ACTL7A - actin like 7A Gene
Also Known as SPGF86
Species: Homo sapiens (human)
Summary
The protein encoded by this gene is a member of a family of actin-related proteins (ARPs) which share significant amino acid sequence identity to conventional actins. Both actins and ARPs have an actin fold, which is an ATP-binding cleft, as a common feature. The ARPs are involved in diverse cellular processes, including vesicular transport, spindle orientation, nuclear migration and chromatin remodeling. This gene (ACTL7A), and related gene, ACTL7B, are intronless, and are located approximately 4 kb apart in a head-to-head orientation within the familial dysautonomia candidate region on 9q31. Based on mutational analysis of the ACTL7A gene in patients with this disorder, it was concluded that it is unlikely to be involved in the pathogenesis of dysautonomia. The ACTL7A gene is expressed in a wide variety of adult tissues, however, its exact function is not known. [provided by RefSeq, Jul 2008]
ACTL7A Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_006687.4 | NP_006678.1 | actin-like protein 7A |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
21278383 | GOA |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| located in acrosomal vesicle |
IDA
IDA: Inferred from direct assay
|
32923619 | GOA |
| located in acrosomal vesicle |
IMP
IMP: Inferred from mutant phenotype
|
34727571 | GOA |
| part of protein-containing complex |
IDA
IDA: Inferred from direct assay
|
21278383 | GOA |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
actin-like protein 7A |
|