TBC1D21 (TBC1 domain family member 21)

2015-11-01  

Identity

HGNC
LOCATION
15q24.1
LOCUSID
ALIAS
MgcRabGAP
FUSION GENES

Other Information

Locus ID:

NCBI: 161514
HGNC: 28536
Ensembl: ENSG00000167139

Variants:

dbSNP: 161514
ClinVar: 161514
TCGA: ENSG00000167139
COSMIC: TBC1D21

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000167139ENST00000300504Q8IYX1
ENSG00000167139ENST00000535547Q8IYX1
ENSG00000167139ENST00000562056H3BTA9

Expression (GTEx)

0
50
100
150

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
329764922020Deficiency of the Tbc1d21 gene causes male infertility with morphological abnormalities of the sperm mitochondria and flagellum in mice.10
329764922020Deficiency of the Tbc1d21 gene causes male infertility with morphological abnormalities of the sperm mitochondria and flagellum in mice.10
249383102014Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population.11
249383102014Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population.11
211289782011Identification and characterization of a novel Rab GTPase-activating protein in spermatids.19
211289782011Identification and characterization of a novel Rab GTPase-activating protein in spermatids.19

Citation

Dessen P

TBC1D21 (TBC1 domain family member 21)

Atlas Genet Cytogenet Oncol Haematol. 2015-11-01

Online version: http://atlasgeneticsoncology.org/gene/55521/tbc1d21-(tbc1-domain-family-member-21)