CASC15 (cancer susceptibility 15)

Gene: CASC15 (cancer susceptibility 15) Homo sapiens

Analyze

Symbol:

CASC15

Name:

cancer susceptibility 15

RGD ID:

5467112

HGNC Page

HGNC:28245

Description:

This gene produces a long non-coding RNA that may regulate cell proliferation. This RNA is upregulated in hepatocellular carcinoma, where it is thought to function as an oncogene. However, some splice variants of this gene may function as a tumor suppressor in neuroblastoma and other tumor types. Circular RNA variants were observed at this gene. [provided by RefSeq, Dec 2017]

Type:

ncrna (Ensembl: lncRNA)

RefSeq Status:

REVIEWED

Previously known as:

cancer susceptibility 15 (non-protein coding); cancer susceptibility candidate 15 (non-protein coding); CANT; FLJ12803; FLJ17254; FLJ22536; FLJ51318; LINC00340; lnc-SOX4-1

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	6	21,666,413 - 22,195,820 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	6	21,664,184 - 22,654,455 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	6	21,666,644 - 22,196,049 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Celera	6	22,900,001 - 23,427,935 (+)	NCBI		Celera
Cytogenetic Map	6	p22.3	NCBI
HuRef	6	21,610,135 - 22,138,081 (+)	NCBI		HuRef
CHM1_1	6	21,669,276 - 22,196,747 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	6	21,539,084 - 22,068,639 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

megacolon (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(+)-catechin (EXP)

17beta-estradiol (EXP)

3-isobutyl-1-methyl-7H-xanthine (EXP)

4,4'-sulfonyldiphenol (EXP)

Aflatoxin B2 alpha (EXP)

arsane (EXP)

arsenic atom (EXP)

benzo[a]pyrene (EXP)

bisphenol A (EXP)

butanal (EXP)

cisplatin (EXP)

cyclosporin A (EXP)

dexamethasone (EXP)

fulvestrant (EXP)

indometacin (EXP)

lipopolysaccharide (EXP)

nickel atom (EXP)

propanal (EXP)

S-(1,2-dichlorovinyl)-L-cysteine (EXP)

serpentine asbestos (EXP)

silicon dioxide (EXP)

sodium arsenate (EXP)

sodium arsenite (EXP)

temozolomide (EXP)

titanium dioxide (EXP)

valproic acid (EXP)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Aganglionic megacolon (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:12477932	PMID:14702039	PMID:16543943	PMID:18463370	PMID:21124317	PMID:21946350	PMID:22941191	PMID:23284291	PMID:24039610	PMID:25367360	PMID:26016895	PMID:26100672
PMID:28330694	PMID:28724437	PMID:29075788	PMID:29207648	PMID:29272000	PMID:29489064	PMID:29804249	PMID:29956772	PMID:30389133	PMID:30720157	PMID:31378128	PMID:31401158
PMID:31665008	PMID:31838468	PMID:32053576	PMID:32329235	PMID:33054061	PMID:33650646	PMID:33760218	PMID:35103883	PMID:35235236	PMID:35342355	PMID:35680788	PMID:35819658
PMID:36111503	PMID:37960753

Genomics

Variants

Variants in CASC15
58 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
NR_015410.1(CASC15):n.455+4431G>C	single nucleotide variant	Lung cancer [RCV000096741]	Chr6:21673330 [GRCh38] Chr6:21673561 [GRCh37] Chr6:6p22.3	uncertain significance
NR_015410.1(CASC15):n.455+51508G>T	single nucleotide variant	Lung cancer [RCV000096742]	Chr6:21720407 [GRCh38] Chr6:21720638 [GRCh37] Chr6:6p22.3	uncertain significance
NR_015410.1(CASC15):n.456-4067G>C	single nucleotide variant	Lung cancer [RCV000096743]	Chr6:21779565 [GRCh38] Chr6:21779796 [GRCh37] Chr6:6p22.3	uncertain significance
NR_015410.1(CASC15):n.456-2012G>A	single nucleotide variant	Lung cancer [RCV000096744]	Chr6:21781620 [GRCh38] Chr6:21781851 [GRCh37] Chr6:6p22.3	uncertain significance
NR_015410.1(CASC15):n.617-12954C>G	single nucleotide variant	Lung cancer [RCV000096745]	Chr6:21896516 [GRCh38] Chr6:21896747 [GRCh37] Chr6:6p22.3	uncertain significance
NR_015410.1(CASC15):n.617-9604G>A	single nucleotide variant	Lung cancer [RCV000096746]	Chr6:21899866 [GRCh38] Chr6:21900097 [GRCh37] Chr6:6p22.3	uncertain significance
NR_015410.1(CASC15):n.751-4732G>A	single nucleotide variant	Lung cancer [RCV000096747]	Chr6:21974213 [GRCh38] Chr6:21974444 [GRCh37] Chr6:6p22.3	uncertain significance
NR_015410.1(CASC15):n.1073-17397G>A	single nucleotide variant	Lung cancer [RCV000096748]	Chr6:22039149 [GRCh38] Chr6:22039378 [GRCh37] Chr6:6p22.3	uncertain significance
GRCh38/hg38 6p25.2-21.33(chr6:3224310-30657190)x3	copy number gain	See cases [RCV000138956]	Chr6:3224310..30657190 [GRCh38] Chr6:3224544..30624967 [GRCh37] Chr6:3169543..30732946 [NCBI36] Chr6:6p25.2-21.33	pathogenic
GRCh38/hg38 6p25.3-12.3(chr6:156974-46789291)x3	copy number gain	See cases [RCV000143497]	Chr6:156974..46789291 [GRCh38] Chr6:156974..46757028 [GRCh37] Chr6:101974..46864987 [NCBI36] Chr6:6p25.3-12.3	pathogenic
GRCh38/hg38 6p24.1-22.3(chr6:13093117-22126024)x3	copy number gain	See cases [RCV000051897]	Chr6:13093117..22126024 [GRCh38] Chr6:13093349..22126253 [GRCh37] Chr6:13201335..22234232 [NCBI36] Chr6:6p24.1-22.3	pathogenic
GRCh38/hg38 6p22.3-21.33(chr6:18120520-30767516)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052180]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052180]\|See cases [RCV000052180]	Chr6:18120520..30767516 [GRCh38] Chr6:18120751..30735293 [GRCh37] Chr6:18228730..30843272 [NCBI36] Chr6:6p22.3-21.33	pathogenic
NC_000006.12:g.22008001_22092880del	deletion	Megacolon [RCV001290054]	Chr6:22008001..22092880 [GRCh38] Chr6:22008230..22093109 [GRCh37] Chr6:6p22.3	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	762
Count of miRNA genes:	506
Interacting mature miRNAs:	538
Transcripts:	ENST00000444265, ENST00000605917, ENST00000606197, ENST00000606336, ENST00000606851, ENST00000607048
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

D6S1588

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,045,415 - 22,045,558	UniSTS	GRCh37
Build 36	6	22,153,394 - 22,153,537	RGD	NCBI36
Celera	6	23,278,776 - 23,278,913	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	21,988,864 - 21,989,005	UniSTS
Marshfield Genetic Map	6	38.24	RGD
Marshfield Genetic Map	6	38.24	UniSTS
Genethon Genetic Map	6	38.1	UniSTS
deCODE Assembly Map	6	44.86	UniSTS
GeneMap99-GB4 RH Map	6	92.62	UniSTS
NCBI RH Map	6	287.0	UniSTS

D6S1029

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,078,011 - 22,078,134	UniSTS	GRCh37
Build 36	6	22,185,990 - 22,186,113	RGD	NCBI36
Celera	6	23,311,367 - 23,311,484	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,021,465 - 22,021,588	UniSTS
Marshfield Genetic Map	6	39.2	RGD
Marshfield Genetic Map	6	39.2	UniSTS
deCODE Assembly Map	6	45.21	UniSTS
Whitehead-YAC Contig Map	6		UniSTS

D6S1686

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,070,770 - 22,071,028	UniSTS	GRCh37
Build 36	6	22,178,749 - 22,179,007	RGD	NCBI36
Celera	6	23,304,127 - 23,304,385	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,014,218 - 22,014,480	UniSTS
Marshfield Genetic Map	6	39.2	RGD
Marshfield Genetic Map	6	39.2	UniSTS
Genethon Genetic Map	6	39.3	UniSTS
GeneMap99-GB4 RH Map	6	92.0	UniSTS
Whitehead-YAC Contig Map	6		UniSTS
NCBI RH Map	6	285.5	UniSTS

D6S1597

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	21,726,308 - 21,726,497	UniSTS	GRCh37
Build 36	6	21,834,287 - 21,834,476	RGD	NCBI36
Celera	6	22,959,634 - 22,959,823	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	21,670,452 - 21,670,643	UniSTS
Marshfield Genetic Map	6	37.79	UniSTS
Marshfield Genetic Map	6	37.79	RGD
Genethon Genetic Map	6	38.0	UniSTS
deCODE Assembly Map	6	43.93	UniSTS

RH46644

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,134,888 - 22,135,036	UniSTS	GRCh37
Build 36	6	22,242,867 - 22,243,015	RGD	NCBI36
Celera	6	23,368,222 - 23,368,370	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,078,339 - 22,078,487	UniSTS
GeneMap99-GB4 RH Map	6	91.79	UniSTS

RH15831

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,133,518 - 22,133,697	UniSTS	GRCh37
Build 36	6	22,241,497 - 22,241,676	RGD	NCBI36
Celera	6	23,366,852 - 23,367,031	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,076,969 - 22,077,148	UniSTS
GeneMap99-GB4 RH Map	6	85.54	UniSTS

D6S2148

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	21,934,588 - 21,934,736	UniSTS	GRCh37
Build 36	6	22,042,567 - 22,042,715	RGD	NCBI36
Celera	6	23,167,912 - 23,168,060	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	21,878,240 - 21,878,388	UniSTS
Stanford-G3 RH Map	6	1033.0	UniSTS
NCBI RH Map	6	281.9	UniSTS

A004M23

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,134,857 - 22,135,093	UniSTS	GRCh37
Build 36	6	22,242,836 - 22,243,072	RGD	NCBI36
Celera	6	23,368,191 - 23,368,427	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,078,308 - 22,078,544	UniSTS
GeneMap99-GB4 RH Map	6	85.38	UniSTS

SHGC-30550

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,151,769 - 22,151,894	UniSTS	GRCh37
Build 36	6	22,259,748 - 22,259,873	RGD	NCBI36
Celera	6	23,385,105 - 23,385,230	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,095,224 - 22,095,349	UniSTS
TNG Radiation Hybrid Map	6	12270.0	UniSTS
GeneMap99-GB4 RH Map	6	85.38	UniSTS
GeneMap99-GB4 RH Map	6	91.79	UniSTS
Whitehead-RH Map	6	121.6	UniSTS
NCBI RH Map	6	285.5	UniSTS
GeneMap99-G3 RH Map	6	1304.0	UniSTS

RH46729

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,133,572 - 22,133,712	UniSTS	GRCh37
Build 36	6	22,241,551 - 22,241,691	RGD	NCBI36
Celera	6	23,366,906 - 23,367,046	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,077,023 - 22,077,163	UniSTS
GeneMap99-GB4 RH Map	6	85.38	UniSTS
NCBI RH Map	6	223.6	UniSTS

WI-12018

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,194,455 - 22,194,604	UniSTS	GRCh37
Build 36	6	22,302,434 - 22,302,583	RGD	NCBI36
Celera	6	23,427,761 - 23,427,910	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,137,909 - 22,138,058	UniSTS
GeneMap99-GB4 RH Map	6	85.38	UniSTS
Whitehead-RH Map	6	121.5	UniSTS

AL008737

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,110,060 - 22,110,225	UniSTS	GRCh37
Build 36	6	22,218,039 - 22,218,204	RGD	NCBI36
Celera	6	23,343,398 - 23,343,563	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,053,509 - 22,053,674	UniSTS

SHGC-80081

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	21,772,917 - 21,773,251	UniSTS	GRCh37
Build 36	6	21,880,896 - 21,881,230	RGD	NCBI36
Celera	6	23,006,234 - 23,006,568	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	21,716,643 - 21,716,977	UniSTS
TNG Radiation Hybrid Map	6	12041.0	UniSTS

SHGC-84864

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	21,847,722 - 21,848,024	UniSTS	GRCh37
Build 36	6	21,955,701 - 21,956,003	RGD	NCBI36
Celera	6	23,081,042 - 23,081,344	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	21,791,668 - 21,791,970	UniSTS
TNG Radiation Hybrid Map	6	12096.0	UniSTS

RH119266

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,073,155 - 22,073,467	UniSTS	GRCh37
Build 36	6	22,181,134 - 22,181,446	RGD	NCBI36
Celera	6	23,306,510 - 23,306,822	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,016,605 - 22,016,917	UniSTS
TNG Radiation Hybrid Map	6	12224.0	UniSTS

RH119598

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	21,681,910 - 21,682,131	UniSTS	GRCh37
Build 36	6	21,789,889 - 21,790,110	RGD	NCBI36
Celera	6	22,915,240 - 22,915,461	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	21,625,397 - 21,625,618	UniSTS

RH121785

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	21,847,791 - 21,848,075	UniSTS	GRCh37
Build 36	6	21,955,770 - 21,956,054	RGD	NCBI36
Celera	6	23,081,111 - 23,081,395	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	21,791,737 - 21,792,021	UniSTS
TNG Radiation Hybrid Map	6	12092.0	UniSTS

G60336

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,070,749 - 22,071,026	UniSTS	GRCh37
Build 36	6	22,178,728 - 22,179,005	RGD	NCBI36
Celera	6	23,304,106 - 23,304,383	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,014,197 - 22,014,478	UniSTS
TNG Radiation Hybrid Map	6	12224.0	UniSTS

G60558

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,045,412 - 22,045,564	UniSTS	GRCh37
Build 36	6	22,153,391 - 22,153,543	RGD	NCBI36
Celera	6	23,278,773 - 23,278,919	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	21,988,861 - 21,989,011	UniSTS
TNG Radiation Hybrid Map	11	35868.0	UniSTS
TNG Radiation Hybrid Map	6	12209.0	UniSTS

RH123746

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	21,755,198 - 21,755,464	UniSTS	GRCh37
Build 36	6	21,863,177 - 21,863,443	RGD	NCBI36
Celera	6	22,988,520 - 22,988,786	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	21,698,916 - 21,699,182	UniSTS
TNG Radiation Hybrid Map	6	12032.0	UniSTS

D6S506

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	21,860,110 - 21,860,245	UniSTS	GRCh37
Build 36	6	21,968,089 - 21,968,224	RGD	NCBI36
Celera	6	23,093,404 - 23,093,539	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	21,803,749 - 21,803,882	UniSTS

D6S507

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	21,814,753 - 21,814,964	UniSTS	GRCh37
Build 36	6	21,922,732 - 21,922,943	RGD	NCBI36
Celera	6	23,048,074 - 23,048,285	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	21,758,675 - 21,758,884	UniSTS

SGC36817

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,134,877 - 22,134,985	UniSTS	GRCh37
Build 36	6	22,242,856 - 22,242,964	RGD	NCBI36
Celera	6	23,368,211 - 23,368,319	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,078,328 - 22,078,436	UniSTS
GeneMap99-GB4 RH Map	6	85.38	UniSTS
Whitehead-RH Map	6	121.6	UniSTS
NCBI RH Map	6	223.6	UniSTS

SHGC-155368

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	21,947,031 - 21,947,303	UniSTS	GRCh37
Build 36	6	22,055,010 - 22,055,282	RGD	NCBI36
Celera	6	23,180,356 - 23,180,628	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	21,890,547 - 21,890,819	UniSTS
TNG Radiation Hybrid Map	6	12143.0	UniSTS

G67601

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	21,963,531 - 21,963,610	UniSTS	GRCh37
Build 36	6	22,071,510 - 22,071,589	RGD	NCBI36
Celera	6	23,196,865 - 23,196,944	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	21,907,043 - 21,907,122	UniSTS

G67602

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	21,963,621 - 21,963,997	UniSTS	GRCh37
Build 36	6	22,071,600 - 22,071,976	RGD	NCBI36
Celera	6	23,196,955 - 23,197,331	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	21,907,133 - 21,907,509	UniSTS

G67600

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	21,805,688 - 21,805,743	UniSTS	GRCh37
Build 36	6	21,913,667 - 21,913,722	RGD	NCBI36
Celera	6	23,039,013 - 23,039,068	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	21,749,584 - 21,749,639	UniSTS

G67604

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,190,917 - 22,191,060	UniSTS	GRCh37
Build 36	6	22,298,896 - 22,299,039	RGD	NCBI36
Celera	6	23,424,220 - 23,424,363	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,134,369 - 22,134,512	UniSTS

G67603

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,140,677 - 22,140,958	UniSTS	GRCh37
Build 36	6	22,248,656 - 22,248,937	RGD	NCBI36
Celera	6	23,374,011 - 23,374,292	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,084,128 - 22,084,409	UniSTS

RH64859

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,134,580 - 22,134,705	UniSTS	GRCh37
Build 36	6	22,242,559 - 22,242,684	RGD	NCBI36
Celera	6	23,367,914 - 23,368,039	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,078,031 - 22,078,156	UniSTS
GeneMap99-GB4 RH Map	6	92.0	UniSTS
NCBI RH Map	6	285.5	UniSTS

D6S2250

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	21,932,187 - 21,932,346	UniSTS	GRCh37
Build 36	6	22,040,166 - 22,040,325	RGD	NCBI36
Celera	6	23,165,498 - 23,165,657	RGD
HuRef	6	21,875,827 - 21,875,986	UniSTS

D6S1501

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,131,342 - 22,131,446	UniSTS	GRCh37
Build 36	6	22,239,321 - 22,239,425	RGD	NCBI36
Celera	6	23,364,676 - 23,364,780	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,074,793 - 22,074,897	UniSTS
Whitehead-RH Map	6	123.3	UniSTS
Whitehead-YAC Contig Map	6		UniSTS

G17038

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,107,651 - 22,107,937	UniSTS	GRCh37
Build 36	6	22,215,630 - 22,215,916	RGD	NCBI36
Celera	6	23,340,992 - 23,341,278	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,051,100 - 22,051,386	UniSTS

WI-18694

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,194,465 - 22,194,614	UniSTS	GRCh37
Build 36	6	22,302,444 - 22,302,593	RGD	NCBI36
Celera	6	23,427,771 - 23,427,920	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,137,919 - 22,138,068	UniSTS
GeneMap99-GB4 RH Map	6	92.0	UniSTS
Whitehead-RH Map	6	123.2	UniSTS
NCBI RH Map	6	285.5	UniSTS

RH66723

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,186,700 - 22,186,821	UniSTS	GRCh37
Build 36	6	22,294,679 - 22,294,800	RGD	NCBI36
Celera	6	23,420,001 - 23,420,122	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,130,150 - 22,130,271	UniSTS
GeneMap99-GB4 RH Map	6	91.79	UniSTS
NCBI RH Map	6	284.7	UniSTS

WI-13536

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	6	22,133,454 - 22,133,582	UniSTS	GRCh37
Build 36	6	22,241,433 - 22,241,561	RGD	NCBI36
Celera	6	23,366,788 - 23,366,916	RGD
Cytogenetic Map	6	p22.3	UniSTS
HuRef	6	22,076,905 - 22,077,033	UniSTS
GeneMap99-GB4 RH Map	6	85.38	UniSTS
Whitehead-RH Map	6	121.6	UniSTS
NCBI RH Map	6	223.6	UniSTS

SHGC-67307

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	15	q22.3	UniSTS
Cytogenetic Map	20	q13.3	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	7	p13	UniSTS
Cytogenetic Map	19	q13.32	UniSTS
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	3	q21.2	UniSTS
Cytogenetic Map	3	p21.3	UniSTS
Cytogenetic Map	18	q11.2	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	X	p11.3	UniSTS
Cytogenetic Map	7	q21.2	UniSTS
Cytogenetic Map	13	q14	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	18	pter-p11.3	UniSTS
Cytogenetic Map	7	p22.2	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	22	q11.21	UniSTS
Cytogenetic Map	4	q13.1	UniSTS
Cytogenetic Map	6	p25	UniSTS
Cytogenetic Map	13	q34	UniSTS
Cytogenetic Map	8	q24.22	UniSTS
Cytogenetic Map	16	q21	UniSTS
Cytogenetic Map	1	p35.2	UniSTS
Cytogenetic Map	1	q25.1	UniSTS
Cytogenetic Map	12	q13.3	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	8	q21.1	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
Cytogenetic Map	1	p13.3	UniSTS
Cytogenetic Map	6	q22.31	UniSTS
Cytogenetic Map	7	p11.2	UniSTS
Cytogenetic Map	7	q34	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	12	q24.23	UniSTS
Cytogenetic Map	9	p13.3	UniSTS
Cytogenetic Map	3	p21.1	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
Cytogenetic Map	2	q24.2	UniSTS
Cytogenetic Map	2	p25.1-p24.1	UniSTS
Cytogenetic Map	5	q32	UniSTS
Cytogenetic Map	5	q31	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
Cytogenetic Map	16	p13.3	UniSTS
Cytogenetic Map	16	q22.2	UniSTS
Cytogenetic Map	1	q32.2-q41	UniSTS
Cytogenetic Map	17	q21.31	UniSTS
Cytogenetic Map	14	q12	UniSTS
Cytogenetic Map	16	q24.3	UniSTS
Cytogenetic Map	17	q24.1	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	16	p13	UniSTS
Cytogenetic Map	1	q32	UniSTS
Cytogenetic Map	X	p22.3	UniSTS
Cytogenetic Map	14	q11.2	UniSTS
Cytogenetic Map	6	p22.3	UniSTS
Cytogenetic Map	6	p25.2	UniSTS
Cytogenetic Map	14	q22.1	UniSTS
Cytogenetic Map	1	p34.3	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	7	p15.3	UniSTS
Cytogenetic Map	1	q25.3	UniSTS
Cytogenetic Map	15	q22.2	UniSTS
Cytogenetic Map	20	q12	UniSTS
Cytogenetic Map	4	p15.32	UniSTS
Cytogenetic Map	19	q13.42	UniSTS
Cytogenetic Map	12	q24.13	UniSTS
Cytogenetic Map	20	q11.22	UniSTS
Cytogenetic Map	6	p12.3	UniSTS
Cytogenetic Map	7	q33	UniSTS
Cytogenetic Map	15	q13.2	UniSTS
Cytogenetic Map	8	q22.1	UniSTS
Cytogenetic Map	17	q21	UniSTS
Cytogenetic Map	22	q11.1	UniSTS
Cytogenetic Map	7	q22	UniSTS
Cytogenetic Map	6	q21	UniSTS
Cytogenetic Map	1	p36.13	UniSTS
Cytogenetic Map	5	p13.3	UniSTS
Cytogenetic Map	2	p23.3	UniSTS
Cytogenetic Map	19	q13	UniSTS
Cytogenetic Map	4	q26	UniSTS
Cytogenetic Map	10	q11.23	UniSTS
Cytogenetic Map	16	p13.12	UniSTS
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	16	q23.1	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	15	q15.3	UniSTS
Cytogenetic Map	2	q35	UniSTS
Cytogenetic Map	22	q13.2	UniSTS
Cytogenetic Map	18	q21.32	UniSTS
Cytogenetic Map	5	q22.1	UniSTS
Cytogenetic Map	1	p36.12	UniSTS
Cytogenetic Map	14	q32.12	UniSTS
Cytogenetic Map	12	q13	UniSTS
Cytogenetic Map	11	q13.1	UniSTS
Cytogenetic Map	14	q32.31	UniSTS
Cytogenetic Map	17	q21.2	UniSTS
Cytogenetic Map	11	q13.5	UniSTS
Cytogenetic Map	15	q25.2	UniSTS
Cytogenetic Map	22	q12.1	UniSTS
Cytogenetic Map	7	p14.3	UniSTS
Cytogenetic Map	20	q13.33	UniSTS
Cytogenetic Map	1	p36.21	UniSTS
TNG Radiation Hybrid Map	4	1213.0	UniSTS

D11S2921

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	16	q22.1	UniSTS
Cytogenetic Map	1	p36.1	UniSTS
Cytogenetic Map	3	p24.2	UniSTS
Cytogenetic Map	1	q23.3	UniSTS
Cytogenetic Map	9	q34.3	UniSTS
Cytogenetic Map	1	p36.31	UniSTS
Cytogenetic Map	3	p25.3	UniSTS
Cytogenetic Map	11	p15.4	UniSTS
Cytogenetic Map	7	p14.1	UniSTS
Cytogenetic Map	2	q22.3	UniSTS
Cytogenetic Map	9	q22.33	UniSTS
Cytogenetic Map	15	q13.2	UniSTS
Cytogenetic Map	16	q24.3	UniSTS
Cytogenetic Map	5	q31	UniSTS
Cytogenetic Map	19	q13.11	UniSTS
Cytogenetic Map	17	p11.2	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	22	q13.33	UniSTS
Cytogenetic Map	14	q13.2	UniSTS
Cytogenetic Map	2	p25.1	UniSTS
Cytogenetic Map	10	q24.33	UniSTS
Cytogenetic Map	5	q23.3-q31.1	UniSTS
Cytogenetic Map	8	p21.3	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	1	p32.3	UniSTS
Cytogenetic Map	17	q11	UniSTS
Cytogenetic Map	1	q24	UniSTS
Cytogenetic Map	11	q14	UniSTS
Cytogenetic Map	17	q25	UniSTS
Cytogenetic Map	X	q13.1	UniSTS
Cytogenetic Map	2	q11.2	UniSTS
Cytogenetic Map	9	p13.3	UniSTS
Cytogenetic Map	19	p13.2	UniSTS
Cytogenetic Map	2	q32.3	UniSTS
Cytogenetic Map	17	q21.31	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
Cytogenetic Map	4	q32.1	UniSTS
Cytogenetic Map	7	q34	UniSTS
Cytogenetic Map	13	q12	UniSTS
Cytogenetic Map	12	p13.31	UniSTS
Cytogenetic Map	3	p21.1	UniSTS
Cytogenetic Map	3	q12.3	UniSTS
Cytogenetic Map	14	q24.3	UniSTS
Cytogenetic Map	6	q22	UniSTS
Cytogenetic Map	22	q13.2	UniSTS
Cytogenetic Map	19	q13.42	UniSTS
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	20	q11	UniSTS
Cytogenetic Map	8	q22.1	UniSTS
Cytogenetic Map	5	q23.3	UniSTS
Cytogenetic Map	20	q11.22	UniSTS
Cytogenetic Map	1	p36.11	UniSTS
Cytogenetic Map	19	q13.43	UniSTS
Cytogenetic Map	17	q21	UniSTS
Cytogenetic Map	11	q25	UniSTS
Cytogenetic Map	3	p21.3	UniSTS
Cytogenetic Map	1	q32.3	UniSTS
Cytogenetic Map	2	q37.3	UniSTS
Cytogenetic Map	12	q21.33	UniSTS
Cytogenetic Map	7	p22.3	UniSTS
Cytogenetic Map	4	p16.3	UniSTS
Cytogenetic Map	17	p13.3	UniSTS
Cytogenetic Map	1	p35.1	UniSTS
Cytogenetic Map	X	p11.4-p11.3	UniSTS
Cytogenetic Map	17	q11.2	UniSTS
Cytogenetic Map	1	p36.33	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	1	q24.1	UniSTS
Cytogenetic Map	14	q11.2	UniSTS
Cytogenetic Map	16	p11.2	UniSTS
Cytogenetic Map	11	q24.2	UniSTS
Cytogenetic Map	10	p15.1	UniSTS
Cytogenetic Map	18	p11.31	UniSTS
Cytogenetic Map	12	p13.32	UniSTS
Cytogenetic Map	19	p13.11	UniSTS
Cytogenetic Map	11	q13.5	UniSTS
Cytogenetic Map	1	p22	UniSTS
Cytogenetic Map	2	q14	UniSTS
Cytogenetic Map	16	q24	UniSTS
Cytogenetic Map	16	p13.3	UniSTS
Cytogenetic Map	7	p22	UniSTS
Cytogenetic Map	14	q32.33	UniSTS
Cytogenetic Map	8	p11.21	UniSTS
Cytogenetic Map	8	q24.11	UniSTS
Cytogenetic Map	4	q12	UniSTS
Cytogenetic Map	9	q22.31	UniSTS
Cytogenetic Map	17	p13.2	UniSTS
Cytogenetic Map	11	p15.5	UniSTS
Cytogenetic Map	2	p11.2	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	5	q31.1	UniSTS
Cytogenetic Map	2	q33-q34	UniSTS
Cytogenetic Map	17	q22.2	UniSTS
Cytogenetic Map	8	q24.13	UniSTS
Cytogenetic Map	22	q11.2	UniSTS
Cytogenetic Map	6	p22.1	UniSTS
Cytogenetic Map	Y	p11.2	UniSTS
Cytogenetic Map	19	q13.2	UniSTS
Cytogenetic Map	18	p11.21	UniSTS
Cytogenetic Map	10	q22	UniSTS
Cytogenetic Map	5	q35.3	UniSTS
Cytogenetic Map	10	q23.1	UniSTS
Cytogenetic Map	2	q37	UniSTS
Cytogenetic Map	18	pter-p11.3	UniSTS
Cytogenetic Map	8	q22.3	UniSTS
Cytogenetic Map	6	p21.33	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	2	q21.3	UniSTS
Cytogenetic Map	2	q21.1	UniSTS
Cytogenetic Map	8	p21.2	UniSTS
Cytogenetic Map	X	q22.1	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
Cytogenetic Map	1	p34.2	UniSTS
Cytogenetic Map	19	q13.41	UniSTS
Cytogenetic Map	14	q32.12	UniSTS
Cytogenetic Map	3	q21.3	UniSTS
Cytogenetic Map	4	q34.1	UniSTS
Cytogenetic Map	10	p13	UniSTS
Cytogenetic Map	17	q25.3	UniSTS
Cytogenetic Map	3	q13.31	UniSTS
Cytogenetic Map	7	q21.12	UniSTS
Cytogenetic Map	15	q22.2	UniSTS
Cytogenetic Map	8	p23.1	UniSTS
Cytogenetic Map	5	q32	UniSTS
Cytogenetic Map	20	q13.12	UniSTS
Cytogenetic Map	12	q23.2	UniSTS
Cytogenetic Map	6	p22	UniSTS
Cytogenetic Map	11	q12.3	UniSTS
Cytogenetic Map	11	p13	UniSTS
Cytogenetic Map	1	q21.3	UniSTS
Cytogenetic Map	16	p13.13	UniSTS
Cytogenetic Map	1	p34	UniSTS
Cytogenetic Map	1	p36.21	UniSTS
Cytogenetic Map	12	q13	UniSTS
Cytogenetic Map	19	q13.31	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
Cytogenetic Map	4	p14	UniSTS
Cytogenetic Map	1	q44	UniSTS
Cytogenetic Map	19	p13.1-p12	UniSTS
Cytogenetic Map	7	q22	UniSTS
Cytogenetic Map	8	q24	UniSTS
Cytogenetic Map	18	p11.31-p11.21	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
Cytogenetic Map	7	p21.2	UniSTS
Cytogenetic Map	12	q23-q24.1	UniSTS
Cytogenetic Map	15	q15.1	UniSTS
Cytogenetic Map	10	q11.23	UniSTS
Cytogenetic Map	5	q14.1	UniSTS
Cytogenetic Map	5	p15.33	UniSTS
Cytogenetic Map	1	q21	UniSTS
Cytogenetic Map	22	q11.21	UniSTS
Cytogenetic Map	8	q24.3	UniSTS
Cytogenetic Map	1	q42.1	UniSTS
Cytogenetic Map	12	p13	UniSTS
Cytogenetic Map	15	q21	UniSTS
Cytogenetic Map	6	p21.3	UniSTS
Cytogenetic Map	8	p11.22	UniSTS
Cytogenetic Map	2	q12.3	UniSTS
Cytogenetic Map	19	q13.3-q13.4	UniSTS
Cytogenetic Map	15	q11.2	UniSTS
Cytogenetic Map	5	q35	UniSTS
Cytogenetic Map	8	p23-p22	UniSTS
Cytogenetic Map	12	p11	UniSTS
Cytogenetic Map	17	q21-q22	UniSTS
Cytogenetic Map	12	q13.12	UniSTS
Cytogenetic Map	2	q36.1	UniSTS
Cytogenetic Map	11	p13-p12	UniSTS
Cytogenetic Map	X	p22.33	UniSTS
Cytogenetic Map	Y	p11.3	UniSTS
Cytogenetic Map	2	q12.1	UniSTS
Cytogenetic Map	3	p21.31	UniSTS
Cytogenetic Map	3	q26.32	UniSTS
Cytogenetic Map	7	q11.21	UniSTS
Cytogenetic Map	10	q11.22	UniSTS
Cytogenetic Map	17	p12	UniSTS
Cytogenetic Map	3	p25.1	UniSTS
Cytogenetic Map	14	q32	UniSTS
Cytogenetic Map	5	q12-q13	UniSTS
Cytogenetic Map	6	p23	UniSTS
Cytogenetic Map	20	p12.3-p11.21	UniSTS
Cytogenetic Map	17	q11.2-q12	UniSTS
Cytogenetic Map	11	q23.3	UniSTS
Cytogenetic Map	12	q13.3	UniSTS
Cytogenetic Map	10	q23-q24	UniSTS
Cytogenetic Map	14	q21.3	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	12	q13-q14	UniSTS
Cytogenetic Map	6	q14.1	UniSTS
Cytogenetic Map	3	q26.33	UniSTS
Cytogenetic Map	X	p22.2	UniSTS
Cytogenetic Map	1	p31	UniSTS
Cytogenetic Map	15	q15-q21.1	UniSTS
Cytogenetic Map	9	q32	UniSTS
Cytogenetic Map	17	p13	UniSTS
Cytogenetic Map	7	q21-q22	UniSTS
Cytogenetic Map	16	q24.1	UniSTS
Cytogenetic Map	2	q33.3	UniSTS
Cytogenetic Map	11	q22.1	UniSTS
Cytogenetic Map	1	p13.3	UniSTS
Cytogenetic Map	20	p13	UniSTS
Cytogenetic Map	6	p21.1	UniSTS
Cytogenetic Map	7	q36.3	UniSTS
Cytogenetic Map	5	q12.3	UniSTS
Cytogenetic Map	2	q33.2	UniSTS
Cytogenetic Map	12	q22	UniSTS
Cytogenetic Map	21	p11.1	UniSTS
Cytogenetic Map	14	q23.2	UniSTS
Cytogenetic Map	6	p22.3-p22.1	UniSTS
Cytogenetic Map	7	p11.2	UniSTS
Cytogenetic Map	6	q15	UniSTS
Cytogenetic Map	X	q25-q26.3	UniSTS
Cytogenetic Map	10	q22.3	UniSTS
Cytogenetic Map	12	q24.31-q24.32	UniSTS
Cytogenetic Map	16	p12.3	UniSTS
Cytogenetic Map	9	q33.2	UniSTS
Cytogenetic Map	15	q23	UniSTS
Cytogenetic Map	12	p12.2-p11.2	UniSTS
Cytogenetic Map	2	q14.3	UniSTS
Cytogenetic Map	X	p11	UniSTS
Cytogenetic Map	19	q13	UniSTS
Cytogenetic Map	17	q22	UniSTS
Cytogenetic Map	3	q21	UniSTS
Cytogenetic Map	20	q13.2	UniSTS
Cytogenetic Map	10	q26	UniSTS
Cytogenetic Map	6	q22.31	UniSTS
Cytogenetic Map	3	q27.1	UniSTS
Cytogenetic Map	7	p13	UniSTS
Cytogenetic Map	22	q13	UniSTS
Cytogenetic Map	11	q13.1	UniSTS
Cytogenetic Map	18	p11.32	UniSTS
Cytogenetic Map	12	q15	UniSTS
Cytogenetic Map	X	q22.3	UniSTS
Cytogenetic Map	2	p25.3	UniSTS
Cytogenetic Map	16	q21	UniSTS
Cytogenetic Map	11	q23.1	UniSTS
Cytogenetic Map	3	q13.13	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	3	q27.3	UniSTS
Cytogenetic Map	4	p13	UniSTS
Cytogenetic Map	16	p12.1	UniSTS
Cytogenetic Map	14	q32.11	UniSTS
Cytogenetic Map	7	p14.3	UniSTS
Cytogenetic Map	16	q12.1	UniSTS
Cytogenetic Map	15	q25.2	UniSTS
Cytogenetic Map	9	q21.13	UniSTS
Cytogenetic Map	2	p23.3	UniSTS
Cytogenetic Map	3	q29	UniSTS
Cytogenetic Map	15	q22.31	UniSTS
Cytogenetic Map	16	q22.2	UniSTS
Cytogenetic Map	19	p13.12	UniSTS
Cytogenetic Map	20	q13.1	UniSTS
Cytogenetic Map	3	p14.3	UniSTS
Cytogenetic Map	10	q23.33	UniSTS
Cytogenetic Map	12	p12	UniSTS
Cytogenetic Map	9	p24.1-p23	UniSTS
Cytogenetic Map	15	q22	UniSTS
Cytogenetic Map	6	p25	UniSTS
Cytogenetic Map	X	q12-q13	UniSTS
Cytogenetic Map	2	p16.1	UniSTS
Cytogenetic Map	14	q23	UniSTS
Cytogenetic Map	2	q31.1	UniSTS
Cytogenetic Map	17	q23.3	UniSTS
Cytogenetic Map	1	q42.1-q43	UniSTS
Cytogenetic Map	7	q31.1-q31.3	UniSTS
Cytogenetic Map	20	q11.21	UniSTS
Cytogenetic Map	20	q12-q13.12	UniSTS
Cytogenetic Map	1	q24-q25.3	UniSTS
Cytogenetic Map	20	p12.1	UniSTS
Cytogenetic Map	14	q32.31	UniSTS
Cytogenetic Map	1	p13.2	UniSTS
Cytogenetic Map	2	p13.3	UniSTS
Cytogenetic Map	6	q25.1-q26	UniSTS
Cytogenetic Map	12	q13.11-q14.3	UniSTS
Cytogenetic Map	7	p11	UniSTS
Cytogenetic Map	12	p11.22	UniSTS
Cytogenetic Map	17	q23.1	UniSTS
Cytogenetic Map	1	p36.13	UniSTS
Cytogenetic Map	9	q34.11	UniSTS
Cytogenetic Map	2	p15	UniSTS
Cytogenetic Map	9	p11	UniSTS
Cytogenetic Map	6	p24.3	UniSTS
Cytogenetic Map	9	p24.1	UniSTS
Cytogenetic Map	12	p13.2	UniSTS
Cytogenetic Map	6	p22.2	UniSTS
Cytogenetic Map	12	q24.2-q24.31	UniSTS
Cytogenetic Map	22	q12.2	UniSTS
Cytogenetic Map	11	p11.11	UniSTS
Cytogenetic Map	11	q22-q23	UniSTS
Cytogenetic Map	11	q14.1	UniSTS
Cytogenetic Map	1	q32.1	UniSTS
Cytogenetic Map	15	q22-q23	UniSTS
Cytogenetic Map	9	p21	UniSTS
Cytogenetic Map	15	q13.1	UniSTS
Cytogenetic Map	15	q22-qter	UniSTS
Cytogenetic Map	10	q25	UniSTS
Cytogenetic Map	6	p22.3	UniSTS
Cytogenetic Map	6	p25.2	UniSTS
Cytogenetic Map	5	p15.1	UniSTS
Cytogenetic Map	2	p21	UniSTS
Cytogenetic Map	22	q13.31	UniSTS
Cytogenetic Map	21	q22.2	UniSTS
Cytogenetic Map	19	q13.33	UniSTS
Cytogenetic Map	14	q24.1	UniSTS
Cytogenetic Map	13	q34	UniSTS
Cytogenetic Map	18	q11.2	UniSTS
Cytogenetic Map	6	q25.1	UniSTS
Cytogenetic Map	20	q11.23	UniSTS
Cytogenetic Map	1	q21.1	UniSTS
Cytogenetic Map	17	q24.3	UniSTS
Cytogenetic Map	16	q11.2	UniSTS
Cytogenetic Map	16	p12.2	UniSTS
Cytogenetic Map	11	q24	UniSTS
Cytogenetic Map	2	q23.3	UniSTS
Cytogenetic Map	1	p31.1	UniSTS
Cytogenetic Map	18	q23	UniSTS
Cytogenetic Map	11	q13.4	UniSTS
Cytogenetic Map	7	p21.1	UniSTS
Cytogenetic Map	2	q37.1	UniSTS
Cytogenetic Map	8	p11.2	UniSTS
Cytogenetic Map	9	q33.3	UniSTS
Cytogenetic Map	4	q22.1	UniSTS
Cytogenetic Map	2	q21.2	UniSTS
Cytogenetic Map	15	q13.3	UniSTS
Cytogenetic Map	7	p15.3	UniSTS
Cytogenetic Map	3	p22.2	UniSTS
Cytogenetic Map	11	q13.2	UniSTS
Cytogenetic Map	19	p13.2-cen	UniSTS
Cytogenetic Map	19	p13.3-p13.2	UniSTS
Cytogenetic Map	13	q32.3	UniSTS
Cytogenetic Map	9	q33	UniSTS
Cytogenetic Map	1	p36-p35	UniSTS
Cytogenetic Map	19	q13.1	UniSTS
Cytogenetic Map	X	q25	UniSTS
Cytogenetic Map	12	q23	UniSTS
Cytogenetic Map	21	q22.13	UniSTS
Cytogenetic Map	2	q24.2	UniSTS
Cytogenetic Map	7	q31.1-q31.2	UniSTS
Cytogenetic Map	22	q11.23	UniSTS
Cytogenetic Map	X	q24	UniSTS
Cytogenetic Map	4	q25-q27	UniSTS
Cytogenetic Map	3	q25.33	UniSTS
Cytogenetic Map	X	q26.2	UniSTS
Cytogenetic Map	8	q13.2	UniSTS
Cytogenetic Map	8	q13.1	UniSTS
Cytogenetic Map	8	q22.2	UniSTS
Cytogenetic Map	6	q21	UniSTS
Cytogenetic Map	5	q23.1	UniSTS
Cytogenetic Map	4	q13.3	UniSTS
Cytogenetic Map	3	p26.1	UniSTS
Cytogenetic Map	1	q21.2	UniSTS
Cytogenetic Map	17	p13.1	UniSTS
Cytogenetic Map	3	p22-p21.3	UniSTS
Cytogenetic Map	12	q	UniSTS
Cytogenetic Map	X	q21.3	UniSTS
Cytogenetic Map	12	q12	UniSTS
Cytogenetic Map	20	p11	UniSTS
Cytogenetic Map	6	p12.3	UniSTS
Cytogenetic Map	5	p13.1-p12	UniSTS
Cytogenetic Map	1	p36.22	UniSTS
Cytogenetic Map	9	q34	UniSTS
Cytogenetic Map	7	q21.13	UniSTS
Cytogenetic Map	20	q13.33	UniSTS
Cytogenetic Map	3	p21.1-p14.3	UniSTS
Cytogenetic Map	2	q33.1	UniSTS
Cytogenetic Map	7	q36.1	UniSTS
Cytogenetic Map	10	q24.31	UniSTS
Cytogenetic Map	2	p25.1-p24.1	UniSTS
Cytogenetic Map	3	q23	UniSTS
Cytogenetic Map	13	q12.11	UniSTS
Cytogenetic Map	12	q14.3	UniSTS
Cytogenetic Map	13	q14.13	UniSTS
Cytogenetic Map	11	p15	UniSTS
Cytogenetic Map	6	q14.3-q16.1	UniSTS
Cytogenetic Map	16	p13.2	UniSTS
Cytogenetic Map	16	q22.3	UniSTS
Cytogenetic Map	1	p32-p31	UniSTS
Cytogenetic Map	12	q13.13	UniSTS
Cytogenetic Map	8	p11	UniSTS
Cytogenetic Map	6	q25	UniSTS
Cytogenetic Map	8	p11.23	UniSTS
Cytogenetic Map	9	p24.3	UniSTS
Cytogenetic Map	7	q35	UniSTS
Cytogenetic Map	11	q22.3	UniSTS
Cytogenetic Map	16	p12	UniSTS
Cytogenetic Map	6	q14.3	UniSTS
Cytogenetic Map	7	q36	UniSTS
Cytogenetic Map	1	q22	UniSTS
Cytogenetic Map	10	p15.3	UniSTS
Cytogenetic Map	8	p12	UniSTS
Cytogenetic Map	13	q12.2	UniSTS
Cytogenetic Map	7	p22.1	UniSTS
Cytogenetic Map	6	p21.2	UniSTS
Cytogenetic Map	18	q21.1	UniSTS
Cytogenetic Map	10	p11.21	UniSTS
Cytogenetic Map	10	p14	UniSTS
Cytogenetic Map	3	p26	UniSTS
Cytogenetic Map	9	q22.3	UniSTS
Cytogenetic Map	17	q21.1-q21.3	UniSTS
Cytogenetic Map	6	q11.1	UniSTS
Cytogenetic Map	5	q13.2	UniSTS
Cytogenetic Map	3	q21.1	UniSTS
Cytogenetic Map	1	q32	UniSTS
Cytogenetic Map	22	q13.1-q13.2	UniSTS
Cytogenetic Map	19	p12	UniSTS
Cytogenetic Map	9	q32-q33.3	UniSTS
Cytogenetic Map	8	q21.2	UniSTS
Cytogenetic Map	18	q12.1	UniSTS
Cytogenetic Map	12	p13.2-p12.3	UniSTS
Cytogenetic Map	1	p36.3-p36.2	UniSTS
Cytogenetic Map	5	q11.2	UniSTS
Cytogenetic Map	1	q25.2	UniSTS
Cytogenetic Map	3	q13.2	UniSTS
Cytogenetic Map	8	p22	UniSTS
Cytogenetic Map	1	q25.1	UniSTS
Cytogenetic Map	18	q21.32	UniSTS
Cytogenetic Map	17	q21.2	UniSTS
Cytogenetic Map	15	q26.2	UniSTS
Cytogenetic Map	14	q22.1	UniSTS
Cytogenetic Map	5	p15.2	UniSTS
Cytogenetic Map	12	q23.1	UniSTS
Cytogenetic Map	10	q24.2	UniSTS
Cytogenetic Map	15	q15.3	UniSTS
Cytogenetic Map	1	p22.2	UniSTS
Cytogenetic Map	7	q32	UniSTS
Cytogenetic Map	5	p13	UniSTS
Cytogenetic Map	16	q23.2	UniSTS
Cytogenetic Map	10	q24-q25	UniSTS
Cytogenetic Map	7	p11.1	UniSTS
Cytogenetic Map	14	q11.2-q21	UniSTS
Cytogenetic Map	14	q12	UniSTS
Cytogenetic Map	12	q24.13	UniSTS
Cytogenetic Map	10	q21-q22	UniSTS
Cytogenetic Map	4	q22	UniSTS
Cytogenetic Map	9	q22.2	UniSTS
Cytogenetic Map	10	q23.31	UniSTS
Cytogenetic Map	2	p13.1	UniSTS
Cytogenetic Map	2	p24.1	UniSTS
Cytogenetic Map	19	p13	UniSTS
Cytogenetic Map	7	p13-p11.1	UniSTS
Cytogenetic Map	7	q21.1-q22	UniSTS
Cytogenetic Map	1	p36.3	UniSTS
Cytogenetic Map	15	q26.1	UniSTS
Cytogenetic Map	2	q32.1	UniSTS
Cytogenetic Map	5	p14.3	UniSTS
Cytogenetic Map	X	p22.13	UniSTS
Cytogenetic Map	13	q14.2	UniSTS
Cytogenetic Map	15	q	UniSTS
Cytogenetic Map	7	q	UniSTS
Cytogenetic Map	17	q25.1	UniSTS
Cytogenetic Map	10	q23	UniSTS
Cytogenetic Map	5	p12	UniSTS
Cytogenetic Map	11	p11.2	UniSTS
Cytogenetic Map	10	q11.21	UniSTS
Cytogenetic Map	20	q13.13	UniSTS
Cytogenetic Map	13	q22.1	UniSTS
Cytogenetic Map	15	q21.2	UniSTS
Cytogenetic Map	X	q28	UniSTS
Cytogenetic Map	9	p13.1	UniSTS
Cytogenetic Map	9	q34.13	UniSTS

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

Low

1671

1336

828

180

177

2017

905

3324

313

1222

870

122

425

1380

Below cutoff

729

1528

838

390

1375

348

2319

1285

334

204

715

779

1408

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NR_015410	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AF086455	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK022865	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK026189	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK094718	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK096633	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK300802	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK310212	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL008732	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL136179	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL136313	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL160260	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL161436	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL359694	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL512344	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC044235	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068272	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY067675	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF458110	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF458112	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KF510947	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KP981381	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA988553	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OA988554	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000444265

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,720 - 22,214,505 (+)	Ensembl

RefSeq Acc Id:

ENST00000561912

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,872 - 22,368,350 (+)	Ensembl

RefSeq Acc Id:

ENST00000567753

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,983 - 22,222,270 (+)	Ensembl

RefSeq Acc Id:

ENST00000605917

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,269 - 22,151,668 (+)	Ensembl

RefSeq Acc Id:

ENST00000606197

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,326 - 22,197,219 (+)	Ensembl

RefSeq Acc Id:

ENST00000606336

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,664,772 - 21,909,837 (+)	Ensembl

RefSeq Acc Id:

ENST00000606851

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,666,444 - 22,194,387 (+)	Ensembl

RefSeq Acc Id:

ENST00000607048

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,668,819 - 22,194,385 (+)	Ensembl

RefSeq Acc Id:

ENST00000636388

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,063,106 - 22,222,457 (+)	Ensembl

RefSeq Acc Id:

ENST00000650720

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,886,119 - 22,030,429 (+)	Ensembl

RefSeq Acc Id:

ENST00000650782

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,667 - 22,194,236 (+)	Ensembl

RefSeq Acc Id:

ENST00000651007

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,954,422 - 22,195,127 (+)	Ensembl

RefSeq Acc Id:

ENST00000651125

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,886,096 - 22,194,412 (+)	Ensembl

RefSeq Acc Id:

ENST00000651277

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,666,404 - 21,671,718 (+)	Ensembl

RefSeq Acc Id:

ENST00000651481

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,664,206 - 21,696,753 (+)	Ensembl

RefSeq Acc Id:

ENST00000651569

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,236,702 - 22,340,790 (+)	Ensembl

RefSeq Acc Id:

ENST00000651620

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,885,656 - 22,194,412 (+)	Ensembl

RefSeq Acc Id:

ENST00000651751

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,461 - 22,196,533 (+)	Ensembl

RefSeq Acc Id:

ENST00000651758

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,647 - 22,194,236 (+)	Ensembl

RefSeq Acc Id:

ENST00000652000

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,203,442 - 22,214,480 (+)	Ensembl

RefSeq Acc Id:

ENST00000652081

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,349,440 - 22,654,455 (+)	Ensembl

RefSeq Acc Id:

ENST00000652256

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,979 - 22,217,178 (+)	Ensembl

RefSeq Acc Id:

ENST00000652717

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,614 - 22,217,719 (+)	Ensembl

RefSeq Acc Id:

ENST00000653010

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,694 - 22,194,224 (+)	Ensembl

RefSeq Acc Id:

ENST00000653161

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,675 - 22,194,234 (+)	Ensembl

RefSeq Acc Id:

ENST00000653246

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,694 - 22,214,502 (+)	Ensembl

RefSeq Acc Id:

ENST00000653320

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,886,154 - 22,063,901 (+)	Ensembl

RefSeq Acc Id:

ENST00000653763

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,706 - 22,222,461 (+)	Ensembl

RefSeq Acc Id:

ENST00000653997

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,666,389 - 22,194,412 (+)	Ensembl

RefSeq Acc Id:

ENST00000654262

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,037 - 22,147,715 (+)	Ensembl

RefSeq Acc Id:

ENST00000654774

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,687 - 22,214,504 (+)	Ensembl

RefSeq Acc Id:

ENST00000654782

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,692 - 22,194,224 (+)	Ensembl

RefSeq Acc Id:

ENST00000654807

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,692 - 22,194,235 (+)	Ensembl

RefSeq Acc Id:

ENST00000654918

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,909,469 - 21,999,360 (+)	Ensembl

RefSeq Acc Id:

ENST00000654942

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,692 - 22,194,230 (+)	Ensembl

RefSeq Acc Id:

ENST00000655154

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,666,388 - 22,194,435 (+)	Ensembl

RefSeq Acc Id:

ENST00000655292

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,675 - 22,194,227 (+)	Ensembl

RefSeq Acc Id:

ENST00000655498

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,687 - 22,194,224 (+)	Ensembl

RefSeq Acc Id:

ENST00000655700

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,616 - 22,196,540 (+)	Ensembl

RefSeq Acc Id:

ENST00000655702

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,782 - 22,214,535 (+)	Ensembl

RefSeq Acc Id:

ENST00000655824

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,687 - 22,194,229 (+)	Ensembl

RefSeq Acc Id:

ENST00000655886

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,675 - 22,194,255 (+)	Ensembl

RefSeq Acc Id:

ENST00000657548

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,572 - 22,195,138 (+)	Ensembl

RefSeq Acc Id:

ENST00000657660

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,673 - 22,194,235 (+)	Ensembl

RefSeq Acc Id:

ENST00000657825

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,571 - 22,191,894 (+)	Ensembl

RefSeq Acc Id:

ENST00000657828

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,326 - 22,196,540 (+)	Ensembl

RefSeq Acc Id:

ENST00000658187

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,886,108 - 21,999,356 (+)	Ensembl

RefSeq Acc Id:

ENST00000658810

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,113,344 - 22,194,419 (+)	Ensembl

RefSeq Acc Id:

ENST00000658841

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,692 - 22,111,011 (+)	Ensembl

RefSeq Acc Id:

ENST00000658974

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,758,478 - 22,194,224 (+)	Ensembl

RefSeq Acc Id:

ENST00000659237

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,180,863 - 22,194,569 (+)	Ensembl

RefSeq Acc Id:

ENST00000659457

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,349,242 - 22,354,384 (+)	Ensembl

RefSeq Acc Id:

ENST00000659720

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,666,404 - 21,784,591 (+)	Ensembl

RefSeq Acc Id:

ENST00000659780

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,569 - 22,196,406 (+)	Ensembl

RefSeq Acc Id:

ENST00000659886

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,648 - 22,111,148 (+)	Ensembl

RefSeq Acc Id:

ENST00000660187

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,675 - 22,110,935 (+)	Ensembl

RefSeq Acc Id:

ENST00000660518

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,673 - 22,194,400 (+)	Ensembl

RefSeq Acc Id:

ENST00000660934

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,675 - 22,194,231 (+)	Ensembl

RefSeq Acc Id:

ENST00000661200

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,615 - 22,214,509 (+)	Ensembl

RefSeq Acc Id:

ENST00000661662

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,147,092 - 22,194,890 (+)	Ensembl

RefSeq Acc Id:

ENST00000661722

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,692 - 21,999,358 (+)	Ensembl

RefSeq Acc Id:

ENST00000661893

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,747 - 22,217,828 (+)	Ensembl

RefSeq Acc Id:

ENST00000662172

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,664,790 - 21,696,759 (+)	Ensembl

RefSeq Acc Id:

ENST00000662187

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,694 - 22,194,224 (+)	Ensembl

RefSeq Acc Id:

ENST00000662510

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,885,656 - 21,999,239 (+)	Ensembl

RefSeq Acc Id:

ENST00000662805

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,574 - 22,194,422 (+)	Ensembl

RefSeq Acc Id:

ENST00000663874

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,571 - 22,194,412 (+)	Ensembl

RefSeq Acc Id:

ENST00000663957

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,647 - 22,194,233 (+)	Ensembl

RefSeq Acc Id:

ENST00000663998

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,113,374 - 22,194,224 (+)	Ensembl

RefSeq Acc Id:

ENST00000664020

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,675 - 22,194,224 (+)	Ensembl

RefSeq Acc Id:

ENST00000664406

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,147,129 - 22,196,427 (+)	Ensembl

RefSeq Acc Id:

ENST00000664431

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,694 - 22,194,174 (+)	Ensembl

RefSeq Acc Id:

ENST00000664500

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,673 - 22,194,232 (+)	Ensembl

RefSeq Acc Id:

ENST00000664560

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,697 - 22,194,231 (+)	Ensembl

RefSeq Acc Id:

ENST00000664625

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,673 - 22,194,234 (+)	Ensembl

RefSeq Acc Id:

ENST00000664716

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,571 - 22,191,895 (+)	Ensembl

RefSeq Acc Id:

ENST00000664756

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,688 - 22,194,174 (+)	Ensembl

RefSeq Acc Id:

ENST00000664780

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,692 - 22,194,231 (+)	Ensembl

RefSeq Acc Id:

ENST00000664808

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,576 - 22,194,412 (+)	Ensembl

RefSeq Acc Id:

ENST00000664889

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,687 - 22,194,219 (+)	Ensembl

RefSeq Acc Id:

ENST00000665014

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,698 - 22,194,224 (+)	Ensembl

RefSeq Acc Id:

ENST00000665902

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,908,313 - 22,111,146 (+)	Ensembl

RefSeq Acc Id:

ENST00000666108

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,630 - 22,194,412 (+)	Ensembl

RefSeq Acc Id:

ENST00000666201

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,566 - 22,196,431 (+)	Ensembl

RefSeq Acc Id:

ENST00000666379

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,627 - 22,218,021 (+)	Ensembl

RefSeq Acc Id:

ENST00000666875

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,113,331 - 22,195,140 (+)	Ensembl

RefSeq Acc Id:

ENST00000667176

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,056,473 - 22,111,011 (+)	Ensembl

RefSeq Acc Id:

ENST00000667291

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,174,046 - 22,222,461 (+)	Ensembl

RefSeq Acc Id:

ENST00000667719

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,687 - 22,194,229 (+)	Ensembl

RefSeq Acc Id:

ENST00000667830

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,688 - 22,194,219 (+)	Ensembl

RefSeq Acc Id:

ENST00000668137

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,566 - 22,222,461 (+)	Ensembl

RefSeq Acc Id:

ENST00000668219

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,694 - 22,194,236 (+)	Ensembl

RefSeq Acc Id:

ENST00000668355

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,671 - 22,194,224 (+)	Ensembl

RefSeq Acc Id:

ENST00000668404

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,661 - 22,194,179 (+)	Ensembl

RefSeq Acc Id:

ENST00000668839

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,686 - 22,194,174 (+)	Ensembl

RefSeq Acc Id:

ENST00000669171

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,675 - 22,214,506 (+)	Ensembl

RefSeq Acc Id:

ENST00000669448

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,326 - 22,195,127 (+)	Ensembl

RefSeq Acc Id:

ENST00000669670

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,147,792 - 22,194,890 (+)	Ensembl

RefSeq Acc Id:

ENST00000669942

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,666,412 - 21,755,639 (+)	Ensembl

RefSeq Acc Id:

ENST00000670293

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,978,973 - 22,194,227 (+)	Ensembl

RefSeq Acc Id:

ENST00000670467

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,668 - 22,194,231 (+)	Ensembl

RefSeq Acc Id:

ENST00000671013

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,692 - 22,194,233 (+)	Ensembl

RefSeq Acc Id:

ENST00000671160

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,664,185 - 22,194,412 (+)	Ensembl

RefSeq Acc Id:

ENST00000671524

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,692 - 22,110,991 (+)	Ensembl

RefSeq Acc Id:

ENST00000671659

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,898,688 - 22,194,232 (+)	Ensembl

RefSeq Acc Id:

ENST00000685436

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,269 - 22,147,731 (+)	Ensembl

RefSeq Acc Id:

ENST00000685576

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,664,184 - 22,195,133 (+)	Ensembl

RefSeq Acc Id:

ENST00000687332

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,883,836 - 22,194,235 (+)	Ensembl

RefSeq Acc Id:

ENST00000688254

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,666,426 - 22,214,506 (+)	Ensembl

RefSeq Acc Id:

ENST00000691204

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,665,509 - 21,669,714 (+)	Ensembl

RefSeq Acc Id:

ENST00000691572

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	21,666,436 - 21,669,714 (+)	Ensembl

RefSeq Acc Id:

ENST00000692274

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,220,781 - 22,222,392 (+)	Ensembl

RefSeq Acc Id:

ENST00000692822

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	6	22,146,569 - 22,147,732 (+)	Ensembl

RefSeq Acc Id:

NR_015410

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	21,666,413 - 22,195,820 (+)	NCBI
GRCh37	6	21,666,675 - 22,194,629 (+)	ENTREZGENE
HuRef	6	21,610,135 - 22,138,081 (+)	ENTREZGENE
CHM1_1	6	21,669,276 - 22,196,747 (+)	NCBI
T2T-CHM13v2.0	6	21,539,084 - 22,068,639 (+)	NCBI

Sequence:

show sequence

GGAGAAACCTGCCGCCGCTCGCCGCCTCTTTGTCTGCTCCGGGACTTGGAACAAAAGGGGGAAC
TCTGATGAACTCTCTTTCCTCCCCTCTCCCCCGGACGCCGGGGTATCTCCCTCTCGCAACTTTG
CCGCCCCGACTTTCTCTGCTGTCAGGCCGGGAAAAAGTGTCCGAACGCCTCGTGGACTGCAGCG
GGGGAAATGTCCCTTAAAAGTGCGACGAAGTGGGGAAGAAGGTGTAATTACTATTATCAGCATC
TAGAAAGCATCATGAATTTGCTGGAGTACTTCCTAGCACTGACCTCCTTCATTCTGCGTTGTTC
TTACTGGATCTTTCCATCAGCCAACAATATGGAAGTACCAATACAAGGTCAAATCATTCCTGGA
TTCATCTGGAGTTGCTTAAAAGTTAAATCATTGGAATTTTTGATGATACCTTTTCTATATGGAT
TACAATTTGATCGCTGGGAATTCTCCACCTTAAAGAAGTACCCTCAGGTGACTACAGATGTGTT
AACACCCAGCATGTTCCGGTAGGAGACTTTCTGGATGGGGAAGATTTCCAGGAATTGGCAACAA
GCTCATTTCACTGGTGGGTTTGCTGAAGCATTATCACAAGACAGTCAGAATGACTGATGAGTGC
TCTTCAGGTGTGAATCATGGCAATACAGTGAAAGACAGTGATTTACTGCTTTTGAGGGCGTGCA
TGTATATGATTAACGGATGGAAGTGCAGGACTCCAAGATTTACTTCCTTCCCTTTCCAGCAGAA
TTACCTGAGACGAGTAAAATCTACTGGTGGAGTCACTCCATTATTCTTATCTGTGGAGATCTAG
ATCTTGATTTGAAAGTTTCTGAGAAAATCTTCAGCTCAGACTTGAGGGTCAACTTTACCAGCTG
AAGGATCTGCATTTACTGCTCAACCACATCTAATTTGATGTCCTCTGCAGATTTAAAATGTGTG
CCTTCTTTTCCGTCACCAAGTCATCCCTGGGTTACTACTGAACATCCTTCTCAATTCCCCCCGA
CCCATGGATGGCTGTTCTCCATTGTCTGTTTCACCAGATGTCCTCAAAACAAACAGACAGAAGA
AGGAAGTGGCTAATGGAGCTGTGGAGTCCAAGTGTGACTGCCAAGAGGAATCCAGCAAAGCCAA
AAAGCCCAAGCATGTAGCCCTGCCCGAAGCACGCCACACGCATGGAAAACCCAGAGGAAATGAG
TGAGGATCAATGGGAAGAAGAGAGCCAGCCAGGAAGTTGAAGATTTGTCCAGGAGCAGATAGCT
GAAGAGAGAGAGAGAGAAGAGAGAACGGCTTACAGCTCAGGTCCTCTCTCCATGCTTAGGAACC
ACTACAAATGCTACTGCCTTGAGTCTCATTTTGTTTCCCTCTGGAAACCACATGTGTACCTTGT
TTGCAACAGTATGGGCTCACAGGCAGAAGGAATTTTCCTTGTCTTGGATGAGACTTTTGACTTG
GACTTTTGGGTTAAGTTCTGGAGACCAGAAGGCCAAAATCAAAAGTATGGGCAGGCTTGATTTC
TTTAGAAGACTCCAGCGGAGAACTGTGTCTCCTTGCTTCTGATTCTACATCTCCATCCATGGGC
CACTGTTTCAGCAACCTCAGCCAGTGCAACACAACCTCAGCCAAGAAGAGTATGCAGAGAAAGG
AGTCCCCTACCTGCCACAAAACTGTTGTCTGAAAACTGTCTCATATTGTCTCAAGTTGTCATTC
ATTGTGAATTAGACCTGTTTAACATGTAATCTGCAACATGCTTCACTGTCTAATTTTCCAGAGC
CCCTCATATAAGGAACTGTATTATTGGTATAATCATCATGGTGAAGAAGTTGGTATGTGGGGGA
GAGATGACAGAAACAGAGAGTAAGTCAGAGCTGGCTGCCTGACAGATAAAAAGGAAATGACCAA
AAAAAAAAAAAAAGACACAGAAGAATACTTTGTTGTCCACACAGAAAAGGGAAGTGTAGGTAAG
ACAGCAGTAGACTAAGATTCTTAAGACTCAAGTTCTAGTCTTATTTATTAGCTATGGGAGGCCT
TGAGGGAGTTCTAGAATTAAGTGATCTCTCTTTATAAAATAGGAACAGTAATAACTTCCTGGCT
AACTCCCTGGCTGTCTCACAATGCTGTAGTAGTAAGAAATAATTTTATAATTAAAGACTATTTT
AGGGCTGATTACATTTTTGGGCAGTGGCTCATACATGTAATTTCAACATTTTGGGAGGCCAAGG
TGGGCGGATTGCTTGAGCCCAGGAATTCAAGACCAGGCTGGGCAACACAGACCTTGTCACTACA
AAAGAAAAAAACATTAGCTAGGCGTGGTGATGTATGCCTGTGGTCCCAGCTACTCAGGAAGCTG
AGACAGGAGGATCACCTGAGCCTGGGAGGTCGAGGCTACAGTGAGCCATGATCACACTACTGCA
CTCCAGCCTGGGAAACAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAGGAATATTTTACACT
TCAAGGTTCTATACAAATGTAAAATATCATTCTATTACTTATTTATAATGCTGATTATTCTTTA
AATGACTTTAAAATGTTAATCTCTGCTTGAGCCTACGGAGAAGTATGTAACAAATTTGTGAAGG
ATTGGCATTAAACATAGTCAAAATAAAACATAGAAATTATGGTAAATAATTTAACTGGTAAAAT
AATCTAAGTGGTAGTTCTCAGGTAAGTGGAAATTCGATTAGCTGATTGTTTAGGATTCTTGGTT
ATAAGTGACAGAGACCTGACTAAAAGTACATGAAGCACATAACTGAGAAGGTTGTGGTATGGCT
CAGCAGAAATGGGAAAATCTTGGGACTGGTTCGTGTTTTATTTACATTATCTTTGTTCCCAGGC
AGTCTCTGCATGTAAGTGGCAAAGATGACTGTCTGAAAATATATACCTACTTTTTTAAAGGGCT
ATCTCAAGCCATTCTGGAGAAGCACCAAAAGCCACTTTGCTTATACTGGGAGAATAGTTTGCTT
TCCCTAATTTGTGATGAGTGAAACACTGAACAGAGACATAGAATAATATTCTGTAGTTCAGGGT
TGGTGTAATATGGCCAGTGGGCGGAATCTGGTCCTCAGACTGATTTTGCAAATAATCTTATAGA
AACACAGCAACACCCATTCATTACATGTTGTTTATGGTTGCTTTGGGGTTACAATGGCAGAGTT
GAGTAGTTGTGACAGAGATCACTAGGCTCACCACATCTGAGATATGTACTGACTGACCCTGTAC
AGAAAGTTTGCTGCTCTTAGAGGAATGTGTGTTTCTAGTGTCAGCAATAAACTTCTTGGATTTG
TTTTGTTTTCTCATCTTTACATGAT

hide sequence

Promoters

RGD ID:

15095992

Promoter ID:

EPDNEWNC_H839

Type:

initiation region

Name:

CASC15_1

Description:

cancer susceptibility 15 [Source:HGNC Symbol;Acc:HGNC:28245]

SO ACC ID:

SO:0000170

Source:

EPDNEWNC (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	21,666,444 - 21,666,504	EPDNEWNC

RGD ID:

15096001

Promoter ID:

EPDNEWNC_H840

Type:

initiation region

Name:

CASC15_2

Description:

cancer susceptibility 15 [Source:HGNC Symbol;Acc:HGNC:28245]

SO ACC ID:

SO:0000170

Source:

EPDNEWNC (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	6	22,146,630 - 22,146,690	EPDNEWNC

Additional Information

External Database Links

Database	Acc Id	Source(s)
COSMIC	CASC15	COSMIC
Ensembl Genes	ENSG00000272168	Ensembl
GTEx	ENSG00000272168	GTEx
HGNC ID	HGNC:28245	ENTREZGENE
Human Proteome Map	CASC15	Human Proteome Map
NCBI Gene	401237	ENTREZGENE
OMIM	616610	OMIM
RNAcentral	URS0000CCE117	RNACentral

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2018-05-22	CASC15	cancer susceptibility 15		cancer susceptibility 15 (non-protein coding)	Symbol and/or name change	5135510	APPROVED
2017-01-31	CASC15	cancer susceptibility 15 (non-protein coding)		cancer susceptibility candidate 15 (non-protein coding)	Symbol and/or name change	5135510	APPROVED
2013-09-03	CASC15	cancer susceptibility candidate 15 (non-protein coding)	LINC00340	long intergenic non-protein coding RNA 340	Symbol and/or name change	5135510	APPROVED

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar