Description

lamin B1 [Source:HGNC Symbol;Acc:HGNC:6637]

Location

Chromosome 5: 126,776,623-126,837,020 forward strand.

GRCh38:CM000667.2

About this gene

This gene has 8 transcripts (splice variants), 69 orthologues, 10 paralogues, is a member of 1 Ensembl protein family and is associated with 2 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
LMNB1-001ENST000002613662878586aaENSP00000261366
 
Protein coding
CCDS4140P20700 NM_001198557
NM_005573
NP_001185486
NP_005564
TSL:1GENCODE basicAPPRIS P1
LMNB1-003ENST000003953541572387aaENSP00000378761
 
Protein coding
-E9PBF6 -TSL:1GENCODE basic
LMNB1-005ENST00000492190738166aaENSP00000486992
 
Protein coding
---CDS 3' incompleteTSL:3
LMNB1-002ENST000004602653475329aaENSP00000486528
 
Nonsense mediated decay
---TSL:1
LMNB1-009ENST000005047881801No protein-
 
Processed transcript
---TSL:2
LMNB1-004ENST00000472034730No protein-
 
Processed transcript
---TSL:3
LMNB1-006ENST00000463908557No protein-
 
Processed transcript
---TSL:4
LMNB1-007ENST00000494185579No protein-
 
Retained intron
---TSL:2

Gene-based displays