DDX55 (DEAD-box helicase 55) - Rat Genome Database

Name: DDX55
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

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Gene: DDX55 (DEAD-box helicase 55) Homo sapiens

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Symbol:

DDX55

Name:

DEAD-box helicase 55

RGD ID:

1323439

HGNC Page

HGNC:20085

Description:

Enables RNA binding activity. Located in cytosol; nucleolus; and nucleoplasm.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

ATP-dependent RNA helicase DDX55; DEAD (Asp-Glu-Ala-Asp) box polypeptide 55; DEAD box protein 55; FLJ16577; KIAA1595; MGC33209

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Ddx55 (DEAD box helicase 55)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Ddx55 (DEAD-box helicase 55)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Ddx55 (DEAD-box helicase 55)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	DDX55 (DEAD-box helicase 55)	NCBI	Ortholog
Canis lupus familiaris (dog):	DDX55 (DEAD-box helicase 55)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Ddx55 (DEAD-box helicase 55)	NCBI	Ortholog
Sus scrofa (pig):	DDX55 (DEAD-box helicase 55)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	DDX55 (DEAD-box helicase 55)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Ddx55 (DEAD-box helicase 55)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Stfa3 (stefin A3)	HGNC	OMA
Alliance orthologs ³
Mus musculus (house mouse):	Ddx55 (DEAD box helicase 55)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Rattus norvegicus (Norway rat):	Ddx55 (DEAD-box helicase 55)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	ddx55 (DEAD (Asp-Glu-Ala-Asp) box polypeptide 55)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Drosophila melanogaster (fruit fly):	CG9630	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Saccharomyces cerevisiae (baker's yeast):	SPB4	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Caenorhabditis elegans (roundworm):	ZK512.2	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	ddx55.S	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	ddx55	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB)

Related Pseudogenes:

DDX55P1 LOC100421344

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	12	123,602,099 - 123,620,943 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	12	123,602,077 - 123,620,943 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	12	124,086,646 - 124,105,490 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	12	122,652,625 - 122,671,435 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	12	122,611,551 - 122,630,362	NCBI
Celera	12	123,683,109 - 123,701,918 (+)	NCBI		Celera
Cytogenetic Map	12	q24.31	NCBI
HuRef	12	121,048,035 - 121,066,826 (+)	NCBI		HuRef
CHM1_1	12	123,907,616 - 123,926,431 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	12	123,600,963 - 123,619,807 (+)	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

short chain acyl-CoA dehydrogenase deficiency (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dimethylhydrazine (ISO)

17beta-estradiol (EXP)

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

2-methylcholine (EXP)

4-phenylbutyric acid (EXP)

acrolein (EXP)

aflatoxin B1 (EXP)

alpha-pinene (EXP)

atrazine (EXP)

bisphenol A (ISO)

bisphenol F (ISO)

caffeine (EXP)

carbamazepine (EXP)

chlorpyrifos (ISO)

choline (ISO)

cyclosporin A (EXP)

DDE (EXP)

Dibutyl phosphate (EXP)

dibutyl phthalate (ISO)

diuron (EXP)

folic acid (ISO)

FR900359 (EXP)

L-methionine (ISO)

ozone (EXP)

paracetamol (ISO)

resveratrol (EXP,ISO)

sodium arsenite (ISO)

T-2 toxin (ISO)

temozolomide (EXP)

titanium dioxide (ISO)

urethane (EXP)

valproic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

chromatin looping (IEA)

chromatin remodeling (IEA)

Cellular Component

cytosol (IDA)

membrane (HDA)

nucleolus (IBA,IDA)

nucleoplasm (IDA)

Molecular Function

ATP binding (IEA)

ATP hydrolysis activity (IEA)

ATP-dependent H2AZ histone chaperone activity (IEA)

ATP-dependent H3-H4 histone complex chaperone activity (IEA)

chromatin extrusion motor activity (IEA)

cohesin loader activity (IEA)

DNA clamp loader activity (IEA)

helicase activity (IEA)

hydrolase activity (IEA)

nucleic acid binding (IEA)

protein binding (IPI)

RNA binding (HDA,IEA)

RNA helicase activity (IEA)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Spastic paraplegia (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:1552844	PMID:10997877	PMID:12477932	PMID:15489334	PMID:15635413	PMID:16344560	PMID:18187620	PMID:19946888	PMID:21081503	PMID:21145461	PMID:21244100	PMID:21832049
PMID:21873635	PMID:22658674	PMID:23449627	PMID:25281560	PMID:25416956	PMID:25921289	PMID:26186194	PMID:26344197	PMID:26496610	PMID:27926873	PMID:28514442	PMID:28515276
PMID:28695742	PMID:28977666	PMID:29298432	PMID:29509190	PMID:29568061	PMID:30196744	PMID:30209976	PMID:30884312	PMID:30940648	PMID:30948266	PMID:31091453	PMID:31343991
PMID:31527615	PMID:31586073	PMID:31665637	PMID:31822558	PMID:32296183	PMID:32433965	PMID:32694731	PMID:32807901	PMID:32877691	PMID:33048000	PMID:33226137	PMID:33306668
PMID:33536335	PMID:33545068	PMID:33742100	PMID:33961781	PMID:34079125	PMID:34189442	PMID:34244565	PMID:34349018	PMID:34373451	PMID:35013218	PMID:35271311	PMID:35575683
PMID:35652658	PMID:35696571	PMID:35850772	PMID:35915203	PMID:35944360	PMID:36089195	PMID:36215168	PMID:36232890	PMID:36244648	PMID:36526897	PMID:36574265	PMID:36912080
PMID:37267103	PMID:37314180	PMID:37689310	PMID:37827155	PMID:38697112	PMID:38777146

Genomics

Comparative Map Data

DDX55
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	12	123,602,099 - 123,620,943 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	12	123,602,077 - 123,620,943 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	12	124,086,646 - 124,105,490 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	12	122,652,625 - 122,671,435 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	12	122,611,551 - 122,630,362	NCBI
Celera	12	123,683,109 - 123,701,918 (+)	NCBI		Celera
Cytogenetic Map	12	q24.31	NCBI
HuRef	12	121,048,035 - 121,066,826 (+)	NCBI		HuRef
CHM1_1	12	123,907,616 - 123,926,431 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	12	123,600,963 - 123,619,807 (+)	NCBI		T2T-CHM13v2.0

Ddx55
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	5	124,690,895 - 124,707,723 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	5	124,690,927 - 124,707,723 (+)	Ensembl		GRCm39 Ensembl
GRCm38	5	124,552,832 - 124,569,660 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	5	124,552,864 - 124,569,660 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	5	125,002,873 - 125,018,947 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	5	124,813,504 - 124,829,590 (+)	NCBI		MGSCv36	mm8
Celera	5	121,629,125 - 121,645,637 (+)	NCBI		Celera
Cytogenetic Map	5	F	NCBI
cM Map	5	63.66	NCBI

Ddx55
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	12	37,695,444 - 37,711,198 (-)	NCBI		GRCr8
mRatBN7.2	12	32,034,462 - 32,050,218 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	12	32,034,462 - 32,050,219 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	12	33,213,387 - 33,229,625 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	12	33,824,708 - 33,840,948 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	12	32,876,575 - 32,892,814 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	12	37,453,005 - 37,468,935 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	12	37,453,005 - 37,468,935 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	12	39,324,015 - 39,339,763 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	12	33,147,211 - 33,162,925 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	12	33,011,099 - 33,026,931 (-)	NCBI
Celera	12	33,723,880 - 33,740,275 (-)	NCBI		Celera
Cytogenetic Map	12	q15	NCBI

Ddx55
(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_004955482	5,389,195 - 5,401,873 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955482	5,389,195 - 5,401,885 (-)	NCBI	ChiLan1.0	ChiLan1.0

DDX55
(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	10	131,675,799 - 131,695,839 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	12	131,672,558 - 131,692,216 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	12	121,187,465 - 121,206,287 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	12	125,414,730 - 125,433,147 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	12	125,414,730 - 125,433,147 (+)	Ensembl	panpan1.1		panPan2

DDX55
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	26	6,022,739 - 6,036,539 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	26	6,023,288 - 6,036,782 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	26	6,185,611 - 6,199,418 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	26	6,272,817 - 6,286,633 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	26	6,272,817 - 6,286,617 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	26	6,206,294 - 6,220,107 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	26	6,298,665 - 6,312,477 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	26	6,251,877 - 6,265,689 (-)	NCBI		UU_Cfam_GSD_1.0

Ddx55
(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_024405118	158,257,907 - 158,282,235 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936558	1,200,064 - 1,221,521 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936558	1,198,281 - 1,221,497 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

DDX55
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	14	29,368,023 - 29,387,776 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	14	29,368,018 - 29,388,785 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	14	31,060,310 - 31,080,076 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

