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Gene: KRTAP12-4 (keratin associated protein 12-4) Homo sapiens
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Symbol: KRTAP12-4
Name: keratin associated protein 12-4
Description: INVOLVED IN keratinization (inferred); ASSOCIATED WITH autistic disorder; autoimmune polyendocrine syndrome type 1; Neurodevelopmental Disorders; FOUND IN cytosol (inferred); intermediate filament (inferred)
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: high sulfur keratin-associated protein 12.4; keratin-associated protein 12-4; keratin-associated protein 12.4; KRTAP12.4; MGC150594
Orthologs:
Pan paniscus (bonobo/pygmy chimpanzee) : LOC106634220 (keratin-associated protein 12-4)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382144,654,213 - 44,654,659 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372146,074,130 - 46,074,576 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362144,898,558 - 44,899,004 (-)NCBINCBI36hg18NCBI36
Build 342144,898,557 - 44,899,004NCBI
Celera2131,181,766 - 31,182,212 (-)NCBI
Cytogenetic Map21q22.3NCBI
HuRef2131,448,308 - 31,448,754 (-)NCBIHuRef
CHM1_12145,634,978 - 45,635,424 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene Ontology Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
 
More on KRTAP12-4
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1347376
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-09-12
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.