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Gene: ZNF135 (zinc finger protein 135) Homo sapiens

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Symbol:

ZNF135

Name:

zinc finger protein 135

RGD ID:

1349048

HGNC Page

HGNC:12919

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:

pHZ-17; pT3; zinc finger protein 135 (clone pHZ-17); zinc finger protein 61; zinc finger protein 78-like 1 (pT3); ZNF61; ZNF78L1

RGD Orthologs

Alliance Orthologs

More Info

more info ...

Related Pseudogenes:

ZNF840P ZNF859P

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	58,059,239 - 58,069,755 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	58,059,238 - 58,086,310 (+)	Ensembl		GRCh38.p14 Ensembl	hg38	GRCh38
GRCh37	19	58,570,607 - 58,581,123 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	63,262,424 - 63,272,588 (+)	NCBI	Build 36	Build 36	hg18	NCBI36
Build 34	19	63,262,423 - 63,272,585	NCBI
Celera	19	55,613,970 - 55,624,470 (+)	NCBI		Celera
Cytogenetic Map	19	q13.43	NCBI
HuRef	19	54,881,599 - 54,892,090 (+)	NCBI		HuRef
CHM1_1	19	58,564,299 - 58,574,790 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	19	61,156,060 - 61,166,554 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

Breast Cancer, Familial (IAGP)

cholangiocarcinoma (IAGP)

melanoma (IAGP)

nonpapillary renal cell carcinoma (IAGP)

Thyroid Carcinoma, Nonmedullary 1 (IAGP)

urinary bladder cancer (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

17beta-estradiol (EXP)

acrylamide (EXP)

benzo[a]pyrene (EXP)

bucladesine (EXP)

cadmium atom (EXP)

cadmium dichloride (EXP)

disodium selenite (EXP)

GSK-J4 (EXP)

medroxyprogesterone acetate (EXP)

niclosamide (EXP)

resveratrol (EXP)

sodium arsenite (EXP)

sunitinib (EXP)

triphenyl phosphate (EXP)

valproic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

negative regulation of DNA-templated transcription (IEA)

regulation of DNA-templated transcription (IEA)

regulation of transcription by RNA polymerase II (IBA)

Cellular Component

cytoplasm (IEA)

nucleus (IBA,IEA)

Molecular Function

DNA-binding transcription factor activity, RNA polymerase II-specific (IBA)

RNA polymerase II cis-regulatory region sequence-specific DNA binding (IBA)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Cholangiocarcinoma (IAGP)

Clear cell renal cell carcinoma (IAGP)

Melanoma (IAGP)

Papillary renal cell carcinoma type 1 (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:1505991	PMID:1946370	PMID:7557990	PMID:8478004	PMID:12477932	PMID:14702039	PMID:15146197	PMID:16344560	PMID:21834987	PMID:21873635	PMID:21900206	PMID:32296183
PMID:36138187

Genomics

Comparative Map Data

ZNF135
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	19	58,059,239 - 58,069,755 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	58,059,238 - 58,086,310 (+)	Ensembl		GRCh38.p14 Ensembl	hg38	GRCh38
GRCh37	19	58,570,607 - 58,581,123 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	63,262,424 - 63,272,588 (+)	NCBI	Build 36	Build 36	hg18	NCBI36
Build 34	19	63,262,423 - 63,272,585	NCBI
Celera	19	55,613,970 - 55,624,470 (+)	NCBI		Celera
Cytogenetic Map	19	q13.43	NCBI
HuRef	19	54,881,599 - 54,892,090 (+)	NCBI		HuRef
CHM1_1	19	58,564,299 - 58,574,790 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	19	61,156,060 - 61,166,554 (+)	NCBI		T2T-CHM13v2.0

Znf135
(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_004955584	837,288 - 844,651 (+)	NCBI	ChiLan1.0	ChiLan1.0

ZNF135
(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	64,333,943 - 64,348,759 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	19	66,126,508 - 66,136,997 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	19	55,071,083 - 55,081,392 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	19	63,898,314 - 63,908,261 (+)	NCBI	PanPan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	19	63,898,314 - 63,908,261 (+)	Ensembl		PanPan1.1 Ensembl	panPan2	panpan1.1

ZNF135
(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	99,820,281 - 99,829,560 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	1	99,819,583 - 99,828,898 (-)	Ensembl		CanFam3.1 Ensembl	canFam3	CanFam3.1
Dog10K_Boxer_Tasha	1	100,214,152 - 100,223,223 (-)	NCBI	Dog10K_Boxer_Tasha	Dog10K_Boxer_Tasha
ROS_Cfam_1.0	1	100,460,147 - 100,469,219 (-)	NCBI	ROS_Cfam_1.0	ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	1	100,460,151 - 100,469,899 (-)	Ensembl				ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	1	100,105,311 - 100,114,381 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	1	99,817,633 - 99,826,699 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	1	100,572,804 - 100,581,877 (-)	NCBI	UU_Cfam_GSD_1.0	UU_Cfam_GSD_1.0

Znf135
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
mIctTri1.hap1	15	641,348 - 645,712 (+)	NCBI		mIctTri1.hap1

ZNF135
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	6	62,754,353 - 62,768,964 (+)	Ensembl		Sscrofa11.1 Ensembl	susScr11	Sscrofa11.1
Sscrofa11.1	6	62,754,034 - 62,769,561 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	6	57,351,839 - 57,364,765 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

ZNF135
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
mChlSab1.0.hap1	6	562,970 - 575,710 (-)	NCBI		mChlSab1.0.hap1
Vero_WHO_p1.0	NW_023666045	3,626,749 - 3,637,660 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0
ChlSab1.1	6	50,365,727 - 50,381,013 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2

