TNRC6C (trinucleotide repeat containing adaptor 6C) - Rat Genome Database

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Gene: TNRC6C (trinucleotide repeat containing adaptor 6C) Homo sapiens
Analyze
Symbol: TNRC6C
Name: trinucleotide repeat containing adaptor 6C
RGD ID: 1349772
HGNC Page HGNC:29318
Description: Predicted to enable RNA binding activity. Involved in miRNA-mediated post-transcriptional gene silencing; positive regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay; and positive regulation of nuclear-transcribed mRNA poly(A) tail shortening. Predicted to be located in cytosol. Predicted to be active in P-body and nucleoplasm.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FLJ20015; KIAA1582; LOC107985010; trinucleotide repeat containing 6C; trinucleotide repeat-containing gene 6C protein; uncharacterized LOC107985010
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Black Rat
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
GRCh381777,957,557 - 78,108,835 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1777,958,624 - 78,108,822 (+)Ensemblhg38GRCh38
GRCh371775,953,639 - 76,104,916 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361773,556,589 - 73,612,616 (+)NCBIBuild 36Build 36hg18NCBI36
Build 341773,556,588 - 73,612,616NCBI
Celera1772,596,318 - 72,700,896 (+)NCBICelera
Cytogenetic Map17q25.3NCBI
HuRef1771,424,371 - 71,528,917 (+)NCBIHuRef
CHM1_11776,065,011 - 76,169,559 (+)NCBICHM1_1
T2T-CHM13v2.01778,851,592 - 79,002,521 (+)NCBIT2T-CHM13v2.0
JBrowse:




Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
cytoplasm  (IEA)
cytosol  (IEA,TAS)
nucleoplasm  (IBA)
P-body  (IBA)
RISC complex  (NAS)

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. Argonaute proteins at a glance. Ender C and Meister G, J Cell Sci. 2010 Jun 1;123(Pt 11):1819-23.
2. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
4. Transcriptomic characteristics of bronchoalveolar lavage fluid and peripheral blood mononuclear cells in COVID-19 patients. Xiong Y, etal., Emerg Microbes Infect. 2020 Dec;9(1):761-770. doi: 10.1080/22221751.2020.1747363.
Additional References at PubMed
PMID:10997877   PMID:12168954   PMID:12477932   PMID:14702039   PMID:15489334   PMID:16344560   PMID:16625196   PMID:16880270   PMID:19304925   PMID:19383768   PMID:19470757   PMID:19716330  
PMID:19838187   PMID:20098421   PMID:20181956   PMID:21063388   PMID:21145461   PMID:21873635   PMID:21981923   PMID:21984184   PMID:21984185   PMID:23172285   PMID:23340509   PMID:23400010  
PMID:23463101   PMID:24768540   PMID:24778252   PMID:26106978   PMID:26186194   PMID:26344197   PMID:26638075   PMID:26673895   PMID:26831064   PMID:27025967   PMID:27542412   PMID:28514442  
PMID:28611215   PMID:28718761   PMID:28781232   PMID:29128334   PMID:29395067   PMID:29507755   PMID:29568061   PMID:30938030   PMID:30997501   PMID:31253590   PMID:31586073   PMID:31670606  
PMID:31699778   PMID:32877691   PMID:33060197   PMID:33417976   PMID:33961781   PMID:34079125   PMID:34108231   PMID:35013218   PMID:35051175   PMID:35140242   PMID:35271311   PMID:35748872  
PMID:35803934   PMID:37499664   PMID:37689310   PMID:37827155   PMID:38360978   PMID:39098523  


Genomics

Comparative Map Data
TNRC6C
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381777,957,557 - 78,108,835 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1777,958,624 - 78,108,822 (+)Ensemblhg38GRCh38
GRCh371775,953,639 - 76,104,916 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361773,556,589 - 73,612,616 (+)NCBIBuild 36Build 36hg18NCBI36
Build 341773,556,588 - 73,612,616NCBI
Celera1772,596,318 - 72,700,896 (+)NCBICelera
Cytogenetic Map17q25.3NCBI
HuRef1771,424,371 - 71,528,917 (+)NCBIHuRef
CHM1_11776,065,011 - 76,169,559 (+)NCBICHM1_1
T2T-CHM13v2.01778,851,592 - 79,002,521 (+)NCBIT2T-CHM13v2.0
Tnrc6c
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3911117,544,529 - 117,654,265 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl11117,545,115 - 117,654,265 (+)EnsemblGRCm39 EnsemblGRCm39
GRCm3811117,653,703 - 117,763,439 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl11117,654,289 - 117,763,439 (+)Ensemblmm10GRCm38
MGSCv3711117,515,603 - 117,624,753 (+)NCBIMGSCv37MGSCv37mm9NCBIm37
MGSCv3611117,470,379 - 117,579,529 (+)NCBIMGSCv36mm8
Celera11129,397,726 - 129,507,237 (+)NCBICelera
Cytogenetic Map11E2NCBI
cM Map1182.96NCBI
Tnrc6c
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr810103,367,498 - 103,478,246 (+)NCBIGRCr8GRCr8GRCr8
GRCr8 Ensembl10103,367,647 - 103,478,246 (+)EnsemblGRCr8
mRatBN7.210102,908,958 - 102,979,543 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl10102,868,828 - 102,978,194 (+)EnsemblmRatBN7.2
Rnor_6.010106,698,359 - 106,763,639 (+)NCBIRnor_6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl10106,712,127 - 106,762,043 (+)Ensemblrn6Rnor6.0
Rnor_5.010106,337,197 - 106,403,097 (+)NCBIRnor_5.0Rnor_5.0rn5
RGSC_v3.410107,829,754 - 107,854,869 (+)NCBIRGSC_v3.4RGSC_v3.4rn4
Celera10101,489,423 - 101,539,688 (+)NCBICelera
Cytogenetic Map10q32.2NCBI
Tnrc6c
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555064,440,555 - 4,559,070 (-)Ensembl
ChiLan1.0NW_0049555064,440,555 - 4,579,642 (-)NCBIChiLan1.0ChiLan1.0
TNRC6C
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21994,007,592 - 94,157,602 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11798,836,243 - 98,986,328 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01772,035,737 - 72,185,489 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11777,634,111 - 77,738,511 (+)NCBIPanPan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1777,633,564 - 77,738,511 (+)EnsemblpanPan2panpan1.1
TNRC6C
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.193,018,599 - 3,122,664 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl93,020,533 - 3,171,471 (-)EnsemblcanFam3CanFam3.1
Dog10K_Boxer_Tasha93,701,674 - 3,805,806 (-)NCBIDog10K_Boxer_TashaDog10K_Boxer_Tasha
ROS_Cfam_1.093,696,277 - 3,800,626 (-)NCBIROS_Cfam_1.0ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl93,698,224 - 3,777,294 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.193,721,379 - 3,823,452 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.093,843,625 - 3,947,774 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.093,925,070 - 4,029,400 (-)NCBIUU_Cfam_GSD_1.0UU_Cfam_GSD_1.0
Tnrc6c
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244056023,670,705 - 3,761,602 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365942,656,045 - 2,741,233 (+)EnsemblSpeTri2.0 Ensembl
SpeTri2.0NW_0049365942,656,079 - 2,741,254 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TNRC6C
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl123,847,901 - 3,935,368 (-)EnsemblsusScr11Sscrofa11.1
Sscrofa11.1123,847,522 - 3,939,054 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
TNRC6C
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11643,610,595 - 43,718,117 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1643,613,223 - 43,717,852 (-)EnsemblChlSab1.1 EnsemblchlSab2Vervet-AGM
Vero_WHO_p1.0NW_02366607714,328,740 - 14,463,687 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Tnrc6c
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248017,552,030 - 7,638,834 (+)EnsemblHetGla_female_1.0 EnsemblhetGla2HetGla_female_1.0 Ensembl
HetGla 1.0NW_0046248017,552,644 - 7,644,755 (+)NCBIHetGla 1.0HetGla 1.0hetGla2
Tnrc6c
(Rattus rattus - black rat)
Black Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rrattus_CSIRO_v1966,306,846 - 66,379,436 (-)NCBIRrattus_CSIRO_v1

Variants

.
Variants in TNRC6C
185 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q25.3(chr17:78092236-83086677)x3 copy number gain See cases [RCV000050685] Chr17:78092236..83086677 [GRCh38]
Chr17:76088317..81044553 [GRCh37]
Chr17:73599912..78637842 [NCBI36]
Chr17:17q25.3		 pathogenic
GRCh38/hg38 17q24.3-25.3(chr17:69209079-83086677)x3 copy number gain See cases [RCV000052486] Chr17:69209079..83086677 [GRCh38]
Chr17:67205220..81044553 [GRCh37]
Chr17:64716815..78637842 [NCBI36]
Chr17:17q24.3-25.3		 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 17q25.3(chr17:78092356-78444214)x1 copy number loss See cases [RCV000139522] Chr17:78092356..78444214 [GRCh38]
Chr17:76088437..76440296 [GRCh37]
Chr17:73600032..73951891 [NCBI36]
Chr17:17q25.3		 likely benign
GRCh38/hg38 17q24.3-25.3(chr17:69916435-83102552)x3 copy number gain See cases [RCV000143342] Chr17:69916435..83102552 [GRCh38]
Chr17:67912576..81048189 [GRCh37]
Chr17:65424171..78653717 [NCBI36]
Chr17:17q24.3-25.3		 pathogenic
GRCh37/hg19 17q25.1-25.3(chr17:73951701-81041938)x3 copy number gain See cases [RCV000447539] Chr17:73951701..81041938 [GRCh37]
Chr17:17q25.1-25.3		 pathogenic
GRCh37/hg19 17q24.2-25.3(chr17:64241326-81041938)x3 copy number gain See cases [RCV000447577] Chr17:64241326..81041938 [GRCh37]
Chr17:17q24.2-25.3		 pathogenic
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 17q25.1-25.3(chr17:73951701-81041938)x3 copy number gain See cases [RCV000510919] Chr17:73951701..81041938 [GRCh37]
Chr17:17q25.1-25.3		 pathogenic
NM_001142640.2(TNRC6C):c.4841C>T (p.Pro1614Leu) single nucleotide variant not specified [RCV004329373] Chr17:78093677 [GRCh38]
Chr17:76089758 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1063A>T (p.Thr355Ser) single nucleotide variant not specified [RCV004311496] Chr17:78049495 [GRCh38]
Chr17:76045576 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2723C>T (p.Pro908Leu) single nucleotide variant not specified [RCV004331212] Chr17:78051155 [GRCh38]
Chr17:76047236 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4970C>T (p.Ser1657Leu) single nucleotide variant not specified [RCV004289692] Chr17:78097787 [GRCh38]
Chr17:76093868 [GRCh37]
Chr17:17q25.3		 uncertain significance
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 17q24.2-25.3(chr17:67002415-81041938)x3 copy number gain See cases [RCV000512573] Chr17:67002415..81041938 [GRCh37]
Chr17:17q24.2-25.3		 pathogenic
GRCh37/hg19 17q24.1-25.3(chr17:63689671-81041938)x3 copy number gain not provided [RCV000683952] Chr17:63689671..81041938 [GRCh37]
Chr17:17q24.1-25.3		 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
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
NM_001142640.2(TNRC6C):c.1652G>A (p.Gly551Glu) single nucleotide variant Intellectual disability [RCV001007802] Chr17:78050084 [GRCh38]
Chr17:76046165 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4714C>T (p.His1572Tyr) single nucleotide variant not specified [RCV004302391] Chr17:78093055 [GRCh38]
Chr17:76089136 [GRCh37]
Chr17:17q25.3		 uncertain significance
GRCh37/hg19 17q24.1-25.3(chr17:62778720-81041938)x3 copy number gain not provided [RCV000849900] Chr17:62778720..81041938 [GRCh37]
Chr17:17q24.1-25.3		 pathogenic
NM_001142640.2(TNRC6C):c.3941G>T (p.Ser1314Ile) single nucleotide variant not specified [RCV004309977] Chr17:78079504 [GRCh38]
Chr17:76075585 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4928G>C (p.Gly1643Ala) single nucleotide variant not specified [RCV004321763] Chr17:78097745 [GRCh38]
Chr17:76093826 [GRCh37]
Chr17:17q25.3		 uncertain significance
GRCh37/hg19 17q25.1-25.3(chr17:73261871-78608763)x3 copy number gain not provided [RCV001006919] Chr17:73261871..78608763 [GRCh37]
Chr17:17q25.1-25.3		 pathogenic
NC_000017.10:g.(?_76004208)_(76127818_?)dup duplication Epidermodysplasia verruciformis [RCV001919196] Chr17:76004208..76127818 [GRCh37]
Chr17:17q25.3		 uncertain significance
GRCh37/hg19 17q25.1-25.3(chr17:73481509-81043199)x3 copy number gain not provided [RCV002276051] Chr17:73481509..81043199 [GRCh37]
Chr17:17q25.1-25.3		 pathogenic
NM_001142640.2(TNRC6C):c.3345A>C (p.Glu1115Asp) single nucleotide variant not specified [RCV004292132] Chr17:78067869 [GRCh38]
Chr17:76063950 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4295C>G (p.Ser1432Cys) single nucleotide variant not specified [RCV004078245] Chr17:78086965 [GRCh38]
Chr17:76083046 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1583A>G (p.Asn528Ser) single nucleotide variant not specified [RCV004189682] Chr17:78050015 [GRCh38]
Chr17:76046096 [GRCh37]
Chr17:17q25.3		 likely benign
NM_001142640.2(TNRC6C):c.2126A>G (p.Asn709Ser) single nucleotide variant not specified [RCV004192794] Chr17:78050558 [GRCh38]
Chr17:76046639 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5614G>T (p.Val1872Leu) single nucleotide variant not specified [RCV004161160] Chr17:78104648 [GRCh38]
Chr17:76100729 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2595G>T (p.Trp865Cys) single nucleotide variant not specified [RCV004164188] Chr17:78051027 [GRCh38]
Chr17:76047108 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2253A>G (p.Ile751Met) single nucleotide variant not specified [RCV004109908] Chr17:78050685 [GRCh38]
Chr17:76046766 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2637C>G (p.Ser879Arg) single nucleotide variant not specified [RCV004149837] Chr17:78051069 [GRCh38]
Chr17:76047150 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5617C>T (p.Arg1873Cys) single nucleotide variant not specified [RCV004125277] Chr17:78104651 [GRCh38]
Chr17:76100732 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1537C>T (p.Pro513Ser) single nucleotide variant not specified [RCV004216449] Chr17:78049969 [GRCh38]
Chr17:76046050 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.865G>A (p.Gly289Arg) single nucleotide variant not specified [RCV004240123] Chr17:78049297 [GRCh38]
Chr17:76045378 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2314G>A (p.Ala772Thr) single nucleotide variant not specified [RCV004214073] Chr17:78050746 [GRCh38]
Chr17:76046827 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1889G>A (p.Arg630Gln) single nucleotide variant not specified [RCV004207275] Chr17:78050321 [GRCh38]
Chr17:76046402 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3589A>G (p.Thr1197Ala) single nucleotide variant not specified [RCV004155927] Chr17:78075186 [GRCh38]
Chr17:76071267 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2267T>G (p.Val756Gly) single nucleotide variant not specified [RCV004215985] Chr17:78050699 [GRCh38]
Chr17:76046780 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1043G>A (p.Gly348Asp) single nucleotide variant not specified [RCV004190469] Chr17:78049475 [GRCh38]
Chr17:76045556 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5479G>T (p.Ala1827Ser) single nucleotide variant not specified [RCV004148471] Chr17:78104513 [GRCh38]
Chr17:76100594 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3341A>G (p.Gln1114Arg) single nucleotide variant not specified [RCV004226492] Chr17:78067865 [GRCh38]
Chr17:76063946 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2559C>A (p.Asn853Lys) single nucleotide variant not specified [RCV004209568] Chr17:78050991 [GRCh38]
Chr17:76047072 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3162C>A (p.His1054Gln) single nucleotide variant not specified [RCV004232599] Chr17:78064867 [GRCh38]
Chr17:76060948 [GRCh37]
Chr17:17q25.3		 likely benign
NM_001142640.2(TNRC6C):c.823T>C (p.Cys275Arg) single nucleotide variant not specified [RCV004203118] Chr17:78049255 [GRCh38]
Chr17:76045336 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2092A>G (p.Asn698Asp) single nucleotide variant not specified [RCV004229964] Chr17:78050524 [GRCh38]
Chr17:76046605 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.841G>A (p.Asp281Asn) single nucleotide variant not specified [RCV004133378] Chr17:78049273 [GRCh38]
Chr17:76045354 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2164G>A (p.Ala722Thr) single nucleotide variant not specified [RCV004171749] Chr17:78050596 [GRCh38]
Chr17:76046677 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5623G>A (p.Asp1875Asn) single nucleotide variant not specified [RCV004220668] Chr17:78104657 [GRCh38]
Chr17:76100738 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5762C>T (p.Pro1921Leu) single nucleotide variant not specified [RCV004240747] Chr17:78104796 [GRCh38]
Chr17:76100877 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2417G>A (p.Gly806Glu) single nucleotide variant not specified [RCV004117013] Chr17:78050849 [GRCh38]
Chr17:76046930 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4277C>T (p.Pro1426Leu) single nucleotide variant not specified [RCV004210125] Chr17:78086947 [GRCh38]
Chr17:76083028 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4558G>A (p.Ala1520Thr) single nucleotide variant not specified [RCV004087200] Chr17:78091574 [GRCh38]
Chr17:76087655 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2176G>A (p.Ala726Thr) single nucleotide variant not specified [RCV004128527] Chr17:78050608 [GRCh38]
Chr17:76046689 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2219C>T (p.Ala740Val) single nucleotide variant not specified [RCV004196208] Chr17:78050651 [GRCh38]
Chr17:76046732 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2204A>G (p.Asp735Gly) single nucleotide variant not specified [RCV004142953] Chr17:78050636 [GRCh38]
Chr17:76046717 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2683G>A (p.Val895Met) single nucleotide variant not specified [RCV004104483] Chr17:78051115 [GRCh38]
Chr17:76047196 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1198A>G (p.Met400Val) single nucleotide variant not specified [RCV004173573] Chr17:78049630 [GRCh38]
Chr17:76045711 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4706C>G (p.Ala1569Gly) single nucleotide variant not specified [RCV004168599] Chr17:78093047 [GRCh38]
Chr17:76089128 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3002C>T (p.Pro1001Leu) single nucleotide variant not specified [RCV004155143] Chr17:78051434 [GRCh38]
Chr17:76047515 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4226A>T (p.His1409Leu) single nucleotide variant not specified [RCV004214157] Chr17:78086896 [GRCh38]
Chr17:76082977 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1445C>T (p.Thr482Ile) single nucleotide variant not specified [RCV004074353] Chr17:78049877 [GRCh38]
Chr17:76045958 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2736G>T (p.Lys912Asn) single nucleotide variant not specified [RCV004179169] Chr17:78051168 [GRCh38]
Chr17:76047249 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1729A>G (p.Ser577Gly) single nucleotide variant not specified [RCV004072178] Chr17:78050161 [GRCh38]
Chr17:76046242 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1373T>C (p.Val458Ala) single nucleotide variant not specified [RCV004172936] Chr17:78049805 [GRCh38]
Chr17:76045886 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1013G>T (p.Ser338Ile) single nucleotide variant not specified [RCV004202086] Chr17:78049445 [GRCh38]
Chr17:76045526 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2938A>G (p.Asn980Asp) single nucleotide variant not specified [RCV004116475] Chr17:78051370 [GRCh38]
Chr17:76047451 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3644A>G (p.Lys1215Arg) single nucleotide variant not specified [RCV004179895] Chr17:78075241 [GRCh38]
Chr17:76071322 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.655A>G (p.Asn219Asp) single nucleotide variant not specified [RCV004082908] Chr17:78049087 [GRCh38]
Chr17:76045168 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2503A>G (p.Arg835Gly) single nucleotide variant not specified [RCV004126957] Chr17:78050935 [GRCh38]
Chr17:76047016 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2035G>A (p.Glu679Lys) single nucleotide variant not specified [RCV004121065] Chr17:78050467 [GRCh38]
Chr17:76046548 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4640T>C (p.Ile1547Thr) single nucleotide variant not specified [RCV004223717] Chr17:78092981 [GRCh38]
Chr17:76089062 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2614G>A (p.Gly872Ser) single nucleotide variant not specified [RCV004116286] Chr17:78051046 [GRCh38]
Chr17:76047127 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4067C>T (p.Thr1356Met) single nucleotide variant not specified [RCV004195663] Chr17:78083135 [GRCh38]
Chr17:76079216 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2467A>G (p.Lys823Glu) single nucleotide variant not specified [RCV004152819] Chr17:78050899 [GRCh38]
Chr17:76046980 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3337T>C (p.Ser1113Pro) single nucleotide variant not specified [RCV004178367] Chr17:78067861 [GRCh38]
Chr17:76063942 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2918C>G (p.Thr973Ser) single nucleotide variant not specified [RCV004095724] Chr17:78051350 [GRCh38]
Chr17:76047431 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4937C>T (p.Pro1646Leu) single nucleotide variant not specified [RCV004180545] Chr17:78097754 [GRCh38]
Chr17:76093835 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.851T>C (p.Met284Thr) single nucleotide variant not specified [RCV004258647] Chr17:78049283 [GRCh38]
Chr17:76045364 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4255G>A (p.Val1419Met) single nucleotide variant not specified [RCV004252499] Chr17:78086925 [GRCh38]
Chr17:76083006 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2602A>C (p.Thr868Pro) single nucleotide variant not specified [RCV004269965] Chr17:78051034 [GRCh38]
Chr17:76047115 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1735A>G (p.Thr579Ala) single nucleotide variant not specified [RCV004277513] Chr17:78050167 [GRCh38]
Chr17:76046248 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5600G>A (p.Ser1867Asn) single nucleotide variant not specified [RCV004284767] Chr17:78104634 [GRCh38]
Chr17:76100715 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1214A>G (p.Asn405Ser) single nucleotide variant not specified [RCV004252629] Chr17:78049646 [GRCh38]
Chr17:76045727 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4064T>C (p.Met1355Thr) single nucleotide variant not specified [RCV004265662] Chr17:78083132 [GRCh38]
Chr17:76079213 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5101G>A (p.Ala1701Thr) single nucleotide variant not specified [RCV004275607] Chr17:78098399 [GRCh38]
Chr17:76094480 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5280C>G (p.Ser1760Arg) single nucleotide variant not specified [RCV004272772] Chr17:78102514 [GRCh38]
Chr17:76098595 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2339C>T (p.Thr780Ile) single nucleotide variant not specified [RCV004263363] Chr17:78050771 [GRCh38]
Chr17:76046852 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4405T>C (p.Phe1469Leu) single nucleotide variant not specified [RCV004283280] Chr17:78087075 [GRCh38]
Chr17:76083156 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2823G>C (p.Trp941Cys) single nucleotide variant not specified [RCV004273171] Chr17:78051255 [GRCh38]
Chr17:76047336 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2099G>T (p.Gly700Val) single nucleotide variant not specified [RCV004263470] Chr17:78050531 [GRCh38]
Chr17:76046612 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5720C>T (p.Pro1907Leu) single nucleotide variant not specified [RCV004258492] Chr17:78104754 [GRCh38]
Chr17:76100835 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2681C>T (p.Ser894Phe) single nucleotide variant not specified [RCV004360137] Chr17:78051113 [GRCh38]
Chr17:76047194 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5257G>A (p.Asp1753Asn) single nucleotide variant not specified [RCV004335438] Chr17:78102491 [GRCh38]
Chr17:76098572 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1758G>T (p.Gln586His) single nucleotide variant not specified [RCV004358036] Chr17:78050190 [GRCh38]
Chr17:76046271 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5507A>G (p.Asn1836Ser) single nucleotide variant not specified [RCV004359597] Chr17:78104541 [GRCh38]
Chr17:76100622 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.875G>A (p.Arg292Lys) single nucleotide variant not provided [RCV003421513] Chr17:78049307 [GRCh38]
Chr17:76045388 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2996G>T (p.Arg999Leu) single nucleotide variant not provided [RCV003421514] Chr17:78051428 [GRCh38]
Chr17:76047509 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3249A>G (p.Gln1083=) single nucleotide variant not provided [RCV003428503] Chr17:78067773 [GRCh38]
Chr17:76063854 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1367A>G (p.Asn456Ser) single nucleotide variant not provided [RCV003886038] Chr17:78049799 [GRCh38]
Chr17:76045880 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2933C>T (p.Thr978Met) single nucleotide variant not specified [RCV004475627] Chr17:78051365 [GRCh38]
Chr17:76047446 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2960C>T (p.Thr987Met) single nucleotide variant not specified [RCV004475628] Chr17:78051392 [GRCh38]
Chr17:76047473 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4192A>T (p.Thr1398Ser) single nucleotide variant not specified [RCV004475640] Chr17:78086862 [GRCh38]
Chr17:76082943 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4433A>G (p.Asn1478Ser) single nucleotide variant not specified [RCV004475642] Chr17:78091449 [GRCh38]
Chr17:76087530 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4490C>T (p.Pro1497Leu) single nucleotide variant not specified [RCV004475643] Chr17:78091506 [GRCh38]
Chr17:76087587 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1018G>A (p.Val340Ile) single nucleotide variant not specified [RCV004475644] Chr17:78049450 [GRCh38]
Chr17:76045531 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4532A>G (p.Asn1511Ser) single nucleotide variant not specified [RCV004475645] Chr17:78091548 [GRCh38]
Chr17:76087629 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4702G>A (p.Val1568Ile) single nucleotide variant not specified [RCV004475647] Chr17:78093043 [GRCh38]
Chr17:76089124 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4727G>A (p.Arg1576His) single nucleotide variant not specified [RCV004475648] Chr17:78093068 [GRCh38]
Chr17:76089149 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1054G>A (p.Gly352Arg) single nucleotide variant not specified [RCV004475649] Chr17:78049486 [GRCh38]
Chr17:76045567 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1055G>T (p.Gly352Val) single nucleotide variant not specified [RCV004475650] Chr17:78049487 [GRCh38]
Chr17:76045568 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5029G>A (p.Ala1677Thr) single nucleotide variant not specified [RCV004475651] Chr17:78097846 [GRCh38]
Chr17:76093927 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5734G>A (p.Asp1912Asn) single nucleotide variant not specified [RCV004475655] Chr17:78104768 [GRCh38]
Chr17:76100849 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2099G>A (p.Gly700Glu) single nucleotide variant not specified [RCV004475618] Chr17:78050531 [GRCh38]
Chr17:76046612 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2192C>A (p.Thr731Lys) single nucleotide variant not specified [RCV004475619] Chr17:78050624 [GRCh38]
Chr17:76046705 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2236G>C (p.Val746Leu) single nucleotide variant not specified [RCV004475620] Chr17:78050668 [GRCh38]
Chr17:76046749 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2595G>C (p.Trp865Cys) single nucleotide variant not specified [RCV004475621] Chr17:78051027 [GRCh38]
Chr17:76047108 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2699C>T (p.Thr900Ile) single nucleotide variant not specified [RCV004475622] Chr17:78051131 [GRCh38]
Chr17:76047212 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3346A>G (p.Ser1116Gly) single nucleotide variant not specified [RCV004475633] Chr17:78067870 [GRCh38]
Chr17:76063951 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3515A>G (p.Asn1172Ser) single nucleotide variant not specified [RCV004475634] Chr17:78073071 [GRCh38]
Chr17:76069152 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3574C>T (p.Arg1192Cys) single nucleotide variant not specified [RCV004475635] Chr17:78075171 [GRCh38]
Chr17:76071252 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4072T>A (p.Leu1358Met) single nucleotide variant not specified [RCV004475637] Chr17:78083140 [GRCh38]
Chr17:76079221 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.976G>A (p.Gly326Arg) single nucleotide variant not specified [RCV004475638] Chr17:78049408 [GRCh38]
Chr17:76045489 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.982G>A (p.Val328Met) single nucleotide variant not specified [RCV004475639] Chr17:78049414 [GRCh38]
Chr17:76045495 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2879C>A (p.Pro960Gln) single nucleotide variant not specified [RCV004475626] Chr17:78051311 [GRCh38]
Chr17:76047392 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.701A>G (p.Asn234Ser) single nucleotide variant not specified [RCV004475659] Chr17:78049133 [GRCh38]
Chr17:76045214 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.712G>A (p.Val238Ile) single nucleotide variant not specified [RCV004475660] Chr17:78049144 [GRCh38]
Chr17:76045225 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1621C>G (p.Pro541Ala) single nucleotide variant not specified [RCV004475661] Chr17:78050053 [GRCh38]
Chr17:76046134 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3113C>T (p.Thr1038Ile) single nucleotide variant not specified [RCV004475629] Chr17:78064818 [GRCh38]
Chr17:76060899 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3133C>G (p.Pro1045Ala) single nucleotide variant not specified [RCV004475631] Chr17:78064838 [GRCh38]
Chr17:76060919 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3250G>A (p.Glu1084Lys) single nucleotide variant not specified [RCV004475632] Chr17:78067774 [GRCh38]
Chr17:76063855 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5529G>T (p.Gln1843His) single nucleotide variant not specified [RCV004475652] Chr17:78104563 [GRCh38]
Chr17:76100644 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1856G>T (p.Gly619Val) single nucleotide variant not specified [RCV004475613] Chr17:78050288 [GRCh38]
Chr17:76046369 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1873G>C (p.Gly625Arg) single nucleotide variant not specified [RCV004475614] Chr17:78050305 [GRCh38]
Chr17:76046386 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1984A>G (p.Thr662Ala) single nucleotide variant not specified [RCV004475615] Chr17:78050416 [GRCh38]
Chr17:76046497 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2042A>T (p.Lys681Ile) single nucleotide variant not specified [RCV004475616] Chr17:78050474 [GRCh38]
Chr17:76046555 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.775G>T (p.Ala259Ser) single nucleotide variant not specified [RCV004475617] Chr17:78049207 [GRCh38]
Chr17:76045288 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2735A>G (p.Lys912Arg) single nucleotide variant not specified [RCV004475623] Chr17:78051167 [GRCh38]
Chr17:76047248 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2798A>G (p.Glu933Gly) single nucleotide variant not specified [RCV004475624] Chr17:78051230 [GRCh38]
Chr17:76047311 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5531C>G (p.Ala1844Gly) single nucleotide variant not specified [RCV004475654] Chr17:78104565 [GRCh38]
Chr17:76100646 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1150G>A (p.Ala384Thr) single nucleotide variant not specified [RCV004475656] Chr17:78049582 [GRCh38]
Chr17:76045663 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1175A>G (p.Asp392Gly) single nucleotide variant not specified [RCV004475657] Chr17:78049607 [GRCh38]
Chr17:76045688 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1508G>A (p.Ser503Asn) single nucleotide variant not specified [RCV004682345] Chr17:78049940 [GRCh38]
Chr17:76046021 [GRCh37]
Chr17:17q25.3		 likely benign
NM_001142640.2(TNRC6C):c.4401C>A (p.Asn1467Lys) single nucleotide variant not specified [RCV004682350] Chr17:78087071 [GRCh38]
Chr17:76083152 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4906C>T (p.Arg1636Cys) single nucleotide variant not specified [RCV004682351] Chr17:78093742 [GRCh38]
Chr17:76089823 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4396C>G (p.Pro1466Ala) single nucleotide variant not specified [RCV004682352] Chr17:78087066 [GRCh38]
Chr17:76083147 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.908A>G (p.Asn303Ser) single nucleotide variant not specified [RCV004682355] Chr17:78049340 [GRCh38]
Chr17:76045421 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4303C>G (p.Pro1435Ala) single nucleotide variant not specified [RCV004687031] Chr17:78086973 [GRCh38]
Chr17:76083054 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4201A>C (p.Asn1401His) single nucleotide variant not specified [RCV004682353] Chr17:78086871 [GRCh38]
Chr17:76082952 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1753G>A (p.Val585Ile) single nucleotide variant not specified [RCV004682338] Chr17:78050185 [GRCh38]
Chr17:76046266 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1877C>T (p.Thr626Met) single nucleotide variant not specified [RCV004682340] Chr17:78050309 [GRCh38]
Chr17:76046390 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2725G>A (p.Val909Ile) single nucleotide variant not specified [RCV004682341] Chr17:78051157 [GRCh38]
Chr17:76047238 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4939C>A (p.Pro1647Thr) single nucleotide variant not specified [RCV004682342] Chr17:78097756 [GRCh38]
Chr17:76093837 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5038G>A (p.Val1680Ile) single nucleotide variant not specified [RCV004682343] Chr17:78097855 [GRCh38]
Chr17:76093936 [GRCh37]
Chr17:17q25.3		 likely benign
NM_001142640.2(TNRC6C):c.1321T>A (p.Ser441Thr) single nucleotide variant not specified [RCV004682344] Chr17:78049753 [GRCh38]
Chr17:76045834 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1514G>C (p.Gly505Ala) single nucleotide variant not specified [RCV004682347] Chr17:78049946 [GRCh38]
Chr17:76046027 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1517A>G (p.Asn506Ser) single nucleotide variant not specified [RCV004682348] Chr17:78049949 [GRCh38]
Chr17:76046030 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2531C>T (p.Thr844Met) single nucleotide variant not specified [RCV004682349] Chr17:78050963 [GRCh38]
Chr17:76047044 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2128A>G (p.Ser710Gly) single nucleotide variant not specified [RCV004682354] Chr17:78050560 [GRCh38]
Chr17:76046641 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2717C>T (p.Pro906Leu) single nucleotide variant not specified [RCV004687033] Chr17:78051149 [GRCh38]
Chr17:76047230 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5566G>A (p.Ala1856Thr) single nucleotide variant not specified [RCV004687034] Chr17:78104600 [GRCh38]
Chr17:76100681 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1258A>G (p.Met420Val) single nucleotide variant not specified [RCV004687035] Chr17:78049690 [GRCh38]
Chr17:76045771 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3596A>G (p.His1199Arg) single nucleotide variant not specified [RCV004883173] Chr17:78075193 [GRCh38]
Chr17:76071274 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1443C>G (p.Asp481Glu) single nucleotide variant not specified [RCV004883174] Chr17:78049875 [GRCh38]
Chr17:76045956 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3575G>A (p.Arg1192His) single nucleotide variant not specified [RCV004883175] Chr17:78075172 [GRCh38]
Chr17:76071253 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4156G>A (p.Gly1386Arg) single nucleotide variant not specified [RCV004883176] Chr17:78086560 [GRCh38]
Chr17:76082641 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3607G>T (p.Ala1203Ser) single nucleotide variant not specified [RCV004883180] Chr17:78075204 [GRCh38]
Chr17:76071285 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.860T>C (p.Met287Thr) single nucleotide variant not specified [RCV004883182] Chr17:78049292 [GRCh38]
Chr17:76045373 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1228A>G (p.Met410Val) single nucleotide variant not specified [RCV004883178] Chr17:78049660 [GRCh38]
Chr17:76045741 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3866G>C (p.Ser1289Thr) single nucleotide variant not specified [RCV004883179] Chr17:78079429 [GRCh38]
Chr17:76075510 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1141T>A (p.Ser381Thr) single nucleotide variant not specified [RCV004883181] Chr17:78049573 [GRCh38]
Chr17:76045654 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4264C>G (p.Pro1422Ala) single nucleotide variant not specified [RCV004883184] Chr17:78086934 [GRCh38]
Chr17:76083015 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5426C>T (p.Ala1809Val) single nucleotide variant not specified [RCV004883186] Chr17:78103529 [GRCh38]
Chr17:76099610 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4912C>T (p.Leu1638Phe) single nucleotide variant not specified [RCV004883187] Chr17:78093748 [GRCh38]
Chr17:76089829 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2906A>G (p.Asn969Ser) single nucleotide variant not specified [RCV004883189] Chr17:78051338 [GRCh38]
Chr17:76047419 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1361T>G (p.Ile454Arg) single nucleotide variant not specified [RCV004883190] Chr17:78049793 [GRCh38]
Chr17:76045874 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1220T>C (p.Ile407Thr) single nucleotide variant not specified [RCV004883171] Chr17:78049652 [GRCh38]
Chr17:76045733 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3836C>T (p.Pro1279Leu) single nucleotide variant not specified [RCV004883172] Chr17:78079399 [GRCh38]
Chr17:76075480 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1738A>C (p.Ser580Arg) single nucleotide variant not specified [RCV004883183] Chr17:78050170 [GRCh38]
Chr17:76046251 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1063A>C (p.Thr355Pro) single nucleotide variant not specified [RCV004883169] Chr17:78049495 [GRCh38]
Chr17:76045576 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.878G>C (p.Ser293Thr) single nucleotide variant not specified [RCV004883185] Chr17:78049310 [GRCh38]
Chr17:76045391 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3832A>G (p.Ile1278Val) single nucleotide variant not specified [RCV005278347] Chr17:78079395 [GRCh38]
Chr17:76075476 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.5606A>G (p.His1869Arg) single nucleotide variant not specified [RCV005278348] Chr17:78104640 [GRCh38]
Chr17:76100721 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2651A>G (p.Asn884Ser) single nucleotide variant not specified [RCV005278345] Chr17:78051083 [GRCh38]
Chr17:76047164 [GRCh37]
Chr17:17q25.3		 likely benign
NM_001142640.2(TNRC6C):c.2870G>T (p.Arg957Ile) single nucleotide variant not specified [RCV005278346] Chr17:78051302 [GRCh38]
Chr17:76047383 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3778C>T (p.Leu1260=) single nucleotide variant not specified [RCV005287671] Chr17:78077281 [GRCh38]
Chr17:76073362 [GRCh37]
Chr17:17q25.3		 likely benign
NM_001142640.2(TNRC6C):c.5641G>A (p.Ala1881Thr) single nucleotide variant not specified [RCV005287670] Chr17:78104675 [GRCh38]
Chr17:76100756 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3037A>G (p.Met1013Val) single nucleotide variant not specified [RCV005287669] Chr17:78064742 [GRCh38]
Chr17:76060823 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2617C>T (p.Pro873Ser) single nucleotide variant not specified [RCV005287673] Chr17:78051049 [GRCh38]
Chr17:76047130 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.1846C>T (p.His616Tyr) single nucleotide variant not specified [RCV005287672] Chr17:78050278 [GRCh38]
Chr17:76046359 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.3994T>G (p.Leu1332Val) single nucleotide variant not specified [RCV005278344] Chr17:78083062 [GRCh38]
Chr17:76079143 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.2165C>A (p.Ala722Glu) single nucleotide variant not specified [RCV005287675] Chr17:78050597 [GRCh38]
Chr17:76046678 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4739A>G (p.Asp1580Gly) single nucleotide variant not specified [RCV005287668] Chr17:78093080 [GRCh38]
Chr17:76089161 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4310C>T (p.Ala1437Val) single nucleotide variant not specified [RCV005287677] Chr17:78086980 [GRCh38]
Chr17:76083061 [GRCh37]
Chr17:17q25.3		 uncertain significance
NM_001142640.2(TNRC6C):c.4655G>A (p.Gly1552Asp) single nucleotide variant not specified [RCV005287676] Chr17:78092996 [GRCh38]
Chr17:76089077 [GRCh37]
Chr17:17q25.3		 uncertain significance
miRNA Target Status (No longer updated)

Predicted Target Of
Summary Value
Count of predictions:7269
Count of miRNA genes:1250
Interacting mature miRNAs:1608
Transcripts:ENST00000301624, ENST00000335749, ENST00000541771, ENST00000544502, ENST00000585438, ENST00000587990, ENST00000588061, ENST00000588549, ENST00000588847, ENST00000591851, ENST00000592251, ENST00000592566
Prediction methods:Microtar, Miranda, Pita, Pita,Targetscan, 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
597208536GWAS1304610_Hmathematical ability QTL GWAS1304610 (human)6e-09mathematical ability177803059078030591Human
596962069GWAS1081588_Hmetabolic syndrome QTL GWAS1081588 (human)8e-09metabolic syndrome177799974877999749Human
597518741GWAS1614815_Hcolorectal cancer QTL GWAS1614815 (human)6e-09colorectal cancer177806700278067003Human
407057161GWAS706137_Hreaction time measurement QTL GWAS706137 (human)0.000003reaction time measurement177806166178061662Human
597134428GWAS1230502_Hmemory performance QTL GWAS1230502 (human)0.000008learning/memory/conditioning trait (VT:0002063)177808235878082359Human
597149147GWAS1245221_Hbody mass index QTL GWAS1245221 (human)9e-10body mass index177799974877999749Human
628431585GWAS2339814_Hmetabolic syndrome QTL GWAS2339814 (human)8e-09metabolic syndrome177799974877999749Human
628671264GWAS2579493_Hbody mass index QTL GWAS2579493 (human)2e-10body size trait (VT:0100005)body mass index (BMI) (CMO:0000105)177799974877999749Human
597137422GWAS1233496_Hbody height QTL GWAS1233496 (human)3e-12body height177807082578070826Human
628571118GWAS2479347_Hbody mass index QTL GWAS2479347 (human)7e-09body size trait (VT:0100005)body mass index (BMI) (CMO:0000105)177799974877999749Human
407320349GWAS969325_HHbA1c measurement QTL GWAS969325 (human)4e-13HbA1c measurement177800839378008394Human
597137421GWAS1233495_Hbody height QTL GWAS1233495 (human)3e-18body height177796543177965432Human
407138329GWAS787305_Hbody mass index QTL GWAS787305 (human)9e-10body mass index177799974877999749Human
407233179GWAS882155_Hbody height QTL GWAS882155 (human)3e-12body height177807082578070826Human
407233178GWAS882154_Hbody height QTL GWAS882154 (human)3e-18body height177796543177965432Human
597056502GWAS1152576_Hreaction time measurement QTL GWAS1152576 (human)0.000003reaction time measurement177806166178061662Human
628857051GWAS2765280_Hbody mass index QTL GWAS2765280 (human)9e-10body size trait (VT:0100005)body mass index (BMI) (CMO:0000105)177799974877999749Human
628665565GWAS2573794_Hcolorectal cancer QTL GWAS2573794 (human)6e-09colorectal cancer177806700278067003Human
597109297GWAS1205371_Hself reported educational attainment QTL GWAS1205371 (human)7e-09self reported educational attainment177800449278004493Human
628423186GWAS2331415_Hreaction time measurement QTL GWAS2331415 (human)0.000003reaction time measurement177806166178061662Human
628839133GWAS2747362_Hsphingomyelin measurement QTL GWAS2747362 (human)3e-08blood phospholipid amount (VT:0006084)177808220778082208Human
597293246GWAS1389320_Hbody mass index QTL GWAS1389320 (human)7e-09body mass index177799974877999749Human
597293875GWAS1389949_Hsphingomyelin measurement QTL GWAS1389949 (human)3e-08sphingomyelin measurement177808220778082208Human
407094760GWAS743736_Hbody mass index QTL GWAS743736 (human)6e-10body mass index177799974877999749Human
598063694GWAS1782993_Hbody height QTL GWAS1782993 (human)3e-18body height177796543177965432Human
407300587GWAS949563_Hcolorectal cancer QTL GWAS949563 (human)6e-09colorectal cancer177806700278067003Human
596987899GWAS1107418_Hbody mass index QTL GWAS1107418 (human)7e-09body mass index177799974877999749Human
597193526GWAS1289600_Hbody mass index QTL GWAS1289600 (human)2e-10body mass index177799974877999749Human
407046060GWAS695036_Hbody mass index QTL GWAS695036 (human)2e-10body mass index177799974877999749Human
407103212GWAS752188_Hmathematical ability QTL GWAS752188 (human)6e-09mathematical ability177803059078030591Human
598063690GWAS1782989_Hbody height QTL GWAS1782989 (human)3e-12body height177807082578070826Human
597242089GWAS1338163_HHbA1c measurement QTL GWAS1338163 (human)4e-13HbA1c measurement177800839378008394Human
628448581GWAS2356810_Hself reported educational attainment QTL GWAS2356810 (human)7e-09self reported educational attainment177800449278004493Human
628980429GWAS2888658_Hbody height QTL GWAS2888658 (human)3e-18body height177796543177965432Human
596981476GWAS1100995_Hmemory performance QTL GWAS1100995 (human)0.000008memory performance177808235878082359Human
617033205GWAS2050704_Hcolorectal cancer QTL GWAS2050704 (human)6e-09colorectal cancer177806700278067003Human
628980430GWAS2888659_Hbody height QTL GWAS2888659 (human)3e-12body height177807082578070826Human
407312115GWAS961091_Hsphingomyelin measurement QTL GWAS961091 (human)3e-08sphingomyelin measurement177808220778082208Human
407111793GWAS760769_Herythrocyte count QTL GWAS760769 (human)8e-10erythrocyte countred blood cell count (CMO:0000025)177801560578015606Human
407105206GWAS754182_Hself reported educational attainment QTL GWAS754182 (human)7e-09self reported educational attainment177800449278004493Human
628741839GWAS2650068_HHbA1c measurement QTL GWAS2650068 (human)4e-13blood hemoglobin amount (VT:0001588)blood hemoglobin A1c level (CMO:0002786)177800839378008394Human
597055983GWAS1152057_Hmetabolic syndrome QTL GWAS1152057 (human)8e-09metabolic syndrome177799974877999749Human
597028207GWAS1124281_Hbody mass index QTL GWAS1124281 (human)6e-10body mass index177799974877999749Human
628453256GWAS2361485_Hmathematical ability QTL GWAS2361485 (human)6e-09cognitive behavior trait (VT:0010450)177803059078030591Human

Markers in Region
RH65140  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371776,008,362 - 76,008,486UniSTSGRCh37
Build 361773,519,957 - 73,520,081RGDNCBI36
Celera1772,604,344 - 72,604,468RGD
Cytogenetic Map17q25.3UniSTS
HuRef1771,432,397 - 71,432,521UniSTS
GeneMap99-GB4 RH Map17500.9UniSTS
SHGC-105798  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371776,005,043 - 76,005,313UniSTSGRCh37
Build 361773,516,638 - 73,516,908RGDNCBI36
Celera1772,601,025 - 72,601,295RGD
Cytogenetic Map17q25.3UniSTS
HuRef1771,429,078 - 71,429,348UniSTS
SHGC-105772  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371776,005,003 - 76,005,301UniSTSGRCh37
Build 361773,516,598 - 73,516,896RGDNCBI36
Celera1772,600,985 - 72,601,283RGD
Cytogenetic Map17q25.3UniSTS
HuRef1771,429,038 - 71,429,336UniSTS
FLJ20015  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371776,101,632 - 76,101,819UniSTSGRCh37
Build 361773,613,227 - 73,613,414RGDNCBI36
Celera1772,697,612 - 72,697,799RGD
D11S3114  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map10q11.1-q24UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic MapXq13.1-q21.1UniSTS
Cytogenetic Map20pter-q12UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map9p23UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map6p12UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map22q12.3-q13.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map4p12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map19q11UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map1p32.2-p32.1UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map4q13.2UniSTS
Cytogenetic Map4q31.23UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map14q24.2UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
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Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS


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
1204 2431 2788 2238 4941 1723 2344 3 622 1922 464 2267 7261 6434 52 3708 847 1730 1611 170

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001142640 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001395508 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001395509 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001395510 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001395511 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001395512 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_018996 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006721996 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006721997 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006722000 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011525088 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017024906 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017024907 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024450848 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047436485 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047436486 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047436487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047436488 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047436489 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047436490 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047436491 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047436492 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047436493 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047436494 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047436495 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047436496 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054316803 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054316804 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054316805 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054316806 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054316807 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054316808 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054316809 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054316810 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054316811 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054316812 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054316813 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054316814 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054316815 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054316816 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB046802 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC015804 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC021593 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI337097 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK000022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK054995 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK056421 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK092762 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK098609 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL834429 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC035105 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC039479 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC045631 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC051468 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471099 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA339992 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DV080590 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HF584111 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF511238 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000301624   ⟹   ENSP00000301624
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1778,005,056 - 78,108,835 (+)Ensembl
Ensembl Acc Id: ENST00000335749   ⟹   ENSP00000336783
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1778,005,056 - 78,108,835 (+)Ensembl
Ensembl Acc Id: ENST00000585438   ⟹   ENSP00000466277
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1778,031,522 - 78,067,910 (+)Ensembl
Ensembl Acc Id: ENST00000587990
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1778,064,894 - 78,075,385 (+)Ensembl
Ensembl Acc Id: ENST00000588061   ⟹   ENSP00000468647
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1778,048,913 - 78,104,940 (+)Ensembl
Ensembl Acc Id: ENST00000588549   ⟹   ENSP00000465707
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1778,041,047 - 78,049,349 (+)Ensembl
Ensembl Acc Id: ENST00000588847   ⟹   ENSP00000467154
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1778,004,167 - 78,031,842 (+)Ensembl
Ensembl Acc Id: ENST00000591851
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1778,051,067 - 78,077,779 (+)Ensembl
Ensembl Acc Id: ENST00000592251
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1778,091,367 - 78,093,299 (+)Ensembl
Ensembl Acc Id: ENST00000592566
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1778,098,342 - 78,102,821 (+)Ensembl
Ensembl Acc Id: ENST00000636222   ⟹   ENSP00000489933
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1777,959,240 - 78,106,037 (+)Ensembl
Ensembl Acc Id: ENST00000696270   ⟹   ENSP00000512514
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1777,958,703 - 78,108,822 (+)Ensembl
Ensembl Acc Id: ENST00000696541   ⟹   ENSP00000512702
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1777,959,180 - 78,106,242 (+)Ensembl
Ensembl Acc Id: ENST00000935185   ⟹   ENSP00000605244
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1777,958,650 - 78,108,820 (+)Ensembl
Ensembl Acc Id: ENST00000935186   ⟹   ENSP00000605245
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1777,958,624 - 78,107,463 (+)Ensembl
Ensembl Acc Id: ENST00000935187   ⟹   ENSP00000605246
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1777,958,690 - 78,107,463 (+)Ensembl
Ensembl Acc Id: ENST00000935188   ⟹   ENSP00000605247
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1777,958,688 - 78,107,460 (+)Ensembl
Ensembl Acc Id: ENST00000935189   ⟹   ENSP00000605248
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1777,958,709 - 78,107,463 (+)Ensembl
Ensembl Acc Id: ENST00000935190   ⟹   ENSP00000605249
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1777,958,705 - 78,107,458 (+)Ensembl
RefSeq Acc Id: NM_001142640   ⟹   NP_001136112
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381777,958,703 - 78,108,822 (+)NCBI
GRCh371776,000,194 - 76,104,916 (+)NCBI
Celera1772,596,318 - 72,700,896 (+)RGD
HuRef1771,424,371 - 71,528,917 (+)ENTREZGENE
CHM1_11776,065,011 - 76,169,559 (+)NCBI
T2T-CHM13v2.01778,852,738 - 79,002,508 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001395508   ⟹   NP_001382437
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381778,040,910 - 78,108,822 (+)NCBI
T2T-CHM13v2.01778,934,610 - 79,002,508 (+)NCBI
RefSeq Acc Id: NM_001395509   ⟹   NP_001382438
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381777,958,703 - 78,108,822 (+)NCBI
T2T-CHM13v2.01778,852,738 - 79,002,508 (+)NCBI
RefSeq Acc Id: NM_001395510   ⟹   NP_001382439
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381777,958,703 - 78,108,822 (+)NCBI
T2T-CHM13v2.01778,852,738 - 79,002,508 (+)NCBI
RefSeq Acc Id: NM_001395511   ⟹   NP_001382440
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381778,040,910 - 78,108,822 (+)NCBI
T2T-CHM13v2.01778,934,610 - 79,002,508 (+)NCBI
RefSeq Acc Id: NM_001395512   ⟹   NP_001382441
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381777,957,557 - 78,108,822 (+)NCBI
T2T-CHM13v2.01778,851,592 - 79,002,508 (+)NCBI
RefSeq Acc Id: NM_018996   ⟹   NP_061869
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381778,004,237 - 78,108,835 (+)NCBI
GRCh371776,000,194 - 76,104,916 (+)NCBI
Build 361773,556,589 - 73,612,616 (+)NCBI Archive
Celera1772,596,318 - 72,700,896 (+)RGD
HuRef1771,424,371 - 71,528,917 (+)ENTREZGENE
CHM1_11776,065,011 - 76,169,559 (+)NCBI
T2T-CHM13v2.01778,897,963 - 79,002,521 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006721996   ⟹   XP_006722059
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381778,004,170 - 78,108,835 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006721997   ⟹   XP_006722060
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381778,004,170 - 78,108,835 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047436485   ⟹   XP_047292441
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381778,004,170 - 78,108,835 (+)NCBI
RefSeq Acc Id: XM_047436486   ⟹   XP_047292442
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381778,004,170 - 78,108,835 (+)NCBI
RefSeq Acc Id: XM_047436487   ⟹   XP_047292443
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381778,004,170 - 78,108,835 (+)NCBI
RefSeq Acc Id: XM_047436488   ⟹   XP_047292444
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381778,004,170 - 78,108,835 (+)NCBI
RefSeq Acc Id: XM_047436489   ⟹   XP_047292445
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381778,004,170 - 78,108,835 (+)NCBI
RefSeq Acc Id: XM_047436490   ⟹   XP_047292446
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381778,004,170 - 78,108,835 (+)NCBI
RefSeq Acc Id: XM_047436491   ⟹   XP_047292447
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381778,004,170 - 78,108,835 (+)NCBI
RefSeq Acc Id: XM_047436492   ⟹   XP_047292448
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381778,004,170 - 78,108,835 (+)NCBI
RefSeq Acc Id: XM_047436493   ⟹   XP_047292449
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381778,004,170 - 78,108,835 (+)NCBI
RefSeq Acc Id: XM_047436494   ⟹   XP_047292450
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381778,004,170 - 78,108,835 (+)NCBI
RefSeq Acc Id: XM_047436495   ⟹   XP_047292451
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381778,004,170 - 78,108,835 (+)NCBI
RefSeq Acc Id: XM_047436496   ⟹   XP_047292452
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381778,004,170 - 78,108,835 (+)NCBI
RefSeq Acc Id: XM_054316803   ⟹   XP_054172778
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01778,897,896 - 79,002,521 (+)NCBI
RefSeq Acc Id: XM_054316804   ⟹   XP_054172779
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01778,897,896 - 79,002,521 (+)NCBI
RefSeq Acc Id: XM_054316805   ⟹   XP_054172780
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01778,897,896 - 79,002,521 (+)NCBI
RefSeq Acc Id: XM_054316806   ⟹   XP_054172781
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01778,897,896 - 79,002,521 (+)NCBI
RefSeq Acc Id: XM_054316807   ⟹   XP_054172782
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01778,897,896 - 79,002,521 (+)NCBI
RefSeq Acc Id: XM_054316808   ⟹   XP_054172783
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01778,897,896 - 79,002,521 (+)NCBI
RefSeq Acc Id: XM_054316809   ⟹   XP_054172784
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01778,897,896 - 79,002,521 (+)NCBI
RefSeq Acc Id: XM_054316810   ⟹   XP_054172785
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01778,897,896 - 79,002,521 (+)NCBI
RefSeq Acc Id: XM_054316811   ⟹   XP_054172786
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01778,897,896 - 79,002,521 (+)NCBI
RefSeq Acc Id: XM_054316812   ⟹   XP_054172787
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01778,897,896 - 79,002,521 (+)NCBI
RefSeq Acc Id: XM_054316813   ⟹   XP_054172788
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01778,897,896 - 79,002,521 (+)NCBI
RefSeq Acc Id: XM_054316814   ⟹   XP_054172789
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01778,897,896 - 79,002,521 (+)NCBI
RefSeq Acc Id: XM_054316815   ⟹   XP_054172790
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01778,897,896 - 79,002,521 (+)NCBI
RefSeq Acc Id: XM_054316816   ⟹   XP_054172791
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01778,897,896 - 79,002,521 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001136112 (Get FASTA)   NCBI Sequence Viewer  
  NP_001382437 (Get FASTA)   NCBI Sequence Viewer  
  NP_001382438 (Get FASTA)   NCBI Sequence Viewer  
  NP_001382439 (Get FASTA)   NCBI Sequence Viewer  
  NP_001382440 (Get FASTA)   NCBI Sequence Viewer  
  NP_001382441 (Get FASTA)   NCBI Sequence Viewer  
  NP_061869 (Get FASTA)   NCBI Sequence Viewer  
  XP_006722059 (Get FASTA)   NCBI Sequence Viewer  
  XP_006722060 (Get FASTA)   NCBI Sequence Viewer  
  XP_047292441 (Get FASTA)   NCBI Sequence Viewer  
  XP_047292442 (Get FASTA)   NCBI Sequence Viewer  
  XP_047292443 (Get FASTA)   NCBI Sequence Viewer  
  XP_047292444 (Get FASTA)   NCBI Sequence Viewer  
  XP_047292445 (Get FASTA)   NCBI Sequence Viewer  
  XP_047292446 (Get FASTA)   NCBI Sequence Viewer  
  XP_047292447 (Get FASTA)   NCBI Sequence Viewer  
  XP_047292448 (Get FASTA)   NCBI Sequence Viewer  
  XP_047292449 (Get FASTA)   NCBI Sequence Viewer  
  XP_047292450 (Get FASTA)   NCBI Sequence Viewer  
  XP_047292451 (Get FASTA)   NCBI Sequence Viewer  
  XP_047292452 (Get FASTA)   NCBI Sequence Viewer  
  XP_054172778 (Get FASTA)   NCBI Sequence Viewer  
  XP_054172779 (Get FASTA)   NCBI Sequence Viewer  
  XP_054172780 (Get FASTA)   NCBI Sequence Viewer  
  XP_054172781 (Get FASTA)   NCBI Sequence Viewer  
  XP_054172782 (Get FASTA)   NCBI Sequence Viewer  
  XP_054172783 (Get FASTA)   NCBI Sequence Viewer  
  XP_054172784 (Get FASTA)   NCBI Sequence Viewer  
  XP_054172785 (Get FASTA)   NCBI Sequence Viewer  
  XP_054172786 (Get FASTA)   NCBI Sequence Viewer  
  XP_054172787 (Get FASTA)   NCBI Sequence Viewer  
  XP_054172788 (Get FASTA)   NCBI Sequence Viewer  
  XP_054172789 (Get FASTA)   NCBI Sequence Viewer  
  XP_054172790 (Get FASTA)   NCBI Sequence Viewer  
  XP_054172791 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH45631 (Get FASTA)   NCBI Sequence Viewer  
  BAA90890 (Get FASTA)   NCBI Sequence Viewer  
  BAB13408 (Get FASTA)   NCBI Sequence Viewer  
  BAB71179 (Get FASTA)   NCBI Sequence Viewer  
  CAD39090 (Get FASTA)   NCBI Sequence Viewer  
  CCQ43608 (Get FASTA)   NCBI Sequence Viewer  
  EAW89480 (Get FASTA)   NCBI Sequence Viewer  
  EAW89481 (Get FASTA)   NCBI Sequence Viewer  
  EAW89482 (Get FASTA)   NCBI Sequence Viewer  
  EAW89483 (Get FASTA)   NCBI Sequence Viewer  
  EAW89484 (Get FASTA)   NCBI Sequence Viewer  
  EAW89485 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000468647
  ENSP00000512514
  ENSP00000512514.1
  ENSP00000512702
  ENSP00000512702.1
  ENSP00000605244
  ENSP00000605245
  ENSP00000605247
  ENSP00000605248
GenBank Protein Q9HCJ0 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_061869   ⟸   NM_018996
- Peptide Label: isoform 2
- UniProtKB: A0AAA9XYZ6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001136112   ⟸   NM_001142640
- Peptide Label: isoform 1
- UniProtKB: Q9HCJ0 (UniProtKB/Swiss-Prot),   Q96MU9 (UniProtKB/Swiss-Prot),   Q8N3D8 (UniProtKB/Swiss-Prot),   Q86UE5 (UniProtKB/Swiss-Prot),   G3XAB8 (UniProtKB/Swiss-Prot),   A0A8Q3SIS0 (UniProtKB/Swiss-Prot),   A0A8Q3SIH5 (UniProtKB/TrEMBL),   A0A1B0GU24 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006722059   ⟸   XM_006721996
- Peptide Label: isoform X3
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006722060   ⟸   XM_006721997
- Peptide Label: isoform X6
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000489933   ⟸   ENST00000636222
Ensembl Acc Id: ENSP00000336783   ⟸   ENST00000335749
Ensembl Acc Id: ENSP00000466277   ⟸   ENST00000585438
Ensembl Acc Id: ENSP00000468647   ⟸   ENST00000588061
Ensembl Acc Id: ENSP00000467154   ⟸   ENST00000588847
Ensembl Acc Id: ENSP00000465707   ⟸   ENST00000588549
Ensembl Acc Id: ENSP00000301624   ⟸   ENST00000301624
RefSeq Acc Id: NP_001382441   ⟸   NM_001395512
- Peptide Label: isoform 7
- UniProtKB: A0AAA9XYZ6 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001382438   ⟸   NM_001395509
- Peptide Label: isoform 4
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001382439   ⟸   NM_001395510
- Peptide Label: isoform 5
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001382440   ⟸   NM_001395511
- Peptide Label: isoform 6
- UniProtKB: A0AAA9XYZ6 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001382437   ⟸   NM_001395508
- Peptide Label: isoform 3
- UniProtKB: A0AAA9XYZ6 (UniProtKB/TrEMBL)
Ensembl Acc Id: ENSP00000512702   ⟸   ENST00000696541
Ensembl Acc Id: ENSP00000512514   ⟸   ENST00000696270
RefSeq Acc Id: XP_047292452   ⟸   XM_047436496
- Peptide Label: isoform X14
- UniProtKB: A0AAA9XYZ6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047292441   ⟸   XM_047436485
- Peptide Label: isoform X1
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047292443   ⟸   XM_047436487
- Peptide Label: isoform X4
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047292446   ⟸   XM_047436490
- Peptide Label: isoform X8
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047292448   ⟸   XM_047436492
- Peptide Label: isoform X10
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047292450   ⟸   XM_047436494
- Peptide Label: isoform X12
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047292442   ⟸   XM_047436486
- Peptide Label: isoform X2
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047292444   ⟸   XM_047436488
- Peptide Label: isoform X5
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047292445   ⟸   XM_047436489
- Peptide Label: isoform X7
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047292447   ⟸   XM_047436491
- Peptide Label: isoform X9
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047292449   ⟸   XM_047436493
- Peptide Label: isoform X11
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047292451   ⟸   XM_047436495
- Peptide Label: isoform X13
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054172791   ⟸   XM_054316816
- Peptide Label: isoform X14
- UniProtKB: A0AAA9XYZ6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054172778   ⟸   XM_054316803
- Peptide Label: isoform X1
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054172780   ⟸   XM_054316805
- Peptide Label: isoform X3
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054172781   ⟸   XM_054316806
- Peptide Label: isoform X4
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054172783   ⟸   XM_054316808
- Peptide Label: isoform X6
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054172785   ⟸   XM_054316810
- Peptide Label: isoform X8
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054172787   ⟸   XM_054316812
- Peptide Label: isoform X10
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054172789   ⟸   XM_054316814
- Peptide Label: isoform X12
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054172779   ⟸   XM_054316804
- Peptide Label: isoform X2
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054172782   ⟸   XM_054316807
- Peptide Label: isoform X5
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054172784   ⟸   XM_054316809
- Peptide Label: isoform X7
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054172786   ⟸   XM_054316811
- Peptide Label: isoform X9
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054172788   ⟸   XM_054316813
- Peptide Label: isoform X11
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054172790   ⟸   XM_054316815
- Peptide Label: isoform X13
- UniProtKB: A0A1B0GU24 (UniProtKB/TrEMBL)
Ensembl Acc Id: ENSP00000605249   ⟸   ENST00000935190
Ensembl Acc Id: ENSP00000605247   ⟸   ENST00000935188
Ensembl Acc Id: ENSP00000605246   ⟸   ENST00000935187
Ensembl Acc Id: ENSP00000605245   ⟸   ENST00000935186
Ensembl Acc Id: ENSP00000605244   ⟸   ENST00000935185
Ensembl Acc Id: ENSP00000605248   ⟸   ENST00000935189
Protein Domains
Argonaute hook   RRM   UBA

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9HCJ0-F1-model_v2 AlphaFold Q9HCJ0 1-1690 view protein structure

Promoters
RGD ID:6811374
Promoter ID:HG_ACW:36557
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   Lymphoblastoid
Transcripts:TNRC6C.BAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 361773,548,484 - 73,548,984 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:29318 AgrOrtholog
COSMIC TNRC6C COSMIC
Ensembl Genes ENSG00000078687 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000588061 ENTREZGENE
  ENST00000696270 ENTREZGENE
  ENST00000696270.1 UniProtKB/Swiss-Prot
  ENST00000696541 ENTREZGENE
  ENST00000696541.1 UniProtKB/Swiss-Prot
  ENST00000935185 ENTREZGENE
  ENST00000935186 ENTREZGENE
  ENST00000935188 ENTREZGENE
  ENST00000935189 ENTREZGENE
Gene3D-CATH 3.30.70.330 UniProtKB/Swiss-Prot
  DNA helicase RuvA subunit, C-terminal domain UniProtKB/Swiss-Prot
GTEx ENSG00000078687 GTEx
HGNC ID HGNC:29318 ENTREZGENE
Human Proteome Map TNRC6C Human Proteome Map
InterPro Argonaute_hook_dom UniProtKB/Swiss-Prot
  GW182_domain UniProtKB/Swiss-Prot
  GW182_M_dom UniProtKB/Swiss-Prot
  Nucleotide-bd_a/b_plait_sf UniProtKB/Swiss-Prot
  RBD_domain_sf UniProtKB/Swiss-Prot
  RRM_dom UniProtKB/Swiss-Prot
  TNR6C_UBA UniProtKB/Swiss-Prot
  TNRC6_PABC-bd UniProtKB/Swiss-Prot
  TNRC6C_RRM UniProtKB/Swiss-Prot
  UBA UniProtKB/Swiss-Prot
  UBA-like_sf UniProtKB/Swiss-Prot
KEGG Report hsa:57690 UniProtKB/Swiss-Prot
NCBI Gene 57690 ENTREZGENE
OMIM 610741 OMIM
PANTHER PTHR13020:SF9 UniProtKB/Swiss-Prot
  TRINUCLEOTIDE REPEAT-CONTAINING GENE 6 UniProtKB/Swiss-Prot
Pfam Ago_hook UniProtKB/Swiss-Prot
  M_domain UniProtKB/Swiss-Prot
  RRM_1 UniProtKB/Swiss-Prot
  TNRC6-PABC_bdg UniProtKB/Swiss-Prot
  UBA UniProtKB/Swiss-Prot
PharmGKB PA134880671 PharmGKB
PROSITE UBA UniProtKB/Swiss-Prot
SMART UBA UniProtKB/Swiss-Prot
Superfamily-SCOP SSF46934 UniProtKB/Swiss-Prot
  SSF54928 UniProtKB/Swiss-Prot
UniProt A0A1B0GU24 ENTREZGENE, UniProtKB/TrEMBL
  A0A8Q3SIH5 ENTREZGENE
  A0A8Q3SIS0 ENTREZGENE
  A0AAA9XYZ6 ENTREZGENE, UniProtKB/TrEMBL
  G3XAB8 ENTREZGENE
  K7EKN9_HUMAN UniProtKB/TrEMBL
  K7ELY5_HUMAN UniProtKB/TrEMBL
  L8EB01_HUMAN UniProtKB/TrEMBL
  Q86UE5 ENTREZGENE
  Q8N3D8 ENTREZGENE
  Q96MU9 ENTREZGENE
  Q9HCJ0 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary A0A8Q3SIH5 UniProtKB/Swiss-Prot
  A0A8Q3SIS0 UniProtKB/Swiss-Prot
  G3XAB8 UniProtKB/Swiss-Prot
  Q86UE5 UniProtKB/Swiss-Prot
  Q8N3D8 UniProtKB/Swiss-Prot
  Q96MU9 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2022-04-14 TNRC6C  trinucleotide repeat containing adaptor 6C  LOC107985010  uncharacterized LOC107985010  Data merged from RGD:38608153 737654 PROVISIONAL
2019-01-15 TNRC6C  trinucleotide repeat containing adaptor 6C    trinucleotide repeat containing 6C  Symbol and/or name change 5135510 APPROVED