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SEMA6D
Expand for information on SEMA6D
SEMA6D
Description
semaphorin 6D
Aliases
Gene Identifiers
mRNA Identifiers
RefSeq (mRNA)
NM_001198999.2; NM_001358351.3; NM_001358352.2; NM_020858.2; NM_024966.3; NM_153616.2; NM_153617.2; NM_153618.2; NM_153619.1; XM_005254685.4; XM_005254689.4; XM_011522075.2; XM_011522076.2; XM_011522077.2; XM_011522078.2; XM_011522079.2; XM_011522080.2; XM_011522081.2; XM_017022617.2; XM_017022618.2; XM_017022619.2; XM_017022620.1; XM_017022621.1; XM_024450073.1; XM_024450074.1; XM_024450075.1; XM_024450076.1
Protein Identifiers
RefSeq (protein)
NP_001185928.1; NP_001345280.1; NP_001345281.1; NP_065909.1; NP_079242.2; NP_705869.1; NP_705870.1; NP_705871.1; NP_705872.1; XP_005254742.1; XP_005254746.1; XP_011520377.1; XP_011520378.1; XP_011520379.1; XP_011520380.1; XP_011520381.1; XP_011520382.1; XP_011520383.1; XP_016878106.1; XP_016878107.1; XP_016878108.1; XP_016878109.1; XP_016878110.1; XP_024305841.1; XP_024305842.1; XP_024305843.1; XP_024305844.1
Uniprot ID
Ensembl protein ID
Protein Architecture
SMART
Disease Mapping
Druggability
- Candidate cancer driver
- Damaged in 77/7921 TCGA samples
- Damaged in 122/1291 cell lines
- Fewer loss of function mutations
- Equal damaging SNVs/indels
- Fewer structural variants