MEIG1 - meiosis/spermiogenesis associated 1 Gene
Also Known as SPATA39; bA2K17.3
Species: Homo sapiens
Gene Type: protein coding
Gene ID: 644890
About MEIG1
Cytogenetic location: 10p13
Genomic coordinates (GRCh38): 10:14,954,228-14,988,050 (from NCBI)
This gene has 5 transcripts (splice variants) and 175 orthologues. Biased expression in testis (RPKM 4.2) and brain (RPKM 0.2).
Summary
Predicted to act upstream of or within cellular protein localization; manchette assembly; and sperm axoneme assembly. Predicted to be located in cytosol and manchette. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]
MEIG1 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_001080836.3 | NP_001074305.1 | meiosis expressed gene 1 protein homolog |
| Molecular Function GO Annotation | Evidence | Verweise | 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
MEIG1 Protein Structure
Meiosis_expr
Meiosis_expr: Meiosis-expressed (11 - 87)
- 0
- 88 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
meiosis expressed gene 1 protein homolog |
|
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Cardiomyopathy, Familial Hypertrophic, 7 |
|
|
Related Agents
- Pre-clinical Phase
Pre-clinical Phase
Bioactive Molecules
(1)
| Art. -Nr. | Produktname |
Wirkung
|
Reinheit |
Rare Diseases
|
|---|---|---|---|---|
| HY-RS08321 | MEIG1 Human Pre-designed siRNA Set A | Pre-designed Set | / | Unkown |
Compound Screening Libraries
Virtual Screening
Customize Your Library
Drug Screening Service