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PKDCC (protein kinase domain containing, cytoplasmic)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
91461
Gene nameGene Name - the full gene name approved by the HGNC.
Protein kinase domain containing, cytoplasmic
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
PKDCC
SynonymsGene synonyms aliases
RLSDF, SGK493, Vlk
ChromosomeChromosome number
2
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p21
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs761532715 C>A Pathogenic, likely-pathogenic Coding sequence variant, stop gained
rs763243200 G>A,T Pathogenic, likely-pathogenic Splice donor variant
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT050335 hsa-miR-25-3p CLASH 23622248
MIRT049360 hsa-miR-92a-3p CLASH 23622248
MIRT1237321 hsa-miR-103a CLIP-seq
MIRT1237322 hsa-miR-107 CLIP-seq
MIRT1237323 hsa-miR-1256 CLIP-seq
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001501 Process Skeletal system development IMP 30478137
GO:0004672 Function Protein kinase activity ISS
GO:0004715 Function Non-membrane spanning protein tyrosine kinase activity IDA 25171405
GO:0005524 Function ATP binding IEA
GO:0005576 Component Extracellular region IDA 25171405
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID Q504Y2
Protein name Extracellular tyrosine-protein kinase PKDCC (EC 2.7.10.2) (Protein kinase domain-containing protein, cytoplasmic) (Protein kinase-like protein SgK493) (Sugen kinase 493) (Vertebrate lonesome kinase)
Protein function Secreted tyrosine-protein kinase that mediates phosphorylation of extracellular proteins and endogenous proteins in the secretory pathway, which is essential for patterning at organogenesis stages. Mediates phosphorylation of MMP1, MMP13, MMP14,
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12260 PIP49_C
191 372
Protein-kinase domain of FAM69
Family
Sequence
MRRRRAAVAAGFCASFLLGSVLNVLFAPGSEPPRPGQSPEPSPAPGPGRRGGRGELARQI
RARYEEVQRYSRGGPGPGAGRPERRRLMDLAPGGPGLPRPRPPWARPLSDGAPGWPPAPG
PGSPGPGPRLGCAALRNVSGAQYMGSGYTKAVYRVRLPGGAAVALKAVDFSGHDLGSCVR
EFGVRRGCYRLAAHKLLKEMVLLERLRHPNVLQLYGYCYQDSEDIPDTLTTITELGAPVE
MIQLLQTSWEDRFRICLSLGRLLHHLAHSPLGSVTLLDFRPRQFVLVDGELKVTDLDDAR
VEETPCAGSTDCILEFPARNFTLPCSAQGWCEGMNEKRNLYNAYRFFFTYLLPHSAPPSL
RPLLDSIVNATG
ELAWGVDETLAQLEKVLHLYRSGQYLQNSTASSSTEYQCIPDSTIPQE
DYRCWPSYHHGSCLLSVFNLAEAVDVCESHAQCRAFVVTNQTTWTGRQLVFFKTGWSQVV
PDPNKTTYVKASG
Sequence length 493
Interactions View interactions
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Multiple congenital anomalies Multiple congenital anomalies rs1057517732 25171405, 19465597, 23792766, 19097194, 23559552
Unknown
Disease name Disease term dbSNP ID References
Dysmorphic features Dysmorphic features 23559552, 19465597, 23792766, 25171405, 19097194

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