MRPL10 (mitochondrial ribosomal protein L10) - Rat Genome Database

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Gene: MRPL10 (mitochondrial ribosomal protein L10) Homo sapiens
Analyze
Symbol: MRPL10
Name: mitochondrial ribosomal protein L10
RGD ID: 1315061
HGNC Page HGNC:14055
Description: Enables RNA binding activity. Predicted to be involved in translation. Located in mitochondrion and nucleoplasm. Part of mitochondrial large ribosomal subunit.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: 39S ribosomal protein L10, mitochondrial; 39S ribosomal protein L8, mitochondrial; L10MT; L8mt; large ribosomal subunit protein uL10m; MGC17973; mitochondrial large ribosomal subunit protein uL10m; mitochondrial ribosomal protein L8; MRP-L10; MRP-L8; MRPL8; RPML8; uL10m
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Related Pseudogenes: LOC348958  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381747,823,272 - 47,831,541 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1747,823,272 - 47,831,541 (-)EnsemblGRCh38hg38GRCh38
GRCh371745,900,638 - 45,908,907 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361743,255,637 - 43,263,902 (-)NCBINCBI36Build 36hg18NCBI36
Build 341743,255,637 - 43,263,902NCBI
Celera1742,353,443 - 42,361,707 (-)NCBICelera
Cytogenetic Map17q21.32NCBI
HuRef1741,269,550 - 41,277,826 (-)NCBIHuRef
CHM1_11745,965,594 - 45,973,847 (-)NCBICHM1_1
T2T-CHM13v2.01748,685,040 - 48,693,314 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:3129699   PMID:9857009   PMID:11543634   PMID:11551941   PMID:12477932   PMID:12706105   PMID:14733910   PMID:15489334   PMID:16169070   PMID:16344560   PMID:18029348   PMID:18854154  
PMID:19913121   PMID:19948975   PMID:20186120   PMID:20379614   PMID:20628086   PMID:20877624   PMID:21832049   PMID:21873635   PMID:22681889   PMID:22939629   PMID:23402259   PMID:23535033  
PMID:24797263   PMID:25278503   PMID:25416956   PMID:25910212   PMID:26186194   PMID:26344197   PMID:26496610   PMID:27023846   PMID:28514442   PMID:28695742   PMID:28712289   PMID:28892042  
PMID:29229926   PMID:29395067   PMID:29509190   PMID:29540532   PMID:29568061   PMID:29802200   PMID:29845934   PMID:30033366   PMID:30209976   PMID:31056398   PMID:31182584   PMID:31617661  
PMID:31980649   PMID:32129710   PMID:32203420   PMID:32628020   PMID:32707033   PMID:32807901   PMID:32877691   PMID:33957083   PMID:33961781   PMID:34079125   PMID:34133714   PMID:34373451  
PMID:34709727   PMID:34800366   PMID:35013218   PMID:35140242   PMID:35271311   PMID:35384245   PMID:36215168   PMID:36538041   PMID:37071682   PMID:37314216   PMID:38113892   PMID:38803224  


Genomics

Comparative Map Data
MRPL10
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381747,823,272 - 47,831,541 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1747,823,272 - 47,831,541 (-)EnsemblGRCh38hg38GRCh38
GRCh371745,900,638 - 45,908,907 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361743,255,637 - 43,263,902 (-)NCBINCBI36Build 36hg18NCBI36
Build 341743,255,637 - 43,263,902NCBI
Celera1742,353,443 - 42,361,707 (-)NCBICelera
Cytogenetic Map17q21.32NCBI
HuRef1741,269,550 - 41,277,826 (-)NCBIHuRef
CHM1_11745,965,594 - 45,973,847 (-)NCBICHM1_1
T2T-CHM13v2.01748,685,040 - 48,693,314 (-)NCBIT2T-CHM13v2.0
Mrpl10
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391196,932,408 - 96,940,039 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1196,932,386 - 96,940,039 (+)EnsemblGRCm39 Ensembl
GRCm381197,041,582 - 97,049,213 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1197,041,560 - 97,049,213 (+)EnsemblGRCm38mm10GRCm38
MGSCv371196,902,900 - 96,910,527 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361196,857,676 - 96,865,303 (+)NCBIMGSCv36mm8
Celera11106,693,044 - 106,700,671 (+)NCBICelera
Cytogenetic Map11DNCBI
