Dedicator of Cytokinesis 8

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OMIM Number

611432

NCBI Gene ID

81704

Uniprot ID

Q8NF50

Length

250,406 bases

No. of Exons

54

No. of isoforms

4

Protein Name

Dedicator of cytokinesis protein 8

Molecular Mass

238529 Da

Amino Acid Count

2099

Genomic Location

chr9:214,854-465,259

Gene Map Locus
9p24.3

Description

The DOCK8 gene encodes a protein belonging to the DOCK180 family of guanine nucleotide exchange factors (GEF).  Members of this family function as activators of small G proteins and are components of intracellular signaling networks.  Similar to other members of this family, DOCK8 is made up of two domains called the DOCK homology regions (DHR).  While DHR1 is responsible for downstream signaling and biological activity, DHR2 contains the catalytic site for GEF activity.

Mutations in the DOCK8 gene are associated with autosomal recessive hyper IgE syndrome (AR-HIES).  This primary immunodeficiency disorder is characterized by recurrent viral infections, chronic eczema, elevated serum IgE levels and defective T cell activation.  The disease has a high morbidity and mortality rate.  AR-HIES patients with DOCK8 mutations usually have little or no DOCK8 protein.  This shortage of DOCK8 is believed to affect T-cell structure and migration, B cell maturation, and antibody production, thereby leaving the individual severely immunocompromised. 

Molecular Genetics

The 214 kb long DOCK8 gene is located on the short arm of chromosome 9.  Its coding sequence is made up of 46 to 48 exons.  The encoded protein product is approximately 238 kDa in size and made up of 2099 amino acids.  Several different isoforms exist due to alternative splicing.  The DOCK8 gene has been found to be highly expressed in cells of the immune system, especially in lymphocytes.  More than 110 DOCK8 mutations (both homozygous and compound heterozygous) have been associated with AR-HIES. Most of these are deletions that result in a truncated protein.  

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_203447.3:c.1498C>TLebanonNC_000009.12:g.339081C>TPathogenicPathogenicNG_017007.1:g.129217C>T; NM_203447.3:c.1498C>T; NP_982272.2:p.Arg500Ter7707483161069888
NM_203447.3:c.3339dupUnited Arab EmiratesNC_000009.12:g.405022dupNG_017007.1:g.195158dup; NM_203447.3:c.3339dup; NP_982272.2:p.Met1114TyrfsTer4748134881
NM_203447.4:c.2248G>TLebanonNC_000009.12:g.377019G>TPathogenicHyper-IgE Recurrent Infection Syndrome 2, Autosomal RecessiveNG_017007.1:g.167155G>T; NM_203447.4:c.2248G>T; NP_982272.2:p.Glu750Ter1192065366
NM_203447.4:c.3220C>AUnited Arab EmiratesNC_000009.12:g.399245C>ALikely Benign, Uncertain SignificanceUncertain SignificanceNG_017007.1:g.189381C>A; NM_203447.4:c.3220C>A; NP_982272.2:p.His1074Asn150298985366969

Other Reports

Lebanon

Engelhardtet al. 2015 studied a cohort of 82 patients from 60 families with autosomal recessive hyper-IgE syndrome (AR-HIES). Three homozygous mutations in DOCK8 gene – p.E750X , >80kb 5’ deletion including Ex1_2del, and Ex29_36del – were identified in three families from Lebanon.

Saudi Arabia

Alsum et al. (2013) studied the clinical and molecular characteristics of 25 patients diagnosed with AR-HIES.  A genetic analysis revealed DOCK8 mutations in 13 of the 17 screened individuals.  Of these, seven patients from three families carried the 5625T>G (Y1875X) mutation in exon 44.  Two patients of the same tribe carried the mutation 5132C>A (S1711X) in exon 40 while one patient had a splice site mutation c.827+6 T>C.  All three mutations were novel and were predicted to result in a truncated protein.  This was confirmed in the patient with the splice site mutation by western blot analysis, which found no DOCK8 expression.  In three patients, large deletions were discovered which would abolish DOCK8 expression.  An additional four patients were assumed to be DOCK8 deficient due to siblings with confirmed DOCK8 mutations and similar clinical presentations.  

Yemen

AlKhater, 2016 described a 6-year-old Yemeni girl, born to consanguineous parents, who presented with eczema, skin abscesses, and recurrent bronchopneumonia.  She also exhibited recurrences of Herpes zoster involving multiple dermatomes and persistent Molluscum contagiosum infections of the skin.  Immunological analysis showed leukocytosis at 31 × 109/L, extreme peripheral eosinophilia as high as 18,000 × 109/L, an elevated IgG level of 2,530 mg/dl, and an elevated serum IgE level of 41,000 IU/ml.  At 8 years of age, she had dysphasia, visual hallucinations, ipsilateral ptosis, acute left eye squinting, and fatigue.  During three-week period she developed excessive sleepiness, dizziness, and unsteady gait.  In addition, she had severe dermatitis on the back and buttocks and eczematous eruptions on the flexures of the arms and popliteal region.  With steroids and mycophenolate mofetil (MMF) treatment, she remained symptom-free, and no vasculitis or infectious flare-ups have occurred.  The patient made remarkable recover of most of her neurological deficits with effective treatments.   By performing polymerase chain reaction (PCR) and multiplex ligation probe amplification (MLPA), a large homozygous deletion of the DOCK8 gene on chromosome 9 was identified.

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