anti-Family with Sequence Similarity 58, Member B (FAM58B) Antibodies

Mutations in FAM58B have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations.

list all antibodies Gene Name GeneID UniProt
FAM58B 92002 Q8N1B3
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Catalog No. Reactivity Host Conjugate Application Quantity Supplier Delivery Price Details
Human Rabbit Un-conjugated ELISA, IHC, WB 100 μg Log in to see 6 to 7 Days
$485.80
Details

FAM58B Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality
Human


More Antibodies against Family with Sequence Similarity 58, Member B Interaction Partners

Human Family with Sequence Similarity 58, Member B (FAM58B) interaction partners

  1. this is the first occurrence of a nonsense variant in FAM58A described in individuals with STAR syndrome and the phenotype in this pedigree suggests that tethered cord and hearing loss are features of STAR syndrome.

  2. Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations.

Family with Sequence Similarity 58, Member B (FAM58B) Antigen Profile

Protein Summary

Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

Gene names and symbols associated with FAM58B

  • family with sequence similarity 58, member A (FAM58A) antibody
  • STAR antibody

Protein level used designations for FAM58B

cyclin M , cyclin-related protein FAM58A

GENE ID SPECIES
92002 Homo sapiens
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