CLRN3 (clarin 3) - Rat Genome Database

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Gene: CLRN3 (clarin 3) Homo sapiens
Analyze
Symbol: CLRN3
Name: clarin 3
RGD ID: 1603923
HGNC Page HGNC:20795
Description: Predicted to be involved in sensory perception of sound. Located in extracellular exosome.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: clarin-3; DKFZp686F11218; MGC32871; TMEM12; transmembrane protein 12; USH3AL1; usher syndrome type-3A-like protein 1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-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
GRCh3810127,877,841 - 127,892,941 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl10127,877,841 - 127,892,941 (-)EnsemblGRCh38hg38GRCh38
GRCh3710129,676,105 - 129,691,205 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 3610129,566,104 - 129,581,201 (-)NCBINCBI36Build 36hg18NCBI36
Celera10123,347,587 - 123,362,681 (-)NCBICelera
Cytogenetic Map10q26.2NCBI
HuRef10123,250,911 - 123,266,000 (-)NCBIHuRef
CHM1_110129,958,532 - 129,973,623 (-)NCBICHM1_1
T2T-CHM13v2.010128,776,372 - 128,791,469 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12080385   PMID:12145752   PMID:12477932   PMID:15164054   PMID:15489334   PMID:16341674   PMID:16385451   PMID:17207965   PMID:19056867   PMID:20379614   PMID:22658654   PMID:23376485  
PMID:24705354   PMID:26186194   PMID:28514442   PMID:32814053   PMID:33961781  


Genomics

Comparative Map Data
CLRN3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3810127,877,841 - 127,892,941 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl10127,877,841 - 127,892,941 (-)EnsemblGRCh38hg38GRCh38
GRCh3710129,676,105 - 129,691,205 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 3610129,566,104 - 129,581,201 (-)NCBINCBI36Build 36hg18NCBI36
Celera10123,347,587 - 123,362,681 (-)NCBICelera
Cytogenetic Map10q26.2NCBI
HuRef10123,250,911 - 123,266,000 (-)NCBIHuRef
CHM1_110129,958,532 - 129,973,623 (-)NCBICHM1_1
T2T-CHM13v2.010128,776,372 - 128,791,469 (-)NCBIT2T-CHM13v2.0
Clrn3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm397135,113,185 - 135,130,383 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl7135,113,195 - 135,130,383 (-)EnsemblGRCm39 Ensembl
GRCm387135,511,456 - 135,528,654 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl7135,511,466 - 135,528,654 (-)EnsemblGRCm38mm10GRCm38
MGSCv377142,703,139 - 142,720,337 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv367135,351,069 - 135,366,985 (-)NCBIMGSCv36mm8
Celera7135,333,741 - 135,351,380 (-)NCBICelera
Cytogenetic Map7F3NCBI
cM Map781.27NCBI
Clrn3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81199,748,863 - 199,764,486 (-)NCBIGRCr8
mRatBN7.21190,319,025 - 190,334,648 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1190,319,026 - 190,334,648 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1198,675,031 - 198,690,589 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01205,833,147 - 205,848,783 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01198,506,610 - 198,522,246 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01207,750,627 - 207,766,250 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1207,750,223 - 207,811,008 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01214,683,449 - 214,699,072 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41195,132,680 - 195,148,303 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11195,282,672 - 195,298,295 (-)NCBI
Celera1188,034,301 - 188,049,855 (-)NCBICelera
Cytogenetic Map1q41NCBI
Clrn3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554775,663,488 - 5,676,459 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554775,663,188 - 5,676,430 (-)NCBIChiLan1.0ChiLan1.0
CLRN3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v28139,755,788 - 139,784,556 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan110139,760,990 - 139,789,910 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v010124,464,925 - 124,493,994 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.110128,714,201 - 128,729,251 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl10128,712,990 - 128,729,560 (-)Ensemblpanpan1.1panPan2
CLRN3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12836,719,441 - 36,734,519 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2836,721,645 - 36,734,623 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2836,775,045 - 36,790,108 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02837,351,065 - 37,366,148 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2837,353,267 - 37,366,218 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12836,831,220 - 36,846,275 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02836,826,012 - 36,841,046 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02837,080,684 - 37,095,782 (-)NCBIUU_Cfam_GSD_1.0
Clrn3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440721310,139,776 - 10,152,939 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493648615,408,689 - 15,421,224 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493648615,408,712 - 15,421,224 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CLRN3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl14137,069,384 - 137,089,197 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.114137,063,671 - 137,089,827 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.214148,976,961 - 148,991,675 (-)NCBISscrofa10.2Sscrofa10.2susScr3
CLRN3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.19120,484,216 - 120,499,937 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl9120,481,843 - 120,499,525 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604881,873,323 - 81,888,472 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Clrn3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473719,140,907 - 19,156,308 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473719,140,954 - 19,154,709 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in CLRN3
19 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 10q25.2-26.3(chr10:111313099-133620674)x3 copy number gain See cases [RCV000051218] Chr10:111313099..133620674 [GRCh38]
Chr10:113072857..135434178 [GRCh37]
Chr10:113062847..135284168 [NCBI36]
Chr10:10q25.2-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:122265252-133620674)x1 copy number loss See cases [RCV000051069] Chr10:122265252..133620674 [GRCh38]
Chr10:124024767..135434178 [GRCh37]
Chr10:124014757..135284168 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.12-26.3(chr10:120454430-133620674)x1 copy number loss See cases [RCV000051103] Chr10:120454430..133620674 [GRCh38]
Chr10:122213942..135434178 [GRCh37]
Chr10:122203932..135284168 [NCBI36]
Chr10:10q26.12-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:123307835-133620674)x1 copy number loss See cases [RCV000051150] Chr10:123307835..133620674 [GRCh38]
Chr10:125067351..135434178 [GRCh37]
Chr10:125057341..135284168 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.2(chr10:127435985-127992839)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051655]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051655]|See cases [RCV000051655] Chr10:127435985..127992839 [GRCh38]
Chr10:129234249..129791103 [GRCh37]
Chr10:129124239..129681093 [NCBI36]
Chr10:10q26.2		 uncertain significance
GRCh38/hg38 10q26.2-26.3(chr10:127852284-129780378)x3 copy number gain See cases [RCV000051656] Chr10:127852284..129780378 [GRCh38]
Chr10:129650548..131578642 [GRCh37]
Chr10:129540538..131468632 [NCBI36]
Chr10:10q26.2-26.3		 uncertain significance
GRCh38/hg38 10q26.2-26.3(chr10:126256585-133613938)x1 copy number loss See cases [RCV000052612] Chr10:126256585..133613938 [GRCh38]
Chr10:127945154..135427442 [GRCh37]
Chr10:127935144..135277432 [NCBI36]
Chr10:10q26.2-26.3		 pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:127500483-133620674)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052613]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052613]|See cases [RCV000052613] Chr10:127500483..133620674 [GRCh38]
Chr10:129298747..135434178 [GRCh37]
Chr10:129188737..135284168 [NCBI36]
Chr10:10q26.2-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.2(chr10:122973296-128210291)x1 copy number loss See cases [RCV000052610] Chr10:122973296..128210291 [GRCh38]
Chr10:124732812..130008555 [GRCh37]
Chr10:124722802..129898545 [NCBI36]
Chr10:10q26.13-26.2		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:123580320-133558988)x1 copy number loss See cases [RCV000052611] Chr10:123580320..133558988 [GRCh38]
Chr10:125339836..135372492 [GRCh37]
Chr10:125329826..135222482 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q23.31-26.3(chr10:91048545-133620674)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053560]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053560]|See cases [RCV000053560] Chr10:91048545..133620674 [GRCh38]
Chr10:92808302..135434178 [GRCh37]
Chr10:92798282..135284168 [NCBI36]
Chr10:10q23.31-26.3		 pathogenic
GRCh38/hg38 10q24.31-26.3(chr10:100194215-132432797)x3 copy number gain See cases [RCV000053564] Chr10:100194215..132432797 [GRCh38]
Chr10:101953972..134246301 [GRCh37]
Chr10:101943962..134096291 [NCBI36]
Chr10:10q24.31-26.3		 pathogenic
GRCh38/hg38 10q25.1-26.3(chr10:106925303-133620815)x3 copy number gain See cases [RCV000053588] Chr10:106925303..133620815 [GRCh38]
Chr10:108685061..135434319 [GRCh37]
Chr10:108675051..135284309 [NCBI36]
Chr10:10q25.1-26.3		 pathogenic
GRCh38/hg38 10q26.11-26.3(chr10:117866565-133554210)x3 copy number gain See cases [RCV000053589] Chr10:117866565..133554210 [GRCh38]
Chr10:119626076..135367714 [GRCh37]
Chr10:119616066..135217704 [NCBI36]
Chr10:10q26.11-26.3		 pathogenic
NM_152311.3(CLRN3):c.216G>A (p.Lys72=) single nucleotide variant Malignant melanoma [RCV000062012] Chr10:127892569 [GRCh38]
Chr10:129690833 [GRCh37]
Chr10:129580823 [NCBI36]
Chr10:10q26.2		 not provided
GRCh38/hg38 10q25.1-26.3(chr10:108102587-133620674)x3 copy number gain See cases [RCV000133688] Chr10:108102587..133620674 [GRCh38]
Chr10:109862345..135434178 [GRCh37]
Chr10:109852335..135284168 [NCBI36]
Chr10:10q25.1-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:125657472-133620674)x1 copy number loss See cases [RCV000133741] Chr10:125657472..133620674 [GRCh38]
Chr10:127346041..135434178 [GRCh37]
Chr10:127336031..135284168 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:126730896-133620609)x1 copy number loss See cases [RCV000134040] Chr10:126730896..133620609 [GRCh38]
Chr10:128419465..135434113 [GRCh37]
Chr10:128409455..135284103 [NCBI36]
Chr10:10q26.2-26.3		 pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:127640489-132776585)x1 copy number loss See cases [RCV000135728] Chr10:127640489..132776585 [GRCh38]
Chr10:129438753..134590089 [GRCh37]
Chr10:129328743..134440079 [NCBI36]
Chr10:10q26.2-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:124473108-133620609)x1 copy number loss See cases [RCV000136028] Chr10:124473108..133620609 [GRCh38]
Chr10:126161677..135434113 [GRCh37]
Chr10:126151667..135284103 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:124834858-133622588)x1 copy number loss See cases [RCV000137653] Chr10:124834858..133622588 [GRCh38]
Chr10:126523427..135436092 [GRCh37]
Chr10:126513417..135286082 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:127849717-133622588)x1 copy number loss See cases [RCV000138160] Chr10:127849717..133622588 [GRCh38]
Chr10:129647981..135436092 [GRCh37]
Chr10:129537971..135286082 [NCBI36]
Chr10:10q26.2-26.3		 pathogenic|likely benign
GRCh38/hg38 10q24.31-26.3(chr10:100600492-133622588)x3 copy number gain See cases [RCV000137747] Chr10:100600492..133622588 [GRCh38]
Chr10:102360249..135436092 [GRCh37]
Chr10:102350239..135286082 [NCBI36]
Chr10:10q24.31-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:122881207-133620609)x1 copy number loss See cases [RCV000138435] Chr10:122881207..133620609 [GRCh38]
Chr10:124640723..135434113 [GRCh37]
Chr10:124630713..135284103 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.12-26.3(chr10:120970558-133622588)x1 copy number loss See cases [RCV000139344] Chr10:120970558..133622588 [GRCh38]
Chr10:122730071..135436092 [GRCh37]
Chr10:122720061..135286082 [NCBI36]
Chr10:10q26.12-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:125316124-130269667)x1 copy number loss See cases [RCV000139127] Chr10:125316124..130269667 [GRCh38]
Chr10:127004693..132067931 [GRCh37]
Chr10:126994683..131957921 [NCBI36]
Chr10:10q26.13-26.3		 likely benign
GRCh38/hg38 10q26.13-26.3(chr10:125021995-133620609)x1 copy number loss See cases [RCV000139588] Chr10:125021995..133620609 [GRCh38]
Chr10:126710564..135434113 [GRCh37]
Chr10:126700554..135284103 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:125452905-133785874)x3 copy number gain See cases [RCV000141337] Chr10:125452905..133785874 [GRCh38]
Chr10:127141474..135523199 [GRCh37]
Chr10:127131464..135373189 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:127664168-133622588)x3 copy number gain See cases [RCV000140974] Chr10:127664168..133622588 [GRCh38]
Chr10:129462432..135436092 [GRCh37]
Chr10:129352422..135286082 [NCBI36]
Chr10:10q26.2-26.3		 likely pathogenic
GRCh38/hg38 10q26.11-26.3(chr10:119707856-133613639)x3 copy number gain See cases [RCV000142005] Chr10:119707856..133613639 [GRCh38]
Chr10:121467368..135427143 [GRCh37]
Chr10:121457358..135277133 [NCBI36]
Chr10:10q26.11-26.3		 pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:127507503-129782976)x3 copy number gain See cases [RCV000141892] Chr10:127507503..129782976 [GRCh38]
Chr10:129305767..131581240 [GRCh37]
Chr10:129195757..131471230 [NCBI36]
Chr10:10q26.2-26.3		 uncertain significance
GRCh38/hg38 10q26.13-26.3(chr10:121588992-133620674)x1 copy number loss See cases [RCV000142441] Chr10:121588992..133620674 [GRCh38]
Chr10:123348506..135434178 [GRCh37]
Chr10:123338496..135284168 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:121918547-133620674)x1 copy number loss See cases [RCV000142737] Chr10:121918547..133620674 [GRCh38]
Chr10:123678062..135434178 [GRCh37]
Chr10:123668052..135284168 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:127435985-133622588)x1 copy number loss See cases [RCV000143241] Chr10:127435985..133622588 [GRCh38]
Chr10:129234249..135436092 [GRCh37]
Chr10:129124239..135286082 [NCBI36]
Chr10:10q26.2-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:123986772-133613639)x1 copy number loss See cases [RCV000143623] Chr10:123986772..133613639 [GRCh38]
Chr10:125746288..135427143 [GRCh37]
Chr10:125736278..135277133 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.13-26.3(chr10:123576393-133613639)x1 copy number loss See cases [RCV000143544] Chr10:123576393..133613639 [GRCh38]
Chr10:125335909..135427143 [GRCh37]
Chr10:125325899..135277133 [NCBI36]
Chr10:10q26.13-26.3		 pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:126794646-133613639)x1 copy number loss See cases [RCV000143615] Chr10:126794646..133613639 [GRCh38]
Chr10:128483215..135427143 [GRCh37]
Chr10:128473205..135277133 [NCBI36]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:123731209-135353867)x1 copy number loss See cases [RCV000203440] Chr10:123731209..135353867 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic|likely pathogenic
GRCh37/hg19 10q24.32-26.3(chr10:103288313-135512075)x3 copy number gain See cases [RCV000240457] Chr10:103288313..135512075 [GRCh37]
Chr10:10q24.32-26.3		 pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122125760-135062972)x3 copy number gain See cases [RCV000449169] Chr10:122125760..135062972 [GRCh37]
Chr10:10q26.12-26.3		 likely pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:124147428-135370736)x1 copy number loss See cases [RCV000449336] Chr10:124147428..135370736 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10q24.32-26.3(chr10:104633712-135427143)x3 copy number gain See cases [RCV000449386] Chr10:104633712..135427143 [GRCh37]
Chr10:10q24.32-26.3		 pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122343861-135427143)x1 copy number loss See cases [RCV000446095] Chr10:122343861..135427143 [GRCh37]
Chr10:10q26.12-26.3		 pathogenic
GRCh37/hg19 10q24.2-26.3(chr10:100780957-135427143)x3 copy number gain See cases [RCV000446733] Chr10:100780957..135427143 [GRCh37]
Chr10:10q24.2-26.3		 pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:128465436-135427143)x1 copy number loss See cases [RCV000447132] Chr10:128465436..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3 copy number gain See cases [RCV000448750] Chr10:93297..135378918 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:127658004-135427143)x1 copy number loss See cases [RCV000511813] Chr10:127658004..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143) copy number gain See cases [RCV000511389] Chr10:100027..135427143 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic|uncertain significance
GRCh37/hg19 10q25.1-26.3(chr10:106003533-135427143)x3 copy number gain See cases [RCV000510813] Chr10:106003533..135427143 [GRCh37]
Chr10:10q25.1-26.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3 copy number gain See cases [RCV000510861] Chr10:100027..135427143 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
GRCh37/hg19 10q23.32-26.3(chr10:93283493-135427143)x3 copy number gain See cases [RCV000510972] Chr10:93283493..135427143 [GRCh37]
Chr10:10q23.32-26.3		 pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:129007673-135427143)x3 copy number gain See cases [RCV000512398] Chr10:129007673..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q11.21-26.3(chr10:42347406-135534747)x1 copy number loss Poly (ADP-Ribose) polymerase inhibitor response [RCV000626438] Chr10:42347406..135534747 [GRCh37]
Chr10:10q11.21-26.3		 drug response
GRCh37/hg19 10q26.13-26.3(chr10:127375792-135427143)x1 copy number loss not provided [RCV000683283] Chr10:127375792..135427143 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:123019239-135427143)x1 copy number loss not provided [RCV000683286] Chr10:123019239..135427143 [GRCh37]
Chr10:10q26.12-26.3		 pathogenic
GRCh37/hg19 10q26.11-26.3(chr10:121269222-135427143)x3 copy number gain not provided [RCV000683288] Chr10:121269222..135427143 [GRCh37]
Chr10:10q26.11-26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:125450893-135427143)x1 copy number loss not provided [RCV000683285] Chr10:125450893..135427143 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10q24.33-26.3(chr10:105613040-135427143)x3 copy number gain not provided [RCV000683290] Chr10:105613040..135427143 [GRCh37]
Chr10:10q24.33-26.3		 pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122509781-135427143)x1 copy number loss not provided [RCV000683287] Chr10:122509781..135427143 [GRCh37]
Chr10:10q26.12-26.3		 pathogenic
GRCh37/hg19 10q23.33-26.3(chr10:94346520-135427143)x3 copy number gain not provided [RCV000683291] Chr10:94346520..135427143 [GRCh37]
Chr10:10q23.33-26.3		 pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122443197-135477883)x1 copy number loss not provided [RCV000737305] Chr10:122443197..135477883 [GRCh37]
Chr10:10q26.12-26.3		 pathogenic
GRCh37/hg19 10q26.2(chr10:129454892-129830216)x1 copy number loss not provided [RCV000737322] Chr10:129454892..129830216 [GRCh37]
Chr10:10q26.2		 benign
GRCh37/hg19 10q26.2-26.3(chr10:129454892-135447971)x1 copy number loss not provided [RCV000737323] Chr10:129454892..135447971 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:73232-135524321)x3 copy number gain not provided [RCV000749464] Chr10:73232..135524321 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:98087-135477883)x3 copy number gain not provided [RCV000749465] Chr10:98087..135477883 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
GRCh37/hg19 10q25.1-26.3(chr10:110022170-135439095) copy number gain not provided [RCV000767665] Chr10:110022170..135439095 [GRCh37]
Chr10:10q25.1-26.3		 pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:129009772-135427143)x1 copy number loss not provided [RCV001006362] Chr10:129009772..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:124988334-135427143)x3 copy number gain not provided [RCV000848791] Chr10:124988334..135427143 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10q25.2-26.3(chr10:114544537-135427143)x3 copy number gain not provided [RCV000847820] Chr10:114544537..135427143 [GRCh37]
Chr10:10q25.2-26.3		 pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:129381095-135427143)x1 copy number loss not provided [RCV001006364] Chr10:129381095..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.2(chr10:129297102-129802813)x3 copy number gain not provided [RCV000846591] Chr10:129297102..129802813 [GRCh37]
Chr10:10q26.2		 uncertain significance
NM_152311.5(CLRN3):c.92A>C (p.Gln31Pro) single nucleotide variant not specified [RCV004308415] Chr10:127892693 [GRCh38]
Chr10:129690957 [GRCh37]
Chr10:10q26.2		 uncertain significance
NM_152311.5(CLRN3):c.392C>T (p.Thr131Ile) single nucleotide variant not specified [RCV004319021] Chr10:127883713 [GRCh38]
Chr10:129681977 [GRCh37]
Chr10:10q26.2		 uncertain significance
GRCh37/hg19 10q26.11-26.3(chr10:119996339-135427143)x3 copy number gain not provided [RCV001006356] Chr10:119996339..135427143 [GRCh37]
Chr10:10q26.11-26.3		 pathogenic
GRCh37/hg19 10q26.2(chr10:129160805-129922819)x3 copy number gain not provided [RCV002473640] Chr10:129160805..129922819 [GRCh37]
Chr10:10q26.2		 uncertain significance
GRCh37/hg19 10q25.3-26.3(chr10:118247181-135435319)x3 copy number gain not provided [RCV001537903] Chr10:118247181..135435319 [GRCh37]
Chr10:10q25.3-26.3		 pathogenic
GRCh37/hg19 10q26.2(chr10:129303032-129814581)x3 copy number gain not provided [RCV001259084] Chr10:129303032..129814581 [GRCh37]
Chr10:10q26.2		 uncertain significance
GRCh37/hg19 10q26.2-26.3(chr10:129031265-135427143)x1 copy number loss not provided [RCV001259085] Chr10:129031265..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:129605105-135427143)x1 copy number loss See cases [RCV002285041] Chr10:129605105..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:129483682-135434178) copy number loss Global developmental delay [RCV001352664] Chr10:129483682..135434178 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
Single allele deletion Distal 10q deletion syndrome [RCV001391670] Chr10:127548166..135440251 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122785023-135457222)x1 copy number loss See cases [RCV001526488] Chr10:122785023..135457222 [GRCh37]
Chr10:10q26.12-26.3		 pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122343861-135427143) copy number loss not specified [RCV002052895] Chr10:122343861..135427143 [GRCh37]
Chr10:10q26.12-26.3		 pathogenic
GRCh37/hg19 10q25.1-26.3(chr10:108455687-135427143) copy number gain not specified [RCV002052891] Chr10:108455687..135427143 [GRCh37]
Chr10:10q25.1-26.3		 pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122125760-135062972) copy number gain not specified [RCV002052894] Chr10:122125760..135062972 [GRCh37]
Chr10:10q26.12-26.3		 likely pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:128465436-135427143) copy number loss not specified [RCV002052902] Chr10:128465436..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:127198625-135427143)x3 copy number gain See cases [RCV002292400] Chr10:127198625..135427143 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:126914469-135427143)x1 copy number loss See cases [RCV002292397] Chr10:126914469..135427143 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10q26.2(chr10:129298285-129812992)x3 copy number gain not provided [RCV002474627] Chr10:129298285..129812992 [GRCh37]
Chr10:10q26.2		 uncertain significance
GRCh37/hg19 10q26.2-26.3(chr10:128877896-131842835)x1 copy number loss not provided [RCV002472530] Chr10:128877896..131842835 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:126662496-133985966)x3 copy number gain not provided [RCV002474692] Chr10:126662496..133985966 [GRCh37]
Chr10:10q26.13-26.3		 uncertain significance
NM_152311.5(CLRN3):c.233T>C (p.Leu78Ser) single nucleotide variant not specified [RCV004077090] Chr10:127883872 [GRCh38]
Chr10:129682136 [GRCh37]
Chr10:10q26.2		 uncertain significance
NM_152311.5(CLRN3):c.221A>T (p.Lys74Met) single nucleotide variant not specified [RCV004236449] Chr10:127892564 [GRCh38]
Chr10:129690828 [GRCh37]
Chr10:10q26.2		 uncertain significance
NM_152311.5(CLRN3):c.269A>G (p.His90Arg) single nucleotide variant not specified [RCV004135942] Chr10:127883836 [GRCh38]
Chr10:129682100 [GRCh37]
Chr10:10q26.2		 uncertain significance
NM_152311.5(CLRN3):c.380C>T (p.Thr127Met) single nucleotide variant not specified [RCV004133875] Chr10:127883725 [GRCh38]
Chr10:129681989 [GRCh37]
Chr10:10q26.2		 likely benign
NM_152311.5(CLRN3):c.623G>A (p.Arg208Gln) single nucleotide variant not specified [RCV004220992] Chr10:127878207 [GRCh38]
Chr10:129676471 [GRCh37]
Chr10:10q26.2		 likely benign
NM_152311.5(CLRN3):c.446C>A (p.Ala149Glu) single nucleotide variant not specified [RCV004165840] Chr10:127878384 [GRCh38]
Chr10:129676648 [GRCh37]
Chr10:10q26.2		 uncertain significance
NM_152311.5(CLRN3):c.559G>A (p.Val187Ile) single nucleotide variant not specified [RCV004089920] Chr10:127878271 [GRCh38]
Chr10:129676535 [GRCh37]
Chr10:10q26.2		 likely benign
NM_152311.5(CLRN3):c.445G>A (p.Ala149Thr) single nucleotide variant not specified [RCV004165839] Chr10:127878385 [GRCh38]
Chr10:129676649 [GRCh37]
Chr10:10q26.2		 uncertain significance
NM_152311.5(CLRN3):c.518C>T (p.Thr173Met) single nucleotide variant not specified [RCV004186315] Chr10:127878312 [GRCh38]
Chr10:129676576 [GRCh37]
Chr10:10q26.2		 uncertain significance
NM_152311.5(CLRN3):c.472G>A (p.Glu158Lys) single nucleotide variant not specified [RCV004134381] Chr10:127878358 [GRCh38]
Chr10:129676622 [GRCh37]
Chr10:10q26.2		 uncertain significance
NM_152311.5(CLRN3):c.82C>G (p.Leu28Val) single nucleotide variant not specified [RCV004077911] Chr10:127892703 [GRCh38]
Chr10:129690967 [GRCh37]
Chr10:10q26.2		 uncertain significance
NM_152311.5(CLRN3):c.348C>G (p.Ile116Met) single nucleotide variant not specified [RCV004223263] Chr10:127883757 [GRCh38]
Chr10:129682021 [GRCh37]
Chr10:10q26.2		 uncertain significance
NM_152311.5(CLRN3):c.587C>A (p.Thr196Asn) single nucleotide variant not specified [RCV004285257] Chr10:127878243 [GRCh38]
Chr10:129676507 [GRCh37]
Chr10:10q26.2		 uncertain significance
NM_152311.5(CLRN3):c.407G>A (p.Gly136Asp) single nucleotide variant not specified [RCV004270091] Chr10:127883698 [GRCh38]
Chr10:129681962 [GRCh37]
Chr10:10q26.2		 uncertain significance
GRCh37/hg19 10q26.12-26.3(chr10:122610933-135439810)x1 copy number loss not provided [RCV003222684] Chr10:122610933..135439810 [GRCh37]
Chr10:10q26.12-26.3		 pathogenic
NM_152311.5(CLRN3):c.452C>T (p.Thr151Met) single nucleotide variant not specified [RCV004300112] Chr10:127878378 [GRCh38]
Chr10:129676642 [GRCh37]
Chr10:10q26.2		 uncertain significance
GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143) copy number loss Distal 10q deletion syndrome [RCV003319583] Chr10:12829206..135427143 [GRCh37]
Chr10:10p13-q26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:123477898-135427143) copy number loss Distal 10q deletion syndrome [RCV003319590] Chr10:123477898..135427143 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143) copy number gain Distal trisomy 10q [RCV003319593] Chr10:11138692..135427143 [GRCh37]
Chr10:10p14-q26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:124895517-135440296)x1 copy number loss Distal 10q deletion syndrome [RCV003329543] Chr10:124895517..135440296 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
NM_152311.5(CLRN3):c.15G>T (p.Lys5Asn) single nucleotide variant not specified [RCV004365923] Chr10:127892770 [GRCh38]
Chr10:129691034 [GRCh37]
Chr10:10q26.2		 uncertain significance
GRCh37/hg19 10q26.2-26.3(chr10:128289206-135427143)x1 copy number loss Distal 10q deletion syndrome [RCV003458182] Chr10:128289206..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q25.1-26.3(chr10:111447991-133435388)x3 copy number gain not provided [RCV003484817] Chr10:111447991..133435388 [GRCh37]
Chr10:10q25.1-26.3		 pathogenic
GRCh37/hg19 10q26.2-26.3(chr10:128925940-135427143)x1 copy number loss not provided [RCV003483108] Chr10:128925940..135427143 [GRCh37]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q25.1-26.3(chr10:111378692-135427143)x3 copy number gain Distal trisomy 10q [RCV003458955] Chr10:111378692..135427143 [GRCh37]
Chr10:10q25.1-26.3		 pathogenic
GRCh38/hg38 10q26.2-26.3(chr10:125976998-133427130)x1 copy number loss Duane syndrome type 1 [RCV003984306] Chr10:125976998..133427130 [GRCh38]
Chr10:10q26.2-26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:125987494-135427143)x1 copy number loss not specified [RCV003986904] Chr10:125987494..135427143 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10q26.13-26.3(chr10:126127397-135427143)x1 copy number loss not specified [RCV003986878] Chr10:126127397..135427143 [GRCh37]
Chr10:10q26.13-26.3		 pathogenic
GRCh37/hg19 10q23.33-26.3(chr10:95078198-135427143)x3 copy number gain not specified [RCV003986893] Chr10:95078198..135427143 [GRCh37]
Chr10:10q23.33-26.3		 pathogenic
GRCh37/hg19 10q26.12-26.3(chr10:122331280-135426386)x1 copy number loss not provided [RCV004442821] Chr10:122331280..135426386 [GRCh37]
Chr10:10q26.12-26.3		 pathogenic
NM_152311.5(CLRN3):c.583G>A (p.Val195Ile) single nucleotide variant not specified [RCV004437326] Chr10:127878247 [GRCh38]
Chr10:129676511 [GRCh37]
Chr10:10q26.2		 uncertain significance
NM_152311.5(CLRN3):c.305T>C (p.Ile102Thr) single nucleotide variant not specified [RCV004437325] Chr10:127883800 [GRCh38]
Chr10:129682064 [GRCh37]
Chr10:10q26.2		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:145
Count of miRNA genes:105
Interacting mature miRNAs:105
Transcripts:ENST00000368671
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

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

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

Markers in Region
RH102083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710129,676,443 - 129,676,581UniSTSGRCh37
Build 3610129,566,433 - 129,566,571RGDNCBI36
Celera10123,347,916 - 123,348,054RGD
Cytogenetic Map10q26.2UniSTS
HuRef10123,251,240 - 123,251,378UniSTS
GeneMap99-GB4 RH Map10556.09UniSTS
SHGC-82601  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710129,685,054 - 129,685,366UniSTSGRCh37
Build 3610129,575,044 - 129,575,356RGDNCBI36
Celera10123,356,525 - 123,356,837RGD
Cytogenetic Map10q26.2UniSTS
HuRef10123,259,844 - 123,260,156UniSTS
TNG Radiation Hybrid Map1034877.0UniSTS
SHGC-83074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3710129,676,056 - 129,676,345UniSTSGRCh37
Build 3610129,566,046 - 129,566,335RGDNCBI36
Celera10123,347,529 - 123,347,818RGD
Cytogenetic Map10q26.2UniSTS
HuRef10123,250,853 - 123,251,142UniSTS
TNG Radiation Hybrid Map1034869.0UniSTS


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage
High
Medium 569 323 323 132 325 1 1 1 208 17 9 4 1
Low 318 18 227 100 94 101 67 7 549 78 101 66 230 34
Below cutoff 768 1091 659 70 656 25 1410 636 2551 71 740 723 49 538 900

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000368671   ⟹   ENSP00000357660
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl10127,877,841 - 127,892,941 (-)Ensembl
RefSeq Acc Id: NM_152311   ⟹   NP_689524
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810127,877,841 - 127,892,941 (-)NCBI
GRCh3710129,676,114 - 129,691,211 (-)RGD
Build 3610129,566,104 - 129,581,201 (-)NCBI Archive
Celera10123,347,587 - 123,362,681 (-)RGD
HuRef10123,250,911 - 123,266,000 (-)RGD
CHM1_110129,958,532 - 129,973,623 (-)NCBI
T2T-CHM13v2.010128,776,372 - 128,791,469 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011539274   ⟹   XP_011537576
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810127,877,841 - 127,892,941 (-)NCBI
Sequence:
RefSeq Acc Id: XM_054364751   ⟹   XP_054220726
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.010128,776,372 - 128,791,469 (-)NCBI
Reference Protein Sequences
RefSeq Acc Id: NP_689524   ⟸   NM_152311
- UniProtKB: Q6MZX8 (UniProtKB/Swiss-Prot),   Q8NCR9 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011537576   ⟸   XM_011539274
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: ENSP00000357660   ⟸   ENST00000368671
RefSeq Acc Id: XP_054220726   ⟸   XM_054364751
- Peptide Label: isoform X1

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8NCR9-F1-model_v2 AlphaFold Q8NCR9 1-226 view protein structure

Promoters
RGD ID:7218999
Promoter ID:EPDNEW_H15244
Type:initiation region
Name:CLRN3_1
Description:clarin 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3810127,892,940 - 127,893,000EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:20795 AgrOrtholog
COSMIC CLRN3 COSMIC
Ensembl Genes ENSG00000180745 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000368671 ENTREZGENE
  ENST00000368671.4 UniProtKB/Swiss-Prot
Gene3D-CATH 1.20.140.150 UniProtKB/Swiss-Prot
GTEx ENSG00000180745 GTEx
HGNC ID HGNC:20795 ENTREZGENE
Human Proteome Map CLRN3 Human Proteome Map
InterPro Clarin UniProtKB/Swiss-Prot
KEGG Report hsa:119467 UniProtKB/Swiss-Prot
NCBI Gene 119467 ENTREZGENE
OMIM 620256 OMIM
PANTHER CLARIN-3 UniProtKB/Swiss-Prot
  PTHR31548 UniProtKB/Swiss-Prot
PharmGKB PA162382510 PharmGKB
UniProt CLRN3_HUMAN UniProtKB/Swiss-Prot
  Q6MZX8 ENTREZGENE
  Q8NCR9 ENTREZGENE
UniProt Secondary Q6MZX8 UniProtKB/Swiss-Prot