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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 Show/Hide all (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.).
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 Reference Evidence Score
COLOR VISION DISORDER — GWAS catalog 37359372
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations