, Lee, Lopes, Fry, MacDougall, Wandinger-Ness: OFD1 and flotillins are integral components of a ciliary signaling protein complex organized by polycystins in renal epithelia and odontoblasts. in PLoS ONE 2014
Show all 2 references for ABIN4341360
polycystins are necessary for assembly of a novel flotillin (show FLOT2 Antibodies)-containing ciliary signaling complex and provide a molecular rationale for the common renal pathologies caused by OFD1 and polycystin mutations.
OFD1 regulation and primary cilium formation are defective in autophagy-deficient cells
loss of BBS1 (show BBS1 Antibodies), BBS4 (show BBS4 Antibodies), or OFD1 led to decreased NF-kappaB (show NFKB1 Antibodies) activity and concomitant IkappaBbeta (show NFKBIB Antibodies) accumulation and that these defects were ameliorated with SFN (show SFN Antibodies) treatment.
Novel OFD1 mutations have been identified in males with orofaciodigital syndromes and ciliary basal body docking impairment.
Identification of a causative splicing mutation in OFD1, through exome sequencing, in a family with three males having an 'unclassified' X-linked lethal congenital malformation syndrome.
Data indicate that although the OFD1 gene apparently escapes X-inactivation, skewed inactivation was observed in seven of 14 patient.
Deep intronic mutation in OFD1 causes a severe form of X-linked retinitis pigmentosa.
Sequence deletion in OFD1 has been identified as the cause of X-linked Joubert syndrome.
A single-base deletion in exon 16 of OFD1 (c.2183delG) leading to a frameshift was detected in proband, her mother, and her sister. All 3 women had similar oral phenotype; new mutation might be involved in development of OFD1 oral manifestations.
Ofd1 acts at the distal centriole to build distal appendages, recruit Ift88 (show IFT88 Antibodies), and stabilize centriolar microtubules at a defined length.
This gene is located on the X chromosome and encodes a centrosomal protein. A knockout mouse model has been used to study the effect of mutations in this gene. The mouse gene is also located on the X chromosome, however, unlike the human gene it is not subject to X inactivation. Mutations in this gene are associated with oral-facial-digital syndrome type I and Simpson-Golabi-Behmel syndrome type 2. Many pseudogenes have been identified\; a single pseudogene is found on chromosome 5 while as many as fifteen have been found on the Y chromosome. Alternatively spliced transcripts have been described for this gene but the biological validity of these transcripts has not been determined.
oral-facial-digital syndrome 1
, oral-facial-digital syndrome 1 protein-like
, oral-facial-digital syndrome 1 protein
, protein 71-7A
, retinitis pigmentosa 23 (X-linked recessive)
, oral-facial-digital syndrome 1 gene homolog