Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
24139
Gene name Gene Name - the full gene name approved by the HGNC.
EMAP like 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
EML2
Synonyms (NCBI Gene) Gene synonyms aliases
ELP70, EMAP-2, EMAP2
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.32
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT962089 hsa-miR-656 CLIP-seq
MIRT1985089 hsa-miR-1236 CLIP-seq
MIRT1985090 hsa-miR-345 CLIP-seq
MIRT1985091 hsa-miR-3622a-3p CLIP-seq
MIRT1985092 hsa-miR-3622b-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000226 Process Microtubule cytoskeleton organization IBA
GO:0005515 Function Protein binding IPI 25416956, 25740311
GO:0005737 Component Cytoplasm IEA
GO:0005819 Component Spindle IEA
GO:0005856 Component Cytoskeleton IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
617494 18035 ENSG00000125746
Protein
UniProt ID O95834
Protein name Echinoderm microtubule-associated protein-like 2 (EMAP-2) (HuEMAP-2)
Protein function Tubulin binding protein that inhibits microtubule nucleation and growth, resulting in shorter microtubules.
PDB 4CGB
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03451 HELP 19 93 HELP motif Family
PF00400 WD40 95 143 WD domain, G-beta repeat Repeat
PF00400 WD40 284 321 WD domain, G-beta repeat Repeat
PF00400 WD40 364 405 WD domain, G-beta repeat Repeat
PF00400 WD40 449 488 WD domain, G-beta repeat Repeat
PF00400 WD40 497 534 WD domain, G-beta repeat Repeat
PF00400 WD40 608 647 WD domain, G-beta repeat Repeat
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. {ECO:0000269|PubMed:10521658}.
Sequence
MSSFGAGKTKEVIFSVEDGSVKMFLRGRPVPMMIPDELAPTYSLDTRSELPSCRLKLEWV
YGYRGRDCRANLYLLPTGEIVYFVASVAVLYSV
EEQRQRHYLGHNDDIKCLAIHPDMVTI
ATGQVAGTTKEGKPLPPHVRIWD
SVSLSTLHVLGLGVFDRAVCCVGFSKSNGGNLLCAVD
ESNDHMLSVWDWAKETKVVDVKCSNEAVLVATFHPTDPTVLITCGKSHIYFWTLEGGSLS
KRQGLFEKHEKPKYVLCVTFLEGGDVVTGDSGGNLYVWGKGGNRITQAVLGAHDGGVFGL
CALRDGTLVSGGGRDRRVVLW
GSDYSKLQEVEVPEDFGPVRTVAEGHGDTLYVGTTRNSI
LQGSVHTGFSLLVQGHVEELWGLATHPSRAQFVTCGQDKLVHLWSSDSHQPLWSRIIEDP
ARSAGFHPSGSVLAVGTVTGRWLLLDTETHDLVAIHTDGNEQISVVSFSPDGAYLAVGSH
DNLVYVYT
VDQGGRKVSRLGKCSGHSSFITHLDWAQDSSCFVTNSGDYEILYWDPATCKQ
ITSADAVRNMEWATATCVLGFGVFGIWSEGADGTDINAVARSHDGKLLASADDFGKVHLF
SYPCCQPRALSHKYGGHSSHVTNVAFLWDDSMALTTGGKDTSVLQWRVV
Sequence length 649
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
Metabolic Syndrome Metabolic syndrome N/A N/A GWAS