MINDY3 (MINDY lysine 48 deubiquitinase 3)

Gene: MINDY3 (MINDY lysine 48 deubiquitinase 3) Homo sapiens

Analyze

Symbol:

MINDY3

Name:

MINDY lysine 48 deubiquitinase 3

RGD ID:

1320032

HGNC Page

HGNC:23578

Description:

Enables K48-linked deubiquitinase activity and cysteine-type deubiquitinase activity. Predicted to be involved in apoptotic process and proteolysis. Located in nuclear membrane and nucleoplasm.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

C10orf97; CARD-containing protein; CARP; caspase recruitment domain containing pro-apoptotic protein; chromosome 10 open reading frame 97; dermal papilla-derived protein 5; DERP5; deubiquitinating enzyme MINDY-3; FAM188A; family with sequence similarity 188 member A; family with sequence similarity 188, member A; FLJ13397; MINDY deubiquitinase 3; MST126; MSTP126; my042; RP11-394I23.1; ubiquitin carboxyl-terminal hydrolase FAM188A; ubiquitin carboxyl-terminal hydrolase MINDY-3

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Mindy3 (MINDY lysine 48 deubiquitinase 3)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Mindy3 (MINDY lysine 48 deubiquitinase 3)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Mindy3 (MINDY lysine 48 deubiquitinase 3)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	MINDY3 (MINDY lysine 48 deubiquitinase 3)	NCBI	Ortholog
Canis lupus familiaris (dog):	MINDY3 (MINDY lysine 48 deubiquitinase 3)	HGNC	HomoloGene, NCBI
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Mindy3 (MINDY lysine 48 deubiquitinase 3)	NCBI	Ortholog
Sus scrofa (pig):	MINDY3 (MINDY lysine 48 deubiquitinase 3)	HGNC	EggNOG, Ensembl, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	MINDY3 (MINDY lysine 48 deubiquitinase 3)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Mindy3 (MINDY lysine 48 deubiquitinase 3)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Rpl36al-ps5 (ribosomal protein L36A, pseudogene 5)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Mindy3 (MINDY lysine 48 deubiquitinase 3)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Mindy3 (MINDY lysine 48 deubiquitinase 3)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Drosophila melanogaster (fruit fly):	CG7332	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	mindy3	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Xenopus laevis (African clawed frog):	mindy3.L	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	mindy3	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	mindy3.S	Alliance	DIOPT (Xenbase)

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	10	15,778,174 - 15,860,507 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	10	15,778,170 - 15,860,507 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	10	15,820,173 - 15,902,506 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	10	15,860,181 - 15,942,525 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	10	15,860,180 - 15,942,525	NCBI
Celera	10	15,753,418 - 15,835,764 (-)	NCBI		Celera
Cytogenetic Map	10	p13	NCBI
HuRef	10	15,732,561 - 15,814,922 (-)	NCBI		HuRef
CHM1_1	10	15,820,225 - 15,902,566 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	10	15,796,178 - 15,878,518 (-)	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

Experimental Liver Cirrhosis (EXP)

hypoparathyroidism-deafness-renal disease syndrome (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dimethylhydrazine (ISO)

1-naphthyl isothiocyanate (ISO)

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

2-hydroxypropanoic acid (EXP)

3-isobutyl-1-methyl-7H-xanthine (EXP)

4,4'-diaminodiphenylmethane (ISO)

4,4'-sulfonyldiphenol (EXP)

6-propyl-2-thiouracil (ISO)

aflatoxin B1 (EXP)

all-trans-retinoic acid (EXP)

arsenite(3-) (EXP)

atrazine (EXP)

benzo[a]pyrene (EXP)

bisphenol A (EXP,ISO)

cadmium atom (EXP)

cadmium dichloride (EXP)

carbon nanotube (ISO)

cisplatin (EXP)

crocidolite asbestos (ISO)

cyclosporin A (EXP)

dexamethasone (EXP)

dibutyl phthalate (ISO)

dorsomorphin (EXP)

epoxiconazole (ISO)

ethyl methanesulfonate (EXP)

flutamide (ISO)

folic acid (ISO)

formaldehyde (EXP)

gentamycin (ISO)

indometacin (EXP)

ivermectin (EXP)

lead(0) (EXP)

methimazole (ISO)

methyl methanesulfonate (EXP)

N-nitrosodimethylamine (ISO)

nefazodone (ISO)

paracetamol (ISO)

rac-lactic acid (EXP)

SB 431542 (EXP)

sodium arsenite (EXP,ISO)

Soman (ISO)

sulfadimethoxine (ISO)

sunitinib (EXP)

temozolomide (EXP)

testosterone (EXP)

thioacetamide (ISO)

triptonide (ISO)

troglitazone (EXP)

tungsten (ISO)

valproic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

apoptotic process (IEA)

proteolysis (IEA)

Cellular Component

nuclear membrane (IDA)

nucleoplasm (IDA)

nucleus (IEA)

Molecular Function

cysteine-type deubiquitinase activity (IDA,IEA)

cysteine-type peptidase activity (IEA)

K48-linked deubiquitinase activity (IBA,IDA,IEA)

protein binding (IPI)

References

References - curated

#	Reference Title	Reference Citation
1.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions
2.	Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.	Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.

Additional References at PubMed

PMID:12054670	PMID:14702039	PMID:16169070	PMID:16344560	PMID:17207965	PMID:17652099	PMID:18029348	PMID:20804422	PMID:21499297	PMID:21873635	PMID:24823311	PMID:24870804
PMID:25260751	PMID:25416956	PMID:25544563	PMID:26186194	PMID:27292798	PMID:28514442	PMID:29576527	PMID:30561431	PMID:31515488	PMID:32296183	PMID:33277362	PMID:33417976
PMID:33961781	PMID:34599178	PMID:35831314	PMID:36168628

Genomics

Comparative Map Data

MINDY3
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	10	15,778,174 - 15,860,507 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	10	15,778,170 - 15,860,507 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	10	15,820,173 - 15,902,506 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	10	15,860,181 - 15,942,525 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	10	15,860,180 - 15,942,525	NCBI
Celera	10	15,753,418 - 15,835,764 (-)	NCBI		Celera
Cytogenetic Map	10	p13	NCBI
HuRef	10	15,732,561 - 15,814,922 (-)	NCBI		HuRef
CHM1_1	10	15,820,225 - 15,902,566 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	10	15,796,178 - 15,878,518 (-)	NCBI		T2T-CHM13v2.0

Mindy3
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	2	12,352,074 - 12,424,298 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	2	12,352,074 - 12,424,281 (-)	Ensembl		GRCm39 Ensembl
GRCm38	2	12,347,263 - 12,419,489 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	2	12,347,263 - 12,419,470 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	2	12,268,891 - 12,341,087 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	2	12,265,117 - 12,337,313 (-)	NCBI		MGSCv36	mm8
Celera	2	12,260,745 - 12,332,603 (-)	NCBI		Celera
Cytogenetic Map	2	A1	NCBI
cM Map	2	9.27	NCBI

Mindy3
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	17	80,454,404 - 80,532,999 (-)	NCBI		GRCr8
mRatBN7.2	17	75,545,286 - 75,623,884 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	17	75,545,286 - 75,623,854 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	17	79,004,991 - 79,083,646 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	17	82,840,328 - 82,918,988 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	17	76,888,261 - 76,966,923 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	17	79,720,534 - 79,798,470 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	17	79,720,535 - 79,798,435 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	17	81,348,947 - 81,426,343 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	17	86,693,496 - 86,771,915 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	17	86,713,857 - 86,956,893 (-)	NCBI
Celera	17	74,921,510 - 74,998,724 (-)	NCBI		Celera
Cytogenetic Map	17	q12.3	NCBI

Mindy3
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0 Ensembl	NW_004955429	11,805,080 - 11,890,103 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955429	11,805,205 - 11,890,103 (+)	NCBI	ChiLan1.0	ChiLan1.0

MINDY3
(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	8	28,627,068 - 28,709,225 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	10	28,632,395 - 28,714,551 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	10	16,101,605 - 16,183,746 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	10	16,377,064 - 16,459,134 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	10	16,377,064 - 16,459,135 (-)	Ensembl	panpan1.1		panPan2

MINDY3
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	2	20,948,946 - 21,014,938 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	2	20,865,946 - 21,014,429 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	2	18,041,164 - 18,125,213 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	2	21,223,797 - 21,307,880 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	2	21,223,812 - 21,307,880 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	2	18,430,539 - 18,514,602 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	2	19,264,996 - 19,349,027 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	2	19,890,285 - 19,974,351 (+)	NCBI		UU_Cfam_GSD_1.0

Mindy3
(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_024409344	16,705,922 - 16,796,909 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936574	6,205,442 - 6,296,345 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936574	6,205,419 - 6,296,385 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

MINDY3
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	10	45,980,111 - 46,062,700 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	10	45,980,088 - 46,062,700 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	10	50,676,092 - 50,758,110 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

MINDY3
(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	9	15,738,104 - 15,820,935 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	9	15,737,625 - 15,820,266 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666051	21,328,221 - 21,410,447 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Mindy3
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624796	11,778,201 - 11,863,318 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624796	11,778,932 - 11,862,882 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in MINDY3
6 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 10p13(chr10:15680938-16480748)x3	copy number gain	See cases [RCV000051623]	Chr10:15680938..16480748 [GRCh38] Chr10:15722937..16522747 [GRCh37] Chr10:15762943..16562753 [NCBI36] Chr10:10p13	uncertain significance
GRCh38/hg38 10p15.1-13(chr10:4802753-16823491)x1	copy number loss	See cases [RCV000052500]	Chr10:4802753..16823491 [GRCh38] Chr10:4844945..16865490 [GRCh37] Chr10:4834945..16905496 [NCBI36] Chr10:10p15.1-13	pathogenic
GRCh38/hg38 10p15.3-12.31(chr10:69261-19184047)x3	copy number gain	See cases [RCV000053507]	Chr10:69261..19184047 [GRCh38] Chr10:224406..19472976 [GRCh37] Chr10:105201..19512982 [NCBI36] Chr10:10p15.3-12.31	pathogenic
GRCh38/hg38 10p15.3-12.2(chr10:90221-22567425)x3	copy number gain	See cases [RCV000053508]	Chr10:90221..22567425 [GRCh38] Chr10:224406..22856354 [GRCh37] Chr10:126161..22896360 [NCBI36] Chr10:10p15.3-12.2	pathogenic
GRCh38/hg38 10p15.3-12.1(chr10:90421-29058318)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053512]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053512]\|See cases [RCV000053512]	Chr10:90421..29058318 [GRCh38] Chr10:224406..29347247 [GRCh37] Chr10:126361..29387253 [NCBI36] Chr10:10p15.3-12.1	pathogenic
GRCh38/hg38 10p13(chr10:15569469-16776796)x3	copy number gain	See cases [RCV000135483]	Chr10:15569469..16776796 [GRCh38] Chr10:15611468..16818795 [GRCh37] Chr10:15651474..16858801 [NCBI36] Chr10:10p13	benign
GRCh38/hg38 10p14-12.31(chr10:7428770-21587752)x1	copy number loss	See cases [RCV000137307]	Chr10:7428770..21587752 [GRCh38] Chr10:7470732..21876681 [GRCh37] Chr10:7510738..21916687 [NCBI36] Chr10:10p14-12.31	pathogenic\|uncertain significance
GRCh38/hg38 10p13(chr10:15727841-16109161)x1	copy number loss	See cases [RCV000137834]	Chr10:15727841..16109161 [GRCh38] Chr10:15769840..16151160 [GRCh37] Chr10:15809846..16191166 [NCBI36] Chr10:10p13	likely benign
GRCh38/hg38 10p15.3-12.1(chr10:90205-26339978)x3	copy number gain	See cases [RCV000138428]	Chr10:90205..26339978 [GRCh38] Chr10:224406..26628907 [GRCh37] Chr10:126145..26668913 [NCBI36] Chr10:10p15.3-12.1	pathogenic
GRCh38/hg38 10p15.1-q11.22(chr10:4604734-48074662)x3	copy number gain	See cases [RCV000141497]	Chr10:4604734..48074662 [GRCh38] Chr10:4646926..47531169 [GRCh37] Chr10:4636926..47125152 [NCBI36] Chr10:10p15.1-q11.22	benign
GRCh38/hg38 10p15.3-12.31(chr10:54086-19336980)x1	copy number loss	See cases [RCV000143703]	Chr10:54086..19336980 [GRCh38] Chr10:100026..19625909 [GRCh37] Chr10:90026..19665915 [NCBI36] Chr10:10p15.3-12.31	pathogenic\|likely pathogenic
GRCh37/hg19 10p15.3-11.23(chr10:100026-30278548)x3	copy number gain	See cases [RCV000447131]	Chr10:100026..30278548 [GRCh37] Chr10:10p15.3-11.23	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3	copy number gain	See cases [RCV000448750]	Chr10:93297..135378918 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)	copy number gain	See cases [RCV000511389]	Chr10:100027..135427143 [GRCh37] Chr10:10p15.3-q26.3	pathogenic\|uncertain significance
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3	copy number gain	See cases [RCV000510861]	Chr10:100027..135427143 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
GRCh37/hg19 10p15.3-q11.23(chr10:100026-50961640)x3	copy number gain	See cases [RCV000510893]	Chr10:100026..50961640 [GRCh37] Chr10:10p15.3-q11.23	pathogenic
GRCh37/hg19 10p13(chr10:15718480-15966080)x3	copy number gain	not provided [RCV000683210]	Chr10:15718480..15966080 [GRCh37] Chr10:10p13	likely benign
GRCh37/hg19 10p13(chr10:15814203-15966080)x1	copy number loss	not provided [RCV000683197]	Chr10:15814203..15966080 [GRCh37] Chr10:10p13	likely benign
GRCh37/hg19 10p13(chr10:15719906-16686551)x1	copy number loss	not provided [RCV000683250]	Chr10:15719906..16686551 [GRCh37] Chr10:10p13	uncertain significance
Single allele	deletion	Hypoparathyroidism, deafness, renal disease syndrome [RCV000735901]	Chr10:4689760..19120882 [GRCh37] Chr10:10p15.1-12.31	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:73232-135524321)x3	copy number gain	not provided [RCV000749464]	Chr10:73232..135524321 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:98087-135477883)x3	copy number gain	not provided [RCV000749465]	Chr10:98087..135477883 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
NM_024948.4(MINDY3):c.1029-5C>T	single nucleotide variant	not provided [RCV000968166]	Chr10:15786653 [GRCh38] Chr10:15828652 [GRCh37] Chr10:10p13	benign
GRCh37/hg19 10p13(chr10:15661517-16163555)x3	copy number gain	not provided [RCV000846101]	Chr10:15661517..16163555 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.956-10dup	duplication	not provided [RCV000961990]	Chr10:15789328..15789329 [GRCh38] Chr10:15831327..15831328 [GRCh37] Chr10:10p13	benign
NM_024948.4(MINDY3):c.731-23GTT[4]	microsatellite	not provided [RCV000883727]	Chr10:15821735..15821737 [GRCh38] Chr10:15863734..15863736 [GRCh37] Chr10:10p13	benign
NM_024948.4(MINDY3):c.1251T>C (p.Asp417=)	single nucleotide variant	not provided [RCV000961989]	Chr10:15779079 [GRCh38] Chr10:15821078 [GRCh37] Chr10:10p13	benign
GRCh37/hg19 10p14-13(chr10:9137489-17227168)	copy number loss	Neurodevelopmental delay [RCV001352639]	Chr10:9137489..17227168 [GRCh37] Chr10:10p14-13	pathogenic
GRCh37/hg19 10p13(chr10:15631365-16749903)	copy number gain	not specified [RCV002052866]	Chr10:15631365..16749903 [GRCh37] Chr10:10p13	uncertain significance
GRCh37/hg19 10p15.1-11.21(chr10:6273934-34732521)	copy number gain	not specified [RCV002052863]	Chr10:6273934..34732521 [GRCh37] Chr10:10p15.1-11.21	pathogenic
GRCh37/hg19 10p15.3-q11.22(chr10:135655-47688677)x4	copy number gain	Mosaic supernumerary isodicentric chromosome 10 [RCV001825164]	Chr10:135655..47688677 [GRCh37] Chr10:10p15.3-q11.22	not provided
NM_024948.4(MINDY3):c.337G>A (p.Gly113Arg)	single nucleotide variant	not specified [RCV004260788]	Chr10:15841498 [GRCh38] Chr10:15883497 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.823C>G (p.Pro275Ala)	single nucleotide variant	not specified [RCV004258114]	Chr10:15816894 [GRCh38] Chr10:15858893 [GRCh37] Chr10:10p13	uncertain significance
GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143)	copy number gain	Distal trisomy 10q [RCV003319593]	Chr10:11138692..135427143 [GRCh37] Chr10:10p14-q26.3	pathogenic
NM_024948.4(MINDY3):c.1283A>G (p.Lys428Arg)	single nucleotide variant	not specified [RCV004324804]	Chr10:15779047 [GRCh38] Chr10:15821046 [GRCh37] Chr10:10p13	uncertain significance
GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143)	copy number loss	Distal 10q deletion syndrome [RCV003319583]	Chr10:12829206..135427143 [GRCh37] Chr10:10p13-q26.3	pathogenic
GRCh37/hg19 10p13(chr10:15595630-16873686)x3	copy number gain	not specified [RCV003986902]	Chr10:15595630..16873686 [GRCh37] Chr10:10p13	uncertain significance
GRCh37/hg19 10p13(chr10:15634150-16873686)x3	copy number gain	not specified [RCV003986905]	Chr10:15634150..16873686 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.868G>A (p.Val290Ile)	single nucleotide variant	not specified [RCV004421958]	Chr10:15816849 [GRCh38] Chr10:15858848 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.1178A>G (p.Tyr393Cys)	single nucleotide variant	not specified [RCV004421944]	Chr10:15782165 [GRCh38] Chr10:15824164 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.421G>T (p.Val141Phe)	single nucleotide variant	not specified [RCV004421948]	Chr10:15838268 [GRCh38] Chr10:15880267 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.448C>T (p.His150Tyr)	single nucleotide variant	not specified [RCV004421949]	Chr10:15838241 [GRCh38] Chr10:15880240 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.520A>G (p.Met174Val)	single nucleotide variant	not specified [RCV004421951]	Chr10:15837260 [GRCh38] Chr10:15879259 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.53G>A (p.Ser18Asn)	single nucleotide variant	not specified [RCV004421952]	Chr10:15860247 [GRCh38] Chr10:15902246 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.830T>A (p.Phe277Tyr)	single nucleotide variant	not specified [RCV004421955]	Chr10:15816887 [GRCh38] Chr10:15858886 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.898G>A (p.Ala300Thr)	single nucleotide variant	not specified [RCV004421959]	Chr10:15796157 [GRCh38] Chr10:15838156 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.899C>T (p.Ala300Val)	single nucleotide variant	not specified [RCV004421960]	Chr10:15796156 [GRCh38] Chr10:15838155 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.611C>T (p.Ala204Val)	single nucleotide variant	not specified [RCV004421953]	Chr10:15834582 [GRCh38] Chr10:15876581 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.853G>A (p.Glu285Lys)	single nucleotide variant	not specified [RCV004421956]	Chr10:15816864 [GRCh38] Chr10:15858863 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.860A>C (p.His287Pro)	single nucleotide variant	not specified [RCV004421957]	Chr10:15816857 [GRCh38] Chr10:15858856 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.260G>A (p.Cys87Tyr)	single nucleotide variant	not specified [RCV004421947]	Chr10:15841575 [GRCh38] Chr10:15883574 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.470C>T (p.Ser157Leu)	single nucleotide variant	not specified [RCV004421950]	Chr10:15837310 [GRCh38] Chr10:15879309 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.744A>G (p.Ile248Met)	single nucleotide variant	not specified [RCV004421954]	Chr10:15821713 [GRCh38] Chr10:15863712 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.1031T>C (p.Ile344Thr)	single nucleotide variant	not specified [RCV004421943]	Chr10:15786646 [GRCh38] Chr10:15828645 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.212A>G (p.Lys71Arg)	single nucleotide variant	not specified [RCV004421945]	Chr10:15843235 [GRCh38] Chr10:15885234 [GRCh37] Chr10:10p13	uncertain significance
NM_024948.4(MINDY3):c.228T>A (p.Asp76Glu)	single nucleotide variant	not specified [RCV004421946]	Chr10:15843219 [GRCh38] Chr10:15885218 [GRCh37] Chr10:10p13	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	942
Count of miRNA genes:	464
Interacting mature miRNAs:	524
Transcripts:	ENST00000277632, ENST00000378036, ENST00000418767, ENST00000436829, ENST00000476912, ENST00000477891
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

WI-17514

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	15,831,017 - 15,831,125	UniSTS	GRCh37
Build 36	10	15,871,023 - 15,871,131	RGD	NCBI36
Celera	10	15,764,260 - 15,764,368	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	15,743,403 - 15,743,511	UniSTS
GeneMap99-GB4 RH Map	10	108.85	UniSTS
Whitehead-RH Map	10	108.1	UniSTS
NCBI RH Map	10	210.8	UniSTS

RH119444

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	15,874,602 - 15,874,914	UniSTS	GRCh37
Build 36	10	15,914,608 - 15,914,920	RGD	NCBI36
Celera	10	15,807,847 - 15,808,159	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	15,786,990 - 15,787,302	UniSTS
TNG Radiation Hybrid Map	10	8615.0	UniSTS

MARC_43417-43418:1095094009:1

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	15,820,192 - 15,820,756	UniSTS	GRCh37
Build 36	10	15,860,198 - 15,860,762	RGD	NCBI36
Celera	10	15,753,435 - 15,753,999	RGD

AB070132

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	15,820,923 - 15,821,023	UniSTS	GRCh37
Build 36	10	15,860,929 - 15,861,029	RGD	NCBI36
Celera	10	15,754,166 - 15,754,266	RGD
HuRef	10	15,733,309 - 15,733,409	UniSTS

WI-13843

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	15,820,185 - 15,820,334	UniSTS	GRCh37
Build 36	10	15,860,191 - 15,860,340	RGD	NCBI36
Celera	10	15,753,428 - 15,753,577	RGD
Cytogenetic Map	10	p13	UniSTS
HuRef	10	15,732,571 - 15,732,720	UniSTS
GeneMap99-GB4 RH Map	10	116.51	UniSTS
Whitehead-RH Map	10	113.4	UniSTS

Expression

RNA-SEQ Expression

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

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

visual system

adipose tissue

appendage

entire extraembryonic component

pharyngeal arch

High

Medium

1758

1373

1215

182

958

105

3289

889

2638

259

1339

1476

1124

1864

Low

680

1591

511

442

967

360

1068

1307

1096

160

121

136

924

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001318330	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_024948	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005252600	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005252602	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_006717508	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519690	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519691	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519693	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011519694	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017016671	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017016672	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017016673	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017016674	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017016675	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017016676	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425772	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425773	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425774	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425775	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047425776	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054366774	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054366775	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054366776	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054366777	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054366778	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054366779	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054366780	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054366781	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054366782	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054366783	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054366784	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001747205	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001747206	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001747207	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_428647	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_930516	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB014761	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF063600	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF176916	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AI573091	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK023459	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL590439	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL833873	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC020605	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC061585	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC067799	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471072	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068268	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CR457315	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA063140	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	OP794525	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000277632 ⟹ ENSP00000277632

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	15,778,174 - 15,860,507 (-)	Ensembl

RefSeq Acc Id:

ENST00000378036 ⟹ ENSP00000367275

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	15,778,170 - 15,818,008 (-)	Ensembl

RefSeq Acc Id:

ENST00000418767 ⟹ ENSP00000388661

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	15,788,828 - 15,837,299 (-)	Ensembl

RefSeq Acc Id:

ENST00000436829 ⟹ ENSP00000389883

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	15,796,120 - 15,838,279 (-)	Ensembl

RefSeq Acc Id:

ENST00000476912

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	15,778,854 - 15,782,335 (-)	Ensembl

RefSeq Acc Id:

ENST00000477891

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	15,778,170 - 15,860,498 (-)	Ensembl

RefSeq Acc Id:

NM_001318330 ⟹ NP_001305259

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	15,778,174 - 15,860,507 (-)	NCBI
CHM1_1	10	15,820,218 - 15,902,579 (-)	NCBI
T2T-CHM13v2.0	10	15,796,178 - 15,878,518 (-)	NCBI

Sequence:

show sequence

ACTTCCGGTACGGAAAACTCGCTGCTGCCCCAACCTGGCTTGACAGGCTTGGTCTCTGCAAGTG
GCTCTCAGCCCCTTCTTCTTTCCTGCCTCACCTTCCAATTCGTTTGCCGCCGCCGTCCCGCAGC
TGCTGTTTCCGGAGTTGCCCCTTCCCCATGTTCCGGGGCAGGAGTCCGCAAAGCGAAGATCCGC
CCGCCGGTTCCTCATCATGTCCGAACTGACTAAAGAGCTGATGGAGCTGGTGTGGGGCACCAAG
AGCAGCCCCGGTCTCTCGGACACCATTTTCTGCCGCTGGACGCAAGGGTTTGTGTTTAGTGAAT
CAGAGGGATCTGCATTAGAACAGTTTGAAGGTGGCCCCTGTGCTGTTATTGCACCTGTTCAGGC
ATTTCTTTTGAAGAAGCTCCTGTTTTCTTCGGAGAAGTCTTCTTGGCGGGATTGTTCAGAGGAA
GAGCAGAAGGAACTCCTTTGTCATACCTTGTGTGATATTTTAGAAAGTGCTTGTTGTGACCACT
CTGGATCATACTGCTTGGTTTCATGGTTAAGAGGAAAGACAACTGAGGAAACTGCTAGTATTTC
TGGGAGTCCTGCAGAGTCTAGTTGCCAAGTGGAACATTCTTAAAAAGATCGTTCAGAAGTTTAC
CAGAATTAAAAGATGCTGTCTTGGACCAGTATTCAATGTGGGGAAATAAATTTGGAGTATTGCT
TTTTCTGTATTCTGTATTACTGACAAAGGGCATTGAAAACATAAAAAACGAAATTGAAGATGCA
AGTGAACCCTTGATAGATCCTGTATATGGACATGGCAGCCAAAGTTTAATTAATCTCCTGCTGA
CGGGACATGCTGTTTCTAATGTATGGGATGGTGATAGAGAGTGCTCAGGAATGAAACTTCTTGG
TATACATGAACAAGCAGCAGTAGGATTTTTAACACTAATGGAAGCTTTAAGATACTGTAAGGTT
GGTTCTTACTTGAAATCTCCAAAATTCCCTATTTGGATTGTTGGCAGTGAGACTCACCTCACCG
TATTTTTTGCCAAGGATATGGCTTTAGTTGCCCCTGAAGCTCCTTCAGAACAAGCCAGAAGAGT
TTTTCAAACCTACGACCCAGAAGATAATGGATTCATACCCGATTCACTTCTGGAAGATGTGATG
AAAGCATTGGACCTTGTTTCAGATCCTGAATATATAAATCTCATGAAGAATAAATTAGATCCAG
AAGGATTAGGAATCATATTATTGGGCCCATTTCTTCAAGAATTTTTTCCTGATCAGGGCTCCAG
TGGTCCAGAATCTTTTACTGTCTACCACTACAATGGATTGAAGCAGTCAAATTATAATGAAAAG
GTCATGTACGTAGAAGGGACTGCAGTTGTGATGGGTTTTGAAGATCCCATGCTACAGACAGATG
ACACTCCTATTAAACGCTGTCTGCAAACCAAATGGCCATACATTGAGTTACTCTGGACCACAGA
TCGCTCTCCTTCACTAAATTAATTTGTCTAAGTATTTATAAGGAAGATCTTAATAACAGATGTT
GAAAGAAGGAGTCAAGACTGGCAATTGGCTGGATTAAGCTAAACACTGGTATCACTGATTAACT
GTAAATAACAATTAAAAACACATTTTCAGTGTTTATGATATGTTTAAATTATTTGTCCTAAAGC
TTTATGTTAAAGATTATCCTATTTTACCCCTTCGTGTGAAATTTACTAGCAAAATTAAGCTTTC
ATCAAAGTTCATCACTTTTGCATTCAGATACTTGGTCATTTACTTACCAAATTACAAACGCAAT
ACTACAGCATTTGTATATTAAGTATCACAGTTACTATTGATAAACTACTTTTGGGTTTTATTTC
ATTGAGGCACTTTTTTTATTGTTTGAATGATTCCGGCTTGTAATATATCAGCCTCTACAATGAA
ATGCAGAAGAGTTCATTTTTCTAAGATCTGTTTTTCATTAGAAATATTGACAAATAACACATTG
TCAACCTGGATCCTTTGACAATTTACTTAACTCTGGCATGTTCACAAAAAGTAGAAACTCTAAG
AGACCATTACCATTTATTCACAGATGTATAGGGGATGTATTCTAAAAACTGACAGAAAAGAGAA
TCTGATAGTCAACACTGTTAACTTTTACTGTGTAATTGCCAAATACACTTTTCCAAATTTGTCC
CAACAGCCCTGTAAGCCAGCTTTCTTCTATATTTATAAACACGATAAATGCATGAGAAGATCTG
TTATTACATTAGTATATTACGTTATTTATTATGATCCTAGTTGATGGCCTAAATAAACACCTTT
TTCTTTAA

hide sequence

RefSeq Acc Id:

NM_024948 ⟹ NP_079224

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	15,778,174 - 15,860,507 (-)	NCBI
GRCh37	10	15,820,173 - 15,902,519 (-)	NCBI
Build 36	10	15,860,181 - 15,942,525 (-)	NCBI Archive
Celera	10	15,753,418 - 15,835,764 (-)	RGD
HuRef	10	15,732,561 - 15,814,922 (-)	ENTREZGENE
CHM1_1	10	15,820,218 - 15,902,579 (-)	NCBI
T2T-CHM13v2.0	10	15,796,178 - 15,878,518 (-)	NCBI

Sequence:

show sequence

ACTTCCGGTACGGAAAACTCGCTGCTGCCCCAACCTGGCTTGACAGGCTTGGTCTCTGCAAGTG
GCTCTCAGCCCCTTCTTCTTTCCTGCCTCACCTTCCAATTCGTTTGCCGCCGCCGTCCCGCAGC
TGCTGTTTCCGGAGTTGCCCCTTCCCCATGTTCCGGGGCAGGAGTCCGCAAAGCGAAGATCCGC
CCGCCGGTTCCTCATCATGTCCGAACTGACTAAAGAGCTGATGGAGCTGGTGTGGGGCACCAAG
AGCAGCCCCGGTCTCTCGGACACCATTTTCTGCCGCTGGACGCAAGGGTTTGTGTTTAGTGAAT
CAGAGGGATCTGCATTAGAACAGTTTGAAGGTGGCCCCTGTGCTGTTATTGCACCTGTTCAGGC
ATTTCTTTTGAAGAAGCTCCTGTTTTCTTCGGAGAAGTCTTCTTGGCGGGATTGTTCAGAGGAA
GAGCAGAAGGAACTCCTTTGTCATACCTTGTGTGATATTTTAGAAAGTGCTTGTTGTGACCACT
CTGGATCATACTGCTTGGTTTCATGGTTAAGAGGAAAGACAACTGAGGAAACTGCTAGTATTTC
TGGGAGTCCTGCAGAGTCTAGTTGCCAAGTGGAACATTCTTCTGCCTTGGCTGTCGAAGAGCTT
GGCTTTGAGCGATTTCATGCATTAATTCAAAAAAGATCGTTCAGAAGTTTACCAGAATTAAAAG
ATGCTGTCTTGGACCAGTATTCAATGTGGGGAAATAAATTTGGAGTATTGCTTTTTCTGTATTC
TGTATTACTGACAAAGGGCATTGAAAACATAAAAAACGAAATTGAAGATGCAAGTGAACCCTTG
ATAGATCCTGTATATGGACATGGCAGCCAAAGTTTAATTAATCTCCTGCTGACGGGACATGCTG
TTTCTAATGTATGGGATGGTGATAGAGAGTGCTCAGGAATGAAACTTCTTGGTATACATGAACA
AGCAGCAGTAGGATTTTTAACACTAATGGAAGCTTTAAGATACTGTAAGGTTGGTTCTTACTTG
AAATCTCCAAAATTCCCTATTTGGATTGTTGGCAGTGAGACTCACCTCACCGTATTTTTTGCCA
AGGATATGGCTTTAGTTGCCCCTGAAGCTCCTTCAGAACAAGCCAGAAGAGTTTTTCAAACCTA
CGACCCAGAAGATAATGGATTCATACCCGATTCACTTCTGGAAGATGTGATGAAAGCATTGGAC
CTTGTTTCAGATCCTGAATATATAAATCTCATGAAGAATAAATTAGATCCAGAAGGATTAGGAA
TCATATTATTGGGCCCATTTCTTCAAGAATTTTTTCCTGATCAGGGCTCCAGTGGTCCAGAATC
TTTTACTGTCTACCACTACAATGGATTGAAGCAGTCAAATTATAATGAAAAGGTCATGTACGTA
GAAGGGACTGCAGTTGTGATGGGTTTTGAAGATCCCATGCTACAGACAGATGACACTCCTATTA
AACGCTGTCTGCAAACCAAATGGCCATACATTGAGTTACTCTGGACCACAGATCGCTCTCCTTC
ACTAAATTAATTTGTCTAAGTATTTATAAGGAAGATCTTAATAACAGATGTTGAAAGAAGGAGT
CAAGACTGGCAATTGGCTGGATTAAGCTAAACACTGGTATCACTGATTAACTGTAAATAACAAT
TAAAAACACATTTTCAGTGTTTATGATATGTTTAAATTATTTGTCCTAAAGCTTTATGTTAAAG
ATTATCCTATTTTACCCCTTCGTGTGAAATTTACTAGCAAAATTAAGCTTTCATCAAAGTTCAT
CACTTTTGCATTCAGATACTTGGTCATTTACTTACCAAATTACAAACGCAATACTACAGCATTT
GTATATTAAGTATCACAGTTACTATTGATAAACTACTTTTGGGTTTTATTTCATTGAGGCACTT
TTTTTATTGTTTGAATGATTCCGGCTTGTAATATATCAGCCTCTACAATGAAATGCAGAAGAGT
TCATTTTTCTAAGATCTGTTTTTCATTAGAAATATTGACAAATAACACATTGTCAACCTGGATC
CTTTGACAATTTACTTAACTCTGGCATGTTCACAAAAAGTAGAAACTCTAAGAGACCATTACCA
TTTATTCACAGATGTATAGGGGATGTATTCTAAAAACTGACAGAAAAGAGAATCTGATAGTCAA
CACTGTTAACTTTTACTGTGTAATTGCCAAATACACTTTTCCAAATTTGTCCCAACAGCCCTGT
AAGCCAGCTTTCTTCTATATTTATAAACACGATAAATGCATGAGAAGATCTGTTATTACATTAG
TATATTACGTTATTTATTATGATCCTAGTTGATGGCCTAAATAAACACCTTTTTCTTTAA

hide sequence

RefSeq Acc Id:

XM_005252600 ⟹ XP_005252657

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	15,778,174 - 15,860,507 (-)	NCBI
GRCh37	10	15,820,173 - 15,902,519 (-)	NCBI

Sequence:

show sequence

ACTTCCGGTACGGAAAACTCGCTGCTGCCCCAACCTGGCTTGACAGGCTTGGTCTCTGCAAGTG
GCTCTCAGCCCCTTCTTCTTTCCTGCCTCACCTTCCAATTCGTTTGCCGCCGCCGTCCCGCAGC
TGCTGTTTCCGGAGTTGCCCCTTCCCCATGTTCCGGGGCAGGAGTCCGCAAAGCGAAGATCCGC
CCGCCGGTTCCTCATCATGTCCGAACTGACTAAAGAGCTGATGGAGCTGGTGTGGGGCACCAAG
AGCAGCCCCGGTCTCTCGGACACCATTTTCTGCCGCTGGACGCAAGGCATTTCTTTTGAAGAAG
CTCCTGTTTTCTTCGGAGAAGTCTTCTTGGCGGGATTGTTCAGAGGAAGAGCAGAAGGAACTCC
TTTGTCATACCTTGTGTGATATTTTAGAAAGTGCTTGTTGTGACCACTCTGGATCATACTGCTT
GGTTTCATGGTTAAGAGGAAAGACAACTGAGGAAACTGCTAGTATTTCTGGGAGTCCTGCAGAG
TCTAGTTGCCAAGTGGAACATTCTTCTGCCTTGGCTGTCGAAGAGCTTGGCTTTGAGCGATTTC
ATGCATTAATTCAAAAAAGATCGTTCAGAAGTTTACCAGAATTAAAAGATGCTGTCTTGGACCA
GTATTCAATGTGGGGAAATAAATTTGGAGTATTGCTTTTTCTGTATTCTGTATTACTGACAAAG
GGCATTGAAAACATAAAAAACGAAATTGAAGATGCAAGTGAACCCTTGATAGATCCTGTATATG
GACATGGCAGCCAAAGTTTAATTAATCTCCTGCTGACGGGACATGCTGTTTCTAATGTATGGGA
TGGTGATAGAGAGTGCTCAGGAATGAAACTTCTTGGTATACATGAACAAGCAGCAGTAGGATTT
TTAACACTAATGGAAGCTTTAAGATACTGTAAGGTTGGTTCTTACTTGAAATCTCCAAAATTCC
CTATTTGGATTGTTGGCAGTGAGACTCACCTCACCGTATTTTTTGCCAAGGATATGGCTTTAGT
TGCCCCTGAAGCTCCTTCAGAACAAGCCAGAAGAGTTTTTCAAACCTACGACCCAGAAGATAAT
GGATTCATACCCGATTCACTTCTGGAAGATGTGATGAAAGCATTGGACCTTGTTTCAGATCCTG
AATATATAAATCTCATGAAGAATAAATTAGATCCAGAAGGATTAGGAATCATATTATTGGGCCC
ATTTCTTCAAGAATTTTTTCCTGATCAGGGCTCCAGTGGTCCAGAATCTTTTACTGTCTACCAC
TACAATGGATTGAAGCAGTCAAATTATAATGAAAAGGTCATGTACGTAGAAGGGACTGCAGTTG
TGATGGGTTTTGAAGATCCCATGCTACAGACAGATGACACTCCTATTAAACGCTGTCTGCAAAC
CAAATGGCCATACATTGAGTTACTCTGGACCACAGATCGCTCTCCTTCACTAAATTAATTTGTC
TAAGTATTTATAAGGAAGATCTTAATAACAGATGTTGAAAGAAGGAGTCAAGACTGGCAATTGG
CTGGATTAAGCTAAACACTGGTATCACTGATTAACTGTAAATAACAATTAAAAACACATTTTCA
GTGTTTATGATATGTTTAAATTATTTGTCCTAAAGCTTTATGTTAAAGATTATCCTATTTTACC
CCTTCGTGTGAAATTTACTAGCAAAATTAAGCTTTCATCAAAGTTCATCACTTTTGCATTCAGA
TACTTGGTCATTTACTTACCAAATTACAAACGCAATACTACAGCATTTGTATATTAAGTATCAC
AGTTACTATTGATAAACTACTTTTGGGTTTTATTTCATTGAGGCACTTTTTTTATTGTTTGAAT
GATTCCGGCTTGTAATATATCAGCCTCTACAATGAAATGCAGAAGAGTTCATTTTTCTAAGATC
TGTTTTTCATTAGAAATATTGACAAATAACACATTGTCAACCTGGATCCTTTGACAATTTACTT
AACTCTGGCATGTTCACAAAAAGTAGAAACTCTAAGAGACCATTACCATTTATTCACAGATGTA
TAGGGGATGTATTCTAAAAACTGACAGAAAAGAGAATCTGATAGTCAACACTGTTAACTTTTAC
TGTGTAATTGCCAAATACACTTTTCCAAATTTGTCCCAACAGCCCTGTAAGCCAGCTTTCTTCT
ATATTTATAAACACGATAAATGCATGAGAAGATCTGTTATTACATTAGTATATTACGTTATTTA
TTATGATCCTAGTTGATGGCCTAAATAAACACCTTTTTCTTTAACTGTA

hide sequence

RefSeq Acc Id:

XM_006717508 ⟹ XP_006717571

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	15,778,174 - 15,860,507 (-)	NCBI

Sequence:

show sequence

AGCACTTCCGGTACGGAAAACTCGCTGCTGCCCCAACCTGGCTTGACAGGCTTGGTCTCTGCAA
GTGGCTCTCAGCCCCTTCTTCTTTCCTGCCTCACCTTCCAATTCGTTTGCCGCCGCCGTCCCGC
AGCTGCTGTTTCCGGAGTTGCCCCTTCCCCATGTTCCGGGGCAGGAGTCCGCAAAGCGAAGATC
CGCCCGCCGGTTCCTCATCATGTCCGAACTGACTAAAGAGCTGATGGAGCTGGTGTGGGGCACC
AAGAGCAGCCCCGGTCTCTCGGACACCATTTTCTGCCGCTGGACGCAAGGGTTTGTGTTTAGTG
AATCAGAGGGATCTGCATTAGAACAGTTTGAAGGTGGCCCCTGTGCTGTTATTGCACCTGTTCA
GGCATTTCTTTTGAAGAAGCTCCTGTTTTCTTCGGAGAAGTCTTCTTGGCGGGATTGTTCAGAG
GAAGAGCAGAAGGAACTCCTTTGTCATACCTTGTGTGATATTTTAGAAAGTGCTTGTTGTGACC
ACTCTGGATCATACTGCTTGGTTTCATGGTTAAGAGGAAAGACAACTGAGGAAACTGCTAGTAT
TTCTGGGAGTCCTGCAGAGTCTAGTTGCCAAGTGGAACATTCTTCTGCCTTGGCTGTCGAAGAG
CTTGGCTTTGAGCGATTTCATGCATTAATTCAAAAAAGATCGTTCAGAAGTTTACCAGAATTAA
AAGATGCTGTCTTGGACCAGTATTCAATGTGGGGAAATAAATTTGGAGTATTGCTTTTTCTGTA
TTCTGTATTACTGACAAAGGGCATTGAAAACATAAAAAACGAAATTGAAGATGCAAGTGAACCC
TTGATAGATCCTGTATATGGACATGGCAGCCAAAGTTTAATTAATCTCCTGCTGACGGGACATG
CTGTTTCTAATGTATGGGATGGTGATAGAGAGTGCTCAGGAATGAAACTTCTTGGTATACATGA
ACAAGCAGCAGTAGGATTTTTAACACTAATGGAAGCTTTAAGATACTGTAAGGATATGGCTTTA
GTTGCCCCTGAAGCTCCTTCAGAACAAGCCAGAAGAGTTTTTCAAACCTACGACCCAGAAGATA
ATGGATTCATACCCGATTCACTTCTGGAAGATGTGATGAAAGCATTGGACCTTGTTTCAGATCC
TGAATATATAAATCTCATGAAGAATAAATTAGATCCAGAAGGATTAGGAATCATATTATTGGGC
CCATTTCTTCAAGAATTTTTTCCTGATCAGGGCTCCAGTGGTCCAGAATCTTTTACTGTCTACC
ACTACAATGGATTGAAGCAGTCAAATTATAATGAAAAGGTCATGTACGTAGAAGGGACTGCAGT
TGTGATGGGTTTTGAAGATCCCATGCTACAGACAGATGACACTCCTATTAAACGCTGTCTGCAA
ACCAAATGGCCATACATTGAGTTACTCTGGACCACAGATCGCTCTCCTTCACTAAATTAATTTG
TCTAAGTATTTATAAGGAAGATCTTAATAACAGATGTTGAAAGAAGGAGTCAAGACTGGCAATT
GGCTGGATTAAGCTAAACACTGGTATCACTGATTAACTGTAAATAACAATTAAAAACACATTTT
CAGTGTTTATGATATGTTTAAATTATTTGTCCTAAAGCTTTATGTTAAAGATTATCCTATTTTA
CCCCTTCGTGTGAAATTTACTAGCAAAATTAAGCTTTCATCAAAGTTCATCACTTTTGCATTCA
GATACTTGGTCATTTACTTACCAAATTACAAACGCAATACTACAGCATTTGTATATTAAGTATC
ACAGTTACTATTGATAAACTACTTTTGGGTTTTATTTCATTGAGGCACTTTTTTTATTGTTTGA
ATGATTCCGGCTTGTAATATATCAGCCTCTACAATGAAATGCAGAAGAGTTCATTTTTCTAAGA
TCTGTTTTTCATTAGAAATATTGACAAATAACACATTGTCAACCTGGATCCTTTGACAATTTAC
TTAACTCTGGCATGTTCACAAAAAGTAGAAACTCTAAGAGACCATTACCATTTATTCACAGATG
TATAGGGGATGTATTCTAAAAACTGACAGAAAAGAGAATCTGATAGTCAACACTGTTAACTTTT
ACTGTGTAATTGCCAAATACACTTTTCCAAATTTGTCCCAACAGCCCTGTAAGCCAGCTTTCTT
CTATATTTATAAACACGATAAATGCATGAGAAGATCTGTTATTACATTAGTATATTACGTTATT
TATTATGATCCTAGTTGATGGCCTAAATAAACACCTTTTTCTTTAACTGTA

hide sequence

RefSeq Acc Id:

XM_011519690 ⟹ XP_011517992

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	15,779,849 - 15,860,507 (-)	NCBI

Sequence:

show sequence

AGCACTTCCGGTACGGAAAACTCGCTGCTGCCCCAACCTGGCTTGACAGGCTTGGTCTCTGCAA
GTGGCTCTCAGCCCCTTCTTCTTTCCTGCCTCACCTTCCAATTCGTTTGCCGCCGCCGTCCCGC
AGCTGCTGTTTCCGGAGTTGCCCCTTCCCCATGTTCCGGGGCAGGAGTCCGCAAAGCGAAGATC
CGCCCGCCGGTTCCTCATCATGTCCGAACTGACTAAAGAGCTGATGGAGCTGGTGTGGGGCACC
AAGAGCAGCCCCGGTCTCTCGGACACCATTTTCTGCCGCTGGACGCAAGGGTTTGTGTTTAGTG
AATCAGAGGGATCTGCATTAGAACAGTTTGAAGGTGGCCCCTGTGCTGTTATTGCACCTGTTCA
GGCATTTCTTTTGAAGAAGCTCCTGTTTTCTTCGGAGAAGTCTTCTTGGCGGGATTGTTCAGAG
GAAGAGCAGAAGGAACTCCTTTGTCATACCTTGTGTGATATTTTAGAAAGTGCTTGTTGTGACC
ACTCTGGATCATACTGCTTGGTTTCATGGTTAAGAGGAAAGACAACTGAGGAAACTGCTAGTAT
TTCTGGGAGTCCTGCAGAGTCTAGTTGCCAAGTGGAACATTCTTCTGCCTTGGCTGTCGAAGAG
CTTGGCTTTGAGCGATTTCATGCATTAATTCAAAAAAGATCGTTCAGAAGTTTACCAGAATTAA
AAGATGCTGTCTTGGACCAGTATTCAATGTGGGGAAATAAATTTGGAGTATTGCTTTTTCTGTA
TTCTGTATTACTGACAAAGGGCATTGAAAACATAAAAAACGAAATTGAAGATGCAAGTGAACCC
TTGATAGATCCTGTATATGGACATGGCAGCCAAAGTTTAATTAATCTCCTGCTGACGGGACATG
CTGTTTCTAATGTATGGGATGGTGATAGAGAGTGCTCAGGAATGAAACTTCTTGGTATACATGA
ACAAGCAGCAGTAGGATTTTTAACACTAATGGAAGCTTTAAGATACTGTAAGGTTGGTTCTTAC
TTGAAATCTCCAAAATTCCCTATTTGGATTGTTGGCAGTGAGACTCACCTCACCGTATTTTTTG
CCAAGGATATGGCTTTAGTTGCCCCTGAAGCTCCTTCAGAACAAGCCAGAAGAGTTTTTCAAAC
CTACGACCCAGAAGATAATGGATTCATACCCGATTCACTTCTGGAAGATGTGATGAAAGCATTG
GACCTTGTTTCAGATCCTGAATATATAAATCTCATGAAGAATAAATTAGATCCAGAAGGATTAG
GAATCATATTATTGGGCCCATTTCTTCAAGAATTTTTTCCTGATCAGGGCTCCAGTGGTCCAGA
ATCTTTTACTGTCTACCACTACAATGGATTGAAGCAGTCAAATTATAATGAAAAGATGAGGCAT
CTGAGACGGGGAGATCAAGTGACTCACCCAGGGTCACACAGCAAGTCATTGGCAGAACAGGGAT
TGGAACTGAGTTCCTGATTCCCAATCCTGTCCTTGGTCTGCTTGGCCACTCTACCTGTATGTAG
TATAAGTTTTCAAATCATGTTTGTGACAAGCTTCTGACACACCAACAAAAAGATTAGAAAACAA
ATAGGATGAACTGTTAAAATGACAGTAATATACAGCAGCTATAAAGCAAAGTATGGATGTCATT
AAGTCACAGAAATATGTTTTGAAGTTAATCAGGAGCTAAAATTATAAGCTGCATAGCAAGGTCC
TGTTAGAAAGGAAACAGACAAAAGGAGAATGCTGGCAAAGTGAGATGGAGTCTGAGCCGCCAGG
CATCCGAGCCTGATTGAGGCCATGGAGGTGGGTCATGGCACCTTGCCCAAGCACTTCTGCTCTA
ATGACATGAGTACATGAAGTTCTTTGTGAAAAATAGGGCCGATTGTATTTAACTTAATAACTTG
AATTATATTCTTTGTGTATAACTTTTCAGAGAAGGCAGTTTTGCTTTGGGGACTGAAAAGCCCG
AGTTGTAGTTTCAATGTCAATTTATTTCATCAACACTAGAAACTAATATATTAACTAAAATAAA
GATGCCAAAAAATGTATTTCACGTTACAATGTATCTTTAGCACTTTCTTAGGAATGAGTAGATT
CATGACACAAGATTATCTGATCTAGTAATATATTCTATTCCTATATTTAATGTGTTTTAGAGGC
AACTACCATTTAAGGATAATAAAGTTGTTTCTTTTGGCTCCTTAAATAGCTTATGGCTTTTATT
TTGGAAGAACATAATTACACTCATGTGTATCAGCCAGTGAATGTGTAAAAATAATTTTATACAC
TTTGGAAGAAGACAGTCGTCTGTATCTGTTTCTTTTAAATTATACAGCATCAGAATTTCTCTTG
GTACAAAAAAGAAATTAACCACCAAGGAGTGCCTTAATGTCCACAGTGAGCCCTTGGTAATGAG
TTAGGGTTTTTGTTGATATGTCCAAAATACTTTTTAAGTATGTTTCATTGTAAATTAATCAGAA
TAAAATTTTTCTTGCTATTCACCTGCCAGTATATATTTCTGTGATCACTGCCACTGCATATACA
GTATCTGGTTAGTTTGATCTTTCAACGTCTCTTTTACTTTTCTTTCTGTCCTGACATCCTTTTT
AATTTTTTTCTCCATGATTTTTCATGCTGTACAGAATGCACTCATGAATTGCATTTCAGGAATA
TTTAATACCATAATAGCAAGTTTTGTTGACAAACATTCAAATTGGTTTCAGCTCTAGAAATTCA
ATACTTAAATTAGAAGGAGACACATGTTCCTCAGAACATAATAGCTATATTCCTTTTATAGCTC
TCCGTTTCATTAGGCAGCATGAGCATCTGAGAACCTCAGTATTAAAGCAGTAGGACCTGTATAA
ATTATATGTAAATATGATAATTAAGCATTTCTTTCCGATGGTATAGATCCGTTGAAGAATGTTT
TTTTTCTTAGAAACAATCTATGTGTTTTAGGATTCACATGATCTTGAATTTTTTAAAAATCACC
TGGCCAGCTAGCAATTAAATATCGTTTACAAATTTACTTTCACATTAATCAGTAAGCAGATATT
CCTTCTCATTTCTAGCAAAATAAAATTACATGTCAAGTTTCATCTGAAACTATGTAATACCTTA
TTTGCTAGCCTCTAAAAATTGTTTTCATTCCACATAAGAATTTGCTAAGACTGTTGCTTGACCT
TGGTGGCTTTATTTTGTT

hide sequence

RefSeq Acc Id:

XM_011519691 ⟹ XP_011517993

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	15,782,234 - 15,860,507 (-)	NCBI

Sequence:

show sequence

AGCACTTCCGGTACGGAAAACTCGCTGCTGCCCCAACCTGGCTTGACAGGCTTGGTCTCTGCAA
GTGGCTCTCAGCCCCTTCTTCTTTCCTGCCTCACCTTCCAATTCGTTTGCCGCCGCCGTCCCGC
AGCTGCTGTTTCCGGAGTTGCCCCTTCCCCATGTTCCGGGGCAGGAGTCCGCAAAGCGAAGATC
CGCCCGCCGGTTCCTCATCATGTCCGAACTGACTAAAGAGCTGATGGAGCTGGTGTGGGGCACC
AAGAGCAGCCCCGGTCTCTCGGACACCATTTTCTGCCGCTGGACGCAAGGGTTTGTGTTTAGTG
AATCAGAGGGATCTGCATTAGAACAGTTTGAAGGTGGCCCCTGTGCTGTTATTGCACCTGTTCA
GGCATTTCTTTTGAAGAAGCTCCTGTTTTCTTCGGAGAAGTCTTCTTGGCGGGATTGTTCAGAG
GAAGAGCAGAAGGAACTCCTTTGTCATACCTTGTGTGATATTTTAGAAAGTGCTTGTTGTGACC
ACTCTGGATCATACTGCTTGGTTTCATGGTTAAGAGGAAAGACAACTGAGGAAACTGCTAGTAT
TTCTGGGAGTCCTGCAGAGTCTAGTTGCCAAGTGGAACATTCTTCTGCCTTGGCTGTCGAAGAG
CTTGGCTTTGAGCGATTTCATGCATTAATTCAAAAAAGATCGTTCAGAAGTTTACCAGAATTAA
AAGATGCTGTCTTGGACCAGTATTCAATGTGGGGAAATAAATTTGGAGTATTGCTTTTTCTGTA
TTCTGTATTACTGACAAAGGGCATTGAAAACATAAAAAACGAAATTGAAGATGCAAGTGAACCC
TTGATAGATCCTGTATATGGACATGGCAGCCAAAGTTTAATTAATCTCCTGCTGACGGGACATG
CTGTTTCTAATGTATGGGATGGTGATAGAGAGTGCTCAGGAATGAAACTTCTTGGTATACATGA
ACAAGCAGCAGTAGGATTTTTAACACTAATGGAAGCTTTAAGATACTGTAAGGTTGGTTCTTAC
TTGAAATCTCCAAAATTCCCTATTTGGATTGTTGGCAGTGAGACTCACCTCACCGTATTTTTTG
CCAAGGATATGGCTTTAGTTGCCCCTGAAGCTCCTTCAGAACAAGCCAGAAGAGTTTTTCAAAC
CTACGACCCAGAAGATAATGGATTCATACCCGATTCACTTCTGGAAGATGTGATGAAAGCATTG
GACCTTGTTTCAGATCCTGAATATATAAATCTCATGAAGAATAAATTAGATCCAGAAGGATTAG
GAATCATATTATTGGGCCCATTTCTTCAAGAATTTTTTCCTGATCAGATATGAGACTGAGAAAA
CACCGTTACATGGAAACCTTCCCAGACAGAGGGAATGTGTGTTCGAATACGGTAACGCAGTGCC
TTGATGGGGAGGGCAGCAGAAGATGACGCAGACACCAGTCTATACACATAATGATACGGAGAGA
ACAGTTCGGAAGTTTGAGGAGTAAAAAGAGAAAGATTCTCTTTCTCCACTCCCACCCCCACTTT
TCTTCTCTCAGGAAGCTGTTAAATACTGTGAGAAGAGGTCAAGGTGGCTGTGGGTAGTAGAAGC
CCCTAGCTAGTGAAGCTAAGCTCCTGGAGAATTAAAACCTAAGTGGGTCTGGGCCGTTTCCCAT
TGGGACATGTCTTCCACTGGGCTTTGATAGGAGCTCAGTTACCTGGAATAGCAGAGGCATCTGG
GCCAACCTGAATGTTTTTGAGTTGTATCTGCATCATTGGCAAGCCAGTTCTATATCCAATACCC
ATCTTTCTGTCTTTGTTCTCTAAGTGAAGCATTTTACCACTAAATCAAATTACTTAACTAGATA
ACAGATATCATGGTCATTTTATCAGATATCAGTATAGTTTGCACTGAAGTTCATTGTTGCAATA
GACATTCCAATTTCTATTTTACCGCTATTATTAGAGAGACATATTGACAAATAGAAAAAATTTA
AAAGCAAGAGGGAAAATTTCAAAATATAATTACTAAAATTCAGAATGTAATTGTTAAAAAAGAT
TGTTAAACTCAAGATAAAATTGTTAAGAAAGAGGTAAGATTCAAAAAGTAACTGAGGATATCAC
AATGTAGACAATGTAGACTACTGGACTTCTTAAAACTTTGGTCTTAAAGCCTTCATGAAAAATT
AGATTTTATTGTCCGACATTAGACCCTTCAGTGTGATATCCTCTTTGTTCACATTCTGACTGGA
TATCTGGATTAATAATACATTATACCATCTTAAACTTTGAGACAGTATTAATTTTAATTATATT
TCAAGGCTGCTATCGGAACTTTTGATAGAAATGTTGATTCTTAGTTATAATAAAAAGAATATTC
CTGTTTTTAATTTAATTTGGGGAAGATTTTGAAAAGTGAGAAATGTAAAGTGAGACAGTTACTT
GTAGTAATTTTTTAGGTAAAAAGAGGGTTCTAGTCCCTTCTCTTTCGCCTGTAACAGACATTTC
CATTTGGTTGTACTGTTTGTTGCCTCTGTGTTCCTCTCTCACTGTTTACTTGTTGCCTGCTATT
CTGAAGACACTCTCCACCTGGGCCTGGTTTGTCTCATTGTCTGTATAGTTCATGCTGTTTGCCT
CCCACGAGCATGTGATCCTGCTCTTGGTTACCTTTAGAGCAGTGAGTTCTCAGTATGATCTCCA
AGAGCTTGTTAGAAATGCTAATTCTCAGGTTTCTCCCTGAAGCAGAGACTTTAAGGGTGGGTGC
AGCAATGTGGTCTAACAAGCCCTGCAAGTGATCTGGAGGCCCAAGTTAGAGAACAGCTGCTTTA
GAGGAAGACCTGTCACAGTCCCACCTATTCCCATCTGTTCCCATCCTATAGCAGCTCAGACGCC
CTCGGTGTCATAGATCTTTTCCGATCATGCCCTACATACCACTGATGTCCCCTTTCCCCTGTAG
CCACAAAATGCATAGTGACTCAACACTCCTTTTGGCAATTAGTCACATACTGCCTTGTCCCTAA
CAGATGAATATAGTGATCATTCCGTAAACTATTTATTTATTTAAGATGGAGTTTCGCTCCTTTA
CCCAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACTGTAACCTCCGCCTCCCTGGTCCAAGCA
ATTCTCCTGCCTCAGCCTCCTGTGTAGCTGGGACTACATATGGTGGCCTGGCTAATTTTTGTAT
CCTTAGTAGAGATGGGGTTTCACCTTGTTGGTCAGGCTGGTCTCAAACTCCTAACCTCAGGTGT
TCCACCCGTCCTGGCCTTCCAAAGTGCTGGGATTACAGGTATGAGCCACCTCACGAGGCCCAGT
AAACATTTATTTAATCAGCCACAAATAAATGAAGTTGCAAAACTGGAGTGACAAGGACAGCCAG
GAAAATATTTAACTTCGGTAATCTTTACAATGCTTCAAGTAGGTCCTGTGGAAGAACACTTATT
TGCTATGATGTAGAGGCTGATGCAGGAAGAAAAAAGTGGTAATATTTATAAGCTTTTCAAGACC
ATTCGTTTAAATAAGAATAGCAGAAGCAGCTCCCCTTTCCCAAGCACATACTCTCCATCAGGCA
CTGTGTGCCTTCCAAACACCATACTATTATCTTCCCCATTTTGACAATGAGGAAATTGAGGATT
AGAGAACTTAAGACGATTGTTGAAGGTCATACACTAGGTATCTTAGTAGCTGATTCAGGAATTT
TTTGACAATGAGGAAATTGAAGATTAGAGAACTTAAGACAATTGTTTAAGGTCATACACTAGGT
ATTTTAGTAGCTGATTCAGAAATCCAATATAGTCTGTCTAACCACAGAGTCTATGCACTTTACC
AGTGGGCTACACTACTTTTTGTTGGTATTTCTGTATTTTATGCCAGTTAATTACTGGAAATAGG
GAATATAAATTATATTCAGTTACAGGAAAATGGTTATTTAAGTTCAAATAATTTAACTCTGATA
GCCAAGAGTCAAATTATGTAACTAATTGCAATGACTCCTGTAATTAAGGAAACGATCAAATTGA
TTTTTCTATTTTCTGTAAGGCATTTTGAGTGGGATACAAAACAATTTTAGGCTTTAGTTGGGAA
TGTAAGACATGAAAAATTAAACAGTCTTTCAAAATAATAGAAGAGATGATACAAAGTAGTACTA
TATGATTCCTTCTCAAATTATTTAGACAATTGTTATGATAAAGGTTAAGTTCCAGTGTAGTAAA
AAACTAACTAGTGTGTCCAGGAAAAACTTTACAGAAAAAGTAAGATTTAAACCAGGTCTGGAAA
AAGGAAGGAGAGGAGGGCATTTTAGAGAAGAGTAAAAAAAAATCATGAATGTGCAAAAGGCCAA
CAAAAGATCTTTTCATGATGAAATGAGTCATGCTTGTCCAAAACAGAATTCAGAAAGGTGAGTA
GTTGGAGATAAGACTAAAAAGGTAGATTAAGCCCTGTATGATTTTAAGACTCATGATTGCAGGT
CACAGAACCTCAGCCTAAATTGGCATAAGTGAGGGGGAAAATACATGAAGGGGAAGGAGTAGCT
CAGGTGAATTGAAGAAGCAAGCACCGGGAAAGTGCTCCTGGAGTCCTTGAACAGCACTGGGAGG
TCTCCACCTCCCATCCCCTGTCTCTAAAGTGGCTACATTCTCACAGCCTATCTTTCTGTAGGAG
CTGAAGCTCCAGTTGCCAGCAGCTGTCTTCCCTTAATTCCAGTTGGAAAAAATTCTAAGGAGGG
CCATGTGCCTGTTTGTATCCATCGGATATGGCCAGGAAGACAAGGGGGATCTATCCAGGCAGAC
TCAGCCAGGGGCCCTGAGGGAAATCACTGGGAGCCAGGCCTGTAATGGCCTTGAACGCCAGGTT
AAGAGGGTTGAACGTGATCTTTAGCTAATTGAAAAGCAAGGTTAAGATAGTGGGAATAACATGA
CCCATTTTTCTACAAGCTTACTCTGTTAGTGATATATAGGATATCCTTTCTTTATTGAATATTA
CTGAAATCGCCTTAAGCATTATAAGTATGTTTTCATTTCTCACAGTGCTCTTTTCACTAATTAA
TGGTTGACAATATTCAAATATTGGATATTTTTTGGAAAAGAAACCACTAATTAAACATCGTGGG
CCAAATTGGAAGTATTGGTACATACTGGAAGTGTATTTAGTCTGAGTAAAAGTGATGCTACTGC
TTTTCTCAATTCATTGAGAGGAACAAATTATTTACATAGAAAAGGAGATATACTTTAGCAAATG
TTTTAGAAGCTTGTCTTTTGAAAAAAGTTATAGTGATACATGCACATAATTAAAAAAAAAA

hide sequence

RefSeq Acc Id:

XM_011519694 ⟹ XP_011517996

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	15,778,174 - 15,860,507 (-)	NCBI

Sequence:

show sequence

AGCACTTCCGGTACGGAAAACTCGCTGCTGCCCCAACCTGGCTTGACAGGCTTGGTCTCTGCAA
GTGGCTCTCAGCCCCTTCTTCTTTCCTGCCTCACCTTCCAATTCGTTTGCCGCCGCCGTCCCGC
AGCTGCTGTTTCCGGAGTTGCCCCTTCCCCATGTTCCGGGGCAGGAGTCCGCAAAGCGAAGATC
CGCCCGCCGGTTCCTCATCATGTCCGAACTGACTAAAGAGCTGATGGAGCTGGTGTGGGGCACC
AAGAGCAGCCCCGGTCTCTCGGACACCATTTTCTGCCGCTGGACGCAAGTCTGTGATCGTGTCT
TCAGTTGACAACTGCAGTCTCATTAGTTTTCTGGAAGCAAGATACAGATGGTTTGTGTTTAGTG
AATCAGAGGGATCTGCATTAGAACAGTTTGAAGGTGGCCCCTGTGCTGTTATTGCACCTGTTCA
GGCATTTCTTTTGAAGAAGCTCCTGTTTTCTTCGGAGAAGTCTTCTTGGCGGGATTGTTCAGAG
GAAGAGCAGAAGGAACTCCTTTGTCATACCTTGTGTGATATTTTAGAAAGTGCTTGTTGTGACC
ACTCTGGATCATACTGCTTGGTTTCATGGTTAAGAGGAAAGACAACTGAGGAAACTGCTAGTAT
TTCTGGGAGTCCTGCAGAGTCTAGTTGCCAAGTGGAACATTCTTCTGCCTTGGCTGTCGAAGAG
CTTGGCTTTGAGCGATTTCATGCATTAATTCAAAAAAGATCGTTCAGAAGTTTACCAGAATTAA
AAGATGCTGTCTTGGACCAGTATTCAATGTGGGGAAATAAATTTGGAGTATTGCTTTTTCTGTA
TTCTGTATTACTGACAAAGGGCATTGAAAACATAAAAAACGAAATTGAAGATGCAAGTGAACCC
TTGATAGATCCTGTATATGGACATGGCAGCCAAAGTTTAATTAATCTCCTGCTGACGGGACATG
CTGTTTCTAATGTATGGGATGGTGATAGAGAGTGCTCAGGAATGAAACTTCTTGGTATACATGA
ACAAGCAGCAGTAGGATTTTTAACACTAATGGAAGCTTTAAGATACTGTAAGGTTGGTTCTTAC
TTGAAATCTCCAAAATTCCCTATTTGGATTGTTGGCAGTGAGACTCACCTCACCGTATTTTTTG
CCAAGGATATGGCTTTAGTTGCCCCTGAAGCTCCTTCAGAACAAGCCAGAAGAGTTTTTCAAAC
CTACGACCCAGAAGATAATGGATTCATACCCGATTCACTTCTGGAAGATGTGATGAAAGCATTG
GACCTTGTTTCAGATCCTGAATATATAAATCTCATGAAGAATAAATTAGATCCAGAAGGATTAG
GAATCATATTATTGGGCCCATTTCTTCAAGAATTTTTTCCTGATCAGGGCTCCAGTGGTCCAGA
ATCTTTTACTGTCTACCACTACAATGGATTGAAGCAGTCAAATTATAATGAAAAGGTCATGTAC
GTAGAAGGGACTGCAGTTGTGATGGGTTTTGAAGATCCCATGCTACAGACAGATGACACTCCTA
TTAAACGCTGTCTGCAAACCAAATGGCCATACATTGAGTTACTCTGGACCACAGATCGCTCTCC
TTCACTAAATTAATTTGTCTAAGTATTTATAAGGAAGATCTTAATAACAGATGTTGAAAGAAGG
AGTCAAGACTGGCAATTGGCTGGATTAAGCTAAACACTGGTATCACTGATTAACTGTAAATAAC
AATTAAAAACACATTTTCAGTGTTTATGATATGTTTAAATTATTTGTCCTAAAGCTTTATGTTA
AAGATTATCCTATTTTACCCCTTCGTGTGAAATTTACTAGCAAAATTAAGCTTTCATCAAAGTT
CATCACTTTTGCATTCAGATACTTGGTCATTTACTTACCAAATTACAAACGCAATACTACAGCA
TTTGTATATTAAGTATCACAGTTACTATTGATAAACTACTTTTGGGTTTTATTTCATTGAGGCA
CTTTTTTTATTGTTTGAATGATTCCGGCTTGTAATATATCAGCCTCTACAATGAAATGCAGAAG
AGTTCATTTTTCTAAGATCTGTTTTTCATTAGAAATATTGACAAATAACACATTGTCAACCTGG
ATCCTTTGACAATTTACTTAACTCTGGCATGTTCACAAAAAGTAGAAACTCTAAGAGACCATTA
CCATTTATTCACAGATGTATAGGGGATGTATTCTAAAAACTGACAGAAAAGAGAATCTGATAGT
CAACACTGTTAACTTTTACTGTGTAATTGCCAAATACACTTTTCCAAATTTGTCCCAACAGCCC
TGTAAGCCAGCTTTCTTCTATATTTATAAACACGATAAATGCATGAGAAGATCTGTTATTACAT
TAGTATATTACGTTATTTATTATGATCCTAGTTGATGGCCTAAATAAACACCTTTTTCTTTAAC
TGTA

hide sequence

RefSeq Acc Id:

XM_017016671 ⟹ XP_016872160

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	15,779,849 - 15,860,507 (-)	NCBI

Sequence:

show sequence

AGCACTTCCGGTACGGAAAACTCGCTGCTGCCCCAACCTGGCTTGACAGGCTTGGTCTCTGCAA
GTGGCTCTCAGCCCCTTCTTCTTTCCTGCCTCACCTTCCAATTCGTTTGCCGCCGCCGTCCCGC
AGCTGCTGTTTCCGGAGTTGCCCCTTCCCCATGTTCCGGGGCAGGAGTCCGCAAAGCGAAGATC
CGCCCGCCGGTTCCTCATCATGTCCGAACTGACTAAAGAGCTGATGGAGCTGGTGTGGGGCACC
AAGAGCAGCCCCGGTCTCTCGGACACCATTTTCTGCCGCTGGACGCAAGGGTTTGTGTTTAGTG
AATCAGAGGGATCTGCATTAGAACAGTTTGAAGGTGGCCCCTGTGCTGTTATTGCACCTGTTCA
GGCATTTCTTTTGAAGAAGCTCCTGTTTTCTTCGGAGAAGTCTTCTTGGCGGGATTGTTCAGAG
GAAGAGCAGAAGGAACTCCTTTGTCATACCTTGTGTGATATTTTAGAAAGTGCTTGTTGTGACC
ACTCTGGATCATACTGCTTGGTTTCATGGTTAAGAGGAAAGACAACTGAGGAAACTGCTAGTAT
TTCTGGGAGTCCTGCAGAGTCTAGTTGCCAAGTGGAACATTCTTCTGCCTTGGCTGTCGAAGAG
CTTGGCTTTGAGCGATTTCATGCATTAATTCAAAAAAGATCGTTCAGAAGTTTACCAGAATTAA
AAGATGCTGTCTTGGACCAGTATTCAATGTGGGGAAATAAATTTGGAGTATTGCTTTTTCTGTA
TTCTGTATTACTGACAAAGGGCATTGAAAACATAAAAAACGAAATTGAAGATGCAAGTGAACCC
TTGATAGATCCTGTATATGGACATGGCAGCCAAAGTTTAATTAATCTCCTGCTGACGGGACATG
CTGTTTCTAATGTATGGGATGGTGATAGAGAGTGCTCAGGAATGAAACTTCTTGGTATACATGA
ACAAGCAGCAGTAGGATTTTTAACACTAATGGAAGCTTTAAGATACTGTAAGGATATGGCTTTA
GTTGCCCCTGAAGCTCCTTCAGAACAAGCCAGAAGAGTTTTTCAAACCTACGACCCAGAAGATA
ATGGATTCATACCCGATTCACTTCTGGAAGATGTGATGAAAGCATTGGACCTTGTTTCAGATCC
TGAATATATAAATCTCATGAAGAATAAATTAGATCCAGAAGGATTAGGAATCATATTATTGGGC
CCATTTCTTCAAGAATTTTTTCCTGATCAGGGCTCCAGTGGTCCAGAATCTTTTACTGTCTACC
ACTACAATGGATTGAAGCAGTCAAATTATAATGAAAAGATGAGGCATCTGAGACGGGGAGATCA
AGTGACTCACCCAGGGTCACACAGCAAGTCATTGGCAGAACAGGGATTGGAACTGAGTTCCTGA
TTCCCAATCCTGTCCTTGGTCTGCTTGGCCACTCTACCTGTATGTAGTATAAGTTTTCAAATCA
TGTTTGTGACAAGCTTCTGACACACCAACAAAAAGATTAGAAAACAAATAGGATGAACTGTTAA
AATGACAGTAATATACAGCAGCTATAAAGCAAAGTATGGATGTCATTAAGTCACAGAAATATGT
TTTGAAGTTAATCAGGAGCTAAAATTATAAGCTGCATAGCAAGGTCCTGTTAGAAAGGAAACAG
ACAAAAGGAGAATGCTGGCAAAGTGAGATGGAGTCTGAGCCGCCAGGCATCCGAGCCTGATTGA
GGCCATGGAGGTGGGTCATGGCACCTTGCCCAAGCACTTCTGCTCTAATGACATGAGTACATGA
AGTTCTTTGTGAAAAATAGGGCCGATTGTATTTAACTTAATAACTTGAATTATATTCTTTGTGT
ATAACTTTTCAGAGAAGGCAGTTTTGCTTTGGGGACTGAAAAGCCCGAGTTGTAGTTTCAATGT
CAATTTATTTCATCAACACTAGAAACTAATATATTAACTAAAATAAAGATGCCAAAAAATGTAT
TTCACGTTACAATGTATCTTTAGCACTTTCTTAGGAATGAGTAGATTCATGACACAAGATTATC
TGATCTAGTAATATATTCTATTCCTATATTTAATGTGTTTTAGAGGCAACTACCATTTAAGGAT
AATAAAGTTGTTTCTTTTGGCTCCTTAAATAGCTTATGGCTTTTATTTTGGAAGAACATAATTA
CACTCATGTGTATCAGCCAGTGAATGTGTAAAAATAATTTTATACACTTTGGAAGAAGACAGTC
GTCTGTATCTGTTTCTTTTAAATTATACAGCATCAGAATTTCTCTTGGTACAAAAAAGAAATTA
ACCACCAAGGAGTGCCTTAATGTCCACAGTGAGCCCTTGGTAATGAGTTAGGGTTTTTGTTGAT
ATGTCCAAAATACTTTTTAAGTATGTTTCATTGTAAATTAATCAGAATAAAATTTTTCTTGCTA
TTCACCTGCCAGTATATATTTCTGTGATCACTGCCACTGCATATACAGTATCTGGTTAGTTTGA
TCTTTCAACGTCTCTTTTACTTTTCTTTCTGTCCTGACATCCTTTTTAATTTTTTTCTCCATGA
TTTTTCATGCTGTACAGAATGCACTCATGAATTGCATTTCAGGAATATTTAATACCATAATAGC
AAGTTTTGTTGACAAACATTCAAATTGGTTTCAGCTCTAGAAATTCAATACTTAAATTAGAAGG
AGACACATGTTCCTCAGAACATAATAGCTATATTCCTTTTATAGCTCTCCGTTTCATTAGGCAG
CATGAGCATCTGAGAACCTCAGTATTAAAGCAGTAGGACCTGTATAAATTATATGTAAATATGA
TAATTAAGCATTTCTTTCCGATGGTATAGATCCGTTGAAGAATGTTTTTTTTCTTAGAAACAAT
CTATGTGTTTTAGGATTCACATGATCTTGAATTTTTTAAAAATCACCTGGCCAGCTAGCAATTA
AATATCGTTTACAAATTTACTTTCACATTAATCAGTAAGCAGATATTCCTTCTCATTTCTAGCA
AAATAAAATTACATGTCAAGTTTCATCTGAAACTATGTAATACCTTATTTGCTAGCCTCTAAAA
ATTGTTTTCATTCCACATAAGAATTTGCTAAGACTGTTGCTTGACCTTGGTGGCTTTATTTTGT
T

hide sequence

RefSeq Acc Id:

XM_047425772 ⟹ XP_047281728

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	15,782,160 - 15,860,507 (-)	NCBI

RefSeq Acc Id:

XM_047425773 ⟹ XP_047281729

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	15,778,174 - 15,838,279 (-)	NCBI

RefSeq Acc Id:

XM_047425774 ⟹ XP_047281730

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	15,778,174 - 15,838,279 (-)	NCBI

RefSeq Acc Id:

XM_047425775 ⟹ XP_047281731

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	15,796,106 - 15,860,507 (-)	NCBI

RefSeq Acc Id:

XM_047425776 ⟹ XP_047281732

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	15,796,106 - 15,860,507 (-)	NCBI

RefSeq Acc Id:

XM_054366774 ⟹ XP_054222749

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	15,797,152 - 15,878,518 (-)	NCBI

RefSeq Acc Id:

XM_054366775 ⟹ XP_054222750

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	15,796,178 - 15,878,518 (-)	NCBI

RefSeq Acc Id:

XM_054366776 ⟹ XP_054222751

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	15,797,152 - 15,878,518 (-)	NCBI

RefSeq Acc Id:

XM_054366777 ⟹ XP_054222752

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	15,800,238 - 15,878,518 (-)	NCBI

RefSeq Acc Id:

XM_054366778 ⟹ XP_054222753

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	15,800,164 - 15,878,518 (-)	NCBI

RefSeq Acc Id:

XM_054366779 ⟹ XP_054222754

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	15,796,178 - 15,856,291 (-)	NCBI

RefSeq Acc Id:

XM_054366780 ⟹ XP_054222755

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	15,796,178 - 15,878,518 (-)	NCBI

RefSeq Acc Id:

XM_054366781 ⟹ XP_054222756

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	15,796,178 - 15,878,518 (-)	NCBI

RefSeq Acc Id:

XM_054366782 ⟹ XP_054222757

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	15,796,178 - 15,856,291 (-)	NCBI

RefSeq Acc Id:

XM_054366783 ⟹ XP_054222758

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	15,814,112 - 15,878,518 (-)	NCBI

RefSeq Acc Id:

XM_054366784 ⟹ XP_054222759

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	15,814,112 - 15,878,518 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_001305259	(Get FASTA)	NCBI Sequence Viewer
	NP_079224	(Get FASTA)	NCBI Sequence Viewer
	XP_005252657	(Get FASTA)	NCBI Sequence Viewer
	XP_006717571	(Get FASTA)	NCBI Sequence Viewer
	XP_011517992	(Get FASTA)	NCBI Sequence Viewer
	XP_011517993	(Get FASTA)	NCBI Sequence Viewer
	XP_011517996	(Get FASTA)	NCBI Sequence Viewer
	XP_016872160	(Get FASTA)	NCBI Sequence Viewer
	XP_047281728	(Get FASTA)	NCBI Sequence Viewer
	XP_047281729	(Get FASTA)	NCBI Sequence Viewer
	XP_047281730	(Get FASTA)	NCBI Sequence Viewer
	XP_047281731	(Get FASTA)	NCBI Sequence Viewer
	XP_047281732	(Get FASTA)	NCBI Sequence Viewer
	XP_054222749	(Get FASTA)	NCBI Sequence Viewer
	XP_054222750	(Get FASTA)	NCBI Sequence Viewer
	XP_054222751	(Get FASTA)	NCBI Sequence Viewer
	XP_054222752	(Get FASTA)	NCBI Sequence Viewer
	XP_054222753	(Get FASTA)	NCBI Sequence Viewer
	XP_054222754	(Get FASTA)	NCBI Sequence Viewer
	XP_054222755	(Get FASTA)	NCBI Sequence Viewer
	XP_054222756	(Get FASTA)	NCBI Sequence Viewer
	XP_054222757	(Get FASTA)	NCBI Sequence Viewer
	XP_054222758	(Get FASTA)	NCBI Sequence Viewer
	XP_054222759	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAG43159	(Get FASTA)	NCBI Sequence Viewer
	AAH20605	(Get FASTA)	NCBI Sequence Viewer
	AAH61585	(Get FASTA)	NCBI Sequence Viewer
	AAH67799	(Get FASTA)	NCBI Sequence Viewer
	AAQ13660	(Get FASTA)	NCBI Sequence Viewer
	BAB14582	(Get FASTA)	NCBI Sequence Viewer
	BAB87802	(Get FASTA)	NCBI Sequence Viewer
	CAD38730	(Get FASTA)	NCBI Sequence Viewer
	CAG33596	(Get FASTA)	NCBI Sequence Viewer
	EAW86233	(Get FASTA)	NCBI Sequence Viewer
	EAW86234	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000277632
	ENSP00000277632.3
	ENSP00000367275.1
	ENSP00000388661.1
	ENSP00000389883.1
GenBank Protein	Q9H8M7	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_079224 ⟸ NM_024948
- Peptide Label:	isoform a
- UniProtKB:	Q8WUF1 (UniProtKB/Swiss-Prot), Q7Z2S1 (UniProtKB/Swiss-Prot), Q6P7P0 (UniProtKB/Swiss-Prot), Q6IA40 (UniProtKB/Swiss-Prot), Q5SZ70 (UniProtKB/Swiss-Prot), Q5SZ69 (UniProtKB/Swiss-Prot), Q5SZ68 (UniProtKB/Swiss-Prot), Q9H3I4 (UniProtKB/Swiss-Prot), Q9H8M7 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MSELTKELMELVWGTKSSPGLSDTIFCRWTQGFVFSESEGSALEQFEGGPCAVIAPVQAFLLKK LLFSSEKSSWRDCSEEEQKELLCHTLCDILESACCDHSGSYCLVSWLRGKTTEETASISGSPAE SSCQVEHSSALAVEELGFERFHALIQKRSFRSLPELKDAVLDQYSMWGNKFGVLLFLYSVLLTK GIENIKNEIEDASEPLIDPVYGHGSQSLINLLLTGHAVSNVWDGDRECSGMKLLGIHEQAAVGF LTLMEALRYCKVGSYLKSPKFPIWIVGSETHLTVFFAKDMALVAPEAPSEQARRVFQTYDPEDN GFIPDSLLEDVMKALDLVSDPEYINLMKNKLDPEGLGIILLGPFLQEFFPDQGSSGPESFTVYH YNGLKQSNYNEKVMYVEGTAVVMGFEDPMLQTDDTPIKRCLQTKWPYIELLWTTDRSPSLN hide sequence

RefSeq Acc Id:	XP_005252657 ⟸ XM_005252600
- Peptide Label:	isoform X7
- UniProtKB:	Q9H8M7 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MWGNKFGVLLFLYSVLLTKGIENIKNEIEDASEPLIDPVYGHGSQSLINLLLTGHAVSNVWDGD RECSGMKLLGIHEQAAVGFLTLMEALRYCKVGSYLKSPKFPIWIVGSETHLTVFFAKDMALVAP EAPSEQARRVFQTYDPEDNGFIPDSLLEDVMKALDLVSDPEYINLMKNKLDPEGLGIILLGPFL QEFFPDQGSSGPESFTVYHYNGLKQSNYNEKVMYVEGTAVVMGFEDPMLQTDDTPIKRCLQTKW PYIELLWTTDRSPSLN hide sequence

RefSeq Acc Id:

XP_006717571 ⟸ XM_006717508

- Peptide Label:

isoform X2

- Sequence:

show sequence

MSELTKELMELVWGTKSSPGLSDTIFCRWTQGFVFSESEGSALEQFEGGPCAVIAPVQAFLLKK
LLFSSEKSSWRDCSEEEQKELLCHTLCDILESACCDHSGSYCLVSWLRGKTTEETASISGSPAE
SSCQVEHSSALAVEELGFERFHALIQKRSFRSLPELKDAVLDQYSMWGNKFGVLLFLYSVLLTK
GIENIKNEIEDASEPLIDPVYGHGSQSLINLLLTGHAVSNVWDGDRECSGMKLLGIHEQAAVGF
LTLMEALRYCKDMALVAPEAPSEQARRVFQTYDPEDNGFIPDSLLEDVMKALDLVSDPEYINLM
KNKLDPEGLGIILLGPFLQEFFPDQGSSGPESFTVYHYNGLKQSNYNEKVMYVEGTAVVMGFED
PMLQTDDTPIKRCLQTKWPYIELLWTTDRSPSLN

hide sequence

RefSeq Acc Id:	XP_011517996 ⟸ XM_011519694
- Peptide Label:	isoform X7
- UniProtKB:	Q9H8M7 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MWGNKFGVLLFLYSVLLTKGIENIKNEIEDASEPLIDPVYGHGSQSLINLLLTGHAVSNVWDGD RECSGMKLLGIHEQAAVGFLTLMEALRYCKVGSYLKSPKFPIWIVGSETHLTVFFAKDMALVAP EAPSEQARRVFQTYDPEDNGFIPDSLLEDVMKALDLVSDPEYINLMKNKLDPEGLGIILLGPFL QEFFPDQGSSGPESFTVYHYNGLKQSNYNEKVMYVEGTAVVMGFEDPMLQTDDTPIKRCLQTKW PYIELLWTTDRSPSLN hide sequence

RefSeq Acc Id:

XP_011517992 ⟸ XM_011519690

- Peptide Label:

isoform X1

- Sequence:

show sequence

MSELTKELMELVWGTKSSPGLSDTIFCRWTQGFVFSESEGSALEQFEGGPCAVIAPVQAFLLKK
LLFSSEKSSWRDCSEEEQKELLCHTLCDILESACCDHSGSYCLVSWLRGKTTEETASISGSPAE
SSCQVEHSSALAVEELGFERFHALIQKRSFRSLPELKDAVLDQYSMWGNKFGVLLFLYSVLLTK
GIENIKNEIEDASEPLIDPVYGHGSQSLINLLLTGHAVSNVWDGDRECSGMKLLGIHEQAAVGF
LTLMEALRYCKVGSYLKSPKFPIWIVGSETHLTVFFAKDMALVAPEAPSEQARRVFQTYDPEDN
GFIPDSLLEDVMKALDLVSDPEYINLMKNKLDPEGLGIILLGPFLQEFFPDQGSSGPESFTVYH
YNGLKQSNYNEKMRHLRRGDQVTHPGSHSKSLAEQGLELSS

hide sequence

RefSeq Acc Id:

XP_011517993 ⟸ XM_011519691

- Peptide Label:

isoform X4

- Sequence:

show sequence

MSELTKELMELVWGTKSSPGLSDTIFCRWTQGFVFSESEGSALEQFEGGPCAVIAPVQAFLLKK
LLFSSEKSSWRDCSEEEQKELLCHTLCDILESACCDHSGSYCLVSWLRGKTTEETASISGSPAE
SSCQVEHSSALAVEELGFERFHALIQKRSFRSLPELKDAVLDQYSMWGNKFGVLLFLYSVLLTK
GIENIKNEIEDASEPLIDPVYGHGSQSLINLLLTGHAVSNVWDGDRECSGMKLLGIHEQAAVGF
LTLMEALRYCKVGSYLKSPKFPIWIVGSETHLTVFFAKDMALVAPEAPSEQARRVFQTYDPEDN
GFIPDSLLEDVMKALDLVSDPEYINLMKNKLDPEGLGIILLGPFLQEFFPDQI

hide sequence

RefSeq Acc Id:	NP_001305259 ⟸ NM_001318330
- Peptide Label:	isoform b precursor
- UniProtKB:	Q9H8M7 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MWGNKFGVLLFLYSVLLTKGIENIKNEIEDASEPLIDPVYGHGSQSLINLLLTGHAVSNVWDGD RECSGMKLLGIHEQAAVGFLTLMEALRYCKVGSYLKSPKFPIWIVGSETHLTVFFAKDMALVAP EAPSEQARRVFQTYDPEDNGFIPDSLLEDVMKALDLVSDPEYINLMKNKLDPEGLGIILLGPFL QEFFPDQGSSGPESFTVYHYNGLKQSNYNEKVMYVEGTAVVMGFEDPMLQTDDTPIKRCLQTKW PYIELLWTTDRSPSLN hide sequence

RefSeq Acc Id:

XP_016872160 ⟸ XM_017016671

- Peptide Label:

isoform X3

- Sequence:

show sequence

MSELTKELMELVWGTKSSPGLSDTIFCRWTQGFVFSESEGSALEQFEGGPCAVIAPVQAFLLKK
LLFSSEKSSWRDCSEEEQKELLCHTLCDILESACCDHSGSYCLVSWLRGKTTEETASISGSPAE
SSCQVEHSSALAVEELGFERFHALIQKRSFRSLPELKDAVLDQYSMWGNKFGVLLFLYSVLLTK
GIENIKNEIEDASEPLIDPVYGHGSQSLINLLLTGHAVSNVWDGDRECSGMKLLGIHEQAAVGF
LTLMEALRYCKDMALVAPEAPSEQARRVFQTYDPEDNGFIPDSLLEDVMKALDLVSDPEYINLM
KNKLDPEGLGIILLGPFLQEFFPDQGSSGPESFTVYHYNGLKQSNYNEKMRHLRRGDQVTHPGS
HSKSLAEQGLELSS

hide sequence

RefSeq Acc Id:

ENSP00000367275 ⟸ ENST00000378036

RefSeq Acc Id:

ENSP00000388661 ⟸ ENST00000418767

RefSeq Acc Id:

ENSP00000277632 ⟸ ENST00000277632

RefSeq Acc Id:

ENSP00000389883 ⟸ ENST00000436829

RefSeq Acc Id:	XP_047281730 ⟸ XM_047425774
- Peptide Label:	isoform X8

RefSeq Acc Id:	XP_047281729 ⟸ XM_047425773
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_047281728 ⟸ XM_047425772
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_047281732 ⟸ XM_047425776
- Peptide Label:	isoform X10

RefSeq Acc Id:	XP_047281731 ⟸ XM_047425775
- Peptide Label:	isoform X9

RefSeq Acc Id:	XP_054222756 ⟸ XM_054366781
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_054222750 ⟸ XM_054366775
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054222755 ⟸ XM_054366780
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_054222757 ⟸ XM_054366782
- Peptide Label:	isoform X8

RefSeq Acc Id:	XP_054222754 ⟸ XM_054366779
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054222751 ⟸ XM_054366776
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054222749 ⟸ XM_054366774
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054222753 ⟸ XM_054366778
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054222752 ⟸ XM_054366777
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054222759 ⟸ XM_054366784
- Peptide Label:	isoform X10

RefSeq Acc Id:	XP_054222758 ⟸ XM_054366783
- Peptide Label:	isoform X9

Protein Domains

Deubiquitinating enzyme MINDY-3/4 conserved

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9H8M7-F1-model_v2	AlphaFold	Q9H8M7	1-445	view protein structure

Promoters

RGD ID:

7217067

Promoter ID:

EPDNEW_H14279

Type:

initiation region

Name:

FAM188A_1

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	10	15,860,507 - 15,860,567	EPDNEW

RGD ID:

6787591

Promoter ID:

HG_KWN:8715

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

Lymphoblastoid

Transcripts:

ENST00000378033

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	10	15,896,531 - 15,897,031 (-)	MPROMDB

RGD ID:

6787510

Promoter ID:

HG_KWN:8719

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

ENST00000277632, UC001IOE.1, UC001IOF.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	10	15,942,216 - 15,942,716 (-)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:23578	AgrOrtholog
COSMIC	MINDY3	COSMIC
Ensembl Genes	ENSG00000148481	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000277632	ENTREZGENE
	ENST00000277632.8	UniProtKB/Swiss-Prot
	ENST00000378036.5	UniProtKB/TrEMBL
	ENST00000418767.5	UniProtKB/TrEMBL
	ENST00000436829.1	UniProtKB/TrEMBL
	ENST00000477891	ENTREZGENE
Gene3D-CATH	EF-hand	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000148481	GTEx
HGNC ID	HGNC:23578	ENTREZGENE
Human Proteome Map	MINDY3	Human Proteome Map
InterPro	DUF4205	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	EF-hand-dom_pair	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	MINY3/4	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:80013	UniProtKB/Swiss-Prot
NCBI Gene	80013	ENTREZGENE
OMIM	611649	OMIM
PANTHER	PTHR12473	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	UBIQUITIN CARBOXYL-TERMINAL HYDROLASE MINDY-3	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	DUF4205	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA165548562	PharmGKB
SMART	DUF4205	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF47473	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	MINY3_HUMAN	UniProtKB/Swiss-Prot
	Q5SZ68	ENTREZGENE
	Q5SZ69	ENTREZGENE
	Q5SZ70	ENTREZGENE
	Q6IA40	ENTREZGENE
	Q6P7P0	ENTREZGENE
	Q7Z2S1	ENTREZGENE
	Q8WUF1	ENTREZGENE
	Q9H3I4	ENTREZGENE
	Q9H8M7	ENTREZGENE
	X6R9S5_HUMAN	UniProtKB/TrEMBL
	X6RC30_HUMAN	UniProtKB/TrEMBL
	X6RC97_HUMAN	UniProtKB/TrEMBL
UniProt Secondary	Q5SZ68	UniProtKB/Swiss-Prot
	Q5SZ69	UniProtKB/Swiss-Prot
	Q5SZ70	UniProtKB/Swiss-Prot
	Q6IA40	UniProtKB/Swiss-Prot
	Q6P7P0	UniProtKB/Swiss-Prot
	Q7Z2S1	UniProtKB/Swiss-Prot
	Q8WUF1	UniProtKB/Swiss-Prot
	Q9H3I4	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2017-02-07	MINDY3	MINDY lysine 48 deubiquitinase 3	FAM188A	family with sequence similarity 188 member A	Symbol and/or name change	5135510	APPROVED
2015-11-24	FAM188A	family with sequence similarity 188 member A	FAM188A	family with sequence similarity 188, member A	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)

Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD

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Imported Disease Annotations - ClinVar

Imported Disease Annotations - CTD