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Gene id 6159
Gene Summary     SNPs    Protein Summary    Gene ontology    KEGG pathways    Diseases    PubMed    

Gene Summary

Gene Symbol RPL29   Gene   UCSC   Ensembl
Aliases HIP, HUMRPL29, L29, RPL29P10, RPL29_3_370
Gene name ribosomal protein L29
Alternate names 60S ribosomal protein L29, HP/HS-interacting protein, cell surface heparin-binding protein HIP, heparin/heparan sulfate-binding protein, heparin/heparan sulfate-interacting protein, large ribosomal subunit protein eL29, ribosomal protein YL43 homologue,
Gene location 3p21.2 (45074577: 45226562)     Exons: 24     NC_000021.9
Gene summary(Entrez) Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a cytoplasmic r
OMIM 601832

SNPs


rs147088100

Strand:    Allele origin:   Allele change:   Mutation type: snv

NC_000023.11   g.70853248G>A
NC_000023.10   g.70073098G>A
NG_012574.2   g.60470C>T
NG_012574.1   g.60470C>T
NM_031276.2   c.405C>T
NM_031276.3   c.405C>T
NM_001003811.1   c.450C>T
NM_001003811.2   c.450C>T
XM_011530994.1   c.405C>T
XM_017029649.1   c.405C>T|SEQ=[G/A]|GE

rs143246552

Strand:    Allele origin:   Allele change:   Mutation type: snv

NC_000023.11   g.70853093T>C
NC_000023.10   g.70072943T>C
NG_012574.2   g.60625A>G
NG_012574.1   g.60625A>G
NM_031276.3   c.466A>G
NM_031276.2   c.466A>G
NM_001003811.2   c.511A>G
NM_001003811.1   c.511A>G
XM_011530994.1   c.466A>G
XM_017029649.1   c.466A>G
NP_112566.2  

rs140984555

Strand:    Allele origin:   Allele change:   Mutation type: snv

NC_000023.11   g.70605421C>T
NC_000023.10   g.69825271C>T
NG_012574.2   g.308297G>A
NG_012574.1   g.308297G>A
NM_031276.2   c.2047G>A
NM_031276.3   c.2047G>A
NM_001003811.1   c.2092G>A
NM_001003811.2   c.2092G>A
XM_017029652.2   c.856G>A
XM_011530994.1   c.2047G>A
XM_01  

rs6525433

Strand:    Allele origin:   Allele change:   Mutation type: snv

NC_000023.11   g.70853309T>C
NC_000023.10   g.70073159T>C
NG_012574.2   g.60409A>G
NG_012574.1   g.60409A>G
NM_031276.3   c.344A>G
NM_031276.2   c.344A>G
NM_001003811.2   c.389A>G
NM_001003811.1   c.389A>G
XM_011530994.1   c.344A>G
XM_017029649.1   c.344A>G
NP_112566.2  

rs4844247

Strand:    Allele origin:   Allele change:   Mutation type: snv

NC_000023.11   g.70670451C>T
NC_000023.10   g.69890301C>T
NG_012574.2   g.243267G>A
NG_012574.1   g.243267G>A
NM_031276.3   c.1306G>A
NM_031276.2   c.1306G>A
NM_001003811.2   c.1351G>A
NM_001003811.1   c.1351G>A
XM_017029652.2   c.115G>A
XM_011530994.1   c.1306G>A
XM_01  

Protein Summary

Protein general information P47914  

Name: 60S ribosomal protein L29 (Cell surface heparin binding protein HIP) (Large ribosomal subunit protein eL29)

Length: 159  Mass: 17752

Sequence MAKSKNHTTHNQSRKWHRNGIKKPRSQRYESLKGVDPKFLRNMRFAKKHNKKGLKKMQANNAKAMSARAEAIKAL
VKPKEVKPKIPKGVSRKLDRLAYIAHPKLGKRARARIAKGLRLCRPKAKAKAKAKDQTKAQAAAPASVPAQAPKR
TQAPTKASE
Structural information
Interpro:  IPR002673  

PDB:  
4UG0 4V6X 5AJ0 5T2C 6EK0 6IP5 6IP6 6IP8 6OLE 6OLF 6OLG 6OLI 6OLZ 6OM0 6OM7 6QZP
PDBsum:   4UG0 4V6X 5AJ0 5T2C 6EK0 6IP5 6IP6 6IP8 6OLE 6OLF 6OLG 6OLI 6OLZ 6OM0 6OM7 6QZP
MINT:  
STRING:   ENSP00000418868
Other Databases GeneCards:  RPL29  Malacards:  RPL29

Gene ontology

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GO accessionTerm nameEvidence codeGo category
GO:0003735 structural constituent of
ribosome
IBA molecular function
GO:0002181 cytoplasmic translation
IBA biological process
GO:0022625 cytosolic large ribosomal
subunit
IBA cellular component
GO:0005840 ribosome
IEA cellular component
GO:0006412 translation
IEA biological process
GO:0003735 structural constituent of
ribosome
IEA molecular function
GO:0005840 ribosome
IEA cellular component
GO:0008201 heparin binding
IEA molecular function
GO:0003723 RNA binding
TAS molecular function
GO:0003735 structural constituent of
ribosome
TAS molecular function
GO:0008201 heparin binding
TAS molecular function
GO:0006412 translation
TAS biological process
GO:0007566 embryo implantation
TAS biological process
GO:0022625 cytosolic large ribosomal
subunit
TAS cellular component
GO:0006413 translational initiation
TAS biological process
GO:0000184 nuclear-transcribed mRNA
catabolic process, nonsen
se-mediated decay
TAS biological process
GO:0005829 cytosol
TAS cellular component
GO:0005829 cytosol
TAS cellular component
GO:0005829 cytosol
TAS cellular component
GO:0005829 cytosol
TAS cellular component
GO:0005829 cytosol
TAS cellular component
GO:0005829 cytosol
TAS cellular component
GO:0005829 cytosol
TAS cellular component
GO:0005829 cytosol
TAS cellular component
GO:0005829 cytosol
TAS cellular component
GO:0005829 cytosol
TAS cellular component
GO:0005829 cytosol
TAS cellular component
GO:0005829 cytosol
TAS cellular component
GO:0005829 cytosol
TAS cellular component
GO:0005829 cytosol
TAS cellular component
GO:0006614 SRP-dependent cotranslati
onal protein targeting to
membrane
TAS biological process
GO:0019083 viral transcription
TAS biological process
GO:0045296 cadherin binding
HDA molecular function
GO:0016020 membrane
HDA cellular component
GO:0006412 translation
NAS biological process
GO:0003723 RNA binding
HDA molecular function
GO:0022625 cytosolic large ribosomal
subunit
HDA cellular component
GO:0003723 RNA binding
HDA molecular function
GO:0003735 structural constituent of
ribosome
NAS molecular function

KEGG pathways

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Pathway idPathway name
hsa03010Ribosome
Associated diseases References
Aberrant CpGs in Low Motility Sperm MIK: 21674046
Teratozoospermia MIK: 17327269

PubMed references

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PMID Condition Mutation Ethnicity Population details Infertility_type Associated_genes Abstract
17327269 Teratozoos
permia

19 (6 controls
, 13 cases)
Male infertility GSE6872 analyzed by GEO2R (cutoff 1.5 fold)
Show abstract
21674046 Aberrant C
pGs in Low
Motility
Sperm

18
Male infertility GSE26881
Show abstract