METTL26 (methyltransferase like 26)

Gene: METTL26 (methyltransferase like 26) Homo sapiens

Analyze

Symbol:

METTL26

Name:

methyltransferase like 26

RGD ID:

1603944

HGNC Page

HGNC:14141

Description:

ASSOCIATED WITH epilepsy; Generalized-onset seizure; idiopathic generalized epilepsy; INTERACTS WITH acrylamide; aristolochic acid A; arsenite(3-)

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

C16orf13; chromosome 16 open reading frame 13; hypothetical protein LOC84326; JFP2; methyltransferase-like 26; MGC13114; UPF0585 protein C16orf13

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):	Mettl26 (methyltransferase like 26)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Mettl26 (methyltransferase like 26)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Mettl26 (methyltransferase like 26)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	METTL26 (methyltransferase like 26)	NCBI	Ortholog
Canis lupus familiaris (dog):	METTL26 (methyltransferase like 26)	HGNC	HomoloGene, NCBI
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Mettl26 (methyltransferase like 26)	NCBI	Ortholog
Sus scrofa (pig):	METTL26 (methyltransferase like 26)	HGNC	Ensembl, NCBI, OrthoDB
Chlorocebus sabaeus (green monkey):	METTL26 (methyltransferase like 26)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Mettl26 (methyltransferase like 26)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	Btbd16 (BTB domain containing 16)	HGNC	OMA
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Mettl26 (methyltransferase like 26)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Mettl26 (methyltransferase like 26)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Drosophila melanogaster (fruit fly):	CG18661	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Caenorhabditis elegans (roundworm):	Y26E6A.3	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	mettl26	Alliance	DIOPT (Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|SonicParanoid\|ZFIN)
Xenopus tropicalis (tropical clawed frog):	mettl26	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|SonicParanoid)
Xenopus laevis (African clawed frog):	mettl26.L	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	16	634,430 - 636,305 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	16	634,427 - 636,366 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	16	684,430 - 686,305 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	16	624,430 - 626,348 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	16	884,563 - 886,515 (-)	NCBI		Celera
Cytogenetic Map	16	p13.3	NCBI
HuRef	16	605,692 - 607,644 (-)	NCBI		HuRef
CHM1_1	16	684,266 - 686,184 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	16	638,463 - 640,372 (-)	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

epilepsy (IAGP)

idiopathic generalized epilepsy (IAGP)

short-rib thoracic dysplasia 9 with or without polydactyly (IAGP)

tuberous sclerosis 2 (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dimethylhydrazine (ISO)

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

4-hydroxyphenyl retinamide (ISO)

acrylamide (EXP,ISO)

aristolochic acid A (EXP)

arsenite(3-) (EXP)

atrazine (ISO)

benzo[a]pyrene (EXP)

bisphenol A (ISO)

chlorpyrifos (ISO)

cisplatin (EXP)

cocaine (ISO)

copper(II) sulfate (EXP)

cyclosporin A (EXP)

dimethyl sulfoxide (EXP)

doxorubicin (EXP)

ethanol (ISO)

fenthion (ISO)

folic acid (ISO)

gentamycin (ISO)

ivermectin (EXP)

lead(0) (EXP)

methyl methanesulfonate (EXP)

resveratrol (EXP)

sunitinib (EXP)

tetrachloroethene (ISO)

thioacetamide (ISO)

triptonide (ISO)

valproic acid (EXP)

vorinostat (EXP)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Generalized-onset seizure (IAGP)

Seizure (IAGP)

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:11157797	PMID:12477932	PMID:14702039	PMID:15342556	PMID:16341674	PMID:22939629	PMID:26561776	PMID:29961565	PMID:33961781	PMID:34315543	PMID:35914814

Genomics

Comparative Map Data

METTL26
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	16	634,430 - 636,305 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	16	634,427 - 636,366 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	16	684,430 - 686,305 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	16	624,430 - 626,348 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	16	884,563 - 886,515 (-)	NCBI		Celera
Cytogenetic Map	16	p13.3	NCBI
HuRef	16	605,692 - 607,644 (-)	NCBI		HuRef
CHM1_1	16	684,266 - 686,184 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	16	638,463 - 640,372 (-)	NCBI		T2T-CHM13v2.0

Mettl26
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	17	26,094,474 - 26,096,137 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	17	26,094,048 - 26,096,143 (+)	Ensembl		GRCm39 Ensembl
GRCm38	17	25,875,500 - 25,877,163 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	17	25,875,074 - 25,877,169 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	17	26,012,445 - 26,014,108 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	17	25,603,117 - 25,604,760 (+)	NCBI		MGSCv36	mm8
Celera	17	26,408,488 - 26,410,151 (+)	NCBI		Celera
Cytogenetic Map	17	A3.3	NCBI
cM Map	17	12.97	NCBI

Mettl26
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	10	15,393,554 - 15,448,003 (+)	NCBI		GRCr8
mRatBN7.2	10	14,894,574 - 14,908,067 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	10	14,894,581 - 14,905,851 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	10	19,633,572 - 19,644,633 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	10	19,122,450 - 19,133,511 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	10	14,622,788 - 14,633,634 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	10	15,239,753 - 15,255,054 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	10	15,241,590 - 15,252,413 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	10	15,052,696 - 15,067,997 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	10	15,139,987 - 15,150,815 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	10	15,139,977 - 15,141,474 (+)	NCBI
Celera	10	14,563,467 - 14,574,295 (+)	NCBI		Celera
Cytogenetic Map	10	q12	NCBI

Mettl26
(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_004955442	16,570,831 - 16,572,780 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955442	16,571,339 - 16,572,780 (+)	NCBI	ChiLan1.0	ChiLan1.0

METTL26
(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	18	874,683 - 877,306 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	16	4,658,600 - 4,661,224 (-)	NCBI		NHGRI_mPanPan1
PanPan1.1	16	647,354 - 649,239 (-)	NCBI	panpan1.1	PanPan1.1	panPan2

METTL26
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	6	39,932,040 - 39,933,659 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	6	39,931,968 - 39,933,670 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	6	41,195,638 - 41,197,260 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	6	40,274,192 - 40,275,814 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	6	40,274,196 - 40,275,820 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	6	39,962,716 - 39,964,338 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	6	39,922,902 - 39,924,524 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	6	40,402,083 - 40,403,705 (+)	NCBI		UU_Cfam_GSD_1.0

Mettl26
(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	112,270,949 - 112,273,215 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936501	368,775 - 371,075 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936501	368,532 - 371,075 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

METTL26
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	3	41,134,246 - 41,141,353 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	3	41,134,246 - 41,135,880 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1

METTL26
(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	5	554,049 - 556,223 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666068	30,582,420 - 30,584,234 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Mettl26
(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_004624913	1,446,569 - 1,447,985 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624913	1,446,569 - 1,448,089 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in METTL26
3 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 16p13.3-13.13(chr16:23141-11296695)x3	copy number gain	See cases [RCV000052367]	Chr16:23141..11296695 [GRCh38] Chr16:73141..11390552 [GRCh37] Chr16:13141..11298053 [NCBI36] Chr16:16p13.3-13.13	pathogenic
GRCh38/hg38 16p13.3(chr16:29941-2560460)x3	copy number gain	See cases [RCV000052368]	Chr16:29941..2560460 [GRCh38] Chr16:79941..2610461 [GRCh37] Chr16:19941..2550462 [NCBI36] Chr16:16p13.3	pathogenic
GRCh38/hg38 16p13.3(chr16:46566-1800860)x3	copy number gain	See cases [RCV000052369]	Chr16:46566..1800860 [GRCh38] Chr16:96566..1850861 [GRCh37] Chr16:36566..1790862 [NCBI36] Chr16:16p13.3	pathogenic
GRCh38/hg38 16p13.3(chr16:46766-3214623)x3	copy number gain	See cases [RCV000052370]	Chr16:46766..3214623 [GRCh38] Chr16:96766..3264623 [GRCh37] Chr16:36766..3204624 [NCBI36] Chr16:16p13.3	pathogenic
GRCh38/hg38 16p13.3(chr16:23141-1773349)x1	copy number loss	See cases [RCV000053251]	Chr16:23141..1773349 [GRCh38] Chr16:73141..1823350 [GRCh37] Chr16:13141..1763351 [NCBI36] Chr16:16p13.3	pathogenic
GRCh38/hg38 16p13.3(chr16:23141-1712523)x1	copy number loss	See cases [RCV000053252]	Chr16:23141..1712523 [GRCh38] Chr16:73141..1762524 [GRCh37] Chr16:13141..1702525 [NCBI36] Chr16:16p13.3	pathogenic
GRCh38/hg38 16p13.3(chr16:46766-1997582)x1	copy number loss	See cases [RCV000053253]	Chr16:46766..1997582 [GRCh38] Chr16:96766..2047583 [GRCh37] Chr16:36766..1987584 [NCBI36] Chr16:16p13.3	pathogenic
GRCh38/hg38 16p13.3(chr16:105429-1499893)x1	copy number loss	See cases [RCV000053267]	Chr16:105429..1499893 [GRCh38] Chr16:155427..1549894 [GRCh37] Chr16:95427..1489895 [NCBI36] Chr16:16p13.3	pathogenic
GRCh38/hg38 16p13.3-13.13(chr16:46766-11525516)x3	copy number gain	See cases [RCV000133780]	Chr16:46766..11525516 [GRCh38] Chr16:96766..11619372 [GRCh37] Chr16:36766..11526873 [NCBI36] Chr16:16p13.3-13.13	pathogenic
GRCh38/hg38 16p13.3(chr16:46766-1544014)x1	copy number loss	See cases [RCV000134917]	Chr16:46766..1544014 [GRCh38] Chr16:96766..1594015 [GRCh37] Chr16:36766..1534016 [NCBI36] Chr16:16p13.3	pathogenic
GRCh38/hg38 16p13.3(chr16:551385-722554)x3	copy number gain	See cases [RCV000135264]	Chr16:551385..722554 [GRCh38] Chr16:601385..772554 [GRCh37] Chr16:541386..712555 [NCBI36] Chr16:16p13.3	likely benign
GRCh38/hg38 16p13.3(chr16:46766-4247185)x3	copy number gain	See cases [RCV000136687]	Chr16:46766..4247185 [GRCh38] Chr16:96766..4297186 [GRCh37] Chr16:36766..4237187 [NCBI36] Chr16:16p13.3	pathogenic
GRCh38/hg38 16p13.3(chr16:46722-1867327)x1	copy number loss	See cases [RCV000137826]	Chr16:46722..1867327 [GRCh38] Chr16:96722..1917328 [GRCh37] Chr16:36722..1857329 [NCBI36] Chr16:16p13.3	pathogenic
GRCh38/hg38 16p13.3(chr16:46766-882211)x1	copy number loss	See cases [RCV000137979]	Chr16:46766..882211 [GRCh38] Chr16:96766..932211 [GRCh37] Chr16:36766..872212 [NCBI36] Chr16:16p13.3	pathogenic\|uncertain significance
GRCh38/hg38 16p13.3(chr16:412341-925326)x3	copy number gain	See cases [RCV000139354]	Chr16:412341..925326 [GRCh38] Chr16:462341..975326 [GRCh37] Chr16:402342..915327 [NCBI36] Chr16:16p13.3	uncertain significance
GRCh38/hg38 16p13.3-13.12(chr16:43732-13326806)x3	copy number gain	See cases [RCV000139166]	Chr16:43732..13326806 [GRCh38] Chr16:93732..13420663 [GRCh37] Chr16:33732..13328164 [NCBI36] Chr16:16p13.3-13.12	pathogenic
GRCh38/hg38 16p13.3(chr16:534395-722554)x3	copy number gain	See cases [RCV000140349]	Chr16:534395..722554 [GRCh38] Chr16:584395..772554 [GRCh37] Chr16:524396..712555 [NCBI36] Chr16:16p13.3	benign
GRCh38/hg38 16p13.3(chr16:59980-1221651)x1	copy number loss	See cases [RCV000141384]	Chr16:59980..1221651 [GRCh38] Chr16:109978..1271651 [GRCh37] Chr16:49978..1211652 [NCBI36] Chr16:16p13.3	pathogenic
GRCh37/hg19 16p13.3(chr16:450686-1007236)x3	copy number gain	See cases [RCV000239842]	Chr16:450686..1007236 [GRCh37] Chr16:16p13.3	uncertain significance
GRCh37/hg19 16p13.3-11.2(chr16:102839-28327676)x3	copy number gain	See cases [RCV000203445]	Chr16:102839..28327676 [GRCh37] Chr16:16p13.3-11.2	pathogenic
GRCh37/hg19 16p13.3(chr16:97494-1257060)x3	copy number gain	Breast ductal adenocarcinoma [RCV000207237]	Chr16:97494..1257060 [GRCh37] Chr16:16p13.3	uncertain significance
GRCh37/hg19 16p13.3(chr16:324072-705832)x3	copy number gain	Breast ductal adenocarcinoma [RCV000207302]	Chr16:324072..705832 [GRCh37] Chr16:16p13.3	uncertain significance
GRCh37/hg19 16p13.3(chr16:88165-1715454)x1	copy number loss	See cases [RCV000239415]	Chr16:88165..1715454 [GRCh37] Chr16:16p13.3	pathogenic
GRCh37/hg19 16p13.3(chr16:72769-1511716)x1	copy number loss	See cases [RCV000240294]	Chr16:72769..1511716 [GRCh37] Chr16:16p13.3	pathogenic
GRCh37/hg19 16p13.3(chr16:239130-841725)x3	copy number gain	See cases [RCV000240506]	Chr16:239130..841725 [GRCh37] Chr16:16p13.3	uncertain significance
GRCh37/hg19 16p13.3(chr16:85880-754083)x1	copy number loss	See cases [RCV000446474]	Chr16:85880..754083 [GRCh37] Chr16:16p13.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3	copy number gain	See cases [RCV000446684]	Chr16:69193..90274381 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-13.2(chr16:78801-9169448)	copy number gain	See cases [RCV000446555]	Chr16:78801..9169448 [GRCh37] Chr16:16p13.3-13.2	pathogenic
GRCh37/hg19 16p13.3(chr16:97133-5122974)x3	copy number gain	See cases [RCV000445663]	Chr16:97133..5122974 [GRCh37] Chr16:16p13.3	pathogenic
GRCh37/hg19 16p13.3(chr16:106859-735154)x3	copy number gain	See cases [RCV000511218]	Chr16:106859..735154 [GRCh37] Chr16:16p13.3	uncertain significance
GRCh37/hg19 16p13.3(chr16:643377-3125125)x3	copy number gain	See cases [RCV000510815]	Chr16:643377..3125125 [GRCh37] Chr16:16p13.3	uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)	copy number gain	See cases [RCV000511296]	Chr16:85881..90155062 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-13.2(chr16:85880-9883129)x3	copy number gain	See cases [RCV000510698]	Chr16:85880..9883129 [GRCh37] Chr16:16p13.3-13.2	pathogenic
GRCh37/hg19 16p13.3-12.2(chr16:85880-22442007)x3	copy number gain	See cases [RCV000511360]	Chr16:85880..22442007 [GRCh37] Chr16:16p13.3-12.2	pathogenic
GRCh37/hg19 16p13.3-12.3(chr16:85880-19806921)x3	copy number gain	See cases [RCV000512194]	Chr16:85880..19806921 [GRCh37] Chr16:16p13.3-12.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3	copy number gain	See cases [RCV000512138]	Chr16:85881..90155062 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3(chr16:85880-1875694)x1	copy number loss	not provided [RCV000683741]	Chr16:85880..1875694 [GRCh37] Chr16:16p13.3	pathogenic
GRCh37/hg19 16p13.3(chr16:85880-1498731)x1	copy number loss	not provided [RCV000683740]	Chr16:85880..1498731 [GRCh37] Chr16:16p13.3	pathogenic
GRCh37/hg19 16p13.3(chr16:85880-3216551)x3	copy number gain	not provided [RCV000683742]	Chr16:85880..3216551 [GRCh37] Chr16:16p13.3	pathogenic
GRCh37/hg19 16p13.3-13.13(chr16:85880-11209288)x3	copy number gain	not provided [RCV000683743]	Chr16:85880..11209288 [GRCh37] Chr16:16p13.3-13.13	pathogenic
NC_000016.10:g.(?_582883)_(648190_?)del	deletion	Epilepsy [RCV000708134]	Chr16:582883..648190 [GRCh38] Chr16:632883..698190 [GRCh37] Chr16:16p13.3	uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90274695)x3	copy number gain	not provided [RCV000738918]	Chr16:88165..90274695 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:61451-90294632)x3	copy number gain	not provided [RCV000738915]	Chr16:61451..90294632 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90163275)x3	copy number gain	not provided [RCV000738917]	Chr16:88165..90163275 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3(chr16:591586-784800)x3	copy number gain	not provided [RCV000738948]	Chr16:591586..784800 [GRCh37] Chr16:16p13.3	benign
GRCh37/hg19 16p13.3(chr16:593277-685708)x3	copy number gain	not provided [RCV000738951]	Chr16:593277..685708 [GRCh37] Chr16:16p13.3	benign
GRCh37/hg19 16p13.3(chr16:610419-776308)x1	copy number loss	not provided [RCV000738955]	Chr16:610419..776308 [GRCh37] Chr16:16p13.3	benign
GRCh37/hg19 16p13.3(chr16:624108-780942)x3	copy number gain	not provided [RCV000738956]	Chr16:624108..780942 [GRCh37] Chr16:16p13.3	benign
GRCh37/hg19 16p13.3(chr16:624108-784800)x3	copy number gain	not provided [RCV000738957]	Chr16:624108..784800 [GRCh37] Chr16:16p13.3	benign
GRCh37/hg19 16p13.3(chr16:682670-685708)x4	copy number gain	not provided [RCV000738958]	Chr16:682670..685708 [GRCh37] Chr16:16p13.3	benign
GRCh37/hg19 16p13.3(chr16:682670-784800)x3	copy number gain	not provided [RCV000738959]	Chr16:682670..784800 [GRCh37] Chr16:16p13.3	benign
GRCh37/hg19 16p13.3(chr16:683959-781623)x3	copy number gain	not provided [RCV000738960]	Chr16:683959..781623 [GRCh37] Chr16:16p13.3	benign
GRCh37/hg19 16p13.3(chr16:683959-784800)x3	copy number gain	not provided [RCV000738961]	Chr16:683959..784800 [GRCh37] Chr16:16p13.3	benign
GRCh37/hg19 16p13.3(chr16:569754-781623)x3	copy number gain	not provided [RCV000751474]	Chr16:569754..781623 [GRCh37] Chr16:16p13.3	benign
GRCh37/hg19 16p13.3(chr16:569754-847743)x3	copy number gain	not provided [RCV000751475]	Chr16:569754..847743 [GRCh37] Chr16:16p13.3	benign
GRCh37/hg19 16p13.3(chr16:570466-781623)x3	copy number gain	not provided [RCV000751476]	Chr16:570466..781623 [GRCh37] Chr16:16p13.3	benign
GRCh37/hg19 16p13.3(chr16:575312-700644)x3	copy number gain	not provided [RCV000751478]	Chr16:575312..700644 [GRCh37] Chr16:16p13.3	benign
GRCh37/hg19 16p13.3(chr16:580124-875402)x1	copy number loss	not provided [RCV000751479]	Chr16:580124..875402 [GRCh37] Chr16:16p13.3	benign
GRCh37/hg19 16p13.3(chr16:61451-1593645)x1	copy number loss	not provided [RCV000751445]	Chr16:61451..1593645 [GRCh37] Chr16:16p13.3	pathogenic
GRCh37/hg19 16p13.3(chr16:450309-951598)x3	copy number gain	not provided [RCV000751466]	Chr16:450309..951598 [GRCh37] Chr16:16p13.3	benign
GRCh37/hg19 16p13.3(chr16:569754-700644)x4	copy number gain	not provided [RCV000751472]	Chr16:569754..700644 [GRCh37] Chr16:16p13.3	benign
GRCh37/hg19 16p13.3(chr16:569754-747013)x3	copy number gain	not provided [RCV000751473]	Chr16:569754..747013 [GRCh37] Chr16:16p13.3	benign
GRCh37/hg19 16p13.3(chr16:109978-4316797)	copy number gain	Chromosome 16p13.3 duplication syndrome [RCV000767731]	Chr16:109978..4316797 [GRCh37] Chr16:16p13.3	pathogenic
NC_000016.9:g.(?_624055)_(2115656_?)del	deletion	Tuberous sclerosis 2 [RCV000811345]	Chr16:624055..2115656 [GRCh37] Chr16:16p13.3	pathogenic
GRCh37/hg19 16p13.3(chr16:85880-1166355)x1	copy number loss	not provided [RCV001006741]	Chr16:85880..1166355 [GRCh37] Chr16:16p13.3	pathogenic
GRCh37/hg19 16p13.3(chr16:85880-2053328)x1	copy number loss	not provided [RCV000849039]	Chr16:85880..2053328 [GRCh37] Chr16:16p13.3	pathogenic
GRCh37/hg19 16p13.3(chr16:85880-1468459)x1	copy number loss	not provided [RCV000848130]	Chr16:85880..1468459 [GRCh37] Chr16:16p13.3	pathogenic
GRCh37/hg19 16p13.3(chr16:85880-830613)x1	copy number loss	not provided [RCV000846660]	Chr16:85880..830613 [GRCh37] Chr16:16p13.3	pathogenic
NC_000016.9:g.(?_624055)_(2148005_?)del	deletion	Tuberous sclerosis 2 [RCV001033183]	Chr16:624055..2148005 [GRCh37] Chr16:16p13.3	pathogenic
GRCh37/hg19 16p13.3(chr16:106988-735154)x3	copy number gain	not provided [RCV001006742]	Chr16:106988..735154 [GRCh37] Chr16:16p13.3	uncertain significance
GRCh37/hg19 16p13.3(chr16:364182-1186480)x3	copy number gain	not provided [RCV001006744]	Chr16:364182..1186480 [GRCh37] Chr16:16p13.3	uncertain significance
NC_000016.9:g.(?_624055)_(2550979_?)dup	duplication	Idiopathic generalized epilepsy [RCV001033790]	Chr16:624055..2550979 [GRCh37] Chr16:16p13.3	uncertain significance
GRCh37/hg19 16p13.3(chr16:84485-5251013)x3	copy number gain	not provided [RCV001537890]	Chr16:84485..5251013 [GRCh37] Chr16:16p13.3	pathogenic
GRCh37/hg19 16p13.3(chr16:85880-5249457)x3	copy number gain	not provided [RCV001259749]	Chr16:85880..5249457 [GRCh37] Chr16:16p13.3	pathogenic
NC_000016.9:g.(?_624055)_(2153916_?)dup	duplication	Epilepsy [RCV001344085]\|Idiopathic generalized epilepsy [RCV001316565]	Chr16:624055..2153916 [GRCh37] Chr16:16p13.3	uncertain significance
NC_000016.9:g.(?_632883)_(698190_?)del	deletion	Epilepsy [RCV001314118]	Chr16:632883..698190 [GRCh37] Chr16:16p13.3	uncertain significance
GRCh37/hg19 16p13.3(chr16:85880-754083)	copy number loss	not specified [RCV002052499]	Chr16:85880..754083 [GRCh37] Chr16:16p13.3	pathogenic
GRCh37/hg19 16p13.3(chr16:85880-1468828)	copy number loss	not specified [RCV002052500]	Chr16:85880..1468828 [GRCh37] Chr16:16p13.3	pathogenic
NC_000016.9:g.(?_256302)_(5971108_?)dup	duplication	Familial Mediterranean fever [RCV001877532]\|Fanconi anemia [RCV001877533]\|not provided [RCV001877531]	Chr16:256302..5971108 [GRCh37] Chr16:16p13.3	uncertain significance
NC_000016.9:g.(?_256302)_(4852572_?)dup	duplication	Epilepsy [RCV003113403]\|Idiopathic generalized epilepsy [RCV003109446]\|Saldino-Mainzer syndrome [RCV003113404]	Chr16:256302..4852572 [GRCh37] Chr16:16p13.3	uncertain significance
NC_000016.9:g.(?_256302)_(1843653_?)del	deletion	Idiopathic generalized epilepsy [RCV003109815]	Chr16:256302..1843653 [GRCh37] Chr16:16p13.3	uncertain significance
NC_000016.9:g.(?_256302)_(1657267_?)del	deletion	Saldino-Mainzer syndrome [RCV003116765]\|not provided [RCV003116766]	Chr16:256302..1657267 [GRCh37] Chr16:16p13.3	pathogenic\|no classifications from unflagged records
NC_000016.9:g.(?_256302)_(1918176_?)del	deletion	not provided [RCV003119703]	Chr16:256302..1918176 [GRCh37] Chr16:16p13.3	uncertain significance
GRCh37/hg19 16p13.3(chr16:111043-6627459)x3	copy number gain	See cases [RCV002292215]	Chr16:111043..6627459 [GRCh37] Chr16:16p13.3	pathogenic
GRCh37/hg19 16p13.3(chr16:85881-1350186)x1	copy number loss	not provided [RCV002474576]	Chr16:85881..1350186 [GRCh37] Chr16:16p13.3	pathogenic
NM_032366.5(METTL26):c.274G>C (p.Glu92Gln)	single nucleotide variant	not specified [RCV004101575]	Chr16:635698 [GRCh38] Chr16:685698 [GRCh37] Chr16:16p13.3	uncertain significance
NM_032366.5(METTL26):c.296C>A (p.Pro99Gln)	single nucleotide variant	not specified [RCV004077229]	Chr16:635676 [GRCh38] Chr16:685676 [GRCh37] Chr16:16p13.3	uncertain significance
NM_032366.5(METTL26):c.300G>C (p.Gln100His)	single nucleotide variant	not specified [RCV004112765]	Chr16:635672 [GRCh38] Chr16:685672 [GRCh37] Chr16:16p13.3	uncertain significance
GRCh37/hg19 16p13.3(chr16:85881-1657611)x1	copy number loss	not provided [RCV003483253]	Chr16:85881..1657611 [GRCh37] Chr16:16p13.3	pathogenic
NM_032366.5(METTL26):c.55C>T (p.Arg19Trp)	single nucleotide variant	not specified [RCV004416879]	Chr16:636236 [GRCh38] Chr16:686236 [GRCh37] Chr16:16p13.3	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	4517
Count of miRNA genes:	833
Interacting mature miRNAs:	1009
Transcripts:	ENST00000301686, ENST00000338401, ENST00000397664, ENST00000397665, ENST00000397666, ENST00000448973, ENST00000456420, ENST00000564039, ENST00000565163, ENST00000565799, ENST00000568077, ENST00000568773, ENST00000568830
Prediction methods:	Microtar, Miranda, Rnahybrid
Result types:	miRGate_prediction

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

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

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

2438

2873

1724

622

1857

463

4356

2168

3733

418

1458

1613

175

1204

2788

Low

118

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001040160	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001040161	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001040162	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001040165	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001288710	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_032366	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_109976	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_109977	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_109978	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_109979	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011522713	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011522714	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047434800	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314189	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314190	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054314191	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AE006464	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AI146806	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK057077	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK293046	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK294482	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK295628	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL022341	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AW027232	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC007207	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC047118	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BG612714	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BI762987	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM827705	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BP273946	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BP276058	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BQ921757	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU539308	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX104467	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	C00865	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471112	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CK904040	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068262	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB499720	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	Z84479	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000301686 ⟹ ENSP00000445926

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	634,430 - 636,305 (-)	Ensembl

RefSeq Acc Id:

ENST00000338401 ⟹ ENSP00000444140

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	634,429 - 636,342 (-)	Ensembl

RefSeq Acc Id:

ENST00000397664 ⟹ ENSP00000440475

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	634,438 - 636,351 (-)	Ensembl

RefSeq Acc Id:

ENST00000397665 ⟹ ENSP00000444460

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	634,526 - 636,290 (-)	Ensembl

RefSeq Acc Id:

ENST00000397666 ⟹ ENSP00000440765

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	634,430 - 636,302 (-)	Ensembl

RefSeq Acc Id:

ENST00000448973

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	634,436 - 636,310 (-)	Ensembl

RefSeq Acc Id:

ENST00000456420 ⟹ ENSP00000454359

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	634,513 - 636,239 (-)	Ensembl

RefSeq Acc Id:

ENST00000564039 ⟹ ENSP00000456393

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	634,626 - 636,278 (-)	Ensembl

RefSeq Acc Id:

ENST00000565163 ⟹ ENSP00000455614

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	634,737 - 636,260 (-)	Ensembl

RefSeq Acc Id:

ENST00000565799

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	635,281 - 636,267 (-)	Ensembl

RefSeq Acc Id:

ENST00000568077 ⟹ ENSP00000456569

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	634,502 - 636,331 (-)	Ensembl

RefSeq Acc Id:

ENST00000568773 ⟹ ENSP00000454993

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	634,664 - 636,235 (-)	Ensembl

RefSeq Acc Id:

ENST00000568830 ⟹ ENSP00000454764

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	634,949 - 636,358 (-)	Ensembl

RefSeq Acc Id:

ENST00000614890 ⟹ ENSP00000482089

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	634,427 - 636,366 (-)	Ensembl

RefSeq Acc Id:

NM_001040160 ⟹ NP_001035250

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	634,430 - 636,305 (-)	NCBI
GRCh37	16	684,429 - 686,371 (-)	NCBI
Build 36	16	624,430 - 626,348 (-)	NCBI Archive
Celera	16	884,563 - 886,515 (-)	RGD
HuRef	16	605,690 - 607,663 (-)	NCBI
CHM1_1	16	684,264 - 686,203 (-)	NCBI
T2T-CHM13v2.0	16	638,463 - 640,372 (-)	NCBI

Sequence:

show sequence

GTTGTTGCTGCCGCGATGCTGGTGGCGGCGGCCGCGGAGCGGAACAAGGATCCCATCTTGCACG
TGCTGCGGCAGTACCTGGATCCGGCCCAGCGTGGCGTCCGCGTCCTCGAGGTGGCCTCGGGCTC
CGGCCAGCACGCAGCGCACTTCGCGCGGGCCTTCCCCCTGGCCGAGTGGCAGCCGTCGGACGTG
GACCAGCGCTGCCTGGACAGCATCGCGGCCACCACGCAAGCCCAGGGCCTGACCAACGTGAAGG
CCCCGCTACACCTGGACGTGACGTGGGGCTGGGAGCACTGGGGCGGGATCCTGCCACAGTCGCT
GGACCTGTTGCTCTGCATCAACATGGCCCATGTCAGCCCCCTGCGCTGCACGGAGGGGCTCTTC
AGAGCAGCAGGACACCTGCTCAAACCCAGGGCCCTGCTCATCACCTACGGGGAACCCAGAATGG
GGGCTTCGGGACACAGCCCTCCTGGAGGACCTGGGAAAGGCCAGTGGCCTGCTCCTGGAGAGGA
TGGTGGACATGCCAGCCAACAACAAATGCCTGATCTTCCGGAAAAACTAAGCCCCTCCTTCACC
CCCGCACACCTGCATCCCTGCCGGAGGCTCTGTGAGGCACGAACCCTGCCTCCCTAGGCCGGAC
CTTGTGGACGACAGCCCCACCCAGTCTGTGCTCTCAGCCGCTGGCCGAAGGGCCCAGCCTGCTC
AGAATAAAGCATGTCCTGCTGCCGG

hide sequence

RefSeq Acc Id:

NM_001040161 ⟹ NP_001035251

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	634,430 - 636,305 (-)	NCBI
GRCh37	16	684,429 - 686,371 (-)	NCBI
Build 36	16	624,430 - 626,348 (-)	NCBI Archive
Celera	16	884,563 - 886,515 (-)	RGD
HuRef	16	605,690 - 607,663 (-)	NCBI
CHM1_1	16	684,264 - 686,203 (-)	NCBI
T2T-CHM13v2.0	16	638,463 - 640,372 (-)	NCBI

Sequence:

show sequence

GTTGTTGCTGCCGCGATGCTGGTGGCGGCGGCCGCGGAGCGGAACAAGGATCCCATCTTGCACG
TGCTGCGGCAGTACCTGGATCCGGCCCAGCGTGGCGTCCGCGTCCTCGAGGTGGCCTCGGGCTC
CGGCCAGCACGCAGCGCACTTCGCGCGGGCCTTCCCCCTGGCCGAGTGGCAGCCGTCGGACGTG
GACCAGCGCTGCCTGGACAGGAACCCAGAATGGGGGCTTCGGGACACAGCCCTCCTGGAGGACC
TGGGAAAGGCCAGTGGCCTGCTCCTGGAGAGGATGGTGGACATGCCAGCCAACAACAAATGCCT
GATCTTCCGGAAAAACTAAGCCCCTCCTTCACCCCCGCACACCTGCATCCCTGCCGGAGGCTCT
GTGAGGCACGAACCCTGCCTCCCTAGGCCGGACCTTGTGGACGACAGCCCCACCCAGTCTGTGC
TCTCAGCCGCTGGCCGAAGGGCCCAGCCTGCTCAGAATAAAGCATGTCCTGCTGCCGG

hide sequence

RefSeq Acc Id:

NM_001040162 ⟹ NP_001035252

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	634,430 - 636,305 (-)	NCBI
GRCh37	16	684,429 - 686,371 (-)	NCBI
Build 36	16	624,430 - 626,348 (-)	NCBI Archive
Celera	16	884,563 - 886,515 (-)	RGD
HuRef	16	605,690 - 607,663 (-)	NCBI
CHM1_1	16	684,264 - 686,203 (-)	NCBI
T2T-CHM13v2.0	16	638,463 - 640,372 (-)	NCBI

Sequence:

show sequence

GTTGTTGCTGCCGCGATGCTGGTGGCGGCGGCCGCGGAGCGGAACAAGGATCCCATCTTGCACG
TGCTGCGGCAGTACCTGGATCCGGCCCAGCGTGGCGTCCGCGTCCTCGAGGTGGCCTCGGGCTC
CGGCCAGCACGCAGCGCACTTCGCGCGGGCCTTCCCCCTGGCCGAGTGGCAGCCGTCGGACGTG
GACCAGCGCTGCCTGGACAGGGGCTCTTCAGAGCAGCAGGACACCTGCTCAAACCCAGGGCCCT
GCTCATCACCTACGGGGAACCCAGAATGGGGGCTTCGGGACACAGCCCTCCTGGAGGACCTGGG
AAAGGCCAGTGGCCTGCTCCTGGAGAGGATGGTGGACATGCCAGCCAACAACAAATGCCTGATC
TTCCGGAAAAACTAAGCCCCTCCTTCACCCCCGCACACCTGCATCCCTGCCGGAGGCTCTGTGA
GGCACGAACCCTGCCTCCCTAGGCCGGACCTTGTGGACGACAGCCCCACCCAGTCTGTGCTCTC
AGCCGCTGGCCGAAGGGCCCAGCCTGCTCAGAATAAAGCATGTCCTGCTGCCGG

hide sequence

RefSeq Acc Id:

NM_001040165 ⟹ NP_001035255

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	634,430 - 636,305 (-)	NCBI
GRCh37	16	684,429 - 686,371 (-)	NCBI
Build 36	16	624,430 - 626,348 (-)	NCBI Archive
Celera	16	884,563 - 886,515 (-)	RGD
HuRef	16	605,690 - 607,663 (-)	NCBI
CHM1_1	16	684,264 - 686,203 (-)	NCBI
T2T-CHM13v2.0	16	638,463 - 640,372 (-)	NCBI

Sequence:

show sequence

GTTGTTGCTGCCGCGATGCTGGTGGCGGCGGCCGCGGAGCGGAACAAGGATCCCATCTTGCACG
TGCTGCGGCAGTACCTGGATCCGGCCCAGCGTGGCGTCCGCGTCCTCGAGGTGGCCTCGGGCTC
CGGCCAGCACGCAGCGCACTTCGCGCGGGCCTTCCCCCTGGCCGAGTGGCAGCCGTCGGACGTG
GACCAGCGCTGCCTGGACAGCATCGCGGCCACCACGCAAGCCCAGGGCCTGACCAACGTGAAGG
CCCCGCTACACCTGGACGTGACGTGGGGCTGGGAGCACTGGGGCGGGATCCTGCCACAGTCGCT
GGACCTGTTGCTCTGCATCAACATGGCCCATGTCAGCCCCCTGCGCTGCACGGAGGAACCCAGA
ATGGGGGCTTCGGGACACAGCCCTCCTGGAGGACCTGGGAAAGGCCAGTGGCCTGCTCCTGGAG
AGGATGGTGGACATGCCAGCCAACAACAAATGCCTGATCTTCCGGAAAAACTAAGCCCCTCCTT
CACCCCCGCACACCTGCATCCCTGCCGGAGGCTCTGTGAGGCACGAACCCTGCCTCCCTAGGCC
GGACCTTGTGGACGACAGCCCCACCCAGTCTGTGCTCTCAGCCGCTGGCCGAAGGGCCCAGCCT
GCTCAGAATAAAGCATGTCCTGCTGCCGG

hide sequence

RefSeq Acc Id:

NM_001288710 ⟹ NP_001275639

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	634,430 - 636,305 (-)	NCBI
HuRef	16	605,690 - 607,663 (-)	NCBI
CHM1_1	16	684,264 - 686,203 (-)	NCBI
T2T-CHM13v2.0	16	638,463 - 640,372 (-)	NCBI

Sequence:

show sequence

GTTGTTGCTGCCGCGATGCTGGTGGCGGCGGCCGCGGAGCGGAACAAGGATCCCATCTTGCACG
TGCTGCGGCAGTACCTGGATCCGGCCCAGCGTGGCGTCCGCGTCCTCGAGGTGGCCTCGGGCTC
CGGCCAGCACGCAGCGCACTTCGCGCGGGCCTTCCCCCTGGCCGAGTGGCAGCCGTCGGACGTG
GACCAGCGCTGCCTGGACAGCATCGCGGCCACCACGCAAGCCCAGGGCCTGACCAACGTGAAGG
CCCCGCTACACCTGGACGTGACGTGGGGCTGGGAGCACTGGGGCGGGATCCTGCCACAGTCGCT
GGACCTGTTGCTCTGCATCAACATGGCCCATGTCAGCCCCCTGCGCTGCACGGAGCCCTATGCC
ATCAATGGGAAGATCTCCCCCCAGAGCAACGTGGACTTTGACCTGATGCTCAGATGCAGGAACC
CAGAATGGGGGCTTCGGGACACAGCCCTCCTGGAGGACCTGGGAAAGGCCAGTGGCCTGCTCCT
GGAGAGGATGGTGGACATGCCAGCCAACAACAAATGCCTGATCTTCCGGAAAAACTAAGCCCCT
CCTTCACCCCCGCACACCTGCATCCCTGCCGGAGGCTCTGTGAGGCACGAACCCTGCCTCCCTA
GGCCGGACCTTGTGGACGACAGCCCCACCCAGTCTGTGCTCTCAGCCGCTGGCCGAAGGGCCCA
GCCTGCTCAGAATAAAGCATGTCCTGCTGCCGG

hide sequence

RefSeq Acc Id:

NM_032366 ⟹ NP_115742

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	634,430 - 636,305 (-)	NCBI
GRCh37	16	684,429 - 686,371 (-)	NCBI
Build 36	16	624,430 - 626,348 (-)	NCBI Archive
Celera	16	884,563 - 886,515 (-)	RGD
HuRef	16	605,690 - 607,663 (-)	NCBI
CHM1_1	16	684,264 - 686,203 (-)	NCBI
T2T-CHM13v2.0	16	638,463 - 640,372 (-)	NCBI

Sequence:

show sequence

GTTGTTGCTGCCGCGATGCTGGTGGCGGCGGCCGCGGAGCGGAACAAGGATCCCATCTTGCACG
TGCTGCGGCAGTACCTGGATCCGGCCCAGCGTGGCGTCCGCGTCCTCGAGGTGGCCTCGGGCTC
CGGCCAGCACGCAGCGCACTTCGCGCGGGCCTTCCCCCTGGCCGAGTGGCAGCCGTCGGACGTG
GACCAGCGCTGCCTGGACAGCATCGCGGCCACCACGCAAGCCCAGGGCCTGACCAACGTGAAGG
CCCCGCTACACCTGGACGTGACGTGGGGCTGGGAGCACTGGGGCGGGATCCTGCCACAGTCGCT
GGACCTGTTGCTCTGCATCAACATGGCCCATGTCAGCCCCCTGCGCTGCACGGAGGGGCTCTTC
AGAGCAGCAGGACACCTGCTCAAACCCAGGGCCCTGCTCATCACCTACGGGCCCTATGCCATCA
ATGGGAAGATCTCCCCCCAGAGCAACGTGGACTTTGACCTGATGCTCAGATGCAGGAACCCAGA
ATGGGGGCTTCGGGACACAGCCCTCCTGGAGGACCTGGGAAAGGCCAGTGGCCTGCTCCTGGAG
AGGATGGTGGACATGCCAGCCAACAACAAATGCCTGATCTTCCGGAAAAACTAAGCCCCTCCTT
CACCCCCGCACACCTGCATCCCTGCCGGAGGCTCTGTGAGGCACGAACCCTGCCTCCCTAGGCC
GGACCTTGTGGACGACAGCCCCACCCAGTCTGTGCTCTCAGCCGCTGGCCGAAGGGCCCAGCCT
GCTCAGAATAAAGCATGTCCTGCTGCCGG

hide sequence

RefSeq Acc Id:

NR_109976

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	634,430 - 636,305 (-)	NCBI
HuRef	16	605,690 - 607,663 (-)	NCBI
CHM1_1	16	684,264 - 686,203 (-)	NCBI
T2T-CHM13v2.0	16	638,463 - 640,372 (-)	NCBI

Sequence:

show sequence

GTTGTTGCTGCCGCGATGCTGGTGGCGGCGGCCGCGGAGCGGAACAAGGATCCCATCTTGCACG
TGCTGCGGCAGTACCTGGATCCGGCCCAGCGTGGCGTCCGCGTCCTCGAGGTGGCCTCGGGCTC
CGGCCAGCACGCAGCGCACTTCGCGCGGGCCTTCCCCCTGGCCGAGTGGCAGCCGTCGGACGTG
GACCAGCGCTGCCTGGACAGGGGCTCTTCAGAGCAGCAGGACACCTGCTCAAACCCAGGGCCCT
GCTCATCACCTACGGGGGAGGGGGTGCCCTTTCATTCTCCAAACCCCAGCCTGCAAGTCTGTCC
CAGGCTCTCTGGGAAATACCCCGACCTTGGTCCAGTGGGCTGTGTCCCCATGCCCACAGCCCTA
TGCCATCAATGGGAAGATCTCCCCCCAGAGCAACGTGGACTTTGACCTGATGCTCAGATGCAGG
AACCCAGAATGGGGGCTTCGGGACACAGCCCTCCTGGAGGACCTGGGAAAGGCCAGTGGCCTGC
TCCTGGAGAGGATGGTGGACATGCCAGCCAACAACAAATGCCTGATCTTCCGGAAAAACTAAGC
CCCTCCTTCACCCCCGCACACCTGCATCCCTGCCGGAGGCTCTGTGAGGCACGAACCCTGCCTC
CCTAGGCCGGACCTTGTGGACGACAGCCCCACCCAGTCTGTGCTCTCAGCCGCTGGCCGAAGGG
CCCAGCCTGCTCAGAATAAAGCATGTCCTGCTGCCGG

hide sequence

RefSeq Acc Id:

NR_109977

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	634,430 - 636,305 (-)	NCBI
HuRef	16	605,690 - 607,663 (-)	NCBI
CHM1_1	16	684,264 - 686,203 (-)	NCBI
T2T-CHM13v2.0	16	638,463 - 640,372 (-)	NCBI

Sequence:

show sequence

GTTGTTGCTGCCGCGATGCTGGTGGCGGCGGCCGCGGAGCGGAACAAGGATCCCATCTTGCACG
TGCTGCGGCAGTACCTGGATCCGGCCCAGCGTGGCGTCCGCGTCCTCGAGGTGGCCTCGGGCTC
CGGCCAGCACGCAGCGCACTTCGCGCGGGCCTTCCCCCTGGCCGAGTGGCAGCCGTCGGACGTG
GACCAGCGCTGCCTGGACAGGGGCTCTTCAGAGCAGCAGGACACCTGCTCAAACCCAGGGCCCT
GCTCATCACCTACGGGCCCTATGCCATCAATGGGAAGATCTCCCCCCAGAGCAACGTGGACTTT
GACCTGATGCTCAGATGCAGGAACCCAGAATGGGGGCTTCGGGACACAGCCCTCCTGGAGGACC
TGGGAAAGGCCAGTGGCCTGCTCCTGGAGAGGATGGTGGACATGCCAGCCAACAACAAATGCCT
GATCTTCCGGAAAAACTAAGCCCCTCCTTCACCCCCGCACACCTGCATCCCTGCCGGAGGCTCT
GTGAGGCACGAACCCTGCCTCCCTAGGCCGGACCTTGTGGACGACAGCCCCACCCAGTCTGTGC
TCTCAGCCGCTGGCCGAAGGGCCCAGCCTGCTCAGAATAAAGCATGTCCTGCTGCCGG

hide sequence

RefSeq Acc Id:

NR_109978

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	634,430 - 636,305 (-)	NCBI
HuRef	16	605,690 - 607,663 (-)	NCBI
CHM1_1	16	684,264 - 686,203 (-)	NCBI
T2T-CHM13v2.0	16	638,463 - 640,372 (-)	NCBI

Sequence:

show sequence

GTTGTTGCTGCCGCGATGCTGGTGGCGGCGGCCGCGGAGCGGAACAAGGATCCCATCTTGCACG
TGCTGCGGCAGTACCTGGATCCGGCCCAGCGTGGCGTCCGCGTCCTCGAGGTGGCCTCGGGCTC
CGGCCAGCACGCAGCGCACTTCGCGCGGGCCTTCCCCCTGGCCGAGTGGCAGCCGTCGGACGTG
GACCAGCGCTGCCTGGACAGCATCGCGGCCACCACGCAAGCCCAGGGCCTGACCAACGTGAAGG
CCCCGCTACACCTGGACGTGACGTGGGGCTGGGAGCACTGGGGCGGGATCCTGCCACAGTCGCT
GGACCTGTTGCTCTGCATCAACATGGCCCATGTCAGCCCCCTGCGCTGCACGGAGGGGCTCTTC
AGAGCAGCAGGACACCTGCTCAAACCCAGGGCCCTGCTCATCACCTACGGGGGAGGGGGTGCCC
TTTCATTCTCCAAACCCCAGCCTGCAAGTCTGTCCCAGGCTCTCTGGGAAATACCCCGACCTTG
GTCCAGTGGGCTGTGTCCCCATGCCCACAGCCCTATGCCATCAATGGGAAGATCTCCCCCCAGA
GCAACGTGGACTTTGACCTGATGCTCAGATGCAGGAACCCAGAATGGGGGCTTCGGGACACAGC
CCTCCTGGAGGACCTGGGAAAGGCCAGTGGCCTGCTCCTGGAGAGGATGGTGGACATGCCAGCC
AACAACAAATGCCTGATCTTCCGGAAAAACTAAGCCCCTCCTTCACCCCCGCACACCTGCATCC
CTGCCGGAGGCTCTGTGAGGCACGAACCCTGCCTCCCTAGGCCGGACCTTGTGGACGACAGCCC
CACCCAGTCTGTGCTCTCAGCCGCTGGCCGAAGGGCCCAGCCTGCTCAGAATAAAGCATGTCCT
GCTGCCGG

hide sequence

RefSeq Acc Id:

NR_109979

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	634,430 - 636,305 (-)	NCBI
HuRef	16	605,690 - 607,663 (-)	NCBI
CHM1_1	16	684,264 - 686,203 (-)	NCBI
T2T-CHM13v2.0	16	638,463 - 640,372 (-)	NCBI

Sequence:

show sequence

GTTGTTGCTGCCGCGATGCTGGTGGCGGCGGCCGCGGAGCGGAACAAGGATCCCATCTTGCACG
TGCTGCGGCAGTACCTGGATCCGGCCCAGCGTGGCGTCCGCGTCCTCGAGGTGGCCTCGGGCTC
CGGCCAGCACGCAGCGCACTTCGCGCGGGCCTTCCCCCTGGCCGAGTGGCAGCCGTCGGACGTG
GACCAGCGCTGCCTGGACAGCCCTATGCCATCAATGGGAAGATCTCCCCCCAGAGCAACGTGGA
CTTTGACCTGATGCTCAGATGCAGGAACCCAGAATGGGGGCTTCGGGACACAGCCCTCCTGGAG
GACCTGGGAAAGGCCAGTGGCCTGCTCCTGGAGAGGATGGTGGACATGCCAGCCAACAACAAAT
GCCTGATCTTCCGGAAAAACTAAGCCCCTCCTTCACCCCCGCACACCTGCATCCCTGCCGGAGG
CTCTGTGAGGCACGAACCCTGCCTCCCTAGGCCGGACCTTGTGGACGACAGCCCCACCCAGTCT
GTGCTCTCAGCCGCTGGCCGAAGGGCCCAGCCTGCTCAGAATAAAGCATGTCCTGCTGCCGG

hide sequence

RefSeq Acc Id:

XM_011522713 ⟹ XP_011521015

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	634,430 - 636,305 (-)	NCBI

Sequence:

show sequence

GCCCCGCGGAAGCCCGGCCACCGCCCCCGACGCGACCCGCGCCGCGTCCGCGGCGGGGAGTTGT
TGCTGCCGCGATGCTGGTGGCGGCGGCCGCGGAGCGGAACAAGGATCCCATCTTGCACGTGCTG
CGGCAGTACCTGGATCCGGCCCAGCGTGGCGTCCGCGTCCTCGAGGTGGCCTCGGGCTCCGGCC
AGCACGCAGCGCACTTCGCGCGGGCCTTCCCCCTGGCCGAGTGGCAGCCGTCGGACGTGGACCA
GCGCTGCCTGGACAGCATCGCGGCCACCACGCAAGCCCAGGGCCTGACCAACGTGAAGGCCCCG
CTACACCTGGACGTGACGTGGGGCTGGGAGCACTGGGGCGGGATCCTGCCACAGTCGCTGGACC
TGTTGCTCTGCATCAACATGGCCCATGTCAGCCCCCTGCGCTGCACGGAGGTCTGTGGGGAGCC
CAGCATGGGTGTCTGCCGTGGCACCACTCACCCTGCATGGGGGCAGCTGGGATGCCAGATTTGC
CCCCATCACAGTCGGGGGGCTCTTCAGAGCAGCAGGACACCTGCTCAAACCCAGGGCCCTGCTC
ATCACCTACGGGGGAGGGGGTGCCCTTTCATTCTCCAAACCCCAGCCTGCAAGTCTGTCCCAGG
CTCTCTGGGAAATACCCCGACCTTGGTCCAGTGGGCTGTGTCCCCATGCCCACAGCCCTATGCC
ATCAATGGGAAGATCTCCCCCCAGAGCAACGTGGACTTTGACCTGATGCTCAGATGCAGGAACC
CAGAATGGGGGCTTCGGGACACAGCCCTCCTGGAGGACCTGGGAAAGGCCAGTGGCCTGCTCCT
GGAGAGGATGGTGGACATGCCAGCCAACAACAAATGCCTGATCTTCCGGAAAAACTAAGCCCCT
CCTTCACCCCCGCACACCTGCATCCCTGCCGGAGGCTCTGTGAGGCACGAACCCTGCCTCCCTA
GGCCGGACCTTGTGGACGACAGCCCCACCCAGTCTGTGCTCTCAGCCGCTGGCCGAAGGGCCCA
GCCTGCTCAGAATAAAGCATGTCCTGCTGCCGGC

hide sequence

RefSeq Acc Id:

XM_011522714 ⟹ XP_011521016

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	634,430 - 636,305 (-)	NCBI

Sequence:

show sequence

GCCCCGCGGAAGCCCGGCCACCGCCCCCGACGCGACCCGCGCCGCGTCCGCGGCGGGGAGTTGT
TGCTGCCGCGATGCTGGTGGCGGCGGCCGCGGAGCGGAACAAGGATCCCATCTTGCACGTGCTG
CGGCAGTACCTGGATCCGGCCCAGCGTGGCGTCCGCGTCCTCGAGGTGGCCTCGGGCTCCGGCC
AGCACGCAGCGCACTTCGCGCGGGCCTTCCCCCTGGCCGAGTGGCAGCCGTCGGACGTGGACCA
GCGCTGCCTGGACAGCATCGCGGCCACCACGCAAGCCCAGGGCCTGACCAACGTGAAGGCCCCG
CTACACCTGGACGTGACGTGGGGCTGGGAGCACTGGGGCGGGATCCTGCCACAGTCGCTGGACC
TGTTGCTCTGCATCAACATGGCCCATGTCAGCCCCCTGCGCTGCACGGAGGTCTGTGGGGAGCC
CAGCATGGGTGTCTGCCGTGGCACCACTCACCCTGCATGGGGGCAGCTGGGATGCCAGATTTGC
CCCCATCACAGTCGGGGGGCTCTTCAGAGCAGCAGGACACCTGCTCAAACCCAGGGCCCTGCTC
ATCACCTACGGGGAACCCAGAATGGGGGCTTCGGGACACAGCCCTCCTGGAGGACCTGGGAAAG
GCCAGTGGCCTGCTCCTGGAGAGGATGGTGGACATGCCAGCCAACAACAAATGCCTGATCTTCC
GGAAAAACTAAGCCCCTCCTTCACCCCCGCACACCTGCATCCCTGCCGGAGGCTCTGTGAGGCA
CGAACCCTGCCTCCCTAGGCCGGACCTTGTGGACGACAGCCCCACCCAGTCTGTGCTCTCAGCC
GCTGGCCGAAGGGCCCAGCCTGCTCAGAATAAAGCATGTCCTGCTGCCGGC

hide sequence

RefSeq Acc Id:

XM_047434800 ⟹ XP_047290756

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	634,430 - 635,774 (-)	NCBI

RefSeq Acc Id:

XM_054314189 ⟹ XP_054170164

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	638,463 - 640,372 (-)	NCBI

RefSeq Acc Id:

XM_054314190 ⟹ XP_054170165

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	638,463 - 640,372 (-)	NCBI

RefSeq Acc Id:

XM_054314191 ⟹ XP_054170166

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	16	638,463 - 639,841 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_001035250	(Get FASTA)	NCBI Sequence Viewer
	NP_001035251	(Get FASTA)	NCBI Sequence Viewer
	NP_001035252	(Get FASTA)	NCBI Sequence Viewer
	NP_001035255	(Get FASTA)	NCBI Sequence Viewer
	NP_001275639	(Get FASTA)	NCBI Sequence Viewer
	NP_115742	(Get FASTA)	NCBI Sequence Viewer
	XP_011521015	(Get FASTA)	NCBI Sequence Viewer
	XP_011521016	(Get FASTA)	NCBI Sequence Viewer
	XP_047290756	(Get FASTA)	NCBI Sequence Viewer
	XP_054170164	(Get FASTA)	NCBI Sequence Viewer
	XP_054170165	(Get FASTA)	NCBI Sequence Viewer
	XP_054170166	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH07207	(Get FASTA)	NCBI Sequence Viewer
	AAH47118	(Get FASTA)	NCBI Sequence Viewer
	AAK61238	(Get FASTA)	NCBI Sequence Viewer
	BAB71362	(Get FASTA)	NCBI Sequence Viewer
	BAF85735	(Get FASTA)	NCBI Sequence Viewer
	BAG57706	(Get FASTA)	NCBI Sequence Viewer
	BAG58505	(Get FASTA)	NCBI Sequence Viewer
	EAW85784	(Get FASTA)	NCBI Sequence Viewer
	EAW85785	(Get FASTA)	NCBI Sequence Viewer
	EAW85786	(Get FASTA)	NCBI Sequence Viewer
	EAW85787	(Get FASTA)	NCBI Sequence Viewer
	EAW85788	(Get FASTA)	NCBI Sequence Viewer
	EAW85789	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000440475
	ENSP00000440475.2
	ENSP00000440765
	ENSP00000440765.2
	ENSP00000444140
	ENSP00000444140.2
	ENSP00000444460
	ENSP00000444460.2
	ENSP00000445926
	ENSP00000445926.2
	ENSP00000454359.1
	ENSP00000454764.1
	ENSP00000454993.1
	ENSP00000455614.1
	ENSP00000456393.1
	ENSP00000456569.1
	ENSP00000482089
	ENSP00000482089.1
GenBank Protein	Q96S19	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001035251 ⟸ NM_001040161
- Peptide Label:	isoform c
- UniProtKB:	Q96S19 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MLVAAAAERNKDPILHVLRQYLDPAQRGVRVLEVASGSGQHAAHFARAFPLAEWQPSDVDQRCL DRNPEWGLRDTALLEDLGKASGLLLERMVDMPANNKCLIFRKN hide sequence

RefSeq Acc Id:	NP_001035252 ⟸ NM_001040162
- Peptide Label:	isoform d
- UniProtKB:	Q96S19 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MLVAAAAERNKDPILHVLRQYLDPAQRGVRVLEVASGSGQHAAHFARAFPLAEWQPSDVDQRCL DRGSSEQQDTCSNPGPCSSPTGNPEWGLRDTALLEDLGKASGLLLERMVDMPANNKCLIFRKN hide sequence

RefSeq Acc Id:	NP_001035255 ⟸ NM_001040165
- Peptide Label:	isoform g
- UniProtKB:	Q96S19 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MLVAAAAERNKDPILHVLRQYLDPAQRGVRVLEVASGSGQHAAHFARAFPLAEWQPSDVDQRCL DSIAATTQAQGLTNVKAPLHLDVTWGWEHWGGILPQSLDLLLCINMAHVSPLRCTEEPRMGASG HSPPGGPGKGQWPAPGEDGGHASQQQMPDLPEKLSPSFTPAHLHPCRRLCEARTLPP hide sequence

RefSeq Acc Id:	NP_001035250 ⟸ NM_001040160
- Peptide Label:	isoform b
- UniProtKB:	Q96S19 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MLVAAAAERNKDPILHVLRQYLDPAQRGVRVLEVASGSGQHAAHFARAFPLAEWQPSDVDQRCL DSIAATTQAQGLTNVKAPLHLDVTWGWEHWGGILPQSLDLLLCINMAHVSPLRCTEGLFRAAGH LLKPRALLITYGEPRMGASGHSPPGGPGKGQWPAPGEDGGHASQQQMPDLPEKLSPSFTPAHLH PCRRLCEARTLPP hide sequence

