KRT24 (keratin 24) - Rat Genome Database

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Gene: KRT24 (keratin 24) Homo sapiens
Analyze
Symbol: KRT24
Name: keratin 24
RGD ID: 1349415
HGNC Page HGNC:18527
Description: Predicted to enable structural molecule activity. Predicted to be involved in epithelial cell differentiation and intermediate filament organization. Located in extracellular exosome.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: CK-24; cytokeratin-24; FLJ20261; K24; KA24; keratin 24, type I; keratin, type I cytoskeletal 24; keratin-24; MGC138169; MGC138173; type I keratin-24
RGD Orthologs
Mouse
Rat
Chinchilla
Dog
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: KRT223P  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
NCBI Annotation Information: Note: Genetic polymorphisms result in both protein coding and non-coding alleles of this gene.
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381740,697,991 - 40,703,752 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1740,697,991 - 40,703,752 (-)EnsemblGRCh38hg38GRCh38
GRCh371738,854,243 - 38,860,004 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361736,107,769 - 36,113,528 (-)NCBINCBI36Build 36hg18NCBI36
Build 341736,107,770 - 36,113,528NCBI
Celera1735,515,802 - 35,521,547 (-)NCBICelera
Cytogenetic Map17q21.2NCBI
HuRef1734,648,584 - 34,654,332 (-)NCBIHuRef
CHM1_11739,089,584 - 39,095,343 (-)NCBICHM1_1
T2T-CHM13v2.01741,562,356 - 41,568,083 (-)NCBIT2T-CHM13v2.0
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
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12230514   PMID:12477932   PMID:16831889   PMID:17317818   PMID:18029348   PMID:19380743   PMID:21145461   PMID:21873635   PMID:23533145   PMID:27107012   PMID:28362807   PMID:29039047  
PMID:29845934   PMID:32296183   PMID:32461654   PMID:32487729   PMID:32822701   PMID:34450690   PMID:35676659  


