KRTAP8-1

keratin associated protein 8-1, the group of Keratin associated proteins

Basic information

Region (hg38): 21:30812697-30813274

Links

ENSG00000183640HGNC:18935Uniprot:Q8IUC2AlphaFoldGenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the KRTAP8-1 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the KRTAP8-1 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
6
clinvar
6
nonsense
0
start loss
0
frameshift
0
inframe indel
0
splice donor/acceptor (+/-2bp)
0
splice region
0
non coding
0
Total 0 0 6 0 0

Variants in KRTAP8-1

This is a list of pathogenic ClinVar variants found in the KRTAP8-1 region.

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

Position Type Phenotype Significance ClinVar
21-30813040-C-T not specified Uncertain significance (Apr 27, 2022)2257388
21-30813045-G-A not specified Uncertain significance (Nov 21, 2023)3117134
21-30813061-A-G not specified Uncertain significance (Jun 02, 2023)2555337
21-30813081-T-C not specified Uncertain significance (Mar 17, 2023)2523247
21-30813102-T-C not specified Uncertain significance (Sep 13, 2023)2623535
21-30813199-C-T not specified Uncertain significance (Dec 19, 2022)2336637

GnomAD

Source: gnomAD

GeneTypeBio TypeTranscript Coding Exons Length
KRTAP8-1protein_codingprotein_codingENST00000329621 1555
pLI Probability
LOF Intolerant
pRec Probability
LOF Recessive
Individuals with
no LOFs
Individuals with
Homozygous LOFs
Individuals with
Heterozygous LOFs
Defined p
0.1030.60200000.00
Z-Score Observed Expected Observed/Expected Mutation Rate Total Possible in Transcript
Missense0.4933139.80.7800.00000235393
Missense in Polyphen1417.1570.81601159
Synonymous-0.1802120.01.050.00000152128
Loss of Function0.19211.230.8135.15e-816

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.;
Pathway
Vitamin D Receptor Pathway (Consensus)

Recessive Scores

pRec
0.0876

Intolerance Scores

loftool
0.564
rvis_EVS
0.32
rvis_percentile_EVS
72.94

Haploinsufficiency Scores

pHI
0.134
hipred
N
hipred_score
0.144
ghis
0.398

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
Krtap8-1
Phenotype

Gene ontology

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