COMMD7 (COMM domain containing 7)

Gene: COMMD7 (COMM domain containing 7) Homo sapiens

Analyze

Symbol:

COMMD7

Name:

COMM domain containing 7

RGD ID:

1317181

HGNC Page

HGNC:16223

Description:

Enables NF-kappaB binding activity. Involved in negative regulation of DNA-templated transcription and tumor necrosis factor-mediated signaling pathway. Predicted to be located in cytoplasmic vesicle and membrane.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

C20orf92; COMM domain-containing protein 7; dJ1085F17.3; FLJ14987; MGC33315

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):	Commd7 (COMM domain containing 7)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther
Rattus norvegicus (Norway rat):	Commd7 (COMM domain containing 7)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Commd7 (COMM domain containing 7)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	COMMD7 (COMM domain containing 7)	NCBI	Ortholog
Canis lupus familiaris (dog):	COMMD7 (COMM domain containing 7)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Commd7 (COMM domain containing 7)	NCBI	Ortholog
Sus scrofa (pig):	NOL4L (nucleolar protein 4 like)	HGNC	NCBI
Chlorocebus sabaeus (green monkey):	COMMD7 (COMM domain containing 7)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Commd7 (COMM domain containing 7)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Commd7 (COMM domain containing 7)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Commd7 (COMM domain containing 7)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	commd7 (COMM domain containing 7)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)

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	32,702,699 - 32,743,467 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	20	32,702,699 - 32,743,467 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	20	31,290,501 - 31,331,273 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	20	30,754,154 - 30,795,475 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	20	30,754,164 - 30,795,036	NCBI
Celera	20	28,045,955 - 28,085,739 (-)	NCBI		Celera
Cytogenetic Map	20	q11.21	NCBI
HuRef	20	28,079,083 - 28,118,793 (-)	NCBI		HuRef
CHM1_1	20	31,195,366 - 31,235,269 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	20	34,431,363 - 34,470,209 (-)	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)

immunodeficiency-centromeric instability-facial anomalies syndrome 1 (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dimethylhydrazine (ISO)

17alpha-ethynylestradiol (ISO)

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

6-propyl-2-thiouracil (ISO)

acrylamide (EXP,ISO)

aflatoxin B1 (EXP)

amitrole (ISO)

arsenite(3-) (EXP)

benzo[a]pyrene (EXP)

bisphenol A (ISO)

CGP 52608 (EXP)

chlorpyrifos (ISO)

choline (ISO)

ciguatoxin CTX1B (ISO)

copper(II) chloride (EXP)

copper(II) sulfate (EXP)

cyclosporin A (EXP)

decabromodiphenyl ether (ISO)

dioxygen (ISO)

folic acid (ISO)

gentamycin (ISO)

inulin (ISO)

L-methionine (ISO)

methimazole (ISO)

paracetamol (EXP,ISO)

perfluorooctane-1-sulfonic acid (ISO)

pregnenolone 16alpha-carbonitrile (ISO)

resveratrol (ISO)

sulfadimethoxine (ISO)

valproic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

negative regulation of DNA-templated transcription (IBA,IDA)

tumor necrosis factor-mediated signaling pathway (IBA,IDA)

Cellular Component

cytoplasmic vesicle (IEA)

membrane (IEA)

Molecular Function

NF-kappaB binding (IBA,IDA)

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:10393949	PMID:11780052	PMID:12477932	PMID:14702039	PMID:15489334	PMID:15799966	PMID:20379614	PMID:20979692	PMID:21778237	PMID:21873635	PMID:22939629	PMID:23049798
PMID:23376485	PMID:23563313	PMID:25355947	PMID:26060140	PMID:26186194	PMID:26344197	PMID:26496610	PMID:27129158	PMID:27350032	PMID:28142122	PMID:28298427	PMID:28514442
PMID:29532873	PMID:30232004	PMID:30833792	PMID:33891561	PMID:33961781	PMID:34917906	PMID:35088190	PMID:35271311	PMID:37057209	PMID:37172566

Genomics

Comparative Map Data

COMMD7
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	20	32,702,699 - 32,743,467 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	20	32,702,699 - 32,743,467 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	20	31,290,501 - 31,331,273 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	20	30,754,154 - 30,795,475 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	20	30,754,164 - 30,795,036	NCBI
Celera	20	28,045,955 - 28,085,739 (-)	NCBI		Celera
Cytogenetic Map	20	q11.21	NCBI
HuRef	20	28,079,083 - 28,118,793 (-)	NCBI		HuRef
CHM1_1	20	31,195,366 - 31,235,269 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	20	34,431,363 - 34,470,209 (-)	NCBI		T2T-CHM13v2.0

Commd7
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	2	153,458,850 - 153,474,712 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	2	153,458,853 - 153,474,701 (-)	Ensembl		GRCm39 Ensembl
GRCm38	2	153,616,930 - 153,632,795 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	2	153,616,933 - 153,632,781 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	2	153,444,570 - 153,458,467 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	2	153,310,275 - 153,324,172 (-)	NCBI		MGSCv36	mm8
MGSCv36	2	154,428,011 - 154,442,033 (-)	NCBI		MGSCv36	mm8
Celera	2	159,461,429 - 159,478,858 (-)	NCBI		Celera
Cytogenetic Map	2	H1	NCBI
cM Map	2	75.73	NCBI

Commd7
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	3	162,559,762 - 162,574,543 (-)	NCBI		GRCr8
mRatBN7.2	3	142,099,566 - 142,114,348 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	3	142,099,251 - 142,114,317 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	3	146,001,750 - 146,016,368 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	3	154,585,556 - 154,600,182 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	3	152,325,856 - 152,340,470 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	3	149,101,242 - 149,115,227 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	3	149,101,243 - 149,115,209 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	3	155,480,860 - 155,495,145 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	3	143,997,788 - 144,012,407 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	3	143,903,047 - 143,918,137 (-)	NCBI
Celera	3	140,841,506 - 140,856,102 (-)	NCBI		Celera
Cytogenetic Map	3	q41	NCBI

Commd7
(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_004955422	28,442,274 - 28,467,057 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955422	28,454,984 - 28,464,885 (+)	NCBI	ChiLan1.0	ChiLan1.0

COMMD7
(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	38,393,081 - 38,434,386 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	20	38,386,179 - 38,427,289 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	20	28,990,068 - 29,031,630 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3

COMMD7
(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	22,035,590 - 22,057,799 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	24	22,035,990 - 22,079,583 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	24	21,681,685 - 21,725,457 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	24	22,722,770 - 22,766,625 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	24	22,722,779 - 22,745,431 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	24	21,998,876 - 22,042,786 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	24	22,107,585 - 22,151,493 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	24	22,538,585 - 22,582,519 (-)	NCBI		UU_Cfam_GSD_1.0

Commd7
(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	171,067,914 - 171,087,117 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936485	19,499,224 - 19,518,481 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936485	19,500,170 - 19,518,481 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

NOL4L
(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	36,300,087 - 36,324,918 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	17	36,256,243 - 36,325,479 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	17	41,092,379 - 41,095,895 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

COMMD7
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	2	37,078,210 - 37,112,012 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	2	37,077,735 - 37,111,556 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666050	89,790,194 - 89,828,112 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Commd7
(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 1.0	NW_004624842	6,520,873 - 6,545,368 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in COMMD7
16 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 20p12.2-q12(chr20:9811433-39316956)x3	copy number gain	See cases [RCV000052999]	Chr20:9811433..39316956 [GRCh38] Chr20:9792081..37945599 [GRCh37] Chr20:9740081..37379013 [NCBI36] Chr20:20p12.2-q12	pathogenic
GRCh38/hg38 20q11.21(chr20:31254983-33473080)x3	copy number gain	See cases [RCV000135358]	Chr20:31254983..33473080 [GRCh38] Chr20:29842786..32060886 [GRCh37] Chr20:29306447..31524547 [NCBI36] Chr20:20q11.21	pathogenic
GRCh38/hg38 20p13-q13.33(chr20:99557-64277321)x3	copy number gain	See cases [RCV000135859]	Chr20:99557..64277321 [GRCh38] Chr20:80198..62908674 [GRCh37] Chr20:28198..62379118 [NCBI36] Chr20:20p13-q13.33	pathogenic
GRCh38/hg38 20q11.21-11.23(chr20:32062768-35906606)x3	copy number gain	See cases [RCV000141833]	Chr20:32062768..35906606 [GRCh38] Chr20:30650571..34494528 [GRCh37] Chr20:30114232..33957942 [NCBI36] Chr20:20q11.21-11.23	pathogenic
GRCh37/hg19 20p12.1-q11.21(chr20:17705775-31600738)x3	copy number gain	See cases [RCV000240436]	Chr20:17705775..31600738 [GRCh37] Chr20:20p12.1-q11.21	pathogenic
GRCh37/hg19 20p11.21-q11.21(chr20:24162775-31820857)x3	copy number gain	See cases [RCV000448977]	Chr20:24162775..31820857 [GRCh37] Chr20:20p11.21-q11.21	likely pathogenic
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)x3	copy number gain	See cases [RCV000510832]	Chr20:61569..62915555 [GRCh37] Chr20:20p13-q13.33	pathogenic
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)	copy number gain	See cases [RCV000512450]	Chr20:61569..62915555 [GRCh37] Chr20:20p13-q13.33	pathogenic
Single allele	duplication	not provided [RCV000677978]	Chr20:17705775..31600738 [GRCh37] Chr20:20p12.1-q11.21	pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62961294)x3	copy number gain	not provided [RCV000741059]	Chr20:63244..62961294 [GRCh37] Chr20:20p13-q13.33	pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62912463)x3	copy number gain	not provided [RCV000741057]	Chr20:63244..62912463 [GRCh37] Chr20:20p13-q13.33	pathogenic
GRCh37/hg19 20p13-q13.33(chr20:63244-62948788)x3	copy number gain	not provided [RCV000741058]	Chr20:63244..62948788 [GRCh37] Chr20:20p13-q13.33	pathogenic
GRCh37/hg19 20q11.21(chr20:31282278-31396065)x1	copy number loss	not provided [RCV001007090]	Chr20:31282278..31396065 [GRCh37] Chr20:20q11.21	uncertain significance
NM_053041.3(COMMD7):c.472T>G (p.Leu158Val)	single nucleotide variant	Inborn genetic diseases [RCV003269891]	Chr20:32704445 [GRCh38] Chr20:31292247 [GRCh37] Chr20:20q11.21	uncertain significance
GRCh37/hg19 20q11.21-11.23(chr20:29833608-35087952)x3	copy number gain	not provided [RCV000849735]	Chr20:29833608..35087952 [GRCh37] Chr20:20q11.21-11.23	pathogenic
NM_053041.3(COMMD7):c.196G>T (p.Gly66Cys)	single nucleotide variant	Inborn genetic diseases [RCV003290941]	Chr20:32727938 [GRCh38] Chr20:31315745 [GRCh37] Chr20:20q11.21	uncertain significance
NM_053041.3(COMMD7):c.526+3G>A	single nucleotide variant	not provided [RCV000958026]	Chr20:32704020 [GRCh38] Chr20:31291822 [GRCh37] Chr20:20q11.21	benign
NC_000020.10:g.(?_30795725)_(31395729_?)dup	duplication	Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency [RCV001300701]	Chr20:30795725..31395729 [GRCh37] Chr20:20q11.21	uncertain significance
GRCh37/hg19 20p11.21-q11.22(chr20:25442597-33761550)	copy number gain	not specified [RCV002052709]	Chr20:25442597..33761550 [GRCh37] Chr20:20p11.21-q11.22	pathogenic
GRCh37/hg19 20p11.21-q11.21(chr20:24162775-31820857)	copy number gain	not specified [RCV002052707]	Chr20:24162775..31820857 [GRCh37] Chr20:20p11.21-q11.21	likely pathogenic
GRCh37/hg19 20p11.23-q11.22(chr20:18665879-33903216)x3	copy number gain	not provided [RCV001829151]	Chr20:18665879..33903216 [GRCh37] Chr20:20p11.23-q11.22	likely pathogenic
NC_000020.10:g.(?_31189994)_(34287210_?)del	deletion	not provided [RCV001956104]	Chr20:31189994..34287210 [GRCh37] Chr20:20q11.21-11.22	pathogenic
NM_053041.3(COMMD7):c.128A>G (p.Glu43Gly)	single nucleotide variant	Inborn genetic diseases [RCV003300083]	Chr20:32728099 [GRCh38] Chr20:31315906 [GRCh37] Chr20:20q11.21	uncertain significance
GRCh37/hg19 20q11.21-11.23(chr20:29833535-34815537)x3	copy number gain	not provided [RCV002474532]	Chr20:29833535..34815537 [GRCh37] Chr20:20q11.21-11.23	likely pathogenic
GRCh37/hg19 20q11.21-11.23(chr20:29652122-35603726)x3	copy number gain	not provided [RCV002475651]	Chr20:29652122..35603726 [GRCh37] Chr20:20q11.21-11.23	likely pathogenic
NM_053041.3(COMMD7):c.500G>T (p.Gly167Val)	single nucleotide variant	Inborn genetic diseases [RCV003004875]	Chr20:32704049 [GRCh38] Chr20:31291851 [GRCh37] Chr20:20q11.21	uncertain significance
NM_053041.3(COMMD7):c.281C>T (p.Ala94Val)	single nucleotide variant	Inborn genetic diseases [RCV002982054]	Chr20:32706721 [GRCh38] Chr20:31294523 [GRCh37] Chr20:20q11.21	uncertain significance
NM_053041.3(COMMD7):c.511G>A (p.Glu171Lys)	single nucleotide variant	Inborn genetic diseases [RCV002645021]	Chr20:32704038 [GRCh38] Chr20:31291840 [GRCh37] Chr20:20q11.21	uncertain significance
NM_053041.3(COMMD7):c.319A>G (p.Thr107Ala)	single nucleotide variant	Inborn genetic diseases [RCV002835884]	Chr20:32706600 [GRCh38] Chr20:31294402 [GRCh37] Chr20:20q11.21	uncertain significance
NM_053041.3(COMMD7):c.538C>T (p.Pro180Ser)	single nucleotide variant	Inborn genetic diseases [RCV002960228]	Chr20:32703447 [GRCh38] Chr20:31291249 [GRCh37] Chr20:20q11.21	uncertain significance
NM_053041.3(COMMD7):c.121C>G (p.Leu41Val)	single nucleotide variant	Inborn genetic diseases [RCV002831842]	Chr20:32728106 [GRCh38] Chr20:31315913 [GRCh37] Chr20:20q11.21	uncertain significance
NM_053041.3(COMMD7):c.503A>G (p.Asn168Ser)	single nucleotide variant	Inborn genetic diseases [RCV003219341]	Chr20:32704046 [GRCh38] Chr20:31291848 [GRCh37] Chr20:20q11.21	uncertain significance
NM_053041.3(COMMD7):c.176C>T (p.Thr59Ile)	single nucleotide variant	Inborn genetic diseases [RCV003181360]	Chr20:32727958 [GRCh38] Chr20:31315765 [GRCh37] Chr20:20q11.21	uncertain significance
NM_053041.3(COMMD7):c.362C>T (p.Ala121Val)	single nucleotide variant	Inborn genetic diseases [RCV003383930]	Chr20:32704879 [GRCh38] Chr20:31292681 [GRCh37] Chr20:20q11.21	uncertain significance
GRCh37/hg19 20q11.21(chr20:29917837-31886619)x3	copy number gain	not specified [RCV003986134]	Chr20:29917837..31886619 [GRCh37] Chr20:20q11.21	uncertain significance
NC_000020.10:g.(?_30795725)_(31395729_?)dup	duplication	Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency [RCV001032627]	Chr20:30795725..31395729 [GRCh37] Chr20:20q11.21	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1241
Count of miRNA genes:	529
Interacting mature miRNAs:	574
Transcripts:	ENST00000278980, ENST00000446419, ENST00000474815, ENST00000610160
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

RH25024

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	31,290,613 - 31,290,769	UniSTS	GRCh37
Build 36	20	30,754,274 - 30,754,430	RGD	NCBI36
Celera	20	28,046,075 - 28,046,231	RGD
Cytogenetic Map	20	q11.21	UniSTS
HuRef	20	28,079,203 - 28,079,359	UniSTS

D20S1117

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	31,290,593 - 31,290,736	UniSTS	GRCh37
Build 36	20	30,754,254 - 30,754,397	RGD	NCBI36
Celera	20	28,046,055 - 28,046,198	RGD
Cytogenetic Map	20	q11.21	UniSTS
HuRef	20	28,079,183 - 28,079,326	UniSTS
Stanford-G3 RH Map	20	1668.0	UniSTS
GeneMap99-GB4 RH Map	20	191.45	UniSTS
NCBI RH Map	20	286.4	UniSTS
GeneMap99-G3 RH Map	20	1701.0	UniSTS

WI-20368

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	20	31,290,544 - 31,290,833	UniSTS	GRCh37
Build 36	20	30,754,205 - 30,754,494	RGD	NCBI36
Celera	20	28,046,006 - 28,046,295	RGD
Cytogenetic Map	20	q11.21	UniSTS
HuRef	20	28,079,134 - 28,079,423	UniSTS
GeneMap99-GB4 RH Map	20	191.21	UniSTS
Whitehead-RH Map	20	196.6	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

2428

2770

1713

612

1798

454

4352

2128

3621

417

1441

1608

171

1204

2785

Low

220

153

113

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001099339	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_053041	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005260299	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005260300	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011528604	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017027685	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017027686	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017027687	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439932	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323080	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323081	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323082	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323083	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323084	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054323085	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AJ012490	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK027893	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK096307	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK097059	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL035071	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY542162	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC000628	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC022073	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC047440	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BG715846	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BQ006261	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX640505	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471077	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068258	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DN993528	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	FQ976907	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000278980 ⟹ ENSP00000278980

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	32,702,699 - 32,743,467 (-)	Ensembl

RefSeq Acc Id:

ENST00000446419 ⟹ ENSP00000395339

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	32,702,703 - 32,743,455 (-)	Ensembl

RefSeq Acc Id:

ENST00000474815 ⟹ ENSP00000476443

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	32,704,474 - 32,743,406 (-)	Ensembl

RefSeq Acc Id:

ENST00000610160 ⟹ ENSP00000476617

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	32,702,703 - 32,743,445 (-)	Ensembl

RefSeq Acc Id:

ENST00000642484 ⟹ ENSP00000496538

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	32,632,183 - 32,743,523 (-)	Ensembl

RefSeq Acc Id:

ENST00000642630 ⟹ ENSP00000494986

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	32,632,183 - 32,743,523 (-)	Ensembl

RefSeq Acc Id:

ENST00000645058 ⟹ ENSP00000494955

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	32,632,183 - 32,743,567 (-)	Ensembl

RefSeq Acc Id:

ENST00000646357 ⟹ ENSP00000493768

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	20	32,632,183 - 32,743,523 (-)	Ensembl

RefSeq Acc Id:

NM_001099339 ⟹ NP_001092809

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	32,702,699 - 32,743,467 (-)	NCBI
GRCh37	20	31,290,493 - 31,331,814 (-)	RGD
Build 36	20	30,754,154 - 30,795,475 (-)	NCBI Archive
Celera	20	28,045,955 - 28,085,739 (-)	RGD
HuRef	20	28,079,083 - 28,118,793 (-)	ENTREZGENE
CHM1_1	20	31,195,366 - 31,235,269 (-)	NCBI
T2T-CHM13v2.0	20	34,431,363 - 34,470,209 (-)	NCBI

Sequence:

show sequence

GGTGGCAGCGGCAGCGGAGGAGGAAGCTGAGCAGGGCGGCGGCGGCGGTGGAACCTGCGGGGCT
GGGGCGCGCGCCATGGGCCGCCTGCACTGCACTGAGGACCCGGTGCCGGAGGCCGTGGGCGGCG
ACATGCAGCAGCTGAACCAGCTGGGCGCGCAGTTCTCAGCCCTGACAGAGGTGCTTTTCCACTT
CCTAACTGAGCCAAAAGAGGTGGAAAGATTTCTGGCTCAGCTCTCTGAATTTGCCACCACCAAT
CAGATCAGTCTTGGCTCCCTCAGAAGCATCGTGAAAAGCCTCCTTCTGGTTCCAAATGGTGCTT
TGAAGAAGAGTCTCACAGCCAAGCAGGTCCAGGCGGATTTCATAACTCTGGGTCTTAGTGAGGA
GAAAGCCACTTACTTTTCTGAAAAGTGGAAGCAGAATGCTCCCACCCTTGCTCGATGGGCCATA
GGTCAGACTCTGATGATTAACCAGCTCATAGATATGGAGTGGAAATTTGGAGTGACATCTGGGA
GCAGCGAATTGGAGAAAGTGGGAAGTATATTTTTACAACTAAAGTTGGTGGTTAAGAAAGGAAA
TCAAACCGAAAATGTGTATATAGAATTAACCTTGCCTCAGTTCTACAGCTTCCTGCACGAGATG
GAGCGAGTCAGAACCAGCATGGAGTGTTTCTGCTGATTTCTGTCCCTGCATCTCCCCTGGCCCC
GTTCCCTGCCCTCCTCCCTTCCCTGGGTGACTGCTCTGAGAGGCACTTCACTCACAGGCCTGTG
GGATGCTCCATGGGGCCCTGCTGGCTCCATGGGGCCCAGGTGCAAAGGGTTTCTGAAAAACAGC
AGGATTAAGTACTGAAAGAGCCCAACACAATTACCCTGTAAACTCTCTGTTAGGGCAACCACCA
CCACCTGTCTTCCAGGACACATTTTTAGATACTCTGACAGGCCACTGCATCTCAGATTCAGGGG
AGAAAATAAGTTGTCACCTCCCCTTCAAAGTTCCAGAGTAAACAAATGGTGCCATCATTCAAGA
TAACATGCTGATCACCCTCCTCCCAAAAAGCAAGAGCTTGTTTATGGCTGAGGAATCGGCGGAT
TGTCTGAATGACACATATACAGAGCCCCCACGGATTTCTGCACACTCTGGGTCTGTGCTGGTGG
AACATTGCCAATCAGTTCTTAATGAGGCACCTGTGTGTAAATACATGCTTGGTCTTCTCTGCAG
AGAACTGAGGCTAAACTCTGTCCCTACTTCTGGTTTTGCCCTGTCATGTCGTAACGAGGTGGGC
CTTTTGAGGCCATTTTAGTTTGAGTTCGAGCCAACCACCTCTGTTGGTTAGATGATGAATAAAA
AGGTTCTGAAGAAAA

hide sequence

RefSeq Acc Id:

NM_053041 ⟹ NP_444269

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	32,702,699 - 32,743,467 (-)	NCBI
GRCh37	20	31,290,493 - 31,331,814 (-)	RGD
Build 36	20	30,754,154 - 30,795,475 (-)	NCBI Archive
Celera	20	28,045,955 - 28,085,739 (-)	RGD
HuRef	20	28,079,083 - 28,118,793 (-)	ENTREZGENE
CHM1_1	20	31,195,366 - 31,235,269 (-)	NCBI
T2T-CHM13v2.0	20	34,431,363 - 34,470,209 (-)	NCBI

Sequence:

show sequence

GGTGGCAGCGGCAGCGGAGGAGGAAGCTGAGCAGGGCGGCGGCGGCGGTGGAACCTGCGGGGCT
GGGGCGCGCGCCATGGGCCGCCTGCACTGCACTGAGGACCCGGTGCCGGAGGCCGTGGGCGGCG
ACATGCAGCAGCTGAACCAGCTGGGCGCGCAGCAGTTCTCAGCCCTGACAGAGGTGCTTTTCCA
CTTCCTAACTGAGCCAAAAGAGGTGGAAAGATTTCTGGCTCAGCTCTCTGAATTTGCCACCACC
AATCAGATCAGTCTTGGCTCCCTCAGAAGCATCGTGAAAAGCCTCCTTCTGGTTCCAAATGGTG
CTTTGAAGAAGAGTCTCACAGCCAAGCAGGTCCAGGCGGATTTCATAACTCTGGGTCTTAGTGA
GGAGAAAGCCACTTACTTTTCTGAAAAGTGGAAGCAGAATGCTCCCACCCTTGCTCGATGGGCC
ATAGGTCAGACTCTGATGATTAACCAGCTCATAGATATGGAGTGGAAATTTGGAGTGACATCTG
GGAGCAGCGAATTGGAGAAAGTGGGAAGTATATTTTTACAACTAAAGTTGGTGGTTAAGAAAGG
AAATCAAACCGAAAATGTGTATATAGAATTAACCTTGCCTCAGTTCTACAGCTTCCTGCACGAG
ATGGAGCGAGTCAGAACCAGCATGGAGTGTTTCTGCTGATTTCTGTCCCTGCATCTCCCCTGGC
CCCGTTCCCTGCCCTCCTCCCTTCCCTGGGTGACTGCTCTGAGAGGCACTTCACTCACAGGCCT
GTGGGATGCTCCATGGGGCCCTGCTGGCTCCATGGGGCCCAGGTGCAAAGGGTTTCTGAAAAAC
AGCAGGATTAAGTACTGAAAGAGCCCAACACAATTACCCTGTAAACTCTCTGTTAGGGCAACCA
CCACCACCTGTCTTCCAGGACACATTTTTAGATACTCTGACAGGCCACTGCATCTCAGATTCAG
GGGAGAAAATAAGTTGTCACCTCCCCTTCAAAGTTCCAGAGTAAACAAATGGTGCCATCATTCA
AGATAACATGCTGATCACCCTCCTCCCAAAAAGCAAGAGCTTGTTTATGGCTGAGGAATCGGCG
GATTGTCTGAATGACACATATACAGAGCCCCCACGGATTTCTGCACACTCTGGGTCTGTGCTGG
TGGAACATTGCCAATCAGTTCTTAATGAGGCACCTGTGTGTAAATACATGCTTGGTCTTCTCTG
CAGAGAACTGAGGCTAAACTCTGTCCCTACTTCTGGTTTTGCCCTGTCATGTCGTAACGAGGTG
GGCCTTTTGAGGCCATTTTAGTTTGAGTTCGAGCCAACCACCTCTGTTGGTTAGATGATGAATA
AAAAGGTTCTGAAGAAAA

hide sequence

RefSeq Acc Id:

XM_005260299 ⟹ XP_005260356

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	32,703,465 - 32,743,467 (-)	NCBI
GRCh37	20	31,290,493 - 31,331,814 (-)	NCBI

Sequence:

show sequence

GCAGCGGTGGCAGCGGCAGCGGAGGAGGAAGCTGAGCAGGGCGGCGGCGGCGGTGGAACCTGCG
GGGCTGGGGCGCGCGCCATGGGCCGCCTGCACTGCACTGAGGACCCGGTGCCGGAGGCCGTGGG
CGGCGACATGCAGCAGCTGAACCAGCTGGGCGCGCAGCAGTTCTCAGCCCTGACAGAGGTGCTT
TTCCACTTCCTAACTGAGCCAAAAGAGGTGGAAAGATTTCTGGCTCAGCTCTCTGAATTTGCCA
CCACCAATCAGATCAGTCTTGGCTCCCTCAGAAGCATCGTGAAAAGCCTCCTTCTGGTTCCAAA
TGGTGCTTTGAAGAAGAGTCTCACAGCCAAGCAGGTCCAGGCGGATTTCATAACTCTGGGTCTT
AGTGAGGAGAAAGCCACTTACTTTTCTGAAAAGTGGAAGCAGAATGCTCCCACCCTTGCTCGAT
GGGCCATAGGTCAGACTCTGATGATTAACCAGCTCATAGATATGGAGTGGAAATTTGGAGTGAC
ATCTGGGAGCAGCGAATTGGAGAAAGTGGGAAGTATATTTTTACAACTAAAGTTGGTGGTTAAG
AAAGGAAATCAAACCGAAAATGTGTATATAGGTGAGTCTGAATTCCCACTTGAGCCTCTTCACC
TTTTTTGTGTTCTCTGCAATCAGGGGCTGGTGACGCTCACCACAAATCATGTCTTCTATAAAAA
CAGTCATTGCCAGCTGTGGAGTAGCTGTTCCACTGCCTTTCCTCTCCTGAAAGATGGCACAAGG
AGTGTTAGAAAGCCACTGGCAGGTTGGAGCCCCCACAGTTGAAGAGCCGTTTTGAAAAAGGGAA
AGGGTGGGAACGGAATGGCTGGGATTGAAGAAGAAGGTTGACGAGCAAGAAGCTCTTGCCATAG
AAGTCACATTGAACATCCCGAATGATACCCTTTCATCTCTTTGTGCCATGGAGCTGTGCCATTT
GAACACTCACTCCCCTTTTTTTTCCTTTGGAGCAGAGAACCTTCTGCATTCAAGTCTCTCAGTT
CTTTATTATGATCAGTTACCCATCAAGAGCTGCTTAGATGTATTAAGCCAAAAAA

hide sequence

RefSeq Acc Id:

XM_005260300 ⟹ XP_005260357

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	32,703,465 - 32,743,467 (-)	NCBI
GRCh37	20	31,290,493 - 31,331,814 (-)	NCBI

Sequence:

show sequence

AGCGGAGGAGGAAGCTGAGCAGGGCGGCGGCGGCGGTGGAACCTGCGGGGCTGGGGCGCGCGCC
ATGGGCCGCCTGCACTGCACTGAGGACCCGGTGCCGGAGGCCGTGGGCGGCGACATGCAGCAGC
TGAACCAGCTGGGCGCGCAGTTCTCAGCCCTGACAGAGGTGCTTTTCCACTTCCTAACTGAGCC
AAAAGAGGTGGAAAGATTTCTGGCTCAGCTCTCTGAATTTGCCACCACCAATCAGATCAGTCTT
GGCTCCCTCAGAAGCATCGTGAAAAGCCTCCTTCTGGTTCCAAATGGTGCTTTGAAGAAGAGTC
TCACAGCCAAGCAGGTCCAGGCGGATTTCATAACTCTGGGTCTTAGTGAGGAGAAAGCCACTTA
CTTTTCTGAAAAGTGGAAGCAGAATGCTCCCACCCTTGCTCGATGGGCCATAGGTCAGACTCTG
ATGATTAACCAGCTCATAGATATGGAGTGGAAATTTGGAGTGACATCTGGGAGCAGCGAATTGG
AGAAAGTGGGAAGTATATTTTTACAACTAAAGTTGGTGGTTAAGAAAGGAAATCAAACCGAAAA
TGTGTATATAGGTGAGTCTGAATTCCCACTTGAGCCTCTTCACCTTTTTTGTGTTCTCTGCAAT
CAGGGGCTGGTGACGCTCACCACAAATCATGTCTTCTATAAAAACAGTCATTGCCAGCTGTGGA
GTAGCTGTTCCACTGCCTTTCCTCTCCTGAAAGATGGCACAAGGAGTGTTAGAAAGCCACTGGC
AGGTTGGAGCCCCCACAGTTGAAGAGCCGTTTTGAAAAAGGGAAAGGGTGGGAACGGAATGGCT
GGGATTGAAGAAGAAGGTTGACGAGCAAGAAGCTCTTGCCATAGAAGTCACATTGAACATCCCG
AATGATACCCTTTCATCTCTTTGTGCCATGGAGCTGTGCCATTTGAACACTCACTCCCCTTTTT
TTTCCTTTGGAGCAGAGAACCTTCTGCATTCAAGTCTCTCAGTTCTTTATTATGATCAGTTACC
CATCAAGAGCTGCTTAGATGTATTAAGCCAAAAAA

hide sequence

RefSeq Acc Id:

XM_011528604 ⟹ XP_011526906

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	32,702,699 - 32,743,467 (-)	NCBI

Sequence:

show sequence

GCAGCGGTGGCAGCGGCAGCGGAGGAGGAAGCTGAGCAGGGCGGCGGCGGCGGTGGAACCTGCG
GGGCTGGGGCGCGCGCCATGGGCCGCCTGCACTGCACTGAGGACCCGGTGCCGGAGGCCGTGGG
CGGCGACATGCAGCAGCTGAACCAGCTGGGCGCGCAGCAGTTCTCAGCCCTGACAGAGGTGCTT
TTCCACTTCCTAACTGAGCCAAAAGAGGTGGAAAGATTTCTGGCTCAGCTCTCTGAATTTGCCA
CCACCAATCAGATCAGTCTTGGCTCCCTCAGAAGCATCGTGAAAAGCCTCCTTCTGGTTCCAAA
TGGTGCTTTGAAGAAGAGTCTCACAGCCAAGCAGGTCCAGGCGGATTTCATAACTCTGGGTCTT
AGTGAGGAGAAAGCCACTTACTTTTCTGAAAAGTGGAAGCAGAATGCTCCCACCCTTGCTCGAT
GGGCCATAGGTCAGACTCTGATGATTAACCAGCTCATAGATATGGAGTGGAAATTTGGAGTGAC
ATCTGGGAGCAGCGAATTGGAGAAAGTGGGAAGTATATTTTTACAACTAAAGTTGGTGGTTAAG
AAAGGAAATCAAACCGAAAATGTGTATATAGTCATTGCCAGCTGTGGAGTAGCTGTTCCACTGC
CTTTCCTCTCCTGAAAGATGGCACAAGGAGTGTTAGAAAGCCACTGGCAGGTTGGAGCCCCCAC
AGTTGAAGAGCCGTTTTGAAAAAGGGAAAGGGTGGGAACGGAATGGCTGGGATTGAAGAAGAAG
GTTGACGAGCAAGAAGCTCTTGCCATAGAAGTCACATTGAACATCCCGAATGATACCCTTTCAT
CTCTTTGTGCCATGGAGCTGTGCCATTTGAACACTCACTCCCCTTTTTTTTCCTTTGGAGCAGA
GAACCTTCTGCATTCAAGTCTCTCAGTTCTTTATTATGATCAGTTACCCATCAAGAGCTGCTTA
GATGTATTAAGCCAAAAAAGAAAAAAAAAATCCTCCGGGTGGAAATTAATTTTCTTGGATGATT
CTGTGGAGTTGGAAACATTTATCTGAAGCTGAATTTTCTCTCCCCAGAATTAACCTTGCCTCAG
TTCTACAGCTTCCTGCACGAGATGGAGCGAGTCAGAACCAGCATGGAGTGTTTCTGCTGATTTC
TGTCCCTGCATCTCCCCTGGCCCCGTTCCCTGCCCTCCTCCCTTCCCTGGGTGACTGCTCTGAG
AGGCACTTCACTCACAGGCCTGTGGGATGCTCCATGGGGCCCTGCTGGCTCCATGGGGCCCAGG
TGCAAAGGGTTTCTGAAAAACAGCAGGATTAAGTACTGAAAGAGCCCAACACAATTACCCTGTA
AACTCTCTGTTAGGGCAACCACCACCACCTGTCTTCCAGGACACATTTTTAGATACTCTGACAG
GCCACTGCATCTCAGATTCAGGGGAGAAAATAAGTTGTCACCTCCCCTTCAAAGTTCCAGAGTA
AACAAATGGTGCCATCATTCAAGATAACATGCTGATCACCCTCCTCCCAAAAAGCAAGAGCTTG
TTTATGGCTGAGGAATCGGCGGATTGTCTGAATGACACATATACAGAGCCCCCACGGATTTCTG
CACACTCTGGGTCTGTGCTGGTGGAACATTGCCAATCAGTTCTTAATGAGGCACCTGTGTGTAA
ATACATGCTTGGTCTTCTCTGCAGAGAACTGAGGCTAAACTCTGTCCCTACTTCTGGTTTTGCC
CTGTCATGTCGTAACGAGGTGGGCCTTTTGAGGCCATTTTAGTTTGAGTTCGAGCCAACCACCT
CTGTTGGTTAGATGATGAATAAAAAGGTTCTGAAGAAAAGGTCTGGA

hide sequence

RefSeq Acc Id:

XM_017027685 ⟹ XP_016883174

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	32,702,699 - 32,743,467 (-)	NCBI

Sequence:

show sequence

AGCGGAGGAGGAAGCTGAGCAGGGCGGCGGCGGCGGTGGAACCTGCGGGGCTGGGGCGCGCGCC
ATGGGCCGCCTGCACTGCACTGAGGACCCGGTGCCGGAGGCCGTGGGCGGCGACATGCAGCAGC
TGAACCAGCTGGGCGCGCAGTTCTCAGCCCTGACAGAGGTGCTTTTCCACTTCCTAACTGAGCC
AAAAGAGGTGGAAAGATTTCTGGCTCAGCTCTCTGAATTTGCCACCACCAATCAGATCAGTCTT
GGCTCCCTCAGAAGCATCGTGAAAAGCCTCCTTCTGGTTCCAAATGGTGCTTTGAAGAAGAGTC
TCACAGCCAAGCAGGTCCAGGCGGATTTCATAACTCTGGGTCTTAGTGAGGAGAAAGCCACTTA
CTTTTCTGAAAAGTGGAAGCAGAATGCTCCCACCCTTGCTCGATGGGCCATAGGTCAGACTCTG
ATGATTAACCAGCTCATAGATATGGAGTGGAAATTTGGAGTGACATCTGGGAGCAGCGAATTGG
AGAAAGTGGGAAGTATATTTTTACAACTAAAGTTGGTGGTTAAGAAAGGAAATCAAACCGAAAA
TGTGTATATAGTCATTGCCAGCTGTGGAGTAGCTGTTCCACTGCCTTTCCTCTCCTGAAAGATG
GCACAAGGAGTGTTAGAAAGCCACTGGCAGGTTGGAGCCCCCACAGTTGAAGAGCCGTTTTGAA
AAAGGGAAAGGGTGGGAACGGAATGGCTGGGATTGAAGAAGAAGGTTGACGAGCAAGAAGCTCT
TGCCATAGAAGTCACATTGAACATCCCGAATGATACCCTTTCATCTCTTTGTGCCATGGAGCTG
TGCCATTTGAACACTCACTCCCCTTTTTTTTCCTTTGGAGCAGAGAACCTTCTGCATTCAAGTC
TCTCAGTTCTTTATTATGATCAGTTACCCATCAAGAGCTGCTTAGATGTATTAAGCCAAAAAAG
AAAAAAAAAATCCTCCGGGTGGAAATTAATTTTCTTGGATGATTCTGTGGAGTTGGAAACATTT
ATCTGAAGCTGAATTTTCTCTCCCCAGAATTAACCTTGCCTCAGTTCTACAGCTTCCTGCACGA
GATGGAGCGAGTCAGAACCAGCATGGAGTGTTTCTGCTGATTTCTGTCCCTGCATCTCCCCTGG
CCCCGTTCCCTGCCCTCCTCCCTTCCCTGGGTGACTGCTCTGAGAGGCACTTCACTCACAGGCC
TGTGGGATGCTCCATGGGGCCCTGCTGGCTCCATGGGGCCCAGGTGCAAAGGGTTTCTGAAAAA
CAGCAGGATTAAGTACTGAAAGAGCCCAACACAATTACCCTGTAAACTCTCTGTTAGGGCAACC
ACCACCACCTGTCTTCCAGGACACATTTTTAGATACTCTGACAGGCCACTGCATCTCAGATTCA
GGGGAGAAAATAAGTTGTCACCTCCCCTTCAAAGTTCCAGAGTAAACAAATGGTGCCATCATTC
AAGATAACATGCTGATCACCCTCCTCCCAAAAAGCAAGAGCTTGTTTATGGCTGAGGAATCGGC
GGATTGTCTGAATGACACATATACAGAGCCCCCACGGATTTCTGCACACTCTGGGTCTGTGCTG
GTGGAACATTGCCAATCAGTTCTTAATGAGGCACCTGTGTGTAAATACATGCTTGGTCTTCTCT
GCAGAGAACTGAGGCTAAACTCTGTCCCTACTTCTGGTTTTGCCCTGTCATGTCGTAACGAGGT
GGGCCTTTTGAGGCCATTTTAGTTTGAGTTCGAGCCAACCACCTCTGTTGGTTAGATGATGAAT
AAAAAGGTTCTGAAGAAAAGGTCTGGA

hide sequence

RefSeq Acc Id:

XM_017027686 ⟹ XP_016883175

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	32,702,699 - 32,743,467 (-)	NCBI

Sequence:

show sequence

AGCGGAGGAGGAAGCTGAGCAGGGCGGCGGCGGCGGTGGAACCTGCGGGGCTGGGGCGCGCGCC
ATGGGCCGCCTGCACTGCACTGAGGACCCGGTGCCGGAGGCCGTGGGCGGCGACATGCAGCAGC
TGAACCAGCTGGGCGCGCAGCAGTTCTCAGCCCTGACAGAGGTGCTTTTCCACTTCCTAACTGA
GCCAAAAGAGGTGGAAAGATTTCTGGCTCAGCTCTCTGAATTTGCCACCACCAATCAGATCAGT
CTTGGCTCCCTCAGAAGCATCGTGAAAAGCCTCCTTCTGGTTCCAAATGGTGCTTTGAAGAAGA
GTCTCACAGCCAAGCAGGTCCAGGCGGATTTCATAACTCTGGGTCTTAGTGAGGAGAAAGCCAC
TTACTTTTCTGAAAAGCTAAAGTTGGTGGTTAAGAAAGGAAATCAAACCGAAAATGTGTATATA
GAATTAACCTTGCCTCAGTTCTACAGCTTCCTGCACGAGATGGAGCGAGTCAGAACCAGCATGG
AGTGTTTCTGCTGATTTCTGTCCCTGCATCTCCCCTGGCCCCGTTCCCTGCCCTCCTCCCTTCC
CTGGGTGACTGCTCTGAGAGGCACTTCACTCACAGGCCTGTGGGATGCTCCATGGGGCCCTGCT
GGCTCCATGGGGCCCAGGTGCAAAGGGTTTCTGAAAAACAGCAGGATTAAGTACTGAAAGAGCC
CAACACAATTACCCTGTAAACTCTCTGTTAGGGCAACCACCACCACCTGTCTTCCAGGACACAT
TTTTAGATACTCTGACAGGCCACTGCATCTCAGATTCAGGGGAGAAAATAAGTTGTCACCTCCC
CTTCAAAGTTCCAGAGTAAACAAATGGTGCCATCATTCAAGATAACATGCTGATCACCCTCCTC
CCAAAAAGCAAGAGCTTGTTTATGGCTGAGGAATCGGCGGATTGTCTGAATGACACATATACAG
AGCCCCCACGGATTTCTGCACACTCTGGGTCTGTGCTGGTGGAACATTGCCAATCAGTTCTTAA
TGAGGCACCTGTGTGTAAATACATGCTTGGTCTTCTCTGCAGAGAACTGAGGCTAAACTCTGTC
CCTACTTCTGGTTTTGCCCTGTCATGTCGTAACGAGGTGGGCCTTTTGAGGCCATTTTAGTTTG
AGTTCGAGCCAACCACCTCTGTTGGTTAGATGATGAATAAAAAGGTTCTGAAGAAAA

hide sequence

RefSeq Acc Id:

XM_047439932 ⟹ XP_047295888

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	32,702,699 - 32,743,467 (-)	NCBI

RefSeq Acc Id:

XM_054323080 ⟹ XP_054179055

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	34,432,129 - 34,470,209 (-)	NCBI

RefSeq Acc Id:

XM_054323081 ⟹ XP_054179056

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	34,432,129 - 34,470,209 (-)	NCBI

RefSeq Acc Id:

XM_054323082 ⟹ XP_054179057

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	34,431,363 - 34,470,209 (-)	NCBI

RefSeq Acc Id:

XM_054323083 ⟹ XP_054179058

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	34,431,363 - 34,470,209 (-)	NCBI

RefSeq Acc Id:

XM_054323084 ⟹ XP_054179059

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	34,431,363 - 34,470,209 (-)	NCBI

RefSeq Acc Id:

XM_054323085 ⟹ XP_054179060

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	20	34,431,363 - 34,470,209 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_001092809	(Get FASTA)	NCBI Sequence Viewer
	NP_444269	(Get FASTA)	NCBI Sequence Viewer
	XP_005260356	(Get FASTA)	NCBI Sequence Viewer
	XP_005260357	(Get FASTA)	NCBI Sequence Viewer
	XP_011526906	(Get FASTA)	NCBI Sequence Viewer
	XP_016883174	(Get FASTA)	NCBI Sequence Viewer
	XP_016883175	(Get FASTA)	NCBI Sequence Viewer
	XP_047295888	(Get FASTA)	NCBI Sequence Viewer
	XP_054179055	(Get FASTA)	NCBI Sequence Viewer
	XP_054179056	(Get FASTA)	NCBI Sequence Viewer
	XP_054179057	(Get FASTA)	NCBI Sequence Viewer
	XP_054179058	(Get FASTA)	NCBI Sequence Viewer
	XP_054179059	(Get FASTA)	NCBI Sequence Viewer
	XP_054179060	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH00628	(Get FASTA)	NCBI Sequence Viewer
	AAH47440	(Get FASTA)	NCBI Sequence Viewer
	AAS22244	(Get FASTA)	NCBI Sequence Viewer
	BAB55436	(Get FASTA)	NCBI Sequence Viewer
	BAG53254	(Get FASTA)	NCBI Sequence Viewer
	EAW76357	(Get FASTA)	NCBI Sequence Viewer
	EAW76358	(Get FASTA)	NCBI Sequence Viewer
	EAW76359	(Get FASTA)	NCBI Sequence Viewer
	EAW76360	(Get FASTA)	NCBI Sequence Viewer
	EAW76361	(Get FASTA)	NCBI Sequence Viewer
	EAW76362	(Get FASTA)	NCBI Sequence Viewer
	EAW76363	(Get FASTA)	NCBI Sequence Viewer
	EAW76364	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000278980
	ENSP00000278980.6
	ENSP00000395339
	ENSP00000395339.1
	ENSP00000476443.1
	ENSP00000476617.1
	ENSP00000493768.1
	ENSP00000494955.1
	ENSP00000494986.1
	ENSP00000496538.1
GenBank Protein	Q86VX2	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_444269 ⟸ NM_053041
- Peptide Label:	isoform 1
- UniProtKB:	Q96SI7 (UniProtKB/Swiss-Prot), Q5JYB0 (UniProtKB/Swiss-Prot), B3KTZ2 (UniProtKB/Swiss-Prot), A2BHJ2 (UniProtKB/Swiss-Prot), Q9BW53 (UniProtKB/Swiss-Prot), Q86VX2 (UniProtKB/Swiss-Prot), A0A2R8Y620 (UniProtKB/TrEMBL)
- Sequence:	show sequence MGRLHCTEDPVPEAVGGDMQQLNQLGAQQFSALTEVLFHFLTEPKEVERFLAQLSEFATTNQIS LGSLRSIVKSLLLVPNGALKKSLTAKQVQADFITLGLSEEKATYFSEKWKQNAPTLARWAIGQT LMINQLIDMEWKFGVTSGSSELEKVGSIFLQLKLVVKKGNQTENVYIELTLPQFYSFLHEMERV RTSMECFC hide sequence

RefSeq Acc Id:	NP_001092809 ⟸ NM_001099339
- Peptide Label:	isoform 2
- UniProtKB:	A0A2R8Y620 (UniProtKB/TrEMBL)
- Sequence:	show sequence MGRLHCTEDPVPEAVGGDMQQLNQLGAQFSALTEVLFHFLTEPKEVERFLAQLSEFATTNQISL GSLRSIVKSLLLVPNGALKKSLTAKQVQADFITLGLSEEKATYFSEKWKQNAPTLARWAIGQTL MINQLIDMEWKFGVTSGSSELEKVGSIFLQLKLVVKKGNQTENVYIELTLPQFYSFLHEMERVR TSMECFC hide sequence

RefSeq Acc Id:

XP_005260357 ⟸ XM_005260300

- Peptide Label:

isoform X2

- Sequence:

show sequence

MGRLHCTEDPVPEAVGGDMQQLNQLGAQFSALTEVLFHFLTEPKEVERFLAQLSEFATTNQISL
GSLRSIVKSLLLVPNGALKKSLTAKQVQADFITLGLSEEKATYFSEKWKQNAPTLARWAIGQTL
MINQLIDMEWKFGVTSGSSELEKVGSIFLQLKLVVKKGNQTENVYIGESEFPLEPLHLFCVLCN
QGLVTLTTNHVFYKNSHCQLWSSCSTAFPLLKDGTRSVRKPLAGWSPHS

hide sequence

RefSeq Acc Id:

XP_005260356 ⟸ XM_005260299

- Peptide Label:

isoform X1

- Sequence:

show sequence

MGRLHCTEDPVPEAVGGDMQQLNQLGAQQFSALTEVLFHFLTEPKEVERFLAQLSEFATTNQIS
LGSLRSIVKSLLLVPNGALKKSLTAKQVQADFITLGLSEEKATYFSEKWKQNAPTLARWAIGQT
LMINQLIDMEWKFGVTSGSSELEKVGSIFLQLKLVVKKGNQTENVYIGESEFPLEPLHLFCVLC
NQGLVTLTTNHVFYKNSHCQLWSSCSTAFPLLKDGTRSVRKPLAGWSPHS

hide sequence

RefSeq Acc Id:	XP_011526906 ⟸ XM_011528604
- Peptide Label:	isoform X3
- UniProtKB:	A0A2R8Y620 (UniProtKB/TrEMBL)
- Sequence:	show sequence MGRLHCTEDPVPEAVGGDMQQLNQLGAQQFSALTEVLFHFLTEPKEVERFLAQLSEFATTNQIS LGSLRSIVKSLLLVPNGALKKSLTAKQVQADFITLGLSEEKATYFSEKWKQNAPTLARWAIGQT LMINQLIDMEWKFGVTSGSSELEKVGSIFLQLKLVVKKGNQTENVYIVIASCGVAVPLPFLS hide sequence

RefSeq Acc Id:	XP_016883174 ⟸ XM_017027685
- Peptide Label:	isoform X4
- UniProtKB:	A0A2R8Y620 (UniProtKB/TrEMBL)
- Sequence:	show sequence MGRLHCTEDPVPEAVGGDMQQLNQLGAQFSALTEVLFHFLTEPKEVERFLAQLSEFATTNQISL GSLRSIVKSLLLVPNGALKKSLTAKQVQADFITLGLSEEKATYFSEKWKQNAPTLARWAIGQTL MINQLIDMEWKFGVTSGSSELEKVGSIFLQLKLVVKKGNQTENVYIVIASCGVAVPLPFLS hide sequence

RefSeq Acc Id:	XP_016883175 ⟸ XM_017027686
- Peptide Label:	isoform X5
- Sequence:	show sequence MGRLHCTEDPVPEAVGGDMQQLNQLGAQQFSALTEVLFHFLTEPKEVERFLAQLSEFATTNQIS LGSLRSIVKSLLLVPNGALKKSLTAKQVQADFITLGLSEEKATYFSEKLKLVVKKGNQTENVYI ELTLPQFYSFLHEMERVRTSMECFC hide sequence

RefSeq Acc Id:

ENSP00000476617 ⟸ ENST00000610160

RefSeq Acc Id:

ENSP00000496538 ⟸ ENST00000642484

RefSeq Acc Id:

ENSP00000494986 ⟸ ENST00000642630

RefSeq Acc Id:

ENSP00000395339 ⟸ ENST00000446419

RefSeq Acc Id:

ENSP00000494955 ⟸ ENST00000645058

RefSeq Acc Id:

ENSP00000278980 ⟸ ENST00000278980

RefSeq Acc Id:

ENSP00000476443 ⟸ ENST00000474815

RefSeq Acc Id:

ENSP00000493768 ⟸ ENST00000646357

RefSeq Acc Id:	XP_047295888 ⟸ XM_047439932
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054179060 ⟸ XM_054323085
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054179058 ⟸ XM_054323083
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054179059 ⟸ XM_054323084
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054179057 ⟸ XM_054323082
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054179056 ⟸ XM_054323081
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054179055 ⟸ XM_054323080
- Peptide Label:	isoform X1

Protein Domains

COMM

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q86VX2-F1-model_v2	AlphaFold	Q86VX2	1-200	view protein structure

Promoters

RGD ID:

6798607

Promoter ID:

HG_KWN:39041

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

NM_001099339, NM_053041, UC002WYB.2

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	20	30,794,871 - 30,795,392 (-)	MPROMDB

RGD ID:

13206663

Promoter ID:

EPDNEW_H26912

Type:

initiation region

Name:

COMMD7_3

Description:

COMM domain containing 7

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H26914 EPDNEW_H26913

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	32,706,727 - 32,706,787	EPDNEW

RGD ID:

13206667

Promoter ID:

EPDNEW_H26913

Type:

initiation region

Name:

COMMD7_1

Description:

COMM domain containing 7

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H26912 EPDNEW_H26914

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	32,743,455 - 32,743,515	EPDNEW

RGD ID:

13206665

Promoter ID:

EPDNEW_H26914

Type:

initiation region

Name:

COMMD7_2

Description:

COMM domain containing 7

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H26912 EPDNEW_H26913

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	20	32,743,947 - 32,744,007	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:16223	AgrOrtholog
COSMIC	COMMD7	COSMIC
Ensembl Genes	ENSG00000149600	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ENSG00000285382	Ensembl, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000278980	ENTREZGENE
	ENST00000278980.11	UniProtKB/Swiss-Prot
	ENST00000446419	ENTREZGENE
	ENST00000446419.6	UniProtKB/Swiss-Prot
	ENST00000474815.2	UniProtKB/TrEMBL
	ENST00000610160.1	UniProtKB/TrEMBL
	ENST00000642484.1	UniProtKB/TrEMBL
	ENST00000642630.1	UniProtKB/TrEMBL
	ENST00000645058.1	UniProtKB/TrEMBL
	ENST00000646357.1	UniProtKB/TrEMBL
GTEx	ENSG00000149600	GTEx
	ENSG00000285382	GTEx
HGNC ID	HGNC:16223	ENTREZGENE
Human Proteome Map	COMMD7	Human Proteome Map
InterPro	COMM	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	COMMD4/6/7/8	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	COMMD7	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:149951	UniProtKB/Swiss-Prot
NCBI Gene	149951	ENTREZGENE
OMIM	616703	OMIM
PANTHER	COMM DOMAIN-CONTAINING PROTEIN 4-8 FAMILY MEMBER	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	COMM DOMAIN-CONTAINING PROTEIN 7	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	COMM_domain	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	COMM_HN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA25799	PharmGKB
PROSITE	COMM	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0A2R8Y455_HUMAN	UniProtKB/TrEMBL
	A0A2R8Y600_HUMAN	UniProtKB/TrEMBL
	A0A2R8Y620	ENTREZGENE, UniProtKB/TrEMBL
	A0A2R8Y7U2_HUMAN	UniProtKB/TrEMBL
	A2BHJ2	ENTREZGENE
	B3KTZ2	ENTREZGENE
	COMD7_HUMAN	UniProtKB/Swiss-Prot
	Q5JYB0	ENTREZGENE
	Q86VX2	ENTREZGENE
	Q96SI7	ENTREZGENE
	Q9BW53	ENTREZGENE
	V9GY66_HUMAN	UniProtKB/TrEMBL
	V9GYC5_HUMAN	UniProtKB/TrEMBL
UniProt Secondary	A2BHJ2	UniProtKB/Swiss-Prot
	B3KTZ2	UniProtKB/Swiss-Prot
	Q5JYB0	UniProtKB/Swiss-Prot
	Q96SI7	UniProtKB/Swiss-Prot
	Q9BW53	UniProtKB/Swiss-Prot

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

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

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

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

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Imported Disease Annotations - ClinVar