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Query results
Results for
PLXNB2
Expand for information on PLXNB2
PLXNB2
Description
plexin B2
Aliases
MM1, Nbla00445, PLEXB2, dJ402G11.3
Gene Identifiers
mRNA Identifiers
RefSeq (mRNA)
NM_001376864.1; NM_001376865.1; NM_001376866.1; NM_001376867.1; NM_001376868.1; NM_001376869.1; NM_001376870.1; NM_001376871.1; NM_001376872.1; NM_001376873.1; NM_001376874.1; NM_001376875.1; NM_001376876.1; NM_001376877.1; NM_001376878.1; NM_001376879.1; NM_001376880.1; NM_001376881.1; NM_001376882.1; NM_001376883.1; NM_001376884.1; NM_001376885.1; NM_001376886.1; NM_012401.4; XM_011530682.2
Protein Identifiers
RefSeq (protein)
NP_001363793.1; NP_001363794.1; NP_001363795.1; NP_001363796.1; NP_001363797.1; NP_001363798.1; NP_001363799.1; NP_001363800.1; NP_001363801.1; NP_001363802.1; NP_001363803.1; NP_001363804.1; NP_001363805.1; NP_001363806.1; NP_001363807.1; NP_001363808.1; NP_001363809.1; NP_001363810.1; NP_001363811.1; NP_001363812.1; NP_001363813.1; NP_001363814.1; NP_001363815.1; NP_036533.2; XP_011528984.1
Uniprot ID
Ensembl protein ID
Protein Architecture
SMART
Disease Mapping
Druggability
- Candidate cancer driver, healthy and TIME driver
- Damaged in 127/7921 TCGA samples
- Damaged in 47/1291 cell lines
- Fewer loss of function mutations
- Equal damaging SNVs/indels
- Fewer structural variants