MEDAG (mesenteric estrogen dependent adipogenesis)

Gene: MEDAG (mesenteric estrogen dependent adipogenesis) Homo sapiens

Analyze

Symbol:

MEDAG

Name:

mesenteric estrogen dependent adipogenesis

RGD ID:

1605918

HGNC Page

HGNC:25926

Description:

Predicted to be involved in positive regulation of fat cell differentiation. Located in cytoplasm.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

activated in W/Wv mouse stomach 3 homolog; AWMS3; C13orf33; FLJ14834; hAWMS3; hypothetical protein LOC84935; MEDA-4; MEDA4; mesenteric estrogen-dependent adipogenesis; mesenteric estrogen-dependent adipogenesis protein; mesenteric estrogen-dependent adipose 4; MGC126673; MGC126675; uncharacterized protein C13orf33

RGD Orthologs

Alliance Genes

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	13	30,906,271 - 30,925,572 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	13	30,906,271 - 30,925,572 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	13	31,480,408 - 31,499,709 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	13	30,378,328 - 30,397,678 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	13	12,546,863 - 12,566,248 (+)	NCBI		Celera
Cytogenetic Map	13	q12.3	NCBI
HuRef	13	12,291,191 - 12,310,577 (+)	NCBI		HuRef
CHM1_1	13	31,447,426 - 31,466,813 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	13	30,128,196 - 30,147,488 (+)	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

(-)-epigallocatechin 3-gallate (EXP)

17beta-estradiol (EXP)

2,4-dibromophenyl 2,4,5-tribromophenyl ether (EXP)

2-palmitoylglycerol (EXP)

3-chloropropane-1,2-diol (ISO)

4,4'-sulfonyldiphenol (ISO)

6-propyl-2-thiouracil (ISO)

8-Br-cAMP (EXP)

all-trans-retinoic acid (EXP)

antirheumatic drug (EXP)

benzo[a]pyrene (EXP,ISO)

bisphenol A (ISO)

bisphenol F (ISO)

cadmium atom (ISO)

cadmium dichloride (ISO)

cantharidin (ISO)

carbon nanotube (ISO)

chromium(6+) (EXP)

diazinon (EXP)

dioxygen (ISO)

diuron (ISO)

dorsomorphin (EXP)

doxorubicin (EXP)

entinostat (EXP)

fenvalerate (ISO)

fluoranthene (ISO)

gentamycin (ISO)

manganese(II) chloride (ISO)

nickel atom (EXP)

nickel sulfate (EXP)

oxybenzone (ISO)

ozone (ISO)

paracetamol (EXP,ISO)

paraquat (ISO)

perfluorohexanesulfonic acid (ISO)

permethrin (EXP)

potassium chromate (EXP)

progesterone (EXP)

rotenone (ISO)

SB 431542 (EXP)

silicon dioxide (EXP)

thimerosal (EXP)

titanium dioxide (ISO)

triclosan (EXP)

valproic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

positive regulation of fat cell differentiation (IEA,ISS)

Cellular Component

cytoplasm (IBA,IDA,IEA)

Molecular Function

protein binding (IPI)

References

References - curated

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

Additional References at PubMed

PMID:12477932	PMID:14702039	PMID:15057823	PMID:15489334	PMID:17207965	PMID:21873635	PMID:22510272	PMID:28005267	PMID:30021884	PMID:32296183	PMID:33728329	PMID:35906200

Genomics

Comparative Map Data

MEDAG
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	13	30,906,271 - 30,925,572 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	13	30,906,271 - 30,925,572 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	13	31,480,408 - 31,499,709 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	13	30,378,328 - 30,397,678 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	13	12,546,863 - 12,566,248 (+)	NCBI		Celera
Cytogenetic Map	13	q12.3	NCBI
HuRef	13	12,291,191 - 12,310,577 (+)	NCBI		HuRef
CHM1_1	13	31,447,426 - 31,466,813 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	13	30,128,196 - 30,147,488 (+)	NCBI		T2T-CHM13v2.0

Medag
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	5	149,335,214 - 149,355,188 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	5	149,335,214 - 149,355,188 (+)	Ensembl		GRCm39 Ensembl
GRCm38	5	149,367,641 - 149,431,723 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	5	149,411,749 - 149,431,723 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	5	150,214,381 - 150,234,278 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	5	149,680,185 - 149,700,082 (+)	NCBI		MGSCv36	mm8
Celera	5	147,412,123 - 147,432,091 (+)	NCBI		Celera
Cytogenetic Map	5	G3	NCBI
cM Map	5	89.18	NCBI

Medag
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	12	10,649,526 - 10,670,913 (-)	NCBI		GRCr8
mRatBN7.2	12	5,613,191 - 5,634,583 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	12	5,613,208 - 5,634,767 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	12	6,279,708 - 6,300,994 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	12	6,903,180 - 6,924,463 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	12	5,930,909 - 5,952,145 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	12	6,711,745 - 6,730,959 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	12	6,711,747 - 6,740,714 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	12	8,808,629 - 8,828,437 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	12	6,104,957 - 6,126,628 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	12	6,104,981 - 6,126,628 (-)	NCBI
Celera	12	7,371,986 - 7,393,743 (-)	NCBI		Celera
Cytogenetic Map	12	p11	NCBI

