Gene Gene information from NCBI Gene database.
Entrez ID 24139
Gene name EMAP like 2
Gene symbol EML2
Synonyms (NCBI Gene)
ELP70EMAP-2EMAP2
Chromosome 19
Chromosome location 19q13.32
miRNA miRNA information provided by mirtarbase database.
25
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
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 identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617494 18035 ENSG00000125746
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Malignant lymphoma, large B-cell, diffuse Uncertain significance rs138590950 RCV005932191