Genomics

Comparative Map Data
KRT24
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381740,697,991 - 40,703,752 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1740,697,991 - 40,703,752 (-)EnsemblGRCh38hg38GRCh38
GRCh371738,854,243 - 38,860,004 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361736,107,769 - 36,113,528 (-)NCBINCBI36Build 36hg18NCBI36
Build 341736,107,770 - 36,113,528NCBI
Celera1735,515,802 - 35,521,547 (-)NCBICelera
Cytogenetic Map17q21.2NCBI
HuRef1734,648,584 - 34,654,332 (-)NCBIHuRef
CHM1_11739,089,584 - 39,095,343 (-)NCBICHM1_1
T2T-CHM13v2.01741,562,356 - 41,568,083 (-)NCBIT2T-CHM13v2.0
Krt24
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391199,170,785 - 99,176,088 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1199,170,785 - 99,176,088 (-)EnsemblGRCm39 Ensembl
GRCm381199,279,959 - 99,285,262 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1199,279,959 - 99,285,262 (-)EnsemblGRCm38mm10GRCm38
MGSCv371199,141,407 - 99,146,552 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361199,096,049 - 99,101,352 (-)NCBIMGSCv36mm8
Celera11108,947,265 - 108,952,409 (-)NCBICelera
Cytogenetic Map11DNCBI
cM Map1162.92NCBI
Krt24
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81084,728,350 - 84,733,486 (-)NCBIGRCr8
mRatBN7.21084,232,163 - 84,237,299 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1084,232,164 - 84,237,299 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1089,175,926 - 89,180,817 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01088,674,041 - 88,678,932 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01084,066,038 - 84,070,929 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01087,190,184 - 87,195,075 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1087,189,934 - 87,195,075 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01086,986,162 - 86,991,053 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41088,180,329 - 88,186,201 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11088,194,698 - 88,200,571 (-)NCBI
Celera1082,971,744 - 82,976,640 (-)NCBICelera
Cytogenetic Map10q31NCBI
Krt24
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495545115,187,764 - 15,191,573 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495545115,187,535 - 15,191,685 (-)NCBIChiLan1.0ChiLan1.0
KRT24
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1921,966,861 - 21,971,905 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl921,967,227 - 21,971,917 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha921,439,913 - 21,444,954 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0922,759,961 - 22,765,014 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl922,760,336 - 22,765,022 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1921,534,514 - 21,539,560 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0921,793,392 - 21,798,445 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0921,917,777 - 21,922,835 (+)NCBIUU_Cfam_GSD_1.0
KRT24
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1221,731,599 - 21,736,525 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11221,731,170 - 21,737,515 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21222,056,216 - 22,061,224 (-)NCBISscrofa10.2Sscrofa10.2susScr3
KRT24
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Vero_WHO_p1.0NW_02366607736,344,422 - 36,347,394 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Krt24
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247952,674,488 - 2,678,297 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247952,674,450 - 2,678,302 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in KRT24
24 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3 copy number gain See cases [RCV000050957] Chr17:36449220..68170214 [GRCh38]
Chr17:48563237..65936105 [GRCh37]
Chr17:45918236..63677950 [NCBI36]
Chr17:17q21.33-24.2		 pathogenic
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|See cases [RCV000052483] Chr17:36449220..83086677 [GRCh38]
Chr17:58617905..81044553 [GRCh37]
Chr17:55972687..78637842 [NCBI36]
Chr17:17q23.2-25.3		 pathogenic
GRCh38/hg38 17q12-21.31(chr17:39199873-45629579)x3 copy number gain See cases [RCV000052479] Chr17:39199873..45629579 [GRCh38]
Chr17:37356126..43706945 [GRCh37]
Chr17:34609652..41062728 [NCBI36]
Chr17:17q12-21.31		 pathogenic
GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3 copy number gain See cases [RCV000137437] Chr17:36449220..75053130 [GRCh38]
Chr17:57595736..73049225 [GRCh37]
Chr17:54950518..70560820 [NCBI36]
Chr17:17q23.1-25.1		 pathogenic
NM_019016.3(KRT24):c.1454G>A (p.Ser485Asn) single nucleotide variant Inborn genetic diseases [RCV003311328] Chr17:40698558 [GRCh38]
