CIAO1 (cytosolic iron-sulfur assembly component 1) - Rat Genome Database

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Gene: CIAO1 (cytosolic iron-sulfur assembly component 1) Homo sapiens
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Symbol: CIAO1
Name: cytosolic iron-sulfur assembly component 1
RGD ID: 1354495
HGNC Page HGNC:14280
Description: Involved in iron-sulfur cluster assembly and protein maturation by iron-sulfur cluster transfer. Located in cytoplasm. Part of MMXD complex and cytosolic [4Fe-4S] assembly targeting complex.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: CIA1; cytosolic iron-sulfur protein assembly 1 homolog; probable cytosolic iron-sulfur protein assembly protein CIAO1; WD repeat domain 39; WD repeat-containing protein 39; WD40 protein Ciao1; WDR39
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38296,266,225 - 96,274,173 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl296,266,159 - 96,274,173 (+)EnsemblGRCh38hg38GRCh38
GRCh37296,931,963 - 96,939,911 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36296,295,611 - 96,303,644 (+)NCBINCBI36Build 36hg18NCBI36
Build 34296,353,757 - 96,361,786NCBI
Celera291,373,072 - 91,381,105 (+)NCBICelera
Cytogenetic Map2q11.2NCBI
HuRef290,893,381 - 90,901,414 (+)NCBIHuRef
CHM1_1296,936,239 - 96,944,254 (+)NCBICHM1_1
T2T-CHM13v2.0296,772,833 - 96,780,781 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

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

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Iron-sulfur cluster biogenesis in mammalian cells: New insights into the molecular mechanisms of cluster delivery. Maio N and Rouault TA, Biochim Biophys Acta. 2015 Jun;1853(6):1493-512. doi: 10.1016/j.bbamcr.2014.09.009. Epub 2014 Sep 19.
3. Biogenesis of cytosolic and nuclear iron-sulfur proteins and their role in genome stability. Paul VD and Lill R, Biochim Biophys Acta. 2015 Jun;1853(6):1528-39. doi: 10.1016/j.bbamcr.2014.12.018. Epub 2015 Jan 10.
4. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
5. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8125298   PMID:9556563   PMID:10493829   PMID:12477932   PMID:14702039   PMID:15489334   PMID:16169070   PMID:16189514   PMID:16751776   PMID:17041588   PMID:17353931   PMID:17937914  
PMID:20797633   PMID:21516116   PMID:21832049   PMID:21873635   PMID:22190034   PMID:22379092   PMID:22678361   PMID:22678362   PMID:22865885   PMID:22939629   PMID:23585563   PMID:23602568  
PMID:23891004   PMID:24130505   PMID:24245804   PMID:24981860   PMID:25416956   PMID:25659154   PMID:26186194   PMID:26344197   PMID:26496610   PMID:26760575   PMID:26972000   PMID:27107014  
PMID:27235625   PMID:27432908   PMID:28178521   PMID:28514442   PMID:28615450   PMID:28675297   PMID:29309586   PMID:29395067   PMID:29467282   PMID:29955894   PMID:30833792   PMID:30884312  
PMID:31091453   PMID:31229404   PMID:31753913   PMID:31796584   PMID:32222833   PMID:32296183   PMID:32632277   PMID:32707033   PMID:33393230   PMID:33853758   PMID:33961781   PMID:34083449  
PMID:34373451   PMID:34569959   PMID:34687317   PMID:34709727   PMID:35241646   PMID:35256949   PMID:35509820   PMID:35831314   PMID:35944360   PMID:36114006   PMID:36215168   PMID:36538041  
PMID:36629882   PMID:36688959   PMID:36724073   PMID:36736316   PMID:37536630   PMID:37689310   PMID:38113892   PMID:38580884   PMID:38803224   PMID:38950322  


Genomics

Comparative Map Data
CIAO1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38296,266,225 - 96,274,173 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl296,266,159 - 96,274,173 (+)EnsemblGRCh38hg38GRCh38
GRCh37296,931,963 - 96,939,911 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36296,295,611 - 96,303,644 (+)NCBINCBI36Build 36hg18NCBI36
Build 34296,353,757 - 96,361,786NCBI
Celera291,373,072 - 91,381,105 (+)NCBICelera
Cytogenetic Map2q11.2NCBI
HuRef290,893,381 - 90,901,414 (+)NCBIHuRef
CHM1_1296,936,239 - 96,944,254 (+)NCBICHM1_1
T2T-CHM13v2.0296,772,833 - 96,780,781 (+)NCBIT2T-CHM13v2.0
Ciao1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm392127,082,858 - 127,089,736 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl2127,082,858 - 127,089,736 (-)EnsemblGRCm39 Ensembl
GRCm382127,240,938 - 127,247,816 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl2127,240,938 - 127,247,816 (-)EnsemblGRCm38mm10GRCm38
MGSCv372127,066,674 - 127,073,552 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv362126,932,379 - 126,939,183 (-)NCBIMGSCv36mm8
Celera2128,480,303 - 128,487,188 (-)NCBICelera
Cytogenetic Map2F1NCBI
cM Map261.86NCBI
Ciao1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr83134,913,639 - 134,919,244 (-)NCBIGRCr8
mRatBN7.23114,458,671 - 114,465,928 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl3114,458,655 - 114,467,009 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx3118,351,884 - 118,357,408 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.03126,947,428 - 126,952,952 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.03124,607,808 - 124,613,332 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.03119,671,778 - 119,677,324 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl3119,671,779 - 119,678,092 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.03126,196,996 - 126,202,542 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.43114,740,676 - 114,746,203 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.13114,646,248 - 114,651,776 (-)NCBI
Celera3113,300,999 - 113,306,382 (-)NCBICelera
Cytogenetic Map3q36NCBI
Ciao1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554703,822,582 - 3,828,563 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554703,822,606 - 3,828,563 (+)NCBIChiLan1.0ChiLan1.0
CIAO1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21232,034,666 - 32,042,638 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12A32,037,475 - 32,045,398 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02A103,041,509 - 103,049,469 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12A97,189,246 - 97,194,576 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2A97,188,949 - 97,194,576 (+)Ensemblpanpan1.1panPan2
CIAO1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11734,507,136 - 34,512,566 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1734,508,662 - 34,512,486 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1734,277,047 - 34,282,512 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01735,278,219 - 35,283,798 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1735,278,225 - 35,283,748 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11734,407,476 - 34,412,941 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01734,476,119 - 34,481,585 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01734,682,825 - 34,688,404 (-)NCBIUU_Cfam_GSD_1.0
Ciao1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440629283,106,283 - 83,111,710 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936744359,258 - 363,585 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936744359,234 - 364,649 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CIAO1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl346,960,881 - 46,966,635 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1346,960,880 - 46,967,003 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2349,102,770 - 49,108,598 (-)NCBISscrofa10.2Sscrofa10.2susScr3
CIAO1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.114685,378 - 690,752 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl14685,321 - 690,544 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666041168,111,923 - 168,117,714 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ciao1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247492,344,743 - 2,351,358 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247492,344,833 - 2,350,986 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in CIAO1