Variants

Variants in ZNF135
70 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3	copy number gain	Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000050883]	Chr19:19q13.33-13.43	pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3	copy number gain	Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000052925]	Chr19:19q13.33-13.43	pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3	copy number gain	See cases [RCV000052926]	Chr19:19q13.41-13.43	pathogenic
GRCh38/hg38 19q13.43(chr19:56363208-58581203)x3	copy number gain	Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000052927]	Chr19:19q13.43	pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3	copy number gain	Failure to thrive [RCV000052915]	Chr19:19q13.33-13.43	pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52612432-58581203)x3	copy number gain	See cases [RCV000134174]	Chr19:19q13.41-13.43	pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52955056-58581203)x3	copy number gain	See cases [RCV000134139]	Chr19:19q13.41-13.43	pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3	copy number gain	Abnormal facial shape [RCV000135843]	Chr19:19q13.33-13.43	pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52143873-58445521)x3	copy number gain	See cases [RCV000142008]	Chr19:19q13.41-13.43	pathogenic
GRCh38/hg38 19q13.43(chr19:56353449-58445521)x3	copy number gain	See cases [RCV000141900]	Chr19:19q13.43	uncertain significance
GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3	copy number gain	Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000052914]	Chr19:19q13.33-13.43	pathogenic
GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3	copy number gain	See cases [RCV000445925]	Chr19:19q13.33-13.43	pathogenic
GRCh37/hg19 19q13.42-13.43(chr19:54344821-58956888)x3	copy number gain	See cases [RCV000448186]	Chr19:54344821..58956888 [GRCh37] Chr19:19q13.42-13.43	pathogenic
GRCh37/hg19 19q13.43(chr19:56706500-58956888)x3	copy number gain	Autism [RCV000512396]	Chr19:19q13.43	uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	copy number gain	Ventricular septal defect [RCV000511289]	Chr19:19p13.3-q13.43	pathogenic\|uncertain significance
NM_001289401.2(ZNF135):c.1427G>A (p.Arg476Gln)	single nucleotide variant	not specified [RCV004333129]	Chr19:58067911 [GRCh38] Chr19:58579279 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.712G>A (p.Gly238Arg)	single nucleotide variant	not specified [RCV004318398]	Chr19:58067196 [GRCh38] Chr19:58578564 [GRCh37] Chr19:19q13.43	uncertain significance
GRCh37/hg19 19q13.43(chr19:58458999-58929684)x3	copy number gain	See Cases [RCV000240566]	Chr19:19q13.43	uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	copy number gain	Abnormality of the ear [RCV000512296]	Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19q13.42-13.43(chr19:54196216-58759679)x3	copy number gain	not provided [RCV000684095]	Chr19:19q13.42-13.43	pathogenic
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
GRCh37/hg19 19q13.33-13.43(chr19:50740074-59097160)x3	copy number gain	not provided [RCV000740208]	Chr19:50740074..59097160 [GRCh37] Chr19:19q13.33-13.43	pathogenic
NM_001289401.2(ZNF135):c.1158G>A (p.Glu386=)	single nucleotide variant	not provided [RCV000898928]	Chr19:58067642 [GRCh38] Chr19:58579010 [GRCh37] Chr19:19q13.43	likely benign
NM_001289401.2(ZNF135):c.-58G>C	single nucleotide variant	not provided [RCV000900398]	Chr19:58059287 [GRCh38] Chr19:58570655 [GRCh37] Chr19:19q13.43	likely benign
NM_001289401.2(ZNF135):c.1612A>G (p.Ile538Val)	single nucleotide variant	not provided [RCV000967544]	Chr19:58068096 [GRCh38] Chr19:58579464 [GRCh37] Chr19:19q13.43	benign
NM_001289401.2(ZNF135):c.645A>G (p.Lys215=)	single nucleotide variant	not provided [RCV000969330]	Chr19:58067129 [GRCh38] Chr19:58578497 [GRCh37] Chr19:19q13.43	benign
NM_001289401.2(ZNF135):c.1788C>T (p.His596=)	single nucleotide variant	not provided [RCV000962781]	Chr19:58068272 [GRCh38] Chr19:58579640 [GRCh37] Chr19:19q13.43	benign
NM_001289401.2(ZNF135):c.589G>T (p.Glu197Ter)	single nucleotide variant	not provided [RCV000923200]	Chr19:58067073 [GRCh38] Chr19:58578441 [GRCh37] Chr19:19q13.43	likely benign\|evidence_only
NM_001289401.2(ZNF135):c.1845T>C (p.Phe615=)	single nucleotide variant	not provided [RCV000962782]	Chr19:58068329 [GRCh38] Chr19:58579697 [GRCh37] Chr19:19q13.43	benign
NM_001289401.2(ZNF135):c.1640A>G (p.Glu547Gly)	single nucleotide variant	not specified [RCV004289121]	Chr19:58068124 [GRCh38] Chr19:58579492 [GRCh37] Chr19:19q13.43	uncertain significance
GRCh37/hg19 19q13.43(chr19:58092045-58686148)x3	copy number gain	not provided [RCV000849080]	Chr19:19q13.43	uncertain significance
GRCh37/hg19 19q13.43(chr19:58369898-58590924)x3	copy number gain	not provided [RCV000848536]	Chr19:19q13.43	uncertain significance
GRCh37/hg19 19q13.43(chr19:57952073-58661581)x3	copy number gain	not provided [RCV000846105]	Chr19:19q13.43	uncertain significance
GRCh37/hg19 19q13.43(chr19:58369898-58590859)x3	copy number gain	not provided [RCV000849787]	Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1834G>A (p.Gly612Arg)	single nucleotide variant	not specified [RCV004316674]	Chr19:58068318 [GRCh38] Chr19:58579686 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.462G>A (p.Thr154=)	single nucleotide variant	not provided [RCV000962780]	Chr19:58066946 [GRCh38] Chr19:58578314 [GRCh37] Chr19:19q13.43	benign
NM_001289401.2(ZNF135):c.196C>T (p.Leu66=)	single nucleotide variant	not provided [RCV000901207]	Chr19:58063481 [GRCh38] Chr19:58574849 [GRCh37] Chr19:19q13.43	benign
NM_001289401.2(ZNF135):c.1731G>A (p.Pro577=)	single nucleotide variant	not provided [RCV000997020]	Chr19:58068215 [GRCh38] Chr19:58579583 [GRCh37] Chr19:19q13.43	likely benign
NM_001289401.2(ZNF135):c.704C>T (p.Thr235Met)	single nucleotide variant	not specified [RCV006669949]	Chr19:58067188 [GRCh38] Chr19:58578556 [GRCh37] Chr19:19q13.43	uncertain significance
t(10;19)(q26.13;q13.43)	translocation	Glioblastoma [RCV001532885]	Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.878C>T (p.Thr293Ile)	single nucleotide variant	not specified [RCV004216045]	Chr19:58067362 [GRCh38] Chr19:58578730 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1460T>C (p.Ile487Thr)	single nucleotide variant	not specified [RCV004242568]	Chr19:58067944 [GRCh38] Chr19:58579312 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1355C>T (p.Ser452Leu)	single nucleotide variant	not specified [RCV004208725]	Chr19:58067839 [GRCh38] Chr19:58579207 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.173C>T (p.Pro58Leu)	single nucleotide variant	not specified [RCV004196987]	Chr19:58063458 [GRCh38] Chr19:58574826 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.574A>C (p.Thr192Pro)	single nucleotide variant	not specified [RCV004133833]	Chr19:58067058 [GRCh38] Chr19:58578426 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.149T>C (p.Leu50Pro)	single nucleotide variant	not specified [RCV004198788]	Chr19:58061695 [GRCh38] Chr19:58573063 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.386C>G (p.Thr129Ser)	single nucleotide variant	not specified [RCV004221034]	Chr19:58066870 [GRCh38] Chr19:58578238 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.764C>T (p.Ser255Leu)	single nucleotide variant	not specified [RCV004095186]	Chr19:58067248 [GRCh38] Chr19:58578616 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.477G>C (p.Gln159His)	single nucleotide variant	not specified [RCV004201082]	Chr19:58066961 [GRCh38] Chr19:58578329 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.850C>T (p.Pro284Ser)	single nucleotide variant	not specified [RCV004172359]	Chr19:58067334 [GRCh38] Chr19:58578702 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1522T>C (p.Ser508Pro)	single nucleotide variant	not specified [RCV004182914]	Chr19:58068006 [GRCh38] Chr19:58579374 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1030C>T (p.His344Tyr)	single nucleotide variant	not specified [RCV004155368]	Chr19:58067514 [GRCh38] Chr19:58578882 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.394C>T (p.His132Tyr)	single nucleotide variant	not specified [RCV004106711]	Chr19:58066878 [GRCh38] Chr19:58578246 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1541G>A (p.Arg514Gln)	single nucleotide variant	not specified [RCV004090407]	Chr19:58068025 [GRCh38] Chr19:58579393 [GRCh37] Chr19:19q13.43	uncertain significance
GRCh37/hg19 19q13.43(chr19:57961308-58704009)x3	copy number gain	not provided [RCV006436495]	Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.572G>A (p.Gly191Glu)	single nucleotide variant	not specified [RCV004331859]	Chr19:58067056 [GRCh38] Chr19:58578424 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.179C>T (p.Pro60Leu)	single nucleotide variant	not specified [RCV004260533]	Chr19:58063464 [GRCh38] Chr19:58574832 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1285C>T (p.Arg429Trp)	single nucleotide variant	not specified [RCV004334023]	Chr19:58067769 [GRCh38] Chr19:58579137 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.893A>G (p.Tyr298Cys)	single nucleotide variant	not specified [RCV005306688]	Chr19:58067377 [GRCh38] Chr19:58578745 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.214C>G (p.Leu72Val)	single nucleotide variant	not specified [RCV005523285]	Chr19:58063499 [GRCh38] Chr19:58574867 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.34-2A>C	single nucleotide variant	Nonpapillary renal cell carcinoma [RCV006146628]	Chr19:58061578 [GRCh38] Chr19:58572946 [GRCh37] Chr19:19q13.43	evidence_only
NM_001289401.2(ZNF135):c.437C>A (p.Pro146Gln)	single nucleotide variant	Melanoma [RCV006146631]	Chr19:58066921 [GRCh38] Chr19:58578289 [GRCh37] Chr19:19q13.43	evidence_only
NM_001289401.2(ZNF135):c.1265G>A (p.Ser422Asn)	single nucleotide variant	not specified [RCV006344677]	Chr19:58067749 [GRCh38] Chr19:58579117 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.257A>G (p.Asp86Gly)	single nucleotide variant	not specified [RCV006344675]	Chr19:58066741 [GRCh38] Chr19:58578109 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.690C>A (p.Ile230=)	single nucleotide variant	Malignant tumor of urinary bladder [RCV006146633]	Chr19:58067174 [GRCh38] Chr19:58578542 [GRCh37] Chr19:19q13.43	evidence_only
NM_001289401.2(ZNF135):c.1384G>A (p.Gly462Arg)	single nucleotide variant	not specified [RCV004354861]	Chr19:58067868 [GRCh38] Chr19:58579236 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.-35+19G>T	single nucleotide variant	Cholangiocarcinoma [RCV006146626]	Chr19:58059329 [GRCh38] Chr19:58570697 [GRCh37] Chr19:19q13.43	evidence_only
NM_001289401.2(ZNF135):c.690C>G (p.Ile230Met)	single nucleotide variant	not specified [RCV005523284]	Chr19:58067174 [GRCh38] Chr19:58578542 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.83G>C (p.Trp28Ser)	single nucleotide variant	not specified [RCV005512387]	Chr19:58061629 [GRCh38] Chr19:58572997 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1721A>G (p.Lys574Arg)	single nucleotide variant	not specified [RCV005512389]	Chr19:58068205 [GRCh38] Chr19:58579573 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.541A>G (p.Thr181Ala)	single nucleotide variant	not specified [RCV004341727]	Chr19:58067025 [GRCh38] Chr19:58578393 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.247G>A (p.Val83Met)	single nucleotide variant	not specified [RCV004357408]	Chr19:58063532 [GRCh38] Chr19:58574900 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1588G>T (p.Ala530Ser)	single nucleotide variant	not specified [RCV004489312]	Chr19:58068072 [GRCh38] Chr19:58579440 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1828G>A (p.Asp610Asn)	single nucleotide variant	not specified [RCV004489313]	Chr19:58068312 [GRCh38] Chr19:58579680 [GRCh37] Chr19:19q13.43	uncertain significance
NM_007134.1(ZNF135):c.32G>A (p.Gly11Asp)	single nucleotide variant	not specified [RCV004489317]	Chr19:58059273 [GRCh38] Chr19:58570641 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1893G>C (p.Glu631Asp)	single nucleotide variant	not specified [RCV004687455]	Chr19:58068377 [GRCh38] Chr19:58579745 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1434C>G (p.Ser478Arg)	single nucleotide variant	not specified [RCV004687454]	Chr19:58067918 [GRCh38] Chr19:58579286 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.301G>T (p.Gly101Cys)	single nucleotide variant	not specified [RCV004687452]	Chr19:58066785 [GRCh38] Chr19:58578153 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1498G>A (p.Gly500Ser)	single nucleotide variant	not specified [RCV004687453]	Chr19:58067982 [GRCh38] Chr19:58579350 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1067G>A (p.Cys356Tyr)	single nucleotide variant	not specified [RCV004687456]	Chr19:58067551 [GRCh38] Chr19:58578919 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.691G>A (p.Glu231Lys)	single nucleotide variant	not specified [RCV004885994]	Chr19:58067175 [GRCh38] Chr19:58578543 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1686C>A (p.Ser562Arg)	single nucleotide variant	not specified [RCV004885996]	Chr19:58068170 [GRCh38] Chr19:58579538 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.689T>C (p.Ile230Thr)	single nucleotide variant	not specified [RCV004886001]	Chr19:58067173 [GRCh38] Chr19:58578541 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.118C>T (p.Arg40Cys)	single nucleotide variant	not specified [RCV004885991]	Chr19:58061664 [GRCh38] Chr19:58573032 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.842A>G (p.Gln281Arg)	single nucleotide variant	not specified [RCV004885992]	Chr19:58067326 [GRCh38] Chr19:58578694 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1736G>C (p.Gly579Ala)	single nucleotide variant	not specified [RCV004885995]	Chr19:58068220 [GRCh38] Chr19:58579588 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1468G>A (p.Gly490Arg)	single nucleotide variant	not specified [RCV004885997]	Chr19:58067952 [GRCh38] Chr19:58579320 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1739G>A (p.Cys580Tyr)	single nucleotide variant	not specified [RCV004885998]	Chr19:58068223 [GRCh38] Chr19:58579591 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1604C>T (p.Ala535Val)	single nucleotide variant	not specified [RCV004885999]	Chr19:58068088 [GRCh38] Chr19:58579456 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1475A>G (p.Lys492Arg)	single nucleotide variant	not specified [RCV004886000]	Chr19:58067959 [GRCh38] Chr19:58579327 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1643A>C (p.Lys548Thr)	single nucleotide variant	not specified [RCV005306690]	Chr19:58068127 [GRCh38] Chr19:58579495 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1648T>C (p.Tyr550His)	single nucleotide variant	not specified [RCV005306692]	Chr19:58068132 [GRCh38] Chr19:58579500 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1696A>G (p.Ile566Val)	single nucleotide variant	not specified [RCV005302638]	Chr19:58068180 [GRCh38] Chr19:58579548 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.129G>T (p.Met43Ile)	single nucleotide variant	not specified [RCV005302639]	Chr19:58061675 [GRCh38] Chr19:58573043 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.851C>T (p.Pro284Leu)	single nucleotide variant	not specified [RCV005302641]	Chr19:58067335 [GRCh38] Chr19:58578703 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.566C>G (p.Thr189Arg)	single nucleotide variant	not specified [RCV005302642]	Chr19:58067050 [GRCh38] Chr19:58578418 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1685G>T (p.Ser562Ile)	single nucleotide variant	not specified [RCV005302643]	Chr19:58068169 [GRCh38] Chr19:58579537 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.320C>A (p.Ser107Tyr)	single nucleotide variant	not specified [RCV005302640]	Chr19:58066804 [GRCh38] Chr19:58578172 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.967G>A (p.Glu323Lys)	single nucleotide variant	not specified [RCV005512388]	Chr19:58067451 [GRCh38] Chr19:58578819 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1903G>A (p.Ala635Thr)	single nucleotide variant	not specified [RCV005512390]	Chr19:58068387 [GRCh38] Chr19:58579755 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1229A>G (p.Tyr410Cys)	single nucleotide variant	not specified [RCV005776767]	Chr19:58067713 [GRCh38] Chr19:58579081 [GRCh37] Chr19:19q13.43	uncertain significance
NM_007134.1(ZNF135):c.31G>T (p.Gly11Cys)	single nucleotide variant	not specified [RCV005776759]	Chr19:58059272 [GRCh38] Chr19:58570640 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.68T>A (p.Phe23Tyr)	single nucleotide variant	not specified [RCV005776757]	Chr19:58061614 [GRCh38] Chr19:58572982 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.875A>C (p.His292Pro)	single nucleotide variant	not specified [RCV005776763]	Chr19:58067359 [GRCh38] Chr19:58578727 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.317T>C (p.Ile106Thr)	single nucleotide variant	not specified [RCV005776764]	Chr19:58066801 [GRCh38] Chr19:58578169 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.587G>T (p.Arg196Met)	single nucleotide variant	not specified [RCV005776766]	Chr19:58067071 [GRCh38] Chr19:58578439 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.44C>T (p.Thr15Met)	single nucleotide variant	not specified [RCV005776768]	Chr19:58061590 [GRCh38] Chr19:58572958 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.-55C>T	single nucleotide variant	not specified [RCV005776771]	Chr19:58059290 [GRCh38] Chr19:58570658 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.433G>C (p.Val145Leu)	single nucleotide variant	not specified [RCV005776772]	Chr19:58066917 [GRCh38] Chr19:58578285 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.69C>A (p.Phe23Leu)	single nucleotide variant	not specified [RCV005776758]	Chr19:58061615 [GRCh38] Chr19:58572983 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1757C>T (p.Ser586Phe)	single nucleotide variant	not specified [RCV005512386]	Chr19:58068241 [GRCh38] Chr19:58579609 [GRCh37] Chr19:19q13.43	uncertain significance
NM_007134.1(ZNF135):c.31G>A (p.Gly11Ser)	single nucleotide variant	not specified [RCV004173575]	Chr19:58059272 [GRCh38] Chr19:58570640 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1384G>C (p.Gly462Arg)	single nucleotide variant	not specified [RCV004259670]	Chr19:58067868 [GRCh38] Chr19:58579236 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1003T>C (p.Phe335Leu)	single nucleotide variant	not specified [RCV005512394]	Chr19:58067487 [GRCh38] Chr19:58578855 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1372C>T (p.Arg458Trp)	single nucleotide variant	not specified [RCV005523282]	Chr19:58067856 [GRCh38] Chr19:58579224 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.700C>T (p.Arg234Trp)	single nucleotide variant	not specified [RCV005523283]	Chr19:58067184 [GRCh38] Chr19:58578552 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.949G>A (p.Glu317Lys)	single nucleotide variant	not specified [RCV006344674]	Chr19:58067433 [GRCh38] Chr19:58578801 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1163G>A (p.Gly388Glu)	single nucleotide variant	not specified [RCV006344679]	Chr19:58067647 [GRCh38] Chr19:58579015 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1313A>G (p.Tyr438Cys)	single nucleotide variant	not specified [RCV006344676]	Chr19:58067797 [GRCh38] Chr19:58579165 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.476A>G (p.Gln159Arg)	single nucleotide variant	not specified [RCV006344678]	Chr19:58066960 [GRCh38] Chr19:58578328 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.256G>A (p.Asp86Asn)	single nucleotide variant	Thyroid cancer, nonmedullary, 1 [RCV006146630]	Chr19:58063541 [GRCh38] Chr19:58574909 [GRCh37] Chr19:19q13.43	evidence_only
NM_001289401.2(ZNF135):c.966C>T (p.Gly322=)	single nucleotide variant	Thyroid cancer, nonmedullary, 1 [RCV006146635]	Chr19:58067450 [GRCh38] Chr19:58578818 [GRCh37] Chr19:19q13.43	evidence_only
NM_001289401.2(ZNF135):c.118C>G (p.Arg40Gly)	single nucleotide variant	not specified [RCV005512391]	Chr19:58061664 [GRCh38] Chr19:58573032 [GRCh37] Chr19:19q13.43	evidence_only\|uncertain significance
NM_001289401.2(ZNF135):c.735C>G (p.His245Gln)	single nucleotide variant	Papillary renal cell carcinoma type 1 [RCV006146634]	Chr19:58067219 [GRCh38] Chr19:58578587 [GRCh37] Chr19:19q13.43	evidence_only
NM_001289401.2(ZNF135):c.*457G>A	single nucleotide variant	Familial cancer of breast [RCV006146636]	Chr19:58068918 [GRCh38] Chr19:58580286 [GRCh37] Chr19:19q13.43	evidence_only
NM_001289401.2(ZNF135):c.149T>A (p.Leu50Gln)	single nucleotide variant	Familial cancer of breast [RCV006146629]	Chr19:58061695 [GRCh38] Chr19:58573063 [GRCh37] Chr19:19q13.43	evidence_only
NM_001289401.2(ZNF135):c.1147G>A (p.Glu383Lys)	single nucleotide variant	not specified [RCV004489310]	Chr19:58067631 [GRCh38] Chr19:58578999 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.221C>T (p.Ala74Val)	single nucleotide variant	not specified [RCV004489316]	Chr19:58063506 [GRCh38] Chr19:58574874 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.946C>T (p.His316Tyr)	single nucleotide variant	not specified [RCV004489309]	Chr19:58067430 [GRCh38] Chr19:58578798 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1490A>G (p.Asn497Ser)	single nucleotide variant	not specified [RCV004489311]	Chr19:58067974 [GRCh38] Chr19:58579342 [GRCh37] Chr19:19q13.43	likely benign
NM_001289401.2(ZNF135):c.1952A>G (p.Lys651Arg)	single nucleotide variant	not specified [RCV004489314]	Chr19:58068436 [GRCh38] Chr19:58579804 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.839A>G (p.Asn280Ser)	single nucleotide variant	not specified [RCV005306691]	Chr19:58067323 [GRCh38] Chr19:58578691 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1954C>G (p.His652Asp)	single nucleotide variant	not specified [RCV005306689]	Chr19:58068438 [GRCh38] Chr19:58579806 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1243T>C (p.Cys415Arg)	single nucleotide variant	not specified [RCV005512393]	Chr19:58067727 [GRCh38] Chr19:58579095 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.559C>G (p.Pro187Ala)	single nucleotide variant	not specified [RCV005523281]	Chr19:58067043 [GRCh38] Chr19:58578411 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1757C>G (p.Ser586Cys)	single nucleotide variant	not specified [RCV005512392]	Chr19:58068241 [GRCh38] Chr19:58579609 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1286G>A (p.Arg429Gln)	single nucleotide variant	not specified [RCV005776760]	Chr19:58067770 [GRCh38] Chr19:58579138 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1721A>C (p.Lys574Thr)	single nucleotide variant	not specified [RCV005776761]	Chr19:58068205 [GRCh38] Chr19:58579573 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.512T>C (p.Leu171Pro)	single nucleotide variant	not specified [RCV005776765]	Chr19:58066996 [GRCh38] Chr19:58578364 [GRCh37] Chr19:19q13.43	uncertain significance
NM_001289401.2(ZNF135):c.1346A>G (p.His449Arg)	single nucleotide variant	not specified [RCV005776769]	Chr19:58067830 [GRCh38] Chr19:58579198 [GRCh37] Chr19:19q13.43	uncertain significance

miRNA Target Status (No longer updated)

Predicted Target Of

	Summary Value
Count of predictions:	3062
Count of miRNA genes:	947
Interacting mature miRNAs:	1126
Transcripts:	ENST00000313434, ENST00000359978, ENST00000401053, ENST00000439855, ENST00000506786, ENST00000511556, ENST00000515535
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

RH39178

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	58,580,349 - 58,580,596	UniSTS	GRCh37
GRCh37	X	101,167,569 - 101,167,816	UniSTS	GRCh37
Build 36	X	101,054,225 - 101,054,472	RGD	NCBI36
Celera	19	55,623,696 - 55,623,943	UniSTS
Celera	X	101,688,119 - 101,688,366	RGD
Cytogenetic Map	19	q13.4	UniSTS
Cytogenetic Map	X	q21	UniSTS
HuRef	19	54,891,316 - 54,891,563	UniSTS
HuRef	X	90,975,232 - 90,975,479	UniSTS

RH98773

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	58,574,887 - 58,575,083	UniSTS	GRCh37
Build 36	19	63,266,699 - 63,266,895	RGD	NCBI36
Celera	19	55,618,234 - 55,618,430	RGD
Cytogenetic Map	19	q13.4	UniSTS
HuRef	19	54,885,854 - 54,886,050	UniSTS
GeneMap99-GB4 RH Map	19	289.46	UniSTS

ZNF135_8743

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	58,579,901 - 58,580,778	UniSTS	GRCh37
Build 36	19	63,271,713 - 63,272,590	RGD	NCBI36
Celera	19	55,623,248 - 55,624,125	RGD
HuRef	19	54,890,868 - 54,891,745	UniSTS

AF020182

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	58,580,583 - 58,580,677	UniSTS	GRCh37
GRCh37	X	101,167,803 - 101,167,897	UniSTS	GRCh37
Build 36	X	101,054,459 - 101,054,553	RGD	NCBI36
Celera	19	55,623,930 - 55,624,024	UniSTS
Celera	X	101,688,353 - 101,688,447	RGD
Cytogenetic Map	X	q21	UniSTS
Cytogenetic Map	19	q13.4	UniSTS
HuRef	19	54,891,550 - 54,891,644	UniSTS
HuRef	X	90,975,466 - 90,975,560	UniSTS

DXS7489

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	19	q13.4	UniSTS
Stanford-G3 RH Map	19	2926.0	UniSTS
Whitehead-YAC Contig Map	X		UniSTS
NCBI RH Map	19	600.5	UniSTS
GeneMap99-G3 RH Map	19	2937.0	UniSTS

Expression

RNA-SEQ Expression

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	2331	2788	2232	4918	1701	2258	6	603	1710	442	2229	6967	6243	43	3719	1	833	1695	1546	166	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001164527	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001164529	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001164530	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001289401	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001289402	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_003436	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_007134	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005259211	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006723362	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006723363	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017027240	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017027241	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017027242	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439362	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439363	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047439364	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054322003	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054322004	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054322005	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054322006	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054322007	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054322008	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC008751	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK094202	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK095796	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK098011	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK295110	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK297226	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL833637	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC046434	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM993886	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX647775	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471135	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CN367970	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068259	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA232862	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB117846	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB304820	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KT584393	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	M88370	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	U09413	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	X65231	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000313434 ⟹ ENSP00000321406

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,282 - 58,069,755 (+)	Ensembl

Ensembl Acc Id:

ENST00000359978 ⟹ ENSP00000369437

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,238 - 58,069,405 (+)	Ensembl

Ensembl Acc Id:

ENST00000401053 ⟹ ENSP00000441410

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,238 - 58,069,755 (+)	Ensembl

Ensembl Acc Id:

ENST00000506786 ⟹ ENSP00000427691

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,280 - 58,069,405 (+)	Ensembl

Ensembl Acc Id:

ENST00000511556 ⟹ ENSP00000422074

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,269 - 58,068,630 (+)	Ensembl

Ensembl Acc Id:

ENST00000515535 ⟹ ENSP00000471344

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,734 - 58,086,310 (+)	Ensembl

Ensembl Acc Id:

ENST00000890101 ⟹ ENSP00000560160

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,244 - 58,069,408 (+)	Ensembl

Ensembl Acc Id:

ENST00000890102 ⟹ ENSP00000560161

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,282 - 58,069,408 (+)	Ensembl

Ensembl Acc Id:

ENST00000890103 ⟹ ENSP00000560162

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,372 - 58,069,408 (+)	Ensembl

Ensembl Acc Id:

ENST00000890104 ⟹ ENSP00000560163

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,347 - 58,069,156 (+)	Ensembl

Ensembl Acc Id:

ENST00000938056 ⟹ ENSP00000608115

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,602 - 58,069,154 (+)	Ensembl

Ensembl Acc Id:

ENST00000988320 ⟹ ENSP00000658137

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,276 - 58,064,741 (+)	Ensembl

Ensembl Acc Id:

ENST00001048131 ⟹ ENSP00000717948

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,276 - 58,086,308 (+)	Ensembl

Ensembl Acc Id:

ENST00001048132 ⟹ ENSP00000717949

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,276 - 58,086,308 (+)	Ensembl

Ensembl Acc Id:

ENST00001048133 ⟹ ENSP00000717950

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,261 - 58,064,714 (+)	Ensembl

Ensembl Acc Id:

ENST00001048134 ⟹ ENSP00000717951

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,269 - 58,064,716 (+)	Ensembl

Ensembl Acc Id:

ENST00001048135 ⟹ ENSP00000717952

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,347 - 58,064,741 (+)	Ensembl

Ensembl Acc Id:

ENST00001095316 ⟹ ENSP00000765122

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,269 - 58,074,018 (+)	Ensembl

Ensembl Acc Id:

ENST00001122233 ⟹ ENSP00000792038

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,259 - 58,074,018 (+)	Ensembl

Ensembl Acc Id:

ENST00001122234 ⟹ ENSP00000792039

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,277 - 58,074,018 (+)	Ensembl

Ensembl Acc Id:

ENST00001130018 ⟹ ENSP00000799823

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	58,059,269 - 58,074,018 (+)	Ensembl

RefSeq Acc Id:

NM_001164527 ⟹ NP_001157999

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,059,239 - 58,063,936 (+)	NCBI
GRCh37	19	58,570,607 - 58,581,123 (+)	RGD
Celera	19	55,613,970 - 55,624,470 (+)	RGD
HuRef	19	54,881,599 - 54,892,090 (+)	ENTREZGENE
CHM1_1	19	58,564,299 - 58,568,971 (+)	NCBI
T2T-CHM13v2.0	19	61,156,060 - 61,160,730 (+)	NCBI

Sequence:

show sequence

GAAATGGAGTTAGGCTCGCGCCGGCGCAGTGTCGGCTGCCGGTGCCGCGGCCTTTGTCTCGCAG
TCAGGAGGGAGCAAGTGACGTTTGAGGACGTGGTAGTGGGCTTCAGCCAGGAGGAGTGGGGGCA
GCTGAAGCCTGCCCAGAGGACCCTGTACCGTGATGTAATGCTGGACACCTTCAGGCTTCTGGTC
TCTGTGGGACATTGGTTACCGAAGCCGAATGTCATCTCCCTGCTGGAGCAAGAGGCAGAGCTGT
GGGCGGTGGAGTCTAGACTTCCCCAAGGCGTGTACCCAGGTGAGATGGGAGCCCTTCGGGGCAG
AGAGAAGCCTGTCCATGCTTGCTTCCTGGTTTCTCCCTCTGCATCTGCTCTCTAATTCTTCAGA
GCAAATTTACTACTCAGTCTTAGTGAAGATTTACCAAGCACCCATTTTGCTGTGAGTGACGACA
CCACGTCCTCATCTCCACTGAATTTATATTCTTGGTGAGGGAGTGGGGGAAACAAACAATAAAT
CGGTAAAATAATAATAATAAAACAAGTTGGATGATTACAGATTGTGATGAATGCCGAGAAAATG
AAAATGAGCAATGAGGTAGACTAGGAGGGGGATGAGTAGACTTTAGCAGAGAGATGAGGGATAG
CCTCTCCAAGGAGGTGACATGTGACTTGAAGCCTGAGCCATGAGGCAGTC

hide sequence

RefSeq Acc Id:

NM_001164529 ⟹ NP_001158001

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,059,239 - 58,069,755 (+)	NCBI
GRCh37	19	58,570,607 - 58,581,123 (+)	RGD
Celera	19	55,613,970 - 55,624,470 (+)	RGD
HuRef	19	54,881,599 - 54,892,090 (+)	ENTREZGENE
CHM1_1	19	58,564,299 - 58,574,790 (+)	NCBI
T2T-CHM13v2.0	19	61,156,060 - 61,166,554 (+)	NCBI

Sequence:

show sequence

GAAATGGAGTTAGGCTCGCGCCGGCGCAGTGTCGGCTGCCGGTGCCGCGGCCTTTGTCTCGCAG
TCAGGAGGGAGCAAGTGACGTTTGAGGACGTGGTAGTGGGCTTCAGCCAGGAGGAGTGGGGGCA
GCTGAAGCCTGCCCAGAGGACCCTGTACCGTGATGTAATGCTGGACACCTTCAGGCTTCTGGTC
TCTGTGGGACATTGGTTACCGAAGCCGAATGTCATCTCCCTGCTGGAGCAAGAGGCAGAGCTGT
GGGCGGTGGAGTCTAGACTTCCCCAAGGCGTGTACCCAGAAAACCTGTGTAAAAGAGAAACCCT
ACAAATGTCAGGAATGCGGAAAGGCCTTTAGTCACAGCTCAGCACTTATCGAACACCACCGGAC
GCACACAGGAGAGAGACCTTACGAATGTCACGAATGCTTAAAAGGCTTCCGGAACAGCTCGGCA
CTTACCAAACACCAGAGAATCCATACTGGGGAGAAACCCTATAAATGCACTCAGTGTGGGAGGA
CCTTCAACCAAATTGCCCCACTGATCCAGCACCAGAGAACTCACACAGGTGAGAAGCCCTATGA
ATGCAGCGAATGTGGGAAATCCTTCAGTTTTAGGTCCTCCTTCAGCCAGCACGAGCGAACTCAC
ACAGGCGAGAAGCCCTACGAGTGCAGTGAGTGTGGGAAAGCCTTCCGGCAAAGCATCCACCTCA
CCCAGCATCTGCGAATCCACACTGGGGAGAAACCCTATCAGTGTGGTGAGTGTGGCAAGGCCTT
CAGCCACAGCTCATCCTTGACCAAACACCAGCGAATCCACACAGGGGAGAAGCCCTACGAGTGC
CATGAGTGTGGAAAAGCCTTCACCCAGATCACACCACTGATTCAGCACCAGAGGACCCACACAG
GAGAAAAGCCCTATGAGTGTGGTGAGTGTGGGAAAGCCTTCAGTCAGAGCACACTCCTGACCGA
GCATCGGAGGATTCACACAGGAGAGAAGCCCTATGGATGCAACGAGTGTGGGAAAACCTTCAGC
CACAGCTCCTCACTCAGCCAGCATGAGCGGACACACACAGGAGAGAAGCCCTATGAGTGCAGTC
AGTGTGGGAAGGCCTTCCGGCAGAGCACACACCTCACCCAACACCAGCGAATCCACACAGGGGA
GAAGCCCTATGAATGCAATGACTGCGGCAAGGCATTCAGTCACAGCTCGTCCCTCACCAAACAT
CAGCGAATCCACACTGGGGAGAAGCCCTACGAATGCAACCAGTGTGGCAGAGCCTTCAGCCAGC
TTGCTCCCCTCATTCAGCATCAGAGGATCCACACAGGAGAGAAACCCTATGAATGTAACCAGTG
TGGCAGAGCCTTCAGCCAGAGCTCCCTTCTCATCGAACACCAGAGGATTCACACCAAGGAAAAG
CCGTATGGGTGCAATGAGTGTGGGAAATCCTTCAGCCACAGCTCCTCGCTCAGCCAGCACGAAA
GGACGCACACTGGGGAAAAGCCCTATGAGTGTCACGATTGCGGAAAGTCCTTTAGGCAGAGCAC
CCACCTCACTCAGCACCGGAGGATCCACACAGGAGAGAAGCCATATGCATGCAGGGACTGTGGA
AAGGCCTTTACCCACAGCTCCTCCCTTACCAAGCACCAGAGAACTCACACTGGATAAACCCACT
CCACATGTGCTGGGGACATAGGAAGACCTTAAGCCATAGCTCATCCCTTTCTAGATTTGACCCA
ATCATACACATGAGAAACGTACATTCATACACAAGCCTTTTCACACAGCACTCCCCTCAGACAC
CCTCAGAGAGTTCACACTGATGGGAAATGACCATGGGACCACCAAGCTCTAGGTCATCCATCTC
TGCATCCAAATAGTAGGGAAACGTGGAGATAATCAACACTCAGGACCTTCAGCCTTGAACGCCC
ATTAGTGCTATGTTATAGAACCTACAAAAAAGAAATGGAACAAATGTAGTGGATCCAGGGAACG
CTTTTGTCCAAGGATTCACCGTATTCCAAACCAGAGATGTTCAAATTGGTGAGAAACCCAACAA
ATGCCTTTCATATATACGAGAACCAAATGAAGTCAGAATTTGCCATTATTGCACATCACATTTT
TGGGGGGGAAAGTGCTTATGAATGGTGCAGGTTGACTCTGATATTCATTCCCAAATGACAGTAT
GGCAGAGTGTTCCAGAAATGAGAGTGGCATCTTTATGGAATCACTGTGGATACTGACTGTCTCA
GTAAACAGCTGTCTTGTCTGTGTGTATATTGTTTGATCAGGGTACATGGCAGCCAGTCACAGAT
TGGAATTACATATGACAAAGTATCAGTGTACTATAAACAGGTTTTTAGTTATCCCTGCATTATT
TTTGCAATTAATCTTTATATGCAATGAGATTGAAAAGCTTTGTATGGGAAGACTCAAAATGTAA
AGCTGCTTCCGTAGAGTCTCACTGATTCTGAGATGGCTTTTGCTGCTCTGTTCTCCCTCTACAT
TTCTCTGCAGAACTCGCGTTAGAAACACAGATATTTGTTTTACAAAAAGGGAGATTTTTCCTTT
GTTAAACCATCGTCTTATAAGCAATAGCAAATTCATGTTAGAAACTTCTGTTTTGCAAGATTCA
TCTTTTTTGGGATATGTTCAAGTTAATCCTCTCAAACTGCTTTTTCATTGTTTTCATACAATTT
AACATTTTGTTAAACCCTAAGTCCACAAATAGCAGTCTTTCTGACAACTATAACCTTTAAATGG
TGACTTGCTGCCCTCATTAGAAATTGCATTGGCTGGCCAGGCGCGGTGACTTATGCCTGTAATC
CCAGCACTTTGGGAGGCCAAGGTGGGAGGATCACCTGAGGTCGGGAGATGGAGGTTGCAGTGAG
CTGAGATCGTACCATTGCACTCCAGCCTGGGCAACAAGAGTGAAACTCTGTCTCAGAAAAAAAA
AAAAAAA

hide sequence

RefSeq Acc Id:

NM_001164530 ⟹ NP_001158002

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,059,239 - 58,069,755 (+)	NCBI
GRCh37	19	58,570,607 - 58,581,123 (+)	RGD
Celera	19	55,613,970 - 55,624,470 (+)	RGD
HuRef	19	54,881,599 - 54,892,090 (+)	ENTREZGENE
CHM1_1	19	58,564,299 - 58,574,790 (+)	NCBI
T2T-CHM13v2.0	19	61,156,060 - 61,166,554 (+)	NCBI

Sequence:

show sequence

GAAATGGAGTTAGGCTCGCGCCGGCGCAGTGTCGGCTGCCGGTGCCGCGGCCTTTGTCTCGCAG
TCAGGAGGGAGCAAGTGACGTTTGAGGACGTGGTAGTGGGCTTCAGCCAGGAGGAGTGGGGGCA
GCTGAAGCCTGCCCAGAGGACCCTGTACCGTGATGTAATGCTGGACACCTTCAGGCTTCTGGTC
TCTGTGGGACATTGGTTACCGAAGCCGAATGTCATCTCCCTGCTGGAGCAAGAGGCAGAGCTGT
GGGCGGTGGAGTCTAGACTTCCCCAAGGCGTGTACCCAGACTTGGAAACTAGACCCAAAGTCAA
ACTGTCAGTTCTAAAGCAAGGCATCTCTGAAGAAATATCCAACAGTGTCATCTTGGTAGAAAGA
TTCCTGTGGGATGGTCTGTGGTACTGCAGGGGTGAGGACACTGAGGGCCACTGGGAATGGAGTT
GTGAGAGTCTAGAGAGCCTGGCAGTGCCGGTGGCCTTCACGCCTGTGAAGACGCCTGTTCTGGA
GCAGTGGCAGAGGAATGGGTTTGGGGAAAACATAAGTCTGAACCCTGATCTCCCACATCAACCA
ATGACTCCTGAAAGACAAAGCCCCCACACATGGGGAACACGTGGAAAAAGGGAGAAGCCAGACC
TAAATGTTTTACAGAAAACCTGTGTAAAAGAGAAACCCTACAAATGTCAGGAATGCGGAAAGGC
CTTTAGTCACAGCTCAGCACTTATCGAACACCACCGGACGCACACAGGAGAGAGACCTTACGAA
TGTCACGAATGCTTAAAAGGCTTCCGGAACAGCTCGGCACTTACCAAACACCAGAGAATCCATA
CTGGGGAGAAACCCTATAAATGCACTCAGTGTGGGAGGACCTTCAACCAAATTGCCCCACTGAT
CCAGCACCAGAGAACTCACACAGGTGAGAAGCCCTATGAATGCAGCGAATGTGGGAAATCCTTC
AGTTTTAGGTCCTCCTTCAGCCAGCACGAGCGAACTCACACAGGCGAGAAGCCCTACGAGTGCA
GTGAGTGTGGGAAAGCCTTCCGGCAAAGCATCCACCTCACCCAGCATCTGCGAATCCACACTGG
GGAGAAACCCTATCAGTGTGGTGAGTGTGGCAAGGCCTTTACCCACAGCTCCTCCCTTACCAAG
CACCAGAGAACTCACACTGGATAAACCCACTCCACATGTGCTGGGGACATAGGAAGACCTTAAG
CCATAGCTCATCCCTTTCTAGATTTGACCCAATCATACACATGAGAAACGTACATTCATACACA
AGCCTTTTCACACAGCACTCCCCTCAGACACCCTCAGAGAGTTCACACTGATGGGAAATGACCA
TGGGACCACCAAGCTCTAGGTCATCCATCTCTGCATCCAAATAGTAGGGAAACGTGGAGATAAT
CAACACTCAGGACCTTCAGCCTTGAACGCCCATTAGTGCTATGTTATAGAACCTACAAAAAAGA
AATGGAACAAATGTAGTGGATCCAGGGAACGCTTTTGTCCAAGGATTCACCGTATTCCAAACCA
GAGATGTTCAAATTGGTGAGAAACCCAACAAATGCCTTTCATATATACGAGAACCAAATGAAGT
CAGAATTTGCCATTATTGCACATCACATTTTTGGGGGGGAAAGTGCTTATGAATGGTGCAGGTT
GACTCTGATATTCATTCCCAAATGACAGTATGGCAGAGTGTTCCAGAAATGAGAGTGGCATCTT
TATGGAATCACTGTGGATACTGACTGTCTCAGTAAACAGCTGTCTTGTCTGTGTGTATATTGTT
TGATCAGGGTACATGGCAGCCAGTCACAGATTGGAATTACATATGACAAAGTATCAGTGTACTA
TAAACAGGTTTTTAGTTATCCCTGCATTATTTTTGCAATTAATCTTTATATGCAATGAGATTGA
AAAGCTTTGTATGGGAAGACTCAAAATGTAAAGCTGCTTCCGTAGAGTCTCACTGATTCTGAGA
TGGCTTTTGCTGCTCTGTTCTCCCTCTACATTTCTCTGCAGAACTCGCGTTAGAAACACAGATA
TTTGTTTTACAAAAAGGGAGATTTTTCCTTTGTTAAACCATCGTCTTATAAGCAATAGCAAATT
CATGTTAGAAACTTCTGTTTTGCAAGATTCATCTTTTTTGGGATATGTTCAAGTTAATCCTCTC
AAACTGCTTTTTCATTGTTTTCATACAATTTAACATTTTGTTAAACCCTAAGTCCACAAATAGC
AGTCTTTCTGACAACTATAACCTTTAAATGGTGACTTGCTGCCCTCATTAGAAATTGCATTGGC
TGGCCAGGCGCGGTGACTTATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGAGGATCA
CCTGAGGTCGGGAGATGGAGGTTGCAGTGAGCTGAGATCGTACCATTGCACTCCAGCCTGGGCA
ACAAGAGTGAAACTCTGTCTCAGAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NM_001289401 ⟹ NP_001276330

