Browse our anti-OFD1 (OFD1) Antibodies

Full name:
anti-Oral-Facial-Digital Syndrome 1 Antibodies (OFD1)
On are 11 Oral-Facial-Digital Syndrome 1 (OFD1) Antibodies from 6 different suppliers available. Additionally we are shipping OFD1 Proteins (3) and many more products for this protein. A total of 15 OFD1 products are currently listed.
71-7A, CXorf5, JBTS10, RGD1562231, RP23, SGBS2
list all antibodies Gene Name GeneID UniProt
OFD1 8481 O75665
OFD1 302661  

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Top referenced anti-OFD1 Antibodies

  1. 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 (PubMed)
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More Antibodies against OFD1 Interaction Partners

Human Oral-Facial-Digital Syndrome 1 (OFD1) interaction partners

  1. The underlying pathogenesis of CHD (show CHDH Antibodies) in OFD1 (and other ciliopathies) probably involves dysfunction of the primary cilia regarding coordination of left-right signalling during early heart development.

  2. 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.

  3. OFD1 regulation and primary cilium formation are defective in autophagy-deficient cells

  4. 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.

  5. Novel OFD1 mutations have been identified in males with orofaciodigital syndromes and ciliary basal body docking impairment.

  6. 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.

  7. Data indicate that although the OFD1 gene apparently escapes X-inactivation, skewed inactivation was observed in seven of 14 patient.

  8. Deep intronic mutation in OFD1 causes a severe form of X-linked retinitis pigmentosa.

  9. Sequence deletion in OFD1 has been identified as the cause of X-linked Joubert syndrome.

  10. 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 Antigen Profile

Antigen Summary

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.

Alternative names and synonyms associated with OFD1

  • oral-facial-digital syndrome 1 (OFD1) antibody
  • oral-facial-digital syndrome 1 (ofd1) antibody
  • oral-facial-digital syndrome 1 (Ofd1) antibody
  • 71-7A antibody
  • CXorf5 antibody
  • JBTS10 antibody
  • RGD1562231 antibody
  • RP23 antibody
  • SGBS2 antibody

Protein level used designations for OFD1

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

100461471 Pongo abelii
100543134 Meleagris gallopavo
100563722 Anolis carolinensis
100591843 Nomascus leucogenys
8481 Homo sapiens
302661 Rattus norvegicus
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