2. Gene
  3. ASZ1 - ankyrin repeat, SAM and basic leucine zipper domain containing 1 Gene

ASZ1 - ankyrin repeat, SAM and basic leucine zipper domain containing 1 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as ALP1; GASZ; Orf3; ANKL1; C7orf7; CT1.19

Gene ID: 136991 | Gene type: protein coding

About ASZ1

Cytogenetic location: 7q31.2 Genomic coordinates (GRCh38): 7:117,363,222-117,427,493 (from NCBI)

This gene has 6 transcripts (splice variants), 201 orthologues and 1 paralogue. Restricted expression toward testis (RPKM 8.9).

Summary

Predicted to be involved in gamete generation and piRNA metabolic process. Predicted to be located in cytoplasm. Predicted to be active in pi-body. [provided by Alliance of Genome Resources, Apr 2022]

ASZ1 Products(3)

mRNA Protein Name
NM_001301821.2 NP_001288750.1 ankyrin repeat, SAM and basic leucine zipper domain-containing protein 1 isoform 2
NM_001301822.2 NP_001288751.1 ankyrin repeat, SAM and basic leucine zipper domain-containing protein 1 isoform 3
NM_130768.3 NP_570124.1 ankyrin repeat, SAM and basic leucine zipper domain-containing protein 1 isoform 1
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

ASZ1 Protein Structure

Ank_2

Ank_2: Ankyrin repeats (3 copies) (53 - 106)

Ank_2

Ank_2: Ankyrin repeats (3 copies) (128 - 210)

SAM_2

SAM_2: SAM domain (Sterile alpha motif) (273 - 334)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 475 a.a.
Protein Preferred Names Protein Names

ankyrin repeat, SAM and basic leucine zipper domain-containing protein 1

ankyrin-like 1

Related Diseases

Diseases Alias
Hepatitis E
Noonan Syndrome 7

NS7

Noonan Syndrome, Type 7
Acute Diarrhea
Noonan Syndrome 12

NS12
Amelogenesis Imperfecta, Type If

Amelogenesis Imperfecta Type 1f

AI1F

Amelogenesis Imperfecta, Hypoplastic Type If

Amelogenesis Imperfecta Type If

Amelogenesis Imperfecta Hypoplastic Type If

Amelogenesis Imperfecta 1f
Erythema Infectiosum

Fifth Disease

Slapped Cheek Syndrome

Parvovirus B19 Infection
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 (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS01117 ASZ1 Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Macaca mulatta ASZ1 VGNC VGNC:70058
Mus musculus ASZ1 MGD MGI:1921318
Felis catus ASZ1 VGNC VGNC:59987
Canis familiaris ASZ1 VGNC VGNC:38199
Bos taurus ASZ1 VGNC VGNC:26231
Rattus norvegicus ASZ1 RGD RGD:621579