KRTAP6-3

protein-coding

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

Gene summary

Predicted to be involved in keratinization. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]

MANE transcript

NM_001433434.1

Inheritance

—

ClinVar variants

U:11B:1

Top phenotype

—

gnomAD constraint

pLI —, LoF o/e 0

Max pathogenic AF

—

Genomic locus

chr21:30,592,440-30,593,075

External References & Databases

Transcript & Mutation Effects

hg38 • Region Span ~0.6 kb
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GenCC Phenotypes & Disease Associations

Curated gene-disease validity assertions and inheritance patterns

No GenCC data available for this gene.

ClinVar Associated Diseases & Phenotypes

Reported disease conditions connected to KRTAP6-3 variants in ClinVar

2 Conditions Cataloged
not specifiedTotal: 11
not providedTotal: 1

ClinVar Variants & Pathogenicity by Type

Statistics based on transcript NM_001433434.1. Only rare variants are included.

We include only reliable ClinVar variants with their consequences to MANE Select, MANE Plus Clinical transcripts, or transcripts with TSL equal to 1. Click a count to filter the variants table below.

Slight differences between displayed counts and ClinVar may occur due to a different transcript/consequence chosen by our variant effect predictor, or because we classify Benign/Likely benign as Likely benign and Pathogenic/Likely pathogenic as Likely pathogenic.

EffectPLPVUSLBBSum
synonymous
0
missense
9
clinvar
1
clinvar
10
nonsense
0
start loss
2
clinvar
2
frameshift
0
splice donor/acceptor (+/-2bp)
0
Total00110112
Loading ClinVar variants...

Transcript Catalog

Annotated transcript isoforms across RefSeq and Ensembl databases

Showing 3 of 3 transcripts
Transcript IDSourceProtein IDCoding ExonsMANE Status
NM_001433434.1RefSeqNP_001420363.11MANE Select
ENST00000391624.1EnsemblENSP00000375482.21MANE Select
ENST00000391624.2EnsemblENSP00000375482.31MANE Select

Gene Ontology (GO) Annotations & Pathways

Biological processes, molecular functions, cellular components and pathways

Biological Process

  • keratinization

Cellular Component

  • cytosol
  • intermediate filament

gnomAD Constraint

Source: gnomAD

Gene type
protein_coding
Transcript type
protein_coding
Transcript
ENST00000391624
Coding exons
1
Length
636
Individuals with no LoFs
0
Homozygous LoFs
0
Heterozygous LoFs
0
Defined
0
p
0.00
Z-ScoreObservedExpectedObserved/ExpectedMutation RateTotal Possible
Missense0.1535053.10.9410.00000245625
Missense (PolyPhen)
Synonymous-0.2472826.41.060.00000151210
Loss of Function1.3202.040.008.47e-831

Population LoF Frequency

PopulationCAFp-valueStatus
African00.0absent
Latino/Admixed American00.0absent
Ashkenazi Jewish00.0absent
East Asian00.0absent
Finnish00.0absent
European (Non-Finnish)00.0absent
South Asian00.0absent
Other00.0absent

dbNSFP Gene Annotations

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.;

Essentials

Essential (CRISPR2)
N
Indispensability pred.
N
Indispensability score
0.000104

Gene Damage Prediction

AllRecessiveDominant
MendelianMediumMediumMedium
Primary ImmunodeficiencyMediumMediumMedium
CancerMediumMediumMedium
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