Krtap13 keratin associated protein 13 [Mus musculus (house mouse)] - Gene

Summary

Official Symbol: Krtap13provided by MGI
Official Full Name: keratin associated protein 13provided by MGI
Primary source: MGI:MGI:1330835
See related: Ensembl:ENSMUSG00000050224 AllianceGenome:MGI:1330835
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Mus musculus
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus
Also known as: 4C32
Summary: Is expressed in skin and tongue. Orthologous to human KRTAP13-3 (keratin associated protein 13-3). [provided by Alliance of Genome Resources, Apr 2022]
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Genomic context

Location:: 16 C3.3; 16 51.4 cM

Exon count:: 1

Annotation release	Status	Assembly	Chr	Location
RS_2024_02	current	GRCm39 (GCF_000001635.27)	16	NC_000082.7 (88547632..88548516, complement)
108.20200622	previous assembly	GRCm38.p6 (GCF_000001635.26)	16	NC_000082.6 (88750744..88751628, complement)

Chromosome 16 - NC_000082.7 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Krtap16 is a hair keratin-associated protein gene complex regulated by Hoxc13; localized to chromosome 16
Title: Krtap16, characterization of a new hair keratin-associated protein (KAP) gene complex on mouse chromosome 16 and evidence for regulation by Hoxc13.

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Variation

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Alleles

Alleles of this type are documented at Mouse Genome Informatics (MGI)

Endonuclease-mediated (1)

General gene information

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General protein information

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Preferred Names: keratin associated protein 13

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.