1. Gene
  2. PKDCC - protein kinase domain containing, cytoplasmic Gene

PKDCC - protein kinase domain containing, cytoplasmic Gene

Homo sapiens

Also known as Vlk; RLSDF; SGK493

Gene ID: 91461 | Gene type: protein coding

About PKDCC

Cytogenetic location: 2p21 Genomic coordinates (GRCh38): 2:42,048,021-42,058,517 (from NCBI)

This gene has 9 transcripts (splice variants), 156 orthologues, 2 paralogues and is associated with 1 phenotype. Broad expression in ovary (RPKM 28.2), endometrium (RPKM 26.6) and 22 other tissues.

Summary

Enables non-membrane spanning protein tyrosine kinase activity. Involved in peptidyl-tyrosine phosphorylation and skeletal system development. Located in extracellular region. [provided by Alliance of Genome Resources, Apr 2022]

PKDCC Products(1)

mRNA Protein Name
NM_138370.3 NP_612379.2 extracellular tyrosine-protein kinase PKDCC precursor

PKDCC Protein Structure

PIP49_C

PIP49_C: Protein-kinase domain of FAM69 (238 - 368)

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  • 493 a.a.
Protein Preferred Names Protein Names

extracellular tyrosine-protein kinase PKDCC

protein kinase domain containing, cytoplasmic homolog

Related Diseases

Diseases Alias
Rhizomelic Limb Shortening With Dysmorphic Features

RLSDF

N Syndrome

NSX

Intellectual Disability, Malformations, Chromosome Breakage, And Development Of T-Cell Leukemia

Amelogenesis Imperfecta, Type Ic

Amelogenesis Imperfecta Type 1c

AI1C

Amelogenesis Imperfecta Type Ic

Amelogenesis Imperfecta, Local Hypoplastic Type, Autosomal Recessive

Amelogenesis Imperfecta, Hypoplastic, With Or Without Open-Bite Malocclusion, Autosomal Recessive

Autosomal Recessive Amelogenesis Imperfecta Hypoplastic With Or Without Openbite Malocclusion

Autosomal Recessive Amelogenesis Imperfecta Local Hypoplastic Type

Amelogenesis Imperfecta 1c

Amelogenesis Imperfecta Hypoplastic With Or Without Openbite Malocclusion Autosomal Recessive

Amelogenesis Imperfecta Local Hypoplastic Type Autosomal Recessive

Cleft Palate, Isolated

Cleft Palate

Isolated Cleft Palate

CPI

Cp

Palatoschisis

Cleft Palate Isolated

Uranostaphyloschisis

Congenital Fissure Of Palate

Cleft Of Secondary Palate

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus PKDCC VGNC VGNC:81149
Macaca mulatta PKDCC VGNC VGNC:106196
Canis familiaris PKDCC VGNC VGNC:44603
Mus musculus PKDCC MGD MGI:2147077
Bos taurus PKDCC VGNC VGNC:32938
Rattus norvegicus PKDCC RGD RGD:1311939