15 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 2q11.1-11.2(chr2:95879602-97029672)x3 copy number gain Global developmental delay [RCV000050366]|See cases [RCV000050366] Chr2:95879602..97029672 [GRCh38]
Chr2:96545350..97695409 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh38/hg38 2q11.1-11.2(chr2:95879602-97285797)x1 copy number loss See cases [RCV000051260] Chr2:95879602..97285797 [GRCh38]
Chr2:96545350..98013866 [GRCh37]
Chr2:95909077..97380005 [NCBI36]
Chr2:2q11.1-11.2		 pathogenic
GRCh38/hg38 2q11.2(chr2:96100812-97285797)x1 copy number loss See cases [RCV000051137] Chr2:96100812..97285797 [GRCh38]
Chr2:96766560..98013866 [GRCh37]
Chr2:96130287..97380005 [NCBI36]
Chr2:2q11.2		 pathogenic
GRCh38/hg38 2q11.1-11.2(chr2:95806265-97285797)x3 copy number gain See cases [RCV000053136] Chr2:95806265..97285797 [GRCh38]
Chr2:96472013..98013866 [GRCh37]
Chr2:95835740..97380005 [NCBI36]
Chr2:2q11.1-11.2		 uncertain significance
GRCh38/hg38 2q11.1-11.2(chr2:95810453-97024341)x3 copy number gain See cases [RCV000053137] Chr2:95810453..97024341 [GRCh38]
Chr2:96476201..97690078 [GRCh37]
Chr2:95839928..97053805 [NCBI36]
Chr2:2q11.1-11.2		 uncertain significance
GRCh38/hg38 2q11.1-11.2(chr2:95880668-97131646)x3 copy number gain See cases [RCV000053138] Chr2:95880668..97131646 [GRCh38]
Chr2:96546416..97797383 [GRCh37]
Chr2:95910143..97161110 [NCBI36]
Chr2:2q11.1-11.2		 uncertain significance
GRCh38/hg38 2q11.1-11.2(chr2:95916534-97024341)x3 copy number gain See cases [RCV000053139] Chr2:95916534..97024341 [GRCh38]
Chr2:96582282..97690078 [GRCh37]
Chr2:95946009..97053805 [NCBI36]
Chr2:2q11.1-11.2		 uncertain significance
GRCh38/hg38 2q11.2(chr2:96100612-97285797)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053140]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053140]|See cases [RCV000053140] Chr2:96100612..97285797 [GRCh38]
Chr2:96766360..98014007 [GRCh37]
Chr2:96130087..97380146 [NCBI36]
Chr2:2q11.2		 uncertain significance
GRCh38/hg38 2q11.1-12.1(chr2:94817406-103252396)x3 copy number gain See cases [RCV000052946] Chr2:94817406..103252396 [GRCh38]
Chr2:95618109..103868854 [GRCh37]
Chr2:94846878..103235286 [NCBI36]
Chr2:2q11.1-12.1		 pathogenic
GRCh38/hg38 2p11.2-q11.2(chr2:91443218-102334856)x3 copy number gain See cases [RCV000052945] Chr2:91443218..102334856 [GRCh38]
Chr2:91617683..102951316 [GRCh37]
Chr2:90981410..102317748 [NCBI36]
Chr2:2p11.2-q11.2		 pathogenic
NM_014014.4(SNRNP200):c.5673C>T (p.Thr1891=) single nucleotide variant Malignant melanoma [RCV000060630] Chr2:96277888 [GRCh38]
Chr2:96943626 [GRCh37]
Chr2:96307353 [NCBI36]
Chr2:2q11.2		 not provided
GRCh38/hg38 2q11.1-11.2(chr2:95493468-96977610)x3 copy number gain See cases [RCV000133839] Chr2:95493468..96977610 [GRCh38]
Chr2:96159216..97643347 [GRCh37]
Chr2:95522943..97007074 [NCBI36]
Chr2:2q11.1-11.2		 uncertain significance
GRCh38/hg38 2q11.1-11.2(chr2:95879602-97029672)x3 copy number gain See cases [RCV000050366] Chr2:95879602..97029672 [GRCh38]
Chr2:96545350..97695409 [GRCh37]
Chr2:95909077..97059136 [NCBI36]
Chr2:2q11.1-11.2		 uncertain significance
GRCh38/hg38 2q11.1-11.2(chr2:95879602-97029672)x1 copy number loss See cases [RCV000134141] Chr2:95879602..97029672 [GRCh38]
Chr2:96545350..97695409 [GRCh37]
Chr2:95909077..97059136 [NCBI36]
Chr2:2q11.1-11.2		 pathogenic
GRCh38/hg38 2q11.2(chr2:96073560-97062710)x1 copy number loss See cases [RCV000135343] Chr2:96073560..97062710 [GRCh38]
Chr2:96739308..97728447 [GRCh37]
Chr2:96103035..97092174 [NCBI36]
Chr2:2q11.2		 pathogenic
GRCh38/hg38 2q11.2(chr2:96100812-97154835)x1 copy number loss See cases [RCV000137012] Chr2:96100812..97154835 [GRCh38]
Chr2:96766560..97820572 [GRCh37]