DDX55
(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	11	118,930,642 - 118,949,331 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	11	118,930,683 - 118,948,814 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666037	126,326,273 - 126,346,294 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Ddx55
(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_004624747	23,401,323 - 23,412,804 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624747	23,401,267 - 23,413,002 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in DDX55
48 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 12q24.23-24.33(chr12:118165459-133182322)x3	copy number gain	See cases [RCV000050866]	Chr12:118165459..133182322 [GRCh38] Chr12:118603264..133758908 [GRCh37] Chr12:117087647..132268981 [NCBI36] Chr12:12q24.23-24.33	pathogenic
GRCh38/hg38 12q24.31-24.33(chr12:122985202-130714574)x1	copy number loss	See cases [RCV000051345]	Chr12:122985202..130714574 [GRCh38] Chr12:123469749..131199119 [GRCh37] Chr12:122035702..129765072 [NCBI36] Chr12:12q24.31-24.33	pathogenic
GRCh38/hg38 12q24.31-24.33(chr12:123444758-133191400)x3	copy number gain	See cases [RCV000051151]	Chr12:123444758..133191400 [GRCh38] Chr12:123929305..133767986 [GRCh37] Chr12:122495258..132278059 [NCBI36] Chr12:12q24.31-24.33	pathogenic
GRCh38/hg38 12q24.21-24.33(chr12:115131583-133166920)x3	copy number gain	See cases [RCV000053689]	Chr12:115131583..133166920 [GRCh38] Chr12:115569388..133743506 [GRCh37] Chr12:114053771..132253579 [NCBI36] Chr12:12q24.21-24.33	pathogenic
GRCh38/hg38 12q24.23-24.33(chr12:119417382-133191400)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053691]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053691]\|See cases [RCV000053691]	Chr12:119417382..133191400 [GRCh38] Chr12:119855187..133767986 [GRCh37] Chr12:118339570..132278059 [NCBI36] Chr12:12q24.23-24.33	pathogenic
GRCh38/hg38 12q24.31-24.33(chr12:123365769-133191400)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053693]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053693]\|See cases [RCV000053693]	Chr12:123365769..133191400 [GRCh38] Chr12:123850316..133767986 [GRCh37] Chr12:122416269..132278059 [NCBI36] Chr12:12q24.31-24.33	pathogenic
GRCh38/hg38 12q24.31(chr12:123509825-123975309)x3	copy number gain	See cases [RCV000134900]	Chr12:123509825..123975309 [GRCh38] Chr12:123994372..124459856 [GRCh37] Chr12:122560325..123025809 [NCBI36] Chr12:12q24.31	uncertain significance
GRCh38/hg38 12q24.31-24.33(chr12:123509825-133191400)x3	copy number gain	See cases [RCV000135535]	Chr12:123509825..133191400 [GRCh38] Chr12:123994372..133767986 [GRCh37] Chr12:122560325..132278059 [NCBI36] Chr12:12q24.31-24.33	pathogenic
GRCh38/hg38 12q24.31-24.33(chr12:120697672-133202490)x3	copy number gain	See cases [RCV000137651]	Chr12:120697672..133202490 [GRCh38] Chr12:121135475..133779076 [GRCh37] Chr12:119619858..132289149 [NCBI36] Chr12:12q24.31-24.33	pathogenic
GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	copy number gain	See cases [RCV000139555]	Chr12:121271..133196807 [GRCh38] Chr12:282465..133773393 [GRCh37] Chr12:100698..132283466 [NCBI36] Chr12:12p13.33-q24.33	pathogenic
GRCh38/hg38 12q24.31-24.32(chr12:120718786-127500215)x1	copy number loss	See cases [RCV000142454]	Chr12:120718786..127500215 [GRCh38] Chr12:121156589..127984760 [GRCh37] Chr12:119640972..126550713 [NCBI36] Chr12:12q24.31-24.32	pathogenic
GRCh38/hg38 12q24.31-24.32(chr12:121917758-127802717)x1	copy number loss	See cases [RCV000143250]	Chr12:121917758..127802717 [GRCh38] Chr12:122355664..128287262 [GRCh37] Chr12:120840047..126853215 [NCBI36] Chr12:12q24.31-24.32	pathogenic
GRCh38/hg38 12q24.21-24.33(chr12:114268403-133201316)x3	copy number gain	See cases [RCV000143656]	Chr12:114268403..133201316 [GRCh38] Chr12:114706208..133777902 [GRCh37] Chr12:113190591..132287975 [NCBI36] Chr12:12q24.21-24.33	pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3	copy number gain	See cases [RCV000258805]	Chr12:1..133851895 [GRCh37] Chr12:12p13.33-q24.33	pathogenic\|likely pathogenic
GRCh37/hg19 12q24.31-24.32(chr12:122726807-127365912)x1	copy number loss	See cases [RCV000449178]	Chr12:122726807..127365912 [GRCh37] Chr12:12q24.31-24.32	likely pathogenic
GRCh37/hg19 12q24.31(chr12:123404920-124192840)	copy number gain	See cases [RCV000446571]	Chr12:123404920..124192840 [GRCh37] Chr12:12q24.31	likely pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3	copy number gain	See cases [RCV000510482]	Chr12:173787..133777902 [GRCh37] Chr12:12p13.33-q24.33	pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)	copy number gain	See cases [RCV000511643]	Chr12:173787..133777902 [GRCh37] Chr12:12p13.33-q24.33	pathogenic
NM_020936.3(DDX55):c.1325G>T (p.Arg442Ile)	single nucleotide variant	not specified [RCV004325684]	Chr12:123618829 [GRCh38] Chr12:124103376 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1759A>G (p.Lys587Glu)	single nucleotide variant	not specified [RCV004290280]	Chr12:123620096 [GRCh38] Chr12:124104643 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.317C>G (p.Thr106Arg)	single nucleotide variant	not specified [RCV004311968]	Chr12:123607502 [GRCh38] Chr12:124092049 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1361G>A (p.Gly454Asp)	single nucleotide variant	not specified [RCV004320613]	Chr12:123619459 [GRCh38] Chr12:124104006 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.52C>G (p.Pro18Ala)	single nucleotide variant	not specified [RCV004307418]	Chr12:123602200 [GRCh38] Chr12:124086747 [GRCh37] Chr12:12q24.31	uncertain significance
GRCh37/hg19 12q24.31(chr12:124097565-124462296)x3	copy number gain	not provided [RCV000683425]	Chr12:124097565..124462296 [GRCh37] Chr12:12q24.31	uncertain significance
GRCh37/hg19 12q24.23-24.33(chr12:120367241-133777645)x3	copy number gain	not provided [RCV000738070]	Chr12:120367241..133777645 [GRCh37] Chr12:12q24.23-24.33	pathogenic
GRCh37/hg19 12q24.31(chr12:122706844-124294517)x3	copy number gain	not provided [RCV000738079]	Chr12:122706844..124294517 [GRCh37] Chr12:12q24.31	uncertain significance
GRCh37/hg19 12p13.33-q24.33(chr12:191619-133777645)x3	copy number gain	not provided [RCV000750246]	Chr12:191619..133777645 [GRCh37] Chr12:12p13.33-q24.33	pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:621220-133779118)x3	copy number gain	not provided [RCV000750253]	Chr12:621220..133779118 [GRCh37] Chr12:12p13.33-q24.33	pathogenic
NM_020936.3(DDX55):c.1385A>G (p.Lys462Arg)	single nucleotide variant	not specified [RCV004311889]	Chr12:123619483 [GRCh38] Chr12:124104030 [GRCh37] Chr12:12q24.31	uncertain significance
GRCh37/hg19 12q24.31-24.32(chr12:122169403-129084163)x1	copy number loss	not provided [RCV000848395]	Chr12:122169403..129084163 [GRCh37] Chr12:12q24.31-24.32	pathogenic
GRCh37/hg19 12q24.31(chr12:123807132-124299781)x3	copy number gain	not provided [RCV001260170]	Chr12:123807132..124299781 [GRCh37] Chr12:12q24.31	uncertain significance
GRCh37/hg19 12q24.31-24.32(chr12:123878845-126829341)	copy number loss	Severe short stature [RCV001352637]	Chr12:123878845..126829341 [GRCh37] Chr12:12q24.31-24.32	pathogenic
NC_000012.11:g.(?_123738222)_(124242579_?)dup	duplication	Combined oxidative phosphorylation defect type 7 [RCV002239168]	Chr12:123738222..124242579 [GRCh37] Chr12:12q24.31	uncertain significance
GRCh37/hg19 12q24.22-24.33(chr12:117461902-133841395)x3	copy number gain	Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures [RCV001801213]	Chr12:117461902..133841395 [GRCh37] Chr12:12q24.22-24.33	likely pathogenic
GRCh37/hg19 12q24.31(chr12:124097565-124278641)	copy number loss	not specified [RCV002053032]	Chr12:124097565..124278641 [GRCh37] Chr12:12q24.31	uncertain significance
GRCh37/hg19 12q24.31(chr12:123807132-124300075)x3	copy number gain	not provided [RCV001834350]	Chr12:123807132..124300075 [GRCh37] Chr12:12q24.31	uncertain significance
NC_000012.11:g.(?_122277634)_(124242579_?)del	deletion	not provided [RCV003111519]	Chr12:122277634..124242579 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.542T>G (p.Phe181Cys)	single nucleotide variant	not specified [RCV004246922]	Chr12:123608820 [GRCh38] Chr12:124093367 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1381C>T (p.Pro461Ser)	single nucleotide variant	not specified [RCV004144859]	Chr12:123619479 [GRCh38] Chr12:124104026 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1304A>G (p.His435Arg)	single nucleotide variant	not specified [RCV004130850]	Chr12:123618808 [GRCh38] Chr12:124103355 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1157A>G (p.Asn386Ser)	single nucleotide variant	not specified [RCV004076985]	Chr12:123617865 [GRCh38] Chr12:124102412 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.52C>T (p.Pro18Ser)	single nucleotide variant	not specified [RCV004172140]	Chr12:123602200 [GRCh38] Chr12:124086747 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.688G>A (p.Val230Met)	single nucleotide variant	not specified [RCV004079709]	Chr12:123610075 [GRCh38] Chr12:124094622 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.296A>G (p.Asp99Gly)	single nucleotide variant	not specified [RCV004238179]	Chr12:123607481 [GRCh38] Chr12:124092028 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.936G>A (p.Met312Ile)	single nucleotide variant	not specified [RCV004240172]	Chr12:123615296 [GRCh38] Chr12:124099843 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.827C>T (p.Thr276Ile)	single nucleotide variant	not specified [RCV004135523]	Chr12:123615187 [GRCh38] Chr12:124099734 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.897T>G (p.Ile299Met)	single nucleotide variant	not specified [RCV004118332]	Chr12:123615257 [GRCh38] Chr12:124099804 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1153A>C (p.Ile385Leu)	single nucleotide variant	not specified [RCV004169340]	Chr12:123617861 [GRCh38] Chr12:124102408 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1575G>C (p.Lys525Asn)	single nucleotide variant	not specified [RCV004236742]	Chr12:123619673 [GRCh38] Chr12:124104220 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1607A>C (p.Glu536Ala)	single nucleotide variant	not specified [RCV004117759]	Chr12:123619705 [GRCh38] Chr12:124104252 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1123A>G (p.Met375Val)	single nucleotide variant	not specified [RCV004150216]	Chr12:123617831 [GRCh38] Chr12:124102378 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.458C>A (p.Ala153Asp)	single nucleotide variant	not specified [RCV004099099]	Chr12:123608736 [GRCh38] Chr12:124093283 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.745T>G (p.Cys249Gly)	single nucleotide variant	not specified [RCV004108575]	Chr12:123613173 [GRCh38] Chr12:124097720 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1076C>T (p.Thr359Ile)	single nucleotide variant	not specified [RCV004099098]	Chr12:123617784 [GRCh38] Chr12:124102331 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1429G>A (p.Val477Met)	single nucleotide variant	not specified [RCV004192425]	Chr12:123619527 [GRCh38] Chr12:124104074 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1050T>A (p.Ser350Arg)	single nucleotide variant	not specified [RCV004189127]	Chr12:123617758 [GRCh38] Chr12:124102305 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1350C>A (p.Ser450Arg)	single nucleotide variant	not specified [RCV004186406]	Chr12:123619448 [GRCh38] Chr12:124103995 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.644C>T (p.Ala215Val)	single nucleotide variant	not specified [RCV004138480]	Chr12:123610031 [GRCh38] Chr12:124094578 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.298G>A (p.Glu100Lys)	single nucleotide variant	not specified [RCV004269294]	Chr12:123607483 [GRCh38] Chr12:124092030 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1448C>T (p.Thr483Met)	single nucleotide variant	not specified [RCV004287250]	Chr12:123619546 [GRCh38] Chr12:124104093 [GRCh37] Chr12:12q24.31	uncertain significance
GRCh37/hg19 12q24.31(chr12:121341598-124103434)x3	copy number gain	See cases [RCV003329531]	Chr12:121341598..124103434 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1193G>A (p.Arg398Lys)	single nucleotide variant	not specified [RCV004365586]	Chr12:123618697 [GRCh38] Chr12:124103244 [GRCh37] Chr12:12q24.31	likely benign
NM_020936.3(DDX55):c.1063C>T (p.Arg355Cys)	single nucleotide variant	not specified [RCV004356756]	Chr12:123617771 [GRCh38] Chr12:124102318 [GRCh37] Chr12:12q24.31	uncertain significance
GRCh37/hg19 12q24.31-24.33(chr12:121551496-133777902)x3	copy number gain	not provided [RCV003484881]	Chr12:121551496..133777902 [GRCh37] Chr12:12q24.31-24.33	pathogenic
GRCh37/hg19 12q24.31-24.33(chr12:120880079-133777902)x3	copy number gain	not provided [RCV003484880]	Chr12:120880079..133777902 [GRCh37] Chr12:12q24.31-24.33	pathogenic
GRCh37/hg19 12q24.31(chr12:123640263-124319101)x1	copy number loss	not specified [RCV003986985]	Chr12:123640263..124319101 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1358G>A (p.Arg453Gln)	single nucleotide variant	not specified [RCV004368059]	Chr12:123619456 [GRCh38] Chr12:124104003 [GRCh37] Chr12:12q24.31	likely benign
NM_020936.3(DDX55):c.704C>T (p.Ala235Val)	single nucleotide variant	not specified [RCV004368064]	Chr12:123610091 [GRCh38] Chr12:124094638 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.974C>T (p.Thr325Ile)	single nucleotide variant	not specified [RCV004368067]	Chr12:123616528 [GRCh38] Chr12:124101075 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1139T>G (p.Ile380Ser)	single nucleotide variant	not specified [RCV004368053]	Chr12:123617847 [GRCh38] Chr12:124102394 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.116C>T (p.Thr39Ile)	single nucleotide variant	not specified [RCV004368055]	Chr12:123605938 [GRCh38] Chr12:124090485 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1201G>C (p.Ala401Pro)	single nucleotide variant	not specified [RCV004368057]	Chr12:123618705 [GRCh38] Chr12:124103252 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1498G>C (p.Glu500Gln)	single nucleotide variant	not specified [RCV004368060]	Chr12:123619596 [GRCh38] Chr12:124104143 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.206A>G (p.Glu69Gly)	single nucleotide variant	not specified [RCV004368061]	Chr12:123606119 [GRCh38] Chr12:124090666 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.280C>G (p.Leu94Val)	single nucleotide variant	not specified [RCV004368062]	Chr12:123607465 [GRCh38] Chr12:124092012 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.943C>T (p.Arg315Cys)	single nucleotide variant	not specified [RCV004368066]	Chr12:123615303 [GRCh38] Chr12:124099850 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1142A>G (p.Asn381Ser)	single nucleotide variant	not specified [RCV004368054]	Chr12:123617850 [GRCh38] Chr12:124102397 [GRCh37] Chr12:12q24.31	likely benign
NM_020936.3(DDX55):c.685G>A (p.Gly229Ser)	single nucleotide variant	not specified [RCV004368063]	Chr12:123610072 [GRCh38] Chr12:124094619 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.988C>T (p.Arg330Trp)	single nucleotide variant	not specified [RCV004368068]	Chr12:123616542 [GRCh38] Chr12:124101089 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.1228A>G (p.Met410Val)	single nucleotide variant	not specified [RCV004368058]	Chr12:123618732 [GRCh38] Chr12:124103279 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.721C>T (p.Arg241Cys)	single nucleotide variant	not specified [RCV004368065]	Chr12:123610108 [GRCh38] Chr12:124094655 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.511G>C (p.Asp171His)	single nucleotide variant	not specified [RCV004611724]	Chr12:123608789 [GRCh38] Chr12:124093336 [GRCh37] Chr12:12q24.31	uncertain significance
NC_000012.11:g.(?_120270555)_(124242579_?)dup	duplication	Deficiency of butyryl-CoA dehydrogenase [RCV004578383]	Chr12:120270555..124242579 [GRCh37] Chr12:12q24.23-24.31	uncertain significance
NM_020936.3(DDX55):c.775G>A (p.Val259Ile)	single nucleotide variant	not specified [RCV004611725]	Chr12:123613203 [GRCh38] Chr12:124097750 [GRCh37] Chr12:12q24.31	uncertain significance
NM_020936.3(DDX55):c.23C>T (p.Ser8Phe)	single nucleotide variant	not specified [RCV004611726]	Chr12:123602171 [GRCh38] Chr12:124086718 [GRCh37] Chr12:12q24.31	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	2924
Count of miRNA genes:	999
Interacting mature miRNAs:	1233
Transcripts:	ENST00000238146, ENST00000354291, ENST00000421670, ENST00000536079, ENST00000538744, ENST00000539934, ENST00000540763, ENST00000541259, ENST00000542286, ENST00000543016, ENST00000544429, ENST00000544738, ENST00000545042
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

QTLs in Region (GRCh38)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
1298449	UAE2_H	Urinary albumin excretion QTL 2 (human)	2	0.005	Urinary albumin excretion	urine albumin:creatinine ratio (ACR)	12	102836889	128836889	Human
407344196	GWAS993172_H	high density lipoprotein cholesterol measurement QTL GWAS993172 (human)		3e-15	high density lipoprotein cholesterol measurement	blood high density lipoprotein cholesterol level (CMO:0000052)	12	123618347	123618348	Human
1643452	BW104_H	Body weight QTL 104 (human)	1.89	0.005	Body fat amount	abdominal visceral	12	102395874	128395874	Human
407237692	GWAS886668_H	apolipoprotein A 1 measurement QTL GWAS886668 (human)		6e-14	apolipoprotein A 1 measurement	blood apolipoprotein AI level (CMO:0000520)	12	123618347	123618348	Human
407036094	GWAS685070_H	alcohol consumption measurement QTL GWAS685070 (human)		7e-11	alcohol consumption measurement	ethanol drink intake rate (CMO:0001407)	12	123620679	123620680	Human
407412374	GWAS1061350_H	alcohol consumption measurement QTL GWAS1061350 (human)		1e-10	alcohol consumption measurement	ethanol drink intake rate (CMO:0001407)	12	123620679	123620680	Human

Markers in Region

WI-12310

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	124,105,592 - 124,105,723	UniSTS	GRCh37
Build 36	12	122,671,545 - 122,671,676	RGD	NCBI36
Celera	12	123,702,028 - 123,702,159	RGD
Cytogenetic Map	12	q24.31	UniSTS
HuRef	12	121,066,936 - 121,067,067	UniSTS
GeneMap99-GB4 RH Map	12	479.33	UniSTS
Whitehead-RH Map	12	600.7	UniSTS
NCBI RH Map	12	777.7	UniSTS

RH98764

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	124,100,762 - 124,100,899	UniSTS	GRCh37
Build 36	12	122,666,715 - 122,666,852	RGD	NCBI36
Celera	12	123,697,198 - 123,697,335	RGD
Cytogenetic Map	12	q24.31	UniSTS
HuRef	12	121,062,126 - 121,062,263	UniSTS
GeneMap99-GB4 RH Map	12	479.55	UniSTS

G64577

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	124,092,069 - 124,092,362	UniSTS	GRCh37
Build 36	12	122,658,022 - 122,658,315	RGD	NCBI36
Celera	12	123,688,505 - 123,688,798	RGD
Cytogenetic Map	12	q24.31	UniSTS
HuRef	12	121,053,434 - 121,053,727	UniSTS

SHGC-149620

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	124,097,202 - 124,097,501	UniSTS	GRCh37
Build 36	12	122,663,155 - 122,663,454	RGD	NCBI36
Celera	12	123,693,638 - 123,693,937	RGD
Cytogenetic Map	12	q24.31	UniSTS
HuRef	12	121,058,566 - 121,058,865	UniSTS
TNG Radiation Hybrid Map	12	61097.0	UniSTS

G20768

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	124,105,663 - 124,105,791	UniSTS	GRCh37
Build 36	12	122,671,616 - 122,671,744	RGD	NCBI36
Celera	12	123,702,099 - 123,702,227	RGD
Cytogenetic Map	12	q24.31	UniSTS
HuRef	12	121,067,007 - 121,067,135	UniSTS

A006F32

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	124,105,663 - 124,105,791	UniSTS	GRCh37
Build 36	12	122,671,616 - 122,671,744	RGD	NCBI36
Celera	12	123,702,099 - 123,702,227	RGD
Cytogenetic Map	12	q24.31	UniSTS
HuRef	12	121,067,007 - 121,067,135	UniSTS
GeneMap99-GB4 RH Map	12	479.33	UniSTS
NCBI RH Map	12	778.6	UniSTS

GC29S0405

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	124,091,865 - 124,092,271	UniSTS	GRCh37
Build 36	12	122,657,818 - 122,658,224	RGD	NCBI36
Celera	12	123,688,301 - 123,688,707	RGD
Cytogenetic Map	12	q24.31	UniSTS
HuRef	12	121,053,230 - 121,053,636	UniSTS

GC29S06

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	124,093,101 - 124,093,454	UniSTS	GRCh37
Build 36	12	122,659,054 - 122,659,407	RGD	NCBI36
Celera	12	123,689,537 - 123,689,890	RGD
HuRef	12	121,054,465 - 121,054,818	UniSTS

GC29S08

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	124,097,586 - 124,097,891	UniSTS	GRCh37
Build 36	12	122,663,539 - 122,663,844	RGD	NCBI36
Celera	12	123,694,022 - 123,694,327	RGD
HuRef	12	121,058,950 - 121,059,255	UniSTS

STS-N26791

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	12	124,105,264 - 124,105,480	UniSTS	GRCh37
Build 36	12	122,671,217 - 122,671,433	RGD	NCBI36
Celera	12	123,701,700 - 123,701,916	RGD
Cytogenetic Map	12	q24.31	UniSTS
HuRef	12	121,066,608 - 121,066,824	UniSTS
GeneMap99-GB4 RH Map	12	479.55	UniSTS
NCBI RH Map	12	776.8	UniSTS

G38154

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	17	q12	UniSTS
Cytogenetic Map	3	q26.1	UniSTS
Cytogenetic Map	18	q21.32	UniSTS
Cytogenetic Map	17	q21.2-q21.3	UniSTS
Cytogenetic Map	19	q13.3	UniSTS
Cytogenetic Map	X	p11.3	UniSTS
Cytogenetic Map	3	q21.2	UniSTS
Cytogenetic Map	19	p13.3	UniSTS
Cytogenetic Map	7	q22.1	UniSTS
Cytogenetic Map	16	q11.2	UniSTS
Cytogenetic Map	11	q13	UniSTS
Cytogenetic Map	11	q23.3	UniSTS
Cytogenetic Map	1	p36.1	UniSTS
Cytogenetic Map	20	q11.2-q13.2	UniSTS
Cytogenetic Map	3	q13.33	UniSTS
Cytogenetic Map	19	p13.12	UniSTS
Cytogenetic Map	7	q36.3	UniSTS
Cytogenetic Map	1	p34.2	UniSTS
Cytogenetic Map	12	q24.31	UniSTS
Cytogenetic Map	7	p11.2	UniSTS
Cytogenetic Map	21	q22.3	UniSTS
Cytogenetic Map	17	q11.2	UniSTS
Cytogenetic Map	3	q23	UniSTS
Cytogenetic Map	16	q22.2	UniSTS
Cytogenetic Map	22	q13.1	UniSTS
Cytogenetic Map	1	p34	UniSTS
Cytogenetic Map	5	q11.2	UniSTS
Cytogenetic Map	7	q32.1	UniSTS
Cytogenetic Map	7	q11.23	UniSTS
Cytogenetic Map	4	p15.31	UniSTS
Cytogenetic Map	20	q11.22	UniSTS
Cytogenetic Map	17	q21	UniSTS
Cytogenetic Map	6	q21	UniSTS
Cytogenetic Map	5	q13.2	UniSTS
Cytogenetic Map	4	q32.3	UniSTS
Cytogenetic Map	3	p14.3	UniSTS
Cytogenetic Map	6	p24.3	UniSTS
Cytogenetic Map	2	q37	UniSTS
Cytogenetic Map	1	p32	UniSTS
Cytogenetic Map	3	p21.1	UniSTS

Expression

RNA-SEQ Expression

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2439	2788	2253	4974	1726	2351	6	624	1951	465	2270	7306	6472	53	3734	1	852	1744	1617	175	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_020936	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_135104	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_135105	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011538608	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019710	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019711	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019712	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019713	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019714	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019715	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019716	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019717	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019718	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019719	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019720	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017019721	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449102	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449103	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449104	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449105	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429221	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429222	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429223	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429224	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429225	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429226	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429227	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429228	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047429229	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372692	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372693	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372694	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372695	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372696	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372697	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372698	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372699	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372700	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372701	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372702	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372703	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372704	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372705	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372706	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372707	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372708	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054372709	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001748821	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001748822	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001748823	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001748824	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001748825	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001748826	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001748827	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001748828	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001748829	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AA403154	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AB046815	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC055713	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC117503	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK074219	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK131442	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK301043	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK307384	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL833756	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC030020	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC035911	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU619784	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471054	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068266	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA806426	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	GQ891432	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000238146 ⟹ ENSP00000238146

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	123,602,099 - 123,620,943 (+)	Ensembl

Ensembl Acc Id:

ENST00000354291 ⟹ ENSP00000346244

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	123,602,130 - 123,616,603 (+)	Ensembl

Ensembl Acc Id:

ENST00000421670 ⟹ ENSP00000442332

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	123,618,016 - 123,620,422 (+)	Ensembl

Ensembl Acc Id:

ENST00000536079

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	123,602,143 - 123,610,070 (+)	Ensembl

Ensembl Acc Id:

ENST00000538744 ⟹ ENSP00000443114

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	123,602,128 - 123,620,144 (+)	Ensembl

Ensembl Acc Id:

ENST00000539934

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	123,604,873 - 123,618,153 (+)	Ensembl

Ensembl Acc Id:

ENST00000540763 ⟹ ENSP00000446255

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	123,602,128 - 123,610,103 (+)	Ensembl

Ensembl Acc Id:

ENST00000541259

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	123,613,215 - 123,619,628 (+)	Ensembl

Ensembl Acc Id:

ENST00000542286

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	123,602,077 - 123,619,716 (+)	Ensembl

Ensembl Acc Id:

ENST00000543016

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	123,616,558 - 123,618,778 (+)	Ensembl

Ensembl Acc Id:

ENST00000544429

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	123,602,097 - 123,607,770 (+)	Ensembl

Ensembl Acc Id:

ENST00000544738 ⟹ ENSP00000442823

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	123,602,125 - 123,617,870 (+)	Ensembl

Ensembl Acc Id:

ENST00000545042

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	12	123,602,099 - 123,607,662 (+)	Ensembl

RefSeq Acc Id:

NM_020936 ⟹ NP_065987

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,620,943 (+)	NCBI
GRCh37	12	124,086,650 - 124,105,482 (+)	NCBI
Build 36	12	122,652,625 - 122,671,435 (+)	NCBI Archive
Celera	12	123,683,109 - 123,701,918 (+)	RGD
HuRef	12	121,048,035 - 121,066,826 (+)	ENTREZGENE
CHM1_1	12	123,907,568 - 123,926,439 (+)	NCBI
T2T-CHM13v2.0	12	123,600,963 - 123,619,807 (+)	NCBI

Sequence:

show sequence

GCACAAGGCGCGTTCGAGCAGCGGCGACCGACGCGGCGAAGGAGCGCGCCATGGAGCATGTGAC
AGAGGGCTCCTGGGAGTCGCTGCCTGTGCCGCTGCACCCGCAGGTGCTGGGCGCGCTGCGGGAG
CTGGGCTTCCCGTACATGACGCCGGTGCAGTCCGCAACCATCCCTCTGTTCATGCGAAACAAAG
ATGTCGCTGCAGAAGCGGTCACAGGTAGTGGCAAAACACTCGCTTTTGTCATCCCCATCCTGGA
AATTCTTCTGAGAAGAGAAGAGAAGTTAAAAAAGAGTCAGGTTGGAGCCATAATCATCACCCCC
ACTCGAGAGCTGGCCATTCAAATAGACGAGGTCCTGTCGCATTTCACGAAGCACTTCCCCGAGT
TCAGCCAGATTCTTTGGATCGGAGGCAGGAATCCTGGAGAAGATGTTGAGAGGTTTAAGCAACA
AGGTGGGAACATCATTGTGGCCACTCCAGGCCGCTTGGAGGACATGTTCCGGAGGAAGGCCGAA
GGCTTGGATCTGGCCAGCTGTGTGCGATCCCTGGATGTCCTGGTGTTGGATGAGGCAGACAGAC
TTCTGGACATGGGGTTTGAGGCAAGCATCAACACCATTCTGGAGTTTTTGCCAAAGCAGAGGAG
AACAGGCCTTTTCTCTGCCACTCAGACGCAGGAAGTGGAGAACCTGGTGAGAGCGGGCCTCCGG
AACCCTGTCCGGGTCTCAGTGAAGGAGAAGGGCGTGGCAGCCAGCAGTGCCCAGAAGACCCCCT
CCCGCCTGGAAAACTACTACATGGTATGCAAGGCAGATGAGAAATTTAATCAGCTGGTCCATTT
TCTTCGCAATCATAAGCAGGAGAAACACCTGGTCTTCTTCAGCACCTGTGCCTGTGTGGAATAC
TATGGGAAGGCTCTGGAAGTGCTGGTGAAGGGCGTGAAGATTATGTGCATTCACGGAAAGATGA
AATATAAACGCAATAAGATCTTCATGGAGTTCCGCAAATTGCAAAGTGGGATTTTAGTGTGCAC
TGATGTGATGGCCCGGGGAATTGATATTCCTGAAGTCAACTGGGTTTTGCAGTATGACCCTCCC
AGCAATGCAAGTGCCTTCGTGCATCGCTGCGGTCGCACAGCTCGCATTGGCCACGGGGGCAGCG
CTCTGGTGTTCCTCCTGCCCATGGAAGAGTCATACATCAATTTCCTTGCAATTAACCAAAAATG
CCCCCTGCAGGAGATGAAGCCCCAGAGAAACACAGCGGACCTTCTGCCAAAACTCAAGTCCATG
GCCCTGGCTGACAGAGCTGTGTTTGAAAAGGGCATGAAAGCTTTTGTGTCATATGTCCAAGCTT
ATGCAAAGCATGAATGCAACCTGATTTTCAGATTAAAGGATCTTGATTTTGCCAGCCTTGCTCG
AGGTTTTGCCCTGCTGAGGATGCCCAAGATGCCAGAATTGAGAGGAAAGCAGTTTCCAGATTTT
GTGCCCGTGGACGTTAATACCGACACGATTCCATTTAAAGATAAAATCAGAGAAAAGCAGAGGC
AGAAACTCCTGGAGCAACAAAGAAGAGAGAAAACAGAAAATGAAGGGAGAAGAAAATTCATAAA
AAATAAAGCTTGGTCAAAGCAGAAGGCCAAAAAAGAAAAGAAGAAAAAAATGAATGAGAAAAGG
AAAAGGGAAGAGGGTTCTGATATTGAAGATGAGGACATGGAAGAACTTCTTAATGACACAAGAC
TCTTGAAAAAACTTAAGAAAGGCAAAATAACTGAAGAAGAATTTGAGAAGGGCTTGTTGACAAC
TGGCAAAAGAACAATCAAGACAGTGGATTTAGGGATCTCAGATTTGGAAGATGACTGCTGATTC
CAGTGCCACAGATGAACCCACAAGGACATAGCTGTTCCCTAACTTGGTGGATGGCTCCAGTTTG
CTTTTAACGAAAATCACAACTTCAGGAGACATCTGAAAAGAATGATGTCTCTGAAAGCTGTCCT
TTCAGATGAGGGAGAAATGAAGGATTTCACACTTCAGAATATTTTACTAAAAACATTCCAGTCT
TGGCCGGGTGCGGTGGCTCCTGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGAGGATCA
CTTGAGCCCAGGAGTTCAAGACCAGCCTGGGAACACAGCGAGACCCTCTCATTAAAAACAACAA
AACAAAACAATTCCAGTCTTGGAGTAGTCTAACAGAAGAAAATGTAAAATTATTTGAGTGTAAA
TAATAGATGTCAGTATTTATCATGATGGGTCACATATAGACATATGTACATATTATATATATAT
ATATATATATATATATATATATATATATATATATATAAGCTCTTTTTTCTGAGGCTATTTTATA
GTTATTTTTAAACATAAAGATACAGAAGTCTTCTTGACTTCTGATTTTCAAAACCATTCCTCAG
TATCTTCAGGCATTTGACCTCCTGAATGTGCTTGGCCCTGGGCTTCAGTTATCCTTTGATGTCC
TGCAGGGGTGGCTAATGTGCTGGGGTTTTTCTGTGTTAATAGTCACAGTATTGTTTTATTGGTG
AATAGCTGAAAAACAGAGGGATTAAGTCATATTCCGGGAAAGAGAATTATAGTTTTTATGCCTC
CTGTTGAATAAATGGTGTCCTGATTGCCTGGG

hide sequence

RefSeq Acc Id:

NR_135104

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,620,943 (+)	NCBI
CHM1_1	12	123,907,568 - 123,926,439 (+)	NCBI
T2T-CHM13v2.0	12	123,600,963 - 123,619,807 (+)	NCBI

