SYNDIG1 (synapse differentiation inducing 1)

Gene: SYNDIG1 (synapse differentiation inducing 1) Homo sapiens

Analyze

Symbol:

SYNDIG1

Name:

synapse differentiation inducing 1

RGD ID:

1321842

HGNC Page

HGNC:15885

Description:

Predicted to enable glutamate receptor binding activity and protein homodimerization activity. Involved in positive regulation of synapse assembly. Located in intracellular membrane-bounded organelle.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

C20orf39; dispanin subfamily C member 2; DSPC2; FLJ14220; IFITMD5; interferon induced transmembrane protein domain containing 5; synapse differentiation induced gene 1; synapse differentiation-inducing gene protein 1; TMEM90B; transmembrane protein 90B

RGD Orthologs

Alliance Genes

More Info

more info ...

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	20	24,469,629 - 24,666,616 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	20	24,469,629 - 24,666,616 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	20	24,450,265 - 24,647,252 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	20	24,397,835 - 24,595,167 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	20	24,397,834 - 24,595,167	NCBI
Celera	20	24,524,151 - 24,721,487 (+)	NCBI		Celera
Cytogenetic Map	20	p11.21	NCBI
HuRef	20	24,405,607 - 24,604,629 (+)	NCBI		HuRef
CHM1_1	20	24,450,308 - 24,648,495 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	20	24,531,610 - 24,729,659 (+)	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

genetic disease (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dichloroethane (ISO)

17beta-estradiol (EXP)

2-palmitoylglycerol (EXP)

4,4'-sulfonyldiphenol (EXP)

acrylamide (EXP,ISO)

aflatoxin B1 (EXP)

Aflatoxin B2 alpha (EXP)

aldehydo-D-glucose (ISO)

arsenite(3-) (EXP)

benzo[a]pyrene (EXP)

benzo[e]pyrene (EXP)

bis(2-ethylhexyl) phthalate (ISO)

bisphenol A (EXP,ISO)

Cuprizon (ISO)

D-glucose (ISO)

diazinon (EXP)

doxorubicin (EXP,ISO)

ethanol (ISO)

fructose (ISO)

fulvestrant (EXP)

furan (ISO)

glucose (ISO)

herbicide (ISO)

iron dichloride (EXP)

methapyrilene (EXP)

methylmercury chloride (EXP)

Monobutylphthalate (ISO)

paraquat (ISO)

silicon dioxide (EXP)

sodium arsenite (EXP)

Soman (ISO)

sunitinib (EXP)

titanium dioxide (ISO)

valproic acid (EXP)

vitamin E (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

intracellular protein transport (IEA,ISS)

positive regulation of synapse assembly (IBA,IDA,IEA)

synaptic vesicle clustering (IBA,IEA,ISS)

Cellular Component

cell body (IEA,ISS)

cell projection (IEA)

dendrite (IEA)

dendritic shaft (IEA,ISS)

dendritic spine (IEA,ISS)

early endosome membrane (IEA,ISS)

endosome (IEA)

excitatory synapse (IBA,IEA,ISS)

Golgi membrane (ISO)

intracellular membrane-bounded organelle (IBA,IDA)

membrane (IEA)

plasma membrane (IEA,ISS)

postsynaptic density (IEA,ISS)

postsynaptic density membrane (IBA,IEA)

postsynaptic membrane (IEA)

synapse (IEA)

synaptic vesicle membrane (IBA,IEA)

Molecular Function

glutamate receptor binding (IEA,ISS)

protein binding (IPI)

protein homodimerization activity (IEA,ISS)

References

References - curated

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

Additional References at PubMed

PMID:11780052	PMID:12477932	PMID:14702039	PMID:15489334	PMID:16169070	PMID:16344560	PMID:17207965	PMID:20152115	PMID:20379614	PMID:21873635	PMID:22363774	PMID:25416956
PMID:26186194	PMID:32296183	PMID:33961781

Genomics

Comparative Map Data

SYNDIG1
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	20	24,469,629 - 24,666,616 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	20	24,469,629 - 24,666,616 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	20	24,450,265 - 24,647,252 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	20	24,397,835 - 24,595,167 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	20	24,397,834 - 24,595,167	NCBI
Celera	20	24,524,151 - 24,721,487 (+)	NCBI		Celera
Cytogenetic Map	20	p11.21	NCBI
HuRef	20	24,405,607 - 24,604,629 (+)	NCBI		HuRef
CHM1_1	20	24,450,308 - 24,648,495 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	20	24,531,610 - 24,729,659 (+)	NCBI		T2T-CHM13v2.0

Syndig1
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	2	149,672,703 - 149,846,312 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	2	149,671,131 - 149,846,312 (+)	Ensembl		GRCm39 Ensembl
GRCm38	2	149,830,783 - 150,004,392 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	2	149,829,211 - 150,004,392 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	2	149,656,519 - 149,830,128 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	2	149,522,238 - 149,695,833 (+)	NCBI		MGSCv36	mm8
Celera	2	151,074,984 - 151,248,632 (+)	NCBI		Celera
Cytogenetic Map	2	G3	NCBI
cM Map	2	73.8	NCBI

Syndig1
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	3	158,491,474 - 158,695,174 (+)	NCBI		GRCr8
mRatBN7.2	3	138,030,995 - 138,234,646 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	3	138,031,769 - 138,198,122 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	3	141,965,844 - 142,132,031 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	3	150,549,574 - 150,715,761 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	3	148,264,722 - 148,431,040 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	3	145,031,427 - 145,199,273 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	3	145,032,200 - 145,199,356 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	3	151,405,855 - 151,571,801 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	3	139,434,170 - 139,834,916 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	3	139,339,742 - 139,740,488 (+)	NCBI
Celera	3	136,716,149 - 136,879,658 (+)	NCBI		Celera
Cytogenetic Map	3	q41	NCBI

Syndig1
(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_004955415	30,909,014 - 31,005,533 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955415	30,909,654 - 31,005,421 (+)	NCBI	ChiLan1.0	ChiLan1.0

SYNDIG1
(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	21	25,333,573 - 25,559,619 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	20	25,330,408 - 25,563,465 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	20	24,402,471 - 24,629,365 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	20	24,751,062 - 24,947,280 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	20	24,825,380 - 24,947,370 (+)	Ensembl	panpan1.1		panPan2

SYNDIG1
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	23	759,787 - 865,659 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	23	685,782 - 865,359 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	23	707,338 - 896,758 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	23	919,502 - 1,109,045 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	23	918,789 - 1,108,951 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	23	819,974 - 925,587 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	23	859,317 - 1,048,759 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	23	848,398 - 1,037,785 (+)	NCBI		UU_Cfam_GSD_1.0

Syndig1
(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_024408640	147,745,538 - 147,938,240 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936620	1,165,709 - 1,359,179 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936620	1,165,312 - 1,359,127 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

SYNDIG1
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	17	30,638,039 - 30,709,382 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	17	30,621,622 - 30,709,387 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	17	34,684,454 - 34,720,447 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

SYNDIG1
(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	2	53,532,455 - 53,682,063 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	2	53,533,174 - 53,682,056 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666050	92,177,743 - 92,250,156 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Syndig1
(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_004624939	560,106 - 661,570 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624939	560,192 - 698,100 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in SYNDIG1
19 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 20p13-11.21(chr20:89939-25697564)x3	copy number gain	See cases [RCV000051227]	Chr20:89939..25697564 [GRCh38] Chr20:70580..25678200 [GRCh37] Chr20:18580..25626200 [NCBI36] Chr20:20p13-11.21	pathogenic
GRCh38/hg38 20p12.2-q12(chr20:9811433-39316956)x3	copy number gain	See cases [RCV000052999]	Chr20:9811433..39316956 [GRCh38] Chr20:9792081..37945599 [GRCh37] Chr20:9740081..37379013 [NCBI36] Chr20:20p12.2-q12	pathogenic
GRCh38/hg38 20p11.22-q11.1(chr20:22061586-30285812)x3	copy number gain	See cases [RCV000053000]	Chr20:22061586..30285812 [GRCh38] Chr20:22042224..29520488 [GRCh37] Chr20:21990224..28134149 [NCBI36] Chr20:20p11.22-q11.1	pathogenic
GRCh38/hg38 20p11.21(chr20:23455796-24880833)x3	copy number gain	See cases [RCV000053001]	Chr20:23455796..24880833 [GRCh38] Chr20:23436433..24861469 [GRCh37] Chr20:23384433..24809469 [NCBI36] Chr20:20p11.21	pathogenic
NM_024893.2(SYNDIG1):c.307G>A (p.Gly103Arg)	single nucleotide variant	Malignant melanoma [RCV000072553]	Chr20:24543404 [GRCh38] Chr20:24524040 [GRCh37] Chr20:24472040 [NCBI36] Chr20:20p11.21	not provided
NM_024893.2(SYNDIG1):c.-78-10155T>G	single nucleotide variant	Lung cancer [RCV000101515]	Chr20:24532865 [GRCh38] Chr20:24513501 [GRCh37] Chr20:20p11.21	uncertain significance
NM_024893.2(SYNDIG1):c.-78-3787T>C	single nucleotide variant	Lung cancer [RCV000101516]	Chr20:24539233 [GRCh38] Chr20:24519869 [GRCh37] Chr20:20p11.21	uncertain significance
GRCh38/hg38 20p13-q11.1(chr20:80106-30227427)x3	copy number gain	See cases [RCV000133996]	Chr20:80106..30227427 [GRCh38] Chr20:60747..29462103 [GRCh37] Chr20:8747..28075764 [NCBI36] Chr20:20p13-q11.1	pathogenic
GRCh38/hg38 20p13-q13.33(chr20:99557-64277321)x3	copy number gain	See cases [RCV000135859]	Chr20:99557..64277321 [GRCh38] Chr20:80198..62908674 [GRCh37] Chr20:28198..62379118 [NCBI36] Chr20:20p13-q13.33	pathogenic
GRCh38/hg38 20p13-11.1(chr20:80927-26324843)x3	copy number gain	See cases [RCV000142017]	Chr20:80927..26324843 [GRCh38] Chr20:61568..26305479 [GRCh37] Chr20:9568..26253479 [NCBI36] Chr20:20p13-11.1	pathogenic
GRCh37/hg19 20p13-11.1(chr20:80198-26075841)x3	copy number gain	See cases [RCV000239954]	Chr20:80198..26075841 [GRCh37] Chr20:20p13-11.1	pathogenic
GRCh37/hg19 20p12.1-q11.21(chr20:17705775-31600738)x3	copy number gain	See cases [RCV000240436]	Chr20:17705775..31600738 [GRCh37] Chr20:20p12.1-q11.21	pathogenic
GRCh37/hg19 20p11.21-q11.21(chr20:24162775-31820857)x3	copy number gain	See cases [RCV000448977]	Chr20:24162775..31820857 [GRCh37] Chr20:20p11.21-q11.21	likely pathogenic
GRCh37/hg19 20p13-q11.21(chr20:80198-26208081)x3	copy number gain	not provided [RCV000487461]	Chr20:80198..26208081 [GRCh37] Chr20:20p13-q11.21	pathogenic
GRCh37/hg19 20p11.23-11.1(chr20:18500917-25847320)x1	copy number loss	See cases [RCV000510621]	Chr20:18500917..25847320 [GRCh37] Chr20:20p11.23-11.1	pathogenic
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)x3	copy number gain	See cases [RCV000510832]	Chr20:61569..62915555 [GRCh37] Chr20:20p13-q13.33	pathogenic
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)	copy number gain	See cases [RCV000512450]	Chr20:61569..62915555 [GRCh37] Chr20:20p13-q13.33	pathogenic
Single allele	duplication	not provided [RCV000677978]	Chr20:17705775..31600738 [GRCh37] Chr20:20p12.1-q11.21	pathogenic
GRCh37/hg19 20p11.21(chr20:23884744-24530547)x1	copy number loss	not provided [RCV000684121]	Chr20:23884744..24530547 [GRCh37] Chr20:20p11.21	likely benign
GRCh37/hg19 20p13-q13.33(chr20:63244-62948788)x3	copy number gain	not provided [RCV000741058]	Chr20:63244..62948788 [GRCh37] Chr20:20p13-q13.33	pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62961294)x3	copy number gain	not provided [RCV000741059]	Chr20:63244..62961294 [GRCh37] Chr20:20p13-q13.33	pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62912463)x3	copy number gain	not provided [RCV000741057]	Chr20:63244..62912463 [GRCh37] Chr20:20p13-q13.33	pathogenic
GRCh37/hg19 20p11.21(chr20:24079491-24681352)x3	copy number gain	not provided [RCV001007087]	Chr20:24079491..24681352 [GRCh37] Chr20:20p11.21	uncertain significance
GRCh37/hg19 20p11.21(chr20:24232978-25520939)x3	copy number gain	not provided [RCV000847453]	Chr20:24232978..25520939 [GRCh37] Chr20:20p11.21	uncertain significance
GRCh37/hg19 20p11.21(chr20:24365369-24488368)x1	copy number loss	not provided [RCV001007088]	Chr20:24365369..24488368 [GRCh37] Chr20:20p11.21	likely benign
GRCh37/hg19 20p13-11.1(chr20:61568-26305479)x3	copy number gain	not provided [RCV001007068]	Chr20:61568..26305479 [GRCh37] Chr20:20p13-11.1	pathogenic
NM_024893.2(SYNDIG1):c.-524C>T	single nucleotide variant	not provided [RCV003431281]	Chr20:24469308 [GRCh38] Chr20:24449944 [GRCh37] Chr20:20p11.21	likely benign
GRCh37/hg19 20p11.23-q11.21(chr20:19750804-30479077)x3	copy number gain	not provided [RCV001258738]	Chr20:19750804..30479077 [GRCh37] Chr20:20p11.23-q11.21	likely pathogenic
GRCh37/hg19 20p11.21-q11.21(chr20:24162775-31820857)	copy number gain	not specified [RCV002052707]	Chr20:24162775..31820857 [GRCh37] Chr20:20p11.21-q11.21	likely pathogenic
GRCh37/hg19 20p11.23-q11.22(chr20:18665879-33903216)x3	copy number gain	not provided [RCV001829151]	Chr20:18665879..33903216 [GRCh37] Chr20:20p11.23-q11.22	likely pathogenic
GRCh37/hg19 20p11.21(chr20:23142478-24824349)x3	copy number gain	not provided [RCV002474920]	Chr20:23142478..24824349 [GRCh37] Chr20:20p11.21	uncertain significance
NM_024893.3(SYNDIG1):c.595G>A (p.Ala199Thr)	single nucleotide variant	Inborn genetic diseases [RCV002776940]	Chr20:24584970 [GRCh38] Chr20:24565606 [GRCh37] Chr20:20p11.21	uncertain significance
NM_024893.3(SYNDIG1):c.582G>C (p.Trp194Cys)	single nucleotide variant	Inborn genetic diseases [RCV002865596]	Chr20:24584957 [GRCh38] Chr20:24565593 [GRCh37] Chr20:20p11.21	uncertain significance
NM_024893.3(SYNDIG1):c.764A>G (p.Asn255Ser)	single nucleotide variant	Inborn genetic diseases [RCV002818530]	Chr20:24665491 [GRCh38] Chr20:24646127 [GRCh37] Chr20:20p11.21	uncertain significance
NM_024893.3(SYNDIG1):c.6T>G (p.Asp2Glu)	single nucleotide variant	Inborn genetic diseases [RCV002951914]	Chr20:24543103 [GRCh38] Chr20:24523739 [GRCh37] Chr20:20p11.21	uncertain significance
NM_024893.3(SYNDIG1):c.226C>G (p.Pro76Ala)	single nucleotide variant	Inborn genetic diseases [RCV002641039]	Chr20:24543323 [GRCh38] Chr20:24523959 [GRCh37] Chr20:20p11.21	uncertain significance
NM_024893.3(SYNDIG1):c.206C>T (p.Pro69Leu)	single nucleotide variant	Inborn genetic diseases [RCV002767845]	Chr20:24543303 [GRCh38] Chr20:24523939 [GRCh37] Chr20:20p11.21	uncertain significance
NM_024893.3(SYNDIG1):c.637A>C (p.Lys213Gln)	single nucleotide variant	Inborn genetic diseases [RCV002921475]	Chr20:24665364 [GRCh38] Chr20:24646000 [GRCh37] Chr20:20p11.21	uncertain significance
NM_024893.3(SYNDIG1):c.92T>C (p.Leu31Ser)	single nucleotide variant	Inborn genetic diseases [RCV003209725]	Chr20:24543189 [GRCh38] Chr20:24523825 [GRCh37] Chr20:20p11.21	uncertain significance
NM_024893.3(SYNDIG1):c.524T>C (p.Met175Thr)	single nucleotide variant	Inborn genetic diseases [RCV003213339]	Chr20:24584899 [GRCh38] Chr20:24565535 [GRCh37] Chr20:20p11.21	uncertain significance
NM_024893.3(SYNDIG1):c.281A>G (p.Tyr94Cys)	single nucleotide variant	Inborn genetic diseases [RCV003197309]	Chr20:24543378 [GRCh38] Chr20:24524014 [GRCh37] Chr20:20p11.21	uncertain significance
NM_024893.3(SYNDIG1):c.536G>A (p.Arg179Gln)	single nucleotide variant	Inborn genetic diseases [RCV003359967]	Chr20:24584911 [GRCh38] Chr20:24565547 [GRCh37] Chr20:20p11.21	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	679
Count of miRNA genes:	536
Interacting mature miRNAs:	576
Transcripts:	ENST00000376862, ENST00000482637
Prediction methods:	Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

Markers in Region

D20S844

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	24,448,342 - 24,448,543	UniSTS	GRCh37
Build 36	20	24,396,342 - 24,396,543	RGD	NCBI36
Celera	20	24,522,658 - 24,522,859	RGD
Cytogenetic Map	20	p11.21	UniSTS
HuRef	20	24,404,104 - 24,404,315	UniSTS
Marshfield Genetic Map	20	49.71	RGD
Marshfield Genetic Map	20	49.71	UniSTS
Genethon Genetic Map	20	49.2	UniSTS
TNG Radiation Hybrid Map	20	13032.0	UniSTS
Whitehead-YAC Contig Map	20		UniSTS

D20S486

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	24,635,134 - 24,635,369	UniSTS	GRCh37
Build 36	20	24,583,134 - 24,583,369	RGD	NCBI36
Celera	20	24,709,455 - 24,709,690	RGD
Cytogenetic Map	20	p11.21	UniSTS
HuRef	20	24,592,455 - 24,592,694	UniSTS
Marshfield Genetic Map	20	49.22	UniSTS
Marshfield Genetic Map	20	49.22	RGD
Whitehead-YAC Contig Map	20		UniSTS

D20S462

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	24,601,986 - 24,602,195	UniSTS	GRCh37
Build 36	20	24,549,986 - 24,550,195	RGD	NCBI36
Celera	20	24,676,306 - 24,676,515	RGD
Cytogenetic Map	20	p11.21	UniSTS
HuRef	20	24,559,313 - 24,559,522	UniSTS
Whitehead-RH Map	20	117.3	UniSTS
Whitehead-YAC Contig Map	20		UniSTS
NCBI RH Map	20	191.0	UniSTS

RH98971

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	24,545,078 - 24,545,232	UniSTS	GRCh37
Build 36	20	24,493,078 - 24,493,232	RGD	NCBI36
Celera	20	24,619,406 - 24,619,560	RGD
Cytogenetic Map	20	p11.21	UniSTS
HuRef	20	24,502,420 - 24,502,574	UniSTS
GeneMap99-GB4 RH Map	20	128.21	UniSTS

RH121314

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	24,589,848 - 24,590,121	UniSTS	GRCh37
Build 36	20	24,537,848 - 24,538,121	RGD	NCBI36
Celera	20	24,664,168 - 24,664,441	RGD
Cytogenetic Map	20	p11.21	UniSTS
HuRef	20	24,547,175 - 24,547,448	UniSTS

SHGC-142801

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	24,525,522 - 24,525,820	UniSTS	GRCh37
Build 36	20	24,473,522 - 24,473,820	RGD	NCBI36
Celera	20	24,599,847 - 24,600,145	RGD
Cytogenetic Map	20	p11.21	UniSTS
HuRef	20	24,482,877 - 24,483,175	UniSTS
TNG Radiation Hybrid Map	20	13063.0	UniSTS

D20S558E

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	24,646,996 - 24,647,112	UniSTS	GRCh37
Build 36	20	24,594,996 - 24,595,112	RGD	NCBI36
Celera	20	24,721,316 - 24,721,432	RGD
Cytogenetic Map	20	p11.21	UniSTS
HuRef	20	24,604,372 - 24,604,488	UniSTS
GeneMap99-GB4 RH Map	20	126.96	UniSTS
NCBI RH Map	20	205.4	UniSTS

D20S1035

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	24,646,992 - 24,647,199	UniSTS	GRCh37
Build 36	20	24,594,992 - 24,595,199	RGD	NCBI36
Celera	20	24,721,312 - 24,721,519	RGD
Cytogenetic Map	20	p11.21	UniSTS
HuRef	20	24,604,368 - 24,604,575	UniSTS
GeneMap99-GB4 RH Map	20	125.69	UniSTS
Whitehead-YAC Contig Map	20		UniSTS
NCBI RH Map	20	207.2	UniSTS

RH48635

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	24,549,552 - 24,549,673	UniSTS	GRCh37
Build 36	20	24,497,552 - 24,497,673	RGD	NCBI36
Celera	20	24,623,880 - 24,624,001	RGD
Cytogenetic Map	20	p11.21	UniSTS
HuRef	20	24,506,888 - 24,507,009	UniSTS
GeneMap99-GB4 RH Map	20	128.43	UniSTS
NCBI RH Map	20	199.4	UniSTS

D20S754

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	24,626,378 - 24,626,627	UniSTS	GRCh37
Build 36	20	24,574,378 - 24,574,627	RGD	NCBI36
Celera	20	24,700,698 - 24,700,947	RGD
Cytogenetic Map	20	p11.21	UniSTS
HuRef	20	24,583,698 - 24,583,947	UniSTS
Whitehead-RH Map	20	110.9	UniSTS
Whitehead-YAC Contig Map	20		UniSTS
NCBI RH Map	20	207.2	UniSTS

STS-AA019613

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	24,523,667 - 24,523,869	UniSTS	GRCh37
Build 36	20	24,471,667 - 24,471,869	RGD	NCBI36
Celera	20	24,597,992 - 24,598,194	RGD
Cytogenetic Map	20	p11.21	UniSTS
HuRef	20	24,481,022 - 24,481,224	UniSTS
GeneMap99-GB4 RH Map	20	125.26	UniSTS

D20S954

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	24,615,036 - 24,615,185	UniSTS	GRCh37
Build 36	20	24,563,036 - 24,563,185	RGD	NCBI36
Celera	20	24,689,356 - 24,689,505	RGD
Cytogenetic Map	20	p11.21	UniSTS
HuRef	20	24,572,364 - 24,572,513	UniSTS
GeneMap99-GB4 RH Map	20	126.96	UniSTS
Whitehead-RH Map	20	111.0	UniSTS
Whitehead-YAC Contig Map	20		UniSTS
NCBI RH Map	20	205.4	UniSTS

G69455

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	24,578,239 - 24,578,476	UniSTS	GRCh37
Build 36	20	24,526,239 - 24,526,476	RGD	NCBI36
Celera	20	24,652,558 - 24,652,795	RGD
Cytogenetic Map	20	p11.21	UniSTS
HuRef	20	24,535,566 - 24,535,803	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

High

Medium

1088

288

805

230

2509

159

311

766

Low

1365

1122

792

456

1456

642

1046

269

1113

977

648

723

Below cutoff

932

475

447

342

563

242

1862

1162

153

118

181

104

538

1155

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001323606	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001323607	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_024893	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_147606	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529347	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529348	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529349	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529350	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529351	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529352	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529353	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529354	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529356	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529358	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017028064	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017028065	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017028066	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017028067	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017028068	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017028069	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440496	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440497	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440498	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440499	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440500	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324015	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324016	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324017	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324018	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324019	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324020	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324021	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324022	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324023	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324024	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324025	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324026	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324027	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324028	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324029	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324030	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324031	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324032	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324033	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054324034	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_937144	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AK024282	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL034426	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL049594	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL157413	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AX883820	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC030637	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471133	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068258	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CR457325	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB306704	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000376862 ⟹ ENSP00000366058

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	24,469,629 - 24,666,616 (+)	Ensembl

RefSeq Acc Id:

ENST00000482637

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	24,584,902 - 24,597,153 (+)	Ensembl

RefSeq Acc Id:

NM_001323606 ⟹ NP_001310535

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,629 - 24,666,616 (+)	NCBI
CHM1_1	20	24,450,308 - 24,648,495 (+)	NCBI
T2T-CHM13v2.0	20	24,531,610 - 24,729,659 (+)	NCBI

Sequence:

show sequence

AGAGGAGGAGAGAGCCTGGCAGCGGAGGAGCAGAGGCGGGCGCCGCACCGCCCCGCACGCTCGC
TCGCTCGGGAGAGTCGCGGGCGGCCGCTTGGGCGCACTTGCCGGGTCACCTTGTCCCGGAGCCC
AGCCCTTGGCACTGTGACATTGCCACAGCTCCCGTCAAGAAGAGGAGGTCCTGGGATCTGGATT
TGGACTGACCCCATAACTGGCTTGGAGCACTACAAGGAAGCGAAAGTGGCGATGGACCCATTCT
GAGGTGGTACAGCCAGCAGCTGTCCAAACATGTCGGTGAGGCTGTAGTGTGCCGATCTACTCCA
GCTGACTGCGGCTTCATCAGTGACCCCAGGAGAGACCAGCCAAGAATCAAGCATCCCAGCGCAG
CTTCACCTGTCAACCCAGAAAATGAGATGACTCCATTTTAACCCACCAACTCTTAGGGTGATTG
GTTACACAACAAGTAATAACACATGGCTAGAAAAAAATGGACTAGAAATATCTCTGCATAATAC
TCTATATTTACACTCAACAATATAGCCCTTGAGTAAACGTTGGAAGGGAATTCAGCTGGTCATT
TATTGCTCCTGCAGAGAGGAAGTGTGGGAAATAATTCAGCCGGGATCCTGGCCCTGGTAAAAGG
CAAGGCACCATGCGAGGCACTGCATTCACAGTGAACCAGACGTGAGAGCCAAACAGACGTTTCC
CATTTGTGCACACATACAAAGTGCTTCGCCCAGTGCCTTGTGGGGTGCCCCCACTTCTCTTCAG
TGCTCCACGTCTGTTTGTAACTCACTGTAGCTCTCACTACCTGGTGGTGTGCCGACAACAATGG
TAGACCAGCTGGACAAGCCCCAGAGTGGGGAGCAGAGGGAACACTTCATCTGCTTCAAGCCCTT
CTGCAGGCTCCAGGCACAAACTGATGAAGGACAGAATTCTTTTGTCCTGCTGGAGCCAGAGGGT
GTGGACACCAGAGGAGCCGTCCCTGGGCATCACATTGGCTCTTGCCCAAGAAAGGAGAAATGGC
TTCCCTGAGGCAAGTGTAACCTACATTCCCAGCCCACCAGCCTGACGCCCAGCCAGGGAGAGAG
TACCATGGATGGCATCATTGAACAGAAGAGCATGCTGGTGCACAGTAAAATCAGTGATGCTGGC
AAGAGGAATGGTTTAATTAACACCAGAAACTTGATGGCCGAGAGCAGAGATGGTCTGGTGTCTG
TTTACCCAGCGCCCCAGTACCAGAGCCACCGGGTGGGGGCCAGCACAGTGCCGGCCAGCCTGGA
CAGCAGCAGGAGTGAGCCGATGCAGCAGCTGCTGGACCCCAACACCCTGCAGCAGTCAGTGGAG
TCCCGCTACCGGCCCAACATCATCCTCTATTCAGAGGGCGTGCTGCGCTCCTGGGGGGACGGTG
TGGCCGCCGACTGCTGCGAGACCACCTTCATCGAGGACCGGTCGCCCACCAAAGACAGCCTCGA
GTACCCGGATGGGAAGTTCATTGACCTCTCAGCTGATGACATAAAAATCCACACCCTGTCCTAC
GATGTGGAGGAGGAGGAGGAGTTCCAGGAGCTGGAGAGCGACTACTCAAGCGACACAGAGAGTG
AGGACAATTTCCTCATGATGCCCCCGCGGGACCACCTGGGCCTCAGTGTCTTCTCCATGCTCTG
CTGCTTCTGGCCTCTGGGCATCGCAGCCTTCTACTTGTCCCATGAGACCAACAAAGCCGTGGCC
AAGGGGGACTTGCACCAGGCCAGCACCAGCTCCCGGCGGGCCCTATTCCTGGCAGTGCTGTCCA
TCACCATTGGGACTGGCGTCTATGTGGGCGTGGCCGTGGCCCTCATCGCCTACCTCTCCAAGAA
CAACCACCTGTGAGCTTCCTGCGAATGGAGGGGGAGCACCCGGGGCCAGGTCTGTGTGGACGTG
GAGGAAGCAGGCATACCGCATGATGCTGTACAGTACAAATGATTGCCAAATGATGCCACGAAGC
CCTGGGATTTCCTACCCATGGATTTATTTTGTTTTTATCCTTTAATTTCATGTTCACAGCACTG
TGTAGAGCACCAGACAGACGGGCACTGCTAATCCTTCCAAAGGAAAGCTCCAAAGATCCCAGCC
CGCAAGGCTGTCTCTGGATGGATTCTGGTGGATGAATGGCAACGCGGCTCTCTGCAGCCTGCCA
GTGCCCAGAGTGCCACCGCATTAGCAATATACAAACAGTCCAAAAAAGTGTTTATTTTTTATGG
AATACGGTGCAATAGGCAGAGGACAAGGGACACATCACTCTTCTGTCTGTGGCCCTGCTGGAGT
CCTTTGTGCCCCCCGGAGTCCACACGCCTTCCCTGCAAGACGAGAATGGGGCTGGGAAGAAAGA
GGCAACACCACGGCTGGCAGGAGCCCCGCTGCACTGCTCTGCAGACCCATTGGCCTGACCCTGA
GAAGCAGAGCCAGCAAAGCCCGGGACCTGCCCCTCTTTCTTTCCCTTCACACCACCCCAGCCTC
AGGATGTCAAGCCACCTCCGGAACGTGTCTACACTCCACAGCTACCCCGCAGCAATACGCACTC
TTGGGACCTCGCTGATCTAGGATGGGGAGGCAGGCCACCGCCCCTCCCAAGACTCCTCAAGAAA
GAGCCCCGCGGTTGCTCCGGAAACTCGAGGCACTGCAGCTATGGGCACTGCCTCAGCCTAAAGA
CACAGGGGCGCCTCCCAATCACCGCGCTGGCGGATGCTCACCCCGTCATAAGCAGAAACTAGTG
ATCCTGGAAATGAGATGGGCCTTACTCTGTCGACTAAATGAATAGCTATTTTCTTGTCATTTTT
TAAAGTGCAACTCTTGCTTCATGCTGCTTAAGTTACCAGATGAATGCTGAGAAATAAGTAATCA
CAGACATTTTAATACCATTTCATTGCTGTTTTACGAGTGTTCATTACTTAACAAAAAATTATCT
TTTAGCTTTTTCGCTTAAGACTTTTCTTTCTGATGAA

hide sequence

RefSeq Acc Id:

NM_001323607 ⟹ NP_001310536

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,873 - 24,666,616 (+)	NCBI
CHM1_1	20	24,450,915 - 24,648,495 (+)	NCBI
T2T-CHM13v2.0	20	24,531,854 - 24,729,659 (+)	NCBI

Sequence:

show sequence

AGTCCTGGCTCCGCCTCGGAGCGCGCAGACCCGGCGGCGGCGTGGCGCCCGCGGAGAAATGGCT
TCCCTGAGGCAAGTGTAACCTACATTCCCAGCCCACCAGCCTGACGCCCAGCCAGGGAGAGAGT
ACCATGGATGGCATCATTGAACAGAAGAGCATGCTGGTGCACAGTAAAATCAGTGATGCTGGCA
AGAGGAATGGTTTAATTAACACCAGAAACTTGATGGCCGAGAGCAGAGATGGTCTGGTGTCTGT
TTACCCAGCGCCCCAGTACCAGAGCCACCGGGTGGGGGCCAGCACAGTGCCGGCCAGCCTGGAC
AGCAGCAGGAGTGAGCCGATGCAGCAGCTGCTGGACCCCAACACCCTGCAGCAGTCAGTGGAGT
CCCGCTACCGGCCCAACATCATCCTCTATTCAGAGGGCGTGCTGCGCTCCTGGGGGGACGGTGT
GGCCGCCGACTGCTGCGAGACCACCTTCATCGAGGACCGGTCGCCCACCAAAGACAGCCTCGAG
TACCCGGATGGGAAGTTCATTGACCTCTCAGCTGATGACATAAAAATCCACACCCTGTCCTACG
ATGTGGAGGAGGAGGAGGAGTTCCAGGAGCTGGAGAGCGACTACTCAAGCGACACAGAGAGTGA
GGACAATTTCCTCATGATGCCCCCGCGGGACCACCTGGGCCTCAGTGTCTTCTCCATGCTCTGC
TGCTTCTGGCCTCTGGGCATCGCAGCCTTCTACTTGTCCCATGAGACCAACAAAGCCGTGGCCA
AGGGGGACTTGCACCAGGCCAGCACCAGCTCCCGGCGGGCCCTATTCCTGGCAGTGCTGTCCAT
CACCATTGGGACTGGCGTCTATGTGGGCGTGGCCGTGGCCCTCATCGCCTACCTCTCCAAGAAC
AACCACCTGTGAGCTTCCTGCGAATGGAGGGGGAGCACCCGGGGCCAGGTCTGTGTGGACGTGG
AGGAAGCAGGCATACCGCATGATGCTGTACAGTACAAATGATTGCCAAATGATGCCACGAAGCC
CTGGGATTTCCTACCCATGGATTTATTTTGTTTTTATCCTTTAATTTCATGTTCACAGCACTGT
GTAGAGCACCAGACAGACGGGCACTGCTAATCCTTCCAAAGGAAAGCTCCAAAGATCCCAGCCC
GCAAGGCTGTCTCTGGATGGATTCTGGTGGATGAATGGCAACGCGGCTCTCTGCAGCCTGCCAG
TGCCCAGAGTGCCACCGCATTAGCAATATACAAACAGTCCAAAAAAGTGTTTATTTTTTATGGA
ATACGGTGCAATAGGCAGAGGACAAGGGACACATCACTCTTCTGTCTGTGGCCCTGCTGGAGTC
CTTTGTGCCCCCCGGAGTCCACACGCCTTCCCTGCAAGACGAGAATGGGGCTGGGAAGAAAGAG
GCAACACCACGGCTGGCAGGAGCCCCGCTGCACTGCTCTGCAGACCCATTGGCCTGACCCTGAG
AAGCAGAGCCAGCAAAGCCCGGGACCTGCCCCTCTTTCTTTCCCTTCACACCACCCCAGCCTCA
GGATGTCAAGCCACCTCCGGAACGTGTCTACACTCCACAGCTACCCCGCAGCAATACGCACTCT
TGGGACCTCGCTGATCTAGGATGGGGAGGCAGGCCACCGCCCCTCCCAAGACTCCTCAAGAAAG
AGCCCCGCGGTTGCTCCGGAAACTCGAGGCACTGCAGCTATGGGCACTGCCTCAGCCTAAAGAC
ACAGGGGCGCCTCCCAATCACCGCGCTGGCGGATGCTCACCCCGTCATAAGCAGAAACTAGTGA
TCCTGGAAATGAGATGGGCCTTACTCTGTCGACTAAATGAATAGCTATTTTCTTGTCATTTTTT
AAAGTGCAACTCTTGCTTCATGCTGCTTAAGTTACCAGATGAATGCTGAGAAATAAGTAATCAC
AGACATTTTAATACCATTTCATTGCTGTTTTACGAGTGTTCATTACTTAACAAAAAATTATCTT
TTAGCTTTTTCGCTTAAGACTTTTCTTTCTGATGAA

hide sequence

RefSeq Acc Id:

NM_024893 ⟹ NP_079169

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,629 - 24,666,616 (+)	NCBI
GRCh37	20	24,449,835 - 24,647,253 (+)	NCBI
Build 36	20	24,397,835 - 24,595,167 (+)	NCBI Archive
Celera	20	24,524,151 - 24,721,487 (+)	RGD
HuRef	20	24,405,607 - 24,604,629 (+)	NCBI
CHM1_1	20	24,450,308 - 24,648,495 (+)	NCBI
T2T-CHM13v2.0	20	24,531,610 - 24,729,659 (+)	NCBI

