Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
57140
Gene name Gene Name - the full gene name approved by the HGNC.
Arginyl aminopeptidase like 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
RNPEPL1
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q37.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT002699 hsa-miR-124-3p Microarray 15685193
MIRT002699 hsa-miR-124-3p Microarray 18668037
MIRT002699 hsa-miR-124-3p Microarray 15685193
MIRT724346 hsa-miR-4308 HITS-CLIP 19536157
MIRT724345 hsa-miR-4292 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:0006508 Process Proteolysis IBA 21873635
GO:0006508 Process Proteolysis IDA 11017071
GO:0008270 Function Zinc ion binding IEA
GO:0070006 Function Metalloaminopeptidase activity IBA 21873635
GO:0070006 Function Metalloaminopeptidase activity IDA 11017071
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605287 10079 ENSG00000142327
Protein
UniProt ID Q9HAU8
Protein name Aminopeptidase RNPEPL1 (EC 3.4.11.-) (Arginyl aminopeptidase-like 1) (Methionyl aminopeptidase) (EC 3.4.11.18)
Protein function Broad specificity aminopeptidase which preferentially hydrolyzes an N-terminal methionine, citrulline or glutamine.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17900 Peptidase_M1_N 133 258 Domain
PF01433 Peptidase_M1 291 501 Peptidase family M1 domain Domain
PF09127 Leuk-A4-hydro_C 560 673 Leukotriene A4 hydrolase, C-terminal Family
Tissue specificity TISSUE SPECIFICITY: Ubiquitously expressed. Expressed at relatively higher levels in heart and skeletal muscle. {ECO:0000269|PubMed:11017071, ECO:0000269|PubMed:19508204}.
Sequence
Sequence length 725
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Colorectal cancer Colorectal Carcinoma rs137854568, rs137854573, rs137854575, rs387906234, rs121908380, rs121908702, rs267606674, rs794729661, rs121909055, rs281865417, rs267606884, rs28934575, rs587776769, rs104893815, rs587776800
View all (467 more)
Unknown
Disease term Disease name Evidence References Source
Bipolar Disorder Bipolar Disorder GWAS