AutismKB 2.0

Annotation Details for SMCR7L


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Basic Information Top
Gene Symbol:SMCR7L ( FLJ20232,HSU79252,dJ1104E15.3 )
Gene Full Name: Smith-Magenis syndrome chromosome region, candidate 7-like
Band: 22q13
Quick LinksEntrez ID:54471; OMIM: NA; Uniprot ID:SMC7L_HUMAN; ENSEMBL ID: ENSG00000100335; HGNC ID:
Relate to Another Database: SFARIGene; denovo-db
Gene Ontology Top
GO ID Evidence Qualifier GO_term References
GO:0005739IDA-mitochondrion23921378
GO:0005741IDA-mitochondrial outer membrane21508961
GO:0005777TASNOTperoxisome23921378
GO:0016021IEA-integral component of membrane-
GO ID Evidence Qualifier GO_term References
GO:0005515IPI-protein binding16189514
GO:0019003IDA-GDP binding24515348
GO:0042802IPI-identical protein binding21701560
GO:0043531IDA-ADP binding24515348
GO ID Evidence Qualifier GO_term References
GO:0000266IMP-mitochondrial fission21701560
GO:0008053IMPNOTmitochondrial fusion23921378
GO:0090141IDA-positive regulation of mitochondrial fission23283981
GO:0090141TAS-positive regulation of mitochondrial fission23921378
GO:0090314IDA-positive regulation of protein targeting to membrane23283981
GO:0090314IDANOTpositive regulation of protein targeting to membrane23921378
Protein-Protein Interaction Top
Gene Symbol Interactant Interaction ID References Description
SMCR7LMAGEA111027416189514 Two-hybrid
SMCR7LMAGEA111997716189514 Two-hybrid
No data
No data
AlzGene, PDGene and SZGene Top
Animal Model Top
  • MGI ID: MGI:2146020
  • Data Attributes: HomoloGene calculated
SELECT * FROM lijr_20110218_zfin_genotype_phenotype WHERE ZFIN_Gene_ID='ZDB-GENE-060810-64'