KRTAP12-2

keratin associated protein 12-2, the group of Keratin associated proteins

Basic information

Region (hg38): 21:44666189-44666927

Links

ENSG00000221864NCBI:353323HGNC:20530Uniprot:P59991AlphaFoldGenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the KRTAP12-2 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the KRTAP12-2 gene is commonly pathogenic or not.

In the table, we include only reliable ClinVar variants with their consequences to MANE Select, Mane Plus Clinical transcripts, or transcripts with TSL equals 1. Click the count to view the source variants.

Warning: slight differences between displayed counts and the number of variants in ClinVar may occur, primarily due to (1) the application of a different transcript and/or consequence by our variant effect predictor or (2) differences in clinical significance: we classify Benign/Likely benign variants as Likely benign and Pathogenic/Likely pathogenic variants as Likely pathogenic.

Variant type Pathogenic Likely pathogenic VUS Likely benign Benign Sum
synonymous
0
missense
12
clinvar
2
clinvar
14
nonsense
0
start loss
0
frameshift
0
inframe indel
0
splice donor/acceptor (+/-2bp)
0
splice region
0
non coding
0
Total 0 0 12 2 0

Variants in KRTAP12-2

This is a list of pathogenic ClinVar variants found in the KRTAP12-2 region.

You can filter this list by clicking the number of variants in the Variants pathogenicity by type table.

Position Type Phenotype Significance ClinVar
21-44666463-T-C not specified Uncertain significance (Jun 21, 2021)2388459
21-44666492-C-T not specified Uncertain significance (Nov 24, 2024)3536434
21-44666514-A-G not specified Uncertain significance (Sep 04, 2024)3116925
21-44666549-A-T not specified Uncertain significance (Jul 17, 2023)2612240
21-44666553-G-A Likely benign (Oct 01, 2023)2652780
21-44666564-A-G not specified Uncertain significance (Nov 25, 2024)3536435
21-44666607-C-T not specified Uncertain significance (Jan 18, 2022)2344969
21-44666655-C-T not specified Uncertain significance (Sep 16, 2021)2211730
21-44666661-C-G not specified Uncertain significance (Nov 08, 2022)3116924
21-44666661-C-T not specified Uncertain significance (Sep 04, 2024)2213939
21-44666715-C-T not specified Uncertain significance (Mar 30, 2024)3289645
21-44666746-G-A not specified Likely benign (Nov 11, 2024)3536432
21-44666748-G-A not specified Uncertain significance (Jul 12, 2023)2602301
21-44666757-C-T not specified Uncertain significance (Sep 11, 2024)3116923
21-44666774-A-G not specified Uncertain significance (Nov 03, 2023)3116922
21-44666799-A-G not specified Uncertain significance (Jan 10, 2022)2271746
21-44666807-G-A not specified Uncertain significance (Mar 04, 2024)3116926
21-44666834-C-T Likely benign (Dec 01, 2022)2652781
21-44666856-G-T not specified Uncertain significance (Aug 11, 2024)3536433
21-44666864-G-A not specified Uncertain significance (Dec 04, 2024)3536431

GnomAD

Source: gnomAD

GeneTypeBio TypeTranscript Coding Exons Length
KRTAP12-2protein_codingprotein_codingENST00000360770 1739
pLI Probability
LOF Intolerant
pRec Probability
LOF Recessive
Individuals with
no LOFs
Individuals with
Homozygous LOFs
Individuals with
Heterozygous LOFs
Defined p
Z-Score Observed Expected Observed/Expected Mutation Rate Total Possible in Transcript
Missense-0.03038281.21.010.00000440920
Missense in Polyphen2422.9991.0435258
Synonymous0.005014040.00.9990.00000268307
Loss of Function

LoF frequencies by population

EthnicitySum of pLOFs p
African & African-American0.000.00
Ashkenazi Jewish
East Asian
Finnish
European (Non-Finnish)
Middle Eastern
South Asian
Other

dbNSFP

Source: dbNSFP

Function
FUNCTION: In the hair cortex, hair keratin intermediate filaments are embedded in an interfilamentous matrix, consisting of hair keratin-associated proteins (KRTAP), which are essential for the formation of a rigid and resistant hair shaft through their extensive disulfide bond cross-linking with abundant cysteine residues of hair keratins. The matrix proteins include the high- sulfur and high-glycine-tyrosine keratins.;
Pathway
Vitamin D Receptor Pathway (Consensus)

Recessive Scores

pRec
0.103

Intolerance Scores

loftool
0.632
rvis_EVS
1.75
rvis_percentile_EVS
96.67

Haploinsufficiency Scores

pHI
hipred
N
hipred_score
0.112
ghis
0.420

Essentials

essential_gene_CRISPR
N
essential_gene_CRISPR2
N
essential_gene_gene_trap
N
gene_indispensability_pred
N
gene_indispensability_score
0.114

Gene Damage Prediction

AllRecessiveDominant
MendelianMediumMediumMedium
Primary ImmunodeficiencyMediumMediumMedium
CancerMediumMediumMedium

Mouse Genome Informatics

Gene name
Gm10142
Phenotype

Gene ontology

Biological process
keratinization
Cellular component
cytosol;keratin filament
Molecular function
protein binding