Flg (filaggrin) - Rat Genome Database

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Gene: Flg (filaggrin) Rattus norvegicus
Analyze
Symbol: Flg
Name: filaggrin
RGD ID: 2620
Description: Predicted to enable keratin filament binding activity. Predicted to be a structural constituent of skin epidermis. Involved in epidermal cell differentiation. Predicted to be located in cytoplasmic ribonucleoprotein granule. Predicted to be active in cornified envelope and keratohyalin granule. Human ortholog(s) of this gene implicated in atopic dermatitis 2 and ichthyosis vulgaris. Orthologous to human FLG (filaggrin); INTERACTS WITH 1,3,5-trinitro-1,3,5-triazinane; acrylamide; ammonium chloride.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: Filaggrin (profilaggrin); LOC679174; Pflg; profilaggrin
RGD Orthologs
Human
Mouse
Bonobo
Dog
Alliance Orthologs
More Info more info ...
Latest Assembly: GRCr8 - GRCr8 Assembly
NCBI Annotation Information: Annotation category: partial on reference assembly
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr82181,583,801 - 181,596,464 (+)NCBIGRCr8
mRatBN7.22178,884,793 - 178,912,986 (+)NCBImRatBN7.2mRatBN7.2
UTH_Rnor_SHR_Utx2186,449,517 - 186,478,945 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.02184,429,834 - 184,448,291 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.02179,092,619 - 179,122,045 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.02193,565,401 - 193,574,297 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.02211,289,344 - 211,294,588 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.42186,307,359 - 186,311,549 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.12186,259,903 - 186,260,929 (+)NCBI
Celera2171,386,515 - 171,395,603 (-)NCBICelera
Cytogenetic Map2q34NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model



  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
FlgRatichthyosis vulgaris  ISOFLG (Homo sapiens)1598947DNA:nonsense mutation more ...RGD 
1 to 15 of 15 rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
FlgRatatopic dermatitis  ISOFLG (Homo sapiens)8554872ClinVar more ...ClinVarPMID:16444271 more ...
FlgRatatopic dermatitis 2  ISOFLG (Homo sapiens)8554872ClinVar more ...ClinVarPMID:16444271 more ...
FlgRatcerebellar hypoplasia  ISOFLG (Homo sapiens)8554872ClinVar Annotator: match by term: Congenital cerebellar hypoplasiaClinVarPMID:25741868
FlgRatEczema  ISOFLG (Homo sapiens)8554872ClinVar Annotator: match by term: EczemaClinVarPMID:16444271 more ...
FlgRatgastrointestinal stromal tumor  ISOFLG (Homo sapiens)8554872ClinVar Annotator: match by term: Gastrointestinal stromal tumorClinVarPMID:28492532
FlgRatgenetic disease  ISOFLG (Homo sapiens)8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:17291859 more ...
FlgRatHyperhidrosis Palmaris Et Plantaris  ISOFLG (Homo sapiens)8554872ClinVar Annotator: match by term: HYPRPPClinVarPMID:25741868
FlgRatichthyosis  ISOFLG (Homo sapiens)8554872ClinVar Annotator: match by term: IchthyosisClinVarPMID:25741868
FlgRatichthyosis vulgaris  ISOFLG (Homo sapiens)8554872ClinVar more ...ClinVarPMID:16444271 more ...
FlgRatimmunodeficiency 42  ISOFLG (Homo sapiens)8554872ClinVar Annotator: match by term: Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiencyClinVarPMID:28492532
FlgRatmegacolon  ISOFLG (Homo sapiens)8554872ClinVar Annotator: match by term: MegacolonClinVarPMID:21681106
FlgRatMHC class II deficiency  ISOFLG (Homo sapiens)8554872ClinVar Annotator: match by term: MHC class II deficiencyClinVarPMID:28492532
FlgRatparathyroid carcinoma  ISOFLG (Homo sapiens)8554872ClinVar Annotator: match by term: Parathyroid carcinomaClinVarPMID:28492532
FlgRatsevere congenital neutropenia 3  ISOFLG (Homo sapiens)8554872ClinVar Annotator: match by term: Kostmann syndromeClinVarPMID:28492532
FlgRatsevere congenital neutropenia 5  ISOFLG (Homo sapiens)8554872ClinVar Annotator: match by term: Congenital neutropenia-myelofibrosis-nephromegaly syndromeClinVarPMID:28492532
1 to 15 of 15 rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
FlgRatatopic dermatitis  ISOFLG (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:19349982 more ...
FlgRatatopic dermatitis 2  ISOFLG (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTD 
FlgRatcontact dermatitis  ISOFLG (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:25724174
FlgRatdermatitis  ISOFLG (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:31330126
FlgRatEczema  ISOFLG (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:17417636
FlgRatichthyosis vulgaris  ISOFLG (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:17417636 and PMID:24061166
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
FlgRatatopic dermatitis 2  ISSFlg (Mus musculus)13592920OMIM:605803MouseDO 
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
FlgRatatopic dermatitis 2 susceptibilityISOFLG (Homo sapiens)7240710 OMIM 
FlgRatichthyosis vulgaris susceptibilityISOFLG (Homo sapiens)7240710 OMIM 

