Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4600
Gene name Gene Name - the full gene name approved by the HGNC.
MX dynamin like GTPase 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MX2
Synonyms (NCBI Gene) Gene synonyms aliases
MXB
Chromosome Chromosome number
21
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
21q22.3
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene has a nuclear and a cytoplasmic form and is a member of both the dynamin family and the family of large GTPases. The nuclear form is localized in a granular pattern in the heterochromatin region beneath the nuclear envelop
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT021267 hsa-miR-146a-5p Microarray 18057241
MIRT628763 hsa-miR-148a-5p HITS-CLIP 19536157
MIRT710678 hsa-miR-511-3p HITS-CLIP 19536157
MIRT628762 hsa-miR-7110-3p HITS-CLIP 19536157
MIRT628761 hsa-miR-6817-3p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0002376 Process Immune system process IEA
GO:0003924 Function GTPase activity IBA
GO:0003924 Function GTPase activity IEA
GO:0003924 Function GTPase activity TAS 8798556
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
147890 7533 ENSG00000183486
Protein
UniProt ID P20592
Protein name Interferon-induced GTP-binding protein Mx2 (Interferon-regulated resistance GTP-binding protein MxB) (Myxovirus resistance protein 2) (p78-related protein)
Protein function Interferon-induced dynamin-like GTPase with potent antiviral activity against human immunodeficiency virus type 1 (HIV-1). Acts by targeting the viral capsid and affects the nuclear uptake and/or stability of the HIV-1 replication complex and th
PDB 4WHJ , 4X0R , 5UOT
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00350 Dynamin_N 121 296 Dynamin family Domain
PF01031 Dynamin_M 307 594 Dynamin central region Family
PF02212 GED 618 709 Dynamin GTPase effector domain Family
Sequence
Sequence length 715
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Viral life cycle - HIV-1
Hepatitis C
Measles
Influenza A
Human papillomavirus infection
Coronavirus disease - COVID-19
  ISG15 antiviral mechanism
Interferon alpha/beta signaling
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Dementia Dementia N/A N/A GWAS
Melanoma Melanoma N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Arthritis Psoriatic Stimulate 25809693
Breast Neoplasms Associate 37286092
Carcinogenesis Associate 33734579
Carcinoma Squamous Cell Associate 35779918
Colitis Ulcerative Associate 36165492
Congenital heart block Associate 28626076
COVID 19 Stimulate 34076249
COVID 19 Associate 34880855
Dermatomyositis Associate 37353938
Diabetes Mellitus Stimulate 34076249