Sequence:

show sequence

GCACAAGGCGCGTTCGAGCAGCGGCGACCGACGCGGCGAAGGAGCGCGCCATGGAGCATGTGAC
AGAGGGCTCCTGGGAGTCGCTGCCTGTGCCGCTGCACCCGCAGGTGCTGGGCGCGCTGCGGGAG
CTGGGCTTCCCGTACATGACGCCGGTGCAGTCCGCAACCATCCCTCTGTTCATGCGAAACAAAG
ATGTCGCTGCAGAAGCGGTCACAGGTAGTGGCAAAACACTCGCTTTTGTCATCCCCATCCTGGA
AATTCTTCTGAGAAGAGAAGAGAAGTTAAAAAAGAGTCAGGTTGGAGCCATAATCATCACCCCC
ACTCGAGAGCTGGCCATTCAAATAGACGAGGTCCTGTCGCATTTCACGAAGCACTTCCCCGAGT
TCAGCCAGATTCTTTGGATCGGAGGCAGGAATCCTGGAGAAGATGTTGAGAGGTTTAAGCAACA
AGGTGGGAACATCATTGTGGCCACTCCAGGCCGCTTGGAGGACATGTTCCGGAGGAAGGCCGAA
GGCTTGGATCTGGCCAGCTGTGTGCGATCCCTGGATGTCCTGGTGTTGGATGAGGCAGACAGAC
TTCTGGACATGGGGTTTGAGGCAAGCATCAACACCATTCTGGAGTTTTTGCCAAAGCAGAGGAG
AACAGGCCTTTTCTCTGCCACTCAGACGCAGGAAGTGGAGAACCTGGTGAGAGCGGGCCTCCGG
AACCCTGTCCGGGTCTCAGTGAAGGAGAAGGGCGTGGCAGCCAGCAGTGCCCAGAAGACCCCCT
CCCGCCTGGAAAACTACTACATGGTATGCAAGGCAGATGAGAAATTTAATCAGCTGGTCCATTT
TCTTCGCAATCATAAGCAGGAGAAACACCTGGTCTTCTTCAGCACCTGTGCCTGTGTGGAATAC
TATGGGAAGGCTCTGGAAGTGCTGGTGAAGGGCGTGAAGATTATGTGCATTCACGGAAAGATGA
AATATAAACGCAATAAGATCTTCATGGAGTTCCGCAAATTGCAAAGTGGGATTTTAGTGTGCAC
TGATGTGATGGCCCGGGGAATTGATATTCCTGAAGTCAACTGGGTTTTGCAGTATGACCCTCCC
AGCAATGCAAGTGCCTTCGTGCATCGCTGCGGTCGCACAGCTCGCATTGGCCACGGGGGCAGCG
CTCTGGTGTTCCTCCTGCCCATGGAAGAGTCATACATCAATTTCCTTGCAATTAACCAAAAAGT
TGTGATGGGGAGCCCTGGGGATATGATGCCAGCCAGGGAAGGTGAGAATGTGGTATGTGTGTGT
GTGTAGTGCCCCCTGCAGGAGATGAAGCCCCAGAGAAACACAGCGGACCTTCTGCCAAAACTCA
AGTCCATGGCCCTGGCTGACAGAGCTGTGTTTGAAAAGGGCATGAAAGCTTTTGTGTCATATGT
CCAAGCTTATGCAAAGCATGAATGCAACCTGATTTTCAGATTAAAGGATCTTGATTTTGCCAGC
CTTGCTCGAGGTTTTGCCCTGCTGAGGATGCCCAAGATGCCAGAATTGAGAGGAAAGCAGTTTC
CAGATTTTGTGCCCGTGGACGTTAATACCGACACGATTCCATTTAAAGATAAAATCAGAGAAAA
GCAGAGGCAGAAACTCCTGGAGCAACAAAGAAGAGAGAAAACAGAAAATGAAGGGAGAAGAAAA
TTCATAAAAAATAAAGCTTGGTCAAAGCAGAAGGCCAAAAAAGAAAAGAAGAAAAAAATGAATG
AGAAAAGGAAAAGGGAAGAGGGTTCTGATATTGAAGATGAGGACATGGAAGAACTTCTTAATGA
CACAAGACTCTTGAAAAAACTTAAGAAAGGCAAAATAACTGAAGAAGAATTTGAGAAGGGCTTG
TTGACAACTGGCAAAAGAACAATCAAGACAGTGGATTTAGGGATCTCAGATTTGGAAGATGACT
GCTGATTCCAGTGCCACAGATGAACCCACAAGGACATAGCTGTTCCCTAACTTGGTGGATGGCT
CCAGTTTGCTTTTAACGAAAATCACAACTTCAGGAGACATCTGAAAAGAATGATGTCTCTGAAA
GCTGTCCTTTCAGATGAGGGAGAAATGAAGGATTTCACACTTCAGAATATTTTACTAAAAACAT
TCCAGTCTTGGCCGGGTGCGGTGGCTCCTGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAG
GAGGATCACTTGAGCCCAGGAGTTCAAGACCAGCCTGGGAACACAGCGAGACCCTCTCATTAAA
AACAACAAAACAAAACAATTCCAGTCTTGGAGTAGTCTAACAGAAGAAAATGTAAAATTATTTG
AGTGTAAATAATAGATGTCAGTATTTATCATGATGGGTCACATATAGACATATGTACATATTAT
ATATATATATATATATATATATATATATATATATATATATATATAAGCTCTTTTTTCTGAGGCT
ATTTTATAGTTATTTTTAAACATAAAGATACAGAAGTCTTCTTGACTTCTGATTTTCAAAACCA
TTCCTCAGTATCTTCAGGCATTTGACCTCCTGAATGTGCTTGGCCCTGGGCTTCAGTTATCCTT
TGATGTCCTGCAGGGGTGGCTAATGTGCTGGGGTTTTTCTGTGTTAATAGTCACAGTATTGTTT
TATTGGTGAATAGCTGAAAAACAGAGGGATTAAGTCATATTCCGGGAAAGAGAATTATAGTTTT
TATGCCTCCTGTTGAATAAATGGTGTCCTGATTGCCTGGG

hide sequence

RefSeq Acc Id:

NR_135105

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,620,943 (+)	NCBI
CHM1_1	12	123,907,568 - 123,926,439 (+)	NCBI
T2T-CHM13v2.0	12	123,600,963 - 123,619,807 (+)	NCBI

Sequence:

show sequence

GCACAAGGCGCGTTCGAGCAGCGGCGACCGACGCGGCGAAGGAGCGCGCCATGGAGCATGTGAC
AGAGGGCTCCTGGGAGTCGCTGCCTGTGCCGCTGCACCCGCAGGTGCTGGGCGCGCTGCGGGAG
CTGGGCTTCCCGTACATGACGCCGGTGCAGTCCGCAACCATCCCTCTGTTCATGCGAAACAAAG
ATGTCGCTGCAGAAGCGGTCACAGGTAGTGGCAAAACACTCGCTTTTGTCATCCCCATCCTGGA
AATTCTTCTGAGAAGAGAAGAGAAGTTAAAAAAGAGTCAGGTTGGAGCCATAATCATCACCCCC
ACTCGAGAGCTGGCCATTCAAATAGACGAGGTCCTGTCGCATTTCACGAAGCACTTCCCCGAGT
TCAGCCAGATTCTTTGGATCGGAGGCAGGAATCCTGGAGAAGATGTTGAGAGGTTTAAGCAACA
AGGTGGGAACATCATTGTGGCCACTCCAGGCCGCTTGGAGGACATGTTCCGGAGGAAGGCCGAA
GGCTTGGATCTGGCCAGCTGTGTGCGATCCCTGGATGTCCTGGTGTTGGATGAGGCAGACAGAC
TTCTGGACATGGGGTTTGAGGCAAGCATCAACACCATTCTGGAGTTTTTGCCAAAGCAGAGGAG
AACAGGCCTTTTCTCTGCCACTCAGACGCAGGAAGTGGAGAACCTGGTGAGAGCGGGCCTCCGG
AACCCTGTCCGGGTCTCAGTGAAGGAGAAGGGCGTGGCAGCCAGCAGTGCCCAGAAGACCCCCT
CCCGCCTGGAAAACTACTACATGGTATGCAAGGCAGATGAGAAATTTAATCAGCTGGTCCATTT
TCTTCGCAATCATAAGCAGGAGAAACACCTGGTCTTCTTCAGCACCTGTGCCTGTGTGGAATAC
TATGGGAAGGCTCTGGAAGTGCTGGTGAAGGGCGTGAAGATTATGTGCATTCACGGAAAGATGA
AATATAAACGCAATAAGATCTTCATGGAGTTCCGCAAATTGCAAAGTGGGATTTTAGTGTGCAC
TGATGTGATGGCCCGGGGAATTGATATTCCTGAAGTCAACTGGGTTTTGCAGTATGACCCTCCC
AGCAATGCAAGTGCCTTCGTGCATCGCTGCGGTCGCACAGCTCGCATTGGCCACGGGGGCAGCG
CTCTGGTGTTCCTCCTGCCCATGGAAGAGTCATACATCAATTTCCTTGCAATTAACCAAAAATG
CCCCCTGCAGGAGATGAAGCCCCAGAGAAACACAGCGGACCTTCTGCCAAAACTCAAGTCCATG
GCCCTGGCTGACAGAGCTGTGTTTGAAAAGGGCATGAAAGCTTTTGTGTCATATGTCCAAGCTT
ATGCAAAGCATGAATGCAACCTGATTTTCAGATTAAAGGCCTTGCTCGAGGTTTTGCCCTGCTG
AGGATGCCCAAGATGCCAGAATTGAGAGGAAAGCAGTTTCCAGATTTTGTGCCCGTGGACGTTA
ATACCGACACGATTCCATTTAAAGATAAAATCAGAGAAAAGCAGAGGCAGAAACTCCTGGAGCA
ACAAAGAAGAGAGAAAACAGAAAATGAAGGGAGAAGAAAATTCATAAAAAATAAAGCTTGGTCA
AAGCAGAAGGCCAAAAAAGAAAAGAAGAAAAAAATGAATGAGAAAAGGAAAAGGGAAGAGGGTT
CTGATATTGAAGATGAGGACATGGAAGAACTTCTTAATGACACAAGACTCTTGAAAAAACTTAA
GAAAGGCAAAATAACTGAAGAAGAATTTGAGAAGGGCTTGTTGACAACTGGCAAAAGAACAATC
AAGACAGTGGATTTAGGGATCTCAGATTTGGAAGATGACTGCTGATTCCAGTGCCACAGATGAA
CCCACAAGGACATAGCTGTTCCCTAACTTGGTGGATGGCTCCAGTTTGCTTTTAACGAAAATCA
CAACTTCAGGAGACATCTGAAAAGAATGATGTCTCTGAAAGCTGTCCTTTCAGATGAGGGAGAA
ATGAAGGATTTCACACTTCAGAATATTTTACTAAAAACATTCCAGTCTTGGCCGGGTGCGGTGG
CTCCTGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGAGGATCACTTGAGCCCAGGAGTT
CAAGACCAGCCTGGGAACACAGCGAGACCCTCTCATTAAAAACAACAAAACAAAACAATTCCAG
TCTTGGAGTAGTCTAACAGAAGAAAATGTAAAATTATTTGAGTGTAAATAATAGATGTCAGTAT
TTATCATGATGGGTCACATATAGACATATGTACATATTATATATATATATATATATATATATAT
ATATATATATATATATATATAAGCTCTTTTTTCTGAGGCTATTTTATAGTTATTTTTAAACATA
AAGATACAGAAGTCTTCTTGACTTCTGATTTTCAAAACCATTCCTCAGTATCTTCAGGCATTTG
ACCTCCTGAATGTGCTTGGCCCTGGGCTTCAGTTATCCTTTGATGTCCTGCAGGGGTGGCTAAT
GTGCTGGGGTTTTTCTGTGTTAATAGTCACAGTATTGTTTTATTGGTGAATAGCTGAAAAACAG
AGGGATTAAGTCATATTCCGGGAAAGAGAATTATAGTTTTTATGCCTCCTGTTGAATAAATGGT
GTCCTGATTGCCTGGG

hide sequence

RefSeq Acc Id:

XM_011538608 ⟹ XP_011536910

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,619,619 (+)	NCBI

Sequence:

show sequence

CGTTGGGGGTGCACAAGGCGCGTTCGAGCAGCGGCGACCGACGCGGCGAAGGAGCGCGCCATGG
AGCATGTGACAGAGGGCTCCTGGGAGTCGCTGCCTGTGCCGCTGCACCCGCAGGTGCTGGGCGC
GCTGCGGGAGCTGGGCTTCCCGTACATGACGCCGGTGCAGTCCGCAACCATCCCTCTGTTCATG
CGAAACAAAGATGTCGCTGCAGAAGCGGTCACAGGTAGTGGCAAAACACTCGCTTTTGTCATCC
CCATCCTGGAAATTCTTCTGAGAAGAGAAGAGAAGTTAAAAAAGAGTCAGGTTGGAGCCATAAT
CATCACCCCCACTCGAGAGCTGGCCATTCAAATAGACGAGGTCCTGTCGCATTTCACGAAGCAC
TTCCCCGAGTTCAGCCAGATTCTTTGGATCGGAGGCAGGAATCCTGGAGAAGATGTTGAGAGGT
TTAAGCAACAAGGTGGGAACATCATTGTGGCCACTCCAGGCCGCTTGGAGGACATGTTCCGGAG
GAAGGCCGAAGGCTTGGATCTGGCCAGCTGTGTGCGATCCCTGGATGTCCTGGTGTTGGATGAG
GCAGACAGACTTCTGGACATGGGGTTTGAGGCAAGCATCAACACCATTCTGGAGTTTTTGCCAA
AGCAGAGGAGAACAGGCCTTTTCTCTGCCACTCAGACGCAGGAAGTGGAGAACCTGGTGAGAGC
GGGCCTCCGGAACCCTGTCCGGGTCTCAGTGAAGGAGAAGGGCGTGGCAGCCAGCAGTGCCCAG
AAGACCCCCTCCCGCCTGGAAAACTACTACATGGTATGCAAGGCAGATGAGAAATTTAATCAGC
TGGTCCATTTTCTTCGCAATCATAAGCAGGAGAAACACCTGGTCTTCTTCAGGTACTCCTCTGG
TCTCTGTGGTAGAGGCATCAGGGATTCAGCCAGAATGTGCAGCACCTGTGCCTGTGTGGAATAC
TATGGGAAGGCTCTGGAAGTGCTGGTGAAGGGCGTGAAGATTATGTGCATTCACGGAAAGATGA
AATATAAACGCAATAAGATCTTCATGGAGTTCCGCAAATTGCAAAGTGGGATTTTAGTGTGCAC
TGATGTGATGGCCCGGGGAATTGATATTCCTGAAGTCAACTGGGTTTTGCAGTATGACCCTCCC
AGCAATGCAAGATCTTGATTTTGCCAGCCTTGCTCGAGGTTTTGCCCTGCTGAGGATGCCCAAG
ATGCCAGAATTGAGAGGAAAGCAGTTTCCAGAT

hide sequence

RefSeq Acc Id:

