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SPAG16 (sperm associated antigen 16)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
79582
Gene nameGene Name - the full gene name approved by the HGNC.
Sperm associated antigen 16
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
SPAG16
SynonymsGene synonyms aliases
PF20, WDR29
ChromosomeChromosome number
2
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q34
SummarySummary of gene provided in NCBI Entrez Gene.
Cilia and flagella are comprised of a microtubular backbone, the axoneme, which is organized by the basal body and surrounded by plasma membrane. SPAG16 encodes 2 major proteins that associate with the axoneme of sperm tail and the nucleus of postmeiotic
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT712970 hsa-miR-3662 HITS-CLIP 19536157
MIRT712969 hsa-miR-651-3p HITS-CLIP 19536157
MIRT712968 hsa-miR-6828-5p HITS-CLIP 19536157
MIRT712970 hsa-miR-3662 HITS-CLIP 19536157
MIRT712969 hsa-miR-651-3p HITS-CLIP 19536157
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005576 Component Extracellular region IEA
GO:0005930 Component Axoneme ISS
GO:0007288 Process Sperm axoneme assembly IEA
GO:0035082 Process Axoneme assembly IBA 21873635
GO:0035082 Process Axoneme assembly IMP 17699735
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID Q8N0X2
Protein name Sperm-associated antigen 16 protein (Pf20 protein homolog)
Protein function Necessary for sperm flagellar function. Plays a role in motile ciliogenesis. May help to recruit STK36 to the cilium or apical surface of the cell to initiate subsequent steps of construction of the central pair apparatus of motile cilia (By sim
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00400 WD40
383 422
WD domain, G-beta repeat
Repeat
PF00400 WD40
426 464
WD domain, G-beta repeat
Repeat
PF00400 WD40
468 506
WD domain, G-beta repeat
Repeat
PF00400 WD40
510 548
WD domain, G-beta repeat
Repeat
PF00400 WD40
594 631
WD domain, G-beta repeat
Repeat
Sequence
MAAQRGMPSSAVRVLEEALGMGLTAAGDARDTADAVAAEGAYYLEQVTITEASEDDYEYE
EIPDDNFSIPEGEEDLAKAIQMAQEQATDTEILERKTVLPSKHAVPEVIEDFLCNFLIKM
GMTRTLDCFQSEWYELIQKGVTELRTVGNVPDVYTQIMLLENENKNLKKDLKHYKQAADK
AREDLLKIQKERDFHRMHHKRIVQEKNKLINDLKGLKLHYASYEPTIRVLHEKHHTLLKE
KMLTSLERDKVVGQISGLQETLKKLQRGHSYHGPQIKVDHSREKENAPEGPTQKGLREAR
EQNKCKTKMKGNTKDSEFPIDMQPNPNLNVSKESLSPAKFDYKLKNIFRLHELPVSCVSM
QPHKDILVSCGEDRLWKVLGLPKCNVLLTGFGHTDWLSDCCFHPSGDKLATSSGDTTVKL
WD
LCKGDCILTFEGHSRAVWSCTWHSCGNFVASSSLDKTSKIWDVNSERCRCTLYGHTDS
VNSIEFFPFSNTLLTSSADKTLSIWD
ARTGICEQSLYGHMHSINDAIFDPRGHMIASCDA
CGVTKLWD
FRKLLPIVSIDIGPSPGNEVNFDSSGRVLAQASGNGVIHLLDLKSGEIHKLM
GHENEAHTVVFSHDGEILFSGGSDGTVRTWS
Sequence length 631
Interactions View interactions
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Attention deficit hyperactivity disorder Attention deficit hyperactivity disorder rs120074176, rs786205019 30478444
Chronic obstructive pulmonary disease Chronic Obstructive Airway Disease rs2227956, rs1008438, rs1043618, rs562047, rs1061581, rs2763979, rs6457452, rs13147758, rs1828591, rs13118928 26634245

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