RefSeq Acc Id:	NP_115742 ⟸ NM_032366
- Peptide Label:	isoform a
- UniProtKB:	Q96IW1 (UniProtKB/Swiss-Prot), F6VM53 (UniProtKB/Swiss-Prot), F6TF62 (UniProtKB/Swiss-Prot), D6REA6 (UniProtKB/Swiss-Prot), B4DIJ3 (UniProtKB/Swiss-Prot), B4DG95 (UniProtKB/Swiss-Prot), A8MZA1 (UniProtKB/Swiss-Prot), A8MWJ8 (UniProtKB/Swiss-Prot), A8MTR1 (UniProtKB/Swiss-Prot), Q96MD6 (UniProtKB/Swiss-Prot), Q96S19 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MLVAAAAERNKDPILHVLRQYLDPAQRGVRVLEVASGSGQHAAHFARAFPLAEWQPSDVDQRCL DSIAATTQAQGLTNVKAPLHLDVTWGWEHWGGILPQSLDLLLCINMAHVSPLRCTEGLFRAAGH LLKPRALLITYGPYAINGKISPQSNVDFDLMLRCRNPEWGLRDTALLEDLGKASGLLLERMVDM PANNKCLIFRKN hide sequence

RefSeq Acc Id:	NP_001275639 ⟸ NM_001288710
- Peptide Label:	isoform h
- UniProtKB:	A0A087WYU2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLVAAAAERNKDPILHVLRQYLDPAQRGVRVLEVASGSGQHAAHFARAFPLAEWQPSDVDQRCL DSIAATTQAQGLTNVKAPLHLDVTWGWEHWGGILPQSLDLLLCINMAHVSPLRCTEPYAINGKI SPQSNVDFDLMLRCRNPEWGLRDTALLEDLGKASGLLLERMVDMPANNKCLIFRKN hide sequence

RefSeq Acc Id:	XP_011521016 ⟸ XM_011522714
- Peptide Label:	isoform X2
- UniProtKB:	H3BNB2 (UniProtKB/TrEMBL)
- Sequence:	show sequence MLVAAAAERNKDPILHVLRQYLDPAQRGVRVLEVASGSGQHAAHFARAFPLAEWQPSDVDQRCL DSIAATTQAQGLTNVKAPLHLDVTWGWEHWGGILPQSLDLLLCINMAHVSPLRCTEVCGEPSMG VCRGTTHPAWGQLGCQICPHHSRGALQSSRTPAQTQGPAHHLRGTQNGGFGTQPSWRTWERPVA CSWRGWWTCQPTTNA hide sequence

RefSeq Acc Id:

XP_011521015 ⟸ XM_011522713

- Peptide Label:

isoform X1

- Sequence:

show sequence

MLVAAAAERNKDPILHVLRQYLDPAQRGVRVLEVASGSGQHAAHFARAFPLAEWQPSDVDQRCL
DSIAATTQAQGLTNVKAPLHLDVTWGWEHWGGILPQSLDLLLCINMAHVSPLRCTEVCGEPSMG
VCRGTTHPAWGQLGCQICPHHSRGALQSSRTPAQTQGPAHHLRGRGCPFILQTPACKSVPGSLG
NTPTLVQWAVSPCPQPYAINGKISPQSNVDFDLMLRCRNPEWGLRDTALLEDLGKASGLLLERM
VDMPANNKCLIFRKN

hide sequence

RefSeq Acc Id:

ENSP00000454359 ⟸ ENST00000456420

RefSeq Acc Id:

ENSP00000444140 ⟸ ENST00000338401

RefSeq Acc Id:

ENSP00000482089 ⟸ ENST00000614890

RefSeq Acc Id:

ENSP00000456393 ⟸ ENST00000564039

RefSeq Acc Id:

ENSP00000445926 ⟸ ENST00000301686

RefSeq Acc Id:

ENSP00000455614 ⟸ ENST00000565163

RefSeq Acc Id:

ENSP00000456569 ⟸ ENST00000568077

RefSeq Acc Id:

ENSP00000440765 ⟸ ENST00000397666

RefSeq Acc Id:

ENSP00000444460 ⟸ ENST00000397665

RefSeq Acc Id:

ENSP00000440475 ⟸ ENST00000397664

RefSeq Acc Id:

ENSP00000454764 ⟸ ENST00000568830

RefSeq Acc Id:

ENSP00000454993 ⟸ ENST00000568773

RefSeq Acc Id:	XP_047290756 ⟸ XM_047434800
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054170165 ⟸ XM_054314190
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054170164 ⟸ XM_054314189
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054170166 ⟸ XM_054314191
- Peptide Label:	isoform X3

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q96S19-F1-model_v2	AlphaFold	Q96S19	1-204	view protein structure

Promoters

RGD ID:

6792861

Promoter ID:

HG_KWN:22627

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

ENST00000301686, ENST00000397664, NM_001040160, NM_001040161, NM_001040162, NM_001040165, NM_032366, OTTHUMT00000109080, OTTHUMT00000109081

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	16	626,251 - 626,982 (-)	MPROMDB

RGD ID:

7230807

Promoter ID:

EPDNEW_H21149

Type:

initiation region

Name:

C16orf13_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	16	636,302 - 636,362	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:14141	AgrOrtholog
COSMIC	METTL26	COSMIC
Ensembl Genes	ENSG00000130731	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000301686	ENTREZGENE
	ENST00000301686.13	UniProtKB/Swiss-Prot
	ENST00000338401	ENTREZGENE
	ENST00000338401.8	UniProtKB/Swiss-Prot
	ENST00000397664	ENTREZGENE
	ENST00000397664.8	UniProtKB/Swiss-Prot
	ENST00000397665	ENTREZGENE
	ENST00000397665.6	UniProtKB/Swiss-Prot
	ENST00000397666	ENTREZGENE
	ENST00000397666.6	UniProtKB/Swiss-Prot
	ENST00000456420	ENTREZGENE
	ENST00000456420.6	UniProtKB/TrEMBL
	ENST00000564039.1	UniProtKB/TrEMBL
	ENST00000565163.5	UniProtKB/TrEMBL
	ENST00000568077	ENTREZGENE
	ENST00000568077.5	UniProtKB/TrEMBL
	ENST00000568773.1	UniProtKB/TrEMBL
	ENST00000568830.1	UniProtKB/TrEMBL
	ENST00000614890	ENTREZGENE
	ENST00000614890.4	UniProtKB/TrEMBL
Gene3D-CATH	3.40.50.150	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000130731	GTEx
HGNC ID	HGNC:14141	ENTREZGENE
Human Proteome Map	METTL26	Human Proteome Map
InterPro	DUF938	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	SAM-dependent_MTases	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:84326	UniProtKB/Swiss-Prot
NCBI Gene	84326	ENTREZGENE
PANTHER	METHYLTRANSFERASE-LIKE 26	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR20974	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	DUF938	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA25526	PharmGKB
Superfamily-SCOP	SSF53335	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0A087WYU2	ENTREZGENE, UniProtKB/TrEMBL
	A8MTR1	ENTREZGENE
	A8MWJ8	ENTREZGENE
	A8MZA1	ENTREZGENE
	B4DG95	ENTREZGENE
	B4DIJ3	ENTREZGENE
	D6REA6	ENTREZGENE
	F6TF62	ENTREZGENE
	F6VM53	ENTREZGENE
	H3BMF3_HUMAN	UniProtKB/TrEMBL
	H3BNB2	ENTREZGENE, UniProtKB/TrEMBL
	H3BNT3_HUMAN	UniProtKB/TrEMBL
	H3BQ55_HUMAN	UniProtKB/TrEMBL
	H3BRT2_HUMAN	UniProtKB/TrEMBL
	H3BS73_HUMAN	UniProtKB/TrEMBL
	MTL26_HUMAN	UniProtKB/Swiss-Prot
	Q96IW1	ENTREZGENE
	Q96MD6	ENTREZGENE
	Q96S19	ENTREZGENE
UniProt Secondary	A8MTR1	UniProtKB/Swiss-Prot
	A8MWJ8	UniProtKB/Swiss-Prot
	A8MZA1	UniProtKB/Swiss-Prot
	B4DG95	UniProtKB/Swiss-Prot
	B4DIJ3	UniProtKB/Swiss-Prot
	D6REA6	UniProtKB/Swiss-Prot
	F6TF62	UniProtKB/Swiss-Prot
	F6VM53	UniProtKB/Swiss-Prot
	Q96IW1	UniProtKB/Swiss-Prot
	Q96MD6	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-06-21	METTL26	methyltransferase like 26	C16orf13	chromosome 16 open reading frame 13	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 Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar