C3orf22 (chromosome 3 open reading frame 22)

Gene: C3orf22 (chromosome 3 open reading frame 22) Homo sapiens

Analyze

Symbol:

C3orf22

Name:

chromosome 3 open reading frame 22

RGD ID:

1603560

HGNC Page

HGNC:28534

Description:

ASSOCIATED WITH alkaptonuria; genetic disease; Primary Lymphedema with Myelodysplasia; INTERACTS WITH (+)-catechin; aflatoxin B1; arsane

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

hypothetical protein LOC152065; MGC34728; uncharacterized protein C3orf22

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	3	126,526,999 - 126,558,932 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	3	126,526,999 - 126,558,965 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	3	126,245,842 - 126,277,775 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	3	127,751,209 - 127,760,448 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	3	124,693,189 - 124,702,399 (-)	NCBI		Celera
Cytogenetic Map	3	q21.3	NCBI
HuRef	3	123,648,905 - 123,658,113 (-)	NCBI		HuRef
CHM1_1	3	126,231,527 - 126,240,737 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	3	129,259,307 - 129,291,738 (-)	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

alkaptonuria (IAGP)

genetic disease (IAGP)

Primary Lymphedema with Myelodysplasia (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(+)-catechin (EXP)

aflatoxin B1 (EXP)

arsane (EXP)

arsenic atom (EXP)

benzo[a]pyrene (EXP)

bisphenol A (ISO)

diazinon (EXP)

fonofos (EXP)

parathion (EXP)

resveratrol (EXP)

tebuconazole (EXP)

terbufos (EXP)

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:12477932	PMID:14702039	PMID:15489334	PMID:16344560

Genomics

Comparative Map Data

C3orf22
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	3	126,526,999 - 126,558,932 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	3	126,526,999 - 126,558,965 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	3	126,245,842 - 126,277,775 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	3	127,751,209 - 127,760,448 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	3	124,693,189 - 124,702,399 (-)	NCBI		Celera
Cytogenetic Map	3	q21.3	NCBI
HuRef	3	123,648,905 - 123,658,113 (-)	NCBI		HuRef
CHM1_1	3	126,231,527 - 126,240,737 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	3	129,259,307 - 129,291,738 (-)	NCBI		T2T-CHM13v2.0

BC048671
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	6	90,278,201 - 90,282,430 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	6	90,278,201 - 90,282,431 (+)	Ensembl		GRCm39 Ensembl
GRCm38	6	90,301,219 - 90,305,448 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	6	90,301,219 - 90,305,449 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	6	90,251,264 - 90,255,442 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	6	90,266,774 - 90,270,952 (+)	NCBI		MGSCv36	mm8
Celera	6	92,195,104 - 92,199,276 (+)	NCBI		Celera
Cytogenetic Map	6	D1	NCBI
cM Map	6	40.12	NCBI

C4h3orf22
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	4	124,374,885 - 124,379,380 (+)	NCBI		GRCr8
mRatBN7.2	4	122,817,681 - 122,822,175 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	4	122,817,681 - 122,822,175 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	4	128,284,375 - 128,288,858 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	4	124,059,148 - 124,063,631 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	4	122,683,362 - 122,687,845 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	4	122,217,505 - 122,221,999 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	4	122,217,505 - 122,221,999 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	4	186,758,874 - 186,763,369 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	4	124,564,593 - 124,569,087 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	4	111,742,535 - 111,746,963 (+)	NCBI		Celera
Cytogenetic Map	4	q34	NCBI

LOC102020573
(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	NW_004955421	21,945,527 - 21,949,229 (+)	NCBI	ChiLan1.0	ChiLan1.0

C2H3orf22
(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	2	124,479,862 - 124,489,154 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	3	124,484,642 - 124,498,688 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	3	123,599,191 - 123,609,230 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	3	130,914,841 - 130,924,133 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	3	130,914,841 - 130,924,133 (-)	Ensembl	panpan1.1		panPan2

C20H3orf22
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	20	752,614 - 758,180 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	20	753,461 - 757,115 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	20	786,766 - 792,311 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	20	764,139 - 769,692 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	20	764,133 - 768,646 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	20	492,041 - 497,588 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	20	821,005 - 826,558 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	20	779,899 - 785,446 (-)	NCBI		UU_Cfam_GSD_1.0

CUNH3orf22
(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_024404942	19,080,330 - 19,082,462 (+)	NCBI		HiC_Itri_2
SpeTri2.0	NW_004936898	608,726 - 610,110 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

CUNH3orf22
(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	22	54,455,637 - 54,465,446 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	22	54,461,735 - 54,465,250 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666041	111,826,162 - 111,835,348 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Variants

Variants in C3orf22
27 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 3q21.3(chr3:126167799-126819908)x3	copy number gain	See cases [RCV000051531]	Chr3:126167799..126819908 [GRCh38] Chr3:125886642..126538751 [GRCh37] Chr3:127369332..128021441 [NCBI36] Chr3:3q21.3	uncertain significance
NM_152533.2(C3orf22):c.-41+2457T>A	single nucleotide variant	Lung cancer [RCV000092885]	Chr3:126556170 [GRCh38] Chr3:126275013 [GRCh37] Chr3:3q21.3	uncertain significance
GRCh38/hg38 3q13.11-29(chr3:103426882-198110178)x3	copy number gain	See cases [RCV000134948]	Chr3:103426882..198110178 [GRCh38] Chr3:103145726..197837049 [GRCh37] Chr3:104628416..199321446 [NCBI36] Chr3:3q13.11-29	pathogenic
GRCh38/hg38 3q13.2-21.3(chr3:112620977-128734134)x1	copy number loss	See cases [RCV000139033]	Chr3:112620977..128734134 [GRCh38] Chr3:112339824..128452977 [GRCh37] Chr3:113822514..129935667 [NCBI36] Chr3:3q13.2-21.3	pathogenic
GRCh38/hg38 3q13.33-21.3(chr3:121925147-126782249)x1	copy number loss	See cases [RCV000140814]	Chr3:121925147..126782249 [GRCh38] Chr3:121643994..126501092 [GRCh37] Chr3:123126684..127983782 [NCBI36] Chr3:3q13.33-21.3	pathogenic
GRCh38/hg38 3q21.3-23(chr3:126106779-140918089)x3	copy number gain	See cases [RCV000142010]	Chr3:126106779..140918089 [GRCh38] Chr3:125825622..140636931 [GRCh37] Chr3:127308312..142119621 [NCBI36] Chr3:3q21.3-23	uncertain significance
GRCh38/hg38 3q11.1-24(chr3:93800620-145695381)x3	copy number gain	See cases [RCV000142340]	Chr3:93800620..145695381 [GRCh38] Chr3:93519464..145413168 [GRCh37] Chr3:95002154..146895858 [NCBI36] Chr3:3q11.1-24	pathogenic
GRCh38/hg38 3q13.32-21.3(chr3:118673898-126540730)x1	copy number loss	See cases [RCV000143695]	Chr3:118673898..126540730 [GRCh38] Chr3:118392745..126259573 [GRCh37] Chr3:119875435..127742263 [NCBI36] Chr3:3q13.32-21.3	pathogenic
GRCh37/hg19 3q21.2-21.3(chr3:124806350-126567150)x4	copy number gain	See cases [RCV000448957]	Chr3:124806350..126567150 [GRCh37] Chr3:3q21.2-21.3	uncertain significance
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3	copy number gain	See cases [RCV000511055]	Chr3:61892..197851986 [GRCh37] Chr3:3p26.3-q29	pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)	copy number gain	See cases [RCV000512358]	Chr3:61892..197851986 [GRCh37] Chr3:3p26.3-q29	pathogenic
NM_152889.3(CHST13):c.748G>T (p.Ala250Ser)	single nucleotide variant	Inborn genetic diseases [RCV003250202]	Chr3:126542300 [GRCh38] Chr3:126261143 [GRCh37] Chr3:3q21.3	uncertain significance
GRCh37/hg19 3p26.3-q29(chr3:61495-197838262)x3	copy number gain	not provided [RCV000742138]	Chr3:61495..197838262 [GRCh37] Chr3:3p26.3-q29	pathogenic
GRCh37/hg19 3p26.3-q29(chr3:60174-197948027)x3	copy number gain	not provided [RCV000742133]	Chr3:60174..197948027 [GRCh37] Chr3:3p26.3-q29	pathogenic
Single allele	deletion	Deafness-lymphedema-leukemia syndrome [RCV001541926]	Chr3:123000000..129700000 [GRCh37] Chr3:3q21.1-22.1	pathogenic
GRCh37/hg19 3q21.2-21.3(chr3:124369671-126423192)	copy number loss	not provided [RCV000767706]	Chr3:124369671..126423192 [GRCh37] Chr3:3q21.2-21.3	likely pathogenic
GRCh37/hg19 3q13.31-26.31(chr3:116620308-172042292)x3	copy number gain	not provided [RCV002472621]	Chr3:116620308..172042292 [GRCh37] Chr3:3q13.31-26.31	pathogenic
GRCh37/hg19 3q21.3(chr3:126269767-126800773)x3	copy number gain	not provided [RCV002472486]	Chr3:126269767..126800773 [GRCh37] Chr3:3q21.3	uncertain significance
Single allele	deletion	Deafness-lymphedema-leukemia syndrome [RCV001541924]	Chr3:120247726..128319968 [GRCh37] Chr3:3q13.33-21.3	pathogenic
GRCh37/hg19 3q21.2-21.3(chr3:124990058-126401548)	copy number gain	not specified [RCV002053372]	Chr3:124990058..126401548 [GRCh37] Chr3:3q21.2-21.3	uncertain significance
NC_000003.11:g.(?_120365818)_(133465047_?)del	deletion	Alkaptonuria [RCV002035459]	Chr3:120365818..133465047 [GRCh37] Chr3:3q13.33-22.1	pathogenic
GRCh37/hg19 3q21.3(chr3:126158843-126683166)x3	copy number gain	not provided [RCV002475843]	Chr3:126158843..126683166 [GRCh37] Chr3:3q21.3	uncertain significance
NM_152889.3(CHST13):c.407G>C (p.Arg136Pro)	single nucleotide variant	Inborn genetic diseases [RCV002822881]	Chr3:126541959 [GRCh38] Chr3:126260802 [GRCh37] Chr3:3q21.3	uncertain significance
NM_152889.3(CHST13):c.608G>T (p.Arg203Leu)	single nucleotide variant	Inborn genetic diseases [RCV002703907]	Chr3:126542160 [GRCh38] Chr3:126261003 [GRCh37] Chr3:3q21.3	uncertain significance
NM_152889.3(CHST13):c.670C>T (p.Arg224Cys)	single nucleotide variant	Inborn genetic diseases [RCV002739706]	Chr3:126542222 [GRCh38] Chr3:126261065 [GRCh37] Chr3:3q21.3	uncertain significance
NM_152889.3(CHST13):c.604G>C (p.Ala202Pro)	single nucleotide variant	Inborn genetic diseases [RCV002929462]	Chr3:126542156 [GRCh38] Chr3:126260999 [GRCh37] Chr3:3q21.3	uncertain significance
NM_152889.3(CHST13):c.483C>A (p.Asn161Lys)	single nucleotide variant	Inborn genetic diseases [RCV002826564]	Chr3:126542035 [GRCh38] Chr3:126260878 [GRCh37] Chr3:3q21.3	uncertain significance
NM_152889.3(CHST13):c.961G>A (p.Asp321Asn)	single nucleotide variant	Inborn genetic diseases [RCV002955336]	Chr3:126542513 [GRCh38] Chr3:126261356 [GRCh37] Chr3:3q21.3	uncertain significance
NM_152889.3(CHST13):c.568C>G (p.Arg190Gly)	single nucleotide variant	Inborn genetic diseases [RCV002788502]	Chr3:126542120 [GRCh38] Chr3:126260963 [GRCh37] Chr3:3q21.3	uncertain significance
NM_152889.3(CHST13):c.868G>A (p.Gly290Arg)	single nucleotide variant	Inborn genetic diseases [RCV002960294]	Chr3:126542420 [GRCh38] Chr3:126261263 [GRCh37] Chr3:3q21.3	uncertain significance
NM_152889.3(CHST13):c.970A>G (p.Lys324Glu)	single nucleotide variant	Inborn genetic diseases [RCV002674611]	Chr3:126542522 [GRCh38] Chr3:126261365 [GRCh37] Chr3:3q21.3	uncertain significance
NM_152889.3(CHST13):c.992A>G (p.Asn331Ser)	single nucleotide variant	Inborn genetic diseases [RCV002677777]	Chr3:126542544 [GRCh38] Chr3:126261387 [GRCh37] Chr3:3q21.3	uncertain significance
NM_152889.3(CHST13):c.385G>A (p.Gly129Ser)	single nucleotide variant	Inborn genetic diseases [RCV003209416]	Chr3:126541937 [GRCh38] Chr3:126260780 [GRCh37] Chr3:3q21.3	uncertain significance
NM_152889.3(CHST13):c.949C>G (p.Arg317Gly)	single nucleotide variant	Inborn genetic diseases [RCV003220644]	Chr3:126542501 [GRCh38] Chr3:126261344 [GRCh37] Chr3:3q21.3	uncertain significance
NM_152889.3(CHST13):c.215A>G (p.Gln72Arg)	single nucleotide variant	Inborn genetic diseases [RCV003202339]	Chr3:126541767 [GRCh38] Chr3:126260610 [GRCh37] Chr3:3q21.3	uncertain significance
NM_152889.3(CHST13):c.294C>G (p.His98Gln)	single nucleotide variant	Inborn genetic diseases [RCV003373545]	Chr3:126541846 [GRCh38] Chr3:126260689 [GRCh37] Chr3:3q21.3	uncertain significance
GRCh37/hg19 3q21.2-21.3(chr3:124119718-127457671)x1	copy number loss	not specified [RCV003986465]	Chr3:124119718..127457671 [GRCh37] Chr3:3q21.2-21.3	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1002
Count of miRNA genes:	559
Interacting mature miRNAs:	628
Transcripts:	ENST00000318225, ENST00000505070
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

RH92341

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	126,268,582 - 126,268,719	UniSTS	GRCh37
Build 36	3	127,751,272 - 127,751,409	RGD	NCBI36
Celera	3	124,693,252 - 124,693,389	RGD
Cytogenetic Map	3	q21.3	UniSTS
HuRef	3	123,648,968 - 123,649,105	UniSTS
GeneMap99-GB4 RH Map	3	457.26	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

adipose tissue

appendage

High

Medium

348

Low

Below cutoff

959

1284

1023

360

547

283

1963

1088

2365

208

650

756

467

1498

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_152533	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_130715	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011512455	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011512457	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017005751	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017005752	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017005753	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054345360	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054345361	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054345362	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054345363	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC024558	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK097841	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC032025	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471052	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068275	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB055549	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HC007152	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000318225 ⟹ ENSP00000316644

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	126,549,692 - 126,558,932 (-)	Ensembl

RefSeq Acc Id:

ENST00000505070 ⟹ ENSP00000422064

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	126,526,999 - 126,558,965 (-)	Ensembl

RefSeq Acc Id:

NM_152533 ⟹ NP_689746

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	126,549,692 - 126,558,932 (-)	NCBI
GRCh37	3	126,245,842 - 126,277,808 (-)	NCBI
Build 36	3	127,751,209 - 127,760,448 (-)	NCBI Archive
Celera	3	124,693,189 - 124,702,399 (-)	RGD
HuRef	3	123,648,905 - 123,658,113 (-)	ENTREZGENE
CHM1_1	3	126,231,527 - 126,240,787 (-)	NCBI
T2T-CHM13v2.0	3	129,282,512 - 129,291,724 (-)	NCBI

Sequence:

show sequence

ACTGCCTGTCCGGGGACCCTGGGGCTGCTGTTCCTGTGGTAATGTGGCAGCTGGGACCATGGCC
AGCTTCAGTCTGCCTGGCGTCACATAAGCCAGCCCACAGGGTCCTGCAGCTTGTCCTTTCTGGC
TGGAAGCTCTGGGCATAGCCTGGGACTGGGTCTTTCCAGAGAGGGCTGTAGCCAGGGCCCTGCC
AGCCTCGGGGGCCACAGCGGCTCTCACACCAGCATCTTGCTGGATAGGAGCAGTTCCAGGACTC
TCTGATCACACCTGATCATCGTCACTGCCAGAATTCAAGGTAGCTGCCTGCCATGGCTGAGAGG
TGTGCCTCAGCTTAACCCACTCAGTGATGGACTCCAGTGCCTGCAAGAAGTCTCACCAGAGTAA
GAAGTGGAGGATCCAGGCCCAGGAGAATTTTGCCAAGAAGTTTCCGTACAGGTTGTCGTGGCTG
ACAGAGCCCGACCCTGAGCCCCTGCAGCCCTGGGAGGTCACAAACGACTCGAACACGGTGCAGC
TGCCCCTGCAGAAGAGGTTGGTGCCAACGAGGTCCATCCCAGTCCGAGGGCTCGGGGCTCCAGA
TTTTACATCACCGTCTGGCTCCTGCCCGGCACCACTACCAGCACCATCACCACCTCCACTGTGC
AACCTTTGGGAACTCAAGTTGCTGAGTCGCCGCTTCCCCAGACAACTCGCCTTCCTGCTGTCCA
CCCGGCACACTGAGGCTGCCTGCCCCCAGACCAGCAAGGCGGCAGGGCTGTCCAGGGGCCTCTC
CTAGAGACTGGGCTCTGTGTGTGGCCTTCTTATTGGCCACCTTCTCCTTGGCAGGCTCTGGGCA
GTAGCCACAGAGACTTTAGTAAAGGGATCAGCCTTCATGGCCATCATAGACCGGGAGTGGTTTG
TGGTCCCCCCAAAAAGCTACACCAAGCTAATAAACTGCGAGTTCCCACCCCA

hide sequence

RefSeq Acc Id:

NR_130715

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	126,526,999 - 126,558,932 (-)	NCBI
CHM1_1	3	126,208,862 - 126,240,787 (-)	NCBI
T2T-CHM13v2.0	3	129,259,307 - 129,291,724 (-)	NCBI

Sequence:

show sequence

ACTGCCTGTCCGGGGACCCTGGGGCTGCTGTTCCTGTGGTAATGTGGCAGCTGGGACCATGGCC
AGCTTCAGTCTGCCTGGCGTCACATAAGCCAGCCCACAGGGTCCTGCAGCTTGTCCTTTCTGGC
TGGAAGCTCTGGGCATAGCCTGGGACTGGGTCTTTCCAGAGAGGGCTGTAGCCAGGGCCCTGCC
AGCCTCGGGGGCCACAGCGGCTCTCACACCAGCATCTTGCTGGATAGGAGCAGTTCCAGGACTC
TCTGATCACACCTGATCATCGTCACTGCCAGAATTCAAGGTAGCTGCCTGCCATGGCTGAGAGG
TGTGCCTCAGCTTAACCCACTCAGTGATGGACTCCAGTGCCTGCAAGAAGTCTCACCAGAGTAA
GAAGTGGAGGATCCAGGCCCAGGAGAATTTTGCCAAGAAGTTTCCGTACAGGTTGTCGTGGCTG
ACAGAGCCCGACCCTGAGCCCCTGCAGCCCTGGGAGGTCACAAACGACTCGAACACGGTGCAGC
TGCCCCTGCAGAAGAGGTTGGTGCCAACGAGGTCCATCCCAGTCCGAGGGGTTGGTGTGAGGAT
TAAAAAGAGCATGAATGTCACTTCTAGGACTTTATCCCAAATGTACACTCACACAGGCAAGTGG
GCCCCATTTCACTGACCCATGAGGAAATACCAGCCCAGGGAAGGAGAGCAGAGAGAGCTGCTCA
AGGCCATGCGATTGCTGCACACAGGACACCCGCACACGTCATGTTGCAAGGCCTCCTCTGCCAA
TCAAGATACCGGGTGAAACACCACACTAGAAACCTACAGCAGAAGCACGACCATCCTCCTCTGC
ACACCCACCTCAGCCAAAGCAGGGCTCGCGCCCTGTGCAGGGATTGCCAATTCCTGTTCTGCAG
AGCCACCCACCTGCCAGCTTGCCTCTTCTCACGGTACTTTCTGGAGGTCCTCTGAACTCGGGAC
ACTCCAGCAGTACCTGAAGATGGACAGCAGCATGGGGAGCATCTACCAATTTGGCTCCAGCAGC
CACTTCCCCTCCCTTTGCCCACCCACCAGAGGAGGATGCCTGCCAGGCCTTCAGCCCATGTGAT
TCCGATAGGCTCCCCTACGCCTCCACCACCTGCTGGGATAGGCATGTGGCCTAGGCCTGTCCAA
TCACAGCCTCCCAGCCCTTCCTGCCACCTGACTGGCTCAGAGACGGGCACTTGAGACCCAGACC
GGGCCAATGGATGCCTCCTTGGGACTTTGGCTGGAATCAGTGGCAAAGGAACCCTCTCTAGCTT
TGGGTTGGAGTTGCTGAACTGGTGCAGCTGAGAGTGAGGCTATGGCAGAGAAAAGCTAAACCAC
AGCTGGAGGTGTGATCTGAACCCCAAGATCTATGCCTGTCCGAGGCAGAGGCACCTGGCCTTTT
CAGTCACAGGCACAGACCCACTCCCTCCCAGCTGAAGGGAGTCTGAATTGGGTTGGGTTTGTCC
TCGCCGAGGCTACCACTGTGTGCCATTGGGTGGCCCACAGTCTTAGCTTCCTTGCCTGCCTAGG
GGTGAGCAGGGGCTGGGATGGGATGCAGAGGCCCACCTGGCTCCAAGAGGAACACCTGTGACTC
CAAACACTGGGACAGATGCTCAGCCCTGCAGCCGCGGGAGTGGAATAGGGGAAGGGGGCTGGTG
CCAACACTGCTCCCGCCGGTGTCTCAGAGGCAGAAGACATAGAGCTGAGATCTTGGGTTTTCAT
ATTAAAAATGTAAGCTCCTC

hide sequence

RefSeq Acc Id:

XM_011512455 ⟹ XP_011510757

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	126,546,620 - 126,558,932 (-)	NCBI

Sequence:

show sequence

AAGGGCTTCTGACCTTGCAGTGAGCTTGTTGGCACTGCCTGTCCGGGGACCCTGGGGCTGCTGT
TCCTGTGGTAATGTGGCAGCTGGGACCATGGCCAGCTTCAGTCTGCCTGGCGTCACATAAGCCA
GCCCACAGGGTCCTGCAGCTTGTCCTTTCTGGCTGGAAGCTCTGGGCATAGCCTGGGACTGGGT
CTTTCCAGAGAGGGCTGTAGCCAGGGCCCTGCCAGCCTCGGGGGCCACAGCGGCTCTCACACCA
GCATCTTGCTGGATAGGAGCAGTTCCAGGACTCTCTGATCACACCTGATCATCGTCACTGCCAG
AATTCAAGGTAGCTGCCTGCCATGGCTGAGAGGTGTGCCTCAGCTTAACCCACTCAGTGATGGA
CTCCAGTGCCTGCAAGAAGTCTCACCAGAGTAAGAAGTGGAGGATCCAGGCCCAGGAGAATTTT
GCCAAGAAGTTTCCGTACAGGTTGTCGTGGCTGACAGAGCCCGACCCTGAGCCCCTGCAGCCCT
GGGAGGTCACAAACGACTCGAACACGGTGCAGCTGCCCCTGCAGAAGAGGTTGGTGCCAACGAG
GTCCATCCCAGTCCGAGGGGTTGGTGTGAGGATTAAAAAGAGCATGAATGTCACTTCTAGGACT
TTATCCCAAATGTACACTCACACAGTTCCAAGGAAGGCTGGACGTCCAAGGTGAAAGTGCTAGC
TGCCTTGGTTCCCTGATGGGGGCTCTCTT

hide sequence

RefSeq Acc Id:

XM_011512457 ⟹ XP_011510759

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	126,545,764 - 126,558,932 (-)	NCBI

Sequence:

show sequence

AAGGGCTTCTGACCTTGCAGTGAGCTTGTTGGCACTGCCTGTCCGGGGACCCTGGGGCTGCTGT
TCCTGTGGTAATGTGGCAGCTGGGACCATGGCCAGCTTCAGTCTGCCTGGCGTCACATAAGCCA
GCCCACAGGGTCCTGCAGCTTGTCCTTTCTGGCTGGAAGCTCTGGGCATAGCCTGGGACTGGGT
CTTTCCAGAGAGGGCTGTAGCCAGGGCCCTGCCAGCCTCGGGGGCCACAGCGGCTCTCACACCA
GCATCTTGCTGGATAGGAGCAGTTCCAGGACTCTCTGATCACACCTGATCATCGTCACTGCCAG
AATTCAAGGTAGCTGCCTGCCATGGCTGAGAGGTGTGCCTCAGCTTAACCCACTCAGTGATGGA
CTCCAGTGCCTGCAAGAAGTCTCACCAGAGTAAGAAGTGGAGGATCCAGGCCCAGGAGAATTTT
GCCAAGAAGTTTCCGTACAGGTTGTCGTGGCTGACAGAGCCCGACCCTGAGCCCCTGCAGCCCT
GGGAGGTCACAAACGACTCGAACACGGTGCAGCTGCCCCTGCAGAAGAGGTTGGTGCCAACGAG
GTCCATCCCAGTCCGAGGGGTTGGTGTGAGGATTAAAAAGAGCATGAATGTCACTTCTAGGACT
TTATCCCAAATGTACACTCACACAGATGGCTGCTTTCTCCCTGTGTGAGAGGGAGAGGCGGGGA
GGGAGAGAGAGAGAACTCTCCAGTGGCTCTGCTTATGAGGACACTAATCCCACCATGGAGACCG
CATCCTCATGACCTCATCTCAACCTGATCACCTCCCAAAGGCCCCATCGCCAAATAGCATCACA
TTGTGGGTGAGGGCTTCCACATAAGACTGGGGAGAACATAATTCAGTCCACAGCAGCCACTGAG
GGCATTTGGTGCCCAGTCCCCGTGGGGAAATCTGGGGCACCATGCAGATTGTGTCTCAATGTCC
TTCATGCAGGGATAAAAGCTGGAGCATTTATCGCCCGACTTCCAACAGATGTAGGTGAGGACTG
CTTCCAGGGGGCACTAACTCCTGCACACCCAGCCTTCTTGTGCCCAGGCCAAGAGGCCTGGTGG
TCAGAGGGAGACTGCGGGAGGGTTGCAGATGCTAGGGAGCGCATTGAGGCACCCGACCTAAAAC
TGGCTGTCAGTTCCCAGACTCCCTTGCCACTGGGAATACAGTGGGCTAGGTTCAGGCCAATGGC
ATTGCACTGGAAATGGAATGGACTGTCCAGTTTGTGTCTTTAAAGCCAGCTTGGGTGCCCTTCT
TTTCCCTTTGACATTGGGATACTTGAAAAGTGAATGGCTCACTCTCATGGAAAAGGGCCAGGCC
CTAGGGACTAGGGAGCAACAAAAGAGAAGGGTCCTGGGCTCCAAGTGGCCCATTGGAGCATCTG
TCCCACCAGCCCTCAGCCCCCTTCCTCTGGATAACAGAAAACACCTTAAACGACTGTCATCAAG
CCTTTGTCCCAGGCAGCCGCACCTTTATCT

hide sequence

RefSeq Acc Id:

XM_017005751 ⟹ XP_016861240

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	126,549,692 - 126,558,932 (-)	NCBI

Sequence:

show sequence

GTGAGCTTGTTGGCACTGCCTGTCCGGGGACCCTGGGGCTGCTGTTCCTGTGGTAATGTGGCAG
CTGGGACCATGGCCAGCTTCAGTCTGCCTGGCGTCACATAAGCCAGCCCACAGGGTCCTGCAGC
TTGTCCTTTCTGGCTGGAAGCTCTGGGCATAGCCTGGGACTGGGTCTTTCCAGAGAGGGCTGTA
GCCAGGGCCCTGCCAGCCTCGGGGGCCACAGCGGCTCTCACACCAGCATCTTGCTGGATAGGAG
CAGTTCCAGGACTCTCTGATCACACCTGATCATCGTCACTGCCAGAATTCAAGCCATGGCTGAG
AGGTGTGCCTCAGCTTAACCCACTCAGTGATGGACTCCAGTGCCTGCAAGAAGTCTCACCAGAG
TAAGAAGTGGAGGATCCAGGCCCAGGAGAATTTTGCCAAGAAGTTTCCGTACAGGTTGTCGTGG
CTGACAGAGCCCGACCCTGAGCCCCTGCAGCCCTGGGAGGTCACAAACGACTCGAACACGGTGC
AGCTGCCCCTGCAGAAGAGGTTGGTGCCAACGAGGTCCATCCCAGTCCGAGGGCTCGGGGCTCC
AGATTTTACATCACCGTCTGGCTCCTGCCCGGCACCACTACCAGCACCATCACCACCTCCACTG
TGCAACCTTTGGGAACTCAAGTTGCTGAGTCGCCGCTTCCCCAGACAACTCGCCTTCCTGCTGT
CCACCCGGCACACTGAGGCTGCCTGCCCCCAGACCAGCAAGGCGGCAGGGCTGTCCAGGGGCCT
CTCCTAGAGACTGGGCTCTGTGTGTGGCCTTCTTATTGGCCACCTTCTCCTTGGCAGGCTCTGG
GCAGTAGCCACAGAGACTTTAGTAAAGGGATCAGCCTTCATGGCCATCATAGACCGGGAGTGGT
TTGTGGTCCCCCCAAAAAGCTACACCAAGCTAATAAACTGCGAGTTCCCACCCCACTTCCAGCT
GGAATGATCA

hide sequence

RefSeq Acc Id:

XM_017005752 ⟹ XP_016861241

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	126,549,692 - 126,558,373 (-)	NCBI

Sequence:

show sequence

CTCAATTCCTGTGGTAATGCTGCTTCCCCGGTTCAGGACTGTTTGAGGCTGCATGGCCCAGCAG
GAGGAGCACAGGCCACCCATCCTGAACCTCTTCCCCGACTCACTGTGTGAATGCAGGCAAATCA
GTTAACTTTCCGGAGCCTCAGTTTCCTCACTTGAATTATGGGGCCATGGCTGAGAGGTGTGCCT
CAGCTTAACCCACTCAGTGATGGACTCCAGTGCCTGCAAGAAGTCTCACCAGAGTAAGAAGTGG
AGGATCCAGGCCCAGGAGAATTTTGCCAAGAAGTTTCCGTACAGGTTGTCGTGGCTGACAGAGC
CCGACCCTGAGCCCCTGCAGCCCTGGGAGGTCACAAACGACTCGAACACGGTGCAGCTGCCCCT
GCAGAAGAGGTTGGTGCCAACGAGGTCCATCCCAGTCCGAGGGCTCGGGGCTCCAGATTTTACA
TCACCGTCTGGCTCCTGCCCGGCACCACTACCAGCACCATCACCACCTCCACTGTGCAACCTTT
GGGAACTCAAGTTGCTGAGTCGCCGCTTCCCCAGACAACTCGCCTTCCTGCTGTCCACCCGGCA
CACTGAGGCTGCCTGCCCCCAGACCAGCAAGGCGGCAGGGCTGTCCAGGGGCCTCTCCTAGAGA
CTGGGCTCTGTGTGTGGCCTTCTTATTGGCCACCTTCTCCTTGGCAGGCTCTGGGCAGTAGCCA
CAGAGACTTTAGTAAAGGGATCAGCCTTCATGGCCATCATAGACCGGGAGTGGTTTGTGGTCCC
CCCAAAAAGCTACACCAAGCTAATAAACTGCGAGTTCCCACCCCACTTCCAGCTGGAATGATCA

hide sequence

RefSeq Acc Id:

XM_054345360 ⟹ XP_054201335

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	129,282,512 - 129,291,738 (-)	NCBI

RefSeq Acc Id:

XM_054345361 ⟹ XP_054201336

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	129,282,512 - 129,291,165 (-)	NCBI

RefSeq Acc Id:

XM_054345362 ⟹ XP_054201337

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	129,279,439 - 129,291,724 (-)	NCBI

RefSeq Acc Id:

XM_054345363 ⟹ XP_054201338

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	129,278,583 - 129,291,724 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_689746	(Get FASTA)	NCBI Sequence Viewer
	XP_011510757	(Get FASTA)	NCBI Sequence Viewer
	XP_011510759	(Get FASTA)	NCBI Sequence Viewer
	XP_016861240	(Get FASTA)	NCBI Sequence Viewer
	XP_016861241	(Get FASTA)	NCBI Sequence Viewer
	XP_054201335	(Get FASTA)	NCBI Sequence Viewer
	XP_054201336	(Get FASTA)	NCBI Sequence Viewer
	XP_054201337	(Get FASTA)	NCBI Sequence Viewer
	XP_054201338	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH32025	(Get FASTA)	NCBI Sequence Viewer
	BAG53541	(Get FASTA)	NCBI Sequence Viewer
	CBH19381	(Get FASTA)	NCBI Sequence Viewer
	EAW79358	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000316644
	ENSP00000316644.2
	ENSP00000422064.1
GenBank Protein	Q8N5N4	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_689746 ⟸ NM_152533
- UniProtKB:	B3KUS9 (UniProtKB/Swiss-Prot), Q8N5N4 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MDSSACKKSHQSKKWRIQAQENFAKKFPYRLSWLTEPDPEPLQPWEVTNDSNTVQLPLQKRLVP TRSIPVRGLGAPDFTSPSGSCPAPLPAPSPPPLCNLWELKLLSRRFPRQLAFLLSTRHTEAACP QTSKAAGLSRGLS hide sequence

RefSeq Acc Id:	XP_011510759 ⟸ XM_011512457
- Peptide Label:	isoform X3
- Sequence:	show sequence MDSSACKKSHQSKKWRIQAQENFAKKFPYRLSWLTEPDPEPLQPWEVTNDSNTVQLPLQKRLVP TRSIPVRGVGVRIKKSMNVTSRTLSQMYTHTDGCFLPV hide sequence

RefSeq Acc Id:	XP_011510757 ⟸ XM_011512455
- Peptide Label:	isoform X2
- Sequence:	show sequence MDSSACKKSHQSKKWRIQAQENFAKKFPYRLSWLTEPDPEPLQPWEVTNDSNTVQLPLQKRLVP TRSIPVRGVGVRIKKSMNVTSRTLSQMYTHTVPRKAGRPR hide sequence

RefSeq Acc Id:	XP_016861240 ⟸ XM_017005751
- Peptide Label:	isoform X1
- UniProtKB:	B3KUS9 (UniProtKB/Swiss-Prot), Q8N5N4 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MDSSACKKSHQSKKWRIQAQENFAKKFPYRLSWLTEPDPEPLQPWEVTNDSNTVQLPLQKRLVP TRSIPVRGLGAPDFTSPSGSCPAPLPAPSPPPLCNLWELKLLSRRFPRQLAFLLSTRHTEAACP QTSKAAGLSRGLS hide sequence

RefSeq Acc Id:	XP_016861241 ⟸ XM_017005752
- Peptide Label:	isoform X1
- UniProtKB:	B3KUS9 (UniProtKB/Swiss-Prot), Q8N5N4 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MDSSACKKSHQSKKWRIQAQENFAKKFPYRLSWLTEPDPEPLQPWEVTNDSNTVQLPLQKRLVP TRSIPVRGLGAPDFTSPSGSCPAPLPAPSPPPLCNLWELKLLSRRFPRQLAFLLSTRHTEAACP QTSKAAGLSRGLS hide sequence

RefSeq Acc Id:

ENSP00000422064 ⟸ ENST00000505070

RefSeq Acc Id:

ENSP00000316644 ⟸ ENST00000318225

RefSeq Acc Id:	XP_054201338 ⟸ XM_054345363
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054201337 ⟸ XM_054345362
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054201335 ⟸ XM_054345360
- Peptide Label:	isoform X1
- UniProtKB:	Q8N5N4 (UniProtKB/Swiss-Prot), B3KUS9 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054201336 ⟸ XM_054345361
- Peptide Label:	isoform X1
- UniProtKB:	Q8N5N4 (UniProtKB/Swiss-Prot), B3KUS9 (UniProtKB/Swiss-Prot)

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q8N5N4-F1-model_v2	AlphaFold	Q8N5N4	1-141	view protein structure

Promoters

RGD ID:

6865550

Promoter ID:

EPDNEW_H5940

Type:

initiation region

Name:

C3orf22_1

Description:

chromosome 3 open reading frame 22

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	126,558,932 - 126,558,992	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:28534	AgrOrtholog
COSMIC	C3orf22	COSMIC
Ensembl Genes	ENSG00000180697	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000318225	ENTREZGENE
	ENST00000318225.3	UniProtKB/Swiss-Prot
	ENST00000505070	ENTREZGENE
	ENST00000505070.5	UniProtKB/Swiss-Prot
GTEx	ENSG00000180697	GTEx
HGNC ID	HGNC:28534	ENTREZGENE
Human Proteome Map	C3orf22	Human Proteome Map
InterPro	C3orf22	UniProtKB/Swiss-Prot
KEGG Report	hsa:152065	UniProtKB/Swiss-Prot
NCBI Gene	152065	ENTREZGENE
PANTHER	HYPOTHETICAL PROTEIN LOC685964	UniProtKB/Swiss-Prot
	PTHR37875	UniProtKB/Swiss-Prot
PharmGKB	PA142672383	PharmGKB
UniProt	B3KUS9	ENTREZGENE
	CC022_HUMAN	UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary	B3KUS9	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