Homo sapiens Protein: KIRREL3
Summary
InnateDB Protein IDBP-585329.2
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol KIRREL3
Protein Name kin of IRRE like 3 (Drosophila)
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000435466
InnateDB Gene IDBG-75885 (KIRREL3)
Protein Structure
UniProt Annotation
Function Could be involved in the hematopoietic supportive capacity of stroma cells. {ECO:0000250}.
Subcellular Localization Cell membrane {ECO:0000269PubMed:19012874}; Single-pass type I membrane protein {ECO:0000269PubMed:19012874}.
Disease Associations Note=A chromosomal aberration involving KIRREL3 and CDH15 is found in a patient with severe mental retardation and dysmorphic facial features. Translocation t(11;16)(q24.2;q24).Mental retardation, autosomal dominant 4 (MRD4) [MIM:612581]: A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. {ECO:0000269PubMed:19012874}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Expressed in fetal and adult brain. Also expressed in kidney, specifically in podocytes of kidney glomeruli. {ECO:0000269PubMed:12424224, ECO:0000269PubMed:19012874}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
GO:0030097 hemopoiesis
Cellular Component
GO:0005576 extracellular region
GO:0005886 plasma membrane
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID
InterPro IPR003598 Immunoglobulin subtype 2
IPR003599 Immunoglobulin subtype
IPR007110 Immunoglobulin-like domain
IPR013098 Immunoglobulin I-set
IPR013151 Immunoglobulin
IPR013162 CD80-like, immunoglobulin C2-set
PFAM PF07679
PF00047
PF08205
PRINTS
PIRSF
SMART SM00408
SM00409
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8IZU9
PhosphoSite PhosphoSite-Q8IZU9
TrEMBL B4DT91
UniProt Splice Variant
Entrez Gene 84623
UniGene Hs.376015
RefSeq NP_115920
HUGO HGNC:23204
OMIM 607761
CCDS CCDS53723
HPRD 09679
IMGT
EMBL AB058770 AF480410 AK300108 AP000741 AP000806 AP001783 AP002832 AP002833 AY358743 AY358760 BC101775 BC101801 CH471065
GenPept AAI01776 AAI01802 AAN73042 AAQ89103 AAQ89120 BAB47496 BAG61903 EAW67698 EAW67699