# KALRN

> protein-coding gene in the species Homo sapiens

**Wikidata**: [Q18033696](https://www.wikidata.org/wiki/Q18033696)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Kalirin)  
**Source**: https://4ort.xyz/entity/kalrn


## References

1. ensembl Release 106
2. Ensembl Release 87
3. Q20641742
4. Online Mendelian Inheritance in Man
5. HomoloGene build68
6. [Orthologous MAtrix](https://omabrowser.org/oma/vps/O60229/)
7. UniProt
8. KALRN: a central regulator of synaptic function and synaptopathies
9. β-Amyloid 42/40 ratio and kalirin expression in Alzheimer disease with psychosis
10. Kalirin is under-expressed in Alzheimer's disease hippocampus.
11. Genetic Variation of the Kalirin Gene is Associated with ICAS in the Chinese Population
12. Association between Serum Kalirin Levels and the KALRN gene rs9289231 Polymorphism in Early-Onset Coronary Artery Disease
13. Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations
14. A Schizophrenia-Linked KALRN Coding Variant Alters Neuron Morphology, Protein Function, and Transcript Stability.
15. A sequence variant in human KALRN impairs protein function and coincides with reduced cortical thickness.
16. Mouse and Human Genetic Analyses Associate Kalirin with Ventral Striatal Activation during Impulsivity and with Alcohol Misuse
17. A polygenic burden of rare disruptive mutations in schizophrenia
18. Resequencing and association analysis of the KALRN and EPHB1 genes and their contribution to schizophrenia susceptibility
19. Both rare and common genetic variants contribute to autism in the Faroe Islands
20. Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
21. Prevalence and architecture of de novo mutations in developmental disorders
22. Genetic Variant of Kalirin Gene Is Associated with Ischemic Stroke in a Chinese Han Population.
23. Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease
24. Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree
25. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069)
26. UMLS 2023
27. [Bgee](https://www.bgee.org/gene/ENSG00000160145)