HEXIM2 (HEXIM P-TEFb complex subunit 2)

Gene: HEXIM2 (HEXIM P-TEFb complex subunit 2) Homo sapiens

Analyze

Symbol:

HEXIM2

Name:

HEXIM P-TEFb complex subunit 2

RGD ID:

1601726

HGNC Page

HGNC:28591

Description:

Enables 7SK snRNA binding activity; cyclin-dependent protein serine/threonine kinase inhibitor activity; and identical protein binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in cytosol and nuclear speck.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

FLJ32384; hexamethylene bis-acetamide inducible 2; hexamethylene bis-acetamide-inducible protein 2; hexamethylene bisacetamide inducible 2; hexamethylene-bis-acetamide-inducible transcript 2; hexamthylene bis-acetamide inducible 2; L3; MAQ1 paralog

RGD Orthologs

Alliance Genes

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	17	45,160,174 - 45,170,040 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	17	45,160,700 - 45,170,040 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	17	43,237,541 - 43,247,407 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	17	40,594,047 - 40,603,189 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	17	39,947,916 - 39,957,031 (+)	NCBI		Celera
Cytogenetic Map	17	q21.31	NCBI
HuRef	17	39,001,091 - 39,009,915 (+)	NCBI		HuRef
CHM1_1	17	43,473,807 - 43,482,952 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	17	46,014,059 - 46,023,937 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

genetic disease (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dimethylhydrazine (ISO)

17beta-estradiol (EXP)

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

3,3',4,4',5-pentachlorobiphenyl (ISO)

4,4'-sulfonyldiphenol (ISO)

arsane (EXP)

arsenic atom (EXP)

benzo[a]pyrene (EXP)

benzo[b]fluoranthene (ISO)

benzo[e]pyrene (EXP)

bisphenol A (EXP,ISO)

bisphenol F (ISO)

caffeine (EXP)

carbon nanotube (ISO)

CGP 52608 (EXP)

chlorpyrifos (ISO)

choline (ISO)

cisplatin (EXP)

copper(II) sulfate (EXP)

cyclosporin A (EXP)

Ethylenethiourea (ISO)

folic acid (ISO)

formaldehyde (EXP)

FR900359 (EXP)

gentamycin (ISO)

iron dichloride (EXP)

L-methionine (ISO)

leflunomide (ISO)

methapyrilene (EXP)

methyl methanesulfonate (EXP)

paracetamol (EXP)

pirinixic acid (ISO)

quercetin (EXP)

silver atom (ISO)

silver(0) (ISO)

sunitinib (EXP)

T-2 toxin (ISO)

temozolomide (EXP)

trichloroethene (ISO)

triptonide (ISO)

tunicamycin (EXP)

urethane (EXP)

valproic acid (EXP,ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

negative regulation of DNA-templated transcription (IDA)

negative regulation of transcription by RNA polymerase II (IBA,IDA,IEA)

Cellular Component

cytoplasm (IBA,IEA,ISS)

cytosol (IDA)

nuclear speck (IDA)

nucleoplasm (IBA,IDA,IEA)

nucleus (IEA,ISS)

Molecular Function

7SK snRNA binding (IBA,IDA,IEA)

cyclin-dependent protein serine/threonine kinase inhibitor activity (IBA,IDA,IEA)

identical protein binding (IPI)

protein binding (IPI)

snRNA binding (IDA,IEA)

References

References - curated

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

Additional References at PubMed

PMID:8889548	PMID:12477932	PMID:12832472	PMID:14702039	PMID:15146197	PMID:15302935	PMID:15334068	PMID:15342556	PMID:15713661	PMID:15713662	PMID:15965233	PMID:15992410
PMID:15994294	PMID:16344560	PMID:17207965	PMID:17643375	PMID:17709395	PMID:18029348	PMID:18281698	PMID:18655042	PMID:19430483	PMID:19883659	PMID:21044950	PMID:21516116
PMID:21873635	PMID:22355797	PMID:22377309	PMID:23455922	PMID:23518577	PMID:24515107	PMID:25416956	PMID:25609649	PMID:26186194	PMID:26673895	PMID:27684187	PMID:28514442
PMID:28611215	PMID:29802200	PMID:29845934	PMID:32296183	PMID:32393512	PMID:32707033	PMID:33961781	PMID:35140242	PMID:35271311	PMID:35944360	PMID:36244648	PMID:36736316

Genomics

Comparative Map Data

HEXIM2
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	17	45,160,174 - 45,170,040 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	17	45,160,700 - 45,170,040 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	17	43,237,541 - 43,247,407 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	17	40,594,047 - 40,603,189 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	17	39,947,916 - 39,957,031 (+)	NCBI		Celera
Cytogenetic Map	17	q21.31	NCBI
HuRef	17	39,001,091 - 39,009,915 (+)	NCBI		HuRef
CHM1_1	17	43,473,807 - 43,482,952 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	17	46,014,059 - 46,023,937 (+)	NCBI		T2T-CHM13v2.0

Hexim2
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	11	103,014,086 - 103,030,734 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	11	103,023,255 - 103,030,702 (+)	Ensembl		GRCm39 Ensembl
GRCm38	11	103,123,260 - 103,139,908 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	11	103,132,429 - 103,139,876 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	11	102,994,653 - 103,001,222 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	11	102,949,404 - 102,955,998 (+)	NCBI		MGSCv36	mm8
Celera	11	114,816,349 - 114,849,525 (+)	NCBI		Celera
Cytogenetic Map	11	E1	NCBI
cM Map	11	66.71	NCBI

Hexim2
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	10	88,572,102 - 88,584,856 (+)	NCBI		GRCr8
mRatBN7.2	10	88,077,870 - 88,084,776 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	10	88,079,014 - 88,084,775 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	10	93,115,155 - 93,120,921 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	10	92,581,799 - 92,587,566 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	10	87,975,151 - 87,980,918 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	10	91,212,296 - 91,222,841 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	10	91,217,079 - 91,222,840 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	10	90,988,728 - 90,994,491 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	10	92,306,494 - 92,312,256 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	10	92,320,794 - 92,329,877 (+)	NCBI
Celera	10	86,780,500 - 86,786,262 (+)	NCBI		Celera
Cytogenetic Map	10	q32.1	NCBI

HEXIM2
(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	19	19,667,571 - 19,676,969 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	17	21,636,155 - 21,646,713 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	17	12,157,392 - 12,167,281 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	17	12,333,957 - 12,343,424 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	17	12,333,957 - 12,343,399 (-)	Ensembl	panpan1.1		panPan2

HEXIM2
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	9	18,373,761 - 18,379,185 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	9	18,373,992 - 18,377,260 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	9	17,758,535 - 17,763,959 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	9	19,046,798 - 19,052,222 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	9	19,046,986 - 19,050,297 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	9	17,925,068 - 17,930,491 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	9	18,103,901 - 18,109,325 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	9	18,259,869 - 18,265,293 (-)	NCBI		UU_Cfam_GSD_1.0

Hexim2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024405602	17,717,605 - 17,722,656 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936541	1,472,027 - 1,477,048 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936541	1,472,041 - 1,476,993 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

HEXIM2
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	12	18,251,428 - 18,258,295 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	12	18,251,424 - 18,263,032 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	12	18,500,139 - 18,509,293 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

HEXIM2
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	16	61,236,919 - 61,251,203 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	16	61,236,566 - 61,248,252 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666077	31,985,644 - 31,996,088 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Variants

Variants in HEXIM2
10 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3	copy number gain	See cases [RCV000050957]	Chr17:36449220..68170214 [GRCh38] Chr17:48563237..65936105 [GRCh37] Chr17:45918236..63677950 [NCBI36] Chr17:17q21.33-24.2	pathogenic
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]\|See cases [RCV000052483]	Chr17:36449220..83086677 [GRCh38] Chr17:58617905..81044553 [GRCh37] Chr17:55972687..78637842 [NCBI36] Chr17:17q23.2-25.3	pathogenic
GRCh38/hg38 17q12-21.31(chr17:39199873-45629579)x3	copy number gain	See cases [RCV000052479]	Chr17:39199873..45629579 [GRCh38] Chr17:37356126..43706945 [GRCh37] Chr17:34609652..41062728 [NCBI36] Chr17:17q12-21.31	pathogenic
GRCh38/hg38 17q21.31-21.33(chr17:44955325-49381173)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052480]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052480]\|See cases [RCV000052480]	Chr17:44955325..49381173 [GRCh38] Chr17:43032693..47458535 [GRCh37] Chr17:40388219..44813534 [NCBI36] Chr17:17q21.31-21.33	pathogenic
GRCh38/hg38 17q21.31(chr17:44928498-45299730)x1	copy number loss	See cases [RCV000053430]	Chr17:44928498..45299730 [GRCh38] Chr17:43005866..43377096 [GRCh37] Chr17:40361392..40732879 [NCBI36] Chr17:17q21.31	pathogenic
GRCh38/hg38 17q21.31(chr17:44906235-45220406)x3	copy number gain	See cases [RCV000054045]	Chr17:44906235..45220406 [GRCh38] Chr17:42983603..43297773 [GRCh37] Chr17:40339129..40653556 [NCBI36] Chr17:17q21.31	uncertain significance
GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3	copy number gain	See cases [RCV000137437]	Chr17:36449220..75053130 [GRCh38] Chr17:57595736..73049225 [GRCh37] Chr17:54950518..70560820 [NCBI36] Chr17:17q23.1-25.1	pathogenic
GRCh37/hg19 17q21.31-25.3(chr17:42580684-81085615)x3	copy number gain	See cases [RCV000447823]	Chr17:42580684..81085615 [GRCh37] Chr17:17q21.31-25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)	copy number gain	See cases [RCV000511439]	Chr17:526..81041938 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
NM_001303441.2(HEXIM2):c.592G>C (p.Glu198Gln)	single nucleotide variant	Inborn genetic diseases [RCV003243745]	Chr17:45169540 [GRCh38] Chr17:43246907 [GRCh37] Chr17:17q21.31	uncertain significance
GRCh37/hg19 17q21.31(chr17:42649083-43659985)x3	copy number gain	See cases [RCV000512371]	Chr17:42649083..43659985 [GRCh37] Chr17:17q21.31	uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3	copy number gain	See cases [RCV000512441]	Chr17:526..81041938 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3	copy number gain	not provided [RCV000739324]	Chr17:8547..81060040 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3	copy number gain	not provided [RCV000739320]	Chr17:7214..81058310 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3	copy number gain	not provided [RCV000739325]	Chr17:12344..81057996 [GRCh37] Chr17:17p13.3-q25.3	pathogenic
NM_001303441.2(HEXIM2):c.80C>G (p.Pro27Arg)	single nucleotide variant	not provided [RCV001813144]	Chr17:45169028 [GRCh38] Chr17:43246395 [GRCh37] Chr17:17q21.31	uncertain significance
NM_001303441.2(HEXIM2):c.752A>G (p.Glu251Gly)	single nucleotide variant	Inborn genetic diseases [RCV003297773]	Chr17:45169700 [GRCh38] Chr17:43247067 [GRCh37] Chr17:17q21.31	uncertain significance
NM_001303441.2(HEXIM2):c.64A>G (p.Lys22Glu)	single nucleotide variant	Inborn genetic diseases [RCV002707592]	Chr17:45162857 [GRCh38] Chr17:43240224 [GRCh37] Chr17:17q21.31	uncertain significance
NM_001303441.2(HEXIM2):c.757G>T (p.Ala253Ser)	single nucleotide variant	Inborn genetic diseases [RCV002916065]	Chr17:45169705 [GRCh38] Chr17:43247072 [GRCh37] Chr17:17q21.31	uncertain significance
NM_001303441.2(HEXIM2):c.169G>C (p.Asp57His)	single nucleotide variant	Inborn genetic diseases [RCV002763295]	Chr17:45169117 [GRCh38] Chr17:43246484 [GRCh37] Chr17:17q21.31	uncertain significance
NM_001303441.2(HEXIM2):c.498C>G (p.His166Gln)	single nucleotide variant	Inborn genetic diseases [RCV002965910]	Chr17:45169446 [GRCh38] Chr17:43246813 [GRCh37] Chr17:17q21.31	uncertain significance
NM_001303441.2(HEXIM2):c.281G>T (p.Arg94Leu)	single nucleotide variant	Inborn genetic diseases [RCV002854717]	Chr17:45169229 [GRCh38] Chr17:43246596 [GRCh37] Chr17:17q21.31	uncertain significance
NM_001303441.2(HEXIM2):c.793C>T (p.Arg265Trp)	single nucleotide variant	Inborn genetic diseases [RCV003210145]	Chr17:45169741 [GRCh38] Chr17:43247108 [GRCh37] Chr17:17q21.31	uncertain significance
NM_001303441.2(HEXIM2):c.836G>T (p.Arg279Leu)	single nucleotide variant	Inborn genetic diseases [RCV003349483]	Chr17:45169784 [GRCh38] Chr17:43247151 [GRCh37] Chr17:17q21.31	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	2322
Count of miRNA genes:	693
Interacting mature miRNAs:	814
Transcripts:	ENST00000307275, ENST00000585340, ENST00000586681, ENST00000589230, ENST00000591070, ENST00000591576, ENST00000592695, ENST00000593138
Prediction methods:	Microtar, Miranda, Rnahybrid, Targetscan
Result types:	miRGate_prediction

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

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

Markers in Region

RH78214

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	43,247,195 - 43,247,347	UniSTS	GRCh37
Build 36	17	40,602,978 - 40,603,130	RGD	NCBI36
Celera	17	39,956,820 - 39,956,972	RGD
Cytogenetic Map	17	q21.31	UniSTS
HuRef	17	39,009,704 - 39,009,856	UniSTS
GeneMap99-GB4 RH Map	17	329.66	UniSTS

SHGC-30043

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	17	43,247,255 - 43,247,388	UniSTS	GRCh37
Build 36	17	40,603,038 - 40,603,171	RGD	NCBI36
Celera	17	39,956,880 - 39,957,013	RGD
Cytogenetic Map	17	q21.31	UniSTS
HuRef	17	39,009,764 - 39,009,897	UniSTS
TNG Radiation Hybrid Map	17	20476.0	UniSTS
Stanford-G3 RH Map	17	1923.0	UniSTS
NCBI RH Map	17	586.3	UniSTS
GeneMap99-G3 RH Map	17	2424.0	UniSTS

Expression

RNA-SEQ Expression

High: > 1000 TPM value Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

adipose tissue

appendage

entire extraembryonic component

High

Medium

211

351

347

443

218

335

Low

2401

2796

1511

608

1807

448

4004

1760

3616

396

1005

1387

168

1201

2453

Below cutoff

180

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001303436	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001303437	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001303438	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001303439	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001303440	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001303441	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001303442	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001303443	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001303444	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_144608	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006721687	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011524306	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011524307	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011524308	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017024167	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017024170	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024450566	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024450567	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024450568	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047435323	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047435324	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315017	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315018	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315019	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315020	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054315021	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AA223138	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC138150	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK056946	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AW340131	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY598322	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC003531	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC012474	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC025970	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BG696988	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BI829228	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BI829844	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BP209696	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BP398345	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU501076	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CA312679	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471178	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CN425800	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068261	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB160394	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY007091	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000307275 ⟹ ENSP00000302276

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	45,160,700 - 45,170,040 (+)	Ensembl

RefSeq Acc Id:

ENST00000585340 ⟹ ENSP00000468251

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	45,160,730 - 45,170,035 (+)	Ensembl

RefSeq Acc Id:

ENST00000586681 ⟹ ENSP00000465086

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	45,161,094 - 45,170,035 (+)	Ensembl

RefSeq Acc Id:

ENST00000589230 ⟹ ENSP00000466200

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	45,161,875 - 45,170,035 (+)	Ensembl

RefSeq Acc Id:

ENST00000591070 ⟹ ENSP00000464807

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	45,161,896 - 45,170,035 (+)	Ensembl

RefSeq Acc Id:

ENST00000591576 ⟹ ENSP00000465727

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	45,161,895 - 45,170,035 (+)	Ensembl

RefSeq Acc Id:

ENST00000592695 ⟹ ENSP00000467517

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	45,161,917 - 45,170,035 (+)	Ensembl

RefSeq Acc Id:

ENST00000593138 ⟹ ENSP00000468773

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	17	45,161,078 - 45,170,035 (+)	Ensembl

RefSeq Acc Id:

NM_001303436 ⟹ NP_001290365

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	45,160,174 - 45,170,040 (+)	NCBI
CHM1_1	17	43,473,084 - 43,482,953 (+)	NCBI
T2T-CHM13v2.0	17	46,014,059 - 46,023,937 (+)	NCBI

Sequence:

show sequence

CAATCTTTAAGAAGCTGCTACAGCTATAATGTAAGGTTAAGAGTTTATTCTTTCAAAGCAGGTC
TCCTCATCTCTTAAACGCTATACATATGAAGTAGATAAAAACTGGTTTCTTTTTTGGTAGCATT
TAGGATCTACAAAAGTGATCCTTCAATTACTTGGAATTTCAAAAAATTGAGGTTACCTAGTAAC
AATGCACCAGTAGAACACAAAATACTCTGACTTTGTTTAGTCTGTGGGAAAAGAAAAATCTTTA
AACTGGAAAGATTTTGTAGTCTTACAAAGATTACATTGGAATTGGAATTACTGTAGTTCGTTTT
TCCCTCTAGGAGGGCAGCCATTTCTCTAAAAGTTGTGTAAAAGTTAAGACTAGGATTTCAAAAT
GCAAGCAGATGTTGATGAAGCATACGAAATGGGCAACTCCGTTTCTATTTCGGAGCCGCAGCGA
CTCCGACTTTGTGCCCCAACCCTGTAAAGGGCAAAACCTCATCCCTTCGGTGTAAACTTTCAAG
AGAAGTGGGGCAGCACACTTTAGGCGTTTCACCAAGAGGCTGGCGACATGCTAGGTCAGGTTGT
CCGGAGAATCGGGGCTGAATGGGAGAGATCTTGAGGGCAAGAGCCTCAGAGACCTTCAGGCACC
GAGCTCGTGAAGGTTTCCAAGTGCCCCTCTCTAGCTGCTCCCAGGGGGAATTAGTGGTTGCTAC
AGTAGTTTAAGAGGGTCGTGGTTTTTCGCAACCCGGGCGGCGAGATGGCGCTTTGGTGTAAGCG
AGGTGTCACTAGTTCCAGGCGTCTGCTGAAAGATTTGGAACAGAAGATGATGGCCACTCCGAAC
CAGACCGCCTGTAATGCAGAGTCACCAGTGGCCCTGGAGGAGGCCAAGACCTCTGGTGCCCCGG
GGAGCCCCCAAACACCCCCTGAGCGTCATGACTCTGGTGGTTCCCTGCCCCTGACACCGCGGAT
GGAGAGCCACTCAGAGGATGAAGATCTTGCTGGGGCTGTCGGTGGCCTGGGCTGGAACAGTAGG
AGTCCCCGGACCCAGAGCCCAGGGGGCTGCTCAGCGGAGGCTGTGCTGGCCCGGAAGAAACACC
GTCGGCGGCCATCGAAGCGCAAAAGGCACTGGCGACCCTACCTGGAGCTGAGCTGGGCTGAGAA
ACAACAGCGGGATGAGAGGCAGAGCCAGAGGGCCTCCCGGGTCCGCGAAGAGATGTTCGCCAAA
GGCCAGCCCGTGGCCCCCTACAACACCACCCAGTTCCTGATGAATGACAGGGACCCGGAGGAGC
CCAACTTGGATGTGCCCCATGGGATCTCCCACCCAGGTTCCAGTGGGGAGAGTGAGGCCGGGGA
CAGTGATGGGCGGGGCCGAGCGCACGGTGAGTTCCAGCGGAAGGACTTCTCTGAGACTTACGAA
CGCTTCCACACCGAGAGCCTGCAGGGCCGCAGCAAGCAGGAGCTGGTGCGAGACTACCTGGAGC
TGGAGAAGCGGCTGTCGCAGGCGGAGGAGGAGACTAGGAGGCTGCAGCAGCTGCAGGCGTGCAC
CGGCCAGCAGTCCTGCCGCCAGGTGGAGGAGCTGGCTGCCGAGGTCCAGAGGCTCCGGACCGAA
AACCAGCGGCTTCGTCAGGAGAACCAGATGTGGAACCGAGAGGGCTGCCGCTGTGATGAGGAGC
CGGGTACCTAGGGGTGCCTCCCAGCCTGGTGGACCCAAGGAGAAGGTCCCATTTCGTGCACACT
CAGGCCAGCTGGGTCTCAAGGAGGCAGGTGGCAGATGAAAACCACCGTCAACACCCTGTGCGCC
CTGAGAACAGCTAAATCGGTTCAGACTCCCACCTCACCGTTTCCATAGTTGGCTCTTTTGTGTC
ATCTTACCCTTTACAGAGAAATTAAATGGCCTTGGTGGGACCAAATGGGAAAAAAAAAAAAAAA
AAA

hide sequence

RefSeq Acc Id:

NM_001303437 ⟹ NP_001290366

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	45,160,174 - 45,170,040 (+)	NCBI
CHM1_1	17	43,473,084 - 43,482,953 (+)	NCBI
T2T-CHM13v2.0	17	46,014,059 - 46,023,937 (+)	NCBI

Sequence:

show sequence

CAATCTTTAAGAAGCTGCTACAGCTATAATGTAAGGTTAAGAGTTTATTCTTTCAAAGCAGGTC
TCCTCATCTCTTAAACGCTATACATATGAAGTAGATAAAAACTGGTTTCTTTTTTGGTAGCATT
TAGGATCTACAAAAGTGATCCTTCAATTACTTGGAATTTCAAAAAATTGAGGTTACCTAGTAAC
AATGCACCAGTAGAACACAAAATACTCTGACTTTGTTTAGTCTGTGGGAAAAGAAAAATCTTTA
AACTGGAAAGATTTTGTAGTCTTACAAAGATTACATTGGAATTGGAATTACTGTAGTTCGTTTT
TCCCTCTAGGAGGGCAGCCATTTCTCTAAAAGTTGTGTAAAAGTTAAGACTAGGATTTCAAAAT
GCAAGCAGATGTTGATGAAGCATACGAAATGGGCAACTCCGTTTCTATTTCGGAGCCGCAGCGA
CTCCGACTTTGTGCCCCAACCCTGTAAAGGGCAAAACCTCATCCCTTCGGTGTAAACTTTCAAG
AGAAGTGGGGCAGCACACTTTAGGCGTTTCACCAAGAGGCTGGCGACATGCTAGGTCAGGTTGT
CCGGAGAATCGGGGCTGAATGGGAGAGATCTTGAGGGCAAGAGCCTCAGAGACCTTCAGGCACC
GAGCTCGTGAAGGTTTCCAAGTGCCCCTCTCTAGCTGCTCCCAGGGGGAATTAGTGGTTGCTAC
AGTAGTTTAAGAGGGTCGTGGTTTTTCGCAACCCGGGCGGCGAGATGGCGCTTTGGTGTAAGCG
AGGTAAGGTGGGTGCACTGGGATCTCCGCTCTCGGAGCCTCCAGCTGACTGCCACGCCGACTTG
TGGCCAGACCTGCGACCTCCGCCCTCCCCCGCGGCGCCAGCCTCTGGAATCTGGCGTCGCCCCC
ACCTCTCCAGTCGAAGTGGGAGTCCCTCTGTGCGGGGCCTCGCCGCCATACCCAGGCCGAATGG
GGGTGGGGAGGGAAGCTGGCAGAGCTCGGCCTCAGGATCCGCGCCCCTGTGGAAAGACCGCAGA
GGGAAGCCGTTTCACCAGCCTCTCCCCTTCTGGGGTCTCGGGAAACACGCGGAGGACAGTACAG
GACATGAGTCCTGGTGAGGGACCCGAGGAGCAGGACAGAGAAGACGGCCCCTGAATCCCATTTG
GCCCCTTGCTGGCTGGAGGTGTGAAAACCAGCGGTGGAGGCAGCCTTCGGGGCCTGCATTTGAG
AATAAGGGTGTCACTAGTTCCAGGCGTCTGCTGAAAGATTTGGAACAGAAGATGATGGCCACTC
CGAACCAGACCGCCTGTAATGCAGAGTCACCAGTGGCCCTGGAGGAGGCCAAGACCTCTGGTGC
CCCGGGGAGCCCCCAAACACCCCCTGAGCGTCATGACTCTGGTGGTTCCCTGCCCCTGACACCG
CGGATGGAGAGCCACTCAGAGGATGAAGATCTTGCTGGGGCTGTCGGTGGCCTGGGCTGGAACA
GTAGGAGTCCCCGGACCCAGAGCCCAGGGGGCTGCTCAGCGGAGGCTGTGCTGGCCCGGAAGAA
ACACCGTCGGCGGCCATCGAAGCGCAAAAGGCACTGGCGACCCTACCTGGAGCTGAGCTGGGCT
GAGAAACAACAGCGGGATGAGAGGCAGAGCCAGAGGGCCTCCCGGGTCCGCGAAGAGATGTTCG
CCAAAGGCCAGCCCGTGGCCCCCTACAACACCACCCAGTTCCTGATGAATGACAGGGACCCGGA
GGAGCCCAACTTGGATGTGCCCCATGGGATCTCCCACCCAGGTTCCAGTGGGGAGAGTGAGGCC
GGGGACAGTGATGGGCGGGGCCGAGCGCACGGTGAGTTCCAGCGGAAGGACTTCTCTGAGACTT
ACGAACGCTTCCACACCGAGAGCCTGCAGGGCCGCAGCAAGCAGGAGCTGGTGCGAGACTACCT
GGAGCTGGAGAAGCGGCTGTCGCAGGCGGAGGAGGAGACTAGGAGGCTGCAGCAGCTGCAGGCG
TGCACCGGCCAGCAGTCCTGCCGCCAGGTGGAGGAGCTGGCTGCCGAGGTCCAGAGGCTCCGGA
CCGAAAACCAGCGGCTTCGTCAGGAGAACCAGATGTGGAACCGAGAGGGCTGCCGCTGTGATGA
GGAGCCGGGTACCTAGGGGTGCCTCCCAGCCTGGTGGACCCAAGGAGAAGGTCCCATTTCGTGC
ACACTCAGGCCAGCTGGGTCTCAAGGAGGCAGGTGGCAGATGAAAACCACCGTCAACACCCTGT
GCGCCCTGAGAACAGCTAAATCGGTTCAGACTCCCACCTCACCGTTTCCATAGTTGGCTCTTTT
GTGTCATCTTACCCTTTACAGAGAAATTAAATGGCCTTGGTGGGACCAAATGGGAAAAAAAAAA
AAAAAAAA

hide sequence

RefSeq Acc Id:

NM_001303438 ⟹ NP_001290367

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	45,160,174 - 45,170,040 (+)	NCBI
CHM1_1	17	43,473,084 - 43,482,953 (+)	NCBI
T2T-CHM13v2.0	17	46,014,059 - 46,023,937 (+)	NCBI

Sequence:

show sequence

CAATCTTTAAGAAGCTGCTACAGCTATAATGTAAGGTTAAGAGTTTATTCTTTCAAAGCAGGTC
TCCTCATCTCTTAAACGCTATACATATGAAGTAGATAAAAACTGGTTTCTTTTTTGGTAGCATT
TAGGATCTACAAAAGTGATCCTTCAATTACTTGGAATTTCAAAAAATTGAGGTTACCTAGTAAC
AATGCACCAGTAGAACACAAAATACTCTGACTTTGTTTAGTCTGTGGGAAAAGAAAAATCTTTA
AACTGGAAAGATTTTGTAGTCTTACAAAGATTACATTGGAATTGGAATTACTGTAGTTCGTTTT
TCCCTCTAGGAGGGCAGCCATTTCTCTAAAAGTTGTGTAAAAGTTAAGACTAGGATTTCAAAAT
GCAAGCAGATGTTGATGAAGCATACGAAATGGGCAACTCCGTTTCTATTTCGGAGCCGCAGCGA
CTCCGACTTTGTGCCCCAACCCTGTAAAGGGCAAAACCTCATCCCTTCGGTGTAAACTTTCAAG
AGAAGTGGGGCAGCACACTTTAGGCGTTTCACCAAGAGGCTGGCGACATGCTAGGTCAGGTTGT
CCGGAGAATCGGGGCTGAATGGGAGAGATCTTGAGGGCAAGAGCCTCAGAGACCTTCAGGCACC
GAGCTCGTGAAGGTTTCCAAGTGCCCCTCTCTAGCTGCTCCCAGGGGGAATTAGTGGTTGCTAC
AGTAGTTTAAGAGGGTCGTGGTTTTTCGCAACCCGGGCGGCGAGATGGCGCTTTGGTGTAAGCG
AGGTAAGGTGGGTGCACTGGGATCTCCGCTCTCGGAGCCTCCAGCTGACTGCCACGCCGACTTG
TGGCCAGACCTGCGACCTCCGCCCTCCCCCGCGGCGCCAGCCTCTGGAATCTGGCGTCGCCCCC
ACCTCTCCAGTCGAAGTGGGAGTCCCTCTGTGCGGGGCCTCGCCGCCATACCCAGGCCGAATGG
GGGTGGGGAGGGAAGCTGGCAGAGCTCGGCCTCAGGATCCGCGCCCCTGTGGAAAGACCGCAGA
GGGAAGCCGTTTCACCAGCCTCTCCCCTTCTGGGGTCTCGGGAAACACGCGGTGTCACTAGTTC
CAGGCGTCTGCTGAAAGATTTGGAACAGAAGATGATGGCCACTCCGAACCAGACCGCCTGTAAT
GCAGAGTCACCAGTGGCCCTGGAGGAGGCCAAGACCTCTGGTGCCCCGGGGAGCCCCCAAACAC
CCCCTGAGCGTCATGACTCTGGTGGTTCCCTGCCCCTGACACCGCGGATGGAGAGCCACTCAGA
GGATGAAGATCTTGCTGGGGCTGTCGGTGGCCTGGGCTGGAACAGTAGGAGTCCCCGGACCCAG
AGCCCAGGGGGCTGCTCAGCGGAGGCTGTGCTGGCCCGGAAGAAACACCGTCGGCGGCCATCGA
AGCGCAAAAGGCACTGGCGACCCTACCTGGAGCTGAGCTGGGCTGAGAAACAACAGCGGGATGA
GAGGCAGAGCCAGAGGGCCTCCCGGGTCCGCGAAGAGATGTTCGCCAAAGGCCAGCCCGTGGCC
CCCTACAACACCACCCAGTTCCTGATGAATGACAGGGACCCGGAGGAGCCCAACTTGGATGTGC
CCCATGGGATCTCCCACCCAGGTTCCAGTGGGGAGAGTGAGGCCGGGGACAGTGATGGGCGGGG
CCGAGCGCACGGTGAGTTCCAGCGGAAGGACTTCTCTGAGACTTACGAACGCTTCCACACCGAG
AGCCTGCAGGGCCGCAGCAAGCAGGAGCTGGTGCGAGACTACCTGGAGCTGGAGAAGCGGCTGT
CGCAGGCGGAGGAGGAGACTAGGAGGCTGCAGCAGCTGCAGGCGTGCACCGGCCAGCAGTCCTG
CCGCCAGGTGGAGGAGCTGGCTGCCGAGGTCCAGAGGCTCCGGACCGAAAACCAGCGGCTTCGT
CAGGAGAACCAGATGTGGAACCGAGAGGGCTGCCGCTGTGATGAGGAGCCGGGTACCTAGGGGT
GCCTCCCAGCCTGGTGGACCCAAGGAGAAGGTCCCATTTCGTGCACACTCAGGCCAGCTGGGTC
TCAAGGAGGCAGGTGGCAGATGAAAACCACCGTCAACACCCTGTGCGCCCTGAGAACAGCTAAA
TCGGTTCAGACTCCCACCTCACCGTTTCCATAGTTGGCTCTTTTGTGTCATCTTACCCTTTACA
GAGAAATTAAATGGCCTTGGTGGGACCAAATGGGAAAAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NM_001303439 ⟹ NP_001290368

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	45,160,174 - 45,170,040 (+)	NCBI
CHM1_1	17	43,473,084 - 43,482,953 (+)	NCBI
T2T-CHM13v2.0	17	46,014,059 - 46,023,937 (+)	NCBI

Sequence:

