Gene Gene information from NCBI Gene database.
Entrez ID 284611
Gene name EEIG family member 2
Gene symbol EEIG2
Synonyms (NCBI Gene)
FAM102BSYM-3B
Chromosome 1
Chromosome location 1p13.3
miRNA miRNA information provided by mirtarbase database.
685
miRTarBase ID miRNA Experiments Reference
MIRT020374 hsa-miR-29c-3p Sequencing 20371350
MIRT703793 hsa-miR-124-3p HITS-CLIP 23313552
MIRT703792 hsa-miR-576-3p HITS-CLIP 23313552
MIRT703791 hsa-miR-5582-5p HITS-CLIP 23313552
MIRT703790 hsa-miR-33b-3p HITS-CLIP 23313552
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5T8I3
Protein name EEIG family member 2 (EEIG2)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10358 NT-C2 3 149 N-terminal C2 in EEIG1 and EHBP1 proteins Domain
Sequence
MMKKKKFKFKVDFELEELSSVPFVNGVLFCKMRLLDGGSFTAESSREVVQANCVRWRKKF
SFMCKMSASAATGILDPCIYRVSVRKELKGGKAYAKLGFADLNLAEFAGSGNTTRRCLLE
GYDTKNTRQDNSILKVLISMQLMSGDPCF
KTPPSTSMSIPIAGESESLQEDRKGGETLKV
HLGIADLSAKSASVPDELGACGHSRTSSYASQQSKVSGYSTCHSRSSSFSELCHRRNTSV
GSTSTGVESILEPCDEIEQKIAEPNLDTADKEDTASEKLSRCPVKQDSVESQLKRVDDTR
VDADDIVEKILQSQDFSLDSSAEEEGLRLFVGPGGSTTFGSHHLPNRVGSGAYEQVVIKR
Sequence length 360
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
LIVER CIRRHOSIS, EXPERIMENTAL CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations