TMEM74B (transmembrane protein 74B)

Gene: TMEM74B (transmembrane protein 74B) Homo sapiens

Analyze

Symbol:

TMEM74B

Name:

transmembrane protein 74B

RGD ID:

1354046

HGNC Page

HGNC:15893

Description:

Predicted to be located in membrane.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

C20orf46; FLJ11190; transmembrane protein C20orf46

RGD Orthologs

Alliance Genes

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Tmem74b (transmembrane protein 74B)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Rattus norvegicus (Norway rat):	Tmem74b (transmembrane protein 74B)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Tmem74b (transmembrane protein 74B)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	TMEM74B (transmembrane protein 74B)	NCBI	Ortholog
Canis lupus familiaris (dog):	TMEM74B (transmembrane protein 74B)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, Panther, PhylomeDB
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Tmem74b (transmembrane protein 74B)	NCBI	Ortholog
Sus scrofa (pig):	TMEM74B (transmembrane protein 74B)	HGNC	Ensembl, NCBI, OrthoDB
Chlorocebus sabaeus (green monkey):	TMEM74B (transmembrane protein 74B)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Tmem74b (transmembrane protein 74B)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Tmem74b (transmembrane protein 74B)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Tmem74b (transmembrane protein 74B)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	tmem74b (transmembrane protein 74B)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Xenopus laevis (African clawed frog):	tmem74b.L	Alliance	DIOPT (Xenbase)
Xenopus laevis (African clawed frog):	tmem74b.S	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	tmem74b	Alliance	DIOPT (Hieranoid\|OrthoFinder\|OrthoInspector\|PANTHER)

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	1,180,570 - 1,189,409 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	20	1,180,561 - 1,185,415 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	20	1,161,214 - 1,166,564 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	20	1,109,215 - 1,113,117 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	20	1,109,214 - 1,113,117	NCBI
Celera	20	1,257,551 - 1,261,455 (-)	NCBI		Celera
Cytogenetic Map	20	p13	NCBI
HuRef	20	1,112,988 - 1,116,894 (-)	NCBI		HuRef
CHM1_1	20	1,161,233 - 1,165,135 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	20	1,227,788 - 1,236,631 (-)	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->4)-beta-D-glucan (ISO)

6-propyl-2-thiouracil (ISO)

acrylamide (EXP,ISO)

aflatoxin B1 (EXP)

aristolochic acid A (EXP)

arsane (EXP)

arsenic atom (EXP)

benzo[a]pyrene (EXP)

bisphenol A (ISO)

bisphenol F (EXP)

chlorpyrifos (ISO)

cisplatin (EXP)

copper(II) sulfate (EXP)

cyclosporin A (EXP)

dioxygen (EXP)

dorsomorphin (EXP)

entinostat (EXP)

ketamine (ISO)

paracetamol (EXP)

perfluorooctane-1-sulfonic acid (ISO)

resveratrol (EXP)

SB 431542 (EXP)

silicon dioxide (EXP)

sodium arsenite (ISO)

sunitinib (EXP)

thimerosal (EXP)

titanium dioxide (ISO)

trichloroethene (ISO)

urethane (EXP)

valproic acid (EXP)

zoledronic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Cellular Component

membrane (IEA)

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:17474147	PMID:20944657	PMID:32393512

Genomics

Comparative Map Data

TMEM74B
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	20	1,180,570 - 1,189,409 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	20	1,180,561 - 1,185,415 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	20	1,161,214 - 1,166,564 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	20	1,109,215 - 1,113,117 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	20	1,109,214 - 1,113,117	NCBI
Celera	20	1,257,551 - 1,261,455 (-)	NCBI		Celera
Cytogenetic Map	20	p13	NCBI
HuRef	20	1,112,988 - 1,116,894 (-)	NCBI		HuRef
CHM1_1	20	1,161,233 - 1,165,135 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	20	1,227,788 - 1,236,631 (-)	NCBI		T2T-CHM13v2.0

Tmem74b
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	2	151,543,294 - 151,558,665 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	2	151,543,928 - 151,554,077 (+)	Ensembl		GRCm39 Ensembl
GRCm38	2	151,701,805 - 151,716,745 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	2	151,702,008 - 151,712,157 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	2	151,527,744 - 151,533,046 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	2	151,393,287 - 151,398,751 (+)	NCBI		MGSCv36	mm8
Celera	2	157,518,887 - 157,524,197 (+)	NCBI		Celera
Cytogenetic Map	2	G3	NCBI
cM Map	2	74.83	NCBI

Tmem74b
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	3	160,679,964 - 160,684,580 (+)	NCBI		GRCr8
mRatBN7.2	3	140,219,592 - 140,224,208 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	3	140,219,412 - 140,235,872 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	3	144,124,133 - 144,128,749 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	3	152,707,940 - 152,712,556 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	3	150,448,291 - 150,452,897 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	3	147,219,442 - 147,226,949 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	3	147,226,004 - 147,226,702 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	3	153,575,272 - 153,579,554 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	3	142,043,961 - 142,047,717 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	3	138,978,306 - 138,982,741 (+)	NCBI		Celera
Cytogenetic Map	3	q41	NCBI

Tmem74b
(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_004955596	424,771 - 427,694 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955596	424,771 - 427,694 (-)	NCBI	ChiLan1.0	ChiLan1.0

TMEM74B
(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	2,218,171 - 2,223,528 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	20	2,215,000 - 2,220,357 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	20	1,334,191 - 1,342,982 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	20	1,105,487 - 1,110,241 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	20	1,105,492 - 1,110,041 (-)	Ensembl	panpan1.1		panPan2

TMEM74B
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	24	19,801,268 - 19,807,157 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	24	19,801,215 - 19,806,879 (+)	NCBI	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	24	19,455,186 - 19,461,450 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	24	20,491,458 - 20,498,234 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	24	20,490,969 - 20,498,315 (+)	Ensembl		ROS_Cfam_1.0 Ensembl

Tmem74b
(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	169,036,434 - 169,049,577 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936485	17,470,871 - 17,471,569 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936485	17,467,626 - 17,478,749 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

TMEM74B
(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	34,101,109 - 34,103,994 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	17	34,099,511 - 34,107,077 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	17	38,648,381 - 38,653,743 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

TMEM74B
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Vero_WHO_p1.0	NW_023666087	1,779,400 - 1,780,140 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Tmem74b
(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_004624741	2,455,466 - 2,460,243 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624741	2,443,929 - 2,460,264 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in TMEM74B
14 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 20p13(chr20:89939-1360110)x1	copy number loss	See cases [RCV000050841]	Chr20:89939..1360110 [GRCh38] Chr20:70580..1340754 [GRCh37] Chr20:18580..1288754 [NCBI36] Chr20:20p13	pathogenic
GRCh38/hg38 20p13(chr20:89939-1852477)x1	copy number loss	See cases [RCV000050373]	Chr20:89939..1852477 [GRCh38] Chr20:70580..1833123 [GRCh37] Chr20:18580..1781123 [NCBI36] Chr20:20p13	pathogenic
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 20p13-11.23(chr20:89939-19146279)x3	copy number gain	See cases [RCV000051041]	Chr20:89939..19146279 [GRCh38] Chr20:70580..19126923 [GRCh37] Chr20:18580..19074923 [NCBI36] Chr20:20p13-11.23	pathogenic
GRCh38/hg38 20p13(chr20:828964-1241192)x3	copy number gain	See cases [RCV000052732]	Chr20:828964..1241192 [GRCh38] Chr20:809607..1221836 [GRCh37] Chr20:757607..1169836 [NCBI36] Chr20:20p13	uncertain significance
GRCh38/hg38 20p13(chr20:89939-1939218)x1	copy number loss	See cases [RCV000052735]	Chr20:89939..1939218 [GRCh38] Chr20:70580..1919864 [GRCh37] Chr20:18580..1867864 [NCBI36] Chr20:20p13	pathogenic
GRCh38/hg38 20p13(chr20:89939-1770567)x1	copy number loss	See cases [RCV000052736]	Chr20:89939..1770567 [GRCh38] Chr20:70580..1751213 [GRCh37] Chr20:18580..1699213 [NCBI36] Chr20:20p13	pathogenic
GRCh38/hg38 20p13(chr20:89939-1668795)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052737]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052737]\|See cases [RCV000052737]	Chr20:89939..1668795 [GRCh38] Chr20:70580..1649441 [GRCh37] Chr20:18580..1597441 [NCBI36] Chr20:20p13	pathogenic
GRCh38/hg38 20p13(chr20:121781-2290194)x1	copy number loss	See cases [RCV000052738]	Chr20:121781..2290194 [GRCh38] Chr20:102422..2270840 [GRCh37] Chr20:50422..2218840 [NCBI36] Chr20:20p13	pathogenic
GRCh38/hg38 20p13-11.23(chr20:89939-19071495)x3	copy number gain	See cases [RCV000052995]	Chr20:89939..19071495 [GRCh38] Chr20:70580..19052139 [GRCh37] Chr20:18580..19000139 [NCBI36] Chr20:20p13-11.23	pathogenic
GRCh38/hg38 20p13-11.22(chr20:89939-21787252)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052996]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052996]\|See cases [RCV000052996]	Chr20:89939..21787252 [GRCh38] Chr20:70580..21767890 [GRCh37] Chr20:18580..21715890 [NCBI36] Chr20:20p13-11.22	pathogenic
GRCh38/hg38 20p13-12.1(chr20:89939-14818511)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052997]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052997]\|See cases [RCV000052997]	Chr20:89939..14818511 [GRCh38] Chr20:70580..14799157 [GRCh37] Chr20:18580..14747157 [NCBI36] Chr20:20p13-12.1	pathogenic
NM_018354.2(TMEM74B):c.134G>A (p.Arg45Lys)	single nucleotide variant	Malignant melanoma [RCV000072526]	Chr20:1181485 [GRCh38] Chr20:1162129 [GRCh37] Chr20:1110129 [NCBI36] Chr20:20p13	not provided
GRCh37/hg19 20p13(chr20:71023-2129746)x1	copy number loss	See cases [RCV000184090]	Chr20:71023..2129746 [GRCh37] Chr20:20p13	pathogenic
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(chr20:89939-1494113)x1	copy number loss	See cases [RCV000135804]	Chr20:89939..1494113 [GRCh38] Chr20:70580..1474759 [GRCh37] Chr20:18580..1422759 [NCBI36] Chr20:20p13	pathogenic
GRCh38/hg38 20p13(chr20:89939-1246891)x3	copy number gain	See cases [RCV000135794]	Chr20:89939..1246891 [GRCh38] Chr20:70580..1227535 [GRCh37] Chr20:18580..1175535 [NCBI36] Chr20:20p13	uncertain significance
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 20p13-12.1(chr20:80106-13029401)x3	copy number gain	See cases [RCV000138677]	Chr20:80106..13029401 [GRCh38] Chr20:60747..13010049 [GRCh37] Chr20:8747..12958049 [NCBI36] Chr20:20p13-12.1	pathogenic
GRCh38/hg38 20p13(chr20:80093-1246766)x1	copy number loss	See cases [RCV000139403]	Chr20:80093..1246766 [GRCh38] Chr20:60734..1227410 [GRCh37] Chr20:8734..1175410 [NCBI36] Chr20:20p13	pathogenic
GRCh38/hg38 20p13-12.3(chr20:80093-6386012)x3	copy number gain	See cases [RCV000139597]	Chr20:80093..6386012 [GRCh38] Chr20:60734..6366659 [GRCh37] Chr20:8734..6314659 [NCBI36] Chr20:20p13-12.3	pathogenic
GRCh38/hg38 20p13-12.3(chr20:84402-6159078)x3	copy number gain	See cases [RCV000141348]	Chr20:84402..6159078 [GRCh38] Chr20:65043..6139725 [GRCh37] Chr20:13043..6087725 [NCBI36] Chr20:20p13-12.3	pathogenic
GRCh38/hg38 20p13(chr20:209424-1852477)x3	copy number gain	See cases [RCV000140876]	Chr20:209424..1852477 [GRCh38] Chr20:190065..1833123 [GRCh37] Chr20:138065..1781123 [NCBI36] Chr20:20p13	uncertain significance
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
GRCh38/hg38 20p13-12.3(chr20:80927-5447679)x3	copy number gain	See cases [RCV000142285]	Chr20:80927..5447679 [GRCh38] Chr20:61568..5428325 [GRCh37] Chr20:9568..5376325 [NCBI36] Chr20:20p13-12.3	uncertain significance
GRCh38/hg38 20p13(chr20:80106-1246891)x1	copy number loss	See cases [RCV000142919]	Chr20:80106..1246891 [GRCh38] Chr20:60747..1227535 [GRCh37] Chr20:8747..1175535 [NCBI36] Chr20:20p13	likely pathogenic
GRCh38/hg38 20p13-11.23(chr20:80928-18688031)x3	copy number gain	See cases [RCV000143426]	Chr20:80928..18688031 [GRCh38] Chr20:61569..18668675 [GRCh37] Chr20:9569..18616675 [NCBI36] Chr20:20p13-11.23	pathogenic
GRCh38/hg38 20p13(chr20:80927-1806080)x1	copy number loss	See cases [RCV000143700]	Chr20:80927..1806080 [GRCh38] Chr20:61568..1786726 [GRCh37] Chr20:9568..1734726 [NCBI36] Chr20:20p13	likely pathogenic\|uncertain significance
GRCh38/hg38 20p13(chr20:89939-1852477)x1	copy number loss	See cases [RCV000148279]	Chr20:89939..1852477 [GRCh38] Chr20:70580..1833123 [GRCh37] Chr20:18580..1781123 [NCBI36] Chr20:20p13	pathogenic
GRCh37/hg19 20p13-12.3(chr20:121521-5564937)x3	copy number gain	See cases [RCV000239772]	Chr20:121521..5564937 [GRCh37] Chr20:20p13-12.3	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 20p13(chr20:61568-4914872)x3	copy number gain	See cases [RCV000446883]	Chr20:61568..4914872 [GRCh37] Chr20:20p13	pathogenic
GRCh37/hg19 20p13(chr20:61568-1823540)x1	copy number loss	See cases [RCV000446902]	Chr20:61568..1823540 [GRCh37] Chr20:20p13	pathogenic
GRCh37/hg19 20p13(chr20:121521-2073612)x1	copy number loss	See cases [RCV000446640]	Chr20:121521..2073612 [GRCh37] Chr20:20p13	pathogenic
GRCh37/hg19 20p13(chr20:61568-1513319)x1	copy number loss	See cases [RCV000445920]	Chr20:61568..1513319 [GRCh37] Chr20:20p13	pathogenic
GRCh37/hg19 20p13(chr20:61568-4904599)x3	copy number gain	See cases [RCV000448397]	Chr20:61568..4904599 [GRCh37] Chr20:20p13	pathogenic
GRCh37/hg19 20p13(chr20:1164613-1229292)x3	copy number gain	See cases [RCV000447748]	Chr20:1164613..1229292 [GRCh37] Chr20:20p13	uncertain significance
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 20p13-12.3(chr20:213423-5483406)x3	copy number gain	See cases [RCV000510531]	Chr20:213423..5483406 [GRCh37] Chr20:20p13-12.3	uncertain significance
GRCh37/hg19 20p13(chr20:381794-1268103)x3	copy number gain	See cases [RCV000510434]	Chr20:381794..1268103 [GRCh37] Chr20:20p13	uncertain significance
GRCh37/hg19 20p13(chr20:61568-1651420)x1	copy number loss	See cases [RCV000510423]	Chr20:61568..1651420 [GRCh37] Chr20:20p13	likely pathogenic
GRCh37/hg19 20p13(chr20:61568-2824960)x3	copy number gain	See cases [RCV000511991]	Chr20:61568..2824960 [GRCh37] Chr20:20p13	uncertain significance
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)x3	copy number gain	See cases [RCV000510832]	Chr20:61569..62915555 [GRCh37] Chr20:20p13-q13.33	pathogenic
NM_001304748.2(TMEM74B):c.89G>C (p.Gly30Ala)	single nucleotide variant	Inborn genetic diseases [RCV003288210]	Chr20:1181530 [GRCh38] Chr20:1162174 [GRCh37] Chr20:20p13	uncertain significance
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)	copy number gain	See cases [RCV000512450]	Chr20:61569..62915555 [GRCh37] Chr20:20p13-q13.33	pathogenic
GRCh37/hg19 20p13-12.2(chr20:61568-10486106)x3	copy number gain	See cases [RCV000512556]	Chr20:61568..10486106 [GRCh37] Chr20:20p13-12.2	likely pathogenic
GRCh37/hg19 20p13(chr20:61568-2010334)x1	copy number loss	not provided [RCV000684132]	Chr20:61568..2010334 [GRCh37] Chr20:20p13	likely pathogenic
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
NM_001304748.2(TMEM74B):c.631G>A (p.Val211Ile)	single nucleotide variant	Inborn genetic diseases [RCV003244862]	Chr20:1180988 [GRCh38] Chr20:1161632 [GRCh37] Chr20:20p13	uncertain significance
GRCh37/hg19 20p13(chr20:61568-2269777)x1	copy number loss	not provided [RCV001007065]	Chr20:61568..2269777 [GRCh37] Chr20:20p13	pathogenic
GRCh37/hg19 20p13(chr20:728577-1237670)x4	copy number gain	not provided [RCV000849650]	Chr20:728577..1237670 [GRCh37] Chr20:20p13	uncertain significance
GRCh37/hg19 20p13(chr20:61568-1305971)x1	copy number loss	not provided [RCV001007067]	Chr20:61568..1305971 [GRCh37] Chr20:20p13	pathogenic
NM_001304748.2(TMEM74B):c.617G>A (p.Arg206His)	single nucleotide variant	Inborn genetic diseases [RCV003248645]	Chr20:1181002 [GRCh38] Chr20:1161646 [GRCh37] Chr20:20p13	uncertain significance
GRCh37/hg19 20p13(chr20:989820-1216980)x3	copy number gain	not provided [RCV001007070]	Chr20:989820..1216980 [GRCh37] Chr20:20p13	uncertain significance
GRCh37/hg19 20p13-11.1(chr20:61568-26305479)x3	copy number gain	not provided [RCV001007068]	Chr20:61568..26305479 [GRCh37] Chr20:20p13-11.1	pathogenic
GRCh37/hg19 20p13(chr20:61568-1823540)	copy number loss	not specified [RCV002052695]	Chr20:61568..1823540 [GRCh37] Chr20:20p13	pathogenic
NM_001304748.2(TMEM74B):c.52G>A (p.Glu18Lys)	single nucleotide variant	Inborn genetic diseases [RCV003286468]	Chr20:1181567 [GRCh38] Chr20:1162211 [GRCh37] Chr20:20p13	uncertain significance
GRCh37/hg19 20p13(chr20:1015167-1403720)x3	copy number gain	not provided [RCV002473606]	Chr20:1015167..1403720 [GRCh37] Chr20:20p13	uncertain significance
NM_001304748.2(TMEM74B):c.356T>C (p.Val119Ala)	single nucleotide variant	Inborn genetic diseases [RCV002731843]	Chr20:1181263 [GRCh38] Chr20:1161907 [GRCh37] Chr20:20p13	uncertain significance
NM_001304748.2(TMEM74B):c.607G>A (p.Glu203Lys)	single nucleotide variant	Inborn genetic diseases [RCV002749870]	Chr20:1181012 [GRCh38] Chr20:1161656 [GRCh37] Chr20:20p13	uncertain significance
NM_001304748.2(TMEM74B):c.470G>A (p.Arg157Gln)	single nucleotide variant	Inborn genetic diseases [RCV002749605]	Chr20:1181149 [GRCh38] Chr20:1161793 [GRCh37] Chr20:20p13	uncertain significance
GRCh37/hg19 20p13(chr20:992980-1481478)x4	copy number gain	not provided [RCV002475623]	Chr20:992980..1481478 [GRCh37] Chr20:20p13	uncertain significance
NM_001304748.2(TMEM74B):c.382G>A (p.Val128Ile)	single nucleotide variant	Inborn genetic diseases [RCV002733903]	Chr20:1181237 [GRCh38] Chr20:1161881 [GRCh37] Chr20:20p13	uncertain significance
NM_001304748.2(TMEM74B):c.225C>G (p.Asn75Lys)	single nucleotide variant	Inborn genetic diseases [RCV002818701]	Chr20:1181394 [GRCh38] Chr20:1162038 [GRCh37] Chr20:20p13	uncertain significance
NM_001304748.2(TMEM74B):c.350G>A (p.Arg117His)	single nucleotide variant	Inborn genetic diseases [RCV003000922]	Chr20:1181269 [GRCh38] Chr20:1161913 [GRCh37] Chr20:20p13	uncertain significance
NM_001304748.2(TMEM74B):c.709G>T (p.Ala237Ser)	single nucleotide variant	Inborn genetic diseases [RCV002897174]	Chr20:1180910 [GRCh38] Chr20:1161554 [GRCh37] Chr20:20p13	uncertain significance
NM_001304748.2(TMEM74B):c.554C>T (p.Thr185Met)	single nucleotide variant	Inborn genetic diseases [RCV002674782]	Chr20:1181065 [GRCh38] Chr20:1161709 [GRCh37] Chr20:20p13	uncertain significance
NM_001304748.2(TMEM74B):c.205C>T (p.His69Tyr)	single nucleotide variant	Inborn genetic diseases [RCV003265446]	Chr20:1181414 [GRCh38] Chr20:1162058 [GRCh37] Chr20:20p13	uncertain significance
GRCh38/hg38 20p13-11.21(chr20:87153-23635465)x3	copy number gain	Renal agenesis [RCV003327640]	Chr20:87153..23635465 [GRCh38] Chr20:20p13-11.21	pathogenic
Single allele	deletion	not provided [RCV003448677]	Chr20:61001..2316914 [GRCh37] Chr20:20p13	pathogenic
GRCh37/hg19 20p13(chr20:61569-1794919)x3	copy number gain	not provided [RCV003485206]	Chr20:61569..1794919 [GRCh37] Chr20:20p13	uncertain significance
GRCh37/hg19 20p13-12.2(chr20:61569-9542361)x3	copy number gain	not provided [RCV003485207]	Chr20:61569..9542361 [GRCh37] Chr20:20p13-12.2	pathogenic
GRCh37/hg19 20p13-12.1(chr20:68351-16142323)x3	copy number gain	not provided [RCV003885494]	Chr20:68351..16142323 [GRCh37] Chr20:20p13-12.1	pathogenic
GRCh37/hg19 20p13-11.21(chr20:68351-23860313)x3	copy number gain	not provided [RCV003885495]	Chr20:68351..23860313 [GRCh37] Chr20:20p13-11.21	pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	733
Count of miRNA genes:	497
Interacting mature miRNAs:	540
Transcripts:	ENST00000381894, ENST00000429036, ENST00000481747
Prediction methods:	Microtar, Miranda, Rnahybrid
Result types:	miRGate_prediction

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

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

Markers in Region

G59692

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	1,162,516 - 1,162,641	UniSTS	GRCh37
Build 36	20	1,110,516 - 1,110,641	RGD	NCBI36
Celera	20	1,258,852 - 1,258,977	RGD
Cytogenetic Map	20	p13	UniSTS
HuRef	20	1,114,289 - 1,114,414	UniSTS
TNG Radiation Hybrid Map	20	760.0	UniSTS

WIAF-2129

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	1,162,512 - 1,162,656	UniSTS	GRCh37
Build 36	20	1,110,512 - 1,110,656	RGD	NCBI36
Celera	20	1,258,848 - 1,258,992	RGD
Cytogenetic Map	20	p13	UniSTS
HuRef	20	1,114,285 - 1,114,429	UniSTS
GeneMap99-GB4 RH Map	20	11.04	UniSTS
NCBI RH Map	20	10.0	UniSTS

