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Gene: CCNI (cyclin I) Homo sapiens

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Symbol:

CCNI

Name:

cyclin I

RGD ID:

1319424

HGNC Page

HGNC:1595

Description:

Predicted to enable cyclin-dependent protein serine/threonine kinase regulator activity. Predicted to be involved in G1/S transition of mitotic cell cycle. Predicted to be located in nuclear membrane. Predicted to be part of cyclin-dependent protein kinase holoenzyme complex. Predicted to be active in cytoplasm and nucleus.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

CCNI1; CYC1; cyclin ITI; cyclin-I; CYI

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):	Ccni (cyclin I)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, Treefam
Rattus norvegicus (Norway rat):	Ccni (cyclin I)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Ccni (cyclin I)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	CCNI (cyclin I)	NCBI	Ortholog
Canis lupus familiaris (dog):	CCNI (cyclin I)	HGNC	HomoloGene, NCBI
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Ccni (cyclin I)	NCBI	Ortholog
Sus scrofa (pig):	CCNI (cyclin I)	HGNC	EggNOG, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	CCNI (cyclin I)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Ccni (cyclin I)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Ccni (cyclin I)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Ccni (cyclin I)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	ccni (cyclin I)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Caenorhabditis elegans (roundworm):	R02F2.1	Alliance	DIOPT (Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	ccni.S	Alliance	DIOPT (Xenbase)
Xenopus tropicalis (tropical clawed frog):	ccni	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB)
Xenopus laevis (African clawed frog):	ccni.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	4	77,047,155 - 77,075,989 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	4	77,047,155 - 77,076,309 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	4	77,968,308 - 77,997,142 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	4	78,188,189 - 78,216,149 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	4	78,326,353 - 78,354,304	NCBI
Celera	4	75,270,553 - 75,298,504 (-)	NCBI		Celera
Cytogenetic Map	4	q21.1	NCBI
HuRef	4	73,720,994 - 73,748,951 (-)	NCBI		HuRef
CHM1_1	4	77,946,423 - 77,974,382 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	4	80,387,967 - 80,416,780 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

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

1,2-dimethylhydrazine (ISO)

17beta-estradiol (EXP,ISO)

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

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

4,4'-sulfonyldiphenol (EXP)

6-propyl-2-thiouracil (ISO)

acrolein (EXP)

aflatoxin B1 (EXP)

alpha-pinene (EXP)

amitrole (ISO)

antirheumatic drug (EXP)

Aroclor 1254 (ISO)

benzo[a]pyrene diol epoxide I (EXP)

bisphenol A (EXP,ISO)

bisphenol F (EXP)

carbon nanotube (EXP,ISO)

chloropicrin (EXP)

clofibrate (ISO)

cobalt dichloride (EXP)

coumestrol (EXP)

Cuprizon (ISO)

cyclosporin A (EXP)

dexamethasone (EXP)

Di-n-octyl phthalate (ISO)

diazinon (ISO)

dioxygen (ISO)

diuron (ISO)

dorsomorphin (EXP)

doxorubicin (EXP)

endosulfan (ISO)

flutamide (ISO)

folic acid (ISO)

gentamycin (ISO)

glafenine (ISO)

indometacin (EXP)

menadione (EXP)

methimazole (ISO)

ozone (EXP)

paracetamol (EXP,ISO)

perfluorooctane-1-sulfonic acid (ISO)

phenobarbital (ISO)

potassium dichromate (ISO)

progesterone (ISO)

SB 431542 (EXP)

sirolimus (ISO)

sodium arsenite (EXP)

sodium fluoride (ISO)

sulfadimethoxine (ISO)

sunitinib (EXP)

titanium dioxide (ISO)

trichloroethene (ISO)

triphenyl phosphate (EXP)

triptonide (ISO)

valproic acid (EXP)

vorinostat (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

G1/S transition of mitotic cell cycle (IBA)

spermatogenesis (NAS)

Cellular Component

cyclin-dependent protein kinase holoenzyme complex (IBA)

cytoplasm (IBA)

membrane (IEA)

nuclear membrane (IEA)

nucleus (IBA,IEA)

Molecular Function

cyclin-dependent protein serine/threonine kinase regulator activity (IBA)

protein binding (IPI)

References

References - curated

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

Additional References at PubMed

PMID:7493655	PMID:8125298	PMID:9705831	PMID:12477932	PMID:15489334	PMID:17043677	PMID:17507299	PMID:19322201	PMID:21873635	PMID:21988832	PMID:22658674	PMID:23907122
PMID:25640309	PMID:25852190	PMID:26698249	PMID:30797814	PMID:32296183	PMID:32456285	PMID:32513696	PMID:33637726	PMID:33961781	PMID:36736316	PMID:37081792

Genomics

Comparative Map Data

CCNI
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	4	77,047,155 - 77,075,989 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	4	77,047,155 - 77,076,309 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	4	77,968,308 - 77,997,142 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	4	78,188,189 - 78,216,149 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	4	78,326,353 - 78,354,304	NCBI
Celera	4	75,270,553 - 75,298,504 (-)	NCBI		Celera
Cytogenetic Map	4	q21.1	NCBI
HuRef	4	73,720,994 - 73,748,951 (-)	NCBI		HuRef
CHM1_1	4	77,946,423 - 77,974,382 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	4	80,387,967 - 80,416,780 (-)	NCBI		T2T-CHM13v2.0

Ccni
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	5	93,329,796 - 93,354,348 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	5	93,329,792 - 93,354,354 (-)	Ensembl		GRCm39 Ensembl
GRCm38	5	93,181,933 - 93,206,495 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	5	93,181,933 - 93,206,495 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	5	93,610,959 - 93,635,521 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	5	94,257,141 - 94,281,232 (-)	NCBI		MGSCv36	mm8
Celera	5	91,335,519 - 91,360,075 (-)	NCBI		Celera
Cytogenetic Map	5	E2	NCBI
cM Map	5	47.29	NCBI