Chr2:96130287..97184299 [NCBI36]
Chr2:2q11.2		 uncertain significance
GRCh38/hg38 2q11.1-11.2(chr2:95337458-99072953)x3 copy number gain See cases [RCV000138012] Chr2:95337458..99072953 [GRCh38]
Chr2:96003206..99689416 [GRCh37]
Chr2:95366933..99055848 [NCBI36]
Chr2:2q11.1-11.2		 uncertain significance
GRCh38/hg38 2q11.1-11.2(chr2:95766541-97589743)x3 copy number gain See cases [RCV000137817] Chr2:95766541..97589743 [GRCh38]
Chr2:96432289..98206206 [GRCh37]
Chr2:95796016..97572638 [NCBI36]
Chr2:2q11.1-11.2		 uncertain significance
GRCh38/hg38 2q11.1-13(chr2:94678532-110602409)x3 copy number gain See cases [RCV000141075] Chr2:94678532..110602409 [GRCh38]
Chr2:95344257..111359986 [GRCh37]
Chr2:94707984..111076455 [NCBI36]
Chr2:2q11.1-13		 pathogenic
GRCh38/hg38 2q11.2(chr2:96066771-97285797)x3 copy number gain See cases [RCV000142146] Chr2:96066771..97285797 [GRCh38]
Chr2:96732519..98079569 [GRCh37]
Chr2:96096246..97432433 [NCBI36]
Chr2:2q11.2		 uncertain significance
GRCh38/hg38 2q11.2(chr2:96100816-97285797)x3 copy number gain See cases [RCV000142814] Chr2:96100816..97285797 [GRCh38]
Chr2:96766564..98013954 [GRCh37]
Chr2:96130291..97380093 [NCBI36]
Chr2:2q11.2		 uncertain significance
GRCh38/hg38 2q11.2(chr2:96073560-97513144)x1 copy number loss See cases [RCV000142800] Chr2:96073560..97513144 [GRCh38]
Chr2:96739308..98066294 [GRCh37]
Chr2:96103035..97496039 [NCBI36]
Chr2:2q11.2		 pathogenic
GRCh38/hg38 2q11.2(chr2:96073560-97589743)x3 copy number gain See cases [RCV000143142] Chr2:96073560..97589743 [GRCh38]
Chr2:96739308..98206206 [GRCh37]
Chr2:96103035..97572638 [NCBI36]
Chr2:2q11.2		 likely benign
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3 copy number gain not provided [RCV000752802] Chr2:14238..243048760 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q11.1-12.3(chr2:95529039-108518266) copy number gain See cases [RCV000449270] Chr2:95529039..108518266 [GRCh37]
Chr2:2q11.1-12.3		 pathogenic
GRCh37/hg19 2q11.1-13(chr2:95327499-111370025)x4 copy number gain See cases [RCV000446842] Chr2:95327499..111370025 [GRCh37]
Chr2:2q11.1-13		 pathogenic
GRCh37/hg19 2q11.1-11.2(chr2:96544602-98118115)x1 copy number loss See cases [RCV000446002] Chr2:96544602..98118115 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:96698012-97757442)x3 copy number gain See cases [RCV000445685] Chr2:96698012..97757442 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:95691600-100587394) copy number gain See cases [RCV000447723] Chr2:95691600..100587394 [GRCh37]
Chr2:2q11.1-11.2		 pathogenic
NC_000002.11:g.(?_96738407)_(97742073_?)del deletion Schizophrenia [RCV000416822] Chr2:96738407..97742073 [GRCh37]
Chr2:96102134..97105800 [NCBI36]
Chr2:2q11.1-11.2		 likely pathogenic
GRCh37/hg19 2q11.1-11.2(chr2:96778661-97757978)x3 copy number gain See cases [RCV000448583] Chr2:96778661..97757978 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384) copy number gain See cases [RCV000512056] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q11.1-11.2(chr2:96468158-97871906)x3 copy number gain See cases [RCV000511375] Chr2:96468158..97871906 [GRCh37]
Chr2:2q11.1-11.2		 likely pathogenic
GRCh37/hg19 2q11.1-11.2(chr2:96097383-97679933)x1 copy number loss See cases [RCV000511715] Chr2:96097383..97679933 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:96732519-98225552)x3 copy number gain See cases [RCV000511635] Chr2:96732519..98225552 [GRCh37]
Chr2:2q11.1-11.2		 likely benign
GRCh37/hg19 2q11.1-11.2(chr2:96712139-98249638)x1 copy number loss See cases [RCV000511596] Chr2:96712139..98249638 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh37/hg19 2q11.1-12.2(chr2:95518497-107186127) copy number gain See cases [RCV000511158] Chr2:95518497..107186127 [GRCh37]
Chr2:2q11.1-12.2		 uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3 copy number gain See cases [RCV000511212] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
