CCDC82 (coiled-coil domain containing 82)

Gene: CCDC82 (coiled-coil domain containing 82) Homo sapiens

Analyze

Symbol:

CCDC82

Name:

coiled-coil domain containing 82

RGD ID:

1602861

HGNC Page

HGNC:26282

Description:

Predicted to be active in nucleus.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

coiled-coil domain-containing protein 82; FLJ23518; HSPC048

RGD Orthologs

Alliance Genes

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Ccdc82 (coiled-coil domain containing 82)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Ccdc82 (coiled-coil domain containing 82)	HGNC	Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Ccdc82 (coiled-coil domain containing 82)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	CCDC82 (coiled-coil domain containing 82)	NCBI	Ortholog
Canis lupus familiaris (dog):	CCDC82 (coiled-coil domain containing 82)	HGNC	Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Ccdc82 (coiled-coil domain containing 82)	NCBI	Ortholog
Sus scrofa (pig):	CCDC82 (coiled-coil domain containing 82)	HGNC	Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	CCDC82 (coiled-coil domain containing 82)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Ccdc82 (coiled-coil domain containing 82)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Ccdc82 (coiled-coil domain containing 82)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Ccdc82 (coiled-coil domain containing 82)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	ccdc82 (coiled-coil domain containing 82)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Drosophila melanogaster (fruit fly):	CG17233	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|PANTHER\|PhylomeDB)
Caenorhabditis elegans (roundworm):	eor-2	Alliance	DIOPT (OrthoFinder\|PANTHER)
Xenopus laevis (African clawed frog):	ccdc82.L	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	ccdc82	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)

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	11	96,352,773 - 96,389,912 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	96,349,241 - 96,389,956 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	96,085,937 - 96,123,076 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	95,725,590 - 95,762,709 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	11	93,386,131 - 93,423,283 (-)	NCBI		Celera
Cytogenetic Map	11	q21	NCBI
HuRef	11	92,152,648 - 92,189,803 (-)	NCBI		HuRef
CHM1_1	11	95,969,288 - 96,006,437 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	11	96,358,768 - 96,395,934 (-)	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

ataxia telangiectasia (IAGP)

genetic disease (IAGP)

intellectual disability (IAGP)

syndromic intellectual disability (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(-)-demecolcine (EXP)

(1->4)-beta-D-glucan (ISO)

1,2-dimethylhydrazine (ISO)

17beta-estradiol (EXP,ISO)

17beta-estradiol 3-benzoate (ISO)

2,3,7,8-tetrachlorodibenzodioxine (EXP,ISO)

acetamide (ISO)

acrolein (EXP)

acrylamide (ISO)

aflatoxin B1 (EXP,ISO)

aflatoxin M1 (EXP)

antirheumatic drug (EXP)

benzo[a]pyrene (ISO)

benzo[a]pyrene diol epoxide I (EXP)

bisphenol A (EXP,ISO)

bortezomib (EXP)

carbon nanotube (ISO)

chlorpyrifos (ISO)

chrysene (ISO)

cyclosporin A (EXP)

dibenzo[a,l]pyrene (ISO)

dicrotophos (EXP)

ethyl methanesulfonate (EXP)

folic acid (ISO)

formaldehyde (EXP)

FR900359 (EXP)

gentamycin (ISO)

hydralazine (EXP)

hydrogen peroxide (EXP)

methotrexate (EXP)

methyl methanesulfonate (EXP)

methylparaben (EXP)

ozone (EXP)

paracetamol (EXP,ISO)

perfluorohexanesulfonic acid (ISO)

perfluorooctane-1-sulfonic acid (EXP,ISO)

pirinixic acid (ISO)

sodium arsenite (EXP)

sunitinib (EXP)

testosterone (ISO)

tetrachloromethane (ISO)

tetraphene (ISO)

theophylline (EXP)

thimerosal (EXP)

trichostatin A (EXP)

valproic acid (EXP)

vinclozolin (ISO)

vincristine (EXP)

vorinostat (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Cellular Component

nucleus (IBA,IEA)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Intellectual disability (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:8889548	PMID:10931946	PMID:11042152	PMID:12477932	PMID:14702039	PMID:15342556	PMID:15489334	PMID:16344560	PMID:17081983	PMID:17353931	PMID:21873635	PMID:23793441
PMID:26496610	PMID:28514442	PMID:32393512	PMID:33961781	PMID:35118659	PMID:35271311	PMID:36215168	PMID:36724073

Genomics

Comparative Map Data

CCDC82
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	11	96,349,241 - 96,389,956 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	11	96,085,937 - 96,123,076 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	11	95,725,590 - 95,762,709 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	11	93,386,131 - 93,423,283 (-)	NCBI		Celera
Cytogenetic Map	11	q21	NCBI
HuRef	11	92,152,648 - 92,189,803 (-)	NCBI		HuRef
CHM1_1	11	95,969,288 - 96,006,437 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	11	96,358,768 - 96,395,934 (-)	NCBI		T2T-CHM13v2.0

Ccdc82
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	9	13,246,573 - 13,292,867 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	9	13,246,536 - 13,292,867 (+)	Ensembl		GRCm39 Ensembl
GRCm38	9	13,246,917 - 13,292,517 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	9	13,246,955 - 13,292,520 (+)	Ensembl	GRCm38		mm10	GRCm38
Celera	9	10,604,678 - 10,650,978 (+)	NCBI		Celera
Cytogenetic Map	9	A1	NCBI

Ccdc82
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	8	18,509,293 - 18,665,008 (+)	NCBI		GRCr8
mRatBN7.2	8	10,227,727 - 10,265,963 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	8	10,228,430 - 10,265,963 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	8	14,212,789 - 14,251,003 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	8	12,510,498 - 12,548,712 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	8	10,488,629 - 10,526,686 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	8	11,888,460 - 11,927,920 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	8	11,888,591 - 11,927,919 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	8	11,845,974 - 11,885,451 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	8	10,118,375 - 10,157,451 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	8	10,118,374 - 10,157,449 (+)	NCBI
Celera	8	11,726,946 - 11,764,927 (+)	NCBI		Celera
Cytogenetic Map	8	q11	NCBI

Ccdc82
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0 Ensembl	NW_004955412	1,174,945 - 1,205,326 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955412	1,178,695 - 1,208,883 (-)	NCBI	ChiLan1.0	ChiLan1.0

CCDC82
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	9	97,200,333 - 97,237,641 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	11	98,292,237 - 98,329,090 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	11	91,359,827 - 91,397,027 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	11	94,884,846 - 94,921,488 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	11	94,884,856 - 94,921,339 (-)	Ensembl	panpan1.1		panPan2

CCDC82
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	21	4,785,169 - 4,818,832 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	21	4,782,389 - 4,817,988 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	21	4,796,008 - 4,830,180 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	21	4,955,528 - 4,989,731 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	21	4,955,560 - 4,989,716 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	21	4,745,691 - 4,779,936 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	21	4,816,051 - 4,850,234 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	21	4,863,849 - 4,898,032 (+)	NCBI		UU_Cfam_GSD_1.0

Ccdc82
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024404947	81,130,429 - 81,163,448 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936700	1,387,332 - 1,415,494 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936700	1,382,272 - 1,415,113 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

CCDC82
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	9	28,376,732 - 28,407,348 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	9	28,376,716 - 28,407,350 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	9	32,410,759 - 32,436,851 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

CCDC82
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	1	87,622,501 - 87,654,789 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	1	87,622,189 - 87,653,838 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666043	38,151,875 - 38,184,230 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Ccdc82
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624735	41,186,413 - 41,216,074 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624735	41,186,413 - 41,217,693 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in CCDC82
29 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 11q14.1-22.3(chr11:78232836-106779420)x1	copy number loss	See cases [RCV000052710]	Chr11:78232836..106779420 [GRCh38] Chr11:77943882..106650146 [GRCh37] Chr11:77621530..106155356 [NCBI36] Chr11:11q14.1-22.3	pathogenic
GRCh38/hg38 11q14.1-22.2(chr11:85242847-102920097)x1	copy number loss	See cases [RCV000052711]	Chr11:85242847..102920097 [GRCh38] Chr11:84953891..102738968 [GRCh37] Chr11:84631539..102296037 [NCBI36] Chr11:11q14.1-22.2	pathogenic
GRCh38/hg38 11q13.5-22.1(chr11:75941754-98357960)x1	copy number loss	See cases [RCV000133838]	Chr11:75941754..98357960 [GRCh38] Chr11:75652798..98228688 [GRCh37] Chr11:75330446..97733898 [NCBI36] Chr11:11q13.5-22.1	pathogenic
GRCh38/hg38 11q14.3-22.3(chr11:91086659-109595582)x1	copy number loss	See cases [RCV000138038]	Chr11:91086659..109595582 [GRCh38] Chr11:90819827..109466308 [GRCh37] Chr11:90459475..108971518 [NCBI36] Chr11:11q14.3-22.3	pathogenic
GRCh37/hg19 11q14.1-21(chr11:80318996-96116221)x1	copy number loss	See cases [RCV000446395]	Chr11:80318996..96116221 [GRCh37] Chr11:11q14.1-21	pathogenic
GRCh37/hg19 11q14.2-22.3(chr11:88152458-109414650)x1	copy number loss	See cases [RCV000510457]	Chr11:88152458..109414650 [GRCh37] Chr11:11q14.2-22.3	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)	copy number gain	See cases [RCV000511729]	Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3	copy number gain	See cases [RCV000510881]	Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
NM_024725.4(CCDC82):c.1294T>C (p.Tyr432His)	single nucleotide variant	Inborn genetic diseases [RCV003247224]	Chr11:96365066 [GRCh38] Chr11:96098230 [GRCh37] Chr11:11q21	likely benign
NM_024725.4(CCDC82):c.1408A>C (p.Ser470Arg)	single nucleotide variant	Inborn genetic diseases [RCV003288527]	Chr11:96359151 [GRCh38] Chr11:96092315 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.215G>C (p.Gly72Ala)	single nucleotide variant	Inborn genetic diseases [RCV003274810]	Chr11:96384533 [GRCh38] Chr11:96117697 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.289A>G (p.Ser97Gly)	single nucleotide variant	Inborn genetic diseases [RCV003275285]	Chr11:96384459 [GRCh38] Chr11:96117623 [GRCh37] Chr11:11q21	uncertain significance
GRCh37/hg19 11q13.4-23.3(chr11:71588805-116680918)x3	copy number gain	not provided [RCV000683374]	Chr11:71588805..116680918 [GRCh37] Chr11:11q13.4-23.3	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3	copy number gain	not provided [RCV000737348]	Chr11:198510..134934063 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3	copy number gain	not provided [RCV000749874]	Chr11:70864..134938470 [GRCh37] Chr11:11p15.5-q25	pathogenic
GRCh37/hg19 11q14.1-23.2(chr11:80053454-113316236)x1	copy number loss	not provided [RCV000737595]	Chr11:80053454..113316236 [GRCh37] Chr11:11q14.1-23.2	pathogenic
GRCh37/hg19 11q21(chr11:95867366-96127385)x3	copy number gain	not provided [RCV000750159]	Chr11:95867366..96127385 [GRCh37] Chr11:11q21	benign
NM_024725.4(CCDC82):c.880A>G (p.Ile294Val)	single nucleotide variant	Inborn genetic diseases [RCV003291672]	Chr11:96383380 [GRCh38] Chr11:96116544 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.1269del (p.Cys424fs)	deletion	not provided [RCV003313435]	Chr11:96365091 [GRCh38] Chr11:96098255 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.205del (p.Ser69fs)	deletion	not provided [RCV003313521]	Chr11:96384543 [GRCh38] Chr11:96117707 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.322A>G (p.Thr108Ala)	single nucleotide variant	not provided [RCV000969068]	Chr11:96384426 [GRCh38] Chr11:96117590 [GRCh37] Chr11:11q21	benign
GRCh37/hg19 11q21-22.1(chr11:95878455-98553076)x1	copy number loss	not provided [RCV001006436]	Chr11:95878455..98553076 [GRCh37] Chr11:11q21-22.1	uncertain significance
GRCh37/hg19 11q21(chr11:95841847-96810072)x3	copy number gain	not provided [RCV001006435]	Chr11:95841847..96810072 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.183del (p.Phe61fs)	deletion	not provided [RCV001267910]	Chr11:96384565 [GRCh38] Chr11:96117729 [GRCh37] Chr11:11q21	pathogenic
GRCh37/hg19 11q21-22.1(chr11:95822513-97875558)x3	copy number gain	not provided [RCV001260147]	Chr11:95822513..97875558 [GRCh37] Chr11:11q21-22.1	uncertain significance
Single allele	deletion	Intellectual disability [RCV001293382]	Chr11:118359328..118372573 [GRCh37] Chr11:11p15.3-q23.3	pathogenic
NC_000011.9:g.(?_94153285)_(111965700_?)del	deletion	Ataxia-telangiectasia syndrome [RCV001389105]	Chr11:94153285..111965700 [GRCh37] Chr11:11q21-23.1	pathogenic
NM_024725.4(CCDC82):c.535C>T (p.Arg179Ter)	single nucleotide variant	Syndromic intellectual disability [RCV001352902]\|not provided [RCV002250375]	Chr11:96384213 [GRCh38] Chr11:96117377 [GRCh37] Chr11:11q21	pathogenic\|uncertain significance
GRCh37/hg19 11q14.1-23.3(chr11:85422071-118022671)x1	copy number loss	not provided [RCV001832892]	Chr11:85422071..118022671 [GRCh37] Chr11:11q14.1-23.3	uncertain significance
GRCh37/hg19 11q14.1-21(chr11:80318996-96116221)	copy number loss	not specified [RCV002052941]	Chr11:80318996..96116221 [GRCh37] Chr11:11q14.1-21	pathogenic
GRCh37/hg19 11q14.1-22.1(chr11:77855209-98002445)	copy number loss	not specified [RCV002052940]	Chr11:77855209..98002445 [GRCh37] Chr11:11q14.1-22.1	pathogenic
NM_024725.4(CCDC82):c.373del (p.Asp125fs)	deletion	not provided [RCV002250391]	Chr11:96384375 [GRCh38] Chr11:96117539 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.67C>T (p.Arg23Ter)	single nucleotide variant	Intellectual disability [RCV002287618]	Chr11:96384681 [GRCh38] Chr11:96117845 [GRCh37] Chr11:11q21	likely pathogenic
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3	copy number gain	MISSED ABORTION [RCV002282973]	Chr11:32799481..134938470 [GRCh37] Chr11:11p13-q25	pathogenic
NM_024725.4(CCDC82):c.653G>T (p.Gly218Val)	single nucleotide variant	Inborn genetic diseases [RCV002727445]	Chr11:96384095 [GRCh38] Chr11:96117259 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.536G>A (p.Arg179Gln)	single nucleotide variant	Inborn genetic diseases [RCV002969124]	Chr11:96384212 [GRCh38] Chr11:96117376 [GRCh37] Chr11:11q21	uncertain significance
GRCh37/hg19 11q14.1-22.3(chr11:81478509-104667040)x1	copy number loss	not provided [RCV002475722]	Chr11:81478509..104667040 [GRCh37] Chr11:11q14.1-22.3	pathogenic
NM_024725.4(CCDC82):c.162G>T (p.Glu54Asp)	single nucleotide variant	Inborn genetic diseases [RCV002793966]	Chr11:96384586 [GRCh38] Chr11:96117750 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.118A>G (p.Ser40Gly)	single nucleotide variant	Inborn genetic diseases [RCV002882562]	Chr11:96384630 [GRCh38] Chr11:96117794 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.631C>T (p.Arg211Cys)	single nucleotide variant	Inborn genetic diseases [RCV002974581]	Chr11:96384117 [GRCh38] Chr11:96117281 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.868G>A (p.Gly290Arg)	single nucleotide variant	Inborn genetic diseases [RCV002684168]	Chr11:96383392 [GRCh38] Chr11:96116556 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.1341G>C (p.Arg447Ser)	single nucleotide variant	Inborn genetic diseases [RCV002992316]	Chr11:96365019 [GRCh38] Chr11:96098183 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.1219G>A (p.Glu407Lys)	single nucleotide variant	Inborn genetic diseases [RCV002691892]	Chr11:96365141 [GRCh38] Chr11:96098305 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.1411C>T (p.Arg471Cys)	single nucleotide variant	Inborn genetic diseases [RCV002978664]	Chr11:96359148 [GRCh38] Chr11:96092312 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.1447T>C (p.Phe483Leu)	single nucleotide variant	Inborn genetic diseases [RCV002757623]	Chr11:96359112 [GRCh38] Chr11:96092276 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.731A>G (p.Lys244Arg)	single nucleotide variant	Inborn genetic diseases [RCV002868344]	Chr11:96384017 [GRCh38] Chr11:96117181 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.1202A>G (p.Gln401Arg)	single nucleotide variant	Inborn genetic diseases [RCV002916286]	Chr11:96371020 [GRCh38] Chr11:96104184 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.265A>G (p.Lys89Glu)	single nucleotide variant	Inborn genetic diseases [RCV002849893]	Chr11:96384483 [GRCh38] Chr11:96117647 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.790T>G (p.Ser264Ala)	single nucleotide variant	Inborn genetic diseases [RCV002930608]	Chr11:96383470 [GRCh38] Chr11:96116634 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.1045A>G (p.Ile349Val)	single nucleotide variant	Inborn genetic diseases [RCV002874704]	Chr11:96373414 [GRCh38] Chr11:96106578 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.475G>A (p.Asp159Asn)	single nucleotide variant	Inborn genetic diseases [RCV002789189]	Chr11:96384273 [GRCh38] Chr11:96117437 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.386A>G (p.His129Arg)	single nucleotide variant	Inborn genetic diseases [RCV002960267]	Chr11:96384362 [GRCh38] Chr11:96117526 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.26C>G (p.Thr9Arg)	single nucleotide variant	Inborn genetic diseases [RCV003356468]	Chr11:96384722 [GRCh38] Chr11:96117886 [GRCh37] Chr11:11q21	uncertain significance
NM_024725.4(CCDC82):c.389T>C (p.Leu130Ser)	single nucleotide variant	Inborn genetic diseases [RCV003355173]	Chr11:96384359 [GRCh38] Chr11:96117523 [GRCh37] Chr11:11q21	likely benign
NM_024725.4(CCDC82):c.100A>G (p.Ile34Val)	single nucleotide variant	not provided [RCV003396030]	Chr11:96384648 [GRCh38] Chr11:96117812 [GRCh37] Chr11:11q21	likely benign

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1041
Count of miRNA genes:	524
Interacting mature miRNAs:	574
Transcripts:	ENST00000278520, ENST00000423339, ENST00000524836, ENST00000525786, ENST00000530106, ENST00000530203, ENST00000538597, ENST00000542662, ENST00000545264
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

Markers in Region

STS-R68789

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	96,085,949 - 96,086,072	UniSTS	GRCh37
Build 36	11	95,725,597 - 95,725,720	RGD	NCBI36
Celera	11	93,386,151 - 93,386,274	RGD
Cytogenetic Map	11	q21	UniSTS
HuRef	11	92,152,668 - 92,152,791	UniSTS
GeneMap99-GB4 RH Map	11	326.69	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

visual system

adipose tissue

appendage

entire extraembryonic component

pharyngeal arch

High

Medium

2016

1477

1166

196

891

2922

1011

3038

215

1265

1484

113

1192

1713

Low

422

1438

560

428

984

373

1434

1186

696

204

195

129

1075

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001318736	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001318737	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001363594	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_024725	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005274292	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006718911	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011542984	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011542987	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011542988	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017018307	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017018310	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024448690	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024448691	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024448692	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024448693	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024448694	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047427602	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047427603	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047427604	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047427605	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047427606	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047427607	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369969	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369970	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369971	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369972	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369973	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369974	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369975	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369976	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369977	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369978	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369979	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054369980	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AF161533	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF245436	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK027171	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK056790	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK074306	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK313893	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK314669	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AP000848	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AP003781	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC018663	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC033726	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM678039	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BP219605	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU742709	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471065	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068267	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA801410	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000278520 ⟹ ENSP00000278520

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,769 - 96,387,904 (-)	Ensembl

RefSeq Acc Id:

ENST00000423339 ⟹ ENSP00000397156

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,353,646 - 96,384,990 (-)	Ensembl

RefSeq Acc Id:

ENST00000524836

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,385,966 - 96,389,923 (-)	Ensembl

RefSeq Acc Id:

ENST00000525786

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,387,140 - 96,389,919 (-)	Ensembl

RefSeq Acc Id:

ENST00000530106 ⟹ ENSP00000495640

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,380,539 - 96,389,956 (-)	Ensembl

RefSeq Acc Id:

ENST00000530203 ⟹ ENSP00000431148

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,777 - 96,389,929 (-)	Ensembl

RefSeq Acc Id:

ENST00000538597 ⟹ ENSP00000442723

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,383,961 - 96,389,412 (-)	Ensembl

RefSeq Acc Id:

ENST00000545264

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,353,448 - 96,359,282 (-)	Ensembl

RefSeq Acc Id:

ENST00000643839 ⟹ ENSP00000495913

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,353,250 - 96,389,936 (-)	Ensembl

RefSeq Acc Id:

ENST00000644312

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,363,128 - 96,389,921 (-)	Ensembl

RefSeq Acc Id:

ENST00000644686 ⟹ ENSP00000495081

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,777 - 96,389,922 (-)	Ensembl

RefSeq Acc Id:

ENST00000645302

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,363,132 - 96,389,566 (-)	Ensembl

RefSeq Acc Id:

ENST00000645366 ⟹ ENSP00000494629

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,779 - 96,389,891 (-)	Ensembl

RefSeq Acc Id:

ENST00000645439 ⟹ ENSP00000495063

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,777 - 96,389,887 (-)	Ensembl

RefSeq Acc Id:

ENST00000645500 ⟹ ENSP00000495485

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,779 - 96,389,948 (-)	Ensembl

RefSeq Acc Id:

ENST00000646050 ⟹ ENSP00000495406

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,805 - 96,389,921 (-)	Ensembl

RefSeq Acc Id:

ENST00000646638 ⟹ ENSP00000494657

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,779 - 96,389,816 (-)	Ensembl

RefSeq Acc Id:

ENST00000646818 ⟹ ENSP00000496393

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,773 - 96,389,912 (-)	Ensembl

RefSeq Acc Id:

ENST00000647080 ⟹ ENSP00000493876

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,787 - 96,389,921 (-)	Ensembl

RefSeq Acc Id:

ENST00000647522

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,363,132 - 96,389,921 (-)	Ensembl

RefSeq Acc Id:

ENST00000679577

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,380,548 - 96,389,779 (-)	Ensembl

RefSeq Acc Id:

ENST00000679616 ⟹ ENSP00000504968

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,358,249 - 96,389,922 (-)	Ensembl

RefSeq Acc Id:

ENST00000679696 ⟹ ENSP00000505581

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,349,241 - 96,389,917 (-)	Ensembl

RefSeq Acc Id:

ENST00000679708 ⟹ ENSP00000506371

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,779 - 96,389,880 (-)	Ensembl

RefSeq Acc Id:

ENST00000679788 ⟹ ENSP00000505510

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,779 - 96,389,905 (-)	Ensembl

RefSeq Acc Id:

ENST00000679823

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,364,649 - 96,373,543 (-)	Ensembl

RefSeq Acc Id:

ENST00000679856 ⟹ ENSP00000505833

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,779 - 96,389,936 (-)	Ensembl

RefSeq Acc Id:

ENST00000679960 ⟹ ENSP00000506164

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,779 - 96,389,921 (-)	Ensembl

RefSeq Acc Id:

ENST00000680049

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,380,548 - 96,389,921 (-)	Ensembl

RefSeq Acc Id:

ENST00000680052 ⟹ ENSP00000505054

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,353,566 - 96,389,922 (-)	Ensembl

RefSeq Acc Id:

ENST00000680171 ⟹ ENSP00000505858

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,779 - 96,389,912 (-)	Ensembl

RefSeq Acc Id:

ENST00000680322

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,153 - 96,389,933 (-)	Ensembl

RefSeq Acc Id:

ENST00000680334

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,363,857 - 96,384,116 (-)	Ensembl

RefSeq Acc Id:

ENST00000680532 ⟹ ENSP00000506206

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,787 - 96,389,865 (-)	Ensembl

RefSeq Acc Id:

ENST00000680728 ⟹ ENSP00000506715

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,781 - 96,389,895 (-)	Ensembl

RefSeq Acc Id:

ENST00000680763 ⟹ ENSP00000504912

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,777 - 96,389,936 (-)	Ensembl

RefSeq Acc Id:

ENST00000680859 ⟹ ENSP00000506687

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,353,250 - 96,389,903 (-)	Ensembl

RefSeq Acc Id:

ENST00000680979 ⟹ ENSP00000505977

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,777 - 96,388,763 (-)	Ensembl

RefSeq Acc Id:

ENST00000681014 ⟹ ENSP00000505643

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,787 - 96,389,868 (-)	Ensembl

RefSeq Acc Id:

ENST00000681164 ⟹ ENSP00000506296

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,779 - 96,389,905 (-)	Ensembl

RefSeq Acc Id:

ENST00000681200 ⟹ ENSP00000505140

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,353,539 - 96,389,919 (-)	Ensembl

RefSeq Acc Id:

ENST00000681238

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,353,447 - 96,371,772 (-)	Ensembl

RefSeq Acc Id:

ENST00000681451 ⟹ ENSP00000506065

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,353,813 - 96,389,921 (-)	Ensembl

RefSeq Acc Id:

ENST00000681745

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,364,287 - 96,389,921 (-)	Ensembl

RefSeq Acc Id:

ENST00000681868

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,380,539 - 96,389,766 (-)	Ensembl

RefSeq Acc Id:

ENST00000681899

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	11	96,352,789 - 96,359,640 (-)	Ensembl

RefSeq Acc Id:

NM_001318736 ⟹ NP_001305665

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI
CHM1_1	11	95,969,288 - 96,006,437 (-)	NCBI
T2T-CHM13v2.0	11	96,358,776 - 96,395,916 (-)	NCBI

Sequence:

show sequence

ATCGCTTGTCCTGAGCTGGTTGCCGGGGCAGGGGCGGAGGCGGAGGCAGAGGTGGAGGCGCTTT
GAAAGAAAACATCGAAGAGGAGTGATGTTTTACACCCAAGAATGGATCCCTCCTGGTAGAATTT
CAAATAATGACCTGGGGTTCCACTGCCTTTCAAATCTGTAAAGTGTTAACTACCACCTGCATTG
TTTATACAGCAACCGTCATTGTGTGGCACTGGACGGGGAATCAAGAGACCCGGTTTCTAATCCC
TGCTCTGTCACTAACAAGCTGCGTGATCTTCGGAAAAAAGTAATCCTCTTGGAAAGCTGGAAAC
ATAGTCCGAAGCTTAAGTGAAAATGATACATGTTAGAAGACATGAAACAAGGAGAAATTCTAAG
AGTCACGTGCCTGAGCAGAAATCTCGAGTTGATTGGAGGCGAACTAAAAGAAGTAGTATCTCAC
AATTACTTGATAGTGATGAAGAGCTTGATAGTGAAGAATTTGATAGTGATGAAGAGCTTGATAG
TGATGAAAGTTTTGAAAATGATGAAGAGCTTGATAGTAACAAGGGACCTGATTGTAATAAAACA
CCAGGAAGTGAAAGAGAGCTCAACTTAAGTAAAATTCAAAGTGAAGGAAATGACAGTAAGTGTC
TCATTAACTCTGGCAACGGTTCAACATATGAAGAAGAAACGAACAAAATCAAACATAGGAATAT
TGACTTACAAGATCAGGAAAAACATTTAAGTCAAGAGGATAATGATCTCAACAAACAAACTGGA
CAAATAATAGAGGATGATCAGGAAAAACATTTAAGTCAAGAGGATAATGATCTCAACAAACAAA
CTGGACAAATAATAGAGGATGATTTAGAAGAAGAAGACATCAAGCGAGGAAAAAGAAAAAGGCT
ATCCTCTGTGATGTGTGACAGTGATGAGAGTGATGACAGCGATATCCTAGTTAGAAAAGTAGGT
GTTAAACGTCCCCGTAGAGTGGTTGAAGATGAAGGTTCTTCAGTGGAAATGGAGCAAAAGACTC
CTGAAAAAACATTAGCTGCACAAAAGCGAGAAAAACTTCAGAAGCTCAAAGAACTCTCAAAACA
AAGATCTCGTCAGAGACGCAGTAGTGGTAGAGATTTTGAGGACTCTGAAAAGGAATCTTGCCCA
AGCAGTGATGAAGTTGATGAGGAGGAAGAAGAGGATAATTATGAATCTGATGAAGATGGAGATG
ATTATATTATCGATGACTTTGTAGTGCAAGATGAGGAGGGTGATGAAGAGAATAAAAACCAACA
AGGAGAAAAATTGACTACATCACAACTGAAATTAGTAAAACAGAATTCTCTTTATTCTTTTAGT
GACCACTATACTCATTTTGAAAGAGTTGTGAAGGCTCTTCTGATCAACGCTTTAGATGAATCTT
TTCTGGGAACATTATATGATGGCACAAGGCAAAAATCATATGCAAAAGATATGCTAACATCTCT
TCATTATTTGGATAACCGCTTTGTTCAGCCTCGTCTAGAGAGCTTGGTATCTAGAAGTCGTTGG
AAAGAGCAATATAAGGAGCGAGTAGAAAATTATTCTAATGTAAGTATTCATTTGAAGAATCCTG
AAAACTGTTCCTGCCAGGCTTGTGGACTGCATCGCTACTGTAAATATTCAGTGCATTTATCAGG
AGAGTTGTATAACACCAGGACCATGCAAATAGATAATTTCATGTCACATGATAAACAGGTGTTC
ACTGTTGGCAGAATTTGTGCCAGCCGTACCAGAATTTATCATAAACTGAAACATTTTAAATTCA
AACTATACCAGGAATGTTGCACCATTGCAATGACAGAAGAAGTTGAAGATGAACAAGTTAAAGA
AACAGTGGAAAGAATTTTCAGGCGGTCAAAAGAAAATGGCTGGATTAAGGAGAAATATGGTCAA
CTTGAAGAATATCTCAATTTTGCGGATTACTTTCAAGAAGAGAAGTTTGAGTTGTAACACATTT
CCATCAGAGAAGATTTTTTAAATTCCTGTAAATGTGAAGATCATGATTCTTGTTTTTCTGTATC
ATGTGACATGTTTGTACATTTTATCTATATCTTCATGGCAAAATATTTTGTTTAAAACATGATT
ATCTTAATTCCTGTGAAGTGGCACTCTACACTCTAATTAAACTTTTATCTGATGTACATAAAAG
CATTATCTTAATTTTTAAGTCTGTAAATATATTTTAAAGTTATATAATAATGGCTTTATAACAG
ATGACTGTCAAGTGAATGAGCTGTTGATATCCTGTCAGTTTAGTCAAAATATATTGTATCTTAA
AAATGTATTTAGACTAACGTCTACATGTATTTTTACGGAATTCCTGTCCAGATCTGTTTATTCT
TTTACAGTATTAAATGATTTTCACTAATATATTTTTTACTGCTATCATCTAAATCAGTGGGCCA
TGGAAGAAACCTCATATATCATTCAGTTCAATCCCATTGCTTCAGAATCAGATCATAGCATATC
TATTCTAAGTAGAGGAATGCTTTTTTCCTTTTCTTGAAAGTTTCTCTTTCAAATAGATTTCAGG
CCTCTAGAGTCTTTCAACCCTCACATTCAGGAATAATTTTATGTAAATTTTCATGCTTTATAAT
GTTCTTACTTTTTTCTATTCAATTTTGTCTATATATTGATGATTAAGATGTATTTTATTTATTT
TTATCCATAGCTTTTTCCATATAAGTATGTATCTTAGGGTCAGAACTGCTGAAAGAGACAAACT
CAGCCAAAAACACTTGGAAAGCATATTTTGGTATCTGCATTGCTTTGCATATCTAAATTTTCCC
ATAAAGTAATAAAGTAAAATGGTTGCAGAGTGAA

hide sequence

RefSeq Acc Id:

NM_001318737 ⟹ NP_001305666

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,380,535 - 96,389,912 (-)	NCBI
CHM1_1	11	95,998,320 - 96,006,437 (-)	NCBI
T2T-CHM13v2.0	11	96,386,539 - 96,395,916 (-)	NCBI

Sequence:

show sequence

ATCGCTTGTCCTGAGCTGGTTGCCGGGGCAGGGGCGGAGGCGGAGGCAGAGGTGGAGGCGCTTT
GAAAGCCGTCATTGTGTGGCACTGGACGGGGAATCAAGAGACCCGGTTTCTAATCCCTGCTCTG
TCACTAACAAGCTGCGTGATCTTCGGAAAAAAGTAATCCTCTTGGAAAGCTGGAAACATAGTCC
GAAGCTTAAGTGAAAATGATACATGTTAGAAGACATGAAACAAGGAGAAATTCTAAGAGTCACG
TGCCTGAGCAGAAATCTCGAGTTGATTGGAGGCGAACTAAAAGAAGTAGTATCTCACAATTACT
TGATAGTGATGAAGAGCTTGATAGTGAAGAATTTGATAGTGATGAAGAGCTTGATAGTGATGAA
AGTTTTGAAAATGATGAAGAGCTTGATAGTAACAAGGGACCTGATTGTAATAAAACACCAGGAA
GTGAAAGAGAGCTCAACTTAAGTAAAATTCAAAGTGAAGGAAATGACAGTAAGTGTCTCATTAA
CTCTGGCAACGGTTCAACATATGAAGAAGAAACGAACAAAATCAAACATAGGAATATTGACTTA
CAAGATCAGGAAAAACATTTAAGTCAAGAGGATAATGATCTCAACAAACAAACTGGACAAATAA
TAGAGGATGATCAGGAAAAACATTTAAGTCAAGAGGATAATGATCTCAACAAACAAACTGGACA
AATAATAGAGGATGATTTAGAAGAAGAAGACATCAAGCGAGGAAAAAGAAAAAGGCTATCCTCT
GTGATGTGTGACAGTGATGAGAGTGATGACAGCGATATCCTAGTTAGAAAAGTAGGTGTTAAAC
GTCCCCGTAGAGTGGTTGAAGATGAAGGTTCTTCAGTGGAAATGGAGCAAAAGACTCCTGAAAA
AACATTAGCTGCACAAAAGCGAGAAAAACTTCAGAAGCTCAAAGAACTCTCAAAACAAAGATCT
CGTCAGAGACGCAGTAGTGGTAGAGATTTTGAGGACTCTGAAAAGGAATCTTGCCCAAGCAGTG
ATGAAGTTGATGAGGAGGAAGAAGAGGATAATTATGAATCTGATGAAGATGGAGATGATTATAT
TATCGATGACTTTGTAGTGCAAGATGAGGAGGGTGATGAAGAGAATAAAAACCAACAAGGAGAA
AAATTGACTACATCACAACTGAAATTAGTAAAACAGAATTCTCTTTGTAAGTTCAATATTAAGA
AAATGTTTCATGAATTGTTCTCATGATATTTTATCAAGTATCAAATTAGCCTTTTAATATCATG
TTCTAAATCATTGACTAGAAACTGTGGTTTCATTTTCAGATAACCTTGTCAGTTTAATAGTTTA
TTCCAGTGGTCTCAGGAACCATTTACATTTTTCAAAATTATTAACCCCAACACGCCTTTACTTC
AATGAGTTATGCCTGTCAATATTTACCATTGTAGAAATCAAAACTCAGAAATTTAAAATATATT
TATTAATTCATTTAAAATAATCCTTAGTAAATTTATTACATTAATGTAAATAACAATTTTATGA
AAAGTAACTATATTTTTCCCCAAAATGTGATAAATGGCATTGTTTTACATTCTTGTAAATCTTT
AATGTCTAGCTTATAGAAGCCAGCTAGATTCTTATATCTGCTTTTACGTTCAGTCTGTTGTGAC
ATGTTGTTTTGGTTGAAGTGTATGAAAACAATTTTGCCTCACACAGGTAGCTGGAAAAGGGAGG
AGTATTTTAATAGTATTTTAAAAATAATTGTTGATATTCTCATTTGATACTATGCCAAAATTTG
ACAAATGATACTGTTTTCTTAAAGATAATATGGAATTCAAAACCATATAAATGAACTTTTAGTA
CTTGCATTACAACCATTGGTCTGTCGTGCAGTTTAAATAGATAATTTCCCCATGCATGATTTTG
TGATAAAATGCATCAGTCATTTGGAAAATACTGGTTCACTGGATGATACAGATCCTCCAAAATA
TTGACATATTTCATTATATATATATTTTTAATTATATTCATTAATATCACCACCAATCCCATGA
GAATATTTCTCAGGTATTGAGAAGCCGTCAGGCTCAGAATAGCACATACAAGTTTTTCAAAATT
CTAATTTCTGCTTTAAAACTTGATTGTTTTCATTGGCGACAAAACACCGAATTGTTCTTTTTGA
ACTGACAGGCTTACTTTGTTCTTTTTTGAGAAAAGTCTGACAGATTCCCAAGTCTGAATAACCA
GAGCTTGTCACTCTTTCTTTCAAATAAAAATGGTATTTCATGAAAAATGAGGCTTTCCCCCCAC
ACACACAGTTGCACAGGTGTTTTTCCCTCAAAACAACCATTGTACTTTGGTATGCAGTATGAGT
GCTTTTTATGCACTTTCCATTTCATCCTATAGAGTACTACAAAGATGTGTACTTCACATTCAAG
ATTTAATACAGTTAATAGTTTTACTGCTTCAACGAGGACATTCTTAAGTGAAAGTGGCTTTTTT
TACTGTGAGTGCATAGTGGTAATGACAGTAATGATTACTAGTAGTTTGATGCTACTGCCATGAT
TCAAGTTAAGGGGCCAGCTGCCTTACCCATCACTGCTTTTACATCATCAATGAAAATGTCAACA
CAGTGAAAAAAGCAAATAAATAATATTGTTATTACTTGAAATCACAGATTTCCTTAAATGGACT
TGGGCACTATCAGGGGTCTGCGGACAAACACTTTGAGAACCATTGGTTTTATCAGACTTTTTGA
AGCTTCTCTCAAACAGTGAAACCTATCAGAGATAGGACGTTACTTACATGAAAATATAAATCAT
GGAACCTGAAAATGTAGGATATATTTAAATTATTATTATTATGATTCCTATAATTCTACAAAAT
TTCAAAGATTGTTTTTATGATGTTTTACAGCTCTGGTAGGAACAAGGTGTTGGATGGATATACT
TTTATTTTTTTTCTTTGAGTGCATTCTTTCCAAATATTTCAGAAAAGGCCATATTGACTAAAAT
AAAGTGTGACATGACTTGATTTATATCTCATGATTTATAATAAAATAGTGGATTTGGAGATATG
AATCAAATTTCAAGAAATTTGGCAGTTATAGAGATGCCAGTTACAGTTATCTCTACACTGCAAG
TTAATGACTGTTTTCCTTATATCAGTAGGCACTGGTTCACTTGCCACCTGGACATTTAAATTAC
AGGGATACTCAATTAGGAGATATCCTATTTTGGGTTATCTAGAATGTGATGGAACATTTGCTGA
GAGATGCCAACTCATATCAACTCCTGCCAATTAATGGAAATAAAAGGCTAGCATATGGGAACTT
CAACTTCTTTACACCTTTTAGTTGTTTTTTTTAAGGGCACTTTTGGAGTTACAGAAATATTGAA
TGGAATGTACAGAGTTCAAATATACTTCCTCACGTACACAGTTTCCCCTATTATTAACCTCTTT
TATTAGTTTGGTACCTCTGTTACAGTTATTAACTGTAGTTCATACTTCACAACAGGGCTCATTT
TTTAGTACCTTTTATGGGTTTTGACAAGTGTGTAATGACATGTATCTACCATTACACTATCATA
CAGAGTAGTTTCATTGTCCTCAAAATGCCCTGTGCTTTAATTCATTCTCCTTTCCTCCCTCCTC
TGAATCACTGATGTTTTTACCCTCTCCATAGTTTTGCTTTTGCCAAACTGTCATATAGTTGGAA
TCACACAGCATATAACTTTTCAGATTGTCTTCTTTCACTTAATAATATGCACTTAGGTTTCCTC
CATGTCTAAATGTGGCTTAATAGCGCATTTCTTTTTATCGCTGAATATTTTTCATTGTATGGAT
GTACCACAGTTTTGTTCATCCATTCACCTATTGAAAGACATCTTGGTTGCTTACAAGTTTTGGC
AATTGTGAATAAAGCTGCTATAAACATT

hide sequence

RefSeq Acc Id:

NM_001363594 ⟹ NP_001350523

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI
T2T-CHM13v2.0	11	96,358,776 - 96,395,916 (-)	NCBI

Sequence:

show sequence

ATCGCTTGTCCTGAGCTGGTTGCCGGGGCAGGGGCGGAGGCGGAGGCAGAGGTGGAGGCGCTTT
GAAAGGTGAGAGCGCGAGGGCGGTGCGGGGCTGTCTCCCGGCTGGGACTCGCTCGCGCTCCCGG
TGCTAATGGTTTATGAGAGGGGCGGGGGAAGCCGTGCCTCCTCGCGGACTAAGAGAAAAATTCC
CGCGGGCGCTCTTTGGGTGGGCCGGAGAACGCCCCTCAGCCCTTTGCGCCTCTAACCCTCCTCA
GCTGAGCTGCAGTGGGCGCGGTGCCCGTTATTTCCGCCTTGGGGAGGTGCTTGGAACTGATGTA
GGGAGCTCGGTTGGTGATTTCTCGGGTTTCTGGCCTTTCCAGACCCTTGTAATTGTTTTCTCGG
TGCAGAGCTCTTTTGGGGTCTGGGGGTTTCCGTCGTCCTGCGCGCGTCATCGCGAAGCTTGGCC
TGAGGGTCCGGTTTCCTAGCTACTGTGCCCCTCCCTCCTGGAGGCAGAGTGACGGACTAGTGGG
CTAGCGGGCGCTGGGTTCCTGCGTCCCGCCAAAGAGGTTTGTAATCATGAAAGTCACCCTTCCG
GGTGTTAATTCCTGAGAGGATCTATTCCACTGTCTACCACTCATTCCTGCTGCATTAACCTTCA
TTGTTAACGGATTTTAATGAATAATATAGTTATCCCGGATACCATGCTGGCAGGATCCACTTTG
CGAAATTGTGGACTGTTGGACTGTGATTCTAAGTGGGGGAAATAGGCTTTCCTCTCTTTATGTT
TATTTTCTTATATCCTATTTCTGTCATGTTCTGTCTTGTTTTCCTGCCAATAGAAGAACTATGA
TAAATTTATTCATAGCAGTGTGATAAGAACTTGATCTTAATCATACACTGTAGCCCTCAAATCG
TGTATTATGCTGGCTTGTTTTTGGTGTCCCTAGTAATTTCATCAGATTGTGAGCTCCTTGGGAG
CAGAGACCATGTTTATTTGAAATGGTGGCAGCACAGTTCCTAGCAGGTGCTTGCATTTTGGTAG
ATATTCAATAATTATTTTTCGGCTTATTAATCTTTGCTCTCCAAACTGCCATATAAAAGAAAAC
ATCGAAGAGGAGTGATGTTTTACACCCAAGAATGGATCCCTCCTGGTAGAATTTCAAATAATGA
CCTGGGGTTCCACTGCCTTTCAAATCTGTAAAGTGTTAACTACCACCTGCATTGTTTATACAGC
AACCGTCATTGTGTGGCACTGGACGGGGAATCAAGAGACCCGGTTTCTAATCCCTGCTCTGTCA
CTAACAAGCTGCGTGATCTTCGGAAAAAAGTAATCCTCTTGGAAAGCTGGAAACATAGTCCGAA
GCTTAAGTGAAAATGATACATGTTAGAAGACATGAAACAAGGAGAAATTCTAAGAGTCACGTGC
CTGAGCAGAAATCTCGAGTTGATTGGAGGCGAACTAAAAGAAGTAGTATCTCACAATTACTTGA
TAGTGATGAAGAGCTTGATAGTGAAGAATTTGATAGTGATGAAGAGCTTGATAGTGATGAAAGT
TTTGAAAATGATGAAGAGCTTGATAGTAACAAGGGACCTGATTGTAATAAAACACCAGGAAGTG
AAAGAGAGCTCAACTTAAGTAAAATTCAAAGTGAAGGAAATGACAGTAAGTGTCTCATTAACTC
TGGCAACGGTTCAACATATGAAGAAGAAACGAACAAAATCAAACATAGGAATATTGACTTACAA
GATCAGGAAAAACATTTAAGTCAAGAGGATAATGATCTCAACAAACAAACTGGACAAATAATAG
AGGATGATTTAGAAGAAGAAGACATCAAGCGAGGAAAAAGAAAAAGGCTATCCTCTGTGATGTG
TGACAGTGATGAGAGTGATGACAGCGATATCCTAGTTAGAAAAGTAGGTGTTAAACGTCCCCGT
AGAGTGGTTGAAGATGAAGGTTCTTCAGTGGAAATGGAGCAAAAGACTCCTGAAAAAACATTAG
CTGCACAAAAGCGAGAAAAACTTCAGAAGCTCAAAGAACTCTCAAAACAAAGATCTCGTCAGAG
ACGCAGTAGTGGTAGAGATTTTGAGGACTCTGAAAAGGAATCTTGCCCAAGCAGTGATGAAGTT
GATGAGGAGGAAGAAGAGGATAATTATGAATCTGATGAAGATGGAGATGATTATATTATCGATG
ACTTTGTAGTGCAAGATGAGGAGGGTGATGAAGAGAATAAAAACCAACAAGGAGAAAAATTGAC
TACATCACAACTGAAATTAGTAAAACAGAATTCTCTTTATTCTTTTAGTGACCACTATACTCAT
TTTGAAAGAGTTGTGAAGGCTCTTCTGATCAACGCTTTAGATGAATCTTTTCTGGGAACATTAT
ATGATGGCACAAGGCAAAAATCATATGCAAAAGATATGCTAACATCTCTTCATTATTTGGATAA
CCGCTTTGTTCAGCCTCGTCTAGAGAGCTTGGTATCTAGAAGTCGTTGGAAAGAGCAATATAAG
GAGCGAGTAGAAAATTATTCTAATGTAAGTATTCATTTGAAGAATCCTGAAAACTGTTCCTGCC
AGGCTTGTGGACTGCATCGCTACTGTAAATATTCAGTGCATTTATCAGGAGAGTTGTATAACAC
CAGGACCATGCAAATAGATAATTTCATGTCACATGATAAACAGGTGTTCACTGTTGGCAGAATT
TGTGCCAGCCGTACCAGAATTTATCATAAACTGAAACATTTTAAATTCAAACTATACCAGGAAT
GTTGCACCATTGCAATGACAGAAGAAGTTGAAGATGAACAAGTTAAAGAAACAGTGGAAAGAAT
TTTCAGGCGGTCAAAAGAAAATGGCTGGATTAAGGAGAAATATGGTCAACTTGAAGAATATCTC
AATTTTGCGGATTACTTTCAAGAAGAGAAGTTTGAGTTGTAACACATTTCCATCAGAGAAGATT
TTTTAAATTCCTGTAAATGTGAAGATCATGATTCTTGTTTTTCTGTATCATGTGACATGTTTGT
ACATTTTATCTATATCTTCATGGCAAAATATTTTGTTTAAAACATGATTATCTTAATTCCTGTG
AAGTGGCACTCTACACTCTAATTAAACTTTTATCTGATGTACATAAAAGCATTATCTTAATTTT
TAAGTCTGTAAATATATTTTAAAGTTATATAATAATGGCTTTATAACAGATGACTGTCAAGTGA
ATGAGCTGTTGATATCCTGTCAGTTTAGTCAAAATATATTGTATCTTAAAAATGTATTTAGACT
AACGTCTACATGTATTTTTACGGAATTCCTGTCCAGATCTGTTTATTCTTTTACAGTATTAAAT
GATTTTCACTAATATATTTTTTACTGCTATCATCTAAATCAGTGGGCCATGGAAGAAACCTCAT
ATATCATTCAGTTCAATCCCATTGCTTCAGAATCAGATCATAGCATATCTATTCTAAGTAGAGG
AATGCTTTTTTCCTTTTCTTGAAAGTTTCTCTTTCAAATAGATTTCAGGCCTCTAGAGTCTTTC
AACCCTCACATTCAGGAATAATTTTATGTAAATTTTCATGCTTTATAATGTTCTTACTTTTTTC
TATTCAATTTTGTCTATATATTGATGATTAAGATGTATTTTATTTATTTTTATCCATAGCTTTT
TCCATATAAGTATGTATCTTAGGGTCAGAACTGCTGAAAGAGACAAACTCAGCCAAAAACACTT
GGAAAGCATATTTTGGTATCTGCATTGCTTTGCATATCTAAATTTTCCCATAAAGTAATAAAGT
AAAATGGTTGCAGAGTGAA

hide sequence

RefSeq Acc Id:

NM_024725 ⟹ NP_079001

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI
GRCh37	11	96,085,929 - 96,123,083 (-)	NCBI
Build 36	11	95,725,590 - 95,762,709 (-)	NCBI Archive
Celera	11	93,386,131 - 93,423,283 (-)	RGD
HuRef	11	92,152,648 - 92,189,803 (-)	ENTREZGENE
CHM1_1	11	95,969,288 - 96,006,437 (-)	NCBI
T2T-CHM13v2.0	11	96,358,776 - 96,395,916 (-)	NCBI

Sequence:

show sequence

ATCGCTTGTCCTGAGCTGGTTGCCGGGGCAGGGGCGGAGGCGGAGGCAGAGGTGGAGGCGCTTT
GAAAGCCGTCATTGTGTGGCACTGGACGGGGAATCAAGAGACCCGGTTTCTAATCCCTGCTCTG
TCACTAACAAGCTGCGTGATCTTCGGAAAAAAGTAATCCTCTTGGAAAGCTGGAAACATAGTCC
GAAGCTTAAGTGAAAATGATACATGTTAGAAGACATGAAACAAGGAGAAATTCTAAGAGTCACG
TGCCTGAGCAGAAATCTCGAGTTGATTGGAGGCGAACTAAAAGAAGTAGTATCTCACAATTACT
TGATAGTGATGAAGAGCTTGATAGTGAAGAATTTGATAGTGATGAAGAGCTTGATAGTGATGAA
AGTTTTGAAAATGATGAAGAGCTTGATAGTAACAAGGGACCTGATTGTAATAAAACACCAGGAA
GTGAAAGAGAGCTCAACTTAAGTAAAATTCAAAGTGAAGGAAATGACAGTAAGTGTCTCATTAA
CTCTGGCAACGGTTCAACATATGAAGAAGAAACGAACAAAATCAAACATAGGAATATTGACTTA
CAAGATCAGGAAAAACATTTAAGTCAAGAGGATAATGATCTCAACAAACAAACTGGACAAATAA
TAGAGGATGATCAGGAAAAACATTTAAGTCAAGAGGATAATGATCTCAACAAACAAACTGGACA
AATAATAGAGGATGATTTAGAAGAAGAAGACATCAAGCGAGGAAAAAGAAAAAGGCTATCCTCT
GTGATGTGTGACAGTGATGAGAGTGATGACAGCGATATCCTAGTTAGAAAAGTAGGTGTTAAAC
GTCCCCGTAGAGTGGTTGAAGATGAAGGTTCTTCAGTGGAAATGGAGCAAAAGACTCCTGAAAA
AACATTAGCTGCACAAAAGCGAGAAAAACTTCAGAAGCTCAAAGAACTCTCAAAACAAAGATCT
CGTCAGAGACGCAGTAGTGGTAGAGATTTTGAGGACTCTGAAAAGGAATCTTGCCCAAGCAGTG
ATGAAGTTGATGAGGAGGAAGAAGAGGATAATTATGAATCTGATGAAGATGGAGATGATTATAT
TATCGATGACTTTGTAGTGCAAGATGAGGAGGGTGATGAAGAGAATAAAAACCAACAAGGAGAA
AAATTGACTACATCACAACTGAAATTAGTAAAACAGAATTCTCTTTATTCTTTTAGTGACCACT
ATACTCATTTTGAAAGAGTTGTGAAGGCTCTTCTGATCAACGCTTTAGATGAATCTTTTCTGGG
AACATTATATGATGGCACAAGGCAAAAATCATATGCAAAAGATATGCTAACATCTCTTCATTAT
TTGGATAACCGCTTTGTTCAGCCTCGTCTAGAGAGCTTGGTATCTAGAAGTCGTTGGAAAGAGC
AATATAAGGAGCGAGTAGAAAATTATTCTAATGTAAGTATTCATTTGAAGAATCCTGAAAACTG
TTCCTGCCAGGCTTGTGGACTGCATCGCTACTGTAAATATTCAGTGCATTTATCAGGAGAGTTG
TATAACACCAGGACCATGCAAATAGATAATTTCATGTCACATGATAAACAGGTGTTCACTGTTG
GCAGAATTTGTGCCAGCCGTACCAGAATTTATCATAAACTGAAACATTTTAAATTCAAACTATA
CCAGGAATGTTGCACCATTGCAATGACAGAAGAAGTTGAAGATGAACAAGTTAAAGAAACAGTG
GAAAGAATTTTCAGGCGGTCAAAAGAAAATGGCTGGATTAAGGAGAAATATGGTCAACTTGAAG
AATATCTCAATTTTGCGGATTACTTTCAAGAAGAGAAGTTTGAGTTGTAACACATTTCCATCAG
AGAAGATTTTTTAAATTCCTGTAAATGTGAAGATCATGATTCTTGTTTTTCTGTATCATGTGAC
ATGTTTGTACATTTTATCTATATCTTCATGGCAAAATATTTTGTTTAAAACATGATTATCTTAA
TTCCTGTGAAGTGGCACTCTACACTCTAATTAAACTTTTATCTGATGTACATAAAAGCATTATC
TTAATTTTTAAGTCTGTAAATATATTTTAAAGTTATATAATAATGGCTTTATAACAGATGACTG
TCAAGTGAATGAGCTGTTGATATCCTGTCAGTTTAGTCAAAATATATTGTATCTTAAAAATGTA
TTTAGACTAACGTCTACATGTATTTTTACGGAATTCCTGTCCAGATCTGTTTATTCTTTTACAG
TATTAAATGATTTTCACTAATATATTTTTTACTGCTATCATCTAAATCAGTGGGCCATGGAAGA
AACCTCATATATCATTCAGTTCAATCCCATTGCTTCAGAATCAGATCATAGCATATCTATTCTA
AGTAGAGGAATGCTTTTTTCCTTTTCTTGAAAGTTTCTCTTTCAAATAGATTTCAGGCCTCTAG
AGTCTTTCAACCCTCACATTCAGGAATAATTTTATGTAAATTTTCATGCTTTATAATGTTCTTA
CTTTTTTCTATTCAATTTTGTCTATATATTGATGATTAAGATGTATTTTATTTATTTTTATCCA
TAGCTTTTTCCATATAAGTATGTATCTTAGGGTCAGAACTGCTGAAAGAGACAAACTCAGCCAA
AAACACTTGGAAAGCATATTTTGGTATCTGCATTGCTTTGCATATCTAAATTTTCCCATAAAGT
AATAAAGTAAAATGGTTGCAGAGTGAA

hide sequence

RefSeq Acc Id:

XM_005274292 ⟹ XP_005274349

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI

Sequence:

show sequence

GGGGGAGGAGCATCGCTTGTCCTGAGCTGGTTGCCGGGGCAGGGGCGGAGGCGGAGGCAGAGGT
GGAGGCGCTTTGAAAGAAGCTTAAGTGAAAATGATACATGTTAGAAGACATGAAACAAGGAGAA
ATTCTAAGAGTCACGTGCCTGAGCAGAAATCTCGAGTTGATTGGAGGCGAACTAAAAGAAGTAG
TATCTCACAATTACTTGATAGTGATGAAGAGCTTGATAGTGAAGAATTTGATAGTGATGAAGAG
CTTGATAGTGATGAAAGTTTTGAAAATGATGAAGAGCTTGATAGTAACAAGGGACCTGATTGTA
ATAAAACACCAGGAAGTGAAAGAGAGCTCAACTTAAGTAAAATTCAAAGTGAAGGAAATGACAG
TAAGTGTCTCATTAACTCTGGCAACGGTTCAACATATGAAGAAGAAACGAACAAAATCAAACAT
AGGAATATTGACTTACAAGATCAGGAAAAACATTTAAGTCAAGAGGATAATGATCTCAACAAAC
AAACTGGACAAATAATAGAGGATGATCAGGAAAAACATTTAAGTCAAGAGGATAATGATCTCAA
CAAACAAACTGGACAAATAATAGAGGATGATTTAGAAGAAGAAGACATCAAGCGAGGAAAAAGA
AAAAGGCTATCCTCTGTGATGTGTGACAGTGATGAGAGTGATGACAGCGATATCCTAGTTAGAA
AAGTAGGTGTTAAACGTCCCCGTAGAGTGGTTGAAGATGAAGGTTCTTCAGTGGAAATGGAGCA
AAAGACTCCTGAAAAAACATTAGCTGCACAAAAGCGAGAAAAACTTCAGAAGCTCAAAGAACTC
TCAAAACAAAGATCTCGTCAGAGACGCAGTAGTGGTAGAGATTTTGAGGACTCTGAAAAGGAAT
CTTGCCCAAGCAGTGATGAAGTTGATGAGGAGGAAGAAGAGGATAATTATGAATCTGATGAAGA
TGGAGATGATTATATTATCGATGACTTTGTAGTGCAAGATGAGGAGGGTGATGAAGAGAATAAA
AACCAACAAGGAGAAAAATTGACTACATCACAACTGAAATTAGTAAAACAGAATTCTCTTTATT
CTTTTAGTGACCACTATACTCATTTTGAAAGAGTTGTGAAGGCTCTTCTGATCAACGCTTTAGA
TGAATCTTTTCTGGGAACATTATATGATGGCACAAGGCAAAAATCATATGCAAAAGATATGCTA
ACATCTCTTCATTATTTGGATAACCGCTTTGTTCAGCCTCGTCTAGAGAGCTTGGTATCTAGAA
GTCGTTGGAAAGAGCAATATAAGGAGCGAGTAGAAAATTATTCTAATGTAAGTATTCATTTGAA
GAATCCTGAAAACTGTTCCTGCCAGGCTTGTGGACTGCATCGCTACTGTAAATATTCAGTGCAT
TTATCAGGAGAGTTGTATAACACCAGGACCATGCAAATAGATAATTTCATGTCACATGATAAAC
AGGTGTTCACTGTTGGCAGAATTTGTGCCAGCCGTACCAGAATTTATCATAAACTGAAACATTT
TAAATTCAAACTATACCAGGAATGTTGCACCATTGCAATGACAGAAGAAGTTGAAGATGAACAA
GTTAAAGAAACAGTGGAAAGAATTTTCAGGCGGTCAAAAGAAAATGGCTGGATTAAGGAGAAAT
ATGGTCAACTTGAAGAATATCTCAATTTTGCGGATTACTTTCAAGAAGAGAAGTTTGAGTTGTA
ACACATTTCCATCAGAGAAGATTTTTTAAATTCCTGTAAATGTGAAGATCATGATTCTTGTTTT
TCTGTATCATGTGACATGTTTGTACATTTTATCTATATCTTCATGGCAAAATATTTTGTTTAAA
ACATGATTATCTTAATTCCTGTGAAGTGGCACTCTACACTCTAATTAAACTTTTATCTGATGTA
CATAAAAGCATTATCTTAATTTTTAAGTCTGTAAATATATTTTAAAGTTATATAATAATGGCTT
TATAACAGATGACTGTCAAGTGAATGAGCTGTTGATATCCTGTCAGTTTAGTCAAAATATATTG
TATCTTAAAAATGTATTTAGACTAACGTCTACATGTATTTTTACGGAATTCCTGTCCAGATCTG
TTTATTCTTTTACAGTATTAAATGATTTTCACTAATATATTTTTTACTGCTATCATCTAAATCA
GTGGGCCATGGAAGAAACCTCATATATCATTCAGTTCAATCCCATTGCTTCAGAATCAGATCAT
AGCATATCTATTCTAAGTAGAGGAATGCTTTTTTCCTTTTCTTGAAAGTTTCTCTTTCAAATAG
ATTTCAGGCCTCTAGAGTCTTTCAACCCTCACATTCAGGAATAATTTTATGTAAATTTTCATGC
TTTATAATGTTCTTACTTTTTTCTATTCAATTTTGTCTATATATTGATGATTAAGATGTATTTT
ATTTATTTTTATCCATAGCTTTTTCCATATAAGTATGTATCTTAGGGTCAGAACTGCTGAAAGA
GACAAACTCAGCCAAAAACACTTGGAAAGCATATTTTGGTATCTGCATTGCTTTGCATATCTAA
ATTTTCCCATAAAGTAATAAAGTAAAATGGTTGCAGAGTGAACAAATGAA

hide sequence

RefSeq Acc Id:

XM_011542984 ⟹ XP_011541286

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI

Sequence:

show sequence

GTGCGGGGCTGTCTCCCGGCTGGGACTCGCTCGCGCTCCCGGTGCTAATGGTTTATGAGAGGGG
CGGGGGAAGCCGTGCCTCCTCGCGGACTAAGAGAAAAATTCCCGCGGGCGCTCTTTGGGTGGGC
CGGAGAACGCCCCTCAGCCCTTTGCGCCTCTAACCCTCCTCAGCTGAGCTGCAGTGGGCGCGGT
GCCCGTTATTTCCGCCTTGGGGAGGTGCTTGGAACTGATGTAGGGAGCTCGGTTGGTGATTTCT
CGGGTTTCTGGCCTTTCCAGACCCTTGTAATTGTTTTCTCGGTGCAGAGCTCTTTTGGGGTCTG
GGGGTTTCCGTCGTCCTGCGCGCGTCATCGCGAAGCTTGGCCTGAGGGTCCGGTTTCCTAGCTA
CTGTGCCCCTCCCTCCTGGAGGCAGAGTGACGGACTAGTGGGCTAGCGGGCGCTGGGTTCCTGC
GTCCCGCCAAAGAGGTTTGTAATCATGAAAGTCACCCTTCCGGGTGTTAATTCCTGAGAGGATC
TATTCCACTGTCTACCACTCATTCCTGCTGCATTAACCTTCATTGTTAACGGATTTTAATGAAT
AATATAGTTATCCCGGATACCATGCTGGCAGGATCCACTTTGCGAAATTGTGGACTGTTGGACT
GTGATTCTAAGTGGGGGAAATAGGCTTTCCTCTCTTTATGTTTATTTTCTTATATCCTATTTCT
GTCATGTTCTGTCTTGTTTTCCTGCCAATAGAAGAACTATGATAAATTTATTCATAGCAGTGTG
ATAAGAACTTGATCTTAATCATACACTGTAGCCCTCAAATCGTGTATTATGCTGGCTTGTTTTT
GGTGTCCCTAGTAATTTCATCAGATTGTGAGCTCCTTGGGAGCAGAGACCATGTTTATTTGAAA
TGGTGGCAGCACAGTTCCTAGCAGGTGCTTGCATTTTGGTAGATATTCAATAATTATTTTTCGG
CTTATTAATCTTTGCTCTCCAAACTGCCATATAAAAGAAAACATCGAAGAGGAGTGATGTTTTA
CACCCAAGAATGGATCCCTCCTGGTAGAATTTCAAATAATGACCTGGGGTTCCACTGCCTTTCA
AATCTGTAAAGTGTTAACTACCACCTGCATTGTTTATACAGCAACCGTCATTGTGTGGCACTGG
ACGGGGAATCAAGAGACCCGGTTTCTAATCCCTGCTCTGTCACTAACAAGCTGCGTGATCTTCG
GAAAAAAGTAATCCTCTTGGAAAGCTGGAAACATAGTCCGAAGCTTAAGTGAAAATGATACATG
TTAGAAGACATGAAACAAGGAGAAATTCTAAGAGTCACGTGCCTGAGCAGAAATCTCGAGTTGA
TTGGAGGCGAACTAAAAGAAGTAGTATCTCACAATTACTTGATAGTGATGAAGAGCTTGATAGT
GAAGAATTTGATAGTGATGAAGAGCTTGATAGTGATGAAAGTTTTGAAAATGATGAAGAGCTTG
ATAGTAACAAGGGACCTGATTGTAATAAAACACCAGGAAGTGAAAGAGAGCTCAACTTAAGTAA
AATTCAAAGTGAAGGAAATGACAGTAAGTGTCTCATTAACTCTGGCAACGGTTCAACATATGAA
GAAGAAACGAACAAAATCAAACATAGGAATATTGACTTACAAGATCAGGAAAAACATTTAAGTC
AAGAGGATAATGATCTCAACAAACAAACTGGACAAATAATAGAGGATGATCAGGAAAAACATTT
AAGTCAAGAGGATAATGATCTCAACAAACAAACTGGACAAATAATAGAGGATGATTTAGAAGAA
GAAGACATCAAGCGAGGAAAAAGAAAAAGGCTATCCTCTGTGATGTGTGACAGTGATGAGAGTG
ATGACAGCGATATCCTAGTTAGAAAAGTAGGTGTTAAACGTCCCCGTAGAGTGGTTGAAGATGA
AGGTTCTTCAGTGGAAATGGAGCAAAAGACTCCTGAAAAAACATTAGCTGCACAAAAGCGAGAA
AAACTTCAGAAGCTCAAAGAACTCTCAAAACAAAGATCTCGTCAGAGACGCAGTAGTGGTAGAG
ATTTTGAGGACTCTGAAAAGGAATCTTGCCCAAGCAGTGATGAAGTTGATGAGGAGGAAGAAGA
GGATAATTATGAATCTGATGAAGATGGAGATGATTATATTATCGATGACTTTGTAGTGCAAGAT
GAGGAGGGTGATGAAGAGAATAAAAACCAACAAGGAGAAAAATTGACTACATCACAACTGAAAT
TAGTAAAACAGAATTCTCTTTATTCTTTTAGTGACCACTATACTCATTTTGAAAGAGTTGTGAA
GGCTCTTCTGATCAACGCTTTAGATGAATCTTTTCTGGGAACATTATATGATGGCACAAGGCAA
AAATCATATGCAAAAGATATGCTAACATCTCTTCATTATTTGGATAACCGCTTTGTTCAGCCTC
GTCTAGAGAGCTTGGTATCTAGAAGTCGTTGGAAAGAGCAATATAAGGAGCGAGTAGAAAATTA
TTCTAATGTAAGTATTCATTTGAAGAATCCTGAAAACTGTTCCTGCCAGGCTTGTGGACTGCAT
CGCTACTGTAAATATTCAGTGCATTTATCAGGAGAGTTGTATAACACCAGGACCATGCAAATAG
ATAATTTCATGTCACATGATAAACAGGTGTTCACTGTTGGCAGAATTTGTGCCAGCCGTACCAG
AATTTATCATAAACTGAAACATTTTAAATTCAAACTATACCAGGAATGTTGCACCATTGCAATG
ACAGAAGAAGTTGAAGATGAACAAGTTAAAGAAACAGTGGAAAGAATTTTCAGGCGGTCAAAAG
AAAATGGCTGGATTAAGGAGAAATATGGTCAACTTGAAGAATATCTCAATTTTGCGGATTACTT
TCAAGAAGAGAAGTTTGAGTTGTAACACATTTCCATCAGAGAAGATTTTTTAAATTCCTGTAAA
TGTGAAGATCATGATTCTTGTTTTTCTGTATCATGTGACATGTTTGTACATTTTATCTATATCT
TCATGGCAAAATATTTTGTTTAAAACATGATTATCTTAATTCCTGTGAAGTGGCACTCTACACT
CTAATTAAACTTTTATCTGATGTACATAAAAGCATTATCTTAATTTTTAAGTCTGTAAATATAT
TTTAAAGTTATATAATAATGGCTTTATAACAGATGACTGTCAAGTGAATGAGCTGTTGATATCC
TGTCAGTTTAGTCAAAATATATTGTATCTTAAAAATGTATTTAGACTAACGTCTACATGTATTT
TTACGGAATTCCTGTCCAGATCTGTTTATTCTTTTACAGTATTAAATGATTTTCACTAATATAT
TTTTTACTGCTATCATCTAAATCAGTGGGCCATGGAAGAAACCTCATATATCATTCAGTTCAAT
CCCATTGCTTCAGAATCAGATCATAGCATATCTATTCTAAGTAGAGGAATGCTTTTTTCCTTTT
CTTGAAAGTTTCTCTTTCAAATAGATTTCAGGCCTCTAGAGTCTTTCAACCCTCACATTCAGGA
ATAATTTTATGTAAATTTTCATGCTTTATAATGTTCTTACTTTTTTCTATTCAATTTTGTCTAT
ATATTGATGATTAAGATGTATTTTATTTATTTTTATCCATAGCTTTTTCCATATAAGTATGTAT
CTTAGGGTCAGAACTGCTGAAAGAGACAAACTCAGCCAAAAACACTTGGAAAGCATATTTTGGT
ATCTGCATTGCTTTGCATATCTAAATTTTCCCATAAAGTAATAAAGTAAAATGGTTGCAGAGTG
AACAAATGAA

hide sequence

RefSeq Acc Id:

XM_011542987 ⟹ XP_011541289

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI

Sequence:

show sequence

GAGGAGCATCGCTTGTCCTGAGCTGGTTGCCGGGGCAGGGGCGGAGGCGGAGGCAGAGGTGGAG
GCGCTTTGAAAGCCGTCATTGTGTGGCACTGGACGGGGAATCAAGAGACCCGGTTTCTAATCCC
TGCTCTGTCACTAACAAGCTGCGTGATCTTCGGAAAAAAGTAATCCTCTTGGAAAGCTGGAAAC
ATAGTCCGATTTTTTATAGTGTGTGGTTTATAGAAAGACTCCAGGAATATTCTGTGCTGTGGTG
GAAATATTGGAATAATCAGCCTCATAAGAAGCTTAAGTGAAAATGATACATGTTAGAAGACATG
AAACAAGGAGAAATTCTAAGAGTCACGTGCCTGAGCAGAAATCTCGAGTTGATTGGAGGCGAAC
TAAAAGAAGTAGTATCTCACAATTACTTGATAGTGATGAAGAGCTTGATAGTGAAGAATTTGAT
AGTGATGAAGAGCTTGATAGTGATGAAAGTTTTGAAAATGATGAAGAGCTTGATAGTAACAAGG
GACCTGATTGTAATAAAACACCAGGAAGTGAAAGAGAGCTCAACTTAAGTAAAATTCAAAGTGA
AGGAAATGACAGTAAGTGTCTCATTAACTCTGGCAACGGTTCAACATATGAAGAAGAAACGAAC
AAAATCAAACATAGGAATATTGACTTACAAGATCAGGAAAAACATTTAAGTCAAGAGGATAATG
ATCTCAACAAACAAACTGGACAAATAATAGAGGATGATCAGGAAAAACATTTAAGTCAAGAGGA
TAATGATCTCAACAAACAAACTGGACAAATAATAGAGGATGATTTAGAAGAAGAAGACATCAAG
CGAGGAAAAAGAAAAAGGCTATCCTCTGTGATGTGTGACAGTGATGAGAGTGATGACAGCGATA
TCCTAGTTAGAAAAGTAGGTGTTAAACGTCCCCGTAGAGTGGTTGAAGATGAAGGTTCTTCAGT
GGAAATGGAGCAAAAGACTCCTGAAAAAACATTAGCTGCACAAAAGCGAGAAAAACTTCAGAAG
CTCAAAGAACTCTCAAAACAAAGATCTCGTCAGAGACGCAGTAGTGGTAGAGATTTTGAGGACT
CTGAAAAGGAATCTTGCCCAAGCAGTGATGAAGTTGATGAGGAGGAAGAAGAGGATAATTATGA
ATCTGATGAAGATGGAGATGATTATATTATCGATGACTTTGTAGTGCAAGATGAGGAGGGTGAT
GAAGAGAATAAAAACCAACAAGGAGAAAAATTGACTACATCACAACTGAAATTAGTAAAACAGA
ATTCTCTTTATTCTTTTAGTGACCACTATACTCATTTTGAAAGAGTTGTGAAGGCTCTTCTGAT
CAACGCTTTAGATGAATCTTTTCTGGGAACATTATATGATGGCACAAGGCAAAAATCATATGCA
AAAGATATGCTAACATCTCTTCATTATTTGGATAACCGCTTTGTTCAGCCTCGTCTAGAGAGCT
TGGTATCTAGAAGTCGTTGGAAAGAGCAATATAAGGAGCGAGTAGAAAATTATTCTAATGTAAG
TATTCATTTGAAGAATCCTGAAAACTGTTCCTGCCAGGCTTGTGGACTGCATCGCTACTGTAAA
TATTCAGTGCATTTATCAGGAGAGTTGTATAACACCAGGACCATGCAAATAGATAATTTCATGT
CACATGATAAACAGGTGTTCACTGTTGGCAGAATTTGTGCCAGCCGTACCAGAATTTATCATAA
ACTGAAACATTTTAAATTCAAACTATACCAGGAATGTTGCACCATTGCAATGACAGAAGAAGTT
GAAGATGAACAAGTTAAAGAAACAGTGGAAAGAATTTTCAGGCGGTCAAAAGAAAATGGCTGGA
TTAAGGAGAAATATGGTCAACTTGAAGAATATCTCAATTTTGCGGATTACTTTCAAGAAGAGAA
GTTTGAGTTGTAACACATTTCCATCAGAGAAGATTTTTTAAATTCCTGTAAATGTGAAGATCAT
GATTCTTGTTTTTCTGTATCATGTGACATGTTTGTACATTTTATCTATATCTTCATGGCAAAAT
ATTTTGTTTAAAACATGATTATCTTAATTCCTGTGAAGTGGCACTCTACACTCTAATTAAACTT
TTATCTGATGTACATAAAAGCATTATCTTAATTTTTAAGTCTGTAAATATATTTTAAAGTTATA
TAATAATGGCTTTATAACAGATGACTGTCAAGTGAATGAGCTGTTGATATCCTGTCAGTTTAGT
CAAAATATATTGTATCTTAAAAATGTATTTAGACTAACGTCTACATGTATTTTTACGGAATTCC
TGTCCAGATCTGTTTATTCTTTTACAGTATTAAATGATTTTCACTAATATATTTTTTACTGCTA
TCATCTAAATCAGTGGGCCATGGAAGAAACCTCATATATCATTCAGTTCAATCCCATTGCTTCA
GAATCAGATCATAGCATATCTATTCTAAGTAGAGGAATGCTTTTTTCCTTTTCTTGAAAGTTTC
TCTTTCAAATAGATTTCAGGCCTCTAGAGTCTTTCAACCCTCACATTCAGGAATAATTTTATGT
AAATTTTCATGCTTTATAATGTTCTTACTTTTTTCTATTCAATTTTGTCTATATATTGATGATT
AAGATGTATTTTATTTATTTTTATCCATAGCTTTTTCCATATAAGTATGTATCTTAGGGTCAGA
ACTGCTGAAAGAGACAAACTCAGCCAAAAACACTTGGAAAGCATATTTTGGTATCTGCATTGCT
TTGCATATCTAAATTTTCCCATAAAGTAATAAAGTAAAATGGTTGCAGAGTGAACAAATGAA

hide sequence

RefSeq Acc Id:

XM_011542988 ⟹ XP_011541290

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI

Sequence:

show sequence

GAGGAGCATCGCTTGTCCTGAGCTGGTTGCCGGGGCAGGGGCGGAGGCGGAGGCAGAGGTGGAG
GCGCTTTGAAAGCCGTCATTGTGTGGCACTGGACGGGGAATCAAGAGACCCGGTTTCTAATCCC
TGCTCTGTCACTAACAAGCTGCGTGATCTTCGAAGCTTAAGTGAAAATGATACATGTTAGAAGA
CATGAAACAAGGAGAAATTCTAAGAGTCACGTGCCTGAGCAGAAATCTCGAGTTGATTGGAGGC
GAACTAAAAGAAGTAGTATCTCACAATTACTTGATAGTGATGAAGAGCTTGATAGTGAAGAATT
TGATAGTGATGAAGAGCTTGATAGTGATGAAAGTTTTGAAAATGATGAAGAGCTTGATAGTAAC
AAGGGACCTGATTGTAATAAAACACCAGGAAGTGAAAGAGAGCTCAACTTAAGTAAAATTCAAA
GTGAAGGAAATGACAGTAAGTGTCTCATTAACTCTGGCAACGGTTCAACATATGAAGAAGAAAC
GAACAAAATCAAACATAGGAATATTGACTTACAAGATCAGGAAAAACATTTAAGTCAAGAGGAT
AATGATCTCAACAAACAAACTGGACAAATAATAGAGGATGATCAGGAAAAACATTTAAGTCAAG
AGGATAATGATCTCAACAAACAAACTGGACAAATAATAGAGGATGATTTAGAAGAAGAAGACAT
CAAGCGAGGAAAAAGAAAAAGGCTATCCTCTGTGATGTGTGACAGTGATGAGAGTGATGACAGC
GATATCCTAGTTAGAAAAGTAGGTGTTAAACGTCCCCGTAGAGTGGTTGAAGATGAAGGTTCTT
CAGTGGAAATGGAGCAAAAGACTCCTGAAAAAACATTAGCTGCACAAAAGCGAGAAAAACTTCA
GAAGCTCAAAGAACTCTCAAAACAAAGATCTCGTCAGAGACGCAGTAGTGGTAGAGATTTTGAG
GACTCTGAAAAGGAATCTTGCCCAAGCAGTGATGAAGTTGATGAGGAGGAAGAAGAGGATAATT
ATGAATCTGATGAAGATGGAGATGATTATATTATCGATGACTTTGTAGTGCAAGATGAGGAGGG
TGATGAAGAGAATAAAAACCAACAAGGAGAAAAATTGACTACATCACAACTGAAATTAGTAAAA
CAGAATTCTCTTTATTCTTTTAGTGACCACTATACTCATTTTGAAAGAGTTGTGAAGGCTCTTC
TGATCAACGCTTTAGATGAATCTTTTCTGGGAACATTATATGATGGCACAAGGCAAAAATCATA
TGCAAAAGATATGCTAACATCTCTTCATTATTTGGATAACCGCTTTGTTCAGCCTCGTCTAGAG
AGCTTGGTATCTAGAAGTCGTTGGAAAGAGCAATATAAGGAGCGAGTAGAAAATTATTCTAATG
TAAGTATTCATTTGAAGAATCCTGAAAACTGTTCCTGCCAGGCTTGTGGACTGCATCGCTACTG
TAAATATTCAGTGCATTTATCAGGAGAGTTGTATAACACCAGGACCATGCAAATAGATAATTTC
ATGTCACATGATAAACAGGTGTTCACTGTTGGCAGAATTTGTGCCAGCCGTACCAGAATTTATC
ATAAACTGAAACATTTTAAATTCAAACTATACCAGGAATGTTGCACCATTGCAATGACAGAAGA
AGTTGAAGATGAACAAGTTAAAGAAACAGTGGAAAGAATTTTCAGGCGGTCAAAAGAAAATGGC
TGGATTAAGGAGAAATATGGTCAACTTGAAGAATATCTCAATTTTGCGGATTACTTTCAAGAAG
AGAAGTTTGAGTTGTAACACATTTCCATCAGAGAAGATTTTTTAAATTCCTGTAAATGTGAAGA
TCATGATTCTTGTTTTTCTGTATCATGTGACATGTTTGTACATTTTATCTATATCTTCATGGCA
AAATATTTTGTTTAAAACATGATTATCTTAATTCCTGTGAAGTGGCACTCTACACTCTAATTAA
ACTTTTATCTGATGTACATAAAAGCATTATCTTAATTTTTAAGTCTGTAAATATATTTTAAAGT
TATATAATAATGGCTTTATAACAGATGACTGTCAAGTGAATGAGCTGTTGATATCCTGTCAGTT
TAGTCAAAATATATTGTATCTTAAAAATGTATTTAGACTAACGTCTACATGTATTTTTACGGAA
TTCCTGTCCAGATCTGTTTATTCTTTTACAGTATTAAATGATTTTCACTAATATATTTTTTACT
GCTATCATCTAAATCAGTGGGCCATGGAAGAAACCTCATATATCATTCAGTTCAATCCCATTGC
TTCAGAATCAGATCATAGCATATCTATTCTAAGTAGAGGAATGCTTTTTTCCTTTTCTTGAAAG
TTTCTCTTTCAAATAGATTTCAGGCCTCTAGAGTCTTTCAACCCTCACATTCAGGAATAATTTT
ATGTAAATTTTCATGCTTTATAATGTTCTTACTTTTTTCTATTCAATTTTGTCTATATATTGAT
GATTAAGATGTATTTTATTTATTTTTATCCATAGCTTTTTCCATATAAGTATGTATCTTAGGGT
CAGAACTGCTGAAAGAGACAAACTCAGCCAAAAACACTTGGAAAGCATATTTTGGTATCTGCAT
TGCTTTGCATATCTAAATTTTCCCATAAAGTAATAAAGTAAAATGGTTGCAGAGTGAACAAATG
AA

hide sequence

RefSeq Acc Id:

XM_017018307 ⟹ XP_016873796

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI

Sequence:

show sequence

GGTGCGGGGCTGTCTCCCGGCTGGGACTCGCTCGCGCTCCCGGTGCTAATGGTTTATGAGAGGG
GCGGGGGAAGCCGTGCCTCCTCGCGGACTAAGAGAAAAATTCCCGCGGGCGCTCTTTGGGTGGG
CCGGAGAACGCCCCTCAGCCCTTTGCGCCTCTAACCCTCCTCAGCTGAGCTGCAGTGGGCGCGG
TGCCCGTTATTTCCGCCTTGGGGAGGTGCTTGGAACTGATGTAGGGAGCTCGGTTGGTGATTTC
TCGGGTTTCTGGCCTTTCCAGACCCTTGTAATTGTTTTCTCGGTGCAGAGCTCTTTTGGGGTCT
GGGGGTTTCCGTCGTCCTGCGCGCGTCATCGCGAAGCTTGGCCTGAGGGTCCGGTTTCCTAGCT
ACTGTGCCCCTCCCTCCTGGAGGCAGAGTGACGGACTAGTGGGCTAGCGGGCGCTGGGTTCCTG
CGTCCCGCCAAAGAGCCGTCATTGTGTGGCACTGGACGGGGAATCAAGAGACCCGGTTTCTAAT
CCCTGCTCTGTCACTAACAAGCTGCGTGATCTTCGGAAAAAAGTAATCCTCTTGGAAAGCTGGA
AACATAGTCCGATTTTTTATAGTGTGTGGTTTATAGAAAGACTCCAGGAATATTCTGTGCTGTG
GTGGAAATATTGGAATAATCAGCCTCATAAGAAGCTTAAGTGAAAATGATACATGTTAGAAGAC
ATGAAACAAGGAGAAATTCTAAGAGTCACGTGCCTGAGCAGAAATCTCGAGTTGATTGGAGGCG
AACTAAAAGAAGTAGTATCTCACAATTACTTGATAGTGATGAAGAGCTTGATAGTGAAGAATTT
GATAGTGATGAAGAGCTTGATAGTGATGAAAGTTTTGAAAATGATGAAGAGCTTGATAGTAACA
AGGGACCTGATTGTAATAAAACACCAGGAAGTGAAAGAGAGCTCAACTTAAGTAAAATTCAAAG
TGAAGGAAATGACAGTAAGTGTCTCATTAACTCTGGCAACGGTTCAACATATGAAGAAGAAACG
AACAAAATCAAACATAGGAATATTGACTTACAAGATCAGGAAAAACATTTAAGTCAAGAGGATA
ATGATCTCAACAAACAAACTGGACAAATAATAGAGGATGATCAGGAAAAACATTTAAGTCAAGA
GGATAATGATCTCAACAAACAAACTGGACAAATAATAGAGGATGATTTAGAAGAAGAAGACATC
AAGCGAGGAAAAAGAAAAAGGCTATCCTCTGTGATGTGTGACAGTGATGAGAGTGATGACAGCG
ATATCCTAGTTAGAAAAGTAGGTGTTAAACGTCCCCGTAGAGTGGTTGAAGATGAAGGTTCTTC
AGTGGAAATGGAGCAAAAGACTCCTGAAAAAACATTAGCTGCACAAAAGCGAGAAAAACTTCAG
AAGCTCAAAGAACTCTCAAAACAAAGATCTCGTCAGAGACGCAGTAGTGGTAGAGATTTTGAGG
ACTCTGAAAAGGAATCTTGCCCAAGCAGTGATGAAGTTGATGAGGAGGAAGAAGAGGATAATTA
TGAATCTGATGAAGATGGAGATGATTATATTATCGATGACTTTGTAGTGCAAGATGAGGAGGGT
GATGAAGAGAATAAAAACCAACAAGGAGAAAAATTGACTACATCACAACTGAAATTAGTAAAAC
AGAATTCTCTTTATTCTTTTAGTGACCACTATACTCATTTTGAAAGAGTTGTGAAGGCTCTTCT
GATCAACGCTTTAGATGAATCTTTTCTGGGAACATTATATGATGGCACAAGGCAAAAATCATAT
GCAAAAGATATGCTAACATCTCTTCATTATTTGGATAACCGCTTTGTTCAGCCTCGTCTAGAGA
GCTTGGTATCTAGAAGTCGTTGGAAAGAGCAATATAAGGAGCGAGTAGAAAATTATTCTAATGT
AAGTATTCATTTGAAGAATCCTGAAAACTGTTCCTGCCAGGCTTGTGGACTGCATCGCTACTGT
AAATATTCAGTGCATTTATCAGGAGAGTTGTATAACACCAGGACCATGCAAATAGATAATTTCA
TGTCACATGATAAACAGGTGTTCACTGTTGGCAGAATTTGTGCCAGCCGTACCAGAATTTATCA
TAAACTGAAACATTTTAAATTCAAACTATACCAGGAATGTTGCACCATTGCAATGACAGAAGAA
GTTGAAGATGAACAAGTTAAAGAAACAGTGGAAAGAATTTTCAGGCGGTCAAAAGAAAATGGCT
GGATTAAGGAGAAATATGGTCAACTTGAAGAATATCTCAATTTTGCGGATTACTTTCAAGAAGA
GAAGTTTGAGTTGTAACACATTTCCATCAGAGAAGATTTTTTAAATTCCTGTAAATGTGAAGAT
CATGATTCTTGTTTTTCTGTATCATGTGACATGTTTGTACATTTTATCTATATCTTCATGGCAA
AATATTTTGTTTAAAACATGATTATCTTAATTCCTGTGAAGTGGCACTCTACACTCTAATTAAA
CTTTTATCTGATGTACATAAAAGCATTATCTTAATTTTTAAGTCTGTAAATATATTTTAAAGTT
ATATAATAATGGCTTTATAACAGATGACTGTCAAGTGAATGAGCTGTTGATATCCTGTCAGTTT
AGTCAAAATATATTGTATCTTAAAAATGTATTTAGACTAACGTCTACATGTATTTTTACGGAAT
TCCTGTCCAGATCTGTTTATTCTTTTACAGTATTAAATGATTTTCACTAATATATTTTTTACTG
CTATCATCTAAATCAGTGGGCCATGGAAGAAACCTCATATATCATTCAGTTCAATCCCATTGCT
TCAGAATCAGATCATAGCATATCTATTCTAAGTAGAGGAATGCTTTTTTCCTTTTCTTGAAAGT
TTCTCTTTCAAATAGATTTCAGGCCTCTAGAGTCTTTCAACCCTCACATTCAGGAATAATTTTA
TGTAAATTTTCATGCTTTATAATGTTCTTACTTTTTTCTATTCAATTTTGTCTATATATTGATG
ATTAAGATGTATTTTATTTATTTTTATCCATAGCTTTTTCCATATAAGTATGTATCTTAGGGTC
AGAACTGCTGAAAGAGACAAACTCAGCCAAAAACACTTGGAAAGCATATTTTGGTATCTGCATT
GCTTTGCATATCTAAATTTTCCCATAAAGTAATAAAGTAAAATGGTTGCAGAGTGAACAAATGA
A

hide sequence

RefSeq Acc Id:

XM_017018310 ⟹ XP_016873799

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI

Sequence:

show sequence

GGGGGGAGGAGCATCGCTTGTCCTGAGCTGGTTGCCGGGGCAGGGGCGGAGGCGGAGGCAGAGG
TGGAGGCGCTTTGAAAGAAGCTTAAGTGAAAATGATACATGTTAGAAGACATGAAACAAGGAGA
AATTCTAAGAGTCACGTGCCTGAGCAGAAATCTCGAGTTGATTGGAGGCGAACTAAAAGAAGTA
GTATCTCACAATTACTTGATAGTGATGAAGAGCTTGATAGTGAAGAATTTGATAGTGATGAAGA
GCTTGATAGTGATGAAAGTTTTGAAAATGATGAAGAGCTTGATAGTAACAAGGGACCTGATTGT
AATAAAACACCAGGAAGTGAAAGAGAGCTCAACTTAAGTAAAATTCAAAGTGAAGGAAATGACA
GTAAGTGTCTCATTAACTCTGGCAACGGTTCAACATATGAAGAAGAAACGAACAAAATCAAACA
TAGGAATATTGACTTACAAGATCAGGAAAAACATTTAAGTCAAGAGGATAATGATCTCAACAAA
CAAACTGGACAAATAATAGAGGATGATCAGGAAAAACATTTAAGTCAAGAGGATAATGATCTCA
ACAAACAAACTGGACAAATAATAGAGGATGATTTAGAAGAAGAAGACATCAAGCGAGGAAAAAG
AAAAAGGCTATCCTCTGTGATGTGTGACAGTGATGAGAGTGATGACAGCGATATCCTAGTTAGA
AAAGTAGGTGTTAAACGTCCCCGTAGAGTGGTTGAAGATGAAGGTTCTTCAGTGGAAATGGAGC
AAAAGACTCCTGAAAAAACATTAGCTGCACAAAAGCGAGAAAAACTTCAGAAGCTCAAAGAACT
CTCAAAACAAAGATCTCGTCAGAGACGCAGTAGTGGTAGAGATTTTGAGGACTCTGAAAAGGAA
TCTTGCCCAAGCAGTGATGAAGTTGATGAGGAGGAAGAAGAGGATAATTATGAATCTGATGAAG
ATGGAGATGATTATATTATCGATGACTTTGTAGTGCAAGATGAGGAGGGTGATGAAGAGAATAA
AAACCAACAAGGAGAAAAATTGACTACATCACAACTGAAATTAGTAAAACAGAATTCTCTTTAT
TCTTTTAGTGACCACTATACTCATTTTGAAAGAGTTGTGAAGGCTCTTCTGATCAACGCTTTAG
ATGAATCTTTTCTGGGAACATTATATGATGGCACAAGGCAAAAATCATATGCAAAAGATATGCT
AACATCTCTTCATTATTTGGATAACCGCTTTGTTCAGCCTCGTCTAGAGAGCTTGGTATCTAGA
AGTCGTTGGAAAGAGCAATATAAGGAGCGAGTAGAAAATTATTCTAATGTAAGTATTCATTTGA
AGAATCCTGAAAACTGTTCCTGCCAGGCTTGTGGACTGCATCGCTACTGTAAATATTCAGTGCA
TTTATCAGGAGAGTTGTATAACACCAGGACCATGCAAATAGATAATTTCATGTCACATGATAAA
CAGGTGTTCACTGTTGGCAGAATTTGTGCCAGCCGTACCAGAATTTATCATAAACTGAAACATT
TTAAATTCAAACTATACCAGGAATGTTGCACCATTGCAATGACAGAAGAAGTTGAAGATGAACA
AGTTAAAGAAACAGTGGAAAGAATTTTCAGGCGGTCAAAAGAAAATGGCTGGATTAAGGAGAAC
AGTTCTTGTGACCTGAGAGTGAAGAAGCACCTGGTGCCAGTCTGAGGAAAGGATCTCGGCTGCC
AGTTCTAATACACCCACATCCTCTTCTTGAGGACATGGGACTGAGCAGTGAGCACTGTAACTGA
AGATCGAGGGGAATGCAGAGGTTTCAGACCACAGCACTGATTTTGATTCCCCCATATCCTATTG
ATCACTAAATTTGATAACAGGAGTAAAGTGGGGGTTTTGAAGAGTGCACTGGATTCCCGAAGAT
CTGCTGGCAGCTTACAAGCTCTGGTCTGCTCACAGAGCTTTTAGAATTGTTTATGGTATATGGA
AAGAATGCTAATACGACTGCAGTCTTCTAAAACAAGTCTAGTTACATGAATGTATAAGAGAGAA
CAAATAGTAGATTTTCAGGCAACTCTTATCAACATTTAATCTTTTAAAGAAAAGAAAAAAGCCT
AACTTGAGATCCATTGCCTGGACTATATCATAGGGAAATTTGTAAAAGAGGAATATAAAAAATA
AGGCAAGAGAGCTTAGGCAGATGGAAAGAAAACAAAACAGAAACTTTTTTAGCACATGTCATAT
TTAGTGGAGGTCTCCCAGTCTAGATAATGACATCATCACTGGTTTCCCTTTGACAATTTTTCTC
CCACCACAAACCACCACCCAGTGATCTTGCCTGCCCCCCACATCTTGATCCTTAAGTCTTTCTC
TCATTTTATTCTTTTCAGCTTTTTGTCTTTTACTTTGCTTCTACTTCTCCTACTCCAAATGCTT
CTCCCTGCTTATCCGTACTTTTTCATTTGCTTTAGGAGAGAGCACTTATTCAATAACTTCCCGT
CTTCATTTTCCTAGACAACATTAAATTCTTAAGTGCTTTTATTGATGCCTTTAAGTGTTGCCAA
CCCTCTAGTGGAACTGCAAAACCTATTGGGATAGCACAGTTATAAAGAATTAGATACTAGGTAT
AGAAAAATCACTGTGCATATACTGTATATGTTATATAATAGTATCATATATGGGGAAGAACTTT
AAACTTCTTGAAGAAAAAAGCATTTCCAAATCATGTATCCTAGAAAAAGCTTAACAAGGTTTAG
GACACCAGAAGGGACCTGGAATTTTAAAGACGTTATTCTTTATGCATAACACTTGGCATTCTTT
TCTTAGGAAAAGAAAGGAGCTTAGGCTTTCTTTTCAAGAAAGCCAAGTGTCATGTTATACATAA
AGAATAACATTTAGCATTAGGCATTGAAGGTATTTCAAGATTGTGCATGTCTAGGACAGTATAC
ACATTTTTTTCCCCATGAAAATACCAAAGACCTTCATTTTTTTGAGATTTCTCCACTTAAAAAA
TTTGTTCCTAGGTTTTCTCAAAAGATTTCCTAGAAACCACAGAGGTTTATAGCCAATATAAACC
CATTTGCAGCTTTTTGTGCTGTAATGAAATTTCAAAATTTGTCACGTGCTCTGACATTTCCCAT
CCTCACTCTGTCTGTCCCTCTCACTGTGTGCCTTTGAGTGATAGCACTGCATGTACTTTGTGAT
GTGTGCTGCCTTTAGCTACAGTCTGGTAGTCACAGTTACTCTAACCCTTTAGAATGCCTGGGGC
TCAGTGTTACTTGAATGCCGTCTCCATGGCACTTTCCGCTCATATTTCCCATTTATGTCAACCC
CTTTTGTTGCCTTACACGTACTATTTGTTCCTGTCTTTCTGCCTCCAGCTTGTATTCCACACCT
TACTTTTTCCCTTACCTGCTTCTTCAGCCATTTTACTTTAATTATCTCAGGATGTCTCAGCATG
TCTTCCCAAAGACATGCCAACTAGACTGACTTCATTCTTTTTGTTCTTCCTTCTAAAGGTTGAA
CTAGGGTGATCCGTTTTTAATGTAATGATACTAAAGGGGTGTAGGAGCAACTTGAGTATAAGAA
AAGAATAGATAATAGGAAAATTATAATAAAACCAAAATATTTAATAAACATAATAATGCATGTC
TTATTCTAAAGAAGAGTTCAATAACATACTCTAATATGACACTGGCAAAATTCTAACGAATATT
TGTTCATTAAGAAGAAAGTGTATATGATGATGGGACTTCCTGGGAAGTTGAAGATAGTATTGTT
GGGATTGGCTGGTGGATGCATAAACACCAGGTAGTAAAGAAAGCATGTCAATAGAAGTATCAGA
TGCCCATTCATACTGTAAATACTGTGTGTAAAACTGTTACAAGTGACAGTTGTATGTAAATTTT
AAATGCACTGATAAATATTGTCATATACATAATAATTTAAAATTATAATTAGATATCCCTTGCC
TTCCTTAAACGCTTCTCTTCTTTTTCCCCTCCTTTTCAACTTTTTCCCTTGCCCCTTTTTTCCC
CACCCCTTAAACTGATGTTTCTCAAAGCATGGCCCTAAACTACCTATATCAGAATCACCTAGAA
GTTTTTGAAAAGTGTATAATCCCCTAGCCTCATCCCAGATTTATTGAATGACAATCCTTGTGGA
TGTTAAACATCCAATATTTTTAGCATTGATGATTCTTAAATAGATAAAAGTTTGAGGATCACTG
CTAAAAAGTACCCGTTAACACTGAATTCTGTCCTCATCCTCTCAAAGTTGCCTTGGCGAATCAA
TTCCCTTCTGCAGTTGTAGCTACTACTTCTGAGTAGAAGATTCCAAACTTCTCTTATATTCTGA
CCTCTTTCCCACACTTCATTTCCACAATTCCAACTGTTTTCATCAGTAGGTCCATCAGGTGTTG
TAAGAGAGTAGTCTTCACTATTAAAATAAGTAGTCTTCACTATTAAAACCCTCCAAATGTTTAG
TAAAGAATTATGAGAGCAGTATCTTTAGGTAGAGAGGATGGCAGAGTAATACTAACTGCAATGT
CTGTGAGTTTCACTTTCCAAGTTTTTTTTTTCTTGCCAAAGCTGCATCCTAGCCACACCATTTA
AATCTCAGAAACAGCATACTCTAAACTGGTTAAAAGTATAAGCTTAAGTATTTGCTTTGCCACT
TACTAGCAGTAGAATTTGGGAGCAAGCTATTTTATTTCTCTTAGCCTAAGTTTTCTCATCTGTA
AAGTAGGAACAAAAACAGTAATAATAATTAGGGTTTTGATTGTGGAGATTAGATATGTAATACG
TTTTAAGCATTTAGTATAGGACCTAGCAATTAGTAAGTGATTGATTAATCTTAGCTGTTACTTG
CAATAAAAGCAAGTAACCTCCTATCTTAGTATAGCTGAGATAGATTTTAATTGTCCTAGCTGTG
TGTGGTGGTGCACAGCTGTAGTCACAGCTACTTGGGAGGCTGAGGTGGTAGAATCGCCTGAGCC
CAGGAGTTCAAGGCCAGCCTGAGCAAGATAGTGAGACCCTGTCTCTTAAAATAATTTTTTTAAT
TTTTAATTTTCCAAAAGAAATTTAATAAATAATAAAGGAATATGAGGAAAGGTAATATGAGAAA
CATAAAAAGTCAAACTTTTAAAGTATAGGTTTCTAATCCTAGAGTACTTTACTTATATCTAATA
AAACCTATCTAAGTACTAGGCCAAAGAAAATTCCTAAGTAGTCCCTAGGCTATTTCCCCTTCTG
TTATGTGTTTCCATCTTTCCTGAGAAGGAGATCCAGTCAGATATCATACGGTTATAAAAAAGAG
TTTCATGGCCTTCAAGGTGTAGAAGGAAAATGCACTTCTCAACATTCCCTTCTGTAGGTCCCTA
TCACCACAAAAGTCAGGGTCACCAGGATCCTCTCTCATTTCACTGAAGATTAAAACACAGTTCA
TAAACAGAGTCAAGAAACTAGTATGTCATTAATCCCCTCACTGAAATAAATACTTTGAACTCTA
TATGTCTGAAACTGAAATCATGATATCTTTCCCTCGCACAAACAACCTGCAAAAGAGCCTGCCA
TTATTCTACTCTGTCAACTTTGAAATCTCTAAATCATTCTTGACCCCTCTCTTAACTTGTTACA
CTTTGTTCTTTACTCTTCATCTTCATTGCCATGACTCAGATTTGGGCCCTCATGACCTAAATTG
TTATCACAGACCCATAACTAGTTGCTGAACTATTCTAGAATGAATGTTTTACCGATTTTCTTAA
AATACACCTGAGATCAGTTCAGTCCCCTGCTCCAAAACCTTTAGCAACTTTCCATTACCTGTCA
AATGATTGTTCAATTCTTTAACCAGTATTTTATAATTTTTGTTCTCTGAACTCAGCCTCTTTGG
TTCAGTCTTAGCTCTCTCTGTTCTCCTAAAAATACTCAGGTTGTAGTCAAATCCCATATTTTCT
TGTCACGTCACTTTGATGGACTGTTCCCTCTTACTGAAAAGTCTTGCCACCAACTCTTTGCCTA
CCAAATCTGTTTTTCCAGGACAACTTAAATGCCACTCTTTACTGCTTACCTCAACTAACCATGA
CCTATCTTCTGAACCCTCATAACAGTGTCTGTACCTCTTTGGCACTTATTACTGATTGTTATTG
GTGTATTACTACTGAACTGTATTCTCCTTAGGGGCAGGAAAAGTATCTTTTAAAAAACACTGTA
CCTAGACAGTCATTAGCAGAGCCTTTGATATATATGTTCAACAAACTTTTTATTAAGTTATTGA
GGTTACTACATTTCTACTGTAATCATGATAATATAAAAATTATAATTTAAAACACAGTTATAAA
ATTAATAATATTCACTTTGATCACTTTCCAATGCTTTCTATATGGAAATATATGAGTTATATAT
GAGTTAGGAATGCTTATTTGAAATTAAGTTCCTGTTTATCATAAAAAGATTTTTGTTCACGATT
ACCATGAAATGGACTTATCCTAATTGTGTCTGTAGTTTGCAAAGGCCCAGTTTGTCTTCATTGC
TTTGAGTAAAATAACTAGCTTTTCTATTGTATATGCAGAAATATGGTCAACTTGAAGAATATCT
CAATTTTGCGGATTACTTTCAAGAAGAGAAGTTTGAGTTGTAACACATTTCCATCAGAGAAGAT
TTTTTAAATTCCTGTAAATGTGAAGATCATGATTCTTGTTTTTCTGTATCATGTGACATGTTTG
TACATTTTATCTATATCTTCATGGCAAAATATTTTGTTTAAAACATGATTATCTTAATTCCTGT
GAAGTGGCACTCTACACTCTAATTAAACTTTTATCTGATGTACATAAAAGCATTATCTTAATTT
TTAAGTCTGTAAATATATTTTAAAGTTATATAATAATGGCTTTATAACAGATGACTGTCAAGTG
AATGAGCTGTTGATATCCTGTCAGTTTAGTCAAAATATATTGTATCTTAAAAATGTATTTAGAC
TAACGTCTACATGTATTTTTACGGAATTCCTGTCCAGATCTGTTTATTCTTTTACAGTATTAAA
TGATTTTCACTAATATATTTTTTACTGCTATCATCTAAATCAGTGGGCCATGGAAGAAACCTCA
TATATCATTCAGTTCAATCCCATTGCTTCAGAATCAGATCATAGCATATCTATTCTAAGTAGAG
GAATGCTTTTTTCCTTTTCTTGAAAGTTTCTCTTTCAAATAGATTTCAGGCCTCTAGAGTCTTT
CAACCCTCACATTCAGGAATAATTTTATGTAAATTTTCATGCTTTATAATGTTCTTACTTTTTT
CTATTCAATTTTGTCTATATATTGATGATTAAGATGTATTTTATTTATTTTTATCCATAGCTTT
TTCCATATAAGTATGTATCTTAGGGTCAGAACTGCTGAAAGAGACAAACTCAGCCAAAAACACT
TGGAAAGCATATTTTGGTATCTGCATTGCTTTGCATATCTAAATTTTCCCATAAAGTAATAAAG
TAAAATGGTTGCAGAGTGAACAAATGAA

hide sequence

RefSeq Acc Id:

XM_024448690 ⟹ XP_024304458

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI

Sequence:

show sequence

GTTGCCGGGGCAGGGGCGGAGGCGGAGGCAGAGGTGGAGGCGCTTTGAAAGGTGAGAGCGCGAG
GGCGGTGCGGGGCTGTCTCCCGGCTGGGACTCGCTCGCGCTCCCGGTGCTAATGGTTTATGAGA
GGGGCGGGGGAAGCCGTGCCTCCTCGCGGACTAAGAGAAAAATTCCCGCGGGCGCTCTTTGGGT
GGGCCGGAGAACGCCCCTCAGCCCTTTGCGCCTCTAACCCTCCTCAGCTGAGCTGCAGTGGGCG
CGGTGCCCGTTATTTCCGCCTTGGGGAGGTGCTTGGAACTGATGTAGGGAGCTCGGTTGGTGAT
TTCTCGGGTTTCTGGCCTTTCCAGACCCTTGTAATTGTTTTCTCGGTGCAGAGCTCTTTTGGGG
TCTGGGGGTTTCCGTCGTCCTGCGCGCGTCATCGCGAAGCTTGGCCTGAGGGTCCGGTTTCCTA
GCTACTGTGCCCCTCCCTCCTGGAGGCAGAGTGACGGACTAGTGGGCTAGCGGGCGCTGGGTTC
CTGCGTCCCGCCAAAGAGCCGTCATTGTGTGGCACTGGACGGGGAATCAAGAGACCCGGTTTCT
AATCCCTGCTCTGTCACTAACAAGCTGCGTGATCTTCGGAAAAAAGTAATCCTCTTGGAAAGCT
GGAAACATAGTCCGAAGCTTAAGTGAAAATGATACATGTTAGAAGACATGAAACAAGGAGAAAT
TCTAAGAGTCACGTGCCTGAGCAGAAATCTCGAGTTGATTGGAGGCGAACTAAAAGAAGTAGTA
TCTCACAATTACTTGATAGTGATGAAGAGCTTGATAGTGAAGAATTTGATAGTGATGAAGAGCT
TGATAGTGATGAAAGTTTTGAAAATGATGAAGAGCTTGATAGTAACAAGGGACCTGATTGTAAT
AAAACACCAGGAAGTGAAAGAGAGCTCAACTTAAGTAAAATTCAAAGTGAAGGAAATGACAGTA
AGTGTCTCATTAACTCTGGCAACGGTTCAACATATGAAGAAGAAACGAACAAAATCAAACATAG
GAATATTGACTTACAAGATCAGGAAAAACATTTAAGTCAAGAGGATAATGATCTCAACAAACAA
ACTGGACAAATAATAGAGGATGATCAGGAAAAACATTTAAGTCAAGAGGATAATGATCTCAACA
AACAAACTGGACAAATAATAGAGGATGATTTAGAAGAAGAAGACATCAAGCGAGGAAAAAGAAA
AAGGCTATCCTCTGTGATGTGTGACAGTGATGAGAGTGATGACAGCGATATCCTAGTTAGAAAA
GTAGGTGTTAAACGTCCCCGTAGAGTGGTTGAAGATGAAGGTTCTTCAGTGGAAATGGAGCAAA
AGACTCCTGAAAAAACATTAGCTGCACAAAAGCGAGAAAAACTTCAGAAGCTCAAAGAACTCTC
AAAACAAAGATCTCGTCAGAGACGCAGTAGTGGTAGAGATTTTGAGGACTCTGAAAAGGAATCT
TGCCCAAGCAGTGATGAAGTTGATGAGGAGGAAGAAGAGGATAATTATGAATCTGATGAAGATG
GAGATGATTATATTATCGATGACTTTGTAGTGCAAGATGAGGAGGGTGATGAAGAGAATAAAAA
CCAACAAGGAGAAAAATTGACTACATCACAACTGAAATTAGTAAAACAGAATTCTCTTTATTCT
TTTAGTGACCACTATACTCATTTTGAAAGAGTTGTGAAGGCTCTTCTGATCAACGCTTTAGATG
AATCTTTTCTGGGAACATTATATGATGGCACAAGGCAAAAATCATATGCAAAAGATATGCTAAC
ATCTCTTCATTATTTGGATAACCGCTTTGTTCAGCCTCGTCTAGAGAGCTTGGTATCTAGAAGT
CGTTGGAAAGAGCAATATAAGGAGCGAGTAGAAAATTATTCTAATGTAAGTATTCATTTGAAGA
ATCCTGAAAACTGTTCCTGCCAGGCTTGTGGACTGCATCGCTACTGTAAATATTCAGTGCATTT
ATCAGGAGAGTTGTATAACACCAGGACCATGCAAATAGATAATTTCATGTCACATGATAAACAG
GTGTTCACTGTTGGCAGAATTTGTGCCAGCCGTACCAGAATTTATCATAAACTGAAACATTTTA
AATTCAAACTATACCAGGAATGTTGCACCATTGCAATGACAGAAGAAGTTGAAGATGAACAAGT
TAAAGAAACAGTGGAAAGAATTTTCAGGCGGTCAAAAGAAAATGGCTGGATTAAGGAGAAATAT
GGTCAACTTGAAGAATATCTCAATTTTGCGGATTACTTTCAAGAAGAGAAGTTTGAGTTGTAAC
ACATTTCCATCAGAGAAGATTTTTTAAATTCCTGTAAATGTGAAGATCATGATTCTTGTTTTTC
TGTATCATGTGACATGTTTGTACATTTTATCTATATCTTCATGGCAAAATATTTTGTTTAAAAC
ATGATTATCTTAATTCCTGTGAAGTGGCACTCTACACTCTAATTAAACTTTTATCTGATGTACA
TAAAAGCATTATCTTAATTTTTAAGTCTGTAAATATATTTTAAAGTTATATAATAATGGCTTTA
TAACAGATGACTGTCAAGTGAATGAGCTGTTGATATCCTGTCAGTTTAGTCAAAATATATTGTA
TCTTAAAAATGTATTTAGACTAACGTCTACATGTATTTTTACGGAATTCCTGTCCAGATCTGTT
TATTCTTTTACAGTATTAAATGATTTTCACTAATATATTTTTTACTGCTATCATCTAAATCAGT
GGGCCATGGAAGAAACCTCATATATCATTCAGTTCAATCCCATTGCTTCAGAATCAGATCATAG
CATATCTATTCTAAGTAGAGGAATGCTTTTTTCCTTTTCTTGAAAGTTTCTCTTTCAAATAGAT
TTCAGGCCTCTAGAGTCTTTCAACCCTCACATTCAGGAATAATTTTATGTAAATTTTCATGCTT
TATAATGTTCTTACTTTTTTCTATTCAATTTTGTCTATATATTGATGATTAAGATGTATTTTAT
TTATTTTTATCCATAGCTTTTTCCATATAAGTATGTATCTTAGGGTCAGAACTGCTGAAAGAGA
CAAACTCAGCCAAAAACACTTGGAAAGCATATTTTGGTATCTGCATTGCTTTGCATATCTAAAT
TTTCCCATAAAGTAATAAAGTAAAATGGTTGCAGAGTGAACAAATGAA

hide sequence

RefSeq Acc Id:

XM_024448693 ⟹ XP_024304461

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI

Sequence:

show sequence

GAGGAGCATCGCTTGTCCTGAGCTGGTTGCCGGGGCAGGGGCGGAGGCGGAGGCAGAGGTGGAG
GCGCTTTGAAAGCCGTCATTGTGTGGCACTGGACGGGGAATCAAGAGACCCGGTTTCTAATCCC
TGCTCTGTCACTAACAAGCTGCGTGATCTTCGGAAAAAAGTAATCCTCTTGGAAAGCTGGAAAC
ATAGTCCGAAGCTTAAGTGAAAATGATACATGTTAGAAGACATGAAACAAGGAGAAATTCTAAG
AGTCACGTGCCTGAGCAGAAATCTCGAGTTGATTGGAGGCGAACTAAAAGAAGTAGTATCTCAC
AATTACTTGATAGTGATGAAGAGCTTGATAGTGAAGAATTTGATAGTGATGAAGAGCTTGATAG
TGATGAAAGTTTTGAAAATGATGAAGAGCTTGATAGTAACAAGGGACCTGATTGTAATAAAACA
CCAGGAAGTGAAAGAGAGCTCAACTTAAGTAAAATTCAAAGTGAAGGAAATGACAGTAAGTGTC
TCATTAACTCTGGCAACGGTTCAACATATGAAGAAGAAACGAACAAAATCAAACATAGGAATAT
TGACTTACAAGATCAGGAAAAACATTTAAGTCAAGAGGATAATGATCTCAACAAACAAACTGGA
CAAATAATAGAGGATGATCAGGAAAAACATTTAAGTCAAGAGGATAATGATCTCAACAAACAAA
CTGGACAAATAATAGAGGATGATTTAGAAGAAGAAGACATCAAGCGAGGAAAAAGAAAAAGGCT
ATCCTCTGTGATGTGTGACAGTGATGAGAGTGATGACAGCGATATCCTAGTTAGAAAAGTAGGT
GTTAAACGTCCCCGTAGAGTGGTTGAAGATGAAGGTTCTTCAGTGGAAATGGAGCAAAAGACTC
CTGAAAAAACATTAGCTGCACAAAAGCGAGAAAAACTTCAGAAGCTCAAAGAACTCTCAAAACA
AAGATCTCGTCAGAGACGCAGTAGTGGTAGAGATTTTGAGGACTCTGAAAAGGAATCTTGCCCA
AGCAGTGATGAAGTTGATGAGGAGGAAGAAGAGGATAATTATGAATCTGATGAAGATGGAGATG
ATTATATTATCGATGACTTTGTAGTGCAAGATGAGGAGGGTGATGAAGAGAATAAAAACCAACA
AGGAGAAAAATTGACTACATCACAACTGAAATTAGTAAAACAGAATTCTCTTTATTCTTTTAGT
GACCACTATACTCATTTTGAAAGAGTTGTGAAGGCTCTTCTGATCAACGCTTTAGATGAATCTT
TTCTGGGAACATTATATGATGGCACAAGGCAAAAATCATATGCAAAAGATATGCTAACATCTCT
TCATTATTTGGATAACCGCTTTGTTCAGCCTCGTCTAGAGAGCTTGGTATCTAGAAGTCGTTGG
AAAGAGCAATATAAGGAGCGAGTAGAAAATTATTCTAATGTAAGTATTCATTTGAAGAATCCTG
AAAACTGTTCCTGCCAGGCTTGTGGACTGCATCGCTACTGTAAATATTCAGTGCATTTATCAGG
AGAGTTGTATAACACCAGGACCATGCAAATAGATAATTTCATGTCACATGATAAACAGGTGTTC
ACTGTTGGCAGAATTTGTGCCAGCCGTACCAGAATTTATCATAAACTGAAACATTTTAAATTCA
AACTATACCAGGAATGTTGCACCATTGCAATGACAGAAGAAGTTGAAGATGAACAAGTTAAAGA
AACAGTGGAAAGAATTTTCAGGCGGTCAAAAGAAAATGGCTGGATTAAGGAGAACAGTTCTTGT
GACCTGAGAGTGAAGAAGCACCTGGTGCCAGTCTGAGGAAAGGATCTCGGCTGCCAGTTCTAAT
ACACCCACATCCTCTTCTTGAGGACATGGGACTGAGCAGTGAGCACTGTAACTGAAGATCGAGG
GGAATGCAGAGGTTTCAGACCACAGCACTGATTTTGATTCCCCCATATCCTATTGATCACTAAA
TTTGATAACAGGAGTAAAGTGGGGGTTTTGAAGAGTGCACTGGATTCCCGAAGATCTGCTGGCA
GCTTACAAGCTCTGGTCTGCTCACAGAGCTTTTAGAATTGTTTATGGTATATGGAAAGAATGCT
AATACGACTGCAGTCTTCTAAAACAAGTCTAGTTACATGAATGTATAAGAGAGAACAAATAGTA
GATTTTCAGGCAACTCTTATCAACATTTAATCTTTTAAAGAAAAGAAAAAAGCCTAACTTGAGA
TCCATTGCCTGGACTATATCATAGGGAAATTTGTAAAAGAGGAATATAAAAAATAAGGCAAGAG
AGCTTAGGCAGATGGAAAGAAAACAAAACAGAAACTTTTTTAGCACATGTCATATTTAGTGGAG
GTCTCCCAGTCTAGATAATGACATCATCACTGGTTTCCCTTTGACAATTTTTCTCCCACCACAA
ACCACCACCCAGTGATCTTGCCTGCCCCCCACATCTTGATCCTTAAGTCTTTCTCTCATTTTAT
TCTTTTCAGCTTTTTGTCTTTTACTTTGCTTCTACTTCTCCTACTCCAAATGCTTCTCCCTGCT
TATCCGTACTTTTTCATTTGCTTTAGGAGAGAGCACTTATTCAATAACTTCCCGTCTTCATTTT
CCTAGACAACATTAAATTCTTAAGTGCTTTTATTGATGCCTTTAAGTGTTGCCAACCCTCTAGT
GGAACTGCAAAACCTATTGGGATAGCACAGTTATAAAGAATTAGATACTAGGTATAGAAAAATC
ACTGTGCATATACTGTATATGTTATATAATAGTATCATATATGGGGAAGAACTTTAAACTTCTT
GAAGAAAAAAGCATTTCCAAATCATGTATCCTAGAAAAAGCTTAACAAGGTTTAGGACACCAGA
AGGGACCTGGAATTTTAAAGACGTTATTCTTTATGCATAACACTTGGCATTCTTTTCTTAGGAA
AAGAAAGGAGCTTAGGCTTTCTTTTCAAGAAAGCCAAGTGTCATGTTATACATAAAGAATAACA
TTTAGCATTAGGCATTGAAGGTATTTCAAGATTGTGCATGTCTAGGACAGTATACACATTTTTT
TCCCCATGAAAATACCAAAGACCTTCATTTTTTTGAGATTTCTCCACTTAAAAAATTTGTTCCT
AGGTTTTCTCAAAAGATTTCCTAGAAACCACAGAGGTTTATAGCCAATATAAACCCATTTGCAG
CTTTTTGTGCTGTAATGAAATTTCAAAATTTGTCACGTGCTCTGACATTTCCCATCCTCACTCT
GTCTGTCCCTCTCACTGTGTGCCTTTGAGTGATAGCACTGCATGTACTTTGTGATGTGTGCTGC
CTTTAGCTACAGTCTGGTAGTCACAGTTACTCTAACCCTTTAGAATGCCTGGGGCTCAGTGTTA
CTTGAATGCCGTCTCCATGGCACTTTCCGCTCATATTTCCCATTTATGTCAACCCCTTTTGTTG
CCTTACACGTACTATTTGTTCCTGTCTTTCTGCCTCCAGCTTGTATTCCACACCTTACTTTTTC
CCTTACCTGCTTCTTCAGCCATTTTACTTTAATTATCTCAGGATGTCTCAGCATGTCTTCCCAA
AGACATGCCAACTAGACTGACTTCATTCTTTTTGTTCTTCCTTCTAAAGGTTGAACTAGGGTGA
TCCGTTTTTAATGTAATGATACTAAAGGGGTGTAGGAGCAACTTGAGTATAAGAAAAGAATAGA
TAATAGGAAAATTATAATAAAACCAAAATATTTAATAAACATAATAATGCATGTCTTATTCTAA
AGAAGAGTTCAATAACATACTCTAATATGACACTGGCAAAATTCTAACGAATATTTGTTCATTA
AGAAGAAAGTGTATATGATGATGGGACTTCCTGGGAAGTTGAAGATAGTATTGTTGGGATTGGC
TGGTGGATGCATAAACACCAGGTAGTAAAGAAAGCATGTCAATAGAAGTATCAGATGCCCATTC
ATACTGTAAATACTGTGTGTAAAACTGTTACAAGTGACAGTTGTATGTAAATTTTAAATGCACT
GATAAATATTGTCATATACATAATAATTTAAAATTATAATTAGATATCCCTTGCCTTCCTTAAA
CGCTTCTCTTCTTTTTCCCCTCCTTTTCAACTTTTTCCCTTGCCCCTTTTTTCCCCACCCCTTA
AACTGATGTTTCTCAAAGCATGGCCCTAAACTACCTATATCAGAATCACCTAGAAGTTTTTGAA
AAGTGTATAATCCCCTAGCCTCATCCCAGATTTATTGAATGACAATCCTTGTGGATGTTAAACA
TCCAATATTTTTAGCATTGATGATTCTTAAATAGATAAAAGTTTGAGGATCACTGCTAAAAAGT
ACCCGTTAACACTGAATTCTGTCCTCATCCTCTCAAAGTTGCCTTGGCGAATCAATTCCCTTCT
GCAGTTGTAGCTACTACTTCTGAGTAGAAGATTCCAAACTTCTCTTATATTCTGACCTCTTTCC
CACACTTCATTTCCACAATTCCAACTGTTTTCATCAGTAGGTCCATCAGGTGTTGTAAGAGAGT
AGTCTTCACTATTAAAATAAGTAGTCTTCACTATTAAAACCCTCCAAATGTTTAGTAAAGAATT
ATGAGAGCAGTATCTTTAGGTAGAGAGGATGGCAGAGTAATACTAACTGCAATGTCTGTGAGTT
TCACTTTCCAAGTTTTTTTTTTCTTGCCAAAGCTGCATCCTAGCCACACCATTTAAATCTCAGA
AACAGCATACTCTAAACTGGTTAAAAGTATAAGCTTAAGTATTTGCTTTGCCACTTACTAGCAG
TAGAATTTGGGAGCAAGCTATTTTATTTCTCTTAGCCTAAGTTTTCTCATCTGTAAAGTAGGAA
CAAAAACAGTAATAATAATTAGGGTTTTGATTGTGGAGATTAGATATGTAATACGTTTTAAGCA
TTTAGTATAGGACCTAGCAATTAGTAAGTGATTGATTAATCTTAGCTGTTACTTGCAATAAAAG
CAAGTAACCTCCTATCTTAGTATAGCTGAGATAGATTTTAATTGTCCTAGCTGTGTGTGGTGGT
GCACAGCTGTAGTCACAGCTACTTGGGAGGCTGAGGTGGTAGAATCGCCTGAGCCCAGGAGTTC
AAGGCCAGCCTGAGCAAGATAGTGAGACCCTGTCTCTTAAAATAATTTTTTTAATTTTTAATTT
TCCAAAAGAAATTTAATAAATAATAAAGGAATATGAGGAAAGGTAATATGAGAAACATAAAAAG
TCAAACTTTTAAAGTATAGGTTTCTAATCCTAGAGTACTTTACTTATATCTAATAAAACCTATC
TAAGTACTAGGCCAAAGAAAATTCCTAAGTAGTCCCTAGGCTATTTCCCCTTCTGTTATGTGTT
TCCATCTTTCCTGAGAAGGAGATCCAGTCAGATATCATACGGTTATAAAAAAGAGTTTCATGGC
CTTCAAGGTGTAGAAGGAAAATGCACTTCTCAACATTCCCTTCTGTAGGTCCCTATCACCACAA
AAGTCAGGGTCACCAGGATCCTCTCTCATTTCACTGAAGATTAAAACACAGTTCATAAACAGAG
TCAAGAAACTAGTATGTCATTAATCCCCTCACTGAAATAAATACTTTGAACTCTATATGTCTGA
AACTGAAATCATGATATCTTTCCCTCGCACAAACAACCTGCAAAAGAGCCTGCCATTATTCTAC
TCTGTCAACTTTGAAATCTCTAAATCATTCTTGACCCCTCTCTTAACTTGTTACACTTTGTTCT
TTACTCTTCATCTTCATTGCCATGACTCAGATTTGGGCCCTCATGACCTAAATTGTTATCACAG
ACCCATAACTAGTTGCTGAACTATTCTAGAATGAATGTTTTACCGATTTTCTTAAAATACACCT
GAGATCAGTTCAGTCCCCTGCTCCAAAACCTTTAGCAACTTTCCATTACCTGTCAAATGATTGT
TCAATTCTTTAACCAGTATTTTATAATTTTTGTTCTCTGAACTCAGCCTCTTTGGTTCAGTCTT
AGCTCTCTCTGTTCTCCTAAAAATACTCAGGTTGTAGTCAAATCCCATATTTTCTTGTCACGTC
ACTTTGATGGACTGTTCCCTCTTACTGAAAAGTCTTGCCACCAACTCTTTGCCTACCAAATCTG
TTTTTCCAGGACAACTTAAATGCCACTCTTTACTGCTTACCTCAACTAACCATGACCTATCTTC
TGAACCCTCATAACAGTGTCTGTACCTCTTTGGCACTTATTACTGATTGTTATTGGTGTATTAC
TACTGAACTGTATTCTCCTTAGGGGCAGGAAAAGTATCTTTTAAAAAACACTGTACCTAGACAG
TCATTAGCAGAGCCTTTGATATATATGTTCAACAAACTTTTTATTAAGTTATTGAGGTTACTAC
ATTTCTACTGTAATCATGATAATATAAAAATTATAATTTAAAACACAGTTATAAAATTAATAAT
ATTCACTTTGATCACTTTCCAATGCTTTCTATATGGAAATATATGAGTTATATATGAGTTAGGA
ATGCTTATTTGAAATTAAGTTCCTGTTTATCATAAAAAGATTTTTGTTCACGATTACCATGAAA
TGGACTTATCCTAATTGTGTCTGTAGTTTGCAAAGGCCCAGTTTGTCTTCATTGCTTTGAGTAA
AATAACTAGCTTTTCTATTGTATATGCAGAAATATGGTCAACTTGAAGAATATCTCAATTTTGC
GGATTACTTTCAAGAAGAGAAGTTTGAGTTGTAACACATTTCCATCAGAGAAGATTTTTTAAAT
TCCTGTAAATGTGAAGATCATGATTCTTGTTTTTCTGTATCATGTGACATGTTTGTACATTTTA
TCTATATCTTCATGGCAAAATATTTTGTTTAAAACATGATTATCTTAATTCCTGTGAAGTGGCA
CTCTACACTCTAATTAAACTTTTATCTGATGTACATAAAAGCATTATCTTAATTTTTAAGTCTG
TAAATATATTTTAAAGTTATATAATAATGGCTTTATAACAGATGACTGTCAAGTGAATGAGCTG
TTGATATCCTGTCAGTTTAGTCAAAATATATTGTATCTTAAAAATGTATTTAGACTAACGTCTA
CATGTATTTTTACGGAATTCCTGTCCAGATCTGTTTATTCTTTTACAGTATTAAATGATTTTCA
CTAATATATTTTTTACTGCTATCATCTAAATCAGTGGGCCATGGAAGAAACCTCATATATCATT
CAGTTCAATCCCATTGCTTCAGAATCAGATCATAGCATATCTATTCTAAGTAGAGGAATGCTTT
TTTCCTTTTCTTGAAAGTTTCTCTTTCAAATAGATTTCAGGCCTCTAGAGTCTTTCAACCCTCA
CATTCAGGAATAATTTTATGTAAATTTTCATGCTTTATAATGTTCTTACTTTTTTCTATTCAAT
TTTGTCTATATATTGATGATTAAGATGTATTTTATTTATTTTTATCCATAGCTTTTTCCATATA
AGTATGTATCTTAGGGTCAGAACTGCTGAAAGAGACAAACTCAGCCAAAAACACTTGGAAAGCA
TATTTTGGTATCTGCATTGCTTTGCATATCTAAATTTTCCCATAAAGTAATAAAGTAAAATGGT
TGCAGAGTGAACAAATGAA

hide sequence

RefSeq Acc Id:

XM_047427602 ⟹ XP_047283558

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI

RefSeq Acc Id:

XM_047427603 ⟹ XP_047283559

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI

RefSeq Acc Id:

XM_047427604 ⟹ XP_047283560

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI

RefSeq Acc Id:

XM_047427605 ⟹ XP_047283561

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI

RefSeq Acc Id:

XM_047427606 ⟹ XP_047283562

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI

RefSeq Acc Id:

XM_047427607 ⟹ XP_047283563

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	11	96,352,773 - 96,389,912 (-)	NCBI

RefSeq Acc Id:

XM_054369969 ⟹ XP_054225944

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	96,358,776 - 96,395,898 (-)	NCBI

RefSeq Acc Id:

XM_054369970 ⟹ XP_054225945

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	96,358,776 - 96,395,916 (-)	NCBI

RefSeq Acc Id:

XM_054369971 ⟹ XP_054225946

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	96,358,776 - 96,395,934 (-)	NCBI

RefSeq Acc Id:

XM_054369972 ⟹ XP_054225947

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	96,358,776 - 96,395,904 (-)	NCBI

RefSeq Acc Id:

XM_054369973 ⟹ XP_054225948

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	96,358,776 - 96,395,916 (-)	NCBI

RefSeq Acc Id:

XM_054369974 ⟹ XP_054225949

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	96,358,776 - 96,395,857 (-)	NCBI

RefSeq Acc Id:

XM_054369975 ⟹ XP_054225950

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	96,358,776 - 96,395,916 (-)	NCBI

RefSeq Acc Id:

XM_054369976 ⟹ XP_054225951

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	96,358,776 - 96,395,916 (-)	NCBI

RefSeq Acc Id:

XM_054369977 ⟹ XP_054225952

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	96,358,768 - 96,395,916 (-)	NCBI

RefSeq Acc Id:

XM_054369978 ⟹ XP_054225953

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	96,358,768 - 96,395,857 (-)	NCBI

RefSeq Acc Id:

XM_054369979 ⟹ XP_054225954

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	96,358,768 - 96,395,899 (-)	NCBI

RefSeq Acc Id:

XM_054369980 ⟹ XP_054225955

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	11	96,358,768 - 96,395,916 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_001305665	(Get FASTA)	NCBI Sequence Viewer
	NP_001305666	(Get FASTA)	NCBI Sequence Viewer
	NP_001350523	(Get FASTA)	NCBI Sequence Viewer
	NP_079001	(Get FASTA)	NCBI Sequence Viewer
	XP_005274349	(Get FASTA)	NCBI Sequence Viewer
	XP_011541286	(Get FASTA)	NCBI Sequence Viewer
	XP_011541289	(Get FASTA)	NCBI Sequence Viewer
	XP_011541290	(Get FASTA)	NCBI Sequence Viewer
	XP_016873796	(Get FASTA)	NCBI Sequence Viewer
	XP_016873799	(Get FASTA)	NCBI Sequence Viewer
	XP_024304458	(Get FASTA)	NCBI Sequence Viewer
	XP_024304461	(Get FASTA)	NCBI Sequence Viewer
	XP_047283558	(Get FASTA)	NCBI Sequence Viewer
	XP_047283559	(Get FASTA)	NCBI Sequence Viewer
	XP_047283560	(Get FASTA)	NCBI Sequence Viewer
	XP_047283561	(Get FASTA)	NCBI Sequence Viewer
	XP_047283562	(Get FASTA)	NCBI Sequence Viewer
	XP_047283563	(Get FASTA)	NCBI Sequence Viewer
	XP_054225944	(Get FASTA)	NCBI Sequence Viewer
	XP_054225945	(Get FASTA)	NCBI Sequence Viewer
	XP_054225946	(Get FASTA)	NCBI Sequence Viewer
	XP_054225947	(Get FASTA)	NCBI Sequence Viewer
	XP_054225948	(Get FASTA)	NCBI Sequence Viewer
	XP_054225949	(Get FASTA)	NCBI Sequence Viewer
	XP_054225950	(Get FASTA)	NCBI Sequence Viewer
	XP_054225951	(Get FASTA)	NCBI Sequence Viewer
	XP_054225952	(Get FASTA)	NCBI Sequence Viewer
	XP_054225953	(Get FASTA)	NCBI Sequence Viewer
	XP_054225954	(Get FASTA)	NCBI Sequence Viewer
	XP_054225955	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAF29020	(Get FASTA)	NCBI Sequence Viewer
	AAG44484	(Get FASTA)	NCBI Sequence Viewer
	AAH18663	(Get FASTA)	NCBI Sequence Viewer
	AAH33726	(Get FASTA)	NCBI Sequence Viewer
	BAB15683	(Get FASTA)	NCBI Sequence Viewer
	BAG36616	(Get FASTA)	NCBI Sequence Viewer
	BAG37226	(Get FASTA)	NCBI Sequence Viewer
	BAG51809	(Get FASTA)	NCBI Sequence Viewer
	EAW66979	(Get FASTA)	NCBI Sequence Viewer
	EAW66980	(Get FASTA)	NCBI Sequence Viewer
	EAW66981	(Get FASTA)	NCBI Sequence Viewer
	EAW66982	(Get FASTA)	NCBI Sequence Viewer
	EAW66983	(Get FASTA)	NCBI Sequence Viewer
	EAW66984	(Get FASTA)	NCBI Sequence Viewer
	EAW66985	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000278520.5
	ENSP00000397156.2
	ENSP00000431148
	ENSP00000431148.2
	ENSP00000442723.1
	ENSP00000493876.1
	ENSP00000494629.1
	ENSP00000494657
	ENSP00000494657.1
	ENSP00000495063
	ENSP00000495063.1
	ENSP00000495081.1
	ENSP00000495406.1
	ENSP00000495485
	ENSP00000495485.1
	ENSP00000495640
	ENSP00000495640.1
	ENSP00000495913
	ENSP00000495913.1
	ENSP00000496393
	ENSP00000496393.1
	ENSP00000504912
	ENSP00000504912.1
	ENSP00000504968.1
	ENSP00000505054.1
	ENSP00000505140.1
	ENSP00000505510.1
	ENSP00000505581.1
	ENSP00000505643.1
	ENSP00000505833
	ENSP00000505833.1
	ENSP00000505858
	ENSP00000505858.1
	ENSP00000505977
	ENSP00000505977.1
	ENSP00000506065.1
	ENSP00000506164
	ENSP00000506164.1
	ENSP00000506206.1
	ENSP00000506296.1
	ENSP00000506371
	ENSP00000506371.1
	ENSP00000506687
	ENSP00000506687.1
	ENSP00000506715
	ENSP00000506715.1
GenBank Protein	Q8N4S0	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_079001 ⟸ NM_024725
- Peptide Label:	isoform a
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MIHVRRHETRRNSKSHVPEQKSRVDWRRTKRSSISQLLDSDEELDSEEFDSDEELDSDESFEND EELDSNKGPDCNKTPGSERELNLSKIQSEGNDSKCLINSGNGSTYEEETNKIKHRNIDLQDQEK HLSQEDNDLNKQTGQIIEDDQEKHLSQEDNDLNKQTGQIIEDDLEEEDIKRGKRKRLSSVMCDS DESDDSDILVRKVGVKRPRRVVEDEGSSVEMEQKTPEKTLAAQKREKLQKLKELSKQRSRQRRS SGRDFEDSEKESCPSSDEVDEEEEEDNYESDEDGDDYIIDDFVVQDEEGDEENKNQQGEKLTTS QLKLVKQNSLYSFSDHYTHFERVVKALLINALDESFLGTLYDGTRQKSYAKDMLTSLHYLDNRF VQPRLESLVSRSRWKEQYKERVENYSNVSIHLKNPENCSCQACGLHRYCKYSVHLSGELYNTRT MQIDNFMSHDKQVFTVGRICASRTRIYHKLKHFKFKLYQECCTIAMTEEVEDEQVKETVERIFR RSKENGWIKEKYGQLEEYLNFADYFQEEKFEL hide sequence

RefSeq Acc Id:	XP_005274349 ⟸ XM_005274292
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MIHVRRHETRRNSKSHVPEQKSRVDWRRTKRSSISQLLDSDEELDSEEFDSDEELDSDESFEND EELDSNKGPDCNKTPGSERELNLSKIQSEGNDSKCLINSGNGSTYEEETNKIKHRNIDLQDQEK HLSQEDNDLNKQTGQIIEDDQEKHLSQEDNDLNKQTGQIIEDDLEEEDIKRGKRKRLSSVMCDS DESDDSDILVRKVGVKRPRRVVEDEGSSVEMEQKTPEKTLAAQKREKLQKLKELSKQRSRQRRS SGRDFEDSEKESCPSSDEVDEEEEEDNYESDEDGDDYIIDDFVVQDEEGDEENKNQQGEKLTTS QLKLVKQNSLYSFSDHYTHFERVVKALLINALDESFLGTLYDGTRQKSYAKDMLTSLHYLDNRF VQPRLESLVSRSRWKEQYKERVENYSNVSIHLKNPENCSCQACGLHRYCKYSVHLSGELYNTRT MQIDNFMSHDKQVFTVGRICASRTRIYHKLKHFKFKLYQECCTIAMTEEVEDEQVKETVERIFR RSKENGWIKEKYGQLEEYLNFADYFQEEKFEL hide sequence

RefSeq Acc Id:	XP_011541290 ⟸ XM_011542988
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MIHVRRHETRRNSKSHVPEQKSRVDWRRTKRSSISQLLDSDEELDSEEFDSDEELDSDESFEND EELDSNKGPDCNKTPGSERELNLSKIQSEGNDSKCLINSGNGSTYEEETNKIKHRNIDLQDQEK HLSQEDNDLNKQTGQIIEDDQEKHLSQEDNDLNKQTGQIIEDDLEEEDIKRGKRKRLSSVMCDS DESDDSDILVRKVGVKRPRRVVEDEGSSVEMEQKTPEKTLAAQKREKLQKLKELSKQRSRQRRS SGRDFEDSEKESCPSSDEVDEEEEEDNYESDEDGDDYIIDDFVVQDEEGDEENKNQQGEKLTTS QLKLVKQNSLYSFSDHYTHFERVVKALLINALDESFLGTLYDGTRQKSYAKDMLTSLHYLDNRF VQPRLESLVSRSRWKEQYKERVENYSNVSIHLKNPENCSCQACGLHRYCKYSVHLSGELYNTRT MQIDNFMSHDKQVFTVGRICASRTRIYHKLKHFKFKLYQECCTIAMTEEVEDEQVKETVERIFR RSKENGWIKEKYGQLEEYLNFADYFQEEKFEL hide sequence

RefSeq Acc Id:	XP_011541289 ⟸ XM_011542987
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MIHVRRHETRRNSKSHVPEQKSRVDWRRTKRSSISQLLDSDEELDSEEFDSDEELDSDESFEND EELDSNKGPDCNKTPGSERELNLSKIQSEGNDSKCLINSGNGSTYEEETNKIKHRNIDLQDQEK HLSQEDNDLNKQTGQIIEDDQEKHLSQEDNDLNKQTGQIIEDDLEEEDIKRGKRKRLSSVMCDS DESDDSDILVRKVGVKRPRRVVEDEGSSVEMEQKTPEKTLAAQKREKLQKLKELSKQRSRQRRS SGRDFEDSEKESCPSSDEVDEEEEEDNYESDEDGDDYIIDDFVVQDEEGDEENKNQQGEKLTTS QLKLVKQNSLYSFSDHYTHFERVVKALLINALDESFLGTLYDGTRQKSYAKDMLTSLHYLDNRF VQPRLESLVSRSRWKEQYKERVENYSNVSIHLKNPENCSCQACGLHRYCKYSVHLSGELYNTRT MQIDNFMSHDKQVFTVGRICASRTRIYHKLKHFKFKLYQECCTIAMTEEVEDEQVKETVERIFR RSKENGWIKEKYGQLEEYLNFADYFQEEKFEL hide sequence

RefSeq Acc Id:	XP_011541286 ⟸ XM_011542984
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MIHVRRHETRRNSKSHVPEQKSRVDWRRTKRSSISQLLDSDEELDSEEFDSDEELDSDESFEND EELDSNKGPDCNKTPGSERELNLSKIQSEGNDSKCLINSGNGSTYEEETNKIKHRNIDLQDQEK HLSQEDNDLNKQTGQIIEDDQEKHLSQEDNDLNKQTGQIIEDDLEEEDIKRGKRKRLSSVMCDS DESDDSDILVRKVGVKRPRRVVEDEGSSVEMEQKTPEKTLAAQKREKLQKLKELSKQRSRQRRS SGRDFEDSEKESCPSSDEVDEEEEEDNYESDEDGDDYIIDDFVVQDEEGDEENKNQQGEKLTTS QLKLVKQNSLYSFSDHYTHFERVVKALLINALDESFLGTLYDGTRQKSYAKDMLTSLHYLDNRF VQPRLESLVSRSRWKEQYKERVENYSNVSIHLKNPENCSCQACGLHRYCKYSVHLSGELYNTRT MQIDNFMSHDKQVFTVGRICASRTRIYHKLKHFKFKLYQECCTIAMTEEVEDEQVKETVERIFR RSKENGWIKEKYGQLEEYLNFADYFQEEKFEL hide sequence

RefSeq Acc Id:	NP_001305665 ⟸ NM_001318736
- Peptide Label:	isoform a
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MIHVRRHETRRNSKSHVPEQKSRVDWRRTKRSSISQLLDSDEELDSEEFDSDEELDSDESFEND EELDSNKGPDCNKTPGSERELNLSKIQSEGNDSKCLINSGNGSTYEEETNKIKHRNIDLQDQEK HLSQEDNDLNKQTGQIIEDDQEKHLSQEDNDLNKQTGQIIEDDLEEEDIKRGKRKRLSSVMCDS DESDDSDILVRKVGVKRPRRVVEDEGSSVEMEQKTPEKTLAAQKREKLQKLKELSKQRSRQRRS SGRDFEDSEKESCPSSDEVDEEEEEDNYESDEDGDDYIIDDFVVQDEEGDEENKNQQGEKLTTS QLKLVKQNSLYSFSDHYTHFERVVKALLINALDESFLGTLYDGTRQKSYAKDMLTSLHYLDNRF VQPRLESLVSRSRWKEQYKERVENYSNVSIHLKNPENCSCQACGLHRYCKYSVHLSGELYNTRT MQIDNFMSHDKQVFTVGRICASRTRIYHKLKHFKFKLYQECCTIAMTEEVEDEQVKETVERIFR RSKENGWIKEKYGQLEEYLNFADYFQEEKFEL hide sequence

RefSeq Acc Id:	NP_001305666 ⟸ NM_001318737
- Peptide Label:	isoform b
- UniProtKB:	Q8N4S0 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MIHVRRHETRRNSKSHVPEQKSRVDWRRTKRSSISQLLDSDEELDSEEFDSDEELDSDESFEND EELDSNKGPDCNKTPGSERELNLSKIQSEGNDSKCLINSGNGSTYEEETNKIKHRNIDLQDQEK HLSQEDNDLNKQTGQIIEDDQEKHLSQEDNDLNKQTGQIIEDDLEEEDIKRGKRKRLSSVMCDS DESDDSDILVRKVGVKRPRRVVEDEGSSVEMEQKTPEKTLAAQKREKLQKLKELSKQRSRQRRS SGRDFEDSEKESCPSSDEVDEEEEEDNYESDEDGDDYIIDDFVVQDEEGDEENKNQQGEKLTTS QLKLVKQNSLCKFNIKKMFHELFS hide sequence

RefSeq Acc Id:	XP_016873799 ⟸ XM_017018310
- Peptide Label:	isoform X2
- UniProtKB:	A0A2R8Y7C3 (UniProtKB/TrEMBL), A0A7P0T881 (UniProtKB/TrEMBL)
- Sequence:	show sequence MIHVRRHETRRNSKSHVPEQKSRVDWRRTKRSSISQLLDSDEELDSEEFDSDEELDSDESFEND EELDSNKGPDCNKTPGSERELNLSKIQSEGNDSKCLINSGNGSTYEEETNKIKHRNIDLQDQEK HLSQEDNDLNKQTGQIIEDDQEKHLSQEDNDLNKQTGQIIEDDLEEEDIKRGKRKRLSSVMCDS DESDDSDILVRKVGVKRPRRVVEDEGSSVEMEQKTPEKTLAAQKREKLQKLKELSKQRSRQRRS SGRDFEDSEKESCPSSDEVDEEEEEDNYESDEDGDDYIIDDFVVQDEEGDEENKNQQGEKLTTS QLKLVKQNSLYSFSDHYTHFERVVKALLINALDESFLGTLYDGTRQKSYAKDMLTSLHYLDNRF VQPRLESLVSRSRWKEQYKERVENYSNVSIHLKNPENCSCQACGLHRYCKYSVHLSGELYNTRT MQIDNFMSHDKQVFTVGRICASRTRIYHKLKHFKFKLYQECCTIAMTEEVEDEQVKETVERIFR RSKENGWIKENSSCDLRVKKHLVPV hide sequence

RefSeq Acc Id:	XP_016873796 ⟸ XM_017018307
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MIHVRRHETRRNSKSHVPEQKSRVDWRRTKRSSISQLLDSDEELDSEEFDSDEELDSDESFEND EELDSNKGPDCNKTPGSERELNLSKIQSEGNDSKCLINSGNGSTYEEETNKIKHRNIDLQDQEK HLSQEDNDLNKQTGQIIEDDQEKHLSQEDNDLNKQTGQIIEDDLEEEDIKRGKRKRLSSVMCDS DESDDSDILVRKVGVKRPRRVVEDEGSSVEMEQKTPEKTLAAQKREKLQKLKELSKQRSRQRRS SGRDFEDSEKESCPSSDEVDEEEEEDNYESDEDGDDYIIDDFVVQDEEGDEENKNQQGEKLTTS QLKLVKQNSLYSFSDHYTHFERVVKALLINALDESFLGTLYDGTRQKSYAKDMLTSLHYLDNRF VQPRLESLVSRSRWKEQYKERVENYSNVSIHLKNPENCSCQACGLHRYCKYSVHLSGELYNTRT MQIDNFMSHDKQVFTVGRICASRTRIYHKLKHFKFKLYQECCTIAMTEEVEDEQVKETVERIFR RSKENGWIKEKYGQLEEYLNFADYFQEEKFEL hide sequence

RefSeq Acc Id:	XP_024304461 ⟸ XM_024448693
- Peptide Label:	isoform X2
- UniProtKB:	A0A2R8Y7C3 (UniProtKB/TrEMBL), A0A7P0T881 (UniProtKB/TrEMBL)
- Sequence:	show sequence MIHVRRHETRRNSKSHVPEQKSRVDWRRTKRSSISQLLDSDEELDSEEFDSDEELDSDESFEND EELDSNKGPDCNKTPGSERELNLSKIQSEGNDSKCLINSGNGSTYEEETNKIKHRNIDLQDQEK HLSQEDNDLNKQTGQIIEDDQEKHLSQEDNDLNKQTGQIIEDDLEEEDIKRGKRKRLSSVMCDS DESDDSDILVRKVGVKRPRRVVEDEGSSVEMEQKTPEKTLAAQKREKLQKLKELSKQRSRQRRS SGRDFEDSEKESCPSSDEVDEEEEEDNYESDEDGDDYIIDDFVVQDEEGDEENKNQQGEKLTTS QLKLVKQNSLYSFSDHYTHFERVVKALLINALDESFLGTLYDGTRQKSYAKDMLTSLHYLDNRF VQPRLESLVSRSRWKEQYKERVENYSNVSIHLKNPENCSCQACGLHRYCKYSVHLSGELYNTRT MQIDNFMSHDKQVFTVGRICASRTRIYHKLKHFKFKLYQECCTIAMTEEVEDEQVKETVERIFR RSKENGWIKENSSCDLRVKKHLVPV hide sequence

RefSeq Acc Id:	XP_024304458 ⟸ XM_024448690
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MIHVRRHETRRNSKSHVPEQKSRVDWRRTKRSSISQLLDSDEELDSEEFDSDEELDSDESFEND EELDSNKGPDCNKTPGSERELNLSKIQSEGNDSKCLINSGNGSTYEEETNKIKHRNIDLQDQEK HLSQEDNDLNKQTGQIIEDDQEKHLSQEDNDLNKQTGQIIEDDLEEEDIKRGKRKRLSSVMCDS DESDDSDILVRKVGVKRPRRVVEDEGSSVEMEQKTPEKTLAAQKREKLQKLKELSKQRSRQRRS SGRDFEDSEKESCPSSDEVDEEEEEDNYESDEDGDDYIIDDFVVQDEEGDEENKNQQGEKLTTS QLKLVKQNSLYSFSDHYTHFERVVKALLINALDESFLGTLYDGTRQKSYAKDMLTSLHYLDNRF VQPRLESLVSRSRWKEQYKERVENYSNVSIHLKNPENCSCQACGLHRYCKYSVHLSGELYNTRT MQIDNFMSHDKQVFTVGRICASRTRIYHKLKHFKFKLYQECCTIAMTEEVEDEQVKETVERIFR RSKENGWIKEKYGQLEEYLNFADYFQEEKFEL hide sequence

RefSeq Acc Id:	NP_001350523 ⟸ NM_001363594
- Peptide Label:	isoform c
- UniProtKB:	A0A7P0TBN6 (UniProtKB/TrEMBL), B2RBH9 (UniProtKB/TrEMBL)

RefSeq Acc Id:

ENSP00000397156 ⟸ ENST00000423339

RefSeq Acc Id:

ENSP00000431148 ⟸ ENST00000530203

RefSeq Acc Id:

ENSP00000495640 ⟸ ENST00000530106

RefSeq Acc Id:

ENSP00000442723 ⟸ ENST00000538597

RefSeq Acc Id:

ENSP00000495913 ⟸ ENST00000643839

RefSeq Acc Id:

ENSP00000495081 ⟸ ENST00000644686

RefSeq Acc Id:

ENSP00000495485 ⟸ ENST00000645500

RefSeq Acc Id:

ENSP00000495063 ⟸ ENST00000645439

RefSeq Acc Id:

ENSP00000494629 ⟸ ENST00000645366

RefSeq Acc Id:

ENSP00000495406 ⟸ ENST00000646050

RefSeq Acc Id:

ENSP00000278520 ⟸ ENST00000278520

RefSeq Acc Id:

ENSP00000496393 ⟸ ENST00000646818

RefSeq Acc Id:

ENSP00000494657 ⟸ ENST00000646638

RefSeq Acc Id:

ENSP00000493876 ⟸ ENST00000647080

RefSeq Acc Id:

ENSP00000506715 ⟸ ENST00000680728

RefSeq Acc Id:

ENSP00000505510 ⟸ ENST00000679788

RefSeq Acc Id:

ENSP00000506687 ⟸ ENST00000680859

RefSeq Acc Id:

ENSP00000505581 ⟸ ENST00000679696

RefSeq Acc Id:

ENSP00000505643 ⟸ ENST00000681014

RefSeq Acc Id:

ENSP00000505977 ⟸ ENST00000680979

RefSeq Acc Id:

ENSP00000504912 ⟸ ENST00000680763

RefSeq Acc Id:

ENSP00000506206 ⟸ ENST00000680532

RefSeq Acc Id:

ENSP00000506296 ⟸ ENST00000681164

RefSeq Acc Id:

ENSP00000505833 ⟸ ENST00000679856

RefSeq Acc Id:

ENSP00000505140 ⟸ ENST00000681200

RefSeq Acc Id:

ENSP00000505858 ⟸ ENST00000680171

RefSeq Acc Id:

ENSP00000506065 ⟸ ENST00000681451

RefSeq Acc Id:

ENSP00000506164 ⟸ ENST00000679960

RefSeq Acc Id:

ENSP00000504968 ⟸ ENST00000679616

RefSeq Acc Id:

ENSP00000506371 ⟸ ENST00000679708

RefSeq Acc Id:

ENSP00000505054 ⟸ ENST00000680052

RefSeq Acc Id:	XP_047283562 ⟸ XM_047427606
- Peptide Label:	isoform X2
- UniProtKB:	A0A2R8Y7C3 (UniProtKB/TrEMBL), A0A7P0T881 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047283561 ⟸ XM_047427605
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047283559 ⟸ XM_047427603
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047283558 ⟸ XM_047427602
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047283563 ⟸ XM_047427607
- Peptide Label:	isoform X2
- UniProtKB:	A0A2R8Y7C3 (UniProtKB/TrEMBL), A0A7P0T881 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047283560 ⟸ XM_047427604
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054225955 ⟸ XM_054369980
- Peptide Label:	isoform X2
- UniProtKB:	A0A2R8Y7C3 (UniProtKB/TrEMBL), A0A7P0T881 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054225952 ⟸ XM_054369977
- Peptide Label:	isoform X2
- UniProtKB:	A0A2R8Y7C3 (UniProtKB/TrEMBL), A0A7P0T881 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054225954 ⟸ XM_054369979
- Peptide Label:	isoform X2
- UniProtKB:	A0A2R8Y7C3 (UniProtKB/TrEMBL), A0A7P0T881 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054225953 ⟸ XM_054369978
- Peptide Label:	isoform X2
- UniProtKB:	A0A2R8Y7C3 (UniProtKB/TrEMBL), A0A7P0T881 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054225946 ⟸ XM_054369971
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054225951 ⟸ XM_054369976
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054225950 ⟸ XM_054369975
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054225948 ⟸ XM_054369973
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054225945 ⟸ XM_054369970
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054225947 ⟸ XM_054369972
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054225944 ⟸ XM_054369969
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054225949 ⟸ XM_054369974
- Peptide Label:	isoform X1
- UniProtKB:	Q9H2Q5 (UniProtKB/Swiss-Prot), Q8WV71 (UniProtKB/Swiss-Prot), Q8N4S0 (UniProtKB/Swiss-Prot), B3KPU7 (UniProtKB/Swiss-Prot), Q9H5E3 (UniProtKB/Swiss-Prot), B2RBH9 (UniProtKB/TrEMBL)

Protein Domains

Coiled-coil DUF4211

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q8N4S0-F1-model_v2	AlphaFold	Q8N4S0	1-544	view protein structure

Promoters

RGD ID:

6788457

Promoter ID:

HG_KWN:14002

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, HeLa_S3, Jurkat, K562, Lymphoblastoid, NB4

Transcripts:

ENST00000361025, NM_003772, NM_024725, UC009YWR.1, UC009YWT.1, UC009YWU.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	11	95,762,581 - 95,766,762 (-)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:26282	AgrOrtholog
COSMIC	CCDC82	COSMIC
Ensembl Genes	ENSG00000149231	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000278520.9	UniProtKB/Swiss-Prot
	ENST00000423339.2	UniProtKB/Swiss-Prot
	ENST00000530106	ENTREZGENE
	ENST00000530106.2	UniProtKB/Swiss-Prot
	ENST00000530203	UniProtKB/TrEMBL
	ENST00000530203.2	UniProtKB/Swiss-Prot
	ENST00000538597.1	UniProtKB/TrEMBL
	ENST00000643839	ENTREZGENE
	ENST00000643839.1	UniProtKB/TrEMBL
	ENST00000644686.1	UniProtKB/Swiss-Prot
	ENST00000645366.1	UniProtKB/Swiss-Prot
	ENST00000645439	ENTREZGENE
	ENST00000645439.1	UniProtKB/Swiss-Prot
	ENST00000645500	ENTREZGENE
	ENST00000645500.1	UniProtKB/Swiss-Prot
	ENST00000646050.1	UniProtKB/TrEMBL
	ENST00000646638	ENTREZGENE
	ENST00000646638.1	UniProtKB/Swiss-Prot
	ENST00000646818	ENTREZGENE
	ENST00000646818.2	UniProtKB/Swiss-Prot
	ENST00000647080.1	UniProtKB/TrEMBL
	ENST00000679616.1	UniProtKB/TrEMBL
	ENST00000679696.1	UniProtKB/TrEMBL
	ENST00000679708	ENTREZGENE
	ENST00000679708.1	UniProtKB/Swiss-Prot
	ENST00000679788.1	UniProtKB/Swiss-Prot
	ENST00000679856	ENTREZGENE
	ENST00000679856.1	UniProtKB/Swiss-Prot
	ENST00000679960	ENTREZGENE
	ENST00000679960.1	UniProtKB/Swiss-Prot
	ENST00000680052.1	UniProtKB/TrEMBL
	ENST00000680171	ENTREZGENE
	ENST00000680171.1	UniProtKB/Swiss-Prot
	ENST00000680532.1	UniProtKB/TrEMBL
	ENST00000680728	ENTREZGENE
	ENST00000680728.1	UniProtKB/TrEMBL
	ENST00000680763	ENTREZGENE
	ENST00000680763.1	UniProtKB/Swiss-Prot
	ENST00000680859	ENTREZGENE
	ENST00000680859.1	UniProtKB/TrEMBL
	ENST00000680979	ENTREZGENE
	ENST00000680979.1	UniProtKB/Swiss-Prot
	ENST00000681014.1	UniProtKB/TrEMBL
	ENST00000681164.1	UniProtKB/Swiss-Prot
	ENST00000681200.1	UniProtKB/TrEMBL
	ENST00000681451.1	UniProtKB/TrEMBL
GTEx	ENSG00000149231	GTEx
HGNC ID	HGNC:26282	ENTREZGENE
Human Proteome Map	CCDC82	Human Proteome Map
InterPro	DUF4196	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	DUF4211	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:79780	UniProtKB/Swiss-Prot
NCBI Gene	79780	ENTREZGENE
OMIM	619870	OMIM
PANTHER	COILED-COIL DOMAIN-CONTAINING PROTEIN 82	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	UNCHARACTERIZED	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	DUF4196	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	DUF4211	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA143485431	PharmGKB
UniProt	A0A024R3B8_HUMAN	UniProtKB/TrEMBL
	A0A2R8Y4L3_HUMAN	UniProtKB/TrEMBL
	A0A2R8Y7C3	ENTREZGENE, UniProtKB/TrEMBL
	A0A2R8YE98_HUMAN	UniProtKB/TrEMBL
	A0A7P0T881	ENTREZGENE, UniProtKB/TrEMBL
	A0A7P0T8E7_HUMAN	UniProtKB/TrEMBL
	A0A7P0T8I8_HUMAN	UniProtKB/TrEMBL
	A0A7P0TAG3_HUMAN	UniProtKB/TrEMBL
	A0A7P0TBN6	ENTREZGENE, UniProtKB/TrEMBL
	B2RBH9	ENTREZGENE, UniProtKB/TrEMBL
	B3KPU7	ENTREZGENE
	CCD82_HUMAN	UniProtKB/Swiss-Prot
	E9PMD6_HUMAN	UniProtKB/TrEMBL
	F5H777_HUMAN	UniProtKB/TrEMBL
	Q8N4S0	ENTREZGENE
	Q8WV71	ENTREZGENE
	Q9H2Q5	ENTREZGENE
	Q9H5E3	ENTREZGENE
UniProt Secondary	B3KPU7	UniProtKB/Swiss-Prot
	Q8WV71	UniProtKB/Swiss-Prot
	Q9H2Q5	UniProtKB/Swiss-Prot
	Q9H5E3	UniProtKB/Swiss-Prot

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)

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Imported Disease Annotations - ClinVar

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