Gene Gene information from NCBI Gene database.
Entrez ID 256364
Gene name EMAP like 3
Gene symbol EML3
Synonyms (NCBI Gene)
ELP95EMAP3EMAP95
Chromosome 11
Chromosome location 11q12.3
miRNA miRNA information provided by mirtarbase database.
1
miRTarBase ID miRNA Experiments Reference
MIRT023979 hsa-miR-1-3p Microarray 18668037
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
22
GO ID Ontology Definition Evidence Reference
GO:0000226 Process Microtubule cytoskeleton organization IBA
GO:0005515 Function Protein binding IPI 25740311, 30723163, 32296183
GO:0005634 Component Nucleus IDA 18445686
GO:0005634 Component Nucleus IEA
GO:0005737 Component Cytoplasm IDA 18445686
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
618118 26666 ENSG00000149499
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q32P44
Protein name Echinoderm microtubule-associated protein-like 3 (EMAP-3)
Protein function Regulates mitotic spindle assembly, microtubule (MT)-kinetochore attachment and chromosome separation via recruitment of HAUS augmin-like complex and TUBG1 to the existing MTs and promoting MT-based MT nucleation (PubMed:30723163). Required for
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03451 HELP 214 285 HELP motif Family
PF00400 WD40 295 343 WD domain, G-beta repeat Repeat
PF00400 WD40 589 625 WD domain, G-beta repeat Repeat
PF00400 WD40 716 754 WD domain, G-beta repeat Repeat
PF00400 WD40 829 868 WD domain, G-beta repeat Repeat
Sequence
MDGAAGPGDGPAREALQSLSQRLRVQEQEMELVKAALAEALRLLRLQVPPSSLQGSGTPA
PPGDSLAAPPGLPPTCTPSLVSRGTQTETEVELKSSPGPPGLSNGPPAPQGASEEPSGTQ
SEGGGSSSSGAGSPGPPGILRPLQPPQRADTPRRNSSSSSSPSERPRQKLSRKAISSANL
LVRSGSTESRGGKDPLSSPGGPGSRRSNYNLEGISVKMFLRGRPITMYIPSGIRSLEELP
SGPPPETLSLDWVYGYRGRDSRSNLFVLRSGEVVYFIACVVVLYR
PGGGPGGPGGGGQRH
YRGHTDCVRCLAVHPDGVRVASGQTAGVDKDGKPLQPVVHIWD
SETLLKLQEIGLGAFER
GVGALAFSAADQGAFLCVVDDSNEHMLSVWDCSRGMKLAEIKSTNDSVLAVGFNPRDSSC
IVTSGKSHVHFWNWSGGVGVPGNGTLTRKQGVFGKYKKPKFIPCFVFLPDGDILTGDSEG
NILTWGRSPSDSKTPGRGGAKETYGIVAQAHAHEGSIFALCLRRDGTVLSGGGRDRRLVQ
WGPGLVALQEAEIPEHFGAVRAIAEGLGSELLVGTTKNALLRGDLAQGFSPVIQGHTDEL
WGLCTHPSQNRFLTCGHDRQLCLWD
GESHALAWSIDLKETGLCADFHPSGAVVAVGLNTG
RWLVLDTETREIVSDVIDGNEQLSVVRYSPDGLYLAIGSHDNVIYIYSVSSDGAKSSRFG
RCMGHSSFITHLDWSKDGNFIMSNSGDYEILYWD
VAGGCKQLKNRYESRDREWATYTCVL
GFHVYGVWPDGSDGTDINSLCRSHNERVVAVADDFCKVHLFQYPCARAKAPSRMYGGHGS
HVTSVRFTHDDSHLVSLGGKDASIFQWR
VLGAGGAGPAPATPSRTPSLSPASSLDV
Sequence length 896
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 Evidence Score
RETINITIS PIGMENTOSA Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations