ZC2HC1C (zinc finger C2HC-type containing 1C)

Gene: ZC2HC1C (zinc finger C2HC-type containing 1C) Homo sapiens

Analyze

Symbol:

ZC2HC1C

Name:

zinc finger C2HC-type containing 1C

RGD ID:

1316129

HGNC Page

HGNC:20354

Description:

Predicted to enable metal ion binding activity.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

C14orf140; chromosome 14 open reading frame 140; FAM164C; family with sequence similarity 164, member C; FLJ23093; hypothetical protein LOC79696; zinc finger C2HC domain-containing protein 1C; zinc finger, C2HC-type containing 1C

RGD Orthologs

Alliance Orthologs

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	14	75,069,641 - 75,079,988 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	14	75,064,109 - 75,119,502 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	14	75,536,344 - 75,546,691 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	14	74,606,052 - 74,614,552 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	14	74,606,107 - 74,614,544	NCBI
Celera	14	55,573,960 - 55,582,456 (+)	NCBI		Celera
Cytogenetic Map	14	q24.3	NCBI
HuRef	14	55,704,470 - 55,712,966 (+)	NCBI		HuRef
CHM1_1	14	75,474,072 - 75,482,572 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	14	69,279,032 - 69,289,387 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

genetic disease (IAGP)

intellectual disability (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(1->4)-beta-D-glucan (ISO)

1,2-dimethylhydrazine (ISO)

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

3,3',5,5'-tetrabromobisphenol A (ISO)

4,4'-sulfonyldiphenol (EXP)

4-hydroxyphenyl retinamide (ISO)

acetamide (ISO)

aflatoxin B1 (ISO)

benzo[a]pyrene (EXP)

bisphenol A (EXP,ISO)

cadmium atom (EXP,ISO)

cadmium dichloride (EXP,ISO)

copper(II) sulfate (EXP)

cyclosporin A (EXP)

dicrotophos (EXP)

doxorubicin (EXP)

gentamycin (ISO)

lipopolysaccharide (EXP)

methylmercury chloride (EXP)

perfluorooctane-1-sulfonic acid (ISO)

pregnenolone 16alpha-carbonitrile (ISO)

quercetin (EXP)

S-(1,2-dichlorovinyl)-L-cysteine (EXP)

sunitinib (EXP)

temozolomide (EXP)

thioacetamide (ISO)

trichloroethene (ISO)

trimellitic anhydride (ISO)

trovafloxacin (ISO)

vinclozolin (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Molecular Function

metal ion binding (IEA)

protein binding (IPI)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Intellectual disability, mild (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:8125298	PMID:12477932	PMID:14702039	PMID:15489334	PMID:16189514	PMID:21516116	PMID:22810586	PMID:24623722	PMID:25416956	PMID:25910212	PMID:27503909	PMID:29676528
PMID:31391242	PMID:31515488	PMID:32296183	PMID:33961781	PMID:36193031

Genomics

Comparative Map Data

ZC2HC1C
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	14	75,069,641 - 75,079,988 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	14	75,064,109 - 75,119,502 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	14	75,536,344 - 75,546,691 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	14	74,606,052 - 74,614,552 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	14	74,606,107 - 74,614,544	NCBI
Celera	14	55,573,960 - 55,582,456 (+)	NCBI		Celera
Cytogenetic Map	14	q24.3	NCBI
HuRef	14	55,704,470 - 55,712,966 (+)	NCBI		HuRef
CHM1_1	14	75,474,072 - 75,482,572 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	14	69,279,032 - 69,289,387 (+)	NCBI		T2T-CHM13v2.0

Zc2hc1c
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	12	85,321,020 - 85,346,132 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	12	85,321,060 - 85,346,132 (+)	Ensembl		GRCm39 Ensembl
GRCm38	12	85,274,243 - 85,299,361 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	12	85,274,286 - 85,299,358 (+)	Ensembl	GRCm38		mm10	GRCm38
GRCm38.p6 Ensembl	12	85,288,591 - 85,299,358 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	12	86,629,541 - 86,640,308 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	12	86,177,756 - 86,188,461 (+)	NCBI		MGSCv36	mm8
Celera	12	86,746,092 - 86,756,859 (+)	NCBI		Celera
Cytogenetic Map	12	D1- D2	NCBI
cM Map	12	39.63	NCBI

Zc2hc1c
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	6	110,663,682 - 110,672,606 (+)	NCBI		GRCr8
mRatBN7.2	6	104,932,631 - 104,941,555 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	6	104,932,631 - 104,941,554 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	6	105,102,235 - 105,111,159 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	6	105,401,107 - 105,410,031 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	6	104,770,769 - 104,779,689 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	6	109,110,534 - 109,119,458 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	6	109,110,534 - 109,119,457 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	6	116,437,583 - 116,446,512 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	6	109,333,912 - 109,343,371 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	6	109,337,367 - 109,346,826 (+)	NCBI
Celera	6	102,755,566 - 102,764,422 (+)	NCBI		Celera
Cytogenetic Map	6	q31	NCBI

Zc2hc1c
(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_004955523	487,564 - 494,537 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955523	487,091 - 494,537 (-)	NCBI	ChiLan1.0	ChiLan1.0

ZC2HC1C
(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	15	76,151,412 - 76,160,296 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	14	75,367,916 - 75,376,800 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	14	55,621,163 - 55,630,779 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	14	74,465,002 - 74,474,694 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	14	74,465,002 - 74,474,694 (+)	Ensembl	panpan1.1		panPan2

ZC2HC1C
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	8	48,169,562 - 48,177,900 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	8	48,170,112 - 48,215,954 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	8	47,853,666 - 47,862,011 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	8	48,397,173 - 48,405,518 (+)	NCBI		ROS_Cfam_1.0
UMICH_Zoey_3.1	8	48,067,951 - 48,076,294 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	8	48,089,222 - 48,097,563 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	8	48,487,919 - 48,496,262 (+)	NCBI		UU_Cfam_GSD_1.0

Zc2hc1c
(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_024408640	27,848,696 - 27,857,345 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936488	4,212,624 - 4,219,131 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936488	4,212,503 - 4,219,314 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

ZC2HC1C
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	7	98,265,274 - 98,273,351 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	7	98,265,252 - 98,273,357 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	7	104,109,337 - 104,117,483 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

ZC2HC1C
(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	24	52,283,909 - 52,341,700 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	24	52,284,827 - 52,292,950 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666053	40,514,580 - 40,524,768 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Zc2hc1c
(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_004624734	26,604,773 - 26,611,732 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624734	26,602,549 - 26,612,649 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in ZC2HC1C
15 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 14q24.3(chr14:73877072-78042422)x1	copy number loss	See cases [RCV000051548]	Chr14:73877072..78042422 [GRCh38] Chr14:74343775..78508765 [GRCh37] Chr14:73413528..77578518 [NCBI36] Chr14:14q24.3	pathogenic
GRCh38/hg38 14q24.2-32.2(chr14:72787506-99596719)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052293]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052293]\|See cases [RCV000052293]	Chr14:72787506..99596719 [GRCh38] Chr14:73254214..100063056 [GRCh37] Chr14:72323967..99132809 [NCBI36] Chr14:14q24.2-32.2	pathogenic
GRCh37/hg19 14q24.2-q24.3(chr14:73152115..77698582)	deletion	Intellectual disability, mild [RCV000190520]	Chr14:73152115..77698582 [GRCh37] Chr14:14q24.2-24.3	pathogenic\|likely pathogenic
GRCh38/hg38 14q24.1-31.1(chr14:69562099-81975384)x1	copy number loss	See cases [RCV000134154]	Chr14:69562099..81975384 [GRCh38] Chr14:70028816..82441728 [GRCh37] Chr14:69098569..81511481 [NCBI36] Chr14:14q24.1-31.1	pathogenic
GRCh38/hg38 14q24.3-32.33(chr14:73655772-106879298)x3	copy number gain	See cases [RCV000134000]	Chr14:73655772..106879298 [GRCh38] Chr14:74122475..107287505 [GRCh37] Chr14:73192228..106358550 [NCBI36] Chr14:14q24.3-32.33	pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3	copy number gain	See cases [RCV000135543]	Chr14:20151149..106855263 [GRCh38] Chr14:20619308..107263478 [GRCh37] Chr14:19689148..106334523 [NCBI36] Chr14:14q11.2-32.33	pathogenic
GRCh38/hg38 14q24.3(chr14:74986195-76399258)x1	copy number loss	See cases [RCV000137114]	Chr14:74986195..76399258 [GRCh38] Chr14:75452898..76865601 [GRCh37] Chr14:74522651..75935354 [NCBI36] Chr14:14q24.3	uncertain significance
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3	copy number gain	See cases [RCV000143373]	Chr14:20043514..106877229 [GRCh38] Chr14:20511673..107285437 [GRCh37] Chr14:19581513..106356482 [NCBI36] Chr14:14q11.2-32.33	pathogenic
GRCh38/hg38 14q24.3-31.1(chr14:73343213-78835059)x1	copy number loss	See cases [RCV000143265]	Chr14:73343213..78835059 [GRCh38] Chr14:73809921..79301402 [GRCh37] Chr14:72879674..78371155 [NCBI36] Chr14:14q24.3-31.1	pathogenic\|likely pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3	copy number gain	See cases [RCV000446256]	Chr14:19794561..107234280 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q23.2-32.33(chr14:62493932-107285437)x3	copy number gain	See cases [RCV000448557]	Chr14:62493932..107285437 [GRCh37] Chr14:14q23.2-32.33	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437)	copy number gain	See cases [RCV000512041]	Chr14:20511673..107285437 [GRCh37] Chr14:14q11.2-32.33	pathogenic
NM_024643.4(ZC2HC1C):c.1037C>T (p.Ser346Leu)	single nucleotide variant	Inborn genetic diseases [RCV003276949]	Chr14:75071610 [GRCh38] Chr14:75538313 [GRCh37] Chr14:14q24.3	likely benign
GRCh37/hg19 14q24.2-32.33(chr14:73750741-107285437)x3	copy number gain	See cases [RCV000512497]	Chr14:73750741..107285437 [GRCh37] Chr14:14q24.2-32.33	pathogenic
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3	copy number gain	not provided [RCV000738412]	Chr14:19000422..107289053 [GRCh37] Chr14:14q11.1-32.33	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3	copy number gain	not provided [RCV000738413]	Chr14:19280733..107287663 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3	copy number gain	not provided [RCV000738414]	Chr14:19327823..107287663 [GRCh37] Chr14:14q11.2-32.33	pathogenic
GRCh37/hg19 14q24.3(chr14:74040231-76368547)	copy number loss	not provided [RCV000767572]	Chr14:74040231..76368547 [GRCh37] Chr14:14q24.3	likely pathogenic
NM_024643.4(ZC2HC1C):c.1141G>A (p.Gly381Ser)	single nucleotide variant	Inborn genetic diseases [RCV003239907]	Chr14:75071714 [GRCh38] Chr14:75538417 [GRCh37] Chr14:14q24.3	uncertain significance
NM_024643.4(ZC2HC1C):c.268G>A (p.Gly90Arg)	single nucleotide variant	Inborn genetic diseases [RCV003275637]	Chr14:75070841 [GRCh38] Chr14:75537544 [GRCh37] Chr14:14q24.3	uncertain significance
GRCh37/hg19 14q22.2-24.3(chr14:54654001-75828024)x3	copy number gain	14q22.2q24.3 duplication [RCV001506967]	Chr14:54654001..75828024 [GRCh37] Chr14:14q22.2-24.3	likely pathogenic
GRCh37/hg19 14q13.3-32.33(chr14:37671058-106985955)x2	copy number gain	See cases [RCV002286356]	Chr14:37671058..106985955 [GRCh37] Chr14:14q13.3-32.33	pathogenic
NM_024643.4(ZC2HC1C):c.242G>A (p.Arg81Gln)	single nucleotide variant	Inborn genetic diseases [RCV002752674]	Chr14:75070815 [GRCh38] Chr14:75537518 [GRCh37] Chr14:14q24.3	likely benign
NM_024643.4(ZC2HC1C):c.1148T>C (p.Ile383Thr)	single nucleotide variant	Inborn genetic diseases [RCV002882742]	Chr14:75071721 [GRCh38] Chr14:75538424 [GRCh37] Chr14:14q24.3	likely benign
NM_024643.4(ZC2HC1C):c.1151A>T (p.Glu384Val)	single nucleotide variant	Inborn genetic diseases [RCV002776859]	Chr14:75071724 [GRCh38] Chr14:75538427 [GRCh37] Chr14:14q24.3	uncertain significance
NM_024643.4(ZC2HC1C):c.233C>T (p.Thr78Ile)	single nucleotide variant	Inborn genetic diseases [RCV002950520]	Chr14:75070806 [GRCh38] Chr14:75537509 [GRCh37] Chr14:14q24.3	uncertain significance
NM_024643.4(ZC2HC1C):c.805C>T (p.Pro269Ser)	single nucleotide variant	Inborn genetic diseases [RCV002783294]	Chr14:75071378 [GRCh38] Chr14:75538081 [GRCh37] Chr14:14q24.3	uncertain significance
NM_024643.4(ZC2HC1C):c.1039G>A (p.Val347Met)	single nucleotide variant	Inborn genetic diseases [RCV002785137]	Chr14:75071612 [GRCh38] Chr14:75538315 [GRCh37] Chr14:14q24.3	likely benign
NM_024643.4(ZC2HC1C):c.604G>A (p.Val202Met)	single nucleotide variant	Inborn genetic diseases [RCV002830968]	Chr14:75071177 [GRCh38] Chr14:75537880 [GRCh37] Chr14:14q24.3	likely benign
NM_024643.4(ZC2HC1C):c.994G>A (p.Val332Ile)	single nucleotide variant	Inborn genetic diseases [RCV002813733]	Chr14:75071567 [GRCh38] Chr14:75538270 [GRCh37] Chr14:14q24.3	uncertain significance
NM_024643.4(ZC2HC1C):c.1234A>G (p.Arg412Gly)	single nucleotide variant	Inborn genetic diseases [RCV003189143]	Chr14:75071807 [GRCh38] Chr14:75538510 [GRCh37] Chr14:14q24.3	uncertain significance
NM_024643.4(ZC2HC1C):c.663G>C (p.Glu221Asp)	single nucleotide variant	Inborn genetic diseases [RCV003309739]	Chr14:75071236 [GRCh38] Chr14:75537939 [GRCh37] Chr14:14q24.3	uncertain significance
NM_024643.4(ZC2HC1C):c.664A>T (p.Ser222Cys)	single nucleotide variant	Inborn genetic diseases [RCV003309740]	Chr14:75071237 [GRCh38] Chr14:75537940 [GRCh37] Chr14:14q24.3	uncertain significance
NM_024643.4(ZC2HC1C):c.1312A>C (p.Asn438His)	single nucleotide variant	Inborn genetic diseases [RCV003383032]	Chr14:75071885 [GRCh38] Chr14:75538588 [GRCh37] Chr14:14q24.3	uncertain significance
GRCh37/hg19 14q24.3(chr14:74883763-77219310)x1	copy number loss	not provided [RCV003483211]	Chr14:74883763..77219310 [GRCh37] Chr14:14q24.3	uncertain significance
GRCh37/hg19 14q23.1-32.33(chr14:58894502-107227240)x3	copy number gain	not provided [RCV003485036]	Chr14:58894502..107227240 [GRCh37] Chr14:14q23.1-32.33	pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	2355
Count of miRNA genes:	669
Interacting mature miRNAs:	769
Transcripts:	ENST00000238686, ENST00000439583, ENST00000524913, ENST00000525046, ENST00000526130, ENST00000526748, ENST00000532198, ENST00000534151, ENST00000554763
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

RH102372

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	75,544,531 - 75,544,670	UniSTS	GRCh37
Build 36	14	74,614,284 - 74,614,423	RGD	NCBI36
Celera	14	55,582,188 - 55,582,327	RGD
Cytogenetic Map	14	q24.3	UniSTS
HuRef	14	55,712,698 - 55,712,837	UniSTS
GeneMap99-GB4 RH Map	14	198.97	UniSTS

G36089

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	14	75,542,811 - 75,542,866	UniSTS	GRCh37
Build 36	14	74,612,564 - 74,612,619	RGD	NCBI36
Celera	14	55,580,472 - 55,580,527	RGD
Cytogenetic Map	14	q24.3	UniSTS
HuRef	14	55,710,982 - 55,711,037	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

414

Low

2389

1903

1636

611

1029

454

3757

2081

3599

378

941

1527

172

799

2564

Below cutoff

1060

873

594

108

114

105

405

224

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001042430	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001330191	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_024643	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_110315	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005268062	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005268063	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011537155	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011537156	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011537157	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017021643	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017021644	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017021645	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449710	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_024449711	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054376715	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054376716	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054376717	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AK026746	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK223359	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK303882	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL049780	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC004259	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BQ061857	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX110341	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471061	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068264	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY031397	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	N62812	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000238686 ⟹ ENSP00000238686

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	75,069,577 - 75,078,423 (+)	Ensembl

RefSeq Acc Id:

ENST00000439583 ⟹ ENSP00000390606

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	75,069,641 - 75,078,089 (+)	Ensembl

RefSeq Acc Id:

ENST00000524913 ⟹ ENSP00000435550

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	75,069,641 - 75,079,988 (+)	Ensembl

RefSeq Acc Id:

ENST00000525046 ⟹ ENSP00000435684

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	75,069,652 - 75,078,089 (+)	Ensembl

RefSeq Acc Id:

ENST00000526130 ⟹ ENSP00000437160

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	75,069,677 - 75,077,991 (+)	Ensembl

RefSeq Acc Id:

ENST00000526748

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	75,069,673 - 75,078,091 (+)	Ensembl

RefSeq Acc Id:

ENST00000532198 ⟹ ENSP00000434733

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	75,069,808 - 75,078,089 (+)	Ensembl

RefSeq Acc Id:

ENST00000534151 ⟹ ENSP00000434997

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	75,064,170 - 75,070,853 (+)	Ensembl

RefSeq Acc Id:

ENST00000554763 ⟹ ENSP00000451195

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	75,069,641 - 75,078,390 (+)	Ensembl

RefSeq Acc Id:

ENST00000673663

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	75,064,109 - 75,078,089 (+)	Ensembl

RefSeq Acc Id:

ENST00000673981 ⟹ ENSP00000501014

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	75,069,625 - 75,119,502 (+)	Ensembl

RefSeq Acc Id:

ENST00000674017 ⟹ ENSP00000501062

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	75,068,743 - 75,079,199 (+)	Ensembl

RefSeq Acc Id:

ENST00000674086 ⟹ ENSP00000501056

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	75,069,662 - 75,078,363 (+)	Ensembl

RefSeq Acc Id:

ENST00000674094 ⟹ ENSP00000501069

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	75,069,677 - 75,078,077 (+)	Ensembl

RefSeq Acc Id:

ENST00000674097 ⟹ ENSP00000501052

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	14	75,068,601 - 75,079,107 (+)	Ensembl

RefSeq Acc Id:

NM_001042430 ⟹ NP_001035895

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	75,069,641 - 75,079,988 (+)	NCBI
GRCh37	14	75,535,935 - 75,544,799 (+)	NCBI
Build 36	14	74,606,052 - 74,614,552 (+)	NCBI Archive
Celera	14	55,573,960 - 55,582,456 (+)	RGD
HuRef	14	55,704,451 - 55,714,856 (+)	NCBI
CHM1_1	14	75,474,053 - 75,484,463 (+)	NCBI
T2T-CHM13v2.0	14	69,279,045 - 69,289,387 (+)	NCBI

Sequence:

show sequence

AGAAGCCAGCTGAGAGCGCCTGCGCGGCTGTCGGTTGATGGGGAGGTCAGGTCTGGGAAACTAG
GCCCTGGGGTTTTCCCTGAGCAGGAGCGGTGCCCGAGGGCCTCAGGCGTCAGTCCAGGCCCTGA
ATGGCTGGTCTCCAGCGGTTGGCGTCACATCTGCCTGTGGGCGTTATGCTCCCACATAATACAA
CGGAAGCTCCAGGGCCCCACTCAGCCAAGCAAGACTCTTACGAACAAGGTGACTCTTCCCAGCA
GTCCTTGAAGGGGCACCTGAGGAACAATTTCCAGAAGCAGCTTTTGAGCAACAAAGAGTTGATT
CTGGATAAAGTCTATACTCACCCCAAATGGAACACCCAAACAAAAGCCCGGAGCTACTCCTATC
CCCACTGTACTGGAATCAGCCAGCAAGATCCAGAAAGTGATTCCCAGGGCCAAGGAAATGGTTT
GTTTTACTCGTCAGGCCCTCAATCCTGGTATCCCAAAGCCAATAACCAGGACTTTATCCCCTTT
ACAAAGAAACGAGTTGGAGTGGACCGGGCGTTCCCATTGAAACCCATGGTCCACAGGAAGTCGT
GCAGTACAGGTGAGGCTGGCACTGATGGGGACCATAATGTCTACCCAAGGCCCCCTGAGCCGAG
AGAGTTTTCATCTAGGAACTTTGGTGTGAGGAACCAGGGCAACTTTTCTGTGGTTGGTACTGTT
CTTGCTGCCACGCAGGCGGAGAAGGCCGTGGCAAACTTTGACAGGACGGAGTGGGTGCAGATCC
GAAGACTAGAAGCTGCAGGGGAGAGCTTAGAGGAGGAAATCCGAAGAAAGCAGATTCTCCTGAG
GGGAAAGCTGAAGAAGACAGAGGAGGAACTCAGAAGGATCCAGACGCAAAAGGAACAGGCCAAG
GAAAATGAAAACGGAGAGCTACAGAAAATTATACTCCCCAGGAGCAGAGTTAAAGGCTGAACCT
CCTCAGAAGAGCAACTGGAGATAGAAGCATGAATCTTTTATCCATACGTTCCGCCAGGCTCGAG
AGGTCCAGCAGGTAACTGCCAAAGGTGGAAACTGTTCACACTTGCCTCCCATCCTGCCTGCAGA
AAACCCAGACTGCATTCAGTGTCCTCAGTGTAGCCACCACTTTGCTCCCAAGGTGGCTGAGCAA
CACATTCCCAAGTGTAAGACCATCAAGAACTGTCTTCCACCTCTAAGGAAGCATTATAGTTGAG
CAGACAACAATGGAAACTTTTGGATAGTTCAGAAAGCTCTGCTTCTCTTCAGCAGTAAATGGGA
GTAGAATTTGATGCAAAGCAGAAAGAAATCAAACAGCTCCCAGATCTGCCTGCAGAGCTAAAAT
CTGTGAGGAGAGAGCCACTGCTAAGCAGCAGGAGGCAGAAGGAAGCCCCAGCTTCCCACTAAAT
TACAACCTTGGGCTGGTATGCTTTATGTTATTGCCCTCAGAATTGATGGGTGAAGACACTGAAG
AGTCATGAGCAGGCTCCATTAAAGCTCTTTTCTTGCATGCCTGACTTGTGGTTTGTGCTAGTTA
AGTGCCTGCATCTGGTTCTGCCTTCTTGTCACTGCATGTATGTTCAGAGTTCCTGTTAACTCTT
GCTTTTGTAGAAGCTGGAGTTATTAGGATGTGTTGGTGTCAGAGGGGCATGATCACCCAGATAG
TAACTCTTATAAAAGATAATACAATTTTGCTATAAGGCATTATTAATGGAAATCTATCCTTGGT
CTCCCTGGTGCATAAGCCTGGCCAAAACCCAATACAAGTATGTAAGGTTAAGGCACCAATGTCT
CCTAAACCTTCCCTATGGTGTACTGTGTAATAAAGGAAAGATCTTTATGTACTTTACAGGGTAG
GGATGGGTGTTGGGGGGGAAACACATTATACTTCTCTCTACTTGTTCTTTTCTAATGGGTTTCA
TATGTTAAGAAAGAAACCTCCATTTTAGCTGTTAGTAGCACTCTACTTTCAAATCGGTTTGGCT
AAATGACTGTTTAGAGGCAGCAAAATCTACCATCAAAGCAAGCTGAGACAGGCTGGTCATGGTG
GCTCATTCCTATAATTCCAGCACTTTGGGAGGCTGAAGTGGGAGGATTGCTTGAGGCCAGGAGT
TCAAGAGCGGCCTCGACAACAAAGCAAGACCCCATCTCAAAACAAAACAAAGCTGGGACACTGC
ACAGTGTCACATGCCCTTGGCAATTATAGCATAGTCAACTTCTATTTCAGAGAGTAAACTTTGA
AGGGAAAGGGATCAAATCTTTTTAATTTTCTCTGTGTAGAATATTGCCTAGCACAAGTTAGACC
TTCAATTAGTGAGGTCTGGAGATTTAAAATTAAACAAGAAGATGAGTGAGTCCTACACTAGTGA
AATCAGAGAACTGATAAGTTAATGTCTGCGAGAGTATTATCAGTTCAGATAGGAGTGAAGTTAG
CACAACAGATAGAAATCTTAGGATTACTGTTCTGTATTACTCAAATTGTTAGTTTAAAATACTG
GAGAAAAACTGCTCAATTTGAGCTAGTCAACAGGGCTAGACAGACAACAAAATCCTATTTTACT
AAGTAACAAATGGCCACTCACTCTTGCTCCATTTCCACTGCACTCCAGCCTGGTGACCTAGTGA
GACTCCATCTCAAAAAAAAAAAAAAAAAAAAGAAAAAAAAATTGGGCTAACAGATCAGACCAAT
TTGAAATGTGAGTTAAGGCTTTAGCGGTGAAGCTGCAGGACACAGGCTGGGAAAAAATCCTATA
TATTTAAATAGGAGCACACATTTCTTTGCACTCTTTTTAATTGTTCCAAAGGAAAGGAGGTATC
ACATAATAAAGCTTTATGGTTAGCCCCTTAAGGAAACCTCACACAGAGATAATGGATATTTAAC
CTAATAGGTACATTCCCTAGGCAAGTTCAATGAAATGTACACTTTAAGTGGGAATGTAAACCAG
TACATTGCAATAGATGGCAAGAGTAAGCTGTGGCCAAGGTCACAAAATGGCAACATGTGGATTG
CTTTGCTCCACAGATGTTTTATTTCGCTGGCCTAGCATTCATAATATGATCTGACATTTAAAAA
CTGGGATATGGAACATCTCTTGAAAAACTGGAAGTTCTGGAAACACTGGGCCAGCAACCCGCAT
GGCACAAATTGGGTGGGGTTTAGAATCAGATGCTCCTCCAGATGGGAATGGTAGCACCAGACCA
CTGCAGTCTCACTTGGCCTGCTTCACTTCTTTACCTTATCTGCCTGGTACCACAGGCACTTGGA
TTTGGGATCGCTGGATGTTAGTAAGGTCATAGATCCGGGCCCTCCAGAGAGAACAAATTGTTGT
TATATGTGGGGAGTGCTTTCTAAAAAGGAAGCAGTTGTTTGCTCTCATTTTGCTAAAGAAATAA
AACAATAGTCAATGCC

hide sequence

RefSeq Acc Id:

NM_001330191 ⟹ NP_001317120

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	75,069,641 - 75,079,988 (+)	NCBI
T2T-CHM13v2.0	14	69,279,045 - 69,289,387 (+)	NCBI

Sequence:

