SPEF2 (sperm flagellar 2)

2014-11-01  

Identity

HGNC
LOCATION
5p13.2
LOCUSID
ALIAS
CT122,KPL2,SPGF43
FUSION GENES

Other Information

Locus ID:

NCBI: 79925
MIM: 610172
HGNC: 26293
Ensembl: ENSG00000152582

Variants:

dbSNP: 79925
ClinVar: 79925
TCGA: ENSG00000152582
COSMIC: SPEF2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000152582ENST00000282469Q9C093
ENSG00000152582ENST00000356031Q9C093
ENSG00000152582ENST00000356031A0A140VKD0
ENSG00000152582ENST00000440995Q9C093
ENSG00000152582ENST00000506526H0YAC0
ENSG00000152582ENST00000508817H0Y8H6
ENSG00000152582ENST00000509059D6REZ4
ENSG00000152582ENST00000510777D6RGZ5
ENSG00000152582ENST00000513078H0Y989
ENSG00000152582ENST00000637061A0A1B0GWC1
ENSG00000152582ENST00000637569A0A1B0GWD8

Expression (GTEx)

0
5
10
15

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
385684622024Novel SPEF2 variants cause male infertility and likely primary ciliary dyskinesia.0
385684622024Novel SPEF2 variants cause male infertility and likely primary ciliary dyskinesia.0
347556992022Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans.5
347556992022Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans.5
310483442020Homozygous mutations in SPEF2 induce multiple morphological abnormalities of the sperm flagella and male infertility.31
315456502020SPEF2- and HYDIN-Mutant Cilia Lack the Central Pair-associated Protein SPEF2, Aiding Primary Ciliary Dyskinesia Diagnostics.36
319426432020Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD.31
310483442020Homozygous mutations in SPEF2 induce multiple morphological abnormalities of the sperm flagella and male infertility.31
315456502020SPEF2- and HYDIN-Mutant Cilia Lack the Central Pair-associated Protein SPEF2, Aiding Primary Ciliary Dyskinesia Diagnostics.36
319426432020Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD.31
311519902019Loss-of-function mutations in SPEF2 cause multiple morphological abnormalities of the sperm flagella (MMAF).30
312787452019Biallelic mutations in Sperm flagellum 2 cause human multiple morphological abnormalities of the sperm flagella (MMAF) phenotype.11
311519902019Loss-of-function mutations in SPEF2 cause multiple morphological abnormalities of the sperm flagella (MMAF).30
312787452019Biallelic mutations in Sperm flagellum 2 cause human multiple morphological abnormalities of the sperm flagella (MMAF) phenotype.11
203796142010Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.78

Citation

Dessen P

SPEF2 (sperm flagellar 2)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/74169/haematological-explorer/cancer-prone-explorer/favicon/apple-touch-icon.png