Version: 8.0.0
Date: Tue Jan 28 2025
426 results for nfatc2ip

Nfatc2ip

(Rattus norvegicus)
Gene
Name: nuclear factor of activated T-cells 2 interacting protein
Synonyms: MGC93987, NFATC2-interacting protein, nuclear factor of activated T-cells, cytoplasmic 2-interacting protein, nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 2 interacting protein
Source: RGD:1359096
Biotype: protein coding gene
Symbol: Nfatc2ip (Rno)
Symbol: Nfatc2ip
Gene Synopsis: Orthologous to human NFATC2IP (nuclear factor of activated T cells 2 interacting protein); INTERACTS
Automated Gene Synopsis: Orthologous to human NFATC2IP (nuclear factor of activated T cells 2 interacting protein).
Strict Orthology Symbols: nfatc2ip

NFATC2IP

(Homo sapiens)
Gene
Name: nuclear factor of activated T cells 2 interacting protein
Synonyms: 45 kDa NF-AT-interacting protein, MGC126790, NFATC2-interacting protein, MGC138387, nuclear factor of activated T-cells, cytoplasmic 2-interacting protein, FLJ14639, 45 kDa NFAT-interacting protein, NIP45, RAD60, ESC2
Source: HGNC:25906
Biotype: protein coding gene
Symbol: NFATC2IP (Hsa)
Symbol: NFATC2IP
Strict Orthology Symbols: nfatc2ip

Nfatc2ip

(Mus musculus)
Gene
Name: nuclear factor of activated T cells, cytoplasmic, calcineurin dependent 2 interacting protein
Synonyms: DNA segment, Chr 7, ERATO Doi 304, expressed, D7Ertd304e, NIP45
Source: MGI:1329015
Biotype: protein coding gene
Symbol: Nfatc2ip (Mmu)
Symbol: Nfatc2ip
Automated Gene Synopsis: Orthologous to human NFATC2IP (nuclear factor of activated T cells 2 interacting protein).
Strict Orthology Symbols: nfatc2ip
Alleles: Nfatc2ip (Mmu)...Nfatc2ip (Mmu)...Nfatc2ip (Mmu)...Nfatc2ip (Mmu)

nfatc2ip

(Danio rerio)
Gene
Name: nuclear factor of activated T cells 2 interacting protein
Synonyms: wu:fj84d09
Source: ZFIN:ZDB-GENE-030131-9520
Biotype: protein coding gene
Symbol: nfatc2ip (Dre)
Symbol: nfatc2ip
Automated Gene Synopsis: Orthologous to human NFATC2IP (nuclear factor of activated T cells 2 interacting protein).
Strict Orthology Symbols: NFATC2IP...Nfatc2ip

NFATC2IP-AS1

(Homo sapiens)
Gene
Name: NFATC2IP antisense RNA 1
Synonyms: Not Available
Source: HGNC:56085
Biotype: ncRNA gene
Symbol: NFATC2IP-AS1 (Hsa)
Symbol: NFATC2IP-AS1

Nfatc2ipem2Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7302984
Genes: Nfatc2ip (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Nfatc2ip (Mmu)
Genes: Nfatc2ip (Mmu)
Symbol: Nfatc2ipem2Gpt

Nfatc2ipem1(IMPC)Ics

(Mus musculus)
Allele/Variant
Source: MGI:6336082
Genes: Nfatc2ip (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Nfatc2ip (Mmu)
Genes: Nfatc2ip (Mmu)
Symbol: Nfatc2ipem1(IMPC)Ics

Nfatc2iptm1.1Glm

(Mus musculus)
Allele/Variant
Source: MGI:4437260
Genes: Nfatc2ip (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Nfatc2ip (Mmu)
Genes: Nfatc2ip (Mmu)
Symbol: Nfatc2iptm1.1Glm