cM Map1160.69NCBI
Mrpl10
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81082,522,470 - 82,530,886 (+)NCBIGRCr8
mRatBN7.21082,026,031 - 82,034,451 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1082,026,031 - 82,034,443 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1086,974,104 - 86,982,361 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01086,472,154 - 86,480,411 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01081,864,737 - 81,872,994 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01084,976,377 - 84,984,793 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1084,976,377 - 84,984,780 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01084,766,862 - 84,775,278 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41085,761,934 - 85,770,350 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1080,787,382 - 80,795,760 (+)NCBICelera
Cytogenetic Map10q31NCBI
Mrpl10
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495545113,281,935 - 13,288,033 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495545113,281,935 - 13,288,033 (+)NCBIChiLan1.0ChiLan1.0
MRPL10
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21917,271,567 - 17,279,706 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11719,237,156 - 19,245,299 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0179,705,709 - 9,713,844 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1179,887,855 - 9,895,969 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl179,887,855 - 9,895,969 (+)Ensemblpanpan1.1panPan2
MRPL10
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1924,156,825 - 24,162,754 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl924,156,555 - 24,163,336 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha923,624,854 - 23,630,783 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0924,951,849 - 24,957,778 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl924,951,852 - 24,958,146 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1923,721,989 - 23,727,918 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0923,982,823 - 23,988,743 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0924,109,493 - 24,115,425 (-)NCBIUU_Cfam_GSD_1.0
Mrpl10
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560223,585,923 - 23,594,119 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493649013,481,097 - 13,489,216 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493649013,481,082 - 13,489,221 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MRPL10
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1224,075,632 - 24,083,052 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11224,076,484 - 24,083,086 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21223,954,339 - 23,960,936 (-)NCBISscrofa10.2Sscrofa10.2susScr3
MRPL10
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11668,224,300 - 68,232,020 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1668,223,846 - 68,231,989 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607739,274,833 - 39,282,682 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Mrpl10
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247954,479,728 - 4,487,366 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247954,481,270 - 4,487,423 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in MRPL10
18 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3 copy number gain See cases [RCV000050957] Chr17:36449220..68170214 [GRCh38]
Chr17:48563237..65936105 [GRCh37]
Chr17:45918236..63677950 [NCBI36]
Chr17:17q21.33-24.2
pathogenic
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|See cases [RCV000052483] Chr17:36449220..83086677 [GRCh38]
Chr17:58617905..81044553 [GRCh37]
Chr17:55972687..78637842 [NCBI36]
Chr17:17q23.2-25.3
pathogenic
GRCh38/hg38 17q21.31-21.33(chr17:44955325-49381173)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052480]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052480]|See cases [RCV000052480] Chr17:44955325..49381173 [GRCh38]
Chr17:43032693..47458535 [GRCh37]
Chr17:40388219..44813534 [NCBI36]
Chr17:17q21.31-21.33
pathogenic
GRCh38/hg38 17q21.32(chr17:47686487-47986961)x1 copy number loss See cases [RCV000134967] Chr17:47686487..47986961 [GRCh38]
Chr17:45763853..46064327 [GRCh37]
Chr17:43118852..43419326 [NCBI36]
Chr17:17q21.32
likely pathogenic|uncertain significance
GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3 copy number gain See cases [RCV000137437] Chr17:36449220..75053130 [GRCh38]
Chr17:57595736..73049225 [GRCh37]
Chr17:54950518..70560820 [NCBI36]
Chr17:17q23.1-25.1
pathogenic
chr17:45008570..45994044 complex variant complex Breast ductal adenocarcinoma [RCV000207217] Chr17:45008570..45994044 [GRCh37]
Chr17:17q21.32
uncertain significance
GRCh37/hg19 17q21.31-25.3(chr17:42580684-81085615)x3 copy number gain See cases [RCV000447823] Chr17:42580684..81085615 [GRCh37]
Chr17:17q21.31-25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17q21.32(chr17:45884442-46124946)x3 copy number gain not provided [RCV000683940] Chr17:45884442..46124946 [GRCh37]
Chr17:17q21.32
uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
NM_145255.4(MRPL10):c.292G>A (p.Val98Ile) single nucleotide variant not specified [RCV004281675] Chr17:47827135 [GRCh38]
Chr17:45904501 [GRCh37]
Chr17:17q21.32
uncertain significance
NM_145255.4(MRPL10):c.240G>C (p.Arg80Ser) single nucleotide variant not specified [RCV004331043] Chr17:47827187 [GRCh38]
Chr17:45904553 [GRCh37]
Chr17:17q21.32
uncertain significance
GRCh37/hg19 17q21.32(chr17:44949883-46507482) copy number gain PNPO-related disorder [RCV003236737] Chr17:44949883..46507482 [GRCh37]
Chr17:17q21.32
likely pathogenic
NM_145255.4(MRPL10):c.110G>A (p.Arg37His) single nucleotide variant not specified [RCV004158632] Chr17:47828613 [GRCh38]
Chr17:45905979 [GRCh37]
Chr17:17q21.32
uncertain significance
NM_145255.4(MRPL10):c.335T>C (p.Met112Thr) single nucleotide variant not specified [RCV004135398] Chr17:47827092 [GRCh38]
Chr17:45904458 [GRCh37]
Chr17:17q21.32
uncertain significance
NM_145255.4(MRPL10):c.250C>T (p.Arg84Trp) single nucleotide variant not specified [RCV004174279] Chr17:47827177 [GRCh38]
Chr17:45904543 [GRCh37]
Chr17:17q21.32
uncertain significance
NM_145255.4(MRPL10):c.721C>T (p.Arg241Cys) single nucleotide variant not specified [RCV004329890] Chr17:47824270 [GRCh38]
Chr17:45901636 [GRCh37]
Chr17:17q21.32
uncertain significance
NM_145255.4(MRPL10):c.668A>G (p.Gln223Arg) single nucleotide variant not specified [RCV004250443] Chr17:47824323 [GRCh38]
Chr17:45901689 [GRCh37]
Chr17:17q21.32
uncertain significance
NM_145255.4(MRPL10):c.172C>T (p.Pro58Ser) single nucleotide variant not specified [RCV004272286] Chr17:47828551 [GRCh38]
Chr17:45905917 [GRCh37]
Chr17:17q21.32
uncertain significance
NM_145255.4(MRPL10):c.215C>G (p.Pro72Arg) single nucleotide variant not specified [RCV004303958] Chr17:47828508 [GRCh38]
Chr17:45905874 [GRCh37]
Chr17:17q21.32
uncertain significance
NM_145255.4(MRPL10):c.655C>T (p.His219Tyr) single nucleotide variant not specified [RCV004339708] Chr17:47824336 [GRCh38]
Chr17:45901702 [GRCh37]
Chr17:17q21.32
uncertain significance
NM_145255.4(MRPL10):c.373G>A (p.Val125Ile) single nucleotide variant MRPL10-related disorder [RCV003982009] Chr17:47827054 [GRCh38]
Chr17:45904420 [GRCh37]
Chr17:17q21.32
benign
NM_145255.4(MRPL10):c.87C>T (p.Gly29=) single nucleotide variant MRPL10-related disorder [RCV003968955] Chr17:47828636 [GRCh38]
Chr17:45906002 [GRCh37]
Chr17:17q21.32
likely benign
NM_145255.4(MRPL10):c.192C>T (p.Cys64=) single nucleotide variant MRPL10-related disorder [RCV003923875] Chr17:47828531 [GRCh38]
Chr17:45905897 [GRCh37]
Chr17:17q21.32
likely benign
NM_145255.4(MRPL10):c.205C>T (p.Pro69Ser) single nucleotide variant not specified [RCV004501992] Chr17:47828518 [GRCh38]
Chr17:45905884 [GRCh37]
Chr17:17q21.32
uncertain significance
NM_145255.4(MRPL10):c.731A>T (p.Asp244Val) single nucleotide variant not specified [RCV004502016] Chr17:47824260 [GRCh38]
Chr17:45901626 [GRCh37]
Chr17:17q21.32
uncertain significance
NM_145255.4(MRPL10):c.349C>T (p.Arg117Trp) single nucleotide variant not specified [RCV004502006] Chr17:47827078 [GRCh38]
Chr17:45904444 [GRCh37]
Chr17:17q21.32
uncertain significance
NM_145255.4(MRPL10):c.101C>G (p.Thr34Ser) single nucleotide variant not specified [RCV004501985] Chr17:47828622 [GRCh38]
Chr17:45905988 [GRCh37]
Chr17:17q21.32
uncertain significance
NM_145255.4(MRPL10):c.756G>T (p.Lys252Asn) single nucleotide variant not specified [RCV004502018] Chr17:47824235 [GRCh38]
Chr17:45901601 [GRCh37]
Chr17:17q21.32
uncertain significance
GRCh37/hg19 17q12-22(chr17:41196270-41277589) copy number loss Breast-ovarian cancer, familial, susceptibility to, 1 [RCV004759419] Chr17:41196270..41277589 [GRCh37]
Chr17:17q12-22
pathogenic
Single allele deletion Breast-ovarian cancer, familial, susceptibility to, 1 [RCV004759420] Chr17:41231503..41277589 [GRCh37]
Chr17:17q21.31-22
pathogenic
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR1301hsa-miR-1301-3pMirtarbaseexternal_infoCLASHFunctional MTI (Weak)23622248

Predicted Target Of
Summary Value
Count of predictions:2874
Count of miRNA genes:864
Interacting mature miRNAs:1013
Transcripts:ENST00000290208, ENST00000351111, ENST00000414011, ENST00000421763, ENST00000423147, ENST00000466016, ENST00000480901
Prediction methods:Miranda, Pita, Rnahybrid, Targetscan
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.

Markers in Region
RH64830  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371745,900,932 - 45,901,090UniSTSGRCh37
Build 361743,255,931 - 43,256,089RGDNCBI36
Celera1742,353,737 - 42,353,895RGD
Cytogenetic Map17q21UniSTS
Cytogenetic Map17q21.32UniSTS
HuRef1741,269,844 - 41,270,002UniSTS
G43163  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371745,900,959 - 45,901,156UniSTSGRCh37
Build 361743,255,958 - 43,256,155RGDNCBI36
Celera1742,353,764 - 42,353,961RGD
Cytogenetic Map17q21.32UniSTS
HuRef1741,269,871 - 41,270,068UniSTS
G59312  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371745,900,961 - 45,901,115UniSTSGRCh37
Build 361743,255,960 - 43,256,114RGDNCBI36
Celera1742,353,766 - 42,353,920RGD
Cytogenetic Map17q21UniSTS
Cytogenetic Map17q21.32UniSTS
HuRef1741,269,873 - 41,270,027UniSTS
MRPL10_2482  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371745,900,808 - 45,901,470UniSTSGRCh37
Build 361743,255,807 - 43,256,469RGDNCBI36
Celera1742,353,613 - 42,354,275RGD
HuRef1741,269,720 - 41,270,382UniSTS
STS-AA039646  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371745,900,866 - 45,901,107UniSTSGRCh37
Build 361743,255,865 - 43,256,106RGDNCBI36
Celera1742,353,671 - 42,353,912RGD
Cytogenetic Map17q21UniSTS
Cytogenetic Map17q21.32UniSTS
HuRef1741,269,778 - 41,270,019UniSTS
GeneMap99-GB4 RH Map17337.7UniSTS
NCBI RH Map17604.8UniSTS
D1S1425  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map2p23-p22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic Map2p11.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map2p12-p11.2UniSTS
Cytogenetic Map3q11.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map2p24UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map15q11-q12UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map12p13.33UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map4q31.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map10p15-p14UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map15q24-q25UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map6q16UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11q23.1-q23.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map16q24.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic MapXq21.1UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2253 4974 1726 2351 6 624 1951 465 2270 7306 6472 53 3734 1 852 1744 1617 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_145255 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_148887 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_037575 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024450575 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054315044 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB051618 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC003665 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI221522 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK127167 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK293624 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL558270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL701268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC015904 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC039852 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC052601 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471109 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA137043 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000290208   ⟹   ENSP00000290208
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1747,823,461 - 47,829,673 (-)Ensembl
Ensembl Acc Id: ENST00000351111   ⟹   ENSP00000324100
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1747,823,272 - 47,831,541 (-)Ensembl
Ensembl Acc Id: ENST00000414011   ⟹   ENSP00000395870
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1747,823,490 - 47,831,534 (-)Ensembl
Ensembl Acc Id: ENST00000421763   ⟹   ENSP00000404039
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1747,823,583 - 47,831,530 (-)Ensembl
Ensembl Acc Id: ENST00000423147   ⟹   ENSP00000390624
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1747,827,074 - 47,831,523 (-)Ensembl
Ensembl Acc Id: ENST00000466016
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1747,826,895 - 47,831,523 (-)Ensembl
Ensembl Acc Id: ENST00000480901
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1747,828,308 - 47,831,525 (-)Ensembl
RefSeq Acc Id: NM_145255   ⟹   NP_660298
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381747,823,272 - 47,831,541 (-)NCBI
GRCh371745,900,638 - 45,908,907 (-)ENTREZGENE
Build 361743,255,637 - 43,263,902 (-)NCBI Archive
Celera1742,353,443 - 42,361,707 (-)RGD
HuRef1741,269,550 - 41,277,826 (-)ENTREZGENE
CHM1_11745,965,594 - 45,973,847 (-)NCBI
T2T-CHM13v2.01748,685,040 - 48,693,314 (-)NCBI
Sequence:
RefSeq Acc Id: NM_148887   ⟹   NP_683685
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381747,823,272 - 47,831,541 (-)NCBI
GRCh371745,900,638 - 45,908,907 (-)ENTREZGENE
Build 361743,255,637 - 43,263,902 (-)NCBI Archive
HuRef1741,269,550 - 41,277,826 (-)ENTREZGENE
CHM1_11745,965,594 - 45,973,847 (-)NCBI
T2T-CHM13v2.01748,685,040 - 48,693,314 (-)NCBI
Sequence:
RefSeq Acc Id: NR_037575
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381747,823,272 - 47,831,541 (-)NCBI
GRCh371745,900,638 - 45,908,907 (-)ENTREZGENE
HuRef1741,269,550 - 41,277,826 (-)ENTREZGENE
CHM1_11745,965,594 - 45,973,847 (-)NCBI
T2T-CHM13v2.01748,685,040 - 48,693,314 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024450575   ⟹   XP_024306343
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381747,823,272 - 47,831,541 (-)NCBI
Sequence:
RefSeq Acc Id: XM_054315044   ⟹   XP_054171019
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01748,685,040 - 48,693,314 (-)NCBI
RefSeq Acc Id: NP_660298   ⟸   NM_145255
- Peptide Label: isoform a precursor
- UniProtKB: Q96Q55 (UniProtKB/Swiss-Prot),   Q96B80 (UniProtKB/Swiss-Prot),   Q7Z7H8 (UniProtKB/Swiss-Prot),   A6NGJ4 (UniProtKB/Swiss-Prot),   B4DEH0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_683685   ⟸   NM_148887
- Peptide Label: isoform b
- UniProtKB: B4DEH0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024306343   ⟸   XM_024450575
- Peptide Label: isoform X1
- UniProtKB: B4DEH0 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000390624   ⟸   ENST00000423147
Ensembl Acc Id: ENSP00000395870   ⟸   ENST00000414011
Ensembl Acc Id: ENSP00000324100   ⟸   ENST00000351111
Ensembl Acc Id: ENSP00000404039   ⟸   ENST00000421763
Ensembl Acc Id: ENSP00000290208   ⟸   ENST00000290208
RefSeq Acc Id: XP_054171019   ⟸   XM_054315044
- Peptide Label: isoform X1

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q7Z7H8-F1-model_v2 AlphaFold Q7Z7H8 1-261 view protein structure

Promoters
RGD ID:6794292
Promoter ID:HG_KWN:26461
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_033413,   NM_145255,   OTTHUMT00000343767,   OTTHUMT00000343768,   OTTHUMT00000343769,   OTTHUMT00000343770,   UC002ILY.1,   UC002IMB.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361743,263,699 - 43,264,199 (+)MPROMDB
RGD ID:6852984
Promoter ID:EP74312
Type:initiation region
Name:HS_MRPL10
Description:Mitochondrial ribosomal protein L10.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Mammalian gene collection (MGC) full-length cDNA cloning
Position:
Human AssemblyChrPosition (strand)Source
Build 361743,263,891 - 43,263,951EPD
RGD ID:7235429
Promoter ID:EPDNEW_H23459
Type:initiation region
Name:MRPL10_1
Description:mitochondrial ribosomal protein L10
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23461  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381747,831,523 - 47,831,583EPDNEW
RGD ID:7235433
Promoter ID:EPDNEW_H23461
Type:initiation region
Name:MRPL10_2
Description:mitochondrial ribosomal protein L10
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23459  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381747,837,731 - 47,837,791EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:14055 AgrOrtholog
COSMIC MRPL10 COSMIC
Ensembl Genes ENSG00000159111 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000290208.11 UniProtKB/Swiss-Prot
  ENST00000351111 ENTREZGENE
  ENST00000351111.7 UniProtKB/Swiss-Prot
  ENST00000414011 ENTREZGENE
  ENST00000414011.1 UniProtKB/Swiss-Prot
  ENST00000421763 ENTREZGENE
  ENST00000421763.5 UniProtKB/TrEMBL
  ENST00000423147.1 UniProtKB/TrEMBL
Gene3D-CATH 3.30.70.1730 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000159111 GTEx
HGNC ID HGNC:14055 ENTREZGENE
Human Proteome Map MRPL10 Human Proteome Map
InterPro Ribosomal_L10-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_L10P UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_uL10_bac_type UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:124995 UniProtKB/Swiss-Prot
NCBI Gene MRPL10 ENTREZGENE
OMIM 611825 OMIM
PANTHER 39S RIBOSOMAL PROTEIN L10, MITOCHONDRIAL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR11560 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Ribosomal_L10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA30939 PharmGKB
Superfamily-SCOP SSF160369 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A6NGJ4 ENTREZGENE
  B4DEH0 ENTREZGENE, UniProtKB/TrEMBL
  F2Z2K7_HUMAN UniProtKB/TrEMBL
  Q7Z7H8 ENTREZGENE
  Q96B80 ENTREZGENE
  Q96Q55 ENTREZGENE
  RM10_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary A6NGJ4 UniProtKB/Swiss-Prot
  Q96B80 UniProtKB/Swiss-Prot
  Q96Q55 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2017-08-16 MRPL10  mitochondrial ribosomal protein L10  MRPL8  mitochondrial ribosomal protein L8  Data merged from RGD:1346687 737654 PROVISIONAL