Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
64434
Gene name Gene Name - the full gene name approved by the HGNC.
Nucleolar protein with MIF4G domain 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NOM1
Synonyms (NCBI Gene) Gene synonyms aliases
C7orf3, PPP1R113, SGD1
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q36.3
Summary Summary of gene provided in NCBI Entrez Gene.
Proteins that contain MIF4G (middle of eIF4G (MIM 600495)) and/or MA3 domains, such as NOM1, function in protein translation. These domains include binding sites for members of the EIF4A family of ATP-dependent DEAD box RNA helicases (see EIF4A1; MIM 6026
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT041667 hsa-miR-484 CLASH 23622248
MIRT626668 hsa-miR-1304-3p HITS-CLIP 23824327
MIRT639692 hsa-miR-4645-3p HITS-CLIP 23824327
MIRT639693 hsa-miR-514a-3p HITS-CLIP 23824327
MIRT639691 hsa-miR-514b-3p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003723 Function RNA binding HDA 22681889
GO:0003723 Function RNA binding IBA
GO:0003723 Function RNA binding IEA
GO:0005515 Function Protein binding IPI 17965019, 21576267, 32296183, 35271311
GO:0005634 Component Nucleus IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
611269 13244 ENSG00000146909
Protein
UniProt ID Q5C9Z4
Protein name Nucleolar MIF4G domain-containing protein 1 (SGD1 homolog)
Protein function Plays a role in targeting PPP1CA to the nucleolus.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02854 MIF4G 362 559 MIF4G domain Family
PF02847 MA3 655 761 MA3 domain Family
Tissue specificity TISSUE SPECIFICITY: Expressed in heart and skeletal muscle. {ECO:0000269|PubMed:10329000}.
Sequence
MAASRSAGEAGPGGSQGRVVRMKRRGGRGPRRGPAGGGEKALKRLKLAVEEFVHATSEGE
APGGCEGRGAPVSFRPGGRKSRKELRKEKRHLRKARRLQRTAGPEQGPGLGGRSGAEEAS
GHRQDTEERARPAPSRDPSPPRKPRPSRVKAKATAATAKTRPSAAATAAARKRALLAANE
EEDREIRKLERCLGLNKRKKKDGSSSVPLSFARDGLDYILGALESGKNSGLYDSSGEEEE
DAGQTLPESDLESDSQDESEEEEEGDVEKEKKAQEAEAQSEDDDEDTEEEQGEEKEKGAQ
EKRRGKRVRFAEDEEKSENSSEDGDITDKSLCGSGEKYIPPHVRQAEETVDFKKKEELER
LKKHVKGLLNRLSEPNMASISGQLEELYMAHSRKDMNDTLTSALMGACVTASAMPSRLMM
EHVLLVSILHHTVGIEVGAHFLEAVVRKFDAIYKYGSEGKECDNLFTVIAHLYNFHVVQS
LLIFDILKKLIGTFTEKDIELILLMLKNVGFSLRKDDALSLKELITEAQTKASGAGSEFQ
DQTRIRFMLETMLALKNND
MRKIPGYDPEPVEKLRKLQRALVRNAGSGSETQLRVSWDSV
LSAEQTGRWWIVGSAWSGAPMIDNSHHTHLQKQLVGTVSSKILELARKQRMNTDIRRNIF
CTIMTSEDFLDAFEKLLKLGLKDQQEREIIHVLMDCCLQEKTYNPFYAFLASKFCEYERR
FQMTFQFSIWDKFRDLENLPATNFSNLVHLVAHLLKTKSLS
LSILKVVEFSELDKPRVRF
LRKVLSILLMETEVEDLSLIFTRVSDNPKLGVLREGLKLFISHFLLKNAQAHRSADEANV
LREKADLATKCLQGKASLRM
Sequence length 860
Interactions View interactions
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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
Diabetes Type 2 diabetes N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Obesity Associate 28207535