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Gene Gene information from NCBI Gene database.
Entrez ID 348801
Gene name Leukemia NUP98 fusion partner 1
Gene symbol LNP1
Synonyms (NCBI Gene)
NP3
Chromosome 3
Chromosome location 3q12.2
miRNA miRNA information provided by mirtarbase database.
6 Show/Hide all (6)
miRTarBase ID miRNA Experiments Reference
MIRT1112413 hsa-miR-1253 CLIP-seq
MIRT1112414 hsa-miR-1305 CLIP-seq
MIRT1112415 hsa-miR-296-3p CLIP-seq
MIRT1112416 hsa-miR-3154 CLIP-seq
MIRT1112417 hsa-miR-3671 CLIP-seq
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
A1A4G5
Protein name Leukemia NUP98 fusion partner 1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15419 LNP1 7 → 175 Leukemia NUP98 fusion partner 1 Family
Sequence
Sequence length 178
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Reference Evidence Score
Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations