CLCC1 (chloride channel CLIC like 1) - Rat Genome Database

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Gene: CLCC1 (chloride channel CLIC like 1) Homo sapiens
Analyze
Symbol: CLCC1
Name: chloride channel CLIC like 1
RGD ID: 1604384
HGNC Page HGNC
Description: Predicted to enable chloride channel activity. Predicted to be involved in chloride transport. Located in endoplasmic reticulum and mitochondria-associated endoplasmic reticulum membrane. Implicated in retinitis pigmentosa 32; INTERACTS WITH (S)-nicotine; 2-methylcholine; aristolochic acid.
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: chloride channel CLIC-like 1; chloride channel CLIC-like protein 1; KIAA0761; MCLC; Mid-1-related chloride channel 1; mid-1-related chloride channel protein 1; Mid1-related chloride channel; RP11-475E11.6; RP32
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1108,927,361 - 108,963,504 (-)EnsemblGRCh38hg38GRCh38
GRCh381108,929,505 - 108,963,484 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371109,472,127 - 109,506,106 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361109,273,653 - 109,307,634 (-)NCBINCBI36hg18NCBI36
Celera1107,741,688 - 107,775,523 (-)NCBI
Cytogenetic Map1p13.3NCBI
HuRef1107,364,991 - 107,398,998 (-)NCBIHuRef
CHM1_11109,587,075 - 109,621,067 (-)NCBICHM1_1
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

Molecular Function

References

References - curated
1. RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9872452   PMID:11279057   PMID:11826282   PMID:12477932   PMID:14702039   PMID:15342556   PMID:16344560   PMID:18029348   PMID:19946888   PMID:20416077   PMID:21145461   PMID:21873635  
PMID:21897333   PMID:22810586   PMID:25582440   PMID:26186194   PMID:26496610   PMID:26549023   PMID:26638075   PMID:27880917   PMID:28514442   PMID:28611215   PMID:28692057   PMID:28718761  
PMID:29128334   PMID:29180619   PMID:29395067   PMID:29568061   PMID:30157172   PMID:30194290   PMID:30833792   PMID:31056421   PMID:31073040   PMID:31177093   PMID:31653868   PMID:31732153  
PMID:32203420   PMID:32249768   PMID:32353859   PMID:32513696   PMID:32694731   PMID:32788342   PMID:32838362   PMID:32877691   PMID:32994395   PMID:33060197   PMID:33144569   PMID:33845483  
PMID:33957083   PMID:33961781   PMID:34079125  


Genomics

Comparative Map Data
CLCC1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1108,927,361 - 108,963,504 (-)EnsemblGRCh38hg38GRCh38
GRCh381108,929,505 - 108,963,484 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371109,472,127 - 109,506,106 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361109,273,653 - 109,307,634 (-)NCBINCBI36hg18NCBI36
Celera1107,741,688 - 107,775,523 (-)NCBI
Cytogenetic Map1p13.3NCBI
HuRef1107,364,991 - 107,398,998 (-)NCBIHuRef
CHM1_11109,587,075 - 109,621,067 (-)NCBICHM1_1
Clcc1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm393108,561,194 - 108,586,156 (+)NCBIGRCm39mm39
GRCm39 Ensembl3108,561,229 - 108,586,156 (+)Ensembl
GRCm383108,653,878 - 108,678,840 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl3108,653,913 - 108,678,840 (+)EnsemblGRCm38mm10GRCm38
MGSCv373108,456,831 - 108,481,758 (+)NCBIGRCm37mm9NCBIm37
MGSCv363108,782,303 - 108,806,068 (+)NCBImm8
Celera3110,988,607 - 111,013,587 (+)NCBICelera
Cytogenetic Map3F3NCBI
Clcc1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.22196,296,350 - 196,326,914 (+)NCBImRatBN7.2
mRatBN7.2 Ensembl2196,296,393 - 196,326,913 (+)Ensembl
Rnor_6.02211,450,426 - 211,479,885 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl2211,450,484 - 211,479,884 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.02230,923,372 - 230,952,836 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.42204,245,357 - 204,278,530 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.12204,208,110 - 204,241,283 (+)NCBI
Celera2188,943,040 - 188,970,221 (+)NCBICelera
Cytogenetic Map2q34NCBI
Clcc1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_00495543512,387,575 - 12,408,801 (-)NCBIChiLan1.0ChiLan1.0
CLCC1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11110,474,158 - 110,505,626 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1110,473,752 - 110,505,613 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01111,309,680 - 111,340,851 (-)NCBIMhudiblu_PPA_v0panPan3
CLCC1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1642,807,432 - 42,829,317 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl642,807,064 - 42,829,273 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha645,582,407 - 45,604,915 (+)NCBI
ROS_Cfam_1.0643,139,838 - 43,162,167 (+)NCBI
UMICH_Zoey_3.1642,870,406 - 42,892,709 (+)NCBI
UNSW_CanFamBas_1.0642,828,824 - 42,851,132 (+)NCBI
UU_Cfam_GSD_1.0643,270,389 - 43,292,703 (+)NCBI
Clcc1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440505819,574,603 - 19,596,108 (+)NCBI
SpeTri2.0NW_004936704518,040 - 539,526 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CLCC1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl4111,080,655 - 111,101,329 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.14111,080,648 - 111,101,007 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.24121,572,770 - 121,592,914 (+)NCBISscrofa10.2Sscrofa10.2susScr3
CLCC1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12024,627,309 - 24,657,684 (+)NCBIChlSab1.1chlSab2
ChlSab1.12024,627,309 - 24,657,684 (+)NCBIChlSab1.1chlSab2
ChlSab1.1 Ensembl2024,610,854 - 24,655,653 (+)EnsemblChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366603833,694,780 - 33,732,055 (-)NCBIVero_WHO_p1.0
Clcc1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247724,705,198 - 4,744,052 (-)NCBIHetGla_female_1.0hetGla2

Position Markers
A004S40  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,480,582 - 109,480,742UniSTSGRCh37
Build 361109,282,105 - 109,282,265RGDNCBI36
Celera1107,749,993 - 107,750,153RGD
Cytogenetic Map1p13.3UniSTS
HuRef1107,373,440 - 107,373,600UniSTS
GeneMap99-GB4 RH Map1339.42UniSTS
Whitehead-RH Map1401.2UniSTS
RH71239  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,472,420 - 109,472,552UniSTSGRCh37
Build 361109,273,943 - 109,274,075RGDNCBI36
Celera1107,741,978 - 107,742,110RGD
Cytogenetic Map1p13.3UniSTS
HuRef1107,365,281 - 107,365,413UniSTS
RH98217  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,473,943 - 109,474,120UniSTSGRCh37
Build 361109,275,466 - 109,275,643RGDNCBI36
Celera1107,743,501 - 107,743,678RGD
Cytogenetic Map1p13.3UniSTS
HuRef1107,366,804 - 107,366,981UniSTS
GeneMap99-GB4 RH Map1337.19UniSTS
G60047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,480,473 - 109,480,661UniSTSGRCh37
Build 361109,281,996 - 109,282,184RGDNCBI36
Celera1107,749,884 - 107,750,072RGD
Cytogenetic Map1p13.3UniSTS
HuRef1107,373,331 - 107,373,519UniSTS
TNG Radiation Hybrid Map159547.0UniSTS
SHGC-75294  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,493,429 - 109,493,615UniSTSGRCh37
Build 361109,294,952 - 109,295,138RGDNCBI36
Celera1107,762,839 - 107,763,025RGD
Cytogenetic Map1p13.3UniSTS
HuRef1107,386,288 - 107,386,474UniSTS
TNG Radiation Hybrid Map159551.0UniSTS
GeneMap99-GB4 RH Map1340.5UniSTS
Whitehead-RH Map1400.4UniSTS
SHGC-37685  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,474,105 - 109,474,245UniSTSGRCh37
