KRTAP1-3

keratin associated protein 1-3, the group of Keratin associated proteins

Basic information

Region (hg38): 17:41033883-41034874

Links

ENSG00000221880 ∙ NCBI:81850 ∙ OMIM:608820 ∙ HGNC:16771 ∙ Uniprot:Q8IUG1 ∙ AlphaFold ∙ GenCC ∙ jax ∙ Sfari ∙ GnomAD ∙ Pubmed ∙ ClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the KRTAP1-3 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the KRTAP1-3 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				1		1
missense			13	2		15
nonsense						0
start loss						0
frameshift						0
inframe indel					2	2
splice donor/acceptor (+/-2bp)						0
splice region						0
non coding						0
Total	0	0	13	3	2

Variants in KRTAP1-3

This is a list of pathogenic ClinVar variants found in the KRTAP1-3 region.

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

Position	Type	Phenotype	Significance	ClinVar
17-41034328-G-A		not specified	Uncertain significance (Oct 29, 2021)
17-41034329-G-A		not specified	Uncertain significance (Dec 16, 2023)
17-41034356-G-C		not specified	Uncertain significance (Jan 10, 2022)
17-41034358-C-T		not specified	Uncertain significance (Aug 15, 2023)
17-41034359-G-A		not specified	Uncertain significance (Jun 07, 2024)
17-41034398-A-C		not specified	Uncertain significance (Sep 16, 2021)
17-41034417-C-G		not specified	Uncertain significance (May 14, 2024)
17-41034428-T-A		not specified	Likely benign (Nov 12, 2021)
17-41034434-G-T		not specified	Uncertain significance (Aug 04, 2023)
17-41034457-G-A		not specified	Uncertain significance (Nov 08, 2022)
17-41034461-G-T		not specified	Uncertain significance (Apr 23, 2024)
17-41034521-C-T		not specified	Uncertain significance (Mar 24, 2023)
17-41034591-C-G		not specified	Uncertain significance (May 14, 2024)
17-41034595-C-T		not specified	Uncertain significance (Apr 07, 2022)
17-41034601-C-A		not specified	Uncertain significance (Mar 28, 2024)
17-41034650-A-G		not specified	Uncertain significance (May 26, 2024)
17-41034677-T-C		not specified	Uncertain significance (Dec 02, 2022)
17-41034701-G-C		See cases • Autism spectrum disorder	Uncertain significance (Sep 23, 2020)
17-41034702-G-A			Likely benign (Sep 01, 2023)
17-41034702-G-GCAGCAGCTTGGCTGGCAGCAGCTGGTCTCA			Benign (Dec 31, 2019)
17-41034710-T-G		not specified	Likely benign (Aug 03, 2022)
17-41034721-C-G		not specified	Uncertain significance (Aug 03, 2022)
17-41034721-C-CAGCTGGTCTCACAGCAGCTTGGCTGGCAGG			Benign (Dec 31, 2019)
17-41034784-C-T		not specified	Uncertain significance (Nov 17, 2023)

GnomAD

Source: gnomAD

Gene	Type	Bio Type	Transcript	Coding Exons	Length
KRTAP1-3	protein_coding	protein_coding	ENST00000344363	1	966

pLI Probability LOF Intolerant	pRec Probability LOF Recessive	Individuals with no LOFs	Individuals with Homozygous LOFs	Individuals with Heterozygous LOFs	Defined	p
0.118	0.788	0	0	0	0	0.00

	Z-Score	Observed	Expected	Observed/Expected	Mutation Rate	Total Possible in Transcript
Missense	0.145	94	98.1	0.959	0.00000548	1090
Missense in Polyphen		1	0.80331	1.2449		9
Synonymous	-1.01	44	36.2	1.21	0.00000194	311
Loss of Function	1.33	2	5.29	0.378	2.31e-7	61

LoF frequencies by population

Ethnicity	Sum of pLOFs	p
African & African-American	0.00	0.00
Ashkenazi Jewish	0.00	0.00
East Asian	0.00	0.00
Finnish	0.00	0.00
European (Non-Finnish)	0.00	0.00
Middle Eastern	0.00	0.00
South Asian	0.00	0.00
Other	0.00	0.00

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.

Intolerance Scores

• loftool: 0.359
• rvis_EVS: 1.17
• rvis_percentile_EVS: 92.68

Haploinsufficiency Scores

• hipred: N
• hipred_score: 0.158

Essentials

• essential_gene_CRISPR: N
• essential_gene_gene_trap: N
• gene_indispensability_pred: N
• gene_indispensability_score: 0.114

Gene Damage Prediction

	All	Recessive	Dominant
Mendelian	Medium	Medium	Medium
Primary Immunodeficiency	Medium	Medium	Medium
Cancer	Medium	Medium	Medium

Mouse Genome Informatics

• Gene name: Krtap1-5

Gene ontology

• Biological process: biological_process;keratinization
• Cellular component: cytosol;keratin filament
• Molecular function: structural constituent of epidermis