IVL (involucrin) - Rat Genome Database

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Gene: IVL (involucrin) Homo sapiens
Analyze
Symbol: IVL
Name: involucrin
RGD ID: 1314662
HGNC Page HGNC
Description: Involved in keratinocyte differentiation; peptide cross-linking; and response to UV-B. Localizes to several cellular components, including centrosome; cornified envelope; and nuclear body.
Type: protein-coding
RefSeq Status: REVIEWED
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1152,908,546 - 152,911,886 (+)EnsemblGRCh38hg38GRCh38
GRCh381152,908,546 - 152,911,886 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371152,881,022 - 152,884,362 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361151,147,663 - 151,150,986 (+)NCBINCBI36hg18NCBI36
Build 341149,694,111 - 149,697,434NCBI
Celera1125,951,304 - 125,954,567 (+)NCBI
Cytogenetic Map1q21.3NCBI
HuRef1124,244,144 - 124,247,467 (+)NCBIHuRef
CHM1_11154,276,405 - 154,279,728 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(-)-demecolcine  (EXP)
(S)-(-)-perillyl alcohol  (EXP)
(S)-nicotine  (EXP)
1,2-dichloroethane  (ISO)
1-chloro-2,4-dinitrobenzene  (EXP)
17beta-estradiol  (EXP,ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
3H-1,2-dithiole-3-thione  (EXP)
8'-apo-beta,psi-caroten-8'-al  (EXP)
9-cis-retinoic acid  (EXP)
aflatoxin B1  (EXP,ISO)
all-trans-4-oxoretinoic acid  (EXP)
all-trans-4-oxoretinol  (EXP)
all-trans-retinoic acid  (EXP)
all-trans-retinol  (EXP)
arotinoid acid  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
arsenite(3-)  (EXP)
arsenous acid  (EXP)
benzo[a]pyrene  (EXP,ISO)
beta-carotene  (EXP)
beta-naphthoflavone  (EXP)
bexarotene  (EXP)
bis(2-chloroethyl) sulfide  (EXP,ISO)
bisphenol A  (EXP,ISO)
cadmium dichloride  (EXP)
calcipotriol  (EXP)
calcitriol  (EXP)
calcium atom  (EXP)
calcium(0)  (EXP)
clofibrate  (ISO)
crocidolite asbestos  (EXP)
curcumin  (EXP)
DAPT  (EXP)
diarsenic trioxide  (EXP)
dipotassium bis[mu-tartrato(4-)]diantimonate(2-) trihydrate  (EXP)
diuron  (ISO)
flavonoids  (ISO)
folic acid  (ISO)
formaldehyde  (EXP)
fulvestrant  (EXP)
gentamycin  (ISO)
hemin  (EXP)
hydroquinone  (EXP)
lycopene  (EXP)
methylparaben  (EXP)
molybdate  (EXP)
N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal  (ISO)
nickel atom  (EXP)
nicotine  (EXP)
oltipraz  (EXP)
paracetamol  (ISO)
perillyl alcohol  (EXP)
phorbol 13-acetate 12-myristate  (EXP,ISO)
pirinixic acid  (ISO)
potassium chromate  (EXP)
potassium dichromate  (ISO)
raloxifene  (EXP)
silicon dioxide  (EXP)
sodium arsenate  (EXP)
sodium arsenite  (EXP)
tamoxifen  (EXP)
tungstate  (EXP)
tyrphostin AG 1478  (EXP)
undecane  (ISO)
ursodeoxycholic acid  (EXP)
valproic acid  (ISO)
vincristine  (EXP)
zinc atom  (ISO)
zinc(0)  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

Additional References at PubMed
PMID:42494   PMID:1601889   PMID:2461365   PMID:2873896   PMID:2985954   PMID:7759510   PMID:8276421   PMID:8380829   PMID:8550612   PMID:8554386   PMID:8999895   PMID:9115270  
PMID:9159190   PMID:9512462   PMID:9651377   PMID:9804813   PMID:10908733   PMID:11443109   PMID:11850802   PMID:12126624   PMID:12397374   PMID:12445200   PMID:12477932   PMID:12810719  
PMID:15037572   PMID:15044435   PMID:15147942   PMID:15191537   PMID:15304097   PMID:15489334   PMID:15586248   PMID:15805105   PMID:16140218   PMID:16374477   PMID:16639001   PMID:16982614  
PMID:17205062   PMID:17330131   PMID:17662274   PMID:17882273   PMID:17943181   PMID:17968567   PMID:18077140   PMID:18166499   PMID:18259765   PMID:18637039   PMID:19199708   PMID:19515043  
PMID:19601998   PMID:19701759   PMID:20208004   PMID:21044950   PMID:21800051   PMID:22197495   PMID:22333115   PMID:22742591   PMID:23283814   PMID:23599428   PMID:24252747   PMID:24515279  