Build 361109,275,628 - 109,275,768RGDNCBI36
Celera1107,743,663 - 107,743,803RGD
Cytogenetic Map1p13.3UniSTS
HuRef1107,366,966 - 107,367,106UniSTS
Stanford-G3 RH Map15102.0UniSTS
GeneMap99-G3 RH Map15058.0UniSTS
SHGC-75269  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,479,309 - 109,479,436UniSTSGRCh37
Build 361109,280,832 - 109,280,959RGDNCBI36
Celera1107,748,720 - 107,748,847RGD
Cytogenetic Map1p13.3UniSTS
HuRef1107,372,167 - 107,372,294UniSTS
TNG Radiation Hybrid Map159547.0UniSTS
GeneMap99-GB4 RH Map1337.99UniSTS
GeneMap99-GB4 RH Map1337.59UniSTS
Whitehead-RH Map1401.5UniSTS
NIB1477  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,480,559 - 109,480,730UniSTSGRCh37
Build 361109,282,082 - 109,282,253RGDNCBI36
Celera1107,749,970 - 107,750,141RGD
Cytogenetic Map1p13.3UniSTS
HuRef1107,373,417 - 107,373,588UniSTS
GeneMap99-GB4 RH Map1339.89UniSTS
Whitehead-RH Map1401.4UniSTS
GPSM2_9599  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,472,380 - 109,473,220UniSTSGRCh37
Build 361109,273,903 - 109,274,743RGDNCBI36
Celera1107,741,938 - 107,742,778RGD
HuRef1107,365,241 - 107,366,081UniSTS
SHGC-58248  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,503,611 - 109,503,822UniSTSGRCh37
Build 361109,305,134 - 109,305,345RGDNCBI36
Celera1107,773,023 - 107,773,234RGD
Cytogenetic Map1p13.3UniSTS
HuRef1107,396,483 - 107,396,694UniSTS
TNG Radiation Hybrid Map159581.0UniSTS
SHGC-75285  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,480,509 - 109,480,665UniSTSGRCh37
Build 361109,282,032 - 109,282,188RGDNCBI36
Celera1107,749,920 - 107,750,076RGD
Cytogenetic Map1p13.3UniSTS
HuRef1107,373,367 - 107,373,523UniSTS
TNG Radiation Hybrid Map159547.0UniSTS
GeneMap99-GB4 RH Map1340.11UniSTS
WI-18680  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,480,641 - 109,480,741UniSTSGRCh37
Build 361109,282,164 - 109,282,264RGDNCBI36
Celera1107,750,052 - 107,750,152RGD
Cytogenetic Map1p13.3UniSTS
HuRef1107,373,499 - 107,373,599UniSTS
GeneMap99-GB4 RH Map1341.53UniSTS
Whitehead-RH Map1402.6UniSTS
SHGC-75299  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371109,476,208 - 109,476,390UniSTSGRCh37
Build 361109,277,731 - 109,277,913RGDNCBI36
Celera1107,745,620 - 107,745,802RGD
Cytogenetic Map1p13.3UniSTS
HuRef1107,369,069 - 107,369,251UniSTS
TNG Radiation Hybrid Map159538.0UniSTS
GeneMap99-GB4 RH Map1341.58UniSTS
L17705  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map5q21UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map18q21.31UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map11q12UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map4p16UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map3q21.3UniSTS
GDB:434012  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map2q31.2-q33.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map5q21UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map1p21.3-p13.1UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1pter-q31.3UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map16p13UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map10p11.1UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map2q11.2-q12UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map4p16UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map14q31UniSTS
L17971  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1q21UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map3p25UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic MapXq22UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map18q21.31UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map20p11.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map9q34.13UniSTS
L17877  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map4p15.31UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map18q21.31UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map20pter-q12UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map9q21.3UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map8q13.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map4p16UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map17q25.3UniSTS
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
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Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
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
D1S1425  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map2p23-p22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic Map2p11.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map2p12-p11.2UniSTS
Cytogenetic Map3q11.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map2p24UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map15q11-q12UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map12p13.33UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map4q31.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map10p15-p14UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map15q24-q25UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map6q16UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11q23.1-q23.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map16q24.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic MapXq21.1UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:8865
Count of miRNA genes:836
Interacting mature miRNAs:958
Transcripts:ENST00000302500, ENST00000348264, ENST00000356970, ENST00000369968, ENST00000369969, ENST00000369970, ENST00000369971, ENST00000369976, ENST00000415331, ENST00000473062, ENST00000482889
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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


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 visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 2299 1857 1409 335 1049 180 4194 1873 2696 210 1344 1561 171 1 1186 2695 6 2
Low 140 1110 317 289 878 285 163 324 1038 209 116 52 4 18 93
Below cutoff 24 24

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001048210 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001278202 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001278203 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001377458 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001377459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001377460 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001377461 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001377462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001377463 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001377464 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001377465 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001377466 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001377467 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001377468 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001377469 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001377470 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_015127 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_165299 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB018304 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB052915 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB052916 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB052917 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB052918 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK090563 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL449266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL550290 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AX965653 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC002939 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP282246 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ685798 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471122 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CS265768 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA247339 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000302500   ⟹   ENSP00000306552
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,932,392 - 108,963,453 (-)Ensembl
RefSeq Acc Id: ENST00000348264   ⟹   ENSP00000337243
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,934,658 - 108,950,448 (-)Ensembl
RefSeq Acc Id: ENST00000356970   ⟹   ENSP00000349456
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,929,508 - 108,963,457 (-)Ensembl
RefSeq Acc Id: ENST00000369968   ⟹   ENSP00000358985
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,927,473 - 108,963,484 (-)Ensembl
RefSeq Acc Id: ENST00000369969   ⟹   ENSP00000358986
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,929,505 - 108,963,484 (-)Ensembl
RefSeq Acc Id: ENST00000369970   ⟹   ENSP00000358987
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,931,986 - 108,963,504 (-)Ensembl
RefSeq Acc Id: ENST00000369976   ⟹   ENSP00000358993
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,929,939 - 108,963,450 (-)Ensembl
RefSeq Acc Id: ENST00000473062
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,929,939 - 108,943,527 (-)Ensembl
RefSeq Acc Id: ENST00000482889
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,929,980 - 108,943,882 (-)Ensembl
RefSeq Acc Id: ENST00000674527   ⟹   ENSP00000501970
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,944,033 - 108,963,480 (-)Ensembl
RefSeq Acc Id: ENST00000674561   ⟹   ENSP00000501591
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,932,014 - 108,962,822 (-)Ensembl
RefSeq Acc Id: ENST00000674849   ⟹   ENSP00000502251
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,932,337 - 108,963,425 (-)Ensembl
RefSeq Acc Id: ENST00000674992   ⟹   ENSP00000501696
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,927,705 - 108,963,504 (-)Ensembl
RefSeq Acc Id: ENST00000675001   ⟹   ENSP00000502551
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,927,719 - 108,963,450 (-)Ensembl
RefSeq Acc Id: ENST00000675018   ⟹   ENSP00000501777
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,927,361 - 108,963,476 (-)Ensembl
RefSeq Acc Id: ENST00000675128   ⟹   ENSP00000501658
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,931,823 - 108,963,504 (-)Ensembl
RefSeq Acc Id: ENST00000675247   ⟹   ENSP00000502042
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,934,627 - 108,947,702 (-)Ensembl
RefSeq Acc Id: ENST00000675451   ⟹   ENSP00000502653
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,932,014 - 108,951,926 (-)Ensembl
RefSeq Acc Id: ENST00000675508   ⟹   ENSP00000502836
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,932,499 - 108,963,484 (-)Ensembl
RefSeq Acc Id: ENST00000675571   ⟹   ENSP00000502527
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,931,828 - 108,963,475 (-)Ensembl
RefSeq Acc Id: ENST00000675584   ⟹   ENSP00000502784
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,932,022 - 108,963,450 (-)Ensembl
RefSeq Acc Id: ENST00000675650   ⟹   ENSP00000502080
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,931,829 - 108,963,504 (-)Ensembl
RefSeq Acc Id: ENST00000675654   ⟹   ENSP00000502648
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,932,015 - 108,963,504 (-)Ensembl
RefSeq Acc Id: ENST00000675790   ⟹   ENSP00000502115
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,932,020 - 108,963,419 (-)Ensembl
RefSeq Acc Id: ENST00000675956   ⟹   ENSP00000502457
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,932,345 - 108,963,427 (-)Ensembl
RefSeq Acc Id: ENST00000676059   ⟹   ENSP00000501775
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,944,057 - 108,963,467 (-)Ensembl
RefSeq Acc Id: ENST00000676306   ⟹   ENSP00000502771
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,933,833 - 108,963,453 (-)Ensembl
RefSeq Acc Id: ENST00000676391   ⟹   ENSP00000502109
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,939,741 - 108,949,893 (-)Ensembl
RefSeq Acc Id: ENST00000676392   ⟹   ENSP00000501566
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,932,106 - 108,963,467 (-)Ensembl
RefSeq Acc Id: ENST00000676454   ⟹   ENSP00000502169
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1108,932,312 - 108,963,413 (-)Ensembl
RefSeq Acc Id: NM_001048210   ⟹   NP_001041675
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,505 - 108,963,484 (-)NCBI
GRCh371109,472,130 - 109,506,121 (-)NCBI
Build 361109,273,653 - 109,307,634 (-)NCBI Archive
Celera1107,741,688 - 107,775,523 (-)RGD
HuRef1107,364,991 - 107,398,998 (-)NCBI
CHM1_11109,587,075 - 109,621,067 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001278202   ⟹   NP_001265131
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,505 - 108,963,484 (-)NCBI
GRCh371109,472,130 - 109,506,121 (-)NCBI
HuRef1107,364,991 - 107,398,998 (-)NCBI
CHM1_11109,587,075 - 109,608,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001278203   ⟹   NP_001265132
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,508 - 108,950,448 (-)NCBI
GRCh371109,472,130 - 109,506,121 (-)NCBI
HuRef1107,364,991 - 107,398,998 (-)NCBI
CHM1_11109,587,075 - 109,608,015 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001377458   ⟹   NP_001364387
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,505 - 108,963,484 (-)NCBI
RefSeq Acc Id: NM_001377459   ⟹   NP_001364388
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,505 - 108,963,484 (-)NCBI
RefSeq Acc Id: NM_001377460   ⟹   NP_001364389
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,505 - 108,963,484 (-)NCBI
RefSeq Acc Id: NM_001377461   ⟹   NP_001364390
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,505 - 108,963,484 (-)NCBI
RefSeq Acc Id: NM_001377462   ⟹   NP_001364391
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,505 - 108,963,484 (-)NCBI
RefSeq Acc Id: NM_001377463   ⟹   NP_001364392
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,505 - 108,963,484 (-)NCBI
RefSeq Acc Id: NM_001377464   ⟹   NP_001364393
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,505 - 108,963,484 (-)NCBI
RefSeq Acc Id: NM_001377465   ⟹   NP_001364394
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,505 - 108,963,484 (-)NCBI
RefSeq Acc Id: NM_001377466   ⟹   NP_001364395
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,505 - 108,963,484 (-)NCBI
RefSeq Acc Id: NM_001377467   ⟹   NP_001364396
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,505 - 108,963,484 (-)NCBI
RefSeq Acc Id: NM_001377468   ⟹   NP_001364397
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,505 - 108,963,484 (-)NCBI
RefSeq Acc Id: NM_001377469   ⟹   NP_001364398
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,505 - 108,963,484 (-)NCBI
RefSeq Acc Id: NM_001377470   ⟹   NP_001364399
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,505 - 108,963,484 (-)NCBI
RefSeq Acc Id: NM_015127   ⟹   NP_055942
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,505 - 108,963,484 (-)NCBI
GRCh371109,472,130 - 109,506,121 (-)NCBI
Build 361109,273,653 - 109,307,634 (-)NCBI Archive
Celera1107,741,688 - 107,775,523 (-)RGD
HuRef1107,364,991 - 107,398,998 (-)NCBI
CHM1_11109,587,075 - 109,621,067 (-)NCBI
Sequence:
RefSeq Acc Id: NR_165299
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,929,505 - 108,963,484 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001041675 (Get FASTA)   NCBI Sequence Viewer  
  NP_001265131 (Get FASTA)   NCBI Sequence Viewer  
  NP_001265132 (Get FASTA)   NCBI Sequence Viewer  
  NP_001364387 (Get FASTA)   NCBI Sequence Viewer  
  NP_001364388 (Get FASTA)   NCBI Sequence Viewer  
  NP_001364389 (Get FASTA)   NCBI Sequence Viewer  
  NP_001364390 (Get FASTA)   NCBI Sequence Viewer  
  NP_001364391 (Get FASTA)   NCBI Sequence Viewer  
  NP_001364392 (Get FASTA)   NCBI Sequence Viewer  
  NP_001364393 (Get FASTA)   NCBI Sequence Viewer  
  NP_001364394 (Get FASTA)   NCBI Sequence Viewer  
  NP_001364395 (Get FASTA)   NCBI Sequence Viewer  
  NP_001364396 (Get FASTA)   NCBI Sequence Viewer  
  NP_001364397 (Get FASTA)   NCBI Sequence Viewer  
  NP_001364398 (Get FASTA)   NCBI Sequence Viewer  
  NP_001364399 (Get FASTA)   NCBI Sequence Viewer  
  NP_055942 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH02939 (Get FASTA)   NCBI Sequence Viewer  
  BAA34481 (Get FASTA)   NCBI Sequence Viewer  
  BAB59018 (Get FASTA)   NCBI Sequence Viewer  
  BAB79261 (Get FASTA)   NCBI Sequence Viewer  
  BAB79262 (Get FASTA)   NCBI Sequence Viewer  
  BAB79263 (Get FASTA)   NCBI Sequence Viewer  
  BAG52186 (Get FASTA)   NCBI Sequence Viewer  
  CAF06563 (Get FASTA)   NCBI Sequence Viewer  
  CAJ78403 (Get FASTA)   NCBI Sequence Viewer  
  EAW56345 (Get FASTA)   NCBI Sequence Viewer  
  EAW56346 (Get FASTA)   NCBI Sequence Viewer  
  EAW56347 (Get FASTA)   NCBI Sequence Viewer  
  EAW56348 (Get FASTA)   NCBI Sequence Viewer  
  EAW56349 (Get FASTA)   NCBI Sequence Viewer  
  Q96S66 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_055942   ⟸   NM_015127
- Peptide Label: isoform 2 precursor
- UniProtKB: Q96S66 (UniProtKB/Swiss-Prot),   A0A024R095 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001041675   ⟸   NM_001048210
- Peptide Label: isoform 1 precursor
- UniProtKB: Q96S66 (UniProtKB/Swiss-Prot),   A0A024R0G0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001265132   ⟸   NM_001278203
- Peptide Label: isoform 4 precursor
- UniProtKB: Q96S66 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001265131   ⟸   NM_001278202
- Peptide Label: isoform 3 precursor
- UniProtKB: Q96S66 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001364393   ⟸   NM_001377464
- Peptide Label: isoform 1 precursor
RefSeq Acc Id: NP_001364391   ⟸   NM_001377462
- Peptide Label: isoform 1 precursor
RefSeq Acc Id: NP_001364396   ⟸   NM_001377467
- Peptide Label: isoform 1 precursor
RefSeq Acc Id: NP_001364395   ⟸   NM_001377466
- Peptide Label: isoform 1 precursor
RefSeq Acc Id: NP_001364394   ⟸   NM_001377465
- Peptide Label: isoform 1 precursor
RefSeq Acc Id: NP_001364392   ⟸   NM_001377463
- Peptide Label: isoform 1 precursor
RefSeq Acc Id: NP_001364397   ⟸   NM_001377468
- Peptide Label: isoform 1 precursor
RefSeq Acc Id: NP_001364398   ⟸   NM_001377469
- Peptide Label: isoform 5 precursor
RefSeq Acc Id: NP_001364390   ⟸   NM_001377461
- Peptide Label: isoform 1 precursor
RefSeq Acc Id: NP_001364389   ⟸   NM_001377460
- Peptide Label: isoform 1 precursor
RefSeq Acc Id: NP_001364399   ⟸   NM_001377470
- Peptide Label: isoform 6
RefSeq Acc Id: NP_001364387   ⟸   NM_001377458
- Peptide Label: isoform 1 precursor
RefSeq Acc Id: NP_001364388   ⟸   NM_001377459
- Peptide Label: isoform 1 precursor
RefSeq Acc Id: ENSP00000337243   ⟸   ENST00000348264
RefSeq Acc Id: ENSP00000358986   ⟸   ENST00000369969
RefSeq Acc Id: ENSP00000358985   ⟸   ENST00000369968
RefSeq Acc Id: ENSP00000358987   ⟸   ENST00000369970
RefSeq Acc Id: ENSP00000358993   ⟸   ENST00000369976
RefSeq Acc Id: ENSP00000306552   ⟸   ENST00000302500
RefSeq Acc Id: ENSP00000349456   ⟸   ENST00000356970
RefSeq Acc Id: ENSP00000501970   ⟸   ENST00000674527
RefSeq Acc Id: ENSP00000501696   ⟸   ENST00000674992
RefSeq Acc Id: ENSP00000502251   ⟸   ENST00000674849
RefSeq Acc Id: ENSP00000501591   ⟸   ENST00000674561
RefSeq Acc Id: ENSP00000502115   ⟸   ENST00000675790
RefSeq Acc Id: ENSP00000502080   ⟸   ENST00000675650
RefSeq Acc Id: ENSP00000502648   ⟸   ENST00000675654
RefSeq Acc Id: ENSP00000502527   ⟸   ENST00000675571
RefSeq Acc Id: ENSP00000502836   ⟸   ENST00000675508
RefSeq Acc Id: ENSP00000502784   ⟸   ENST00000675584
RefSeq Acc Id: ENSP00000502653   ⟸   ENST00000675451
RefSeq Acc Id: ENSP00000502457   ⟸   ENST00000675956
RefSeq Acc Id: ENSP00000502042   ⟸   ENST00000675247
RefSeq Acc Id: ENSP00000501658   ⟸   ENST00000675128
RefSeq Acc Id: ENSP00000501777   ⟸   ENST00000675018
RefSeq Acc Id: ENSP00000502551   ⟸   ENST00000675001
RefSeq Acc Id: ENSP00000501775   ⟸   ENST00000676059
RefSeq Acc Id: ENSP00000502169   ⟸   ENST00000676454
RefSeq Acc Id: ENSP00000502771   ⟸   ENST00000676306
RefSeq Acc Id: ENSP00000501566   ⟸   ENST00000676392
RefSeq Acc Id: ENSP00000502109   ⟸   ENST00000676391

Promoters
RGD ID:6856456
Promoter ID:EPDNEW_H1393
Type:initiation region
Name:CLCC1_3
Description:chloride channel CLIC like 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H1394  EPDNEW_H1395  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,947,691 - 108,947,751EPDNEW
RGD ID:6856458
Promoter ID:EPDNEW_H1394
Type:multiple initiation site
Name:CLCC1_2
Description:chloride channel CLIC like 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H1393  EPDNEW_H1395  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,949,900 - 108,949,960EPDNEW
RGD ID:6856460
Promoter ID:EPDNEW_H1395
Type:initiation region
Name:CLCC1_1
Description:chloride channel CLIC like 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H1393  EPDNEW_H1394  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381108,963,453 - 108,963,513EPDNEW
RGD ID:6784924
Promoter ID:HG_KWN:3953
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000356970,   ENST00000369976,   NM_001048210,   NM_015127,   UC001DWE.1,   UC001DWH.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361109,307,256 - 109,307,756 (-)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1p21.2-13.2(chr1:101618097-111703028)x1 copy number loss See cases [RCV000053879] Chr1:101618097..111703028 [GRCh38]
Chr1:102083653..112245650 [GRCh37]
Chr1:101856241..112047173 [NCBI36]
Chr1:1p21.2-13.2
pathogenic
GRCh38/hg38 1p21.1-13.3(chr1:106074587-110144290)x1 copy number loss See cases [RCV000053881] Chr1:106074587..110144290 [GRCh38]
Chr1:106617209..110686912 [GRCh37]
Chr1:106418732..110488435 [NCBI36]
Chr1:1p21.1-13.3
pathogenic
GRCh38/hg38 1p21.3-13.3(chr1:97410602-110670510)x1 copy number loss See cases [RCV000053877] Chr1:97410602..110670510 [GRCh38]
Chr1:97876158..111213132 [GRCh37]
Chr1:97648746..111014655 [NCBI36]
Chr1:1p21.3-13.3
pathogenic
NM_013296.5(GPSM2):c.2043G>A (p.Ser681=) single nucleotide variant Chudley-McCullough syndrome [RCV001097788]|not provided [RCV000728743]|not specified [RCV000038782] Chr1:108929928 [GRCh38]
Chr1:109472550 [GRCh37]
Chr1:1p13.3
benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001377458.1(CLCC1):c.855C>G (p.Leu285=) single nucleotide variant not provided [RCV001394445] Chr1:108940084 [GRCh38]
Chr1:109482706 [GRCh37]
Chr1:1p13.3
likely benign
GRCh38/hg38 1p13.3(chr1:108807502-109134584)x3 copy number gain See cases [RCV000136126] Chr1:108807502..109134584 [GRCh38]
Chr1:109350124..109677206 [GRCh37]
Chr1:109151647..109478729 [NCBI36]
Chr1:1p13.3
uncertain significance
GRCh38/hg38 1p21.1-12(chr1:104325484-119977655)x3 copy number gain See cases [RCV000142953] Chr1:104325484..119977655 [GRCh38]
Chr1:104868106..120471049 [GRCh37]
Chr1:104669629..120321801 [NCBI36]
Chr1:1p21.1-12
pathogenic
GRCh38/hg38 1p21.1-13.2(chr1:105468292-112190626)x1 copy number loss See cases [RCV000142760] Chr1:105468292..112190626 [GRCh38]
Chr1:106010914..112733248 [GRCh37]
Chr1:105812437..112534771 [NCBI36]
Chr1:1p21.1-13.2
pathogenic
NM_013296.5(GPSM2):c.1816-8A>G single nucleotide variant not provided [RCV000972365]|not specified [RCV000150795] Chr1:108929693 [GRCh38]
Chr1:109472315 [GRCh37]
Chr1:1p13.3
benign|likely benign|conflicting interpretations of pathogenicity
NM_013296.5(GPSM2):c.1820C>T (p.Ser607Phe) single nucleotide variant not provided [RCV000514772]|not specified [RCV000150796] Chr1:108929705 [GRCh38]
Chr1:109472327 [GRCh37]
Chr1:1p13.3
benign|likely benign
NM_013296.5(GPSM2):c.1876G>C (p.Val626Leu) single nucleotide variant Hearing impairment [RCV001375230]|not specified [RCV000150797] Chr1:108929761 [GRCh38]
Chr1:109472383 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_013296.5(GPSM2):c.1909C>T (p.Arg637Trp) single nucleotide variant Chudley-McCullough syndrome [RCV000764929]|not specified [RCV000193105] Chr1:108929794 [GRCh38]
Chr1:109472416 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_013296.5(GPSM2):c.2040A>G (p.Lys680=) single nucleotide variant Chudley-McCullough syndrome [RCV000378661] Chr1:108929925 [GRCh38]
Chr1:109472547 [GRCh37]
Chr1:1p13.3
uncertain significance
GRCh37/hg19 1p36.12-12(chr1:20608823-120546301)x3 copy number loss not provided [RCV000762767] Chr1:20608823..120546301 [GRCh37]
Chr1:1p36.12-12
likely benign
NM_013296.5(GPSM2):c.1910G>A (p.Arg637Gln) single nucleotide variant Chudley-McCullough syndrome [RCV000340491] Chr1:108929795 [GRCh38]
Chr1:109472417 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_013296.5(GPSM2):c.*455C>T single nucleotide variant Chudley-McCullough syndrome [RCV000299988] Chr1:108930395 [GRCh38]
Chr1:109473017 [GRCh37]
Chr1:1p13.3
benign|likely benign
NM_003895.3(SYNJ1):c.3486A>G (p.Pro1162=) single nucleotide variant Chudley-McCullough syndrome [RCV000335054]|not provided [RCV001683169] Chr1:108930191 [GRCh38]
Chr1:109472813 [GRCh37]
Chr1:1p13.3
benign|likely benign
NM_013296.5(GPSM2):c.*211G>A single nucleotide variant Chudley-McCullough syndrome [RCV000286644]|not provided [RCV001537426] Chr1:108930151 [GRCh38]
Chr1:109472773 [GRCh37]
Chr1:1p13.3
benign|likely benign
NM_013296.5(GPSM2):c.*467G>T single nucleotide variant Chudley-McCullough syndrome [RCV000406922] Chr1:108930407 [GRCh38]
Chr1:109473029 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_013296.5(GPSM2):c.*468T>G single nucleotide variant Chudley-McCullough syndrome [RCV000312911] Chr1:108930408 [GRCh38]
Chr1:109473030 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_013296.5(GPSM2):c.*322T>C single nucleotide variant Chudley-McCullough syndrome [RCV000401009] Chr1:108930262 [GRCh38]
Chr1:109472884 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_013296.5(GPSM2):c.*476dup duplication Nonsyndromic Hearing Loss, Recessive [RCV000338622] Chr1:108930407..108930408 [GRCh38]
Chr1:109473029..109473030 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_013296.5(GPSM2):c.*359T>G single nucleotide variant Chudley-McCullough syndrome [RCV001099584] Chr1:108930299 [GRCh38]
Chr1:109472921 [GRCh37]
Chr1:1p13.3
likely benign
NM_013296.5(GPSM2):c.*474T>C single nucleotide variant Chudley-McCullough syndrome [RCV001099585] Chr1:108930414 [GRCh38]
Chr1:109473036 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_013296.5(GPSM2):c.*7T>C single nucleotide variant Chudley-McCullough syndrome [RCV001097789]|not provided [RCV001721299] Chr1:108929947 [GRCh38]
Chr1:109472569 [GRCh37]
Chr1:1p13.3
likely benign|uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p13.3(chr1:109343840-109868178)x3 copy number gain See cases [RCV000510931] Chr1:109343840..109868178 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_013296.5(GPSM2):c.1872G>A (p.Pro624=) single nucleotide variant not specified [RCV000608941] Chr1:108929757 [GRCh38]
Chr1:109472379 [GRCh37]
Chr1:1p13.3
likely benign
GRCh37/hg19 1p22.1-11.2(chr1:93837992-121343783)x3 copy number gain See cases [RCV000512354] Chr1:93837992..121343783 [GRCh37]
Chr1:1p22.1-11.2
pathogenic
GRCh37/hg19 1p13.3(chr1:109428017-109779697)x3 copy number gain not provided [RCV000709949] Chr1:109428017..109779697 [GRCh37]
Chr1:1p13.3
not provided
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44
pathogenic
NC_000001.11:g.(?_103175204)_(111410059_?)del deletion Autistic disorder of childhood onset [RCV000754122] Chr1:103175204..111410059 [GRCh38]
Chr1:1p21.1-13.2
likely pathogenic
GRCh37/hg19 1p13.3(chr1:109498401-109501001)x1 copy number loss not provided [RCV000736639] Chr1:109498401..109501001 [GRCh37]
Chr1:1p13.3
benign
GRCh37/hg19 1p13.3(chr1:109497897-109501001)x0 copy number loss not provided [RCV000736638] Chr1:109497897..109501001 [GRCh37]
Chr1:1p13.3
benign
GRCh37/hg19 1p22.1-13.3(chr1:94054724-111671707)x3 copy number gain not provided [RCV000749068] Chr1:94054724..111671707 [GRCh37]
Chr1:1p22.1-13.3
pathogenic
GRCh37/hg19 1p13.3(chr1:109428249-109789795)x3 copy number gain not provided [RCV000749138] Chr1:109428249..109789795 [GRCh37]
Chr1:1p13.3
benign
NM_001377458.1(CLCC1):c.741G>A (p.Met247Ile) single nucleotide variant not provided [RCV001038871] Chr1:108941460 [GRCh38]
Chr1:109484082 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1600G>A (p.Ala534Thr) single nucleotide variant not provided [RCV001048536] Chr1:108934726 [GRCh38]
Chr1:109477348 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.927G>A (p.Thr309=) single nucleotide variant not provided [RCV001049514] Chr1:108939750 [GRCh38]
Chr1:109482372 [GRCh37]
Chr1:1p13.3
uncertain significance
GRCh37/hg19 1p13.3(chr1:109396970-109807574)x1 copy number loss not provided [RCV001005129] Chr1:109396970..109807574 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1448C>T (p.Pro483Leu) single nucleotide variant not provided [RCV001036539] Chr1:108934878 [GRCh38]
Chr1:109477500 [GRCh37]
Chr1:1p13.3
uncertain significance
Single allele deletion 1p13.3 deletion syndrome [RCV000786772] Chr1:107779092..111199205 [GRCh37]
Chr1:1p13.3
likely pathogenic
