1. Gene
  2. HCLS1 - hematopoietic cell-specific Lyn substrate 1 Gene

HCLS1 - hematopoietic cell-specific Lyn substrate 1 Gene

Homo sapiens

Also known as HS1; p75; CTTNL; lckBP1

Gene ID: 3059 | Gene type: protein coding

About HCLS1

Cytogenetic location: 3q13.33 Genomic coordinates (GRCh38): 3:121,631,399-121,660,903 (from NCBI)

This gene has 12 transcripts (splice variants), 202 orthologues and 4 paralogues. Broad expression in spleen (RPKM 118.5), lymph node (RPKM 107.3) and 16 other tissues.

Summary

Enables RNA polymerase II-specific DNA-binding transcription factor binding activity and protein kinase binding activity. Involved in several processes, including positive regulation of intracellular signal transduction; positive regulation of protein phosphorylation; and regulation of transcription, DNA-templated. Located in cytosol; nucleus; and plasma membrane. Part of transcription regulator complex. [provided by Alliance of Genome Resources, Apr 2022]

HCLS1 Products(2)

mRNA Protein Name
NM_001292041.2 NP_001278970.2 hematopoietic lineage cell-specific protein isoform 2
NM_005335.6 NP_005326.3 hematopoietic lineage cell-specific protein isoform 1

HCLS1 Protein Structure

HS1_rep

HS1_rep: Repeat in HS1/Cortactin (82 - 118)

HS1_rep

HS1_rep: Repeat in HS1/Cortactin (119 - 155)

HS1_rep

HS1_rep: Repeat in HS1/Cortactin (156 - 192)

HS1_rep

HS1_rep: Repeat in HS1/Cortactin (193 - 213)

SH3_1

SH3_1: SH3 domain (434 - 479)

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  • 486 a.a.
Protein Preferred Names Protein Names

hematopoietic lineage cell-specific protein

Recombinant HCLS1 Proteins

Cat. No. Product Name Accession Purity
HY-P70289 HCLS1 Protein, Human (HEK293, His) P14317 (M1-E486) ≥95%

Related Diseases

Diseases Alias
Severe Congenital Neutropenia 3

Kostmann Syndrome

Infantile Agranulocytosis

Kostmann Disease

Scn3

Severe Congenital Neutropenia Type 3

Severe Congenital Neutropenia

Congenital Neutropenia

Neutropenia, Severe Congenital

Congenital Agranulocytosis

Infantile Genetic Agranulocytosis

Kostmann Disease

Kostmann'S Agranulocytosis

Kostmann'S Syndrome

Severe Infantile Genetic Neutropenia

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
Canis familiaris HCLS1 VGNC VGNC:41619
Felis catus HCLS1 VGNC VGNC:67543
Bos taurus HCLS1 VGNC VGNC:29775
Rattus norvegicus HCLS1 RGD RGD:1304754
Mus musculus HCLS1 MGD MGI:104568
Macaca mulatta HCLS1 VGNC VGNC:73354
Others HCLS1 NCBI