RPL8 (ribosomal protein L8) - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Gene: RPL8 (ribosomal protein L8) Homo sapiens
Analyze
Symbol: RPL8
Name: ribosomal protein L8
RGD ID: 735772
HGNC Page HGNC
Description: Exhibits RNA binding activity. Involved in cytoplasmic translation. Localizes to cytosolic large ribosomal subunit; polysomal ribosome; and postsynaptic density.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: 60S ribosomal protein L8; L8; large ribosomal subunit protein uL2
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: RPL8P1   RPL8P2   RPL8P3   RPL8P4   RPL8P5  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl8144,789,765 - 144,792,587 (-)EnsemblGRCh38hg38GRCh38
GRCh388144,789,769 - 144,792,390 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh378146,015,154 - 146,017,775 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 368145,985,958 - 145,988,609 (-)NCBINCBI36hg18NCBI36
Build 348145,985,958 - 145,988,533NCBI
Celera8142,192,658 - 142,195,309 (-)NCBI
Cytogenetic Map8q24.3NCBI
HuRef8141,130,731 - 141,133,382 (-)NCBIHuRef
CHM1_18146,053,726 - 146,056,407 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

Additional References at PubMed
PMID:8722009   PMID:9531480   PMID:9582194   PMID:11790298   PMID:11875025   PMID:12477932   PMID:12777385   PMID:12962325   PMID:14567916   PMID:14743216   PMID:15064750   PMID:15189156  
PMID:15231747   PMID:15489334   PMID:15592455   PMID:15635413   PMID:16169070   PMID:16341674   PMID:16712791   PMID:17361185   PMID:18457437   PMID:19449377   PMID:19596686   PMID:19738201  
PMID:19946888   PMID:20020773   PMID:21081503   PMID:21145461   PMID:21170055   PMID:21182205   PMID:21280222   PMID:21319273   PMID:21423176   PMID:21873635   PMID:21900206   PMID:21951318  
PMID:21988832   PMID:22268729   PMID:22586326   PMID:22623428   PMID:22658674   PMID:22681889   PMID:22863883   PMID:22939629   PMID:23071613   PMID:23084401   PMID:23125841   PMID:23151878  
PMID:23246001   PMID:23398456   PMID:23443559   PMID:23463506   PMID:24140279   PMID:24244333   PMID:24457600   PMID:24625528   PMID:24657165   PMID:24711643   PMID:24999758   PMID:25144556  
PMID:25147182   PMID:25315684   PMID:25324306   PMID:25437307   PMID:25798074   PMID:25893343   PMID:25921289   PMID:25957688   PMID:26170170   PMID:26186194   PMID:26327385   PMID:26344197  
PMID:26460568   PMID:26487511   PMID:26496610   PMID:26549023   PMID:26618866   PMID:26673895   PMID:26725010   PMID:26816005   PMID:26831064   PMID:26979993   PMID:27025967   PMID:27049334  
PMID:27129302   PMID:27591049   PMID:27684187   PMID:27976729   PMID:28077445   PMID:28302793   PMID:28330616   PMID:28416769   PMID:28443643   PMID:28514442   PMID:28515276   PMID:28561026  
PMID:28581483   PMID:28700943   PMID:28902428   PMID:28927264   PMID:28977470   PMID:28977666   PMID:29117863   PMID:29180619   PMID:29229926   PMID:29298432   PMID:29331416   PMID:29467282  
PMID:29507755   PMID:29511296   PMID:29568061   PMID:29721183   PMID:29802200   PMID:29845934   PMID:29991511   PMID:30021884   PMID:30033366   PMID:30209976   PMID:30293783   PMID:30320934  
PMID:30344098   PMID:30349055   PMID:30463901   PMID:30575818   PMID:30804502   PMID:30940648   PMID:30948266   PMID:31048545   PMID:31059266   PMID:31091453   PMID:31180492   PMID:31239290  
PMID:31253590   PMID:31586073   PMID:31732153   PMID:31796584   PMID:31980649   PMID:31995728   PMID:32041737   PMID:32129710   PMID:32457219   PMID:32529326   PMID:32788342  


Genomics

Comparative Map Data
RPL8
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl8144,789,765 - 144,792,587 (-)EnsemblGRCh38hg38GRCh38
GRCh388144,789,769 - 144,792,390 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh378146,015,154 - 146,017,775 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 368145,985,958 - 145,988,609 (-)NCBINCBI36hg18NCBI36
Build 348145,985,958 - 145,988,533NCBI
Celera8142,192,658 - 142,195,309 (-)NCBI
Cytogenetic Map8q24.3NCBI
HuRef8141,130,731 - 141,133,382 (-)NCBIHuRef
CHM1_18146,053,726 - 146,056,407 (-)NCBICHM1_1
Rpl8
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391576,788,271 - 76,790,518 (+)NCBIGRCm39mm39
GRCm39 Ensembl1576,788,278 - 76,790,514 (+)Ensembl
GRCm381576,904,071 - 76,906,318 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1576,904,078 - 76,906,314 (+)EnsemblGRCm38mm10GRCm38
MGSCv371576,734,501 - 76,736,748 (+)NCBIGRCm37mm9NCBIm37
MGSCv361576,731,354 - 76,733,569 (+)NCBImm8
Celera1578,399,102 - 78,401,349 (+)NCBICelera
Cytogenetic Map15D3NCBI
Rpl8
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.27108,626,194 - 108,628,485 (+)NCBI
Rnor_6.0 Ensembl33,389,612 - 3,390,443 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0 Ensembl7118,507,224 - 118,509,256 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0 Ensembl7117,967,818 - 117,969,850 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.07117,967,608 - 117,969,886 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.07118,499,676 - 118,501,954 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.47114,954,061 - 114,956,339 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.17114,988,277 - 114,990,567 (+)NCBI
Celera7104,975,054 - 104,977,332 (+)NCBICelera
Cytogenetic Map7q34NCBI
Rpl8
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554543,397,893 - 3,400,275 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554543,397,893 - 3,400,275 (+)NCBIChiLan1.0ChiLan1.0
RPL8
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.18144,543,354 - 144,546,044 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl8144,543,354 - 144,545,974 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v08141,562,162 - 141,564,885 (-)NCBIMhudiblu_PPA_v0panPan3
RPL8
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11338,101,879 - 38,104,772 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1338,102,010 - 38,104,770 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1338,062,599 - 38,065,478 (+)NCBI
ROS_Cfam_1.01338,575,636 - 38,578,520 (+)NCBI
UMICH_Zoey_3.11338,267,134 - 38,270,012 (+)NCBI
UNSW_CanFamBas_1.01338,375,990 - 38,378,868 (+)NCBI
UU_Cfam_GSD_1.01338,851,293 - 38,854,172 (+)NCBI
Rpl8
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405303112,736 - 115,171 (-)NCBI
SpeTri2.0NW_0049364707,538,835 - 7,541,192 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
RPL8
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl4136,105 - 138,977 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.14136,105 - 138,651 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.24206,963 - 209,523 (+)NCBISscrofa10.2Sscrofa10.2susScr3
RPL8
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.18138,990,088 - 138,992,564 (-)NCBI
ChlSab1.1 Ensembl8138,989,165 - 138,992,554 (-)Ensembl
Rpl8
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462473512,090,624 - 12,093,127 (-)NCBI

Position Markers
STS-Z28407  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372131,636,007 - 31,636,148UniSTSGRCh37
GRCh378146,016,690 - 146,016,830UniSTSGRCh37
Build 368145,987,494 - 145,987,634RGDNCBI36
Celera2116,819,141 - 16,819,282UniSTS
Celera8142,194,194 - 142,194,334RGD
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map21q22.11UniSTS
HuRef2117,044,965 - 17,045,106UniSTS
HuRef8141,132,267 - 141,132,407UniSTS
GeneMap99-GB4 RH Map8563.39UniSTS
D3S2824E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372131,635,968 - 31,636,066UniSTSGRCh37
GRCh373142,546,201 - 142,546,299UniSTSGRCh37
Build 363144,028,891 - 144,028,989RGDNCBI36
Celera2116,819,102 - 16,819,200UniSTS
Celera3140,969,704 - 140,969,802RGD
