anti-Family with Sequence Similarity 58, Member B 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.

Type
  • 1
    Primary
Antigen
  • 1
Reactivity
  • 1
Application
  • 1
  • 1
  • 1
Host
  • 1
Clonality
  • 1
Format
  • 1
1 Product
ReactivityHuman
Application ELISA, IHC, WB
Order details Cat. No. ABIN4889081
$525.06
Plus shipping costs $45.00
Delivery in 6 to 7 Business Days
  • <
  • 1
  • >

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 B (Fam58b) antibody
  • 1810009O10Rik antibody
  • Fam58a antibody
  • RGD1305651 antibody

Protein level used designations for FAM58B

cyclin M , cyclin-related protein FAM58A , cyclin-related protein FAM58B

GENE ID SPECIES
69109 Mus musculus
303321 Rattus norvegicus