Version: 8.1.0
Date: Fri Apr 18 2025
581 results for Fancd2os

Fancd2os

(Mus musculus)
Gene
Name: Fancd2 opposite strand
Synonyms: RGD1565997, RIKEN cDNA 4931417G12 gene, 4931417G12Rik
Source: MGI:1918229
Biotype: protein coding gene
Symbol: Fancd2os (Mmu)
Symbol: Fancd2os
Automated Gene Synopsis: Orthologous to human FANCD2OS (FANCD2 opposite strand).
Strict Orthology Symbols: Fancd2os
Alleles: Fancd2os (Mmu)

FANCD2OS

(Homo sapiens)
Gene
Name: FANCD2 opposite strand
Synonyms: MGC40179, Fanconi anemia group D2 protein opposite strand transcript protein, FANCD2 opposite strand protein, uncharacterized protein C3orf24, hypothetical protein LOC115795, C3orf24
Source: HGNC:28623
Biotype: protein coding gene
Symbol: FANCD2OS (Hsa)
Symbol: FANCD2OS
Strict Orthology Symbols: Fancd2os

Fancd2os

(Rattus norvegicus)
Gene
Name: FANCD2 opposite strand
Synonyms: RGD1565997, uncharacterized protein LOC500294, LOC500294, hypothetical protein LOC500294, similar to 4931417G12Rik protein
Source: RGD:1565997
Biotype: protein coding gene
Symbol: Fancd2os (Rno)
Symbol: Fancd2os
Gene Synopsis: Orthologous to human FANCD2OS (FANCD2 opposite strand); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine
Automated Gene Synopsis: Orthologous to human FANCD2OS (FANCD2 opposite strand).
Strict Orthology Symbols: Fancd2os

fancd2os

(Xenopus tropicalis)
Gene
Name: FANCD2 opposite strand
Synonyms: FANCD2 opposite strand, fancd2os
Source: Xenbase:XB-GENE-965507
Biotype: gene
Symbol: fancd2os (Xtr)
Symbol: fancd2os
Automated Gene Synopsis: Orthologous to human FANCD2OS (FANCD2 opposite strand).
Synonyms: fancd2os...fancd2os
Strict Orthology Symbols: Fancd2os

Fancd2osl2

(Rattus norvegicus)
Gene
Name: FANCD2 opposite strand like 2
Synonyms: FANCD2 opposite strand protein-like, LOC686095, hypothetical protein LOC686095
Source: RGD:1586601
Biotype: protein coding gene
Symbol: Fancd2osl2 (Rno)
Automated Gene Synopsis: Orthologous to human FANCD2OS (FANCD2 opposite strand).
Strict Orthology Symbols: Fancd2os
Symbol: Fancd2osl2

Fancd2osl1

(Rattus norvegicus)
Gene
Name: FANCD2 opposite strand like 1
Synonyms: LOC100910824, uncharacterized LOC100910824, LOC686031, hypothetical protein LOC686031, uncharacterized protein LOC686031
Source: RGD:1586665
Biotype: protein coding gene
Symbol: Fancd2osl1 (Rno)
Automated Gene Synopsis: Orthologous to human FANCD2OS (FANCD2 opposite strand).
Strict Orthology Symbols: Fancd2os
Symbol: Fancd2osl1

fancd2os.L

(Xenopus laevis)
Gene
Name: FANCD2 opposite strand
Synonyms: FANCD2 opposite strand, fancd2os.L
Source: Xenbase:XB-GENE-965510
Biotype: gene
Symbol: fancd2os.L (Xla)
Automated Gene Synopsis: Orthologous to human FANCD2OS (FANCD2 opposite strand).
Strict Orthology Symbols: FANCD2OS...fancd2os
Symbol: fancd2os.L

Fancd2ostm2a(EUCOMM)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:4840597
Genes: Fancd2os (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Fancd2os (Mmu)
Genes: Fancd2os (Mmu)
Symbol: Fancd2ostm2a(EUCOMM)Wtsi

LOC686042

(Rattus norvegicus)
Gene
Name: hypothetical protein LOC686042
Synonyms: FANCD2 opposite strand protein-like
Source: RGD:1586654
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human FANCD2OS (FANCD2 opposite strand).
Strict Orthology Symbols: Fancd2os

cellular_component

Gene Ontology
Source: GO:0005575
Synonyms:
  • cell or subcellular entity
  • cellular component
Branch: cellular component
Genes: Fancd2os (Mmu)

biological_process

Gene Ontology
Source: GO:0008150
Synonyms:
  • biological process
  • physiological process
Branch: biological process
Genes: Fancd2os (Mmu)

molecular_function

Gene Ontology
Source: GO:0003674
Synonyms:
  • molecular function
Branch: molecular function
Genes: Fancd2os (Mmu)

(GRCh38)3:10104414A>G

(Homo sapiens)
Allele/Variant
Source: rs138382980
Genes: FANCD2OS (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)3:10104414A>G

(GRCh38)3:10104764T>C

(Homo sapiens)
Allele/Variant
Source: rs148056567
Genes: FANCD2OS (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)3:10104764T>C

(GRCh38)3:10104621A>G

(Homo sapiens)
Allele/Variant
Source: rs371552916
Genes: FANCD2OS (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)3:10104621A>G

(GRCh38)3:10104729T>A

(Homo sapiens)
Allele/Variant
Source: rs534604820
Genes: FANCD2OS (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)3:10104729T>A

(GRCh38)3:10104537G>A

(Homo sapiens)
Allele/Variant
Source: rs141930678
Genes: FANCD2OS (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)3:10104537G>A

(GRCh38)3:10104647G>A

(Homo sapiens)
Allele/Variant
Source: rs185109881
Genes: FANCD2OS (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)3:10104647G>A

(GRCh38)3:10104693A>T

(Homo sapiens)
Allele/Variant
Source: rs745717436
Genes: FANCD2OS (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)3:10104693A>T

(GRCh38)3:10104312T>G

(Homo sapiens)
Allele/Variant
Source: NC_000003.12:g.10104312T>G
Genes: FANCD2OS (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)3:10104312T>G

(GRCh38)3:10104292C>G

(Homo sapiens)
Allele/Variant
Source: rs898418412
Genes: FANCD2OS (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)3:10104292C>G

(GRCh38)3:10104405A>G

(Homo sapiens)
Allele/Variant
Source: NC_000003.12:g.10104405A>G
Genes: FANCD2OS (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)3:10104405A>G

(GRCh38)3:10104380C>G

(Homo sapiens)
Allele/Variant
Source: rs139498249
Genes: FANCD2OS (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)3:10104380C>G

(mRatBN7.2)4:146746555C>G

(Rattus norvegicus)
Allele/Variant
Source: rs106731051
Genes: Fancd2os (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146746555C>G

(mRatBN7.2)4:146747547C>G

(Rattus norvegicus)
Allele/Variant
Source: rs106249619
Genes: Fancd2os (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146747547C>G

(GRCm39)6:113574359A>G

(Mus musculus)
Allele/Variant
Source: rs214283306
Genes: Fancd2os (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)6:113574359A>G

(GRCm39)6:113577701T>C

(Mus musculus)
Allele/Variant
Source: rs232857464
Genes: Fancd2os (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)6:113577701T>C

(GRCm39)6:113577117G>A

(Mus musculus)
Allele/Variant
Source: rs246839610
Genes: Fancd2os (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)6:113577117G>A

(GRCm39)6:113576370G>A

(Mus musculus)
Allele/Variant
Source: rs36747274
Genes: Fancd2os (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)6:113576370G>A

(GRCm39)6:113575202C>A

(Mus musculus)
Allele/Variant
Source: rs259591873
Genes: Fancd2os (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)6:113575202C>A

(GRCm39)6:113575518A>G

(Mus musculus)
Allele/Variant
Source: rs256694587
Genes: Fancd2os (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)6:113575518A>G

(GRCm39)6:113575911T>C

(Mus musculus)
Allele/Variant
Source: rs219918222
Genes: Fancd2os (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)6:113575911T>C

(GRCm39)6:113576437T>G

(Mus musculus)
Allele/Variant
Source: rs215611033
Genes: Fancd2os (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)6:113576437T>G

(mRatBN7.2)4:146743881T>G

(Rattus norvegicus)
Allele/Variant
Source: rs106485188
Genes: Fancd2os (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146743881T>G

(mRatBN7.2)4:146744478G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320316130
Genes: Fancd2os (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146744478G>A

(mRatBN7.2)4:146745721T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320316167
Genes: Fancd2os (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146745721T>C

(mRatBN7.2)4:146745839A>G

(Rattus norvegicus)
Allele/Variant
Source: rs199343847
Genes: Fancd2os (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146745839A>G

(mRatBN7.2)4:146744519G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320298334
Genes: Fancd2os (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146744519G>A

(mRatBN7.2)4:146747325A>G

(Rattus norvegicus)
Allele/Variant
Source: rs107149685
Genes: Fancd2os (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146747325A>G

(mRatBN7.2)4:146744356C>A

(Rattus norvegicus)
Allele/Variant
Source: rs105094003
Genes: Fancd2os (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146744356C>A

(GRCm39)6:113575101A>T

(Mus musculus)
Allele/Variant
Source: rs246824472
Genes: Fancd2os (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)6:113575101A>T

(GRCm39)6:113575103C>A

(Mus musculus)
Allele/Variant
Source: rs226949007
Genes: Fancd2os (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)6:113575103C>A

(GRCm39)6:113575517C>T

(Mus musculus)
Allele/Variant
Source: rs228204113
Genes: Fancd2os (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)6:113575517C>T

(mRatBN7.2)4:146746452A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106651640
Genes: Fancd2os (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146746452A>G

(mRatBN7.2)4:146746471G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198932707
Genes: Fancd2os (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146746471G>A

(mRatBN7.2)4:146744119A>T

(Rattus norvegicus)
Allele/Variant
Source: rs107393878
Genes: Fancd2os (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146744119A>T

(mRatBN7.2)4:146745563G>T

(Rattus norvegicus)
Allele/Variant
Source: rs106487283
Genes: Fancd2os (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146745563G>T

(mRatBN7.2)4:146745576G>A

(Rattus norvegicus)
Allele/Variant
Source: rs106302905
Genes: Fancd2os (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146745576G>A

(mRatBN7.2)4:146744523T>C

(Rattus norvegicus)
Allele/Variant
Source: rs105135643
Genes: Fancd2os (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146744523T>C

(GRCm39)6:113575192G>A

(Mus musculus)
Allele/Variant
Source: rs239037715
Genes: Fancd2os (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)6:113575192G>A