Cytogenetic Map3q23UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map3q21-q24UniSTS
HuRef3139,918,920 - 139,919,018UniSTS
HuRef2117,044,926 - 17,045,024UniSTS
D3S4174  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh373142,545,946 - 142,546,187UniSTSGRCh37
GRCh378146,015,197 - 146,015,831UniSTSGRCh37
Build 363144,028,636 - 144,028,877RGDNCBI36
Celera8142,192,701 - 142,193,335UniSTS
Celera3140,969,449 - 140,969,690RGD
Cytogenetic Map3q23UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map3q21-q24UniSTS
HuRef8141,130,774 - 141,131,408UniSTS
HuRef3139,918,665 - 139,918,906UniSTS
UniSTS:70780  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378146,017,283 - 146,017,504UniSTSGRCh37
Build 368145,988,087 - 145,988,308RGDNCBI36
Celera8142,194,787 - 142,195,008RGD
HuRef8141,132,860 - 141,133,081UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3872
Count of miRNA genes:731
Interacting mature miRNAs:842
Transcripts:ENST00000262584, ENST00000394920, ENST00000525232, ENST00000526668, ENST00000527914, ENST00000528296, ENST00000528957, ENST00000529163, ENST00000529920, ENST00000531767, ENST00000531975, ENST00000532702, ENST00000533397, ENST00000534781
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High 2097 1559 1144 260 1253 105 3702 1158 1017 285 1062 1497 168 1104 2183 2
Medium 342 1432 582 364 698 360 655 1039 2717 134 398 116 7 1 100 605 4 2
Low
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_000973 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001317771 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001317782 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_033301 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB007168 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB061821 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF235103 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK289459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301073 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC000047 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC000077 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC012197 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC013104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC030151 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC093064 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG480561 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI461661 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM783910 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ929065 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT007379 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB128790 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471162 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR457046 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z28407 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000262584   ⟹   ENSP00000262584
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,789,770 - 144,792,587 (-)Ensembl
RefSeq Acc Id: ENST00000394920   ⟹   ENSP00000378378
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,789,769 - 144,792,389 (-)Ensembl
RefSeq Acc Id: ENST00000525232
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,791,113 - 144,792,421 (-)Ensembl
RefSeq Acc Id: ENST00000526668
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,789,768 - 144,791,959 (-)Ensembl
RefSeq Acc Id: ENST00000527914   ⟹   ENSP00000436460
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,789,769 - 144,792,423 (-)Ensembl
RefSeq Acc Id: ENST00000528296
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,789,769 - 144,792,125 (-)Ensembl
RefSeq Acc Id: ENST00000528957   ⟹   ENSP00000433464
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,789,785 - 144,792,351 (-)Ensembl
