Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23306
Gene name Gene Name - the full gene name approved by the HGNC.
Nuclear envelope integral membrane protein 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NEMP1
Synonyms (NCBI Gene) Gene synonyms aliases
TMEM194, TMEM194A
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q13.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT439433 hsa-miR-155-5p HITS-CLIP 22473208
MIRT439433 hsa-miR-155-5p HITS-CLIP 22473208
MIRT726297 hsa-miR-92a-3p HITS-CLIP 22473208
MIRT726296 hsa-miR-92b-3p HITS-CLIP 22473208
MIRT726295 hsa-miR-32-5p HITS-CLIP 22473208
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:0005634 Component Nucleus IEA
GO:0005635 Component Nuclear envelope IBA
GO:0005635 Component Nuclear envelope IEA
GO:0005635 Component Nuclear envelope ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616496 29001 ENSG00000166881
Protein
UniProt ID O14524
Protein name Nuclear envelope integral membrane protein 1
Protein function Together with EMD, contributes to nuclear envelope stiffness in germ cells (PubMed:32923640). Required for female fertility (By similarity). Essential for normal erythropoiesis (By similarity). Required for efficient nuclear envelope opening and
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10225 NEMP 152 398 NEMP family Family
Sequence
MAGGMKVAVSPAVGPGPWGSGVGGGGTVRLLLILSGCLVYGTAETDVNVVMLQESQVCEK
RASQQFCYTNVLIPKWHDIWTRIQIRVNSSRLVRVTQVENEEKLKELEQFSIWNFFSSFL
KEKLNDTYVNVGLYSTKTCLKVEIIEKDTKYSVIVIRRFDPKLFLVFLLGLMLFFCGDLL
SRSQIFYYSTGMTVGIVASLLIIIFILSKFMPKKSPIYVILVGGWSFSLYLIQLVFKNLQ
EIWRCYWQYLLSYVLTVGFMSFAVCYKYGPLENERSINLLTWTLQLMGLCFMYSGIQIPH
IALAIIIIALCTKNLEHPIQWLYITCRKVCKGAEKPVPPRLLTEEEYRIQGEVETRKALE
ELREFCNSPDCSAWKTVSRIQSPKRFADFVEGSSHLTP
NEVSVHEQEYGLGSIIAQDEIY
EEASSEEEDSYSRCPAITQNNFLT
Sequence length 444
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
Asthma Asthma N/A N/A GWAS
Insomnia Insomnia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 31854049