SOLH2 Rabbit Polyclonal Antibody, 100ul Antibody Development Mutations in this gene cause

Mutations in this gene cause mitochondrial complex I deficiency

Don't let restrictions hold you back - take control and make your mark with Esp3I(BsmBI) and ADCF

Translocations between MLF1 and nucleophosmin have been associated with myelodysplastic syndrome and acute myeloid leukemia

Stimulates cAMP production

Pseudogenes of this gene are located on the long arm of chromosome 13 and the short arm of chromosome 19

SOLH2 Rabbit Polyclonal Antibody, 100ul Antibody Development Mutations in this gene causeThis gene encodes one of testis specific transcription factors which are essential for spermatogenesis oogenesis and folliculogenesis. This gene is located on chromosome 13. The proteins encoded by this gene and another testis specific transcription factor SOHLH1 can form heterodimers in addition to homodimers. There is a read through locus (GeneID: 100526761) that shares sequence identity with this gene and the upstream CCDC169 (GeneID: 728591).