SPEM1 - spermatid maturation 1 Gene

Homo sapiens

Also known as C17orf83

Gene ID: 374768 | Gene type: protein coding

About SPEM1

Cytogenetic location: 17p13.1 Genomic coordinates (GRCh38): 17:7,420,324-7,421,632 (from NCBI)

This gene has 1 transcript (splice variant), 1 gene allele and 79 orthologues. Restricted expression toward testis (RPKM 24.6).

Summary

Predicted to be involved in flagellated sperm motility and sperm individualization. Predicted to act upstream of or within spermatogenesis. Predicted to be integral component of membrane. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

SPEM1 Products(1)

mRNA	Protein	Name
NM_199339.3	NP_955371.2	spermatid maturation protein 1

Protein Preferred Names

Protein Names

spermatid maturation protein 1

SPEM1 Protein-protein interaction Information

Type Cross Intra	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	Reference
Intra	SPEM1	Q8N4L4	PPP1R1A	Homo sapiens	Q13522	Anti Tag CoIP	33961781
Intra	SPEM1	Q8N4L4	PPP1R1A	Homo sapiens	Q13522	Anti Tag CoIP	28514442

Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases

Alias

Spermatogenic Failure 9

Male Infertility Due To Globozoospermia	SPGF9
Male Infertility Due To Round-Headed Spermatozoa	Globozoospermia, Complete
Globozoospermia, Total	Globozoospermia
Globozoospermia Syndrome	Round-Headed Sperm Syndrome
Globozoospermia Complete	Globozoospermia Total

Spermatogenic Failure

Azoospermia	Spgf
Spermatogenic Failure, Susceptibility To	Absent Sperm
Aspermatogenesis	Infertility Due To Azoospermia
Hypospermatogenesis	Azoospermatism

Oligospermia

Primary Ciliary Dyskinesia

Immotile Cilia Syndrome	Kartagener Syndrome
Dextrocardia Bronchiectasis And Sinusitis	Pcd
Ciliary Motility Disorders	Ciliary Motility Disorder
Immotile Ciliary Syndrome	Ciliary Dyskinesia Primary
Ics	Polynesian Bronchiectasis
Dextrocardia-Bronchiectasis-Sinusitis Syndrome	Immotile Cilia Syndrome, Kartagener Type
Primary Ciliary Dyskinesia And Situs Inversus	Primary Ciliary Dyskinesia, Kartagener Type
Siewert Syndrome	Dyskinesia, Ciliary, Primary

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-RS13659	SPEM1 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	SPEM1	RGD	RGD:1593311
Mus musculus	SPEM1	MGD	MGI:1921538
Bos taurus	SPEM1	VGNC	VGNC:35203
Felis catus	SPEM1	VGNC	VGNC:99463
Macaca mulatta	SPEM1	VGNC	VGNC:78031

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