Sequence:

show sequence

AGAGGAGGAGAGAGCCTGGCAGCGGAGGAGCAGAGGCGGGCGCCGCACCGCCCCGCACGCTCGC
TCGCTCGGGAGAGTCGCGGGCGGCCGCTTGGGCGCACTTGCCGGGTCACCTTGTCCCGGAGGAG
AAATGGCTTCCCTGAGGCAAGTGTAACCTACATTCCCAGCCCACCAGCCTGACGCCCAGCCAGG
GAGAGAGTACCATGGATGGCATCATTGAACAGAAGAGCATGCTGGTGCACAGTAAAATCAGTGA
TGCTGGCAAGAGGAATGGTTTAATTAACACCAGAAACTTGATGGCCGAGAGCAGAGATGGTCTG
GTGTCTGTTTACCCAGCGCCCCAGTACCAGAGCCACCGGGTGGGGGCCAGCACAGTGCCGGCCA
GCCTGGACAGCAGCAGGAGTGAGCCGATGCAGCAGCTGCTGGACCCCAACACCCTGCAGCAGTC
AGTGGAGTCCCGCTACCGGCCCAACATCATCCTCTATTCAGAGGGCGTGCTGCGCTCCTGGGGG
GACGGTGTGGCCGCCGACTGCTGCGAGACCACCTTCATCGAGGACCGGTCGCCCACCAAAGACA
GCCTCGAGTACCCGGATGGGAAGTTCATTGACCTCTCAGCTGATGACATAAAAATCCACACCCT
GTCCTACGATGTGGAGGAGGAGGAGGAGTTCCAGGAGCTGGAGAGCGACTACTCAAGCGACACA
GAGAGTGAGGACAATTTCCTCATGATGCCCCCGCGGGACCACCTGGGCCTCAGTGTCTTCTCCA
TGCTCTGCTGCTTCTGGCCTCTGGGCATCGCAGCCTTCTACTTGTCCCATGAGACCAACAAAGC
CGTGGCCAAGGGGGACTTGCACCAGGCCAGCACCAGCTCCCGGCGGGCCCTATTCCTGGCAGTG
CTGTCCATCACCATTGGGACTGGCGTCTATGTGGGCGTGGCCGTGGCCCTCATCGCCTACCTCT
CCAAGAACAACCACCTGTGAGCTTCCTGCGAATGGAGGGGGAGCACCCGGGGCCAGGTCTGTGT
GGACGTGGAGGAAGCAGGCATACCGCATGATGCTGTACAGTACAAATGATTGCCAAATGATGCC
ACGAAGCCCTGGGATTTCCTACCCATGGATTTATTTTGTTTTTATCCTTTAATTTCATGTTCAC
AGCACTGTGTAGAGCACCAGACAGACGGGCACTGCTAATCCTTCCAAAGGAAAGCTCCAAAGAT
CCCAGCCCGCAAGGCTGTCTCTGGATGGATTCTGGTGGATGAATGGCAACGCGGCTCTCTGCAG
CCTGCCAGTGCCCAGAGTGCCACCGCATTAGCAATATACAAACAGTCCAAAAAAGTGTTTATTT
TTTATGGAATACGGTGCAATAGGCAGAGGACAAGGGACACATCACTCTTCTGTCTGTGGCCCTG
CTGGAGTCCTTTGTGCCCCCCGGAGTCCACACGCCTTCCCTGCAAGACGAGAATGGGGCTGGGA
AGAAAGAGGCAACACCACGGCTGGCAGGAGCCCCGCTGCACTGCTCTGCAGACCCATTGGCCTG
ACCCTGAGAAGCAGAGCCAGCAAAGCCCGGGACCTGCCCCTCTTTCTTTCCCTTCACACCACCC
CAGCCTCAGGATGTCAAGCCACCTCCGGAACGTGTCTACACTCCACAGCTACCCCGCAGCAATA
CGCACTCTTGGGACCTCGCTGATCTAGGATGGGGAGGCAGGCCACCGCCCCTCCCAAGACTCCT
CAAGAAAGAGCCCCGCGGTTGCTCCGGAAACTCGAGGCACTGCAGCTATGGGCACTGCCTCAGC
CTAAAGACACAGGGGCGCCTCCCAATCACCGCGCTGGCGGATGCTCACCCCGTCATAAGCAGAA
ACTAGTGATCCTGGAAATGAGATGGGCCTTACTCTGTCGACTAAATGAATAGCTATTTTCTTGT
CATTTTTTAAAGTGCAACTCTTGCTTCATGCTGCTTAAGTTACCAGATGAATGCTGAGAAATAA
GTAATCACAGACATTTTAATACCATTTCATTGCTGTTTTACGAGTGTTCATTACTTAACAAAAA
ATTATCTTTTAGCTTTTTCGCTTAAGACTTTTCTTTCTGATGAA

hide sequence

RefSeq Acc Id:

NR_147606

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,873 - 24,666,616 (+)	NCBI
T2T-CHM13v2.0	20	24,531,854 - 24,729,659 (+)	NCBI

Sequence:

show sequence

AGTCCTGGCTCCGCCTCGGAGCGCGCAGACCCGGCGGCGGCGTGGCGCCCGCGGTAAGTCCGGG
TGGTCGCCGCGACGAGACTTGGGAGACACGGGGTCGCAGGGCGGGAGGGGGAGCTGAGCCGGCA
GAGAAAATGCCCAGGAAGGGGTCGATGCTGGCCTGGGCTGCACCTTGGTGCCTTGCCACCCCGG
GAGACGCGAAGGGGCTGCTGTGCGAATTCGATGGGAGCTGGTGAGACCGAGAACTGAGAGCGTA
GCGGAGCCAGGCTGCCCAGCAGGGCCATGAGGGCGCGCGGCGGGCCAAGGCTCTGCGGGTTCGG
GCTGCCCCTCGGAGTGACCCGAAGGAGACCAGCCAGGGCTGGAGAAATGGCTTCCCTGAGGCAA
GTGTAACCTACATTCCCAGCCCACCAGCCTGACGCCCAGCCAGGGAGAGAGTACCATGGATGGC
ATCATTGAACAGAAGAGCATGCTGGTGCACAGTAAAATCAGTGATGCTGGCAAGAGGAATGGTT
TAATTAACACCAGAAACTTGATGGCCGAGAGCAGAGATGGTCTGGTGTCTGTTTACCCAGCGCC
CCAGTACCAGAGCCACCGGGTGGGGGCCAGCACAGTGCCGGCCAGCCTGGACAGCAGCAGGAGT
GAGCCGATGCAGCAGCTGCTGGACCCCAACACCCTGCAGCAGTCAGTGGAGTCCCGCTACCGGC
CCAACATCATCCTCTATTCAGAGGGCGTGCTGCGCTCCTGGGGGGACGGTGTGGCCGCCGACTG
CTGCGAGACCACCTTCATCGAGGACCGGTCGCCCACCAAAGACAGCCTCGAGTACCCGGATGGG
AAGTTCATTGACCTCTCAGCTGATGACATAAAAATCCACACCCTGTCCTACGATGTGGAGGAGG
AGGAGGAGTTCCAGGAGCTGGAGAGCGACTACTCAAGCGACACAGAGAGTGAGGACAATTTCCT
CATGATGCCCCCGCGGGACCACCTGGGCCTCAGTGTCTTCTCCATGCTCTGCTGCTTCTGGCCT
CTGGGCATCGCAGCCTTCTACTTGTCCCATGAGGTTGCAGGACATCTCCCTTGGGGGCTACGTC
TGATGCCCTGCAGCCAGCCCTGCCGATGGAGCCCAGCTGCTTCCTGCGTTCTCAATGATGAGTC
CTTGTGCCCTGGGCTGTTAAGGCTGTGCCTCTGCTGTGAGCTGAAACGCTTTCTCTGAAGAGCC
CTTACAGTGCAGAAATAGTGTCTTTGGGTCCTGCTGAGCCCCTACCCCCAGCCCACCGCTGGCA
CAAGGTGCAGGCACTGGGCACTGCTTGGGGCTTCGCCAGTCACCTGCACTTTCTAACCGCCTGC
ACTTATTTTCCAATGAAAGGCCAATAAAGTCACAAACTTCACTTGCAACCTGTTGGCAAAAGAC
AGGGAAGGAAAACCAGCCACAAGAAATAACAATCTTGACAAACTTTTTTGCACCTACACACAAA
GCCTTGCCTTCAGCTCAGAGACTCTTGGACTCAAGACAGTTTGCCCTGCCCTCATGCACACCAA
AAATCTTGTCAAAGAGCCAGGAGCTTTCGTCCAGCAGCTGTCAGGATGGAAACGTGTCTTCCCA
TTTGCACCCTGCCAAAGGAATGAGCAAGCTGTTTCACAGCCACAGTTATCCATTTTCTGAGACA
AAAGGTTCATATCAGACCAACAAAGCCGTGGCCAAGGGGGACTTGCACCAGGCCAGCACCAGCT
CCCGGCGGGCCCTATTCCTGGCAGTGCTGTCCATCACCATTGGGACTGGCGTCTATGTGGGCGT
GGCCGTGGCCCTCATCGCCTACCTCTCCAAGAACAACCACCTGTGAGCTTCCTGCGAATGGAGG
GGGAGCACCCGGGGCCAGGTCTGTGTGGACGTGGAGGAAGCAGGCATACCGCATGATGCTGTAC
AGTACAAATGATTGCCAAATGATGCCACGAAGCCCTGGGATTTCCTACCCATGGATTTATTTTG
TTTTTATCCTTTAATTTCATGTTCACAGCACTGTGTAGAGCACCAGACAGACGGGCACTGCTAA
TCCTTCCAAAGGAAAGCTCCAAAGATCCCAGCCCGCAAGGCTGTCTCTGGATGGATTCTGGTGG
ATGAATGGCAACGCGGCTCTCTGCAGCCTGCCAGTGCCCAGAGTGCCACCGCATTAGCAATATA
CAAACAGTCCAAAAAAGTGTTTATTTTTTATGGAATACGGTGCAATAGGCAGAGGACAAGGGAC
ACATCACTCTTCTGTCTGTGGCCCTGCTGGAGTCCTTTGTGCCCCCCGGAGTCCACACGCCTTC
CCTGCAAGACGAGAATGGGGCTGGGAAGAAAGAGGCAACACCACGGCTGGCAGGAGCCCCGCTG
CACTGCTCTGCAGACCCATTGGCCTGACCCTGAGAAGCAGAGCCAGCAAAGCCCGGGACCTGCC
CCTCTTTCTTTCCCTTCACACCACCCCAGCCTCAGGATGTCAAGCCACCTCCGGAACGTGTCTA
CACTCCACAGCTACCCCGCAGCAATACGCACTCTTGGGACCTCGCTGATCTAGGATGGGGAGGC
AGGCCACCGCCCCTCCCAAGACTCCTCAAGAAAGAGCCCCGCGGTTGCTCCGGAAACTCGAGGC
ACTGCAGCTATGGGCACTGCCTCAGCCTAAAGACACAGGGGCGCCTCCCAATCACCGCGCTGGC
GGATGCTCACCCCGTCATAAGCAGAAACTAGTGATCCTGGAAATGAGATGGGCCTTACTCTGTC
GACTAAATGAATAGCTATTTTCTTGTCATTTTTTAAAGTGCAACTCTTGCTTCATGCTGCTTAA
GTTACCAGATGAATGCTGAGAAATAAGTAATCACAGACATTTTAATACCATTTCATTGCTGTTT
TACGAGTGTTCATTACTTAACAAAAAATTATCTTTTAGCTTTTTCGCTTAAGACTTTTCTTTCT
GATGAA

hide sequence

RefSeq Acc Id:

XM_011529347 ⟹ XP_011527649

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,629 - 24,634,588 (+)	NCBI

Sequence:

show sequence

AGAGGAGGAGAGAGCCTGGCAGCGGAGGAGCAGAGGCGGGCGCCGCACCGCCCCGCACGCTCGC
TCGCTCGGGAGAGTCGCGGGCGGCCGCTTGGGCGCACTTGCCGGGTCACCTTGTCCCGGAGGAG
AAATGGCTTCCCTGAGGCAAGTGTAACCTACATTCCCAGCCCACCAGCCTGACGCCCAGCCAGG
GAGAGAGTACCATGGATGGCATCATTGAACAGAAGAGCATGCTGGTGCACAGTAAAATCAGTGA
TGCTGGCAAGAGGAATGGTTTAATTAACACCAGAAACTTGATGGCCGAGAGCAGAGATGGTCTG
GTGTCTGTTTACCCAGCGCCCCAGTACCAGAGCCACCGGGTGGGGGCCAGCACAGTGCCGGCCA
GCCTGGACAGCAGCAGGAGTGAGCCGATGCAGCAGCTGCTGGACCCCAACACCCTGCAGCAGTC
AGTGGAGTCCCGCTACCGGCCCAACATCATCCTCTATTCAGAGGGCGTGCTGCGCTCCTGGGGG
GACGGTGTGGCCGCCGACTGCTGCGAGACCACCTTCATCGAGGACCGGTCGCCCACCAAAGACA
GCCTCGAGTACCCGGATGGGAAGTTCATTGACCTCTCAGCTGATGACATAAAAATCCACACCCT
GTCCTACGATGTGGAGGAGGAGGAGGAGTTCCAGGAGCTGGAGAGCGACTACTCAAGCGACACA
GAGAGTGAGGACAATTTCCTCATGATGCCCCCGCGGGACCACCTGGGCCTCAGTGTCTTCTCCA
TGCTCTGCTGCTTCTGGCCTCTGGGCATCGCAGCCTTCTACTTGTCCCATGAGTTGATCACCCT
GGAAGAAATGGCAGCATTCAATTCCTCCATCCTTTTTTCCAGTTCGCAAGGGCTGGTTCCCTGG
ACCAGCAGCATCAGGGTCATCTGGGAACGTTTTAGGATCGTGAAGTCTCGTCAGCTCCCAAGAC
CTGCTGACTCGGAAGCTCTGGGGACGGGGCTGGCAGTCTGGGTGTGAATGCCCTCTGAGGTTGC
TGTGGAGACTCCTGAGGTAACACATGCTGAAGTCAGCCTGTCCTAATGGACCAGGCTCTTGGTT
AGGAGCCCCAGCACCTAGGGGAGGCCGTGGTTCAGGGTTGTTGGGGTGTGGGCACAGCACGTGA
CACCCGCACCAGCCGCTCTCACCTTTTCACTCCTGCCCTCCCAGGTCACCTGCATCCGCCAAAC
TCTGCCTGGGGTTCCCTTCGTTATCAGCAGAGCACATAGACACATGTCTGGATTTGTTTATTCA
TTGTCTTTTCAAATATAGTGTACTCAACTTGGAAAACAGAAGGAGGAGGAAGAGAATGGAGAAA
GAAAGCATGAAAACTGAACCTCTCCTCCATGCCCCTTTCTCAAAGCCCCTCCTCCAGGGGGACC
CCGTCTTTCTGTGCCTTTATCAATGTGTGTGTGGGCAGTTTTGATTTACACGTAGAAGACCATC
AAAGTGCAATGCAGCTTGCTTTTTCACATAATGTAAATACTTCTGGTATCTGCATATAAACACC
AGCATTGACATTTTTAATGATTTTGTAGCATTTTGATGTATGAATTGCAATAATTTCATTACAG
TAATGTTTTCCCTAAAAATGGACATATCAATTGTTTTCAACTTCTCCTTTTGCAAATATAGGAT
ATCCACAAGTGAAATTCCACCAAGTCAAAGGTTATTCACATGTAAATTTAGCTACATACTGTAA
CTTCTCCTCCAGAAGTCCGTACCAGTTTTCATTCCTATTAACAAAATGTGAATGCCTGTCTTTC
CCACCTGAGCTCAGTGTTCCATTTTCAACAATCTGATAGATAAAATAAAAGATATTGTCAGTT

hide sequence

RefSeq Acc Id:

XM_011529348 ⟹ XP_011527650

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,629 - 24,634,588 (+)	NCBI

Sequence:

show sequence

AGAGGAGGAGAGAGCCTGGCAGCGGAGGAGCAGAGGCGGGCGCCGCACCGCCCCGCACGCTCGC
TCGCTCGGGAGAGTCGCGGGCGGCCGCTTGGGCGCACTTGCCGGGTCACCTTGTCCCGGAGGAG
AAATGGCTTCCCTGAGGCAAGTGTAACCTACATTCCCAGCCCACCAGCCTGACGCCCAGCCAGG
GAGAGAGTACCATGGATGGCATCATTGAACAGAAGAGCATGCTGGTGCACAGTAAAATCAGTGA
TGCTGGCAAGAGGAATGGTTTAATTAACACCAGAAACTTGATGGCCGAGAGCAGAGATGGTCTG
GTGTCTGTTTACCCAGCGCCCCAGTACCAGAGCCACCGGGTGGGGGCCAGCACAGTGCCGGCCA
GCCTGGACAGCAGCAGGAGTGAGCCGATGCAGCAGCTGCTGGACCCCAACACCCTGCAGCAGTC
AGTGGAGTCCCGCTACCGGCCCAACATCATCCTCTATTCAGAGGGCGTGCTGCGCTCCTGGGGG
GACGGTGTGGCCGCCGACTGCTGCGAGACCACCTTCATCGAGGACCGGTCGCCCACCAAAGACA
GCCTCGAGTACCCGGATGGGAAGTTCATTGACCTCTCAGCTGATGACATAAAAATCCACACCCT
GTCCTACGATGTGGAGGAGGAGGAGGAGTTCCAGGAGCTGGAGAGCGACTACTCAAGCGACACA
GAGAGTGAGGACAATTTCCTCATGATGCCCCCGCGGGACCACCTGGGCCTCAGTGTCTTCTCCA
TGCTCTGCTGCTTCTGGCCTCTGGGCATCGCAGCCTTCTACTTGTCCCATGAGTTGATCACCCT
GGAAGAAATGGCAGCATTCAATTCCTCCATCCTTTTTTCCAGTTCGCAAGGGCTGGTTCCCTGG
ACCAGCAGCATCAGGGTCATCTGGGAACGTTTTAGGATCGTGAAGTCTCGTCAGCTCCCAAGAC
CTGCTGACTCGGAAGCTCTGGGGACGGGGCTGGCAGTCTGGGTGTGAATGCCCTCTGAGGTTGC
TGTGGAGACTCCTGAGGTCACCTGCATCCGCCAAACTCTGCCTGGGGTTCCCTTCGTTATCAGC
AGAGCACATAGACACATGTCTGGATTTGTTTATTCATTGTCTTTTCAAATATAGTGTACTCAAC
TTGGAAAACAGAAGGAGGAGGAAGAGAATGGAGAAAGAAAGCATGAAAACTGAACCTCTCCTCC
ATGCCCCTTTCTCAAAGCCCCTCCTCCAGGGGGACCCCGTCTTTCTGTGCCTTTATCAATGTGT
GTGTGGGCAGTTTTGATTTACACGTAGAAGACCATCAAAGTGCAATGCAGCTTGCTTTTTCACA
TAATGTAAATACTTCTGGTATCTGCATATAAACACCAGCATTGACATTTTTAATGATTTTGTAG
CATTTTGATGTATGAATTGCAATAATTTCATTACAGTAATGTTTTCCCTAAAAATGGACATATC
AATTGTTTTCAACTTCTCCTTTTGCAAATATAGGATATCCACAAGTGAAATTCCACCAAGTCAA
AGGTTATTCACATGTAAATTTAGCTACATACTGTAACTTCTCCTCCAGAAGTCCGTACCAGTTT
TCATTCCTATTAACAAAATGTGAATGCCTGTCTTTCCCACCTGAGCTCAGTGTTCCATTTTCAA
CAATCTGATAGATAAAATAAAAGATATTGTCAGTT

hide sequence

RefSeq Acc Id:

XM_011529350 ⟹ XP_011527652

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,629 - 24,634,588 (+)	NCBI

Sequence:

show sequence

AGGAGAGAGCCTGGCAGCGGAGGAGCAGAGGCGGGCGCCGCACCGCCCCGCACGCTCGCTCGCT
CGGGAGAGTCGCGGGCGGCCGCTTGGGCGCACTTGCCGGGTCACCTTGTCCCGGAGCCCAGCCC
TTGGCACTGTGACATTGCCACAGCTCCCGTCAAGAAGAGGAGGTCCTGGGATCTGGATTTGGAC
TGACCCCATAACTGGCTTGGAGCACTACAAGGAAGCGAAAGTGGCGATGGACCCATTCTGAGGT
GGTACAGCCAGCAGCTGTCCAAACATGTCGGTGAGGCTGTAGTGTGCCGATCTACTCCAGCTGA
CTGCGGCTTCATCAGTGACCCCAGGAGAGACCAGCCAAGAATCAAGCATCCCAGCGCAGCTTCA
CCTGTCAACCCAGAAAATGAGATGACTCCATTTTAACCCACCAACTCTTAGGGTGATTGGTTAC
ACAACAAGTAATAACACATGGCTAGAAAAAAATGGACTAGAAATATCTCTGCATAATACTCTAT
ATTTACACTCAACAATATAGCCCTTGAGTAAACGTTGGAAGGGAATTCAGCTGGTCATTTATTG
CTCCTGCAGAGAGGAAGTGTGGGAAATAATTCAGCCGGGATCCTGGCCCTGGTAAAAGGCAAGG
CACCATGCGAGGCACTGCATTCACAGTGAACCAGACGTGAGAGCCAAACAGACGTTTCCCATTT
GTGCACACATACAAAGTGCTTCGCCCAGTGCCTTGTGGGGTGCCCCCACTTCTCTTCAGTGCTC
CACGTCTGTTTGTAACTCACTGTAGCTCTCACTACCTGGTGGTGTGCCGACAACAATGGTAGAC
CAGCTGGACAAGCCCCAGAGTGGGGAGCAGAGGGAACACTTCATCTGCTTCAAGCCCTTCTGCA
GGCTCCAGGCACAAACTGATGAAGGACAGAATTCTTTTGTCCTGCTGGAGCCAGAGGGTGTGGA
CACCAGAGGAGCCGTCCCTGGGCATCACATTGGCTCTTGCCCAAGAAAGGAGAAATGGCTTCCC
TGAGGCAAGTGTAACCTACATTCCCAGCCCACCAGCCTGACGCCCAGCCAGGGAGAGAGTACCA
TGGATGGCATCATTGAACAGAAGAGCATGCTGGTGCACAGTAAAATCAGTGATGCTGGCAAGAG
GAATGGTTTAATTAACACCAGAAACTTGATGGCCGAGAGCAGAGATGGTCTGGTGTCTGTTTAC
CCAGCGCCCCAGTACCAGAGCCACCGGGTGGGGGCCAGCACAGTGCCGGCCAGCCTGGACAGCA
GCAGGAGTGAGCCGATGCAGCAGCTGCTGGACCCCAACACCCTGCAGCAGTCAGTGGAGTCCCG
CTACCGGCCCAACATCATCCTCTATTCAGAGGGCGTGCTGCGCTCCTGGGGGGACGGTGTGGCC
GCCGACTGCTGCGAGACCACCTTCATCGAGGACCGGTCGCCCACCAAAGACAGCCTCGAGTACC
CGGATGGGAAGTTCATTGACCTCTCAGCTGATGACATAAAAATCCACACCCTGTCCTACGATGT
GGAGGAGGAGGAGGAGTTCCAGGAGCTGGAGAGCGACTACTCAAGCGACACAGAGAGTGAGGAC
AATTTCCTCATGATGCCCCCGCGGGACCACCTGGGCCTCAGTGTCTTCTCCATGCTCTGCTGCT
TCTGGCCTCTGGGCATCGCAGCCTTCTACTTGTCCCATGAGTTGATCACCCTGGAAGAAATGGC
AGCATTCAATTCCTCCATCCTTTTTTCCAGTTCGCAAGGGCTGGTTCCCTGGACCAGCAGCATC
AGGGTCATCTGGGAACGTTTTAGGATCGTGAAGTCTCGTCAGCTCCCAAGACCTGCTGACTCGG
AAGCTCTGGGGACGGGGCTGGCAGTCTGGGTGTGAATGCCCTCTGAGGTTGCTGTGGAGACTCC
TGAGGTAACACATGCTGAAGTCAGCCTGTCCTAATGGACCAGGCTCTTGGTTAGGAGCCCCAGC
ACCTAGGGGAGGCCGTGGTTCAGGGTTGTTGGGGTGTGGGCACAGCACGTGACACCCGCACCAG
CCGCTCTCACCTTTTCACTCCTGCCCTCCCAGGTCACCTGCATCCGCCAAACTCTGCCTGGGGT
TCCCTTCGTTATCAGCAGAGCACATAGACACATGTCTGGATTTGTTTATTCATTGTCTTTTCAA
ATATAGTGTACTCAACTTGGAAAACAGAAGGAGGAGGAAGAGAATGGAGAAAGAAAGCATGAAA
ACTGAACCTCTCCTCCATGCCCCTTTCTCAAAGCCCCTCCTCCAGGGGGACCCCGTCTTTCTGT
GCCTTTATCAATGTGTGTGTGGGCAGTTTTGATTTACACGTAGAAGACCATCAAAGTGCAATGC
AGCTTGCTTTTTCACATAATGTAAATACTTCTGGTATCTGCATATAAACACCAGCATTGACATT
TTTAATGATTTTGTAGCATTTTGATGTATGAATTGCAATAATTTCATTACAGTAATGTTTTCCC
TAAAAATGGACATATCAATTGTTTTCAACTTCTCCTTTTGCAAATATAGGATATCCACAAGTGA
AATTCCACCAAGTCAAAGGTTATTCACATGTAAATTTAGCTACATACTGTAACTTCTCCTCCAG
AAGTCCGTACCAGTTTTCATTCCTATTAACAAAATGTGAATGCCTGTCTTTCCCACCTGAGCTC
AGTGTTCCATTTTCAACAATCTGATAGATAAAATAAAAGATATTGTCAGTT

hide sequence

RefSeq Acc Id:

XM_011529351 ⟹ XP_011527653

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,873 - 24,634,588 (+)	NCBI

Sequence:

show sequence

AGACCCGGCGGCGGCGTGGCGCCCGCGCCCAGCCCTTGGCACTGTGACATTGCCACAGCTCCCG
TCAAGAAGAGGAGGTCCTGGGATCTGGATTTGGACTGACCCCATAACTGGCTTGGAGCACTACA
AGGAAGCGAAAGTGGCGATGGACCCATTCTGAGGTGGTACAGCCAGCAGCTGTCCAAACATGTC
GGTGAGGCTGTAGTGTGCCGATCTACTCCAGCTGACTGCGGCTTCATCAGTGACCCCAGGAGAG
ACCAGCCAAGAATCAAGCATCCCAGCGCAGCTTCACCTGTCAACCCAGAAAATGAGATGACTCC
ATTTTAACCCACCAACTCTTAGGGTGATTGGTTACACAACAAGTAATAACACATGGCTAGAAAA
AAATGGACTAGAAATATCTCTGCATAATACTCTATATTTACACTCAACAATATAGCCCTTGAGT
AAACGTTGGAAGGGAATTCAGCTGGTCATTTATTGCTCCTGCAGAGAGGAAGTGTGGGAAATAA
TTCAGCCGGGATCCTGGCCCTGGTAAAAGGCAAGGCACCATGCGAGGCACTGCATTCACAGTGA
ACCAGACGTGAGAGCCAAACAGACGTTTCCCATTTGTGCACACATACAAAGTGCTTCGCCCAGT
GCCTTGTGGGGTGCCCCCACTTCTCTTCAGTGCTCCACGTCTGTTTGTAACTCACTGTAGCTCT
CACTACCTGGTGGTGTGCCGACAACAATGGTAGACCAGCTGGACAAGCCCCAGAGTGGGGAGCA
GAGGGAACACTTCATCTGCTTCAAGCCCTTCTGCAGGCTCCAGGCACAAACTGATGAAGGACAG
AATTCTTTTGTCCTGCTGGAGCCAGAGGGTGTGGACACCAGAGGAGCCGTCCCTGGGCATCACA
TTGGCTCTTGCCCAAGAAAGGAGAAATGGCTTCCCTGAGGCAAGTGTAACCTACATTCCCAGCC
CACCAGCCTGACGCCCAGCCAGGGAGAGAGTACCATGGATGGCATCATTGAACAGAAGAGCATG
CTGGTGCACAGTAAAATCAGTGATGCTGGCAAGAGGAATGGTTTAATTAACACCAGAAACTTGA
TGGCCGAGAGCAGAGATGGTCTGGTGTCTGTTTACCCAGCGCCCCAGTACCAGAGCCACCGGGT
GGGGGCCAGCACAGTGCCGGCCAGCCTGGACAGCAGCAGGAGTGAGCCGATGCAGCAGCTGCTG
GACCCCAACACCCTGCAGCAGTCAGTGGAGTCCCGCTACCGGCCCAACATCATCCTCTATTCAG
AGGGCGTGCTGCGCTCCTGGGGGGACGGTGTGGCCGCCGACTGCTGCGAGACCACCTTCATCGA
GGACCGGTCGCCCACCAAAGACAGCCTCGAGTACCCGGATGGGAAGTTCATTGACCTCTCAGCT
GATGACATAAAAATCCACACCCTGTCCTACGATGTGGAGGAGGAGGAGGAGTTCCAGGAGCTGG
AGAGCGACTACTCAAGCGACACAGAGAGTGAGGACAATTTCCTCATGATGCCCCCGCGGGACCA
CCTGGGCCTCAGTGTCTTCTCCATGCTCTGCTGCTTCTGGCCTCTGGGCATCGCAGCCTTCTAC
TTGTCCCATGAGTTGATCACCCTGGAAGAAATGGCAGCATTCAATTCCTCCATCCTTTTTTCCA
GTTCGCAAGGGCTGGTTCCCTGGACCAGCAGCATCAGGGTCATCTGGGAACGTTTTAGGATCGT
GAAGTCTCGTCAGCTCCCAAGACCTGCTGACTCGGAAGCTCTGGGGACGGGGCTGGCAGTCTGG
GTGTGAATGCCCTCTGAGGTTGCTGTGGAGACTCCTGAGGTAACACATGCTGAAGTCAGCCTGT
CCTAATGGACCAGGCTCTTGGTTAGGAGCCCCAGCACCTAGGGGAGGCCGTGGTTCAGGGTTGT
TGGGGTGTGGGCACAGCACGTGACACCCGCACCAGCCGCTCTCACCTTTTCACTCCTGCCCTCC
CAGGTCACCTGCATCCGCCAAACTCTGCCTGGGGTTCCCTTCGTTATCAGCAGAGCACATAGAC
ACATGTCTGGATTTGTTTATTCATTGTCTTTTCAAATATAGTGTACTCAACTTGGAAAACAGAA
GGAGGAGGAAGAGAATGGAGAAAGAAAGCATGAAAACTGAACCTCTCCTCCATGCCCCTTTCTC
AAAGCCCCTCCTCCAGGGGGACCCCGTCTTTCTGTGCCTTTATCAATGTGTGTGTGGGCAGTTT
TGATTTACACGTAGAAGACCATCAAAGTGCAATGCAGCTTGCTTTTTCACATAATGTAAATACT
TCTGGTATCTGCATATAAACACCAGCATTGACATTTTTAATGATTTTGTAGCATTTTGATGTAT
GAATTGCAATAATTTCATTACAGTAATGTTTTCCCTAAAAATGGACATATCAATTGTTTTCAAC
TTCTCCTTTTGCAAATATAGGATATCCACAAGTGAAATTCCACCAAGTCAAAGGTTATTCACAT
GTAAATTTAGCTACATACTGTAACTTCTCCTCCAGAAGTCCGTACCAGTTTTCATTCCTATTAA
CAAAATGTGAATGCCTGTCTTTCCCACCTGAGCTCAGTGTTCCATTTTCAACAATCTGATAGAT
AAAATAAAAGATATTGTCAGTT

hide sequence

RefSeq Acc Id:

XM_011529353 ⟹ XP_011527655

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,873 - 24,634,588 (+)	NCBI

Sequence:

show sequence

TGGTGAGACCGAGAACTGAGAGCGTAGCGGAGCCAGGCTGCCCAGCAGGGCCATGAGGGCGCGC
GGCGGGCCAAGGCTCTGCGGGTTCGGGCTGCCCCTCGGAGTGACCCGAAGGAGACCAGCCAGGG
CTGGAGAAATGGCTTCCCTGAGGCAAGTGTAACCTACATTCCCAGCCCACCAGCCTGACGCCCA
GCCAGGGAGAGAGTACCATGGATGGCATCATTGAACAGAAGAGCATGCTGGTGCACAGTAAAAT
CAGTGATGCTGGCAAGAGGAATGGTTTAATTAACACCAGAAACTTGATGGCCGAGAGCAGAGAT
GGTCTGGTGTCTGTTTACCCAGCGCCCCAGTACCAGAGCCACCGGGTGGGGGCCAGCACAGTGC
CGGCCAGCCTGGACAGCAGCAGGAGTGAGCCGATGCAGCAGCTGCTGGACCCCAACACCCTGCA
GCAGTCAGTGGAGTCCCGCTACCGGCCCAACATCATCCTCTATTCAGAGGGCGTGCTGCGCTCC
TGGGGGGACGGTGTGGCCGCCGACTGCTGCGAGACCACCTTCATCGAGGACCGGTCGCCCACCA
AAGACAGCCTCGAGTACCCGGATGGGAAGTTCATTGACCTCTCAGCTGATGACATAAAAATCCA
CACCCTGTCCTACGATGTGGAGGAGGAGGAGGAGTTCCAGGAGCTGGAGAGCGACTACTCAAGC
GACACAGAGAGTGAGGACAATTTCCTCATGATGCCCCCGCGGGACCACCTGGGCCTCAGTGTCT
TCTCCATGCTCTGCTGCTTCTGGCCTCTGGGCATCGCAGCCTTCTACTTGTCCCATGAGTTGAT
CACCCTGGAAGAAATGGCAGCATTCAATTCCTCCATCCTTTTTTCCAGTTCGCAAGGGCTGGTT
CCCTGGACCAGCAGCATCAGGGTCATCTGGGAACGTTTTAGGATCGTGAAGTCTCGTCAGCTCC
CAAGACCTGCTGACTCGGAAGCTCTGGGGACGGGGCTGGCAGTCTGGGTGTGAATGCCCTCTGA
GGTTGCTGTGGAGACTCCTGAGGTAACACATGCTGAAGTCAGCCTGTCCTAATGGACCAGGCTC
TTGGTTAGGAGCCCCAGCACCTAGGGGAGGCCGTGGTTCAGGGTTGTTGGGGTGTGGGCACAGC
ACGTGACACCCGCACCAGCCGCTCTCACCTTTTCACTCCTGCCCTCCCAGGTCACCTGCATCCG
CCAAACTCTGCCTGGGGTTCCCTTCGTTATCAGCAGAGCACATAGACACATGTCTGGATTTGTT
TATTCATTGTCTTTTCAAATATAGTGTACTCAACTTGGAAAACAGAAGGAGGAGGAAGAGAATG
GAGAAAGAAAGCATGAAAACTGAACCTCTCCTCCATGCCCCTTTCTCAAAGCCCCTCCTCCAGG
GGGACCCCGTCTTTCTGTGCCTTTATCAATGTGTGTGTGGGCAGTTTTGATTTACACGTAGAAG
ACCATCAAAGTGCAATGCAGCTTGCTTTTTCACATAATGTAAATACTTCTGGTATCTGCATATA
AACACCAGCATTGACATTTTTAATGATTTTGTAGCATTTTGATGTATGAATTGCAATAATTTCA
TTACAGTAATGTTTTCCCTAAAAATGGACATATCAATTGTTTTCAACTTCTCCTTTTGCAAATA
TAGGATATCCACAAGTGAAATTCCACCAAGTCAAAGGTTATTCACATGTAAATTTAGCTACATA
CTGTAACTTCTCCTCCAGAAGTCCGTACCAGTTTTCATTCCTATTAACAAAATGTGAATGCCTG
TCTTTCCCACCTGAGCTCAGTGTTCCATTTTCAACAATCTGATAGATAAAATAAAAGATATTGT
CAGTT

hide sequence

RefSeq Acc Id:

XM_011529354 ⟹ XP_011527656

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,873 - 24,634,588 (+)	NCBI

Sequence:

show sequence

GCCGGCAGAGAAAATGCCCAGGAAGGGGTCGATGCTGGCCTGGGCTGCACCTTGGTGCCTTGCC
ACCCCGGGAGACGCGAAGGGGCTGCTGTGCGAATTCGATGGGAGCTGGAGAAATGGCTTCCCTG
AGGCAAGTGTAACCTACATTCCCAGCCCACCAGCCTGACGCCCAGCCAGGGAGAGAGTACCATG
GATGGCATCATTGAACAGAAGAGCATGCTGGTGCACAGTAAAATCAGTGATGCTGGCAAGAGGA
ATGGTTTAATTAACACCAGAAACTTGATGGCCGAGAGCAGAGATGGTCTGGTGTCTGTTTACCC
AGCGCCCCAGTACCAGAGCCACCGGGTGGGGGCCAGCACAGTGCCGGCCAGCCTGGACAGCAGC
AGGAGTGAGCCGATGCAGCAGCTGCTGGACCCCAACACCCTGCAGCAGTCAGTGGAGTCCCGCT
ACCGGCCCAACATCATCCTCTATTCAGAGGGCGTGCTGCGCTCCTGGGGGGACGGTGTGGCCGC
CGACTGCTGCGAGACCACCTTCATCGAGGACCGGTCGCCCACCAAAGACAGCCTCGAGTACCCG
GATGGGAAGTTCATTGACCTCTCAGCTGATGACATAAAAATCCACACCCTGTCCTACGATGTGG
AGGAGGAGGAGGAGTTCCAGGAGCTGGAGAGCGACTACTCAAGCGACACAGAGAGTGAGGACAA
TTTCCTCATGATGCCCCCGCGGGACCACCTGGGCCTCAGTGTCTTCTCCATGCTCTGCTGCTTC
TGGCCTCTGGGCATCGCAGCCTTCTACTTGTCCCATGAGTTGATCACCCTGGAAGAAATGGCAG
CATTCAATTCCTCCATCCTTTTTTCCAGTTCGCAAGGGCTGGTTCCCTGGACCAGCAGCATCAG
GGTCATCTGGGAACGTTTTAGGATCGTGAAGTCTCGTCAGCTCCCAAGACCTGCTGACTCGGAA
GCTCTGGGGACGGGGCTGGCAGTCTGGGTGTGAATGCCCTCTGAGGTTGCTGTGGAGACTCCTG
AGGTAACACATGCTGAAGTCAGCCTGTCCTAATGGACCAGGCTCTTGGTTAGGAGCCCCAGCAC
CTAGGGGAGGCCGTGGTTCAGGGTTGTTGGGGTGTGGGCACAGCACGTGACACCCGCACCAGCC
GCTCTCACCTTTTCACTCCTGCCCTCCCAGGTCACCTGCATCCGCCAAACTCTGCCTGGGGTTC
CCTTCGTTATCAGCAGAGCACATAGACACATGTCTGGATTTGTTTATTCATTGTCTTTTCAAAT
ATAGTGTACTCAACTTGGAAAACAGAAGGAGGAGGAAGAGAATGGAGAAAGAAAGCATGAAAAC
TGAACCTCTCCTCCATGCCCCTTTCTCAAAGCCCCTCCTCCAGGGGGACCCCGTCTTTCTGTGC
CTTTATCAATGTGTGTGTGGGCAGTTTTGATTTACACGTAGAAGACCATCAAAGTGCAATGCAG
CTTGCTTTTTCACATAATGTAAATACTTCTGGTATCTGCATATAAACACCAGCATTGACATTTT
TAATGATTTTGTAGCATTTTGATGTATGAATTGCAATAATTTCATTACAGTAATGTTTTCCCTA
AAAATGGACATATCAATTGTTTTCAACTTCTCCTTTTGCAAATATAGGATATCCACAAGTGAAA
TTCCACCAAGTCAAAGGTTATTCACATGTAAATTTAGCTACATACTGTAACTTCTCCTCCAGAA
GTCCGTACCAGTTTTCATTCCTATTAACAAAATGTGAATGCCTGTCTTTCCCACCTGAGCTCAG
TGTTCCATTTTCAACAATCTGATAGATAAAATAAAAGATATTGTCAGTT

hide sequence

RefSeq Acc Id:

XM_011529356 ⟹ XP_011527658

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,629 - 24,660,267 (+)	NCBI

Sequence:

show sequence

AGAGGAGGAGAGAGCCTGGCAGCGGAGGAGCAGAGGCGGGCGCCGCACCGCCCCGCACGCTCGC
TCGCTCGGGAGAGTCGCGGGCGGCCGCTTGGGCGCACTTGCCGGGTCACCTTGTCCCGGAGGAG
AAATGGCTTCCCTGAGGCAAGTGTAACCTACATTCCCAGCCCACCAGCCTGACGCCCAGCCAGG
GAGAGAGTACCATGGATGGCATCATTGAACAGAAGAGCATGCTGGTGCACAGTAAAATCAGTGA
TGCTGGCAAGAGGAATGGTTTAATTAACACCAGAAACTTGATGGCCGAGAGCAGAGATGGTCTG
GTGTCTGTTTACCCAGCGCCCCAGTACCAGAGCCACCGGGTGGGGGCCAGCACAGTGCCGGCCA
GCCTGGACAGCAGCAGGAGTGAGCCGATGCAGCAGCTGCTGGACCCCAACACCCTGCAGCAGTC
AGTGGAGTCCCGCTACCGGCCCAACATCATCCTCTATTCAGAGGGCGTGCTGCGCTCCTGGGGG
GACGGTGTGGCCGCCGACTGCTGCGAGACCACCTTCATCGAGGACCGGTCGCCCACCAAAGACA
GCCTCGAGTACCCGGATGGGAAGTTCATTGACCTCTCAGCTGATGACATAAAAATCCACACCCT
GTCCTACGATGTGGAGGAGGAGGAGGAGTTCCAGGAGCTGGAGAGCGACTACTCAAGCGACACA
GAGAGTGAGGACAATTTCCTCATGATGCCCCCGCGGGACCACCTGGGCCTCAGTGTCTTCTCCA
TGCTCTGCTGCTTCTGGCCTCTGGGCATCGCAGCCTTCTACTTGTCCCATGAGTTACCGTTCCT
TCCCAGAAGTATCCATGAACCTGTTTCCATGCCAACAGCAGAGGCAACTTGGGCCTGTTTTGTG
CTGTAGATAATAGGATGCCGAGTCCGGCTTCGTTTGTTCATCACTGTGTCTCTGAAATTTATTC
CATGACTATCTGGGTGTCATGACGGCTTGCCCTTCTATCGCTGGCACTCAGAGGGCTTCCAGGT
CAGGGCAACCATGAGTCAGATTCCTTTGAACATTCCTACAGATGTGTTTTGTGAATACATGAAT
AATTCTTATTGGGTATTTACACAAATAAATGTCCACTCATTTACGGGAGTGGAATTGTTGTTGC
GTGATGTATCTATATGTTCAGCTATAAGAAATGCTGACCATTTCCCCAAGTGGTGGTACCAATT
TGTATCCCACCAGGAGTGCAGGGGAATTTTGGTTTTTCCACATTGTCTGTGACACTTCCTGTTG
CCTCTTGGCCTTGCTGGAGGGTCCATGTACAGCATGTTCTAAGCATGGGTTGGGCATGGCTGCA
CACACAGCAGGCCTGGCCTCAGGAGGAAGGGCCTCCTCTCTTCCCCTCCTCCTCCCCACTCGTC
AGCCACAGTGTCTGCCCCTGTGGACAAGGTGCGGTTGGCAGGAGCAGATAGGAGACAGAGATGT
CACAGCCACCCCAAACTCACATTGTCACAGGAGGCTTGTGCTCTCGTACACGGCTTGCTTTCTC
ATCTGGGCACTTGGCAGGTTCTTCTCAGGCCCACGCTCACCTTCGCATCCCCAGCTTCAGCCTG
CTGGCACAGGCCCTGTGTGTCCATCCACTTGCCCCTCAGCTGGGCTCTACTGGATAGGACCCAA
GACCATGTCTGGTCCCTGGAGAACACCTAGGCCTTTGTTCCCTGCCCAGCCAGGGGCTGGTCAT
CTCCACAGAGCAGCACCCTCCTGGCCCCACCCCTGAGGGGGCCGGTCAGCCGCTTGCCTTTCAG
AGTCTCCAGGTAGGAACCGGCTGGTCACCCGCCCGCAGTGCTGGACATGCATGGAGCCAGCAGG
GTCCCATGGCAGCTGCACCCCCACAGCCTGAGTGAAAAGCAAATGCCTTCCTTCTGTGGATGGG
ACCCAGGCTCAGCACACCGTCAGTCCTTCAAAATGCTTCTCAGCCTCCAAACC

hide sequence

RefSeq Acc Id:

XM_011529358 ⟹ XP_011527660

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,629 - 24,646,662 (+)	NCBI

Sequence:

show sequence

AGAGGAGGAGAGAGCCTGGCAGCGGAGGAGCAGAGGCGGGCGCCGCACCGCCCCGCACGCTCGC
TCGCTCGGGAGAGTCGCGGGCGGCCGCTTGGGCGCACTTGCCGGGTCACCTTGTCCCGGAGGAG
AAATGGCTTCCCTGAGGCAAGTGTAACCTACATTCCCAGCCCACCAGCCTGACGCCCAGCCAGG
GAGAGAGTACCATGGATGGCATCATTGAACAGAAGAGCATGCTGGTGCACAGTAAAATCAGTGA
TGCTGGCAAGAGGAATGGTTTAATTAACACCAGAAACTTGATGGCCGAGAGCAGAGATGGTCTG
GTGTCTGTTTACCCAGCGCCCCAGTACCAGAGCCACCGGGTGGGGGCCAGCACAGTGCCGGCCA
GCCTGGACAGCAGCAGGAGTGAGCCGATGCAGCAGCTGCTGGACCCCAACACCCTGCAGCAGTC
AGTGGAGTCCCGCTACCGGCCCAACATCATCCTCTATTCAGAGGGCGTGCTGCGCTCCTGGGGG
GACGGTGTGGCCGCCGACTGCTGCGAGACCACCTTCATCGAGGACCGGTCGCCCACCAAAGACA
GCCTCGAGTACCCGGATGGGAAGTTCATTGACCTCTCAGCTGATGACATAAAAATCCACACCCT
GTCCTACGATGTGGAGGAGGAGGAGGAGTTCCAGGAGCTGGAGAGCGACTACTCAAGCGACACA
GAGAGTGAGGACAATTTCCTCATGATGCCCCCGCGGGACCACCTGGGCCTCAGTGTCTTCTCCA
TGCTCTGCTGCTTCTGGCCTCTGGGCATCGCAGCCTTCTACTTGTCCCATGAGTGAGTCGAAGC
AGCCCGAGGTCCTCACCATATGCAGATGCTCAGTATTTTTTTTTTTTTGAGATCCACTCTCACT
CTGTCAC

hide sequence

RefSeq Acc Id:

XM_017028064 ⟹ XP_016883553

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,488,664 - 24,634,588 (+)	NCBI

Sequence:

show sequence

CACATGCTTAAACAGACATACATTCACCACACACACTTATATGGACACAGAAATGCACACACAG
GCACACTTATAACCTGAACAGTAACCTCCCACCTCTGTGAATGTCACTGCGGCATGGAGGGAGG
AGGGAGTTGCCACTGGGGAGCCAGGGGCCTCCAGCCAAAGGACAGTGTGCGGTTCAGGGACAGA
CTCGAGCAGCAAGTCAAGAACCAGAAGTTCTGATCACAGCCACTGGAGTGCGTTAAGAAGCCCT
GTGGGCTGTTTTGTGTCATCACCAAGCAGGCCTGGCCGCTGGTGCTGCAGTGCATAGGAGCCCC
AGATTCATCTGGTGAGGGTGAGGGTGCCATCTGTGTGTGGCCCCCGAGCTGAATCCACCACATC
TGCTCCCACAAATAACAGAAGAGAGAGGCAGGGGAGTATGCAGCCAGGGACAGGGGCCAGAGAG
GCACCCTCCAGGATACCTTTGGGGCCCTGCACCCTTTCCTGTTCCATCCACATGCTGTGGGCAG
TGACAGGGGCAGGGCAGAAGGCCCAGCGGAGTGCCTCTGCGGGTCTGGTTTGTCATGGAGGGAT
CAGTGTGTTTCCATGCCTGAATGAGGAACACGCAGATCACAGTTCCCAGAGTACTTTATGTAAA
GCTCGTCTTTGCGGCTTCTTGATTTTTATTTATAGAGAGCTATTTCACCTAAAATAGCAGTTAT
GCCTTGCCTATGAGCCCATGAGGATGGGATTTGCTCTTGGCAGTTTGGAAATGAGGAGAGGCCT
AGAGGAGGGGAAACCAAGTCACAGTCCTCATGGGAAAGGTGGTTTGGGGCTGGAGTGGGCAGTG
GAAGGGGCTAGGCATAAAGAAGGTTGTATCTGGGGCTCTGCTGCCAATGTGCCCGGGCTTGGAC
CCTGGCTCGCCCCTAGCCCTTGGGAGATCATTCAACCTCTCTGTGCCTCGGTTTCCTTATGAAT
GAAGCGAGCACGCCAGTTACCCCTCCATGGTGTCGTCGGGGCAATTACCTGGATGAGAGATGTG
CAGTGCTCAGCAGGATTGTCACGAAGCAGGGGCCGGCATGACAGCTGTGGCTAGGACTCCTTAT
GTGGGGCCTCAGCCAAGGCTAGCACCAGGGAATGGGCTGATCGGGGCCCTTCATATGGCAGGTG
AAGCTCTGCTAGGAACCTGGAAGCGCCAGGCTCCAGGGCAGCACAGAGGAGGGCAGGCAGATGT
CAATCAGCAAGCCAAGCCCCACAGTCTGGAAATTTGCACCAGTGTGAGTGGAGGTGGAGCCAGG
GAGGAAGTAAATCCCAGAGGAGAAGGCCTGGGCCAACATTTTAGAGCCCAGCGGCAGTACTGAG
CCCACTTAGGGAGGTGCCATGGAGTCGTGGCCCCTGGAGCTCCTCGTGCGTCTGGTTGCTGTGG
CAGGTAAGGGTCGGCCTTTGAGGTCCAGGGTCAGGAAAGGACAGGCGCCATGGCGTGCAATAAC
CCTTATGGGATTGATAGTAAAACATACAGAAAATATGTTTCAATAGCAAGCACCACTGCCTCAG
TCCTTAAGATGCTAACCAGTTGGCTCCAATGAGTGTGAGGTCAGCCGCGATCCATTTTGGGAAT
TCTTTGAAGGCACAAGTGGTGACTCGTGGAATACTTAATAAAACAAAGTAAGGGTTGCCCCTGG
AGAACAGAGGTCTGTACAGGCTGGGAGAGCAGCCAGGAGAGGACAGGATGCTCAAGTCTTTTTG
CAGGGCCAGTCATGTCCGAACAACGCCAATTCACTTGCCGTAGGTTGACAGGTGCAGAAGATGA
AAGAGTGGCGAGCCTCAGATGCTATTGCCTTGATGTTATTAGCTCCTGATTCTGACAGCGCAGG
GCCTGGCCCAGGGCACAGCTGCGCACAGGGTGAGCAGCATGCCCTGCTGCAGGAGGGATTTGCC
TTGTCACCATCCCCATAGCAGACCCAGGACAAGGTCCGTCACGTTCCTGATGCCAGGGGATGTG
ACATGTACCTCCCTCAGTGGCTTCCAGGTGCAGACCCAACACTGACACTGACCTTACAGTCAAA
TGGCAAAGTAGAAAATCCAACTGTAACACCAGCAAAGGACACTAGCTTGACAGCACTTTGGAGT
ATCTGGAGGAAATTAAAAGTATGGTTATGCTTGAAGACATTTCACTAAGTCATAAGTCTCTGGG
CTCCTGGGCACATCAAGATTTGTGTCATGCACTTTCTGGGAAGAAAACAAAATGGAAAATGAGG
ACCTTCCATCAGGAAGCTGATCGTTTCCTTCAATGCAAGTACTCTTTGGAAACAAAAGCAAAAC
AAAACAAAAACCATAAAAAATACAAGAACAAGAAATGCTGAAGACAGGTGGAAAGAATGAAAAT
AGGACTGAAGCAGGCCTGTGCCCTAGGCAGAGCCAGGCACACGCCTGCTGAGAGGACCCCACTA
ACAGGTGACCCAGGCAAGAGGCCCCCGGCCGGCTCCGTGTGAACAGATCCTCCCATCTTGTCGC
GTCCGTGTCCACAGTGAAACTCCAGGCACCGCAGGGACGCTGGGGAGAGCCTTCTCTCCACACC
CCCTTGGAATGTGCCCCCCACTTTTCGCTGTTCTGGTGGGCTTTTGGTTTCTTGTCAGGGTTGG
GGCTCTGCCAAGTAGCCACAGTGAACACAGAAAGCAGCCCTTGAGCCTGGCCTTCAGCGAGAGT
TGCTAAGGGGTGGCTAGGAGATGAGGAGGGTAGGCTCGGCCCCGCCGCCTCTGCTGTCTGGTTC
GAGATCAGCTGCTGGCCACCACAGGGGACATGTGCATTGTCATCTATCTTGGGAAAGACTTTGG
TAAACATCCAAGTTTCAAAGGAAAAACAAAACCTCACGGTGGCTCCCCTGCAGGATAAAGGACA
GCACTGCCTTCTCTTTTCTTCAGAGGCTGGCTTGAGCCAGGTTTGCATAATCCCCCACCTAGCC
CTGAGGTGGGGAGAGAGTGTAAGAAGAGCAGCTTCAGGTGGGGTCCTTAGATCCTTAGTGCAGT
CCCCACAACCGCCCCCTCCACCCCTCCTTCCCCCGCTACATTGCTGGAGTGTGAGGGGCCTATA
AGGCCAAAGGGCTGCCCAGGGGAGGGGCCCAGCACCCAGCTTACCACCTGCACGCCCATCCCCC
TTTCTCCATCTTCCTTCCCCTTTGCCTTGCCTCTCCCTGCATCCAGCCAAAGTCCAACTCTGCC
CTTCAACCTGAAAGCCAAATCCTCTAAGCAAAAGAACTGACACATTTTGGAAAGTGGCAGGAAT
TCAAGGTGCTGATGCACGTGATGCTGGGCATGGCTTTGTGTGAGATTGAAGCATTGGTGGTGAT
GATCCTGTTGTGCTAATTTCACTAATGACTGGAGAAGAGAAAATCTACAAGGCTTCAGGCAGGA
GAAATGGCTTCCCTGAGGCAAGTGTAACCTACATTCCCAGCCCACCAGCCTGACGCCCAGCCAG
GGAGAGAGTACCATGGATGGCATCATTGAACAGAAGAGCATGCTGGTGCACAGTAAAATCAGTG
ATGCTGGCAAGAGGAATGGTTTAATTAACACCAGAAACTTGATGGCCGAGAGCAGAGATGGTCT
GGTGTCTGTTTACCCAGCGCCCCAGTACCAGAGCCACCGGGTGGGGGCCAGCACAGTGCCGGCC
AGCCTGGACAGCAGCAGGAGTGAGCCGATGCAGCAGCTGCTGGACCCCAACACCCTGCAGCAGT
CAGTGGAGTCCCGCTACCGGCCCAACATCATCCTCTATTCAGAGGGCGTGCTGCGCTCCTGGGG
GGACGGTGTGGCCGCCGACTGCTGCGAGACCACCTTCATCGAGGACCGGTCGCCCACCAAAGAC
AGCCTCGAGTACCCGGATGGGAAGTTCATTGACCTCTCAGCTGATGACATAAAAATCCACACCC
TGTCCTACGATGTGGAGGAGGAGGAGGAGTTCCAGGAGCTGGAGAGCGACTACTCAAGCGACAC
AGAGAGTGAGGACAATTTCCTCATGATGCCCCCGCGGGACCACCTGGGCCTCAGTGTCTTCTCC
ATGCTCTGCTGCTTCTGGCCTCTGGGCATCGCAGCCTTCTACTTGTCCCATGAGTTGATCACCC
TGGAAGAAATGGCAGCATTCAATTCCTCCATCCTTTTTTCCAGTTCGCAAGGGCTGGTTCCCTG
GACCAGCAGCATCAGGGTCATCTGGGAACGTTTTAGGATCGTGAAGTCTCGTCAGCTCCCAAGA
CCTGCTGACTCGGAAGCTCTGGGGACGGGGCTGGCAGTCTGGGTGTGAATGCCCTCTGAGGTTG
CTGTGGAGACTCCTGAGGTAACACATGCTGAAGTCAGCCTGTCCTAATGGACCAGGCTCTTGGT
TAGGAGCCCCAGCACCTAGGGGAGGCCGTGGTTCAGGGTTGTTGGGGTGTGGGCACAGCACGTG
ACACCCGCACCAGCCGCTCTCACCTTTTCACTCCTGCCCTCCCAGGTCACCTGCATCCGCCAAA
CTCTGCCTGGGGTTCCCTTCGTTATCAGCAGAGCACATAGACACATGTCTGGATTTGTTTATTC
ATTGTCTTTTCAAATATAGTGTACTCAACTTGGAAAACAGAAGGAGGAGGAAGAGAATGGAGAA
AGAAAGCATGAAAACTGAACCTCTCCTCCATGCCCCTTTCTCAAAGCCCCTCCTCCAGGGGGAC
CCCGTCTTTCTGTGCCTTTATCAATGTGTGTGTGGGCAGTTTTGATTTACACGTAGAAGACCAT
CAAAGTGCAATGCAGCTTGCTTTTTCACATAATGTAAATACTTCTGGTATCTGCATATAAACAC
CAGCATTGACATTTTTAATGATTTTGTAGCATTTTGATGTATGAATTGCAATAATTTCATTACA
GTAATGTTTTCCCTAAAAATGGACATATCAATTGTTTTCAACTTCTCCTTTTGCAAATATAGGA
TATCCACAAGTGAAATTCCACCAAGTCAAAGGTTATTCACATGTAAATTTAGCTACATACTGTA
ACTTCTCCTCCAGAAGTCCGTACCAGTTTTCATTCCTATTAACAAAATGTGAATGCCTGTCTTT
CCCACCTGAGCTCAGTGTTCCATTTTCAACAATCTGATAGATAAAATAAAAGATATTGTCAGTT

hide sequence

RefSeq Acc Id:

XM_017028065 ⟹ XP_016883554

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,873 - 24,666,616 (+)	NCBI

Sequence:

show sequence

AGACCCGGCGGCGGCGTGGCGCCCGCGCCCAGCCCTTGGCACTGTGACATTGCCACAGCTCCCG
TCAAGAAGAGGAGGTCCTGGGATCTGGATTTGGACTGACCCCATAACTGGCTTGGAGCACTACA
AGGAAGCGAAAGTGGCGATGGACCCATTCTGAGGTGGTACAGCCAGCAGCTGTCCAAACATGTC
GGTGAGGCTGTAGTGTGCCGATCTACTCCAGCTGACTGCGGCTTCATCAGTGACCCCAGGAGAG
ACCAGCCAAGAATCAAGCATCCCAGCGCAGCTTCACCTGTCAACCCAGAAAATGAGATGACTCC
ATTTTAACCCACCAACTCTTAGGGTGATTGGTTACACAACAAGTAATAACACATGGCTAGAAAA
AAATGGACTAGAAATATCTCTGCATAATACTCTATATTTACACTCAACAATATAGCCCTTGAGT
AAACGTTGGAAGGGAATTCAGCTGGTCATTTATTGCTCCTGCAGAGAGGAAGTGTGGGAAATAA
TTCAGCCGGGATCCTGGCCCTGGTAAAAGGCAAGGCACCATGCGAGGCACTGCATTCACAGTGA
ACCAGACGTGAGAGCCAAACAGACGTTTCCCATTTGTGCACACATACAAAGTGCTTCGCCCAGT
GCCTTGTGGGGTGCCCCCACTTCTCTTCAGTGCTCCACGTCTGTTTGTAACTCACTGTAGCTCT
CACTACCTGGTGGTGTGCCGACAACAATGGTAGACCAGCTGGACAAGCCCCAGAGTGGGGAGCA
GAGGGAACACTTCATCTGCTTCAAGCCCTTCTGCAGGCTCCAGGCACAAACTGATGAAGGACAG
AATTCTTTTGTCCTGCTGGAGCCAGAGGGTGTGGACACCAGAGGAGCCGTCCCTGGGCATCACA
TTGGCTCTTGCCCAAGAAAGGAGAAATGGCTTCCCTGAGGCAAGTGTAACCTACATTCCCAGCC
CACCAGCCTGACGCCCAGCCAGGGAGAGAGTACCATGGATGGCATCATTGAACAGAAGAGCATG
CTGGTGCACAGTAAAATCAGTGATGCTGGCAAGAGGAATGGTTTAATTAACACCAGAAACTTGA
TGGCCGAGAGCAGAGATGGTCTGGTGTCTGTTTACCCAGCGCCCCAGTACCAGAGCCACCGGGT
GGGGGCCAGCACAGTGCCGGCCAGCCTGGACAGCAGCAGGAGTGAGCCGATGCAGCAGCTGCTG
GACCCCAACACCCTGCAGCAGTCAGTGGAGTCCCGCTACCGGCCCAACATCATCCTCTATTCAG
AGGGCGTGCTGCGCTCCTGGGGGGACGGTGTGGCCGCCGACTGCTGCGAGACCACCTTCATCGA
GGACCGGTCGCCCACCAAAGACAGCCTCGAGTACCCGGATGGGAAGTTCATTGACCTCTCAGCT
GATGACATAAAAATCCACACCCTGTCCTACGATGTGGAGGAGGAGGAGGAGTTCCAGGAGCTGG
AGAGCGACTACTCAAGCGACACAGAGAGTGAGGACAATTTCCTCATGATGCCCCCGCGGGACCA
CCTGGGCCTCAGTGTCTTCTCCATGCTCTGCTGCTTCTGGCCTCTGGGCATCGCAGCCTTCTAC
TTGTCCCATGAGACCAACAAAGCCGTGGCCAAGGGGGACTTGCACCAGGCCAGCACCAGCTCCC
GGCGGGCCCTATTCCTGGCAGTGCTGTCCATCACCATTGGGACTGGCGTCTATGTGGGCGTGGC
CGTGGCCCTCATCGCCTACCTCTCCAAGAACAACCACCTGTGAGCTTCCTGCGAATGGAGGGGG
AGCACCCGGGGCCAGGTCTGTGTGGACGTGGAGGAAGCAGGCATACCGCATGATGCTGTACAGT
ACAAATGATTGCCAAATGATGCCACGAAGCCCTGGGATTTCCTACCCATGGATTTATTTTGTTT
TTATCCTTTAATTTCATGTTCACAGCACTGTGTAGAGCACCAGACAGACGGGCACTGCTAATCC
TTCCAAAGGAAAGCTCCAAAGATCCCAGCCCGCAAGGCTGTCTCTGGATGGATTCTGGTGGATG
AATGGCAACGCGGCTCTCTGCAGCCTGCCAGTGCCCAGAGTGCCACCGCATTAGCAATATACAA
ACAGTCCAAAAAAGTGTTTATTTTTTATGGAATACGGTGCAATAGGCAGAGGACAAGGGACACA
TCACTCTTCTGTCTGTGGCCCTGCTGGAGTCCTTTGTGCCCCCCGGAGTCCACACGCCTTCCCT
GCAAGACGAGAATGGGGCTGGGAAGAAAGAGGCAACACCACGGCTGGCAGGAGCCCCGCTGCAC
TGCTCTGCAGACCCATTGGCCTGACCCTGAGAAGCAGAGCCAGCAAAGCCCGGGACCTGCCCCT
CTTTCTTTCCCTTCACACCACCCCAGCCTCAGGATGTCAAGCCACCTCCGGAACGTGTCTACAC
TCCACAGCTACCCCGCAGCAATACGCACTCTTGGGACCTCGCTGATCTAGGATGGGGAGGCAGG
CCACCGCCCCTCCCAAGACTCCTCAAGAAAGAGCCCCGCGGTTGCTCCGGAAACTCGAGGCACT
GCAGCTATGGGCACTGCCTCAGCCTAAAGACACAGGGGCGCCTCCCAATCACCGCGCTGGCGGA
TGCTCACCCCGTCATAAGCAGAAACTAGTGATCCTGGAAATGAGATGGGCCTTACTCTGTCGAC
TAAATGAATAGCTATTTTCTTGTCATTTTTTAAAGTGCAACTCTTGCTTCATGCTGCTTAAGTT
ACCAGATGAATGCTGAGAAATAAGTAATCACAGACATTTTAATACCATTTCATTGCTGTTTTAC
GAGTGTTCATTACTTAACAAAAAATTATCTTTTAGCTTTTT

hide sequence

RefSeq Acc Id:

XM_017028066 ⟹ XP_016883555

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,873 - 24,666,616 (+)	NCBI

Sequence:

show sequence

GAGACTTGGGAGACACGGGGTCGCAGGGCGGGAGGGGGAGCTGAGCCGGCAGAGAAAATGCCCA
GGAAGGGGTCGATGCTGGCCTGGGCTGCACCTTGGTGCCTTGCCACCCCGGGAGACGCGAAGGG
GCTGCTGTGCGAATTCGATGGGAGCTGGTGAGACCGAGAACTGAGAGCGTAGCGGAGCCAGGCT
GCCCAGCAGGGCCATGAGGGCGCGCGGCGGGCCAAGGCTCTGCGGGTTCGGGCTGCCCCTCGGA
GTGACCCGAAGGAGACCAGCCAGGGCTGGAGAAATGGCTTCCCTGAGGCAAGTGTAACCTACAT
TCCCAGCCCACCAGCCTGACGCCCAGCCAGGGAGAGAGTACCATGGATGGCATCATTGAACAGA
AGAGCATGCTGGTGCACAGTAAAATCAGTGATGCTGGCAAGAGGAATGGTTTAATTAACACCAG
AAACTTGATGGCCGAGAGCAGAGATGGTCTGGTGTCTGTTTACCCAGCGCCCCAGTACCAGAGC
CACCGGGTGGGGGCCAGCACAGTGCCGGCCAGCCTGGACAGCAGCAGGAGTGAGCCGATGCAGC
AGCTGCTGGACCCCAACACCCTGCAGCAGTCAGTGGAGTCCCGCTACCGGCCCAACATCATCCT
CTATTCAGAGGGCGTGCTGCGCTCCTGGGGGGACGGTGTGGCCGCCGACTGCTGCGAGACCACC
TTCATCGAGGACCGGTCGCCCACCAAAGACAGCCTCGAGTACCCGGATGGGAAGTTCATTGACC
TCTCAGCTGATGACATAAAAATCCACACCCTGTCCTACGATGTGGAGGAGGAGGAGGAGTTCCA
GGAGCTGGAGAGCGACTACTCAAGCGACACAGAGAGTGAGGACAATTTCCTCATGATGCCCCCG
CGGGACCACCTGGGCCTCAGTGTCTTCTCCATGCTCTGCTGCTTCTGGCCTCTGGGCATCGCAG
CCTTCTACTTGTCCCATGAGACCAACAAAGCCGTGGCCAAGGGGGACTTGCACCAGGCCAGCAC
CAGCTCCCGGCGGGCCCTATTCCTGGCAGTGCTGTCCATCACCATTGGGACTGGCGTCTATGTG
GGCGTGGCCGTGGCCCTCATCGCCTACCTCTCCAAGAACAACCACCTGTGAGCTTCCTGCGAAT
GGAGGGGGAGCACCCGGGGCCAGGTCTGTGTGGACGTGGAGGAAGCAGGCATACCGCATGATGC
TGTACAGTACAAATGATTGCCAAATGATGCCACGAAGCCCTGGGATTTCCTACCCATGGATTTA
TTTTGTTTTTATCCTTTAATTTCATGTTCACAGCACTGTGTAGAGCACCAGACAGACGGGCACT
GCTAATCCTTCCAAAGGAAAGCTCCAAAGATCCCAGCCCGCAAGGCTGTCTCTGGATGGATTCT
GGTGGATGAATGGCAACGCGGCTCTCTGCAGCCTGCCAGTGCCCAGAGTGCCACCGCATTAGCA
ATATACAAACAGTCCAAAAAAGTGTTTATTTTTTATGGAATACGGTGCAATAGGCAGAGGACAA
GGGACACATCACTCTTCTGTCTGTGGCCCTGCTGGAGTCCTTTGTGCCCCCCGGAGTCCACACG
CCTTCCCTGCAAGACGAGAATGGGGCTGGGAAGAAAGAGGCAACACCACGGCTGGCAGGAGCCC
CGCTGCACTGCTCTGCAGACCCATTGGCCTGACCCTGAGAAGCAGAGCCAGCAAAGCCCGGGAC
CTGCCCCTCTTTCTTTCCCTTCACACCACCCCAGCCTCAGGATGTCAAGCCACCTCCGGAACGT
GTCTACACTCCACAGCTACCCCGCAGCAATACGCACTCTTGGGACCTCGCTGATCTAGGATGGG
GAGGCAGGCCACCGCCCCTCCCAAGACTCCTCAAGAAAGAGCCCCGCGGTTGCTCCGGAAACTC
GAGGCACTGCAGCTATGGGCACTGCCTCAGCCTAAAGACACAGGGGCGCCTCCCAATCACCGCG
CTGGCGGATGCTCACCCCGTCATAAGCAGAAACTAGTGATCCTGGAAATGAGATGGGCCTTACT
CTGTCGACTAAATGAATAGCTATTTTCTTGTCATTTTTTAAAGTGCAACTCTTGCTTCATGCTG
CTTAAGTTACCAGATGAATGCTGAGAAATAAGTAATCACAGACATTTTAATACCATTTCATTGC
TGTTTTACGAGTGTTCATTACTTAACAAAAAATTATCTTTTAGCTTTTT

hide sequence

RefSeq Acc Id:

XM_017028067 ⟹ XP_016883556

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,873 - 24,666,616 (+)	NCBI

Sequence:

show sequence

GCGGTAAGTCCGGGTGGTCGCCGCGACGAGACTTGGGAGACACGGGGTCGCAGGGCGGGAGGGG
GAGCTGAGCCGGCAGAGAAAATGCCCAGGAAGGGGTCGATGCTGGCCTGGGCTGCACCTTGGTG
CCTTGCCACCCCGGGAGACGCGAAGGGGCTGCTGTGCGAATTCGATGGGAGCTGGAGAAATGGC
TTCCCTGAGGCAAGTGTAACCTACATTCCCAGCCCACCAGCCTGACGCCCAGCCAGGGAGAGAG
TACCATGGATGGCATCATTGAACAGAAGAGCATGCTGGTGCACAGTAAAATCAGTGATGCTGGC
AAGAGGAATGGTTTAATTAACACCAGAAACTTGATGGCCGAGAGCAGAGATGGTCTGGTGTCTG
TTTACCCAGCGCCCCAGTACCAGAGCCACCGGGTGGGGGCCAGCACAGTGCCGGCCAGCCTGGA
CAGCAGCAGGAGTGAGCCGATGCAGCAGCTGCTGGACCCCAACACCCTGCAGCAGTCAGTGGAG
TCCCGCTACCGGCCCAACATCATCCTCTATTCAGAGGGCGTGCTGCGCTCCTGGGGGGACGGTG
TGGCCGCCGACTGCTGCGAGACCACCTTCATCGAGGACCGGTCGCCCACCAAAGACAGCCTCGA
GTACCCGGATGGGAAGTTCATTGACCTCTCAGCTGATGACATAAAAATCCACACCCTGTCCTAC
GATGTGGAGGAGGAGGAGGAGTTCCAGGAGCTGGAGAGCGACTACTCAAGCGACACAGAGAGTG
AGGACAATTTCCTCATGATGCCCCCGCGGGACCACCTGGGCCTCAGTGTCTTCTCCATGCTCTG
CTGCTTCTGGCCTCTGGGCATCGCAGCCTTCTACTTGTCCCATGAGACCAACAAAGCCGTGGCC
AAGGGGGACTTGCACCAGGCCAGCACCAGCTCCCGGCGGGCCCTATTCCTGGCAGTGCTGTCCA
TCACCATTGGGACTGGCGTCTATGTGGGCGTGGCCGTGGCCCTCATCGCCTACCTCTCCAAGAA
CAACCACCTGTGAGCTTCCTGCGAATGGAGGGGGAGCACCCGGGGCCAGGTCTGTGTGGACGTG
GAGGAAGCAGGCATACCGCATGATGCTGTACAGTACAAATGATTGCCAAATGATGCCACGAAGC
CCTGGGATTTCCTACCCATGGATTTATTTTGTTTTTATCCTTTAATTTCATGTTCACAGCACTG
TGTAGAGCACCAGACAGACGGGCACTGCTAATCCTTCCAAAGGAAAGCTCCAAAGATCCCAGCC
CGCAAGGCTGTCTCTGGATGGATTCTGGTGGATGAATGGCAACGCGGCTCTCTGCAGCCTGCCA
GTGCCCAGAGTGCCACCGCATTAGCAATATACAAACAGTCCAAAAAAGTGTTTATTTTTTATGG
AATACGGTGCAATAGGCAGAGGACAAGGGACACATCACTCTTCTGTCTGTGGCCCTGCTGGAGT
CCTTTGTGCCCCCCGGAGTCCACACGCCTTCCCTGCAAGACGAGAATGGGGCTGGGAAGAAAGA
GGCAACACCACGGCTGGCAGGAGCCCCGCTGCACTGCTCTGCAGACCCATTGGCCTGACCCTGA
GAAGCAGAGCCAGCAAAGCCCGGGACCTGCCCCTCTTTCTTTCCCTTCACACCACCCCAGCCTC
AGGATGTCAAGCCACCTCCGGAACGTGTCTACACTCCACAGCTACCCCGCAGCAATACGCACTC
TTGGGACCTCGCTGATCTAGGATGGGGAGGCAGGCCACCGCCCCTCCCAAGACTCCTCAAGAAA
GAGCCCCGCGGTTGCTCCGGAAACTCGAGGCACTGCAGCTATGGGCACTGCCTCAGCCTAAAGA
CACAGGGGCGCCTCCCAATCACCGCGCTGGCGGATGCTCACCCCGTCATAAGCAGAAACTAGTG
ATCCTGGAAATGAGATGGGCCTTACTCTGTCGACTAAATGAATAGCTATTTTCTTGTCATTTTT
TAAAGTGCAACTCTTGCTTCATGCTGCTTAAGTTACCAGATGAATGCTGAGAAATAAGTAATCA
CAGACATTTTAATACCATTTCATTGCTGTTTTACGAGTGTTCATTACTTAACAAAAAATTATCT
TTTAGCTTTTT

hide sequence

RefSeq Acc Id:

XM_017028068 ⟹ XP_016883557

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,488,670 - 24,666,616 (+)	NCBI

Sequence:

show sequence

AGGAAGCTGATCGTTTCCTTCAATGCAAGTACTCTTTGGAAACAAAAGCAAAACAAAACAAAAA
CCATAAAAAATACAAGAACAAGAAATGCTGAAGACAGGTGGAAAGAATGAAAATAGGACTGAAG
CAGGCCTGTGCCCTAGGCAGAGCCAGGCACACGCCTGCTGAGAGGACCCCACTAACAGGTGACC
CAGGCAAGAGGCCCCCGGCCGGCTCCGTGTGAACAGATCCTCCCATCTTGTCGCGTCCGTGTCC
ACAGTGAAACTCCAGGCACCGCAGGGACGCTGGGGAGAGCCTTCTCTCCACACCCCCTTGGAAT
GTGCCCCCCACTTTTCGCTGTTCTGGTGGGCTTTTGGTTTCTTGTCAGGGTTGGGGCTCTGCCA
AGTAGCCACAGTGAACACAGAAAGCAGCCCTTGAGCCTGGCCTTCAGCGAGAGTTGCTAAGGGG
TGGCTAGGAGATGAGGAGGGTAGGCTCGGCCCCGCCGCCTCTGCTGTCTGGTTCGAGATCAGCT
GCTGGCCACCACAGGGGACATGTGCATTGTCATCTATCTTGGGAAAGACTTTGGTAAACATCCA
AGTTTCAAAGGAAAAACAAAACCTCACGGTGGCTCCCCTGCAGGATAAAGGACAGCACTGCCTT
CTCTTTTCTTCAGAGGCTGGCTTGAGCCAGGTTTGCATAATCCCCCACCTAGCCCTGAGGTGGG
GAGAGAGTGTAAGAAGAGCAGCTTCAGGTGGGGTCCTTAGATCCTTAGTGCAGTCCCCACAACC
GCCCCCTCCACCCCTCCTTCCCCCGCTACATTGCTGGAGTGTGAGGGGCCTATAAGGCCAAAGG
GCTGCCCAGGGGAGGGGCCCAGCACCCAGCTTACCACCTGCACGCCCATCCCCCTTTCTCCATC
TTCCTTCCCCTTTGCCTTGCCTCTCCCTGCATCCAGCCAAAGTCCAACTCTGCCCTTCAACCTG
AAAGCCAAATCCTCTAAGCAAAAGAACTGACACATTTTGGAAAGTGGCAGGAATTCAAGGTGCT
GATGCACGTGATGCTGGGCATGGCTTTGTGTGAGATTGAAGCATTGGTGGTGATGATCCTGTTG
TGCTAATTTCACTAATGACTGGAGAAGAGAAAATCTACAAGGCTTCAGGCAGGAGAAATGGCTT
CCCTGAGGCAAGTGTAACCTACATTCCCAGCCCACCAGCCTGACGCCCAGCCAGGGAGAGAGTA
CCATGGATGGCATCATTGAACAGAAGAGCATGCTGGTGCACAGTAAAATCAGTGATGCTGGCAA
GAGGAATGGTTTAATTAACACCAGAAACTTGATGGCCGAGAGCAGAGATGGTCTGGTGTCTGTT
TACCCAGCGCCCCAGTACCAGAGCCACCGGGTGGGGGCCAGCACAGTGCCGGCCAGCCTGGACA
GCAGCAGGAGTGAGCCGATGCAGCAGCTGCTGGACCCCAACACCCTGCAGCAGTCAGTGGAGTC
CCGCTACCGGCCCAACATCATCCTCTATTCAGAGGGCGTGCTGCGCTCCTGGGGGGACGGTGTG
GCCGCCGACTGCTGCGAGACCACCTTCATCGAGGACCGGTCGCCCACCAAAGACAGCCTCGAGT
ACCCGGATGGGAAGTTCATTGACCTCTCAGCTGATGACATAAAAATCCACACCCTGTCCTACGA
TGTGGAGGAGGAGGAGGAGTTCCAGGAGCTGGAGAGCGACTACTCAAGCGACACAGAGAGTGAG
GACAATTTCCTCATGATGCCCCCGCGGGACCACCTGGGCCTCAGTGTCTTCTCCATGCTCTGCT
GCTTCTGGCCTCTGGGCATCGCAGCCTTCTACTTGTCCCATGAGACCAACAAAGCCGTGGCCAA
GGGGGACTTGCACCAGGCCAGCACCAGCTCCCGGCGGGCCCTATTCCTGGCAGTGCTGTCCATC
ACCATTGGGACTGGCGTCTATGTGGGCGTGGCCGTGGCCCTCATCGCCTACCTCTCCAAGAACA
ACCACCTGTGAGCTTCCTGCGAATGGAGGGGGAGCACCCGGGGCCAGGTCTGTGTGGACGTGGA
GGAAGCAGGCATACCGCATGATGCTGTACAGTACAAATGATTGCCAAATGATGCCACGAAGCCC
TGGGATTTCCTACCCATGGATTTATTTTGTTTTTATCCTTTAATTTCATGTTCACAGCACTGTG
TAGAGCACCAGACAGACGGGCACTGCTAATCCTTCCAAAGGAAAGCTCCAAAGATCCCAGCCCG
CAAGGCTGTCTCTGGATGGATTCTGGTGGATGAATGGCAACGCGGCTCTCTGCAGCCTGCCAGT
GCCCAGAGTGCCACCGCATTAGCAATATACAAACAGTCCAAAAAAGTGTTTATTTTTTATGGAA
TACGGTGCAATAGGCAGAGGACAAGGGACACATCACTCTTCTGTCTGTGGCCCTGCTGGAGTCC
TTTGTGCCCCCCGGAGTCCACACGCCTTCCCTGCAAGACGAGAATGGGGCTGGGAAGAAAGAGG
CAACACCACGGCTGGCAGGAGCCCCGCTGCACTGCTCTGCAGACCCATTGGCCTGACCCTGAGA
AGCAGAGCCAGCAAAGCCCGGGACCTGCCCCTCTTTCTTTCCCTTCACACCACCCCAGCCTCAG
GATGTCAAGCCACCTCCGGAACGTGTCTACACTCCACAGCTACCCCGCAGCAATACGCACTCTT
GGGACCTCGCTGATCTAGGATGGGGAGGCAGGCCACCGCCCCTCCCAAGACTCCTCAAGAAAGA
GCCCCGCGGTTGCTCCGGAAACTCGAGGCACTGCAGCTATGGGCACTGCCTCAGCCTAAAGACA
CAGGGGCGCCTCCCAATCACCGCGCTGGCGGATGCTCACCCCGTCATAAGCAGAAACTAGTGAT
CCTGGAAATGAGATGGGCCTTACTCTGTCGACTAAATGAATAGCTATTTTCTTGTCATTTTTTA
AAGTGCAACTCTTGCTTCATGCTGCTTAAGTTACCAGATGAATGCTGAGAAATAAGTAATCACA
GACATTTTAATACCATTTCATTGCTGTTTTACGAGTGTTCATTACTTAACAAAAAATTATCTTT
TAGCTTTTT

hide sequence

RefSeq Acc Id:

XM_017028069 ⟹ XP_016883558

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,629 - 24,548,629 (+)	NCBI

Sequence:

show sequence

AGAGGAGGAGAGAGCCTGGCAGCGGAGGAGCAGAGGCGGGCGCCGCACCGCCCCGCACGCTCGC
TCGCTCGGGAGAGTCGCGGGCGGCCGCTTGGGCGCACTTGCCGGGTCACCTTGTCCCGGAGGAG
AAATGGCTTCCCTGAGGCAAGTGTAACCTACATTCCCAGCCCACCAGCCTGACGCCCAGCCAGG
GAGAGAGTACCATGGATGGCATCATTGAACAGAAGAGCATGCTGGTGCACAGTAAAATCAGTGA
TGCTGGCAAGAGGAATGGTTTAATTAACACCAGAAACTTGATGGCCGAGAGCAGAGATGGTCTG
GTGTCTGTTTACCCAGCGCCCCAGTACCAGAGCCACCGGGTGGGGGCCAGCACAGTGCCGGCCA
GCCTGGACAGCAGCAGGAGTGAGCCGATGCAGCAGCTGCTGGACCCCAACACCCTGCAGCAGTC
AGTGGAGTCCCGCTACCGGCCCAACATCATCCTCTATTCAGAGGGCGTGCTGCGCTCCTGGGGG
GACGGTGTGGCCGCCGACTGCTGCGAGACCACCTTCATCGAGGACCGGTCGCCCACCAAAGACA
GCCTCGAGTACCCGGATGGGAAGTTCATTGACCTCTCAGCTGATGACATAAAAATCCACACCCT
GTCCTACGATGTGGAGGAGGAGGAGGAGTTCCAGGAGCTGGAGTGACTTTTGAATATAACGTAA
GATGGAGCATGTTGGCATTTATACTAAAGTAACATCGATGAAACAGCAAGTTGTTTACTTAGGC
ACTTTAGTGAGACTTTCTGGTCGGCTTCCAAGGAGCTCACCTGGACCAAGAAATGGCCCCTTCC
ACAGGCTCTGAGCAGAAGGAATGGAGACACATTATGGCTGCTGCTGCTTCTACATGCGGCTCAG
GATGCCAAGGAGGATTTCAGAGCCTCACCACGGTGGTTAACTTCGTCCTTTTTCTCTGAAAACA
AAGATTTTCTCAGAAACATTCTTACAGTATAGCTATGGTGCTTTTCATTCCCTTCTTCGGTAAT
TAACAAAATACTAATGACTGGTTAGAAGTGTCATTGAACATGCAGTAGCTGTTCTTTGGTTTAC
TGTTTTCTCCATTCCATTAAATAATAAAGGGTCATGTATTGGTTAGCATTTGCTGCATAACAAA
TCACCCCCAAAACACAGTGCCTTAACAACTCTTTCTTCAGCTTATGATTTCTGAGGGTCGGCAA
TTGAGCTGGGCTCAGCTGGGTGATTGTTCTGCTGGTCTCACCTGGGCTCACTCACTTGTCCATA
GCTAGCTGTGATAGGCTGGGAAGCCAGCCTCTGGTGGGCTGTTGGCTGCAGTGACAGAGGTAAC
TGCATCACCCAGCTGTCACCCATCCTGTCCCAGGCTTCATTTTGCGGCAGCCAGAGAGGTGGGG
CCCACTTTGTGAGGGCTTGTCAAGTCTTTGCCTGTGTCCTGCATGTTACTATCTCATTGACCAG
AGCAGGTCCCACAGCCAAGCTCAGTCAGTGTGGGAGAGACTGCTTAGGGTCACAATATAGGGAA
GTGATAACAAATTGGGTGCCAGTACTGCAACCACAGAGCCAAAAACCATAGACTTTTGGCATCA
TTTTTTTTTTCAGATGGTCTAACTGAACAGAATGACAACTACTGAAACAAAAGAACAGTGAATA
CTGATCTGAGCTCTTTCCAGAAGGCAGTTCTACTCAGCCAAAAAAGAAAAAAAAATGTGATTTT
TAACTTCTTTGAGTATTGTATAGCTTCACTTGGTTTATAGCAAATGGATACTGTTTCCCAAATA
ATGCCGTTTTCAAAAAGCCATTGCCCTGGTTCAGAATGGGGCCCCCTCATTGCCCTTGTTCAGA
GGGGGCCACCTCATTGCCCTTGTTCAGGGCCCCTCCCATTGCCCTGGTTCAGAGTGGGGCCTTC
TCATTGTCCTGGGTCAGAGCAGGGCCCCCTCATTGCCCTGGTTCAGAGCAGGGCCCCTCGTTTC
CCTGGTTCTGAGCGGGGCTCCCTTGCTGGAGCTCCTGGGCACTGGGTGGCTGGCTGTGTTTTCC
CCAATCACTTTCCCAAGACAGGTGCATCCCTGGCATTTATGAAGGAGCCTCTCCAGGTCCGAAG
AGGTCGGCCTGTCTGACATATGTTTGCAAGGGCATGTGGAGCGTTCAGTTTGCCTTCGAGGTTG
TGGTAGTAACAAGAACAGGTTCTATGGCTAACTTTGAGAATATTTATGGGAGGTTCTCAACTAT
TCGGCAAGTGTTTATGATCTGTCCTGCTCCACCTTAAGTCGCCAAGTAGAGCATGGCTTGACAT
TAGACAGGTAGATGTAGGGGACCTCTGGGGCTTTGCGGGAGTGCAGAGGTGCCATGCCGCTCAT
TATCTAGTGCCACTGCGCTCAGGGTGACAAGACAGGCATCCTGTGGGGGTGCCCTCAGGGCATC
CTGGGTAGTGATAATTGGGCCTGATGTCCGACAGCCCAGGCCTCTTCCCAGGTATGTGAACACT
GCTTCATCCACTTCCCAGCCAGTAGCTAAAAACTGCTGTCTCTGGGAATACCAGCAGTGGGAAG
CCACTTCTCCTTTCACACAAATAAACTCAGAGAGACTTCAGGGACAAGTAATGAAGTAGGTCTA
CAAAATATACAATTTGAGTTTACAGCCATGAAATGAAGTGGATGGAGTCCAGGTGCAGAGGCCT
GACCACCCTCCTGCCCTTAGAGATGGTGACCAGATGTTGAATGGCACTTACCTGTGGCAATGCA
AAACCTCTCAGACCTGAAGTACATGACGGTCACCACCTAGAAGCGGTGCCCATGGGGGCTGAGC
CTTTTCTTCACTGAAGGAAGAAGGGGGAAGGGAACGCTCATCGATGGAGCACCTTTTCTGCCAC
GCCCTCCAAGTGCACTTGGCCATCGAATCCTCGAAGCGCTTGGGGATGGGTCATGGTGCTGTCC
TCATCCTACACGTGGAGAGACAGAAACTTGGGGTGTTTCCAAGATCACACACGTGGCTCTGCTG
TCAGCCCTTGGATCTGAGACAGATCTCCTGACTTTAGACTCTGTCTCCTCATGATGATGCTGTT
CTTTCTACATTAGGGGGAAAAATGTGTTCCAGTAAACTTCTGTTTCAGCATTATGCCAGAGTCC
AAGGACAAAGCAGGAAGAGACGGCACCAGGACTTCACTTCTGTGAACTCTCCGCCAAGCTTTCC
AAGGCCTTCCAGTCTGTCTTCCCATGTAAAAACTTGAAAGCTGTTGGAGGACACAGAATTCTAT
AACTGCAATAGAGCACTTTACATATACCTCAGTCATAAGTATGGAAAGAGGGGCGAGGACTCAA
CACACATGTGAAGAAAACCCAAAAGCATGAATGAGACAGAACAACAACAAATAGAACAGTTGAC
CCAGAGGAAAGAGAAAGAGTTCAGAAAATAATAAACAGCATTTTGAAAATTATTTTTAGTATCT
CCAGAGAGATTTGAGGTGCTGCTGATTTGGGTGGAAGGAAATTTGGGGGTTTTGTTTTGCTCAT
TTGTTTGTTTACCTCATAGCACTGGCCAGAACCTCAAATACATTGTTTAGTGTGAGTGAACGAA
CATCCTTGCCTTGCTCCTGATCTTAGGGGGAGCTTTTAGCTTTCATGATGAAAGGTGATGTTTT
TGTAGTTCTTTGTAGACACTCATAATCAGGTATAGGAAGTTCCCTTTGTCACTACTTTGTTGAA
GAGGTTTTTTATTTTATTTTTTATTTAATTTTATTTTTTAATAGACAAATAAATGGGATATTCA
TATTCATGGGGTATATAGTGATGTTTTGATACATGTAACATATGGTGATCAGATCAGGGTAATT
AGCATATTCATTATCTCAAACTTTGATCATTGCTTTGTGTTGGGAGCATTCAATAACCTCCTCT
TAGCTATTTGAAACTGCATAATATATTATTTTTCAACTGTTTTCATGCTACAGTGCTGTAGAAC
ACTGGAAGTTATTCATATCTAGCTGTAATTTTGTATGTTTTAATACATCTCTTCCTATCTCTCC
CTTCCTCCTACTCTGCCCACTCTCTACTATTCTTCCTTCTACTTTTACTTCTATAAAATTAACT
CCTTTTAGCTTCCACGAGTGGAACATGCAATGCTTAACTTTCCCTCCTGACTTATTTCATTTAA
CATAATGTCCTCCAGTTTCATCCATATTTGCTGCAAATGACATAATTTCATTATTTTTTTATGG
CTGAATAGTATCCTGTGGTGTTGAAATGGGAGAGTTCCCTGATTCCCCTTGCAGGACGTGGGGT
GGGTGTGGTTCACCTGTTCTGTTGCTGCTCAAACCCCTTGCAGGACTGGAGCATGCAGAAGGGC
AGGTGCAGAGGCTGGGGCGAGTGCTTTATGCTCTGGCCTTGCAGTAGTGTCTAGGGGTGGGTGA
CTGCAACCCCACTGTTACAAAGCTCTTTCAGCTTTGCTGTCCACAGACGGCTTGAATACTAACA
GGCTCAATGGGCCCTTTGCCTTTTCGCAAGGACAGAGGGCTGGATCCAGAGCTGTTGCCCAGCA
TCCTGGAAAAATCAGGTCACATACGGGCTTGAAGGATGAATGTGAAGTTTTTTTGAGTGGTAGA
GGTGGTTTTCAGTGGGATGGATGTGGAGCCGGGAAGGATACTGGAGTGGGAAGGTGATCCTCCC
CTGGACTTGGGCCACCCAGTGGCTGGACTCCTCTCTGACCATCCCCAACCAAACTCCTCTCGGC
ATTCAGATGTTCCTCCTCTTCTCCCTTTCTCTGCCATGTTGTTCTGCCATCTGTCTATTTGCTG
GTCTTCTGGCTTGCTAGTCTGCTTCTGGGTCCTGGGTTTCAGGGTTTATATGGGTGTAGGCATG
CGGGCCAAAATACAACTTTTTGGGTACAAAAACAGGAATGCCTTTTCTCACTTAGGGCCACAGA
TATCCAGGCTTGAGGATGGGGCTTTGCCAGGAAACTGCCCTCTTCTACCCAGTATTTCCCTGAT
TCCTGTCCTATCAGTGTACAACTACCCCATTTTCTTTATCCATTTATCTGTTTGTTGTTGGAGA
CCTAGGTTAATCCCATATCTTGGATATTGCGAATAGCACTGCAACAAACGCATGGTGTAGATGT
CTCTCTAATATACTGATTTCGTTTCCTTTGGATAAATGCCAAGTAGTGGGGTTGCTGGATTGTA
TGGTAGTTCTATTTGTGGTTTTTCTAGGGAGTTGCATATGGGTGTTCAATTCGTCAGGTACTAC
TTAGGTAATCATGTGTGGTGTTTCTTTGTTGTCCTTTATTTTTTCATCCTTTAATCATGTGGTA
TATTACGTTAACTGCTTTTTTTTTTTTTTGAGACGGAGTCTCTCTCTGTCGCCCAGG

hide sequence

RefSeq Acc Id:

XM_047440496 ⟹ XP_047296452

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,629 - 24,634,588 (+)	NCBI

RefSeq Acc Id:

XM_047440497 ⟹ XP_047296453

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,873 - 24,634,588 (+)	NCBI

RefSeq Acc Id:

XM_047440498 ⟹ XP_047296454

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,873 - 24,634,588 (+)	NCBI

RefSeq Acc Id:

XM_047440499 ⟹ XP_047296455

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,629 - 24,663,067 (+)	NCBI

RefSeq Acc Id:

XM_047440500 ⟹ XP_047296456

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,873 - 24,548,629 (+)	NCBI

RefSeq Acc Id:

XM_054324015 ⟹ XP_054179990

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,610 - 24,697,409 (+)	NCBI

RefSeq Acc Id:

XM_054324016 ⟹ XP_054179991

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,610 - 24,697,409 (+)	NCBI

RefSeq Acc Id:

XM_054324017 ⟹ XP_054179992

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,610 - 24,697,409 (+)	NCBI

RefSeq Acc Id:

XM_054324018 ⟹ XP_054179993

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,610 - 24,697,409 (+)	NCBI

RefSeq Acc Id:

XM_054324019 ⟹ XP_054179994

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,854 - 24,697,409 (+)	NCBI

RefSeq Acc Id:

XM_054324020 ⟹ XP_054179995

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,854 - 24,697,409 (+)	NCBI

RefSeq Acc Id:

XM_054324021 ⟹ XP_054179996

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,854 - 24,697,409 (+)	NCBI

RefSeq Acc Id:

XM_054324022 ⟹ XP_054179997

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,854 - 24,697,409 (+)	NCBI

RefSeq Acc Id:

XM_054324023 ⟹ XP_054179998

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,906 - 24,697,409 (+)	NCBI

RefSeq Acc Id:

XM_054324024 ⟹ XP_054179999

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,854 - 24,697,409 (+)	NCBI

RefSeq Acc Id:

XM_054324025 ⟹ XP_054180000

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,550,647 - 24,697,409 (+)	NCBI

RefSeq Acc Id:

XM_054324026 ⟹ XP_054180001

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,854 - 24,729,659 (+)	NCBI

RefSeq Acc Id:

XM_054324027 ⟹ XP_054180002

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,854 - 24,729,659 (+)	NCBI

RefSeq Acc Id:

XM_054324028 ⟹ XP_054180003

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,550,653 - 24,729,659 (+)	NCBI

RefSeq Acc Id:

XM_054324029 ⟹ XP_054180004

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,904 - 24,729,659 (+)	NCBI

RefSeq Acc Id:

XM_054324030 ⟹ XP_054180005

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,610 - 24,726,110 (+)	NCBI

RefSeq Acc Id:

XM_054324031 ⟹ XP_054180006

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,610 - 24,724,042 (+)	NCBI

RefSeq Acc Id:

XM_054324032 ⟹ XP_054180007

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,610 - 24,709,478 (+)	NCBI

RefSeq Acc Id:

XM_054324033 ⟹ XP_054180008

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,610 - 24,613,377 (+)	NCBI

RefSeq Acc Id:

XM_054324034 ⟹ XP_054180009

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	24,531,854 - 24,613,377 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001310535	(Get FASTA)	NCBI Sequence Viewer
	NP_001310536	(Get FASTA)	NCBI Sequence Viewer
	NP_079169	(Get FASTA)	NCBI Sequence Viewer
	XP_011527649	(Get FASTA)	NCBI Sequence Viewer
	XP_011527650	(Get FASTA)	NCBI Sequence Viewer
	XP_011527652	(Get FASTA)	NCBI Sequence Viewer
	XP_011527653	(Get FASTA)	NCBI Sequence Viewer
	XP_011527655	(Get FASTA)	NCBI Sequence Viewer
	XP_011527656	(Get FASTA)	NCBI Sequence Viewer
	XP_011527658	(Get FASTA)	NCBI Sequence Viewer
	XP_011527660	(Get FASTA)	NCBI Sequence Viewer
	XP_016883553	(Get FASTA)	NCBI Sequence Viewer
	XP_016883554	(Get FASTA)	NCBI Sequence Viewer
	XP_016883555	(Get FASTA)	NCBI Sequence Viewer
	XP_016883556	(Get FASTA)	NCBI Sequence Viewer
	XP_016883557	(Get FASTA)	NCBI Sequence Viewer
	XP_016883558	(Get FASTA)	NCBI Sequence Viewer
	XP_047296452	(Get FASTA)	NCBI Sequence Viewer
	XP_047296453	(Get FASTA)	NCBI Sequence Viewer
	XP_047296454	(Get FASTA)	NCBI Sequence Viewer
	XP_047296455	(Get FASTA)	NCBI Sequence Viewer
	XP_047296456	(Get FASTA)	NCBI Sequence Viewer
	XP_054179990	(Get FASTA)	NCBI Sequence Viewer
	XP_054179991	(Get FASTA)	NCBI Sequence Viewer
	XP_054179992	(Get FASTA)	NCBI Sequence Viewer
	XP_054179993	(Get FASTA)	NCBI Sequence Viewer
	XP_054179994	(Get FASTA)	NCBI Sequence Viewer
	XP_054179995	(Get FASTA)	NCBI Sequence Viewer
	XP_054179996	(Get FASTA)	NCBI Sequence Viewer
	XP_054179997	(Get FASTA)	NCBI Sequence Viewer
	XP_054179998	(Get FASTA)	NCBI Sequence Viewer
	XP_054179999	(Get FASTA)	NCBI Sequence Viewer
	XP_054180000	(Get FASTA)	NCBI Sequence Viewer
	XP_054180001	(Get FASTA)	NCBI Sequence Viewer
	XP_054180002	(Get FASTA)	NCBI Sequence Viewer
	XP_054180003	(Get FASTA)	NCBI Sequence Viewer
	XP_054180004	(Get FASTA)	NCBI Sequence Viewer
	XP_054180005	(Get FASTA)	NCBI Sequence Viewer
	XP_054180006	(Get FASTA)	NCBI Sequence Viewer
	XP_054180007	(Get FASTA)	NCBI Sequence Viewer
	XP_054180008	(Get FASTA)	NCBI Sequence Viewer
	XP_054180009	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH30637	(Get FASTA)	NCBI Sequence Viewer
	BAB14872	(Get FASTA)	NCBI Sequence Viewer
	CAE92125	(Get FASTA)	NCBI Sequence Viewer
	CAG33606	(Get FASTA)	NCBI Sequence Viewer
	EAX10117	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000366058
	ENSP00000366058.3
GenBank Protein	Q9H7V2	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:

NP_079169 ⟸ NM_024893

- UniProtKB:

Q6IA30 (UniProtKB/Swiss-Prot), Q9H514 (UniProtKB/Swiss-Prot), Q9H7V2 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MDGIIEQKSMLVHSKISDAGKRNGLINTRNLMAESRDGLVSVYPAPQYQSHRVGASTVPASLDS
SRSEPMQQLLDPNTLQQSVESRYRPNIILYSEGVLRSWGDGVAADCCETTFIEDRSPTKDSLEY
PDGKFIDLSADDIKIHTLSYDVEEEEEFQELESDYSSDTESEDNFLMMPPRDHLGLSVFSMLCC
FWPLGIAAFYLSHETNKAVAKGDLHQASTSSRRALFLAVLSITIGTGVYVGVAVALIAYLSKNN
HL

hide sequence

RefSeq Acc Id:

XP_011527658 ⟸ XM_011529356

- Peptide Label:

isoform X4

- Sequence:

show sequence

MDGIIEQKSMLVHSKISDAGKRNGLINTRNLMAESRDGLVSVYPAPQYQSHRVGASTVPASLDS
SRSEPMQQLLDPNTLQQSVESRYRPNIILYSEGVLRSWGDGVAADCCETTFIEDRSPTKDSLEY
PDGKFIDLSADDIKIHTLSYDVEEEEEFQELESDYSSDTESEDNFLMMPPRDHLGLSVFSMLCC
FWPLGIAAFYLSHELPFLPRSIHEPVSMPTAEATWACFVL

hide sequence

RefSeq Acc Id:

XP_011527660 ⟸ XM_011529358

- Peptide Label:

isoform X5

- Sequence:

show sequence

MDGIIEQKSMLVHSKISDAGKRNGLINTRNLMAESRDGLVSVYPAPQYQSHRVGASTVPASLDS
SRSEPMQQLLDPNTLQQSVESRYRPNIILYSEGVLRSWGDGVAADCCETTFIEDRSPTKDSLEY
PDGKFIDLSADDIKIHTLSYDVEEEEEFQELESDYSSDTESEDNFLMMPPRDHLGLSVFSMLCC
FWPLGIAAFYLSHE

hide sequence

RefSeq Acc Id:

XP_011527649 ⟸ XM_011529347

- Peptide Label:

isoform X1

- Sequence:

show sequence

MDGIIEQKSMLVHSKISDAGKRNGLINTRNLMAESRDGLVSVYPAPQYQSHRVGASTVPASLDS
SRSEPMQQLLDPNTLQQSVESRYRPNIILYSEGVLRSWGDGVAADCCETTFIEDRSPTKDSLEY
PDGKFIDLSADDIKIHTLSYDVEEEEEFQELESDYSSDTESEDNFLMMPPRDHLGLSVFSMLCC
FWPLGIAAFYLSHELITLEEMAAFNSSILFSSSQGLVPWTSSIRVIWERFRIVKSRQLPRPADS
EALGTGLAVWV

hide sequence

RefSeq Acc Id:

XP_011527650 ⟸ XM_011529348

- Peptide Label:

isoform X1

- Sequence:

show sequence

MDGIIEQKSMLVHSKISDAGKRNGLINTRNLMAESRDGLVSVYPAPQYQSHRVGASTVPASLDS
SRSEPMQQLLDPNTLQQSVESRYRPNIILYSEGVLRSWGDGVAADCCETTFIEDRSPTKDSLEY
PDGKFIDLSADDIKIHTLSYDVEEEEEFQELESDYSSDTESEDNFLMMPPRDHLGLSVFSMLCC
FWPLGIAAFYLSHELITLEEMAAFNSSILFSSSQGLVPWTSSIRVIWERFRIVKSRQLPRPADS
EALGTGLAVWV

hide sequence

RefSeq Acc Id:

XP_011527652 ⟸ XM_011529350

- Peptide Label:

isoform X1

- Sequence:

show sequence

MDGIIEQKSMLVHSKISDAGKRNGLINTRNLMAESRDGLVSVYPAPQYQSHRVGASTVPASLDS
SRSEPMQQLLDPNTLQQSVESRYRPNIILYSEGVLRSWGDGVAADCCETTFIEDRSPTKDSLEY
PDGKFIDLSADDIKIHTLSYDVEEEEEFQELESDYSSDTESEDNFLMMPPRDHLGLSVFSMLCC
FWPLGIAAFYLSHELITLEEMAAFNSSILFSSSQGLVPWTSSIRVIWERFRIVKSRQLPRPADS
EALGTGLAVWV

hide sequence

RefSeq Acc Id:

XP_011527653 ⟸ XM_011529351

- Peptide Label:

isoform X1

- Sequence:

show sequence

MDGIIEQKSMLVHSKISDAGKRNGLINTRNLMAESRDGLVSVYPAPQYQSHRVGASTVPASLDS
SRSEPMQQLLDPNTLQQSVESRYRPNIILYSEGVLRSWGDGVAADCCETTFIEDRSPTKDSLEY
PDGKFIDLSADDIKIHTLSYDVEEEEEFQELESDYSSDTESEDNFLMMPPRDHLGLSVFSMLCC
FWPLGIAAFYLSHELITLEEMAAFNSSILFSSSQGLVPWTSSIRVIWERFRIVKSRQLPRPADS
EALGTGLAVWV

hide sequence

RefSeq Acc Id:

XP_011527656 ⟸ XM_011529354

- Peptide Label:

isoform X1

- Sequence:

show sequence

MDGIIEQKSMLVHSKISDAGKRNGLINTRNLMAESRDGLVSVYPAPQYQSHRVGASTVPASLDS
SRSEPMQQLLDPNTLQQSVESRYRPNIILYSEGVLRSWGDGVAADCCETTFIEDRSPTKDSLEY
PDGKFIDLSADDIKIHTLSYDVEEEEEFQELESDYSSDTESEDNFLMMPPRDHLGLSVFSMLCC
FWPLGIAAFYLSHELITLEEMAAFNSSILFSSSQGLVPWTSSIRVIWERFRIVKSRQLPRPADS
EALGTGLAVWV

hide sequence

RefSeq Acc Id:

XP_011527655 ⟸ XM_011529353

- Peptide Label:

isoform X1

- Sequence:

show sequence

MDGIIEQKSMLVHSKISDAGKRNGLINTRNLMAESRDGLVSVYPAPQYQSHRVGASTVPASLDS
SRSEPMQQLLDPNTLQQSVESRYRPNIILYSEGVLRSWGDGVAADCCETTFIEDRSPTKDSLEY
PDGKFIDLSADDIKIHTLSYDVEEEEEFQELESDYSSDTESEDNFLMMPPRDHLGLSVFSMLCC
FWPLGIAAFYLSHELITLEEMAAFNSSILFSSSQGLVPWTSSIRVIWERFRIVKSRQLPRPADS
EALGTGLAVWV

hide sequence

RefSeq Acc Id:

NP_001310535 ⟸ NM_001323606

- UniProtKB:

Q6IA30 (UniProtKB/Swiss-Prot), Q9H514 (UniProtKB/Swiss-Prot), Q9H7V2 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MDGIIEQKSMLVHSKISDAGKRNGLINTRNLMAESRDGLVSVYPAPQYQSHRVGASTVPASLDS
SRSEPMQQLLDPNTLQQSVESRYRPNIILYSEGVLRSWGDGVAADCCETTFIEDRSPTKDSLEY
PDGKFIDLSADDIKIHTLSYDVEEEEEFQELESDYSSDTESEDNFLMMPPRDHLGLSVFSMLCC
FWPLGIAAFYLSHETNKAVAKGDLHQASTSSRRALFLAVLSITIGTGVYVGVAVALIAYLSKNN
HL

hide sequence

RefSeq Acc Id:

NP_001310536 ⟸ NM_001323607

- UniProtKB:

Q6IA30 (UniProtKB/Swiss-Prot), Q9H514 (UniProtKB/Swiss-Prot), Q9H7V2 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MDGIIEQKSMLVHSKISDAGKRNGLINTRNLMAESRDGLVSVYPAPQYQSHRVGASTVPASLDS
SRSEPMQQLLDPNTLQQSVESRYRPNIILYSEGVLRSWGDGVAADCCETTFIEDRSPTKDSLEY
PDGKFIDLSADDIKIHTLSYDVEEEEEFQELESDYSSDTESEDNFLMMPPRDHLGLSVFSMLCC
FWPLGIAAFYLSHETNKAVAKGDLHQASTSSRRALFLAVLSITIGTGVYVGVAVALIAYLSKNN
HL

hide sequence

RefSeq Acc Id:	XP_016883558 ⟸ XM_017028069
- Peptide Label:	isoform X6
- Sequence:	show sequence MDGIIEQKSMLVHSKISDAGKRNGLINTRNLMAESRDGLVSVYPAPQYQSHRVGASTVPASLDS SRSEPMQQLLDPNTLQQSVESRYRPNIILYSEGVLRSWGDGVAADCCETTFIEDRSPTKDSLEY PDGKFIDLSADDIKIHTLSYDVEEEEEFQELE hide sequence

RefSeq Acc Id:	XP_016883554 ⟸ XM_017028065
- Peptide Label:	isoform X2
- UniProtKB:	Q6IA30 (UniProtKB/Swiss-Prot), Q9H514 (UniProtKB/Swiss-Prot), Q9H7V2 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MDGIIEQKSMLVHSKISDAGKRNGLINTRNLMAESRDGLVSVYPAPQYQSHRVGASTVPASLDS SRSEPMQQLLDPNTLQQSVESRYRPNIILYSEGVLRSWGDGVAADCCETTFIEDRSPTKDSLEY PDGKFIDLSADDIKIHTLSYDVEEEEEFQELESDYSSDTESEDNFLMMPPRDHLGLSVFSMLCC FWPLGIAAFYLSHETNKAVAKGDLHQASTSSRRALFLAVLSITIGTGVYVGVAVALIAYLSKNN HL hide sequence

RefSeq Acc Id:	XP_016883556 ⟸ XM_017028067
- Peptide Label:	isoform X2
- UniProtKB:	Q6IA30 (UniProtKB/Swiss-Prot), Q9H514 (UniProtKB/Swiss-Prot), Q9H7V2 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MDGIIEQKSMLVHSKISDAGKRNGLINTRNLMAESRDGLVSVYPAPQYQSHRVGASTVPASLDS SRSEPMQQLLDPNTLQQSVESRYRPNIILYSEGVLRSWGDGVAADCCETTFIEDRSPTKDSLEY PDGKFIDLSADDIKIHTLSYDVEEEEEFQELESDYSSDTESEDNFLMMPPRDHLGLSVFSMLCC FWPLGIAAFYLSHETNKAVAKGDLHQASTSSRRALFLAVLSITIGTGVYVGVAVALIAYLSKNN HL hide sequence

RefSeq Acc Id:	XP_016883555 ⟸ XM_017028066
- Peptide Label:	isoform X2
- UniProtKB:	Q6IA30 (UniProtKB/Swiss-Prot), Q9H514 (UniProtKB/Swiss-Prot), Q9H7V2 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MDGIIEQKSMLVHSKISDAGKRNGLINTRNLMAESRDGLVSVYPAPQYQSHRVGASTVPASLDS SRSEPMQQLLDPNTLQQSVESRYRPNIILYSEGVLRSWGDGVAADCCETTFIEDRSPTKDSLEY PDGKFIDLSADDIKIHTLSYDVEEEEEFQELESDYSSDTESEDNFLMMPPRDHLGLSVFSMLCC FWPLGIAAFYLSHETNKAVAKGDLHQASTSSRRALFLAVLSITIGTGVYVGVAVALIAYLSKNN HL hide sequence

RefSeq Acc Id:

XP_016883553 ⟸ XM_017028064

- Peptide Label:

isoform X1

- Sequence:

show sequence

MDGIIEQKSMLVHSKISDAGKRNGLINTRNLMAESRDGLVSVYPAPQYQSHRVGASTVPASLDS
SRSEPMQQLLDPNTLQQSVESRYRPNIILYSEGVLRSWGDGVAADCCETTFIEDRSPTKDSLEY
PDGKFIDLSADDIKIHTLSYDVEEEEEFQELESDYSSDTESEDNFLMMPPRDHLGLSVFSMLCC
FWPLGIAAFYLSHELITLEEMAAFNSSILFSSSQGLVPWTSSIRVIWERFRIVKSRQLPRPADS
EALGTGLAVWV

hide sequence

RefSeq Acc Id:	XP_016883557 ⟸ XM_017028068
- Peptide Label:	isoform X2
- UniProtKB:	Q6IA30 (UniProtKB/Swiss-Prot), Q9H514 (UniProtKB/Swiss-Prot), Q9H7V2 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MDGIIEQKSMLVHSKISDAGKRNGLINTRNLMAESRDGLVSVYPAPQYQSHRVGASTVPASLDS SRSEPMQQLLDPNTLQQSVESRYRPNIILYSEGVLRSWGDGVAADCCETTFIEDRSPTKDSLEY PDGKFIDLSADDIKIHTLSYDVEEEEEFQELESDYSSDTESEDNFLMMPPRDHLGLSVFSMLCC FWPLGIAAFYLSHETNKAVAKGDLHQASTSSRRALFLAVLSITIGTGVYVGVAVALIAYLSKNN HL hide sequence

RefSeq Acc Id:

ENSP00000366058 ⟸ ENST00000376862

RefSeq Acc Id:	XP_047296455 ⟸ XM_047440499
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047296452 ⟸ XM_047440496
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_047296453 ⟸ XM_047440497
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_047296454 ⟸ XM_047440498
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_047296456 ⟸ XM_047440500
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054180005 ⟸ XM_054324030
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054180006 ⟸ XM_054324031
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054180007 ⟸ XM_054324032
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054179992 ⟸ XM_054324017
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054179993 ⟸ XM_054324018
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054179990 ⟸ XM_054324015
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054179991 ⟸ XM_054324016
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054180008 ⟸ XM_054324033
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054180002 ⟸ XM_054324027
- Peptide Label:	isoform X2
- UniProtKB:	Q9H7V2 (UniProtKB/Swiss-Prot), Q6IA30 (UniProtKB/Swiss-Prot), Q9H514 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054180001 ⟸ XM_054324026
- Peptide Label:	isoform X2
- UniProtKB:	Q9H7V2 (UniProtKB/Swiss-Prot), Q6IA30 (UniProtKB/Swiss-Prot), Q9H514 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054179999 ⟸ XM_054324024
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054179994 ⟸ XM_054324019
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054179995 ⟸ XM_054324020
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054179996 ⟸ XM_054324021
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054179997 ⟸ XM_054324022
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054180009 ⟸ XM_054324034
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054180004 ⟸ XM_054324029
- Peptide Label:	isoform X2
- UniProtKB:	Q9H7V2 (UniProtKB/Swiss-Prot), Q6IA30 (UniProtKB/Swiss-Prot), Q9H514 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054179998 ⟸ XM_054324023
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054180000 ⟸ XM_054324025
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054180003 ⟸ XM_054324028
- Peptide Label:	isoform X2
- UniProtKB:	Q9H7V2 (UniProtKB/Swiss-Prot), Q6IA30 (UniProtKB/Swiss-Prot), Q9H514 (UniProtKB/Swiss-Prot)

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9H7V2-F1-model_v2	AlphaFold	Q9H7V2	1-258	view protein structure

Promoters

RGD ID:

13206555

Promoter ID:

EPDNEW_H26858

Type:

initiation region

Name:

SYNDIG1_1

Description:

synapse differentiation inducing 1

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H26859

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,469,192 - 24,469,252	EPDNEW

RGD ID:

13206559

Promoter ID:

EPDNEW_H26859

Type:

multiple initiation site

Name:

SYNDIG1_2

Description:

synapse differentiation inducing 1

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H26858

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	24,528,954 - 24,529,014	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:15885	AgrOrtholog
COSMIC	SYNDIG1	COSMIC
Ensembl Genes	ENSG00000101463	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000376862	ENTREZGENE
	ENST00000376862.4	UniProtKB/Swiss-Prot
GTEx	ENSG00000101463	GTEx
HGNC ID	HGNC:15885	ENTREZGENE
Human Proteome Map	SYNDIG1	Human Proteome Map
InterPro	CD225/Dispanin_fam	UniProtKB/Swiss-Prot
KEGG Report	hsa:79953	UniProtKB/Swiss-Prot
NCBI Gene	79953	ENTREZGENE
OMIM	614311	OMIM
PANTHER	SYNAPSE DIFFERENTIATION-INDUCING GENE PROTEIN 1	UniProtKB/Swiss-Prot
	UPF0338 PROTEIN	UniProtKB/Swiss-Prot
Pfam	CD225	UniProtKB/Swiss-Prot
PharmGKB	PA25752	PharmGKB
UniProt	Q6IA30	ENTREZGENE
	Q9H514	ENTREZGENE
	Q9H7V2	ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary	Q6IA30	UniProtKB/Swiss-Prot
	Q9H514	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2011-07-27	SYNDIG1	synapse differentiation inducing 1	TMEM90B	transmembrane protein 90B	Symbol and/or name change	5135510	APPROVED

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

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

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

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

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Imported Disease Annotations - ClinVar