The TRIM37 gene homepage

General information
Gene symbol TRIM37
Gene name tripartite motif containing 37
Chromosome 17
Chromosomal band q
Imprinted Unknown
Genomic reference NG_009298.1
Transcript reference NM_001005207.2, NM_015294.3
Exon/intron information NM_001005207.2 exon/intron table
Associated with diseases Mulibrey nanism
Citation reference(s) PubMed: Avela et al. 2000, PubMed: Jagiello et al. 2003, PubMed: Hämäläinen et al. 2004, PubMed: Hämäläinen et al. 2006, PubMed: Doğanc et al. 2007
Refseq URL Genomic reference sequence
Curators (1) Kaisa Kettunen
Total number of public variants reported 66
Unique public DNA variants reported 57
Individuals with public variants 6
Hidden variants 14
Download all this gene's data Download all data
Notes The establishment of this gene variant database (LSDB) was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement nº 200754 - the GEN2PHEN project.
Date created August 28, 2012
Date last updated February 08, 2021
Version TRIM37:210208

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_001005207.2.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
External URL Finnish Disease Database (Findis)
HGNC 7523
Entrez Gene 4591
PubMed articles TRIM37
OMIM - Gene 605073
OMIM - Diseases Mulibrey nanism (Mulibrey nanism (muscle-liver-brain-eye dwarfism))
GeneCards TRIM37
GeneTests TRIM37
Orphanet TRIM37

Active transcripts




NCBI ID     

NCBI Protein ID     

00000271 17 transcript variant 1 NM_015294.3 NP_056109.1 65
00000273 17 transcript variant 2 NM_001005207.2 NP_001005207.1 45

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