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,059,282 - 58,069,755 (+)	NCBI
HuRef	19	54,881,599 - 54,892,090 (+)	NCBI
CHM1_1	19	58,564,299 - 58,574,790 (+)	NCBI
T2T-CHM13v2.0	19	61,156,103 - 61,166,554 (+)	NCBI

Sequence:

show sequence

GCCGCGGCCTTTGTCTCGCAGTCAGGAGGAGCAGGGCCAGCCGTTCCTGCCAGAAGCCAGGGCA
TGACCCCTGGGGTGCGCGTCTCCACAGACCCGGAGCAAGTGACGTTTGAGGACGTGGTAGTGGG
CTTCAGCCAGGAGGAGTGGGGGCAGCTGAAGCCTGCCCAGAGGACCCTGTACCGTGATGTAATG
CTGGACACCTTCAGGCTTCTGGTCTCTGTGGGACATTGGTTACCGAAGCCGAATGTCATCTCCC
TGCTGGAGCAAGAGGCAGAGCTGTGGGCGGTGGAGTCTAGACTTCCCCAAGGCGTGTACCCAGA
CTTGGAAACTAGACCCAAAGTCAAACTGTCAGTTCTAAAGCAAGGCATCTCTGAAGAAATATCC
AACAGTGTCATCTTGGTAGAAAGATTCCTGTGGGATGGTCTGTGGTACTGCAGGGGTGAGGACA
CTGAGGGCCACTGGGAATGGAGTTGTGAGAGTCTAGAGAGCCTGGCAGTGCCGGTGGCCTTCAC
GCCTGTGAAGACGCCTGTTCTGGAGCAGTGGCAGAGGAATGGGTTTGGGGAAAACATAAGTCTG
AACCCTGATCTCCCACATCAACCAATGACTCCTGAAAGACAAAGCCCCCACACATGGGGAACAC
GTGGAAAAAGGGAGAAGCCAGACCTAAATGTTTTACAGAAAACCTGTGTAAAAGAGAAACCCTA
CAAATGTCAGGAATGCGGAAAGGCCTTTAGTCACAGCTCAGCACTTATCGAACACCACCGGACG
CACACAGGAGAGAGACCTTACGAATGTCACGAATGCTTAAAAGGCTTCCGGAACAGCTCGGCAC
TTACCAAACACCAGAGAATCCATACTGGGGAGAAACCCTATAAATGCACTCAGTGTGGGAGGAC
CTTCAACCAAATTGCCCCACTGATCCAGCACCAGAGAACTCACACAGGTGAGAAGCCCTATGAA
TGCAGCGAATGTGGGAAATCCTTCAGTTTTAGGTCCTCCTTCAGCCAGCACGAGCGAACTCACA
CAGGCGAGAAGCCCTACGAGTGCAGTGAGTGTGGGAAAGCCTTCCGGCAAAGCATCCACCTCAC
CCAGCATCTGCGAATCCACACTGGGGAGAAACCCTATCAGTGTGGTGAGTGTGGCAAGGCCTTC
AGCCACAGCTCATCCTTGACCAAACACCAGCGAATCCACACAGGGGAGAAGCCCTACGAGTGCC
ATGAGTGTGGAAAAGCCTTCACCCAGATCACACCACTGATTCAGCACCAGAGGACCCACACAGG
AGAAAAGCCCTATGAGTGTGGTGAGTGTGGGAAAGCCTTCAGTCAGAGCACACTCCTGACCGAG
CATCGGAGGATTCACACAGGAGAGAAGCCCTATGGATGCAACGAGTGTGGGAAAACCTTCAGCC
ACAGCTCCTCACTCAGCCAGCATGAGCGGACACACACAGGAGAGAAGCCCTATGAGTGCAGTCA
GTGTGGGAAGGCCTTCCGGCAGAGCACACACCTCACCCAACACCAGCGAATCCACACAGGGGAG
AAGCCCTATGAATGCAATGACTGCGGCAAGGCATTCAGTCACAGCTCGTCCCTCACCAAACATC
AGCGAATCCACACTGGGGAGAAGCCCTACGAATGCAACCAGTGTGGCAGAGCCTTCAGCCAGCT
TGCTCCCCTCATTCAGCATCAGAGGATCCACACAGGAGAGAAACCCTATGAATGTAACCAGTGT
GGCAGAGCCTTCAGCCAGAGCTCCCTTCTCATCGAACACCAGAGGATTCACACCAAGGAAAAGC
CGTATGGGTGCAATGAGTGTGGGAAATCCTTCAGCCACAGCTCCTCGCTCAGCCAGCACGAAAG
GACGCACACTGGGGAAAAGCCCTATGAGTGTCACGATTGCGGAAAGTCCTTTAGGCAGAGCACC
CACCTCACTCAGCACCGGAGGATCCACACAGGAGAGAAGCCATATGCATGCAGGGACTGTGGAA
AGGCCTTTACCCACAGCTCCTCCCTTACCAAGCACCAGAGAACTCACACTGGATAAACCCACTC
CACATGTGCTGGGGACATAGGAAGACCTTAAGCCATAGCTCATCCCTTTCTAGATTTGACCCAA
TCATACACATGAGAAACGTACATTCATACACAAGCCTTTTCACACAGCACTCCCCTCAGACACC
CTCAGAGAGTTCACACTGATGGGAAATGACCATGGGACCACCAAGCTCTAGGTCATCCATCTCT
GCATCCAAATAGTAGGGAAACGTGGAGATAATCAACACTCAGGACCTTCAGCCTTGAACGCCCA
TTAGTGCTATGTTATAGAACCTACAAAAAAGAAATGGAACAAATGTAGTGGATCCAGGGAACGC
TTTTGTCCAAGGATTCACCGTATTCCAAACCAGAGATGTTCAAATTGGTGAGAAACCCAACAAA
TGCCTTTCATATATACGAGAACCAAATGAAGTCAGAATTTGCCATTATTGCACATCACATTTTT
GGGGGGGAAAGTGCTTATGAATGGTGCAGGTTGACTCTGATATTCATTCCCAAATGACAGTATG
GCAGAGTGTTCCAGAAATGAGAGTGGCATCTTTATGGAATCACTGTGGATACTGACTGTCTCAG
TAAACAGCTGTCTTGTCTGTGTGTATATTGTTTGATCAGGGTACATGGCAGCCAGTCACAGATT
GGAATTACATATGACAAAGTATCAGTGTACTATAAACAGGTTTTTAGTTATCCCTGCATTATTT
TTGCAATTAATCTTTATATGCAATGAGATTGAAAAGCTTTGTATGGGAAGACTCAAAATGTAAA
GCTGCTTCCGTAGAGTCTCACTGATTCTGAGATGGCTTTTGCTGCTCTGTTCTCCCTCTACATT
TCTCTGCAGAACTCGCGTTAGAAACACAGATATTTGTTTTACAAAAAGGGAGATTTTTCCTTTG
TTAAACCATCGTCTTATAAGCAATAGCAAATTCATGTTAGAAACTTCTGTTTTGCAAGATTCAT
CTTTTTTGGGATATGTTCAAGTTAATCCTCTCAAACTGCTTTTTCATTGTTTTCATACAATTTA
ACATTTTGTTAAACCCTAAGTCCACAAATAGCAGTCTTTCTGACAACTATAACCTTTAAATGGT
GACTTGCTGCCCTCATTAGAAATTGCATTGGCTGGCCAGGCGCGGTGACTTATGCCTGTAATCC
CAGCACTTTGGGAGGCCAAGGTGGGAGGATCACCTGAGGTCGGGAGATGGAGGTTGCAGTGAGC
TGAGATCGTACCATTGCACTCCAGCCTGGGCAACAAGAGTGAAACTCTGTCTCAGAAAAAAAAA
AAAAAA

hide sequence

RefSeq Acc Id:

NM_001289402 ⟹ NP_001276331

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,059,282 - 58,069,755 (+)	NCBI
HuRef	19	54,881,599 - 54,892,090 (+)	NCBI
CHM1_1	19	58,564,299 - 58,574,790 (+)	NCBI
T2T-CHM13v2.0	19	61,156,103 - 61,166,554 (+)	NCBI

Sequence:

show sequence

GCCGCGGCCTTTGTCTCGCAGTCAGGAGGAGCAGGGCCAGCCGTTCCTGCCAGAAGCCAGGGCA
TGACCCCTGGGGTGCGCGTCTCCACAGACCCGGTGAGAATCTCGGCCTCCTTGCGCGTGTCCTC
CACCTCGTGCCCGGCCTCCTCGCGCGCGGCCTTCTCACGCCCGGCCTCCTCTTTGCACCCCGTC
CCTACTCGCGCTCAGCCTCCTCCTTGTGCCCGGCCCCTACTTGCGTGCCCGGCCCCTACTCGTG
CCCGGCCTCTACTCGCACAACTGGCCTCTACTCGCGCACCTGGCCTCTACTGGTGCCCGGCCTC
TACTCGTGCCCGGCCTCTATTTGCACATCTAGCCTCTACTCGTGTCCGGCCTCTACCTGCACAC
CCGGCCTCCTAAAGTCCGCGCCAAGCTCCCCAACCACAGCCTGCCTCTGAAAGGACCGCCCACG
CCGCGCTGGAGGAGCAAGTGACGTTTGAGGACGTGGTAGTGGGCTTCAGCCAGGAGGAGTGGGG
GCAGCTGAAGCCTGCCCAGAGGACCCTGTACCGTGATGTAATGCTGGACACCTTCAGGCTTCTG
GTCTCTGTGGGACATTGGTTACCGAAGCCGAATGTCATCTCCCTGCTGGAGCAAGAGGCAGAGC
TGTGGGCGGTGGAGTCTAGACTTCCCCAAGGCGTGTACCCAGACTTGGAAACTAGACCCAAAGT
CAAACTGTCAGTTCTAAAGCAAGGCATCTCTGAAGAAATATCCAACAGTGTCATCTTGGTAGAA
AGATTCCTGTGGGATGGTCTGTGGTACTGCAGGGGTGAGGACACTGAGGGCCACTGGGAATGGA
GTTGTGAGAGTCTAGAGAGCCTGGCAGTGCCGGTGGCCTTCACGCCTGTGAAGACGCCTGTTCT
GGAGCAGTGGCAGAGGAATGGGTTTGGGGAAAACATAAGTCTGAACCCTGATCTCCCACATCAA
CCAATGACTCCTGAAAGACAAAGCCCCCACACATGGGGAACACGTGGAAAAAGGGAGAAGCCAG
ACCTAAATGTTTTACAGAAAACCTGTGTAAAAGAGAAACCCTACAAATGTCAGGAATGCGGAAA
GGCCTTTAGTCACAGCTCAGCACTTATCGAACACCACCGGACGCACACAGGAGAGAGACCTTAC
GAATGTCACGAATGCTTAAAAGGCTTCCGGAACAGCTCGGCACTTACCAAACACCAGAGAATCC
ATACTGGGGAGAAACCCTATAAATGCACTCAGTGTGGGAGGACCTTCAACCAAATTGCCCCACT
GATCCAGCACCAGAGAACTCACACAGGTGAGAAGCCCTATGAATGCAGCGAATGTGGGAAATCC
TTCAGTTTTAGGTCCTCCTTCAGCCAGCACGAGCGAACTCACACAGGCGAGAAGCCCTACGAGT
GCAGTGAGTGTGGGAAAGCCTTCCGGCAAAGCATCCACCTCACCCAGCATCTGCGAATCCACAC
TGGGGAGAAACCCTATCAGTGTGGTGAGTGTGGCAAGGCCTTCAGCCACAGCTCATCCTTGACC
AAACACCAGCGAATCCACACAGGGGAGAAGCCCTACGAGTGCCATGAGTGTGGAAAAGCCTTCA
CCCAGATCACACCACTGATTCAGCACCAGAGGACCCACACAGGAGAAAAGCCCTATGAGTGTGG
TGAGTGTGGGAAAGCCTTCAGTCAGAGCACACTCCTGACCGAGCATCGGAGGATTCACACAGGA
GAGAAGCCCTATGGATGCAACGAGTGTGGGAAAACCTTCAGCCACAGCTCCTCACTCAGCCAGC
ATGAGCGGACACACACAGGAGAGAAGCCCTATGAGTGCAGTCAGTGTGGGAAGGCCTTCCGGCA
GAGCACACACCTCACCCAACACCAGCGAATCCACACAGGGGAGAAGCCCTATGAATGCAATGAC
TGCGGCAAGGCATTCAGTCACAGCTCGTCCCTCACCAAACATCAGCGAATCCACACTGGGGAGA
AGCCCTACGAATGCAACCAGTGTGGCAGAGCCTTCAGCCAGCTTGCTCCCCTCATTCAGCATCA
GAGGATCCACACAGGAGAGAAACCCTATGAATGTAACCAGTGTGGCAGAGCCTTCAGCCAGAGC
TCCCTTCTCATCGAACACCAGAGGATTCACACCAAGGAAAAGCCGTATGGGTGCAATGAGTGTG
GGAAATCCTTCAGCCACAGCTCCTCGCTCAGCCAGCACGAAAGGACGCACACTGGGGAAAAGCC
CTATGAGTGTCACGATTGCGGAAAGTCCTTTAGGCAGAGCACCCACCTCACTCAGCACCGGAGG
ATCCACACAGGAGAGAAGCCATATGCATGCAGGGACTGTGGAAAGGCCTTTACCCACAGCTCCT
CCCTTACCAAGCACCAGAGAACTCACACTGGATAAACCCACTCCACATGTGCTGGGGACATAGG
AAGACCTTAAGCCATAGCTCATCCCTTTCTAGATTTGACCCAATCATACACATGAGAAACGTAC
ATTCATACACAAGCCTTTTCACACAGCACTCCCCTCAGACACCCTCAGAGAGTTCACACTGATG
GGAAATGACCATGGGACCACCAAGCTCTAGGTCATCCATCTCTGCATCCAAATAGTAGGGAAAC
GTGGAGATAATCAACACTCAGGACCTTCAGCCTTGAACGCCCATTAGTGCTATGTTATAGAACC
TACAAAAAAGAAATGGAACAAATGTAGTGGATCCAGGGAACGCTTTTGTCCAAGGATTCACCGT
ATTCCAAACCAGAGATGTTCAAATTGGTGAGAAACCCAACAAATGCCTTTCATATATACGAGAA
CCAAATGAAGTCAGAATTTGCCATTATTGCACATCACATTTTTGGGGGGGAAAGTGCTTATGAA
TGGTGCAGGTTGACTCTGATATTCATTCCCAAATGACAGTATGGCAGAGTGTTCCAGAAATGAG
AGTGGCATCTTTATGGAATCACTGTGGATACTGACTGTCTCAGTAAACAGCTGTCTTGTCTGTG
TGTATATTGTTTGATCAGGGTACATGGCAGCCAGTCACAGATTGGAATTACATATGACAAAGTA
TCAGTGTACTATAAACAGGTTTTTAGTTATCCCTGCATTATTTTTGCAATTAATCTTTATATGC
AATGAGATTGAAAAGCTTTGTATGGGAAGACTCAAAATGTAAAGCTGCTTCCGTAGAGTCTCAC
TGATTCTGAGATGGCTTTTGCTGCTCTGTTCTCCCTCTACATTTCTCTGCAGAACTCGCGTTAG
AAACACAGATATTTGTTTTACAAAAAGGGAGATTTTTCCTTTGTTAAACCATCGTCTTATAAGC
AATAGCAAATTCATGTTAGAAACTTCTGTTTTGCAAGATTCATCTTTTTTGGGATATGTTCAAG
TTAATCCTCTCAAACTGCTTTTTCATTGTTTTCATACAATTTAACATTTTGTTAAACCCTAAGT
CCACAAATAGCAGTCTTTCTGACAACTATAACCTTTAAATGGTGACTTGCTGCCCTCATTAGAA
ATTGCATTGGCTGGCCAGGCGCGGTGACTTATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGG
TGGGAGGATCACCTGAGGTCGGGAGATGGAGGTTGCAGTGAGCTGAGATCGTACCATTGCACTC
CAGCCTGGGCAACAAGAGTGAAACTCTGTCTCAGAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NM_003436 ⟹ NP_003427

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,059,282 - 58,069,755 (+)	NCBI
GRCh37	19	58,570,607 - 58,581,123 (+)	RGD
Build 36	19	63,262,424 - 63,272,588 (+)	NCBI Archive
Celera	19	55,613,970 - 55,624,470 (+)	RGD
HuRef	19	54,881,599 - 54,892,090 (+)	ENTREZGENE
CHM1_1	19	58,564,299 - 58,574,790 (+)	NCBI
T2T-CHM13v2.0	19	61,156,103 - 61,166,554 (+)	NCBI

Sequence:

show sequence

GCCGCGGCCTTTGTCTCGCAGTCAGGAGGGGCCAGCCGTTCCTGCCAGAAGCCAGGGCATGACC
CCTGGGGTGCGCGTCTCCACAGACCCGGAGCAAGTGACGTTTGAGGACGTGGTAGTGGGCTTCA
GCCAGGAGGAGTGGGGGCAGCTGAAGCCTGCCCAGAGGACCCTGTACCGTGATGTAATGCTGGA
CACCTTCAGGCTTCTGGTCTCTGTGGGACATTGGTTACCGAAGCCGAATGTCATCTCCCTGCTG
GAGCAAGAGGCAGAGCTGTGGGCGGTGGAGTCTAGACTTCCCCAAGGCGTGTACCCAGAGATTA
AGGGACATTTCCAGTTTTTGCTTCTTTCAGACTTGGAAACTAGACCCAAAGTCAAACTGTCAGT
TCTAAAGCAAGGCATCTCTGAAGAAATATCCAACAGTGTCATCTTGGTAGAAAGATTCCTGTGG
GATGGTCTGTGGTACTGCAGGGGTGAGGACACTGAGGGCCACTGGGAATGGAGTTGTGAGAGTC
TAGAGAGCCTGGCAGTGCCGGTGGCCTTCACGCCTGTGAAGACGCCTGTTCTGGAGCAGTGGCA
GAGGAATGGGTTTGGGGAAAACATAAGTCTGAACCCTGATCTCCCACATCAACCAATGACTCCT
GAAAGACAAAGCCCCCACACATGGGGAACACGTGGAAAAAGGGAGAAGCCAGACCTAAATGTTT
TACAGAAAACCTGTGTAAAAGAGAAACCCTACAAATGTCAGGAATGCGGAAAGGCCTTTAGTCA
CAGCTCAGCACTTATCGAACACCACCGGACGCACACAGGAGAGAGACCTTACGAATGTCACGAA
TGCTTAAAAGGCTTCCGGAACAGCTCGGCACTTACCAAACACCAGAGAATCCATACTGGGGAGA
AACCCTATAAATGCACTCAGTGTGGGAGGACCTTCAACCAAATTGCCCCACTGATCCAGCACCA
GAGAACTCACACAGGTGAGAAGCCCTATGAATGCAGCGAATGTGGGAAATCCTTCAGTTTTAGG
TCCTCCTTCAGCCAGCACGAGCGAACTCACACAGGCGAGAAGCCCTACGAGTGCAGTGAGTGTG
GGAAAGCCTTCCGGCAAAGCATCCACCTCACCCAGCATCTGCGAATCCACACTGGGGAGAAACC
CTATCAGTGTGGTGAGTGTGGCAAGGCCTTCAGCCACAGCTCATCCTTGACCAAACACCAGCGA
ATCCACACAGGGGAGAAGCCCTACGAGTGCCATGAGTGTGGAAAAGCCTTCACCCAGATCACAC
CACTGATTCAGCACCAGAGGACCCACACAGGAGAAAAGCCCTATGAGTGTGGTGAGTGTGGGAA
AGCCTTCAGTCAGAGCACACTCCTGACCGAGCATCGGAGGATTCACACAGGAGAGAAGCCCTAT
GGATGCAACGAGTGTGGGAAAACCTTCAGCCACAGCTCCTCACTCAGCCAGCATGAGCGGACAC
ACACAGGAGAGAAGCCCTATGAGTGCAGTCAGTGTGGGAAGGCCTTCCGGCAGAGCACACACCT
CACCCAACACCAGCGAATCCACACAGGGGAGAAGCCCTATGAATGCAATGACTGCGGCAAGGCA
TTCAGTCACAGCTCGTCCCTCACCAAACATCAGCGAATCCACACTGGGGAGAAGCCCTACGAAT
GCAACCAGTGTGGCAGAGCCTTCAGCCAGCTTGCTCCCCTCATTCAGCATCAGAGGATCCACAC
AGGAGAGAAACCCTATGAATGTAACCAGTGTGGCAGAGCCTTCAGCCAGAGCTCCCTTCTCATC
GAACACCAGAGGATTCACACCAAGGAAAAGCCGTATGGGTGCAATGAGTGTGGGAAATCCTTCA
GCCACAGCTCCTCGCTCAGCCAGCACGAAAGGACGCACACTGGGGAAAAGCCCTATGAGTGTCA
CGATTGCGGAAAGTCCTTTAGGCAGAGCACCCACCTCACTCAGCACCGGAGGATCCACACAGGA
GAGAAGCCATATGCATGCAGGGACTGTGGAAAGGCCTTTACCCACAGCTCCTCCCTTACCAAGC
ACCAGAGAACTCACACTGGATAAACCCACTCCACATGTGCTGGGGACATAGGAAGACCTTAAGC
CATAGCTCATCCCTTTCTAGATTTGACCCAATCATACACATGAGAAACGTACATTCATACACAA
GCCTTTTCACACAGCACTCCCCTCAGACACCCTCAGAGAGTTCACACTGATGGGAAATGACCAT
GGGACCACCAAGCTCTAGGTCATCCATCTCTGCATCCAAATAGTAGGGAAACGTGGAGATAATC
AACACTCAGGACCTTCAGCCTTGAACGCCCATTAGTGCTATGTTATAGAACCTACAAAAAAGAA
ATGGAACAAATGTAGTGGATCCAGGGAACGCTTTTGTCCAAGGATTCACCGTATTCCAAACCAG
AGATGTTCAAATTGGTGAGAAACCCAACAAATGCCTTTCATATATACGAGAACCAAATGAAGTC
AGAATTTGCCATTATTGCACATCACATTTTTGGGGGGGAAAGTGCTTATGAATGGTGCAGGTTG
ACTCTGATATTCATTCCCAAATGACAGTATGGCAGAGTGTTCCAGAAATGAGAGTGGCATCTTT
ATGGAATCACTGTGGATACTGACTGTCTCAGTAAACAGCTGTCTTGTCTGTGTGTATATTGTTT
GATCAGGGTACATGGCAGCCAGTCACAGATTGGAATTACATATGACAAAGTATCAGTGTACTAT
AAACAGGTTTTTAGTTATCCCTGCATTATTTTTGCAATTAATCTTTATATGCAATGAGATTGAA
AAGCTTTGTATGGGAAGACTCAAAATGTAAAGCTGCTTCCGTAGAGTCTCACTGATTCTGAGAT
GGCTTTTGCTGCTCTGTTCTCCCTCTACATTTCTCTGCAGAACTCGCGTTAGAAACACAGATAT
TTGTTTTACAAAAAGGGAGATTTTTCCTTTGTTAAACCATCGTCTTATAAGCAATAGCAAATTC
ATGTTAGAAACTTCTGTTTTGCAAGATTCATCTTTTTTGGGATATGTTCAAGTTAATCCTCTCA
AACTGCTTTTTCATTGTTTTCATACAATTTAACATTTTGTTAAACCCTAAGTCCACAAATAGCA
GTCTTTCTGACAACTATAACCTTTAAATGGTGACTTGCTGCCCTCATTAGAAATTGCATTGGCT
GGCCAGGCGCGGTGACTTATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGAGGATCAC
CTGAGGTCGGGAGATGGAGGTTGCAGTGAGCTGAGATCGTACCATTGCACTCCAGCCTGGGCAA
CAAGAGTGAAACTCTGTCTCAGAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NM_007134 ⟹ NP_009065

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,059,239 - 58,069,755 (+)	NCBI
GRCh37	19	58,570,607 - 58,581,123 (+)	RGD
Celera	19	55,613,970 - 55,624,470 (+)	RGD
HuRef	19	54,881,599 - 54,892,090 (+)	ENTREZGENE
CHM1_1	19	58,564,299 - 58,574,790 (+)	NCBI
T2T-CHM13v2.0	19	61,156,060 - 61,166,554 (+)	NCBI

Sequence:

show sequence

GAAATGGAGTTAGGCTCGCGCCGGCGCAGTGTCGGCTGCCGGTGCCGCGGCCTTTGTCTCGCAG
TCAGGAGGGAGCAAGTGACGTTTGAGGACGTGGTAGTGGGCTTCAGCCAGGAGGAGTGGGGGCA
GCTGAAGCCTGCCCAGAGGACCCTGTACCGTGATGTAATGCTGGACACCTTCAGGCTTCTGGTC
TCTGTGGGACATTGGTTACCGAAGCCGAATGTCATCTCCCTGCTGGAGCAAGAGGCAGAGCTGT
GGGCGGTGGAGTCTAGACTTCCCCAAGGCGTGTACCCAGAGATTAAGGGACATTTCCAGTTTTT
GCTTCTTTCAGACTTGGAAACTAGACCCAAAGTCAAACTGTCAGTTCTAAAGCAAGGCATCTCT
GAAGAAATATCCAACAGTGTCATCTTGGTAGAAAGATTCCTGTGGGATGGTCTGTGGTACTGCA
GGGGTGAGGACACTGAGGGCCACTGGGAATGGAGTTGTGAGAGTCTAGAGAGCCTGGCAGTGCC
GGTGGCCTTCACGCCTGTGAAGACGCCTGTTCTGGAGCAGTGGCAGAGGAATGGGTTTGGGGAA
AACATAAGTCTGAACCCTGATCTCCCACATCAACCAATGACTCCTGAAAGACAAAGCCCCCACA
CATGGGGAACACGTGGAAAAAGGGAGAAGCCAGACCTAAATGTTTTACAGAAAACCTGTGTAAA
AGAGAAACCCTACAAATGTCAGGAATGCGGAAAGGCCTTTAGTCACAGCTCAGCACTTATCGAA
CACCACCGGACGCACACAGGAGAGAGACCTTACGAATGTCACGAATGCTTAAAAGGCTTCCGGA
ACAGCTCGGCACTTACCAAACACCAGAGAATCCATACTGGGGAGAAACCCTATAAATGCACTCA
GTGTGGGAGGACCTTCAACCAAATTGCCCCACTGATCCAGCACCAGAGAACTCACACAGGTGAG
AAGCCCTATGAATGCAGCGAATGTGGGAAATCCTTCAGTTTTAGGTCCTCCTTCAGCCAGCACG
AGCGAACTCACACAGGCGAGAAGCCCTACGAGTGCAGTGAGTGTGGGAAAGCCTTCCGGCAAAG
CATCCACCTCACCCAGCATCTGCGAATCCACACTGGGGAGAAACCCTATCAGTGTGGTGAGTGT
GGCAAGGCCTTCAGCCACAGCTCATCCTTGACCAAACACCAGCGAATCCACACAGGGGAGAAGC
CCTACGAGTGCCATGAGTGTGGAAAAGCCTTCACCCAGATCACACCACTGATTCAGCACCAGAG
GACCCACACAGGAGAAAAGCCCTATGAGTGTGGTGAGTGTGGGAAAGCCTTCAGTCAGAGCACA
CTCCTGACCGAGCATCGGAGGATTCACACAGGAGAGAAGCCCTATGGATGCAACGAGTGTGGGA
AAACCTTCAGCCACAGCTCCTCACTCAGCCAGCATGAGCGGACACACACAGGAGAGAAGCCCTA
TGAGTGCAGTCAGTGTGGGAAGGCCTTCCGGCAGAGCACACACCTCACCCAACACCAGCGAATC
CACACAGGGGAGAAGCCCTATGAATGCAATGACTGCGGCAAGGCATTCAGTCACAGCTCGTCCC
TCACCAAACATCAGCGAATCCACACTGGGGAGAAGCCCTACGAATGCAACCAGTGTGGCAGAGC
CTTCAGCCAGCTTGCTCCCCTCATTCAGCATCAGAGGATCCACACAGGAGAGAAACCCTATGAA
TGTAACCAGTGTGGCAGAGCCTTCAGCCAGAGCTCCCTTCTCATCGAACACCAGAGGATTCACA
CCAAGGAAAAGCCGTATGGGTGCAATGAGTGTGGGAAATCCTTCAGCCACAGCTCCTCGCTCAG
CCAGCACGAAAGGACGCACACTGGGGAAAAGCCCTATGAGTGTCACGATTGCGGAAAGTCCTTT
AGGCAGAGCACCCACCTCACTCAGCACCGGAGGATCCACACAGGAGAGAAGCCATATGCATGCA
GGGACTGTGGAAAGGCCTTTACCCACAGCTCCTCCCTTACCAAGCACCAGAGAACTCACACTGG
ATAAACCCACTCCACATGTGCTGGGGACATAGGAAGACCTTAAGCCATAGCTCATCCCTTTCTA
GATTTGACCCAATCATACACATGAGAAACGTACATTCATACACAAGCCTTTTCACACAGCACTC
CCCTCAGACACCCTCAGAGAGTTCACACTGATGGGAAATGACCATGGGACCACCAAGCTCTAGG
TCATCCATCTCTGCATCCAAATAGTAGGGAAACGTGGAGATAATCAACACTCAGGACCTTCAGC
CTTGAACGCCCATTAGTGCTATGTTATAGAACCTACAAAAAAGAAATGGAACAAATGTAGTGGA
TCCAGGGAACGCTTTTGTCCAAGGATTCACCGTATTCCAAACCAGAGATGTTCAAATTGGTGAG
AAACCCAACAAATGCCTTTCATATATACGAGAACCAAATGAAGTCAGAATTTGCCATTATTGCA
CATCACATTTTTGGGGGGGAAAGTGCTTATGAATGGTGCAGGTTGACTCTGATATTCATTCCCA
AATGACAGTATGGCAGAGTGTTCCAGAAATGAGAGTGGCATCTTTATGGAATCACTGTGGATAC
TGACTGTCTCAGTAAACAGCTGTCTTGTCTGTGTGTATATTGTTTGATCAGGGTACATGGCAGC
CAGTCACAGATTGGAATTACATATGACAAAGTATCAGTGTACTATAAACAGGTTTTTAGTTATC
CCTGCATTATTTTTGCAATTAATCTTTATATGCAATGAGATTGAAAAGCTTTGTATGGGAAGAC
TCAAAATGTAAAGCTGCTTCCGTAGAGTCTCACTGATTCTGAGATGGCTTTTGCTGCTCTGTTC
TCCCTCTACATTTCTCTGCAGAACTCGCGTTAGAAACACAGATATTTGTTTTACAAAAAGGGAG
ATTTTTCCTTTGTTAAACCATCGTCTTATAAGCAATAGCAAATTCATGTTAGAAACTTCTGTTT
TGCAAGATTCATCTTTTTTGGGATATGTTCAAGTTAATCCTCTCAAACTGCTTTTTCATTGTTT
TCATACAATTTAACATTTTGTTAAACCCTAAGTCCACAAATAGCAGTCTTTCTGACAACTATAA
CCTTTAAATGGTGACTTGCTGCCCTCATTAGAAATTGCATTGGCTGGCCAGGCGCGGTGACTTA
TGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGAGGATCACCTGAGGTCGGGAGATGGAG
GTTGCAGTGAGCTGAGATCGTACCATTGCACTCCAGCCTGGGCAACAAGAGTGAAACTCTGTCT
CAGAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

XM_005259211 ⟹ XP_005259268

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,059,239 - 58,069,755 (+)	NCBI
GRCh37	19	58,570,607 - 58,581,123 (+)	NCBI

Sequence:

show sequence

GAAATGGAGTTAGGCTCGCGCCGGCGCAGTGTCGGCTGCCGGTGCCGCGGCCTTTGTCTCGCAG
TCAGGAGGGAGCAAGTGACGTTTGAGGACGTGGTAGTGGGCTTCAGCCAGGAGGAGTGGGGGCA
GCTGAAGCCTGCCCAGAGGACCCTGTACCGTGATGTAATGCTGGACACCTTCAGGCTTCTGGTC
TCTGTGGGACATTGGTTACCGAAGCCGAATGTCATCTCCCTGCTGGAGCAAGAGGCAGAGCTGT
GGGCGGTGGAGTCTAGACTTCCCCAAGGCGTGTACCCAGACTTGGAAACTAGACCCAAAGTCAA
ACTGTCAGTTCTAAAGCAAGGCATCTCTGAAGAAATATCCAACAGTGTCATCTTGGTAGAAAGA
TTCCTGTGGGATGGTCTGTGGTACTGCAGGGGTGAGGACACTGAGGGCCACTGGGAATGGAGTT
GTGAGAGTCTAGAGAGCCTGGCAGTGCCGGTGGCCTTCACGCCTGTGAAGACGCCTGTTCTGGA
GCAGTGGCAGAGGAATGGGTTTGGGGAAAACATAAGTCTGAACCCTGATCTCCCACATCAACCA
ATGACTCCTGAAAGACAAAGCCCCCACACATGGGGAACACGTGGAAAAAGGGAGAAGCCAGACC
TAAATGTTTTACAGAAAACCTGTGTAAAAGAGAAACCCTACAAATGTCAGGAATGCGGAAAGGC
CTTTAGTCACAGCTCAGCACTTATCGAACACCACCGGACGCACACAGGAGAGAGACCTTACGAA
TGTCACGAATGCTTAAAAGGCTTCCGGAACAGCTCGGCACTTACCAAACACCAGAGAATCCATA
CTGGGGAGAAACCCTATAAATGCACTCAGTGTGGGAGGACCTTCAACCAAATTGCCCCACTGAT
CCAGCACCAGAGAACTCACACAGGTGAGAAGCCCTATGAATGCAGCGAATGTGGGAAATCCTTC
AGTTTTAGGTCCTCCTTCAGCCAGCACGAGCGAACTCACACAGGCGAGAAGCCCTACGAGTGCA
GTGAGTGTGGGAAAGCCTTCCGGCAAAGCATCCACCTCACCCAGCATCTGCGAATCCACACTGG
GGAGAAACCCTATCAGTGTGGTGAGTGTGGCAAGGCCTTCAGCCACAGCTCATCCTTGACCAAA
CACCAGCGAATCCACACAGGGGAGAAGCCCTACGAGTGCCATGAGTGTGGAAAAGCCTTCACCC
AGATCACACCACTGATTCAGCACCAGAGGACCCACACAGGAGAAAAGCCCTATGAGTGTGGTGA
GTGTGGGAAAGCCTTCAGTCAGAGCACACTCCTGACCGAGCATCGGAGGATTCACACAGGAGAG
AAGCCCTATGGATGCAACGAGTGTGGGAAAACCTTCAGCCACAGCTCCTCACTCAGCCAGCATG
AGCGGACACACACAGGAGAGAAGCCCTATGAGTGCAGTCAGTGTGGGAAGGCCTTCCGGCAGAG
CACACACCTCACCCAACACCAGCGAATCCACACAGGGGAGAAGCCCTATGAATGCAATGACTGC
GGCAAGGCATTCAGTCACAGCTCGTCCCTCACCAAACATCAGCGAATCCACACTGGGGAGAAGC
CCTACGAATGCAACCAGTGTGGCAGAGCCTTCAGCCAGCTTGCTCCCCTCATTCAGCATCAGAG
GATCCACACAGGAGAGAAACCCTATGAATGTAACCAGTGTGGCAGAGCCTTCAGCCAGAGCTCC
CTTCTCATCGAACACCAGAGGATTCACACCAAGGAAAAGCCGTATGGGTGCAATGAGTGTGGGA
AATCCTTCAGCCACAGCTCCTCGCTCAGCCAGCACGAAAGGACGCACACTGGGGAAAAGCCCTA
TGAGTGTCACGATTGCGGAAAGTCCTTTAGGCAGAGCACCCACCTCACTCAGCACCGGAGGATC
CACACAGGAGAGAAGCCATATGCATGCAGGGACTGTGGAAAGGCCTTTACCCACAGCTCCTCCC
TTACCAAGCACCAGAGAACTCACACTGGATAAACCCACTCCACATGTGCTGGGGACATAGGAAG
ACCTTAAGCCATAGCTCATCCCTTTCTAGATTTGACCCAATCATACACATGAGAAACGTACATT
CATACACAAGCCTTTTCACACAGCACTCCCCTCAGACACCCTCAGAGAGTTCACACTGATGGGA
AATGACCATGGGACCACCAAGCTCTAGGTCATCCATCTCTGCATCCAAATAGTAGGGAAACGTG
GAGATAATCAACACTCAGGACCTTCAGCCTTGAACGCCCATTAGTGCTATGTTATAGAACCTAC
AAAAAAGAAATGGAACAAATGTAGTGGATCCAGGGAACGCTTTTGTCCAAGGATTCACCGTATT
CCAAACCAGAGATGTTCAAATTGGTGAGAAACCCAACAAATGCCTTTCATATATACGAGAACCA
AATGAAGTCAGAATTTGCCATTATTGCACATCACATTTTTGGGGGGGAAAGTGCTTATGAATGG
TGCAGGTTGACTCTGATATTCATTCCCAAATGACAGTATGGCAGAGTGTTCCAGAAATGAGAGT
GGCATCTTTATGGAATCACTGTGGATACTGACTGTCTCAGTAAACAGCTGTCTTGTCTGTGTGT
ATATTGTTTGATCAGGGTACATGGCAGCCAGTCACAGATTGGAATTACATATGACAAAGTATCA
GTGTACTATAAACAGGTTTTTAGTTATCCCTGCATTATTTTTGCAATTAATCTTTATATGCAAT
GAGATTGAAAAGCTTTGTATGGGAAGACTCAAAATGTAAAGCTGCTTCCGTAGAGTCTCACTGA
TTCTGAGATGGCTTTTGCTGCTCTGTTCTCCCTCTACATTTCTCTGCAGAACTCGCGTTAGAAA
CACAGATATTTGTTTTACAAAAAGGGAGATTTTTCCTTTGTTAAACCATCGTCTTATAAGCAAT
AGCAAATTCATGTTAGAAACTTC

hide sequence

RefSeq Acc Id:

XM_006723362 ⟹ XP_006723425

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,059,239 - 58,069,755 (+)	NCBI

Sequence:

show sequence

GGAAATGGAGTTAGGCTCGCGCCGGCGCAGTGTCGGCTGCCGGTGCCGCGGCCTTTGTCTCGCA
GTCAGGAGGAGCAGGGCCAGCCGTTCCTGCCAGAAGCCAGGGCATGACCCCTGGGGTGCGCGTC
TCCACAGACCCGGAGCAAGTGACGTTTGAGGACGTGGTAGTGGGCTTCAGCCAGGAGGAGTGGG
GGCAGCTGAAGCCTGCCCAGAGGACCCTGTACCGTGATGTAATGCTGGACACCTTCAGGCTTCT
GGTCTCTGTGGGACATTGGTTACCGAAGCCGAATGTCATCTCCCTGCTGGAGCAAGAGGCAGAG
CTGTGGGCGGTGGAGTCTAGACTTCCCCAAGGCGTGTACCCAGAGATTAAGGGACATTTCCAGT
TTTTGCTTCTTTCAGACTTGGAAACTAGACCCAAAGTCAAACTGTCAGTTCTAAAGCAAGGCAT
CTCTGAAGAAATATCCAACAGTGTCATCTTGGTAGAAAGATTCCTGTGGGATGGTCTGTGGTAC
TGCAGGGGTGAGGACACTGAGGGCCACTGGGAATGGAGTTGTGAGAGTCTAGAGAGCCTGGCAG
TGCCGGTGGCCTTCACGCCTGTGAAGACGCCTGTTCTGGAGCAGTGGCAGAGGAATGGGTTTGG
GGAAAACATAAGTCTGAACCCTGATCTCCCACATCAACCAATGACTCCTGAAAGACAAAGCCCC
CACACATGGGGAACACGTGGAAAAAGGGAGAAGCCAGACCTAAATGTTTTACAGAAAACCTGTG
TAAAAGAGAAACCCTACAAATGTCAGGAATGCGGAAAGGCCTTTAGTCACAGCTCAGCACTTAT
CGAACACCACCGGACGCACACAGGAGAGAGACCTTACGAATGTCACGAATGCTTAAAAGGCTTC
CGGAACAGCTCGGCACTTACCAAACACCAGAGAATCCATACTGGGGAGAAACCCTATAAATGCA
CTCAGTGTGGGAGGACCTTCAACCAAATTGCCCCACTGATCCAGCACCAGAGAACTCACACAGG
TGAGAAGCCCTATGAATGCAGCGAATGTGGGAAATCCTTCAGTTTTAGGTCCTCCTTCAGCCAG
CACGAGCGAACTCACACAGGCGAGAAGCCCTACGAGTGCAGTGAGTGTGGGAAAGCCTTCCGGC
AAAGCATCCACCTCACCCAGCATCTGCGAATCCACACTGGGGAGAAACCCTATCAGTGTGGTGA
GTGTGGCAAGGCCTTCAGCCACAGCTCATCCTTGACCAAACACCAGCGAATCCACACAGGGGAG
AAGCCCTACGAGTGCCATGAGTGTGGAAAAGCCTTCACCCAGATCACACCACTGATTCAGCACC
AGAGGACCCACACAGGAGAAAAGCCCTATGAGTGTGGTGAGTGTGGGAAAGCCTTCAGTCAGAG
CACACTCCTGACCGAGCATCGGAGGATTCACACAGGAGAGAAGCCCTATGGATGCAACGAGTGT
GGGAAAACCTTCAGCCACAGCTCCTCACTCAGCCAGCATGAGCGGACACACACAGGAGAGAAGC
CCTATGAGTGCAGTCAGTGTGGGAAGGCCTTCCGGCAGAGCACACACCTCACCCAACACCAGCG
AATCCACACAGGGGAGAAGCCCTATGAATGCAATGACTGCGGCAAGGCATTCAGTCACAGCTCG
TCCCTCACCAAACATCAGCGAATCCACACTGGGGAGAAGCCCTACGAATGCAACCAGTGTGGCA
GAGCCTTCAGCCAGCTTGCTCCCCTCATTCAGCATCAGAGGATCCACACAGGAGAGAAACCCTA
TGAATGTAACCAGTGTGGCAGAGCCTTCAGCCAGAGCTCCCTTCTCATCGAACACCAGAGGATT
CACACCAAGGAAAAGCCGTATGGGTGCAATGAGTGTGGGAAATCCTTCAGCCACAGCTCCTCGC
TCAGCCAGCACGAAAGGACGCACACTGGGGAAAAGCCCTATGAGTGTCACGATTGCGGAAAGTC
CTTTAGGCAGAGCACCCACCTCACTCAGCACCGGAGGATCCACACAGGAGAGAAGCCATATGCA
TGCAGGGACTGTGGAAAGGCCTTTACCCACAGCTCCTCCCTTACCAAGCACCAGAGAACTCACA
CTGGATAAACCCACTCCACATGTGCTGGGGACATAGGAAGACCTTAAGCCATAGCTCATCCCTT
TCTAGATTTGACCCAATCATACACATGAGAAACGTACATTCATACACAAGCCTTTTCACACAGC
ACTCCCCTCAGACACCCTCAGAGAGTTCACACTGATGGGAAATGACCATGGGACCACCAAGCTC
TAGGTCATCCATCTCTGCATCCAAATAGTAGGGAAACGTGGAGATAATCAACACTCAGGACCTT
CAGCCTTGAACGCCCATTAGTGCTATGTTATAGAACCTACAAAAAAGAAATGGAACAAATGTAG
TGGATCCAGGGAACGCTTTTGTCCAAGGATTCACCGTATTCCAAACCAGAGATGTTCAAATTGG
TGAGAAACCCAACAAATGCCTTTCATATATACGAGAACCAAATGAAGTCAGAATTTGCCATTAT
TGCACATCACATTTTTGGGGGGGAAAGTGCTTATGAATGGTGCAGGTTGACTCTGATATTCATT
CCCAAATGACAGTATGGCAGAGTGTTCCAGAAATGAGAGTGGCATCTTTATGGAATCACTGTGG
ATACTGACTGTCTCAGTAAACAGCTGTCTTGTCTGTGTGTATATTGTTTGATCAGGGTACATGG
CAGCCAGTCACAGATTGGAATTACATATGACAAAGTATCAGTGTACTATAAACAGGTTTTTAGT
TATCCCTGCATTATTTTTGCAATTAATCTTTATATGCAATGAGATTGAAAAGCTTTGTATGGGA
AGACTCAAAATGTAAAGCTGCTTCCGTAGAGTCTCACTGATTCTGAGATGGCTTTTGCTGCTCT
GTTCTCCCTCTACATTTCTCTGCAGAACTCGCGTTAGAAACACAGATATTTGTTTTACAAAAAG
GGAGATTTTTCCTTTGTTAAACCATCGTCTTATAAGCAATAGCAAATTCATGTTAGAAACTTC

hide sequence

RefSeq Acc Id:

XM_006723363 ⟹ XP_006723426

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,059,282 - 58,069,755 (+)	NCBI

Sequence:

show sequence

GTTTCCAGCAGCGCGCGTCTGTGTGGAGTCCGTTTTGCTGCCCGGGGCCTGGGGAAGGCCGTTT
CGGGGCTGGCGGGGGCAGGCTTTGCGGGGCATCCCTAGTCTGAGAGGAGGGCGGGGCCCAACGC
CCAGCTGGACAGGAGCTGCTCCGACGGCCCCTGAGGGAACGCGCGCCCCGCCCCTGGCCCCACC
TCTGCCCCACACCGGGCACTGGGCCGCCACCTTTGTTGATGGAAGAGAGAAACTGAGGCATAGT
GCCCAGGGCCAGGGGACCGCAACCACCCGGCCCTTGTCACTGTAGCGTTAAGGCTCAGAGTCTG
CGCAGCAGATATGTGTCCGCACCCGCCAGGCCTTCAGCTTCCCTCAGACAGGCGGGAAAACCCT
AGGCTGCCCTTCTCCGAGCGGAGGGCCGCCCCACACACAGCAGGCGCTTAAACGGAGCAGGGCC
AGCCGTTCCTGCCAGAAGCCAGGGCATGACCCCTGGGGTGCGCGTCTCCACAGACCCGGAGCAA
GTGACGTTTGAGGACGTGGTAGTGGGCTTCAGCCAGGAGGAGTGGGGGCAGCTGAAGCCTGCCC
AGAGGACCCTGTACCGTGATGTAATGCTGGACACCTTCAGGCTTCTGGTCTCTGTGGGACATTG
GTTACCGAAGCCGAATGTCATCTCCCTGCTGGAGCAAGAGGCAGAGCTGTGGGCGGTGGAGTCT
AGACTTCCCCAAGGCGTGTACCCAGAGATTAAGGGACATTTCCAGTTTTTGCTTCTTTCAGACT
TGGAAACTAGACCCAAAGTCAAACTGTCAGTTCTAAAGCAAGGCATCTCTGAAGAAATATCCAA
CAGTGTCATCTTGGTAGAAAGATTCCTGTGGGATGGTCTGTGGTACTGCAGGGGTGAGGACACT
GAGGGCCACTGGGAATGGAGTTGTGAGAGTCTAGAGAGCCTGGCAGTGCCGGTGGCCTTCACGC
CTGTGAAGACGCCTGTTCTGGAGCAGTGGCAGAGGAATGGGTTTGGGGAAAACATAAGTCTGAA
CCCTGATCTCCCACATCAACCAATGACTCCTGAAAGACAAAGCCCCCACACATGGGGAACACGT
GGAAAAAGGGAGAAGCCAGACCTAAATGTTTTACAGAAAACCTGTGTAAAAGAGAAACCCTACA
AATGTCAGGAATGCGGAAAGGCCTTTAGTCACAGCTCAGCACTTATCGAACACCACCGGACGCA
CACAGGAGAGAGACCTTACGAATGTCACGAATGCTTAAAAGGCTTCCGGAACAGCTCGGCACTT
ACCAAACACCAGAGAATCCATACTGGGGAGAAACCCTATAAATGCACTCAGTGTGGGAGGACCT
TCAACCAAATTGCCCCACTGATCCAGCACCAGAGAACTCACACAGGTGAGAAGCCCTATGAATG
CAGCGAATGTGGGAAATCCTTCAGTTTTAGGTCCTCCTTCAGCCAGCACGAGCGAACTCACACA
GGCGAGAAGCCCTACGAGTGCAGTGAGTGTGGGAAAGCCTTCCGGCAAAGCATCCACCTCACCC
AGCATCTGCGAATCCACACTGGGGAGAAACCCTATCAGTGTGGTGAGTGTGGCAAGGCCTTCAG
CCACAGCTCATCCTTGACCAAACACCAGCGAATCCACACAGGGGAGAAGCCCTACGAGTGCCAT
GAGTGTGGAAAAGCCTTCACCCAGATCACACCACTGATTCAGCACCAGAGGACCCACACAGGAG
AAAAGCCCTATGAGTGTGGTGAGTGTGGGAAAGCCTTCAGTCAGAGCACACTCCTGACCGAGCA
TCGGAGGATTCACACAGGAGAGAAGCCCTATGGATGCAACGAGTGTGGGAAAACCTTCAGCCAC
AGCTCCTCACTCAGCCAGCATGAGCGGACACACACAGGAGAGAAGCCCTATGAGTGCAGTCAGT
GTGGGAAGGCCTTCCGGCAGAGCACACACCTCACCCAACACCAGCGAATCCACACAGGGGAGAA
GCCCTATGAATGCAATGACTGCGGCAAGGCATTCAGTCACAGCTCGTCCCTCACCAAACATCAG
CGAATCCACACTGGGGAGAAGCCCTACGAATGCAACCAGTGTGGCAGAGCCTTCAGCCAGCTTG
CTCCCCTCATTCAGCATCAGAGGATCCACACAGGAGAGAAACCCTATGAATGTAACCAGTGTGG
CAGAGCCTTCAGCCAGAGCTCCCTTCTCATCGAACACCAGAGGATTCACACCAAGGAAAAGCCG
TATGGGTGCAATGAGTGTGGGAAATCCTTCAGCCACAGCTCCTCGCTCAGCCAGCACGAAAGGA
CGCACACTGGGGAAAAGCCCTATGAGTGTCACGATTGCGGAAAGTCCTTTAGGCAGAGCACCCA
CCTCACTCAGCACCGGAGGATCCACACAGGAGAGAAGCCATATGCATGCAGGGACTGTGGAAAG
GCCTTTACCCACAGCTCCTCCCTTACCAAGCACCAGAGAACTCACACTGGATAAACCCACTCCA
CATGTGCTGGGGACATAGGAAGACCTTAAGCCATAGCTCATCCCTTTCTAGATTTGACCCAATC
ATACACATGAGAAACGTACATTCATACACAAGCCTTTTCACACAGCACTCCCCTCAGACACCCT
CAGAGAGTTCACACTGATGGGAAATGACCATGGGACCACCAAGCTCTAGGTCATCCATCTCTGC
ATCCAAATAGTAGGGAAACGTGGAGATAATCAACACTCAGGACCTTCAGCCTTGAACGCCCATT
AGTGCTATGTTATAGAACCTACAAAAAAGAAATGGAACAAATGTAGTGGATCCAGGGAACGCTT
TTGTCCAAGGATTCACCGTATTCCAAACCAGAGATGTTCAAATTGGTGAGAAACCCAACAAATG
CCTTTCATATATACGAGAACCAAATGAAGTCAGAATTTGCCATTATTGCACATCACATTTTTGG
GGGGGAAAGTGCTTATGAATGGTGCAGGTTGACTCTGATATTCATTCCCAAATGACAGTATGGC
AGAGTGTTCCAGAAATGAGAGTGGCATCTTTATGGAATCACTGTGGATACTGACTGTCTCAGTA
AACAGCTGTCTTGTCTGTGTGTATATTGTTTGATCAGGGTACATGGCAGCCAGTCACAGATTGG
AATTACATATGACAAAGTATCAGTGTACTATAAACAGGTTTTTAGTTATCCCTGCATTATTTTT
GCAATTAATCTTTATATGCAATGAGATTGAAAAGCTTTGTATGGGAAGACTCAAAATGTAAAGC
TGCTTCCGTAGAGTCTCACTGATTCTGAGATGGCTTTTGCTGCTCTGTTCTCCCTCTACATTTC
TCTGCAGAACTCGCGTTAGAAACACAGATATTTGTTTTACAAAAAGGGAGATTTTTCCTTTGTT
AAACCATCGTCTTATAAGCAATAGCAAATTCATGTTAGAAACTTC

hide sequence

RefSeq Acc Id:

XM_047439362 ⟹ XP_047295318

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,059,239 - 58,069,755 (+)	NCBI

RefSeq Acc Id:

XM_047439363 ⟹ XP_047295319

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,059,282 - 58,069,755 (+)	NCBI

RefSeq Acc Id:

XM_047439364 ⟹ XP_047295320

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	58,060,069 - 58,069,755 (+)	NCBI

RefSeq Acc Id:

XM_054322003 ⟹ XP_054177978

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	61,156,060 - 61,166,554 (+)	NCBI

RefSeq Acc Id:

XM_054322004 ⟹ XP_054177979

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	61,156,246 - 61,166,554 (+)	NCBI

RefSeq Acc Id:

XM_054322005 ⟹ XP_054177980

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	61,156,060 - 61,166,554 (+)	NCBI

RefSeq Acc Id:

XM_054322006 ⟹ XP_054177981

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	61,156,060 - 61,166,554 (+)	NCBI

RefSeq Acc Id:

XM_054322007 ⟹ XP_054177982

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	61,156,155 - 61,166,554 (+)	NCBI

RefSeq Acc Id:

XM_054322008 ⟹ XP_054177983

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	61,156,895 - 61,166,554 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001157999	(Get FASTA)	NCBI Sequence Viewer
	NP_001158001	(Get FASTA)	NCBI Sequence Viewer
	NP_001158002	(Get FASTA)	NCBI Sequence Viewer
	NP_001276330	(Get FASTA)	NCBI Sequence Viewer
	NP_001276331	(Get FASTA)	NCBI Sequence Viewer
	NP_003427	(Get FASTA)	NCBI Sequence Viewer
	NP_009065	(Get FASTA)	NCBI Sequence Viewer
	XP_005259268	(Get FASTA)	NCBI Sequence Viewer
	XP_006723425	(Get FASTA)	NCBI Sequence Viewer
	XP_006723426	(Get FASTA)	NCBI Sequence Viewer
	XP_047295318	(Get FASTA)	NCBI Sequence Viewer
	XP_047295319	(Get FASTA)	NCBI Sequence Viewer
	XP_047295320	(Get FASTA)	NCBI Sequence Viewer
	XP_054177978	(Get FASTA)	NCBI Sequence Viewer
	XP_054177979	(Get FASTA)	NCBI Sequence Viewer
	XP_054177980	(Get FASTA)	NCBI Sequence Viewer
	XP_054177981	(Get FASTA)	NCBI Sequence Viewer
	XP_054177982	(Get FASTA)	NCBI Sequence Viewer
	XP_054177983	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAA61328	(Get FASTA)	NCBI Sequence Viewer
	AAC50254	(Get FASTA)	NCBI Sequence Viewer
	AAH46434	(Get FASTA)	NCBI Sequence Viewer
	BAC04309	(Get FASTA)	NCBI Sequence Viewer
	BAC05214	(Get FASTA)	NCBI Sequence Viewer
	BAG58141	(Get FASTA)	NCBI Sequence Viewer
	BAG59709	(Get FASTA)	NCBI Sequence Viewer
	CAA46338	(Get FASTA)	NCBI Sequence Viewer
	EAW72552	(Get FASTA)	NCBI Sequence Viewer
	EAW72553	(Get FASTA)	NCBI Sequence Viewer
	EAW72554	(Get FASTA)	NCBI Sequence Viewer
	EAW72555	(Get FASTA)	NCBI Sequence Viewer
	EAW72556	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000321406
	ENSP00000321406.5
	ENSP00000369437
	ENSP00000369437.4
	ENSP00000422074
	ENSP00000422074.1
	ENSP00000427691
	ENSP00000441410
	ENSP00000441410.1
	ENSP00000560160
	ENSP00000560160.1
	ENSP00000560161
	ENSP00000560161.1
	ENSP00000560162
	ENSP00000560162.1
	ENSP00000560163.1
	ENSP00000608115
	ENSP00000608115.1
GenBank Protein	P52742	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_003427 ⟸ NM_003436
- Peptide Label:	isoform 2
- UniProtKB:	P52742 (UniProtKB/Swiss-Prot), Q8N9M3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTPGVRVSTDPEQVTFEDVVVGFSQEEWGQLKPAQRTLYRDVMLDTFRLLVSVGHWLPKPNVIS LLEQEAELWAVESRLPQGVYPEIKGHFQFLLLSDLETRPKVKLSVLKQGISEEISNSVILVERF LWDGLWYCRGEDTEGHWEWSCESLESLAVPVAFTPVKTPVLEQWQRNGFGENISLNPDLPHQPM TPERQSPHTWGTRGKREKPDLNVLQKTCVKEKPYKCQECGKAFSHSSALIEHHRTHTGERPYEC HECLKGFRNSSALTKHQRIHTGEKPYKCTQCGRTFNQIAPLIQHQRTHTGEKPYECSECGKSFS FRSSFSQHERTHTGEKPYECSECGKAFRQSIHLTQHLRIHTGEKPYQCGECGKAFSHSSSLTKH QRIHTGEKPYECHECGKAFTQITPLIQHQRTHTGEKPYECGECGKAFSQSTLLTEHRRIHTGEK PYGCNECGKTFSHSSSLSQHERTHTGEKPYECSQCGKAFRQSTHLTQHQRIHTGEKPYECNDCG KAFSHSSSLTKHQRIHTGEKPYECNQCGRAFSQLAPLIQHQRIHTGEKPYECNQCGRAFSQSSL LIEHQRIHTKEKPYGCNECGKSFSHSSSLSQHERTHTGEKPYECHDCGKSFRQSTHLTQHRRIH TGEKPYACRDCGKAFTHSSSLTKHQRTHTG hide sequence

RefSeq Acc Id:	NP_009065 ⟸ NM_007134
- Peptide Label:	isoform 1
- UniProtKB:	P52742 (UniProtKB/Swiss-Prot), Q8N9M3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MELGSRRRSVGCRCRGLCLAVRREQVTFEDVVVGFSQEEWGQLKPAQRTLYRDVMLDTFRLLVS VGHWLPKPNVISLLEQEAELWAVESRLPQGVYPEIKGHFQFLLLSDLETRPKVKLSVLKQGISE EISNSVILVERFLWDGLWYCRGEDTEGHWEWSCESLESLAVPVAFTPVKTPVLEQWQRNGFGEN ISLNPDLPHQPMTPERQSPHTWGTRGKREKPDLNVLQKTCVKEKPYKCQECGKAFSHSSALIEH HRTHTGERPYECHECLKGFRNSSALTKHQRIHTGEKPYKCTQCGRTFNQIAPLIQHQRTHTGEK PYECSECGKSFSFRSSFSQHERTHTGEKPYECSECGKAFRQSIHLTQHLRIHTGEKPYQCGECG KAFSHSSSLTKHQRIHTGEKPYECHECGKAFTQITPLIQHQRTHTGEKPYECGECGKAFSQSTL LTEHRRIHTGEKPYGCNECGKTFSHSSSLSQHERTHTGEKPYECSQCGKAFRQSTHLTQHQRIH TGEKPYECNDCGKAFSHSSSLTKHQRIHTGEKPYECNQCGRAFSQLAPLIQHQRIHTGEKPYEC NQCGRAFSQSSLLIEHQRIHTKEKPYGCNECGKSFSHSSSLSQHERTHTGEKPYECHDCGKSFR QSTHLTQHRRIHTGEKPYACRDCGKAFTHSSSLTKHQRTHTG hide sequence

RefSeq Acc Id:	NP_001158001 ⟸ NM_001164529
- Peptide Label:	isoform 4
- UniProtKB:	P52742 (UniProtKB/Swiss-Prot), Q8N9M3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MELGSRRRSVGCRCRGLCLAVRREQVTFEDVVVGFSQEEWGQLKPAQRTLYRDVMLDTFRLLVS VGHWLPKPNVISLLEQEAELWAVESRLPQGVYPENLCKRETLQMSGMRKGL hide sequence

RefSeq Acc Id:	NP_001158002 ⟸ NM_001164530
- Peptide Label:	isoform 5
- UniProtKB:	P52742 (UniProtKB/Swiss-Prot), B4DLZ7 (UniProtKB/TrEMBL), Q8N9M3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MELGSRRRSVGCRCRGLCLAVRREQVTFEDVVVGFSQEEWGQLKPAQRTLYRDVMLDTFRLLVS VGHWLPKPNVISLLEQEAELWAVESRLPQGVYPDLETRPKVKLSVLKQGISEEISNSVILVERF LWDGLWYCRGEDTEGHWEWSCESLESLAVPVAFTPVKTPVLEQWQRNGFGENISLNPDLPHQPM TPERQSPHTWGTRGKREKPDLNVLQKTCVKEKPYKCQECGKAFSHSSALIEHHRTHTGERPYEC HECLKGFRNSSALTKHQRIHTGEKPYKCTQCGRTFNQIAPLIQHQRTHTGEKPYECSECGKSFS FRSSFSQHERTHTGEKPYECSECGKAFRQSIHLTQHLRIHTGEKPYQCGECGKAFTHSSSLTKH QRTHTG hide sequence

RefSeq Acc Id:	NP_001157999 ⟸ NM_001164527
- Peptide Label:	isoform 3
- UniProtKB:	Q8N9M3 (UniProtKB/TrEMBL)
- Sequence:	show sequence MELGSRRRSVGCRCRGLCLAVRREQVTFEDVVVGFSQEEWGQLKPAQRTLYRDVMLDTFRLLVS VGHWLPKPNVISLLEQEAELWAVESRLPQGVYPGEMGALRGREKPVHACFLVSPSASAL hide sequence

RefSeq Acc Id:

XP_005259268 ⟸ XM_005259211

- Peptide Label:

isoform X2

- Sequence:

show sequence

MELGSRRRSVGCRCRGLCLAVRREQVTFEDVVVGFSQEEWGQLKPAQRTLYRDVMLDTFRLLVS
VGHWLPKPNVISLLEQEAELWAVESRLPQGVYPDLETRPKVKLSVLKQGISEEISNSVILVERF
LWDGLWYCRGEDTEGHWEWSCESLESLAVPVAFTPVKTPVLEQWQRNGFGENISLNPDLPHQPM
TPERQSPHTWGTRGKREKPDLNVLQKTCVKEKPYKCQECGKAFSHSSALIEHHRTHTGERPYEC
HECLKGFRNSSALTKHQRIHTGEKPYKCTQCGRTFNQIAPLIQHQRTHTGEKPYECSECGKSFS
FRSSFSQHERTHTGEKPYECSECGKAFRQSIHLTQHLRIHTGEKPYQCGECGKAFSHSSSLTKH
QRIHTGEKPYECHECGKAFTQITPLIQHQRTHTGEKPYECGECGKAFSQSTLLTEHRRIHTGEK
PYGCNECGKTFSHSSSLSQHERTHTGEKPYECSQCGKAFRQSTHLTQHQRIHTGEKPYECNDCG
KAFSHSSSLTKHQRIHTGEKPYECNQCGRAFSQLAPLIQHQRIHTGEKPYECNQCGRAFSQSSL
LIEHQRIHTKEKPYGCNECGKSFSHSSSLSQHERTHTGEKPYECHDCGKSFRQSTHLTQHRRIH
TGEKPYACRDCGKAFTHSSSLTKHQRTHTG

hide sequence

RefSeq Acc Id:	NP_001276331 ⟸ NM_001289402
- Peptide Label:	isoform 7
- UniProtKB:	Q8N9M3 (UniProtKB/TrEMBL), F6QNB9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLDTFRLLVSVGHWLPKPNVISLLEQEAELWAVESRLPQGVYPDLETRPKVKLSVLKQGISEEI SNSVILVERFLWDGLWYCRGEDTEGHWEWSCESLESLAVPVAFTPVKTPVLEQWQRNGFGENIS LNPDLPHQPMTPERQSPHTWGTRGKREKPDLNVLQKTCVKEKPYKCQECGKAFSHSSALIEHHR THTGERPYECHECLKGFRNSSALTKHQRIHTGEKPYKCTQCGRTFNQIAPLIQHQRTHTGEKPY ECSECGKSFSFRSSFSQHERTHTGEKPYECSECGKAFRQSIHLTQHLRIHTGEKPYQCGECGKA FSHSSSLTKHQRIHTGEKPYECHECGKAFTQITPLIQHQRTHTGEKPYECGECGKAFSQSTLLT EHRRIHTGEKPYGCNECGKTFSHSSSLSQHERTHTGEKPYECSQCGKAFRQSTHLTQHQRIHTG EKPYECNDCGKAFSHSSSLTKHQRIHTGEKPYECNQCGRAFSQLAPLIQHQRIHTGEKPYECNQ CGRAFSQSSLLIEHQRIHTKEKPYGCNECGKSFSHSSSLSQHERTHTGEKPYECHDCGKSFRQS THLTQHRRIHTGEKPYACRDCGKAFTHSSSLTKHQRTHTG hide sequence

RefSeq Acc Id:	NP_001276330 ⟸ NM_001289401
- Peptide Label:	isoform 6
- UniProtKB:	Q5U5L3 (UniProtKB/Swiss-Prot), I3L0B3 (UniProtKB/Swiss-Prot), F5GYY9 (UniProtKB/Swiss-Prot), E9PEV2 (UniProtKB/Swiss-Prot), B4DHH9 (UniProtKB/Swiss-Prot), Q8N1I7 (UniProtKB/Swiss-Prot), P52742 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MTPGVRVSTDPEQVTFEDVVVGFSQEEWGQLKPAQRTLYRDVMLDTFRLLVSVGHWLPKPNVIS LLEQEAELWAVESRLPQGVYPDLETRPKVKLSVLKQGISEEISNSVILVERFLWDGLWYCRGED TEGHWEWSCESLESLAVPVAFTPVKTPVLEQWQRNGFGENISLNPDLPHQPMTPERQSPHTWGT RGKREKPDLNVLQKTCVKEKPYKCQECGKAFSHSSALIEHHRTHTGERPYECHECLKGFRNSSA LTKHQRIHTGEKPYKCTQCGRTFNQIAPLIQHQRTHTGEKPYECSECGKSFSFRSSFSQHERTH TGEKPYECSECGKAFRQSIHLTQHLRIHTGEKPYQCGECGKAFSHSSSLTKHQRIHTGEKPYEC HECGKAFTQITPLIQHQRTHTGEKPYECGECGKAFSQSTLLTEHRRIHTGEKPYGCNECGKTFS HSSSLSQHERTHTGEKPYECSQCGKAFRQSTHLTQHQRIHTGEKPYECNDCGKAFSHSSSLTKH QRIHTGEKPYECNQCGRAFSQLAPLIQHQRIHTGEKPYECNQCGRAFSQSSLLIEHQRIHTKEK PYGCNECGKSFSHSSSLSQHERTHTGEKPYECHDCGKSFRQSTHLTQHRRIHTGEKPYACRDCG KAFTHSSSLTKHQRTHTG hide sequence

RefSeq Acc Id:	XP_006723425 ⟸ XM_006723362
- Peptide Label:	isoform X1
- UniProtKB:	P52742 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MTPGVRVSTDPEQVTFEDVVVGFSQEEWGQLKPAQRTLYRDVMLDTFRLLVSVGHWLPKPNVIS LLEQEAELWAVESRLPQGVYPEIKGHFQFLLLSDLETRPKVKLSVLKQGISEEISNSVILVERF LWDGLWYCRGEDTEGHWEWSCESLESLAVPVAFTPVKTPVLEQWQRNGFGENISLNPDLPHQPM TPERQSPHTWGTRGKREKPDLNVLQKTCVKEKPYKCQECGKAFSHSSALIEHHRTHTGERPYEC HECLKGFRNSSALTKHQRIHTGEKPYKCTQCGRTFNQIAPLIQHQRTHTGEKPYECSECGKSFS FRSSFSQHERTHTGEKPYECSECGKAFRQSIHLTQHLRIHTGEKPYQCGECGKAFSHSSSLTKH QRIHTGEKPYECHECGKAFTQITPLIQHQRTHTGEKPYECGECGKAFSQSTLLTEHRRIHTGEK PYGCNECGKTFSHSSSLSQHERTHTGEKPYECSQCGKAFRQSTHLTQHQRIHTGEKPYECNDCG KAFSHSSSLTKHQRIHTGEKPYECNQCGRAFSQLAPLIQHQRIHTGEKPYECNQCGRAFSQSSL LIEHQRIHTKEKPYGCNECGKSFSHSSSLSQHERTHTGEKPYECHDCGKSFRQSTHLTQHRRIH TGEKPYACRDCGKAFTHSSSLTKHQRTHTG hide sequence

RefSeq Acc Id:	XP_006723426 ⟸ XM_006723363
- Peptide Label:	isoform X1
- UniProtKB:	P52742 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MTPGVRVSTDPEQVTFEDVVVGFSQEEWGQLKPAQRTLYRDVMLDTFRLLVSVGHWLPKPNVIS LLEQEAELWAVESRLPQGVYPEIKGHFQFLLLSDLETRPKVKLSVLKQGISEEISNSVILVERF LWDGLWYCRGEDTEGHWEWSCESLESLAVPVAFTPVKTPVLEQWQRNGFGENISLNPDLPHQPM TPERQSPHTWGTRGKREKPDLNVLQKTCVKEKPYKCQECGKAFSHSSALIEHHRTHTGERPYEC HECLKGFRNSSALTKHQRIHTGEKPYKCTQCGRTFNQIAPLIQHQRTHTGEKPYECSECGKSFS FRSSFSQHERTHTGEKPYECSECGKAFRQSIHLTQHLRIHTGEKPYQCGECGKAFSHSSSLTKH QRIHTGEKPYECHECGKAFTQITPLIQHQRTHTGEKPYECGECGKAFSQSTLLTEHRRIHTGEK PYGCNECGKTFSHSSSLSQHERTHTGEKPYECSQCGKAFRQSTHLTQHQRIHTGEKPYECNDCG KAFSHSSSLTKHQRIHTGEKPYECNQCGRAFSQLAPLIQHQRIHTGEKPYECNQCGRAFSQSSL LIEHQRIHTKEKPYGCNECGKSFSHSSSLSQHERTHTGEKPYECHDCGKSFRQSTHLTQHRRIH TGEKPYACRDCGKAFTHSSSLTKHQRTHTG hide sequence

Ensembl Acc Id:

ENSP00000369437 ⟸ ENST00000359978

Ensembl Acc Id:

ENSP00000427691 ⟸ ENST00000506786

Ensembl Acc Id:

ENSP00000441410 ⟸ ENST00000401053

Ensembl Acc Id:

ENSP00000321406 ⟸ ENST00000313434

Ensembl Acc Id:

ENSP00000422074 ⟸ ENST00000511556

Ensembl Acc Id:

ENSP00000471344 ⟸ ENST00000515535

RefSeq Acc Id:	XP_047295318 ⟸ XM_047439362
- Peptide Label:	isoform X3
- UniProtKB:	Q5U5L3 (UniProtKB/Swiss-Prot), P52742 (UniProtKB/Swiss-Prot), I3L0B3 (UniProtKB/Swiss-Prot), F5GYY9 (UniProtKB/Swiss-Prot), E9PEV2 (UniProtKB/Swiss-Prot), B4DHH9 (UniProtKB/Swiss-Prot), Q8N1I7 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047295319 ⟸ XM_047439363
- Peptide Label:	isoform X3
- UniProtKB:	Q5U5L3 (UniProtKB/Swiss-Prot), P52742 (UniProtKB/Swiss-Prot), I3L0B3 (UniProtKB/Swiss-Prot), F5GYY9 (UniProtKB/Swiss-Prot), E9PEV2 (UniProtKB/Swiss-Prot), B4DHH9 (UniProtKB/Swiss-Prot), Q8N1I7 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047295320 ⟸ XM_047439364
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054177978 ⟸ XM_054322003
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054177981 ⟸ XM_054322006
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054177980 ⟸ XM_054322005
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054177982 ⟸ XM_054322007
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054177979 ⟸ XM_054322004
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054177983 ⟸ XM_054322008
- Peptide Label:	isoform X4

Ensembl Acc Id:

ENSP00000560161 ⟸ ENST00000890102

Ensembl Acc Id:

ENSP00000608115 ⟸ ENST00000938056

Ensembl Acc Id:

ENSP00000560163 ⟸ ENST00000890104

Ensembl Acc Id:

ENSP00000560160 ⟸ ENST00000890101

Ensembl Acc Id:

ENSP00000560162 ⟸ ENST00000890103

Ensembl Acc Id:

ENSP00000799823 ⟸ ENST00001130018

Ensembl Acc Id:

ENSP00000717951 ⟸ ENST00001048134

Ensembl Acc Id:

ENSP00000658137 ⟸ ENST00000988320

Ensembl Acc Id:

ENSP00000717952 ⟸ ENST00001048135

Ensembl Acc Id:

ENSP00000717948 ⟸ ENST00001048131

Ensembl Acc Id:

ENSP00000792039 ⟸ ENST00001122234

Ensembl Acc Id:

ENSP00000792038 ⟸ ENST00001122233

Ensembl Acc Id:

ENSP00000717950 ⟸ ENST00001048133

Ensembl Acc Id:

ENSP00000717949 ⟸ ENST00001048132

Ensembl Acc Id:

ENSP00000765122 ⟸ ENST00001095316

Protein Domains

C2H2-type KRAB

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-P52742-F1-model_v2	AlphaFold	P52742	1-658	view protein structure

Promoters

RGD ID:

13205957

Promoter ID:

EPDNEW_H26559

Type:

initiation region

Name:

ZNF135_1

Description:

zinc finger protein 135

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	19	58,059,282 - 58,059,342	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:12919	AgrOrtholog
COSMIC	ZNF135	COSMIC
Ensembl Genes	ENSG00000176293	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000313434	ENTREZGENE
	ENST00000313434.10	UniProtKB/Swiss-Prot
	ENST00000359978	ENTREZGENE
	ENST00000359978.10	UniProtKB/Swiss-Prot
	ENST00000401053	ENTREZGENE
	ENST00000401053.8	UniProtKB/Swiss-Prot
	ENST00000506786	ENTREZGENE
	ENST00000511556	ENTREZGENE
	ENST00000511556.5	UniProtKB/Swiss-Prot
	ENST00000890101	ENTREZGENE
	ENST00000890101.1	UniProtKB/Swiss-Prot
	ENST00000890102	ENTREZGENE
	ENST00000890102.1	UniProtKB/Swiss-Prot
	ENST00000890103	ENTREZGENE
	ENST00000890103.1	UniProtKB/Swiss-Prot
	ENST00000890104.1	UniProtKB/Swiss-Prot
	ENST00000938056	ENTREZGENE
	ENST00000938056.1	UniProtKB/Swiss-Prot
Gene3D-CATH	6.10.140.140	UniProtKB/Swiss-Prot
	Classic Zinc Finger	UniProtKB/Swiss-Prot
GTEx	ENSG00000176293	GTEx
HGNC ID	HGNC:12919	ENTREZGENE
Human Proteome Map	ZNF135	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:7694	UniProtKB/Swiss-Prot
NCBI Gene	7694	ENTREZGENE
OMIM	604077	OMIM
PANTHER	ZINC FINGER PROTEIN	UniProtKB/Swiss-Prot
	ZINC FINGER PROTEIN 606	UniProtKB/Swiss-Prot
Pfam	KRAB	UniProtKB/Swiss-Prot
	zf-C2H2	UniProtKB/Swiss-Prot
PharmGKB	PA37507	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	B4DHH9	ENTREZGENE
	B4DLZ7	ENTREZGENE, UniProtKB/TrEMBL
	E9PEV2	ENTREZGENE
	F5GYY9	ENTREZGENE
	F6QNB9	ENTREZGENE, UniProtKB/TrEMBL
	I3L0B3	ENTREZGENE
	M0R0N7_HUMAN	UniProtKB/TrEMBL
	P52742	ENTREZGENE
	Q5U5L3	ENTREZGENE
	Q8N1I7	ENTREZGENE
	Q8N9M3	ENTREZGENE, UniProtKB/TrEMBL
	ZN135_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	B4DHH9	UniProtKB/Swiss-Prot
	E9PEV2	UniProtKB/Swiss-Prot
	F5GYY9	UniProtKB/Swiss-Prot
	I3L0B3	UniProtKB/Swiss-Prot
	Q5U5L3	UniProtKB/Swiss-Prot
	Q8N1I7	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-03-31	ZNF135	zinc finger protein 135	ZNF78L1	zinc finger protein 78-like 1 (pT3)	Data merged from RGD:1344887	737654	PROVISIONAL

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)

Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

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