show sequence

CAATCTTTAAGAAGCTGCTACAGCTATAATGTAAGGTTAAGAGTTTATTCTTTCAAAGCAGGTC
TCCTCATCTCTTAAACGCTATACATATGAAGTAGATAAAAACTGGTTTCTTTTTTGGTAGCATT
TAGGATCTACAAAAGTGATCCTTCAATTACTTGGAATTTCAAAAAATTGAGGTTACCTAGTAAC
AATGCACCAGTAGAACACAAAATACTCTGACTTTGTTTAGTCTGTGGGAAAAGAAAAATCTTTA
AACTGGAAAGATTTTGTAGTCTTACAAAGATTACATTGGAATTGGAATTACTGTAGTTCGTTTT
TCCCTCTAGGAGGGCAGCCATTTCTCTAAAAGTTGTGTAAAAGTTAAGACTAGGATTTCAAAAT
GCAAGCAGATGTTGATGAAGCATACGAAATGGGCAACTCCGTTTCTATTTCGGAGCCGCAGCGA
CTCCGACTTTGTGCCCCAACCCTGTAAAGGGCAAAACCTCATCCCTTCGGTGTAAACTTTCAAG
AGAAGTGGGGCAGCACACTTTAGGCGTTTCACCAAGAGGCTGGCGACATGCTAGGTCAGGTTGT
CCGGAGAATCGGGGCTGAATGGGAGAGATCTTGAGGGCAAGAGCCTCAGAGACCTTCAGGCACC
GAGCTCGTGAAGGTTTCCAAGTGCCCCTCTCTAGCTGCTCCCAGGGGGAATTAGTGGTTGCTAC
AGTAGTTTAAGAGGGTCGTGGTTTTTCGCAACCCGGGCGGCGAGATGGCGCTTTGGTGTAAGCG
AGGTAAGGTGGGTGCACTGGGATCTCCGCTCTCGGAGCCTCCAGCTGACTGCCACGCCGACTTG
TGGCCAGACCTGCGACCTCCGCCCTCCCCCGCGGCGCCAGCCTCTGGAATCTGGCGTCGCCCCC
ACCTCTCCAGTCGAAGTGGGAGTCCCTCTGTGCGGGGCCTCGCCGCCATACCCAGGCCGAATGG
GGGTGGGGAGGGAAGCTGGCAGAGCTCGGCCTCAGGATCCGCGCCCCTGTGGAAAGACCGCAGA
GGGAAGCCGTTTCACCAGCCTCTCCCCTTCTGGGGTCTCGGGAAACACGCGGTAATTACCGAAG
AACCCCGCACTCTGTGAGAGGCGAGGCTGCGGGGCTGCCGGGACGGTTTGAGGACCGGGCTCGG
CCGAGGAGACTCCAACCTTCACCCTCCCTGGCCCCCGGTCCCACTTCCCGCCGTCTCCCGGCGC
CGCCACTTCAGGTGTCACTAGTTCCAGGCGTCTGCTGAAAGATTTGGAACAGAAGATGATGGCC
ACTCCGAACCAGACCGCCTGTAATGCAGAGTCACCAGTGGCCCTGGAGGAGGCCAAGACCTCTG
GTGCCCCGGGGAGCCCCCAAACACCCCCTGAGCGTCATGACTCTGGTGGTTCCCTGCCCCTGAC
ACCGCGGATGGAGAGCCACTCAGAGGATGAAGATCTTGCTGGGGCTGTCGGTGGCCTGGGCTGG
AACAGTAGGAGTCCCCGGACCCAGAGCCCAGGGGGCTGCTCAGCGGAGGCTGTGCTGGCCCGGA
AGAAACACCGTCGGCGGCCATCGAAGCGCAAAAGGCACTGGCGACCCTACCTGGAGCTGAGCTG
GGCTGAGAAACAACAGCGGGATGAGAGGCAGAGCCAGAGGGCCTCCCGGGTCCGCGAAGAGATG
TTCGCCAAAGGCCAGCCCGTGGCCCCCTACAACACCACCCAGTTCCTGATGAATGACAGGGACC
CGGAGGAGCCCAACTTGGATGTGCCCCATGGGATCTCCCACCCAGGTTCCAGTGGGGAGAGTGA
GGCCGGGGACAGTGATGGGCGGGGCCGAGCGCACGGTGAGTTCCAGCGGAAGGACTTCTCTGAG
ACTTACGAACGCTTCCACACCGAGAGCCTGCAGGGCCGCAGCAAGCAGGAGCTGGTGCGAGACT
ACCTGGAGCTGGAGAAGCGGCTGTCGCAGGCGGAGGAGGAGACTAGGAGGCTGCAGCAGCTGCA
GGCGTGCACCGGCCAGCAGTCCTGCCGCCAGGTGGAGGAGCTGGCTGCCGAGGTCCAGAGGCTC
CGGACCGAAAACCAGCGGCTTCGTCAGGAGAACCAGATGTGGAACCGAGAGGGCTGCCGCTGTG
ATGAGGAGCCGGGTACCTAGGGGTGCCTCCCAGCCTGGTGGACCCAAGGAGAAGGTCCCATTTC
GTGCACACTCAGGCCAGCTGGGTCTCAAGGAGGCAGGTGGCAGATGAAAACCACCGTCAACACC
CTGTGCGCCCTGAGAACAGCTAAATCGGTTCAGACTCCCACCTCACCGTTTCCATAGTTGGCTC
TTTTGTGTCATCTTACCCTTTACAGAGAAATTAAATGGCCTTGGTGGGACCAAATGGGAAAAAA
AAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NM_001303440 ⟹ NP_001290369

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	45,161,875 - 45,170,035 (+)	NCBI
CHM1_1	17	43,474,755 - 43,482,953 (+)	NCBI
T2T-CHM13v2.0	17	46,015,760 - 46,023,932 (+)	NCBI

Sequence:

show sequence

CTCTCTTCCCCCCCATCTTAGTGGCCTGAGCGGCTTGACCAGAGCTGCTGCAACTGCAGCAAGA
GGTAGGGCTCAGGCGTTGGGAATTGCACCGACAGGCAGTCGCACAGAAAGGCACACAGATGTAG
TGGTGTGCATAGCCCTTGACAGCGAATAGGTGTCACTAGTTCCAGGCGTCTGCTGAAAGATTTG
GAACAGAAGATGATGGCCACTCCGAACCAGACCGCCTGTAATGCAGAGTCACCAGTGGCCCTGG
AGGAGGCCAAGACCTCTGGTGCCCCGGGGAGCCCCCAAACACCCCCTGAGCGTCATGACTCTGG
TGGTTCCCTGCCCCTGACACCGCGGATGGAGAGCCACTCAGAGGATGAAGATCTTGCTGGGGCT
GTCGGTGGCCTGGGCTGGAACAGTAGGAGTCCCCGGACCCAGAGCCCAGGGGGCTGCTCAGCGG
AGGCTGTGCTGGCCCGGAAGAAACACCGTCGGCGGCCATCGAAGCGCAAAAGGCACTGGCGACC
CTACCTGGAGCTGAGCTGGGCTGAGAAACAACAGCGGGATGAGAGGCAGAGCCAGAGGGCCTCC
CGGGTCCGCGAAGAGATGTTCGCCAAAGGCCAGCCCGTGGCCCCCTACAACACCACCCAGTTCC
TGATGAATGACAGGGACCCGGAGGAGCCCAACTTGGATGTGCCCCATGGGATCTCCCACCCAGG
TTCCAGTGGGGAGAGTGAGGCCGGGGACAGTGATGGGCGGGGCCGAGCGCACGGTGAGTTCCAG
CGGAAGGACTTCTCTGAGACTTACGAACGCTTCCACACCGAGAGCCTGCAGGGCCGCAGCAAGC
AGGAGCTGGTGCGAGACTACCTGGAGCTGGAGAAGCGGCTGTCGCAGGCGGAGGAGGAGACTAG
GAGGCTGCAGCAGCTGCAGGCGTGCACCGGCCAGCAGTCCTGCCGCCAGGTGGAGGAGCTGGCT
GCCGAGGTCCAGAGGCTCCGGACCGAAAACCAGCGGCTTCGTCAGGAGAACCAGATGTGGAACC
GAGAGGGCTGCCGCTGTGATGAGGAGCCGGGTACCTAGGGGTGCCTCCCAGCCTGGTGGACCCA
AGGAGAAGGTCCCATTTCGTGCACACTCAGGCCAGCTGGGTCTCAAGGAGGCAGGTGGCAGATG
AAAACCACCGTCAACACCCTGTGCGCCCTGAGAACAGCTAAATCGGTTCAGACTCCCACCTCAC
CGTTTCCATAGTTGGCTCTTTTGTGTCATCTTACCCTTTACAGAGAAATTAAATGGCCTTGGTG
GGACCAAA

hide sequence

RefSeq Acc Id:

NM_001303441 ⟹ NP_001290370

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	45,161,875 - 45,170,035 (+)	NCBI
CHM1_1	17	43,474,755 - 43,482,953 (+)	NCBI
T2T-CHM13v2.0	17	46,015,760 - 46,023,932 (+)	NCBI

Sequence:

show sequence

CTCTCTTCCCCCCCATCTTAGTGGCCTGAGCGGCTTGACCAGAGCTGCTGCAACTGCAGCAAGA
GGTAGGGCTCAGGCGTTGGGAATTGCACCGACAGGCAGTCGCACAGAAAGGCACACAGATGTAG
TGGTGTGCATAGCCCTTGACAGCGAATAGGAGGACAGTACAGGACATGAGTCCTGGTGAGGGAC
CCGAGGAGCAGGACAGAGAAGACGGCCCCTGAATCCCATTTGGCCCCTTGCTGGCTGGAGGTGT
GAAAACCAGCGGTGGAGGCAGCCTTCGGGGCCTGCATTTGAGAATAAGGGTGTCACTAGTTCCA
GGCGTCTGCTGAAAGATTTGGAACAGAAGATGATGGCCACTCCGAACCAGACCGCCTGTAATGC
AGAGTCACCAGTGGCCCTGGAGGAGGCCAAGACCTCTGGTGCCCCGGGGAGCCCCCAAACACCC
CCTGAGCGTCATGACTCTGGTGGTTCCCTGCCCCTGACACCGCGGATGGAGAGCCACTCAGAGG
ATGAAGATCTTGCTGGGGCTGTCGGTGGCCTGGGCTGGAACAGTAGGAGTCCCCGGACCCAGAG
CCCAGGGGGCTGCTCAGCGGAGGCTGTGCTGGCCCGGAAGAAACACCGTCGGCGGCCATCGAAG
CGCAAAAGGCACTGGCGACCCTACCTGGAGCTGAGCTGGGCTGAGAAACAACAGCGGGATGAGA
GGCAGAGCCAGAGGGCCTCCCGGGTCCGCGAAGAGATGTTCGCCAAAGGCCAGCCCGTGGCCCC
CTACAACACCACCCAGTTCCTGATGAATGACAGGGACCCGGAGGAGCCCAACTTGGATGTGCCC
CATGGGATCTCCCACCCAGGTTCCAGTGGGGAGAGTGAGGCCGGGGACAGTGATGGGCGGGGCC
GAGCGCACGGTGAGTTCCAGCGGAAGGACTTCTCTGAGACTTACGAACGCTTCCACACCGAGAG
CCTGCAGGGCCGCAGCAAGCAGGAGCTGGTGCGAGACTACCTGGAGCTGGAGAAGCGGCTGTCG
CAGGCGGAGGAGGAGACTAGGAGGCTGCAGCAGCTGCAGGCGTGCACCGGCCAGCAGTCCTGCC
GCCAGGTGGAGGAGCTGGCTGCCGAGGTCCAGAGGCTCCGGACCGAAAACCAGCGGCTTCGTCA
GGAGAACCAGATGTGGAACCGAGAGGGCTGCCGCTGTGATGAGGAGCCGGGTACCTAGGGGTGC
CTCCCAGCCTGGTGGACCCAAGGAGAAGGTCCCATTTCGTGCACACTCAGGCCAGCTGGGTCTC
AAGGAGGCAGGTGGCAGATGAAAACCACCGTCAACACCCTGTGCGCCCTGAGAACAGCTAAATC
GGTTCAGACTCCCACCTCACCGTTTCCATAGTTGGCTCTTTTGTGTCATCTTACCCTTTACAGA
GAAATTAAATGGCCTTGGTGGGACCAAA

hide sequence

RefSeq Acc Id:

NM_001303442 ⟹ NP_001290371

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	45,161,875 - 45,170,035 (+)	NCBI
CHM1_1	17	43,474,769 - 43,482,953 (+)	NCBI
T2T-CHM13v2.0	17	46,015,760 - 46,023,932 (+)	NCBI

Sequence:

show sequence

CTCTCTTCCCCCCCATCTTAGTGGCCTGAGCGGCTTGACCAGAGCTGCTGCAACTGCAGCAAGA
GGTGTCACTAGTTCCAGGCGTCTGCTGAAAGATTTGGAACAGAAGATGATGGCCACTCCGAACC
AGACCGCCTGTAATGCAGAGTCACCAGTGGCCCTGGAGGAGGCCAAGACCTCTGGTGCCCCGGG
GAGCCCCCAAACACCCCCTGAGCGTCATGACTCTGGTGGTTCCCTGCCCCTGACACCGCGGATG
GAGAGCCACTCAGAGGATGAAGATCTTGCTGGGGCTGTCGGTGGCCTGGGCTGGAACAGTAGGA
GTCCCCGGACCCAGAGCCCAGGGGGCTGCTCAGCGGAGGCTGTGCTGGCCCGGAAGAAACACCG
TCGGCGGCCATCGAAGCGCAAAAGGCACTGGCGACCCTACCTGGAGCTGAGCTGGGCTGAGAAA
CAACAGCGGGATGAGAGGCAGAGCCAGAGGGCCTCCCGGGTCCGCGAAGAGATGTTCGCCAAAG
GCCAGCCCGTGGCCCCCTACAACACCACCCAGTTCCTGATGAATGACAGGGACCCGGAGGAGCC
CAACTTGGATGTGCCCCATGGGATCTCCCACCCAGGTTCCAGTGGGGAGAGTGAGGCCGGGGAC
AGTGATGGGCGGGGCCGAGCGCACGGTGAGTTCCAGCGGAAGGACTTCTCTGAGACTTACGAAC
GCTTCCACACCGAGAGCCTGCAGGGCCGCAGCAAGCAGGAGCTGGTGCGAGACTACCTGGAGCT
GGAGAAGCGGCTGTCGCAGGCGGAGGAGGAGACTAGGAGGCTGCAGCAGCTGCAGGCGTGCACC
GGCCAGCAGTCCTGCCGCCAGGTGGAGGAGCTGGCTGCCGAGGTCCAGAGGCTCCGGACCGAAA
ACCAGCGGCTTCGTCAGGAGAACCAGATGTGGAACCGAGAGGGCTGCCGCTGTGATGAGGAGCC
GGGTACCTAGGGGTGCCTCCCAGCCTGGTGGACCCAAGGAGAAGGTCCCATTTCGTGCACACTC
AGGCCAGCTGGGTCTCAAGGAGGCAGGTGGCAGATGAAAACCACCGTCAACACCCTGTGCGCCC
TGAGAACAGCTAAATCGGTTCAGACTCCCACCTCACCGTTTCCATAGTTGGCTCTTTTGTGTCA
TCTTACCCTTTACAGAGAAATTAAATGGCCTTGGTGGGACCAAA

hide sequence

RefSeq Acc Id:

NM_001303443 ⟹ NP_001290372

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	45,161,875 - 45,170,035 (+)	NCBI
CHM1_1	17	43,474,769 - 43,482,953 (+)	NCBI
T2T-CHM13v2.0	17	46,015,760 - 46,023,932 (+)	NCBI

Sequence:

show sequence

CTCTCTTCCCCCCCATCTTAGTGGCCTGAGCGGCTTGACCAGAGCTGCTGCAACTGCAGCAAGA
GGAGGACAGTACAGGACATGAGTCCTGGTGAGGGACCCGAGGAGCAGGACAGAGAAGACGGCCC
CTGAATCCCATTTGGCCCCTTGCTGGCTGGAGGTGTGAAAACCAGCGGTGGAGGCAGCCTTCGG
GGCCTGCATTTGAGAATAAGGGTGTCACTAGTTCCAGGCGTCTGCTGAAAGATTTGGAACAGAA
GATGATGGCCACTCCGAACCAGACCGCCTGTAATGCAGAGTCACCAGTGGCCCTGGAGGAGGCC
AAGACCTCTGGTGCCCCGGGGAGCCCCCAAACACCCCCTGAGCGTCATGACTCTGGTGGTTCCC
TGCCCCTGACACCGCGGATGGAGAGCCACTCAGAGGATGAAGATCTTGCTGGGGCTGTCGGTGG
CCTGGGCTGGAACAGTAGGAGTCCCCGGACCCAGAGCCCAGGGGGCTGCTCAGCGGAGGCTGTG
CTGGCCCGGAAGAAACACCGTCGGCGGCCATCGAAGCGCAAAAGGCACTGGCGACCCTACCTGG
AGCTGAGCTGGGCTGAGAAACAACAGCGGGATGAGAGGCAGAGCCAGAGGGCCTCCCGGGTCCG
CGAAGAGATGTTCGCCAAAGGCCAGCCCGTGGCCCCCTACAACACCACCCAGTTCCTGATGAAT
GACAGGGACCCGGAGGAGCCCAACTTGGATGTGCCCCATGGGATCTCCCACCCAGGTTCCAGTG
GGGAGAGTGAGGCCGGGGACAGTGATGGGCGGGGCCGAGCGCACGGTGAGTTCCAGCGGAAGGA
CTTCTCTGAGACTTACGAACGCTTCCACACCGAGAGCCTGCAGGGCCGCAGCAAGCAGGAGCTG
GTGCGAGACTACCTGGAGCTGGAGAAGCGGCTGTCGCAGGCGGAGGAGGAGACTAGGAGGCTGC
AGCAGCTGCAGGCGTGCACCGGCCAGCAGTCCTGCCGCCAGGTGGAGGAGCTGGCTGCCGAGGT
CCAGAGGCTCCGGACCGAAAACCAGCGGCTTCGTCAGGAGAACCAGATGTGGAACCGAGAGGGC
TGCCGCTGTGATGAGGAGCCGGGTACCTAGGGGTGCCTCCCAGCCTGGTGGACCCAAGGAGAAG
GTCCCATTTCGTGCACACTCAGGCCAGCTGGGTCTCAAGGAGGCAGGTGGCAGATGAAAACCAC
CGTCAACACCCTGTGCGCCCTGAGAACAGCTAAATCGGTTCAGACTCCCACCTCACCGTTTCCA
TAGTTGGCTCTTTTGTGTCATCTTACCCTTTACAGAGAAATTAAATGGCCTTGGTGGGACCAAA

hide sequence

RefSeq Acc Id:

NM_001303444 ⟹ NP_001290373

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	45,161,875 - 45,170,035 (+)	NCBI
CHM1_1	17	43,474,769 - 43,482,953 (+)	NCBI
T2T-CHM13v2.0	17	46,015,760 - 46,023,932 (+)	NCBI

Sequence:

show sequence

CTCTCTTCCCCCCCATCTTAGTGGCCTGAGCGGCTTGACCAGAGCTGCTGCAACTGCAGCAAGA
GCAGGTGTCACTAGTTCCAGGCGTCTGCTGAAAGATTTGGAACAGAAGATGATGGCCACTCCGA
ACCAGACCGCCTGTAATGCAGAGTCACCAGTGGCCCTGGAGGAGGCCAAGACCTCTGGTGCCCC
GGGGAGCCCCCAAACACCCCCTGAGCGTCATGACTCTGGTGGTTCCCTGCCCCTGACACCGCGG
ATGGAGAGCCACTCAGAGGATGAAGATCTTGCTGGGGCTGTCGGTGGCCTGGGCTGGAACAGTA
GGAGTCCCCGGACCCAGAGCCCAGGGGGCTGCTCAGCGGAGGCTGTGCTGGCCCGGAAGAAACA
CCGTCGGCGGCCATCGAAGCGCAAAAGGCACTGGCGACCCTACCTGGAGCTGAGCTGGGCTGAG
AAACAACAGCGGGATGAGAGGCAGAGCCAGAGGGCCTCCCGGGTCCGCGAAGAGATGTTCGCCA
AAGGCCAGCCCGTGGCCCCCTACAACACCACCCAGTTCCTGATGAATGACAGGGACCCGGAGGA
GCCCAACTTGGATGTGCCCCATGGGATCTCCCACCCAGGTTCCAGTGGGGAGAGTGAGGCCGGG
GACAGTGATGGGCGGGGCCGAGCGCACGGTGAGTTCCAGCGGAAGGACTTCTCTGAGACTTACG
AACGCTTCCACACCGAGAGCCTGCAGGGCCGCAGCAAGCAGGAGCTGGTGCGAGACTACCTGGA
GCTGGAGAAGCGGCTGTCGCAGGCGGAGGAGGAGACTAGGAGGCTGCAGCAGCTGCAGGCGTGC
ACCGGCCAGCAGTCCTGCCGCCAGGTGGAGGAGCTGGCTGCCGAGGTCCAGAGGCTCCGGACCG
AAAACCAGCGGCTTCGTCAGGAGAACCAGATGTGGAACCGAGAGGGCTGCCGCTGTGATGAGGA
GCCGGGTACCTAGGGGTGCCTCCCAGCCTGGTGGACCCAAGGAGAAGGTCCCATTTCGTGCACA
CTCAGGCCAGCTGGGTCTCAAGGAGGCAGGTGGCAGATGAAAACCACCGTCAACACCCTGTGCG
CCCTGAGAACAGCTAAATCGGTTCAGACTCCCACCTCACCGTTTCCATAGTTGGCTCTTTTGTG
TCATCTTACCCTTTACAGAGAAATTAAATGGCCTTGGTGGGACCAAA

hide sequence

RefSeq Acc Id:

NM_144608 ⟹ NP_653209

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	45,160,174 - 45,170,040 (+)	NCBI
GRCh37	17	43,237,502 - 43,247,406 (+)	NCBI
Build 36	17	40,594,047 - 40,603,189 (+)	NCBI Archive
Celera	17	39,947,916 - 39,957,031 (+)	RGD
HuRef	17	39,001,091 - 39,009,915 (+)	ENTREZGENE
CHM1_1	17	43,473,084 - 43,482,953 (+)	NCBI
T2T-CHM13v2.0	17	46,014,059 - 46,023,937 (+)	NCBI

Sequence:

show sequence

CAATCTTTAAGAAGCTGCTACAGCTATAATGTAAGGTTAAGAGTTTATTCTTTCAAAGCAGGTC
TCCTCATCTCTTAAACGCTATACATATGAAGTAGATAAAAACTGGTTTCTTTTTTGGTAGCATT
TAGGATCTACAAAAGTGATCCTTCAATTACTTGGAATTTCAAAAAATTGAGGTTACCTAGTAAC
AATGCACCAGTAGAACACAAAATACTCTGACTTTGTTTAGTCTGTGGGAAAAGAAAAATCTTTA
AACTGGAAAGATTTTGTAGTCTTACAAAGATTACATTGGAATTGGAATTACTGTAGTTCGTTTT
TCCCTCTAGGAGGGCAGCCATTTCTCTAAAAGTTGTGTAAAAGTTAAGACTAGGATTTCAAAAT
GCAAGCAGATGTTGATGAAGCATACGAAATGGGCAACTCCGTTTCTATTTCGGAGCCGCAGCGA
CTCCGACTTTGTGCCCCAACCCTGTAAAGGGCAAAACCTCATCCCTTCGGTGTAAACTTTCAAG
AGAAGTGGGGCAGCACACTTTAGGCGTTTCACCAAGAGGCTGGCGACATGCTAGGTCAGGTTGT
CCGGAGAATCGGGGCTGAATGGGAGAGATCTTGAGGGCAAGAGCCTCAGAGACCTTCAGGCACC
GAGCTCGTGAAGGTTTCCAAGTGCCCCTCTCTAGCTGCTCCCAGGGGGAATTAGTGGTTGCTAC
AGTAGTTTAAGAGGGTCGTGGTTTTTCGCAACCCGGGCGGCGAGATGGCGCTTTGGTGTAAGCG
AGGAGGACAGTACAGGACATGAGTCCTGGTGAGGGACCCGAGGAGCAGGACAGAGAAGACGGCC
CCTGAATCCCATTTGGCCCCTTGCTGGCTGGAGGTGTGAAAACCAGCGGTGGAGGCAGCCTTCG
GGGCCTGCATTTGAGAATAAGGGTGTCACTAGTTCCAGGCGTCTGCTGAAAGATTTGGAACAGA
AGATGATGGCCACTCCGAACCAGACCGCCTGTAATGCAGAGTCACCAGTGGCCCTGGAGGAGGC
CAAGACCTCTGGTGCCCCGGGGAGCCCCCAAACACCCCCTGAGCGTCATGACTCTGGTGGTTCC
CTGCCCCTGACACCGCGGATGGAGAGCCACTCAGAGGATGAAGATCTTGCTGGGGCTGTCGGTG
GCCTGGGCTGGAACAGTAGGAGTCCCCGGACCCAGAGCCCAGGGGGCTGCTCAGCGGAGGCTGT
GCTGGCCCGGAAGAAACACCGTCGGCGGCCATCGAAGCGCAAAAGGCACTGGCGACCCTACCTG
GAGCTGAGCTGGGCTGAGAAACAACAGCGGGATGAGAGGCAGAGCCAGAGGGCCTCCCGGGTCC
GCGAAGAGATGTTCGCCAAAGGCCAGCCCGTGGCCCCCTACAACACCACCCAGTTCCTGATGAA
TGACAGGGACCCGGAGGAGCCCAACTTGGATGTGCCCCATGGGATCTCCCACCCAGGTTCCAGT
GGGGAGAGTGAGGCCGGGGACAGTGATGGGCGGGGCCGAGCGCACGGTGAGTTCCAGCGGAAGG
ACTTCTCTGAGACTTACGAACGCTTCCACACCGAGAGCCTGCAGGGCCGCAGCAAGCAGGAGCT
GGTGCGAGACTACCTGGAGCTGGAGAAGCGGCTGTCGCAGGCGGAGGAGGAGACTAGGAGGCTG
CAGCAGCTGCAGGCGTGCACCGGCCAGCAGTCCTGCCGCCAGGTGGAGGAGCTGGCTGCCGAGG
TCCAGAGGCTCCGGACCGAAAACCAGCGGCTTCGTCAGGAGAACCAGATGTGGAACCGAGAGGG
CTGCCGCTGTGATGAGGAGCCGGGTACCTAGGGGTGCCTCCCAGCCTGGTGGACCCAAGGAGAA
GGTCCCATTTCGTGCACACTCAGGCCAGCTGGGTCTCAAGGAGGCAGGTGGCAGATGAAAACCA
CCGTCAACACCCTGTGCGCCCTGAGAACAGCTAAATCGGTTCAGACTCCCACCTCACCGTTTCC
ATAGTTGGCTCTTTTGTGTCATCTTACCCTTTACAGAGAAATTAAATGGCCTTGGTGGGACCAA
ATGGGAAAAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

XM_006721687 ⟹ XP_006721750

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	45,160,174 - 45,170,040 (+)	NCBI

Sequence:

show sequence

AGACTCATCACAAGGTACCCACAAAATTCACTGCCAGTCACTCTGCTACGTCAAAGCCTCTCCT
ACTTCAGCACCTACCTAGGCATAATTTTAACTGACATTTTAGCAATAAAACTTTTATTTGAAGA
TATCCTTGAGCCACAAATCTCTCTGGATTTAGATTTCAAGCAGTAGGAAGTAAGATGGTTTAAC
CTGCAATTCAATAAAAGAACTTCACATCAAACTTCAATCTTTAAGAAGCTGCTACAGCTATAAT
GTAAGGTTAAGAGTTTATTCTTTCAAAGCAGGTCTCCTCATCTCTTAAACGCTATACATATGAA
GTAGATAAAAACTGGTTTCTTTTTTGGTAGCATTTAGGATCTACAAAAGTGATCCTTCAATTAC
TTGGAATTTCAAAAAATTGAGGTTACCTAGTAACAATGCACCAGTAGAACACAAAATACTCTGA
CTTTGTTTAGTCTGTGGGAAAAGAAAAATCTTTAAACTGGAAAGATTTTGTAGTCTTACAAAGA
TTACATTGGAATTGGAATTACTGTAGTTCGTTTTTCCCTCTAGGAGGGCAGCCATTTCTCTAAA
AGTTGTGTAAAAGTTAAGACTAGGATTTCAAAATGCAAGCAGATGTTGATGAAGCATACGAAAT
GGGCAACTCCGTTTCTATTTCGGAGCCGCAGCGACTCCGACTTTGTGCCCCAACCCTGTAAAGG
GCAAAACCTCATCCCTTCGGTGTAAACTTTCAAGAGAAGTGGGGCAGCACACTTTAGGCGTTTC
ACCAAGAGGCTGGCGACATGCTAGGTCAGGTTGTCCGGAGAATCGGGGCTGAATGGGAGAGATC
TTGAGGGCAAGAGCCTCAGAGACCTTCAGGCACCGAGCTCGTGAAGGTTTCCAAGTGCCCCTCT
CTAGCTGCTCCCAGGGGGAATTAGTGGTTGCTACAGTAGTTTAAGAGGGTCGTGGTTTTTCGCA
ACCCGGGCGGCGAGATGGCGCTTTGGTGTAAGCGAGCAGGTGTCACTAGTTCCAGGCGTCTGCT
GAAAGATTTGGAACAGAAGATGATGGCCACTCCGAACCAGACCGCCTGTAATGCAGAGTCACCA
GTGGCCCTGGAGGAGGCCAAGACCTCTGGTGCCCCGGGGAGCCCCCAAACACCCCCTGAGCGTC
ATGACTCTGGTGGTTCCCTGCCCCTGACACCGCGGATGGAGAGCCACTCAGAGGATGAAGATCT
TGCTGGGGCTGTCGGTGGCCTGGGCTGGAACAGTAGGAGTCCCCGGACCCAGAGCCCAGGGGGC
TGCTCAGCGGAGGCTGTGCTGGCCCGGAAGAAACACCGTCGGCGGCCATCGAAGCGCAAAAGGC
ACTGGCGACCCTACCTGGAGCTGAGCTGGGCTGAGAAACAACAGCGGGATGAGAGGCAGAGCCA
GAGGGCCTCCCGGGTCCGCGAAGAGATGTTCGCCAAAGGCCAGCCCGTGGCCCCCTACAACACC
ACCCAGTTCCTGATGAATGACAGGGACCCGGAGGAGCCCAACTTGGATGTGCCCCATGGGATCT
CCCACCCAGGTTCCAGTGGGGAGAGTGAGGCCGGGGACAGTGATGGGCGGGGCCGAGCGCACGG
TGAGTTCCAGCGGAAGGACTTCTCTGAGACTTACGAACGCTTCCACACCGAGAGCCTGCAGGGC
CGCAGCAAGCAGGAGCTGGTGCGAGACTACCTGGAGCTGGAGAAGCGGCTGTCGCAGGCGGAGG
AGGAGACTAGGAGGCTGCAGCAGCTGCAGGCGTGCACCGGCCAGCAGTCCTGCCGCCAGGTGGA
GGAGCTGGCTGCCGAGGTCCAGAGGCTCCGGACCGAAAACCAGCGGCTTCGTCAGGAGAACCAG
ATGTGGAACCGAGAGGGCTGCCGCTGTGATGAGGAGCCGGGTACCTAGGGGTGCCTCCCAGCCT
GGTGGACCCAAGGAGAAGGTCCCATTTCGTGCACACTCAGGCCAGCTGGGTCTCAAGGAGGCAG
GTGGCAGATGAAAACCACCGTCAACACCCTGTGCGCCCTGAGAACAGCTAAATCGGTTCAGACT
CCCACCTCACCGTTTCCATAGTTGGCTCTTTTGTGTCATCTTACCCTTTACAGAGAAATTAAAT
GGCCTTGGTGGGACCAAATGGGA

hide sequence

RefSeq Acc Id:

XM_011524307 ⟹ XP_011522609

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	45,160,174 - 45,170,040 (+)	NCBI

Sequence:

show sequence

GTGGGGAGGGAAGCTGGCAGAGCTCGGCCTCAGGATCCGCGCCCCTGTGGAAAGACCGCAGAGG
GAAGCCGTTTCACCAGCCTCTCCCCTTCTGGGGTCTCGGGAAACACGCGGCCAGAAGAACTACA
ATCCCCAGCAGGCACCGCGCGTCCAGGCTCTCTCTTCCCCCCCATCTTAGTGGCCTGAGCGGCT
TGACCAGAGCTGCTGCAACTGCAGCAAGAGGTGTCACTAGTTCCAGGCGTCTGCTGAAAGATTT
GGAACAGAAGATGATGGCCACTCCGAACCAGACCGCCTGTAATGCAGAGTCACCAGTGGCCCTG
GAGGAGGCCAAGACCTCTGGTGCCCCGGGGAGCCCCCAAACACCCCCTGAGCGTCATGACTCTG
GTGGTTCCCTGCCCCTGACACCGCGGATGGAGAGCCACTCAGAGGATGAAGATCTTGCTGGGGC
TGTCGGTGGCCTGGGCTGGAACAGTAGGAGTCCCCGGACCCAGAGCCCAGGGGGCTGCTCAGCG
GAGGCTGTGCTGGCCCGGAAGAAACACCGTCGGCGGCCATCGAAGCGCAAAAGGCACTGGCGAC
CCTACCTGGAGCTGAGCTGGGCTGAGAAACAACAGCGGGATGAGAGGCAGAGCCAGAGGGCCTC
CCGGGTCCGCGAAGAGATGTTCGCCAAAGGCCAGCCCGTGGCCCCCTACAACACCACCCAGTTC
CTGATGAATGACAGGGACCCGGAGGAGCCCAACTTGGATGTGCCCCATGGGATCTCCCACCCAG
GTTCCAGTGGGGAGAGTGAGGCCGGGGACAGTGATGGGCGGGGCCGAGCGCACGGTGAGTTCCA
GCGGAAGGACTTCTCTGAGACTTACGAACGCTTCCACACCGAGAGCCTGCAGGGCCGCAGCAAG
CAGGAGCTGGTGCGAGACTACCTGGAGCTGGAGAAGCGGCTGTCGCAGGCGGAGGAGGAGACTA
GGAGGCTGCAGCAGCTGCAGGCGTGCACCGGCCAGCAGTCCTGCCGCCAGGTGGAGGAGCTGGC
TGCCGAGGTCCAGAGGCTCCGGACCGAAAACCAGCGGCTTCGTCAGGAGAACCAGATGTGGAAC
CGAGAGGGCTGCCGCTGTGATGAGGAGCCGGGTACCTAGGGGTGCCTCCCAGCCTGGTGGACCC
AAGGAGAAGGTCCCATTTCGTGCACACTCAGGCCAGCTGGGTCTCAAGGAGGCAGGTGGCAGAT
GAAAACCACCGTCAACACCCTGTGCGCCCTGAGAACAGCTAAATCGGTTCAGACTCCCACCTCA
CCGTTTCCATAGTTGGCTCTTTTGTGTCATCTTACCCTTTACAGAGAAATTAAATGGCCTTGGT
GGGACCAAATGGGA

hide sequence

RefSeq Acc Id:

XM_011524308 ⟹ XP_011522610

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	45,160,174 - 45,170,040 (+)	NCBI

Sequence:

show sequence

GTGGGGAGGGAAGCTGGCAGAGCTCGGCCTCAGGATCCGCGCCCCTGTGGAAAGACCGCAGAGG
GAAGCCGTTTCACCAGCCTCTCCCCTTCTGGGGTCTCGGGAAACACGCGGCCAGAAGAACTACA
ATCCCCAGCAGGCACCGCGCGTCCAGGCTCTCTCTTCCCCCCCATCTTAGTGGCCTGAGCGGCT
TGACCAGAGCTGCTGCAACTGCAGCAAGAGCAGGTGTCACTAGTTCCAGGCGTCTGCTGAAAGA
TTTGGAACAGAAGATGATGGCCACTCCGAACCAGACCGCCTGTAATGCAGAGTCACCAGTGGCC
CTGGAGGAGGCCAAGACCTCTGGTGCCCCGGGGAGCCCCCAAACACCCCCTGAGCGTCATGACT
CTGGTGGTTCCCTGCCCCTGACACCGCGGATGGAGAGCCACTCAGAGGATGAAGATCTTGCTGG
GGCTGTCGGTGGCCTGGGCTGGAACAGTAGGAGTCCCCGGACCCAGAGCCCAGGGGGCTGCTCA
GCGGAGGCTGTGCTGGCCCGGAAGAAACACCGTCGGCGGCCATCGAAGCGCAAAAGGCACTGGC
GACCCTACCTGGAGCTGAGCTGGGCTGAGAAACAACAGCGGGATGAGAGGCAGAGCCAGAGGGC
CTCCCGGGTCCGCGAAGAGATGTTCGCCAAAGGCCAGCCCGTGGCCCCCTACAACACCACCCAG
TTCCTGATGAATGACAGGGACCCGGAGGAGCCCAACTTGGATGTGCCCCATGGGATCTCCCACC
CAGGTTCCAGTGGGGAGAGTGAGGCCGGGGACAGTGATGGGCGGGGCCGAGCGCACGGTGAGTT
CCAGCGGAAGGACTTCTCTGAGACTTACGAACGCTTCCACACCGAGAGCCTGCAGGGCCGCAGC
AAGCAGGAGCTGGTGCGAGACTACCTGGAGCTGGAGAAGCGGCTGTCGCAGGCGGAGGAGGAGA
CTAGGAGGCTGCAGCAGCTGCAGGCGTGCACCGGCCAGCAGTCCTGCCGCCAGGTGGAGGAGCT
GGCTGCCGAGGTCCAGAGGCTCCGGACCGAAAACCAGCGGCTTCGTCAGGAGAACCAGATGTGG
AACCGAGAGGGCTGCCGCTGTGATGAGGAGCCGGGTACCTAGGGGTGCCTCCCAGCCTGGTGGA
CCCAAGGAGAAGGTCCCATTTCGTGCACACTCAGGCCAGCTGGGTCTCAAGGAGGCAGGTGGCA
GATGAAAACCACCGTCAACACCCTGTGCGCCCTGAGAACAGCTAAATCGGTTCAGACTCCCACC
TCACCGTTTCCATAGTTGGCTCTTTTGTGTCATCTTACCCTTTACAGAGAAATTAAATGGCCTT
GGTGGGACCAAATGGGA

hide sequence

RefSeq Acc Id:

XM_047435323 ⟹ XP_047291279

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	45,160,174 - 45,170,040 (+)	NCBI

RefSeq Acc Id:

XM_047435324 ⟹ XP_047291280

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	45,160,174 - 45,170,040 (+)	NCBI

RefSeq Acc Id:

XM_054315017 ⟹ XP_054170992

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	46,014,059 - 46,023,937 (+)	NCBI

RefSeq Acc Id:

XM_054315018 ⟹ XP_054170993

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	46,014,059 - 46,023,937 (+)	NCBI

RefSeq Acc Id:

XM_054315019 ⟹ XP_054170994

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	46,014,059 - 46,023,937 (+)	NCBI

RefSeq Acc Id:

XM_054315020 ⟹ XP_054170995

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	46,014,059 - 46,023,937 (+)	NCBI

RefSeq Acc Id:

XM_054315021 ⟹ XP_054170996

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	17	46,014,059 - 46,023,937 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001290365	(Get FASTA)	NCBI Sequence Viewer
	NP_001290366	(Get FASTA)	NCBI Sequence Viewer
	NP_001290367	(Get FASTA)	NCBI Sequence Viewer
	NP_001290368	(Get FASTA)	NCBI Sequence Viewer
	NP_001290369	(Get FASTA)	NCBI Sequence Viewer
	NP_001290370	(Get FASTA)	NCBI Sequence Viewer
	NP_001290371	(Get FASTA)	NCBI Sequence Viewer
	NP_001290372	(Get FASTA)	NCBI Sequence Viewer
	NP_001290373	(Get FASTA)	NCBI Sequence Viewer
	NP_653209	(Get FASTA)	NCBI Sequence Viewer
	XP_006721750	(Get FASTA)	NCBI Sequence Viewer
	XP_011522609	(Get FASTA)	NCBI Sequence Viewer
	XP_011522610	(Get FASTA)	NCBI Sequence Viewer
	XP_047291279	(Get FASTA)	NCBI Sequence Viewer
	XP_047291280	(Get FASTA)	NCBI Sequence Viewer
	XP_054170992	(Get FASTA)	NCBI Sequence Viewer
	XP_054170993	(Get FASTA)	NCBI Sequence Viewer
	XP_054170994	(Get FASTA)	NCBI Sequence Viewer
	XP_054170995	(Get FASTA)	NCBI Sequence Viewer
	XP_054170996	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH03531	(Get FASTA)	NCBI Sequence Viewer
	AAH12474	(Get FASTA)	NCBI Sequence Viewer
	AAH25970	(Get FASTA)	NCBI Sequence Viewer
	AAT06733	(Get FASTA)	NCBI Sequence Viewer
	BAB71319	(Get FASTA)	NCBI Sequence Viewer
	EAW51541	(Get FASTA)	NCBI Sequence Viewer
	EAW51542	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000302276
	ENSP00000302276.2
	ENSP00000464807
	ENSP00000464807.2
	ENSP00000465086
	ENSP00000465086.2
	ENSP00000465727
	ENSP00000465727.1
	ENSP00000466200
	ENSP00000466200.2
	ENSP00000467517
	ENSP00000467517.1
	ENSP00000468251
	ENSP00000468251.2
	ENSP00000468773
	ENSP00000468773.2
GenBank Protein	Q96MH2	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_653209 ⟸ NM_144608
- Peptide Label:	isoform 1
- UniProtKB:	D3DX66 (UniProtKB/Swiss-Prot), Q96MH2 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MMATPNQTACNAESPVALEEAKTSGAPGSPQTPPERHDSGGSLPLTPRMESHSEDEDLAGAVGG LGWNSRSPRTQSPGGCSAEAVLARKKHRRRPSKRKRHWRPYLELSWAEKQQRDERQSQRASRVR EEMFAKGQPVAPYNTTQFLMNDRDPEEPNLDVPHGISHPGSSGESEAGDSDGRGRAHGEFQRKD FSETYERFHTESLQGRSKQELVRDYLELEKRLSQAEEETRRLQQLQACTGQQSCRQVEELAAEV QRLRTENQRLRQENQMWNREGCRCDEEPGT hide sequence

RefSeq Acc Id:

XP_006721750 ⟸ XM_006721687

- Peptide Label:

isoform X3

- Sequence:

show sequence

MALWCKRAGVTSSRRLLKDLEQKMMATPNQTACNAESPVALEEAKTSGAPGSPQTPPERHDSGG
SLPLTPRMESHSEDEDLAGAVGGLGWNSRSPRTQSPGGCSAEAVLARKKHRRRPSKRKRHWRPY
LELSWAEKQQRDERQSQRASRVREEMFAKGQPVAPYNTTQFLMNDRDPEEPNLDVPHGISHPGS
SGESEAGDSDGRGRAHGEFQRKDFSETYERFHTESLQGRSKQELVRDYLELEKRLSQAEEETRR
LQQLQACTGQQSCRQVEELAAEVQRLRTENQRLRQENQMWNREGCRCDEEPGT

hide sequence

RefSeq Acc Id:	NP_001290368 ⟸ NM_001303439
- Peptide Label:	isoform 1
- UniProtKB:	D3DX66 (UniProtKB/Swiss-Prot), Q96MH2 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MMATPNQTACNAESPVALEEAKTSGAPGSPQTPPERHDSGGSLPLTPRMESHSEDEDLAGAVGG LGWNSRSPRTQSPGGCSAEAVLARKKHRRRPSKRKRHWRPYLELSWAEKQQRDERQSQRASRVR EEMFAKGQPVAPYNTTQFLMNDRDPEEPNLDVPHGISHPGSSGESEAGDSDGRGRAHGEFQRKD FSETYERFHTESLQGRSKQELVRDYLELEKRLSQAEEETRRLQQLQACTGQQSCRQVEELAAEV QRLRTENQRLRQENQMWNREGCRCDEEPGT hide sequence

RefSeq Acc Id:	NP_001290366 ⟸ NM_001303437
- Peptide Label:	isoform 1
- UniProtKB:	D3DX66 (UniProtKB/Swiss-Prot), Q96MH2 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MMATPNQTACNAESPVALEEAKTSGAPGSPQTPPERHDSGGSLPLTPRMESHSEDEDLAGAVGG LGWNSRSPRTQSPGGCSAEAVLARKKHRRRPSKRKRHWRPYLELSWAEKQQRDERQSQRASRVR EEMFAKGQPVAPYNTTQFLMNDRDPEEPNLDVPHGISHPGSSGESEAGDSDGRGRAHGEFQRKD FSETYERFHTESLQGRSKQELVRDYLELEKRLSQAEEETRRLQQLQACTGQQSCRQVEELAAEV QRLRTENQRLRQENQMWNREGCRCDEEPGT hide sequence

RefSeq Acc Id:	NP_001290367 ⟸ NM_001303438
- Peptide Label:	isoform 1
- UniProtKB:	D3DX66 (UniProtKB/Swiss-Prot), Q96MH2 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MMATPNQTACNAESPVALEEAKTSGAPGSPQTPPERHDSGGSLPLTPRMESHSEDEDLAGAVGG LGWNSRSPRTQSPGGCSAEAVLARKKHRRRPSKRKRHWRPYLELSWAEKQQRDERQSQRASRVR EEMFAKGQPVAPYNTTQFLMNDRDPEEPNLDVPHGISHPGSSGESEAGDSDGRGRAHGEFQRKD FSETYERFHTESLQGRSKQELVRDYLELEKRLSQAEEETRRLQQLQACTGQQSCRQVEELAAEV QRLRTENQRLRQENQMWNREGCRCDEEPGT hide sequence

RefSeq Acc Id:	NP_001290365 ⟸ NM_001303436
- Peptide Label:	isoform 2
- UniProtKB:	Q96MH2 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MALWCKRGVTSSRRLLKDLEQKMMATPNQTACNAESPVALEEAKTSGAPGSPQTPPERHDSGGS LPLTPRMESHSEDEDLAGAVGGLGWNSRSPRTQSPGGCSAEAVLARKKHRRRPSKRKRHWRPYL ELSWAEKQQRDERQSQRASRVREEMFAKGQPVAPYNTTQFLMNDRDPEEPNLDVPHGISHPGSS GESEAGDSDGRGRAHGEFQRKDFSETYERFHTESLQGRSKQELVRDYLELEKRLSQAEEETRRL QQLQACTGQQSCRQVEELAAEVQRLRTENQRLRQENQMWNREGCRCDEEPGT hide sequence

RefSeq Acc Id:	NP_001290370 ⟸ NM_001303441
- Peptide Label:	isoform 1
- UniProtKB:	D3DX66 (UniProtKB/Swiss-Prot), Q96MH2 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MMATPNQTACNAESPVALEEAKTSGAPGSPQTPPERHDSGGSLPLTPRMESHSEDEDLAGAVGG LGWNSRSPRTQSPGGCSAEAVLARKKHRRRPSKRKRHWRPYLELSWAEKQQRDERQSQRASRVR EEMFAKGQPVAPYNTTQFLMNDRDPEEPNLDVPHGISHPGSSGESEAGDSDGRGRAHGEFQRKD FSETYERFHTESLQGRSKQELVRDYLELEKRLSQAEEETRRLQQLQACTGQQSCRQVEELAAEV QRLRTENQRLRQENQMWNREGCRCDEEPGT hide sequence

RefSeq Acc Id:	NP_001290369 ⟸ NM_001303440
- Peptide Label:	isoform 1
- UniProtKB:	D3DX66 (UniProtKB/Swiss-Prot), Q96MH2 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MMATPNQTACNAESPVALEEAKTSGAPGSPQTPPERHDSGGSLPLTPRMESHSEDEDLAGAVGG LGWNSRSPRTQSPGGCSAEAVLARKKHRRRPSKRKRHWRPYLELSWAEKQQRDERQSQRASRVR EEMFAKGQPVAPYNTTQFLMNDRDPEEPNLDVPHGISHPGSSGESEAGDSDGRGRAHGEFQRKD FSETYERFHTESLQGRSKQELVRDYLELEKRLSQAEEETRRLQQLQACTGQQSCRQVEELAAEV QRLRTENQRLRQENQMWNREGCRCDEEPGT hide sequence

RefSeq Acc Id:	NP_001290372 ⟸ NM_001303443
- Peptide Label:	isoform 1
- UniProtKB:	D3DX66 (UniProtKB/Swiss-Prot), Q96MH2 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MMATPNQTACNAESPVALEEAKTSGAPGSPQTPPERHDSGGSLPLTPRMESHSEDEDLAGAVGG LGWNSRSPRTQSPGGCSAEAVLARKKHRRRPSKRKRHWRPYLELSWAEKQQRDERQSQRASRVR EEMFAKGQPVAPYNTTQFLMNDRDPEEPNLDVPHGISHPGSSGESEAGDSDGRGRAHGEFQRKD FSETYERFHTESLQGRSKQELVRDYLELEKRLSQAEEETRRLQQLQACTGQQSCRQVEELAAEV QRLRTENQRLRQENQMWNREGCRCDEEPGT hide sequence

RefSeq Acc Id:	NP_001290373 ⟸ NM_001303444
- Peptide Label:	isoform 1
- UniProtKB:	D3DX66 (UniProtKB/Swiss-Prot), Q96MH2 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MMATPNQTACNAESPVALEEAKTSGAPGSPQTPPERHDSGGSLPLTPRMESHSEDEDLAGAVGG LGWNSRSPRTQSPGGCSAEAVLARKKHRRRPSKRKRHWRPYLELSWAEKQQRDERQSQRASRVR EEMFAKGQPVAPYNTTQFLMNDRDPEEPNLDVPHGISHPGSSGESEAGDSDGRGRAHGEFQRKD FSETYERFHTESLQGRSKQELVRDYLELEKRLSQAEEETRRLQQLQACTGQQSCRQVEELAAEV QRLRTENQRLRQENQMWNREGCRCDEEPGT hide sequence

RefSeq Acc Id:	NP_001290371 ⟸ NM_001303442
- Peptide Label:	isoform 1
- UniProtKB:	D3DX66 (UniProtKB/Swiss-Prot), Q96MH2 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MMATPNQTACNAESPVALEEAKTSGAPGSPQTPPERHDSGGSLPLTPRMESHSEDEDLAGAVGG LGWNSRSPRTQSPGGCSAEAVLARKKHRRRPSKRKRHWRPYLELSWAEKQQRDERQSQRASRVR EEMFAKGQPVAPYNTTQFLMNDRDPEEPNLDVPHGISHPGSSGESEAGDSDGRGRAHGEFQRKD FSETYERFHTESLQGRSKQELVRDYLELEKRLSQAEEETRRLQQLQACTGQQSCRQVEELAAEV QRLRTENQRLRQENQMWNREGCRCDEEPGT hide sequence

RefSeq Acc Id:

XP_011522610 ⟸ XM_011524308

- Peptide Label:

isoform X1

- Sequence:

show sequence

MMATPNQTACNAESPVALEEAKTSGAPGSPQTPPERHDSGGSLPLTPRMESHSEDEDLAGAVGG
LGWNSRSPRTQSPGGCSAEAVLARKKHRRRPSKRKRHWRPYLELSWAEKQQRDERQSQRASRVR
EEMFAKGQPVAPYNTTQFLMNDRDPEEPNLDVPHGISHPGSSGESEAGDSDGRGRAHGEFQRKD
FSETYERFHTESLQGRSKQELVRDYLELEKRLSQAEEETRRLQQLQACTGQQSCRQVEELAAEV
QRLRTENQRLRQENQMWNREGCRCDEEPGT

hide sequence

RefSeq Acc Id:

XP_011522609 ⟸ XM_011524307

- Peptide Label:

isoform X2

- Sequence:

show sequence

MMATPNQTACNAESPVALEEAKTSGAPGSPQTPPERHDSGGSLPLTPRMESHSEDEDLAGAVGG
LGWNSRSPRTQSPGGCSAEAVLARKKHRRRPSKRKRHWRPYLELSWAEKQQRDERQSQRASRVR
EEMFAKGQPVAPYNTTQFLMNDRDPEEPNLDVPHGISHPGSSGESEAGDSDGRGRAHGEFQRKD
FSETYERFHTESLQGRSKQELVRDYLELEKRLSQAEEETRRLQQLQACTGQQSCRQVEELAAEV
QRLRTENQRLRQENQMWNREGCRCDEEPGT

hide sequence

RefSeq Acc Id:

ENSP00000302276 ⟸ ENST00000307275

RefSeq Acc Id:

ENSP00000468251 ⟸ ENST00000585340

RefSeq Acc Id:

ENSP00000465086 ⟸ ENST00000586681

RefSeq Acc Id:

ENSP00000466200 ⟸ ENST00000589230

RefSeq Acc Id:

ENSP00000465727 ⟸ ENST00000591576

RefSeq Acc Id:

ENSP00000464807 ⟸ ENST00000591070

RefSeq Acc Id:

ENSP00000467517 ⟸ ENST00000592695

RefSeq Acc Id:

ENSP00000468773 ⟸ ENST00000593138

RefSeq Acc Id:	XP_047291279 ⟸ XM_047435323
- Peptide Label:	isoform X4
- UniProtKB:	Q96MH2 (UniProtKB/Swiss-Prot), D3DX66 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047291280 ⟸ XM_047435324
- Peptide Label:	isoform X4
- UniProtKB:	Q96MH2 (UniProtKB/Swiss-Prot), D3DX66 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054170992 ⟸ XM_054315017
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054170993 ⟸ XM_054315018
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054170995 ⟸ XM_054315020
- Peptide Label:	isoform X4
- UniProtKB:	Q96MH2 (UniProtKB/Swiss-Prot), D3DX66 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054170996 ⟸ XM_054315021
- Peptide Label:	isoform X4
- UniProtKB:	Q96MH2 (UniProtKB/Swiss-Prot), D3DX66 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054170994 ⟸ XM_054315019
- Peptide Label:	isoform X3

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q96MH2-F1-model_v2	AlphaFold	Q96MH2	1-286	view protein structure

Promoters

RGD ID:

6794198

Promoter ID:

HG_KWN:26356

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, Jurkat, K562, Lymphoblastoid

Transcripts:

NM_144608, UC010DAF.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	17	40,593,694 - 40,594,194 (+)	MPROMDB

RGD ID:

6794200

Promoter ID:

HG_KWN:26357

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

UC002III.1, UC002IIJ.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	17	40,594,116 - 40,595,142 (+)	MPROMDB

RGD ID:

7235321

Promoter ID:

EPDNEW_H23406

Type:

initiation region

Name:

HEXIM2_2

Description:

hexamethylene bisacetamide inducible 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H23407

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	45,160,702 - 45,160,762	EPDNEW

RGD ID:

7235325

Promoter ID:

EPDNEW_H23407

Type:

initiation region

Name:

HEXIM2_1

Description:

hexamethylene bisacetamide inducible 2

SO ACC ID:

SO:0000170

Source:

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

Alternative Promoters:

null; see alsoEPDNEW_H23406

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	17	45,161,894 - 45,161,954	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:28591	AgrOrtholog
COSMIC	HEXIM2	COSMIC
Ensembl Genes	ENSG00000168517	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000307275	ENTREZGENE
	ENST00000307275.7	UniProtKB/Swiss-Prot
	ENST00000585340	UniProtKB/TrEMBL
	ENST00000585340.2	UniProtKB/Swiss-Prot
	ENST00000586681	ENTREZGENE, UniProtKB/TrEMBL
	ENST00000586681.6	UniProtKB/Swiss-Prot
	ENST00000589230	ENTREZGENE, UniProtKB/TrEMBL
	ENST00000589230.6	UniProtKB/Swiss-Prot
	ENST00000591070	ENTREZGENE, UniProtKB/TrEMBL
	ENST00000591070.6	UniProtKB/Swiss-Prot
	ENST00000591576	ENTREZGENE
	ENST00000591576.5	UniProtKB/Swiss-Prot
	ENST00000592695	ENTREZGENE
	ENST00000592695.1	UniProtKB/Swiss-Prot
	ENST00000593138	ENTREZGENE, UniProtKB/TrEMBL
	ENST00000593138.6	UniProtKB/Swiss-Prot
Gene3D-CATH	6.10.250.2910	UniProtKB/Swiss-Prot
GTEx	ENSG00000168517	GTEx
HGNC ID	HGNC:28591	ENTREZGENE
Human Proteome Map	HEXIM2	Human Proteome Map
InterPro	HEXIM	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:124790	UniProtKB/Swiss-Prot
NCBI Gene	124790	ENTREZGENE
OMIM	615695	OMIM
PANTHER	PTHR13469	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR13469:SF3	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	HEXIM	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA142671695	PharmGKB
PRINTS	HEXIMFAMILY	UniProtKB/Swiss-Prot
UniProt	D3DX66	ENTREZGENE
	HEXI2_HUMAN	UniProtKB/Swiss-Prot
	K7EIM4_HUMAN	UniProtKB/TrEMBL
	K7EJA3_HUMAN	UniProtKB/TrEMBL
	K7ELS4_HUMAN	UniProtKB/TrEMBL
	K7ERG7_HUMAN	UniProtKB/TrEMBL
	K7ESM2_HUMAN	UniProtKB/TrEMBL
	Q96MH2	ENTREZGENE
UniProt Secondary	D3DX66	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2018-11-29	HEXIM2	HEXIM P-TEFb complex subunit 2		hexamethylene bisacetamide inducible 2	Symbol and/or name change	5135510	APPROVED
2016-04-12	HEXIM2	hexamethylene bisacetamide inducible 2		hexamethylene bis-acetamide inducible 2	Symbol and/or name change	5135510	APPROVED
2011-08-02	HEXIM2	hexamethylene bis-acetamide inducible 2	HEXIM2	hexamthylene bis-acetamide inducible 2	Symbol and/or name change	5135510	APPROVED

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

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

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

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

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Imported Disease Annotations - ClinVar