FX4L5 Polyclonal Antibody, 20ul Peptide Library Haploinsufficiency for this protein may

Haploinsufficiency for this protein may contribute to the mental retardation found in haemoglobin H-related mental retardation (ART-16 syndrome)

The WAP-type| follistatin type| Kunitz-type| and NTR-type protease inhibitory domains may control the action of multiple types of proteases

Multiple alternatively spliced transcript variants of this gene

This gene is a member of the ABC1 subfamily and is clustered with four other ABC1 family members on chromosome 17q24

Two other genes have been identified

FX4L5 Polyclonal Antibody, 20ul Peptide Library Haploinsufficiency for this protein maymiscellaneous: 5 FOXD4 like proteins (FOXD4L2, FOXD4L3, FOXD4L4, FOXD4L5 and FOXD4L6) are encoded by a strongly repeated region of the 9q12 chromosome region. They are very similar and it is therefore difficult to provide a clear and unambiguous protein sequence. Our sequences are in agreement with HGNC nomenclature.,Contains 1 fork head DNA binding domain.,