Version: 8.0.0
Date: Tue Jan 28 2025
715 results for foxn4
Allele/Variant

Foxn4em1(IMPC)Ccpcz

(Mus musculus)
Allele/Variant
Source: MGI:7431369
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Foxn4 (Mmu)
Genes: Foxn4 (Mmu)
Symbol: Foxn4em1(IMPC)Ccpcz

Foxn4tm1Xia

(Mus musculus)
Allele/Variant
Source: MGI:3054789
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Foxn4 (Mmu)
Genes: Foxn4 (Mmu)
Symbol: Foxn4tm1Xia

Foxn4em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7299243
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Foxn4 (Mmu)
Genes: Foxn4 (Mmu)
Symbol: Foxn4em1Gpt

tm117c

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-980203-1815
Genes: foxn4 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: foxn4 (Dre)

Tg(Foxn4-icre)1Smal

(Mus musculus)
Allele/Variant
Source: MGI:4838412
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Tg(Foxn4-icre)1Smal
Construct Regulatory Region: Foxn4

Tg(Foxn4-cre)1Xia

(Mus musculus)
Allele/Variant
Source: MGI:4867445
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Tg(Foxn4-cre)1Xia
Construct Regulatory Region: Foxn4 (Mmu)

(GRCh38)12:109279819G>A

(Homo sapiens)
Allele/Variant
Source: rs761568029
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109279819G>A
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109281685C>G

(Homo sapiens)
Allele/Variant
Source: rs769676620
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109281685C>G
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109285333G>T

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.109285333G>T
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109285333G>T
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109290186C>A

(Homo sapiens)
Allele/Variant
Source: rs1332686599
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109290186C>A
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109287939C>T

(Homo sapiens)
Allele/Variant
Source: rs551517487
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109287939C>T
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109281437C>T

(Homo sapiens)
Allele/Variant
Source: rs757089691
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109281437C>T
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109281538G>A

(Homo sapiens)
Allele/Variant
Source: rs778183505
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109281538G>A
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109290252C>T

(Homo sapiens)
Allele/Variant
Source: rs1297168227
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109290252C>T
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109279835C>T

(Homo sapiens)
Allele/Variant
Source: rs1002698716
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109279835C>T
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109281774G>C

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.109281774G>C
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109281774G>C
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109285436T>G

(Homo sapiens)
Allele/Variant
Source: rs147176302
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109285436T>G
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109287436A>C

(Homo sapiens)
Allele/Variant
Source: rs999794714
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109287436A>C
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109281776C>T

(Homo sapiens)
Allele/Variant
Source: rs267603292
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109281776C>T
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109285418G>A

(Homo sapiens)
Allele/Variant
Source: rs756382561
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109285418G>A
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109285510G>A

(Homo sapiens)
Allele/Variant
Source: rs764687840
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109285510G>A
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109287434G>A

(Homo sapiens)
Allele/Variant
Source: rs999160211
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109287434G>A
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109279834C>A

(Homo sapiens)
Allele/Variant
Source: rs375715687
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109279834C>A
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109281638A>G

(Homo sapiens)
Allele/Variant
Source: rs757579785
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109281638A>G
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109281736T>C

(Homo sapiens)
Allele/Variant
Source: rs1385671217
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109281736T>C
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109287485G>A

(Homo sapiens)
Allele/Variant
Source: rs958198313
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109287485G>A
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109281509G>T

(Homo sapiens)
Allele/Variant
Source: rs201494583
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109281509G>T
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109281749C>T

(Homo sapiens)
Allele/Variant
Source: rs748968074
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109281749C>T
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109281755G>A

(Homo sapiens)
Allele/Variant
Source: rs139066057
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109281755G>A
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109290203A>G

(Homo sapiens)
Allele/Variant
Source: rs2047754073
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109290203A>G
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109285334C>T

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.109285334C>T
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109285334C>T
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109288135C>T

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.109288135C>T
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109288135C>T
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109308239T>C

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.109308239T>C
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109308239T>C
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109281718A>G

(Homo sapiens)
Allele/Variant
Source: rs762356924
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109281718A>G
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109286689C>T

(Homo sapiens)
Allele/Variant
Source: rs750462584
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109286689C>T
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109279877C>T

(Homo sapiens)
Allele/Variant
Source: rs144504080
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109279877C>T
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109281617G>A

(Homo sapiens)
Allele/Variant
Source: rs571119975
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109281617G>A
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109287502C>T

(Homo sapiens)
Allele/Variant
Source: rs751654854
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109287502C>T
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109287905G>A

(Homo sapiens)
Allele/Variant
Source: rs763259820
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109287905G>A
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109279753G>A

(Homo sapiens)
Allele/Variant
Source: rs750298439
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109279753G>A
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109287857G>A

(Homo sapiens)
Allele/Variant
Source: rs745671013
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109287857G>A
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109287866G>A

(Homo sapiens)
Allele/Variant
Source: rs982248955
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109287866G>A
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109281416C>T

(Homo sapiens)
Allele/Variant
Source: rs200750509
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109281416C>T
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109281464C>T

(Homo sapiens)
Allele/Variant
Source: rs369321450
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109281464C>T
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109285491C>T

(Homo sapiens)
Allele/Variant
Source: rs267603293
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109285491C>T
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109281725G>A

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.109281725G>A
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109281725G>A
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

(GRCh38)12:109281590G>C

(Homo sapiens)
Allele/Variant
Source: rs765143345
Genes: FOXN4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109281590G>C
Gene Synonyms: forkhead/winged helix transcription factor FOXN4

sa33562

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-2476
Genes: foxn4 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: foxn4 (Dre)

s644

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-080710-1
Genes: foxn4 (Dre)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: frameshift_variant
Diseases: Not Available
Variant Name: Not Available
Genes: foxn4 (Dre)

(mRatBN7.2)12:42347901G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321894333
Genes: Foxn4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:42347901G>A