Single allele deletion not provided [RCV000844956] Chr1:108926313..111266497 [GRCh37]
Chr1:1p13.3
not provided
NM_013296.5(GPSM2):c.1816-10A>G single nucleotide variant Chudley-McCullough syndrome [RCV001096017] Chr1:108929691 [GRCh38]
Chr1:109472313 [GRCh37]
Chr1:1p13.3
uncertain significance
GRCh37/hg19 1p13.3(chr1:109425142-109703243)x3 copy number gain not provided [RCV000846908] Chr1:109425142..109703243 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1261G>C (p.Glu421Gln) single nucleotide variant not provided [RCV001231109] Chr1:108937199 [GRCh38]
Chr1:109479821 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.425A>G (p.Asn142Ser) single nucleotide variant not provided [RCV001208153] Chr1:108943972 [GRCh38]
Chr1:109486594 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.402G>T (p.Leu134Phe) single nucleotide variant not provided [RCV001240203] Chr1:108943995 [GRCh38]
Chr1:109486617 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1328G>A (p.Arg443Gln) single nucleotide variant not provided [RCV001241920] Chr1:108937132 [GRCh38]
Chr1:109479754 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1385A>G (p.His462Arg) single nucleotide variant not provided [RCV001231021] Chr1:108934941 [GRCh38]
Chr1:109477563 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.362T>C (p.Met121Thr) single nucleotide variant not provided [RCV001240573] Chr1:108944035 [GRCh38]
Chr1:109486657 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.740T>C (p.Met247Thr) single nucleotide variant not provided [RCV001235374] Chr1:108941461 [GRCh38]
Chr1:109484083 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1105G>A (p.Glu369Lys) single nucleotide variant not provided [RCV001201552] Chr1:108937355 [GRCh38]
Chr1:109479977 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_013296.5(GPSM2):c.1871C>T (p.Pro624Leu) single nucleotide variant not provided [RCV001577719] Chr1:108929756 [GRCh38]
Chr1:109472378 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1634C>T (p.Pro545Leu) single nucleotide variant not provided [RCV001212647] Chr1:108934692 [GRCh38]
Chr1:109477314 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.871A>G (p.Ile291Val) single nucleotide variant not provided [RCV001245219] Chr1:108940068 [GRCh38]
Chr1:109482690 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_013296.5(GPSM2):c.*351C>T single nucleotide variant Chudley-McCullough syndrome [RCV001097791] Chr1:108930291 [GRCh38]
Chr1:109472913 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1041+3T>G single nucleotide variant not provided [RCV001061974] Chr1:108939633 [GRCh38]
Chr1:109482255 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1129C>T (p.Arg377Trp) single nucleotide variant not provided [RCV001060347] Chr1:108937331 [GRCh38]
Chr1:109479953 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1606G>C (p.Gly536Arg) single nucleotide variant not provided [RCV001211264] Chr1:108934720 [GRCh38]
Chr1:109477342 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.586G>A (p.Val196Met) single nucleotide variant not provided [RCV001061232] Chr1:108943591 [GRCh38]
Chr1:109486213 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.227A>G (p.Tyr76Cys) single nucleotide variant not provided [RCV001204953] Chr1:108949824 [GRCh38]
Chr1:109492446 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.926C>T (p.Thr309Met) single nucleotide variant not provided [RCV001207648] Chr1:108939751 [GRCh38]
Chr1:109482373 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.623G>A (p.Arg208His) single nucleotide variant not provided [RCV001069831] Chr1:108943554 [GRCh38]
Chr1:109486176 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.518G>T (p.Arg173Leu) single nucleotide variant not provided [RCV001230847] Chr1:108943879 [GRCh38]
Chr1:109486501 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1212G>A (p.Met404Ile) single nucleotide variant not provided [RCV001237040] Chr1:108937248 [GRCh38]
Chr1:109479870 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.562-1G>A single nucleotide variant not provided [RCV001204939] Chr1:108943616 [GRCh38]
Chr1:109486238 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.883C>A (p.Pro295Thr) single nucleotide variant not provided [RCV001218073] Chr1:108940056 [GRCh38]
Chr1:109482678 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1519G>C (p.Glu507Gln) single nucleotide variant not provided [RCV001064818] Chr1:108934807 [GRCh38]
Chr1:109477429 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.733G>A (p.Ala245Thr) single nucleotide variant not provided [RCV001245555] Chr1:108941468 [GRCh38]
Chr1:109484090 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1327C>T (p.Arg443Trp) single nucleotide variant not provided [RCV001046616] Chr1:108937133 [GRCh38]
Chr1:109479755 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1314C>A (p.Ser438Arg) single nucleotide variant not provided [RCV001066649] Chr1:108937146 [GRCh38]
Chr1:109479768 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_013296.5(GPSM2):c.*208A>G single nucleotide variant Chudley-McCullough syndrome [RCV001097790] Chr1:108930148 [GRCh38]
Chr1:109472770 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1226A>C (p.Gln409Pro) single nucleotide variant not provided [RCV001228450] Chr1:108937234 [GRCh38]
Chr1:109479856 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.75C>A (p.Asp25Glu) single nucleotide variant Retinitis pigmentosa 32 [RCV001248856] Chr1:108950363 [GRCh38]
Chr1:109492985 [GRCh37]
Chr1:1p13.3
pathogenic
NM_001377458.1(CLCC1):c.518G>A (p.Arg173Gln) single nucleotide variant not provided [RCV001338501] Chr1:108943879 [GRCh38]
Chr1:109486501 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1063_1083del (p.Lys355_Arg361del) deletion not provided [RCV001350585] Chr1:108937377..108937397 [GRCh38]
Chr1:109479999..109480019 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.601A>G (p.Thr201Ala) single nucleotide variant not provided [RCV001327042] Chr1:108943576 [GRCh38]
Chr1:109486198 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.962A>C (p.Glu321Ala) single nucleotide variant not provided [RCV001299202] Chr1:108939715 [GRCh38]
Chr1:109482337 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.526_527del (p.Asp176fs) deletion not provided [RCV001342830] Chr1:108943870..108943871 [GRCh38]
Chr1:109486492..109486493 [GRCh37]
Chr1:1p13.3
uncertain significance
NC_000001.10:g.(?_109428145)_(109816671_?)dup duplication not provided [RCV001308191] Chr1:109428145..109816671 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.281A>G (p.Asn94Ser) single nucleotide variant not provided [RCV001343793] Chr1:108947669 [GRCh38]
Chr1:109490291 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.461C>T (p.Ala154Val) single nucleotide variant not provided [RCV001300778] Chr1:108943936 [GRCh38]
Chr1:109486558 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1362G>A (p.Glu454=) single nucleotide variant not provided [RCV001433044] Chr1:108937098 [GRCh38]
Chr1:109479720 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.1408A>C (p.Lys470Gln) single nucleotide variant not provided [RCV001325125] Chr1:108934918 [GRCh38]
Chr1:109477540 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1530C>T (p.Pro510=) single nucleotide variant not provided [RCV001413108] Chr1:108934796 [GRCh38]
Chr1:109477418 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.1432C>T (p.Leu478=) single nucleotide variant not provided [RCV001414434] Chr1:108934894 [GRCh38]
Chr1:109477516 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.621A>T (p.Val207=) single nucleotide variant not provided [RCV001392418] Chr1:108943556 [GRCh38]
Chr1:109486178 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.912C>G (p.Phe304Leu) single nucleotide variant not provided [RCV001370582] Chr1:108939765 [GRCh38]
Chr1:109482387 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1244C>T (p.Thr415Met) single nucleotide variant not provided [RCV001349937] Chr1:108937216 [GRCh38]
Chr1:109479838 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1180G>A (p.Gly394Ser) single nucleotide variant not provided [RCV001317822] Chr1:108937280 [GRCh38]
Chr1:109479902 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1564G>A (p.Ala522Thr) single nucleotide variant not provided [RCV001301773] Chr1:108934762 [GRCh38]
Chr1:109477384 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.229_233del (p.Tyr76_Lys77insTer) deletion not provided [RCV001301807] Chr1:108949820..108949824 [GRCh38]
Chr1:109492442..109492446 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.478A>G (p.Ile160Val) single nucleotide variant not provided [RCV001322495] Chr1:108943919 [GRCh38]
Chr1:109486541 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.902C>G (p.Ala301Gly) single nucleotide variant not provided [RCV001313604] Chr1:108939775 [GRCh38]
Chr1:109482397 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1454A>C (p.Glu485Ala) single nucleotide variant not provided [RCV001322656] Chr1:108934872 [GRCh38]
Chr1:109477494 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1027G>A (p.Ala343Thr) single nucleotide variant not provided [RCV001370828] Chr1:108939650 [GRCh38]
Chr1:109482272 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.846C>T (p.Tyr282=) single nucleotide variant not provided [RCV001395979] Chr1:108940093 [GRCh38]
Chr1:109482715 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.340C>T (p.Pro114Ser) single nucleotide variant not provided [RCV001309242] Chr1:108944057 [GRCh38]
Chr1:109486679 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.402G>C (p.Leu134Phe) single nucleotide variant not provided [RCV001366671] Chr1:108943995 [GRCh38]
Chr1:109486617 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.510G>A (p.Trp170Ter) single nucleotide variant not provided [RCV001366820] Chr1:108943887 [GRCh38]
Chr1:109486509 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.92A>G (p.Asn31Ser) single nucleotide variant not provided [RCV001366897] Chr1:108950346 [GRCh38]
Chr1:109492968 [GRCh37]
Chr1:1p13.3
uncertain significance
NM_001377458.1(CLCC1):c.1542G>A (p.Lys514=) single nucleotide variant not provided [RCV001413966] Chr1:108934784 [GRCh38]
Chr1:109477406 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.1556C>A (p.Ser519Tyr) single nucleotide variant not provided [RCV001365615] Chr1:108934770 [GRCh38]
Chr1:109477392 [GRCh37]
Chr1:1p13.3
uncertain significance
GRCh37/hg19 1p21.2-12(chr1:102021465-119737478) copy number loss Seizures [RCV001352640] Chr1:102021465..119737478 [GRCh37]
Chr1:1p21.2-12
pathogenic
NM_001377458.1(CLCC1):c.1464T>G (p.Thr488=) single nucleotide variant not provided [RCV001485498] Chr1:108934862 [GRCh38]
Chr1:109477484 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.630C>T (p.Tyr210=) single nucleotide variant not provided [RCV001394262] Chr1:108943547 [GRCh38]
Chr1:109486169 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.562-4del deletion not provided [RCV001514918] Chr1:108943619 [GRCh38]
Chr1:109486241 [GRCh37]
Chr1:1p13.3
benign
NM_001377458.1(CLCC1):c.340-6_340-2del microsatellite not provided [RCV001439709] Chr1:108944059..108944063 [GRCh38]
Chr1:109486681..109486685 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.1486C>G (p.Pro496Ala) single nucleotide variant not provided [RCV001453339] Chr1:108934840 [GRCh38]
Chr1:109477462 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.478A>C (p.Ile160Leu) single nucleotide variant not provided [RCV001467132] Chr1:108943919 [GRCh38]
Chr1:109486541 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.466A>G (p.Ser156Gly) single nucleotide variant not provided [RCV001522032] Chr1:108943931 [GRCh38]
Chr1:109486553 [GRCh37]
Chr1:1p13.3
benign
NM_001377458.1(CLCC1):c.462A>G (p.Ala154=) single nucleotide variant not provided [RCV001522033] Chr1:108943935 [GRCh38]
Chr1:109486557 [GRCh37]
Chr1:1p13.3
benign
NM_001377458.1(CLCC1):c.1384-5T>C single nucleotide variant not provided [RCV001470891] Chr1:108934947 [GRCh38]
Chr1:109477569 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.1599C>T (p.Pro533=) single nucleotide variant not provided [RCV001481663] Chr1:108934727 [GRCh38]
Chr1:109477349 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.1123C>T (p.Arg375Trp) single nucleotide variant not provided [RCV001513108] Chr1:108937337 [GRCh38]
Chr1:109479959 [GRCh37]
Chr1:1p13.3
benign
NM_001377458.1(CLCC1):c.895-7G>A single nucleotide variant not provided [RCV001392872] Chr1:108939789 [GRCh38]
Chr1:109482411 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.1041+7A>G single nucleotide variant not provided [RCV001423617] Chr1:108939629 [GRCh38]
Chr1:109482251 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.797-8C>T single nucleotide variant not provided [RCV001408677] Chr1:108940150 [GRCh38]
Chr1:109482772 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.1449G>A (p.Pro483=) single nucleotide variant not provided [RCV001419530] Chr1:108934877 [GRCh38]
Chr1:109477499 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.934T>C (p.Leu312=) single nucleotide variant not provided [RCV001401696] Chr1:108939743 [GRCh38]
Chr1:109482365 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.522C>T (p.Phe174=) single nucleotide variant not provided [RCV001429794] Chr1:108943875 [GRCh38]
Chr1:109486497 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.995C>T (p.Ala332Val) single nucleotide variant not provided [RCV001519090] Chr1:108939682 [GRCh38]
Chr1:109482304 [GRCh37]
Chr1:1p13.3
benign
NM_001377458.1(CLCC1):c.1635G>C (p.Pro545=) single nucleotide variant not provided [RCV001505882] Chr1:108934691 [GRCh38]
Chr1:109477313 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.895-8C>T single nucleotide variant not provided [RCV001476286] Chr1:108939790 [GRCh38]
Chr1:109482412 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.130-9_130-8del microsatellite not provided [RCV001499917] Chr1:108949929..108949930 [GRCh38]
Chr1:109492551..109492552 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.1155T>C (p.Ile385=) single nucleotide variant not provided [RCV001466449] Chr1:108937305 [GRCh38]
Chr1:109479927 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.1478C>T (p.Ser493Leu) single nucleotide variant not provided [RCV001517639] Chr1:108934848 [GRCh38]
Chr1:109477470 [GRCh37]
Chr1:1p13.3
benign
NM_001377458.1(CLCC1):c.1377A>G (p.Val459=) single nucleotide variant not provided [RCV001471278] Chr1:108937083 [GRCh38]
Chr1:109479705 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.909A>C (p.Thr303=) single nucleotide variant not provided [RCV001426776] Chr1:108939768 [GRCh38]
Chr1:109482390 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.897A>G (p.Ala299=) single nucleotide variant not provided [RCV001441971] Chr1:108939780 [GRCh38]
Chr1:109482402 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.903A>G (p.Ala301=) single nucleotide variant not provided [RCV001436129] Chr1:108939774 [GRCh38]
Chr1:109482396 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.1347C>T (p.Asp449=) single nucleotide variant not provided [RCV001403331] Chr1:108937113 [GRCh38]
Chr1:109479735 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.1080G>A (p.Leu360=) single nucleotide variant not provided [RCV001429472] Chr1:108937380 [GRCh38]
Chr1:109480002 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.357C>T (p.Gly119=) single nucleotide variant not provided [RCV001514113] Chr1:108944040 [GRCh38]
Chr1:109486662 [GRCh37]
Chr1:1p13.3
benign
NM_001377458.1(CLCC1):c.232-10A>G single nucleotide variant not provided [RCV001455834] Chr1:108947728 [GRCh38]
Chr1:109490350 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.996G>A (p.Ala332=) single nucleotide variant not provided [RCV001521487] Chr1:108939681 [GRCh38]
Chr1:109482303 [GRCh37]
Chr1:1p13.3
benign
NM_001377458.1(CLCC1):c.1556C>G (p.Ser519Cys) single nucleotide variant not provided [RCV001505193] Chr1:108934770 [GRCh38]
Chr1:109477392 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.819C>G (p.Thr273=) single nucleotide variant not provided [RCV001499470] Chr1:108940120 [GRCh38]
Chr1:109482742 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.643C>T (p.Arg215Cys) single nucleotide variant not provided [RCV001478641] Chr1:108943534 [GRCh38]
Chr1:109486156 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.1596C>T (p.Ser532=) single nucleotide variant not provided [RCV001400006] Chr1:108934730 [GRCh38]
Chr1:109477352 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.1104C>A (p.Ser368Arg) single nucleotide variant not provided [RCV001514916] Chr1:108937356 [GRCh38]
Chr1:109479978 [GRCh37]
Chr1:1p13.3
benign
NM_001377458.1(CLCC1):c.603T>C (p.Thr201=) single nucleotide variant not provided [RCV001514917] Chr1:108943574 [GRCh38]
Chr1:109486196 [GRCh37]
Chr1:1p13.3
benign
NM_001377458.1(CLCC1):c.195A>G (p.Ser65=) single nucleotide variant not provided [RCV001521798] Chr1:108949856 [GRCh38]
Chr1:109492478 [GRCh37]
Chr1:1p13.3
benign
NM_001377458.1(CLCC1):c.1480G>A (p.Ala494Thr) single nucleotide variant not provided [RCV001404631] Chr1:108934846 [GRCh38]
Chr1:109477468 [GRCh37]
Chr1:1p13.3
likely benign
NM_001377458.1(CLCC1):c.1253G>A (p.Gly418Asp) single nucleotide variant not provided [RCV001522031] Chr1:108937207 [GRCh38]
Chr1:109479829 [GRCh37]
Chr1:1p13.3
benign
NM_001377458.1(CLCC1):c.231+9T>C single nucleotide variant not provided [RCV001463854] Chr1:108949811 [GRCh38]
Chr1:109492433 [GRCh37]
Chr1:1p13.3
likely benign

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:29675 AgrOrtholog
COSMIC CLCC1 COSMIC
Ensembl Genes ENSG00000121940 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000306552 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000337243 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000349456 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000358985 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000358986 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000358987 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000358993 UniProtKB/TrEMBL
  ENSP00000501566 UniProtKB/TrEMBL
  ENSP00000501591 UniProtKB/TrEMBL
  ENSP00000501658 UniProtKB/TrEMBL
  ENSP00000501696 UniProtKB/TrEMBL
  ENSP00000501775 UniProtKB/TrEMBL
  ENSP00000501777 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000501970 UniProtKB/TrEMBL
  ENSP00000502042 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000502080 UniProtKB/TrEMBL
  ENSP00000502109 UniProtKB/TrEMBL
  ENSP00000502115 UniProtKB/TrEMBL
  ENSP00000502169 UniProtKB/TrEMBL
  ENSP00000502251 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000502457 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000502527 UniProtKB/TrEMBL
  ENSP00000502551 UniProtKB/TrEMBL
  ENSP00000502648 UniProtKB/Swiss-Prot
  ENSP00000502653 UniProtKB/TrEMBL
  ENSP00000502771 UniProtKB/TrEMBL
  ENSP00000502784 UniProtKB/TrEMBL
  ENSP00000502836 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000302500 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000348264 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000356970 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000369968 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000369969 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000369970 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000369976 UniProtKB/TrEMBL
  ENST00000674527 UniProtKB/TrEMBL
  ENST00000674561 UniProtKB/TrEMBL
  ENST00000674849 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000674992 UniProtKB/TrEMBL
  ENST00000675001 UniProtKB/TrEMBL
  ENST00000675018 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000675128 UniProtKB/TrEMBL
  ENST00000675247 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000675451 UniProtKB/TrEMBL
  ENST00000675508 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000675571 UniProtKB/TrEMBL
  ENST00000675584 UniProtKB/TrEMBL
  ENST00000675650 UniProtKB/TrEMBL
  ENST00000675654 UniProtKB/Swiss-Prot
  ENST00000675790 UniProtKB/TrEMBL
  ENST00000675956 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000676059 UniProtKB/TrEMBL
  ENST00000676306 UniProtKB/TrEMBL
  ENST00000676391 UniProtKB/TrEMBL
  ENST00000676392 UniProtKB/TrEMBL
  ENST00000676454 UniProtKB/TrEMBL
GTEx ENSG00000121940 GTEx
HGNC ID HGNC:29675 ENTREZGENE
Human Proteome Map CLCC1 Human Proteome Map
InterPro Chloride_chnl_CLIC-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:23155 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 23155 ENTREZGENE
OMIM 609913 OMIM
  617539 OMIM
PANTHER PTHR34093 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam MCLC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA142672105 PharmGKB
UniProt A0A024R095 ENTREZGENE, UniProtKB/TrEMBL
  A0A024R0G0 ENTREZGENE, UniProtKB/TrEMBL
  A0A6Q8PEZ7_HUMAN UniProtKB/TrEMBL
  A0A6Q8PF11_HUMAN UniProtKB/TrEMBL
  A0A6Q8PF97_HUMAN UniProtKB/TrEMBL
  A0A6Q8PFF7_HUMAN UniProtKB/TrEMBL
  A0A6Q8PFH1_HUMAN UniProtKB/TrEMBL
  A0A6Q8PFT6_HUMAN UniProtKB/TrEMBL
  A0A6Q8PG14_HUMAN UniProtKB/TrEMBL
  A0A6Q8PG30_HUMAN UniProtKB/TrEMBL
  A0A6Q8PG68_HUMAN UniProtKB/TrEMBL
  A0A6Q8PG75_HUMAN UniProtKB/TrEMBL
  A0A6Q8PGA4_HUMAN UniProtKB/TrEMBL
  A0A6Q8PHQ1_HUMAN UniProtKB/TrEMBL
  CLCC1_HUMAN UniProtKB/Swiss-Prot
  Q5T1P5_HUMAN UniProtKB/TrEMBL
  Q96S66 ENTREZGENE
UniProt Secondary A6NGP0 UniProtKB/TrEMBL
  O94861 UniProtKB/Swiss-Prot
  Q8WYP8 UniProtKB/Swiss-Prot
  Q8WYP9 UniProtKB/Swiss-Prot
  Q9BU25 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-01-26 CLCC1  chloride channel CLIC like 1    chloride channel CLIC-like 1  Symbol and/or name change 5135510 APPROVED