Nfatc2ipem1Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7291294
Genes: Nfatc2ip (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Nfatc2ip (Mmu)
Genes: Nfatc2ip (Mmu)
Symbol: Nfatc2ipem1Smoc

Nfatc2ipem1(IMPC)Ics/Nfatc2ipem1(IMPC)Ics [background:] C57BL/6N-Nfatc2ipem1(IMPC)Ics/Ics

(Mus musculus)
Model
Id: MGI:6408532
Synonyms: Not Available
Symbol: Nfatc2ip/Nfatc2ip [background:] C57BL/6N-Nfatc2ip/Ics (Mmu
Genes: Nfatc2ip (Mmu)
Alleles: Nfatc2ip (Mmu)
Name: Nfatc2ip/Nfatc2ip [background:] C57BL/6N-Nfatc2ip/Ics

Nfatc2iptm1.1Glm/Nfatc2iptm1.1Glm [background:] either: B6.129-Nfatc2iptm1.1Glm or C.129-Nfatc2iptm1.1Glm

(Mus musculus)
Model
Id: MGI:4437262
Synonyms: Not Available
Symbol: Nfatc2ip/Nfatc2ip [background:] either: B6.129-Nfatc2ip or C.129-Nfatc2ip
Genes: Nfatc2ip (Mmu)
Alleles: Nfatc2ip (Mmu)
Name: Nfatc2ip/Nfatc2ip [background:] either: B6.129-Nfatc2ip or C.129-Nfatc2ip

cytokine production

Gene Ontology
Source: GO:0001816
Synonyms:
  • cytokine biosynthetic process
  • cytokine metabolic process
Branch: biological process
Genes: Nfatc2ip (Mmu)

protein sumoylation

Gene Ontology
Source: GO:0016925
Synonyms:
  • SUMO-protein conjugation
  • Smt3-protein conjugation
Branch: biological process
Genes: NFATC2IP (Hsa)

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: Nfatc2ip (Rno)...NFATC2IP (Hsa)...Nfatc2ip (Mmu)...nfatc2ip (Dre)

sa38377

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-15871
Genes: nfatc2ip (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_region_variant, stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: nfatc2ip (Dre)

sa40020

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-6336
Genes: nfatc2ip (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: nfatc2ip (Dre)

cytoplasm

Gene Ontology
Source: GO:0005737
Synonyms: Not Available
Branch: cellular component
Genes: Nfatc2ip (Mmu)...Nfatc2ip (Rno)...NFATC2IP (Hsa)

protein binding

Gene Ontology
Source: GO:0005515
Synonyms:
  • glycoprotein binding
  • protein amino acid binding
Branch: molecular function
Genes: NFATC2IP (Hsa)...Nfatc2ip (Mmu)

(GRCh38)16:28951022C>T

(Homo sapiens)
Allele/Variant
Source: rs552799873
Genes: NFATC2IP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28951022C>T

(GRCh38)16:28956031C>T

(Homo sapiens)
Allele/Variant
Source: rs138977975
Genes: NFATC2IP (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)16:28956031C>T

(GRCh38)16:28951340G>T

(Homo sapiens)
Allele/Variant
Source: rs940951480
Genes: NFATC2IP (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)16:28951340G>T

(GRCh38)16:28951184T>G

(Homo sapiens)
Allele/Variant
Source: rs1020176693
Genes: NFATC2IP (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)16:28951184T>G

(GRCh38)16:28952199A>C

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.28952199A>C
Genes: NFATC2IP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28952199A>C

(GRCh38)16:28951394G>A

(Homo sapiens)
Allele/Variant
Source: rs1303198814
Genes: NFATC2IP (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)16:28951394G>A

(GRCh38)16:28951153G>A

(Homo sapiens)
Allele/Variant
Source: rs766415125
Genes: NFATC2IP (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)16:28951153G>A

(GRCh38)16:28963727T>G

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.28963727T>G
Genes: NFATC2IP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28963727T>G

