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Gene: KRTAP10-9 (keratin associated protein 10-9) Homo sapiens
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Symbol: KRTAP10-9
Name: keratin associated protein 10-9
Description: INVOLVED IN keratinization (inferred); ASSOCIATED WITH autistic disorder; autoimmune polyendocrine syndrome type 1; Neurodevelopmental Disorders; FOUND IN cytosol (inferred); keratin filament (inferred); INTERACTS WITH bisphenol A (ortholog)
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: high sulfur keratin-associated protein 10.9; KAP10.9; KAP18.9; keratin associated protein 18-9; keratin-associated protein 10-9; keratin-associated protein 10.9; keratin-associated protein 18-9; keratin-associated protein 18.9; KRTAP18-9
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382144,627,093 - 44,628,378 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372146,047,040 - 46,048,295 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362144,871,468 - 44,872,723 (+)NCBINCBI36hg18NCBI36
Celera2131,154,676 - 31,155,931 (+)NCBI
Cytogenetic Map21q22.3NCBI
HuRef2131,421,207 - 31,422,462 (+)NCBIHuRef
CHM1_12145,607,647 - 45,608,901 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
 
More on KRTAP10-9
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1605521
Created: 2007-04-28
Species: Homo sapiens
Last Modified: 2019-10-08
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.