104 results for foxn4
Allele/Variant Molecular Consequence: intron 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)

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

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

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

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

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)12:42359769A>T

(Rattus norvegicus)
Allele/Variant
Source: rs107507561
Genes: Foxn4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:42359769A>T

(mRatBN7.2)12:42353319G>A

(Rattus norvegicus)
Allele/Variant
Source: rs107006826
Genes: Foxn4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:42353319G>A

Allele/Variant
Source: rs213540675
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114394934A>G

Allele/Variant
Source: rs248925923
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114397874T>C

Allele/Variant
Source: rs223645865
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114412482C>T

Allele/Variant
Source: rs247437732
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114392581T>C

Allele/Variant
Source: rs255850903
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114393158T>C

Allele/Variant
Source: rs241494395
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114392480G>T

Allele/Variant
Source: rs29728631
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114392730G>A

Allele/Variant
Source: rs214473805
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114393478G>A

(mRatBN7.2)12:42358721G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322284600
Genes: Foxn4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:42358721G>A

Allele/Variant
Source: rs230992984
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114412300A>G

Allele/Variant
Source: rs211930143
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114392977T>C

Allele/Variant
Source: rs263732762
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114394862A>C

Allele/Variant
Source: rs223063822
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114411764G>A

Allele/Variant
Source: rs251709037
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114393305G>A

Allele/Variant
Source: rs243008922
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114399204G>A

Allele/Variant
Source: rs219275691
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114393744G>C

Allele/Variant
Source: rs33168262
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114401137A>C

Allele/Variant
Source: rs224761473
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114399249T>A

(mRatBN7.2)12:42337824T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322090734
Genes: Foxn4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:42337824T>C

Allele/Variant
Source: rs216540873
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114393633G>A

Allele/Variant
Source: rs261813850
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114411923T>A

Allele/Variant
Source: rs578447704
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114392260A>T

Allele/Variant
Source: rs48798524
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114392909C>G

Allele/Variant
Source: rs33116175
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114393049T>C

Allele/Variant
Source: rs46179798
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114393147A>G

Allele/Variant
Source: rs232488167
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114399006G>A

Allele/Variant
Source: rs219600609
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114396660C>T

Allele/Variant
Source: rs263739988
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114392528C>T

Allele/Variant
Source: rs33195720
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114393518A>G

Allele/Variant
Source: rs245675848
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114411919C>T

Allele/Variant
Source: rs265519377
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114412297A>T

Allele/Variant
Source: rs585260386
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114392838C>T

Allele/Variant
Source: rs49910156
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114393123C>T

Allele/Variant
Source: rs232745320
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114392802T>C

Allele/Variant
Source: rs262243005
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114393149G>A

Allele/Variant
Source: rs224911869
Genes: Foxn4 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)5:114394963A>G