PMID:24550385   PMID:24981860   PMID:25324306   PMID:25468996   PMID:26186194   PMID:27173435   PMID:28514442   PMID:30021884   PMID:30561431   PMID:31180492   PMID:31594818   PMID:32751111  


Genomics

Comparative Map Data
IVL
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1152,908,546 - 152,911,886 (+)EnsemblGRCh38hg38GRCh38
GRCh381152,908,546 - 152,911,886 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371152,881,022 - 152,884,362 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361151,147,663 - 151,150,986 (+)NCBINCBI36hg18NCBI36
Build 341149,694,111 - 149,697,434NCBI
Celera1125,951,304 - 125,954,567 (+)NCBI
Cytogenetic Map1q21.3NCBI
HuRef1124,244,144 - 124,247,467 (+)NCBIHuRef
CHM1_11154,276,405 - 154,279,728 (+)NCBICHM1_1
Ivl
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39392,478,206 - 92,481,097 (-)NCBIGRCm39mm39
GRCm39 Ensembl392,478,209 - 92,481,042 (-)Ensembl
GRCm38392,570,899 - 92,573,790 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl392,570,902 - 92,573,735 (-)EnsemblGRCm38mm10GRCm38
MGSCv37392,374,824 - 92,377,637 (-)NCBIGRCm37mm9NCBIm37
MGSCv36392,656,305 - 92,659,118 (-)NCBImm8
Celera394,509,236 - 94,512,049 (+)NCBICelera
Cytogenetic Map3F1NCBI
cM Map340.14NCBI
Ivl
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.22178,146,694 - 178,160,807 (-)NCBI
Rnor_6.0 Ensembl2192,761,538 - 192,763,577 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.02192,761,171 - 192,773,346 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.02212,096,984 - 212,109,138 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.42185,556,271 - 185,558,310 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.12185,506,376 - 185,508,416 (-)NCBI
Celera2172,109,346 - 172,111,385 (+)NCBICelera
Cytogenetic Map2q34NCBI
Ivl
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_004955592522,730 - 525,728 (-)NCBIChiLan1.0ChiLan1.0
IVL
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11131,884,571 - 131,886,131 (+)NCBIpanpan1.1PanPan1.1panPan2
Mhudiblu_PPA_v01128,254,139 - 128,256,893 (+)NCBIMhudiblu_PPA_v0panPan3
IVL
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11761,714,470 - 61,716,961 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1761,182,296 - 61,184,801 (+)NCBI
ROS_Cfam_1.01762,859,431 - 62,861,928 (+)NCBI
UMICH_Zoey_3.11761,590,286 - 61,592,786 (+)NCBI
UNSW_CanFamBas_1.01761,660,013 - 61,662,512 (+)NCBI
UU_Cfam_GSD_1.01762,417,479 - 62,419,989 (+)NCBI
Ivl
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440505823,860,740 - 23,863,905 (+)NCBI
SpeTri2.0NW_0049365802,892,316 - 2,894,085 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
IVL
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl496,656,033 - 96,658,737 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1496,656,033 - 96,658,737 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.24105,591,862 - 105,594,575 (-)NCBISscrofa10.2Sscrofa10.2susScr3
Pig Cytomap4q22-q23NCBI
IVL
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12010,809,528 - 10,814,646 (-)NCBI
Vero_WHO_p1.0NW_02366603810,282,380 - 10,284,080 (-)NCBI
Ivl
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_004624885375,035 - 375,967 (+)NCBI

Position Markers
RH80799  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371152,884,027 - 152,884,261UniSTSGRCh37
Build 361151,150,651 - 151,150,885RGDNCBI36
Celera1125,954,232 - 125,954,466RGD
Cytogenetic Map1q21UniSTS
GeneMap99-GB4 RH Map1538.95UniSTS
RH18018  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371152,880,756 - 152,880,972UniSTSGRCh37
Build 361151,147,380 - 151,147,596RGDNCBI36
Celera1125,951,021 - 125,951,237RGD
Cytogenetic Map1q21UniSTS
HuRef1124,243,861 - 124,244,077UniSTS
GeneMap99-GB4 RH Map1552.04UniSTS
NCBI RH Map11256.8UniSTS
RH69071  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371152,884,029 - 152,884,254UniSTSGRCh37
