Human (GRCh37.p13)
Description

LEM domain containing 3 [Source:HGNC Symbol;Acc:28887]

Gene Synonyms

MAN1

Location

Chromosome 12: 65,563,351-65,642,107 forward strand.

GRCh37:CM000674.1

About this gene

This gene has 6 transcripts (splice variants), 1 paralogue and is associated with 8 phenotypes.

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000308330.2LEMD3-0014764911aa
 
Protein coding
CCDS8972B4DI45 Q9Y2U8 NM_014319.4Ensembl CanonicalGENCODE Basic
ENST00000541171.1LEMD3-002856No protein
 
Processed transcript
---
ENST00000539442.1LEMD3-005932No protein
 
Retained intron
---
ENST00000542032.1LEMD3-003645No protein
 
Retained intron
---
ENST00000545026.1LEMD3-004619No protein
 
Retained intron
---
ENST00000544506.1LEMD3-006412No protein
 
Retained intron
---
Name

LEMD3 (HGNC Symbol)

UniProtKB

This gene has proteins that correspond to the following UniProtKB identifiers: Q9Y2U8

CCDS

This gene is a member of the Human CCDS set: CCDS8972.1

Ensembl version

ENSG00000174106.2

Other assemblies

This gene maps to 65,169,571-65,248,327 in GRCh38 coordinates.

Gene type

Protein coding

Annotation method

Annotation for this gene includes both automatic annotation from Ensembl and Havana manual curation, see article.

Alternative genes

This gene corresponds to the following database identifiers:

Havana gene:
OTTHUMG00000168840 (version 2)

Basic Gene Annotations from GENCODE 19

The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

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Basic Gene Annotations from GENCODE 19

The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

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Contigs

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