Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
151963
Gene name Gene Name - the full gene name approved by the HGNC.
Mab-21 domain containing 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MB21D2
Synonyms (NCBI Gene) Gene synonyms aliases
C3orf59, D2A, hMB21D2
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q29
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT020219 hsa-miR-130b-3p Sequencing 20371350
MIRT031178 hsa-miR-19b-3p Sequencing 20371350
MIRT042369 hsa-miR-484 CLASH 23622248
MIRT566809 hsa-miR-1277-5p PAR-CLIP 20371350
MIRT566808 hsa-miR-4517 PAR-CLIP 20371350
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0044877 Function Protein-containing complex binding IDA 23209302
GO:0045296 Function Cadherin binding HDA 25468996
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
620914 30438 ENSG00000180611
Protein
UniProt ID Q8IYB1
Protein name Nucleotidyltransferase MB21D2 (EC 2.7.7.-) (Mab-21 domain-containing protein 2) (hMB21D2)
Protein function Probable nucleotidyltransferase that catalyzes the formation of cyclic dinucleotide second messenger in response to some unknown stimulus.
PDB 7LT1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03281 Mab-21 108 402 Mab-21 protein Family
Sequence
MKMAAPTANKAASLGCNNKPAFPELDFRSGARVEELNKLIQEFTKHDQREYDDQRALEIH
TAKDFIFSMLGMVQKLDQKLPVANEYLLLSGGVREGVVDLDLDELNVYARGTDYDMDFTL
LVPALKLHDRNQPVTLDMRHSALCHSWLSLRLFDEGTISKWKDCCTIVDHINGATNYFFS
PTKVADWFYDSISIVLSEIQKKPQRGMPKVEKVEKNGTIISIILGVGSSRMLYDIVPVVS
FKGWPAVAQSWLMENHFWDGKITEEEVISGFYLVPACSYKGKKDNEWRLSFARSEVQLKK
CISSSLMQAYQACKAIIIKLLSRPKAISPYHLRSMMLWACDRLPANYLAQEDYAAHFLLG
LIDDLQHCLVNKMCPNYFIPQCNMLEHLSEETVMLHARKLSS
VRSDPAEHLRTAIEHVKA
ANRLTLELQRRGSTTSIPSPQSDGGDPNQPDDRLAKKLQQLVTENPGKSISVFINPDDVT
RPHFRIDDKFF
Sequence length 491
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Autoimmune diseases Autoimmune Diseases, AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1, AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 rs869025224 30595370
Hypothyroidism Hypothyroidism rs869320723, rs121908862, rs121908863, rs121908865, rs121908866, rs121908867, rs121908870, rs121908871, rs121908872, rs2140110277, rs121908881, rs121908884, rs121908885, rs786205080, rs1586182912
View all (22 more)
30595370
Unknown
Disease term Disease name Evidence References Source
Alzheimer disease Alzheimer disease GWAS
Rheumatoid arthritis Rheumatoid arthritis GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma Associate 35046897