show sequence

AGAAGCCAGCTGAGAGCGCCTGCGCGGCTGTCGGTTGATGGGGAGGTCAGGTCTGGGAAACTAG
GCCCTGGGGTTTTCCCTGAGCAGGAGCGGTGCCCGAGGGCCTCAGGCGTCAGTCCAGGCCCTGA
ATGGCTGGTCTCCAGCGGTTGGCGTCACATCTGCCTGTGGGCGTTATGCTCCCACATAATACAA
CGGAAGCTCCAGGGCCCCACTCAGCCAAGCAAGACTCTTACGAACAAGGTGACTCTTCCCAGCA
GTCCTTGAAGGGGCACCTGAGGAACAATTTCCAGAAGCAGCTTTTGAGCAACAAAGAGTTGATT
CTGGATAAAGTCTATACTCACCCCAAATGGAACACCCAAACAAAAGCCCGGAGCTACTCCTATC
CCCACTGTACTGGAATCAGCCAGCAAGATCCAGAAAGTGATTCCCAGGGCCAAGGAAATGGTTT
GTTTTACTCGTCAGGCCCTCAATCCTGGTATCCCAAAGCCAATAACCAGGACTTTATCCCCTTT
ACAAAGAAACGAGTTGGAGTGGACCGGGCGTTCCCATTGAAACCCATGGTCCACAGGAAGTCGT
GCAGTACAGGTGAGGCTGGCACTGATGGGGACCATAATGTCTACCCAAGGCCCCCTGAGCCGAG
AGAGTTTTCATCTAGGAACTTTGGTGTGAGGAACCAGGGCAACTTTTCTGTGGTTGGTACTGTT
CTTGCTGCCACGCAGGCGGAGAAGGCCGTGGCAAACTTTGACAGGACGGAGTGGGTGCAGATCC
GAAGACTAGAAGCTGCAGGGGAGAGCTTAGAGGAGGAAATCCGAAGAAAGCAGATTCTCCTGAG
GGGAAAGCTGAAGAAGACAGAGGAGGAACTCAGAAGGATCCAGACGCAAAAGGAACAGGCCAAG
GAAAATGAAAACGGAGAGCTACAGAAAATTATACTCCCCAGGAGCAGAGTTAAAGGTAATAAAA
GCAACACCATGTACAAACCTATCTTCTCCCCAGAATTTGAGTTTGAGGAAGAATTTAGTAGAGA
CAGGAGAGAGGATGAAACTTGGGGACGGTCTCAACAAAATTCAGGTCCATTCCAGTTCTCTGAT
TATAGAATCCAGAGGCTCAAAAGGGAAAGGCTGGTAGCAAGCAATAATAAAATTCGAGACCCAG
TCTCAGAGCCATCGGTGGAGAAATTCTCCCCGCCTTCAGAAACACCAGTCGGTGCTTTGCAGGG
ATCCGCCAGAAATTCCAGCCTGTCCATGGCACCAGACTCCTCAGGTTCCAGCGGCTCCATTGAA
GAGCCACAGCTGGGCTGAACCTCCTCAGAAGAGCAACTGGAGATAGAAGCATGAATCTTTTATC
CATACGTTCCGCCAGGCTCGAGAGGTCCAGCAGGTAACTGCCAAAGGTGGAAACTGTTCACACT
TGCCTCCCATCCTGCCTGCAGAAAACCCAGACTGCATTCAGTGTCCTCAGTGTAGCCACCACTT
TGCTCCCAAGGTGGCTGAGCAACACATTCCCAAGTGTAAGACCATCAAGAACTGTCTTCCACCT
CTAAGGAAGCATTATAGTTGAGCAGACAACAATGGAAACTTTTGGATAGTTCAGAAAGCTCTGC
TTCTCTTCAGCAGTAAATGGGAGTAGAATTTGATGCAAAGCAGAAAGAAATCAAACAGCTCCCA
GATCTGCCTGCAGAGCTAAAATCTGTGAGGAGAGAGCCACTGCTAAGCAGCAGGAGGCAGAAGG
AAGCCCCAGCTTCCCACTAAATTACAACCTTGGGCTGGTATGCTTTATGTTATTGCCCTCAGAA
TTGATGGGTGAAGACACTGAAGAGTCATGAGCAGGCTCCATTAAAGCTCTTTTCTTGCATGCCT
GACTTGTGGTTTGTGCTAGTTAAGTGCCTGCATCTGGTTCTGCCTTCTTGTCACTGCATGTATG
TTCAGAGTTCCTGTTAACTCTTGCTTTTGTAGAAGCTGGAGTTATTAGGATGTGTTGGTGTCAG
AGGGGCATGATCACCCAGATAGTAACTCTTATAAAAGATAATACAATTTTGCTATAAGGCATTA
TTAATGGAAATCTATCCTTGGTCTCCCTGGTGCATAAGCCTGGCCAAAACCCAATACAAGTATG
TAAGGTTAAGGCACCAATGTCTCCTAAACCTTCCCTATGGTGTACTGTGTAATAAAGGAAAGAT
CTTTATGTACTTTACAGGGTAGGGATGGGTGTTGGGGGGGAAACACATTATACTTCTCTCTACT
TGTTCTTTTCTAATGGGTTTCATATGTTAAGAAAGAAACCTCCATTTTAGCTGTTAGTAGCACT
CTACTTTCAAATCGGTTTGGCTAAATGACTGTTTAGAGGCAGCAAAATCTACCATCAAAGCAAG
CTGAGACAGGCTGGTCATGGTGGCTCATTCCTATAATTCCAGCACTTTGGGAGGCTGAAGTGGG
AGGATTGCTTGAGGCCAGGAGTTCAAGAGCGGCCTCGACAACAAAGCAAGACCCCATCTCAAAA
CAAAACAAAGCTGGGACACTGCACAGTGTCACATGCCCTTGGCAATTATAGCATAGTCAACTTC
TATTTCAGAGAGTAAACTTTGAAGGGAAAGGGATCAAATCTTTTTAATTTTCTCTGTGTAGAAT
ATTGCCTAGCACAAGTTAGACCTTCAATTAGTGAGGTCTGGAGATTTAAAATTAAACAAGAAGA
TGAGTGAGTCCTACACTAGTGAAATCAGAGAACTGATAAGTTAATGTCTGCGAGAGTATTATCA
GTTCAGATAGGAGTGAAGTTAGCACAACAGATAGAAATCTTAGGATTACTGTTCTGTATTACTC
AAATTGTTAGTTTAAAATACTGGAGAAAAACTGCTCAATTTGAGCTAGTCAACAGGGCTAGACA
GACAACAAAATCCTATTTTACTAAGTAACAAATGGCCACTCACTCTTGCTCCATTTCCACTGCA
CTCCAGCCTGGTGACCTAGTGAGACTCCATCTCAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAT
TGGGCTAACAGATCAGACCAATTTGAAATGTGAGTTAAGGCTTTAGCGGTGAAGCTGCAGGACA
CAGGCTGGGAAAAAATCCTATATATTTAAATAGGAGCACACATTTCTTTGCACTCTTTTTAATT
GTTCCAAAGGAAAGGAGGTATCACATAATAAAGCTTTATGGTTAGCCCCTTAAGGAAACCTCAC
ACAGAGATAATGGATATTTAACCTAATAGGTACATTCCCTAGGCAAGTTCAATGAAATGTACAC
TTTAAGTGGGAATGTAAACCAGTACATTGCAATAGATGGCAAGAGTAAGCTGTGGCCAAGGTCA
CAAAATGGCAACATGTGGATTGCTTTGCTCCACAGATGTTTTATTTCGCTGGCCTAGCATTCAT
AATATGATCTGACATTTAAAAACTGGGATATGGAACATCTCTTGAAAAACTGGAAGTTCTGGAA
ACACTGGGCCAGCAACCCGCATGGCACAAATTGGGTGGGGTTTAGAATCAGATGCTCCTCCAGA
TGGGAATGGTAGCACCAGACCACTGCAGTCTCACTTGGCCTGCTTCACTTCTTTACCTTATCTG
CCTGGTACCACAGGCACTTGGATTTGGGATCGCTGGATGTTAGTAAGGTCATAGATCCGGGCCC
TCCAGAGAGAACAAATTGTTGTTATATGTGGGGAGTGCTTTCTAAAAAGGAAGCAGTTGTTTGC
TCTCATTTTGCTAAAGAAATAAAACAATAGTCAATGCC

hide sequence

RefSeq Acc Id:

NM_024643 ⟹ NP_078919

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	75,069,641 - 75,079,988 (+)	NCBI
GRCh37	14	75,535,935 - 75,544,799 (+)	NCBI
Build 36	14	74,606,052 - 74,614,552 (+)	NCBI Archive
Celera	14	55,573,960 - 55,582,456 (+)	RGD
HuRef	14	55,704,451 - 55,714,856 (+)	NCBI
CHM1_1	14	75,474,053 - 75,484,463 (+)	NCBI
T2T-CHM13v2.0	14	69,279,045 - 69,289,387 (+)	NCBI

Sequence:

show sequence

AGAAGCCAGCTGAGAGCGCCTGCGCGGCTGTCGGTTGATGGGGAGGTCAGGTCTGGGAAACTAG
GCCCTGGGGTTTTCCCTGAGCAGGAGCGGTGCCCGAGGGCCTCAGGCGTCAGTCCAGGCCCTGA
ATGGCTGGTCTCCAGCGGTTGGCGTCACATCTGCCTGTGGGCGTTATGCTCCCACATAATACAA
CGGAAGCTCCAGGGCCCCACTCAGCCAAGCAAGACTCTTACGAACAAGGTGACTCTTCCCAGCA
GTCCTTGAAGGGGCACCTGAGGAACAATTTCCAGAAGCAGCTTTTGAGCAACAAAGAGTTGATT
CTGGATAAAGTCTATACTCACCCCAAATGGAACACCCAAACAAAAGCCCGGAGCTACTCCTATC
CCCACTGTACTGGAATCAGCCAGCAAGATCCAGAAAGTGATTCCCAGGGCCAAGGAAATGGTTT
GTTTTACTCGTCAGGCCCTCAATCCTGGTATCCCAAAGCCAATAACCAGGACTTTATCCCCTTT
ACAAAGAAACGAGTTGGAGTGGACCGGGCGTTCCCATTGAAACCCATGGTCCACAGGAAGTCGT
GCAGTACAGGTGAGGCTGGCACTGATGGGGACCATAATGTCTACCCAAGGCCCCCTGAGCCGAG
AGAGTTTTCATCTAGGAACTTTGGTGTGAGGAACCAGGGCAACTTTTCTGTGGTTGGTACTGTT
CTTGCTGCCACGCAGGCGGAGAAGGCCGTGGCAAACTTTGACAGGACGGAGTGGGTGCAGATCC
GAAGACTAGAAGCTGCAGGGGAGAGCTTAGAGGAGGAAATCCGAAGAAAGCAGATTCTCCTGAG
GGGAAAGCTGAAGAAGACAGAGGAGGAACTCAGAAGGATCCAGACGCAAAAGGAACAGGCCAAG
GAAAATGAAAACGGAGAGCTACAGAAAATTATACTCCCCAGGAGCAGAGTTAAAGGTAATAAAA
GCAACACCATGTACAAACCTATCTTCTCCCCAGAATTTGAGTTTGAGGAAGAATTTAGTAGAGA
CAGGAGAGAGGATGAAACTTGGGGACGGTCTCAACAAAATTCAGGTCCATTCCAGTTCTCTGAT
TATAGAATCCAGAGGCTCAAAAGGGAAAGGCTGGTAGCAAGCAATAATAAAATTCGAGACCCAG
TCTCAGAGCCATCGGTGGAGAAATTCTCCCCGCCTTCAGAAACACCAGTCGGTGCTTTGCAGGG
ATCCGCCAGAAATTCCAGCCTGTCCATGGCACCAGACTCCTCAGGTTCCAGCGGCTCCATTGAA
GAGCCACAGCTGGGTGAGTGCAGCCACTGTGGGCGCAAATTCCTCTCGTTCAGGCTGGAGAGAC
ACTCCAACATCTGCAGCAGGATGCGGGGTTCCAAGAGGAAAGTGTTTGACTCCTCCAGGGCCCG
GGCTAAGGGCACAGAACTAGAGCAGTACTTGAACTGGAAGGGGCCAGCTTCAGCCAAGGCTGAA
CCTCCTCAGAAGAGCAACTGGAGATAGAAGCATGAATCTTTTATCCATACGTTCCGCCAGGCTC
GAGAGGTCCAGCAGGTAACTGCCAAAGGTGGAAACTGTTCACACTTGCCTCCCATCCTGCCTGC
AGAAAACCCAGACTGCATTCAGTGTCCTCAGTGTAGCCACCACTTTGCTCCCAAGGTGGCTGAG
CAACACATTCCCAAGTGTAAGACCATCAAGAACTGTCTTCCACCTCTAAGGAAGCATTATAGTT
GAGCAGACAACAATGGAAACTTTTGGATAGTTCAGAAAGCTCTGCTTCTCTTCAGCAGTAAATG
GGAGTAGAATTTGATGCAAAGCAGAAAGAAATCAAACAGCTCCCAGATCTGCCTGCAGAGCTAA
AATCTGTGAGGAGAGAGCCACTGCTAAGCAGCAGGAGGCAGAAGGAAGCCCCAGCTTCCCACTA
AATTACAACCTTGGGCTGGTATGCTTTATGTTATTGCCCTCAGAATTGATGGGTGAAGACACTG
AAGAGTCATGAGCAGGCTCCATTAAAGCTCTTTTCTTGCATGCCTGACTTGTGGTTTGTGCTAG
TTAAGTGCCTGCATCTGGTTCTGCCTTCTTGTCACTGCATGTATGTTCAGAGTTCCTGTTAACT
CTTGCTTTTGTAGAAGCTGGAGTTATTAGGATGTGTTGGTGTCAGAGGGGCATGATCACCCAGA
TAGTAACTCTTATAAAAGATAATACAATTTTGCTATAAGGCATTATTAATGGAAATCTATCCTT
GGTCTCCCTGGTGCATAAGCCTGGCCAAAACCCAATACAAGTATGTAAGGTTAAGGCACCAATG
TCTCCTAAACCTTCCCTATGGTGTACTGTGTAATAAAGGAAAGATCTTTATGTACTTTACAGGG
TAGGGATGGGTGTTGGGGGGGAAACACATTATACTTCTCTCTACTTGTTCTTTTCTAATGGGTT
TCATATGTTAAGAAAGAAACCTCCATTTTAGCTGTTAGTAGCACTCTACTTTCAAATCGGTTTG
GCTAAATGACTGTTTAGAGGCAGCAAAATCTACCATCAAAGCAAGCTGAGACAGGCTGGTCATG
GTGGCTCATTCCTATAATTCCAGCACTTTGGGAGGCTGAAGTGGGAGGATTGCTTGAGGCCAGG
AGTTCAAGAGCGGCCTCGACAACAAAGCAAGACCCCATCTCAAAACAAAACAAAGCTGGGACAC
TGCACAGTGTCACATGCCCTTGGCAATTATAGCATAGTCAACTTCTATTTCAGAGAGTAAACTT
TGAAGGGAAAGGGATCAAATCTTTTTAATTTTCTCTGTGTAGAATATTGCCTAGCACAAGTTAG
ACCTTCAATTAGTGAGGTCTGGAGATTTAAAATTAAACAAGAAGATGAGTGAGTCCTACACTAG
TGAAATCAGAGAACTGATAAGTTAATGTCTGCGAGAGTATTATCAGTTCAGATAGGAGTGAAGT
TAGCACAACAGATAGAAATCTTAGGATTACTGTTCTGTATTACTCAAATTGTTAGTTTAAAATA
CTGGAGAAAAACTGCTCAATTTGAGCTAGTCAACAGGGCTAGACAGACAACAAAATCCTATTTT
ACTAAGTAACAAATGGCCACTCACTCTTGCTCCATTTCCACTGCACTCCAGCCTGGTGACCTAG
TGAGACTCCATCTCAAAAAAAAAAAAAAAAAAAAGAAAAAAAAATTGGGCTAACAGATCAGACC
AATTTGAAATGTGAGTTAAGGCTTTAGCGGTGAAGCTGCAGGACACAGGCTGGGAAAAAATCCT
ATATATTTAAATAGGAGCACACATTTCTTTGCACTCTTTTTAATTGTTCCAAAGGAAAGGAGGT
ATCACATAATAAAGCTTTATGGTTAGCCCCTTAAGGAAACCTCACACAGAGATAATGGATATTT
AACCTAATAGGTACATTCCCTAGGCAAGTTCAATGAAATGTACACTTTAAGTGGGAATGTAAAC
CAGTACATTGCAATAGATGGCAAGAGTAAGCTGTGGCCAAGGTCACAAAATGGCAACATGTGGA
TTGCTTTGCTCCACAGATGTTTTATTTCGCTGGCCTAGCATTCATAATATGATCTGACATTTAA
AAACTGGGATATGGAACATCTCTTGAAAAACTGGAAGTTCTGGAAACACTGGGCCAGCAACCCG
CATGGCACAAATTGGGTGGGGTTTAGAATCAGATGCTCCTCCAGATGGGAATGGTAGCACCAGA
CCACTGCAGTCTCACTTGGCCTGCTTCACTTCTTTACCTTATCTGCCTGGTACCACAGGCACTT
GGATTTGGGATCGCTGGATGTTAGTAAGGTCATAGATCCGGGCCCTCCAGAGAGAACAAATTGT
TGTTATATGTGGGGAGTGCTTTCTAAAAAGGAAGCAGTTGTTTGCTCTCATTTTGCTAAAGAAA
TAAAACAATAGTCAATGCC

hide sequence

RefSeq Acc Id:

NR_110315

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	75,069,641 - 75,079,988 (+)	NCBI
HuRef	14	55,704,451 - 55,714,856 (+)	NCBI
CHM1_1	14	75,474,053 - 75,484,463 (+)	NCBI
T2T-CHM13v2.0	14	69,279,045 - 69,289,387 (+)	NCBI

Sequence:

show sequence

AGAAGCCAGCTGAGAGCGCCTGCGCGGCTGTCGGTTGATGGGGAGGTCAGGTCTGGGAAACTAG
GCCCTGGGGTTTTCCCTGAGCAGGAGCGGTGCCCGAGGGCCTCAGGCTGAACCTCCTCAGAAGA
GCAACTGGAGATAGAAGCATGAATCTTTTATCCATACGTTCCGCCAGGCTCGAGAGGTCCAGCA
GGTAACTGCCAAAGGTGGAAACTGTTCACACTTGCCTCCCATCCTGCCTGCAGAAAACCCAGAC
TGCATTCAGTGTCCTCAGTGTAGCCACCACTTTGCTCCCAAGGTGGCTGAGCAACACATTCCCA
AGTGTAAGACCATCAAGAACTGTCTTCCACCTCTAAGGAAGCATTATAGTTGAGCAGACAACAA
TGGAAACTTTTGGATAGTTCAGAAAGCTCTGCTTCTCTTCAGCAGTAAATGGGAGTAGAATTTG
ATGCAAAGCAGAAAGAAATCAAACAGCTCCCAGATCTGCCTGCAGAGCTAAAATCTGTGAGGAG
AGAGCCACTGCTAAGCAGCAGGAGGCAGAAGGAAGCCCCAGCTTCCCACTAAATTACAACCTTG
GGCTGGTATGCTTTATGTTATTGCCCTCAGAATTGATGGGTGAAGACACTGAAGAGTCATGAGC
AGGCTCCATTAAAGCTCTTTTCTTGCATGCCTGACTTGTGGTTTGTGCTAGTTAAGTGCCTGCA
TCTGGTTCTGCCTTCTTGTCACTGCATGTATGTTCAGAGTTCCTGTTAACTCTTGCTTTTGTAG
AAGCTGGAGTTATTAGGATGTGTTGGTGTCAGAGGGGCATGATCACCCAGATAGTAACTCTTAT
AAAAGATAATACAATTTTGCTATAAGGCATTATTAATGGAAATCTATCCTTGGTCTCCCTGGTG
CATAAGCCTGGCCAAAACCCAATACAAGTATGTAAGGTTAAGGCACCAATGTCTCCTAAACCTT
CCCTATGGTGTACTGTGTAATAAAGGAAAGATCTTTATGTACTTTACAGGGTAGGGATGGGTGT
TGGGGGGGAAACACATTATACTTCTCTCTACTTGTTCTTTTCTAATGGGTTTCATATGTTAAGA
AAGAAACCTCCATTTTAGCTGTTAGTAGCACTCTACTTTCAAATCGGTTTGGCTAAATGACTGT
TTAGAGGCAGCAAAATCTACCATCAAAGCAAGCTGAGACAGGCTGGTCATGGTGGCTCATTCCT
ATAATTCCAGCACTTTGGGAGGCTGAAGTGGGAGGATTGCTTGAGGCCAGGAGTTCAAGAGCGG
CCTCGACAACAAAGCAAGACCCCATCTCAAAACAAAACAAAGCTGGGACACTGCACAGTGTCAC
ATGCCCTTGGCAATTATAGCATAGTCAACTTCTATTTCAGAGAGTAAACTTTGAAGGGAAAGGG
ATCAAATCTTTTTAATTTTCTCTGTGTAGAATATTGCCTAGCACAAGTTAGACCTTCAATTAGT
GAGGTCTGGAGATTTAAAATTAAACAAGAAGATGAGTGAGTCCTACACTAGTGAAATCAGAGAA
CTGATAAGTTAATGTCTGCGAGAGTATTATCAGTTCAGATAGGAGTGAAGTTAGCACAACAGAT
AGAAATCTTAGGATTACTGTTCTGTATTACTCAAATTGTTAGTTTAAAATACTGGAGAAAAACT
GCTCAATTTGAGCTAGTCAACAGGGCTAGACAGACAACAAAATCCTATTTTACTAAGTAACAAA
TGGCCACTCACTCTTGCTCCATTTCCACTGCACTCCAGCCTGGTGACCTAGTGAGACTCCATCT
CAAAAAAAAAAAAAAAAAAAAGAAAAAAAAATTGGGCTAACAGATCAGACCAATTTGAAATGTG
AGTTAAGGCTTTAGCGGTGAAGCTGCAGGACACAGGCTGGGAAAAAATCCTATATATTTAAATA
GGAGCACACATTTCTTTGCACTCTTTTTAATTGTTCCAAAGGAAAGGAGGTATCACATAATAAA
GCTTTATGGTTAGCCCCTTAAGGAAACCTCACACAGAGATAATGGATATTTAACCTAATAGGTA
CATTCCCTAGGCAAGTTCAATGAAATGTACACTTTAAGTGGGAATGTAAACCAGTACATTGCAA
TAGATGGCAAGAGTAAGCTGTGGCCAAGGTCACAAAATGGCAACATGTGGATTGCTTTGCTCCA
CAGATGTTTTATTTCGCTGGCCTAGCATTCATAATATGATCTGACATTTAAAAACTGGGATATG
GAACATCTCTTGAAAAACTGGAAGTTCTGGAAACACTGGGCCAGCAACCCGCATGGCACAAATT
GGGTGGGGTTTAGAATCAGATGCTCCTCCAGATGGGAATGGTAGCACCAGACCACTGCAGTCTC
ACTTGGCCTGCTTCACTTCTTTACCTTATCTGCCTGGTACCACAGGCACTTGGATTTGGGATCG
CTGGATGTTAGTAAGGTCATAGATCCGGGCCCTCCAGAGAGAACAAATTGTTGTTATATGTGGG
GAGTGCTTTCTAAAAAGGAAGCAGTTGTTTGCTCTCATTTTGCTAAAGAAATAAAACAATAGTC
AATGCC

hide sequence

RefSeq Acc Id:

XM_005268062 ⟹ XP_005268119

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	75,069,641 - 75,079,988 (+)	NCBI
GRCh37	14	75,535,935 - 75,544,799 (+)	NCBI

Sequence:

show sequence

GATGGGGAGGTCAGGTCTGGGAAACTAGGCCCTGGGGTTTTCCCTGAGCAGGAGCGGTGCCCGA
GGGCCTCAGGTACGCAGAAGGGCGGGGAGACATGGGATCAGCACCTCCACCTCCTAAGGGACCG
AAGGGCAGGAGAGCGAGAGGACTTGTCCCCAGAGGTGGAGTCCGAAGTGGGGGCGCCCCAGTTG
ACCCTTCGGGACAAAACGTGACTTCAGCCTTAAGGATCTAAAACCGGCCGCGGTCAGGCGTCAG
TCCAGGCCCTGAATGGCTGGTCTCCAGCGGTTGGCGTCACATCTGCCTGTGGGCGTTATGCTCC
CACATAATACAACGGAAGCTCCAGGGCCCCACTCAGCCAAGCAAGACTCTTACGAACAAGGTGA
CTCTTCCCAGCAGTCCTTGAAGGGGCACCTGAGGAACAATTTCCAGAAGCAGCTTTTGAGCAAC
AAAGAGTTGATTCTGGATAAAGTCTATACTCACCCCAAATGGAACACCCAAACAAAAGCCCGGA
GCTACTCCTATCCCCACTGTACTGGAATCAGCCAGCAAGATCCAGAAAGTGATTCCCAGGGCCA
AGGAAATGGTTTGTTTTACTCGTCAGGCCCTCAATCCTGGTATCCCAAAGCCAATAACCAGGAC
TTTATCCCCTTTACAAAGAAACGAGTTGGAGTGGACCGGGCGTTCCCATTGAAACCCATGGTCC
ACAGGAAGTCGTGCAGTACAGGTGAGGCTGGCACTGATGGGGACCATAATGTCTACCCAAGGCC
CCCTGAGCCGAGAGAGTTTTCATCTAGGAACTTTGGTGTGAGGAACCAGGGCAACTTTTCTGTG
GTTGGTACTGTTCTTGCTGCCACGCAGGCGGAGAAGGCCGTGGCAAACTTTGACAGGACGGAGT
GGGTGCAGATCCGAAGACTAGAAGCTGCAGGGGAGAGCTTAGAGGAGGAAATCCGAAGAAAGCA
GATTCTCCTGAGGGGAAAGCTGAAGAAGACAGAGGAGGAACTCAGAAGGATCCAGACGCAAAAG
GAACAGGCCAAGGAAAATGAAAACGGAGAGCTACAGAAAATTATACTCCCCAGGAGCAGAGTTA
AAGGTAATAAAAGCAACACCATGTACAAACCTATCTTCTCCCCAGAATTTGAGTTTGAGGAAGA
ATTTAGTAGAGACAGGAGAGAGGATGAAACTTGGGGACGGTCTCAACAAAATTCAGGTCCATTC
CAGTTCTCTGATTATAGAATCCAGAGGCTCAAAAGGGAAAGGCTGGTAGCAAGCAATAATAAAA
TTCGAGACCCAGTCTCAGAGCCATCGGTGGAGAAATTCTCCCCGCCTTCAGAAACACCAGTCGG
TGCTTTGCAGGGATCCGCCAGAAATTCCAGCCTGTCCATGGCACCAGACTCCTCAGGTTCCAGC
GGCTCCATTGAAGAGCCACAGCTGGGTGAGTGCAGCCACTGTGGGCGCAAATTCCTCTCGTTCA
GGCTGGAGAGACACTCCAACATCTGCAGCAGGATGCGGGGTTCCAAGAGGAAAGTGTTTGACTC
CTCCAGGGCCCGGGCTAAGGGCACAGAACTAGAGCAGTACTTGAACTGGAAGGGGCCAGCTTCA
GCCAAGGCTGAACCTCCTCAGAAGAGCAACTGGAGATAGAAGCATGAATCTTTTATCCATACGT
TCCGCCAGGCTCGAGAGGTCCAGCAGGTAACTGCCAAAGGTGGAAACTGTTCACACTTGCCTCC
CATCCTGCCTGCAGAAAACCCAGACTGCATTCAGTGTCCTCAGTGTAGCCACCACTTTGCTCCC
AAGGTGGCTGAGCAACACATTCCCAAGTGTAAGACCATCAAGAACTGTCTTCCACCTCTAAGGA
AGCATTATAGTTGAGCAGACAACAATGGAAACTTTTGGATAGTTCAGAAAGCTCTGCTTCTCTT
CAGCAGTAAATGGGAGTAGAATTTGATGCAAAGCAGAAAGAAATCAAACAGCTCCCAGATCTGC
CTGCAGAGCTAAAATCTGTGAGGAGAGAGCCACTGCTAAGCAGCAGGAGGCAGAAGGAAGCCCC
AGCTTCCCACTAAATTACAACCTTGGGCTGGTATGCTTTATGTTATTGCCCTCAGAATTGATGG
GTGAAGACACTGAAGAGTCATGAGCAGGCTCCATTAAAGCTCTTTTCTTGCATGCCTGA

hide sequence

RefSeq Acc Id:

XM_011537155 ⟹ XP_011535457

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	75,069,641 - 75,079,988 (+)	NCBI

Sequence:

show sequence

CGAGGGCCTCAGGTACGCAGAAGGGCGGGGAGACATGGGATCAGCACCTCCACCTCCTAAGGGA
CCGAAGGGCAGGAGAGCGAGAGGACTTGTCCCCAGAGGTGGAGTCCGAAGTGGGGGCGCCCCAG
TTGACCCTTCGGGACAAAACGTGACTTCAGCCTTAAGGATCTAAAACCGGCCGCGGTCAGGTCA
GGTGGCCCTCAACGCTCAGGCGTCAGTCCAGGCCCTGAATGGCTGGTCTCCAGCGGTTGGCGTC
ACATCTGCCTGTGGGCGTTATGCTCCCACATAATACAACGGAAGCTCCAGGGCCCCACTCAGCC
AAGCAAGACTCTTACGAACAAGGTGACTCTTCCCAGCAGTCCTTGAAGGGGCACCTGAGGAACA
ATTTCCAGAAGCAGCTTTTGAGCAACAAAGAGTTGATTCTGGATAAAGTCTATACTCACCCCAA
ATGGAACACCCAAACAAAAGCCCGGAGCTACTCCTATCCCCACTGTACTGGAATCAGCCAGCAA
GATCCAGAAAGTGATTCCCAGGGCCAAGGAAATGGTTTGTTTTACTCGTCAGGCCCTCAATCCT
GGTATCCCAAAGCCAATAACCAGGACTTTATCCCCTTTACAAAGAAACGAGTTGGAGTGGACCG
GGCGTTCCCATTGAAACCCATGGTCCACAGGAAGTCGTGCAGTACAGGTGAGGCTGGCACTGAT
GGGGACCATAATGTCTACCCAAGGCCCCCTGAGCCGAGAGAGTTTTCATCTAGGAACTTTGGTG
TGAGGAACCAGGGCAACTTTTCTGTGGTTGGTACTGTTCTTGCTGCCACGCAGGCGGAGAAGGC
CGTGGCAAACTTTGACAGGACGGAGTGGGTGCAGATCCGAAGACTAGAAGCTGCAGGGGAGAGC
TTAGAGGAGGAAATCCGAAGAAAGCAGATTCTCCTGAGGGGAAAGCTGAAGAAGACAGAGGAGG
AACTCAGAAGGATCCAGACGCAAAAGGAACAGGCCAAGGAAAATGAAAACGGAGAGCTACAGAA
AATTATACTCCCCAGGAGCAGAGTTAAAGGTAATAAAAGCAACACCATGTACAAACCTATCTTC
TCCCCAGAATTTGAGTTTGAGGAAGAATTTAGTAGAGACAGGAGAGAGGATGAAACTTGGGGAC
GGTCTCAACAAAATTCAGGTCCATTCCAGTTCTCTGATTATAGAATCCAGAGGCTCAAAAGGGA
AAGGCTGGTAGCAAGCAATAATAAAATTCGAGACCCAGTCTCAGAGCCATCGGTGGAGAAATTC
TCCCCGCCTTCAGAAACACCAGTCGGTGCTTTGCAGGGATCCGCCAGAAATTCCAGCCTGTCCA
TGGCACCAGACTCCTCAGGTTCCAGCGGCTCCATTGAAGAGCCACAGCTGGGTGAGTGCAGCCA
CTGTGGGCGCAAATTCCTCTCGTTCAGGCTGGAGAGACACTCCAACATCTGCAGCAGGATGCGG
GGTTCCAAGAGGAAAGTGTTTGACTCCTCCAGGGCCCGGGCTAAGGGCACAGAACTAGAGCAGT
ACTTGAACTGGAAGGGGCCAGCTTCAGCCAAGGCTGAACCTCCTCAGAAGAGCAACTGGAGATA
GAAGCATGAATCTTTTATCCATACGTTCCGCCAGGCTCGAGAGGTCCAGCAGGTAACTGCCAAA
GGTGGAAACTGTTCACACTTGCCTCCCATCCTGCCTGCAGAAAACCCAGACTGCATTCAGTGTC
CTCAGTGTAGCCACCACTTTGCTCCCAAGGTGGCTGAGCAACACATTCCCAAGTGTAAGACCAT
CAAGAACTGTCTTCCACCTCTAAGGAAGCATTATAGTTGAGCAGACAACAATGGAAACTTTTGG
ATAGTTCAGAAAGCTCTGCTTCTCTTCAGCAGTAAATGGGAGTAGAATTTGATGCAAAGCAGAA
AGAAATCAAACAGCTCCCAGATCTGCCTGCAGAGCTAAAATCTGTGAGGAGAGAGCCACTGCTA
AGCAGCAGGAGGCAGAAGGAAGCCCCAGCTTCCCACTAAATTACAACCTTGGGCTGGTATGCTT
TATGTTATTGCCCTCAGAATTGATGGGTGAAGACACTGAAGAGTCATGAGCAGGCTCCATTAAA
GCTCTTTTCTTGCA

hide sequence

RefSeq Acc Id:

XM_011537156 ⟹ XP_011535458

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	14	75,069,641 - 75,079,988 (+)	NCBI

Sequence:

show sequence

CACCGGGAATAACAGAAGCCAGCTGAGAGCGCCTGCGCGGCTGTCGGTTGATGGGGAGGCGTCA
GTCCAGGCCCTGAATGGCTGGTCTCCAGCGGTTGGCGTCACATCTGCCTGTGGGCGTTATGCTC
CCACATAATACAACGGAAGCTCCAGGGCCCCACTCAGCCAAGCAAGACTCTTACGAACAAGGTG
ACTCTTCCCAGCAGTCCTTGAAGGGGCACCTGAGGAACAATTTCCAGAAGCAGCTTTTGAGCAA
CAAAGAGTTGATTCTGGATAAAGTCTATACTCACCCCAAATGGAACACCCAAACAAAAGCCCGG
AGCTACTCCTATCCCCACTGTACTGGAATCAGCCAGCAAGATCCAGAAAGTGATTCCCAGGGCC
AAGGAAATGGTTTGTTTTACTCGTCAGGCCCTCAATCCTGGTATCCCAAAGCCAATAACCAGGA
CTTTATCCCCTTTACAAAGAAACGAGTTGGAGTGGACCGGGCGTTCCCATTGAAACCCATGGTC
CACAGGAAGTCGTGCAGTACAGGTGAGGCTGGCACTGATGGGGACCATAATGTCTACCCAAGGC
CCCCTGAGCCGAGAGAGTTTTCATCTAGGAACTTTGGTGTGAGGAACCAGGGCAACTTTTCTGT
GGTTGGTACTGTTCTTGCTGCCACGCAGGCGGAGAAGGCCGTGGCAAACTTTGACAGGACGGAG
TGGGTGCAGATCCGAAGACTAGAAGCTGCAGGGGAGAGCTTAGAGGAGGAAATCCGAAGAAAGC
AGATTCTCCTGAGGGGAAAGCTGAAGAAGACAGAGGAGGAACTCAGAAGGATCCAGACGCAAAA
GGAACAGGCCAAGGAAAATGAAAACGGAGAGCTACAGAAAATTATACTCCCCAGGAGCAGAGTT
AAAGGTAATAAAAGCAACACCATGTACAAACCTATCTTCTCCCCAGAATTTGAGTTTGAGGAAG
AATTTAGTAGAGACAGGAGAGAGGATGAAACTTGGGGACGGTCTCAACAAAATTCAGGTCCATT
CCAGTTCTCTGATTATAGAATCCAGAGGCTCAAAAGGGAAAGGCTGGTAGCAAGCAATAATAAA
ATTCGAGACCCAGTCTCAGAGCCATCGGTGGAGAAATTCTCCCCGCCTTCAGAAACACCAGTCG
GTGCTTTGCAGGGATCCGCCAGAAATTCCAGCCTGTCCATGGCACCAGACTCCTCAGGTTCCAG
CGGCTCCATTGAAGAGCCACAGCTGGGTGAGTGCAGCCACTGTGGGCGCAAATTCCTCTCGTTC
AGGCTGGAGAGACACTCCAACATCTGCAGCAGGATGCGGGGTTCCAAGAGGAAAGTGTTTGACT
CCTCCAGGGCCCGGGCTAAGGGCACAGAACTAGAGCAGTACTTGAACTGGAAGGGGCCAGCTTC
AGCCAAGGCTGAACCTCCTCAGAAGAGCAACTGGAGATAGAAGCATGAATCTTTTATCCATACG
TTCCGCCAGGCTCGAGAGGTCCAGCAGGTAACTGCCAAAGGTGGAAACTGTTCACACTTGCCTC
CCATCCTGCCTGCAGAAAACCCAGACTGCATTCAGTGTCCTCAGTGTAGCCACCACTTTGCTCC
CAAGGTGGCTGAGCAACACATTCCCAAGTGTAAGACCATCAAGAACTGTCTTCCACCTCTAAGG
AAGCATTATAGTTGAGCAGACAACAATGGAAACTTTTGGATAGTTCAGAAAGCTCTGCTTCTCT
TCAGCAGTAAATGGGAGTAGAATTTGATGCAAAGCAGAAAGAAATCAAACAGCTCCCAGATCTG
CCTGCAGAGCTAAAATCTGTGAGGAGAGAGCCACTGCTAAGCAGCAGGAGGCAGAAGGAAGCCC
CAGCTTCCCACTAAATTACAACCTTGGGCTGGTATGCTTTATGTTATTGCCCTCAGAATTGATG
GGTGAAGACACTGAAGAGTCATGAGCAGGCTCCATTAAAGCTCTTTTCTTGCATGCCTGA

hide sequence

RefSeq Acc Id:

XM_054376715 ⟹ XP_054232690

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	69,279,034 - 69,289,387 (+)	NCBI

RefSeq Acc Id:

XM_054376716 ⟹ XP_054232691

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	69,279,034 - 69,289,387 (+)	NCBI

RefSeq Acc Id:

XM_054376717 ⟹ XP_054232692

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	14	69,279,032 - 69,289,387 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001035895	(Get FASTA)	NCBI Sequence Viewer
	NP_001317120	(Get FASTA)	NCBI Sequence Viewer
	NP_078919	(Get FASTA)	NCBI Sequence Viewer
	XP_005268119	(Get FASTA)	NCBI Sequence Viewer
	XP_011535457	(Get FASTA)	NCBI Sequence Viewer
	XP_011535458	(Get FASTA)	NCBI Sequence Viewer
	XP_054232690	(Get FASTA)	NCBI Sequence Viewer
	XP_054232691	(Get FASTA)	NCBI Sequence Viewer
	XP_054232692	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH04259	(Get FASTA)	NCBI Sequence Viewer
	BAB15541	(Get FASTA)	NCBI Sequence Viewer
	BAD97079	(Get FASTA)	NCBI Sequence Viewer
	BAG64818	(Get FASTA)	NCBI Sequence Viewer
	EAW81217	(Get FASTA)	NCBI Sequence Viewer
	EAW81218	(Get FASTA)	NCBI Sequence Viewer
	EAW81219	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000238686
	ENSP00000238686.8
	ENSP00000390606
	ENSP00000390606.2
	ENSP00000434733.2
	ENSP00000434997.1
	ENSP00000435550
	ENSP00000435550.1
	ENSP00000435684.2
	ENSP00000437160.2
	ENSP00000451195.2
	ENSP00000501014.1
	ENSP00000501052.1
	ENSP00000501056
	ENSP00000501056.1
	ENSP00000501062.1
	ENSP00000501069.1
GenBank Protein	Q53FD0	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001035895 ⟸ NM_001042430
- Peptide Label:	isoform b
- UniProtKB:	H0YE08 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAGLQRLASHLPVGVMLPHNTTEAPGPHSAKQDSYEQGDSSQQSLKGHLRNNFQKQLLSNKELI LDKVYTHPKWNTQTKARSYSYPHCTGISQQDPESDSQGQGNGLFYSSGPQSWYPKANNQDFIPF TKKRVGVDRAFPLKPMVHRKSCSTGEAGTDGDHNVYPRPPEPREFSSRNFGVRNQGNFSVVGTV LAATQAEKAVANFDRTEWVQIRRLEAAGESLEEEIRRKQILLRGKLKKTEEELRRIQTQKEQAK ENENGELQKIILPRSRVKG hide sequence

RefSeq Acc Id:	NP_078919 ⟸ NM_024643
- Peptide Label:	isoform a
- UniProtKB:	Q9BTA8 (UniProtKB/Swiss-Prot), E9PJQ0 (UniProtKB/Swiss-Prot), Q9H5S9 (UniProtKB/Swiss-Prot), Q53FD0 (UniProtKB/Swiss-Prot), B4E1K6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAGLQRLASHLPVGVMLPHNTTEAPGPHSAKQDSYEQGDSSQQSLKGHLRNNFQKQLLSNKELI LDKVYTHPKWNTQTKARSYSYPHCTGISQQDPESDSQGQGNGLFYSSGPQSWYPKANNQDFIPF TKKRVGVDRAFPLKPMVHRKSCSTGEAGTDGDHNVYPRPPEPREFSSRNFGVRNQGNFSVVGTV LAATQAEKAVANFDRTEWVQIRRLEAAGESLEEEIRRKQILLRGKLKKTEEELRRIQTQKEQAK ENENGELQKIILPRSRVKGNKSNTMYKPIFSPEFEFEEEFSRDRREDETWGRSQQNSGPFQFSD YRIQRLKRERLVASNNKIRDPVSEPSVEKFSPPSETPVGALQGSARNSSLSMAPDSSGSSGSIE EPQLGECSHCGRKFLSFRLERHSNICSRMRGSKRKVFDSSRARAKGTELEQYLNWKGPASAKAE PPQKSNWR hide sequence

RefSeq Acc Id:	XP_005268119 ⟸ XM_005268062
- Peptide Label:	isoform X1
- UniProtKB:	Q9BTA8 (UniProtKB/Swiss-Prot), E9PJQ0 (UniProtKB/Swiss-Prot), Q9H5S9 (UniProtKB/Swiss-Prot), Q53FD0 (UniProtKB/Swiss-Prot), B4E1K6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAGLQRLASHLPVGVMLPHNTTEAPGPHSAKQDSYEQGDSSQQSLKGHLRNNFQKQLLSNKELI LDKVYTHPKWNTQTKARSYSYPHCTGISQQDPESDSQGQGNGLFYSSGPQSWYPKANNQDFIPF TKKRVGVDRAFPLKPMVHRKSCSTGEAGTDGDHNVYPRPPEPREFSSRNFGVRNQGNFSVVGTV LAATQAEKAVANFDRTEWVQIRRLEAAGESLEEEIRRKQILLRGKLKKTEEELRRIQTQKEQAK ENENGELQKIILPRSRVKGNKSNTMYKPIFSPEFEFEEEFSRDRREDETWGRSQQNSGPFQFSD YRIQRLKRERLVASNNKIRDPVSEPSVEKFSPPSETPVGALQGSARNSSLSMAPDSSGSSGSIE EPQLGECSHCGRKFLSFRLERHSNICSRMRGSKRKVFDSSRARAKGTELEQYLNWKGPASAKAE PPQKSNWR hide sequence

RefSeq Acc Id:	XP_011535457 ⟸ XM_011537155
- Peptide Label:	isoform X1
- UniProtKB:	Q9BTA8 (UniProtKB/Swiss-Prot), E9PJQ0 (UniProtKB/Swiss-Prot), Q9H5S9 (UniProtKB/Swiss-Prot), Q53FD0 (UniProtKB/Swiss-Prot), B4E1K6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAGLQRLASHLPVGVMLPHNTTEAPGPHSAKQDSYEQGDSSQQSLKGHLRNNFQKQLLSNKELI LDKVYTHPKWNTQTKARSYSYPHCTGISQQDPESDSQGQGNGLFYSSGPQSWYPKANNQDFIPF TKKRVGVDRAFPLKPMVHRKSCSTGEAGTDGDHNVYPRPPEPREFSSRNFGVRNQGNFSVVGTV LAATQAEKAVANFDRTEWVQIRRLEAAGESLEEEIRRKQILLRGKLKKTEEELRRIQTQKEQAK ENENGELQKIILPRSRVKGNKSNTMYKPIFSPEFEFEEEFSRDRREDETWGRSQQNSGPFQFSD YRIQRLKRERLVASNNKIRDPVSEPSVEKFSPPSETPVGALQGSARNSSLSMAPDSSGSSGSIE EPQLGECSHCGRKFLSFRLERHSNICSRMRGSKRKVFDSSRARAKGTELEQYLNWKGPASAKAE PPQKSNWR hide sequence

RefSeq Acc Id:	XP_011535458 ⟸ XM_011537156
- Peptide Label:	isoform X1
- UniProtKB:	Q9BTA8 (UniProtKB/Swiss-Prot), E9PJQ0 (UniProtKB/Swiss-Prot), Q9H5S9 (UniProtKB/Swiss-Prot), Q53FD0 (UniProtKB/Swiss-Prot), B4E1K6 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAGLQRLASHLPVGVMLPHNTTEAPGPHSAKQDSYEQGDSSQQSLKGHLRNNFQKQLLSNKELI LDKVYTHPKWNTQTKARSYSYPHCTGISQQDPESDSQGQGNGLFYSSGPQSWYPKANNQDFIPF TKKRVGVDRAFPLKPMVHRKSCSTGEAGTDGDHNVYPRPPEPREFSSRNFGVRNQGNFSVVGTV LAATQAEKAVANFDRTEWVQIRRLEAAGESLEEEIRRKQILLRGKLKKTEEELRRIQTQKEQAK ENENGELQKIILPRSRVKGNKSNTMYKPIFSPEFEFEEEFSRDRREDETWGRSQQNSGPFQFSD YRIQRLKRERLVASNNKIRDPVSEPSVEKFSPPSETPVGALQGSARNSSLSMAPDSSGSSGSIE EPQLGECSHCGRKFLSFRLERHSNICSRMRGSKRKVFDSSRARAKGTELEQYLNWKGPASAKAE PPQKSNWR hide sequence

RefSeq Acc Id:	NP_001317120 ⟸ NM_001330191
- Peptide Label:	isoform c
- UniProtKB:	J3KMY6 (UniProtKB/TrEMBL), A0A669KB15 (UniProtKB/TrEMBL)
- Sequence:	show sequence MAGLQRLASHLPVGVMLPHNTTEAPGPHSAKQDSYEQGDSSQQSLKGHLRNNFQKQLLSNKELI LDKVYTHPKWNTQTKARSYSYPHCTGISQQDPESDSQGQGNGLFYSSGPQSWYPKANNQDFIPF TKKRVGVDRAFPLKPMVHRKSCSTGEAGTDGDHNVYPRPPEPREFSSRNFGVRNQGNFSVVGTV LAATQAEKAVANFDRTEWVQIRRLEAAGESLEEEIRRKQILLRGKLKKTEEELRRIQTQKEQAK ENENGELQKIILPRSRVKGNKSNTMYKPIFSPEFEFEEEFSRDRREDETWGRSQQNSGPFQFSD YRIQRLKRERLVASNNKIRDPVSEPSVEKFSPPSETPVGALQGSARNSSLSMAPDSSGSSGSIE EPQLG hide sequence

RefSeq Acc Id:

ENSP00000501014 ⟸ ENST00000673981

RefSeq Acc Id:

ENSP00000501052 ⟸ ENST00000674097

RefSeq Acc Id:

ENSP00000501056 ⟸ ENST00000674086

RefSeq Acc Id:

ENSP00000501069 ⟸ ENST00000674094

RefSeq Acc Id:

ENSP00000501062 ⟸ ENST00000674017

RefSeq Acc Id:

ENSP00000390606 ⟸ ENST00000439583

RefSeq Acc Id:

ENSP00000434733 ⟸ ENST00000532198

RefSeq Acc Id:

ENSP00000434997 ⟸ ENST00000534151

RefSeq Acc Id:

ENSP00000435550 ⟸ ENST00000524913

RefSeq Acc Id:

ENSP00000435684 ⟸ ENST00000525046

RefSeq Acc Id:

ENSP00000437160 ⟸ ENST00000526130

RefSeq Acc Id:

ENSP00000238686 ⟸ ENST00000238686

RefSeq Acc Id:

ENSP00000451195 ⟸ ENST00000554763

RefSeq Acc Id:	XP_054232692 ⟸ XM_054376717
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054232690 ⟸ XM_054376715
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054232691 ⟸ XM_054376716
- Peptide Label:	isoform X1

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q53FD0-F1-model_v2	AlphaFold	Q53FD0	1-456	view protein structure

Promoters

RGD ID:

6791584

Promoter ID:

HG_KWN:19808

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

NM_001042430, NM_024643

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	14	74,605,561 - 74,606,061 (+)	MPROMDB

RGD ID:

7228171

Promoter ID:

EPDNEW_H19831

Type:

initiation region

Name:

ZC2HC1C_1

Description:

zinc finger C2HC-type containing 1C

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	14	75,069,641 - 75,069,701	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:20354	AgrOrtholog
COSMIC	ZC2HC1C	COSMIC
Ensembl Genes	ENSG00000119703	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000238686	ENTREZGENE
	ENST00000238686.8	UniProtKB/TrEMBL
	ENST00000439583	ENTREZGENE
	ENST00000439583.2	UniProtKB/Swiss-Prot
	ENST00000524913	ENTREZGENE
	ENST00000524913.3	UniProtKB/Swiss-Prot
	ENST00000525046.2	UniProtKB/Swiss-Prot
	ENST00000526130.2	UniProtKB/Swiss-Prot
	ENST00000532198.2	UniProtKB/TrEMBL
	ENST00000534151.1	UniProtKB/TrEMBL
	ENST00000554763.2	UniProtKB/Swiss-Prot
	ENST00000673981.1	UniProtKB/Swiss-Prot
	ENST00000674017.1	UniProtKB/Swiss-Prot
	ENST00000674086	ENTREZGENE
	ENST00000674086.1	UniProtKB/Swiss-Prot
	ENST00000674094.1	UniProtKB/TrEMBL
	ENST00000674097.1	UniProtKB/Swiss-Prot
Gene3D-CATH	Classic Zinc Finger	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000119703	GTEx
HGNC ID	HGNC:20354	ENTREZGENE
Human Proteome Map	ZC2HC1C	Human Proteome Map
InterPro	ZNF_C2HC_dom_1C	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:79696	UniProtKB/Swiss-Prot
NCBI Gene	79696	ENTREZGENE
PANTHER	PTHR14649	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ZINC FINGER C2HC DOMAIN-CONTAINING PROTEIN 1C	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA162386996	PharmGKB
PROSITE	ZF_C2HC_C3H	UniProtKB/Swiss-Prot
UniProt	A0A669KB15	ENTREZGENE, UniProtKB/TrEMBL
	B4E1K6	ENTREZGENE, UniProtKB/TrEMBL
	E9PJQ0	ENTREZGENE
	E9PMG6_HUMAN	UniProtKB/TrEMBL
	H0YE08	ENTREZGENE, UniProtKB/TrEMBL
	J3KMY6	ENTREZGENE, UniProtKB/TrEMBL
	Q53FD0	ENTREZGENE
	Q9BTA8	ENTREZGENE
	Q9H5S9	ENTREZGENE
	ZC21C_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	E9PJQ0	UniProtKB/Swiss-Prot
	Q9BTA8	UniProtKB/Swiss-Prot
	Q9H5S9	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-02-16	ZC2HC1C	zinc finger C2HC-type containing 1C		zinc finger, C2HC-type containing 1C	Symbol and/or name change	5135510	APPROVED
2012-03-13	ZC2HC1C	zinc finger, C2HC-type containing 1C	FAM164C	family with sequence similarity 164, member C	Symbol and/or name change	5135510	APPROVED

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

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

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

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

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