Chr17:38854810 [GRCh37]
Chr17:17q21.2		 uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
NM_019016.3(KRT24):c.38G>A (p.Gly13Glu) single nucleotide variant Inborn genetic diseases [RCV003291457] Chr17:40703656 [GRCh38]
Chr17:38859908 [GRCh37]
Chr17:17q21.2		 uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
NM_019016.3(KRT24):c.1252T>C (p.Trp418Arg) single nucleotide variant not provided [RCV000881624] Chr17:40699553 [GRCh38]
Chr17:38855805 [GRCh37]
Chr17:17q21.2		 benign
NM_019016.3(KRT24):c.1244G>A (p.Cys415Tyr) single nucleotide variant not provided [RCV000881625] Chr17:40699561 [GRCh38]
Chr17:38855813 [GRCh37]
Chr17:17q21.2		 benign
NM_019016.3(KRT24):c.27C>T (p.Ser9=) single nucleotide variant not provided [RCV000901197] Chr17:40703667 [GRCh38]
Chr17:38859919 [GRCh37]
Chr17:17q21.2		 likely benign
NM_019016.3(KRT24):c.282C>T (p.Gly94=) single nucleotide variant not provided [RCV000962590] Chr17:40703412 [GRCh38]
Chr17:38859664 [GRCh37]
Chr17:17q21.2		 benign
NM_019016.3(KRT24):c.1503T>C (p.Thr501=) single nucleotide variant not provided [RCV000881623] Chr17:40698312 [GRCh38]
Chr17:38854564 [GRCh37]
Chr17:17q21.2		 benign
NM_019016.3(KRT24):c.853G>A (p.Glu285Lys) single nucleotide variant Inborn genetic diseases [RCV003249369] Chr17:40701142 [GRCh38]
Chr17:38857394 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_019016.3(KRT24):c.684T>A (p.Asp228Glu) single nucleotide variant Inborn genetic diseases [RCV003250033] Chr17:40701865 [GRCh38]
Chr17:38858117 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_019016.3(KRT24):c.552A>G (p.Gly184=) single nucleotide variant not provided [RCV000881626] Chr17:40703142 [GRCh38]
Chr17:38859394 [GRCh37]
Chr17:17q21.2		 benign
NM_019016.3(KRT24):c.343G>A (p.Ala115Thr) single nucleotide variant not provided [RCV000968353] Chr17:40703351 [GRCh38]
Chr17:38859603 [GRCh37]
Chr17:17q21.2		 benign
NM_019016.3(KRT24):c.556G>A (p.Gly186Ser) single nucleotide variant Inborn genetic diseases [RCV002992236] Chr17:40703138 [GRCh38]
Chr17:38859390 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_019016.3(KRT24):c.461A>G (p.Tyr154Cys) single nucleotide variant Inborn genetic diseases [RCV002906876] Chr17:40703233 [GRCh38]
Chr17:38859485 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_019016.3(KRT24):c.1214C>T (p.Thr405Met) single nucleotide variant Inborn genetic diseases [RCV003001632] Chr17:40699591 [GRCh38]
Chr17:38855843 [GRCh37]
Chr17:17q21.2		 likely benign
NM_019016.3(KRT24):c.527A>G (p.Tyr176Cys) single nucleotide variant Inborn genetic diseases [RCV002822732] Chr17:40703167 [GRCh38]
Chr17:38859419 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_019016.3(KRT24):c.870G>T (p.Met290Ile) single nucleotide variant Inborn genetic diseases [RCV002844075] Chr17:40700369 [GRCh38]
Chr17:38856621 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_019016.3(KRT24):c.817A>T (p.Thr273Ser) single nucleotide variant Inborn genetic diseases [RCV002977570] Chr17:40701178 [GRCh38]
Chr17:38857430 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_019016.3(KRT24):c.1192G>C (p.Ala398Pro) single nucleotide variant Inborn genetic diseases [RCV002699629] Chr17:40699613 [GRCh38]
Chr17:38855865 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_019016.3(KRT24):c.727A>G (p.Ser243Gly) single nucleotide variant Inborn genetic diseases [RCV002789207] Chr17:40701268 [GRCh38]
Chr17:38857520 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_019016.3(KRT24):c.1003C>T (p.Arg335Trp) single nucleotide variant Inborn genetic diseases [RCV002874381] Chr17:40700236 [GRCh38]
Chr17:38856488 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_019016.3(KRT24):c.1481G>C (p.Ser494Thr) single nucleotide variant Inborn genetic diseases [RCV002808897] Chr17:40698334 [GRCh38]
Chr17:38854586 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_019016.3(KRT24):c.1447T>C (p.Ser483Pro) single nucleotide variant Inborn genetic diseases [RCV003184430] Chr17:40698565 [GRCh38]
Chr17:38854817 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_019016.3(KRT24):c.829G>C (p.Ala277Pro) single nucleotide variant Inborn genetic diseases [RCV003180763] Chr17:40701166 [GRCh38]
Chr17:38857418 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_019016.3(KRT24):c.448C>T (p.Arg150Cys) single nucleotide variant Inborn genetic diseases [RCV003347500] Chr17:40703246 [GRCh38]
Chr17:38859498 [GRCh37]
Chr17:17q21.2		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:114
Count of miRNA genes:85
Interacting mature miRNAs:91
Transcripts:ENST00000264651
Prediction methods:Microtar, 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.

