KIRREL3

KIRREL3
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 2CRY
Identifiers
Aliases	KIRREL3, KIRRE, MRD4, NEPH2, PRO4502, kin of IRRE like 3 (Drosophila), Kin of IRRE-like protein 3
External IDs	MGI: 1914953 HomoloGene: 57050 GeneCards: KIRREL3
Genetically Related Diseases
attention deficit hyperactivity disorder, Conduct disorder[1]
Gene ontology Molecular function • protein binding Cellular component • dendritic shaft • integral component of membrane • extracellular region • axon • plasma membrane • membrane • dendrite Biological process • hemopoiesis • neuron projection morphogenesis • neuron migration • inter-male aggressive behavior • principal sensory nucleus of trigeminal nerve development • glomerulus morphogenesis • hippocampus development • homophilic cell adhesion via plasma membrane adhesion molecules • synapse assembly Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	84623	67703
Ensembl	ENSG00000149571	ENSMUSG00000032036
UniProt	Q8IZU9	Q8BR86
RefSeq (mRNA)	NM_001161707 NM_001301097 NM_032531	NM_001190911 NM_001190912 NM_001190913 NM_001190914 NM_026324
RefSeq (protein)	NP_001155179.1 NP_115920.1	NP_001177840.1 NP_001177841.1 NP_001177842.1 NP_080600.1
Location (UCSC)	Chr 11: 126.42 – 127 Mb	Chr 9: 34.49 – 35.04 Mb
PubMed search	[2]	[3]
Wikidata

View/Edit Human

View/Edit Mouse

Kin of IRRE-like protein 3 (KIRREL3) also known as kin of irregular chiasm-like protein 3 or NEPH2 is a protein that in humans is encoded by the KIRREL3 gene.^[4]

NEPH2 is a member of the NEPH protein family of transmembrane proteins, which includes NEPH1 (KIRREL) and NEPH3 (KIRREL2). The NEPH proteins can interact with nephrin and CASK.

Function

NEPH2 has been implicated in synapse formation.^[5] Disruption of KIRREL3 gene function had been associated with abnormal brain function.^[6]

NEPH1 and NEPH2 are involved in the blood filtration function of the kidney and are located in the slit diaphragm.^[7]

References

1. "Diseases that are genetically associated with KIRREL3 view/edit references on wikidata".
2. "Human PubMed Reference:".
3. "Mouse PubMed Reference:".
4. "Entrez Gene: kin of IRRE like 3 (Drosophila)".
5. Gerke P, Benzing T, Höhne M, Kispert A, Frotscher M, Walz G, Kretz O (Oct 2006). "Neuronal expression and interaction with the synaptic protein CASK suggest a role for Neph1 and Neph2 in synaptogenesis". The Journal of Comparative Neurology. 498 (4): 466–75. doi:10.1002/cne.21064. PMID 16874800.
6. Bhalla K, Luo Y, Buchan T, Beachem MA, Guzauskas GF, Ladd S, Bratcher SJ, Schroer RJ, Balsamo J, DuPont BR, Lilien J, Srivastava AK (Dec 2008). "Alterations in CDH15 and KIRREL3 in patients with mild to severe intellectual disability". American Journal of Human Genetics. 83 (6): 703–13. doi:10.1016/j.ajhg.2008.10.020. PMC 2668064. PMID 19012874.
7. Neumann-Haefelin E, Kramer-Zucker A, Slanchev K, Hartleben B, Noutsou F, Martin K, Wanner N, Ritter A, Gödel M, Pagel P, Fu X, Müller A, Baumeister R, Walz G, Huber TB (Jun 2010). "A model organism approach: defining the role of Neph proteins as regulators of neuron and kidney morphogenesis". Human Molecular Genetics. 19 (12): 2347–59. doi:10.1093/hmg/ddq108. PMID 20233749.

Further reading

• Davila S, Froeling FE, Tan A, Bonnard C, Boland GJ, Snippe H, Hibberd ML, Seielstad M (Apr 2010). "New genetic associations detected in a host response study to hepatitis B vaccine". Genes and Immunity. 11 (3): 232–8. doi:10.1038/gene.2010.1. PMID 20237496.
• Anney RJ, Lasky-Su J, O'Dúshláine C, Kenny E, Neale BM, Mulligan A, Franke B, Zhou K, Chen W, Christiansen H, Arias-Vásquez A, Banaschewski T, Buitelaar J, Ebstein R, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Steinhausen H, Asherson P, Faraone SV, Gill M (Dec 2008). "Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study". American Journal of Medical Genetics Part B. 147B (8): 1369–78. doi:10.1002/ajmg.b.30871. PMID 18951430.
• Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR. "Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score". Molecular Medicine. 16 (7-8): 247–53. doi:10.2119/molmed.2009.00159. PMC 2896464. PMID 20379614.
• Eriksson N, Macpherson JM, Tung JY, Hon LS, Naughton B, Saxonov S, Avey L, Wojcicki A, Pe'er I, Mountain J (Jun 2010). "Web-based, participant-driven studies yield novel genetic associations for common traits". PLoS Genetics. 6 (6): e1000993. doi:10.1371/journal.pgen.1000993. PMC 2891811. PMID 20585627.
• Bonaldo MF, Lennon G, Soares MB (Sep 1996). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Research. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
• Clark HF, Gurney AL, Abaya E, Baker K, Baldwin D, Brush J, Chen J, Chow B, Chui C, Crowley C, Currell B, Deuel B, Dowd P, Eaton D, Foster J, Grimaldi C, Gu Q, Hass PE, Heldens S, Huang A, Kim HS, Klimowski L, Jin Y, Johnson S, Lee J, Lewis L, Liao D, Mark M, Robbie E, Sanchez C, Schoenfeld J, Seshagiri S, Simmons L, Singh J, Smith V, Stinson J, Vagts A, Vandlen R, Watanabe C, Wieand D, Woods K, Xie MH, Yansura D, Yi S, Yu G, Yuan J, Zhang M, Zhang Z, Goddard A, Wood WI, Godowski P, Gray A (Oct 2003). "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment". Genome Research. 13 (10): 2265–70. doi:10.1101/gr.1293003. PMC 403697. PMID 12975309.
• Sellin L, Huber TB, Gerke P, Quack I, Pavenstädt H, Walz G (Jan 2003). "NEPH1 defines a novel family of podocin interacting proteins". FASEB Journal. 17 (1): 115–7. doi:10.1096/fj.02-0242fje. PMID 12424224.
• Adkins DE, Aberg K, McClay JL, Bukszár J, Zhao Z, Jia P, Stroup TS, Perkins D, McEvoy JP, Lieberman JA, Sullivan PF, van den Oord EJ (Mar 2011). "Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs". Molecular Psychiatry. 16 (3): 321–32. doi:10.1038/mp.2010.14. PMC 2891163. PMID 20195266.