XM_017019710 ⟹ XP_016875199

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,620,581 (+)	NCBI

Sequence:

show sequence

TGGGGGTGCACAAGGCGCGTTCGAGCAGCGGCGACCGACGCGGCGAAGGAGCGCGCCATGGAGC
ATGTGACAGAGGGCTCCTGGGAGTCGCTGCCTGTGCCGCTGCACCCGCAGGTGCTGGGCGCGCT
GCGGGAGCTGGGCTTCCCGTACATGACGCCGGTGCAGTCCGCAACCATCCCTCTGTTCATGCGA
AACAAAGATGTCGCTGCAGAAGCGGTCACAGGTAGTGGCAAAACACTCGCTTTTGTCATCCCCA
TCCTGGAAATTCTTCTGAGAAGAGAAGAGAAGTTAAAAAAGAGTCAGGTTGGAGCCATAATCAT
CACCCCCACTCGAGAGCTGGCCATTCAAATAGACGAGGTCCTGTCGCATTTCACGAAGCACTTC
CCCGAGTTCAGCCAGATTCTTTGGATCGGAGGCAGGAATCCTGGAGAAGATGTTGAGAGGTTTA
AGCAACAAGGTGGGAACATCATTGTGGCCACTCCAGGCCGCTTGGAGGACATGTTCCGGAGGAA
GGCCGAAGGCTTGGATCTGGCCAGCTGTGTGCGATCCCTGGATGTCCTGGTGTTGGATGAGGCA
GACAGACTTCTGGACATGGGGTTTGAGGCAAGCATCAACACCATTCTGGAGTTTTTGCCAAAGC
AGAGGAGAACAGGCCTTTTCTCTGCCACTCAGACGCAGGAAGTGGAGAACCTGGTGAGAGCGGG
CCTCCGGAACCCTGTCCGGGTCTCAGTGAAGGAGAAGGGCGTGGCAGCCAGCAGTGCCCAGAAG
ACCCCCTCCCGCCTGGAAAACTACTACATGGTATGCAAGGCAGATGAGAAATTTAATCAGCTGG
TCCATTTTCTTCGCAATCATAAGCAGGAGAAACACCTGGTCTTCTTCAGGTACTCCTCTGGTCT
CTGTGGTAGAGGCATCAGGGATTCAGCCAGAATGTGCAGCACCTGTGCCTGTGTGGAATACTAT
GGGAAGGCTCTGGAAGTGCTGGTGAAGGGCGTGAAGATTATGTGCATTCACGGAAAGATGAAAT
ATAAACGCAATAAGATCTTCATGGAGTTCCGCAAATTGCAAAGTGGGATTTTAGTGTGCACTGA
TGTGATGGCCCGGGGAATTGATATTCCTGAAGTCAACTGGGTTTTGCAGTATGACCCTCCCAGC
AATGCAAGTGCCTTCGTGCATCGCTGCGGTCGCACAGCTCGCATTGGCCACGGGGGCAGCGCTC
TGGTGTTCCTCCTGCCCATGGAAGAGTCATACATCAATTTCCTTGCAATTAACCAAAAATGCCC
CCTGCAGGAGATGAAGCCCCAGAGAAACACAGCGGACCTTCTGCCAAAACTCAAGTCCATGGCC
CTGGCTGACAGAGCTGTGTTTGAAAAGGGCATGAAAGCTTTTGTGTCATATGTCCAAGCTTATG
CAAAGCATGAATGCAACCTGATTTTCAGATTAAAGGATCTTGATTTTGCCAGCCTTGCTCGAGG
TTTTGCCCTGCTGAGGATGCCCAAGATGCCAGAATTGAGAGGAAAGCAGTTTCCAGATTTTGTG
CCCGTGGACGTTAATACCGACACGATTCCATTTAAAGATAAAATCAGAGAAAAGCAGAGGCAGA
AACTCCTGGAGCAACAAAGAAGAGAGAAAACAGAAAATGAAGGGAGAAGAAAATTCATAAAAAA
TAAAGCTTGGTCAAAGCAGAAGGCCAAAAAAGAAAAGAAGAAAAAAATGAATGAGAAAAGGAAA
AGGGAAGAGGGTTCTGATATTGAAGATGAGGACATGGAAGAACTTCTTAATGACACAAGACTCT
TGAAAAAACTTAAGAAAGGCAAAATAACTGAAGAAGAATTTGAGAAGGGCTTGTTGACAACTGG
CAAAAGAACAATCAAGACAGTGGATTTAGGGATCTCAGATTTGGAAGATGACTGCTGATTCCAG
TGCCACAGATGAACCCACAAGGACATAGCTGTTCCCTAACTTGGTGGATGGCTCCAGTTTGCTT
TTAACGAAAATCACAACTTCAGGAGACATCTGAAAAGAATGATGTCTCTGAAAGCTGTCCTTTC
AGATGAGGGAGAAATGAAGGATTTCACACTTCAGAATATTTTACTAAAAACATTCCAGTCTTGG
CCGGGTGCGGTGGCTCCTGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGAGGATCACTT
GAGCCCAGGAGTTCAAGACCAGCCTGGGAACACAGCGAGACCCTCTCATTAAAAACAACAAAAC
AAAACAATTCCAGTCTTGGAGTAGTCTAACAGAAGAAAATGTAAAATTATTTGAGTGTAAATAA
TAGATGTCAGTATTTATCATGATGGGTCACATATAGACATATGTACATATTATATATATATATA
TATATATATATATATATATATATATATATATATAAGCTCTTTTTTCTGAGGCTATTTTATAGTT
ATTTTTAAACATAAAGATACAGAAGTCTTCTTGACTTCTGATTTTCAAAACCATTCCTCAGTAT
CTTCAGGCATTTGACCTCCTGAATGTGCTTGGCCCTGGGCTTCAGTTATCCTTTGATGTCCTGC
AGGGGTGGCTAATGTGCTGGGGTTTTTCTGTGTTAATAGTCACAGTATTGTTTTATTGGTGAAT
AGCTGAAAAACAGAGGGATTAAGTCATATTCCGGGAAAGAGAATTATAGTTTTTATGCCTCCTG
TTGAATAAATGGTGTCCTGATTGCCTGGG

hide sequence

RefSeq Acc Id:

XM_017019711 ⟹ XP_016875200

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,620,581 (+)	NCBI

Sequence:

show sequence

CTGCACCCGCAGGTGCTGGGCGCGCTGCGGGAGCTGGGCTTCCCGTACATGACGCCGGTGCAGG
GCTTCGGGTCTCACCTGTGAATTGATGGCATCCTTTAACCAGTGCTTTGCAATCTCTCTCTTTA
GTCCGCAACCATCCCTCTGTTCATGCGAAACAAAGATGTCGCTGCAGAAGCGGTGAGTGCCTCG
GGTATGTGCAGCCTGTCCTCGTGTTCTCCCTCAGATGAACTCTGAGGAAGAAAGGGAAACCAAA
ACTCTCTGTTTGCAGGTCACAGGTAGTGGCAAAACACTCGCTTTTGTCATCCCCATCCTGGAAA
TTCTTCTGAGAAGAGAAGAGAAGTTAAAAAAGAGTCAGGTTGGAGCCATAATCATCACCCCCAC
TCGAGAGCTGGCCATTCAAATAGACGAGGTCCTGTCGCATTTCACGAAGCACTTCCCCGAGTTC
AGCCAGATTCTTTGGATCGGAGGCAGGAATCCTGGAGAAGATGTTGAGAGGTTTAAGCAACAAG
GTGGGAACATCATTGTGGCCACTCCAGGCCGCTTGGAGGACATGTTCCGGAGGAAGGCCGAAGG
CTTGGATCTGGCCAGCTGTGTGCGATCCCTGGATGTCCTGGTGTTGGATGAGGCAGACAGACTT
CTGGACATGGGGTTTGAGGCAAGCATCAACACCATTCTGGAGTTTTTGCCAAAGCAGAGGAGAA
CAGGCCTTTTCTCTGCCACTCAGACGCAGGAAGTGGAGAACCTGGTGAGAGCGGGCCTCCGGAA
CCCTGTCCGGGTCTCAGTGAAGGAGAAGGGCGTGGCAGCCAGCAGTGCCCAGAAGACCCCCTCC
CGCCTGGAAAACTACTACATGGTATGCAAGGCAGATGAGAAATTTAATCAGCTGGTCCATTTTC
TTCGCAATCATAAGCAGGAGAAACACCTGGTCTTCTTCAGGTACTCCTCTGGTCTCTGTGGTAG
AGGCATCAGGGATTCAGCCAGAATGTGCAGCACCTGTGCCTGTGTGGAATACTATGGGAAGGCT
CTGGAAGTGCTGGTGAAGGGCGTGAAGATTATGTGCATTCACGGAAAGATGAAATATAAACGCA
ATAAGATCTTCATGGAGTTCCGCAAATTGCAAAGTGGGATTTTAGTGTGCACTGATGTGATGGC
CCGGGGAATTGATATTCCTGAAGTCAACTGGGTTTTGCAGTATGACCCTCCCAGCAATGCAAGT
GCCTTCGTGCATCGCTGCGGTCGCACAGCTCGCATTGGCCACGGGGGCAGCGCTCTGGTGTTCC
TCCTGCCCATGGAAGAGTCATACATCAATTTCCTTGCAATTAACCAAAAATGCCCCCTGCAGGA
GATGAAGCCCCAGAGAAACACAGCGGACCTTCTGCCAAAACTCAAGTCCATGGCCCTGGCTGAC
AGAGCTGTGTTTGAAAAGGGCATGAAAGCTTTTGTGTCATATGTCCAAGCTTATGCAAAGCATG
AATGCAACCTGATTTTCAGATTAAAGGATCTTGATTTTGCCAGCCTTGCTCGAGGTTTTGCCCT
GCTGAGGATGCCCAAGATGCCAGAATTGAGAGGAAAGCAGTTTCCAGATTTTGTGCCCGTGGAC
GTTAATACCGACACGATTCCATTTAAAGATAAAATCAGAGAAAAGCAGAGGCAGAAACTCCTGG
AGCAACAAAGAAGAGAGAAAACAGAAAATGAAGGGAGAAGAAAATTCATAAAAAATAAAGCTTG
GTCAAAGCAGAAGGCCAAAAAAGAAAAGAAGAAAAAAATGAATGAGAAAAGGAAAAGGGAAGAG
GGTTCTGATATTGAAGATGAGGACATGGAAGAACTTCTTAATGACACAAGACTCTTGAAAAAAC
TTAAGAAAGGCAAAATAACTGAAGAAGAATTTGAGAAGGGCTTGTTGACAACTGGCAAAAGAAC
AATCAAGACAGTGGATTTAGGGATCTCAGATTTGGAAGATGACTGCTGATTCCAGTGCCACAGA
TGAACCCACAAGGACATAGCTGTTCCCTAACTTGGTGGATGGCTCCAGTTTGCTTTTAACGAAA
ATCACAACTTCAGGAGACATCTGAAAAGAATGATGTCTCTGAAAGCTGTCCTTTCAGATGAGGG
AGAAATGAAGGATTTCACACTTCAGAATATTTTACTAAAAACATTCCAGTCTTGGCCGGGTGCG
GTGGCTCCTGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGAGGATCACTTGAGCCCAGG
AGTTCAAGACCAGCCTGGGAACACAGCGAGACCCTCTCATTAAAAACAACAAAACAAAACAATT
CCAGTCTTGGAGTAGTCTAACAGAAGAAAATGTAAAATTATTTGAGTGTAAATAATAGATGTCA
GTATTTATCATGATGGGTCACATATAGACATATGTACATATTATATATATATATATATATATAT
ATATATATATATATATATATATATAAGCTCTTTTTTCTGAGGCTATTTTATAGTTATTTTTAAA
CATAAAGATACAGAAGTCTTCTTGACTTCTGATTTTCAAAACCATTCCTCAGTATCTTCAGGCA
TTTGACCTCCTGAATGTGCTTGGCCCTGGGCTTCAGTTATCCTTTGATGTCCTGCAGGGGTGGC
TAATGTGCTGGGGTTTTTCTGTGTTAATAGTCACAGTATTGTTTTATTGGTGAATAGCTGAAAA
ACAGAGGGATTAAGTCATATTCCGGGAAAGAGAATTATAGTTTTTATGCCTCCTGTTGAATAAA
TGGTGTCCTGATTGCCTGGG

hide sequence

RefSeq Acc Id:

XM_017019712 ⟹ XP_016875201

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,604,021 - 123,620,581 (+)	NCBI

Sequence:

show sequence

TTGAACTCCTGACCTCAGTCCGCAACCATCCCTCTGTTCATGCGAAACAAAGATGTCGCTGCAG
AAGCGGTCACAGGTAGTGGCAAAACACTCGCTTTTGTCATCCCCATCCTGGAAATTCTTCTGAG
AAGAGAAGAGAAGTTAAAAAAGAGTCAGGTTGGAGCCATAATCATCACCCCCACTCGAGAGCTG
GCCATTCAAATAGACGAGGTCCTGTCGCATTTCACGAAGCACTTCCCCGAGTTCAGCCAGATTC
TTTGGATCGGAGGCAGGAATCCTGGAGAAGATGTTGAGAGGTTTAAGCAACAAGGTGGGAACAT
CATTGTGGCCACTCCAGGCCGCTTGGAGGACATGTTCCGGAGGAAGGCCGAAGGCTTGGATCTG
GCCAGCTGTGTGCGATCCCTGGATGTCCTGGTGTTGGATGAGGCAGACAGACTTCTGGACATGG
GGTTTGAGGCAAGCATCAACACCATTCTGGAGTTTTTGCCAAAGCAGAGGAGAACAGGCCTTTT
CTCTGCCACTCAGACGCAGGAAGTGGAGAACCTGGTGAGAGCGGGCCTCCGGAACCCTGTCCGG
GTCTCAGTGAAGGAGAAGGGCGTGGCAGCCAGCAGTGCCCAGAAGACCCCCTCCCGCCTGGAAA
ACTACTACATGGTATGCAAGGCAGATGAGAAATTTAATCAGCTGGTCCATTTTCTTCGCAATCA
TAAGCAGGAGAAACACCTGGTCTTCTTCAGGTACTCCTCTGGTCTCTGTGGTAGAGGCATCAGG
GATTCAGCCAGAATGTGCAGCACCTGTGCCTGTGTGGAATACTATGGGAAGGCTCTGGAAGTGC
TGGTGAAGGGCGTGAAGATTATGTGCATTCACGGAAAGATGAAATATAAACGCAATAAGATCTT
CATGGAGTTCCGCAAATTGCAAAGTGGGATTTTAGTGTGCACTGATGTGATGGCCCGGGGAATT
GATATTCCTGAAGTCAACTGGGTTTTGCAGTATGACCCTCCCAGCAATGCAAGTGCCTTCGTGC
ATCGCTGCGGTCGCACAGCTCGCATTGGCCACGGGGGCAGCGCTCTGGTGTTCCTCCTGCCCAT
GGAAGAGTCATACATCAATTTCCTTGCAATTAACCAAAAATGCCCCCTGCAGGAGATGAAGCCC
CAGAGAAACACAGCGGACCTTCTGCCAAAACTCAAGTCCATGGCCCTGGCTGACAGAGCTGTGT
TTGAAAAGGGCATGAAAGCTTTTGTGTCATATGTCCAAGCTTATGCAAAGCATGAATGCAACCT
GATTTTCAGATTAAAGGATCTTGATTTTGCCAGCCTTGCTCGAGGTTTTGCCCTGCTGAGGATG
CCCAAGATGCCAGAATTGAGAGGAAAGCAGTTTCCAGATTTTGTGCCCGTGGACGTTAATACCG
ACACGATTCCATTTAAAGATAAAATCAGAGAAAAGCAGAGGCAGAAACTCCTGGAGCAACAAAG
AAGAGAGAAAACAGAAAATGAAGGGAGAAGAAAATTCATAAAAAATAAAGCTTGGTCAAAGCAG
AAGGCCAAAAAAGAAAAGAAGAAAAAAATGAATGAGAAAAGGAAAAGGGAAGAGGGTTCTGATA
TTGAAGATGAGGACATGGAAGAACTTCTTAATGACACAAGACTCTTGAAAAAACTTAAGAAAGG
CAAAATAACTGAAGAAGAATTTGAGAAGGGCTTGTTGACAACTGGCAAAAGAACAATCAAGACA
GTGGATTTAGGGATCTCAGATTTGGAAGATGACTGCTGATTCCAGTGCCACAGATGAACCCACA
AGGACATAGCTGTTCCCTAACTTGGTGGATGGCTCCAGTTTGCTTTTAACGAAAATCACAACTT
CAGGAGACATCTGAAAAGAATGATGTCTCTGAAAGCTGTCCTTTCAGATGAGGGAGAAATGAAG
GATTTCACACTTCAGAATATTTTACTAAAAACATTCCAGTCTTGGCCGGGTGCGGTGGCTCCTG
CCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGAGGATCACTTGAGCCCAGGAGTTCAAGAC
CAGCCTGGGAACACAGCGAGACCCTCTCATTAAAAACAACAAAACAAAACAATTCCAGTCTTGG
AGTAGTCTAACAGAAGAAAATGTAAAATTATTTGAGTGTAAATAATAGATGTCAGTATTTATCA
TGATGGGTCACATATAGACATATGTACATATTATATATATATATATATATATATATATATATAT
ATATATATATATATAAGCTCTTTTTTCTGAGGCTATTTTATAGTTATTTTTAAACATAAAGATA
CAGAAGTCTTCTTGACTTCTGATTTTCAAAACCATTCCTCAGTATCTTCAGGCATTTGACCTCC
TGAATGTGCTTGGCCCTGGGCTTCAGTTATCCTTTGATGTCCTGCAGGGGTGGCTAATGTGCTG
GGGTTTTTCTGTGTTAATAGTCACAGTATTGTTTTATTGGTGAATAGCTGAAAAACAGAGGGAT
TAAGTCATATTCCGGGAAAGAGAATTATAGTTTTTATGCCTCCTGTTGAATAAATGGTGTCCTG
ATTGCCTGGG

hide sequence

RefSeq Acc Id:

XM_017019715 ⟹ XP_016875204

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,620,581 (+)	NCBI

Sequence:

show sequence

TTGGGGGTGCACAAGGCGCGTTCGAGCAGCGGCGACCGACGCGGCGAAGGAGCGCGCCATGGAG
CATGTGACAGAGGGCTCCTGGGAGTCGCTGCCTGTGCCGCTGCACCCGCAGGTGCTGGGCGCGC
TGCGGGAGCTGGGCTTCCCGTACATGACGCCGGTGCAGTCCGCAACCATCCCTCTGTTCATGCG
AAACAAAGATGTCGCTGCAGAAGCGGTCACAGGTAGTGGCAAAACACTCGCTTTTGTCATCCCC
ATCCTGGAAATTCTTCTGAGAAGAGAAGAGAAGTTAAAAAAGAGTCAGGTTGGAGCCATAATCA
TCACCCCCACTCGAGAGCTGGCCATTCAAATAGACGAGGTCCTGTCGCATTTCACGAAGCACTT
CCCCGAGTTCAGCCAGATTCTTTGGATCGGAGGCAGGAATCCTGGAGAAGATGTTGAGAGGTTT
AAGCAACAAGGTGGGAACATCATTGTGGCCACTCCAGGCCGCTTGGAGGACATGTTCCGGAGGA
AGGCCGAAGGCTTGGATCTGGCCAGCTGTGTGCGATCCCTGGATGTCCTGGTGTTGGATGAGGC
AGACAGACTTCTGGACATGGGGTTTGAGGCAAGCATCAACACCATTCTGGAGTTTTTGCCAAAG
CAGAGGAGAACAGGCCTTTTCTCTGCCACTCAGACGCAGGAAGTGGAGAACCTGGTGAGAGCGG
GCCTCCGGAACCCTGTCCGGGTCTCAGTGAAGGAGAAGGGCGTGGCAGCCAGCAGTGCCCAGAA
GACCCCCTCCCGCCTGGAAAACTACTACATGGTATGCAAGGCAGATGAGAAATTTAATCAGCTG
GTCCATTTTCTTCGCAATCATAAGCAGGAGAAACACCTGGTCTTCTTCAGGTACTCCTCTGGTC
TCTGTGGTAGAGGCATCAGGGATTCAGCCAGAATGTGCAGCACCTGTGCCTGTGTGGAATACTA
TGGGAAGGCTCTGGAAGTGCTGGTGAAGGGCGTGAAGATTATGTGCATTCACGGAAAGATGAAA
TATAAACGCAATAAGATCTTCATGGAGTTCCGCAAATTGCAAAGTGGGATTTTAGTGTGCACTG
ATGTGATGGCCCGGGGAATTGATATTCCTGAAGTCAACTGGGTTTTGCAGTATGACCCTCCCAG
CAATGCAAGCCTTGCTCGAGGTTTTGCCCTGCTGAGGATGCCCAAGATGCCAGAATTGAGAGGA
AAGCAGTTTCCAGATTTTGTGCCCGTGGACGTTAATACCGACACGATTCCATTTAAAGATAAAA
TCAGAGAAAAGCAGAGGCAGAAACTCCTGGAGCAACAAAGAAGAGAGAAAACAGAAAATGAAGG
GAGAAGAAAATTCATAAAAAATAAAGCTTGGTCAAAGCAGAAGGCCAAAAAAGAAAAGAAGAAA
AAAATGAATGAGAAAAGGAAAAGGGAAGAGGGTTCTGATATTGAAGATGAGGACATGGAAGAAC
TTCTTAATGACACAAGACTCTTGAAAAAACTTAAGAAAGGCAAAATAACTGAAGAAGAATTTGA
GAAGGGCTTGTTGACAACTGGCAAAAGAACAATCAAGACAGTGGATTTAGGGATCTCAGATTTG
GAAGATGACTGCTGATTCCAGTGCCACAGATGAACCCACAAGGACATAGCTGTTCCCTAACTTG
GTGGATGGCTCCAGTTTGCTTTTAACGAAAATCACAACTTCAGGAGACATCTGAAAAGAATGAT
GTCTCTGAAAGCTGTCCTTTCAGATGAGGGAGAAATGAAGGATTTCACACTTCAGAATATTTTA
CTAAAAACATTCCAGTCTTGGCCGGGTGCGGTGGCTCCTGCCTATAATCCCAGCACTTTGGGAG
GCTGAGGCAGGAGGATCACTTGAGCCCAGGAGTTCAAGACCAGCCTGGGAACACAGCGAGACCC
TCTCATTAAAAACAACAAAACAAAACAATTCCAGTCTTGGAGTAGTCTAACAGAAGAAAATGTA
AAATTATTTGAGTGTAAATAATAGATGTCAGTATTTATCATGATGGGTCACATATAGACATATG
TACATATTATATATATATATATATATATATATATATATATATATATATATATATAAGCTCTTTT
TTCTGAGGCTATTTTATAGTTATTTTTAAACATAAAGATACAGAAGTCTTCTTGACTTCTGATT
TTCAAAACCATTCCTCAGTATCTTCAGGCATTTGACCTCCTGAATGTGCTTGGCCCTGGGCTTC
AGTTATCCTTTGATGTCCTGCAGGGGTGGCTAATGTGCTGGGGTTTTTCTGTGTTAATAGTCAC
AGTATTGTTTTATTGGTGAATAGCTGAAAAACAGAGGGATTAAGTCATATTCCGGGAAAGAGAA
TTATAGTTTTTATGCCTCCTGTTGAATAAATGGTGTCCTGATTGCCTGGG

hide sequence

RefSeq Acc Id:

XM_017019716 ⟹ XP_016875205

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,620,581 (+)	NCBI

Sequence:

show sequence

TGGGGGTGCACAAGGCGCGTTCGAGCAGCGGCGACCGACGCGGCGAAGGAGCGCGCCATGGAGC
ATGTGACAGAGGGCTCCTGGGAGTCGCTGCCTGTGCCGCTGCACCCGCAGGTGCTGGGCGCGCT
GCGGGAGCTGGGCTTCCCGTACATGACGCCGGTGCAGTCCGCAACCATCCCTCTGTTCATGCGA
AACAAAGATGTCGCTGCAGAAGCGGTCACAGGTAGTGGCAAAACACTCGCTTTTGTCATCCCCA
TCCTGGAAATTCTTCTGAGAAGAGAAGAGAAGTTAAAAAAGAGTCAGGTTGGAGCCATAATCAT
CACCCCCACTCGAGAGCTGGCCATTCAAATAGACGAGGTCCTGTCGCATTTCACGAAGCACTTC
CCCGAGTTCAGCCAGATTCTTTGGATCGGAGGCAGGAATCCTGGAGAAGATGTTGAGAGGTTTA
AGCAACAAGGTGGGAACATCATTGTGGCCACTCCAGGCCGCTTGGAGGACATGTTCCGGAGGAA
GGCCGAAGGCTTGGATCTGGCCAGCTGTGTGCGATCCCTGGATGTCCTGGTGTTGGATGAGGCA
GACAGACTTCTGGACATGGGGTTTGAGGCAAGCATCAACACCATTCTGGAGTTTTTGCCAAAGC
AGAGGAGAACAGGCCTTTTCTCTGCCACTCAGACGCAGGAAGTGGAGAACCTGGTGAGAGCGGG
CCTCCGGAACCCTGTCCGGGTCTCAGTGAAGGAGAAGGGCGTGGCAGCCAGCAGTGCCCAGAAG
ACCCCCTCCCGCCTGGAAAACTACTACATGGTATGCAAGGCAGATGAGAAATTTAATCAGCTGG
TCCATTTTCTTCGCAATCATAAGCAGGAGAAACACCTGGTCTTCTTCAGCACCTGTGCCTGTGT
GGAATACTATGGGAAGGCTCTGGAAGTGCTGGTGAAGGGCGTGAAGATTATGTGCATTCACGGA
AAGATGAAATATAAACGCAATAAGATCTTCATGGAGTTCCGCAAATTGCAAAGTGGGATTTTAG
TGTGCACTGATGTGATGGCCCGGGGAATTGATATTCCTGAAGTCAACTGGGTTTTGCAGTATGA
CCCTCCCAGCAATGCAAGCCTTGCTCGAGGTTTTGCCCTGCTGAGGATGCCCAAGATGCCAGAA
TTGAGAGGAAAGCAGTTTCCAGATTTTGTGCCCGTGGACGTTAATACCGACACGATTCCATTTA
AAGATAAAATCAGAGAAAAGCAGAGGCAGAAACTCCTGGAGCAACAAAGAAGAGAGAAAACAGA
AAATGAAGGGAGAAGAAAATTCATAAAAAATAAAGCTTGGTCAAAGCAGAAGGCCAAAAAAGAA
AAGAAGAAAAAAATGAATGAGAAAAGGAAAAGGGAAGAGGGTTCTGATATTGAAGATGAGGACA
TGGAAGAACTTCTTAATGACACAAGACTCTTGAAAAAACTTAAGAAAGGCAAAATAACTGAAGA
AGAATTTGAGAAGGGCTTGTTGACAACTGGCAAAAGAACAATCAAGACAGTGGATTTAGGGATC
TCAGATTTGGAAGATGACTGCTGATTCCAGTGCCACAGATGAACCCACAAGGACATAGCTGTTC
CCTAACTTGGTGGATGGCTCCAGTTTGCTTTTAACGAAAATCACAACTTCAGGAGACATCTGAA
AAGAATGATGTCTCTGAAAGCTGTCCTTTCAGATGAGGGAGAAATGAAGGATTTCACACTTCAG
AATATTTTACTAAAAACATTCCAGTCTTGGCCGGGTGCGGTGGCTCCTGCCTATAATCCCAGCA
CTTTGGGAGGCTGAGGCAGGAGGATCACTTGAGCCCAGGAGTTCAAGACCAGCCTGGGAACACA
GCGAGACCCTCTCATTAAAAACAACAAAACAAAACAATTCCAGTCTTGGAGTAGTCTAACAGAA
GAAAATGTAAAATTATTTGAGTGTAAATAATAGATGTCAGTATTTATCATGATGGGTCACATAT
AGACATATGTACATATTATATATATATATATATATATATATATATATATATATATATATATATA
AGCTCTTTTTTCTGAGGCTATTTTATAGTTATTTTTAAACATAAAGATACAGAAGTCTTCTTGA
CTTCTGATTTTCAAAACCATTCCTCAGTATCTTCAGGCATTTGACCTCCTGAATGTGCTTGGCC
CTGGGCTTCAGTTATCCTTTGATGTCCTGCAGGGGTGGCTAATGTGCTGGGGTTTTTCTGTGTT
AATAGTCACAGTATTGTTTTATTGGTGAATAGCTGAAAAACAGAGGGATTAAGTCATATTCCGG
GAAAGAGAATTATAGTTTTTATGCCTCCTGTTGAATAAATGGTGTCCTGATTGCCTGGG

hide sequence

RefSeq Acc Id:

