C10orf55 (chromosome 10 putative open reading frame 55) - Rat Genome Database

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Gene: C10orf55 (chromosome 10 putative open reading frame 55) Homo sapiens
Analyze
Symbol: C10orf55
Name: chromosome 10 putative open reading frame 55
RGD ID: 1348811
HGNC Page HGNC:31008
Description: Enables identical protein binding activity.
Type: ncrna (Ensembl: lncRNA)
RefSeq Status: VALIDATED
Previously known as: bA417O11.3; chromosome 10 open reading frame 55; chromosome 10 open reading frame 55 (putative); hypothetical protein LOC414236; uncharacterized protein C10orf55
RGD Orthologs
Green Monkey
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
GRCh381073,909,969 - 73,922,777 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1073,908,103 - 73,922,810 (-)EnsemblGRCh38hg38GRCh38
GRCh371075,669,727 - 75,682,535 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361075,339,740 - 75,341,994 (-)NCBINCBI36Build 36hg18NCBI36
Build 341075,339,739 - 75,341,994NCBI
Celera1068,953,043 - 68,965,862 (-)NCBICelera
Cytogenetic Map10q22.2NCBI
HuRef1069,664,662 - 69,677,397 (-)NCBIHuRef
CHM1_11075,951,489 - 75,964,310 (-)NCBICHM1_1
T2T-CHM13v2.01074,781,360 - 74,794,168 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

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

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:14702039   PMID:15164054   PMID:15489334   PMID:16344560   PMID:19913121   PMID:20628086   PMID:21145461   PMID:23128233   PMID:26186194   PMID:28301587   PMID:28514442  
PMID:32296183   PMID:33961781   PMID:36724073  


Genomics

Comparative Map Data
C10orf55
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381073,909,969 - 73,922,777 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1073,908,103 - 73,922,810 (-)EnsemblGRCh38hg38GRCh38
GRCh371075,669,727 - 75,682,535 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361075,339,740 - 75,341,994 (-)NCBINCBI36Build 36hg18NCBI36
Build 341075,339,739 - 75,341,994NCBI
Celera1068,953,043 - 68,965,862 (-)NCBICelera
Cytogenetic Map10q22.2NCBI
HuRef1069,664,662 - 69,677,397 (-)NCBIHuRef
CHM1_11075,951,489 - 75,964,310 (-)NCBICHM1_1
T2T-CHM13v2.01074,781,360 - 74,794,168 (-)NCBIT2T-CHM13v2.0
LOC103215982
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1957,458,340 - 57,458,820 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366604818,034,352 - 18,034,865 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in C10orf55
110 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 10q21.2-22.2(chr10:62229688-74468143)x1 copy number loss See cases [RCV000052530] Chr10:62229688..74468143 [GRCh38]
Chr10:63989447..76227901 [GRCh37]
Chr10:63659453..75897907 [NCBI36]
Chr10:10q21.2-22.2		 pathogenic
GRCh38/hg38 10q22.1-22.2(chr10:72720628-75612374)x1 copy number loss See cases [RCV000052531] Chr10:72720628..75612374 [GRCh38]
Chr10:74480386..77372132 [GRCh37]
Chr10:74150392..77042138 [NCBI36]
Chr10:10q22.1-22.2		 pathogenic
GRCh38/hg38 10q21.1-22.2(chr10:58436466-74415216)x1 copy number loss See cases [RCV000052511] Chr10:58436466..74415216 [GRCh38]
Chr10:60196226..76174974 [GRCh37]
Chr10:59866232..75844980 [NCBI36]
Chr10:10q21.1-22.2		 pathogenic
NM_002658.6(PLAU):c.422= (p.Leu141=) single nucleotide variant Alzheimer disease, late-onset, susceptibility to [RCV000013052]|not provided [RCV000948375] Chr10:73913343 [GRCh38]
Chr10:75673101 [GRCh37]
Chr10:10q22.2		 risk factor|benign
NC_000010.9:g.75329022_75406959dup duplication Quebec platelet disorder [RCV000022812] Chr10:73899258..73977195 [GRCh38]
Chr10:75659016..75736953 [GRCh37]
Chr10:75329022..75406959 [NCBI36]
Chr10:10q22.2		 pathogenic
GRCh38/hg38 10q21.3-22.3(chr10:67196567-79422057)x3 copy number gain See cases [RCV000135438] Chr10:67196567..79422057 [GRCh38]
Chr10:68956325..81181813 [GRCh37]
Chr10:68626331..80851819 [NCBI36]
Chr10:10q21.3-22.3		 pathogenic
GRCh38/hg38 10q21.3-22.2(chr10:63402579-75296099)x1 copy number loss See cases [RCV000136658] Chr10:63402579..75296099 [GRCh38]
Chr10:65162339..77055857 [GRCh37]
Chr10:64832345..76725863 [NCBI36]
Chr10:10q21.3-22.2		 pathogenic|likely benign
GRCh38/hg38 10q11.23-23.2(chr10:50729367-87147204)x3 copy number gain See cases [RCV000138007] Chr10:50729367..87147204 [GRCh38]
Chr10:52489127..88906961 [GRCh37]
Chr10:52159133..88896941 [NCBI36]
Chr10:10q11.23-23.2		 pathogenic
GRCh38/hg38 10q22.2(chr10:73881750-73942272)x1 copy number loss See cases [RCV000141182] Chr10:73881750..73942272 [GRCh38]
Chr10:75641508..75702030 [GRCh37]
Chr10:75311514..75372036 [NCBI36]
Chr10:10q22.2		 likely benign
NM_002658.6(PLAU):c.172G>A (p.Gly58Arg) single nucleotide variant Hirschsprung disease, susceptibility to, 1 [RCV000201293]|Quebec platelet disorder [RCV000365591]|not provided [RCV000971917] Chr10:73912301 [GRCh38]
Chr10:73912301..73912302 [GRCh38]
Chr10:75672059 [GRCh37]
Chr10:75672059..75672060 [GRCh37]
Chr10:10q22.2		 benign|likely benign|uncertain significance
NM_002658.6(PLAU):c.*355C>T single nucleotide variant Quebec platelet disorder [RCV000321485] Chr10:73916920 [GRCh38]
Chr10:75676678 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.1048T>C (p.Tyr350His) single nucleotide variant PLAU-related disorder [RCV003977867]|Quebec platelet disorder [RCV000344642]|not provided [RCV000951111] Chr10:73915328 [GRCh38]
Chr10:75675086 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.1222G>A (p.Val408Ile) single nucleotide variant Quebec platelet disorder [RCV000369055] Chr10:73916491 [GRCh38]
Chr10:75676249 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.*520G>T single nucleotide variant Quebec platelet disorder [RCV000322787] Chr10:73917085 [GRCh38]
Chr10:75676843 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.*60A>C single nucleotide variant Quebec platelet disorder [RCV000370180] Chr10:73916625 [GRCh38]
Chr10:75676383 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.*444T>A single nucleotide variant Quebec platelet disorder [RCV000286448] Chr10:73917009 [GRCh38]
Chr10:75676767 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.*753C>T single nucleotide variant Quebec platelet disorder [RCV000347880] Chr10:73917318 [GRCh38]
Chr10:75677076 [GRCh37]
Chr10:10q22.2		 likely benign|uncertain significance
NM_002658.6(PLAU):c.581C>T (p.Ala194Val) single nucleotide variant Quebec platelet disorder [RCV000372309]|not provided [RCV004718308] Chr10:73913659 [GRCh38]
Chr10:75673417 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.162A>G (p.Pro54=) single nucleotide variant PLAU-related disorder [RCV003957564]|Quebec platelet disorder [RCV000269937]|not provided [RCV000970461] Chr10:73912291 [GRCh38]
Chr10:75672049 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.236G>A (p.Arg79Gln) single nucleotide variant Quebec platelet disorder [RCV000271088]|not provided [RCV004791398] Chr10:73912966 [GRCh38]
Chr10:75672724 [GRCh37]
Chr10:10q22.2		 benign|likely benign|uncertain significance
NM_002658.6(PLAU):c.57+6T>C single nucleotide variant Quebec platelet disorder [RCV000305546] Chr10:73911618 [GRCh38]
Chr10:75671376 [GRCh37]
Chr10:10q22.2		 likely benign|uncertain significance
NM_002658.6(PLAU):c.163A>G (p.Lys55Glu) single nucleotide variant PLAU-related disorder [RCV004755859]|Quebec platelet disorder [RCV000306361] Chr10:73912292 [GRCh38]
Chr10:75672050 [GRCh37]
Chr10:10q22.2		 benign|likely benign|uncertain significance
NM_002658.6(PLAU):c.*398C>T single nucleotide variant Quebec platelet disorder [RCV000376246] Chr10:73916963 [GRCh38]
Chr10:75676721 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.691A>C (p.Lys231Gln) single nucleotide variant Quebec platelet disorder [RCV000377952]|not provided [RCV004718309] Chr10:73913990 [GRCh38]
Chr10:75673748 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.878G>A (p.Arg293Gln) single nucleotide variant Quebec platelet disorder [RCV000308085]|not provided [RCV001355163] Chr10:73914824 [GRCh38]
Chr10:75674582 [GRCh37]
Chr10:10q22.2		 benign|likely benign|uncertain significance
NM_002658.6(PLAU):c.1092C>T (p.Asp364=) single nucleotide variant Quebec platelet disorder [RCV000309659]|not provided [RCV000879758] Chr10:73915372 [GRCh38]
Chr10:75675130 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.308C>T (p.Thr103Met) single nucleotide variant Quebec platelet disorder [RCV000330967] Chr10:73913038 [GRCh38]
Chr10:75672796 [GRCh37]
Chr10:10q22.2		 benign|uncertain significance
NM_002658.6(PLAU):c.581C>A (p.Ala194Glu) single nucleotide variant Quebec platelet disorder [RCV000332164] Chr10:73913659 [GRCh38]
Chr10:75673417 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.*266T>C single nucleotide variant Quebec platelet disorder [RCV000356504] Chr10:73916831 [GRCh38]
Chr10:75676589 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.1053C>T (p.Tyr351=) single nucleotide variant Quebec platelet disorder [RCV000404445] Chr10:73915333 [GRCh38]
Chr10:75675091 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.43G>T (p.Val15Leu) single nucleotide variant Quebec platelet disorder [RCV000404874]|not provided [RCV004718307] Chr10:73911598 [GRCh38]
Chr10:75671356 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.368+6G>C single nucleotide variant Quebec platelet disorder [RCV000277129] Chr10:73913104 [GRCh38]
Chr10:75672862 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.*844del deletion Quebec platelet disorder [RCV000406801] Chr10:73917409 [GRCh38]
Chr10:75677167 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.*335G>A single nucleotide variant Quebec platelet disorder [RCV000261684] Chr10:73916900 [GRCh38]
Chr10:75676658 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.*141C>T single nucleotide variant Quebec platelet disorder [RCV000261471]|not provided [RCV001672432] Chr10:73916706 [GRCh38]
Chr10:75676464 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.-25C>T single nucleotide variant Quebec platelet disorder [RCV000334715]|not provided [RCV003417975] Chr10:73911531 [GRCh38]
Chr10:75671289 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.681-7C>T single nucleotide variant Quebec platelet disorder [RCV000337376]|not provided [RCV001689998] Chr10:73913973 [GRCh38]
Chr10:75673731 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.111A>G (p.Gly37=) single nucleotide variant Quebec platelet disorder [RCV000360245] Chr10:73912240 [GRCh38]
Chr10:75671998 [GRCh37]
Chr10:10q22.2		 benign|uncertain significance
NM_002658.6(PLAU):c.-32+9C>G single nucleotide variant Quebec platelet disorder [RCV000279693]|not provided [RCV004692927] Chr10:73911227 [GRCh38]
Chr10:75670985 [GRCh37]
Chr10:10q22.2		 likely benign|uncertain significance
NM_002658.6(PLAU):c.*52T>A single nucleotide variant Quebec platelet disorder [RCV000315536] Chr10:73916617 [GRCh38]
Chr10:75676375 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.17C>A (p.Ala6Glu) single nucleotide variant Quebec platelet disorder [RCV000340376]|not specified [RCV004021481] Chr10:73911572 [GRCh38]
Chr10:75671330 [GRCh37]
Chr10:10q22.2		 benign|uncertain significance
NM_002658.6(PLAU):c.-18C>A single nucleotide variant Quebec platelet disorder [RCV000299746]|not provided [RCV004718306] Chr10:73911538 [GRCh38]
Chr10:75671296 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.-20A>G single nucleotide variant Quebec platelet disorder [RCV000391405] Chr10:73911536 [GRCh38]
Chr10:75671294 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.602G>T (p.Arg201Leu) single nucleotide variant Quebec platelet disorder [RCV000282402] Chr10:73913680 [GRCh38]
Chr10:75673438 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.706A>G (p.Ile236Val) single nucleotide variant Quebec platelet disorder [RCV000283375] Chr10:73914005 [GRCh38]
Chr10:75673763 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.822C>T (p.Asn274=) single nucleotide variant Quebec platelet disorder [RCV000393582]|not provided [RCV001642931] Chr10:73914121 [GRCh38]
Chr10:75673879 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.*3G>A single nucleotide variant Quebec platelet disorder [RCV000274497] Chr10:73916568 [GRCh38]
Chr10:75676326 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.*176G>T single nucleotide variant Quebec platelet disorder [RCV000315691] Chr10:73916741 [GRCh38]
Chr10:75676499 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.*631C>T single nucleotide variant Quebec platelet disorder [RCV000382111] Chr10:73917196 [GRCh38]
Chr10:75676954 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.*880T>A single nucleotide variant Quebec platelet disorder [RCV000294098] Chr10:73917445 [GRCh38]
Chr10:75677203 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.*900A>G single nucleotide variant Quebec platelet disorder [RCV000348895] Chr10:73917465 [GRCh38]
Chr10:75677223 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.316G>C (p.Ala106Pro) single nucleotide variant Quebec platelet disorder [RCV000385437] Chr10:73913046 [GRCh38]
Chr10:75672804 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.-41G>A single nucleotide variant Quebec platelet disorder [RCV000352310] Chr10:73911209 [GRCh38]
Chr10:75670967 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.-32G>A single nucleotide variant Quebec platelet disorder [RCV000388238] Chr10:73911218 [GRCh38]
Chr10:75670976 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.4(PLAU):c.*935A>G single nucleotide variant Quebec platelet disorder [RCV000390583] Chr10:73917500 [GRCh38]
Chr10:75677258 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.*688C>T single nucleotide variant Quebec platelet disorder [RCV000288271] Chr10:73917253 [GRCh38]
Chr10:75677011 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.750G>C (p.Gly250=) single nucleotide variant Quebec platelet disorder [RCV000343093] Chr10:73914049 [GRCh38]
Chr10:75673807 [GRCh37]
Chr10:10q22.2		 uncertain significance
GRCh37/hg19 10q22.2-22.3(chr10:75542067-79428995)x1 copy number loss See cases [RCV000447510] Chr10:75542067..79428995 [GRCh37]
Chr10:10q22.2-22.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3 copy number gain See cases [RCV000448750] Chr10:93297..135378918 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143) copy number gain See cases [RCV000511389] Chr10:100027..135427143 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic|uncertain significance
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3 copy number gain See cases [RCV000510861] Chr10:100027..135427143 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
GRCh37/hg19 10q22.2(chr10:75179409-76009153)x3 copy number gain See cases [RCV000511191] Chr10:75179409..76009153 [GRCh37]
Chr10:10q22.2		 uncertain significance
GRCh37/hg19 10q11.21-26.3(chr10:42347406-135534747)x1 copy number loss Poly (ADP-Ribose) polymerase inhibitor response [RCV000626438] Chr10:42347406..135534747 [GRCh37]
Chr10:10q11.21-26.3		 drug response
NM_002658.6(PLAU):c.571C>T (p.Pro191Ser) single nucleotide variant not specified [RCV004299161] Chr10:73913649 [GRCh38]
Chr10:75673407 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.721C>T (p.Arg241Cys) single nucleotide variant not specified [RCV004284578] Chr10:73914020 [GRCh38]
Chr10:75673778 [GRCh37]
Chr10:10q22.2		 uncertain significance
GRCh37/hg19 10q21.3-23.32(chr10:69040366-93194993)x3 copy number gain not provided [RCV000683289] Chr10:69040366..93194993 [GRCh37]
Chr10:10q21.3-23.32		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:73232-135524321)x3 copy number gain not provided [RCV000749464] Chr10:73232..135524321 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:98087-135477883)x3 copy number gain not provided [RCV000749465] Chr10:98087..135477883 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
NM_002658.6(PLAU):c.194-207A>G single nucleotide variant not provided [RCV001541184] Chr10:73912717 [GRCh38]
Chr10:75672475 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.680+80C>T single nucleotide variant not provided [RCV001666396] Chr10:73913838 [GRCh38]
Chr10:75673596 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.1159C>T (p.Arg387Cys) single nucleotide variant not specified [RCV004285992] Chr10:73916428 [GRCh38]
Chr10:75676186 [GRCh37]
Chr10:10q22.2		 uncertain significance
GRCh37/hg19 10q22.2(chr10:75251395-75763287)x1 copy number loss not provided [RCV000849346] Chr10:75251395..75763287 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.143T>A (p.Ile48Asn) single nucleotide variant Quebec platelet disorder [RCV001108612] Chr10:73912272 [GRCh38]
Chr10:75672030 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.972C>T (p.Thr324=) single nucleotide variant Quebec platelet disorder [RCV001108684] Chr10:73915252 [GRCh38]
Chr10:75675010 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.85+49G>A single nucleotide variant not provided [RCV001640909] Chr10:73912117 [GRCh38]
Chr10:75671875 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.-31-121G>T single nucleotide variant not provided [RCV001639533] Chr10:73911404 [GRCh38]
Chr10:75671162 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.744G>A (p.Thr248=) single nucleotide variant not provided [RCV000976202] Chr10:73914043 [GRCh38]
Chr10:75673801 [GRCh37]
Chr10:10q22.2		 likely benign
NM_002658.6(PLAU):c.1221C>T (p.Gly407=) single nucleotide variant not provided [RCV000930114] Chr10:73916490 [GRCh38]
Chr10:75676248 [GRCh37]
Chr10:10q22.2		 likely benign
NM_002658.6(PLAU):c.445C>T (p.His149Tyr) single nucleotide variant Quebec platelet disorder [RCV001105355]|not provided [RCV004584850] Chr10:73913366 [GRCh38]
Chr10:75673124 [GRCh37]
Chr10:10q22.2		 benign|likely benign
NM_002658.6(PLAU):c.*538G>A single nucleotide variant Quebec platelet disorder [RCV001105458] Chr10:73917103 [GRCh38]
Chr10:75676861 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.193+297_193+298insT insertion not provided [RCV001710508] Chr10:73912619..73912620 [GRCh38]
Chr10:75672377..75672378 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.369-87G>A single nucleotide variant not provided [RCV001721784] Chr10:73913203 [GRCh38]
Chr10:75672961 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.735C>A (p.Asn245Lys) single nucleotide variant Quebec platelet disorder [RCV001106495] Chr10:73914034 [GRCh38]
Chr10:75673792 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.830-13T>C single nucleotide variant Quebec platelet disorder [RCV001106496] Chr10:73914763 [GRCh38]
Chr10:75674521 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.845G>A (p.Arg282His) single nucleotide variant Quebec platelet disorder [RCV001106497] Chr10:73914791 [GRCh38]
Chr10:75674549 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.1193G>T (p.Arg398Leu) single nucleotide variant Quebec platelet disorder [RCV001108685] Chr10:73916462 [GRCh38]
Chr10:75676220 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.970+66C>T single nucleotide variant not provided [RCV001611432] Chr10:73914982 [GRCh38]
Chr10:75674740 [GRCh37]
Chr10:10q22.2		 benign
NM_002658.6(PLAU):c.453C>T (p.Cys151=) single nucleotide variant Quebec platelet disorder [RCV001105356] Chr10:73913374 [GRCh38]
Chr10:75673132 [GRCh37]
Chr10:10q22.2		 likely benign
NM_002658.6(PLAU):c.*474G>A single nucleotide variant Quebec platelet disorder [RCV001105457] Chr10:73917039 [GRCh38]
Chr10:75676797 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.*917G>A single nucleotide variant Quebec platelet disorder [RCV001106604] Chr10:73917482 [GRCh38]
Chr10:75677240 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.*921T>C single nucleotide variant Quebec platelet disorder [RCV001106605] Chr10:73917486 [GRCh38]
Chr10:75677244 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.194A>G (p.Asp65Gly) single nucleotide variant Quebec platelet disorder [RCV001103432] Chr10:73912924 [GRCh38]
Chr10:75672682 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.236G>C (p.Arg79Pro) single nucleotide variant Quebec platelet disorder [RCV001103433] Chr10:73912966 [GRCh38]
Chr10:75672724 [GRCh37]
Chr10:10q22.2		 likely benign
NM_002658.6(PLAU):c.*309T>C single nucleotide variant Quebec platelet disorder [RCV001103523] Chr10:73916874 [GRCh38]
Chr10:75676632 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.559A>G (p.Ile187Val) single nucleotide variant Quebec platelet disorder [RCV001105357]|not specified [RCV004032109] Chr10:73913637 [GRCh38]
Chr10:75673395 [GRCh37]
Chr10:10q22.2		 benign|uncertain significance
NM_002658.6(PLAU):c.1229C>T (p.Thr410Met) single nucleotide variant Quebec platelet disorder [RCV001330951] Chr10:73916498 [GRCh38]
Chr10:75676256 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.193+298G>T single nucleotide variant not provided [RCV001614192] Chr10:73912620 [GRCh38]
Chr10:75672378 [GRCh37]
Chr10:10q22.2		 benign
GRCh37/hg19 10q21.3-22.3(chr10:68735254-78885714) copy number loss not specified [RCV002052875] Chr10:68735254..78885714 [GRCh37]
Chr10:10q21.3-22.3		 pathogenic
NC_000010.10:g.(?_75671314)_(79799964_?)dup duplication Genitopatellar syndrome [RCV003116588] Chr10:75671314..79799964 [GRCh37]
Chr10:10q22.2-22.3		 uncertain significance
NM_002658.6(PLAU):c.467dup (p.Pro157fs) duplication Quebec platelet disorder [RCV002266808] Chr10:73913539..73913540 [GRCh38]
Chr10:75673297..75673298 [GRCh37]
Chr10:10q22.2		 uncertain significance
NC_000010.10:g.(?_75670858)_(75677260_?)dup duplication Quebec platelet disorder [RCV002302494] Chr10:75670858..75677260 [GRCh37]
Chr10:10q22.2		 pathogenic
NM_002658.6(PLAU):c.724T>C (p.Ser242Pro) single nucleotide variant not specified [RCV004104588] Chr10:73914023 [GRCh38]
Chr10:75673781 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.260T>C (p.Met87Thr) single nucleotide variant not specified [RCV004114527] Chr10:73912990 [GRCh38]
Chr10:75672748 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.587T>C (p.Ile196Thr) single nucleotide variant not specified [RCV004134586] Chr10:73913665 [GRCh38]
Chr10:75673423 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.527G>A (p.Arg176His) single nucleotide variant not specified [RCV004112685] Chr10:73913605 [GRCh38]
Chr10:75673363 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.902C>T (p.Pro301Leu) single nucleotide variant not specified [RCV004212814] Chr10:73914848 [GRCh38]
Chr10:75674606 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.190A>T (p.Ile64Leu) single nucleotide variant not specified [RCV004257142] Chr10:73912319 [GRCh38]
Chr10:75672077 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.754A>T (p.Met252Leu) single nucleotide variant Quebec platelet disorder [RCV003142682]|not specified [RCV004246043] Chr10:73914053 [GRCh38]
Chr10:75673811 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.601C>T (p.Arg201Trp) single nucleotide variant not specified [RCV004252228] Chr10:73913679 [GRCh38]
Chr10:75673437 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.548A>G (p.Glu183Gly) single nucleotide variant Quebec platelet disorder [RCV003134957] Chr10:73913626 [GRCh38]
Chr10:75673384 [GRCh37]
Chr10:10q22.2		 uncertain significance
GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143) copy number gain Distal trisomy 10q [RCV003319593] Chr10:11138692..135427143 [GRCh37]
Chr10:10p14-q26.3		 pathogenic
GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143) copy number loss Distal 10q deletion syndrome [RCV003319583] Chr10:12829206..135427143 [GRCh37]
Chr10:10p13-q26.3		 pathogenic
NM_002658.6(PLAU):c.539T>C (p.Ile180Thr) single nucleotide variant Quebec platelet disorder [RCV003333893]|not specified [RCV004334122] Chr10:73913617 [GRCh38]
Chr10:75673375 [GRCh37]
Chr10:10q22.2		 uncertain significance
GRCh37/hg19 10q11.21-24.2(chr10:42709645-100834951)x3 copy number gain not provided [RCV003484798] Chr10:42709645..100834951 [GRCh37]
Chr10:10q11.21-24.2		 pathogenic
NM_002658.6(PLAU):c.861G>T (p.Arg287Ser) single nucleotide variant PLAU-related disorder [RCV003421155]|not specified [RCV004690407] Chr10:73914807 [GRCh38]
Chr10:75674565 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.1007T>C (p.Val336Ala) single nucleotide variant not specified [RCV004511674] Chr10:73915287 [GRCh38]
Chr10:75675045 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.383G>A (p.Arg128Gln) single nucleotide variant not specified [RCV004511679] Chr10:73913304 [GRCh38]
Chr10:75673062 [GRCh37]
Chr10:10q22.2		 likely benign
NM_002658.6(PLAU):c.1234G>C (p.Val412Leu) single nucleotide variant not specified [RCV004511677] Chr10:73916503 [GRCh38]
Chr10:75676261 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.1259G>A (p.Arg420His) single nucleotide variant not specified [RCV004511678] Chr10:73916528 [GRCh38]
Chr10:75676286 [GRCh37]
Chr10:10q22.2		 likely benign
NM_002658.6(PLAU):c.571C>A (p.Pro191Thr) single nucleotide variant not specified [RCV004511680] Chr10:73913649 [GRCh38]
Chr10:75673407 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.983A>G (p.Tyr328Cys) single nucleotide variant Quebec platelet disorder [RCV003989077] Chr10:73915263 [GRCh38]
Chr10:75675021 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.745C>A (p.Gln249Lys) single nucleotide variant not specified [RCV004511681] Chr10:73914044 [GRCh38]
Chr10:75673802 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.423G>A (p.Leu141=) single nucleotide variant PLAU-related disorder [RCV003981695] Chr10:73913344 [GRCh38]
Chr10:75673102 [GRCh37]
Chr10:10q22.2		 likely benign
NC_000010.11:g.73912917C>G single nucleotide variant C10orf55-related disorder [RCV003981334] Chr10:73912917 [GRCh38]
Chr10:75672675 [GRCh37]
Chr10:10q22.2		 likely benign
NR_160937.1(C10orf55):n.499C>A single nucleotide variant C10orf55-related disorder [RCV003982112] Chr10:73912216 [GRCh38]
Chr10:75671974 [GRCh37]
Chr10:10q22.2		 likely benign
NM_002658.6(PLAU):c.1041G>C (p.Gln347His) single nucleotide variant not specified [RCV004511676] Chr10:73915321 [GRCh38]
Chr10:75675079 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.827T>C (p.Ile276Thr) single nucleotide variant not specified [RCV004651089] Chr10:73914126 [GRCh38]
Chr10:75673884 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.1028G>A (p.Arg343Gln) single nucleotide variant not specified [RCV004651090] Chr10:73915308 [GRCh38]
Chr10:75675066 [GRCh37]
Chr10:10q22.2		 likely benign
NM_002658.6(PLAU):c.608G>C (p.Gly203Ala) single nucleotide variant not specified [RCV004651091] Chr10:73913686 [GRCh38]
Chr10:75673444 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.1120-14C>G single nucleotide variant not specified [RCV004690669] Chr10:73916375 [GRCh38]
Chr10:75676133 [GRCh37]
Chr10:10q22.2		 likely benign
NM_002658.6(PLAU):c.265C>G (p.Arg89Gly) single nucleotide variant not provided [RCV004793276] Chr10:73912995 [GRCh38]
Chr10:75672753 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.1212C>G (p.Asp404Glu) single nucleotide variant not provided [RCV004793277] Chr10:73916481 [GRCh38]
Chr10:75676239 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.98G>C (p.Cys33Ser) single nucleotide variant PLAU-related disorder [RCV004756926] Chr10:73912227 [GRCh38]
Chr10:75671985 [GRCh37]
Chr10:10q22.2		 uncertain significance
NM_002658.6(PLAU):c.351G>A (p.Gly117=) single nucleotide variant not specified [RCV004699815] Chr10:73913081 [GRCh38]
Chr10:75672839 [GRCh37]
Chr10:10q22.2		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2262
Count of miRNA genes:584
Interacting mature miRNAs:677
Transcripts:ENST00000409178, ENST00000412307
Prediction methods:Microtar, Miranda, 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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
597497145GWAS1593219_Hurokinase plasminogen activator surface receptor measurement QTL GWAS1593219 (human)3e-21urokinase plasminogen activator surface receptor measurement107391895773918958Human
597077811GWAS1173885_Hblood protein measurement QTL GWAS1173885 (human)1e-23blood protein amount (VT:0005416)blood protein measurement (CMO:0000028)107391334373913344Human
597518555GWAS1614629_Hintraocular pressure measurement QTL GWAS1614629 (human)9e-09intraocular pressure measurement107391190073911901Human
597182675GWAS1278749_Hurokinase-type plasminogen activator measurement QTL GWAS1278749 (human)1e-116urokinase-type plasminogen activator measurement107391271773912718Human
597359127GWAS1455201_Hvenous thromboembolism QTL GWAS1455201 (human)0.000002venous thromboembolism107392207173922072Human
597475314GWAS1571388_Hblood protein measurement QTL GWAS1571388 (human)2e-96blood protein amount (VT:0005416)blood protein measurement (CMO:0000028)107391230173912302Human
597348298GWAS1444372_HAbdominal Aortic Aneurysm QTL GWAS1444372 (human)2e-12Abdominal Aortic Aneurysm107391334373913344Human
597021095GWAS1117169_HCrohn's disease QTL GWAS1117169 (human)2e-09intestine integrity trait (VT:0010554)107391334373913344Human
597037890GWAS1133964_Hblood protein measurement QTL GWAS1133964 (human)4e-50blood protein amount (VT:0005416)blood protein measurement (CMO:0000028)107391334373913344Human
407022069GWAS671045_Hinflammatory bowel disease QTL GWAS671045 (human)7e-10inflammatory bowel disease107391334373913344Human
597490948GWAS1587022_HRS-warfarin measurement QTL GWAS1587022 (human)0.0000003RS-warfarin measurement107391181373911814Human
597522561GWAS1618635_Hprotein measurement QTL GWAS1618635 (human)4e-29protein measurement107391284973912850Human
597442465GWAS1538539_Hurokinase-type plasminogen activator measurement QTL GWAS1538539 (human)9e-20urokinase-type plasminogen activator measurement107391230173912302Human
597506051GWAS1602125_Hurokinase-type plasminogen activator measurement QTL GWAS1602125 (human)2e-27urokinase-type plasminogen activator measurement107391230173912302Human
597455715GWAS1551789_Hurokinase-type plasminogen activator measurement QTL GWAS1551789 (human)1e-08urokinase-type plasminogen activator measurement107391230173912302Human
597122760GWAS1218834_Hblood protein measurement QTL GWAS1218834 (human)2e-81blood protein amount (VT:0005416)blood protein measurement (CMO:0000028)107391334373913344Human
597473891GWAS1569965_Hprotein measurement QTL GWAS1569965 (human)2e-39protein measurement107392241873922419Human

Markers in Region
RH92165  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371075,670,118 - 75,670,252UniSTSGRCh37
Build 361075,340,124 - 75,340,258RGDNCBI36
Celera1068,953,434 - 68,953,568RGD
Cytogenetic Map10q22.2UniSTS
HuRef1069,665,053 - 69,665,187UniSTS
GeneMap99-GB4 RH Map10380.97UniSTS
GDB:181547  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371075,672,812 - 75,673,296UniSTSGRCh37
Build 361075,342,818 - 75,343,302RGDNCBI36
Celera1068,956,129 - 68,956,613RGD
Cytogenetic Map10q22.2UniSTS
HuRef1069,667,749 - 69,668,233UniSTS
PMC229370P1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371075,671,802 - 75,672,728UniSTSGRCh37
Build 361075,341,808 - 75,342,734RGDNCBI36
Celera1068,955,118 - 68,956,045RGD
Cytogenetic Map10q22.2UniSTS
HuRef1069,666,737 - 69,667,665UniSTS
SHGC-31374  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10q22.2UniSTS
HuRef1069,671,333 - 69,671,558UniSTS
Stanford-G3 RH Map103441.0UniSTS
GeneMap99-G3 RH Map103417.0UniSTS
PLAU  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371075,672,009 - 75,672,774UniSTSGRCh37
Celera1068,955,325 - 68,956,091UniSTS
HuRef1069,666,944 - 69,667,711UniSTS


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
renal system
reproductive system
respiratory system
sensory system
1200 2297 2644 2138 3846 1426 2065 1 425 1558 267 2203 6364 5923 33 2655 797 1540 1536 167

Sequence


Ensembl Acc Id: ENST00000409178
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1073,909,969 - 73,922,777 (-)Ensembl
Ensembl Acc Id: ENST00000412307   ⟹   ENSP00000409225
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1073,909,978 - 73,916,642 (-)Ensembl
Ensembl Acc Id: ENST00000721915
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1073,908,106 - 73,922,777 (-)Ensembl
Ensembl Acc Id: ENST00000721916
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1073,908,153 - 73,922,794 (-)Ensembl
Ensembl Acc Id: ENST00000721917
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1073,908,176 - 73,922,810 (-)Ensembl
Ensembl Acc Id: ENST00000721918
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1073,908,170 - 73,922,777 (-)Ensembl
Ensembl Acc Id: ENST00000721919
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1073,908,170 - 73,922,773 (-)Ensembl
Ensembl Acc Id: ENST00000721920
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1073,908,176 - 73,922,777 (-)Ensembl
Ensembl Acc Id: ENST00000721921
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1073,908,172 - 73,922,767 (-)Ensembl
Ensembl Acc Id: ENST00000721922
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1073,908,106 - 73,911,022 (-)Ensembl
Ensembl Acc Id: ENST00000721923
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1073,908,106 - 73,909,646 (-)Ensembl
Ensembl Acc Id: ENST00000721924
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1073,908,103 - 73,909,296 (-)Ensembl
RefSeq Acc Id: NR_160937
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381073,909,969 - 73,922,777 (-)NCBI
T2T-CHM13v2.01074,781,360 - 74,794,168 (-)NCBI
Sequence:
RefSeq Acc Id: NR_160938
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381073,909,969 - 73,922,777 (-)NCBI
T2T-CHM13v2.01074,781,360 - 74,794,168 (-)NCBI
Sequence:
Protein Sequences
GenBank Protein AAH49374 (Get FASTA)   NCBI Sequence Viewer  
  BAC03908 (Get FASTA)   NCBI Sequence Viewer  
  EAW54546 (Get FASTA)   NCBI Sequence Viewer  
  Q5SWW7 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Acc Id: ENSP00000409225   ⟸   ENST00000412307

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q5SWW7-F1-model_v2 AlphaFold Q5SWW7 1-151 view protein structure

Promoters
RGD ID:7217891
Promoter ID:EPDNEW_H14691
Type:multiple initiation site
Name:C10orf55_1
Description:chromosome 10 open reading frame 55
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381073,922,777 - 73,922,837EPDNEW

Additional Information

Database Acc Id Source(s)
COSMIC C10orf55 COSMIC
Ensembl Genes ENSG00000222047 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000409178 ENTREZGENE
GTEx ENSG00000222047 GTEx
HGNC ID HGNC:31008 ENTREZGENE
Human Proteome Map C10orf55 Human Proteome Map
NCBI Gene 414236 ENTREZGENE
PharmGKB PA134866694 PharmGKB
RNAcentral URS00007BBDBC RNACentral
  URS0000E60A0D RNACentral
UniProt CJ055_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary Q3KRG4 UniProtKB/Swiss-Prot
  Q8NAK4 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2020-08-10 C10orf55  chromosome 10 putative open reading frame 55  C10orf55  chromosome 10 open reading frame 55  Symbol and/or name change 19259463 PROVISIONAL
2020-08-03 C10orf55  chromosome 10 open reading frame 55  C10orf55  chromosome 10 open reading frame 55 (putative)  Symbol and/or name change 19259463 PROVISIONAL
2019-09-24 C10orf55  chromosome 10 open reading frame 55 (putative)  C10orf55  chromosome 10 open reading frame 55  Symbol and/or name change 5135510 APPROVED