1 to 20 of 116 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
FlgRat1,3,5-trinitro-1,3,5-triazinane increases expressionEXP 6480464cyclonite results in increased expression of FLG mRNACTDPMID:25559034
FlgRat17beta-estradiol increases expressionISOFlg (Mus musculus)6480464Estradiol results in increased expression of FLG mRNACTDPMID:19484750
FlgRat17beta-estradiol decreases expressionISOFLG (Homo sapiens)6480464Estradiol results in decreased expression of FLG mRNACTDPMID:28701262
FlgRat17beta-estradiol multiple interactionsISOFLG (Homo sapiens)6480464[Estradiol co-treated with TGFB1 protein] results in increased expression of FLG mRNA more ...CTDPMID:28701262 more ...
FlgRat2,3,7,8-tetrachlorodibenzodioxine multiple interactionsISOFlg (Mus musculus)6480464AHR protein affects the reaction [Tetrachlorodibenzodioxin results in increased expression of FLG protein]CTDPMID:12151643
FlgRat2,3,7,8-tetrachlorodibenzodioxine decreases expressionISOFLG (Homo sapiens)6480464Tetrachlorodibenzodioxin results in decreased expression of FLG proteinCTDPMID:24161567
FlgRat2,3,7,8-tetrachlorodibenzodioxine increases expressionISOFlg (Mus musculus)6480464Tetrachlorodibenzodioxin results in increased expression of FLG proteinCTDPMID:12151643
FlgRat2,3,7,8-tetrachlorodibenzodioxine increases expressionISOFLG (Homo sapiens)6480464Tetrachlorodibenzodioxin results in increased expression of FLG mRNA and Tetrachlorodibenzodioxin results in increased expression of FLG proteinCTDPMID:21835898 and PMID:23152189
FlgRat2,3,7,8-tetrachlorodibenzodioxine multiple interactionsISOFLG (Homo sapiens)6480464[alpha-naphthoflavone binds to and results in decreased activity of AHR protein] inhibits the reaction [Tetrachlorodibenzodioxin results in increased expression of FLG mRNA] more ...CTDPMID:21835898
FlgRat2,4,5-trichlorophenol multiple interactionsISOFLG (Homo sapiens)6480464[FLG gene mutant form affects the susceptibility to 2 more ...CTDPMID:30245359
FlgRat2,4,5-trichlorophenol affects response to substanceISOFLG (Homo sapiens)6480464FLG gene mutant form affects the susceptibility to 2 more ...CTDPMID:30245359
FlgRat2,4-D multiple interactionsISOFlg (Mus musculus)6480464[lard co-treated with Cholesterol more ...CTDPMID:37567420
FlgRat2,4-Dihydroxybenzophenone multiple interactionsISOFLG (Homo sapiens)6480464[FLG gene mutant form affects the susceptibility to 2 more ...CTDPMID:30245359
FlgRat2,4-Dihydroxybenzophenone affects response to substanceISOFLG (Homo sapiens)6480464FLG gene mutant form affects the susceptibility to 2 and 4-dihydroxybenzophenoneCTDPMID:30245359
FlgRat2,6-dimethoxyphenol multiple interactionsISOFLG (Homo sapiens)6480464[pyrogallol 1 more ...CTDPMID:38598786
FlgRat4-Hydroxybenzophenone multiple interactionsISOFLG (Homo sapiens)6480464[FLG gene mutant form affects the susceptibility to 4-hydroxybenzophenone] which results in decreased secretion of FSHB protein and [FLG gene mutant form affects the susceptibility to 4-hydroxybenzophenone] which results in increased secretion of EstradiolCTDPMID:30245359
FlgRat4-Hydroxybenzophenone affects response to substanceISOFLG (Homo sapiens)6480464FLG gene mutant form affects the susceptibility to 4-hydroxybenzophenoneCTDPMID:30245359
FlgRat9-cis-retinoic acid decreases expressionISOFLG (Homo sapiens)6480464Alitretinoin results in decreased expression of FLG mRNACTDPMID:15982314
FlgRatacrylamide increases expressionEXP 6480464Acrylamide results in increased expression of FLG mRNACTDPMID:28959563
FlgRataflatoxin B1 decreases methylationISOFLG (Homo sapiens)6480464Aflatoxin B1 results in decreased methylation of FLG geneCTDPMID:27153756

