KRTAP3-4P keratin associated protein 3-4, pseudogene [Homo sapiens (human)] - Gene

Summary

Official Symbol: KRTAP3-4Pprovided by HGNC
Official Full Name: keratin associated protein 3-4, pseudogeneprovided by HGNC
Primary source: HGNC:HGNC:18919
See related: Ensembl:ENSG00000226776 AllianceGenome:HGNC:18919
Gene type: pseudo
RefSeq status: INFERRED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: KAP3A; KRTAP3P1
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Genomic context

Location:: 17q21.2

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	17	NC_000017.11 (41004520..41004759, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	17	NC_060941.1 (41868984..41869223, complement)
105.20220307	previous assembly	GRCh37.p13 (GCF_000001405.25)	17	NC_000017.10 (39160772..39161011, complement)

Chromosome 17 - NC_000017.11 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

These findings therefore reveal new substrates of BRK and define KAP3A as a physiological substrate of BRK during cell migration.
Title: Breast tumor kinase BRK requires kinesin-2 subunit KAP3A in modulation of cell migration.

Submit: New GeneRIF Correction

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Other Names

keratin associated protein 3 pseudogene 1
keratin-associated protein 3A pseudogene

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.