Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
64395
Gene name Gene Name - the full gene name approved by the HGNC.
Germ cell-less 1, spermatogenesis associated
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
GMCL1
Synonyms (NCBI Gene) Gene synonyms aliases
BTBD13, GCL, GCL1, SPATA29
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p13.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a nuclear envelope protein that appears to be involved in spermatogenesis, either directly or by influencing genes that play a more direct role in the process. This multi-exon locus is the homolog of the mouse and drosophila germ cell-le
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT022371 hsa-miR-124-3p Microarray 18668037
MIRT679415 hsa-miR-3664-5p HITS-CLIP 23824327
MIRT679414 hsa-miR-4639-3p HITS-CLIP 23824327
MIRT679413 hsa-miR-1304-3p HITS-CLIP 23824327
MIRT679412 hsa-miR-3135a HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 21145461, 21516116, 25910212, 26871637, 27107012, 28514442, 31515488, 32296183, 32814053
GO:0005634 Component Nucleus IBA 21873635
GO:0007275 Process Multicellular organism development IEA
GO:0007281 Process Germ cell development IEA
GO:0007283 Process Spermatogenesis IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
618627 23843 ENSG00000087338
Protein
UniProt ID Q96IK5
Protein name Germ cell-less protein-like 1 (Spermatogenesis-associated protein 29)
Protein function Possible function in spermatogenesis. Enhances the degradation of MDM2 and increases the amount of p53 probably by modulating the nucleocytoplasmic transport (By similarity).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00651 BTB 98 208 BTB/POZ domain Domain
PF07707 BACK 213 301 BTB And C-terminal Kelch Domain
Sequence
MGSLSSRVLRQPRPALAQQAQGARAGGSARRPDTGDDAAGHGFCYCAGSHKRKRSSGSFC
YCHPDSETDEDEEEGDEQQRLLNTPRRKKLKSTSKYIYQTLFLNGENSDIKICALGEEWS
LHKIYLCQSGYFSSMFSGSWKESSMNIIELEIPDQNIDVEALQVAFGSLYRDDVLIKPSR
VVAILAAACLLQLDGLIQQCGETMKETV
NVKTVCGYYTSAGTYGLDSVKKKCLEWLLNNL
MTHQNVELFKELSINVMKQLIGSSNLFVMQVEMDIYTALKKWMFLQLVPSWNGSLKQLLT
E
TDVWFSKQRKDFEGMAFLETEQGKPFVSVFRHLRLQYIISDLASARIIEQDAVVPSEWL
SSVYKQQWFAMLRAEQDSEVGPQEINKEELEGNSMRCGRKLAKDGEYCWRWTGFNFGFDL
LVTYTNRYIIFKRNTLNQPCSGSVSLQPRRSIAFRLRLASFDSSGKLICSRTTGYQILTL
EKDQEQVVMNLDSRLLIFPLYICCNFLYISPEKKN
Sequence length 515
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Atrial fibrillation Atrial Fibrillation rs120074192, rs121908590, rs121908593, rs121434558, rs587776851, rs387906612, rs387906613, rs387906614, rs387906615, rs199472687, rs199472705, rs199473324, rs587777336, rs587777339, rs587777557
View all (6 more)
30061737
Unknown
Disease term Disease name Evidence References Source
Atrial Fibrillation Atrial Fibrillation GWAS
Associations from Text Mining
Disease Name Relationship Type References
Asthenozoospermia Associate 30544396
Carotid Body Tumor Associate 30967136
Hypospadias Associate 32728162
Lymphoma Large B Cell Diffuse Associate 20432501