Gene: BRSK2

Alternate names for this Gene: C11orf7|PEN11B|SAD1|SADA|STK29

Gene Summary:

Gene is located in Chromosome: 11

Location in Chromosome : 11p15.5

Description of this Gene: BR serine/threonine kinase 2

Type of Gene: protein-coding

Gene: LOC107984298

Alternate names for this Gene:

Gene Summary:

Gene is located in Chromosome:

Location in Chromosome :

Description of this Gene:

Type of Gene:

rs1554904159 in BRSK2;LOC107984298 gene and Abnormally large globe PMID 30879638 2019 Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder.

rs1554904159 in BRSK2;LOC107984298 gene and Apraxia of Phonation PMID 30879638 2019 Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder.

rs1554904159 in BRSK2;LOC107984298 gene and Autistic behavior PMID 30879638 2019 Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder.

rs1554904159 in BRSK2;LOC107984298 gene and Cerebellar Ataxia PMID 30879638 2019 Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder.

rs1554904159 in BRSK2;LOC107984298 gene and Convex nasal ridge PMID 30879638 2019 Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder.

rs1554904159 in BRSK2;LOC107984298 gene and Delayed fine motor development PMID 30879638 2019 Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder.

rs1554904159 in BRSK2;LOC107984298 gene and Delayed speech and language development PMID 30879638 2019 Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder.

rs1554904159 in BRSK2;LOC107984298 gene and Global developmental delay PMID 30879638 2019 Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder.

rs1554904159 in BRSK2;LOC107984298 gene and Gross motor development delay PMID 30879638 2019 Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder.

rs1554904159 in BRSK2;LOC107984298 gene and Large head (disorder) PMID 30879638 2019 Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder.

rs1554904159 in BRSK2;LOC107984298 gene and Tall stature PMID 30879638 2019 Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder.