LRRC37B (leucine rich repeat containing 37B)

2014-08-01  

Identity

HGNC
LOCATION
17q11.2
LOCUSID
ALIAS
LRRC37
FUSION GENES

Other Information

Locus ID:

NCBI: 114659
MIM: 616558
HGNC: 29070
Ensembl: ENSG00000185158

Variants:

dbSNP: 114659
ClinVar: 114659
TCGA: ENSG00000185158
COSMIC: LRRC37B

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000185158ENST00000327564J3QSU1
ENSG00000185158ENST00000341671Q96QE4
ENSG00000185158ENST00000394713Q96QE4
ENSG00000185158ENST00000543378F5H5K1
ENSG00000185158ENST00000578674J3QLI7
ENSG00000185158ENST00000579206J3QL10
ENSG00000185158ENST00000582117J3QKM3
ENSG00000185158ENST00000583342J3QLE7
ENSG00000185158ENST00000584368J3KTP0

Expression (GTEx)

0
5
10
15
20
25
30

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
381348742023LRRC37B is a human modifier of voltage-gated sodium channels and axon excitability in cortical neurons.2
381348742023LRRC37B is a human modifier of voltage-gated sodium channels and axon excitability in cortical neurons.2
192917642009RNF135 mutations are not present in patients with Sotos syndrome-like features.4
192917642009RNF135 mutations are not present in patients with Sotos syndrome-like features.4

Citation

Dessen P

LRRC37B (leucine rich repeat containing 37B)

Atlas Genet Cytogenet Oncol Haematol. 2014-08-01

Online version: http://atlasgeneticsoncology.org/gene/54431/css/lib/favicon/js/web-card-_common.js