Medag
(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_004955431	14,916,369 - 14,937,385 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955431	14,918,560 - 14,937,385 (-)	NCBI	ChiLan1.0	ChiLan1.0

MEDAG
(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	14	30,487,042 - 30,506,616 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	13	21,593,822 - 21,613,941 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	13	12,180,622 - 12,200,123 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	13	30,614,989 - 30,634,048 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	13	30,614,989 - 30,632,912 (+)	Ensembl	panpan1.1		panPan2

MEDAG
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	25	9,182,441 - 9,201,235 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	25	9,183,443 - 9,200,051 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	25	9,224,982 - 9,242,610 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	25	9,287,047 - 9,305,980 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	25	9,287,076 - 9,304,969 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	25	9,185,976 - 9,203,593 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	25	9,194,040 - 9,211,661 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	25	9,236,109 - 9,253,732 (-)	NCBI		UU_Cfam_GSD_1.0

Medag
(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_024404945	170,298,447 - 170,317,740 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936472	25,634,349 - 25,653,823 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936472	25,634,444 - 25,653,708 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

MEDAG
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	11	7,545,494 - 7,562,737 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	11	7,545,400 - 7,562,741 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	11	7,396,838 - 7,414,378 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

MEDAG
(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	3	9,779,644 - 9,799,113 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666057	34,569,194 - 34,588,583 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Medag
(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_004624776	7,278,545 - 7,300,602 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624776	7,280,321 - 7,300,505 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in MEDAG
10 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 13q12.3-13.1(chr13:29654134-32858245)x1	copy number loss	See cases [RCV000051372]	Chr13:29654134..32858245 [GRCh38] Chr13:30228271..33432383 [GRCh37] Chr13:29126271..32330383 [NCBI36] Chr13:13q12.3-13.1	pathogenic
GRCh38/hg38 13q12.3-21.33(chr13:30697728-69471973)x1	copy number loss	See cases [RCV000051373]	Chr13:30697728..69471973 [GRCh38] Chr13:31271865..70046105 [GRCh37] Chr13:30169865..68944106 [NCBI36] Chr13:13q12.3-21.33	pathogenic
GRCh38/hg38 13q12.11-34(chr13:18946182-114304628)x3	copy number gain	See cases [RCV000053726]	Chr13:18946182..114304628 [GRCh38] Chr13:19520322..115070103 [GRCh37] Chr13:18418322..114088205 [NCBI36] Chr13:13q12.11-34	pathogenic
GRCh38/hg38 13q12.11-12.3(chr13:18958091-31090460)x3	copy number gain	See cases [RCV000053729]	Chr13:18958091..31090460 [GRCh38] Chr13:19532231..31664597 [GRCh37] Chr13:18430231..30562597 [NCBI36] Chr13:13q12.11-12.3	pathogenic
GRCh38/hg38 13q12.11-34(chr13:19837395-114327173)x3	copy number gain	See cases [RCV000053731]	Chr13:19837395..114327173 [GRCh38] Chr13:20411535..115085141 [GRCh37] Chr13:19309535..114110750 [NCBI36] Chr13:13q12.11-34	pathogenic
GRCh38/hg38 13q12.3-31.1(chr13:30318913-83610426)x3	copy number gain	See cases [RCV000053737]	Chr13:30318913..83610426 [GRCh38] Chr13:30893050..84184561 [GRCh37] Chr13:29791050..83082562 [NCBI36] Chr13:13q12.3-31.1	pathogenic
GRCh38/hg38 13q11-34(chr13:18565048-114327173)x3	copy number gain	See cases [RCV000053719]	Chr13:18565048..114327173 [GRCh38] Chr13:19139188..115085141 [GRCh37] Chr13:18037188..114110750 [NCBI36] Chr13:13q11-34	pathogenic
GRCh38/hg38 13q11-13.3(chr13:18676442-37656039)x3	copy number gain	See cases [RCV000053721]	Chr13:18676442..37656039 [GRCh38] Chr13:19250582..38230176 [GRCh37] Chr13:18148582..37128176 [NCBI36] Chr13:13q11-13.3	pathogenic
GRCh38/hg38 13q11-34(chr13:18850545-114327173)x3	copy number gain	See cases [RCV000053723]	Chr13:18850545..114327173 [GRCh38] Chr13:19296527..115085141 [GRCh37] Chr13:18194527..114110750 [NCBI36] Chr13:13q11-34	pathogenic
GRCh38/hg38 13q12.11-34(chr13:19833130-114298614)x3	copy number gain	See cases [RCV000134104]	Chr13:19833130..114298614 [GRCh38] Chr13:20407270..115064089 [GRCh37] Chr13:19305270..114082191 [NCBI36] Chr13:13q12.11-34	pathogenic
GRCh38/hg38 13q11-34(chr13:18445862-114327173)x1	copy number loss	See cases [RCV000135610]	Chr13:18445862..114327173 [GRCh38] Chr13:19020001..115085141 [GRCh37] Chr13:10098739..114110750 [NCBI36] Chr13:13q11-34	pathogenic
GRCh38/hg38 13q12.11-14.11(chr13:19671934-40914767)x3	copy number gain	See cases [RCV000137892]	Chr13:19671934..40914767 [GRCh38] Chr13:20246074..41488903 [GRCh37] Chr13:19144074..40386903 [NCBI36] Chr13:13q12.11-14.11	pathogenic
GRCh38/hg38 13q12.3-13.3(chr13:29073320-36556014)x1	copy number loss	See cases [RCV000137923]	Chr13:29073320..36556014 [GRCh38] Chr13:29647457..37130151 [GRCh37] Chr13:28545457..36028151 [NCBI36] Chr13:13q12.3-13.3	pathogenic
GRCh38/hg38 13q12.3-13.3(chr13:30313809-39267681)x1	copy number loss	See cases [RCV000139225]	Chr13:30313809..39267681 [GRCh38] Chr13:30887946..39841818 [GRCh37] Chr13:29785946..38739818 [NCBI36] Chr13:13q12.3-13.3	pathogenic
GRCh38/hg38 13q12.11-34(chr13:19833130-114327106)x3	copy number gain	See cases [RCV000139078]	Chr13:19833130..114327106 [GRCh38] Chr13:20407270..115085141 [GRCh37] Chr13:19305270..114110683 [NCBI36] Chr13:13q12.11-34	pathogenic
GRCh38/hg38 13q11-34(chr13:18456040-114340285)x3	copy number gain	See cases [RCV000140004]	Chr13:18456040..114340285 [GRCh38] Chr13:19030180..115105760 [GRCh37] Chr13:17928180..114123862 [NCBI36] Chr13:13q11-34	pathogenic
GRCh38/hg38 13q11-13.2(chr13:18862146-33577351)x3	copy number gain	See cases [RCV000141867]	Chr13:18862146..33577351 [GRCh38] Chr13:19436286..34151488 [GRCh37] Chr13:18334286..33049488 [NCBI36] Chr13:13q11-13.2	pathogenic
GRCh38/hg38 13q12.11-34(chr13:19671934-114340331)x3	copy number gain	See cases [RCV000142924]	Chr13:19671934..114340331 [GRCh38] Chr13:20246074..115085141 [GRCh37] Chr13:19144074..114123908 [NCBI36] Chr13:13q12.11-34	pathogenic
GRCh38/hg38 13q12.3-13.3(chr13:29321454-36995348)x3	copy number gain	See cases [RCV000142869]	Chr13:29321454..36995348 [GRCh38] Chr13:29895591..37569485 [GRCh37] Chr13:28793591..36467485 [NCBI36] Chr13:13q12.3-13.3	pathogenic
GRCh38/hg38 13q11-34(chr13:18862146-114342258)x3	copy number gain	See cases [RCV000143462]	Chr13:18862146..114342258 [GRCh38] Chr13:19436286..115107733 [GRCh37] Chr13:18334286..114125835 [NCBI36] Chr13:13q11-34	pathogenic
GRCh38/hg38 13q12.11-34(chr13:19837395-114327173)x3	copy number gain	See cases [RCV000148126]	Chr13:19837395..114327173 [GRCh38] Chr13:20411535..115085141 [GRCh37] Chr13:19309535..114110750 [NCBI36] Chr13:13q12.11-34	pathogenic
GRCh37/hg19 13q12.11-34(chr13:19571503-115092569)x3	copy number gain	See cases [RCV000240150]	Chr13:19571503..115092569 [GRCh37] Chr13:13q12.11-34	pathogenic
GRCh37/hg19 13q12.11-34(chr13:19571503-115092510)	copy number gain	See cases [RCV000449142]	Chr13:19571503..115092510 [GRCh37] Chr13:13q12.11-34	pathogenic
GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3	copy number gain	See cases [RCV000445886]	Chr13:19436286..115107733 [GRCh37] Chr13:13q11-34	pathogenic
GRCh37/hg19 13q11-34(chr13:19436287-115107733)	copy number gain	See cases [RCV000510405]	Chr13:19436287..115107733 [GRCh37] Chr13:13q11-34	pathogenic
GRCh37/hg19 13q11-34(chr13:19436287-115107733)x3	copy number gain	See cases [RCV000511880]	Chr13:19436287..115107733 [GRCh37] Chr13:13q11-34	pathogenic
NM_032849.4(MEDAG):c.577G>T (p.Ala193Ser)	single nucleotide variant	Inborn genetic diseases [RCV003307005]	Chr13:30921636 [GRCh38] Chr13:31495773 [GRCh37] Chr13:13q12.3	uncertain significance
GRCh37/hg19 13q12.12-13.2(chr13:24080918-34361992)x1	copy number loss	Poly (ADP-Ribose) polymerase inhibitor response [RCV000626443]	Chr13:24080918..34361992 [GRCh37] Chr13:13q12.12-13.2	drug response
GRCh37/hg19 13q11-22.1(chr13:19436286-74045459)x3	copy number gain	not provided [RCV000683572]	Chr13:19436286..74045459 [GRCh37] Chr13:13q11-22.1	pathogenic
GRCh37/hg19 13q11-34(chr13:19058717-115103529)x3	copy number gain	not provided [RCV000738115]	Chr13:19058717..115103529 [GRCh37] Chr13:13q11-34	pathogenic
GRCh37/hg19 13q11-34(chr13:19031237-115107157)x3	copy number gain	not provided [RCV000750643]	Chr13:19031237..115107157 [GRCh37] Chr13:13q11-34	pathogenic
GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3	copy number gain	not provided [RCV000849129]	Chr13:19436286..115107733 [GRCh37] Chr13:13q11-34	pathogenic
GRCh37/hg19 13q12.3(chr13:31498706-31566543)x1	copy number loss	not provided [RCV001006556]	Chr13:31498706..31566543 [GRCh37] Chr13:13q12.3	uncertain significance
NM_032849.4(MEDAG):c.233T>A (p.Val78Glu)	single nucleotide variant	Inborn genetic diseases [RCV003269969]	Chr13:30906748 [GRCh38] Chr13:31480885 [GRCh37] Chr13:13q12.3	uncertain significance
GRCh37/hg19 13q12.3-13.2(chr13:28925153-34061696)x1	copy number loss	not provided [RCV001537908]	Chr13:28925153..34061696 [GRCh37] Chr13:13q12.3-13.2	pathogenic
GRCh37/hg19 13p13-q34(chr13:1-115169878)	copy number gain	Complete trisomy 13 syndrome [RCV002280659]	Chr13:1..115169878 [GRCh37] Chr13:13p13-q34	pathogenic
GRCh37/hg19 13q11-34(chr13:19053605-115108528)x3	copy number gain	See cases [RCV001353184]	Chr13:19053605..115108528 [GRCh37] Chr13:13q11-34	pathogenic
GRCh37/hg19 13p13-q34(chr13:1-115169878)x3	copy number gain	See cases [RCV001780076]	Chr13:1..115169878 [GRCh37] Chr13:13p13-q34	pathogenic
GRCh38/hg38 13q12.3(chr13:30194283-31591879)	copy number loss	Diaphragmatic hernia [RCV001823064]	Chr13:30194283..31591879 [GRCh38] Chr13:13q12.3	uncertain significance
GRCh37/hg19 13q11-34(chr13:19436286-114981726)	copy number gain	not specified [RCV002053035]	Chr13:19436286..114981726 [GRCh37] Chr13:13q11-34	pathogenic
GRCh37/hg19 13q11-34(chr13:19436286-115107733)	copy number gain	not specified [RCV002053036]	Chr13:19436286..115107733 [GRCh37] Chr13:13q11-34	pathogenic
GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3	copy number gain	not provided [RCV001834436]	Chr13:19436286..115107733 [GRCh37] Chr13:13q11-34	pathogenic
NC_000013.10:g.(?_31033232)_(33638323_?)dup	duplication	not provided [RCV003113598]	Chr13:31033232..33638323 [GRCh37] Chr13:13q12.3-13.1	uncertain significance
GRCh37/hg19 13q11-34(chr13:19253848-115108937)x3	copy number gain	not provided [RCV002291540]	Chr13:19253848..115108937 [GRCh37] Chr13:13q11-34	pathogenic
GRCh37/hg19 13q12.3(chr13:31267070-31483281)x3	copy number gain	not provided [RCV002472479]	Chr13:31267070..31483281 [GRCh37] Chr13:13q12.3	uncertain significance
NM_032849.4(MEDAG):c.73C>A (p.Leu25Met)	single nucleotide variant	Inborn genetic diseases [RCV002685254]	Chr13:30906588 [GRCh38] Chr13:31480725 [GRCh37] Chr13:13q12.3	uncertain significance
NM_032849.4(MEDAG):c.750C>A (p.Ser250Arg)	single nucleotide variant	Inborn genetic diseases [RCV002992760]	Chr13:30921809 [GRCh38] Chr13:31495946 [GRCh37] Chr13:13q12.3	uncertain significance
NM_032849.4(MEDAG):c.413A>T (p.Asn138Ile)	single nucleotide variant	Inborn genetic diseases [RCV002849584]	Chr13:30921038 [GRCh38] Chr13:31495175 [GRCh37] Chr13:13q12.3	uncertain significance
NM_032849.4(MEDAG):c.479T>C (p.Ile160Thr)	single nucleotide variant	Inborn genetic diseases [RCV002783000]	Chr13:30921104 [GRCh38] Chr13:31495241 [GRCh37] Chr13:13q12.3	uncertain significance
NM_032849.4(MEDAG):c.650T>C (p.Val217Ala)	single nucleotide variant	Inborn genetic diseases [RCV002697014]	Chr13:30921709 [GRCh38] Chr13:31495846 [GRCh37] Chr13:13q12.3	uncertain significance
NM_032849.4(MEDAG):c.733C>G (p.Pro245Ala)	single nucleotide variant	Inborn genetic diseases [RCV002673341]	Chr13:30921792 [GRCh38] Chr13:31495929 [GRCh37] Chr13:13q12.3	uncertain significance
NM_032849.4(MEDAG):c.244G>A (p.Gly82Arg)	single nucleotide variant	Inborn genetic diseases [RCV003352118]	Chr13:30906759 [GRCh38] Chr13:31480896 [GRCh37] Chr13:13q12.3	uncertain significance
NM_032849.4(MEDAG):c.396G>A (p.Thr132=)	single nucleotide variant	not provided [RCV003390349]	Chr13:30921021 [GRCh38] Chr13:31495158 [GRCh37] Chr13:13q12.3	likely benign
GRCh37/hg19 13q12.3-13.1(chr13:29933399-32792968)x3	copy number gain	not provided [RCV003885456]	Chr13:29933399..32792968 [GRCh37] Chr13:13q12.3-13.1	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	521
Count of miRNA genes:	425
Interacting mature miRNAs:	466
Transcripts:	ENST00000380482, ENST00000428944
Prediction methods:	Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

Markers in Region

D13S1229

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	13	31,484,262 - 31,484,396	UniSTS	GRCh37
Build 36	13	30,382,262 - 30,382,396	RGD	NCBI36
Celera	13	12,550,812 - 12,550,947	RGD
Cytogenetic Map	13	q12.3	UniSTS
HuRef	13	12,295,144 - 12,295,280	UniSTS
Marshfield Genetic Map	13	21.51	RGD
Marshfield Genetic Map	13	21.51	UniSTS
Genethon Genetic Map	13	23.5	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

1571

1709

782

127

125

3246

1238

725

652

1066

125

1193

2135

Low

728

645

656

228

454

184

1016

911

1318

264

703

353

630

Below cutoff

583

259

245

817

247

1620

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_032849	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017020801	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054375073	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB055407	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK027740	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK055635	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL353680	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC040165	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC101624	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC101626	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471075	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068265	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000380482 ⟹ ENSP00000369849

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	13	30,906,271 - 30,925,572 (+)	Ensembl

RefSeq Acc Id:

ENST00000428944 ⟹ ENSP00000416838

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	13	30,906,706 - 30,924,449 (+)	Ensembl

RefSeq Acc Id:

NM_032849 ⟹ NP_116238

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	13	30,906,271 - 30,925,572 (+)	NCBI
GRCh37	13	31,480,312 - 31,499,709 (+)	RGD
Build 36	13	30,378,328 - 30,397,678 (+)	NCBI Archive
Celera	13	12,546,863 - 12,566,248 (+)	RGD
HuRef	13	12,291,191 - 12,310,577 (+)	RGD
CHM1_1	13	31,447,426 - 31,466,813 (+)	NCBI
T2T-CHM13v2.0	13	30,128,196 - 30,147,488 (+)	NCBI

Sequence:

