IMD64
MCID: IMM202
MIFTS: 16

Immunodeficiency 64 (IMD64)

Categories: Genetic diseases, Immune diseases, Infectious diseases

Aliases & Classifications for Immunodeficiency 64

MalaCards integrated aliases for Immunodeficiency 64:

Name: Immunodeficiency 64 56 73 6
Imd64 56 73

Classifications:



External Ids:

OMIM 56 618534
OMIM Phenotypic Series 56 PS300755
MeSH 43 D007153
MedGen 41 CN262189

Summaries for Immunodeficiency 64

OMIM : 56 Immunodeficiency-64 (IMD64) is an autosomal recessive primary immunodeficiency characterized by onset of recurrent bacterial, viral, and fungal infections in early childhood. Laboratory studies show variably decreased numbers of T cells, with lesser deficiencies of B and NK cells. There is impaired T-cell proliferation and activation; functional defects in B cells and NK cells may also be observed. Patients have increased susceptibility to EBV infection and may develop lymphoproliferation or EBV-associated lymphoma. Some patients may develop features of autoimmunity (summary by Salzer et al., 2016, Mao et al., 2018, and Winter et al., 2018). (618534)

MalaCards based summary : Immunodeficiency 64, is also known as imd64. An important gene associated with Immunodeficiency 64 is RASGRP1 (RAS Guanyl Releasing Protein 1). Affiliated tissues include t cells, nk cells and b cells.

UniProtKB/Swiss-Prot : 73 Immunodeficiency 64: An autosomal recessive primary immunodeficiency characterized by recurrent bacterial, viral and fungal infections, variably decreased numbers of T cells, deficiencies of B and NK cells, and increased susceptibility to Epstein-Barr virus (EBV) infection. Patients may develop lymphoproliferation or EBV-associated lymphoma. Some patients may develop features of autoimmunity.

Related Diseases for Immunodeficiency 64

Symptoms & Phenotypes for Immunodeficiency 64

Clinical features from OMIM:

618534

Drugs & Therapeutics for Immunodeficiency 64

Search Clinical Trials , NIH Clinical Center for Immunodeficiency 64

Genetic Tests for Immunodeficiency 64

Anatomical Context for Immunodeficiency 64

MalaCards organs/tissues related to Immunodeficiency 64:

40
T Cells, Nk Cells, B Cells

Publications for Immunodeficiency 64

Articles related to Immunodeficiency 64:

# Title Authors PMID Year
1
RASGRP1 mutation in autoimmune lymphoproliferative syndrome-like disease. 56 6
29155103 2018
2
Loss of RASGRP1 in humans impairs T-cell expansion leading to Epstein-Barr virus susceptibility. 56 6
29282224 2018
3
Combined immunodeficiency with EBV positive B cell lymphoma and epidermodysplasia verruciformis due to a novel homozygous mutation in RASGRP1. 56 6
28822832 2017
4
RASGRP1 deficiency causes immunodeficiency with impaired cytoskeletal dynamics. 56 6
27776107 2016
5
Chronic immunodeficiency in mice lacking RasGRP1 results in CD4 T cell immune activation and exhaustion. 56
17675473 2007

Variations for Immunodeficiency 64

ClinVar genetic disease variations for Immunodeficiency 64:

6 ‎‎ ‎‎ ‎‎ ‎‎ ‎‎
# Gene Name Type Significance ClinVarId dbSNP ID GRCh37 Pos GRCh38 Pos
1 RASGRP1 NM_005739.4(RASGRP1):c.736C>T (p.Arg246Ter)SNV Pathogenic 666277 15:38805097-38805097 15:38512896-38512896
2 RASGRP1 NM_005739.4(RASGRP1):c.771G>A (p.Trp257Ter)SNV Pathogenic 666278 15:38805062-38805062 15:38512861-38512861
3 RASGRP1 NM_005739.4(RASGRP1):c.641C>T (p.Thr214Ile)SNV Pathogenic 666279 15:38808432-38808432 15:38516231-38516231
4 RASGRP1 NM_005739.4(RASGRP1):c.964A>T (p.Lys322Ter)SNV Pathogenic 666280 15:38803807-38803807 15:38511606-38511606
5 RASGRP1 NM_005739.4(RASGRP1):c.1910_1911insAG (p.Ala638fs)insertion Pathogenic 666281 15:38786931-38786932 15:38494730-38494731

Expression for Immunodeficiency 64

Search GEO for disease gene expression data for Immunodeficiency 64.

Pathways for Immunodeficiency 64

GO Terms for Immunodeficiency 64

Sources for Immunodeficiency 64

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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