Version: 8.0.0
Date: Tue Jan 28 2025
391 results for fam92b

cibar2.L

(Xenopus laevis)
Gene
Name: CBY1 interacting BAR domain containing 2
Synonyms: fam92b, CBY1 interacting BAR domain containing 2, cibar2.L
Source: Xenbase:XB-GENE-6488495
Biotype: gene
Synonyms: fam92b...fam92b...fam92b

cibar2.S

(Xenopus laevis)
Gene
Name: CBY1 interacting BAR domain containing 2
Synonyms: fam92b, cibar2.S, CBY1 interacting BAR domain containing 2
Source: Xenbase:XB-GENE-17346393
Biotype: gene
Synonyms: fam92b...fam92b...fam92b

cibar2

(Xenopus tropicalis)
Gene
Name: CBY1 interacting BAR domain containing 2
Synonyms: cibar2, fam92b, CBY1 interacting BAR domain containing 2
Source: Xenbase:XB-GENE-6044519
Biotype: gene
Synonyms: fam92b...fam92b...fam92b

CIBAR2

(Homo sapiens)
Gene
Name: CBY1 interacting BAR domain containing 2
Synonyms: family with sequence similarity 92, member B, FLJ44299, MGC138149, CBY1-interacting BAR domain-containing protein 2, family with sequence similarity 92 member B, FAM92B, hypothetical protein LOC339145
Source: HGNC:24781
Biotype: protein coding gene
Synonyms: FAM92B...FAM92B

Cibar2

(Mus musculus)
Gene
Name: CBY1 interacting BAR domain containing 2
Synonyms: family with sequence similarity 92, member B, RGD1560673, 1700120B06Rik, RIKEN cDNA 1700120B06 gene, Fam92b
Source: MGI:3588213
Biotype: protein coding gene
Synonyms: Fam92b...Fam92b

Cibar2

(Rattus norvegicus)
Gene
Name: CBY1 interacting BAR domain containing 2
Synonyms: LOC361423, family with sequence similarity 92, member B, similar to FLJ44299 protein, RGD1560673, CBY1-interacting BAR domain-containing protein 2, Fam92b
Source: RGD:1560673
Biotype: protein coding gene
Synonyms: Fam92b...Fam92b

Cibar2tm1e(EUCOMM)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:5296610
Genes: Cibar2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Fam92b

Cibar2em1Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7750507
Genes: Cibar2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Fam92b

(GRCh38)16:85102245A>C

(Homo sapiens)
Allele/Variant
Source: rs372377482
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85102245A>C
Gene Synonyms: FAM92B

(GRCh38)16:85102294C>A

(Homo sapiens)
Allele/Variant
Source: rs779231383
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85102294C>A
Gene Synonyms: FAM92B

(GRCh38)16:85100179G>C

(Homo sapiens)
Allele/Variant
Source: rs148969047
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85100179G>C
Gene Synonyms: FAM92B

(GRCh38)16:85107898A>C

(Homo sapiens)
Allele/Variant
Source: rs144820922
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85107898A>C
Gene Synonyms: FAM92B

(GRCh38)16:85110257A>G

(Homo sapiens)
Allele/Variant
Source: rs1375125387
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85110257A>G
Gene Synonyms: FAM92B

(GRCh38)16:85110272C>T

(Homo sapiens)
Allele/Variant
Source: rs140432540
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85110272C>T
Gene Synonyms: FAM92B

(GRCh38)16:85100156G>A

(Homo sapiens)
Allele/Variant
Source: rs553906448
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85100156G>A
Gene Synonyms: FAM92B

(GRCh38)16:85107946G>C

(Homo sapiens)
Allele/Variant
Source: rs1037408892
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85107946G>C
Gene Synonyms: FAM92B

(GRCh38)16:85108092C>T

(Homo sapiens)
Allele/Variant
Source: rs2074011634
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85108092C>T
Gene Synonyms: FAM92B

(GRCh38)16:85108083G>A

(Homo sapiens)
Allele/Variant
Source: rs776711053
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85108083G>A
Gene Synonyms: FAM92B

(GRCh38)16:85110294C>T

(Homo sapiens)
Allele/Variant
Source: rs750472893
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85110294C>T
Gene Synonyms: FAM92B

(GRCh38)16:85105391C>T

(Homo sapiens)
Allele/Variant
Source: rs371379522
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85105391C>T
Gene Synonyms: FAM92B

(GRCh38)16:85107862G>A

(Homo sapiens)
Allele/Variant
Source: rs769846324
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85107862G>A
Gene Synonyms: FAM92B

(GRCh38)16:85108054C>T

(Homo sapiens)
Allele/Variant
Source: rs199599166
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85108054C>T
Gene Synonyms: FAM92B

(GRCh38)16:85099318G>T

(Homo sapiens)
Allele/Variant
Source: rs557088845
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85099318G>T
Gene Synonyms: FAM92B

(GRCh38)16:85112343C>T

(Homo sapiens)
Allele/Variant
Source: rs141128357
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85112343C>T
Gene Synonyms: FAM92B

(GRCh38)16:85102303T>C

(Homo sapiens)
Allele/Variant
Source: rs764104108
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85102303T>C
Gene Synonyms: FAM92B

(GRCh38)16:85107896C>T

(Homo sapiens)
Allele/Variant
Source: rs267604672
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained
Diseases: Not Available
Variant Name: (GRCh38)16:85107896C>T
Gene Synonyms: FAM92B

(GRCh38)16:85099343T>C

(Homo sapiens)
Allele/Variant
Source: rs570833878
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85099343T>C
Gene Synonyms: FAM92B

(GRCh38)16:85102232G>C

(Homo sapiens)
Allele/Variant
Source: rs61740642
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85102232G>C
Gene Synonyms: FAM92B

(GRCh38)16:85102240T>C

(Homo sapiens)
Allele/Variant
Source: rs368472969
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85102240T>C
Gene Synonyms: FAM92B

(GRCh38)16:85107856T>G

(Homo sapiens)
Allele/Variant
Source: rs771505314
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85107856T>G
Gene Synonyms: FAM92B

(GRCh38)16:85110318C>T

(Homo sapiens)
Allele/Variant
Source: rs141444139
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85110318C>T
Gene Synonyms: FAM92B

(GRCh38)16:85110359C>A

(Homo sapiens)
Allele/Variant
Source: rs748006465
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85110359C>A
Gene Synonyms: FAM92B

(GRCh38)16:85110423T>C

(Homo sapiens)
Allele/Variant
Source: rs769416097
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85110423T>C
Gene Synonyms: FAM92B

(GRCh38)16:85099192G>C

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.85099192G>C
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85099192G>C
Gene Synonyms: FAM92B

(GRCh38)16:85099195T>C

(Homo sapiens)
Allele/Variant
Source: rs767350357
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85099195T>C
Gene Synonyms: FAM92B

(GRCh38)16:85099220C>T

(Homo sapiens)
Allele/Variant
Source: rs375070462
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85099220C>T
Gene Synonyms: FAM92B

(GRCh38)16:85100221T>A

(Homo sapiens)
Allele/Variant
Source: rs1370956718
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained
Diseases: Not Available
Variant Name: (GRCh38)16:85100221T>A
Gene Synonyms: FAM92B

(GRCh38)16:85108051C>T

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.85108051C>T
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85108051C>T
Gene Synonyms: FAM92B

(GRCh38)16:85110455C>A

(Homo sapiens)
Allele/Variant
Source: rs1004244141
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85110455C>A
Gene Synonyms: FAM92B

(GRCh38)16:85110386A>C

(Homo sapiens)
Allele/Variant
Source: rs773751395
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85110386A>C
Gene Synonyms: FAM92B

(GRCh38)16:85110407A>T

(Homo sapiens)
Allele/Variant
Source: rs199902827
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85110407A>T
Gene Synonyms: FAM92B

(GRCh38)16:85110371C>T

(Homo sapiens)
Allele/Variant
Source: rs758180795
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85110371C>T
Gene Synonyms: FAM92B

(GRCh38)16:85099319C>A

(Homo sapiens)
Allele/Variant
Source: rs999155595
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85099319C>A
Gene Synonyms: FAM92B

(GRCh38)16:85100147C>T

(Homo sapiens)
Allele/Variant
Source: rs759998712
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85100147C>T
Gene Synonyms: FAM92B

(GRCh38)16:85108032C>T

(Homo sapiens)
Allele/Variant
Source: rs148587987
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85108032C>T
Gene Synonyms: FAM92B

(GRCh38)16:85110365G>A

(Homo sapiens)
Allele/Variant
Source: rs201987292
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85110365G>A
Gene Synonyms: FAM92B

(GRCh38)16:85099298G>T

(Homo sapiens)
Allele/Variant
Source: rs1173482017
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85099298G>T
Gene Synonyms: FAM92B

(GRCh38)16:85110298G>T

(Homo sapiens)
Allele/Variant
Source: rs145597678
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85110298G>T
Gene Synonyms: FAM92B

(GRCh38)16:85102326T>C

(Homo sapiens)
Allele/Variant
Source: rs375222323
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85102326T>C
Gene Synonyms: FAM92B

(GRCh38)16:85110297G>A

(Homo sapiens)
Allele/Variant
Source: rs149617066
Genes: CIBAR2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:85110297G>A
Gene Synonyms: FAM92B