show sequence

GCTTTCTCCGCGCGGTGCCTGCAGGGCTCCCAGCGAGTGGCAGCTTGGGAGGGGCCGCCCGGGC
GGTCAGACTGGCACCTGAGCGGCCACCGCGTCCCGGCCAGGCGGGCAGACCGACCCCCTCCTCA
CCTCGCGCGCGGCTGACGCAGGCAGGGCGCCCGGCCCCTCCTGGGGACCATCAGGTGCCGGCTG
GGGGCTGTAGGCACCGGACGGAAGCAGGCGGTGTGAGGACCGACGACGCGGGCATGGCGGGGGC
GGCCTGCGAGCCGGTGGCCAGGCCGAGCCTGACCTCCATCTCGTCTGGGGAGCTTCGCAGCCTG
TGGACCTGCGACTGCGAGCTGGCCCTGCTGCCGCTGGCTCAGCTGCTGCGCCTGCAGCCCGGTG
CCTTCCAGCTGAGCGGCGACCAGCTCGTGGTGGCCAGGCCCGGGGAGCCGGCGGCGGCGCGGGG
GGGCTTCAACGTCTTCGGTGACGGCCTCGTGCGCCTCGACGGGCAGCTCTACCGCCTCAGCAGC
TACATCAAGAGGTATGTGGAACTGACCAACTACTGTGATTATAAAGACTACAGGGAAACTATAT
TGAGCAAACCAATGTTGTTCTTTATTAATGTACAGACCAAAAAAGACACCTCAAAAGAAAGGAC
GTACGCGTTTCTTGTAAACACGAGGCACCCCAAGATAAGAAGACAGATAGAGCAAGGGATGGAC
ATGGTCATCTCCTCAGTGATTGGAGAAAGTTACCGGCTTCAGTTTGATTTTCAAGAGGCAGTGA
AGAATTTCTTCCCCCCAGGAAATGAAGTGGTTAATGGAGAAAATTTAAGCTTTGCATATGAATT
CAAAGCTGATGCATTATTTGATTTCTTCTATTGGTTTGGGCTCAGTAATTCCGTTGTAAAAGTA
AATGGAAAAGTTCTGAATTTGTCAAGTACAAGTCCAGAAAAGAAGGAGACGATTAAGTTATTTC
TGGAAAAAATGAGTGAGCCTTTAATCCGAAGGAGCAGTTTCTCTGACCGAAAGTTCAGTGTAAC
TTCCAGAGGTTCAATAGATGATGTTTTTAACTGCAATCTGTCACCCAGATCATCTCTGACAGAG
CCTCTTTTGGCAGAATTACCATTTCCAAGTGTTCTGGAATCTGAAGAGACACCCAACCAATTTA
TCTGATTGAACTGAACATTGTAGCAGTTGCTCCCGCACTCCAGGCCTGTGCTAGACTATAGGCT
GGGGGGAGGGTAGGAGGTGGGAGGCAGATACTTCCACCTGCGTGTCAATCTCCGGCTCCTCCAT
GGCTTCTATGGAGGACTCCTCTCTTCTGCTTCTGTGGATGTGATGCCCTGGCAGGCCCAGGGCA
GCTGATTCCCCTAAAACTTATGATTACCAGGATGGAAAGGCCTTGGTCCCATGGCACTGGGTGG
GGCTGGGGGATATTCTCTACTTTGAACACTTCTCCAAAGAGGCAGAAGGGCCACAGAGTTCTGC
CACCCTGAACATTTTTCTCAGTTCCCTGGGAGTTTTTGTGGCAGCCTTTGTGGGAGTGGTCTGA
CTGGCTGTTGACCTAGCATGCTTCATAAATCAGGGTTTGGCCCTCTGCTTGGAGCATCCAACCC
CTTGAACTCAAACCTGTCGAGCAAGGGGTTAAGAGTTCTGTTCTCTTGCCAACCTGGCTGGGCA
AAAGCCTGTGCCATCTTTCACTGGGAGGCAAATATGTTTTTCATCCTGCCATATGACACCTATG
AGAAACGTTCACAGTGAGGAGTAGCCAGGTTGCTAGGACAGTAACCCTGCCACACACTGCCTGA
AATCGGAACTCCCTTGGCCTCCCTCTTAACTAAGTGACCCATGTAGAAGGAAGCCAGGAGATAT
GGTACCGAACAATGACAGGGGAAGGGTATTGGACACGGCAGCGTCCTCCTTATTGAAAACACAT
TATGTCAGTTGGGAATTTTAAATAAGCTTTTAGCAAACCTAACACTAAAAGCAAAATAGAAGAA
AGCTATACCATTACCATAATACATTTTTCATCTCATGGCTACAATGGAATTCTTGAAAAGGAAA
AAAAAATCCTATCTACATATAAAAACCTGCATGAATGAATCACTACATATGCTTATAATGAGGA
AGAGTTATGGGTCCTGAGTGTAATTTTTTATCCTTTCTTAAAAAGTTTCTGTATTATGCATTTT
GATAACACTACTGATGATCCTTCCACTTATATTTGAAATGTTATGTACCACATTTGCACAATTA
AAACTTTTCTTAGCATTCAACCTAGAATTGATTAAATTTATGACTGAGGCTTCA

hide sequence

RefSeq Acc Id:

XM_017020801 ⟹ XP_016876290

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	13	30,917,879 - 30,925,572 (+)	NCBI

Sequence:

