Version: 8.0.0
Date: Tue Jan 28 2025
332 results for nkrf

Nkrf

(Mus musculus)
Gene
Name: NF-kappaB repressing factor
Synonyms: 9430034D17Rik, AW124770, C80287, expressed sequence AW124770, expressed sequence C80287, RIKEN cDNA 9430034D17 gene
Source: MGI:1924536
Biotype: protein coding gene
Symbol: Nkrf (Mmu)
Symbol: Nkrf
Automated Gene Synopsis: Orthologous to human NKRF (NFKB repressing factor).
Strict Orthology Symbols: nkrf
Alleles: Nkrf (Mmu)...Nkrf (Mmu)...Nkrf (Mmu)...Nkrf (Mmu)

nkrf

(Danio rerio)
Gene
Name: NFKB repressing factor
Synonyms: wu:fb75e05, si:bz46j2.5, nrf, fb75e05
Source: ZFIN:ZDB-GENE-030616-73
Biotype: protein coding gene
Symbol: nkrf (Dre)
Symbol: nkrf
Automated Gene Synopsis: Orthologous to human NKRF (NFKB repressing factor).
Strict Orthology Symbols: nkrf

NKRF

(Homo sapiens)
Gene
Name: NFKB repressing factor
Synonyms: ITBA4, nf-kappab repressing factor, NRF, NF-kappa-B-repressing factor, transcription factor NRF
Source: HGNC:19374
Biotype: protein coding gene
Symbol: NKRF (Hsa)
Symbol: NKRF
Strict Orthology Symbols: nkrf

Nkrf

(Rattus norvegicus)
Gene
Name: NFKB repressing factor
Synonyms: NF-kappa-B-repressing factor, LOC100910054, NF-kappa-B-repressing factor-like, NF-kappaB repressing factor
Source: RGD:6500424
Biotype: protein coding gene
Symbol: Nkrf (Rno)
Symbol: Nkrf
Gene Synopsis: Orthologous to human NKRF (NFKB repressing factor); INTERACTS WITH 17alpha-ethynylestradiol; amphetamine
Automated Gene Synopsis: Orthologous to human NKRF (NFKB repressing factor).
Strict Orthology Symbols: nkrf

nkrf

(Xenopus tropicalis)
Gene
Name: NFKB repressing factor
Synonyms: nkrf, NFKB repressing factor
Source: Xenbase:XB-GENE-877251
Biotype: gene
Symbol: nkrf
Symbol: nkrf (Xtr)
Automated Gene Synopsis: Orthologous to human NKRF (NFKB repressing factor).
Synonyms: nkrf...nkrf...nkrf
Strict Orthology Symbols: nkrf

nkrf.S

(Xenopus laevis)
Gene
Name: NFKB repressing factor
Synonyms: NFKB repressing factor, nkrf.S
Source: Xenbase:XB-GENE-17340659
Biotype: gene
Symbol: nkrf.S (Xla)
Automated Gene Synopsis: Orthologous to human NKRF (NFKB repressing factor).
Strict Orthology Symbols: nkrf
Symbol: nkrf.S

nkrf.L

(Xenopus laevis)
Gene
Name: NFKB repressing factor
Synonyms: nkrf.L, NFKB repressing factor
Source: Xenbase:XB-GENE-877259
Biotype: gene
Symbol: nkrf.L (Xla)
Automated Gene Synopsis: Orthologous to human NKRF (NFKB repressing factor).
Strict Orthology Symbols: nkrf
Symbol: nkrf.L

Nkrfem1Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7291319
Genes: Nkrf (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Nkrf (Mmu)
Genes: Nkrf (Mmu)
Symbol: Nkrfem1Smoc

Nkrftm1Hjh

(Mus musculus)
Allele/Variant
Source: MGI:3612956
Genes: Nkrf (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Nkrf (Mmu)
Genes: Nkrf (Mmu)
Symbol: Nkrftm1Hjh

Nkrftm1.1Hjh

(Mus musculus)
Allele/Variant
Source: MGI:3612957
Genes: Nkrf (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Nkrf (Mmu)
Genes: Nkrf (Mmu)
Symbol: Nkrftm1.1Hjh