Markers in Region
RH91917  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371738,854,399 - 38,854,535UniSTSGRCh37
Build 361736,107,925 - 36,108,061RGDNCBI36
Celera1735,515,958 - 35,516,094RGD
Cytogenetic Map17q21.2UniSTS
HuRef1734,648,740 - 34,648,876UniSTS
GeneMap99-GB4 RH Map17309.55UniSTS
KRT24_2966  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371738,854,105 - 38,854,643UniSTSGRCh37
Build 361736,107,631 - 36,108,169RGDNCBI36
Celera1735,515,664 - 35,516,202RGD
HuRef1734,648,446 - 34,648,984UniSTS


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 visual system adipose tissue appendage entire extraembryonic component
High
Medium 231 3 13 4 4 34 1 3 65 2 13 1 4 2
Low 1279 83 64 29 49 1 1168 549 414 37 158 102 32 1 138 777 3
Below cutoff 682 1823 1110 257 604 160 2282 944 1810 161 904 1073 100 986 1432 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000264651   ⟹   ENSP00000264651
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1740,697,991 - 40,703,752 (-)Ensembl
RefSeq Acc Id: NM_019016   ⟹   NP_061889
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381740,697,991 - 40,703,752 (-)NCBI
GRCh371738,854,243 - 38,860,002 (-)RGD
Build 361736,107,769 - 36,113,528 (-)NCBI Archive
Celera1735,515,802 - 35,521,547 (-)RGD
HuRef1734,648,584 - 34,654,332 (-)ENTREZGENE
CHM1_11739,089,584 - 39,095,343 (-)NCBI
T2T-CHM13v2.01741,562,356 - 41,568,083 (-)NCBI
Sequence:
RefSeq Acc Id: NR_178196
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01741,562,356 - 41,568,083 (-)NCBI
Protein Sequences
Protein RefSeqs NP_061889 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAI11969 (Get FASTA)   NCBI Sequence Viewer  
  BAA91044 (Get FASTA)   NCBI Sequence Viewer  
  EAW60675 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000264651
  ENSP00000264651.2
GenBank Protein Q2M2I5 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_061889   ⟸   NM_019016
- UniProtKB: Q9NXG7 (UniProtKB/Swiss-Prot),   Q2M2I5 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000264651   ⟸   ENST00000264651
Protein Domains
IF rod

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q2M2I5-F1-model_v2 AlphaFold Q2M2I5 1-525 view protein structure

Promoters
RGD ID:7234949
Promoter ID:EPDNEW_H23220
Type:multiple initiation site
Name:KRT24_1
Description:keratin 24
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
GRCh381740,703,752 - 40,703,812EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:18527 AgrOrtholog
COSMIC KRT24 COSMIC
Ensembl Genes ENSG00000167916 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000264651 ENTREZGENE
  ENST00000264651.3 UniProtKB/Swiss-Prot
Gene3D-CATH 1.20.5.170 UniProtKB/Swiss-Prot
  Single helix bin UniProtKB/Swiss-Prot
  Vasodilator-stimulated phosphoprotein UniProtKB/Swiss-Prot
GTEx ENSG00000167916 GTEx
HGNC ID HGNC:18527 ENTREZGENE
Human Proteome Map KRT24 Human Proteome Map
InterPro IF_conserved UniProtKB/Swiss-Prot
  IF_rod_dom UniProtKB/Swiss-Prot
  Keratin_I UniProtKB/Swiss-Prot
KEGG Report hsa:192666 UniProtKB/Swiss-Prot
NCBI Gene 192666 ENTREZGENE
OMIM 607742 OMIM
PANTHER KERATIN, TYPE I CYTOSKELETAL 24 UniProtKB/Swiss-Prot
  PTHR23239 UniProtKB/Swiss-Prot
Pfam Filament UniProtKB/Swiss-Prot
PharmGKB PA38344 PharmGKB
PRINTS TYPE1KERATIN UniProtKB/Swiss-Prot
PROSITE IF_ROD_1 UniProtKB/Swiss-Prot
  IF_ROD_2 UniProtKB/Swiss-Prot
SMART Filament UniProtKB/Swiss-Prot
Superfamily-SCOP Intermediate filament protein, coiled coil region UniProtKB/Swiss-Prot
  Prefoldin UniProtKB/Swiss-Prot
UniProt K1C24_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q9NXG7 ENTREZGENE
UniProt Secondary Q9NXG7 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-14 KRT24  keratin 24  KRT24  keratin 24, type I  Symbol and/or name change 5135510 APPROVED
2015-01-27 KRT24  keratin 24, type I  KRT24  keratin 24  Symbol and/or name change 5135510 APPROVED