PDIK1L - PDLIM1 interacting kinase 1 like Gene

Homo sapiens

Also known as CLIK1L; STK35L2

Gene ID: 149420 | Gene type: protein coding

About PDIK1L

Cytogenetic location: 1p36.11 Genomic coordinates (GRCh38): 1:26,111,162-26,125,555 (from NCBI)

This gene has 4 transcripts (splice variants), 203 orthologues and 8 paralogues. Ubiquitous expression in thyroid (RPKM 7.2), bone marrow (RPKM 4.5) and 25 other tissues.

Summary

Predicted to enable protein serine/threonine kinase activity. Predicted to be involved in meiotic cell cycle. Located in nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

PDIK1L Products(3)

mRNA	Protein	Name
NM_001243532.2	NP_001230461.1	serine/threonine-protein kinase PDIK1L
NM_001243533.2	NP_001230462.1	serine/threonine-protein kinase PDIK1L
NM_152835.5	NP_690048.1	serine/threonine-protein kinase PDIK1L

PDIK1L Protein Structure

Pkinase

0
100
200
300
341 a.a.

Protein Preferred Names

Protein Names

serine/threonine-protein kinase PDIK1L

casein kinase

Related Diseases

Diseases

Alias

Axenfeld-Rieger Syndrome, Type 1

Axenfeld-Rieger Syndrome Type 1	RIEG1
Rieg	Rgs
Rieger Syndrome Type 1	Rieger Syndrome, Type 1
Axenfeld-Rieger Syndrome 1	Iridogoniodysgenesis With Somatic Anomalies

Acromesomelic Dysplasia 2c

Acromesomelic Dysplasia, Hunter-Thompson Type	Acromesomelic Dysplasia 2c, Hunter-Thompson Type
AMD2C	Acromesomelic Dwarfism
Amdh Acromesomelic Dwarfism	Acromesomelic Dysplasia-2c
Acromesomelic Dysplasia Hunter Thompson Type	Acromesomelic Chondrodysplasia, Hunter-Thompson Type
Amdh	Dysplasia, Acromesomelic, Type 2c, Hunter-Thompson
Acromesomelic Dysplasia Hunter-Thompson Type

Nail Disorder, Nonsyndromic Congenital, 4

Anonychia Congenita	Anonychia
Hyponychia Congenita	NDNC4
Anonychia/Hyponychia Congenita	Nonsyndromic Congenital Nail Disorder 4
Isolated Congenital Anonychia	Anonychia Congenita Totalis
Anonychia Totalis	Autosomal Recessive Nonsyndromic Congenital Nail Disorder-4
Congenital Anonychia	Nonsyndromic Congenital Nail Disorder, 4
Absent Nails	Aplastic Nails
Congenital Absence Of Nails	Isolated Anonychia
Nail Disorder, Non-Syndromic Congenital, 4	Nail Disorder, Nonsyndromic, Congenital, Type 4

Nonsyndromic Congenital Nail Disorder

Nail Disorder, Nonsyndromic Congenital

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

Related Agents

Pre-clinical Phase

Bioactive Molecules (2)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-148061	DB1113		99.28%	Unkown
HY-RS10272	PDIK1L Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Macaca mulatta	PDIK1L	VGNC	VGNC:75830
Bos taurus	PDIK1L	VGNC	VGNC:32701
Mus musculus	PDIK1L	MGD	MGI:2385213
Canis familiaris	PDIK1L	VGNC	VGNC:44379
Rattus norvegicus	PDIK1L	RGD	RGD:1307476
Felis catus	PDIK1L	VGNC	VGNC:64087

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