SERPINB10 (serpin family B member 10) - Rat Genome Database

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Gene: SERPINB10 (serpin family B member 10) Homo sapiens
Analyze
Symbol: SERPINB10
Name: serpin family B member 10
RGD ID: 733342
HGNC Page HGNC:8942
Description: Predicted to enable serine-type endopeptidase inhibitor activity. Located in cytosol and nucleoplasm.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: bomapin; peptidase inhibitor 10; PI-10; PI10; protease inhibitor 10 (ovalbumin type); protease inhibitor 10 (ovalbumin type, bomapin); serine (or cysteine) proteinase inhibitor, clade B (ovalbumin), member 10; serpin B10; serpin peptidase inhibitor, clade B (ovalbumin), member 10
RGD Orthologs
Mouse
Rat
Bonobo
Dog
Squirrel
Pig
Green Monkey
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
GRCh381863,907,958 - 63,936,111 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1863,907,958 - 63,936,111 (+)EnsemblGRCh38hg38GRCh38
GRCh371861,575,192 - 61,603,345 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361859,733,725 - 59,753,456 (+)NCBINCBI36Build 36hg18NCBI36
Build 341859,733,724 - 59,753,456NCBI
Celera1858,303,195 - 58,322,926 (+)NCBICelera
Cytogenetic Map18q22.1NCBI
HuRef1858,283,872 - 58,303,602 (+)NCBIHuRef
CHM1_11861,578,935 - 61,598,658 (+)NCBICHM1_1
T2T-CHM13v2.01864,113,032 - 64,141,170 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
5. Transcriptomic characteristics of bronchoalveolar lavage fluid and peripheral blood mononuclear cells in COVID-19 patients. Xiong Y, etal., Emerg Microbes Infect. 2020 Dec;9(1):761-770. doi: 10.1080/22221751.2020.1747363.
Additional References at PubMed
PMID:2690952   PMID:7592909   PMID:9268635   PMID:10196205   PMID:10871600   PMID:12477932   PMID:15489334   PMID:16172807   PMID:20433722   PMID:21873635   PMID:22020285   PMID:22465717  
PMID:23602568   PMID:24172014   PMID:30382768   PMID:33961781   PMID:34445206   PMID:35156780   PMID:35526531   PMID:36398030  


Genomics

Comparative Map Data
SERPINB10
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381863,907,958 - 63,936,111 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1863,907,958 - 63,936,111 (+)EnsemblGRCh38hg38GRCh38
GRCh371861,575,192 - 61,603,345 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361859,733,725 - 59,753,456 (+)NCBINCBI36Build 36hg18NCBI36
Build 341859,733,724 - 59,753,456NCBI
Celera1858,303,195 - 58,322,926 (+)NCBICelera
Cytogenetic Map18q22.1NCBI
HuRef1858,283,872 - 58,303,602 (+)NCBIHuRef
CHM1_11861,578,935 - 61,598,658 (+)NCBICHM1_1
T2T-CHM13v2.01864,113,032 - 64,141,170 (+)NCBIT2T-CHM13v2.0
Serpinb10
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391107,456,724 - 107,488,469 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1107,456,757 - 107,477,001 (+)EnsemblGRCm39 Ensembl
GRCm381107,528,994 - 107,560,742 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1107,529,003 - 107,549,271 (+)EnsemblGRCm38mm10GRCm38
MGSCv371109,425,580 - 109,445,848 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361109,356,550 - 109,374,775 (+)NCBIMGSCv36mm8
Celera1110,367,621 - 110,387,897 (+)NCBICelera
Cytogenetic Map1E2.1NCBI
cM Map150.34NCBI
Serpinb10
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81324,067,971 - 24,085,814 (+)NCBIGRCr8
mRatBN7.21323,553,348 - 23,571,182 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1323,553,430 - 23,571,182 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1323,923,746 - 23,941,500 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01325,208,206 - 25,225,958 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01323,893,933 - 23,911,689 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01327,466,036 - 27,483,789 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1327,465,930 - 27,483,799 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01332,615,876 - 32,633,626 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41313,644,626 - 13,662,376 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11313,619,235 - 13,636,986 (+)NCBI
Celera1323,398,735 - 23,416,948 (+)NCBICelera
Cytogenetic Map13p11NCBI
SERPINB10
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21781,412,650 - 81,441,367 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11867,106,752 - 67,133,985 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01857,262,514 - 57,289,744 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11860,573,607 - 60,600,569 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1860,573,580 - 60,599,697 (+)Ensemblpanpan1.1panPan2
SERPINB10
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1113,233,715 - 13,256,289 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl113,234,402 - 13,256,238 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha114,194,436 - 14,217,040 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0113,088,789 - 13,111,392 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl113,089,377 - 13,111,313 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1113,127,369 - 13,149,973 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0113,056,624 - 13,079,227 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0113,305,669 - 13,328,274 (-)NCBIUU_Cfam_GSD_1.0
LOC101971699
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494426,543,128 - 26,561,355 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364971,782,116 - 1,800,307 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364971,782,142 - 1,797,968 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SERPINB10
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1157,841,510 - 157,866,913 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11157,841,487 - 157,866,913 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21175,328,930 - 175,354,354 (-)NCBISscrofa10.2Sscrofa10.2susScr3
SERPINB10
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11815,878,552 - 15,903,891 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1815,878,191 - 15,894,609 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660609,790,738 - 9,814,961 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in SERPINB10
11 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 18q21.1-23(chr18:50068129-80252149)x3 copy number gain See cases [RCV000050989] Chr18:50068129..80252149 [GRCh38]
Chr18:47594499..78010032 [GRCh37]
Chr18:45848497..76111023 [NCBI36]
Chr18:18q21.1-23		 pathogenic
GRCh38/hg38 18q21.31-23(chr18:56618038-80252149)x1 copy number loss See cases [RCV000051032] Chr18:56618038..80252149 [GRCh38]
Chr18:54285269..78010032 [GRCh37]
Chr18:52436267..76111023 [NCBI36]
Chr18:18q21.31-23		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80252149)x3 copy number gain See cases [RCV000051048] Chr18:148963..80252149 [GRCh38]
Chr18:148963..78010032 [GRCh37]
Chr18:138963..76111023 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q11.1-23(chr18:20960320-80234429)x3 copy number gain See cases [RCV000052543] Chr18:20960320..80234429 [GRCh38]
Chr18:18540281..77992312 [GRCh37]
Chr18:16794279..76093303 [NCBI36]
Chr18:18q11.1-23		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:53345-80209986)x3 copy number gain See cases [RCV000052501] Chr18:53345..80209986 [GRCh38]
Chr18:53345..77967869 [GRCh37]
Chr18:43345..76068860 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q11.1-23(chr18:20989762-80209986)x3 copy number gain See cases [RCV000052549] Chr18:20989762..80209986 [GRCh38]
Chr18:18569723..77967869 [GRCh37]
Chr18:16823721..76068860 [NCBI36]
Chr18:18q11.1-23		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148763-80252290)x3 copy number gain See cases [RCV000052507] Chr18:148763..80252290 [GRCh38]
Chr18:148763..78010173 [GRCh37]
Chr18:138763..76111164 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q12.1-22.1(chr18:29249202-65448117)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052563]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052563]|See cases [RCV000052563] Chr18:29249202..65448117 [GRCh38]
Chr18:26829167..63115353 [GRCh37]
Chr18:25083165..61266333 [NCBI36]
Chr18:18q12.1-22.1		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80244381)x3 copy number gain See cases [RCV000052514] Chr18:148963..80244381 [GRCh38]
Chr18:148963..78002264 [GRCh37]
Chr18:138963..76103255 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q21.33-23(chr18:63195579-80234429)x3 copy number gain See cases [RCV000052572] Chr18:63195579..80234429 [GRCh38]
Chr18:60862812..77992312 [GRCh37]
Chr18:59013792..76093303 [NCBI36]
Chr18:18q21.33-23		 pathogenic
GRCh38/hg38 18q21.2-23(chr18:53637007-80252149)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053869]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053869]|See cases [RCV000053869] Chr18:53637007..80252149 [GRCh38]
Chr18:51163377..78010032 [GRCh37]
Chr18:49417375..76111023 [NCBI36]
Chr18:18q21.2-23		 pathogenic
GRCh38/hg38 18q21.31-23(chr18:56353040-80209986)x1 copy number loss See cases [RCV000053873] Chr18:56353040..80209986 [GRCh38]
Chr18:54020271..77967869 [GRCh37]
Chr18:52171269..76068860 [NCBI36]
Chr18:18q21.31-23		 pathogenic
GRCh38/hg38 18q21.33-23(chr18:62999696-80209986)x1 copy number loss See cases [RCV000053875] Chr18:62999696..80209986 [GRCh38]
Chr18:60666929..77967869 [GRCh37]
Chr18:58817909..76068860 [NCBI36]
Chr18:18q21.33-23		 pathogenic
GRCh38/hg38 18q21.2-23(chr18:51605752-80252149)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053834]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053834]|See cases [RCV000053834] Chr18:51605752..80252149 [GRCh38]
Chr18:49132122..78010032 [GRCh37]
Chr18:47386120..76111023 [NCBI36]
Chr18:18q21.2-23		 pathogenic
GRCh38/hg38 18q21.2-22.1(chr18:52156899-65408762)x1 copy number loss See cases [RCV000053836] Chr18:52156899..65408762 [GRCh38]
Chr18:49683269..63075998 [GRCh37]
Chr18:47937267..61226978 [NCBI36]
Chr18:18q21.2-22.1		 pathogenic
NM_005024.1(SERPINB10):c.547C>A (p.Leu183Met) single nucleotide variant Malignant melanoma [RCV000071878] Chr18:63930101 [GRCh38]
Chr18:61597335 [GRCh37]
Chr18:59748315 [NCBI36]
Chr18:18q22.1		 not provided
NM_005024.1(SERPINB10):c.1085G>A (p.Arg362Gln) single nucleotide variant Malignant melanoma [RCV000071879] Chr18:63935133 [GRCh38]
Chr18:61602367 [GRCh37]
Chr18:59753347 [NCBI36]
Chr18:18q22.1		 not provided
NM_005024.1(SERPINB10):c.71A>G (p.Gln24Arg) single nucleotide variant Malignant melanoma [RCV000063404] Chr18:63915581 [GRCh38]
Chr18:61582815 [GRCh37]
Chr18:59733795 [NCBI36]
Chr18:18q22.1		 not provided
GRCh38/hg38 18q21.32-23(chr18:59567681-80252149)x1 copy number loss See cases [RCV000133689] Chr18:59567681..80252149 [GRCh38]
Chr18:57234913..78010032 [GRCh37]
Chr18:55385893..76111023 [NCBI36]
Chr18:18q21.32-23		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:149089-80234391)x3 copy number gain See cases [RCV000134110] Chr18:149089..80234391 [GRCh38]
Chr18:149089..77992274 [GRCh37]
Chr18:139089..76093265 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q21.33-23(chr18:63306200-80252149)x1 copy number loss See cases [RCV000135838] Chr18:63306200..80252149 [GRCh38]
Chr18:60973433..78010032 [GRCh37]
Chr18:59124413..76111023 [NCBI36]
Chr18:18q21.33-23		 pathogenic
GRCh38/hg38 18q21.33-22.1(chr18:63846473-66558774)x1 copy number loss See cases [RCV000135443] Chr18:63846473..66558774 [GRCh38]
Chr18:61513707..64226011 [GRCh37]
Chr18:59664687..62376991 [NCBI36]
Chr18:18q21.33-22.1		 pathogenic
GRCh38/hg38 18q21.33-23(chr18:61576009-80252149)x1 copy number loss See cases [RCV000135616] Chr18:61576009..80252149 [GRCh38]
Chr18:59243242..78010032 [GRCh37]
Chr18:57394222..76111023 [NCBI36]
Chr18:18q21.33-23		 pathogenic
GRCh38/hg38 18q21.2-23(chr18:51190429-80252149)x1 copy number loss See cases [RCV000135413] Chr18:51190429..80252149 [GRCh38]
Chr18:48716799..78010032 [GRCh37]
Chr18:46970797..76111023 [NCBI36]
Chr18:18q21.2-23		 pathogenic
GRCh38/hg38 18q21.33-23(chr18:61827111-80252149)x1 copy number loss See cases [RCV000135567] Chr18:61827111..80252149 [GRCh38]
Chr18:59494344..78010032 [GRCh37]
Chr18:57645324..76111023 [NCBI36]
Chr18:18q21.33-23		 pathogenic|uncertain significance
GRCh38/hg38 18q12.2-22.1(chr18:38794728-65632804)x3 copy number gain See cases [RCV000136910] Chr18:38794728..65632804 [GRCh38]
Chr18:36374692..63300040 [GRCh37]
Chr18:34628690..61451020 [NCBI36]
Chr18:18q12.2-22.1		 pathogenic
GRCh38/hg38 18q12.1-23(chr18:32123105-80252149)x3 copy number gain See cases [RCV000136890] Chr18:32123105..80252149 [GRCh38]
Chr18:29703068..78010032 [GRCh37]
Chr18:27957066..76111023 [NCBI36]
Chr18:18q12.1-23		 pathogenic
GRCh38/hg38 18q21.2-23(chr18:53865057-80252149)x1 copy number loss See cases [RCV000136674] Chr18:53865057..80252149 [GRCh38]
Chr18:51391427..78010032 [GRCh37]
Chr18:49645425..76111023 [NCBI36]
Chr18:18q21.2-23		 pathogenic
GRCh38/hg38 18q21.1-23(chr18:49199411-80254946)x3 copy number gain See cases [RCV000137342] Chr18:49199411..80254946 [GRCh38]
Chr18:46725781..78012829 [GRCh37]
Chr18:44979779..76113817 [NCBI36]
Chr18:18q21.1-23		 pathogenic
GRCh38/hg38 18q21.2-23(chr18:55179364-80254946)x1 copy number loss See cases [RCV000137375] Chr18:55179364..80254946 [GRCh38]
Chr18:52846595..78012829 [GRCh37]
Chr18:50997593..76113817 [NCBI36]
Chr18:18q21.2-23		 pathogenic
GRCh38/hg38 18q12.3-23(chr18:42651392-80254946)x3 copy number gain See cases [RCV000138034] Chr18:42651392..80254946 [GRCh38]
Chr18:40231357..78012829 [GRCh37]
Chr18:38485355..76113817 [NCBI36]
Chr18:18q12.3-23		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:118760-80254946)x3 copy number gain See cases [RCV000138656] Chr18:118760..80254946 [GRCh38]
Chr18:118760..78012829 [GRCh37]
Chr18:108760..76113817 [NCBI36]
Chr18:18p11.32-q23		 pathogenic|conflicting data from submitters
GRCh38/hg38 18p11.32-q23(chr18:149089-80254936)x3 copy number gain See cases [RCV000139397] Chr18:149089..80254936 [GRCh38]
Chr18:149089..78012819 [GRCh37]
Chr18:139089..76113807 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q21.2-23(chr18:52421052-80254946)x1 copy number loss See cases [RCV000139134] Chr18:52421052..80254946 [GRCh38]
Chr18:49947422..78012829 [GRCh37]
Chr18:48201420..76113817 [NCBI36]
Chr18:18q21.2-23		 pathogenic
GRCh38/hg38 18q21.33-22.1(chr18:63144445-64588458)x3 copy number gain See cases [RCV000139938] Chr18:63144445..64588458 [GRCh38]
Chr18:60811678..62255693 [GRCh37]
Chr18:58962658..60406673 [NCBI36]
Chr18:18q21.33-22.1		 uncertain significance
GRCh38/hg38 18q21.2-23(chr18:53959828-80254936)x3 copy number gain See cases [RCV000139496] Chr18:53959828..80254936 [GRCh38]
Chr18:51486198..78012819 [GRCh37]
Chr18:49740196..76113807 [NCBI36]
Chr18:18q21.2-23		 pathogenic
GRCh38/hg38 18q21.32-23(chr18:59996934-80254946)x1 copy number loss See cases [RCV000139669] Chr18:59996934..80254946 [GRCh38]
Chr18:57664166..78012829 [GRCh37]
Chr18:55815146..76113817 [NCBI36]
Chr18:18q21.32-23		 pathogenic
GRCh38/hg38 18q21.33-23(chr18:63756916-80254946)x1 copy number loss See cases [RCV000139464] Chr18:63756916..80254946 [GRCh38]
Chr18:61424150..78012829 [GRCh37]
Chr18:59575130..76113817 [NCBI36]
Chr18:18q21.33-23		 pathogenic
GRCh38/hg38 18q21.33-23(chr18:61613338-80252090)x1 copy number loss See cases [RCV000141429] Chr18:61613338..80252090 [GRCh38]
Chr18:59280571..78009973 [GRCh37]
Chr18:57431551..76110964 [NCBI36]
Chr18:18q21.33-23		 pathogenic
GRCh38/hg38 18q21.2-23(chr18:51167159-80256240)x1 copy number loss See cases [RCV000140925] Chr18:51167159..80256240 [GRCh38]
Chr18:48693529..78014123 [GRCh37]
Chr18:46947527..76115097 [NCBI36]
Chr18:18q21.2-23		 pathogenic
GRCh38/hg38 18q21.33-22.1(chr18:63819028-66637566)x1 copy number loss See cases [RCV000141990] Chr18:63819028..66637566 [GRCh38]
Chr18:61486262..64304803 [GRCh37]
Chr18:59637242..62455783 [NCBI36]
Chr18:18q21.33-22.1		 uncertain significance
GRCh38/hg38 18p11.32-q23(chr18:136227-80256240)x3 copy number gain See cases [RCV000142244] Chr18:136227..80256240 [GRCh38]
Chr18:136227..78014123 [GRCh37]
Chr18:126227..76115097 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18q12.3-23(chr18:40367455-80256240)x3 copy number gain See cases [RCV000142227] Chr18:40367455..80256240 [GRCh38]
Chr18:37947419..78014123 [GRCh37]
Chr18:36201417..76115097 [NCBI36]
Chr18:18q12.3-23		 pathogenic
GRCh38/hg38 18q11.1-22.3(chr18:20962119-74691446)x3 copy number gain See cases [RCV000143057] Chr18:20962119..74691446 [GRCh38]
Chr18:18542080..72403402 [GRCh37]
Chr18:16796078..70532390 [NCBI36]
Chr18:18q11.1-22.3		 pathogenic
GRCh38/hg38 18q21.32-22.3(chr18:59909593-72609801)x3 copy number gain See cases [RCV000143195] Chr18:59909593..72609801 [GRCh38]
Chr18:57576825..70277036 [GRCh37]
Chr18:55727805..68428016 [NCBI36]
Chr18:18q21.32-22.3		 likely pathogenic
GRCh38/hg38 18p11.32-q23(chr18:136226-80256240)x3 copy number gain See cases [RCV000143218] Chr18:136226..80256240 [GRCh38]
Chr18:136226..78014123 [GRCh37]
Chr18:126226..76115097 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh38/hg38 18p11.32-q23(chr18:148963-80252149)x3 copy number gain See cases [RCV000148072] Chr18:148963..80252149 [GRCh38]
Chr18:148963..78010032 [GRCh37]
Chr18:138963..76111023 [NCBI36]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:163323-78005236)x3 copy number gain See cases [RCV000240130] Chr18:163323..78005236 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
Single allele complex Breast ductal adenocarcinoma [RCV000207027] Chr18:61387312..63489378 [GRCh37]
Chr18:18q21.33-22.1		 uncertain significance
GRCh37/hg19 18q21.32-22.2(chr18:58014591-68158862)x1 copy number loss See cases [RCV000240432] Chr18:58014591..68158862 [GRCh37]
Chr18:18q21.32-22.2		 pathogenic
GRCh37/hg19 18q11.1-23(chr18:18548019-77954165)x3 copy number gain See cases [RCV000240476] Chr18:18548019..77954165 [GRCh37]
Chr18:18q11.1-23		 pathogenic
GRCh37/hg19 18q21.32-23(chr18:58525322-78005236)x3 copy number gain See cases [RCV000240296] Chr18:58525322..78005236 [GRCh37]
Chr18:18q21.32-23		 pathogenic
GRCh37/hg19 18q21.33-23(chr18:59461447-78010032)x1 copy number loss not provided [RCV000416006] Chr18:59461447..78010032 [GRCh37]
Chr18:18q21.33-23		 likely pathogenic
GRCh37/hg19 18q21.31-22.3(chr18:55793243-68705548)x1 copy number loss See cases [RCV000449209] Chr18:55793243..68705548 [GRCh37]
Chr18:18q21.31-22.3		 pathogenic
GRCh37/hg19 18q21.33-23(chr18:59332806-78014123)x1 copy number loss See cases [RCV000449163] Chr18:59332806..78014123 [GRCh37]
Chr18:18q21.33-23		 pathogenic
GRCh37/hg19 18q21.2-22.1(chr18:50739715-63705988)x1 copy number loss See cases [RCV000446087] Chr18:50739715..63705988 [GRCh37]
Chr18:18q21.2-22.1		 pathogenic
GRCh37/hg19 18q21.33-23(chr18:60641553-78014123)x1 copy number loss See cases [RCV000447127] Chr18:60641553..78014123 [GRCh37]
Chr18:18q21.33-23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:136226-78014123)x3 copy number gain See cases [RCV000446047] Chr18:136226..78014123 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18q21.33-23(chr18:60796196-78014123)x1 copy number loss See cases [RCV000446171] Chr18:60796196..78014123 [GRCh37]
Chr18:18q21.33-23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:163323-78005185)x3 copy number gain See cases [RCV000445851] Chr18:163323..78005185 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18q21.33-22.1(chr18:61249958-62516230)x3 copy number gain See cases [RCV000445966] Chr18:61249958..62516230 [GRCh37]
Chr18:18q21.33-22.1		 likely benign
GRCh37/hg19 18q21.2-23(chr18:50224898-78014123)x1 copy number loss See cases [RCV000510720] Chr18:50224898..78014123 [GRCh37]
Chr18:18q21.2-23		 likely pathogenic
GRCh37/hg19 18q21.2-23(chr18:53100584-78014123)x1 copy number loss See cases [RCV000445943] Chr18:53100584..78014123 [GRCh37]
Chr18:18q21.2-23		 pathogenic
GRCh37/hg19 18q21.1-23(chr18:47656799-78014123)x1 copy number loss See cases [RCV000447931] Chr18:47656799..78014123 [GRCh37]
Chr18:18q21.1-23		 pathogenic
GRCh37/hg19 18q21.2-23(chr18:52837852-77989426)x1 copy number loss See cases [RCV000448656] Chr18:52837852..77989426 [GRCh37]
Chr18:18q21.2-23		 pathogenic
GRCh37/hg19 18q21.31-23(chr18:54462182-78014123)x1 copy number loss See cases [RCV000512059] Chr18:54462182..78014123 [GRCh37]
Chr18:18q21.31-23		 pathogenic
GRCh37/hg19 18q12.2-23(chr18:33417216-78014123)x3 copy number gain See cases [RCV000512081] Chr18:33417216..78014123 [GRCh37]
Chr18:18q12.2-23		 pathogenic
GRCh37/hg19 18q21.1-23(chr18:47454437-78014123)x3 copy number gain See cases [RCV000510655] Chr18:47454437..78014123 [GRCh37]
Chr18:18q21.1-23		 pathogenic
GRCh37/hg19 18q21.33-23(chr18:59809990-78014123)x1 copy number loss See cases [RCV000510685] Chr18:59809990..78014123 [GRCh37]
Chr18:18q21.33-23		 pathogenic
GRCh37/hg19 18q21.1-23(chr18:43776770-78014123)x3 copy number gain See cases [RCV000511394] Chr18:43776770..78014123 [GRCh37]
Chr18:18q21.1-23		 pathogenic
GRCh37/hg19 18q11.1-22.1(chr18:18521285-64495798)x3 copy number gain See cases [RCV000511734] Chr18:18521285..64495798 [GRCh37]
Chr18:18q11.1-22.1		 pathogenic
GRCh37/hg19 18p11.21-q23(chr18:14869204-78014123)x3 copy number gain See cases [RCV000512030] Chr18:14869204..78014123 [GRCh37]
Chr18:18p11.21-q23		 pathogenic
GRCh37/hg19 18q21.1-23(chr18:46177798-78014123)x1 copy number loss See cases [RCV000511759] Chr18:46177798..78014123 [GRCh37]
Chr18:18q21.1-23		 pathogenic
GRCh37/hg19 18q12.3-23(chr18:42930373-78014123)x3 copy number gain See cases [RCV000511203] Chr18:42930373..78014123 [GRCh37]
Chr18:18q12.3-23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:136227-78014123) copy number gain See cases [RCV000511189] Chr18:136227..78014123 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18q21.33-23(chr18:59876469-78014123)x1 copy number loss See cases [RCV000511105] Chr18:59876469..78014123 [GRCh37]
Chr18:18q21.33-23		 pathogenic
Single allele deletion Deletion of long arm of chromosome 18 [RCV000768454] Chr18:58024137..77996821 [GRCh37]
Chr18:18q21.32-23		 pathogenic
GRCh37/hg19 18q12.1-23(chr18:31879854-78014123)x3 copy number gain See cases [RCV000512425] Chr18:31879854..78014123 [GRCh37]
Chr18:18q12.1-23		 pathogenic
GRCh37/hg19 18q21.32-23(chr18:58768873-78014123)x1 copy number loss See cases [RCV000512579] Chr18:58768873..78014123 [GRCh37]
Chr18:18q21.32-23		 pathogenic
GRCh37/hg19 18q21.33-22.1(chr18:61486262-64304803)x1 copy number loss not provided [RCV000684033] Chr18:61486262..64304803 [GRCh37]
Chr18:18q21.33-22.1		 uncertain significance
GRCh37/hg19 18q21.31-22.3(chr18:55083032-72743857)x1 copy number loss not provided [RCV000684056] Chr18:55083032..72743857 [GRCh37]
Chr18:18q21.31-22.3		 pathogenic
GRCh37/hg19 18q21.32-23(chr18:56905884-78014123)x1 copy number loss not provided [RCV000684058] Chr18:56905884..78014123 [GRCh37]
Chr18:18q21.32-23		 pathogenic
GRCh37/hg19 18q21.31-23(chr18:55298900-78014123)x1 copy number loss not provided [RCV000684059] Chr18:55298900..78014123 [GRCh37]
Chr18:18q21.31-23		 pathogenic
GRCh37/hg19 18q21.1-23(chr18:46942427-78014123)x1 copy number loss not provided [RCV000684060] Chr18:46942427..78014123 [GRCh37]
Chr18:18q21.1-23		 pathogenic
GRCh37/hg19 18q21.33-23(chr18:60416709-78014123)x1 copy number loss not provided [RCV000684055] Chr18:60416709..78014123 [GRCh37]
Chr18:18q21.33-23		 pathogenic
GRCh37/hg19 18q21.2-23(chr18:52802515-78015180)x1 copy number loss not provided [RCV000739824] Chr18:52802515..78015180 [GRCh37]
Chr18:18q21.2-23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:12842-78015180)x3 copy number gain not provided [RCV000752245] Chr18:12842..78015180 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:13034-78015180)x3 copy number gain not provided [RCV000752246] Chr18:13034..78015180 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18q21.32-22.1(chr18:57244903-63722436)x1 copy number loss not provided [RCV000752355] Chr18:57244903..63722436 [GRCh37]
Chr18:18q21.32-22.1		 benign
GRCh37/hg19 18q21.32-23(chr18:57244903-77325446)x1 copy number loss not provided [RCV000752356] Chr18:57244903..77325446 [GRCh37]
Chr18:18q21.32-23		 pathogenic
GRCh37/hg19 18q21.33-23(chr18:59585959-78015180)x1 copy number loss not provided [RCV000752366] Chr18:59585959..78015180 [GRCh37]
Chr18:18q21.33-23		 pathogenic
GRCh37/hg19 18q21.33-23(chr18:60098018-78014123)x1 copy number loss not provided [RCV001007019] Chr18:60098018..78014123 [GRCh37]
Chr18:18q21.33-23		 pathogenic
Single allele deletion Deletion of long arm of chromosome 18 [RCV002280357] Chr18:61490305..80247612 [GRCh38]
Chr18:18q21.33-23		 pathogenic
GRCh37/hg19 18q21.33-22.1(chr18:61388176-62052163)x1 copy number loss not provided [RCV000847942] Chr18:61388176..62052163 [GRCh37]
Chr18:18q21.33-22.1		 uncertain significance
GRCh37/hg19 18q21.32-23(chr18:56750525-78014123)x1 copy number loss not provided [RCV001007018] Chr18:56750525..78014123 [GRCh37]
Chr18:18q21.32-23		 pathogenic
GRCh37/hg19 18q21.2-23(chr18:49460596-78014123)x1 copy number loss not provided [RCV001007016] Chr18:49460596..78014123 [GRCh37]
Chr18:18q21.2-23		 pathogenic
GRCh37/hg19 18q21.31-23(chr18:55458425-78014123)x1 copy number loss not provided [RCV001007017] Chr18:55458425..78014123 [GRCh37]
Chr18:18q21.31-23		 pathogenic
NM_005024.3(SERPINB10):c.543G>T (p.Met181Ile) single nucleotide variant Inborn genetic diseases [RCV003251743] Chr18:63930097 [GRCh38]
Chr18:61597331 [GRCh37]
Chr18:18q22.1		 uncertain significance
NM_005024.3(SERPINB10):c.977C>T (p.Ser326Phe) single nucleotide variant Inborn genetic diseases [RCV003274623] Chr18:63935025 [GRCh38]
Chr18:61602259 [GRCh37]
Chr18:18q22.1		 uncertain significance
GRCh37/hg19 18q21.33-22.1(chr18:61483089-64304841)x1 copy number loss not provided [RCV002473560] Chr18:61483089..64304841 [GRCh37]
Chr18:18q21.33-22.1		 uncertain significance
GRCh37/hg19 18q11.2-23(chr18:23626739-78014976)x3 copy number gain not provided [RCV001537911] Chr18:23626739..78014976 [GRCh37]
Chr18:18q11.2-23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:1-78077248) copy number gain Trisomy 18 [RCV002280660] Chr18:1..78077248 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18q21.2-23(chr18:51925586-78010032) copy number gain Global developmental delay [RCV001352665] Chr18:51925586..78010032 [GRCh37]
Chr18:18q21.2-23		 pathogenic
GRCh37/hg19 18q21.31-23(chr18:54285235-77960815)x1 copy number loss not provided [RCV001531449] Chr18:54285235..77960815 [GRCh37]
Chr18:18q21.31-23		 pathogenic
GRCh37/hg19 18q21.33-23(chr18:61289055-78014123) copy number loss Deletion of long arm of chromosome 18 [RCV002280712] Chr18:61289055..78014123 [GRCh37]
Chr18:18q21.33-23		 pathogenic
GRCh37/hg19 18q21.1-23(chr18:47656799-78014123) copy number loss not specified [RCV002052636] Chr18:47656799..78014123 [GRCh37]
Chr18:18q21.1-23		 pathogenic
GRCh37/hg19 18q21.2-23(chr18:52837852-77989426) copy number loss not specified [RCV002052642] Chr18:52837852..77989426 [GRCh37]
Chr18:18q21.2-23		 pathogenic
GRCh37/hg19 18q21.2-23(chr18:53100584-78014123) copy number loss not specified [RCV002052643] Chr18:53100584..78014123 [GRCh37]
Chr18:18q21.2-23		 pathogenic
GRCh37/hg19 18q21.2-23(chr18:53309113-78014123) copy number loss not specified [RCV002052646] Chr18:53309113..78014123 [GRCh37]
Chr18:18q21.2-23		 pathogenic
GRCh37/hg19 18p11.32-q23(chr18:136226-78014123) copy number gain not specified [RCV002052616] Chr18:136226..78014123 [GRCh37]
Chr18:18p11.32-q23		 pathogenic
GRCh37/hg19 18q21.2-23(chr18:52675201-78014123) copy number loss not specified [RCV002052641] Chr18:52675201..78014123 [GRCh37]
Chr18:18q21.2-23		 pathogenic
GRCh37/hg19 18q21.32-23(chr18:58305972-78014123) copy number loss not specified [RCV002052647] Chr18:58305972..78014123 [GRCh37]
Chr18:18q21.32-23		 pathogenic
GRCh37/hg19 18q21.2-22.1(chr18:50739715-63705988) copy number loss not specified [RCV002052639] Chr18:50739715..63705988 [GRCh37]
Chr18:18q21.2-22.1		 pathogenic
GRCh37/hg19 18q21.33-23(chr18:59332806-78014123) copy number loss not specified [RCV002052649] Chr18:59332806..78014123 [GRCh37]
Chr18:18q21.33-23		 pathogenic
NC_000018.9:g.(?_59713089)_(61654512_?)del deletion Multiple congenital anomalies-hypotonia-seizures syndrome 1 [RCV001898809]|not provided [RCV001909119] Chr18:59713089..61654512 [GRCh37]
Chr18:18q21.33-22.1		 pathogenic|no classifications from unflagged records
NC_000018.9:g.(?_59713089)_(61654512_?)dup duplication Multiple congenital anomalies-hypotonia-seizures syndrome 1 [RCV002029497] Chr18:59713089..61654512 [GRCh37]
Chr18:18q21.33-22.1		 uncertain significance
GRCh37/hg19 18q21.2-23(chr18:53624405-78014123)x1 copy number loss not provided [RCV002473956] Chr18:53624405..78014123 [GRCh37]
Chr18:18q21.2-23		 pathogenic
GRCh37/hg19 18q21.33-23(chr18:61520071-78014123)x1 copy number loss not provided [RCV002472513] Chr18:61520071..78014123 [GRCh37]
Chr18:18q21.33-23		 pathogenic
NM_005024.3(SERPINB10):c.1112A>G (p.Asn371Ser) single nucleotide variant Inborn genetic diseases [RCV003012762] Chr18:63935160 [GRCh38]
Chr18:61602394 [GRCh37]
Chr18:18q22.1		 uncertain significance
NM_005024.3(SERPINB10):c.551T>G (p.Val184Gly) single nucleotide variant Inborn genetic diseases [RCV002661761] Chr18:63930105 [GRCh38]
Chr18:61597339 [GRCh37]
Chr18:18q22.1		 uncertain significance
NM_005024.3(SERPINB10):c.734G>A (p.Ser245Asn) single nucleotide variant Inborn genetic diseases [RCV002809349] Chr18:63933148 [GRCh38]
Chr18:61600382 [GRCh37]
Chr18:18q22.1		 likely benign
NM_005024.3(SERPINB10):c.251A>G (p.Asn84Ser) single nucleotide variant Inborn genetic diseases [RCV003191739] Chr18:63917981 [GRCh38]
Chr18:61585215 [GRCh37]
Chr18:18q22.1		 uncertain significance
GRCh37/hg19 18q21.33-23(chr18:60771809-78014123)x1 copy number loss not provided [RCV003483341] Chr18:60771809..78014123 [GRCh37]
Chr18:18q21.33-23		 pathogenic
GRCh37/hg19 18q21.32-22.3(chr18:58508272-70495604)x3 copy number gain not specified [RCV003986100] Chr18:58508272..70495604 [GRCh37]
Chr18:18q21.32-22.3		 likely pathogenic
GRCh37/hg19 18q21.2-23(chr18:48766173-78014123)x1 copy number loss not specified [RCV003986103] Chr18:48766173..78014123 [GRCh37]
Chr18:18q21.2-23		 pathogenic
GRCh37/hg19 18q21.31-23(chr18:55363398-78014123)x1 copy number loss not specified [RCV003987273] Chr18:55363398..78014123 [GRCh37]
Chr18:18q21.31-23		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:290
Count of miRNA genes:230
Interacting mature miRNAs:237
Transcripts:ENST00000238508, ENST00000397996, ENST00000418725
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

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

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

Markers in Region
RH118875  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,597,147 - 61,597,469UniSTSGRCh37
Build 361859,748,127 - 59,748,449RGDNCBI36
Celera1858,317,597 - 58,317,919RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,298,274 - 58,298,596UniSTS
D18S80  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,602,417 - 61,602,582UniSTSGRCh37
Build 361859,753,397 - 59,753,562RGDNCBI36
Celera1858,322,867 - 58,323,032RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,303,543 - 58,303,708UniSTS
ECD00046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,585,596 - 61,586,544UniSTSGRCh37
Build 361859,736,576 - 59,737,524RGDNCBI36
Celera1858,306,046 - 58,306,994RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,286,722 - 58,287,670UniSTS
ECD00078  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,583,631 - 61,584,571UniSTSGRCh37
Build 361859,734,611 - 59,735,551RGDNCBI36
Celera1858,304,081 - 58,305,021RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,284,757 - 58,285,697UniSTS
ECD00885  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,586,581 - 61,587,466UniSTSGRCh37
Build 361859,737,561 - 59,738,446RGDNCBI36
Celera1858,307,031 - 58,307,916RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,287,707 - 58,288,592UniSTS
ECD03508  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,584,704 - 61,585,496UniSTSGRCh37
Build 361859,735,684 - 59,736,476RGDNCBI36
Celera1858,305,154 - 58,305,946RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,285,830 - 58,286,622UniSTS
ECD06245  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,595,071 - 61,595,784UniSTSGRCh37
Build 361859,746,051 - 59,746,764RGDNCBI36
Celera1858,315,521 - 58,316,234RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,296,197 - 58,296,910UniSTS
ECD07162  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,600,671 - 61,601,359UniSTSGRCh37
Build 361859,751,651 - 59,752,339RGDNCBI36
Celera1858,321,121 - 58,321,809RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,301,798 - 58,302,485UniSTS
ECD07242  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,582,780 - 61,583,466UniSTSGRCh37
Build 361859,733,760 - 59,734,446RGDNCBI36
Celera1858,303,230 - 58,303,916RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,283,907 - 58,284,593UniSTS
ECD08470  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,601,519 - 61,602,172UniSTSGRCh37
Build 361859,752,499 - 59,753,152RGDNCBI36
Celera1858,321,969 - 58,322,622RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,302,645 - 58,303,298UniSTS
ECD09863  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,597,051 - 61,597,668UniSTSGRCh37
Build 361859,748,031 - 59,748,648RGDNCBI36
Celera1858,317,501 - 58,318,118RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,298,178 - 58,298,795UniSTS
ECD11820  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,600,050 - 61,600,610UniSTSGRCh37
Build 361859,751,030 - 59,751,590RGDNCBI36
Celera1858,320,500 - 58,321,060RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,301,177 - 58,301,737UniSTS
ECD12357  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,590,218 - 61,590,763UniSTSGRCh37
Build 361859,741,198 - 59,741,743RGDNCBI36
Celera1858,310,668 - 58,311,213RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,291,344 - 58,291,889UniSTS
ECD14285  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,589,424 - 61,589,920UniSTSGRCh37
Build 361859,740,404 - 59,740,900RGDNCBI36
Celera1858,309,874 - 58,310,370RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,290,550 - 58,291,046UniSTS
ECD15663  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,598,354 - 61,598,818UniSTSGRCh37
Build 361859,749,334 - 59,749,798RGDNCBI36
Celera1858,318,804 - 58,319,268RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,299,481 - 58,299,945UniSTS
ECD16782  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,602,229 - 61,602,654UniSTSGRCh37
Build 361859,753,209 - 59,753,634RGDNCBI36
Celera1858,322,679 - 58,323,104RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,303,355 - 58,303,780UniSTS
ECD18152  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,597,878 - 61,598,248UniSTSGRCh37
Build 361859,748,858 - 59,749,228RGDNCBI36
Celera1858,318,328 - 58,318,698RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,299,005 - 58,299,375UniSTS
ECD19339  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,596,562 - 61,596,886UniSTSGRCh37
GRCh371018,318,376 - 18,318,700UniSTSGRCh37
Build 361018,358,382 - 18,358,706RGDNCBI36
Celera1858,317,012 - 58,317,336UniSTS
Celera1018,004,867 - 18,005,191RGD
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map18q21.3UniSTS
HuRef1858,297,688 - 58,298,012UniSTS
HuRef1017,984,398 - 17,984,722UniSTS
ECD20867  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,591,393 - 61,591,661UniSTSGRCh37
Build 361859,742,373 - 59,742,641RGDNCBI36
Celera1858,311,843 - 58,312,111RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,292,519 - 58,292,787UniSTS
ECD21712  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,596,178 - 61,596,419UniSTSGRCh37
GRCh371018,318,843 - 18,319,084UniSTSGRCh37
Build 361018,358,849 - 18,359,090RGDNCBI36
Celera1858,316,628 - 58,316,869UniSTS
Celera1018,005,334 - 18,005,575RGD
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map18q21.3UniSTS
HuRef1858,297,304 - 58,297,545UniSTS
HuRef1017,984,865 - 17,985,106UniSTS
ECD21886  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,582,035 - 61,582,270UniSTSGRCh37
Build 361859,733,015 - 59,733,250RGDNCBI36
Celera1858,302,485 - 58,302,720RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,283,162 - 58,283,397UniSTS
ECD21986  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,594,201 - 61,594,433UniSTSGRCh37
Build 361859,745,181 - 59,745,413RGDNCBI36
Celera1858,314,651 - 58,314,883RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,295,327 - 58,295,559UniSTS
ECD22762  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,591,885 - 61,592,093UniSTSGRCh37
Build 361859,742,865 - 59,743,073RGDNCBI36
Celera1858,312,335 - 58,312,543RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,293,011 - 58,293,219UniSTS
REN11850  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,580,785 - 61,581,010UniSTSGRCh37
Build 361859,731,765 - 59,731,990RGDNCBI36
Celera1858,301,244 - 58,301,469RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,281,921 - 58,282,146UniSTS
REN11851  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,580,971 - 61,581,233UniSTSGRCh37
Build 361859,731,951 - 59,732,213RGDNCBI36
Celera1858,301,430 - 58,301,684RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,282,107 - 58,282,361UniSTS
REN11852  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,581,214 - 61,581,438UniSTSGRCh37
Build 361859,732,194 - 59,732,418RGDNCBI36
Celera1858,301,664 - 58,301,888RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,282,341 - 58,282,565UniSTS
REN11853  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,581,405 - 61,581,638UniSTSGRCh37
Build 361859,732,385 - 59,732,618RGDNCBI36
Celera1858,301,855 - 58,302,088RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,282,532 - 58,282,765UniSTS
REN11854  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,581,540 - 61,581,764UniSTSGRCh37
Build 361859,732,520 - 59,732,744RGDNCBI36
Celera1858,301,990 - 58,302,214RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,282,667 - 58,282,891UniSTS
REN11855  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,581,737 - 61,581,961UniSTSGRCh37
Build 361859,732,717 - 59,732,941RGDNCBI36
Celera1858,302,187 - 58,302,411RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,282,864 - 58,283,088UniSTS
REN11856  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,581,936 - 61,582,205UniSTSGRCh37
Build 361859,732,916 - 59,733,185RGDNCBI36
Celera1858,302,386 - 58,302,655RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,283,063 - 58,283,332UniSTS
REN11857  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,582,193 - 61,582,442UniSTSGRCh37
Build 361859,733,173 - 59,733,422RGDNCBI36
Celera1858,302,643 - 58,302,892RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,283,320 - 58,283,569UniSTS
REN11858  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,582,414 - 61,582,638UniSTSGRCh37
Build 361859,733,394 - 59,733,618RGDNCBI36
Celera1858,302,864 - 58,303,088RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,283,541 - 58,283,765UniSTS
REN11859  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,582,633 - 61,582,878UniSTSGRCh37
Build 361859,733,613 - 59,733,858RGDNCBI36
Celera1858,303,083 - 58,303,328RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,283,760 - 58,284,005UniSTS
REN11860  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,582,845 - 61,583,096UniSTSGRCh37
Build 361859,733,825 - 59,734,076RGDNCBI36
Celera1858,303,295 - 58,303,546RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,283,972 - 58,284,223UniSTS
REN11861  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,583,059 - 61,583,296UniSTSGRCh37
Build 361859,734,039 - 59,734,276RGDNCBI36
Celera1858,303,509 - 58,303,746RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,284,186 - 58,284,423UniSTS
REN11862  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,583,271 - 61,583,522UniSTSGRCh37
Build 361859,734,251 - 59,734,502RGDNCBI36
Celera1858,303,721 - 58,303,972RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,284,398 - 58,284,649UniSTS
REN11863  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,583,497 - 61,583,740UniSTSGRCh37
Build 361859,734,477 - 59,734,720RGDNCBI36
Celera1858,303,947 - 58,304,190RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,284,624 - 58,284,866UniSTS
REN11864  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,583,719 - 61,583,974UniSTSGRCh37
Build 361859,734,699 - 59,734,954RGDNCBI36
Celera1858,304,169 - 58,304,424RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,284,845 - 58,285,100UniSTS
REN11865  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,583,954 - 61,584,207UniSTSGRCh37
Build 361859,734,934 - 59,735,187RGDNCBI36
Celera1858,304,404 - 58,304,657RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,285,080 - 58,285,333UniSTS
REN11866  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,584,184 - 61,584,438UniSTSGRCh37
Build 361859,735,164 - 59,735,418RGDNCBI36
Celera1858,304,634 - 58,304,888RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,285,310 - 58,285,564UniSTS
REN11867  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,584,425 - 61,584,675UniSTSGRCh37
Build 361859,735,405 - 59,735,655RGDNCBI36
Celera1858,304,875 - 58,305,125RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,285,551 - 58,285,801UniSTS
REN11868  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,584,585 - 61,584,855UniSTSGRCh37
Build 361859,735,565 - 59,735,835RGDNCBI36
Celera1858,305,035 - 58,305,305RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,285,711 - 58,285,981UniSTS
REN11869  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,584,824 - 61,585,048UniSTSGRCh37
Build 361859,735,804 - 59,736,028RGDNCBI36
Celera1858,305,274 - 58,305,498RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,285,950 - 58,286,174UniSTS
REN11870  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,585,020 - 61,585,270UniSTSGRCh37
Build 361859,736,000 - 59,736,250RGDNCBI36
Celera1858,305,470 - 58,305,720RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,286,146 - 58,286,396UniSTS
REN11871  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,585,264 - 61,585,518UniSTSGRCh37
Build 361859,736,244 - 59,736,498RGDNCBI36
Celera1858,305,714 - 58,305,968RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,286,390 - 58,286,644UniSTS
REN11872  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,585,494 - 61,585,746UniSTSGRCh37
Build 361859,736,474 - 59,736,726RGDNCBI36
Celera1858,305,944 - 58,306,196RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,286,620 - 58,286,872UniSTS
REN11873  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,585,713 - 61,585,944UniSTSGRCh37
Build 361859,736,693 - 59,736,924RGDNCBI36
Celera1858,306,163 - 58,306,394RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,286,839 - 58,287,070UniSTS
REN11874  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,585,918 - 61,586,173UniSTSGRCh37
Build 361859,736,898 - 59,737,153RGDNCBI36
Celera1858,306,368 - 58,306,623RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,287,044 - 58,287,299UniSTS
REN11875  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,586,168 - 61,586,415UniSTSGRCh37
Build 361859,737,148 - 59,737,395RGDNCBI36
Celera1858,306,618 - 58,306,865RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,287,294 - 58,287,541UniSTS
REN11876  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,586,392 - 61,586,634UniSTSGRCh37
Build 361859,737,372 - 59,737,614RGDNCBI36
Celera1858,306,842 - 58,307,084RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,287,518 - 58,287,760UniSTS
REN11877  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,586,611 - 61,586,861UniSTSGRCh37
Build 361859,737,591 - 59,737,841RGDNCBI36
Celera1858,307,061 - 58,307,311RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,287,737 - 58,287,987UniSTS
REN11878  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,586,829 - 61,587,078UniSTSGRCh37
Build 361859,737,809 - 59,738,058RGDNCBI36
Celera1858,307,279 - 58,307,528RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,287,955 - 58,288,204UniSTS
REN11879  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,587,062 - 61,587,324UniSTSGRCh37
Build 361859,738,042 - 59,738,304RGDNCBI36
Celera1858,307,512 - 58,307,774RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,288,188 - 58,288,450UniSTS
REN11880  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,587,296 - 61,587,522UniSTSGRCh37
Build 361859,738,276 - 59,738,502RGDNCBI36
Celera1858,307,746 - 58,307,972RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,288,422 - 58,288,648UniSTS
REN11881  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,587,490 - 61,587,754UniSTSGRCh37
Build 361859,738,470 - 59,738,734RGDNCBI36
Celera1858,307,940 - 58,308,204RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,288,616 - 58,288,880UniSTS
REN11882  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,587,736 - 61,587,967UniSTSGRCh37
Build 361859,738,716 - 59,738,947RGDNCBI36
Celera1858,308,186 - 58,308,417RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,288,862 - 58,289,093UniSTS
REN11883  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,587,944 - 61,588,209UniSTSGRCh37
Build 361859,738,924 - 59,739,189RGDNCBI36
Celera1858,308,394 - 58,308,659RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,289,070 - 58,289,335UniSTS
REN11884  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,588,135 - 61,588,373UniSTSGRCh37
Build 361859,739,115 - 59,739,353RGDNCBI36
Celera1858,308,585 - 58,308,823RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,289,261 - 58,289,499UniSTS
REN11885  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,588,350 - 61,588,592UniSTSGRCh37
Build 361859,739,330 - 59,739,572RGDNCBI36
Celera1858,308,800 - 58,309,042RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,289,476 - 58,289,718UniSTS
REN11886  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,588,586 - 61,588,835UniSTSGRCh37
Build 361859,739,566 - 59,739,815RGDNCBI36
Celera1858,309,036 - 58,309,285RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,289,712 - 58,289,961UniSTS
REN11887  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,588,815 - 61,589,046UniSTSGRCh37
Build 361859,739,795 - 59,740,026RGDNCBI36
Celera1858,309,265 - 58,309,496RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,289,941 - 58,290,172UniSTS
REN11888  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,588,999 - 61,589,243UniSTSGRCh37
Build 361859,739,979 - 59,740,223RGDNCBI36
Celera1858,309,449 - 58,309,693RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,290,125 - 58,290,369UniSTS
REN11889  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,589,229 - 61,589,479UniSTSGRCh37
Build 361859,740,209 - 59,740,459RGDNCBI36
Celera1858,309,679 - 58,309,929RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,290,355 - 58,290,605UniSTS
REN11890  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,589,442 - 61,589,704UniSTSGRCh37
Build 361859,740,422 - 59,740,684RGDNCBI36
Celera1858,309,892 - 58,310,154RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,290,568 - 58,290,830UniSTS
REN11891  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,589,699 - 61,589,957UniSTSGRCh37
Build 361859,740,679 - 59,740,937RGDNCBI36
Celera1858,310,149 - 58,310,407RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,290,825 - 58,291,083UniSTS
REN11892  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,589,948 - 61,590,191UniSTSGRCh37
Build 361859,740,928 - 59,741,171RGDNCBI36
Celera1858,310,398 - 58,310,641RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,291,074 - 58,291,317UniSTS
REN11893  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,590,182 - 61,590,434UniSTSGRCh37
Build 361859,741,162 - 59,741,414RGDNCBI36
Celera1858,310,632 - 58,310,884RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,291,308 - 58,291,560UniSTS
REN11894  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,590,393 - 61,590,642UniSTSGRCh37
Build 361859,741,373 - 59,741,622RGDNCBI36
Celera1858,310,843 - 58,311,092RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,291,519 - 58,291,768UniSTS
REN11895  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,590,597 - 61,590,846UniSTSGRCh37
Build 361859,741,577 - 59,741,826RGDNCBI36
Celera1858,311,047 - 58,311,296RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,291,723 - 58,291,972UniSTS
REN11896  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,590,821 - 61,591,071UniSTSGRCh37
Build 361859,741,801 - 59,742,051RGDNCBI36
Celera1858,311,271 - 58,311,521RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,291,947 - 58,292,197UniSTS
REN11897  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,591,068 - 61,591,327UniSTSGRCh37
Build 361859,742,048 - 59,742,307RGDNCBI36
Celera1858,311,518 - 58,311,777RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,292,194 - 58,292,453UniSTS
REN11898  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,591,304 - 61,591,549UniSTSGRCh37
Build 361859,742,284 - 59,742,529RGDNCBI36
Celera1858,311,754 - 58,311,999RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,292,430 - 58,292,675UniSTS
REN11899  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,591,532 - 61,591,784UniSTSGRCh37
Build 361859,742,512 - 59,742,764RGDNCBI36
Celera1858,311,982 - 58,312,234RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,292,658 - 58,292,910UniSTS
REN11900  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,591,760 - 61,592,007UniSTSGRCh37
Build 361859,742,740 - 59,742,987RGDNCBI36
Celera1858,312,210 - 58,312,457RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,292,886 - 58,293,133UniSTS
REN11901  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,591,909 - 61,592,150UniSTSGRCh37
Build 361859,742,889 - 59,743,130RGDNCBI36
Celera1858,312,359 - 58,312,600RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,293,035 - 58,293,276UniSTS
REN11902  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,592,118 - 61,592,362UniSTSGRCh37
Build 361859,743,098 - 59,743,342RGDNCBI36
Celera1858,312,568 - 58,312,812RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,293,244 - 58,293,488UniSTS
REN11903  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,592,336 - 61,592,570UniSTSGRCh37
Build 361859,743,316 - 59,743,550RGDNCBI36
Celera1858,312,786 - 58,313,020RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,293,462 - 58,293,696UniSTS
REN11904  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,592,547 - 61,592,794UniSTSGRCh37
Build 361859,743,527 - 59,743,774RGDNCBI36
Celera1858,312,997 - 58,313,244RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,293,673 - 58,293,920UniSTS
REN11905  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,592,778 - 61,593,005UniSTSGRCh37
Build 361859,743,758 - 59,743,985RGDNCBI36
Celera1858,313,228 - 58,313,455RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,293,904 - 58,294,131UniSTS
REN11906  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,592,970 - 61,593,233UniSTSGRCh37
Build 361859,743,950 - 59,744,213RGDNCBI36
Celera1858,313,420 - 58,313,683RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,294,096 - 58,294,359UniSTS
REN11907  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,593,225 - 61,593,493UniSTSGRCh37
Build 361859,744,205 - 59,744,473RGDNCBI36
Celera1858,313,675 - 58,313,943RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,294,351 - 58,294,619UniSTS
REN11908  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,593,485 - 61,593,727UniSTSGRCh37
Build 361859,744,465 - 59,744,707RGDNCBI36
Celera1858,313,935 - 58,314,177RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,294,611 - 58,294,853UniSTS
REN11909  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,593,704 - 61,593,964UniSTSGRCh37
Build 361859,744,684 - 59,744,944RGDNCBI36
Celera1858,314,154 - 58,314,414RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,294,830 - 58,295,090UniSTS
REN11910  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,593,957 - 61,594,227UniSTSGRCh37
Build 361859,744,937 - 59,745,207RGDNCBI36
Celera1858,314,407 - 58,314,677RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,295,083 - 58,295,353UniSTS
REN11911  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,594,202 - 61,594,433UniSTSGRCh37
Build 361859,745,182 - 59,745,413RGDNCBI36
Celera1858,314,652 - 58,314,883RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,295,328 - 58,295,559UniSTS
REN11912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,594,373 - 61,594,612UniSTSGRCh37
Build 361859,745,353 - 59,745,592RGDNCBI36
Celera1858,314,823 - 58,315,062RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,295,499 - 58,295,738UniSTS
REN11913  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,594,607 - 61,594,866UniSTSGRCh37
Build 361859,745,587 - 59,745,846RGDNCBI36
Celera1858,315,057 - 58,315,316RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,295,733 - 58,295,992UniSTS
REN11914  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,594,864 - 61,595,103UniSTSGRCh37
Build 361859,745,844 - 59,746,083RGDNCBI36
Celera1858,315,314 - 58,315,553RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,295,990 - 58,296,229UniSTS
REN11915  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,595,060 - 61,595,292UniSTSGRCh37
Build 361859,746,040 - 59,746,272RGDNCBI36
Celera1858,315,510 - 58,315,742RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,296,186 - 58,296,418UniSTS
REN11916  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,595,259 - 61,595,517UniSTSGRCh37
Build 361859,746,239 - 59,746,497RGDNCBI36
Celera1858,315,709 - 58,315,967RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,296,385 - 58,296,643UniSTS
REN11917  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,595,494 - 61,595,743UniSTSGRCh37
Build 361859,746,474 - 59,746,723RGDNCBI36
Celera1858,315,944 - 58,316,193RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,296,620 - 58,296,869UniSTS
REN11918  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,595,607 - 61,595,854UniSTSGRCh37
Build 361859,746,587 - 59,746,834RGDNCBI36
Celera1858,316,057 - 58,316,304RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,296,733 - 58,296,980UniSTS
REN11919  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,596,166 - 61,596,406UniSTSGRCh37
Build 361859,747,146 - 59,747,386RGDNCBI36
Celera1858,316,616 - 58,316,856RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,297,292 - 58,297,532UniSTS
REN11920  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,596,244 - 61,596,471UniSTSGRCh37
GRCh371018,318,791 - 18,319,018UniSTSGRCh37
Build 361018,358,797 - 18,359,024RGDNCBI36
Celera1858,316,694 - 58,316,921UniSTS
Celera1018,005,282 - 18,005,509RGD
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map18q21.3UniSTS
HuRef1858,297,370 - 58,297,597UniSTS
HuRef1017,984,813 - 17,985,040UniSTS
REN11921  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,596,454 - 61,596,696UniSTSGRCh37
GRCh371018,318,566 - 18,318,808UniSTSGRCh37
Build 361018,358,572 - 18,358,814RGDNCBI36
Celera1858,316,904 - 58,317,146UniSTS
Celera1018,005,057 - 18,005,299RGD
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map18q21.3UniSTS
HuRef1858,297,580 - 58,297,822UniSTS
HuRef1017,984,588 - 17,984,830UniSTS
REN11922  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,596,674 - 61,596,904UniSTSGRCh37
GRCh371018,318,358 - 18,318,588UniSTSGRCh37
Build 361018,358,364 - 18,358,594RGDNCBI36
Celera1858,317,124 - 58,317,354UniSTS
Celera1018,004,849 - 18,005,079RGD
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map18q21.3UniSTS
HuRef1858,297,800 - 58,298,030UniSTS
HuRef1017,984,380 - 17,984,610UniSTS
REN11923  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,596,892 - 61,597,134UniSTSGRCh37
Build 361859,747,872 - 59,748,114RGDNCBI36
Celera1858,317,342 - 58,317,584RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,298,018 - 58,298,261UniSTS
REN11924  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,597,109 - 61,597,354UniSTSGRCh37
Build 361859,748,089 - 59,748,334RGDNCBI36
Celera1858,317,559 - 58,317,804RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,298,236 - 58,298,481UniSTS
REN11925  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,597,331 - 61,597,583UniSTSGRCh37
Build 361859,748,311 - 59,748,563RGDNCBI36
Celera1858,317,781 - 58,318,033RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,298,458 - 58,298,710UniSTS
REN11926  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,597,582 - 61,597,835UniSTSGRCh37
Build 361859,748,562 - 59,748,815RGDNCBI36
Celera1858,318,032 - 58,318,285RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,298,709 - 58,298,962UniSTS
REN11927  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,597,796 - 61,598,040UniSTSGRCh37
Build 361859,748,776 - 59,749,020RGDNCBI36
Celera1858,318,246 - 58,318,490RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,298,923 - 58,299,167UniSTS
REN11928  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,598,039 - 61,598,287UniSTSGRCh37
Build 361859,749,019 - 59,749,267RGDNCBI36
Celera1858,318,489 - 58,318,737RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,299,166 - 58,299,414UniSTS
REN11929  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,598,278 - 61,598,542UniSTSGRCh37
Build 361859,749,258 - 59,749,522RGDNCBI36
Celera1858,318,728 - 58,318,992RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,299,405 - 58,299,669UniSTS
REN11930  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,598,538 - 61,598,796UniSTSGRCh37
Build 361859,749,518 - 59,749,776RGDNCBI36
Celera1858,318,988 - 58,319,246RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,299,665 - 58,299,923UniSTS
REN11931  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,598,773 - 61,599,038UniSTSGRCh37
Build 361859,749,753 - 59,750,018RGDNCBI36
Celera1858,319,223 - 58,319,488RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,299,900 - 58,300,165UniSTS
REN11932  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,599,019 - 61,599,257UniSTSGRCh37
Build 361859,749,999 - 59,750,237RGDNCBI36
Celera1858,319,469 - 58,319,707RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,300,146 - 58,300,384UniSTS
REN11933  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,599,191 - 61,599,415UniSTSGRCh37
Build 361859,750,171 - 59,750,395RGDNCBI36
Celera1858,319,641 - 58,319,865RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,300,318 - 58,300,542UniSTS
REN11934  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,599,387 - 61,599,636UniSTSGRCh37
Build 361859,750,367 - 59,750,616RGDNCBI36
Celera1858,319,837 - 58,320,086RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,300,514 - 58,300,763UniSTS
REN11935  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,599,634 - 61,599,888UniSTSGRCh37
Build 361859,750,614 - 59,750,868RGDNCBI36
Celera1858,320,084 - 58,320,338RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,300,761 - 58,301,015UniSTS
REN11936  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,599,881 - 61,600,119UniSTSGRCh37
Build 361859,750,861 - 59,751,099RGDNCBI36
Celera1858,320,331 - 58,320,569RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,301,008 - 58,301,246UniSTS
REN11937  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,600,096 - 61,600,359UniSTSGRCh37
Build 361859,751,076 - 59,751,339RGDNCBI36
Celera1858,320,546 - 58,320,809RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,301,223 - 58,301,486UniSTS
REN11938  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,600,355 - 61,600,611UniSTSGRCh37
Build 361859,751,335 - 59,751,591RGDNCBI36
Celera1858,320,805 - 58,321,061RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,301,482 - 58,301,738UniSTS
REN11939  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,600,581 - 61,600,818UniSTSGRCh37
Build 361859,751,561 - 59,751,798RGDNCBI36
Celera1858,321,031 - 58,321,268RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,301,708 - 58,301,945UniSTS
REN11940  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,600,789 - 61,601,037UniSTSGRCh37
Build 361859,751,769 - 59,752,017RGDNCBI36
Celera1858,321,239 - 58,321,487RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,301,916 - 58,302,164UniSTS
REN11941  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,601,022 - 61,601,271UniSTSGRCh37
Build 361859,752,002 - 59,752,251RGDNCBI36
Celera1858,321,472 - 58,321,721RGD
Cytogenetic Map18q21.3UniSTS
REN11942  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,601,084 - 61,601,355UniSTSGRCh37
Build 361859,752,064 - 59,752,335RGDNCBI36
Celera1858,321,534 - 58,321,805RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,302,211 - 58,302,481UniSTS
REN11943  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,601,332 - 61,601,579UniSTSGRCh37
Build 361859,752,312 - 59,752,559RGDNCBI36
Celera1858,321,782 - 58,322,029RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,302,458 - 58,302,705UniSTS
REN11944  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,601,557 - 61,601,815UniSTSGRCh37
Build 361859,752,537 - 59,752,795RGDNCBI36
Celera1858,322,007 - 58,322,265RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,302,683 - 58,302,941UniSTS
REN11945  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,601,791 - 61,602,015UniSTSGRCh37
Build 361859,752,771 - 59,752,995RGDNCBI36
Celera1858,322,241 - 58,322,465RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,302,917 - 58,303,141UniSTS
REN11946  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,601,953 - 61,602,203UniSTSGRCh37
Build 361859,752,933 - 59,753,183RGDNCBI36
Celera1858,322,403 - 58,322,653RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,303,079 - 58,303,329UniSTS
REN11947  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,602,198 - 61,602,440UniSTSGRCh37
Build 361859,753,178 - 59,753,420RGDNCBI36
Celera1858,322,648 - 58,322,890RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,303,324 - 58,303,566UniSTS
REN11948  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,602,399 - 61,602,654UniSTSGRCh37
Build 361859,753,379 - 59,753,634RGDNCBI36
Celera1858,322,849 - 58,323,104RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,303,525 - 58,303,780UniSTS
REN11949  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,602,645 - 61,602,890UniSTSGRCh37
Build 361859,753,625 - 59,753,870RGDNCBI36
Celera1858,323,095 - 58,323,340RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,303,771 - 58,304,016UniSTS
RH18042  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,602,098 - 61,602,236UniSTSGRCh37
Build 361859,753,078 - 59,753,216RGDNCBI36
Celera1858,322,548 - 58,322,686RGD
Cytogenetic Map18q21.3UniSTS
HuRef1858,303,224 - 58,303,362UniSTS
GeneMap99-GB4 RH Map18427.25UniSTS
stSG619537  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,582,034 - 61,583,139UniSTSGRCh37
Build 361859,733,014 - 59,734,119RGDNCBI36
Celera1858,302,484 - 58,303,589RGD
HuRef1858,283,161 - 58,284,266UniSTS
stSG619538  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,583,118 - 61,583,338UniSTSGRCh37
Build 361859,734,098 - 59,734,318RGDNCBI36
Celera1858,303,568 - 58,303,788RGD
HuRef1858,284,245 - 58,284,465UniSTS
stSG619539  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,583,367 - 61,584,570UniSTSGRCh37
Build 361859,734,347 - 59,735,550RGDNCBI36
Celera1858,303,817 - 58,305,020RGD
HuRef1858,284,494 - 58,285,696UniSTS
stSG619540  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,584,552 - 61,585,615UniSTSGRCh37
Build 361859,735,532 - 59,736,595RGDNCBI36
Celera1858,305,002 - 58,306,065RGD
HuRef1858,285,678 - 58,286,741UniSTS
stSG619541  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,585,596 - 61,586,890UniSTSGRCh37
Build 361859,736,576 - 59,737,870RGDNCBI36
Celera1858,306,046 - 58,307,340RGD
HuRef1858,286,722 - 58,288,016UniSTS
stSG619542  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,586,871 - 61,588,151UniSTSGRCh37
Build 361859,737,851 - 59,739,131RGDNCBI36
Celera1858,307,321 - 58,308,601RGD
HuRef1858,287,997 - 58,289,277UniSTS
stSG619543  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,588,133 - 61,589,534UniSTSGRCh37
Build 361859,739,113 - 59,740,514RGDNCBI36
Celera1858,308,583 - 58,309,984RGD
HuRef1858,289,259 - 58,290,660UniSTS
stSG619544  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,589,687 - 61,590,763UniSTSGRCh37
Build 361859,740,667 - 59,741,743RGDNCBI36
Celera1858,310,137 - 58,311,213RGD
HuRef1858,290,813 - 58,291,889UniSTS
stSG619545  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,590,744 - 61,591,919UniSTSGRCh37
Build 361859,741,724 - 59,742,899RGDNCBI36
Celera1858,311,194 - 58,312,369RGD
HuRef1858,291,870 - 58,293,045UniSTS
stSG619546  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,591,902 - 61,592,087UniSTSGRCh37
Build 361859,742,882 - 59,743,067RGDNCBI36
Celera1858,312,352 - 58,312,537RGD
HuRef1858,293,028 - 58,293,213UniSTS
stSG619547  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,594,257 - 61,595,256UniSTSGRCh37
Build 361859,745,237 - 59,746,236RGDNCBI36
Celera1858,314,707 - 58,315,706RGD
HuRef1858,295,383 - 58,296,382UniSTS
stSG619548  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,595,237 - 61,596,560UniSTSGRCh37
Build 361859,746,217 - 59,747,540RGDNCBI36
Celera1858,315,687 - 58,317,010RGD
HuRef1858,296,363 - 58,297,686UniSTS
stSG619549  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,596,562 - 61,597,585UniSTSGRCh37
Build 361859,747,542 - 59,748,565RGDNCBI36
Celera1858,317,012 - 58,318,035RGD
HuRef1858,297,688 - 58,298,712UniSTS
stSG619550  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,597,583 - 61,598,802UniSTSGRCh37
Build 361859,748,563 - 59,749,782RGDNCBI36
Celera1858,318,033 - 58,319,252RGD
HuRef1858,298,710 - 58,299,929UniSTS
stSG619551  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,598,799 - 61,600,202UniSTSGRCh37
Build 361859,749,779 - 59,751,182RGDNCBI36
Celera1858,319,249 - 58,320,652RGD
HuRef1858,299,926 - 58,301,329UniSTS
stSG619552  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,600,289 - 61,601,360UniSTSGRCh37
Build 361859,751,269 - 59,752,340RGDNCBI36
Celera1858,320,739 - 58,321,810RGD
HuRef1858,301,416 - 58,302,486UniSTS
stSG619553  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,601,347 - 61,602,473UniSTSGRCh37
Build 361859,752,327 - 59,753,453RGDNCBI36
Celera1858,321,797 - 58,322,923RGD
HuRef1858,302,473 - 58,303,599UniSTS
SERPINB10_2979  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371861,602,009 - 61,602,629UniSTSGRCh37
Build 361859,752,989 - 59,753,609RGDNCBI36
Celera1858,322,459 - 58,323,079RGD
HuRef1858,303,135 - 58,303,755UniSTS


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component
High
Medium 2 98 399 4 1 1 1
Low 12 583 9 23 827 4 789 11 43 12 66 200 25 164 457
Below cutoff 562 677 485 196 375 115 1675 510 1147 102 617 661 83 686 1001 3

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_005024 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526027 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526028 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017025793 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017025794 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054318688 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054318689 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054318690 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA993220 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC009802 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC072051 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK314936 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC096217 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC096218 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC096219 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC096220 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471096 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068260 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U35459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000238508   ⟹   ENSP00000238508
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1863,907,958 - 63,936,111 (+)Ensembl
RefSeq Acc Id: ENST00000397996   ⟹   ENSP00000381082
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1863,897,174 - 63,917,490 (+)Ensembl
RefSeq Acc Id: ENST00000418725   ⟹   ENSP00000392381
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1863,897,174 - 63,917,490 (+)Ensembl
RefSeq Acc Id: ENST00000619595   ⟹   ENSP00000479385
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1863,915,511 - 63,935,242 (+)Ensembl
RefSeq Acc Id: NM_005024   ⟹   NP_005015
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381863,907,958 - 63,936,111 (+)NCBI
GRCh371861,575,224 - 61,602,948 (+)NCBI
Build 361859,733,725 - 59,753,456 (+)NCBI Archive
Celera1858,303,195 - 58,322,926 (+)RGD
HuRef1858,283,872 - 58,303,602 (+)RGD
CHM1_11861,571,423 - 61,599,527 (+)NCBI
T2T-CHM13v2.01864,113,032 - 64,141,170 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011526027   ⟹   XP_011524329
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381863,907,958 - 63,936,111 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011526028   ⟹   XP_011524330
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381863,918,018 - 63,936,111 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017025793   ⟹   XP_016881282
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381863,907,958 - 63,936,111 (+)NCBI
Sequence:
RefSeq Acc Id: XM_054318688   ⟹   XP_054174663
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01864,113,032 - 64,141,170 (+)NCBI
RefSeq Acc Id: XM_054318689   ⟹   XP_054174664
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01864,113,032 - 64,141,170 (+)NCBI
RefSeq Acc Id: XM_054318690   ⟹   XP_054174665
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01864,123,080 - 64,141,170 (+)NCBI
Reference Protein Sequences
RefSeq Acc Id: NP_005015   ⟸   NM_005024
- UniProtKB: Q4VAX4 (UniProtKB/Swiss-Prot),   Q4VAX7 (UniProtKB/Swiss-Prot),   P48595 (UniProtKB/Swiss-Prot),   Q4VAX6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011524329   ⟸   XM_011526027
- Peptide Label: isoform X1
- UniProtKB: Q4VAX4 (UniProtKB/Swiss-Prot),   Q4VAX7 (UniProtKB/Swiss-Prot),   P48595 (UniProtKB/Swiss-Prot),   Q4VAX6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011524330   ⟸   XM_011526028
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_016881282   ⟸   XM_017025793
- Peptide Label: isoform X2
- UniProtKB: Q4VAX6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000392381   ⟸   ENST00000418725
RefSeq Acc Id: ENSP00000479385   ⟸   ENST00000619595
RefSeq Acc Id: ENSP00000238508   ⟸   ENST00000238508
RefSeq Acc Id: ENSP00000381082   ⟸   ENST00000397996
RefSeq Acc Id: XP_054174663   ⟸   XM_054318688
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054174664   ⟸   XM_054318689
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054174665   ⟸   XM_054318690
- Peptide Label: isoform X3
Protein Domains
SERPIN

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P48595-F1-model_v2 AlphaFold P48595 1-397 view protein structure

Promoters
RGD ID:6794988
Promoter ID:HG_KWN:28172
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:UC010DQI.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361859,725,889 - 59,726,389 (+)MPROMDB
RGD ID:7237531
Promoter ID:EPDNEW_H24510
Type:initiation region
Name:SERPINB10_1
Description:serpin family B member 10
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381863,907,981 - 63,908,041EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:8942 AgrOrtholog
COSMIC SERPINB10 COSMIC
Ensembl Genes ENSG00000242550 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000238508 ENTREZGENE
  ENST00000238508.8 UniProtKB/Swiss-Prot
Gene3D-CATH 2.30.39.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.30.497.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000242550 GTEx
HGNC ID HGNC:8942 ENTREZGENE
Human Proteome Map SERPINB10 Human Proteome Map
InterPro Serpin_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Serpin_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Serpin_fam UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Serpin_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Serpin_sf_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Serpin_sf_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:5273 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 5273 ENTREZGENE
OMIM 602058 OMIM
PANTHER PTHR11461 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SERPIN B10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Serpin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA35510 PharmGKB
PROSITE SERPIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART SERPIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF56574 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt B2RC45_HUMAN UniProtKB/TrEMBL
  P48595 ENTREZGENE
  Q4VAX4 ENTREZGENE
  Q4VAX6 ENTREZGENE, UniProtKB/TrEMBL
  Q4VAX7 ENTREZGENE
  SPB10_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary Q4VAX4 UniProtKB/Swiss-Prot
  Q4VAX7 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-04-12 SERPINB10  serpin family B member 10    serpin peptidase inhibitor, clade B (ovalbumin), member 10  Symbol and/or name change 5135510 APPROVED