XM_017019721 ⟹ XP_016875210

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,619,619 (+)	NCBI

Sequence:

show sequence

TTGGGGGTGCACAAGGCGCGTTCGAGCAGCGGCGACCGACGCGGCGAAGGAGCGCGCCATGGAG
CATGTGACAGAGGGCTCCTGGGAGTCGCTGCCTGTGCCGCTGCACCCGCAGGTGCTGGGCGCGC
TGCGGGAGCTGGGCTTCCCGTACATGACGCCGGTGCAGTCCGCAACCATCCCTCTGTTCATGCG
AAACAAAGATGTCGCTGCAGAAGCGGTCACAGGTAGTGGCAAAACACTCGCTTTTGTCATCCCC
ATCCTGGAAATTCTTCTGAGAAGAGAAGAGAAGTTAAAAAAGAGTCAGGTTGGAGCCATAATCA
TCACCCCCACTCGAGAGCTGGCCATTCAAATAGACGAGGTCCTGTCGCATTTCACGAAGCACTT
CCCCGAGTTCAGCCAGATTCTTTGGATCGGAGGCAGGAATCCTGGAGAAGATGTTGAGAGGTTT
AAGCAACAAGGTGGGAACATCATTGTGGCCACTCCAGGCCGCTTGGAGGACATGTTCCGGAGGA
AGGCCGAAGGCTTGGATCTGGCCAGCTGTGTGCGATCCCTGGATGTCCTGGTGTTGGATGAGGC
AGACAGACTTCTGGACATGGGGTTTGAGGCAAGCATCAACACCATTCTGGAGTTTTTGCCAAAG
CAGAGGAGAACAGGCCTTTTCTCTGCCACTCAGACGCAGGAAGTGGAGAACCTGGTGAGAGCGG
GCCTCCGGAACCCTGTCCGGGTCTCAGTGAAGGAGAAGGGCGTGGCAGCCAGCAGTGCCCAGAA
GACCCCCTCCCGCCTGGAAAACTACTACATGGTATGCAAGGCAGATGAGAAATTTAATCAGCTG
GTCCATTTTCTTCGCAATCATAAGCAGGAGAAACACCTGGTCTTCTTCAGCACCTGTGCCTGTG
TGGAATACTATGGGAAGGCTCTGGAAGTGCTGGTGAAGGGCGTGAAGATTATGTGCATTCACGG
AAAGATGAAATATAAACGCAATAAGATCTTCATGGAGTTCCGCAAATTGCAAAGTGGGATTTTA
GTGTGCACTGATGTGATGGCCCGGGGAATTGATATTCCTGAAGTCAACTGGGTTTTGCAGTATG
ACCCTCCCAGCAATGCAAGATCTTGATTTTGCCAGCCTTGCTCGAGGTTTTGCCCTGCTGAGGA
TGCCCAAGATGCCAGAATTGAGAGGAAAGCAGTTTCCAGATTTTGTGCCCGTGGACGTTAATAC
CGACACGATTCCATTTAAAGATAAAATCAGAGAAAAGCAGAGGCAGAAACTCCTGGAGCAACAA
AGAAGAGAGAAAACAGAAAATGAAGGGAG

hide sequence

RefSeq Acc Id:

XM_047429221 ⟹ XP_047285177

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,620,581 (+)	NCBI

RefSeq Acc Id:

XM_047429222 ⟹ XP_047285178

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,620,581 (+)	NCBI

RefSeq Acc Id:

XM_047429223 ⟹ XP_047285179

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,606,072 - 123,620,581 (+)	NCBI

RefSeq Acc Id:

XM_047429224 ⟹ XP_047285180

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,619,619 (+)	NCBI

RefSeq Acc Id:

XM_047429225 ⟹ XP_047285181

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,618,779 (+)	NCBI

RefSeq Acc Id:

XM_047429226 ⟹ XP_047285182

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,618,778 (+)	NCBI

RefSeq Acc Id:

XM_047429227 ⟹ XP_047285183

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,619,619 (+)	NCBI

RefSeq Acc Id:

XM_047429228 ⟹ XP_047285184

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,618,746 (+)	NCBI

RefSeq Acc Id:

XM_047429229 ⟹ XP_047285185

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,618,790 (+)	NCBI

RefSeq Acc Id:

XM_054372692 ⟹ XP_054228667

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,600,963 - 123,619,447 (+)	NCBI

RefSeq Acc Id:

XM_054372693 ⟹ XP_054228668

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,600,963 - 123,619,447 (+)	NCBI

RefSeq Acc Id:

XM_054372694 ⟹ XP_054228669

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,600,963 - 123,619,447 (+)	NCBI

RefSeq Acc Id:

XM_054372695 ⟹ XP_054228670

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,602,888 - 123,619,447 (+)	NCBI

RefSeq Acc Id:

XM_054372696 ⟹ XP_054228671

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,600,963 - 123,619,447 (+)	NCBI

RefSeq Acc Id:

XM_054372697 ⟹ XP_054228672

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,600,963 - 123,619,447 (+)	NCBI

RefSeq Acc Id:

XM_054372698 ⟹ XP_054228673

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,600,963 - 123,619,447 (+)	NCBI

RefSeq Acc Id:

XM_054372699 ⟹ XP_054228674

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,600,963 - 123,619,447 (+)	NCBI

RefSeq Acc Id:

XM_054372700 ⟹ XP_054228675

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,600,963 - 123,618,548 (+)	NCBI

RefSeq Acc Id:

XM_054372701 ⟹ XP_054228676

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,600,963 - 123,619,447 (+)	NCBI

RefSeq Acc Id:

XM_054372702 ⟹ XP_054228677

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,600,963 - 123,617,645 (+)	NCBI

RefSeq Acc Id:

XM_054372703 ⟹ XP_054228678

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,600,963 - 123,617,644 (+)	NCBI

RefSeq Acc Id:

XM_054372704 ⟹ XP_054228679

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,600,963 - 123,618,548 (+)	NCBI

RefSeq Acc Id:

XM_054372705 ⟹ XP_054228680

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,600,963 - 123,617,612 (+)	NCBI

RefSeq Acc Id:

XM_054372706 ⟹ XP_054228681

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,600,963 - 123,617,656 (+)	NCBI

RefSeq Acc Id:

XM_054372707 ⟹ XP_054228682

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,600,963 - 123,618,391 (+)	NCBI

RefSeq Acc Id:

XM_054372708 ⟹ XP_054228683

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,600,963 - 123,618,548 (+)	NCBI

RefSeq Acc Id:

XM_054372709 ⟹ XP_054228684

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	12	123,600,963 - 123,618,548 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_065987	(Get FASTA)	NCBI Sequence Viewer
	XP_011536910	(Get FASTA)	NCBI Sequence Viewer
	XP_016875199	(Get FASTA)	NCBI Sequence Viewer
	XP_016875200	(Get FASTA)	NCBI Sequence Viewer
	XP_016875201	(Get FASTA)	NCBI Sequence Viewer
	XP_016875204	(Get FASTA)	NCBI Sequence Viewer
	XP_016875205	(Get FASTA)	NCBI Sequence Viewer
	XP_016875210	(Get FASTA)	NCBI Sequence Viewer
	XP_047285177	(Get FASTA)	NCBI Sequence Viewer
	XP_047285178	(Get FASTA)	NCBI Sequence Viewer
	XP_047285179	(Get FASTA)	NCBI Sequence Viewer
	XP_047285180	(Get FASTA)	NCBI Sequence Viewer
	XP_047285181	(Get FASTA)	NCBI Sequence Viewer
	XP_047285182	(Get FASTA)	NCBI Sequence Viewer
	XP_047285183	(Get FASTA)	NCBI Sequence Viewer
	XP_047285184	(Get FASTA)	NCBI Sequence Viewer
	XP_047285185	(Get FASTA)	NCBI Sequence Viewer
	XP_054228667	(Get FASTA)	NCBI Sequence Viewer
	XP_054228668	(Get FASTA)	NCBI Sequence Viewer
	XP_054228669	(Get FASTA)	NCBI Sequence Viewer
	XP_054228670	(Get FASTA)	NCBI Sequence Viewer
	XP_054228671	(Get FASTA)	NCBI Sequence Viewer
	XP_054228672	(Get FASTA)	NCBI Sequence Viewer
	XP_054228673	(Get FASTA)	NCBI Sequence Viewer
	XP_054228674	(Get FASTA)	NCBI Sequence Viewer
	XP_054228675	(Get FASTA)	NCBI Sequence Viewer
	XP_054228676	(Get FASTA)	NCBI Sequence Viewer
	XP_054228677	(Get FASTA)	NCBI Sequence Viewer
	XP_054228678	(Get FASTA)	NCBI Sequence Viewer
	XP_054228679	(Get FASTA)	NCBI Sequence Viewer
	XP_054228680	(Get FASTA)	NCBI Sequence Viewer
	XP_054228681	(Get FASTA)	NCBI Sequence Viewer
	XP_054228682	(Get FASTA)	NCBI Sequence Viewer
	XP_054228683	(Get FASTA)	NCBI Sequence Viewer
	XP_054228684	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH30020	(Get FASTA)	NCBI Sequence Viewer
	AAH35911	(Get FASTA)	NCBI Sequence Viewer
	ADO22294	(Get FASTA)	NCBI Sequence Viewer
	BAB13421	(Get FASTA)	NCBI Sequence Viewer
	BAB85021	(Get FASTA)	NCBI Sequence Viewer
	BAG62656	(Get FASTA)	NCBI Sequence Viewer
	CAH56233	(Get FASTA)	NCBI Sequence Viewer
	EAW98419	(Get FASTA)	NCBI Sequence Viewer
	EAW98420	(Get FASTA)	NCBI Sequence Viewer
	EAW98421	(Get FASTA)	NCBI Sequence Viewer
	EAW98422	(Get FASTA)	NCBI Sequence Viewer
	EAW98423	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000238146
	ENSP00000238146.3
	ENSP00000346244.4
	ENSP00000442332.1
	ENSP00000442823.1
	ENSP00000443114.1
	ENSP00000446255.1
GenBank Protein	Q8NHQ9	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:

NP_065987 ⟸ NM_020936

- UniProtKB:

Q8IYH0 (UniProtKB/Swiss-Prot), Q658L6 (UniProtKB/Swiss-Prot), Q9HCH7 (UniProtKB/Swiss-Prot), Q8NHQ9 (UniProtKB/Swiss-Prot), A0A384N652 (UniProtKB/TrEMBL)

- Sequence:

show sequence

MEHVTEGSWESLPVPLHPQVLGALRELGFPYMTPVQSATIPLFMRNKDVAAEAVTGSGKTLAFV
IPILEILLRREEKLKKSQVGAIIITPTRELAIQIDEVLSHFTKHFPEFSQILWIGGRNPGEDVE
RFKQQGGNIIVATPGRLEDMFRRKAEGLDLASCVRSLDVLVLDEADRLLDMGFEASINTILEFL
PKQRRTGLFSATQTQEVENLVRAGLRNPVRVSVKEKGVAASSAQKTPSRLENYYMVCKADEKFN
QLVHFLRNHKQEKHLVFFSTCACVEYYGKALEVLVKGVKIMCIHGKMKYKRNKIFMEFRKLQSG
ILVCTDVMARGIDIPEVNWVLQYDPPSNASAFVHRCGRTARIGHGGSALVFLLPMEESYINFLA
INQKCPLQEMKPQRNTADLLPKLKSMALADRAVFEKGMKAFVSYVQAYAKHECNLIFRLKDLDF
ASLARGFALLRMPKMPELRGKQFPDFVPVDVNTDTIPFKDKIREKQRQKLLEQQRREKTENEGR
RKFIKNKAWSKQKAKKEKKKKMNEKRKREEGSDIEDEDMEELLNDTRLLKKLKKGKITEEEFEK
GLLTTGKRTIKTVDLGISDLEDDC

hide sequence

RefSeq Acc Id:	XP_011536910 ⟸ XM_011538608
- Peptide Label:	isoform X14
- UniProtKB:	Q8TEC9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEHVTEGSWESLPVPLHPQVLGALRELGFPYMTPVQSATIPLFMRNKDVAAEAVTGSGKTLAFV IPILEILLRREEKLKKSQVGAIIITPTRELAIQIDEVLSHFTKHFPEFSQILWIGGRNPGEDVE RFKQQGGNIIVATPGRLEDMFRRKAEGLDLASCVRSLDVLVLDEADRLLDMGFEASINTILEFL PKQRRTGLFSATQTQEVENLVRAGLRNPVRVSVKEKGVAASSAQKTPSRLENYYMVCKADEKFN QLVHFLRNHKQEKHLVFFRYSSGLCGRGIRDSARMCSTCACVEYYGKALEVLVKGVKIMCIHGK MKYKRNKIFMEFRKLQSGILVCTDVMARGIDIPEVNWVLQYDPPSNARS hide sequence

RefSeq Acc Id:	XP_016875204 ⟸ XM_017019715
- Peptide Label:	isoform X5
- UniProtKB:	F5H5U2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEHVTEGSWESLPVPLHPQVLGALRELGFPYMTPVQSATIPLFMRNKDVAAEAVTGSGKTLAFV IPILEILLRREEKLKKSQVGAIIITPTRELAIQIDEVLSHFTKHFPEFSQILWIGGRNPGEDVE RFKQQGGNIIVATPGRLEDMFRRKAEGLDLASCVRSLDVLVLDEADRLLDMGFEASINTILEFL PKQRRTGLFSATQTQEVENLVRAGLRNPVRVSVKEKGVAASSAQKTPSRLENYYMVCKADEKFN QLVHFLRNHKQEKHLVFFRYSSGLCGRGIRDSARMCSTCACVEYYGKALEVLVKGVKIMCIHGK MKYKRNKIFMEFRKLQSGILVCTDVMARGIDIPEVNWVLQYDPPSNASLARGFALLRMPKMPEL RGKQFPDFVPVDVNTDTIPFKDKIREKQRQKLLEQQRREKTENEGRRKFIKNKAWSKQKAKKEK KKKMNEKRKREEGSDIEDEDMEELLNDTRLLKKLKKGKITEEEFEKGLLTTGKRTIKTVDLGIS DLEDDC hide sequence

RefSeq Acc Id:	XP_016875210 ⟸ XM_017019721
- Peptide Label:	isoform X15
- UniProtKB:	Q8TEC9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEHVTEGSWESLPVPLHPQVLGALRELGFPYMTPVQSATIPLFMRNKDVAAEAVTGSGKTLAFV IPILEILLRREEKLKKSQVGAIIITPTRELAIQIDEVLSHFTKHFPEFSQILWIGGRNPGEDVE RFKQQGGNIIVATPGRLEDMFRRKAEGLDLASCVRSLDVLVLDEADRLLDMGFEASINTILEFL PKQRRTGLFSATQTQEVENLVRAGLRNPVRVSVKEKGVAASSAQKTPSRLENYYMVCKADEKFN QLVHFLRNHKQEKHLVFFSTCACVEYYGKALEVLVKGVKIMCIHGKMKYKRNKIFMEFRKLQSG ILVCTDVMARGIDIPEVNWVLQYDPPSNARS hide sequence

RefSeq Acc Id:	XP_016875199 ⟸ XM_017019710
- Peptide Label:	isoform X1
- UniProtKB:	A0A384N652 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEHVTEGSWESLPVPLHPQVLGALRELGFPYMTPVQSATIPLFMRNKDVAAEAVTGSGKTLAFV IPILEILLRREEKLKKSQVGAIIITPTRELAIQIDEVLSHFTKHFPEFSQILWIGGRNPGEDVE RFKQQGGNIIVATPGRLEDMFRRKAEGLDLASCVRSLDVLVLDEADRLLDMGFEASINTILEFL PKQRRTGLFSATQTQEVENLVRAGLRNPVRVSVKEKGVAASSAQKTPSRLENYYMVCKADEKFN QLVHFLRNHKQEKHLVFFRYSSGLCGRGIRDSARMCSTCACVEYYGKALEVLVKGVKIMCIHGK MKYKRNKIFMEFRKLQSGILVCTDVMARGIDIPEVNWVLQYDPPSNASAFVHRCGRTARIGHGG SALVFLLPMEESYINFLAINQKCPLQEMKPQRNTADLLPKLKSMALADRAVFEKGMKAFVSYVQ AYAKHECNLIFRLKDLDFASLARGFALLRMPKMPELRGKQFPDFVPVDVNTDTIPFKDKIREKQ RQKLLEQQRREKTENEGRRKFIKNKAWSKQKAKKEKKKKMNEKRKREEGSDIEDEDMEELLNDT RLLKKLKKGKITEEEFEKGLLTTGKRTIKTVDLGISDLEDDC hide sequence

RefSeq Acc Id:	XP_016875205 ⟸ XM_017019716
- Peptide Label:	isoform X6
- UniProtKB:	F5H5U2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MEHVTEGSWESLPVPLHPQVLGALRELGFPYMTPVQSATIPLFMRNKDVAAEAVTGSGKTLAFV IPILEILLRREEKLKKSQVGAIIITPTRELAIQIDEVLSHFTKHFPEFSQILWIGGRNPGEDVE RFKQQGGNIIVATPGRLEDMFRRKAEGLDLASCVRSLDVLVLDEADRLLDMGFEASINTILEFL PKQRRTGLFSATQTQEVENLVRAGLRNPVRVSVKEKGVAASSAQKTPSRLENYYMVCKADEKFN QLVHFLRNHKQEKHLVFFSTCACVEYYGKALEVLVKGVKIMCIHGKMKYKRNKIFMEFRKLQSG ILVCTDVMARGIDIPEVNWVLQYDPPSNASLARGFALLRMPKMPELRGKQFPDFVPVDVNTDTI PFKDKIREKQRQKLLEQQRREKTENEGRRKFIKNKAWSKQKAKKEKKKKMNEKRKREEGSDIED EDMEELLNDTRLLKKLKKGKITEEEFEKGLLTTGKRTIKTVDLGISDLEDDC hide sequence

RefSeq Acc Id:	XP_016875200 ⟸ XM_017019711
- Peptide Label:	isoform X2
- UniProtKB:	A0A384N652 (UniProtKB/TrEMBL)
- Sequence:	show sequence MNSEEERETKTLCLQVTGSGKTLAFVIPILEILLRREEKLKKSQVGAIIITPTRELAIQIDEVL SHFTKHFPEFSQILWIGGRNPGEDVERFKQQGGNIIVATPGRLEDMFRRKAEGLDLASCVRSLD VLVLDEADRLLDMGFEASINTILEFLPKQRRTGLFSATQTQEVENLVRAGLRNPVRVSVKEKGV AASSAQKTPSRLENYYMVCKADEKFNQLVHFLRNHKQEKHLVFFRYSSGLCGRGIRDSARMCST CACVEYYGKALEVLVKGVKIMCIHGKMKYKRNKIFMEFRKLQSGILVCTDVMARGIDIPEVNWV LQYDPPSNASAFVHRCGRTARIGHGGSALVFLLPMEESYINFLAINQKCPLQEMKPQRNTADLL PKLKSMALADRAVFEKGMKAFVSYVQAYAKHECNLIFRLKDLDFASLARGFALLRMPKMPELRG KQFPDFVPVDVNTDTIPFKDKIREKQRQKLLEQQRREKTENEGRRKFIKNKAWSKQKAKKEKKK KMNEKRKREEGSDIEDEDMEELLNDTRLLKKLKKGKITEEEFEKGLLTTGKRTIKTVDLGISDL EDDC hide sequence

RefSeq Acc Id:	XP_016875201 ⟸ XM_017019712
- Peptide Label:	isoform X3
- UniProtKB:	A0A384N652 (UniProtKB/TrEMBL)
- Sequence:	show sequence MRNKDVAAEAVTGSGKTLAFVIPILEILLRREEKLKKSQVGAIIITPTRELAIQIDEVLSHFTK HFPEFSQILWIGGRNPGEDVERFKQQGGNIIVATPGRLEDMFRRKAEGLDLASCVRSLDVLVLD EADRLLDMGFEASINTILEFLPKQRRTGLFSATQTQEVENLVRAGLRNPVRVSVKEKGVAASSA QKTPSRLENYYMVCKADEKFNQLVHFLRNHKQEKHLVFFRYSSGLCGRGIRDSARMCSTCACVE YYGKALEVLVKGVKIMCIHGKMKYKRNKIFMEFRKLQSGILVCTDVMARGIDIPEVNWVLQYDP PSNASAFVHRCGRTARIGHGGSALVFLLPMEESYINFLAINQKCPLQEMKPQRNTADLLPKLKS MALADRAVFEKGMKAFVSYVQAYAKHECNLIFRLKDLDFASLARGFALLRMPKMPELRGKQFPD FVPVDVNTDTIPFKDKIREKQRQKLLEQQRREKTENEGRRKFIKNKAWSKQKAKKEKKKKMNEK RKREEGSDIEDEDMEELLNDTRLLKKLKKGKITEEEFEKGLLTTGKRTIKTVDLGISDLEDDC hide sequence

Ensembl Acc Id:

ENSP00000442823 ⟸ ENST00000544738

Ensembl Acc Id:

ENSP00000443114 ⟸ ENST00000538744

Ensembl Acc Id:

ENSP00000346244 ⟸ ENST00000354291

Ensembl Acc Id:

ENSP00000238146 ⟸ ENST00000238146

Ensembl Acc Id:

ENSP00000442332 ⟸ ENST00000421670

Ensembl Acc Id:

ENSP00000446255 ⟸ ENST00000540763

RefSeq Acc Id:	XP_047285177 ⟸ XM_047429221
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_047285178 ⟸ XM_047429222
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_047285183 ⟸ XM_047429227
- Peptide Label:	isoform X11

RefSeq Acc Id:	XP_047285180 ⟸ XM_047429224
- Peptide Label:	isoform X8

RefSeq Acc Id:	XP_047285185 ⟸ XM_047429229
- Peptide Label:	isoform X13

RefSeq Acc Id:	XP_047285181 ⟸ XM_047429225
- Peptide Label:	isoform X9

RefSeq Acc Id:	XP_047285182 ⟸ XM_047429226
- Peptide Label:	isoform X10

RefSeq Acc Id:	XP_047285184 ⟸ XM_047429228
- Peptide Label:	isoform X12

RefSeq Acc Id:	XP_047285179 ⟸ XM_047429223
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_054228668 ⟸ XM_054372693
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054228671 ⟸ XM_054372696
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054228676 ⟸ XM_054372701
- Peptide Label:	isoform X16

RefSeq Acc Id:	XP_054228674 ⟸ XM_054372699
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_054228669 ⟸ XM_054372694
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054228667 ⟸ XM_054372692
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054228672 ⟸ XM_054372697
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054228673 ⟸ XM_054372698
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054228679 ⟸ XM_054372704
- Peptide Label:	isoform X11

RefSeq Acc Id:	XP_054228683 ⟸ XM_054372708
- Peptide Label:	isoform X17

RefSeq Acc Id:	XP_054228675 ⟸ XM_054372700
- Peptide Label:	isoform X8

RefSeq Acc Id:	XP_054228684 ⟸ XM_054372709
- Peptide Label:	isoform X15

RefSeq Acc Id:	XP_054228682 ⟸ XM_054372707
- Peptide Label:	isoform X14

RefSeq Acc Id:	XP_054228681 ⟸ XM_054372706
- Peptide Label:	isoform X13

RefSeq Acc Id:	XP_054228677 ⟸ XM_054372702
- Peptide Label:	isoform X9

RefSeq Acc Id:	XP_054228678 ⟸ XM_054372703
- Peptide Label:	isoform X10

RefSeq Acc Id:	XP_054228680 ⟸ XM_054372705
- Peptide Label:	isoform X12

RefSeq Acc Id:	XP_054228670 ⟸ XM_054372695
- Peptide Label:	isoform X3

Protein Domains

DEAD-box RNA helicase Q Helicase ATP-binding Helicase C-terminal

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q8NHQ9-F1-model_v2	AlphaFold	Q8NHQ9	1-600	view protein structure

Promoters

RGD ID:

6790182

Promoter ID:

HG_KWN:16961

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

ENST00000354291, NM_020936, UC001UFH.2

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	12	122,652,409 - 122,652,909 (+)	MPROMDB

RGD ID:

6790181

Promoter ID:

HG_KWN:16962

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, Lymphoblastoid

Transcripts:

UC001UFJ.1, UC001UFK.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	12	122,656,381 - 122,658,017 (+)	MPROMDB

RGD ID:

6789850

Promoter ID:

HG_KWN:16964

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, HeLa_S3, Lymphoblastoid, NB4

Transcripts:

UC001UFL.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	12	122,668,216 - 122,669,332 (+)	MPROMDB

RGD ID:

7225799

Promoter ID:

EPDNEW_H18645

Type:

initiation region

Name:

DDX55_1

Description:

DEAD-box helicase 55

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	12	123,602,099 - 123,602,159	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:20085	AgrOrtholog
COSMIC	DDX55	COSMIC
Ensembl Genes	ENSG00000111364	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000238146	ENTREZGENE
	ENST00000238146.9	UniProtKB/Swiss-Prot
	ENST00000354291.8	UniProtKB/TrEMBL
	ENST00000421670.3	UniProtKB/Swiss-Prot
	ENST00000538744.5	UniProtKB/TrEMBL
	ENST00000540763.5	UniProtKB/TrEMBL
	ENST00000544738.5	UniProtKB/TrEMBL
Gene3D-CATH	3.40.50.300	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000111364	GTEx
HGNC ID	HGNC:20085	ENTREZGENE
Human Proteome Map	DDX55	Human Proteome Map
InterPro	DEAD/DEAH_box_helicase_dom	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	DUF4217	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Helicase_ATP-bd	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Helicase_C	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	P-loop_NTPase	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	RNA-helicase_DEAD-box_CS	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	RNA_helicase_DEAD_Q_motif	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:57696	UniProtKB/Swiss-Prot
NCBI Gene	57696	ENTREZGENE
OMIM	620176	OMIM
PANTHER	ATP-DEPENDENT RNA HELICASE DDX55	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	RNA HELICASE	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	DEAD	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	DUF4217	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Helicase_C	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA134984021	PharmGKB
PROSITE	DEAD_ATP_HELICASE	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	HELICASE_ATP_BIND_1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	HELICASE_CTER	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Q_MOTIF	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	DEXDc	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	DUF4217	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	HELICc	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF52540	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0A384N652	ENTREZGENE, UniProtKB/TrEMBL
	DDX55_HUMAN	UniProtKB/Swiss-Prot
	E7EX41_HUMAN	UniProtKB/TrEMBL
	F5H2I2_HUMAN	UniProtKB/TrEMBL
	F5H5U2	ENTREZGENE, UniProtKB/TrEMBL
	F5H735_HUMAN	UniProtKB/TrEMBL
	Q658L6	ENTREZGENE
	Q8IYH0	ENTREZGENE
	Q8NHQ9	ENTREZGENE
	Q8TEC9	ENTREZGENE, UniProtKB/TrEMBL
	Q9HCH7	ENTREZGENE
UniProt Secondary	Q658L6	UniProtKB/Swiss-Prot
	Q8IYH0	UniProtKB/Swiss-Prot
	Q9HCH7	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-01-12	DDX55	DEAD-box helicase 55		DEAD (Asp-Glu-Ala-Asp) box polypeptide 55	Symbol and/or name change	5135510	APPROVED

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

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

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

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

Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar