Gene Gene information from NCBI Gene database.
Entrez ID 84063
Gene name Kirre like nephrin family adhesion molecule 2
Gene symbol KIRREL2
Synonyms (NCBI Gene)
FILTRINNEPH3NLG1
Chromosome 19
Chromosome location 19q13.12
Summary This gene encodes a type I transmembrane protein and member of the immunoglobulin superfamily of cell adhesion molecules. The encoded protein localizes to adherens junctions in pancreatic beta cells and regulates insulin secretion. Autoantibodies against
miRNA miRNA information provided by mirtarbase database.
25
miRTarBase ID miRNA Experiments Reference
MIRT023144 hsa-miR-124-3p Microarray 18668037
MIRT1095275 hsa-miR-4477a CLIP-seq
MIRT1095276 hsa-miR-4795-3p CLIP-seq
MIRT1095277 hsa-miR-4803 CLIP-seq
MIRT2558208 hsa-miR-1238 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 32296183
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane ISS
GO:0005886 Component Plasma membrane TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607762 18816 ENSG00000126259
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6UWL6
Protein name Kin of IRRE-like protein 2 (Kin of irregular chiasm-like protein 2) (Nephrin-like protein 3)
Protein function May regulate basal insulin secretion.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07679 I-set 24 121 Immunoglobulin I-set domain Domain
PF08205 C2-set_2 126 214 CD80-like C2-set immunoglobulin domain Domain
PF13927 Ig_3 312 378 Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed in beta-cells of the pancreatic islets. {ECO:0000269|PubMed:12837264}.
Sequence
MLRMRVPALLVLLFCFRGRAGPSPHFLQQPEDLVVLLGEEARLPCALGAYWGLVQWTKSG
LALGGQRDLPGWSRYWISGNAANGQHDLHIRPVELEDEASYECQATQAGLRSRPAQLHVL
V
PPEAPQVLGGPSVSLVAGVPANLTCRSRGDARPTPELLWFRDGVLLDGATFHQTLLKEG
TPGSVESTLTLTPFSHDDGATFVCRARSQALPTG
RDTAITLSLQYPPEVTLSASPHTVQE
GEKVIFLCQATAQPPVTGYRWAKGGSPVLGARGPRLEVVADASFLTEPVSCEVSNAVGSA
NRSTALDVLFGPILQAKPEPVSVDVGEDASFSCAWRGNPLPRVTWTRRGGAQVLGSGATL
RLPSVGPEDAGDYVCRAE
AGLSGLRGGAAEARLTVNAPPVVTALHSAPAFLRGPARLQCL
VFASPAPDAVVWSWDEGFLEAGSQGRFLVETFPAPESRGGLGPGLISVLHISGTQESDFS
RSFNCSARNRLGEGGAQASLGRRDLLPTVRIVAGVAAATTTLLMVITGVALCCWRHSKAS
ASFSEQKNLMRIPGSSDGSSSRGPEEEETGSREDRGPIVHTDHSDLVLEEKGTLETKDPT
NGYYKVRGVSVSLSLGEAPGGGLFLPPPSPLGPPGTPTFYDFNPHLGMVPPCRLYRARAG
YLTTPHPRAFTSYIKPTSFGPPDLAPGTPPFPYAAFPTPSHPRLQTHV
Sequence length 708
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Nephrin family interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
4
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Adrenocortical carcinoma, hereditary Benign rs34494265 RCV005909830
Epilepsy Uncertain significance rs1335997487 RCV001253040
Neurodevelopmental delay Uncertain significance rs1335997487 RCV001253040
Uterine corpus endometrial carcinoma Benign rs34494265 RCV005909831
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Albuminuria Associate 28334007
Hematuria Benign Familial Associate 28334007
Kidney Failure Chronic Associate 28334007
Medulloblastoma Associate 35771282
Nephritis Hereditary Associate 28334007
Paraparesis Tropical Spastic Associate 34446027
Polycystic Ovary Syndrome Associate 39314522
Renal Insufficiency Associate 28334007