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Gene: ZNF790 (zinc finger protein 790) Homo sapiens

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Symbol:

ZNF790

Name:

zinc finger protein 790

RGD ID:

1603835

HGNC Page

HGNC:33114

Description:

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

FLJ20350; MGC62100

RGD Orthologs

Alliance Orthologs

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	19	36,817,428 - 36,850,792 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	36,817,428 - 36,850,787 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	37,308,330 - 37,341,694 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	42,000,170 - 42,021,124 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	19	34,092,627 - 34,113,574 (-)	NCBI		Celera
Cytogenetic Map	19	q13.12	NCBI
HuRef	19	33,778,026 - 33,810,213 (-)	NCBI		HuRef
CHM1_1	19	37,309,707 - 37,342,149 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	19	39,493,114 - 39,526,474 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZNF790	Human	2,3',4,4',5-Pentachlorobiphenyl	increases expression	ISO	RGD:1556944	6480464	2,3',4,4',5-pentachlorobiphenyl results in increased expression of ZFP790 mRNA	CTD	PMID:31388691
ZNF790	Human	2,3,7,8-tetrachlorodibenzodioxine	affects expression	ISO	RGD:1556944	6480464	Tetrachlorodibenzodioxin affects the expression of ZFP790 mRNA	CTD	PMID:21570461
ZNF790	Human	2,3,7,8-tetrachlorodibenzodioxine	multiple interactions	ISO	RGD:1556944	6480464	[TIPARP gene mutant form results in increased susceptibility to Tetrachlorodibenzodioxin] which results in decreased expression more ...	CTD	PMID:25975270
ZNF790	Human	2-hydroxypropanoic acid	decreases expression	EXP		6480464	Lactic Acid results in decreased expression of ZNF790 mRNA	CTD	PMID:30851411
ZNF790	Human	acrolein	multiple interactions	EXP		6480464	[Acrolein co-treated with methacrylaldehyde co-treated with alpha-pinene co-treated with Ozone] results in increased oxidation of more ...	CTD	PMID:32699268
ZNF790	Human	aflatoxin B1	increases expression	ISO	RGD:1556944	6480464	Aflatoxin B1 results in increased expression of ZFP790 mRNA	CTD	PMID:19770486
ZNF790	Human	alpha-pinene	multiple interactions	EXP		6480464	[Acrolein co-treated with methacrylaldehyde co-treated with alpha-pinene co-treated with Ozone] results in increased oxidation of more ...	CTD	PMID:32699268
ZNF790	Human	amphetamine	decreases expression	ISO	RGD:150344952	6480464	Amphetamine results in decreased expression of ZFP790 mRNA	CTD	PMID:30779732
ZNF790	Human	arsane	multiple interactions	EXP		6480464	[[sodium arsenite results in increased abundance of Arsenic] co-treated with [manganese chloride results in increased more ...	CTD	PMID:39836092
ZNF790	Human	arsenic atom	multiple interactions	EXP		6480464	[[sodium arsenite results in increased abundance of Arsenic] co-treated with [manganese chloride results in increased more ...	CTD	PMID:39836092
ZNF790	Human	benzo[a]pyrene	decreases methylation	EXP		6480464	Benzo(a)pyrene results in decreased methylation of ZNF790 promoter	CTD	PMID:27901495
ZNF790	Human	benzo[a]pyrene	multiple interactions	EXP		6480464	[AHR gene mutant form affects the susceptibility to Benzo(a)pyrene] which results in decreased expression of more ...	CTD	PMID:38036013
ZNF790	Human	benzo[a]pyrene	increases methylation	ISO	RGD:1556944	6480464	Benzo(a)pyrene results in increased methylation of ZFP790 exon; Benzo(a)pyrene results in increased methylation of ZFP790 more ...	CTD	PMID:27901495
ZNF790	Human	beta-lapachone	decreases expression	EXP		6480464	beta-lapachone results in decreased expression of ZNF790 mRNA	CTD	PMID:38218311
ZNF790	Human	cadmium dichloride	decreases expression	EXP		6480464	Cadmium Chloride results in decreased expression of ZNF790 mRNA	CTD	PMID:38568856
ZNF790	Human	Dibutyl phosphate	affects expression	EXP		6480464	di-n-butylphosphoric acid affects the expression of ZNF790 mRNA	CTD	PMID:37042841
ZNF790	Human	folic acid	decreases expression	ISO	RGD:1556944	6480464	Folic Acid results in decreased expression of ZFP790 mRNA	CTD	PMID:25629700
ZNF790	Human	GSK-J4	decreases expression	EXP		6480464	GSK-J4 results in decreased expression of ZNF790 mRNA	CTD	PMID:29301935
ZNF790	Human	manganese atom	multiple interactions	EXP		6480464	[[sodium arsenite results in increased abundance of Arsenic] co-treated with [manganese chloride results in increased more ...	CTD	PMID:39836092
ZNF790	Human	manganese(0)	multiple interactions	EXP		6480464	[[sodium arsenite results in increased abundance of Arsenic] co-treated with [manganese chloride results in increased more ...	CTD	PMID:39836092
ZNF790	Human	manganese(II) chloride	multiple interactions	EXP		6480464	[[sodium arsenite results in increased abundance of Arsenic] co-treated with [manganese chloride results in increased more ...	CTD	PMID:39836092
ZNF790	Human	okadaic acid	decreases expression	EXP		6480464	Okadaic Acid results in decreased expression of ZNF790 mRNA	CTD	PMID:38832940
ZNF790	Human	ozone	multiple interactions	EXP		6480464	[Acrolein co-treated with methacrylaldehyde co-treated with alpha-pinene co-treated with Ozone] results in increased oxidation of more ...	CTD	PMID:32699268
ZNF790	Human	rac-lactic acid	decreases expression	EXP		6480464	Lactic Acid results in decreased expression of ZNF790 mRNA	CTD	PMID:30851411
ZNF790	Human	sodium arsenite	increases expression	EXP		6480464	sodium arsenite results in increased expression of ZNF790 mRNA	CTD	PMID:38568856
ZNF790	Human	sodium arsenite	multiple interactions	EXP		6480464	[[sodium arsenite results in increased abundance of Arsenic] co-treated with [manganese chloride results in increased more ...	CTD	PMID:39836092
ZNF790	Human	triphenyl phosphate	affects expression	EXP		6480464	triphenyl phosphate affects the expression of ZNF790 mRNA	CTD	PMID:37042841
ZNF790	Human	troglitazone	decreases expression	ISO	RGD:1556944	6480464	troglitazone results in decreased expression of ZNF790 mRNA	CTD	PMID:28973697
ZNF790	Human	tungsten	decreases expression	ISO	RGD:1556944	6480464	Tungsten results in decreased expression of ZFP790 mRNA	CTD	PMID:30912803
ZNF790	Human	vinclozolin	increases expression	ISO	RGD:150344952	6480464	vinclozolin results in increased expression of ZFP790 mRNA	CTD	PMID:23034163

Biological Process

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZNF790	Human	regulation of DNA-templated transcription	involved_in	IEA	InterPro:IPR001909\|InterPro:IPR036051	150520179		InterPro	GO_REF:0000002
ZNF790	Human	regulation of transcription by RNA polymerase II	involved_in	IBA	MGI:1351476\|MGI:1916754\|MGI:2142347\|MGI:2389445\|MGI:3044162\|PANTHER:PTN001225435\|RGD:2967\|RGD:2985\|UniProtKB:P52737\|UniProtKB:P52738\|UniProtKB:Q96CS4\|UniProtKB:Q96RE9\|UniProtKB:Q9HCX3	150520179		GO_Central	GO_REF:0000033

Cellular Component

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZNF790	Human	nucleus	located_in	IEA	UniProtKB-SubCell:SL-0191	150520179		UniProt	GO_REF:0000044
ZNF790	Human	nucleus	is_active_in	IBA	MGI:105921\|MGI:1328322\|MGI:1353621\|MGI:1916754\|MGI:2142347\|MGI:2143362\|MGI:2389445\|MGI:2444763\|MGI:3040700\|MGI:99206\|PANTHER:PTN001225435\|UniProtKB:O60765\|UniProtKB:P17014\|UniProtKB:P17020\|UniProtKB:P17032\|UniProtKB:Q09FC8\|UniProtKB:Q15072\|UniProtKB:Q16587\|UniProtKB:Q3ZCT1\|UniProtKB:Q5FWF6\|UniProtKB:Q6ECI4\|UniProtKB:Q7Z3V5\|UniProtKB:Q86Y25\|UniProtKB:Q8IZ26\|UniProtKB:Q8N720\|UniProtKB:Q8NDQ6\|UniProtKB:Q8TF45\|UniProtKB:Q8WV37\|UniProtKB:Q96CS4\|UniProtKB:Q96RE9\|UniProtKB:Q9BX82\|UniProtKB:Q9ULD5\|UniProtKB:Q9Y2P7	150520179		GO_Central	GO_REF:0000033
ZNF790	Human	nucleus	located_in	IEA	UniProtKB-KW:KW-0539	150520179		UniProt	GO_REF:0000043

Molecular Function

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
ZNF790	Human	DNA binding	enables	IEA	UniProtKB-KW:KW-0238	150520179		UniProt	GO_REF:0000043
ZNF790	Human	DNA-binding transcription factor activity, RNA polymerase II-specific	enables	IBA	PANTHER:PTN001225435\|UniProtKB:P35789\|UniProtKB:P52738\|UniProtKB:Q86Y25\|UniProtKB:Q96RE9	150520179		GO_Central	GO_REF:0000033
ZNF790	Human	metal ion binding	enables	IEA	UniProtKB-KW:KW-0479	150520179		UniProt	GO_REF:0000043
ZNF790	Human	RNA polymerase II cis-regulatory region sequence-specific DNA binding	enables	IBA	MGI:1916754\|PANTHER:PTN001225435	150520179		GO_Central	GO_REF:0000033
ZNF790	Human	zinc ion binding	enables	IEA	UniProtKB-KW:KW-0863	150520179		UniProt	GO_REF:0000043

#	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

PMID:12477932	PMID:15489334	PMID:16344560	PMID:17207965	PMID:21044950	PMID:21873635

ZNF790
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	19	36,817,428 - 36,850,792 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	36,817,428 - 36,850,787 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	37,308,330 - 37,341,694 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	42,000,170 - 42,021,124 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	19	34,092,627 - 34,113,574 (-)	NCBI		Celera
Cytogenetic Map	19	q13.12	NCBI
HuRef	19	33,778,026 - 33,810,213 (-)	NCBI		HuRef
CHM1_1	19	37,309,707 - 37,342,149 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	19	39,493,114 - 39,526,474 (-)	NCBI		T2T-CHM13v2.0

Zfp790
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	7	29,510,862 - 29,531,467 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	7	29,515,539 - 29,530,430 (+)	Ensembl		GRCm39 Ensembl
GRCm38	7	29,811,437 - 29,832,042 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	7	29,816,114 - 29,831,005 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	7	30,601,091 - 30,617,061 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	7	29,524,879 - 29,539,700 (+)	NCBI		MGSCv36	mm8
Celera	7	24,371,589 - 24,390,090 (+)	NCBI		Celera
Cytogenetic Map	7	B1	NCBI
cM Map	7	17.26	NCBI

Zfp790
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	1	94,166,366 - 94,180,766 (+)	NCBI		GRCr8
mRatBN7.2	1	85,038,923 - 85,053,325 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	1	85,038,911 - 85,052,143 (+)	Ensembl		mRatBN7.2 Ensembl
Rnor_6.0	1	87,665,844 - 87,711,398 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Celera	1	79,380,790 - 79,429,707 (+)	NCBI		Celera
Cytogenetic Map	1	q21	NCBI

ZNF790
(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	20	42,939,749 - 42,993,059 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	19	44,824,868 - 44,877,788 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	19	33,762,837 - 33,811,305 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	19	42,956,493 - 43,004,721 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	19	42,980,457 - 42,988,373 (+)	Ensembl	panpan1.1		panPan2

ZNF790
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	1	115,694,742 - 115,722,622 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	1	115,702,397 - 115,721,845 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	1	115,104,560 - 115,132,877 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	1	116,299,197 - 116,327,580 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	1	116,307,099 - 116,326,959 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	1	115,869,444 - 115,897,764 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	1	115,488,344 - 115,516,662 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	1	116,538,941 - 116,567,287 (+)	NCBI		UU_Cfam_GSD_1.0

ZNF790
(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	6	31,658,741 - 31,686,601 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	6	31,658,883 - 31,664,367 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666073	9,578,950 - 9,607,473 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Variants in ZNF790
54 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 19q13.12(chr19:36439647-37163160)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051288]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051288]\|See cases [RCV000051288]	Chr19:36439647..37163160 [GRCh38] Chr19:36930549..37654062 [GRCh37] Chr19:41622389..42345902 [NCBI36] Chr19:19q13.12	uncertain significance
NM_001242800.1(ZNF790):c.1542C>T (p.Ala514=)	single nucleotide variant	Malignant melanoma [RCV000072104]	Chr19:36818802 [GRCh38] Chr19:37309704 [GRCh37] Chr19:42001544 [NCBI36] Chr19:19q13.12	not provided
NM_001242800.1(ZNF790):c.521A>T (p.Glu174Val)	single nucleotide variant	Malignant melanoma [RCV000072105]	Chr19:36819823 [GRCh38] Chr19:37310725 [GRCh37] Chr19:42002565 [NCBI36] Chr19:19q13.12	not provided
NM_206894.3(ZNF790):c.764A>G (p.Lys255Arg)	single nucleotide variant	Malignant melanoma [RCV000063521]	Chr19:36819580 [GRCh38] Chr19:37310482 [GRCh37] Chr19:42002322 [NCBI36] Chr19:19q13.12	not provided
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	copy number gain	See cases [RCV000133888]	Chr19:11227942..44626354 [GRCh38] Chr19:11338618..45129651 [GRCh37] Chr19:11199618..49821491 [NCBI36] Chr19:19p13.2-q13.31	pathogenic
GRCh38/hg38 19q12-13.13(chr19:29661858-38114723)x1	copy number loss	See cases [RCV000135879]	Chr19:29661858..38114723 [GRCh38] Chr19:30152765..38605363 [GRCh37] Chr19:34844605..43297203 [NCBI36] Chr19:19q12-13.13	pathogenic
GRCh38/hg38 19q12-13.13(chr19:29671324-37902990)x1	copy number loss	See cases [RCV000136794]	Chr19:29671324..37902990 [GRCh38] Chr19:30162231..38393630 [GRCh37] Chr19:34854071..43085470 [NCBI36] Chr19:19q12-13.13	pathogenic
GRCh37/hg19 19q13.12-13.2(chr19:36685995-38708166)x1	copy number loss	Breast ductal adenocarcinoma [RCV000207200]	Chr19:36685995..38708166 [GRCh37] Chr19:19q13.12-13.2	uncertain significance
chr19:36674305-38652962 complex variant	complex	Breast ductal adenocarcinoma [RCV000207036]	Chr19:36674305..38652962 [GRCh37] Chr19:19q13.12-13.13	uncertain significance
GRCh37/hg19 19q13.12-13.13(chr19:36475577-38399402)x3	copy number gain	See cases [RCV000240597]	Chr19:36475577..38399402 [GRCh37] Chr19:19q13.12-13.13	uncertain significance
GRCh37/hg19 19q13.12(chr19:36910874-37705345)x1	copy number loss	See cases [RCV000447259]	Chr19:36910874..37705345 [GRCh37] Chr19:19q13.12	uncertain significance
GRCh37/hg19 19q13.12(chr19:37130813-37342652)x3	copy number gain	See cases [RCV000447637]	Chr19:37130813..37342652 [GRCh37] Chr19:19q13.12	benign
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	copy number gain	See cases [RCV000512296]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
NM_206894.4(ZNF790):c.925C>T (p.Pro309Ser)	single nucleotide variant	not specified [RCV004321042]	Chr19:36819419 [GRCh38] Chr19:37310321 [GRCh37] Chr19:19q13.12	uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	copy number gain	See cases [RCV000511289]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic\|uncertain significance
NM_206894.4(ZNF790):c.1435G>A (p.Glu479Lys)	single nucleotide variant	not specified [RCV004329000]	Chr19:36818909 [GRCh38] Chr19:37309811 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1838T>C (p.Phe613Ser)	single nucleotide variant	not specified [RCV004304833]	Chr19:36818506 [GRCh38] Chr19:37309408 [GRCh37] Chr19:19q13.12	uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3	copy number gain	not provided [RCV000752444]	Chr19:260912..59097160 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3	copy number gain	not provided [RCV000752439]	Chr19:68029..59110290 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
NM_206894.4(ZNF790):c.1488C>G (p.His496Gln)	single nucleotide variant	not specified [RCV004296282]	Chr19:36818856 [GRCh38] Chr19:37309758 [GRCh37] Chr19:19q13.12	uncertain significance
GRCh37/hg19 19q13.11-13.12(chr19:35111811-37744992)	copy number loss	Generalized epilepsy with febrile seizures plus, type 1 [RCV000767768]	Chr19:35111811..37744992 [GRCh37] Chr19:19q13.11-13.12	pathogenic
NM_206894.4(ZNF790):c.821G>A (p.Arg274Gln)	single nucleotide variant	not specified [RCV004332886]	Chr19:36819523 [GRCh38] Chr19:37310425 [GRCh37] Chr19:19q13.12	uncertain significance
GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3	copy number gain	not provided [RCV000845733]	Chr19:28271106..49213832 [GRCh37] Chr19:19q11-13.33	pathogenic
GRCh37/hg19 19q13.12(chr19:37325796-37516374)x1	copy number loss	not provided [RCV001007044]	Chr19:37325796..37516374 [GRCh37] Chr19:19q13.12	likely benign
GRCh37/hg19 19p13.11-q13.2(chr19:19546923-41313229)x3	copy number gain	Specific learning disability [RCV001801194]	Chr19:19546923..41313229 [GRCh37] Chr19:19p13.11-q13.2	pathogenic
GRCh37/hg19 19q13.12(chr19:36910874-37705345)	copy number loss	not specified [RCV002052681]	Chr19:36910874..37705345 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1299G>C (p.Trp433Cys)	single nucleotide variant	not specified [RCV004239812]	Chr19:36819045 [GRCh38] Chr19:37309947 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1885A>G (p.Ser629Gly)	single nucleotide variant	not specified [RCV004239965]	Chr19:36818459 [GRCh38] Chr19:37309361 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1552G>C (p.Gly518Arg)	single nucleotide variant	not specified [RCV004129724]	Chr19:36818792 [GRCh38] Chr19:37309694 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1402C>T (p.His468Tyr)	single nucleotide variant	not specified [RCV004211528]	Chr19:36818942 [GRCh38] Chr19:37309844 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.35T>A (p.Val12Glu)	single nucleotide variant	not specified [RCV004132056]	Chr19:36823765 [GRCh38] Chr19:37314667 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1529A>G (p.Glu510Gly)	single nucleotide variant	not specified [RCV004204318]	Chr19:36818815 [GRCh38] Chr19:37309717 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.334C>G (p.Leu112Val)	single nucleotide variant	not specified [RCV004128903]	Chr19:36820010 [GRCh38] Chr19:37310912 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1393T>C (p.Phe465Leu)	single nucleotide variant	not specified [RCV004207206]	Chr19:36818951 [GRCh38] Chr19:37309853 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.971A>T (p.His324Leu)	single nucleotide variant	not specified [RCV004179059]	Chr19:36819373 [GRCh38] Chr19:37310275 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1603G>A (p.Val535Ile)	single nucleotide variant	not specified [RCV004237038]	Chr19:36818741 [GRCh38] Chr19:37309643 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.970C>A (p.His324Asn)	single nucleotide variant	not specified [RCV004179057]	Chr19:36819374 [GRCh38] Chr19:37310276 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1130G>A (p.Arg377His)	single nucleotide variant	not specified [RCV004189578]	Chr19:36819214 [GRCh38] Chr19:37310116 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.720T>A (p.Ser240Arg)	single nucleotide variant	not specified [RCV004102195]	Chr19:36819624 [GRCh38] Chr19:37310526 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1324A>G (p.Lys442Glu)	single nucleotide variant	not specified [RCV004156195]	Chr19:36819020 [GRCh38] Chr19:37309922 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.373A>G (p.Thr125Ala)	single nucleotide variant	not specified [RCV004193494]	Chr19:36819971 [GRCh38] Chr19:37310873 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1781A>C (p.Tyr594Ser)	single nucleotide variant	not specified [RCV004180671]	Chr19:36818563 [GRCh38] Chr19:37309465 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1391A>G (p.Glu464Gly)	single nucleotide variant	not specified [RCV004250724]	Chr19:36818953 [GRCh38] Chr19:37309855 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.347G>A (p.Cys116Tyr)	single nucleotide variant	not specified [RCV004277060]	Chr19:36819997 [GRCh38] Chr19:37310899 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.931G>C (p.Glu311Gln)	single nucleotide variant	not specified [RCV004275882]	Chr19:36819413 [GRCh38] Chr19:37310315 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1421G>C (p.Gly474Ala)	single nucleotide variant	not specified [RCV004351947]	Chr19:36818923 [GRCh38] Chr19:37309825 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.315A>C (p.Arg105Ser)	single nucleotide variant	not specified [RCV004357349]	Chr19:36820029 [GRCh38] Chr19:37310931 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.401A>C (p.Gln134Pro)	single nucleotide variant	not specified [RCV004356753]	Chr19:36819943 [GRCh38] Chr19:37310845 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.989G>T (p.Arg330Ile)	single nucleotide variant	not specified [RCV004354442]	Chr19:36819355 [GRCh38] Chr19:37310257 [GRCh37] Chr19:19q13.12	uncertain significance
GRCh37/hg19 19q13.12(chr19:36804753-37720742)x1	copy number loss	not provided [RCV003483353]	Chr19:36804753..37720742 [GRCh37] Chr19:19q13.12	uncertain significance
Single allele	deletion	not provided [RCV003448708]	Chr19:35225414..37357598 [GRCh37] Chr19:19q13.11-13.12	pathogenic
GRCh37/hg19 19q11-13.2(chr19:28271146-41508851)x3	copy number gain	not specified [RCV003986115]	Chr19:28271146..41508851 [GRCh37] Chr19:19q11-13.2	pathogenic
NM_206894.4(ZNF790):c.466G>A (p.Val156Met)	single nucleotide variant	not specified [RCV004492821]	Chr19:36819878 [GRCh38] Chr19:37310780 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1829T>G (p.Ile610Ser)	single nucleotide variant	not specified [RCV004492816]	Chr19:36818515 [GRCh38] Chr19:37309417 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.55T>G (p.Trp19Gly)	single nucleotide variant	not specified [RCV004492822]	Chr19:36823745 [GRCh38] Chr19:37314647 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1267G>C (p.Glu423Gln)	single nucleotide variant	not specified [RCV004492813]	Chr19:36819077 [GRCh38] Chr19:37309979 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1523G>A (p.Cys508Tyr)	single nucleotide variant	not specified [RCV004492815]	Chr19:36818821 [GRCh38] Chr19:37309723 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.249G>C (p.Gln83His)	single nucleotide variant	not specified [RCV004492818]	Chr19:36820095 [GRCh38] Chr19:37310997 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.307A>T (p.Ile103Leu)	single nucleotide variant	not specified [RCV004492819]	Chr19:36820037 [GRCh38] Chr19:37310939 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.32C>G (p.Ala11Gly)	single nucleotide variant	not specified [RCV004492820]	Chr19:36823768 [GRCh38] Chr19:37314670 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.920A>G (p.Glu307Gly)	single nucleotide variant	not specified [RCV004492823]	Chr19:36819424 [GRCh38] Chr19:37310326 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.952G>A (p.Ala318Thr)	single nucleotide variant	not specified [RCV004492824]	Chr19:36819392 [GRCh38] Chr19:37310294 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1852G>A (p.Glu618Lys)	single nucleotide variant	not specified [RCV004602058]	Chr19:36818492 [GRCh38] Chr19:37309394 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1385G>A (p.Gly462Asp)	single nucleotide variant	not specified [RCV004602060]	Chr19:36818959 [GRCh38] Chr19:37309861 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1774A>G (p.Thr592Ala)	single nucleotide variant	not specified [RCV004602059]	Chr19:36818570 [GRCh38] Chr19:37309472 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1114G>A (p.Gly372Arg)	single nucleotide variant	not specified [RCV004602061]	Chr19:36819230 [GRCh38] Chr19:37310132 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.856G>C (p.Glu286Gln)	single nucleotide variant	not specified [RCV004886829]	Chr19:36819488 [GRCh38] Chr19:37310390 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1340G>A (p.Arg447Lys)	single nucleotide variant	not specified [RCV004886830]	Chr19:36819004 [GRCh38] Chr19:37309906 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1895T>G (p.Phe632Cys)	single nucleotide variant	not specified [RCV004886832]	Chr19:36818449 [GRCh38] Chr19:37309351 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.312G>A (p.Met104Ile)	single nucleotide variant	not specified [RCV004886833]	Chr19:36820032 [GRCh38] Chr19:37310934 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.725C>G (p.Thr242Ser)	single nucleotide variant	not specified [RCV004886836]	Chr19:36819619 [GRCh38] Chr19:37310521 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.1577G>T (p.Arg526Ile)	single nucleotide variant	not specified [RCV004886831]	Chr19:36818767 [GRCh38] Chr19:37309669 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.478C>T (p.His160Tyr)	single nucleotide variant	not specified [RCV004886828]	Chr19:36819866 [GRCh38] Chr19:37310768 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.208G>A (p.Glu70Lys)	single nucleotide variant	not specified [RCV004886834]	Chr19:36823306 [GRCh38] Chr19:37314208 [GRCh37] Chr19:19q13.12	uncertain significance
NM_206894.4(ZNF790):c.875G>A (p.Ser292Asn)	single nucleotide variant	not specified [RCV004886835]	Chr19:36819469 [GRCh38] Chr19:37310371 [GRCh37] Chr19:19q13.12	uncertain significance
GRCh37/hg19 19q11-13.13(chr19:28271107-38637350)x1	copy number loss	not provided [RCV004819395]	Chr19:28271107..38637350 [GRCh37] Chr19:19q11-13.13	pathogenic

Predicted Target Of

	Summary Value
Count of predictions:	784
Count of miRNA genes:	535
Interacting mature miRNAs:	584
Transcripts:	ENST00000356725, ENST00000525288, ENST00000527645, ENST00000528994, ENST00000586323
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.

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
1300034	BP50_H	Blood pressure QTL 50 (human)	2.1	0.00094	Blood pressure	systolic	19	11089463	37089463	Human
1559110	SCL22_H	Serum cholesterol level QTL 22 (human)	3.59	0.000241	Lipid level	LDL cholesterol	19	31907594	57907594	Human
1331657	COPD9_H	Chronic obstructive pulmonary disease QTL 9 (human)	1.94		Chronic airflow obstruction	post-bronchodilator FEV1	19	31021760	57021760	Human

G09801

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	37,309,121 - 37,309,253	UniSTS	GRCh37
Build 36	19	42,000,961 - 42,001,093	RGD	NCBI36
Celera	19	34,093,418 - 34,093,550	RGD
Cytogenetic Map	19	q13.13	UniSTS
Cytogenetic Map	19	q13.12	UniSTS
HuRef	19	33,777,926 - 33,778,055	UniSTS

D19S657E

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	37,320,974 - 37,321,085	UniSTS	GRCh37
Build 36	19	42,012,814 - 42,012,925	RGD	NCBI36
Celera	19	34,105,271 - 34,105,382	RGD
Cytogenetic Map	19	q13.12	UniSTS
HuRef	19	33,789,512 - 33,789,623	UniSTS

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

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2420	2788	2251	4969	1726	2346	6	624	1937	465	2265	7281	6460	50	3733	1	852	1738	1612	173	1


RefSeq Transcripts	NM_001242800	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001242801	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001242802	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_206894	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005258903	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011526950	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047438798	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047438799	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047438800	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047438801	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054320953	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054320954	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054320955	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054320956	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054320957	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054320958	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC008733	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC020928	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AI808437	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK297474	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC057245	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BF132049	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM473790	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068259	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA819130	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC307556	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC308617	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC324605	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC352882	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DC377558	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	EL735861	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000356725 ⟹ ENSP00000349161

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	36,817,428 - 36,838,387 (-)	Ensembl

Ensembl Acc Id:

ENST00000525288 ⟹ ENSP00000433389

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	36,819,937 - 36,838,095 (-)	Ensembl

Ensembl Acc Id:

ENST00000527645 ⟹ ENSP00000434537

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	36,823,365 - 36,838,027 (-)	Ensembl

Ensembl Acc Id:

ENST00000528994 ⟹ ENSP00000435944

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	36,819,807 - 36,850,313 (-)	Ensembl

Ensembl Acc Id:

ENST00000586323 ⟹ ENSP00000467684

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	36,819,924 - 36,850,787 (-)	Ensembl

Ensembl Acc Id:

ENST00000613249 ⟹ ENSP00000480764

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	36,818,322 - 36,850,787 (-)	Ensembl

Ensembl Acc Id:

ENST00000614179 ⟹ ENSP00000480834

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	36,818,322 - 36,850,267 (-)	Ensembl

Ensembl Acc Id:

ENST00000615484 ⟹ ENSP00000478852

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	36,818,322 - 36,838,027 (-)	Ensembl

RefSeq Acc Id:

NM_001242800 ⟹ NP_001229729

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	36,817,428 - 36,850,792 (-)	NCBI
GRCh37	19	37,309,224 - 37,341,689 (-)	ENTREZGENE
HuRef	19	33,778,026 - 33,810,213 (-)	ENTREZGENE
CHM1_1	19	37,309,707 - 37,342,149 (-)	NCBI
T2T-CHM13v2.0	19	39,493,114 - 39,526,474 (-)	NCBI

Sequence:

show sequence

AGTCCAGAAAGCGACAGGTTGCCGAAAGCTACAGCCCAGCCATCCCGATTCCCCTGGCGCGGACTCTGGCACCAACAAAACTATCTCTTTGAGCTCTGCTTTCCCAGCACGCTGCCTCACCAAGAAAG
AATCCAGAGAAGGACTGGTGGACTTGGAATGTTAAGTCATGGCCCATTTGATGATGTTCAGGGATGTGGCTGTAGATTTCTCTCAGGAGGAGTGGGAGTGCCTGGACCTGGAACAGAGGGATTTATAT
AGAGATGTGATGTTGGAGAACTACAGCAACATGGTCTCACTGGGTTTTTGCATTTATCAGCCAGAAGCGTTCTCTTTATTGGAGAAAGGGAAAGAGCCCTGGAAGATTTTGAGGGATGAGACAAGAGG
ACCTTGCCCAGACATGCAGTCGAGGTGTCAGACCAAGAAGTTATTACCAAAAAATGGCATTTTTGAGAGAGAAATAGCCCAATTGGAAATAATGAGAATTTGTAAAAACCACAGCCTTGACTGTTTAT
GTTTTAGAGGTGACTGGGAAGGCAACACTCAGTTTCAAACACTTCAAGATAATCAAGAGGAATGCTTCAAGCAGGTGATACGCACCTGTGAAAAAAGGCCCACTTTTAACCAGCATACAGTGTTTAAT
CTACACCAGAGACTTAATACAGGAGACAAACTGAATGAATTTAAAGAACTGGGGAAAGCCTTTATTTCTGGTTCAGATCATACTCAACATCAGTTAATTCACACAAGTGAGAAATTCTGTGGAGATAA
AGAATGTGGGAATACCTTTCTTCCTGATTCAGAAGTTATTCAATATCAGACAGTTCACACTGTTAAGAAAACATATGAATGTAAAGAATGTGGGAAGTCTTTTAGTTTACGTTCGAGTCTTACTGGTC
ATAAGAGAATTCATACCGGTGAGAAACCTTTTAAATGTAAGGATTGTGGGAAAGCCTTTAGATTTCATTCACAACTTAGTGTCCATAAGCGAATTCATACTGGTGAGAAATCTTATGAATGTAAGGAA
TGTGGGAAGGCCTTTAGTTGTGGCTCAGATCTTACTCGACATCAGAGAATTCATACTGGTGAAAAACCCTATGAATGTAATGAATGTAGAAAGGCCTTTAGTCAGCGATCACATCTTATTAAACATCA
GAGAATTCACACTGGTGAAAAACCTTATGAATGTAAGGAGTGTGGGAAAGCTTTTACTCGTGGATCACACCTAACTCAGCATCAGAGAATTCATACTGGTGAGAAATCTCATGAGTGTAAGGAATGTG
GAAAAGCCTTTATTCGTGGTTCAAATCTTGCTCAACATCAGAATGTTCATGTTGGTAGGAAACCTTATAAATGTGAGAAATGTGGGAAAGCCTATATTTGGAGCTCACACCTTGCTCGACATCAGCGA
ATTCATACTGGCAGGAAACCTTATGAATGTAAGCAATGCGGGAAGACTTTTACTTGGGCTTCGTATCTTGCTCAACATGAGAAAATTCACAATGAGAGGAAATCCTATGAATGTAAGGAATGTGGAAA
GACCTTTCTTCATGGCTCAGAGTTTAATCGACATCAGAAAATTCATACTGGTGAGAGAAACTATGAATGTAAGGAATGTGGAAAGACCTTTTTTCGTGGTTCAGAACTTAATCGACACCAGAAAATTC
ATACTGGAAAGAGGCCATATGAATGTGAAGAATGTGGAAAAGCCTTTCTCTGGGGTTCACAACTTACTCGACATCAGAGAATGCATACTGGTGAGGAACCTTACGTATGTAAAGAATGTGGGAAATCT
TTTATCTGGGGTTCACAGCTTACACGACATAAGAAAATTCATACTGATGCAGAACCTTATGGATGCAAGAAAAGTAGCCACATCTTTAGTCACCATTCATATTTTACTGAACAAAAAATTCATAATAG
TGCAAATCTCTGTGAATGGACAGACTATGGGAACACCTTTAGTCATGAGTCAAACTTTGCTCAACACCAGAATATTTACACTTTTGAGAAATCCTATGAATTTAAAGATTTTGAGAAAGCATTTTCTT
CAAGCTCTCACTTCATTTCACTCTTGTGAAATATTATATAAAAGTGTAGGAAGGGCTTTATTCATGACTCATTAATTGATGTCATTTATTTTTTTCTCTTGAGGAACACCACAAATGTAAGTAATATT
GGAAGGCATTTTAACAGAGCACACATCCAGCAGCAGCAGCAGCAGCAGCAGCAGAGAATTCATCATGCAATCAATATAGGAAAGAAATTACTGATCAGTTATCAATTGCAGAATATCAGGGTAAAATT
TTATGAGATAGCATGAATTCTTTTTGAATCATTCTCAAAACATTCTCATCAGAGATGTTGCATAAAGAATTTATATATAATTTGGCCAAGCATGGTGGCTCACACCTGTTATCCTAGCACTTTGGGAA
ACAGAGGTGGGTGGATCACCTGAGGTCAGGGGTTCGAGACCAGCCTGACCAACATGGTGAAACCCTGTCTCTACTAAATATACAAAAATTAGCCGGGCGTGGTAGCACACGCCTGTAGTCCCAGCTAC
TCGGGAGGCCGAGGCATGAGAATTCCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCAAGATCACATCACTGCACTCCAGCCTGGGTGATAGAACAAGACTCCATCTCAAAAACAAAAACCCACAAG
AATTTATATATAATTCATTTTGGAAATCTTTCATCATTAGCAAAATTCTGTTGTATTTCCACAAAAATCATGTAATTAATCTAGAAAAGCCTTGAACTATGTCATACAATTTATTTGGCATGTCTTGT
TTCAATACATCCTGCCTCTATTTTTTTTTTTTGGAAAGTATCTTAAATCTATGTCTGTTTAATCGTATTCATTAGATTATAAGGGTTGAATGATTTGAGATTTACATGACTTAGTGACTGTCATTTGT
ATTGGTATTAAGCCATTTTATGAGAGGAGGACTTTTAAGACTATAATGATTATAGACAAATATGTCATCTCTATTTATGTCTTACTGAACATCAGAATGTTAATTCTGAAAAAAAATCAGTAAAATAC
AATGAAGAAA

hide sequence

RefSeq Acc Id:

NM_001242801 ⟹ NP_001229730

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	36,817,428 - 36,850,285 (-)	NCBI
GRCh37	19	37,309,224 - 37,341,689 (-)	ENTREZGENE
HuRef	19	33,778,026 - 33,810,213 (-)	ENTREZGENE
CHM1_1	19	37,309,707 - 37,341,629 (-)	NCBI
T2T-CHM13v2.0	19	39,493,114 - 39,525,967 (-)	NCBI

Sequence:

show sequence

AAACGTAGTCCAAGCCTCGCCGGGGATAGATGGGCCCAACTAAAGTGTGCTGCGTTCTCTGGGT
CCTGAGGCGGCAGTCTGGCCGCAGTGACCAGACTAACTGTGCCCCGGAGGCTGCTTGGAATTCCACTTAACGCTGGAAGCACGCAGACGCTCTTGAGGCGGGCAGCTGCGTAGCGTGTGGAGGAGCCG
GGAGAGCGCACCCCAATGTGGCACCTGAGCGTCTGGGACCGAACCAGCATGGGGAGTCGGAAGGGGACAAATCCGCGATCCCAGTCATGCATCTCTGCTTTCCCAGCACGCTGCCTCACCAAGAAAGA
ATCCAGAGAAGGACTGGTGGACTTGGAATGTTAAGTCATGGCCCATTTGATGATGTTCAGGGATGTGGCTGTAGATTTCTCTCAGGAGGAGTGGGAGTGCCTGGACCTGGAACAGAGGGATTTATATA
GAGATGTGATGTTGGAGAACTACAGCAACATGGTCTCACTGGGTTTTTGCATTTATCAGCCAGAAGCGTTCTCTTTATTGGAGAAAGGGAAAGAGCCCTGGAAGATTTTGAGGGATGAGACAAGAGGA
CCTTGCCCAGACATGCAGTCGAGGTGTCAGACCAAGAAGTTATTACCAAAAAATGGCATTTTTGAGAGAGAAATAGCCCAATTGGAAATAATGAGAATTTGTAAAAACCACAGCCTTGACTGTTTATG
TTTTAGAGGTGACTGGGAAGGCAACACTCAGTTTCAAACACTTCAAGATAATCAAGAGGAATGCTTCAAGCAGGTGATACGCACCTGTGAAAAAAGGCCCACTTTTAACCAGCATACAGTGTTTAATC
TACACCAGAGACTTAATACAGGAGACAAACTGAATGAATTTAAAGAACTGGGGAAAGCCTTTATTTCTGGTTCAGATCATACTCAACATCAGTTAATTCACACAAGTGAGAAATTCTGTGGAGATAAA
GAATGTGGGAATACCTTTCTTCCTGATTCAGAAGTTATTCAATATCAGACAGTTCACACTGTTAAGAAAACATATGAATGTAAAGAATGTGGGAAGTCTTTTAGTTTACGTTCGAGTCTTACTGGTCA
TAAGAGAATTCATACCGGTGAGAAACCTTTTAAATGTAAGGATTGTGGGAAAGCCTTTAGATTTCATTCACAACTTAGTGTCCATAAGCGAATTCATACTGGTGAGAAATCTTATGAATGTAAGGAAT
GTGGGAAGGCCTTTAGTTGTGGCTCAGATCTTACTCGACATCAGAGAATTCATACTGGTGAAAAACCCTATGAATGTAATGAATGTAGAAAGGCCTTTAGTCAGCGATCACATCTTATTAAACATCAG
AGAATTCACACTGGTGAAAAACCTTATGAATGTAAGGAGTGTGGGAAAGCTTTTACTCGTGGATCACACCTAACTCAGCATCAGAGAATTCATACTGGTGAGAAATCTCATGAGTGTAAGGAATGTGG
AAAAGCCTTTATTCGTGGTTCAAATCTTGCTCAACATCAGAATGTTCATGTTGGTAGGAAACCTTATAAATGTGAGAAATGTGGGAAAGCCTATATTTGGAGCTCACACCTTGCTCGACATCAGCGAA
TTCATACTGGCAGGAAACCTTATGAATGTAAGCAATGCGGGAAGACTTTTACTTGGGCTTCGTATCTTGCTCAACATGAGAAAATTCACAATGAGAGGAAATCCTATGAATGTAAGGAATGTGGAAAG
ACCTTTCTTCATGGCTCAGAGTTTAATCGACATCAGAAAATTCATACTGGTGAGAGAAACTATGAATGTAAGGAATGTGGAAAGACCTTTTTTCGTGGTTCAGAACTTAATCGACACCAGAAAATTCA
TACTGGAAAGAGGCCATATGAATGTGAAGAATGTGGAAAAGCCTTTCTCTGGGGTTCACAACTTACTCGACATCAGAGAATGCATACTGGTGAGGAACCTTACGTATGTAAAGAATGTGGGAAATCTT
TTATCTGGGGTTCACAGCTTACACGACATAAGAAAATTCATACTGATGCAGAACCTTATGGATGCAAGAAAAGTAGCCACATCTTTAGTCACCATTCATATTTTACTGAACAAAAAATTCATAATAGT
GCAAATCTCTGTGAATGGACAGACTATGGGAACACCTTTAGTCATGAGTCAAACTTTGCTCAACACCAGAATATTTACACTTTTGAGAAATCCTATGAATTTAAAGATTTTGAGAAAGCATTTTCTTC
AAGCTCTCACTTCATTTCACTCTTGTGAAATATTATATAAAAGTGTAGGAAGGGCTTTATTCATGACTCATTAATTGATGTCATTTATTTTTTTCTCTTGAGGAACACCACAAATGTAAGTAATATTG
GAAGGCATTTTAACAGAGCACACATCCAGCAGCAGCAGCAGCAGCAGCAGCAGAGAATTCATCATGCAATCAATATAGGAAAGAAATTACTGATCAGTTATCAATTGCAGAATATCAGGGTAAAATTT
TATGAGATAGCATGAATTCTTTTTGAATCATTCTCAAAACATTCTCATCAGAGATGTTGCATAAAGAATTTATATATAATTTGGCCAAGCATGGTGGCTCACACCTGTTATCCTAGCACTTTGGGAAA
CAGAGGTGGGTGGATCACCTGAGGTCAGGGGTTCGAGACCAGCCTGACCAACATGGTGAAACCCTGTCTCTACTAAATATACAAAAATTAGCCGGGCGTGGTAGCACACGCCTGTAGTCCCAGCTACT
CGGGAGGCCGAGGCATGAGAATTCCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCAAGATCACATCACTGCACTCCAGCCTGGGTGATAGAACAAGACTCCATCTCAAAAACAAAAACCCACAAGA
ATTTATATATAATTCATTTTGGAAATCTTTCATCATTAGCAAAATTCTGTTGTATTTCCACAAAAATCATGTAATTAATCTAGAAAAGCCTTGAACTATGTCATACAATTTATTTGGCATGTCTTGTT
TCAATACATCCTGCCTCTATTTTTTTTTTTTGGAAAGTATCTTAAATCTATGTCTGTTTAATCGTATTCATTAGATTATAAGGGTTGAATGATTTGAGATTTACATGACTTAGTGACTGTCATTTGTA
TTGGTATTAAGCCATTTTATGAGAGGAGGACTTTTAAGACTATAATGATTATAGACAAATATGTCATCTCTATTTATGTCTTACTGAACATCAGAATGTTAATTCTGAAAAAAAATCAGTAAAATACA
ATGAAGAAA

hide sequence

RefSeq Acc Id:

NM_001242802 ⟹ NP_001229731

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	36,817,428 - 36,838,027 (-)	NCBI
GRCh37	19	37,309,224 - 37,341,689 (-)	ENTREZGENE
HuRef	19	33,778,026 - 33,810,213 (-)	ENTREZGENE
CHM1_1	19	37,309,707 - 37,329,411 (-)	NCBI
T2T-CHM13v2.0	19	39,493,114 - 39,513,707 (-)	NCBI

Sequence:

show sequence

ATGACTGCGTCGCGTTGTGCGTGACCACGTTCGTAAAGGTGGTGATAGCAGCCGCTATGGGGCC
AAAAACAAAGAATTGAGCTTTGCGTTGAGTGACAGGCATAGTCCTTCGTGAATGTGTGGGGAGCAGTTTTTGTGCTGGCCCGTAGCTGGATTGGAGTGGGGGCAACCTAGAAGGAGGGGAGAAGAATG
GGACACAGTGTAGACAACATAGTTCAAGAGTTTCTCCGTAAATTAGAGCAGAGAAATGGAGCAGCAGGTTGGGGTAGAGGGCTGGGGAAGACGGCTGGGGAACAACCACCCATCAACATGTTGTTGGA
AATGAGCCACGAGAGGGGGGAAAAGTCCAGGCAAGGCTCTGCTTTCCCAGCACGCTGCCTCACCAAGAAAGAATCCAGAGAAGGACTGGTGGACTTGGAATGTTAAGTCATGGCCCATTTGATGATGT
TCAGGGATGTGGCTGTAGATTTCTCTCAGGAGGAGTGGGAGTGCCTGGACCTGGAACAGAGGGATTTATATAGAGATGTGATGTTGGAGAACTACAGCAACATGGTCTCACTGGGTTTTTGCATTTAT
CAGCCAGAAGCGTTCTCTTTATTGGAGAAAGGGAAAGAGCCCTGGAAGATTTTGAGGGATGAGACAAGAGGACCTTGCCCAGACATGCAGTCGAGGTGTCAGACCAAGAAGTTATTACCAAAAAATGG
CATTTTTGAGAGAGAAATAGCCCAATTGGAAATAATGAGAATTTGTAAAAACCACAGCCTTGACTGTTTATGTTTTAGAGGTGACTGGGAAGGCAACACTCAGTTTCAAACACTTCAAGATAATCAAG
AGGAATGCTTCAAGCAGGTGATACGCACCTGTGAAAAAAGGCCCACTTTTAACCAGCATACAGTGTTTAATCTACACCAGAGACTTAATACAGGAGACAAACTGAATGAATTTAAAGAACTGGGGAAA
GCCTTTATTTCTGGTTCAGATCATACTCAACATCAGTTAATTCACACAAGTGAGAAATTCTGTGGAGATAAAGAATGTGGGAATACCTTTCTTCCTGATTCAGAAGTTATTCAATATCAGACAGTTCA
CACTGTTAAGAAAACATATGAATGTAAAGAATGTGGGAAGTCTTTTAGTTTACGTTCGAGTCTTACTGGTCATAAGAGAATTCATACCGGTGAGAAACCTTTTAAATGTAAGGATTGTGGGAAAGCCT
TTAGATTTCATTCACAACTTAGTGTCCATAAGCGAATTCATACTGGTGAGAAATCTTATGAATGTAAGGAATGTGGGAAGGCCTTTAGTTGTGGCTCAGATCTTACTCGACATCAGAGAATTCATACT
GGTGAAAAACCCTATGAATGTAATGAATGTAGAAAGGCCTTTAGTCAGCGATCACATCTTATTAAACATCAGAGAATTCACACTGGTGAAAAACCTTATGAATGTAAGGAGTGTGGGAAAGCTTTTAC
TCGTGGATCACACCTAACTCAGCATCAGAGAATTCATACTGGTGAGAAATCTCATGAGTGTAAGGAATGTGGAAAAGCCTTTATTCGTGGTTCAAATCTTGCTCAACATCAGAATGTTCATGTTGGTA
GGAAACCTTATAAATGTGAGAAATGTGGGAAAGCCTATATTTGGAGCTCACACCTTGCTCGACATCAGCGAATTCATACTGGCAGGAAACCTTATGAATGTAAGCAATGCGGGAAGACTTTTACTTGG
GCTTCGTATCTTGCTCAACATGAGAAAATTCACAATGAGAGGAAATCCTATGAATGTAAGGAATGTGGAAAGACCTTTCTTCATGGCTCAGAGTTTAATCGACATCAGAAAATTCATACTGGTGAGAG
AAACTATGAATGTAAGGAATGTGGAAAGACCTTTTTTCGTGGTTCAGAACTTAATCGACACCAGAAAATTCATACTGGAAAGAGGCCATATGAATGTGAAGAATGTGGAAAAGCCTTTCTCTGGGGTT
CACAACTTACTCGACATCAGAGAATGCATACTGGTGAGGAACCTTACGTATGTAAAGAATGTGGGAAATCTTTTATCTGGGGTTCACAGCTTACACGACATAAGAAAATTCATACTGATGCAGAACCT
TATGGATGCAAGAAAAGTAGCCACATCTTTAGTCACCATTCATATTTTACTGAACAAAAAATTCATAATAGTGCAAATCTCTGTGAATGGACAGACTATGGGAACACCTTTAGTCATGAGTCAAACTT
TGCTCAACACCAGAATATTTACACTTTTGAGAAATCCTATGAATTTAAAGATTTTGAGAAAGCATTTTCTTCAAGCTCTCACTTCATTTCACTCTTGTGAAATATTATATAAAAGTGTAGGAAGGGCT
TTATTCATGACTCATTAATTGATGTCATTTATTTTTTTCTCTTGAGGAACACCACAAATGTAAGTAATATTGGAAGGCATTTTAACAGAGCACACATCCAGCAGCAGCAGCAGCAGCAGCAGCAGAGA
ATTCATCATGCAATCAATATAGGAAAGAAATTACTGATCAGTTATCAATTGCAGAATATCAGGGTAAAATTTTATGAGATAGCATGAATTCTTTTTGAATCATTCTCAAAACATTCTCATCAGAGATG
TTGCATAAAGAATTTATATATAATTTGGCCAAGCATGGTGGCTCACACCTGTTATCCTAGCACTTTGGGAAACAGAGGTGGGTGGATCACCTGAGGTCAGGGGTTCGAGACCAGCCTGACCAACATGG
TGAAACCCTGTCTCTACTAAATATACAAAAATTAGCCGGGCGTGGTAGCACACGCCTGTAGTCCCAGCTACTCGGGAGGCCGAGGCATGAGAATTCCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGC
CAAGATCACATCACTGCACTCCAGCCTGGGTGATAGAACAAGACTCCATCTCAAAAACAAAAACCCACAAGAATTTATATATAATTCATTTTGGAAATCTTTCATCATTAGCAAAATTCTGTTGTATT
TCCACAAAAATCATGTAATTAATCTAGAAAAGCCTTGAACTATGTCATACAATTTATTTGGCATGTCTTGTTTCAATACATCCTGCCTCTATTTTTTTTTTTTGGAAAGTATCTTAAATCTATGTCTG
TTTAATCGTATTCATTAGATTATAAGGGTTGAATGATTTGAGATTTACATGACTTAGTGACTGTCATTTGTATTGGTATTAAGCCATTTTATGAGAGGAGGACTTTTAAGACTATAATGATTATAGAC
AAATATGTCATCTCTATTTATGTCTTACTGAACATCAGAATGTTAATTCTGAAAAAAAATCAGTAAAATACAATGAAGAAA

hide sequence

RefSeq Acc Id:

NM_206894 ⟹ NP_996777

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	36,817,428 - 36,838,387 (-)	NCBI
GRCh37	19	37,309,224 - 37,341,689 (-)	ENTREZGENE
Build 36	19	42,000,170 - 42,021,124 (-)	NCBI Archive
Celera	19	34,092,627 - 34,113,574 (-)	RGD
HuRef	19	33,778,026 - 33,810,213 (-)	ENTREZGENE
CHM1_1	19	37,309,707 - 37,329,766 (-)	NCBI
T2T-CHM13v2.0	19	39,493,114 - 39,514,065 (-)	NCBI

Sequence:

show sequence

GTTAATAGAAAGATCGCGGAACCTTCCACCATCAAGGGACCGCAGGGCCGGCTCTGCTTTCCCAGCACGCTGCCTCACCAAGAAAGAATCCAGAGAAGGACTGGTGGACTTGGAATGTTAAGTCATGG
CCCATTTGATGATGTTCAGGGATGTGGCTGTAGATTTCTCTCAGGAGGAGTGGGAGTGCCTGGACCTGGAACAGAGGGATTTATATAGAGATGTGATGTTGGAGAACTACAGCAACATGGTCTCACTG
GGTTTTTGCATTTATCAGCCAGAAGCGTTCTCTTTATTGGAGAAAGGGAAAGAGCCCTGGAAGATTTTGAGGGATGAGACAAGAGGACCTTGCCCAGACATGCAGTCGAGGTGTCAGACCAAGAAGTT
ATTACCAAAAAATGGCATTTTTGAGAGAGAAATAGCCCAATTGGAAATAATGAGAATTTGTAAAAACCACAGCCTTGACTGTTTATGTTTTAGAGGTGACTGGGAAGGCAACACTCAGTTTCAAACAC
TTCAAGATAATCAAGAGGAATGCTTCAAGCAGGTGATACGCACCTGTGAAAAAAGGCCCACTTTTAACCAGCATACAGTGTTTAATCTACACCAGAGACTTAATACAGGAGACAAACTGAATGAATTT
AAAGAACTGGGGAAAGCCTTTATTTCTGGTTCAGATCATACTCAACATCAGTTAATTCACACAAGTGAGAAATTCTGTGGAGATAAAGAATGTGGGAATACCTTTCTTCCTGATTCAGAAGTTATTCA
ATATCAGACAGTTCACACTGTTAAGAAAACATATGAATGTAAAGAATGTGGGAAGTCTTTTAGTTTACGTTCGAGTCTTACTGGTCATAAGAGAATTCATACCGGTGAGAAACCTTTTAAATGTAAGG
ATTGTGGGAAAGCCTTTAGATTTCATTCACAACTTAGTGTCCATAAGCGAATTCATACTGGTGAGAAATCTTATGAATGTAAGGAATGTGGGAAGGCCTTTAGTTGTGGCTCAGATCTTACTCGACAT
CAGAGAATTCATACTGGTGAAAAACCCTATGAATGTAATGAATGTAGAAAGGCCTTTAGTCAGCGATCACATCTTATTAAACATCAGAGAATTCACACTGGTGAAAAACCTTATGAATGTAAGGAGTG
TGGGAAAGCTTTTACTCGTGGATCACACCTAACTCAGCATCAGAGAATTCATACTGGTGAGAAATCTCATGAGTGTAAGGAATGTGGAAAAGCCTTTATTCGTGGTTCAAATCTTGCTCAACATCAGA
ATGTTCATGTTGGTAGGAAACCTTATAAATGTGAGAAATGTGGGAAAGCCTATATTTGGAGCTCACACCTTGCTCGACATCAGCGAATTCATACTGGCAGGAAACCTTATGAATGTAAGCAATGCGGG
AAGACTTTTACTTGGGCTTCGTATCTTGCTCAACATGAGAAAATTCACAATGAGAGGAAATCCTATGAATGTAAGGAATGTGGAAAGACCTTTCTTCATGGCTCAGAGTTTAATCGACATCAGAAAAT
TCATACTGGTGAGAGAAACTATGAATGTAAGGAATGTGGAAAGACCTTTTTTCGTGGTTCAGAACTTAATCGACACCAGAAAATTCATACTGGAAAGAGGCCATATGAATGTGAAGAATGTGGAAAAG
CCTTTCTCTGGGGTTCACAACTTACTCGACATCAGAGAATGCATACTGGTGAGGAACCTTACGTATGTAAAGAATGTGGGAAATCTTTTATCTGGGGTTCACAGCTTACACGACATAAGAAAATTCAT
ACTGATGCAGAACCTTATGGATGCAAGAAAAGTAGCCACATCTTTAGTCACCATTCATATTTTACTGAACAAAAAATTCATAATAGTGCAAATCTCTGTGAATGGACAGACTATGGGAACACCTTTAG
TCATGAGTCAAACTTTGCTCAACACCAGAATATTTACACTTTTGAGAAATCCTATGAATTTAAAGATTTTGAGAAAGCATTTTCTTCAAGCTCTCACTTCATTTCACTCTTGTGAAATATTATATAAA
AGTGTAGGAAGGGCTTTATTCATGACTCATTAATTGATGTCATTTATTTTTTTCTCTTGAGGAACACCACAAATGTAAGTAATATTGGAAGGCATTTTAACAGAGCACACATCCAGCAGCAGCAGCAG
CAGCAGCAGCAGAGAATTCATCATGCAATCAATATAGGAAAGAAATTACTGATCAGTTATCAATTGCAGAATATCAGGGTAAAATTTTATGAGATAGCATGAATTCTTTTTGAATCATTCTCAAAACA
TTCTCATCAGAGATGTTGCATAAAGAATTTATATATAATTTGGCCAAGCATGGTGGCTCACACCTGTTATCCTAGCACTTTGGGAAACAGAGGTGGGTGGATCACCTGAGGTCAGGGGTTCGAGACCA
GCCTGACCAACATGGTGAAACCCTGTCTCTACTAAATATACAAAAATTAGCCGGGCGTGGTAGCACACGCCTGTAGTCCCAGCTACTCGGGAGGCCGAGGCATGAGAATTCCTTGAACCTGGGAGGTG
GAGGTTGCAGTGAGCCAAGATCACATCACTGCACTCCAGCCTGGGTGATAGAACAAGACTCCATCTCAAAAACAAAAACCCACAAGAATTTATATATAATTCATTTTGGAAATCTTTCATCATTAGCA
AAATTCTGTTGTATTTCCACAAAAATCATGTAATTAATCTAGAAAAGCCTTGAACTATGTCATACAATTTATTTGGCATGTCTTGTTTCAATACATCCTGCCTCTATTTTTTTTTTTTGGAAAGTATC
TTAAATCTATGTCTGTTTAATCGTATTCATTAGATTATAAGGGTTGAATGATTTGAGATTTACATGACTTAGTGACTGTCATTTGTATTGGTATTAAGCCATTTTATGAGAGGAGGACTTTTAAGACT
ATAATGATTATAGACAAATATGTCATCTCTATTTATGTCTTACTGAACATCAGAATGTTAATTCTGAAAAAAAATCAGTAAAATACAATGAAGAAA

hide sequence

RefSeq Acc Id:

XM_005258903 ⟹ XP_005258960

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	36,817,428 - 36,838,701 (-)	NCBI
GRCh37	19	37,309,224 - 37,341,689 (-)	NCBI

Sequence:

show sequence

TTGGAGGATGGGAATAAGGTATTAGGAAGAGTTCTCATGGATTCCCAGACAGGGTACCCCTATAGGGCTGGGCATGTAGCTGTGTCCCATGGATCGTTTCCCCTTCGTTCTATCCCAGGCTGGTACTT
GTGGGACAAGAGGTGTCCACCCAGCCGGGCCGAGGCTCGGGCAGAGACGGGACAGACTCGCCACTCGCTTGGCACAGTCTTGTAGGACTTTCCCGCCATGCCACATAGGTCAGAGGCCCACGCAGCGA
GCTCCTACTGAAAACCATCGCACCATCCCCCCGGGGCATTTCTGCAGTGTTCCAGGCTCTGGACTACATTTCCCAGGGCCGTCGGGACCAAGGTTACTTCCAGCCTAAGATGGCCTGGGCTTACTGTC
CTGTTCCCAGGGCTGGGAGCCTTTTGCAGAGCTCTGCTTTCCCAGCACGCTGCCTCACCAAGAAAGAATCCAGAGAAGGACTGGTGGACTTGGAATGTTAAGTCATGGCCCATTTGATGATGTTCAGG
GATGTGGCTGTAGATTTCTCTCAGGAGGAGTGGGAGTGCCTGGACCTGGAACAGAGGGATTTATATAGAGATGTGATGTTGGAGAACTACAGCAACATGGTCTCACTGGGTTTTTGCATTTATCAGCC
AGAAGCGTTCTCTTTATTGGAGAAAGGGAAAGAGCCCTGGAAGATTTTGAGGGATGAGACAAGAGGACCTTGCCCAGACATGCAGTCGAGGTGTCAGACCAAGAAGTTATTACCAAAAAATGGCATTT
TTGAGAGAGAAATAGCCCAATTGGAAATAATGAGAATTTGTAAAAACCACAGCCTTGACTGTTTATGTTTTAGAGGTGACTGGGAAGGCAACACTCAGTTTCAAACACTTCAAGATAATCAAGAGGAA
TGCTTCAAGCAGGTGATACGCACCTGTGAAAAAAGGCCCACTTTTAACCAGCATACAGTGTTTAATCTACACCAGAGACTTAATACAGGAGACAAACTGAATGAATTTAAAGAACTGGGGAAAGCCTT
TATTTCTGGTTCAGATCATACTCAACATCAGTTAATTCACACAAGTGAGAAATTCTGTGGAGATAAAGAATGTGGGAATACCTTTCTTCCTGATTCAGAAGTTATTCAATATCAGACAGTTCACACTG
TTAAGAAAACATATGAATGTAAAGAATGTGGGAAGTCTTTTAGTTTACGTTCGAGTCTTACTGGTCATAAGAGAATTCATACCGGTGAGAAACCTTTTAAATGTAAGGATTGTGGGAAAGCCTTTAGA
TTTCATTCACAACTTAGTGTCCATAAGCGAATTCATACTGGTGAGAAATCTTATGAATGTAAGGAATGTGGGAAGGCCTTTAGTTGTGGCTCAGATCTTACTCGACATCAGAGAATTCATACTGGTGA
AAAACCCTATGAATGTAATGAATGTAGAAAGGCCTTTAGTCAGCGATCACATCTTATTAAACATCAGAGAATTCACACTGGTGAAAAACCTTATGAATGTAAGGAGTGTGGGAAAGCTTTTACTCGTG
GATCACACCTAACTCAGCATCAGAGAATTCATACTGGTGAGAAATCTCATGAGTGTAAGGAATGTGGAAAAGCCTTTATTCGTGGTTCAAATCTTGCTCAACATCAGAATGTTCATGTTGGTAGGAAA
CCTTATAAATGTGAGAAATGTGGGAAAGCCTATATTTGGAGCTCACACCTTGCTCGACATCAGCGAATTCATACTGGCAGGAAACCTTATGAATGTAAGCAATGCGGGAAGACTTTTACTTGGGCTTC
GTATCTTGCTCAACATGAGAAAATTCACAATGAGAGGAAATCCTATGAATGTAAGGAATGTGGAAAGACCTTTCTTCATGGCTCAGAGTTTAATCGACATCAGAAAATTCATACTGGTGAGAGAAACT
ATGAATGTAAGGAATGTGGAAAGACCTTTTTTCGTGGTTCAGAACTTAATCGACACCAGAAAATTCATACTGGAAAGAGGCCATATGAATGTGAAGAATGTGGAAAAGCCTTTCTCTGGGGTTCACAA
CTTACTCGACATCAGAGAATGCATACTGGTGAGGAACCTTACGTATGTAAAGAATGTGGGAAATCTTTTATCTGGGGTTCACAGCTTACACGACATAAGAAAATTCATACTGATGCAGAACCTTATGG
ATGCAAGAAAAGTAGCCACATCTTTAGTCACCATTCATATTTTACTGAACAAAAAATTCATAATAGTGCAAATCTCTGTGAATGGACAGACTATGGGAACACCTTTAGTCATGAGTCAAACTTTGCTC
AACACCAGAATATTTACACTTTTGAGAAATCCTATGAATTTAAAGATTTTGAGAAAGCATTTTCTTCAAGCTCTCACTTCATTTCACTCTTGTGAAATATTATATAAAAGTGTAGGAAGGGCTTTATT
CATGACTCATTAATTGATGTCATTTATTTTTTTCTCTTGAGGAACACCACAAATGTAAGTAATATTGGAAGGCATTTTAACAGAGCACACATCCAGCAGCAGCAGCAGCAGCAGCAGCAGAGAATTCA
TCATGCAATCAATATAGGAAAGAAATTACTGATCAGTTATCAATTGCAGAATATCAGGGTAAAATTTTATGAGATAGCATGAATTCTTTTTGAATCATTCTCAAAACATTCTCATCAGAGATGTTGCA
TAAAGAATTTATATATAATTTGGCCAAGCATGGTGGCTCACACCTGTTATCCTAGCACTTTGGGAAACAGAGGTGGGTGGATCACCTGAGGTCAGGGGTTCGAGACCAGCCTGACCAACATGGTGAAA
CCCTGTCTCTACTAAATATACAAAAATTAGCCGGGCGTGGTAGCACACGCCTGTAGTCCCAGCTACTCGGGAGGCCGAGGCATGAGAATTCCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCAAGA
TCACATCACTGCACTCCAGCCTGGGTGATAGAACAAGACTCCATCTCAAAAACAAAAACCCACAAGAATTTATATATAATTCATTTTGGAAATCTTTCATCATTAGCAAAATTCTGTTGTATTTCCAC
AAAAATCATGTAATTAATCTAGAAAAGCCTTGAACTATGTCATACAATTTATTTGGCATGTCTTGTTTCAATACATCCTGCCTCTATTTTTTTTTTTTGGAAAGTATCTTAAATCTATGTCTGTTTAA
TCGTATTCATTAGATTATAAGGGTTGAATGATTTGAGATTTACATGACTTAGTGACTGTCATTTGTATTGGTATTAAGCCATTTTATGAGAGGAGGACTTTTAAGACTATAATGATTATAGACAAATA
TGTCATCTCTATTTATGTCTTACTGAACATCAGAATGTTAATTCTGAAAAAAAATCAGTAAAATACAATGAAGAAAGCTTTGAATATTAATTTCACATGCTACATCAAAAAAA

hide sequence

RefSeq Acc Id:

XM_011526950 ⟹ XP_011525252

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	36,817,428 - 36,838,701 (-)	NCBI

Sequence:

show sequence

GGCCTGGGCTTACTGTCCTGTTCCCAGGGCTGGGAGCCTTTTGCAGAGGTAGGGCAGCCTGCATGCCTCCGCTGAAGCTTCCTAAACGCGGCCTGGAATTCTGGAAGCTCTCGGCAGCAGATGTGAGC
GCTCTGCTTTCCCAGCACGCTGCCTCACCAAGAAAGAATCCAGAGAAGGACTGGTGGACTTGGAATGTTAAGTCATGGCCCATTTGATGATGTTCAGGGATGTGGCTGTAGATTTCTCTCAGGAGGAG
TGGGAGTGCCTGGACCTGGAACAGAGGGATTTATATAGAGATGTGATGTTGGAGAACTACAGCAACATGGTCTCACTGGGTTTTTGCATTTATCAGCCAGAAGCGTTCTCTTTATTGGAGAAAGGGAA
AGAGCCCTGGAAGATTTTGAGGGATGAGACAAGAGGACCTTGCCCAGACATGCAGTCGAGGTGTCAGACCAAGAAGTTATTACCAAAAAATGGCATTTTTGAGAGAGAAATAGCCCAATTGGAAATAA
TGAGAATTTGTAAAAACCACAGCCTTGACTGTTTATGTTTTAGAGGTGACTGGGAAGGCAACACTCAGTTTCAAACACTTCAAGATAATCAAGAGGAATGCTTCAAGCAGGTGATACGCACCTGTGAA
AAAAGGCCCACTTTTAACCAGCATACAGTGTTTAATCTACACCAGAGACTTAATACAGGAGACAAACTGAATGAATTTAAAGAACTGGGGAAAGCCTTTATTTCTGGTTCAGATCATACTCAACATCA
GTTAATTCACACAAGTGAGAAATTCTGTGGAGATAAAGAATGTGGGAATACCTTTCTTCCTGATTCAGAAGTTATTCAATATCAGACAGTTCACACTGTTAAGAAAACATATGAATGTAAAGAATGTG
GGAAGTCTTTTAGTTTACGTTCGAGTCTTACTGGTCATAAGAGAATTCATACCGGTGAGAAACCTTTTAAATGTAAGGATTGTGGGAAAGCCTTTAGATTTCATTCACAACTTAGTGTCCATAAGCGA
ATTCATACTGGTGAGAAATCTTATGAATGTAAGGAATGTGGGAAGGCCTTTAGTTGTGGCTCAGATCTTACTCGACATCAGAGAATTCATACTGGTGAAAAACCCTATGAATGTAATGAATGTAGAAA
GGCCTTTAGTCAGCGATCACATCTTATTAAACATCAGAGAATTCACACTGGTGAAAAACCTTATGAATGTAAGGAGTGTGGGAAAGCTTTTACTCGTGGATCACACCTAACTCAGCATCAGAGAATTC
ATACTGGTGAGAAATCTCATGAGTGTAAGGAATGTGGAAAAGCCTTTATTCGTGGTTCAAATCTTGCTCAACATCAGAATGTTCATGTTGGTAGGAAACCTTATAAATGTGAGAAATGTGGGAAAGCC
TATATTTGGAGCTCACACCTTGCTCGACATCAGCGAATTCATACTGGCAGGAAACCTTATGAATGTAAGCAATGCGGGAAGACTTTTACTTGGGCTTCGTATCTTGCTCAACATGAGAAAATTCACAA
TGAGAGGAAATCCTATGAATGTAAGGAATGTGGAAAGACCTTTCTTCATGGCTCAGAGTTTAATCGACATCAGAAAATTCATACTGGTGAGAGAAACTATGAATGTAAGGAATGTGGAAAGACCTTTT
TTCGTGGTTCAGAACTTAATCGACACCAGAAAATTCATACTGGAAAGAGGCCATATGAATGTGAAGAATGTGGAAAAGCCTTTCTCTGGGGTTCACAACTTACTCGACATCAGAGAATGCATACTGGT
GAGGAACCTTACGTATGTAAAGAATGTGGGAAATCTTTTATCTGGGGTTCACAGCTTACACGACATAAGAAAATTCATACTGATGCAGAACCTTATGGATGCAAGAAAAGTAGCCACATCTTTAGTCA
CCATTCATATTTTACTGAACAAAAAATTCATAATAGTGCAAATCTCTGTGAATGGACAGACTATGGGAACACCTTTAGTCATGAGTCAAACTTTGCTCAACACCAGAATATTTACACTTTTGAGAAAT
CCTATGAATTTAAAGATTTTGAGAAAGCATTTTCTTCAAGCTCTCACTTCATTTCACTCTTGTGAAATATTATATAAAAGTGTAGGAAGGGCTTTATTCATGACTCATTAATTGATGTCATTTATTTT
TTTCTCTTGAGGAACACCACAAATGTAAGTAATATTGGAAGGCATTTTAACAGAGCACACATCCAGCAGCAGCAGCAGCAGCAGCAGCAGAGAATTCATCATGCAATCAATATAGGAAAGAAATTACT
GATCAGTTATCAATTGCAGAATATCAGGGTAAAATTTTATGAGATAGCATGAATTCTTTTTGAATCATTCTCAAAACATTCTCATCAGAGATGTTGCATAAAGAATTTATATATAATTTGGCCAAGCA
TGGTGGCTCACACCTGTTATCCTAGCACTTTGGGAAACAGAGGTGGGTGGATCACCTGAGGTCAGGGGTTCGAGACCAGCCTGACCAACATGGTGAAACCCTGTCTCTACTAAATATACAAAAATTAG
CCGGGCGTGGTAGCACACGCCTGTAGTCCCAGCTACTCGGGAGGCCGAGGCATGAGAATTCCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCAAGATCACATCACTGCACTCCAGCCTGGGTGATA
GAACAAGACTCCATCTCAAAAACAAAAACCCACAAGAATTTATATATAATTCATTTTGGAAATCTTTCATCATTAGCAAAATTCTGTTGTATTTCCACAAAAATCATGTAATTAATCTAGAAAAGCCT
TGAACTATGTCATACAATTTATTTGGCATGTCTTGTTTCAATACATCCTGCCTCTATTTTTTTTTTTTGGAAAGTATCTTAAATCTATGTCTGTTTAATCGTATTCATTAGATTATAAGGGTTGAATG
ATTTGAGATTTACATGACTTAGTGACTGTCATTTGTATTGGTATTAAGCCATTTTATGAGAGGAGGACTTTTAAGACTATAATGATTATAGACAAATATGTCATCTCTATTTATGTCTTACTGAACAT
CAGAATGTTAATTCTGAAAAAAAATCAGTAAAATACAATGAAGAAAGCTTTGAATATTAATTTCACATGCTACATCAAAAAAA

hide sequence

RefSeq Acc Id:

XM_047438798 ⟹ XP_047294754

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	36,817,428 - 36,823,992 (-)	NCBI

RefSeq Acc Id:

XM_047438799 ⟹ XP_047294755

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	36,817,428 - 36,838,701 (-)	NCBI

RefSeq Acc Id:

XM_047438800 ⟹ XP_047294756

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	36,817,428 - 36,847,113 (-)	NCBI

RefSeq Acc Id:

XM_047438801 ⟹ XP_047294757

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	36,817,428 - 36,838,387 (-)	NCBI

RefSeq Acc Id:

XM_054320953 ⟹ XP_054176928

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	39,493,114 - 39,499,672 (-)	NCBI

RefSeq Acc Id:

XM_054320954 ⟹ XP_054176929

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	39,493,114 - 39,514,386 (-)	NCBI

RefSeq Acc Id:

XM_054320955 ⟹ XP_054176930

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	39,493,114 - 39,514,387 (-)	NCBI

RefSeq Acc Id:

XM_054320956 ⟹ XP_054176931

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	39,493,114 - 39,514,368 (-)	NCBI

RefSeq Acc Id:

XM_054320957 ⟹ XP_054176932

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	39,493,114 - 39,522,794 (-)	NCBI

RefSeq Acc Id:

XM_054320958 ⟹ XP_054176933

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	39,493,114 - 39,514,033 (-)	NCBI


Protein RefSeqs	NP_001229729	(Get FASTA)	NCBI Sequence Viewer
	NP_001229730	(Get FASTA)	NCBI Sequence Viewer
	NP_001229731	(Get FASTA)	NCBI Sequence Viewer
	NP_996777	(Get FASTA)	NCBI Sequence Viewer
	XP_005258960	(Get FASTA)	NCBI Sequence Viewer
	XP_011525252	(Get FASTA)	NCBI Sequence Viewer
	XP_047294754	(Get FASTA)	NCBI Sequence Viewer
	XP_047294755	(Get FASTA)	NCBI Sequence Viewer
	XP_047294756	(Get FASTA)	NCBI Sequence Viewer
	XP_047294757	(Get FASTA)	NCBI Sequence Viewer
	XP_054176928	(Get FASTA)	NCBI Sequence Viewer
	XP_054176929	(Get FASTA)	NCBI Sequence Viewer
	XP_054176930	(Get FASTA)	NCBI Sequence Viewer
	XP_054176931	(Get FASTA)	NCBI Sequence Viewer
	XP_054176932	(Get FASTA)	NCBI Sequence Viewer
	XP_054176933	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH57245	(Get FASTA)	NCBI Sequence Viewer
	BAG59895	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000349161
	ENSP00000349161.3
	ENSP00000478852
	ENSP00000478852.1
	ENSP00000480764
	ENSP00000480764.1
	ENSP00000480834
	ENSP00000480834.1
GenBank Protein	Q6PG37	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:

NP_996777 ⟸ NM_206894

- UniProtKB:

Q6PG37 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MAHLMMFRDVAVDFSQEEWECLDLEQRDLYRDVMLENYSNMVSLGFCIYQPEAFSLLEKGKEPWKILRDETRGPCPDMQSRCQTKKLLPKNGIFEREIAQLEIMRICKNHSLDCLCFRGDWEGNTQFQ
TLQDNQEECFKQVIRTCEKRPTFNQHTVFNLHQRLNTGDKLNEFKELGKAFISGSDHTQHQLIHTSEKFCGDKECGNTFLPDSEVIQYQTVHTVKKTYECKECGKSFSLRSSLTGHKRIHTGEKPFKC
KDCGKAFRFHSQLSVHKRIHTGEKSYECKECGKAFSCGSDLTRHQRIHTGEKPYECNECRKAFSQRSHLIKHQRIHTGEKPYECKECGKAFTRGSHLTQHQRIHTGEKSHECKECGKAFIRGSNLAQH
QNVHVGRKPYKCEKCGKAYIWSSHLARHQRIHTGRKPYECKQCGKTFTWASYLAQHEKIHNERKSYECKECGKTFLHGSEFNRHQKIHTGERNYECKECGKTFFRGSELNRHQKIHTGKRPYECEECG
KAFLWGSQLTRHQRMHTGEEPYVCKECGKSFIWGSQLTRHKKIHTDAEPYGCKKSSHIFSHHSYFTEQKIHNSANLCEWTDYGNTFSHESNFAQHQNIYTFEKSYEFKDFEKAFSSSSHFISLL

hide sequence

RefSeq Acc Id:

NP_001229729 ⟸ NM_001242800

- UniProtKB:

Q6PG37 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MAHLMMFRDVAVDFSQEEWECLDLEQRDLYRDVMLENYSNMVSLGFCIYQPEAFSLLEKGKEPWKILRDETRGPCPDMQSRCQTKKLLPKNGIFEREIAQLEIMRICKNHSLDCLCFRGDWEGNTQFQ
TLQDNQEECFKQVIRTCEKRPTFNQHTVFNLHQRLNTGDKLNEFKELGKAFISGSDHTQHQLIHTSEKFCGDKECGNTFLPDSEVIQYQTVHTVKKTYECKECGKSFSLRSSLTGHKRIHTGEKPFKC
KDCGKAFRFHSQLSVHKRIHTGEKSYECKECGKAFSCGSDLTRHQRIHTGEKPYECNECRKAFSQRSHLIKHQRIHTGEKPYECKECGKAFTRGSHLTQHQRIHTGEKSHECKECGKAFIRGSNLAQH
QNVHVGRKPYKCEKCGKAYIWSSHLARHQRIHTGRKPYECKQCGKTFTWASYLAQHEKIHNERKSYECKECGKTFLHGSEFNRHQKIHTGERNYECKECGKTFFRGSELNRHQKIHTGKRPYECEECG
KAFLWGSQLTRHQRMHTGEEPYVCKECGKSFIWGSQLTRHKKIHTDAEPYGCKKSSHIFSHHSYFTEQKIHNSANLCEWTDYGNTFSHESNFAQHQNIYTFEKSYEFKDFEKAFSSSSHFISLL

hide sequence

RefSeq Acc Id:

NP_001229730 ⟸ NM_001242801

- UniProtKB:

Q6PG37 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MAHLMMFRDVAVDFSQEEWECLDLEQRDLYRDVMLENYSNMVSLGFCIYQPEAFSLLEKGKEPWKILRDETRGPCPDMQSRCQTKKLLPKNGIFEREIAQLEIMRICKNHSLDCLCFRGDWEGNTQFQ
TLQDNQEECFKQVIRTCEKRPTFNQHTVFNLHQRLNTGDKLNEFKELGKAFISGSDHTQHQLIHTSEKFCGDKECGNTFLPDSEVIQYQTVHTVKKTYECKECGKSFSLRSSLTGHKRIHTGEKPFKC
KDCGKAFRFHSQLSVHKRIHTGEKSYECKECGKAFSCGSDLTRHQRIHTGEKPYECNECRKAFSQRSHLIKHQRIHTGEKPYECKECGKAFTRGSHLTQHQRIHTGEKSHECKECGKAFIRGSNLAQH
QNVHVGRKPYKCEKCGKAYIWSSHLARHQRIHTGRKPYECKQCGKTFTWASYLAQHEKIHNERKSYECKECGKTFLHGSEFNRHQKIHTGERNYECKECGKTFFRGSELNRHQKIHTGKRPYECEECG
KAFLWGSQLTRHQRMHTGEEPYVCKECGKSFIWGSQLTRHKKIHTDAEPYGCKKSSHIFSHHSYFTEQKIHNSANLCEWTDYGNTFSHESNFAQHQNIYTFEKSYEFKDFEKAFSSSSHFISLL

hide sequence

RefSeq Acc Id:

NP_001229731 ⟸ NM_001242802

- UniProtKB:

Q6PG37 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MAHLMMFRDVAVDFSQEEWECLDLEQRDLYRDVMLENYSNMVSLGFCIYQPEAFSLLEKGKEPWKILRDETRGPCPDMQSRCQTKKLLPKNGIFEREIAQLEIMRICKNHSLDCLCFRGDWEGNTQFQ
TLQDNQEECFKQVIRTCEKRPTFNQHTVFNLHQRLNTGDKLNEFKELGKAFISGSDHTQHQLIHTSEKFCGDKECGNTFLPDSEVIQYQTVHTVKKTYECKECGKSFSLRSSLTGHKRIHTGEKPFKC
KDCGKAFRFHSQLSVHKRIHTGEKSYECKECGKAFSCGSDLTRHQRIHTGEKPYECNECRKAFSQRSHLIKHQRIHTGEKPYECKECGKAFTRGSHLTQHQRIHTGEKSHECKECGKAFIRGSNLAQH
QNVHVGRKPYKCEKCGKAYIWSSHLARHQRIHTGRKPYECKQCGKTFTWASYLAQHEKIHNERKSYECKECGKTFLHGSEFNRHQKIHTGERNYECKECGKTFFRGSELNRHQKIHTGKRPYECEECG
KAFLWGSQLTRHQRMHTGEEPYVCKECGKSFIWGSQLTRHKKIHTDAEPYGCKKSSHIFSHHSYFTEQKIHNSANLCEWTDYGNTFSHESNFAQHQNIYTFEKSYEFKDFEKAFSSSSHFISLL

hide sequence

RefSeq Acc Id:	XP_005258960 ⟸ XM_005258903
- Peptide Label:	isoform X2
- UniProtKB:	Q6PG37 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAHLMMFRDVAVDFSQEEWECLDLEQRDLYRDVMLENYSNMVSLGFCIYQPEAFSLLEKGKEPWKILRDETRGPCPDMQSRCQTKKLLPKNGIFEREIAQLEIMRICKNHSLDCLCFRGDWEGNTQFQ TLQDNQEECFKQVIRTCEKRPTFNQHTVFNLHQRLNTGDKLNEFKELGKAFISGSDHTQHQLIHTSEKFCGDKECGNTFLPDSEVIQYQTVHTVKKTYECKECGKSFSLRSSLTGHKRIHTGEKPFKC KDCGKAFRFHSQLSVHKRIHTGEKSYECKECGKAFSCGSDLTRHQRIHTGEKPYECNECRKAFSQRSHLIKHQRIHTGEKPYECKECGKAFTRGSHLTQHQRIHTGEKSHECKECGKAFIRGSNLAQH QNVHVGRKPYKCEKCGKAYIWSSHLARHQRIHTGRKPYECKQCGKTFTWASYLAQHEKIHNERKSYECKECGKTFLHGSEFNRHQKIHTGERNYECKECGKTFFRGSELNRHQKIHTGKRPYECEECG KAFLWGSQLTRHQRMHTGEEPYVCKECGKSFIWGSQLTRHKKIHTDAEPYGCKKSSHIFSHHSYFTEQKIHNSANLCEWTDYGNTFSHESNFAQHQNIYTFEKSYEFKDFEKAFSSSSHFISLL hide sequence

Protein Domains

C2H2-type KRAB

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q6PG37-F1-model_v2	AlphaFold	Q6PG37	1-636	view protein structure

RGD ID:

6796428

Promoter ID:

HG_KWN:29756

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

NM_206894

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	19	42,020,691 - 42,021,191 (-)	MPROMDB

Database	Acc Id	Source(s)
COSMIC	ZNF790	COSMIC
Ensembl Genes	ENSG00000197863	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000356725	ENTREZGENE
	ENST00000356725.9	UniProtKB/Swiss-Prot
	ENST00000613249	ENTREZGENE
	ENST00000613249.4	UniProtKB/Swiss-Prot
	ENST00000614179	ENTREZGENE
	ENST00000614179.4	UniProtKB/Swiss-Prot
	ENST00000615484	ENTREZGENE
	ENST00000615484.4	UniProtKB/Swiss-Prot
Gene3D-CATH	6.10.140.140	UniProtKB/Swiss-Prot
	Classic Zinc Finger	UniProtKB/Swiss-Prot
GTEx	ENSG00000197863	GTEx
HGNC ID	HGNC:33114	ENTREZGENE
Human Proteome Map	ZNF790	Human Proteome Map
InterPro	KRAB	UniProtKB/Swiss-Prot
	KRAB_dom_sf	UniProtKB/Swiss-Prot
	Znf_C2H2_sf	UniProtKB/Swiss-Prot
	Znf_C2H2_type	UniProtKB/Swiss-Prot
KEGG Report	hsa:388536	UniProtKB/Swiss-Prot
NCBI Gene	388536	ENTREZGENE
PANTHER	ZINC FINGER PROTEIN	UniProtKB/Swiss-Prot
	ZINC FINGER PROTEIN 566	UniProtKB/Swiss-Prot
Pfam	KRAB	UniProtKB/Swiss-Prot
	zf-C2H2	UniProtKB/Swiss-Prot
PharmGKB	PA162410507	PharmGKB
PROSITE	KRAB	UniProtKB/Swiss-Prot
	ZINC_FINGER_C2H2_1	UniProtKB/Swiss-Prot
	ZINC_FINGER_C2H2_2	UniProtKB/Swiss-Prot
SMART	KRAB	UniProtKB/Swiss-Prot
	ZnF_C2H2	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF109640	UniProtKB/Swiss-Prot
	SSF57667	UniProtKB/Swiss-Prot
UniProt	B4DMI3_HUMAN	UniProtKB/TrEMBL
	E9PL27_HUMAN	UniProtKB/TrEMBL
	E9PQ03_HUMAN	UniProtKB/TrEMBL
	E9PRR6_HUMAN	UniProtKB/TrEMBL
	K7EQ58_HUMAN	UniProtKB/TrEMBL
	Q6PG37	ENTREZGENE, UniProtKB/Swiss-Prot

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


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


Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
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MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable

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