Build 361151,150,653 - 151,150,878RGDNCBI36
Celera1125,954,234 - 125,954,459RGD
Cytogenetic Map1q21UniSTS
GeneMap99-GB4 RH Map1545.88UniSTS
NCBI RH Map11254.4UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:479
Count of miRNA genes:225
Interacting mature miRNAs:233
Transcripts:ENST00000368764, ENST00000392667
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component
High 9 8 23 9 2
Medium 27 1 11 37 159 1 1306 16 3 37 128 69 42 7 695
Low 232 104 93 33 261 11 136 197 111 25 210 227 26 67 86
Below cutoff 1807 2469 1184 293 1073 207 2300 1684 2695 127 851 1034 86 1007 1732 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000368764   ⟹   ENSP00000357753
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1152,908,546 - 152,911,886 (+)Ensembl
RefSeq Acc Id: NM_005547   ⟹   NP_005538
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381152,908,546 - 152,911,886 (+)NCBI
GRCh371152,881,039 - 152,884,362 (+)ENTREZGENE
Build 361151,147,663 - 151,150,986 (+)NCBI Archive
HuRef1124,244,144 - 124,247,467 (+)ENTREZGENE
CHM1_11154,276,405 - 154,279,728 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_005538   ⟸   NM_005547
- UniProtKB: P07476 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000357753   ⟸   ENST00000368764

Promoters
RGD ID:6785809
Promoter ID:HG_KWN:5133
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000034664
Position:
Human AssemblyChrPosition (strand)Source
Build 361151,147,136 - 151,147,636 (+)MPROMDB
RGD ID:6849550
Promoter ID:EP16037
Type:single initiation site
Name:HS_IVL
Description:Involucrin.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Tissues & Cell Lines:keratinocytes
Experiment Methods:Sequencing of a full-length cDNA
Position:
Human AssemblyChrPosition (strand)Source
Build 361151,147,647 - 151,147,707EPD
RGD ID:6857154
Promoter ID:EPDNEW_H1742
Type:multiple initiation site
Name:IVL_1
Description:involucrin
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381152,908,547 - 152,908,607EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_005547.2(IVL):c.6C>T (p.Ser2=) single nucleotide variant Malignant melanoma [RCV000064168] Chr1:152909803 [GRCh38]
Chr1:152882279 [GRCh37]
Chr1:151148903 [NCBI36]
Chr1:1q21.3
not provided
NM_005547.2(IVL):c.7C>T (p.Gln3Ter) single nucleotide variant Malignant melanoma [RCV000064169] Chr1:152909804 [GRCh38]
Chr1:152882280 [GRCh37]
Chr1:151148904 [NCBI36]
Chr1:1q21.3
not provided
NM_005547.2(IVL):c.441G>A (p.Met147Ile) single nucleotide variant Malignant melanoma [RCV000064170] Chr1:152910238 [GRCh38]
Chr1:152882714 [GRCh37]
Chr1:151149338 [NCBI36]
Chr1:1q21.3
not provided
NM_005547.2(IVL):c.508G>A (p.Glu170Lys) single nucleotide variant Malignant melanoma [RCV000064171] Chr1:152910305 [GRCh38]
Chr1:152882781 [GRCh37]
Chr1:151149405 [NCBI36]
Chr1:1q21.3
not provided
NM_005547.2(IVL):c.1567C>T (p.Leu523=) single nucleotide variant Malignant melanoma [RCV000064172] Chr1:152911364 [GRCh38]
Chr1:152883840 [GRCh37]
Chr1:151150464 [NCBI36]
Chr1:1q21.3
not provided
GRCh38/hg38 1q21.2-25.2(chr1:149854269-180267197)x3 copy number gain See cases [RCV000143515] Chr1:149854269..180267197 [GRCh38]
Chr1:149825831..180236332 [GRCh37]
Chr1:148092455..178502955 [NCBI36]
Chr1:1q21.2-25.2
pathogenic
NM_005547.3(IVL):c.1209G>A (p.Leu403=) single nucleotide variant not provided [RCV000936434] Chr1:152911006 [GRCh38]
Chr1:152883482 [GRCh37]
Chr1:1q21.3
likely benign
GRCh37/hg19 1q21.1-21.3(chr1:144927578-153223600)x3 copy number gain Chromosome 1q21.1 duplication syndrome [RCV000223957] Chr1:144927578..153223600 [GRCh37]
Chr1:1q21.1-21.3
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1q21.3(chr1:150853044-154647786)x3 copy number gain not provided [RCV000684655] Chr1:150853044..154647786 [GRCh37]
Chr1:1q21.3
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44
pathogenic
NM_005547.3(IVL):c.882G>T (p.Lys294Asn) single nucleotide variant not provided [RCV000893873] Chr1:152910679 [GRCh38]
Chr1:152883155 [GRCh37]
Chr1:1q21.3
likely benign
NM_005547.3(IVL):c.709C>G (p.Gln237Glu) single nucleotide variant not provided [RCV000948562] Chr1:152910506 [GRCh38]
Chr1:152882982 [GRCh37]
Chr1:1q21.3
benign
NM_005547.3(IVL):c.957G>A (p.Gln319=) single nucleotide variant not provided [RCV000943013] Chr1:152910754 [GRCh38]
Chr1:152883230 [GRCh37]
Chr1:1q21.3
likely benign
NM_005547.3(IVL):c.1374G>A (p.Gly458=) single nucleotide variant not provided [RCV000903680] Chr1:152911171 [GRCh38]
Chr1:152883647 [GRCh37]
Chr1:1q21.3
benign
NM_005547.3(IVL):c.1513C>G (p.Gln505Glu) single nucleotide variant not provided [RCV000948563] Chr1:152911310 [GRCh38]
Chr1:152883786 [GRCh37]
Chr1:1q21.3
benign
NM_005547.3(IVL):c.492G>A (p.Lys164=) single nucleotide variant not provided [RCV000894410] Chr1:152910289 [GRCh38]
Chr1:152882765 [GRCh37]
Chr1:1q21.3
benign
NM_005547.3(IVL):c.633G>A (p.Gly211=) single nucleotide variant not provided [RCV000898681] Chr1:152910430 [GRCh38]
Chr1:152882906 [GRCh37]
Chr1:1q21.3
likely benign
NM_005547.3(IVL):c.375A>G (p.Glu125=) single nucleotide variant not provided [RCV000895776] Chr1:152910172 [GRCh38]
Chr1:152882648 [GRCh37]
Chr1:1q21.3
likely benign
NM_005547.3(IVL):c.513_542del (p.Lys174_Leu183del) deletion not provided [RCV000953646] Chr1:152910296..152910325 [GRCh38]
Chr1:152882772..152882801 [GRCh37]
Chr1:1q21.3
likely benign
NM_005547.3(IVL):c.864G>A (p.Gln288=) single nucleotide variant not provided [RCV000893872] Chr1:152910661 [GRCh38]
Chr1:152883137 [GRCh37]
Chr1:1q21.3
benign
NM_005547.3(IVL):c.933G>A (p.Gly311=) single nucleotide variant not provided [RCV000931015] Chr1:152910730 [GRCh38]
Chr1:152883206 [GRCh37]
Chr1:1q21.3
likely benign
NM_005547.3(IVL):c.1044G>T (p.Gln348His) single nucleotide variant not provided [RCV000893874] Chr1:152910841 [GRCh38]
Chr1:152883317 [GRCh37]
Chr1:1q21.3
likely benign
NM_005547.3(IVL):c.538G>A (p.Glu180Lys) single nucleotide variant not provided [RCV000955783] Chr1:152910335 [GRCh38]
Chr1:152882811 [GRCh37]
Chr1:1q21.3
benign
NM_005547.3(IVL):c.763C>T (p.Leu255Phe) single nucleotide variant not provided [RCV000955784] Chr1:152910560 [GRCh38]
Chr1:152883036 [GRCh37]
Chr1:1q21.3
benign
NM_005547.3(IVL):c.1347G>A (p.Gln449=) single nucleotide variant not provided [RCV000955785] Chr1:152911144 [GRCh38]
Chr1:152883620 [GRCh37]
Chr1:1q21.3
benign
NM_005547.3(IVL):c.1348T>A (p.Leu450Met) single nucleotide variant not provided [RCV000955786] Chr1:152911145 [GRCh38]
Chr1:152883621 [GRCh37]
Chr1:1q21.3
benign
NC_000001.10:g.(?_130980840)_(248900000_?)dup duplication Gastrointestinal stromal tumor [RCV001300221]|Parathyroid carcinoma [RCV001341077] Chr1:130980840..248900000 [GRCh37]
Chr1:1q12-44
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:6187 AgrOrtholog
COSMIC IVL COSMIC
Ensembl Genes ENSG00000163207 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Protein ENSP00000357753 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000368764 ENTREZGENE, UniProtKB/Swiss-Prot
GTEx ENSG00000163207 GTEx
HGNC ID HGNC:6187 ENTREZGENE
Human Proteome Map IVL Human Proteome Map
InterPro Involucrin UniProtKB/Swiss-Prot
  Involucrin_CS UniProtKB/Swiss-Prot
  Involucrin_N UniProtKB/Swiss-Prot
  Involucrin_rpt UniProtKB/Swiss-Prot
KEGG Report hsa:3713 UniProtKB/Swiss-Prot
NCBI Gene 3713 ENTREZGENE
OMIM 147360 OMIM
PANTHER PTHR36910:SF9 UniProtKB/Swiss-Prot
Pfam Involucrin UniProtKB/Swiss-Prot
  Involucrin_N UniProtKB/Swiss-Prot
PharmGKB PA29985 PharmGKB
PROSITE INVOLUCRIN UniProtKB/Swiss-Prot
UniProt INVO_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary Q5T7P4 UniProtKB/Swiss-Prot