Expression

RNA-SEQ Expression

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

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

visual system

adipose tissue

appendage

entire extraembryonic component

pharyngeal arch

High

Medium

285

352

132

982

1776

129

692

290

660

Low

2118

1925

1345

558

553

418

3150

2075

1914

339

1276

859

152

914

1965

Below cutoff

935

1020

208

163

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001304748	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001304749	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001387329	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001387330	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001387331	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001387332	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001387333	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001387334	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_018354	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529281	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529282	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529283	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011529284	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017027923	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017027924	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017027925	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047440257	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323618	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323619	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323620	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323621	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323622	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323623	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323624	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AA861530	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK002052	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK126837	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL031665	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AW628999	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AX405830	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AX878080	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM545116	(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

RefSeq Acc Id:

ENST00000381894 ⟹ ENSP00000371318

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	1,180,561 - 1,184,473 (-)	Ensembl

RefSeq Acc Id:

ENST00000429036 ⟹ ENSP00000400552

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	1,180,570 - 1,184,981 (-)	Ensembl

RefSeq Acc Id:

ENST00000481747

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	1,181,284 - 1,185,415 (-)	Ensembl

RefSeq Acc Id:

NM_001304748 ⟹ NP_001291677

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	1,180,570 - 1,184,981 (-)	NCBI
CHM1_1	20	1,161,223 - 1,165,337 (-)	NCBI
T2T-CHM13v2.0	20	1,227,788 - 1,232,203 (-)	NCBI

Sequence:

show sequence

GCCTTCCGGGTCCCGCGTCTGTGGGCAAGGGCAGGAGCAGGGGGTGTGGACTGGGCCGGCGGGA
GCGGGCGCGGTGGGCAGCCGGCGTGCTGGGGCTTTCTGCGCGCAACTTTGGGTACAACAGCGTG
GACCTGCGTGTGCGTATCTGCGCGCCCCAAGGCTTTGTGTACAACTCGTGCGTGTGTCTATCGA
CTGGGTTTTGTGAAGCTTCACCCACAGCCGCTGTGCGTCCCTCTCTCCGGGTGTCAGTGCGCGC
GGCGGGTGGGGTATTGGGCCCCTGCGGGTCTTGGTGGATCTGGCTTGGGTCTCACTCCCAGGGG
CACTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGCGCGTGTGCGTGTGACGGGGT
ACTCGCGTGGCCCGAAGATCCGAGGGTCACACTACGTGACTTCTGGGTGTCTGTGGGTACTGCT
GTGGGAACAGCTGCTGGGGGAGTGTGTGTGGAACTGGAGTGTTCCTTTCAGGACCTGTCTGACT
GCAGATGAAATTAGTAACTGGTGGGGTCGTGGGGTGTGAATGGTGGGCGGGAGCAGCTATGTCA
GTTGGTGTGTTTCTGCTTATGTTAGGGTAATTGGGCACGGCCTTTGTGTAACTGGTGAATATCT
CTGAACCTGGGCATGAAACAGAGAGATGTCCTAACTCTGGTAAAAGCAGTCTGGGCGCAGGCTG
GGGACCCAGATGGAATTCAAACTTATGCCTGCTCTCAAGGTGCTCACGGTTGCTGATAAACAGC
TGGATAAAATGAAGAGTCTATGAGTGAGGGATGCAGAGCCAGGGAAGGCTGGTGGAGTGATGCC
ACCAGCACAGGGGTATGAGTTTGCAGCTGCCAAGGGGCCAAGGGATGAGCTGGGGCCCTCCTTC
CCAATGGCATCTCCCCCTGGTCTGGAACTGAAGACACTGAGCAATGGTCCCCAAGCCCCAAGGA
GATCAGCTCCCCTGGGCCCAGTGGCCCCAACCAGGGAGGGTGTGGAGAATGCCTGCTTCTCCTC
AGAGGAGCATGAGACCCATTTCCAGAACCCTGGGAACACGAGACTGGGCAGCTCACCCAGTCCC
CCTGGGGGTGTCTCCTCACTGCCCCGATCCCAGCGGGATGATCTGTCCCTTCATTCAGAGGAGG
GGCCAGCCCTGGAGCCCGTGAGCCGCCCGGTGGATTATGGCTTTGTTTCCGCCCTCGTTTTCCT
GGTGAGTGGGATTCTTCTGGTGGTGACAGCATACGCCATCCCCCGTGAGGCTCGAGTCAATCCG
GACACAGTGACAGCGCGGGAGATGGAACGACTGGAGATGTACTACGCCCGCCTAGGCTCCCACC
TGGACAGGTGCATCATCGCAGGCCTCGGGCTGCTCACGGTGGGCGGCATGCTCTTGTCGGTGCT
GCTCATGGTCTCCCTGTGCAAGGGCGAGCTGTACCGCCGGAGGACCTTCGTCCCCGGCAAGGGC
TCCAGGAAGACCTACGGCTCCATTAACCTGCGCATGAGACAGCTCAATGGGGATGGGGGCCAGG
CCCTGGTGGAGAATGAAGTTGTCCAGGTCTCAGAGACTAGCCACACCCTCCAGAGGTCTTAAGA
ACTAGCCCACCTTATCTGGCTGCTTTAGCTCCAGTGCTACAAGGTCCACCCCCTGCTCCCGCCC
ACCTGACCCCTGCCAAGGCCCTGGGGTTTTAAACTGAGCTCACATAGGGCCTTGTGGAAGAAGT
ACTGGGTGCTGGAGGGAGAGCTCGGGGCCCAGCCCATGCCCCACACGGGCAAGCAGCCCACTGA
TCTGTTTTGTAGCTGAGGTTTTGCATACGGTTTTGTTTGGAGGATGGCTTCTGCTGCTAAAAAT
ACAAAAGTTTGGAAACCGCT

hide sequence

RefSeq Acc Id:

NM_001304749 ⟹ NP_001291678

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	1,180,570 - 1,185,920 (-)	NCBI
CHM1_1	20	1,161,223 - 1,166,095 (-)	NCBI
T2T-CHM13v2.0	20	1,227,788 - 1,233,142 (-)	NCBI

Sequence:

show sequence

GAGCCACGGAGCCGCAAGCGCCCGAGGAGACCGTCCCGACCTAAGGACCTCGGAGAGGACCCGG
GGTCCTACCTGGGGGCTGCGTGCGGGGTGGGGGTGGGGGGAAGGGGAAGTGGCAGAGTGGGGGT
GAGGAGTGGGGAGGCACCTGCGCTTGGCGCAATAGGGGCTCTCCGGTGGTGGGGAGGGATCTTC
TTCAGCAGCCCCCGCCCGCCCCGCCCCTGCGCCCGTGGACCGCGGGCTCCAAGCCCCAGTTCCC
TAAGCCCAGGCGCCGGCGATCCAGATCTGCCTGGAGGGGAGGGGAGGACGGTGGATCGGAGCCC
CCGCACCCTCGCCCCAGCCCATCACCCGCCTTCCTGTCCCTCTCCTTGCTAACTCTCCGGGCGC
CCTCGCCGGCCGCGGGCGGAGCTCCCTCCGCGGCGCTCGGCGAGCCCCGGCCCCCGCCCCTTCT
CCCGTCCCTCCGTCCCCGGATCCCCCCCCCGCCTCCCCAGCGGCCGCCACCGCCGCCGTACAGC
TCCGCGCGGCGCGAGTAGGTACGTGCGCCTCGGCAGTGGCTCCGGGCCGGGCCGGGAAGGGGGC
GGGAGACCGGGAGGGCGAGGCGGTGGCGGCCGGGCCCGCGCCCTCCGGGCTGCGCCGCAGGAGA
GAGACCCCCGCAGGCGAGACCCCCGCAGGCGTACGCCGGCTGCAGGAAGGCGGACGGGCACCGG
AGAGGACGCACCCTCGCCCGCCGGCGGCCGGGCGCCCTTCGCCCCAGCGTGGTGAGGCGGGGAG
GGAGGCCCGGCACAGCTGCCAAGGGGCCAAGGGATGAGCTGGGGCCCTCCTTCCCAATGGCATC
TCCCCCTGGTCTGGAACTGAAGACACTGAGCAATGGTCCCCAAGCCCCAAGGAGATCAGCTCCC
CTGGGCCCAGTGGCCCCAACCAGGGAGGGTGTGGAGAATGCCTGCTTCTCCTCAGAGGAGCATG
AGACCCATTTCCAGAACCCTGGGAACACGAGACTGGGCAGCTCACCCAGTCCCCCTGGGGGTGT
CTCCTCACTGCCCCGATCCCAGCGGGATGATCTGTCCCTTCATTCAGAGGAGGGGCCAGCCCTG
GAGCCCGTGAGCCGCCCGGTGGATTATGGCTTTGTTTCCGCCCTCGTTTTCCTGGTGAGTGGGA
TTCTTCTGGTGGTGACAGCATACGCCATCCCCCGTGAGGCTCGAGTCAATCCGGACACAGTGAC
AGCGCGGGAGATGGAACGACTGGAGATGTACTACGCCCGCCTAGGCTCCCACCTGGACAGGTGC
ATCATCGCAGGCCTCGGGCTGCTCACGGTGGGCGGCATGCTCTTGTCGGTGCTGCTCATGGTCT
CCCTGTGCAAGGGCGAGCTGTACCGCCGGAGGACCTTCGTCCCCGGCAAGGGCTCCAGGAAGAC
CTACGGCTCCATTAACCTGCGCATGAGACAGCTCAATGGGGATGGGGGCCAGGCCCTGGTGGAG
AATGAAGTTGTCCAGGTCTCAGAGACTAGCCACACCCTCCAGAGGTCTTAAGAACTAGCCCACC
TTATCTGGCTGCTTTAGCTCCAGTGCTACAAGGTCCACCCCCTGCTCCCGCCCACCTGACCCCT
GCCAAGGCCCTGGGGTTTTAAACTGAGCTCACATAGGGCCTTGTGGAAGAAGTACTGGGTGCTG
GAGGGAGAGCTCGGGGCCCAGCCCATGCCCCACACGGGCAAGCAGCCCACTGATCTGTTTTGTA
GCTGAGGTTTTGCATACGGTTTTGTTTGGAGGATGGCTTCTGCTGCTAAAAATACAAAAGTTTG
GAAACCGCT

hide sequence

RefSeq Acc Id:

NM_001387329 ⟹ NP_001374258

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	1,180,570 - 1,185,920 (-)	NCBI
T2T-CHM13v2.0	20	1,227,788 - 1,233,142 (-)	NCBI

Sequence:

show sequence

GAGCCACGGAGCCGCAAGCGCCCGAGGAGACCGTCCCGACCTAAGGACCTCGGAGAGGACCCGG
GGTCCTACCTGGGGGCTGCGTGCGGGGTGGGGGTGGGGGGAAGGGGAAGTGGCAGAGTGGGGGT
GAGGAGTGGGGAGGCACCTGCGCTTGGCGCAATAGGGGCTCTCCGGTGGTGGGGAGGGATCTTC
TTCAGCAGCCCCCGCCCGCCCCGCCCCTGCGCCCGTGGACCGCGGGCTCCAAGCCCCAGTTCCC
TAAGCCCAGGCGCCGGCGATCCAGATCTGCCTGGAGGGGAGGGGAGGACGGTGGATCGGAGCCC
CCGCACCCTCGCCCCAGCCCATCACCCGCCTTCCTGTCCCTCTCCTTGCTAACTCTCCGGGCGC
CCTCGCCGGCCGCGGGCGGAGCTCCCTCCGCGGCGCTCGGCGAGCCCCGGCCCCCGCCCCTTCT
CCCGTCCCTCCGTCCCCGGATCCCCCCCCCGCCTCCCCAGCGGCCGCCACCGCCGCCGTACAGC
TCCGCGCGGCGCGAGTAGCTGCCAAGGGGCCAAGGGATGAGCTGGGGCCCTCCTTCCCAATGGC
ATCTCCCCCTGGTCTGGAACTGAAGACACTGAGCAATGGTCCCCAAGCCCCAAGGAGATCAGCT
CCCCTGGGCCCAGTGGCCCCAACCAGGGAGGGTGTGGAGAATGCCTGCTTCTCCTCAGAGGAGC
ATGAGACCCATTTCCAGAACCCTGGGAACACGAGACTGGGCAGCTCACCCAGTCCCCCTGGGGG
TGTCTCCTCACTGCCCCGATCCCAGCGGGATGATCTGTCCCTTCATTCAGAGGAGGGGCCAGCC
CTGGAGCCCGTGAGCCGCCCGGTGGATTATGGCTTTGTTTCCGCCCTCGTTTTCCTGGTGAGTG
GGATTCTTCTGGTGGTGACAGCATACGCCATCCCCCGTGAGGCTCGAGTCAATCCGGACACAGT
GACAGCGCGGGAGATGGAACGACTGGAGATGTACTACGCCCGCCTAGGCTCCCACCTGGACAGG
TGCATCATCGCAGGCCTCGGGCTGCTCACGGTGGGCGGCATGCTCTTGTCGGTGCTGCTCATGG
TCTCCCTGTGCAAGGGCGAGCTGTACCGCCGGAGGACCTTCGTCCCCGGCAAGGGCTCCAGGAA
GACCTACGGCTCCATTAACCTGCGCATGAGACAGCTCAATGGGGATGGGGGCCAGGCCCTGGTG
GAGAATGAAGTTGTCCAGGTCTCAGAGACTAGCCACACCCTCCAGAGGTCTTAAGAACTAGCCC
ACCTTATCTGGCTGCTTTAGCTCCAGTGCTACAAGGTCCACCCCCTGCTCCCGCCCACCTGACC
CCTGCCAAGGCCCTGGGGTTTTAAACTGAGCTCACATAGGGCCTTGTGGAAGAAGTACTGGGTG
CTGGAGGGAGAGCTCGGGGCCCAGCCCATGCCCCACACGGGCAAGCAGCCCACTGATCTGTTTT
GTAGCTGAGGTTTTGCATACGGTTTTGTTTGGAGGATGGCTTCTGCTGCTAAAAATACAAAAGT
TTGGAAACCGCT

hide sequence

RefSeq Acc Id:

NM_001387330 ⟹ NP_001374259

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	1,180,570 - 1,185,920 (-)	NCBI
T2T-CHM13v2.0	20	1,227,788 - 1,233,142 (-)	NCBI

Sequence:

show sequence

GAGCCACGGAGCCGCAAGCGCCCGAGGAGACCGTCCCGACCTAAGGACCTCGGAGAGGACCCGG
GGTCCTACCTGGGGGCTGCGTGCGGGGTGGGGGTGGGGGGAAGGGGAAGTGGCAGAGTGGGGGT
GAGGAGTGGGGAGGCACCTGCGCTTGGCGCAATAGGGGCTCTCCGGTGGTGGGGAGGGATCTTC
TTCAGCAGCCCCCGCCCGCCCCGCCCCTGCGCCCGTGGACCGCGGGCTCCAAGCCCCAGTTCCC
TAAGCCCAGGCGCCGGCGATCCAGATCTGCCTGGAGGGGAGGGGAGGACGGTGGATCGGAGCCC
CCGCACCCTCGCCCCAGCCCATCACCCGCCTTCCTGTCCCTCTCCTTGCTAACTCTCCGGGCGC
CCTCGCCGGCCGCGGGCGGAGCTCCCTCCGCGGCGCTCGGCGAGCCCCGGCCCCCGCCCCTTCT
CCCGTCCCTCCGTCCCCGGATCCCCCCCCCGCCTCCCCAGCGGCCGCCACCGCCGCCGTACAGC
TCCGCGCGGCGCGAGTAGGTACGTGCGCCTCGGCAGTGGCTCCGGGCCGGGCCGGGAAGGGGGC
GGGAGACCGGGAGGGCGAGGCGGTGGCGGCCGGGCCCGCGCCCTCCGGGCTGCGCCGCAGGAGA
GAGACCCCCGCAGGCGAGACCCCCGCAGGCGTACGCCGGCTGCAGGAAGGCGGACGGGCACCGG
AGAGGACGCACCCTCGCCCGCCGGCGGCCGGGCGCCCTTCGCCCCAGCGTGGTGAGGCGGGGAG
GGAGGCCCGGCACAGGGTAATTGGGCACGGCCTTTGTGTAACTGGTGAATATCTCTGAACCTGG
GCATGAAACAGAGAGATGTCCTAACTCTGGTAAAAGCAGTCTGGGCGCAGGCTGGGGACCCAGA
TGGAATTCAAACTTATGCCTGCTCTCAAGGTGCTCACGGTTGCTGATAAACAGCTGGATAAAAT
GAAGAGTCTATGAGTGAGGGATGCAGAGCCAGGGAAGGCTGGTGGAGTGATGCCACCAGCACAG
GGGTATGAGTTTGCAGCTGCCAAGGGGCCAAGGGATGAGCTGGGGCCCTCCTTCCCAATGGCAT
CTCCCCCTGGTCTGGAACTGAAGACACTGAGCAATGGTCCCCAAGCCCCAAGGAGATCAGCTCC
CCTGGGCCCAGTGGCCCCAACCAGGGAGGGTGTGGAGAATGCCTGCTTCTCCTCAGAGGAGCAT
GAGACCCATTTCCAGAACCCTGGGAACACGAGACTGGGCAGCTCACCCAGTCCCCCTGGGGGTG
TCTCCTCACTGCCCCGATCCCAGCGGGATGATCTGTCCCTTCATTCAGAGGAGGGGCCAGCCCT
GGAGCCCGTGAGCCGCCCGGTGGATTATGGCTTTGTTTCCGCCCTCGTTTTCCTGGTGAGTGGG
ATTCTTCTGGTGGTGACAGCATACGCCATCCCCCGTGAGGCTCGAGTCAATCCGGACACAGTGA
CAGCGCGGGAGATGGAACGACTGGAGATGTACTACGCCCGCCTAGGCTCCCACCTGGACAGGTG
CATCATCGCAGGCCTCGGGCTGCTCACGGTGGGCGGCATGCTCTTGTCGGTGCTGCTCATGGTC
TCCCTGTGCAAGGGCGAGCTGTACCGCCGGAGGACCTTCGTCCCCGGCAAGGGCTCCAGGAAGA
CCTACGGCTCCATTAACCTGCGCATGAGACAGCTCAATGGGGATGGGGGCCAGGCCCTGGTGGA
GAATGAAGTTGTCCAGGTCTCAGAGACTAGCCACACCCTCCAGAGGTCTTAAGAACTAGCCCAC
CTTATCTGGCTGCTTTAGCTCCAGTGCTACAAGGTCCACCCCCTGCTCCCGCCCACCTGACCCC
TGCCAAGGCCCTGGGGTTTTAAACTGAGCTCACATAGGGCCTTGTGGAAGAAGTACTGGGTGCT
GGAGGGAGAGCTCGGGGCCCAGCCCATGCCCCACACGGGCAAGCAGCCCACTGATCTGTTTTGT
AGCTGAGGTTTTGCATACGGTTTTGTTTGGAGGATGGCTTCTGCTGCTAAAAATACAAAAGTTT
GGAAACCGCT

hide sequence

RefSeq Acc Id:

NM_001387331 ⟹ NP_001374260

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	1,180,570 - 1,185,920 (-)	NCBI
T2T-CHM13v2.0	20	1,227,788 - 1,233,142 (-)	NCBI

Sequence:

show sequence

GAGCCACGGAGCCGCAAGCGCCCGAGGAGACCGTCCCGACCTAAGGACCTCGGAGAGGACCCGG
GGTCCTACCTGGGGGCTGCGTGCGGGGTGGGGGTGGGGGGAAGGGGAAGTGGCAGAGTGGGGGT
GAGGAGTGGGGAGGCACCTGCGCTTGGCGCAATAGGGGCTCTCCGGTGGTGGGGAGGGATCTTC
TTCAGCAGCCCCCGCCCGCCCCGCCCCTGCGCCCGTGGACCGCGGGCTCCAAGCCCCAGTTCCC
TAAGCCCAGGCGCCGGCGATCCAGATCTGCCTGGAGGGGAGGGGAGGACGGTGGATCGGAGCCC
CCGCACCCTCGCCCCAGCCCATCACCCGCCTTCCTGTCCCTCTCCTTGCTAACTCTCCGGGCGC
CCTCGCCGGCCGCGGGCGGAGCTCCCTCCGCGGCGCTCGGCGAGCCCCGGCCCCCGCCCCTTCT
CCCGTCCCTCCGTCCCCGGATCCCCCCCCCGCCTCCCCAGCGGCCGCCACCGCCGCCGTACAGC
TCCGCGCGGCGCGAGTAGGTACGTGCGCCTCGGCAGTGGCTCCGGGCCGGGCCGGGAAGGGGGC
GGGAGACCGGGAGGGCGAGGCGGTGGCGGCCGGGCCCGCGCCCTCCGGGCTGCGCCGCAGGAGA
GAGACCCCCGCAGGCGAGACCCCCGCAGGCGTACGCCGGCTGCAGGAAGGCGGACGGGCACCGG
AGAGGACGCACCCTCGCCCGCCGGCGGCCGGGCGCCCTTCGCCCCAGCGTGGTGAGGCGGGGAG
GGAGGCCCGGCACAGGGTAATTGGGCACGGCCTTTGTGTAACTGGTGAATATCTCTGAACCTGG
GCATGAAACAGAGAGATGTCCTAACTCTGGGTGCTCACGGTTGCTGATAAACAGCTGGATAAAA
TGAAGAGTCTATGAGTGAGGGATGCAGAGCCAGGGAAGGCTGGTGGAGTGATGCCACCAGCACA
GGGGTATGAGTTTGCAGCTGCCAAGGGGCCAAGGGATGAGCTGGGGCCCTCCTTCCCAATGGCA
TCTCCCCCTGGTCTGGAACTGAAGACACTGAGCAATGGTCCCCAAGCCCCAAGGAGATCAGCTC
CCCTGGGCCCAGTGGCCCCAACCAGGGAGGGTGTGGAGAATGCCTGCTTCTCCTCAGAGGAGCA
TGAGACCCATTTCCAGAACCCTGGGAACACGAGACTGGGCAGCTCACCCAGTCCCCCTGGGGGT
GTCTCCTCACTGCCCCGATCCCAGCGGGATGATCTGTCCCTTCATTCAGAGGAGGGGCCAGCCC
TGGAGCCCGTGAGCCGCCCGGTGGATTATGGCTTTGTTTCCGCCCTCGTTTTCCTGGTGAGTGG
GATTCTTCTGGTGGTGACAGCATACGCCATCCCCCGTGAGGCTCGAGTCAATCCGGACACAGTG
ACAGCGCGGGAGATGGAACGACTGGAGATGTACTACGCCCGCCTAGGCTCCCACCTGGACAGGT
GCATCATCGCAGGCCTCGGGCTGCTCACGGTGGGCGGCATGCTCTTGTCGGTGCTGCTCATGGT
CTCCCTGTGCAAGGGCGAGCTGTACCGCCGGAGGACCTTCGTCCCCGGCAAGGGCTCCAGGAAG
ACCTACGGCTCCATTAACCTGCGCATGAGACAGCTCAATGGGGATGGGGGCCAGGCCCTGGTGG
AGAATGAAGTTGTCCAGGTCTCAGAGACTAGCCACACCCTCCAGAGGTCTTAAGAACTAGCCCA
CCTTATCTGGCTGCTTTAGCTCCAGTGCTACAAGGTCCACCCCCTGCTCCCGCCCACCTGACCC
CTGCCAAGGCCCTGGGGTTTTAAACTGAGCTCACATAGGGCCTTGTGGAAGAAGTACTGGGTGC
TGGAGGGAGAGCTCGGGGCCCAGCCCATGCCCCACACGGGCAAGCAGCCCACTGATCTGTTTTG
TAGCTGAGGTTTTGCATACGGTTTTGTTTGGAGGATGGCTTCTGCTGCTAAAAATACAAAAGTT
TGGAAACCGCT

hide sequence

RefSeq Acc Id:

NM_001387332 ⟹ NP_001374261

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	1,180,570 - 1,185,920 (-)	NCBI
T2T-CHM13v2.0	20	1,227,788 - 1,233,142 (-)	NCBI

Sequence:

show sequence

GAGCCACGGAGCCGCAAGCGCCCGAGGAGACCGTCCCGACCTAAGGACCTCGGAGAGGACCCGG
GGTCCTACCTGGGGGCTGCGTGCGGGGTGGGGGTGGGGGGAAGGGGAAGTGGCAGAGTGGGGGT
GAGGAGTGGGGAGGCACCTGCGCTTGGCGCAATAGGGGCTCTCCGGTGGTGGGGAGGGATCTTC
TTCAGCAGCCCCCGCCCGCCCCGCCCCTGCGCCCGTGGACCGCGGGCTCCAAGCCCCAGTTCCC
TAAGCCCAGGCGCCGGCGATCCAGATCTGCCTGGAGGGGAGGGGAGGACGGTGGATCGGAGCCC
CCGCACCCTCGCCCCAGCCCATCACCCGCCTTCCTGTCCCTCTCCTTGCTAACTCTCCGGGCGC
CCTCGCCGGCCGCGGGCGGAGCTCCCTCCGCGGCGCTCGGCGAGCCCCGGCCCCCGCCCCTTCT
CCCGTCCCTCCGTCCCCGGATCCCCCCCCCGCCTCCCCAGCGGCCGCCACCGCCGCCGTACAGC
TCCGCGCGGCGCGAGTAGGTGCTCACGGTTGCTGATAAACAGCTGGATAAAATGAAGAGTCTAT
GAGTGAGGGATGCAGAGCCAGGGAAGGCTGGTGGAGTGATGCCACCAGCACAGGGGTATGAGTT
TGCAGCTGCCAAGGGGCCAAGGGATGAGCTGGGGCCCTCCTTCCCAATGGCATCTCCCCCTGGT
CTGGAACTGAAGACACTGAGCAATGGTCCCCAAGCCCCAAGGAGATCAGCTCCCCTGGGCCCAG
TGGCCCCAACCAGGGAGGGTGTGGAGAATGCCTGCTTCTCCTCAGAGGAGCATGAGACCCATTT
CCAGAACCCTGGGAACACGAGACTGGGCAGCTCACCCAGTCCCCCTGGGGGTGTCTCCTCACTG
CCCCGATCCCAGCGGGATGATCTGTCCCTTCATTCAGAGGAGGGGCCAGCCCTGGAGCCCGTGA
GCCGCCCGGTGGATTATGGCTTTGTTTCCGCCCTCGTTTTCCTGGTGAGTGGGATTCTTCTGGT
GGTGACAGCATACGCCATCCCCCGTGAGGCTCGAGTCAATCCGGACACAGTGACAGCGCGGGAG
ATGGAACGACTGGAGATGTACTACGCCCGCCTAGGCTCCCACCTGGACAGGTGCATCATCGCAG
GCCTCGGGCTGCTCACGGTGGGCGGCATGCTCTTGTCGGTGCTGCTCATGGTCTCCCTGTGCAA
GGGCGAGCTGTACCGCCGGAGGACCTTCGTCCCCGGCAAGGGCTCCAGGAAGACCTACGGCTCC
ATTAACCTGCGCATGAGACAGCTCAATGGGGATGGGGGCCAGGCCCTGGTGGAGAATGAAGTTG
TCCAGGTCTCAGAGACTAGCCACACCCTCCAGAGGTCTTAAGAACTAGCCCACCTTATCTGGCT
GCTTTAGCTCCAGTGCTACAAGGTCCACCCCCTGCTCCCGCCCACCTGACCCCTGCCAAGGCCC
TGGGGTTTTAAACTGAGCTCACATAGGGCCTTGTGGAAGAAGTACTGGGTGCTGGAGGGAGAGC
TCGGGGCCCAGCCCATGCCCCACACGGGCAAGCAGCCCACTGATCTGTTTTGTAGCTGAGGTTT
TGCATACGGTTTTGTTTGGAGGATGGCTTCTGCTGCTAAAAATACAAAAGTTTGGAAACCGCT

hide sequence

RefSeq Acc Id:

NM_001387333 ⟹ NP_001374262

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	1,180,570 - 1,185,920 (-)	NCBI
T2T-CHM13v2.0	20	1,227,788 - 1,233,142 (-)	NCBI

Sequence:

show sequence

GAGCCACGGAGCCGCAAGCGCCCGAGGAGACCGTCCCGACCTAAGGACCTCGGAGAGGACCCGG
GGTCCTACCTGGGGGCTGCGTGCGGGGTGGGGGTGGGGGGAAGGGGAAGTGGCAGAGTGGGGGT
GAGGAGTGGGGAGGCACCTGCGCTTGGCGCAATAGGGGCTCTCCGGTGGTGGGGAGGGATCTTC
TTCAGCAGCCCCCGCCCGCCCCGCCCCTGCGCCCGTGGACCGCGGGCTCCAAGCCCCAGTTCCC
TAAGCCCAGGCGCCGGCGATCCAGATCTGCCTGGAGGGGAGGGGAGGACGGTGGATCGGAGCCC
CCGCACCCTCGCCCCAGCCCATCACCCGCCTTCCTGTCCCTCTCCTTGCTAACTCTCCGGGCGC
CCTCGCCGGCCGCGGGCGGAGCTCCCTCCGCGGCGCTCGGCGAGCCCCGGCCCCCGCCCCTTCT
CCCGTCCCTCCGTCCCCGGATCCCCCCCCCGCCTCCCCAGCGGCCGCCACCGCCGCCGTACAGC
TCCGCGCGGCGCGAGTAGTAAAAGCAGTCTGGGCGCAGGCTGGGGACCCAGATGGAATTCAAAC
TTATGCCTGCTCTCAAGGTGCTCACGGTTGCTGATAAACAGCTGGATAAAATGAAGAGTCTATG
AGTGAGGGATGCAGAGCCAGGGAAGGCTGGTGGAGTGATGCCACCAGCACAGGGGTATGAGTTT
GCAGCTGCCAAGGGGCCAAGGGATGAGCTGGGGCCCTCCTTCCCAATGGCATCTCCCCCTGGTC
TGGAACTGAAGACACTGAGCAATGGTCCCCAAGCCCCAAGGAGATCAGCTCCCCTGGGCCCAGT
GGCCCCAACCAGGGAGGGTGTGGAGAATGCCTGCTTCTCCTCAGAGGAGCATGAGACCCATTTC
CAGAACCCTGGGAACACGAGACTGGGCAGCTCACCCAGTCCCCCTGGGGGTGTCTCCTCACTGC
CCCGATCCCAGCGGGATGATCTGTCCCTTCATTCAGAGGAGGGGCCAGCCCTGGAGCCCGTGAG
CCGCCCGGTGGATTATGGCTTTGTTTCCGCCCTCGTTTTCCTGGTGAGTGGGATTCTTCTGGTG
GTGACAGCATACGCCATCCCCCGTGAGGCTCGAGTCAATCCGGACACAGTGACAGCGCGGGAGA
TGGAACGACTGGAGATGTACTACGCCCGCCTAGGCTCCCACCTGGACAGGTGCATCATCGCAGG
CCTCGGGCTGCTCACGGTGGGCGGCATGCTCTTGTCGGTGCTGCTCATGGTCTCCCTGTGCAAG
GGCGAGCTGTACCGCCGGAGGACCTTCGTCCCCGGCAAGGGCTCCAGGAAGACCTACGGCTCCA
TTAACCTGCGCATGAGACAGCTCAATGGGGATGGGGGCCAGGCCCTGGTGGAGAATGAAGTTGT
CCAGGTCTCAGAGACTAGCCACACCCTCCAGAGGTCTTAAGAACTAGCCCACCTTATCTGGCTG
CTTTAGCTCCAGTGCTACAAGGTCCACCCCCTGCTCCCGCCCACCTGACCCCTGCCAAGGCCCT
GGGGTTTTAAACTGAGCTCACATAGGGCCTTGTGGAAGAAGTACTGGGTGCTGGAGGGAGAGCT
CGGGGCCCAGCCCATGCCCCACACGGGCAAGCAGCCCACTGATCTGTTTTGTAGCTGAGGTTTT
GCATACGGTTTTGTTTGGAGGATGGCTTCTGCTGCTAAAAATACAAAAGTTTGGAAACCGCT

hide sequence

RefSeq Acc Id:

NM_001387334 ⟹ NP_001374263

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	1,180,570 - 1,185,920 (-)	NCBI
T2T-CHM13v2.0	20	1,227,788 - 1,233,142 (-)	NCBI

Sequence:

show sequence

GAGCCACGGAGCCGCAAGCGCCCGAGGAGACCGTCCCGACCTAAGGACCTCGGAGAGGACCCGG
GGTCCTACCTGGGGGCTGCGTGCGGGGTGGGGGTGGGGGGAAGGGGAAGTGGCAGAGTGGGGGT
GAGGAGTGGGGAGGCACCTGCGCTTGGCGCAATAGGGGCTCTCCGGTGGTGGGGAGGGATCTTC
TTCAGCAGCCCCCGCCCGCCCCGCCCCTGCGCCCGTGGACCGCGGGCTCCAAGCCCCAGTTCCC
TAAGCCCAGGCGCCGGCGATCCAGATCTGCCTGGAGGGGAGGGGAGGACGGTGGATCGGAGCCC
CCGCACCCTCGCCCCAGCCCATCACCCGCCTTCCTGTCCCTCTCCTTGCTAACTCTCCGGGCGC
CCTCGCCGGCCGCGGGCGGAGCTCCCTCCGCGGCGCTCGGCGAGCCCCGGCCCCCGCCCCTTCT
CCCGTCCCTCCGTCCCCGGATCCCCCCCCCGCCTCCCCAGCGGCCGCCACCGCCGCCGTACAGC
TCCGCGCGGCGCGAGTAGGTACGTGCGCCTCGGCAGTGGCTCCGGGCCGGGCCGGGAAGGGGGC
GGGAGACCGGGAGGGCGAGGCGGTGGCGGCCGGGCCCGCGCCCTCCGGGCTGCGCCGCAGGAGA
GAGACCCCCGCAGGCGAGACCCCCGCAGGCGTACGCCGGCTGCAGGAAGGCGGACGGGCACCGG
AGAGGACGCACCCTCGCCCGCCGGCGGCCGGGCGCCCTTCGCCCCAGCGTGGTGAGGCGGGGAG
GGAGGCCCGGCACAGTAAAAGCAGTCTGGGCGCAGGCTGGGGACCCAGATGGAATTCAAACTTA
TGCCTGCTCTCAAGGTGCTCACGGTTGCTGATAAACAGCTGGATAAAATGAAGAGTCTATGAGT
GAGGGATGCAGAGCCAGGGAAGGCTGGTGGAGTGATGCCACCAGCACAGGGGTATGAGTTTGCA
GCTGCCAAGGGGCCAAGGGATGAGCTGGGGCCCTCCTTCCCAATGGCATCTCCCCCTGGTCTGG
AACTGAAGACACTGAGCAATGGTCCCCAAGCCCCAAGGAGATCAGCTCCCCTGGGCCCAGTGGC
CCCAACCAGGGAGGGTGTGGAGAATGCCTGCTTCTCCTCAGAGGAGCATGAGACCCATTTCCAG
AACCCTGGGAACACGAGACTGGGCAGCTCACCCAGTCCCCCTGGGGGTGTCTCCTCACTGCCCC
GATCCCAGCGGGATGATCTGTCCCTTCATTCAGAGGAGGGGCCAGCCCTGGAGCCCGTGAGCCG
CCCGGTGGATTATGGCTTTGTTTCCGCCCTCGTTTTCCTGGTGAGTGGGATTCTTCTGGTGGTG
ACAGCATACGCCATCCCCCGTGAGGCTCGAGTCAATCCGGACACAGTGACAGCGCGGGAGATGG
AACGACTGGAGATGTACTACGCCCGCCTAGGCTCCCACCTGGACAGGTGCATCATCGCAGGCCT
CGGGCTGCTCACGGTGGGCGGCATGCTCTTGTCGGTGCTGCTCATGGTCTCCCTGTGCAAGGGC
GAGCTGTACCGCCGGAGGACCTTCGTCCCCGGCAAGGGCTCCAGGAAGACCTACGGCTCCATTA
ACCTGCGCATGAGACAGCTCAATGGGGATGGGGGCCAGGCCCTGGTGGAGAATGAAGTTGTCCA
GGTCTCAGAGACTAGCCACACCCTCCAGAGGTCTTAAGAACTAGCCCACCTTATCTGGCTGCTT
TAGCTCCAGTGCTACAAGGTCCACCCCCTGCTCCCGCCCACCTGACCCCTGCCAAGGCCCTGGG
GTTTTAAACTGAGCTCACATAGGGCCTTGTGGAAGAAGTACTGGGTGCTGGAGGGAGAGCTCGG
GGCCCAGCCCATGCCCCACACGGGCAAGCAGCCCACTGATCTGTTTTGTAGCTGAGGTTTTGCA
TACGGTTTTGTTTGGAGGATGGCTTCTGCTGCTAAAAATACAAAAGTTTGGAAACCGCT

hide sequence

RefSeq Acc Id:

NM_018354 ⟹ NP_060824

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	1,180,570 - 1,184,981 (-)	NCBI
GRCh37	20	1,161,213 - 1,166,077 (-)	NCBI
Build 36	20	1,109,215 - 1,113,117 (-)	NCBI Archive
Celera	20	1,257,551 - 1,261,455 (-)	RGD
HuRef	20	1,112,988 - 1,116,894 (-)	RGD
CHM1_1	20	1,161,223 - 1,165,135 (-)	NCBI
T2T-CHM13v2.0	20	1,227,788 - 1,232,203 (-)	NCBI

Sequence:

show sequence

GCCTTCCGGGTCCCGCGTCTGTGGGCAAGGGCAGGAGCAGGGGGTGTGGACTGGGCCGGCGGGA
GCGGGCGCGGTGGGCAGCCGGCGTGCTGGGGCTTTCTGCGCGCAACTTTGGGTACAACAGCGTG
GACCTGCGTGTGCGTATCTGCGCGCCCCAAGGCTTTGTGTACAACTCGTGCGTGTGTCTATCGA
CTGGGTTTTGTGAAGCTTCACCCACAGCCGCTGTGCGTCCCTCTCTCCGGGTGTCAGTGCGCGC
GGCGGGTGGGGTATTGGGCCCCTGCGGGTCTTGGTGGATCTGGCTTGGGTCTCACTCCCAGGGG
CACTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGCGCGTGTGCGTGTGACGGGGT
ACTCGCGTGGCCCGAAGATCCGAGGGTCACACTACGTGACTTCTGGGTGTCTGTGGGTACTGCT
GTGGGAACAGCTGCTGGGGGAGTGTGTGTGGAACTGGAGTGTTCCTTTCAGGACCTGTCTGACT
GCAGATGAAATTAGTAACTGGTGGGGTCGTGGGGTGTGAATGGTGGGCGGGAGCAGCTATGTCA
GTTGGTGTGTTTCTGCTTATGTTAGGGTAATTGGGCACGGCCTTTGTGTAACTGGTGAATATCT
CTGAACCTGGGCATGAAACAGAGAGATGTCCTAACTCTGGGTGAGAGGAATCCTCATTTTTCTC
TGCCCTCTCACTGTGGCATCCTAAGAAAAAAGTTTTGGGTTCCTGCAGCATGAAGGAGAGCTCT
GCTCCCAGAATTTGGGAGCTCCAGATTTCTTCCAGGGTGTGGAGGCATCAATATATCAGTCTGG
GAAAGGGGTTCCTGGGCCACTCCAGGAGCTGAGTTGGGTGGAAGGTGCTGAGGGTGTGGGTGGG
GGCCACTTCTGAGCACCCATGTGGCACCCACTGCTGGTCCCTGTTTGTGGCTGGGCACTCAGGA
AAATGTTTTTGGTGCTAAGAGTAAAAAGCCAACCAACAAACACATCTCTTTTTTCTGTCTATTC
ACTGGAAAGTAAAAGCAGTCTGGGCGCAGGCTGGGGACCCAGATGGAATTCAAACTTATGCCTG
CTCTCAAGGTGCTCACGGTTGCTGATAAACAGCTGGATAAAATGAAGAGTCTATGAGTGAGGGA
TGCAGAGCCAGGGAAGGCTGGTGGAGTGATGCCACCAGCACAGGGGTATGAGTTTGCAGCTGCC
AAGGGGCCAAGGGATGAGCTGGGGCCCTCCTTCCCAATGGCATCTCCCCCTGGTCTGGAACTGA
AGACACTGAGCAATGGTCCCCAAGCCCCAAGGAGATCAGCTCCCCTGGGCCCAGTGGCCCCAAC
CAGGGAGGGTGTGGAGAATGCCTGCTTCTCCTCAGAGGAGCATGAGACCCATTTCCAGAACCCT
GGGAACACGAGACTGGGCAGCTCACCCAGTCCCCCTGGGGGTGTCTCCTCACTGCCCCGATCCC
AGCGGGATGATCTGTCCCTTCATTCAGAGGAGGGGCCAGCCCTGGAGCCCGTGAGCCGCCCGGT
GGATTATGGCTTTGTTTCCGCCCTCGTTTTCCTGGTGAGTGGGATTCTTCTGGTGGTGACAGCA
TACGCCATCCCCCGTGAGGCTCGAGTCAATCCGGACACAGTGACAGCGCGGGAGATGGAACGAC
TGGAGATGTACTACGCCCGCCTAGGCTCCCACCTGGACAGGTGCATCATCGCAGGCCTCGGGCT
GCTCACGGTGGGCGGCATGCTCTTGTCGGTGCTGCTCATGGTCTCCCTGTGCAAGGGCGAGCTG
TACCGCCGGAGGACCTTCGTCCCCGGCAAGGGCTCCAGGAAGACCTACGGCTCCATTAACCTGC
GCATGAGACAGCTCAATGGGGATGGGGGCCAGGCCCTGGTGGAGAATGAAGTTGTCCAGGTCTC
AGAGACTAGCCACACCCTCCAGAGGTCTTAAGAACTAGCCCACCTTATCTGGCTGCTTTAGCTC
CAGTGCTACAAGGTCCACCCCCTGCTCCCGCCCACCTGACCCCTGCCAAGGCCCTGGGGTTTTA
AACTGAGCTCACATAGGGCCTTGTGGAAGAAGTACTGGGTGCTGGAGGGAGAGCTCGGGGCCCA
GCCCATGCCCCACACGGGCAAGCAGCCCACTGATCTGTTTTGTAGCTGAGGTTTTGCATACGGT
TTTGTTTGGAGGATGGCTTCTGCTGCTAAAAATACAAAAGTTTGGAAACCGCT

hide sequence

RefSeq Acc Id:

XM_011529281 ⟹ XP_011527583

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	1,180,570 - 1,189,409 (-)	NCBI

Sequence:

show sequence

CTTTCTGTATGTAATCATCTGCATCTATATTAAGCTAAACATGAGTTCATTCTGGTATCTCCAA
TTCTAATCTGTTGCCACATGGATCATTCTAGCCTCCTCCTCAGGGGTCATTTTTATCAGAAGCA
ATGTTGCTTAGTAACATAGCAGACATATGTTTATCTGTTTCCAGGAAACAGAGCTTCCAAAGGT
CAAATTCTCATGCAAAAGAGGAAAAGGTTTTGTTAACCCTTTACTTACATTCATCAGTGAGGCT
CTCCACTGCTCTGAGGATAAAGAACAAATTACTTGGCCTGTAAGGCTCTGCAGTGACCTGACCT
GCTAAGCCCAGGCTCGTCTCCTACCAGGTTCCTTATCAGGCCCTCCATGACAACCATACTGGTC
TCCTGCAACTCTCAAACTCGTCACACACTTCCTTCTACCCCAAGGTCTTCGCCTATGCTAGGCG
CTCTGCTGGACTTCTCTTTCCTCCCCTCTTTATCTGGTTGCCTTCTACTCATCCTTCTAATCTC
AGCTCAGTCCACACTTTTACAGGAAGCCATTCCTATCCCCAAGACTAGGTTGGCACCCTTGTTT
GAGGCTTGCACTCTATACTTTTATTTGGTAGCATTTACTATAACTGCAATGTTACATTTACTTA
TCCTTTTCTCCCACTAGAATACAAGCTTCCTGAGTGTAGGGATGGAGTCTACCTAGCTAACTAG
TATATAATATTTGCCCATTTTCTCTGTTCTTTATTCAGTGAGCACTTATCCAGAGCTTCCTAGG
TGTTAGCCCCTTTTCTAGTGTCTGGGGATACTGCAGGGAGGGAAACAGGCAAAAACCCTCTTCT
TTTGGCACTTATTTTTTAGGGGAGGTGGCAATAAGCAAACAGAAACTAATGTCAGTTGGTAAGT
GCTATAGAGAAAAATTCAGAGTGAGGGAGTAAAGAGTGCTGGGGCACTGCTATTTTTGAAAGGA
TGGCCTGGAATGGCGTCTCTGAGAAGGTGGCATTTGAGCAAAGACTTGAAGGAAGTGAGGGAAG
GGGGTGAGTGCGGGAAATATCAGAAAGAAAAACGTCCCAGGCAGAAGGAACAGCCAGCGCAAAG
GCTGAGGTAGGACAGCGCATGACTGAGGGAAGGAACAGTGAGTGCTTTAAAGGCGGTATCTCAT
CCCATTCCCATAACACTTCCTACATCCGTTTCACAGAGGAGGAAACCGAGCTCCAGGAGGGCAG
TCCTTTACACCAGGGCACCCAGCTGTGGGGGTGGAGCTGGGATTTGAACAGGAGTGTGGTGCCA
GGGCTAGCATCCCTTTGAAGTCTCTAACAACGGGCCAGGCCTCTGCAAGGCTGGGAGGAAATGG
AGGCCTTCCCAGCCCTGGTGGACCTGCCTAGGGCTAGGCTATGCTGGCCTTGAAGGCACAGGCA
TCCATCATCCAGGGTGACTTCCAGTCTCCTGGTTGGGGAGGGCTGCACAGAACTTTGGAGGAGG
GCAGGTCAGGCTCCGCTCATGAGGTGGCCGAGGAGCAGGACATGGCACACTCATTCGCCTGTCC
TTCCACATGGCCAACTTCTGCTGGCCTTCCCAGAGCCCTCAAAGCCTGCACATTCACAATCCTC
ATGGACAGAAGTGGATACAGGCTCAGAGGCCAGAGGAGCTGCCAATCCGATGGAGGAGGCTGAC
CCTTAAACAAAATCACGACCGTCAGAGACAAGAGCAAACAGTGCGGGCAAAAGGAGAGCCCAGA
TGGAGGGGCCCGTGGGCTGCCAAGGGGCCAAGGGATGAGCTGGGGCCCTCCTTCCCAATGGCAT
CTCCCCCTGGTCTGGAACTGAAGACACTGAGCAATGGTCCCCAAGCCCCAAGGAGATCAGCTCC
CCTGGGCCCAGTGGCCCCAACCAGGGAGGGTGTGGAGAATGCCTGCTTCTCCTCAGAGGAGCAT
GAGACCCATTTCCAGAACCCTGGGAACACGAGACTGGGCAGCTCACCCAGTCCCCCTGGGGGTG
TCTCCTCACTGCCCCGATCCCAGCGGGATGATCTGTCCCTTCATTCAGAGGAGGGGCCAGCCCT
GGAGCCCGTGAGCCGCCCGGTGGATTATGGCTTTGTTTCCGCCCTCGTTTTCCTGGTGAGTGGG
ATTCTTCTGGTGGTGACAGCATACGCCATCCCCCGTGAGGCTCGAGTCAATCCGGACACAGTGA
CAGCGCGGGAGATGGAACGACTGGAGATGTACTACGCCCGCCTAGGCTCCCACCTGGACAGGTG
CATCATCGCAGGCCTCGGGCTGCTCACGGTGGGCGGCATGCTCTTGTCGGTGCTGCTCATGGTC
TCCCTGTGCAAGGGCGAGCTGTACCGCCGGAGGACCTTCGTCCCCGGCAAGGGCTCCAGGAAGA
CCTACGGCTCCATTAACCTGCGCATGAGACAGCTCAATGGGGATGGGGGCCAGGCCCTGGTGGA
GAATGAAGTTGTCCAGGTCTCAGAGACTAGCCACACCCTCCAGAGGTCTTAAGAACTAGCCCAC
CTTATCTGGCTGCTTTAGCTCCAGTGCTACAAGGTCCACCCCCTGCTCCCGCCCACCTGACCCC
TGCCAAGGCCCTGGGGTTTTAAACTGAGCTCACATAGGGCCTTGTGGAAGAAGTACTGGGTGCT
GGAGGGAGAGCTCGGGGCCCAGCCCATGCCCCACACGGGCAAGCAGCCCACTGATCTGTTTTGT
AGCTGAGGTTTTGCATACGGTTTTGTTTGGAGGATGGCTTCTGCTGCTAAAAATACAAAAGTTT
GGAAACCGCTG

hide sequence

RefSeq Acc Id:

XM_017027923 ⟹ XP_016883412

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	1,180,570 - 1,186,460 (-)	NCBI

Sequence:

show sequence

AACTTCTGCTGGCCTTCCCAGAGCCCTCAAAGCCTGCACATTCACAATCCTCATGGACAGAAGT
GGATACAGGCTCAGAGGCCAGAGGTACTAACCGAGACCACACGATTCAGCTGGTCACCGTGTCT
TCCCGGAACCTGCACGATTCAGACCAAAGCTGTCTCTGGGGTTGGCGTGTGTTCCCCAAAGAGG
AAACGTCTCCATGAATTTGGTCTTCTAGGTGATCAGACATGGGTCCTGCTCTCCAGGAGCTGCC
AATCCGATGGAGGAGGCTGACCCTTAAACAAAATCACGACCGTCAGAGACAAGAGCAAACAGTG
CGGGCAAAAGGAGAGCCCAGATGGAGGGGCCCGTGGGCTGCCAAGGGGCCAAGGGATGAGCTGG
GGCCCTCCTTCCCAATGGCATCTCCCCCTGGTCTGGAACTGAAGACACTGAGCAATGGTCCCCA
AGCCCCAAGGAGATCAGCTCCCCTGGGCCCAGTGGCCCCAACCAGGGAGGGTGTGGAGAATGCC
TGCTTCTCCTCAGAGGAGCATGAGACCCATTTCCAGAACCCTGGGAACACGAGACTGGGCAGCT
CACCCAGTCCCCCTGGGGGTGTCTCCTCACTGCCCCGATCCCAGCGGGATGATCTGTCCCTTCA
TTCAGAGGAGGGGCCAGCCCTGGAGCCCGTGAGCCGCCCGGTGGATTATGGCTTTGTTTCCGCC
CTCGTTTTCCTGGTGAGTGGGATTCTTCTGGTGGTGACAGCATACGCCATCCCCCGTGAGGCTC
GAGTCAATCCGGACACAGTGACAGCGCGGGAGATGGAACGACTGGAGATGTACTACGCCCGCCT
AGGCTCCCACCTGGACAGGTGCATCATCGCAGGCCTCGGGCTGCTCACGGTGGGCGGCATGCTC
TTGTCGGTGCTGCTCATGGTCTCCCTGTGCAAGGGCGAGCTGTACCGCCGGAGGACCTTCGTCC
CCGGCAAGGGCTCCAGGAAGACCTACGGCTCCATTAACCTGCGCATGAGACAGCTCAATGGGGA
TGGGGGCCAGGCCCTGGTGGAGAATGAAGTTGTCCAGGTCTCAGAGACTAGCCACACCCTCCAG
AGGTCTTAAGAACTAGCCCACCTTATCTGGCTGCTTTAGCTCCAGTGCTACAAGGTCCACCCCC
TGCTCCCGCCCACCTGACCCCTGCCAAGGCCCTGGGGTTTTAAACTGAGCTCACATAGGGCCTT
GTGGAAGAAGTACTGGGTGCTGGAGGGAGAGCTCGGGGCCCAGCCCATGCCCCACACGGGCAAG
CAGCCCACTGATCTGTTTTGTAGCTGAGGTTTTGCATACGGTTTTGTTTGGAGGATGGCTTCTG
CTGCTAAAAATACAAAAGTTTGGAAACCGCTG

hide sequence

RefSeq Acc Id:

XM_017027924 ⟹ XP_016883413

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	1,180,570 - 1,185,920 (-)	NCBI

Sequence:

show sequence

ACCGGGAGGGCGAGGCGGTGGCGGCCGGGCCCGCGCCCTCCGGGCTGCGCCGCAGGAGAGAGAC
CCCCGCAGGCGAGACCCCCGCAGGCGTACGCCGGCTGCAGGAAGGCGGACGGGCACCGGAGAGG
ACGCACCCTCGCCCGCCGGCGGCCGGGCGCCCTTCGCCCCAGCGTGGTGAGGCGGGGAGGGAGG
CCCGGCACAGGTGCTCACGGTTGCTGATAAACAGCTGGATAAAATGAAGAGTCTATGAGTGAGG
GATGCAGAGCCAGGGAAGGCTGGTGGAGTGATGCCACCAGCACAGGGGTATGAGTTTGCAGCTG
CCAAGGGGCCAAGGGATGAGCTGGGGCCCTCCTTCCCAATGGCATCTCCCCCTGGTCTGGAACT
GAAGACACTGAGCAATGGTCCCCAAGCCCCAAGGAGATCAGCTCCCCTGGGCCCAGTGGCCCCA
ACCAGGGAGGGTGTGGAGAATGCCTGCTTCTCCTCAGAGGAGCATGAGACCCATTTCCAGAACC
CTGGGAACACGAGACTGGGCAGCTCACCCAGTCCCCCTGGGGGTGTCTCCTCACTGCCCCGATC
CCAGCGGGATGATCTGTCCCTTCATTCAGAGGAGGGGCCAGCCCTGGAGCCCGTGAGCCGCCCG
GTGGATTATGGCTTTGTTTCCGCCCTCGTTTTCCTGGTGAGTGGGATTCTTCTGGTGGTGACAG
CATACGCCATCCCCCGTGAGGCTCGAGTCAATCCGGACACAGTGACAGCGCGGGAGATGGAACG
ACTGGAGATGTACTACGCCCGCCTAGGCTCCCACCTGGACAGGTGCATCATCGCAGGCCTCGGG
CTGCTCACGGTGGGCGGCATGCTCTTGTCGGTGCTGCTCATGGTCTCCCTGTGCAAGGGCGAGC
TGTACCGCCGGAGGACCTTCGTCCCCGGCAAGGGCTCCAGGAAGACCTACGGCTCCATTAACCT
GCGCATGAGACAGCTCAATGGGGATGGGGGCCAGGCCCTGGTGGAGAATGAAGTTGTCCAGGTC
TCAGAGACTAGCCACACCCTCCAGAGGTCTTAAGAACTAGCCCACCTTATCTGGCTGCTTTAGC
TCCAGTGCTACAAGGTCCACCCCCTGCTCCCGCCCACCTGACCCCTGCCAAGGCCCTGGGGTTT
TAAACTGAGCTCACATAGGGCCTTGTGGAAGAAGTACTGGGTGCTGGAGGGAGAGCTCGGGGCC
CAGCCCATGCCCCACACGGGCAAGCAGCCCACTGATCTGTTTTGTAGCTGAGGTTTTGCATACG
GTTTTGTTTGGAGGATGGCTTCTGCTGCTAAAAATACAAAAGTTTGGAAACCGCTG

hide sequence

RefSeq Acc Id:

XM_017027925 ⟹ XP_016883414

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	1,180,570 - 1,184,981 (-)	NCBI

Sequence:

show sequence

CGAAGGACGGCGAGCCTGACCTCGCGGCCCGCCGAAGGACATGCGACCAGGGGACCCGGCCTCC
CCGGGCCTCCGCCTGGTCCGGTTCGGCCTTCCGGGTCCCGCGTCTGTGGGCAAGGGCAGGAGCA
GGGGGTGTGGACTGGGCCGGCGGGAGCGGGCGCGGTGGGCAGCCGGCGTGCTGGGGCTTTCTGC
GCGCAACTTTGGGTACAACAGCGTGGACCTGCGTGTGCGTATCTGCGCGCCCCAAGGCTTTGTG
TACAACTCGTGCGTGTGTCTATCGACTGGGTTTTGTGAAGCTTCACCCACAGCCGCTGTGCGTC
CCTCTCTCCGGGTGTCAGTGCGCGCGGCGGGTGGGGTATTGGGCCCCTGCGGGTCTTGGTGGAT
CTGGCTTGGGTCTCACTCCCAGGGGCACTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
TACGCGCGTGTGCGTGTGACGGGGTACTCGCGTGGCCCGAAGATCCGAGGGTCACACTACGTGA
CTTCTGGGTGTCTGTGGGTACTGCTGTGGGAACAGCTGCTGGGGGAGTGTGTGTGGAACTGGAG
TGTTCCTTTCAGGACCTGTCTGACTGCAGATGAAATTAGTAACTGGTGGGGTCGTGGGGTGTGA
ATGGTGGGCGGGAGCAGCTATGTCAGTTGGTGTGTTTCTGCTTATGTTAGGGTAATTGGGCACG
GCCTTTGTGTAACTGGTGAATATCTCTGAACCTGGGCATGAAACAGAGAGATGTCCTAACTCTG
GTAAAAGCAGTCTGGGCGCAGGCTGGGGACCCAGATGGAATTCAAACTTATGCCTGCTCTCAAG
GTGCTCACGGTTGCTGATAAACAGCTGGATAAAATGAAGAGTCTATGAGTGAGGGATGCAGAGC
CAGGGAAGGCTGGTGGAGTGATGCCACCAGCACAGGGCTGCCAAGGGGCCAAGGGATGAGCTGG
GGCCCTCCTTCCCAATGGCATCTCCCCCTGGTCTGGAACTGAAGACACTGAGCAATGGTCCCCA
AGCCCCAAGGAGATCAGCTCCCCTGGGCCCAGTGGCCCCAACCAGGGAGGGTGTGGAGAATGCC
TGCTTCTCCTCAGAGGAGCATGAGACCCATTTCCAGAACCCTGGGAACACGAGACTGGGCAGCT
CACCCAGTCCCCCTGGGGGTGTCTCCTCACTGCCCCGATCCCAGCGGGATGATCTGTCCCTTCA
TTCAGAGGAGGGGCCAGCCCTGGAGCCCGTGAGCCGCCCGGTGGATTATGGCTTTGTTTCCGCC
CTCGTTTTCCTGGTGAGTGGGATTCTTCTGGTGGTGACAGCATACGCCATCCCCCGTGAGGCTC
GAGTCAATCCGGACACAGTGACAGCGCGGGAGATGGAACGACTGGAGATGTACTACGCCCGCCT
AGGCTCCCACCTGGACAGGTGCATCATCGCAGGCCTCGGGCTGCTCACGGTGGGCGGCATGCTC
TTGTCGGTGCTGCTCATGGTCTCCCTGTGCAAGGGCGAGCTGTACCGCCGGAGGACCTTCGTCC
CCGGCAAGGGCTCCAGGAAGACCTACGGCTCCATTAACCTGCGCATGAGACAGCTCAATGGGGA
TGGGGGCCAGGCCCTGGTGGAGAATGAAGTTGTCCAGGTCTCAGAGACTAGCCACACCCTCCAG
AGGTCTTAAGAACTAGCCCACCTTATCTGGCTGCTTTAGCTCCAGTGCTACAAGGTCCACCCCC
TGCTCCCGCCCACCTGACCCCTGCCAAGGCCCTGGGGTTTTAAACTGAGCTCACATAGGGCCTT
GTGGAAGAAGTACTGGGTGCTGGAGGGAGAGCTCGGGGCCCAGCCCATGCCCCACACGGGCAAG
CAGCCCACTGATCTGTTTTGTAGCTGAGGTTTTGCATACGGTTTTGTTTGGAGGATGGCTTCTG
CTGCTAAAAATACAAAAGTTTGGAAACCGCTG

hide sequence

RefSeq Acc Id:

XM_047440257 ⟹ XP_047296213

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	1,180,570 - 1,185,070 (-)	NCBI

RefSeq Acc Id:

XM_054323618 ⟹ XP_054179593

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	1,227,788 - 1,236,631 (-)	NCBI

RefSeq Acc Id:

XM_054323619 ⟹ XP_054179594

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	1,227,788 - 1,233,903 (-)	NCBI

RefSeq Acc Id:

XM_054323620 ⟹ XP_054179595

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	1,227,788 - 1,233,682 (-)	NCBI

RefSeq Acc Id:

XM_054323621 ⟹ XP_054179596

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	1,227,788 - 1,233,436 (-)	NCBI

RefSeq Acc Id:

XM_054323622 ⟹ XP_054179597

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	1,227,788 - 1,232,292 (-)	NCBI

RefSeq Acc Id:

XM_054323623 ⟹ XP_054179598

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	1,227,788 - 1,233,142 (-)	NCBI

RefSeq Acc Id:

XM_054323624 ⟹ XP_054179599

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	1,227,788 - 1,232,203 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_001291677	(Get FASTA)	NCBI Sequence Viewer
	NP_001291678	(Get FASTA)	NCBI Sequence Viewer
	NP_001374258	(Get FASTA)	NCBI Sequence Viewer
	NP_001374259	(Get FASTA)	NCBI Sequence Viewer
	NP_001374260	(Get FASTA)	NCBI Sequence Viewer
	NP_001374261	(Get FASTA)	NCBI Sequence Viewer
	NP_001374262	(Get FASTA)	NCBI Sequence Viewer
	NP_001374263	(Get FASTA)	NCBI Sequence Viewer
	NP_060824	(Get FASTA)	NCBI Sequence Viewer
	XP_011527583	(Get FASTA)	NCBI Sequence Viewer
	XP_016883412	(Get FASTA)	NCBI Sequence Viewer
	XP_016883413	(Get FASTA)	NCBI Sequence Viewer
	XP_016883414	(Get FASTA)	NCBI Sequence Viewer
	XP_047296213	(Get FASTA)	NCBI Sequence Viewer
	XP_054179593	(Get FASTA)	NCBI Sequence Viewer
	XP_054179594	(Get FASTA)	NCBI Sequence Viewer
	XP_054179595	(Get FASTA)	NCBI Sequence Viewer
	XP_054179596	(Get FASTA)	NCBI Sequence Viewer
	XP_054179597	(Get FASTA)	NCBI Sequence Viewer
	XP_054179598	(Get FASTA)	NCBI Sequence Viewer
	XP_054179599	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	BAA92058	(Get FASTA)	NCBI Sequence Viewer
	CAD34937	(Get FASTA)	NCBI Sequence Viewer
	CAE90001	(Get FASTA)	NCBI Sequence Viewer
	EAX10647	(Get FASTA)	NCBI Sequence Viewer
	EAX10648	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000371318
	ENSP00000371318.3
	ENSP00000400552
	ENSP00000400552.2
GenBank Protein	Q9NUR3	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_060824 ⟸ NM_018354
- Peptide Label:	isoform 1
- UniProtKB:	D3DVW5 (UniProtKB/Swiss-Prot), Q9NUR3 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MPPAQGYEFAAAKGPRDELGPSFPMASPPGLELKTLSNGPQAPRRSAPLGPVAPTREGVENACF SSEEHETHFQNPGNTRLGSSPSPPGGVSSLPRSQRDDLSLHSEEGPALEPVSRPVDYGFVSALV FLVSGILLVVTAYAIPREARVNPDTVTAREMERLEMYYARLGSHLDRCIIAGLGLLTVGGMLLS VLLMVSLCKGELYRRRTFVPGKGSRKTYGSINLRMRQLNGDGGQALVENEVVQVSETSHTLQRS hide sequence

RefSeq Acc Id:	NP_001291678 ⟸ NM_001304749
- Peptide Label:	isoform 2
- UniProtKB:	Q9NUR3 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MASPPGLELKTLSNGPQAPRRSAPLGPVAPTREGVENACFSSEEHETHFQNPGNTRLGSSPSPP GGVSSLPRSQRDDLSLHSEEGPALEPVSRPVDYGFVSALVFLVSGILLVVTAYAIPREARVNPD TVTAREMERLEMYYARLGSHLDRCIIAGLGLLTVGGMLLSVLLMVSLCKGELYRRRTFVPGKGS RKTYGSINLRMRQLNGDGGQALVENEVVQVSETSHTLQRS hide sequence

RefSeq Acc Id:	NP_001291677 ⟸ NM_001304748
- Peptide Label:	isoform 1
- UniProtKB:	D3DVW5 (UniProtKB/Swiss-Prot), Q9NUR3 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MPPAQGYEFAAAKGPRDELGPSFPMASPPGLELKTLSNGPQAPRRSAPLGPVAPTREGVENACF SSEEHETHFQNPGNTRLGSSPSPPGGVSSLPRSQRDDLSLHSEEGPALEPVSRPVDYGFVSALV FLVSGILLVVTAYAIPREARVNPDTVTAREMERLEMYYARLGSHLDRCIIAGLGLLTVGGMLLS VLLMVSLCKGELYRRRTFVPGKGSRKTYGSINLRMRQLNGDGGQALVENEVVQVSETSHTLQRS hide sequence

RefSeq Acc Id:

XP_011527583 ⟸ XM_011529281

- Peptide Label:

isoform X1

- Sequence:

show sequence

MANFCWPSQSPQSLHIHNPHGQKWIQAQRPEELPIRWRRLTLKQNHDRQRQEQTVRAKGEPRWR
GPWAAKGPRDELGPSFPMASPPGLELKTLSNGPQAPRRSAPLGPVAPTREGVENACFSSEEHET
HFQNPGNTRLGSSPSPPGGVSSLPRSQRDDLSLHSEEGPALEPVSRPVDYGFVSALVFLVSGIL
LVVTAYAIPREARVNPDTVTAREMERLEMYYARLGSHLDRCIIAGLGLLTVGGMLLSVLLMVSL
CKGELYRRRTFVPGKGSRKTYGSINLRMRQLNGDGGQALVENEVVQVSETSHTLQRS

hide sequence

RefSeq Acc Id:

XP_016883412 ⟸ XM_017027923

- Peptide Label:

isoform X2

- Sequence:

show sequence

MGPALQELPIRWRRLTLKQNHDRQRQEQTVRAKGEPRWRGPWAAKGPRDELGPSFPMASPPGLE
LKTLSNGPQAPRRSAPLGPVAPTREGVENACFSSEEHETHFQNPGNTRLGSSPSPPGGVSSLPR
SQRDDLSLHSEEGPALEPVSRPVDYGFVSALVFLVSGILLVVTAYAIPREARVNPDTVTAREME
RLEMYYARLGSHLDRCIIAGLGLLTVGGMLLSVLLMVSLCKGELYRRRTFVPGKGSRKTYGSIN
LRMRQLNGDGGQALVENEVVQVSETSHTLQRS

hide sequence

RefSeq Acc Id:	XP_016883413 ⟸ XM_017027924
- Peptide Label:	isoform X3
- UniProtKB:	D3DVW5 (UniProtKB/Swiss-Prot), Q9NUR3 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MPPAQGYEFAAAKGPRDELGPSFPMASPPGLELKTLSNGPQAPRRSAPLGPVAPTREGVENACF SSEEHETHFQNPGNTRLGSSPSPPGGVSSLPRSQRDDLSLHSEEGPALEPVSRPVDYGFVSALV FLVSGILLVVTAYAIPREARVNPDTVTAREMERLEMYYARLGSHLDRCIIAGLGLLTVGGMLLS VLLMVSLCKGELYRRRTFVPGKGSRKTYGSINLRMRQLNGDGGQALVENEVVQVSETSHTLQRS hide sequence

RefSeq Acc Id:

XP_016883414 ⟸ XM_017027925

- Peptide Label:

isoform X4

- Sequence:

show sequence

MASPPGLELKTLSNGPQAPRRSAPLGPVAPTREGVENACFSSEEHETHFQNPGNTRLGSSPSPP
GGVSSLPRSQRDDLSLHSEEGPALEPVSRPVDYGFVSALVFLVSGILLVVTAYAIPREARVNPD
TVTAREMERLEMYYARLGSHLDRCIIAGLGLLTVGGMLLSVLLMVSLCKGELYRRRTFVPGKGS
RKTYGSINLRMRQLNGDGGQALVENEVVQVSETSHTLQRS

hide sequence

RefSeq Acc Id:

ENSP00000400552 ⟸ ENST00000429036

RefSeq Acc Id:

ENSP00000371318 ⟸ ENST00000381894

RefSeq Acc Id:	NP_001374258 ⟸ NM_001387329
- Peptide Label:	isoform 2

RefSeq Acc Id:	NP_001374261 ⟸ NM_001387332
- Peptide Label:	isoform 1
- UniProtKB:	Q9NUR3 (UniProtKB/Swiss-Prot), D3DVW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001374262 ⟸ NM_001387333
- Peptide Label:	isoform 1
- UniProtKB:	Q9NUR3 (UniProtKB/Swiss-Prot), D3DVW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001374263 ⟸ NM_001387334
- Peptide Label:	isoform 1
- UniProtKB:	Q9NUR3 (UniProtKB/Swiss-Prot), D3DVW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001374260 ⟸ NM_001387331
- Peptide Label:	isoform 1
- UniProtKB:	Q9NUR3 (UniProtKB/Swiss-Prot), D3DVW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	NP_001374259 ⟸ NM_001387330
- Peptide Label:	isoform 1
- UniProtKB:	Q9NUR3 (UniProtKB/Swiss-Prot), D3DVW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047296213 ⟸ XM_047440257
- Peptide Label:	isoform X3
- UniProtKB:	Q9NUR3 (UniProtKB/Swiss-Prot), D3DVW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054179593 ⟸ XM_054323618
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054179594 ⟸ XM_054323619
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054179595 ⟸ XM_054323620
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054179596 ⟸ XM_054323621
- Peptide Label:	isoform X3
- UniProtKB:	Q9NUR3 (UniProtKB/Swiss-Prot), D3DVW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054179598 ⟸ XM_054323623
- Peptide Label:	isoform X3
- UniProtKB:	Q9NUR3 (UniProtKB/Swiss-Prot), D3DVW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054179597 ⟸ XM_054323622
- Peptide Label:	isoform X3
- UniProtKB:	Q9NUR3 (UniProtKB/Swiss-Prot), D3DVW5 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054179599 ⟸ XM_054323624
- Peptide Label:	isoform X4

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9NUR3-F1-model_v2	AlphaFold	Q9NUR3	1-256	view protein structure

Promoters

RGD ID:

6798585

Promoter ID:

HG_KWN:38318

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

OTTHUMT00000077497

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	20	1,113,811 - 1,114,312 (-)	MPROMDB

RGD ID:

13206103

Promoter ID:

EPDNEW_H26632

Type:

initiation region

Name:

TMEM74B_2

Description:

transmembrane protein 74B

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H26633

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	1,184,418 - 1,184,478	EPDNEW

RGD ID:

13206105

Promoter ID:

EPDNEW_H26633

Type:

initiation region

Name:

TMEM74B_1

Description:

transmembrane protein 74B

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H26632

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	1,185,515 - 1,185,575	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:15893	AgrOrtholog
COSMIC	TMEM74B	COSMIC
Ensembl Genes	ENSG00000125895	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000381894	ENTREZGENE
	ENST00000381894.3	UniProtKB/Swiss-Prot
	ENST00000429036	ENTREZGENE, UniProtKB/TrEMBL
	ENST00000429036.2	UniProtKB/Swiss-Prot
GTEx	ENSG00000125895	GTEx
HGNC ID	HGNC:15893	ENTREZGENE
Human Proteome Map	TMEM74B	Human Proteome Map
InterPro	TMEM74-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:55321	UniProtKB/Swiss-Prot
NCBI Gene	55321	ENTREZGENE
PANTHER	PTHR16125	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	TRANSMEMBRANE PROTEIN 74B	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA25759	PharmGKB
UniProt	D3DVW5	ENTREZGENE
	Q5QPM3_HUMAN	UniProtKB/TrEMBL
	Q9NUR3	ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary	D3DVW5	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2011-11-29	TMEM74B	transmembrane protein 74B	C20orf46	chromosome 20 open reading frame 46	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