NM_004804.3(CIAO1):c.1016T>C (p.Leu339Pro) single nucleotide variant not specified [RCV004314295] Chr2:96271347 [GRCh38]
Chr2:96937085 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_004804.3(CIAO1):c.646C>T (p.Arg216Cys) single nucleotide variant not specified [RCV004331093] Chr2:96268613 [GRCh38]
Chr2:96934351 [GRCh37]
Chr2:2q11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:96735977-98258828)x1 copy number loss not provided [RCV000682130] Chr2:96735977..98258828 [GRCh37]
Chr2:2q11.1-11.2		 likely pathogenic
GRCh37/hg19 2q11.1-11.2(chr2:96544602-98138405)x1 copy number loss not provided [RCV000682132] Chr2:96544602..98138405 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh37/hg19 2q11.1-13(chr2:96353030-114045463)x3 copy number gain not provided [RCV000682168] Chr2:96353030..114045463 [GRCh37]
Chr2:2q11.1-13		 pathogenic
Single allele deletion not provided [RCV000714264] Chr2:40608411..146900718 [GRCh37]
Chr2:2p22.1-q22.3		 likely pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3 copy number gain not provided [RCV000752804] Chr2:15672..243101834 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
NC_000002.12:g.(?_96063558)_(97079140_?)del deletion Schizophrenia [RCV000754268] Chr2:96063558..97079140 [GRCh38]
Chr2:2q11.2		 likely pathogenic
NC_000002.11:g.(?_96780545)_(96971175_?)dup duplication not provided [RCV001031839] Chr2:96780545..96971175 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
NC_000002.11:g.(?_96780545)_(96994037_?)dup duplication not provided [RCV001031880] Chr2:96780545..96994037 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:96712139-98254657)x1 copy number loss not provided [RCV001005295] Chr2:96712139..98254657 [GRCh37]
Chr2:2q11.1-11.2		 likely pathogenic|uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:96747466-98193473)x1 copy number loss See cases [RCV000790587] Chr2:96747466..98193473 [GRCh37]
Chr2:2q11.1-11.2		 likely pathogenic
GRCh37/hg19 2q11.1-11.2(chr2:96552903-98118115)x1 copy number loss not provided [RCV000848564] Chr2:96552903..98118115 [GRCh37]
Chr2:2q11.1-11.2		 pathogenic
GRCh37/hg19 2q11.1-11.2(chr2:96732519-98118115)x3 copy number gain not provided [RCV001005296] Chr2:96732519..98118115 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:96737083-98193473)x3 copy number gain See cases [RCV001194576] Chr2:96737083..98193473 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:96515883-98025634)x3 copy number gain not provided [RCV000845755] Chr2:96515883..98025634 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:96628608-96981369)x3 copy number gain not provided [RCV002472784] Chr2:96628608..96981369 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh37/hg19 2q11.2(chr2:96939073-97086456)x1 copy number loss not provided [RCV001005297] Chr2:96939073..97086456 [GRCh37]
Chr2:2q11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:96737083-98261802)x1 copy number loss See cases [RCV001194515] Chr2:96737083..98261802 [GRCh37]
Chr2:2q11.1-11.2		 likely pathogenic
NC_000002.12:g.(?_96267321)_(96305437_?)del deletion not provided [RCV001033650] Chr2:96933059..96971175 [GRCh37]
Chr2:2q11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:96515883-98162176)x3 copy number gain not provided [RCV001259641] Chr2:96515883..98162176 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:96421161-97765561)x1 copy number loss not provided [RCV001259642] Chr2:96421161..97765561 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:96544602-97706860)x3 copy number gain not provided [RCV001259643] Chr2:96544602..97706860 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:96755045-98021592) copy number loss Fetal growth restriction [RCV001352673] Chr2:96755045..98021592 [GRCh37]
Chr2:2q11.1-11.2		 pathogenic
Single allele deletion Intellectual disability [RCV001293378] Chr2:96737083..98193473 [GRCh37]
Chr2:2q11.1-11.2		 pathogenic
GRCh37/hg19 2q11.1-11.2(chr2:96544603-98025634)x3 copy number gain not provided [RCV001832989] Chr2:96544603..98025634 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
NC_000002.11:g.(?_96780545)_(97475254_?)dup duplication not provided [RCV001981292] Chr2:96780545..97475254 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373) copy number gain Mosaic trisomy 2 [RCV002280628] Chr2:1..243199373 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2p25.1-q13(chr2:11504318-111365996)x1 copy number loss See cases [RCV002287563] Chr2:11504318..111365996 [GRCh37]
Chr2:2p25.1-q13		 pathogenic
NM_004804.3(CIAO1):c.150G>T (p.Trp50Cys) single nucleotide variant not specified [RCV004322980] Chr2:96267331 [GRCh38]
Chr2:96933069 [GRCh37]
Chr2:2q11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:95341388-100340514)x3 copy number gain not provided [RCV002473932] Chr2:95341388..100340514 [GRCh37]
Chr2:2q11.1-11.2		 likely pathogenic
NM_004804.3(CIAO1):c.98C>T (p.Ser33Leu) single nucleotide variant not specified [RCV004204107] Chr2:96266448 [GRCh38]
Chr2:96932186 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_004804.3(CIAO1):c.683A>G (p.Asn228Ser) single nucleotide variant not specified [RCV004160391] Chr2:96268650 [GRCh38]
Chr2:96934388 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_004804.3(CIAO1):c.440A>G (p.Asn147Ser) single nucleotide variant not specified [RCV004144191] Chr2:96267875 [GRCh38]
Chr2:96933613 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_004804.3(CIAO1):c.217G>A (p.Gly73Ser) single nucleotide variant not specified [RCV004209467] Chr2:96267398 [GRCh38]
Chr2:96933136 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_004804.3(CIAO1):c.77C>T (p.Pro26Leu) single nucleotide variant not specified [RCV004112749] Chr2:96266427 [GRCh38]
Chr2:96932165 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_004804.3(CIAO1):c.829C>T (p.Arg277Cys) single nucleotide variant not specified [RCV004212549] Chr2:96271160 [GRCh38]
Chr2:96936898 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_004804.3(CIAO1):c.349G>A (p.Gly117Ser) single nucleotide variant not specified [RCV004078719] Chr2:96267685 [GRCh38]
Chr2:96933423 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_004804.3(CIAO1):c.655C>T (p.Arg219Cys) single nucleotide variant not specified [RCV004184503] Chr2:96268622 [GRCh38]
Chr2:96934360 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_004804.3(CIAO1):c.487G>C (p.Glu163Gln) single nucleotide variant not specified [RCV004256500] Chr2:96267922 [GRCh38]
Chr2:96933660 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_004804.3(CIAO1):c.1004G>A (p.Arg335Gln) single nucleotide variant not specified [RCV004347139] Chr2:96271335 [GRCh38]
Chr2:96937073 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_004804.3(CIAO1):c.68C>G (p.Ala23Gly) single nucleotide variant not specified [RCV004334649] Chr2:96266418 [GRCh38]
Chr2:96932156 [GRCh37]
Chr2:2q11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:96732520-97671333)x3 copy number gain not provided [RCV003484070] Chr2:96732520..97671333 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
Single allele deletion not provided [RCV003448678] Chr2:96555654..97769352 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:95773428-102550061)x3 copy number gain not provided [RCV003484069] Chr2:95773428..102550061 [GRCh37]
Chr2:2q11.1-11.2		 likely pathogenic
GRCh37/hg19 2q11.1-11.2(chr2:96732520-99142320)x3 copy number gain not provided [RCV003484071] Chr2:96732520..99142320 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
NM_004804.3(CIAO1):c.303C>T (p.Leu101=) single nucleotide variant not provided [RCV003427134] Chr2:96267639 [GRCh38]
Chr2:96933377 [GRCh37]
Chr2:2q11.2		 benign
GRCh37/hg19 2q11.1-11.2(chr2:96735977-98212850)x3 copy number gain not specified [RCV003986352] Chr2:96735977..98212850 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
GRCh37/hg19 2q11.2(chr2:96917560-96934823)x1 copy number loss not specified [RCV003987272] Chr2:96917560..96934823 [GRCh37]
Chr2:2q11.2		 pathogenic
NM_004804.3(CIAO1):c.958G>A (p.Ala320Thr) single nucleotide variant not specified [RCV004441722] Chr2:96271289 [GRCh38]
Chr2:96937027 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_004804.3(CIAO1):c.1006C>G (p.Pro336Ala) single nucleotide variant not specified [RCV004441720] Chr2:96271337 [GRCh38]
Chr2:96937075 [GRCh37]
Chr2:2q11.2		 uncertain significance
GRCh37/hg19 2q11.1-11.2(chr2:96780545-98098961)x1 copy number loss not provided [RCV003885488] Chr2:96780545..98098961 [GRCh37]
Chr2:2q11.1-11.2		 pathogenic
GRCh37/hg19 2q11.1-11.2(chr2:96555654-98024790)x1 copy number loss not provided [RCV004577457] Chr2:96555654..98024790 [GRCh37]
Chr2:2q11.1-11.2		 uncertain significance
NM_004804.3(CIAO1):c.745G>A (p.Gly249Ser) single nucleotide variant not specified [RCV004610618] Chr2:96269321 [GRCh38]
Chr2:96935059 [GRCh37]
Chr2:2q11.2		 uncertain significance
NM_004804.3(CIAO1):c.454G>T (p.Asp152Tyr) single nucleotide variant not specified [RCV004610619] Chr2:96267889 [GRCh38]
Chr2:96933627 [GRCh37]
Chr2:2q11.2		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:900
Count of miRNA genes:595
Interacting mature miRNAs:659
Transcripts:ENST00000272402, ENST00000469320, ENST00000488633, ENST00000491394
Prediction methods: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.

Markers in Region
SHGC-33807  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37296,940,093 - 96,940,242UniSTSGRCh37
Build 36296,303,820 - 96,303,969RGDNCBI36
Celera291,381,281 - 91,381,430RGD
Cytogenetic Map2q11.2UniSTS
HuRef290,901,590 - 90,901,739UniSTS
GeneMap99-GB4 RH Map2356.07UniSTS
Whitehead-RH Map2484.3UniSTS
GeneMap99-G3 RH Map25042.0UniSTS
RH75344  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37296,937,028 - 96,937,246UniSTSGRCh37
Build 36296,300,755 - 96,300,973RGDNCBI36
Celera291,378,216 - 91,378,434RGD
Cytogenetic Map2q11.2UniSTS
HuRef290,898,525 - 90,898,743UniSTS
G29219  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37296,937,099 - 96,937,238UniSTSGRCh37
Build 36296,300,826 - 96,300,965RGDNCBI36
Celera291,378,287 - 91,378,426RGD
Cytogenetic Map2q11.2UniSTS
HuRef290,898,596 - 90,898,735UniSTS
MARC_3297-3298:991936980:1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37296,932,088 - 96,933,079UniSTSGRCh37
Build 36296,295,815 - 96,296,806RGDNCBI36
Celera291,373,276 - 91,374,267RGD
D15S1477  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map4q32-q35UniSTS
Cytogenetic Map5q11UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.1-p11.2UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map16p13.13-p13.12UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q23UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map2q31UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q11.21UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map1q31.3UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map9p13UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map3p25-p24UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map3p12UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map6p21.1-p12.2UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map14q11.1UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map9p22.1UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p24UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q13.1-q13.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map10q25UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map15q21-q23UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map11q12UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map20p11.22-p11.1UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map</