1 to 20 of 116 rows

Biological Process

  

Cellular Component

  

Molecular Function

  


1 to 12 of 12 rows
#
Reference Title
Reference Citation
1. Rat ISS GO annotations from GOA human gene data--August 2006 GOA data from the GO Consortium
2. Filaggrin, an intermediate filament-associated protein: structural and functional implications from the sequence of a cDNA from rat. Haydock PV and Dale BA, DNA Cell Biol 1990 May;9(4):251-61.
3. Antisense profilaggrin RNA delays and decreases profilaggrin expression and alters in vitro differentiation of rat epidermal keratinocytes. Haydock PV, etal., J Invest Dermatol. 1993 Aug;101(2):118-26.
4. Induction of selected lipid metabolic enzymes and differentiation-linked structural proteins by air exposure in fetal rat skin explants. Komuves LG, etal., J Invest Dermatol. 1999 Mar;112(3):303-9.
5. Rat ISS GO annotations from MGI mouse gene data--August 2006 MGD data from the GO Consortium
6. Electronic Transfer of LocusLink and RefSeq Data NCBI rat LocusLink and RefSeq merged data July 26, 2002
7. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
8. Functional analysis of the profilaggrin N-terminal peptide: identification of domains that regulate nuclear and cytoplasmic distribution. Pearton DJ, etal., J Invest Dermatol. 2002 Sep;119(3):661-9.
9. GOA pipeline RGD automated data pipeline
10. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
11. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
12. Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris. Smith FJ, etal., Nat Genet. 2006 Mar;38(3):337-42. Epub 2006 Jan 29.
1 to 12 of 12 rows
PMID:1429717   PMID:4557539   PMID:6170061   PMID:6174530   PMID:7543090   PMID:11572870   PMID:12850301   PMID:20376063   PMID:21464233   PMID:21630459   PMID:21744336   PMID:22366455  
PMID:23403047   PMID:24084074   PMID:33450132  



