PLXND1 - plexin D1 Gene
Also Known as PLEXD1
生物種: Homo sapiens
About PLXND1
This gene has 17 transcripts (splice variants), 191 orthologues, 8 paralogues and is associated with 4 phenotypes. Broad expression in placenta (RPKM 37.7), fat (RPKM 32.1) and 23 other tissues.
Summary
Enables protein domain specific binding activity. Predicted to be involved in several processes, including endothelial cell migration; nervous system development; and regulation of angiogenesis. Predicted to act upstream of or within several processes, including circulatory system development; dichotomous subdivision of terminal units involved in salivary gland branching; and positive regulation of protein binding activity. Located in lamellipodium. [provided by Alliance of Genome Resources, Apr 2022]
PLXND1 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_015103.3 | NP_055918.3 | plexin-D1 precursor |
| Molecular Function GO Annotation | Evidence | 参考文献 | 由来 |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
17318185 | GOA |
| enables protein domain specific binding |
IPI
IPI: Inferred from physical interaction
|
24841563 | GOA |
| Cellular Component GO Annotation | Evidence | 参考文献 | 由来 |
|---|---|---|---|
| located in lamellipodium |
IDA
IDA: Inferred from direct assay
|
24841563 | GOA |
PLXND1 Protein Structure
Sema: Sema domain (63 - 155)
Sema: Sema domain (279 - 521)
PSI: Plexin repeat (549 - 601)
PSI: Plexin repeat (702 - 753)
TIG: IPT/TIG domain (891 - 976)
TIG: IPT/TIG domain (981 - 1063)
TIG: IPT/TIG domain (1069 - 1143)
Plexin_cytopl: Plexin cytoplasmic RasGAP domain (1344 - 1888)
- 0
- 300
- 600
- 900
- 1200
- 1500
- 1800
- 1925 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
plexin-D1 |
|
PLXND1 Protein-protein interaction Information
|
Type
|
タンパク質名 | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | 参考文献 |
|---|---|---|---|---|---|---|---|
|
Intra
|
PLXND1 | Q9Y4D7 | NR4A1 | Homo sapiens | P22736 | 24139859 | |
|
Intra
|
PLXND1 | Q9Y4D7 | NR4A1 | Homo sapiens | P22736 | 24139859 | |
|
Cross
|
PLXND1 | Q9Y4D7 | Sema3e | Mus musculus | P70275 | 24139859 | |
|
Cross
|
PLXND1 | Q9Y4D7 | Sema3e | Mus musculus | P70275 | 24139859 |
関連疾患
| Diseases | Alias | |
|---|---|---|
| Moebius Syndrome |
|
|
| Conotruncal Heart Malformations |
|
|
| Carey-Fineman-Ziter Syndrome 1 |
|
|
| Spinocerebellar Ataxia 44 |
|
|
| Spondylocostal Dysostosis 1, Autosomal Recessive |
|
|
| Congenital Fibrosis Of The Extraocular Muscles |
|
|
| Kallmann Syndrome |
|
|
Orthologs Information
| 生物種 | Symbol | 由来 | ID |
|---|---|---|---|
| Rattus norvegicus | PLXND1 | RGD | RGD:1310796 |
| Macaca mulatta | PLXND1 | VGNC | VGNC:76191 |
| Bos taurus | PLXND1 | VGNC | VGNC:33065 |
| Canis familiaris | PLXND1 | VGNC | VGNC:44726 |
| Mus musculus | PLXND1 | MGD | MGI:2154244 |
| Felis catus | PLXND1 | VGNC | VGNC:80659 |
| Others | PLXND1 | NCBI |