Nkrfem1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7376920
Genes: Nkrf (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Nkrf (Mmu)
Genes: Nkrf (Mmu)
Symbol: Nkrfem1Gpt

Nkrftm1.1Hjh/Y [background:] involves: 129P2/OlaHsd * C57BL/6

(Mus musculus)
Model
Id: MGI:3616180
Synonyms: Not Available
Symbol: Nkrf/Y [background:] involves: 129P2/OlaHsd * C57BL/6 (Mmu)
Genes: Nkrf (Mmu)
Alleles: Nkrf (Mmu)
Name: Nkrf/Y [background:] involves: 129P2/OlaHsd * C57BL/6

Nkrftm1.1Hjh/Nkrftm1.1Hjh [background:] involves: 129P2/OlaHsd * C57BL/6

(Mus musculus)
Model
Id: MGI:3616179
Synonyms: Not Available
Symbol: Nkrf/Nkrf [background:] involves: 129P2/OlaHsd * C57BL/6 (Mmu)
Genes: Nkrf (Mmu)
Alleles: Nkrf (Mmu)
Name: Nkrf/Nkrf [background:] involves: 129P2/OlaHsd * C57BL/6

CG31301

(Drosophila melanogaster)
Gene
Name: Not Available
Synonyms: CG12258
Source: FB:FBgn0051301
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human NKRF (NFKB repressing factor).
Strict Orthology Symbols: nkrf

la012571Tg

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-120806-11169
Genes: nkrf (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: nkrf (Dre)

sa31995

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-1388
Genes: nkrf (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: nkrf (Dre)

ATPase activator activity

Gene Ontology
Source: GO:0001671
Synonyms:
  • ATPase stimulator activity
Branch: molecular function
Genes: NKRF (Hsa)...Nkrf (Mmu)...Nkrf (Rno)

DNA-binding transcription activator activity, RNA polymerase II-specific

Gene Ontology
Source: GO:0001228
Synonyms:
  • RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in positive regulation of transcription
  • RNA polymerase II distal enhancer sequence-specific DNA-binding transcription factor activity involved in positive regulation of transcription
Branch: molecular function
Genes: Nkrf (Rno)...NKRF (Hsa)...Nkrf (Mmu)

negative regulation of DNA-templated transcription

Gene Ontology
Source: GO:0045892
Synonyms:
  • down regulation of gene-specific transcription
  • down regulation of transcription, DNA-dependent
Branch: biological process
Genes: Nkrf (Rno)...NKRF (Hsa)...Nkrf (Mmu)

nucleolus

Gene Ontology
Source: GO:0005730
Synonyms: Not Available
Branch: cellular component
Genes: nkrf (Dre)...Nkrf (Mmu)...Nkrf (Rno)...NKRF (Hsa)

nucleic acid binding

Gene Ontology
Source: GO:0003676
Synonyms:
  • base pairing
Branch: molecular function
Genes: NKRF (Hsa)...nkrf (Dre)

positive regulation of transcription by RNA polymerase II

Gene Ontology
Source: GO:0045944
Synonyms:
  • activation of global transcription from RNA polymerase II promoter
  • activation of transcription from RNA polymerase II promoter
Branch: biological process
Genes: Nkrf (Mmu)...Nkrf (Rno)...NKRF (Hsa)

RNA polymerase II cis-regulatory region sequence-specific DNA binding

Gene Ontology
Source: GO:0000978
Synonyms:
  • RNA polymerase II core promoter proximal region sequence-specific DNA binding
  • RNA polymerase II distal enhancer sequence-specific DNA binding
Branch: molecular function
Genes: Nkrf (Mmu)...Nkrf (Rno)...NKRF (Hsa)

sa16364

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-4844
Genes: nkrf (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: nkrf (Dre)

nucleoplasm

Gene Ontology
Source: GO:0005654
Synonyms: Not Available
Branch: cellular component
Genes: nkrf (Dre)...Nkrf (Rno)...NKRF (Hsa)...Nkrf (Mmu)

sa16160

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-4668
Genes: nkrf (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: nkrf (Dre)

DNA binding

Gene Ontology
Source: GO:0003677
Synonyms:
  • microtubule/chromatin interaction
  • plasmid binding
Branch: molecular function
Genes: NKRF (Hsa)...Nkrf (Mmu)

RNA binding

Gene Ontology
Source: GO:0003723
Synonyms:
  • base pairing with RNA
  • poly(A) RNA binding
Branch: molecular function
Genes: NKRF (Hsa)

protein binding

Gene Ontology
Source: GO:0005515
Synonyms:
  • glycoprotein binding
  • protein amino acid binding
Branch: molecular function
Genes: NKRF (Hsa)

(GRCh38)X:119591267G>A

(Homo sapiens)
Allele/Variant
Source: rs199789706
Genes: NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119591267G>A

(GRCh38)X:119591313T>C

(Homo sapiens)
Allele/Variant
Source: rs376333657
Genes: NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119591313T>C

(GRCh38)X:119591202G>T

(Homo sapiens)
Allele/Variant
Source: rs775960180
Genes: NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119591202G>T

(GRCh38)X:119591248A>G

(Homo sapiens)
Allele/Variant
Source: rs371715100
Genes: NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119591248A>G

(GRCh38)X:119591223T>C

(Homo sapiens)
Allele/Variant
Source: rs1206472204
Genes: NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119591223T>C

(GRCh38)X:119605889T>A

(Homo sapiens)
Allele/Variant
Source: rs1031779475
Genes: NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119605889T>A

(GRCh38)X:119591264C>A

(Homo sapiens)
Allele/Variant
Source: rs2053523070
Genes: NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119591264C>A

(GRCh38)X:119591172C>T

(Homo sapiens)
Allele/Variant
Source: rs142683271
Genes: NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119591172C>T

(GRCh38)X:119605775G>C

(Homo sapiens)
Allele/Variant
Source: rs901890792
Genes: NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119605775G>C

(GRCh38)X:119605916C>G

(Homo sapiens)
Allele/Variant
Source: rs1309058454
Genes: NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119605916C>G

(GRCh38)X:119591250G>T

(Homo sapiens)
Allele/Variant
Source: NC_000023.11:g.119591250G>T
Genes: NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119591250G>T

(GRCh38)X:119592405T>C

(Homo sapiens)
Allele/Variant
Source: rs753806420
Genes: NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119592405T>C

(GRCh38)X:119589490A>G

(Homo sapiens)
Allele/Variant
Source: rs141456610
Genes: UBE2A (Hsa), NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119589490A>G

(GRCh38)X:119590450G>A

(Homo sapiens)
Allele/Variant
Source: rs2233498
Genes: UBE2A (Hsa), NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119590450G>A

(GRCh38)X:119589783G>T

(Homo sapiens)
Allele/Variant
Source: rs973390424
Genes: UBE2A (Hsa), NKRF (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)X:119589783G>T

(GRCh38)X:119590716T>C

(Homo sapiens)
Allele/Variant
Source: NC_000023.11:g.119590716T>C
Genes: UBE2A (Hsa), NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_retained_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119590716T>C

(GRCh38)X:119590377T>C

(Homo sapiens)
Allele/Variant
Source: rs2147389680
Genes: UBE2A (Hsa), NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119590377T>C

(GRCh38)X:119590542G>C

(Homo sapiens)
Allele/Variant
Source: rs145900751
Genes: UBE2A (Hsa), NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119590542G>C

(GRCh38)X:119590575G>A

(Homo sapiens)
Allele/Variant
Source: rs142006983
Genes: UBE2A (Hsa), NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119590575G>A

(GRCh38)X:119590812G>A

(Homo sapiens)
Allele/Variant
Source: NC_000023.11:g.119590812G>A
Genes: UBE2A (Hsa), NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119590812G>A

(GRCh38)X:119589771C>T

(Homo sapiens)
Allele/Variant
Source: NC_000023.11:g.119589771C>T
Genes: UBE2A (Hsa), NKRF (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:119589771C>T