KRTAP6-3

keratin associated protein 6-3, the group of Keratin associated proteins

Basic information

Region (hg38): 21:30592439-30593075

Links

ENSG00000212938NCBI:337968HGNC:18933Uniprot:Q3LI67AlphaFoldGenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the KRTAP6-3 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the KRTAP6-3 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
7
clinvar
1
clinvar
8
nonsense
0
start loss
0
frameshift
0
inframe indel
0
splice donor/acceptor (+/-2bp)
0
splice region
0
non coding
0
Total 0 0 7 0 1

Variants in KRTAP6-3

This is a list of pathogenic ClinVar variants found in the KRTAP6-3 region.

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

Position Type Phenotype Significance ClinVar
21-30592469-G-A not specified Uncertain significance (Oct 25, 2023)3117129
21-30592469-G-T not specified Uncertain significance (Oct 05, 2022)2317200
21-30592555-G-A not specified Uncertain significance (Jun 10, 2024)3289766
21-30592570-G-T not specified Uncertain significance (May 22, 2023)2549353
21-30592582-G-A not specified Uncertain significance (Sep 22, 2023)3117128
21-30592588-G-T Benign (Jul 06, 2018)773370
21-30592596-T-G not specified Uncertain significance (Aug 02, 2021)2240670
21-30592710-C-T not specified Uncertain significance (Sep 22, 2023)3117130
21-30592726-G-A not specified Uncertain significance (Sep 17, 2021)2348445

GnomAD

Source: gnomAD

GeneTypeBio TypeTranscript Coding Exons Length
KRTAP6-3protein_codingprotein_codingENST00000391624 1636
pLI Probability
LOF Intolerant
pRec Probability
LOF Recessive
Individuals with
no LOFs
Individuals with
Homozygous LOFs
Individuals with
Heterozygous LOFs
Defined p
0.5120.42600000.00
Z-Score Observed Expected Observed/Expected Mutation Rate Total Possible in Transcript
Missense0.1535053.10.9410.00000245625
Missense in Polyphen
Synonymous-0.2472826.41.060.00000151210
Loss of Function1.3202.040.008.47e-831

LoF frequencies by population

EthnicitySum of pLOFs p
African & African-American0.000.00
Ashkenazi Jewish0.000.00
East Asian0.000.00
Finnish0.000.00
European (Non-Finnish)0.000.00
Middle Eastern0.000.00
South Asian0.000.00
Other0.000.00

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.;

Haploinsufficiency Scores

pHI
0.381
hipred
N
hipred_score
0.123
ghis

Essentials

essential_gene_CRISPR
essential_gene_CRISPR2
N
essential_gene_gene_trap
gene_indispensability_pred
N
gene_indispensability_score
0.000104

Gene Damage Prediction

AllRecessiveDominant
MendelianMediumMediumMedium
Primary ImmunodeficiencyMediumMediumMedium
CancerMediumMediumMedium

Gene ontology

Biological process
keratinization
Cellular component
cytosol;intermediate filament
Molecular function