Version: 8.0.0Date: Tue Jan 28 2025
Category
Frmd4a
(Rattus norvegicus)Gene
Name: FERM domain containing 4A
Synonyms: similar to mKIAA1294 protein, RGD1309050, LOC307128, FERM domain-containing protein 4A
Source: RGD:1309050
Biotype: protein coding gene
Symbol: Frmd4a (Rno)
Symbol: Frmd4a
Gene Synopsis: Orthologous to human FRMD4A (FERM domain containing 4A); INTERACTS WITH 2,4-dinitrotoluene; 6-propyl-
Automated Gene Synopsis: Orthologous to human FRMD4A (FERM domain containing 4A).
Strict Orthology Symbols: frmd4a
FRMD4A
(Homo sapiens)Gene
Name: FERM domain containing 4A
Synonyms: CCAFCA, FRMD4, bA295P9.4, FLJ10210, FERM domain containing 4, RP11-397C18.4, FERM domain-containing protein 4A, KIAA1294
Source: HGNC:25491
Biotype: protein coding gene
Symbol: FRMD4A (Hsa)
Symbol: FRMD4A
Strict Orthology Symbols: frmd4a
Frmd4a
(Mus musculus)Gene
Name: FERM domain containing 4A
Synonyms: predicted gene, OTTMUSG00000010806, RIKEN cDNA 2700017I06 gene, C230040M21Rik, Gm13190, OTTMUSG00000010806, RIKEN cDNA C230040M21 gene, RGD1309050, 2700017I06Rik, predicted gene 13190, expressed sequence AI594879, AI594879, mKIAA1294
Source: MGI:1919850
Biotype: protein coding gene
Symbol: Frmd4a (Mmu)
Symbol: Frmd4a
Automated Gene Synopsis: Orthologous to human FRMD4A (FERM domain containing 4A).
Strict Orthology Symbols: frmd4a
Alleles: Frmd4a
frmd4a
(Danio rerio)Gene
Name: FERM domain containing 4A
Synonyms: si:ch211-220f12.1
Source: ZFIN:ZDB-GENE-050419-154
Biotype: protein coding gene
Symbol: frmd4a (Dre)
Symbol: frmd4a
Automated Gene Synopsis: Orthologous to human FRMD4A (FERM domain containing 4A).
Strict Orthology Symbols: frmd4a
frmd4a
(Xenopus tropicalis)Gene
Name: FERM domain containing 4A
Synonyms: frmd4a, LOC108712345, FERM domain containing 4A
Source: Xenbase:XB-GENE-5922925
Biotype: gene
Symbol: frmd4a
Symbol: frmd4a (Xtr)
Automated Gene Synopsis: Orthologous to human FRMD4A (FERM domain containing 4A).
Synonyms: frmd4a...frmd4a...frmd4a
Strict Orthology Symbols: frmd4a
FRMD4A-AS1
(Homo sapiens)Gene
Name: FRMD4A antisense RNA 1
Synonyms: Not Available
Source: HGNC:56672
Biotype: ncRNA gene
Symbol: FRMD4A-AS1 (Hsa)
Symbol: FRMD4A-AS1
frmd4a.L
(Xenopus laevis)Gene
Name: FERM domain containing 4A
Synonyms: frmd4a.L, LOC108712345, FERM domain containing 4A
Source: Xenbase:XB-GENE-6487777
Biotype: gene
Symbol: frmd4a.L (Xla)
Automated Gene Synopsis: Orthologous to human FRMD4A (FERM domain containing 4A).
Strict Orthology Symbols: frmd4a
Symbol: frmd4a.L
Frmd4aem1(IMPC)J
(Mus musculus)Allele/Variant
Source: MGI:6158930
Genes: Frmd4a (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Frmd4a
Genes: Frmd4a (Mmu)
Symbol: Frmd4aem1(IMPC)J
Model
Id: MGI:7267015
Synonyms: Not Available
Symbol: Frmd4a/Frmd4a<+> [background:] C57BL/6NJ-Frmd4a/Mmjax (Mmu)
Genes: Frmd4a (Mmu)
Alleles: Frmd4a
Name: Frmd4a/Frmd4a<+> [background:] C57BL/6NJ-Frmd4a/Mmjax
Id: MGI:7316990
Synonyms: Not Available
Symbol: Frmd4a/Frmd4a [background:] C57BL/6NJ-Frmd4a/Mmjax (Mmu)
Genes: Frmd4a (Mmu)
Alleles: Frmd4a
Name: Frmd4a/Frmd4a [background:] C57BL/6NJ-Frmd4a/Mmjax
F07C6.4
(Caenorhabditis elegans)Gene
Name: FERM domain-containing protein
Synonyms: CELE_F07C6.4
Source: WB:WBGene00008555
Biotype: protein coding gene
Gene Synopsis: Is an ortholog of human FRMD4A (FERM domain containing 4A) and FRMD4B (FERM domain containing 4B).
Automated Gene Synopsis: Orthologous to human FRMD4A (FERM domain containing 4A) and FRMD4B (FERM domain containing 4B).