Flg
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr82181,583,801 - 181,596,464 (+)NCBIGRCr8
mRatBN7.22178,884,793 - 178,912,986 (+)NCBImRatBN7.2mRatBN7.2
UTH_Rnor_SHR_Utx2186,449,517 - 186,478,945 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.02184,429,834 - 184,448,291 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.02179,092,619 - 179,122,045 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.02193,565,401 - 193,574,297 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.02211,289,344 - 211,294,588 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.42186,307,359 - 186,311,549 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.12186,259,903 - 186,260,929 (+)NCBI
Celera2171,386,515 - 171,395,603 (-)NCBICelera
Cytogenetic Map2q34NCBI
FLG
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381152,302,165 - 152,325,239 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1152,302,165 - 152,325,239 (-)EnsemblGRCh38hg38GRCh38
GRCh371152,274,641 - 152,297,715 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361150,541,275 - 150,564,303 (-)NCBINCBI36Build 36hg18NCBI36
Celera1125,386,606 - 125,408,667 (-)NCBICelera
Cytogenetic Map1q21.3NCBI
HuRef1123,649,333 - 123,671,391 (-)NCBIHuRef
CHM1_11153,670,002 - 153,693,030 (-)NCBICHM1_1
T2T-CHM13v2.01151,437,741 - 151,461,789 (-)NCBIT2T-CHM13v2.0
Flg
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39393,180,853 - 93,200,996 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl393,180,830 - 93,200,993 (+)EnsemblGRCm39 Ensembl
GRCm38393,273,546 - 93,293,689 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl393,273,523 - 93,293,686 (+)EnsemblGRCm38mm10GRCm38
MGSCv37393,089,108 - 93,097,615 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36393,367,872 - 93,379,097 (+)NCBIMGSCv36mm8
Celera393,804,333 - 93,822,603 (-)NCBICelera
Cytogenetic Map3F2.1NCBI
cM Map340.16NCBI
FLG
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2197,536,576 - 97,547,401 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1197,286,770 - 97,298,567 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01127,634,416 - 127,649,659 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11131,276,648 - 131,285,336 (-)NCBIpanpan1.1PanPan1.1panPan2
FLG
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11761,217,915 - 61,233,068 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1760,662,290 - 60,679,224 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01762,238,036 - 62,255,220 (-)NCBIROS_Cfam_1.0
UMICH_Zoey_3.11761,075,602 - 61,083,175 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01761,151,018 - 61,170,965 (-)NCBIUNSW_CanFamBas_1.0

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Variants in Flg
45 total Variants

1 to 10 of 65 rows
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
1578648Bss11Bone structure and strength QTL 114.7femur morphology trait (VT:0000559)femoral neck cortical cross-sectional area (CMO:0001702)2114837527211674221Rat
1358356Srcrt1Stress Responsive Cort QTL13.66blood corticosterone amount (VT:0005345)plasma corticosterone level (CMO:0001173)2161699179222436696Rat
1331734Bp204Blood pressure QTL 2043.61192arterial blood pressure trait (VT:2000000)mean arterial blood pressure (CMO:0000009)2168358098223265385Rat
1298074Bp164Blood pressure QTL 1640.003arterial blood pressure trait (VT:2000000)systolic blood pressure (CMO:0000004)242804607202447032Rat
1354648Bp239Blood pressure QTL 2390.001arterial blood pressure trait (VT:2000000)systolic blood pressure (CMO:0000004)266118463226797303Rat
1354649Kidm17Kidney mass QTL 172.9kidney mass (VT:0002707)calculated kidney weight (CMO:0000160)281754530227146641Rat
10755499Bp389Blood pressure QTL 3892.61arterial blood pressure trait (VT:2000000)diastolic blood pressure (CMO:0000005)218960362228801039Rat
1298076Bp166Blood pressure QTL 1660.0009arterial blood pressure trait (VT:2000000)systolic blood pressure (CMO:0000004)2136445150202447032Rat
152025245Scl81Serum cholesterol level QTL 813.49blood cholesterol amount (VT:0000180)2122609194206936711Rat
70162Bp63Blood pressure QTL 635.64arterial blood pressure trait (VT:2000000)blood pressure measurement (CMO:0000003)2169745596214745596Rat

1 to 10 of 65 rows
Flg  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.22178,909,027 - 178,909,309 (+)MAPPERmRatBN7.2
mRatBN7.22178,891,975 - 178,892,257 (+)MAPPERmRatBN7.2
mRatBN7.22178,893,193 - 178,893,475 (+)MAPPERmRatBN7.2
mRatBN7.22178,899,283 - 178,899,565 (+)MAPPERmRatBN7.2
mRatBN7.22178,900,501 - 178,900,783 (+)MAPPERmRatBN7.2
mRatBN7.22178,904,155 - 178,904,437 (+)MAPPERmRatBN7.2
mRatBN7.22178,905,373 - 178,905,655 (+)MAPPERmRatBN7.2
mRatBN7.22178,906,591 - 178,906,873 (+)MAPPERmRatBN7.2
mRatBN7.22178,907,809 - 178,908,091 (+)MAPPERmRatBN7.2
mRatBN7.22178,890,757 - 178,891,039 (+)MAPPERmRatBN7.2
mRatBN7.22178,910,245 - 178,910,527 (+)MAPPERmRatBN7.2
mRatBN7.22178,911,463 - 178,911,745 (+)MAPPERmRatBN7.2
mRatBN7.22178,898,065 - 178,898,347 (+)MAPPERmRatBN7.2
mRatBN7.22178,896,847 - 178,897,129 (+)MAPPERmRatBN7.2
mRatBN7.22178,895,629 - 178,895,911 (+)MAPPERmRatBN7.2
mRatBN7.22178,894,411 - 178,894,693 (+)MAPPERmRatBN7.2
Rnor_6.02193,572,763 - 193,573,044NCBIRnor6.0
Rnor_5.02211,292,237 - 211,292,518UniSTSRnor5.0
Cytogenetic Map2q34UniSTS







RefSeq Acc Id: NM_001393766   ⟹   NP_001380695
RefSeq Status: VALIDATED
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr82181,583,801 - 181,596,464 (+)NCBI
mRatBN7.22178,884,793 - 178,912,986 (+)NCBI
Protein RefSeqs NP_001380695 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA41161 (Get FASTA)   NCBI Sequence Viewer  
  AAM54369 (Get FASTA)   NCBI Sequence Viewer  
  EDL87862 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001380695   ⟸   NM_001393766
EF-hand



1 to 23 of 23 rows
Database
Acc Id
Source(s)
BioCyc Gene G2FUF-52243 BioCyc
Gene3D-CATH EF-hand UniProtKB/TrEMBL
InterPro EF-hand-dom_pair UniProtKB/TrEMBL
  EF_Hand_1_Ca_BS UniProtKB/TrEMBL
  EF_hand_dom UniProtKB/TrEMBL
  Filaggrin UniProtKB/TrEMBL
  S-100_dom UniProtKB/TrEMBL
  S100-fused_Epidermal_Struct UniProtKB/TrEMBL
  S100/CaBP-9k_CS UniProtKB/TrEMBL
  S100_Ca-bd_sub UniProtKB/TrEMBL
NCBI Gene 24641 ENTREZGENE
PANTHER FILAGGRIN UniProtKB/TrEMBL
  FILAGGRIN-RELATED UniProtKB/TrEMBL
Pfam Filaggrin UniProtKB/TrEMBL
  S_100 UniProtKB/TrEMBL
PhenoGen Flg PhenoGen
PROSITE EF_HAND_1 UniProtKB/TrEMBL
  EF_HAND_2 UniProtKB/TrEMBL
  S100_CABP UniProtKB/TrEMBL
SMART S_100 UniProtKB/TrEMBL
Superfamily-SCOP SSF47473 UniProtKB/TrEMBL
UniProt A6KMN2_RAT UniProtKB/TrEMBL
  Q8CIU0_RAT UniProtKB/TrEMBL
1 to 23 of 23 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2013-03-29 Flg  filaggrin  LOC679174  similar to filaggrin  Data merged from RGD:1591824 737654 PROVISIONAL
2006-11-20 LOC679174  similar to filaggrin      Symbol and Name status set to provisional 70820 PROVISIONAL
2002-11-06 Flg  filaggrin    Filaggrin (profilaggrin)  Name updated 625702 APPROVED
2002-06-10 Flg  Filaggrin (profilaggrin)      Symbol and Name status set to approved 70586 APPROVED

Note Type Note Reference
gene_domains contains two repeats of 406 amino acid with a filaggrin domain in each repeat 632675
gene_expression expressed in fully cornified cells of the mammalian epidermis, mRNA highly expressed only in keratinizing epithelia 632675
gene_process responsible for epidermal differentiation 632675
gene_transcript cDNA is 2,314 bp long and has a 1,875 bp long coding region ending with an A-T rich 3' noncoding region 632675