show sequence

GGACACAAATCCAAACCATATCAGTATATAAATAGTTTTGGTTTGGTCCTTGCTGGGACCAAAC
TGGGCTGAGGTGTGGACTGATGAGCAGGGCAGAAATCAGCTTGTGACAAGGTAGACAGCAAGGA
GCCTGGTGGGTGAGGCCACCTGAAACACAGCACATGCCTGCAGAACAAACCCCTCAATGATCCT
AGGGCAGAAGCCACCTGTCTGGGAGCTTCTTTTCTACTTCTTGCCTAGGTGGGAAGTGATCTGA
CATTCTGAGCCTTTGGAGGTTGCAGAAATGACTAGAGTGATGAGGATGATATATAACATGCTCT
ACCACGTATCAAACACCTACTATGTCTAAGAAGTGCTCTAATGTAATGGATCACCACAACAACT
TTGTAGGGCTTATCAATTCAGGACGTTATGAACATGAACATCATTACTATCAATAATTATTCTG
GGAAGAAGGTATAAACTGACCCGGGCAAACTAGGATGCGTAATTATCCCACTTAGGAGGTGCTT
ACACTATTCCCATTTTATAGATGAGGAAACTAAGAAAATAAATAGCCATTGTGGATGCTTTTCT
GTTTCATGCCATGATGTTGGAATGTCATGTTTAGACACATCTCTTCATTGTTTCTTCCAAGAAA
TCAGATTAGCTGGTAGCAACTATATTAAACCAAATTTCAGTATGAAAATGTCTCCATTTTGCCT
TCCTCCTCCTGCTCAGAATGATATGTGGGGGAAGTCATGGGCATAACGTTCTGTAATAGAAGTA
GAATTTCTTAAACTTGCTTCTAACTAACATTCTTAAAATGAGTCCAAGGAAATAAGAAATGATC
TACGAATTTCAAATAGATTTCCCCAAACATTCACTCTCATTCAAATTTGTGGAGCTCTCTCTGC
TCATTTGACAATAAAAAGTCATGATGTTCTTTCTGCAGGAGAGGCCAGGAACAGAATGCCCAGT
AACAAGAAGTGCTCATTAGAACATCTGAAGCCCACGTGTTCTTTGGCTTGATTATAACCAGAAA
GCCAGATAGTTCTTTAGGAATGTAATTCACAGCTGTATCAAGTACACCTCCTGCACCGATCACT
CAGGAGGAATCTAAAAAAAGAAAAGGACGTACGCGTTTCTTGTAAACACGAGGCACCCCAAGAT
AAGAAGACAGATAGAGCAAGGGATGGACATGGTCATCTCCTCAGTGATTGGAGAAAGTTACCGG
CTTCAGTTTGATTTTCAAGAGGCAGTGAAGAATTTCTTCCCCCCAGGAAATGAAGTGGTTAATG
GAGAAAATTTAAGCTTTGCATATGAATTCAAAGCTGATGCATTATTTGATTTCTTCTATTGGTT
TGGGCTCAGTAATTCCGTTGTAAAAGTAAATGGAAAAGTTCTGAATTTGTCAAGTACAAGTCCA
GAAAAGAAGGAGACGATTAAGTTATTTCTGGAAAAAATGAGTGAGCCTTTAATCCGAAGGAGCA
GTTTCTCTGACCGAAAGTTCAGTGTAACTTCCAGAGGTTCAATAGATGATGTTTTTAACTGCAA
TCTGTCACCCAGATCATCTCTGACAGAGCCTCTTTTGGCAGAATTACCATTTCCAAGTGTTCTG
GAATCTGAAGAGACACCCAACCAATTTATCTGATTGAACTGAACATTGTAGCAGTTGCTCCCGC
ACTCCAGGCCTGTGCTAGACTATAGGCTGGGGGGAGGGTAGGAGGTGGGAGGCAGATACTTCCA
CCTGCGTGTCAATCTCCGGCTCCTCCATGGCTTCTATGGAGGACTCCTCTCTTCTGCTTCTGTG
GATGTGATGCCCTGGCAGGCCCAGGGCAGCTGATTCCCCTAAAACTTATGATTACCAGGATGGA
AAGGCCTTGGTCCCATGGCACTGGGTGGGGCTGGGGGATATTCTCTACTTTGAACACTTCTCCA
AAGAGGCAGAAGGGCCACAGAGTTCTGCCACCCTGAACATTTTTCTCAGTTCCCTGGGAGTTTT
TGTGGCAGCCTTTGTGGGAGTGGTCTGACTGGCTGTTGACCTAGCATGCTTCATAAATCAGGGT
TTGGCCCTCTGCTTGGAGCATCCAACCCCTTGAACTCAAACCTGTCGAGCAAGGGGTTAAGAGT
TCTGTTCTCTTGCCAACCTGGCTGGGCAAAAGCCTGTGCCATCTTTCACTGGGAGGCAAATATG
TTTTTCATCCTGCCATATGACACCTATGAGAAACGTTCACAGTGAGGAGTAGCCAGGTTGCTAG
GACAGTAACCCTGCCACACACTGCCTGAAATCGGAACTCCCTTGGCCTCCCTCTTAACTAAGTG
ACCCATGTAGAAGGAAGCCAGGAGATATGGTACCGAACAATGACAGGGGAAGGGTATTGGACAC
GGCAGCGTCCTCCTTATTGAAAACACATTATGTCAGTTGGGAATTTTAAATAAGCTTTTAGCAA
ACCTAACACTAAAAGCAAAATAGAAGAAAGCTATACCATTACCATAATACATTTTTCATCTCAT
GGCTACAATGGAATTCTTGAAAAGGAAAAAAAAATCCTATCTACATATAAAAACCTGCATGAAT
GAATCACTACATATGCTTATAATGAGGAAGAGTTATGGGTCCTGAGTGTAATTTTTTATCCTTT
CTTAAAAAGTTTCTGTATTATGCATTTTGATAACACTACTGATGATCCTTCCACTTATATTTGA
AATGTTATGTACCACATTTGCACAATTAAAACTTTTCTTAGCATTCAACCTAGAATTGATTAAA
TTTATGACTGAGGCTTCATGTGA

hide sequence

RefSeq Acc Id:

XM_054375073 ⟹ XP_054231048

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	13	30,139,795 - 30,147,488 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_116238	(Get FASTA)	NCBI Sequence Viewer
	XP_016876290	(Get FASTA)	NCBI Sequence Viewer
	XP_054231048	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH40165	(Get FASTA)	NCBI Sequence Viewer
	AAI01625	(Get FASTA)	NCBI Sequence Viewer
	AAI01627	(Get FASTA)	NCBI Sequence Viewer
	BAB70975	(Get FASTA)	NCBI Sequence Viewer
	BAC53805	(Get FASTA)	NCBI Sequence Viewer
	EAX08473	(Get FASTA)	NCBI Sequence Viewer
	EAX08474	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000369849
	ENSP00000369849.4
	ENSP00000416838.1
GenBank Protein	Q5VYS4	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:

NP_116238 ⟸ NM_032849

- UniProtKB:

Q96K26 (UniProtKB/Swiss-Prot), Q8IXF1 (UniProtKB/Swiss-Prot), Q5VYS4 (UniProtKB/Swiss-Prot), Q96NC8 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MAGAACEPVARPSLTSISSGELRSLWTCDCELALLPLAQLLRLQPGAFQLSGDQLVVAGPGEPA
AARGGFNVFGDGLVRLDGQLYRLSSYIKRYVELTNYCDYKDYRETILSKPMLFFINVQTKKDTS
KERTYAFLVNTRHPKIRRQIEQGMDMVISSVIGESYRLQFDFQEAVKNFFPPGNEVVNGENLSF
AYEFKADALFDFFYWFGLSNSVVKVNGKVLNLSSTSPEKKETIKLFLEKMSEPLIRRSSFSDRK
FSVTSRGSIDDVFNCNLSPRSSLTEPLLAELPFPSVLESEETPNQFI

hide sequence

RefSeq Acc Id:	XP_016876290 ⟸ XM_017020801
- Peptide Label:	isoform X1
- Sequence:	show sequence MDMVISSVIGESYRLQFDFQEAVKNFFPPGNEVVNGENLSFAYEFKADALFDFFYWFGLSNSVV KVNGKVLNLSSTSPEKKETIKLFLEKMSEPLIRRSSFSDRKFSVTSRGSIDDVFNCNLSPRSSL TEPLLAELPFPSVLESEETPNQFI hide sequence

RefSeq Acc Id:

ENSP00000416838 ⟸ ENST00000428944

RefSeq Acc Id:

ENSP00000369849 ⟸ ENST00000380482

RefSeq Acc Id:	XP_054231048 ⟸ XM_054375073
- Peptide Label:	isoform X1

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q5VYS4-F1-model_v2	AlphaFold	Q5VYS4	1-303	view protein structure

Promoters

RGD ID:

7226163

Promoter ID:

EPDNEW_H18827

Type:

multiple initiation site

Name:

MEDAG_1

Description:

mesenteric estrogen dependent adipogenesis

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H18825 EPDNEW_H18826

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	13	30,906,278 - 30,906,338	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:25926	AgrOrtholog
COSMIC	MEDAG	COSMIC
Ensembl Genes	ENSG00000102802	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000380482	ENTREZGENE
	ENST00000380482.9	UniProtKB/Swiss-Prot
	ENST00000428944.1	UniProtKB/TrEMBL
GTEx	ENSG00000102802	GTEx
HGNC ID	HGNC:25926	ENTREZGENE
Human Proteome Map	MEDAG	Human Proteome Map
InterPro	MEDAG/TEX26	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:84935	UniProtKB/Swiss-Prot
NCBI Gene	84935	ENTREZGENE
PANTHER	PTHR33769	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR33769:SF3	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA147358556	PharmGKB
UniProt	H0Y831_HUMAN	UniProtKB/TrEMBL
	MEDAG_HUMAN	UniProtKB/Swiss-Prot, ENTREZGENE
	Q8IXF1	ENTREZGENE
	Q96K26	ENTREZGENE
	Q96NC8	ENTREZGENE
UniProt Secondary	Q8IXF1	UniProtKB/Swiss-Prot
	Q96K26	UniProtKB/Swiss-Prot
	Q96NC8	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-04-12	MEDAG	mesenteric estrogen dependent adipogenesis		mesenteric estrogen-dependent adipogenesis	Symbol and/or name change	5135510	APPROVED
2012-10-02	MEDAG	mesenteric estrogen-dependent adipogenesis	C13orf33	chromosome 13 open reading frame 33	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)

Send us a Message

Imported Disease Annotations - ClinVar