Human (GRCh38.p14)
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), 187 orthologues, 68 paralogues and is associated with 5 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000261366.10LMNB1-2012890586aaENSP00000261366.5
 
Protein coding
CCDS4140P20700 NM_005573.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000395354.1LMNB1-2021572387aaENSP00000378761.1
 
Protein coding
E9PBF6 -GENCODE basicTSL:1
ENST00000492190.5LMNB1-206738166aaENSP00000486992.1
 
Protein coding
A0A0D9SFY5 -TSL:3CDS 3' incomplete
ENST00000460265.5LMNB1-2033475329aaENSP00000486528.1
 
Nonsense mediated decay
A0A0D9SFE5 -TSL:1
ENST00000504788.5LMNB1-2081801No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000472034.5LMNB1-205730No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000463908.2LMNB1-204557No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000494185.1LMNB1-207579No protein-
 
Retained intron
--TSL:2