(GRCh38)16:28951091G>C

(Homo sapiens)
Allele/Variant
Source: rs886706741
Genes: NFATC2IP (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)16:28951091G>C

(GRCh38)16:28951235C>G

(Homo sapiens)
Allele/Variant
Source: rs1008261550
Genes: NFATC2IP (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)16:28951235C>G

(GRCh38)16:28951253C>T

(Homo sapiens)
Allele/Variant
Source: rs1331244609
Genes: NFATC2IP (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)16:28951253C>T

(GRCh38)16:28951127C>T

(Homo sapiens)
Allele/Variant
Source: rs1964960631
Genes: NFATC2IP (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)16:28951127C>T

(GRCh38)16:28956299C>T

(Homo sapiens)
Allele/Variant
Source: rs555198250
Genes: NFATC2IP (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)16:28956299C>T

(GRCh38)16:28958843G>A

(Homo sapiens)
Allele/Variant
Source: rs1596730286
Genes: NFATC2IP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28958843G>A

(GRCh38)16:28956039C>T

(Homo sapiens)
Allele/Variant
Source: rs149606880
Genes: NFATC2IP (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)16:28956039C>T

(GRCh38)16:28956275C>T

(Homo sapiens)
Allele/Variant
Source: rs150870153
Genes: NFATC2IP (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)16:28956275C>T

(GRCh38)16:28956306G>A

(Homo sapiens)
Allele/Variant
Source: rs1231809953
Genes: NFATC2IP (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)16:28956306G>A

(GRCh38)16:28954583C>T

(Homo sapiens)
Allele/Variant
Source: rs376638547
Genes: NFATC2IP (Hsa), NFATC2IP-AS1 (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)16:28954583C>T

(mRatBN7.2)1:180961678A>G

(Rattus norvegicus)
Allele/Variant
Source: rs198325555
Genes: Nfatc2ip (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:180961678A>G

(mRatBN7.2)1:180968100G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319132627
Genes: Nfatc2ip (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:180968100G>A

(mRatBN7.2)1:180968852T>C

(Rattus norvegicus)
Allele/Variant
Source: rs105048499
Genes: Nfatc2ip (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:180968852T>C

(mRatBN7.2)1:180963199T>C

(Rattus norvegicus)
Allele/Variant
Source: rs107498976
Genes: Nfatc2ip (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:180963199T>C

(mRatBN7.2)1:180964731C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105775288
Genes: Nfatc2ip (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:180964731C>T

(mRatBN7.2)1:180965989G>A

(Rattus norvegicus)
Allele/Variant
Source: rs199405500
Genes: Nfatc2ip (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:180965989G>A

(mRatBN7.2)1:180970966T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3319108654
Genes: Nfatc2ip (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:180970966T>C

(mRatBN7.2)1:180971675T>C

(Rattus norvegicus)
Allele/Variant
Source: rs199267050
Genes: Nfatc2ip (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:180971675T>C

(GRCm39)7:125987618C>T

(Mus musculus)
Allele/Variant
Source: rs215299226
Genes: Nfatc2ip (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)7:125987618C>T

(GRCm39)7:125991413C>A

(Mus musculus)
Allele/Variant
Source: rs234672850
Genes: Nfatc2ip (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)7:125991413C>A

(mRatBN7.2)1:180969707T>C

(Rattus norvegicus)
Allele/Variant
Source: rs198143918
Genes: Nfatc2ip (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:180969707T>C

(mRatBN7.2)1:180966482G>A

(Rattus norvegicus)
Allele/Variant
Source: rs107417325
Genes: Nfatc2ip (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:180966482G>A

(mRatBN7.2)1:180968580C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105598627
Genes: Nfatc2ip (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:180968580C>T

(mRatBN7.2)1:180956078C>T

(Rattus norvegicus)
Allele/Variant
Source: rs104935643
Genes: Nfatc2ip (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:180956078C>T