SNHG10 (small nucleolar RNA host gene 10) - Rat Genome Database

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Gene: SNHG10 (small nucleolar RNA host gene 10) Homo sapiens
Analyze
Symbol: SNHG10
Name: small nucleolar RNA host gene 10
RGD ID: 1603252
HGNC Page HGNC:27510
Description: Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus.
Type: ncrna (Ensembl: lncRNA)
RefSeq Status: REVIEWED
Previously known as: C14orf62; chromosome 14 open reading frame 62; FLJ40557; LINC00063; NCRNA00063; TP53LC16
RGD Orthologs
Mouse
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381495,532,912 - 95,534,872 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1495,521,943 - 95,534,889 (-)EnsemblGRCh38hg38GRCh38
GRCh371495,999,249 - 96,001,209 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361495,069,002 - 95,070,962 (-)NCBINCBI36Build 36hg18NCBI36
Celera1476,054,937 - 76,056,896 (-)NCBICelera
Cytogenetic Map14q32.13NCBI
HuRef1476,184,906 - 76,186,865 (-)NCBIHuRef
CHM1_11495,937,172 - 95,939,132 (-)NCBICHM1_1
T2T-CHM13v2.01489,763,605 - 89,765,564 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
Cajal body  (IEA)
nucleolus  (IEA)

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:8889548   PMID:12477932   PMID:14702039   PMID:31101763   PMID:32319822   PMID:32712782   PMID:32843060   PMID:32920660   PMID:33081752   PMID:34456184   PMID:34613933   PMID:35506202  
PMID:37884162  


Genomics

Comparative Map Data
SNHG10
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381495,532,912 - 95,534,872 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1495,521,943 - 95,534,889 (-)EnsemblGRCh38hg38GRCh38
GRCh371495,999,249 - 96,001,209 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361495,069,002 - 95,070,962 (-)NCBINCBI36Build 36hg18NCBI36
Celera1476,054,937 - 76,056,896 (-)NCBICelera
Cytogenetic Map14q32.13NCBI
HuRef1476,184,906 - 76,186,865 (-)NCBIHuRef
CHM1_11495,937,172 - 95,939,132 (-)NCBICHM1_1
T2T-CHM13v2.01489,763,605 - 89,765,564 (-)NCBIT2T-CHM13v2.0
Snhg10
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3912104,996,876 - 104,998,538 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl12104,996,875 - 104,998,567 (-)EnsemblGRCm39 Ensembl
GRCm3812105,030,617 - 105,032,279 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl12105,030,617 - 105,032,279 (-)EnsemblGRCm38mm10GRCm38
MGSCv3712106,268,827 - 106,270,489 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3612106,268,845 - 106,270,489 (-)NCBIMGSCv36mm8
Celera12106,263,062 - 106,264,724 (-)NCBICelera
Cytogenetic Map12ENCBI
cM Map1255.04NCBI

Variants

.
Variants in SNHG10
3 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 14q31.2-32.33(chr14:83912345-106855405)x3 copy number gain See cases [RCV000052294] Chr14:83912345..106855405 [GRCh38]
Chr14:84378689..107263620 [GRCh37]
Chr14:83448442..106334665 [NCBI36]
Chr14:14q31.2-32.33		 pathogenic
GRCh38/hg38 14q32.13-32.33(chr14:94628219-106451054)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052298]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052298]|See cases [RCV000052298] Chr14:94628219..106451054 [GRCh38]
Chr14:95094556..106906960 [GRCh37]
Chr14:94164309..105978005 [NCBI36]
Chr14:14q32.13-32.33		 pathogenic
GRCh38/hg38 14q24.2-32.2(chr14:72787506-99596719)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052293]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052293]|See cases [RCV000052293] Chr14:72787506..99596719 [GRCh38]
Chr14:73254214..100063056 [GRCh37]
Chr14:72323967..99132809 [NCBI36]
Chr14:14q24.2-32.2		 pathogenic
GRCh38/hg38 14q31.3-32.33(chr14:86094030-106832642)x3 copy number gain See cases [RCV000052295] Chr14:86094030..106832642 [GRCh38]
Chr14:86560374..107240869 [GRCh37]
Chr14:85630127..106311914 [NCBI36]
Chr14:14q31.3-32.33		 pathogenic
GRCh38/hg38 14q32.12-32.33(chr14:91455861-106832642)x3 copy number gain See cases [RCV000052296] Chr14:91455861..106832642 [GRCh38]
Chr14:91922205..107240869 [GRCh37]
Chr14:90991958..106311914 [NCBI36]
Chr14:14q32.12-32.33		 pathogenic
GRCh38/hg38 14q24.3-32.33(chr14:73655772-106879298)x3 copy number gain See cases [RCV000134000] Chr14:73655772..106879298 [GRCh38]
Chr14:74122475..107287505 [GRCh37]
Chr14:73192228..106358550 [NCBI36]
Chr14:14q24.3-32.33		 pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3 copy number gain See cases [RCV000135543] Chr14:20151149..106855263 [GRCh38]
Chr14:20619308..107263478 [GRCh37]
Chr14:19689148..106334523 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh38/hg38 14q32.12-32.33(chr14:92540983-104863658)x3 copy number gain See cases [RCV000135896] Chr14:92540983..104863658 [GRCh38]
Chr14:93007328..105329995 [GRCh37]
Chr14:92077081..104401040 [NCBI36]
Chr14:14q32.12-32.33		 pathogenic
GRCh38/hg38 14q32.13-32.33(chr14:95524407-106879501)x1 copy number loss See cases [RCV000136032] Chr14:95524407..106879501 [GRCh38]
Chr14:95990744..107287708 [GRCh37]
Chr14:95060497..106358753 [NCBI36]
Chr14:14q32.13-32.33		 pathogenic
GRCh38/hg38 14q24.3-32.33(chr14:77222795-106879298)x3 copy number gain See cases [RCV000138230] Chr14:77222795..106879298 [GRCh38]
Chr14:77689138..107287505 [GRCh37]
Chr14:76758891..106358550 [NCBI36]
Chr14:14q24.3-32.33		 pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3 copy number gain See cases [RCV000143373] Chr14:20043514..106877229 [GRCh38]
Chr14:20511673..107285437 [GRCh37]
Chr14:19581513..106356482 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3 copy number gain See cases [RCV000446256] Chr14:19794561..107234280 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q23.2-32.33(chr14:62493932-107285437)x3 copy number gain See cases [RCV000448557] Chr14:62493932..107285437 [GRCh37]
Chr14:14q23.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437) copy number gain See cases [RCV000512041] Chr14:20511673..107285437 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q32.12-32.13(chr14:93498930-96059698)x3 copy number gain See cases [RCV000511246] Chr14:93498930..96059698 [GRCh37]
Chr14:14q32.12-32.13		 uncertain significance
GRCh37/hg19 14q24.2-32.33(chr14:73750741-107285437)x3 copy number gain See cases [RCV000512497] Chr14:73750741..107285437 [GRCh37]
Chr14:14q24.2-32.33		 pathogenic
GRCh37/hg19 14q31.2-32.2(chr14:84783137-96908198)x1 copy number loss not provided [RCV000683625] Chr14:84783137..96908198 [GRCh37]
Chr14:14q31.2-32.2		 pathogenic
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3 copy number gain not provided [RCV000738412] Chr14:19000422..107289053 [GRCh37]
Chr14:14q11.1-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3 copy number gain not provided [RCV000738413] Chr14:19280733..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3 copy number gain not provided [RCV000738414] Chr14:19327823..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
NM_016417.2(GLRX5):c.-277T>A single nucleotide variant not provided [RCV000833033] Chr14:95534813 [GRCh38]
Chr14:96001150 [GRCh37]
Chr14:14q32.13		 likely benign
GRCh37/hg19 14q32.12-32.33(chr14:91969028-107285437)x3 copy number gain not provided [RCV000848687] Chr14:91969028..107285437 [GRCh37]
Chr14:14q32.12-32.33		 pathogenic
GRCh37/hg19 14q31.2-32.33(chr14:84537502-107285437)x3 copy number gain not provided [RCV002472581] Chr14:84537502..107285437 [GRCh37]
Chr14:14q31.2-32.33		 pathogenic
GRCh37/hg19 14q31.2-32.2(chr14:84783523-96907490)x1 copy number loss Deletion syndrome [RCV001004048] Chr14:84783523..96907490 [GRCh37]
Chr14:14q31.2-32.2		 pathogenic
NR_001459.2(SNHG10):n.39C>T single nucleotide variant not provided [RCV001652800] Chr14:95534834 [GRCh38]
Chr14:96001171 [GRCh37]
Chr14:14q32.13		 benign
GRCh37/hg19 14q32.12-32.13(chr14:94400492-96192218) copy number gain not specified [RCV002052453] Chr14:94400492..96192218 [GRCh37]
Chr14:14q32.12-32.13		 uncertain significance
GRCh37/hg19 14q32.13-32.31(chr14:95871795-102457523)x1 copy number loss not provided [RCV001827727] Chr14:95871795..102457523 [GRCh37]
Chr14:14q32.13-32.31		 pathogenic
NC_000014.8:g.(?_90429459)_(97347545_?)dup duplication not provided [RCV003109490] Chr14:90429459..97347545 [GRCh37]
Chr14:14q32.11-32.2		 uncertain significance
NC_000014.8:g.(?_95080779)_(97347545_?)dup duplication not provided [RCV003113847] Chr14:95080779..97347545 [GRCh37]
Chr14:14q32.13-32.2		 uncertain significance
GRCh37/hg19 14q13.3-32.33(chr14:37671058-106985955)x2 copy number gain See cases [RCV002286356] Chr14:37671058..106985955 [GRCh37]
Chr14:14q13.3-32.33		 pathogenic
GRCh37/hg19 14q31.1-32.2(chr14:81593708-97059276)x3 copy number gain not provided [RCV002472541] Chr14:81593708..97059276 [GRCh37]
Chr14:14q31.1-32.2		 likely pathogenic
GRCh37/hg19 14q23.1-32.33(chr14:58894502-107227240)x3 copy number gain not provided [RCV003485036] Chr14:58894502..107227240 [GRCh37]
Chr14:14q23.1-32.33		 pathogenic
GRCh37/hg19 14q31.3-32.33(chr14:88580184-107285437)x3 copy number gain not provided [RCV003485051] Chr14:88580184..107285437 [GRCh37]
Chr14:14q31.3-32.33		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:403
Count of miRNA genes:284
Interacting mature miRNAs:309
Transcripts:ENST00000500370, ENST00000553559, ENST00000554169, ENST00000555866
Prediction methods: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.

Markers in Region
RH98225  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371495,999,440 - 95,999,561UniSTSGRCh37
Build 361495,069,193 - 95,069,314RGDNCBI36
Celera1476,055,128 - 76,055,249RGD
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q32.12UniSTS
GeneMap99-GB4 RH Map14259.66UniSTS
RH93740  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371495,999,440 - 95,999,561UniSTSGRCh37
Build 361495,069,193 - 95,069,314RGDNCBI36
Celera1476,055,128 - 76,055,249RGD
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q32.12UniSTS
HuRef1476,185,097 - 76,185,218UniSTS
GeneMap99-GB4 RH Map14259.76UniSTS


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 adipose tissue appendage entire extraembryonic component
High
Medium 211 286 912 31 389 30 541 71 1008 57 969 891 6 8 436 2
Low 2221 2608 812 591 1484 434 3815 2109 2699 360 481 718 164 1196 2352 3
Below cutoff 3 92 1 77 14 14 2 4 3 1 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000500370
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,297 - 95,534,800 (-)Ensembl
RefSeq Acc Id: ENST00000553559
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,914 - 95,534,872 (-)Ensembl
RefSeq Acc Id: ENST00000554169
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,634 - 95,534,642 (-)Ensembl
RefSeq Acc Id: ENST00000555866
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,914 - 95,534,586 (-)Ensembl
RefSeq Acc Id: ENST00000654925
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,522,136 - 95,534,043 (-)Ensembl
RefSeq Acc Id: ENST00000658932
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,222 - 95,534,751 (-)Ensembl
RefSeq Acc Id: ENST00000660378
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,834 - 95,534,889 (-)Ensembl
RefSeq Acc Id: ENST00000663212
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,521,943 - 95,524,457 (-)Ensembl
RefSeq Acc Id: ENST00000667310
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,521,958 - 95,534,642 (-)Ensembl
RefSeq Acc Id: ENST00000667668
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,531,968 - 95,534,235 (-)Ensembl
RefSeq Acc Id: ENST00000671157
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,521,988 - 95,534,652 (-)Ensembl
RefSeq Acc Id: ENST00000685307
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,834 - 95,534,804 (-)Ensembl
RefSeq Acc Id: ENST00000685703
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,912 - 95,534,639 (-)Ensembl
RefSeq Acc Id: ENST00000687146
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,838 - 95,534,642 (-)Ensembl
RefSeq Acc Id: ENST00000688138
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,912 - 95,534,621 (-)Ensembl
RefSeq Acc Id: ENST00000688462
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,912 - 95,534,619 (-)Ensembl
RefSeq Acc Id: ENST00000688965
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,915 - 95,534,627 (-)Ensembl
RefSeq Acc Id: ENST00000689247
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,838 - 95,534,642 (-)Ensembl
RefSeq Acc Id: ENST00000689442
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,912 - 95,534,621 (-)Ensembl
RefSeq Acc Id: ENST00000689758
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,912 - 95,534,783 (-)Ensembl
RefSeq Acc Id: ENST00000689823
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,912 - 95,534,621 (-)Ensembl
RefSeq Acc Id: ENST00000690868
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,912 - 95,534,783 (-)Ensembl
RefSeq Acc Id: ENST00000690961
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,912 - 95,534,621 (-)Ensembl
RefSeq Acc Id: ENST00000691606
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,915 - 95,534,627 (-)Ensembl
RefSeq Acc Id: ENST00000691619
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,834 - 95,534,624 (-)Ensembl
RefSeq Acc Id: ENST00000693219
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,834 - 95,534,627 (-)Ensembl
RefSeq Acc Id: ENST00000693520
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,912 - 95,534,642 (-)Ensembl
RefSeq Acc Id: ENST00000693718
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1495,532,912 - 95,534,619 (-)Ensembl
RefSeq Acc Id: NR_001459
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381495,532,912 - 95,534,872 (-)NCBI
GRCh371495,999,249 - 96,001,209 (-)RGD
Build 361495,069,002 - 95,070,962 (-)NCBI Archive
Celera1476,054,937 - 76,056,896 (-)RGD
HuRef1476,184,906 - 76,186,865 (-)ENTREZGENE
CHM1_11495,937,172 - 95,939,132 (-)NCBI
T2T-CHM13v2.01489,763,605 - 89,765,564 (-)NCBI
Sequence:
RefSeq Acc Id: NR_003138
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381495,532,912 - 95,534,872 (-)NCBI
GRCh371495,999,249 - 96,001,209 (-)RGD
Build 361495,069,002 - 95,070,962 (-)NCBI Archive
Celera1476,054,937 - 76,056,896 (-)RGD
HuRef1476,184,906 - 76,186,865 (-)ENTREZGENE
CHM1_11495,937,172 - 95,939,132 (-)NCBI
T2T-CHM13v2.01489,763,605 - 89,765,564 (-)NCBI
Sequence:
Promoters
RGD ID:6791890
Promoter ID:HG_KWN:20104
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_016417,   NR_001459
Position:
Human AssemblyChrPosition (strand)Source
Build 361495,069,291 - 95,071,947 (-)MPROMDB
RGD ID:15096838
Promoter ID:EPDNEWNC_H1670
Type:initiation region
Name:SNHG10_1
Description:small nucleolar RNA host gene 10 [Source:HGNCSymbol;Acc:HGNC:27510]
SO ACC ID:SO:0000170
Source:EPDNEWNC (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381495,534,244 - 95,534,304EPDNEWNC
RGD ID:15096836
Promoter ID:EPDNEWNC_H1671
Type:initiation region
Name:SNHG10_2
Description:small nucleolar RNA host gene 10 [Source:HGNCSymbol;Acc:HGNC:27510]
SO ACC ID:SO:0000170
Source:EPDNEWNC (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381495,534,751 - 95,534,811EPDNEWNC

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:27510 AgrOrtholog
COSMIC SNHG10 COSMIC
Ensembl Genes ENSG00000247092 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000685307 ENTREZGENE
GTEx ENSG00000247092 GTEx
HGNC ID HGNC:27510 ENTREZGENE
Human Proteome Map SNHG10 Human Proteome Map
NCBI Gene 283596 ENTREZGENE
PharmGKB PA162404106 PharmGKB
RNAcentral URS000075DE81 RNACentral
  URS000075E815 RNACentral


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-04-05 SNHG10  small nucleolar RNA host gene 10  C14orf62  chromosome 14 open reading frame 62  Data merged from RGD:1348359 737654 PROVISIONAL
2015-02-24 SNHG10  small nucleolar RNA host gene 10    small nucleolar RNA host gene 10 (non-protein coding)  Symbol and/or name change 5135510 APPROVED