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SPEF2

SPEF2
Identifiers
Aliases SPEF2, CT122, KPL2, sperm flagellar 2
External IDs MGI: 2443727 HomoloGene: 23371 GeneCards: SPEF2
Gene location (Human)
Chromosome 5 (human)
Chr. Chromosome 5 (human)
Chromosome 5 (human)
Genomic location for SPEF2
Genomic location for SPEF2
Band No data available Start 35,617,844 bp
End 35,814,611 bp
RNA expression pattern
PBB GE FLJ23577 gnf1h00440 at fs.png

PBB GE FLJ23577 gnf1h00434 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_024867
NM_144722

NM_177123
NM_001305042
NM_001305044

RefSeq (protein)

NP_079143
NP_653323

NP_001291971
NP_001291973
NP_796097

Location (UCSC) Chr 5: 35.62 – 35.81 Mb Chr 5: 9.58 – 9.75 Mb
PubMed search

NM_024867
NM_144722

NM_177123
NM_001305042
NM_001305044

NP_079143
NP_653323

NP_001291971
NP_001291973
NP_796097

Sperm flagellar protein 2 is a protein that in humans is encoded by the SPEF2 gene.

SPEF2 plays an important role in spermatogenesis and flagellar assembly. SPEF2 is expressed in all ciliated cells and is required for cilia function. Sperm contain cilia, and a mutation in the SPEF2 gene can cause male infertility due to immobile sperm. In a pig animal model, a SPEF2 mutation affects the sperm tail development. And a loss of function mutation in SPEF2 in mice causes the big giant head phenotype. SPEF2 mRNA and protein products are localized in germ and sertoli cells. Within these cells, SPEF2 is localized in the golgi complex, manchette, basal body and mid piece of the sperm tail. SPEF2 has been shown to interact with the intracellular transport protein IFT20 in the testis.


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