RefSeq Acc Id: ENST00000529163
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,789,767 - 144,792,390 (-)Ensembl
RefSeq Acc Id: ENST00000529920   ⟹   ENSP00000433703
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,789,802 - 144,792,143 (-)Ensembl
RefSeq Acc Id: ENST00000531767
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,791,507 - 144,792,420 (-)Ensembl
RefSeq Acc Id: ENST00000531975   ⟹   ENSP00000437062
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,789,766 - 144,792,057 (-)Ensembl
RefSeq Acc Id: ENST00000532702   ⟹   ENSP00000434535
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,790,355 - 144,792,384 (-)Ensembl
RefSeq Acc Id: ENST00000533397   ⟹   ENSP00000435313
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,789,809 - 144,792,153 (-)Ensembl
RefSeq Acc Id: ENST00000534781
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,789,765 - 144,790,872 (-)Ensembl
RefSeq Acc Id: NM_000973   ⟹   NP_000964
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388144,789,769 - 144,792,390 (-)NCBI
GRCh378146,015,152 - 146,017,805 (-)NCBI
Build 368145,985,958 - 145,988,609 (-)NCBI Archive
Celera8142,192,658 - 142,195,309 (-)RGD
HuRef8141,130,731 - 141,133,382 (-)ENTREZGENE
CHM1_18146,053,726 - 146,056,407 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001317771   ⟹   NP_001304700
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388144,789,769 - 144,792,390 (-)NCBI
CHM1_18146,053,726 - 146,056,350 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001317782   ⟹   NP_001304711
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388144,789,769 - 144,792,390 (-)NCBI
CHM1_18146,053,726 - 146,056,350 (-)NCBI
Sequence:
RefSeq Acc Id: NM_033301   ⟹   NP_150644
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388144,789,769 - 144,792,390 (-)NCBI
GRCh378146,015,152 - 146,017,805 (-)NCBI
Build 368145,985,958 - 145,988,533 (-)NCBI Archive
Celera8142,192,658 - 142,195,309 (-)RGD
HuRef8141,130,731 - 141,133,382 (-)ENTREZGENE
CHM1_18146,053,726 - 146,056,350 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_000964   ⟸   NM_000973
- UniProtKB: P62917 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_150644   ⟸   NM_033301
- UniProtKB: P62917 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001304700   ⟸   NM_001317771
- UniProtKB: P62917 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001304711   ⟸   NM_001317782
- UniProtKB: P62917 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000437062   ⟸   ENST00000531975
RefSeq Acc Id: ENSP00000434535   ⟸   ENST00000532702
RefSeq Acc Id: ENSP00000435313   ⟸   ENST00000533397
RefSeq Acc Id: ENSP00000378378   ⟸   ENST00000394920
RefSeq Acc Id: ENSP00000262584   ⟸   ENST00000262584
RefSeq Acc Id: ENSP00000436460   ⟸   ENST00000527914
RefSeq Acc Id: ENSP00000433464   ⟸   ENST00000528957
RefSeq Acc Id: ENSP00000433703   ⟸   ENST00000529920
Protein Domains
Ribosomal_L2_C

Promoters
RGD ID:7214533
Promoter ID:EPDNEW_H13003
Type:initiation region
Name:RPL8_2
Description:ribosomal protein L8
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H13004  EPDNEW_H13005  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh388144,791,889 - 144,791,949EPDNEW
RGD ID:7214515
Promoter ID:EPDNEW_H13004
Type:initiation region
Name:RPL8_3
Description:ribosomal protein L8
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H13005  EPDNEW_H13003  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh388144,792,134 - 144,792,194EPDNEW
RGD ID:7214517
Promoter ID:EPDNEW_H13005
Type:initiation region
Name:RPL8_1
Description:ribosomal protein L8
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H13004  EPDNEW_H13003  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh388144,792,390 - 144,792,450EPDNEW
RGD ID:6813507
Promoter ID:HG_ACW:79468
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_12Hour,   K562,   Lymphoblastoid
Transcripts:RPL8.RAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 368145,987,041 - 145,987,947 (-)MPROMDB
RGD ID:6852494
Promoter ID:EP74059
Type:multiple initiation site
Name:HS_RPL8_2
Description:Ribosomal protein L8.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:alternative promoter #2 of 2; 5' exon 1; site 2; major promoter.; see alsoEP74058  
Experiment Methods:Mammalian gene collection (MGC) full-length cDNA cloning
Position:
Human AssemblyChrPosition (strand)Source
Build 368145,988,323 - 145,988,383EPD
RGD ID:6807009
Promoter ID:HG_KWN:62371
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_000973,   NM_033301,   UC003ZDZ.1,   UC003ZEA.1,   UC010MGC.1
Position:
Human AssemblyChrPosition (strand)Source
Build 368145,988,461 - 145,989,542 (-)MPROMDB
RGD ID:6852492
Promoter ID:EP74058
Type:initiation region
Name:HS_RPL8_1
Description:Ribosomal protein L8.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:alternative promoter #1 of 2; 5' exon 1; site 1.; see alsoEP74059  
Experiment Methods:Mammalian gene collection (MGC) full-length cDNA cloning
Position:
Human AssemblyChrPosition (strand)Source
Build 368145,988,563 - 145,988,623EPD

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 8q24.21-24.3(chr8:128220912-145049449)x3 copy number gain See cases [RCV000050830] Chr8:128220912..145049449 [GRCh38]
Chr8:129233158..146274835 [GRCh37]
Chr8:129302340..146245639 [NCBI36]
Chr8:8q24.21-24.3
pathogenic
GRCh38/hg38 8q24.3(chr8:144002671-144796947)x3 copy number gain See cases [RCV000050640] Chr8:144002671..144796947 [GRCh38]
Chr8:145076839..146022332 [GRCh37]
Chr8:145148827..145993136 [NCBI36]
Chr8:8q24.3
pathogenic
GRCh38/hg38 8q23.3-24.3(chr8:113580402-145054634)x3 copy number gain See cases [RCV000050638] Chr8:113580402..145054634 [GRCh38]
Chr8:114592631..146280020 [GRCh37]
Chr8:114661807..146250824 [NCBI36]
Chr8:8q23.3-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3 copy number gain See cases [RCV000051206] Chr8:241530..145049449 [GRCh38]
Chr8:191530..146274835 [GRCh37]
Chr8:181530..146245639 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q24.3(chr8:144002671-145054634)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053702]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053702]|See cases [RCV000053702] Chr8:144002671..145054634 [GRCh38]
Chr8:145076839..146280020 [GRCh37]
Chr8:145148827..146250824 [NCBI36]
Chr8:8q24.3
pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:95606052-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]|See cases [RCV000053677] Chr8:95606052..145054775 [GRCh38]
Chr8:96618280..146280161 [GRCh37]
Chr8:96687456..146250965 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124514090-145054634)x3 copy number gain See cases [RCV000053678] Chr8:124514090..145054634 [GRCh38]
Chr8:125526331..146280020 [GRCh37]
Chr8:125595512..146250824 [NCBI36]
Chr8:8q24.13-24.3
pathogenic
GRCh38/hg38 8q24.3(chr8:139447227-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053701]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053701]|See cases [RCV000053701] Chr8:139447227..145054775 [GRCh38]
Chr8:140459470..146280161 [GRCh37]
Chr8:140528652..146250965 [NCBI36]
Chr8:8q24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000053602] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|See cases [RCV000053604] Chr8:244417..145054775 [GRCh38]
Chr8:194417..146280161 [GRCh37]
Chr8:184417..146250965 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q24.3(chr8:144002471-145054775)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054311]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054311]|See cases [RCV000054311] Chr8:144002471..145054775 [GRCh38]
Chr8:145076639..146280161 [GRCh37]
Chr8:145148627..146250965 [NCBI36]
Chr8:8q24.3
pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:94682154-145068656)x3 copy number gain See cases [RCV000134353] Chr8:94682154..145068656 [GRCh38]
Chr8:95694382..146294042 [GRCh37]
Chr8:95763558..146264846 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q24.22-24.3(chr8:130639182-145068712)x3 copy number gain See cases [RCV000137644] Chr8:130639182..145068712 [GRCh38]
Chr8:131651428..146294098 [GRCh37]
Chr8:131720610..146264902 [NCBI36]
Chr8:8q24.22-24.3
pathogenic|conflicting data from submitters
GRCh38/hg38 8q24.3(chr8:139236824-145068712)x3 copy number gain See cases [RCV000137466] Chr8:139236824..145068712 [GRCh38]
Chr8:140249067..146294098 [GRCh37]
Chr8:140318249..146264902 [NCBI36]
Chr8:8q24.3
likely pathogenic
GRCh38/hg38 8q24.3(chr8:139004218-145049449)x3 copy number gain See cases [RCV000137340] Chr8:139004218..145049449 [GRCh38]
Chr8:140016461..146274835 [GRCh37]
Chr8:140085643..146245639 [NCBI36]
Chr8:8q24.3
likely pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124498498-145068712)x3 copy number gain See cases [RCV000137346] Chr8:124498498..145068712 [GRCh38]
Chr8:125510739..146294098 [GRCh37]
Chr8:125579920..146264902 [NCBI36]
Chr8:8q24.13-24.3
pathogenic
GRCh38/hg38 8q21.3-24.3(chr8:87931152-145068712)x3 copy number gain See cases [RCV000138551] Chr8:87931152..145068712 [GRCh38]
Chr8:88943380..146294098 [GRCh37]
Chr8:89012496..146264902 [NCBI36]
Chr8:8q21.3-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3 copy number gain See cases [RCV000138643] Chr8:241605..145054781 [GRCh38]
Chr8:191605..146280167 [GRCh37]
Chr8:181605..146250971 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:77480050-145068712)x3 copy number gain See cases [RCV000139036] Chr8:77480050..145068712 [GRCh38]
Chr8:78392286..146294098 [GRCh37]
Chr8:78554841..146264902 [NCBI36]
Chr8:8q21.13-24.3
pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:97382873-145070385)x3 copy number gain See cases [RCV000140447] Chr8:97382873..145070385 [GRCh38]
Chr8:98395101..146295771 [GRCh37]
Chr8:98464277..146266575 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q22.3-24.3(chr8:100867343-145070385)x3 copy number gain See cases [RCV000141694] Chr8:100867343..145070385 [GRCh38]
Chr8:101879571..146295771 [GRCh37]
Chr8:101948747..146266575 [NCBI36]
Chr8:8q22.3-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3 copy number gain See cases [RCV000141808] Chr8:208048..145070385 [GRCh38]
Chr8:158048..146295771 [GRCh37]
Chr8:148048..146266575 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3 copy number gain See cases [RCV000142021] Chr8:21291522..145070385 [GRCh38]
Chr8:21149033..146295771 [GRCh37]
Chr8:21193313..146266575 [NCBI36]
Chr8:8p21.3-q24.3
pathogenic
GRCh38/hg38 8q22.3-24.3(chr8:103306336-145068712)x3 copy number gain See cases [RCV000142810] Chr8:103306336..145068712 [GRCh38]
Chr8:104318564..146294098 [GRCh37]
Chr8:104387740..146264902 [NCBI36]
Chr8:8q22.3-24.3
pathogenic|likely pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3 copy number gain See cases [RCV000142858] Chr8:226452..145068712 [GRCh38]
Chr8:176452..146294098 [GRCh37]
Chr8:166452..146264902 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:78614077-145054634)x3 copy number gain See cases [RCV000142597] Chr8:78614077..145054634 [GRCh38]
Chr8:79526312..146280020 [GRCh37]
Chr8:79688867..146250824 [NCBI36]
Chr8:8q21.13-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000148092] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.2-24.3(chr8:85765999-145070385)x3 copy number gain See cases [RCV000143659] Chr8:85765999..145070385 [GRCh38]
Chr8:86778228..146295771 [GRCh37]
Chr8:86863079..146266575 [NCBI36]
Chr8:8q21.2-24.3
pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124514090-145054634)x3 copy number gain See cases [RCV000148117] Chr8:124514090..145054634 [GRCh38]
Chr8:125526331..146280020 [GRCh37]
Chr8:125595512..146250824 [NCBI36]
Chr8:8q24.13-24.3
pathogenic
GRCh37/hg19 8p12-q24.3(chr8:31936551-146295771)x3 copy number gain not provided [RCV000848192] Chr8:31936551..146295771 [GRCh37]
Chr8:8p12-q24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3 copy number gain See cases [RCV000447507] Chr8:158991..146280828 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q22.1-24.3(chr8:98432250-146222672)x4 copy number gain See cases [RCV000448954] Chr8:98432250..146222672 [GRCh37]
Chr8:8q22.1-24.3
pathogenic
GRCh37/hg19 8q24.22-24.3(chr8:134825277-146280828)x3 copy number gain See cases [RCV000448348] Chr8:134825277..146280828 [GRCh37]
Chr8:8q24.22-24.3
pathogenic
GRCh37/hg19 8q24.3(chr8:144779442-146113113)x3 copy number gain See cases [RCV000510396] Chr8:144779442..146113113 [GRCh37]
Chr8:8q24.3
uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771) copy number gain See cases [RCV000510234] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q24.22-24.3(chr8:136378789-146295771)x3 copy number gain See cases [RCV000512003] Chr8:136378789..146295771 [GRCh37]
Chr8:8q24.22-24.3
likely pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3 copy number gain See cases [RCV000511095] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q21.2-24.3(chr8:86841154-146295771)x3 copy number gain See cases [RCV000511002] Chr8:86841154..146295771 [GRCh37]
Chr8:8q21.2-24.3
pathogenic
GRCh37/hg19 8q24.3(chr8:142840194-146280020) copy number gain Intellectual disability [RCV000626547] Chr8:142840194..146280020 [GRCh37]
Chr8:8q24.3
pathogenic
GRCh37/hg19 8q23.3-24.3(chr8:114853126-146295771)x3 copy number gain See cases [RCV000512401] Chr8:114853126..146295771 [GRCh37]
Chr8:8q23.3-24.3
pathogenic
GRCh37/hg19 8p23.1-q24.3(chr8:12490999-146295771)x3 copy number gain See cases [RCV000512169] Chr8:12490999..146295771 [GRCh37]
Chr8:8p23.1-q24.3
pathogenic
GRCh37/hg19 8q24.3(chr8:143815037-146295771)x3 copy number gain not provided [RCV000683020] Chr8:143815037..146295771 [GRCh37]
Chr8:8q24.3
pathogenic
GRCh37/hg19 8q24.3(chr8:145778769-146025924)x3 copy number gain not provided [RCV000682955] Chr8:145778769..146025924 [GRCh37]
Chr8:8q24.3
likely benign
GRCh37/hg19 8q24.12-24.3(chr8:121694649-146295771)x3 copy number gain not provided [RCV000683044] Chr8:121694649..146295771 [GRCh37]
Chr8:8q24.12-24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:164984-146293414)x3 copy number gain not provided [RCV000747254] Chr8:164984..146293414 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:10213-146293414)x3 copy number gain not provided [RCV000747248] Chr8:10213..146293414 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q24.3(chr8:145955543-146147494)x3 copy number gain not provided [RCV000748044] Chr8:145955543..146147494 [GRCh37]
Chr8:8q24.3
benign
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3 copy number gain not provided [RCV000848478] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3
pathogenic
GRCh37/hg19 8q24.12-24.3(chr8:122193546-146295771)x3 copy number gain not provided [RCV000849762] Chr8:122193546..146295771 [GRCh37]
Chr8:8q24.12-24.3
pathogenic
GRCh37/hg19 8q24.3(chr8:145897164-146109987)x3 copy number gain not provided [RCV000846187] Chr8:145897164..146109987 [GRCh37]
Chr8:8q24.3
uncertain significance
GRCh37/hg19 8q24.22-24.3(chr8:136059859-146295771)x3 copy number gain not provided [RCV000847171] Chr8:136059859..146295771 [GRCh37]
Chr8:8q24.22-24.3
pathogenic
GRCh37/hg19 8q24.3(chr8:144190206-146295771)x3 copy number gain not provided [RCV000847854] Chr8:144190206..146295771 [GRCh37]
Chr8:8q24.3
uncertain significance
GRCh37/hg19 8q24.3(chr8:145939952-146050283)x3 copy number gain not provided [RCV000848017] Chr8:145939952..146050283 [GRCh37]
Chr8:8q24.3
uncertain significance
GRCh37/hg19 8q24.23-24.3(chr8:139188797-146295771)x3 copy number gain not provided [RCV000846814] Chr8:139188797..146295771 [GRCh37]
Chr8:8q24.23-24.3
pathogenic
GRCh37/hg19 8q24.13-24.3(chr8:125496223-146295771)x3 copy number gain not provided [RCV000845705] Chr8:125496223..146295771 [GRCh37]
Chr8:8q24.13-24.3
pathogenic
GRCh37/hg19 8q24.21-24.3(chr8:128877995-146295771)x3 copy number gain not provided [RCV001006146] Chr8:128877995..146295771 [GRCh37]
Chr8:8q24.21-24.3
pathogenic
GRCh37/hg19 8q24.12-24.3(chr8:121042467-146295771)x3 copy number gain not provided [RCV001006140] Chr8:121042467..146295771 [GRCh37]
Chr8:8q24.12-24.3
pathogenic
GRCh37/hg19 8q24.3(chr8:144262042-146295771)x3 copy number gain not provided [RCV001259034] Chr8:144262042..146295771 [GRCh37]
Chr8:8q24.3
likely pathogenic
GRCh37/hg19 8q24.3(chr8:145033244-146297937)x3 copy number gain not provided [RCV001270667] Chr8:145033244..146297937 [GRCh37]
Chr8:8q24.3
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:10368 AgrOrtholog
COSMIC RPL8 COSMIC
Ensembl Genes ENSG00000161016 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000262584 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000378378 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000433464 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000433703 UniProtKB/TrEMBL
  ENSP00000434535 UniProtKB/TrEMBL
  ENSP00000435313 UniProtKB/TrEMBL
  ENSP00000436460 UniProtKB/TrEMBL
  ENSP00000437062 UniProtKB/TrEMBL
Ensembl Transcript ENST00000262584 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000394920 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000527914 UniProtKB/TrEMBL
  ENST00000528957 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000529920 UniProtKB/TrEMBL
  ENST00000531975 UniProtKB/TrEMBL
  ENST00000532702 UniProtKB/TrEMBL
  ENST00000533397 UniProtKB/TrEMBL
Gene3D-CATH 2.30.30.30 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  4.10.950.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000161016 GTEx
HGNC ID HGNC:10368 ENTREZGENE
Human Proteome Map RPL8 Human Proteome Map
InterPro NA-bd_OB-fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Rbsml_prot_L2_RNA-bd_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Rib_L2_dom2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_L2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_L2_arc UniProtKB/Swiss-Prot
  Ribosomal_L2_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_L2_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_L2_dom3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Translation_prot_SH3-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:6132 UniProtKB/Swiss-Prot
NCBI Gene 6132 ENTREZGENE
OMIM 604177 OMIM
PANTHER PTHR13691 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Ribosomal_L2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_L2_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA34768 PharmGKB
PIRSF Ribosomal_L2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE RIBOSOMAL_L2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART Ribosomal_L2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_L2_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF50104 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF50249 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt E9PKU4_HUMAN UniProtKB/TrEMBL
  E9PKZ0_HUMAN UniProtKB/TrEMBL
  E9PP36_HUMAN UniProtKB/TrEMBL
  G3V1A1_HUMAN UniProtKB/TrEMBL
  H0YF23_HUMAN UniProtKB/TrEMBL
  P62917 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary A8K094 UniProtKB/Swiss-Prot
  D3DWN2 UniProtKB/Swiss-Prot
  P25120 UniProtKB/Swiss-Prot
  Q567Q7 UniProtKB/Swiss-Prot
  Q969V7 UniProtKB/Swiss-Prot
  Q9BWQ9 UniProtKB/Swiss-Prot