Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
84173
Gene name Gene Name - the full gene name approved by the HGNC.
ELMO domain containing 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ELMOD3
Synonyms (NCBI Gene) Gene synonyms aliases
DFNA81, DFNB88, LST3, RBED1, RBM29
Disease Acronyms (UniProt) Disease acronyms from UniProt database
DFNA81, DFNB88
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p11.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the engulfment and cell motility family of GTPase-activating proteins that regulate Arf GTPase proteins. Members of this family are defined by a conserved engulfment and cell motility domain. In rat cochlea, the encoded prote
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs587777040 T>C Pathogenic Missense variant, non coding transcript variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT961100 hsa-miR-1184 CLIP-seq
MIRT961101 hsa-miR-1205 CLIP-seq
MIRT961102 hsa-miR-1224-3p CLIP-seq
MIRT961103 hsa-miR-1260 CLIP-seq
MIRT961104 hsa-miR-1260b CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005096 Function GTPase activator activity IDA 17452337
GO:0005515 Function Protein binding IPI 25416956
GO:0005737 Component Cytoplasm IEA
GO:0005856 Component Cytoskeleton IEA
GO:0005886 Component Plasma membrane IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
615427 26158 ENSG00000115459
Protein
UniProt ID Q96FG2
Protein name ELMO domain-containing protein 3 (RNA-binding motif and ELMO domain-containing protein 1) (RNA-binding motif protein 29) (RNA-binding protein 29)
Protein function Acts as a GTPase-activating protein (GAP) for ARL2 with low specific activity.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04727 ELMO_CED12 155 313 ELMO/CED-12 family Family
Tissue specificity TISSUE SPECIFICITY: Both isoform 1 and isoform 6 are widely expressed. {ECO:0000269|PubMed:24039609}.
Sequence
MNEKSCSFHSKEELRDGQGERLSAGYSPSYDKDKSVLAFRGIPISELKNHGILQALTTEA
YEWEPRVVSTEVVRAQEEWEAVDTIQPETGSQASSEQPGQLISFSEALQHFQTVDLSPFK
KRIQPTIRRTGLAALRHYLFGPPKLHQRLREERDLVLTIAQCGLDSQDPVHGRVLQTIYK
KLTGSKFDCALHGNHWEDLGFQGANPATDLRGAGFLALLHLLYLVMDSKTLPMAQEIFRL
SRHHIQQFPFCLMSVNITHIAIQALREECLSRECNRQQKVIPVVNSFYAATFLHLAHVWR
TQRKTISDSGFVL
KELEVLAKKSPRRLLKTLELYLARVSKGQASLLGAQKCYGPEAPPFK
DLTFTGESDLQSHSSEGVWLI
Sequence length 381
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Deafness DEAFNESS, AUTOSOMAL RECESSIVE 88 rs267607135, rs387906219, rs387906220, rs387906221, rs387906222, rs606231120, rs267606855, rs121918370, rs137853185, rs137853186, rs137853187, rs137853188, rs587776522, rs587776523, rs200781822
View all (1019 more)
24039609
Nonsyndromic deafness Nonsyndromic Deafness rs606231410, rs794729665, rs730880338, rs1566538321 24039609
Associations from Text Mining
Disease Name Relationship Type References
Autism Spectrum Disorder Associate 31800155
Breast Neoplasms Associate 27993161
Hearing Loss Associate 37708136
Nonsyndromic sensorineural hearing loss Associate 37708136