Strict Orthology Symbols: frmd4a
Gene Ontology
Source: GO:0090162
Synonyms: Not Available
Branch: biological process
Genes: Frmd4a (Rno)...FRMD4A (Hsa)...Frmd4a (Mmu)...frmd4a (Dre)
Gene Ontology
Source: GO:0050709
Synonyms:
- down regulation of protein secretion
- down-regulation of protein secretion
Branch: biological process
Genes: Frmd4a (Rno)...FRMD4A (Hsa)...Frmd4a (Mmu)
Gene Ontology
Source: GO:0050714
Synonyms:
- activation of protein secretion
- stimulation of protein secretion
Branch: biological process
Genes: Frmd4a (Rno)...FRMD4A (Hsa)...Frmd4a (Mmu)
Gene Ontology
Source: GO:0005923
Synonyms:
- zonula occludens
Branch: cellular component
Genes: frmd4a (Dre)...Frmd4a (Mmu)...Frmd4a (Rno)...FRMD4A (Hsa)
Gene Ontology
Source: GO:0005912
Synonyms:
- cell-cell adherens junction
Branch: cellular component
Genes: frmd4a (Dre)...Frmd4a (Mmu)...Frmd4a (Rno)...FRMD4A (Hsa)
Gene Ontology
Source: GO:0030674
Synonyms:
- protein binding, bridging
- protein complex scaffold activity
Branch: molecular function
Genes: Frmd4a (Mmu)...Frmd4a (Rno)...FRMD4A (Hsa)
Gene Ontology
Source: GO:0005856
Synonyms: Not Available
Branch: cellular component
Genes: Frmd4a (Mmu)...Frmd4a (Rno)...FRMD4A (Hsa)...frmd4a (Dre)
sa7451
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-161003-20773
Genes: frmd4a (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
Genes: frmd4a (Dre)
sa43047
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-160601-8675
Genes: frmd4a (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: frmd4a (Dre)
sa36573
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-160601-4723
Genes: frmd4a (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: frmd4a (Dre)
sa666
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-161003-20732
Genes: frmd4a (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: frmd4a (Dre)
Gene Ontology
Source: GO:0005737
Synonyms: Not Available
Branch: cellular component
Genes: Frmd4a (Rno)...FRMD4A (Hsa)...frmd4a (Dre)...Frmd4a (Mmu)
(GRCh38)10:14283518A>G
(Homo sapiens)Allele/Variant
Source: rs207470703
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:14283518A>G
(GRCh38)10:13670464C>T
(Homo sapiens)Allele/Variant
Source: rs1443470519
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13670464C>T
(GRCh38)10:13810846C>T
(Homo sapiens)Allele/Variant
Source: rs770116608
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13810846C>T
(GRCh38)10:13796604A>G
(Homo sapiens)Allele/Variant
Source: rs3740121
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13796604A>G
(GRCh38)10:13693926G>A
(Homo sapiens)Allele/Variant
Source: rs751351710
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13693926G>A
(GRCh38)10:13701427C>T
(Homo sapiens)Allele/Variant
Source: rs779028865
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13701427C>T
(GRCh38)10:13670496G>A
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.13670496G>A
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13670496G>A
(GRCh38)10:14008050C>T
(Homo sapiens)Allele/Variant
Source: rs376698792
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:14008050C>T
(GRCh38)10:13858870T>A
(Homo sapiens)Allele/Variant
Source: rs1380612395
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13858870T>A
(GRCh38)10:13670449G>A
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.13670449G>A
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13670449G>A
(GRCh38)10:13737898C>T
(Homo sapiens)Allele/Variant
Source: rs61755072
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13737898C>T
(GRCh38)10:13810915G>A
(Homo sapiens)Allele/Variant
Source: rs150076465
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13810915G>A
(GRCh38)10:13858853T>G
(Homo sapiens)Allele/Variant
Source: rs140383155
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13858853T>G
(GRCh38)10:13858896C>T
(Homo sapiens)Allele/Variant
Source: rs376872935
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13858896C>T
(GRCh38)10:13674954C>T
(Homo sapiens)Allele/Variant
Source: rs369326023
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13674954C>T
(GRCh38)10:13693935C>T
(Homo sapiens)Allele/Variant
Source: rs200763410
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13693935C>T
(GRCh38)10:13694015G>T
(Homo sapiens)Allele/Variant
Source: rs141316396
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13694015G>T
(GRCh38)10:13796567C>G
(Homo sapiens)Allele/Variant
Source: rs144014913
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13796567C>G
(GRCh38)10:13675028A>G
(Homo sapiens)Allele/Variant
Source: rs1418467357
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13675028A>G
(GRCh38)10:13707070T>C
(Homo sapiens)Allele/Variant
Source: rs777898155
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13707070T>C
(GRCh38)10:13694043G>C
(Homo sapiens)Allele/Variant
Source: rs372163447
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13694043G>C
(GRCh38)10:13670455A>G
(Homo sapiens)Allele/Variant
Source: rs970495988
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13670455A>G
(GRCh38)10:13701444C>T
(Homo sapiens)Allele/Variant
Source: rs368993550
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13701444C>T
(GRCh38)10:13782943G>A
(Homo sapiens)Allele/Variant
Source: rs10160188
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13782943G>A
(GRCh38)10:13670453C>T
(Homo sapiens)Allele/Variant
Source: rs371981770
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13670453C>T
(GRCh38)10:13858848T>C
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.13858848T>C
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13858848T>C
(GRCh38)10:13674976C>T
(Homo sapiens)Allele/Variant
Source: rs372988841
Genes: FRMD4A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)10:13674976C>T