KRT32 (keratin 32) - Rat Genome Database

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Gene: KRT32 (keratin 32) Homo sapiens
Analyze
Symbol: KRT32
Name: keratin 32
RGD ID: 1313247
HGNC Page HGNC:6449
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: HA2; hair keratin, type I Ha2; hard keratin, type I, 2; hHa2; HKA2; K32; keratin 32, type I; keratin, hair, acidic, 2; keratin, type I cuticular Ha2; keratin-32; KRTHA2; type I cuticular hair keratin
RGD Orthologs
Mouse
Rat
Bonobo
Dog
Squirrel
Pig
Green Monkey
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381741,459,513 - 41,467,386 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1741,459,513 - 41,467,386 (-)EnsemblGRCh38hg38GRCh38
GRCh371739,615,765 - 39,623,638 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361736,869,291 - 36,877,164 (-)NCBINCBI36Build 36hg18NCBI36
Build 341736,869,587 - 36,877,164NCBI
Celera1736,268,990 - 36,276,862 (-)NCBICelera
Cytogenetic Map17q21.2NCBI
HuRef1735,379,379 - 35,387,251 (-)NCBIHuRef
CHM1_11739,851,077 - 39,858,950 (-)NCBICHM1_1
T2T-CHM13v2.01742,315,065 - 42,322,938 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease 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. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:2456239   PMID:7556444   PMID:7686952   PMID:8823373   PMID:10391933   PMID:12543931   PMID:16831889   PMID:17353931   PMID:19380743   PMID:19490893   PMID:21873635   PMID:23533145  
PMID:23686814   PMID:25963833   PMID:28977666   PMID:29507755   PMID:29845934   PMID:30575818   PMID:32296183   PMID:33961781   PMID:34591612   PMID:35864588   PMID:36217029   PMID:36724073  
PMID:36949045  


Genomics

Comparative Map Data
KRT32
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381741,459,513 - 41,467,386 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1741,459,513 - 41,467,386 (-)EnsemblGRCh38hg38GRCh38
GRCh371739,615,765 - 39,623,638 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361736,869,291 - 36,877,164 (-)NCBINCBI36Build 36hg18NCBI36
Build 341736,869,587 - 36,877,164NCBI
Celera1736,268,990 - 36,276,862 (-)NCBICelera
Cytogenetic Map17q21.2NCBI
HuRef1735,379,379 - 35,387,251 (-)NCBIHuRef
CHM1_11739,851,077 - 39,858,950 (-)NCBICHM1_1
T2T-CHM13v2.01742,315,065 - 42,322,938 (-)NCBIT2T-CHM13v2.0
Krt32
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391199,971,674 - 99,979,095 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1199,971,674 - 99,979,100 (-)EnsemblGRCm39 Ensembl
GRCm3811100,080,848 - 100,088,269 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl11100,080,848 - 100,088,226 (-)EnsemblGRCm38mm10GRCm38
MGSCv371199,942,377 - 99,949,429 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361199,896,947 - 99,904,205 (-)NCBIMGSCv36mm8
Celera11110,697,424 - 110,704,467 (-)NCBICelera
Cytogenetic Map11DNCBI
cM Map1163.4NCBI
Krt32
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81085,513,951 - 85,520,978 (-)NCBIGRCr8
mRatBN7.21085,013,551 - 85,020,578 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1085,013,554 - 85,020,534 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1090,031,763 - 90,038,792 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01089,529,896 - 89,536,923 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01084,921,856 - 84,928,883 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01087,993,569 - 88,000,818 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1087,993,551 - 88,000,534 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01087,785,771 - 87,792,744 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41089,020,219 - 89,025,644 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11089,034,588 - 89,040,014 (-)NCBI
Celera1083,734,752 - 83,740,178 (-)NCBICelera
Cytogenetic Map10q31NCBI
KRT32
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21923,516,040 - 23,525,382 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11725,406,015 - 25,415,355 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01715,847,992 - 15,857,334 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11716,066,796 - 16,074,742 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1716,066,796 - 16,074,742 (+)Ensemblpanpan1.1panPan2
KRT32
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1921,300,125 - 21,306,580 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl921,300,187 - 21,306,272 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha920,761,969 - 20,768,298 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0922,021,140 - 22,027,482 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl922,021,140 - 22,027,528 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1920,807,129 - 20,813,464 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0921,073,145 - 21,079,466 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0921,176,948 - 21,183,269 (+)NCBIUU_Cfam_GSD_1.0
Krt32
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560220,686,310 - 20,693,143 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493649016,382,244 - 16,388,812 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493649016,382,244 - 16,388,812 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
KRT32
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1221,176,089 - 21,184,892 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11221,176,984 - 21,185,014 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21221,426,286 - 21,441,689 (-)NCBISscrofa10.2Sscrofa10.2susScr3
KRT32
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11664,772,775 - 64,781,504 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1664,773,498 - 64,780,717 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607735,618,358 - 35,626,237 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in KRT32
23 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
NM_002278.3(KRT32):c.873G>A (p.Met291Ile) single nucleotide variant Malignant melanoma [RCV000071472] Chr17:41464201 [GRCh38]
Chr17:39620453 [GRCh37]
Chr17:36873979 [NCBI36]
Chr17:17q21.2		 not provided
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
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_002278.3(KRT32):c.1222C>A (p.Pro408Thr) single nucleotide variant not specified [RCV004310401] Chr17:41460235 [GRCh38]
Chr17:39616487 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.523A>C (p.Lys175Gln) single nucleotide variant not specified [RCV004290548] Chr17:41466122 [GRCh38]
Chr17:39622374 [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_002278.3(KRT32):c.1117G>C (p.Glu373Gln) single nucleotide variant not specified [RCV004216928] Chr17:41462930 [GRCh38]
Chr17:39619182 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.773C>T (p.Pro258Leu) single nucleotide variant not specified [RCV004215213] Chr17:41464379 [GRCh38]
Chr17:39620631 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.1022C>T (p.Thr341Met) single nucleotide variant not specified [RCV004220845] Chr17:41463025 [GRCh38]
Chr17:39619277 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.1069A>G (p.Met357Val) single nucleotide variant not specified [RCV004235668] Chr17:41462978 [GRCh38]
Chr17:39619230 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.1300C>T (p.Arg434Cys) single nucleotide variant not specified [RCV004214479] Chr17:41460157 [GRCh38]
Chr17:39616409 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.58C>T (p.Arg20Trp) single nucleotide variant not specified [RCV004191624] Chr17:41467268 [GRCh38]
Chr17:39623520 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.373G>A (p.Glu125Lys) single nucleotide variant not specified [RCV004155451] Chr17:41466953 [GRCh38]
Chr17:39623205 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.806G>A (p.Arg269Gln) single nucleotide variant not specified [RCV004160806] Chr17:41464346 [GRCh38]
Chr17:39620598 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.1324C>A (p.Pro442Thr) single nucleotide variant not specified [RCV004216934] Chr17:41460133 [GRCh38]
Chr17:39616385 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.1108G>A (p.Ala370Thr) single nucleotide variant not specified [RCV004137775] Chr17:41462939 [GRCh38]
Chr17:39619191 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.952A>G (p.Thr318Ala) single nucleotide variant not specified [RCV004170888] Chr17:41464122 [GRCh38]
Chr17:39620374 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.1207G>A (p.Glu403Lys) single nucleotide variant not specified [RCV004118415] Chr17:41462840 [GRCh38]
Chr17:39619092 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.742C>T (p.Arg248Cys) single nucleotide variant not specified [RCV004221968] Chr17:41464410 [GRCh38]
Chr17:39620662 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.68C>T (p.Ser23Leu) single nucleotide variant not specified [RCV004074485] Chr17:41467258 [GRCh38]
Chr17:39623510 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.169C>T (p.Arg57Trp) single nucleotide variant not specified [RCV004077717] Chr17:41467157 [GRCh38]
Chr17:39623409 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.959A>G (p.Asn320Ser) single nucleotide variant not specified [RCV004318873] Chr17:41464115 [GRCh38]
Chr17:39620367 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.130A>C (p.Met44Leu) single nucleotide variant not specified [RCV004266677] Chr17:41467196 [GRCh38]
Chr17:39623448 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.1163G>A (p.Arg388Gln) single nucleotide variant not specified [RCV004294643] Chr17:41462884 [GRCh38]
Chr17:39619136 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.59G>A (p.Arg20Gln) single nucleotide variant not specified [RCV004330191] Chr17:41467267 [GRCh38]
Chr17:39623519 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.85G>A (p.Val29Met) single nucleotide variant not specified [RCV004340853] Chr17:41467241 [GRCh38]
Chr17:39623493 [GRCh37]
Chr17:17q21.2		 likely benign
NM_002278.3(KRT32):c.1120C>T (p.Arg374Trp) single nucleotide variant not specified [RCV004412315] Chr17:41462927 [GRCh38]
Chr17:39619179 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.1141G>C (p.Val381Leu) single nucleotide variant not specified [RCV004412316] Chr17:41462906 [GRCh38]
Chr17:39619158 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.608G>A (p.Arg203His) single nucleotide variant not specified [RCV004412317] Chr17:41465873 [GRCh38]
Chr17:39622125 [GRCh37]
Chr17:17q21.2		 uncertain significance
NM_002278.3(KRT32):c.743G>A (p.Arg248His) single nucleotide variant not specified [RCV004412318] Chr17:41464409 [GRCh38]
Chr17:39620661 [GRCh37]
Chr17:17q21.2		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:255
Count of miRNA genes:236
Interacting mature miRNAs:246
Transcripts:ENST00000225899
Prediction methods:Miranda, Rnahybrid
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
STS-X81419  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371739,616,227 - 39,616,364UniSTSGRCh37
Build 361736,869,753 - 36,869,890RGDNCBI36
Celera1736,269,452 - 36,269,588RGD
Cytogenetic Map17q21.2UniSTS
HuRef1735,379,841 - 35,379,977UniSTS
GeneMap99-GB4 RH Map17308.41UniSTS
NCBI RH Map17472.6UniSTS
KRTHA2__6358  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371739,615,867 - 39,616,483UniSTSGRCh37
Build 361736,869,393 - 36,870,009RGDNCBI36
Celera1736,269,092 - 36,269,707RGD
HuRef1735,379,481 - 35,380,096UniSTS


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
High 1
Medium 1 213 5 1 5 89
Low 57 24 49 39 14 3 868 82 260 25 234 70 38 6 585
Below cutoff 1174 1087 614 196 476 80 1883 1346 1784 140 828 627 123 504 1338

Sequence


Ensembl Acc Id: ENST00000225899   ⟹   ENSP00000225899
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1741,459,513 - 41,467,386 (-)Ensembl
RefSeq Acc Id: NM_002278   ⟹   NP_002269
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381741,459,513 - 41,467,386 (-)NCBI
GRCh371739,615,765 - 39,623,638 (-)RGD
Build 361736,869,291 - 36,877,164 (-)NCBI Archive
Celera1736,268,990 - 36,276,862 (-)RGD
HuRef1735,379,379 - 35,387,251 (-)ENTREZGENE
CHM1_11739,851,077 - 39,858,950 (-)NCBI
T2T-CHM13v2.01742,315,065 - 42,322,938 (-)NCBI
Sequence:
RefSeq Acc Id: XR_008484817
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01742,319,911 - 42,322,938 (-)NCBI
RefSeq Acc Id: XR_934457
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381741,464,359 - 41,467,386 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_002269 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein CAA57179 (Get FASTA)   NCBI Sequence Viewer  
  CAA62284 (Get FASTA)   NCBI Sequence Viewer  
  EAW60735 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000225899
  ENSP00000225899.3
GenBank Protein Q14532 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_002269   ⟸   NM_002278
- UniProtKB: Q14532 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSP00000225899   ⟸   ENST00000225899
Protein Domains
IF rod

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q14532-F1-model_v2 AlphaFold Q14532 1-448 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:6449 AgrOrtholog
COSMIC KRT32 COSMIC
Ensembl Genes ENSG00000108759 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000225899 ENTREZGENE
  ENST00000225899.4 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 ENSG00000108759 GTEx
HGNC ID HGNC:6449 ENTREZGENE
Human Proteome Map KRT32 Human Proteome Map
InterPro Growth_fac_rcpt_cys_sf UniProtKB/Swiss-Prot
  IF_conserved UniProtKB/Swiss-Prot
  IF_rod_dom UniProtKB/Swiss-Prot
  Keratin_I UniProtKB/Swiss-Prot
KEGG Report hsa:3882 UniProtKB/Swiss-Prot
NCBI Gene 3882 ENTREZGENE
OMIM 602760 OMIM
PANTHER KERATIN, TYPE I CUTICULAR HA2 UniProtKB/Swiss-Prot
  PTHR23239 UniProtKB/Swiss-Prot
Pfam Filament UniProtKB/Swiss-Prot
PharmGKB PA30238 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
  SSF57184 UniProtKB/Swiss-Prot
UniProt K1H2_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-14 KRT32  keratin 32  KRT32  keratin 32, type I  Symbol and/or name change 5135510 APPROVED
2015-01-27 KRT32  keratin 32, type I  KRT32  keratin 32  Symbol and/or name change 5135510 APPROVED