AIPL1 Products

Antibodies
Lysates
AIPL1 Overexpression Lysate
AIPL1 Overexpression Lysate
NBL1-07416
Species: Hu
Applications: WB
Proteins
Recombinant Human AIPL1 GST ( ...
Recombinant Human AIPL1 GST (N-Ter...
H00023746-Q01
Species: Hu
Applications: WB, ELISA, PA, PAGE, AP
Recombinant Human AIPL1 GST ( ...
Recombinant Human AIPL1 GST (N-Ter...
H00023746-P01
Species: Hu
Applications: WB, ELISA, PA, AP
AIPL1 Recombinant Protein Ant ...
AIPL1 Recombinant Protein Antigen
NBP2-55506PEP
Species: Hu
Applications: AC

Description

Leber congenital amaurosis (LCA) accounts for at least 5% of all inherited retinal disease and is the most severe inherited retinopathy with the earliest age of onset. Individuals affected with LCA are diagnosed at birth or in the first few months of life with severely impaired vision or blindness, nystagmus and an abnormal or flat electroretinogram. The photoreceptor/pineal -expressed gene, AIPL1, encoding aryl-hydrocarbon interacting protein-like 1, was mapped within the LCA4 candidate region. The protein contains three tetratricopeptide motifs, consistent with nuclear transport or chaperone activity. AIPL1 mutations may cause approximately 20% of recessive LCA. [provided by RefSeq]

Bioinformatics

Entrez Human
Uniprot Human
Human
Human
Human
Human
Product By Gene ID 23746
Alternate Names
  • aryl-hydrocarbon-interacting protein-like 1
  • AIPL2
  • aryl hydrocarbon receptor-interacting protein-like 1
  • LCA4
  • aryl hydrocarbon receptor interacting protein-like 1

Research Areas for AIPL1

Find related products by research area and learn more about each of the different research areas below.

Vision

PTMs for AIPL1

Learn more about PTMs related to AIPL1.

Farnesylation
Phosphorylation
Prenylation

Bioinformatics Tool for AIPL1

Discover related pathways, diseases and genes to AIPL1. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.
 
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