Version: 8.0.0Date: Tue Jan 28 2025
Category
fam189b
(Danio rerio)Gene
Name: family with sequence similarity 189 member B
Synonyms: si:dkey-7f3.9
Source: ZFIN:ZDB-GENE-100922-197
Biotype: protein coding gene
Symbol: fam189b (Dre)
Symbol: fam189b
ENTREP3
(Homo sapiens)Gene
Name: endosomal transmembrane epsin interactor 3
Synonyms: hypothetical protein LOC10712, COTE1, FAM189B, C1orf2, family with sequence similarity 189, member B, family with sequence similarity 189 member B
Source: HGNC:1233
Biotype: protein coding gene
Synonyms: FAM189B...FAM189B
Strict Orthology Symbols: fam189b
entrep3
(Xenopus tropicalis)Gene
Name: endosomal transmembrane epsin interactor 3
Synonyms: cote1, entrep3, endosomal transmembrane epsin interactor 3, fam189b, c1orf2
Source: Xenbase:XB-GENE-939998
Biotype: gene
Synonyms: fam189b...fam189b...fam189b
entrep3.L
(Xenopus laevis)Gene
Name: endosomal transmembrane epsin interactor 3
Synonyms: entrep3.L, cote1, endosomal transmembrane epsin interactor 3, fam189b, c1orf2
Source: Xenbase:XB-GENE-17344671
Biotype: gene
Synonyms: fam189b...fam189b...fam189b
Entrep3
(Mus musculus)Gene
Name: endosomal transmembrane epsin interactor 3
Synonyms: Fam189b, family with sequence similarity 189, member B, RGD1306107, RIKEN cDNA 1110013L07 gene, 1110013L07Rik
Source: MGI:1915771
Biotype: protein coding gene
Synonyms: Fam189b...Fam189b
Strict Orthology Symbols: fam189b
Entrep3
(Rattus norvegicus)Gene
Name: endosomal transmembrane epsin interactor 3
Synonyms: hypothetical protein LOC310640, Fam189b, similar to chromosome 1 open reading frame 2, family with sequence similarity 189, member B, RGD1306107, uncharacterized protein LOC310640, LOC310640
Source: RGD:1306107
Biotype: protein coding gene
Synonyms: Fam189b...Fam189b
Strict Orthology Symbols: fam189b
Entrep3em1(IMPC)Wtsi
(Mus musculus)Allele/Variant
Source: MGI:6281930
Genes: Entrep3 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Fam189b
(GRCh38)1:155247898C>T
(Homo sapiens)Allele/Variant
Source: rs201581173
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155247898C>T
Gene Synonyms: FAM189B
(GRCh38)1:155248222C>T
(Homo sapiens)Allele/Variant
Source: rs374893297
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155248222C>T
Gene Synonyms: FAM189B
(GRCh38)1:155254771G>A
(Homo sapiens)Allele/Variant
Source: rs139227082
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155254771G>A
Gene Synonyms: FAM189B
(GRCh38)1:155247853G>A
(Homo sapiens)Allele/Variant
Source: rs769066320
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155247853G>A
Gene Synonyms: FAM189B
(GRCh38)1:155250395C>A
(Homo sapiens)Allele/Variant
Source: rs1327518406
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155250395C>A
Gene Synonyms: FAM189B
(GRCh38)1:155250459C>A
(Homo sapiens)Allele/Variant
Source: rs926463771
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155250459C>A
Gene Synonyms: FAM189B
(GRCh38)1:155251844G>A
(Homo sapiens)Allele/Variant
Source: rs1290641562
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155251844G>A
Gene Synonyms: FAM189B
(GRCh38)1:155250627C>T
(Homo sapiens)Allele/Variant
Source: rs1240159655
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155250627C>T
Gene Synonyms: FAM189B
(GRCh38)1:155250804A>C
(Homo sapiens)Allele/Variant
Source: rs1672509873
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155250804A>C
Gene Synonyms: FAM189B
(GRCh38)1:155247808C>G
(Homo sapiens)Allele/Variant
Source: rs1281874766
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155247808C>G
Gene Synonyms: FAM189B
(GRCh38)1:155251892C>T
(Homo sapiens)Allele/Variant
Source: rs764049650
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155251892C>T
Gene Synonyms: FAM189B
(GRCh38)1:155253633C>T
(Homo sapiens)Allele/Variant
Source: rs754157328
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155253633C>T
Gene Synonyms: FAM189B
(GRCh38)1:155248262G>T
(Homo sapiens)Allele/Variant
Source: rs896478611
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155248262G>T
Gene Synonyms: FAM189B
(GRCh38)1:155250493C>A
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.155250493C>A
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155250493C>A
Gene Synonyms: FAM189B
(GRCh38)1:155253633C>G
(Homo sapiens)Allele/Variant
Source: rs754157328
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155253633C>G
Gene Synonyms: FAM189B
(GRCh38)1:155250405G>A
(Homo sapiens)Allele/Variant
Source: rs201687408
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155250405G>A
Gene Synonyms: FAM189B
(GRCh38)1:155251856G>T
(Homo sapiens)Allele/Variant
Source: rs374300931
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155251856G>T
Gene Synonyms: FAM189B
(GRCh38)1:155250576A>C
(Homo sapiens)Allele/Variant
Source: rs964087093
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155250576A>C
Gene Synonyms: FAM189B
(GRCh38)1:155248114C>T
(Homo sapiens)Allele/Variant
Source: rs201013021
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155248114C>T
Gene Synonyms: FAM189B
(GRCh38)1:155250608C>T
(Homo sapiens)Allele/Variant
Source: rs911612235
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155250608C>T
Gene Synonyms: FAM189B
(GRCh38)1:155247900C>A
(Homo sapiens)Allele/Variant
Source: rs750576160
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155247900C>A
Gene Synonyms: FAM189B
(GRCh38)1:155250357G>A
(Homo sapiens)Allele/Variant
Source: rs1192442103
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155250357G>A
Gene Synonyms: FAM189B
(GRCh38)1:155250674C>G
(Homo sapiens)Allele/Variant
Source: rs1313184100
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155250674C>G
Gene Synonyms: FAM189B
(GRCh38)1:155253638T>G
(Homo sapiens)Allele/Variant
Source: rs375507400
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155253638T>G
Gene Synonyms: FAM189B
(GRCh38)1:155250645C>T
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.155250645C>T
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155250645C>T
Gene Synonyms: FAM189B
(GRCh38)1:155251874A>C
(Homo sapiens)Allele/Variant
Source: rs775224298
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155251874A>C
Gene Synonyms: FAM189B
(GRCh38)1:155254787G>C
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.155254787G>C
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155254787G>C
Gene Synonyms: FAM189B
(GRCh38)1:155254733C>T
(Homo sapiens)Allele/Variant
Source: rs760569060
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155254733C>T
Gene Synonyms: FAM189B
(GRCh38)1:155247832G>A
(Homo sapiens)Allele/Variant
Source: rs539290757
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155247832G>A
Gene Synonyms: FAM189B
(GRCh38)1:155253915G>C
(Homo sapiens)Allele/Variant
Source: rs1311773662
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155253915G>C
Gene Synonyms: FAM189B
(GRCh38)1:155254093C>A
(Homo sapiens)Allele/Variant
Source: rs760232987
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155254093C>A
Gene Synonyms: FAM189B
(GRCh38)1:155254804C>T
(Homo sapiens)Allele/Variant
Source: rs1557921906
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155254804C>T
Gene Synonyms: FAM189B
(GRCh38)1:155250702C>T
(Homo sapiens)Allele/Variant
Source: rs1553221053
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155250702C>T
Gene Synonyms: FAM189B
(GRCh38)1:155254103T>G
(Homo sapiens)Allele/Variant
Source: rs545510572
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155254103T>G
Gene Synonyms: FAM189B
(GRCh38)1:155251838G>A
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.155251838G>A
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155251838G>A
Gene Synonyms: FAM189B
(GRCh38)1:155248154C>T
(Homo sapiens)Allele/Variant
Source: rs141883731
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155248154C>T
Gene Synonyms: FAM189B
(GRCh38)1:155250371G>A
(Homo sapiens)Allele/Variant
Source: rs1000466806
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155250371G>A
Gene Synonyms: FAM189B
(GRCh38)1:155254861C>G
(Homo sapiens)Allele/Variant
Source: rs1005762321
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155254861C>G
Gene Synonyms: FAM189B
(GRCh38)1:155250396T>C
(Homo sapiens)Allele/Variant
Source: rs1171140514
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155250396T>C
Gene Synonyms: FAM189B
(GRCh38)1:155251119C>G
(Homo sapiens)Allele/Variant
Source: rs1317123081
Genes: ENTREP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:155251119C>G
Gene Synonyms: FAM189B
(GRCm39)3:89091887C>T
(Mus musculus)Allele/Variant
Source: rs240589076
Genes: Entrep3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:89091887C>T
Gene Synonyms: Fam189b
(GRCm39)3:89092350G>T
(Mus musculus)Allele/Variant
Source: rs247268624
Genes: Entrep3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:89092350G>T
Gene Synonyms: Fam189b
(GRCm39)3:89090476T>A
(Mus musculus)Allele/Variant
Source: rs250827454
Genes: Entrep3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)3:89090476T>A
Gene Synonyms: Fam189b