Ccni
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	14	15,164,047 - 15,186,885 (+)	NCBI		GRCr8
mRatBN7.2	14	14,879,698 - 14,902,510 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	14	14,879,717 - 14,902,510 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	14	14,888,988 - 14,911,658 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	14	16,208,004 - 16,230,674 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	14	14,903,257 - 14,925,929 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	14	16,341,510 - 16,364,326 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	14	16,341,536 - 16,364,326 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	14	16,267,506 - 16,290,318 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	14	16,437,340 - 16,460,130 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	14	16,437,274 - 16,460,127 (+)	NCBI
Celera	14	14,282,201 - 14,304,991 (+)	NCBI		Celera
Cytogenetic Map	14	p22	NCBI

Ccni
(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_004955433	1,698,568 - 1,735,196 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955433	1,698,568 - 1,735,196 (-)	NCBI	ChiLan1.0	ChiLan1.0

CCNI
(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	3	52,986,685 - 53,022,812 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	4	53,182,420 - 53,215,473 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	4	47,129,542 - 47,158,419 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	4	52,968,082 - 52,996,932 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	4	52,968,082 - 52,996,932 (+)	Ensembl	panpan1.1		panPan2

CCNI
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	32	1,612,590 - 1,650,661 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	32	1,608,330 - 1,645,352 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	32	40,236,220 - 40,274,002 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	32	1,642,080 - 1,680,282 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	32	1,637,827 - 1,680,282 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	32	1,634,137 - 1,672,319 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	32	1,589,677 - 1,627,852 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	32	38,547,915 - 38,585,702 (+)	NCBI		UU_Cfam_GSD_1.0

Ccni
(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_024405285	10,538,770 - 10,559,788 (+)	NCBI		HiC_Itri_2
SpeTri2.0	NW_004936676	947,455 - 968,479 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

CCNI
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	8	72,686,106 - 72,719,065 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	8	72,686,095 - 72,719,307 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	8	76,887,178 - 76,919,644 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

CCNI
(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	7	25,547,692 - 25,576,412 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666037	3,901,103 - 3,931,303 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Ccni
(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 1.0	NW_004624757	13,887,997 - 13,927,712 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in CCNI
7 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 4q21.1-21.23(chr4:75453111-84094295)x1	copy number loss	See cases [RCV000050786]	Chr4:75453111..84094295 [GRCh38] Chr4:76378321..85015448 [GRCh37] Chr4:76597345..85234472 [NCBI36] Chr4:4q21.1-21.23	pathogenic
GRCh38/hg38 4q13.3-21.21(chr4:71128874-78099088)x3	copy number gain	See cases [RCV000051774]	Chr4:71128874..78099088 [GRCh38] Chr4:71994591..79020242 [GRCh37] Chr4:72213455..79239266 [NCBI36] Chr4:4q13.3-21.21	pathogenic
GRCh38/hg38 4q12-22.3(chr4:51831622-97505618)x3	copy number gain	See cases [RCV000051772]	Chr4:51831622..97505618 [GRCh38] Chr4:52697788..98426769 [GRCh37] Chr4:52392545..98645792 [NCBI36] Chr4:4q12-22.3	pathogenic
GRCh38/hg38 4q13.2-21.23(chr4:67869564-85517308)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053294]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053294]\|See cases [RCV000053294]	Chr4:67869564..85517308 [GRCh38] Chr4:68735282..86438461 [GRCh37] Chr4:68417877..86657485 [NCBI36] Chr4:4q13.2-21.23	pathogenic
GRCh38/hg38 4q13.3-21.22(chr4:71079179-81802208)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053295]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053295]\|See cases [RCV000053295]	Chr4:71079179..81802208 [GRCh38] Chr4:71944896..82723361 [GRCh37] Chr4:72163760..82942385 [NCBI36] Chr4:4q13.3-21.22	pathogenic
GRCh38/hg38 4q13.3-22.1(chr4:74031395-90421127)x1	copy number loss	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053296]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053296]\|See cases [RCV000053296]	Chr4:74031395..90421127 [GRCh38] Chr4:74897112..91342278 [GRCh37] Chr4:75115976..91561301 [NCBI36] Chr4:4q13.3-22.1	pathogenic
GRCh38/hg38 4q13.3-21.3(chr4:72262258-86002147)x3	copy number gain	See cases [RCV000138312]	Chr4:72262258..86002147 [GRCh38] Chr4:73127975..86923300 [GRCh37] Chr4:73346839..87142324 [NCBI36] Chr4:4q13.3-21.3	pathogenic
GRCh38/hg38 4q21.1-21.21(chr4:75801143-79005805)x3	copy number gain	See cases [RCV000141486]	Chr4:75801143..79005805 [GRCh38] Chr4:76722296..79926959 [GRCh37] Chr4:76941320..80145983 [NCBI36] Chr4:4q21.1-21.21	pathogenic
GRCh38/hg38 4q13.2-22.3(chr4:68686088-95294456)x3	copy number gain	See cases [RCV000143458]	Chr4:68686088..95294456 [GRCh38] Chr4:69551806..96215607 [GRCh37] Chr4:69234401..96434630 [NCBI36] Chr4:4q13.2-22.3	pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:12440-190904441)x3	copy number gain	See cases [RCV000446653]	Chr4:12440..190904441 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)	copy number gain	See cases [RCV000510453]	Chr4:68346..190957473 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
NM_006835.3(CCNI):c.568G>A (p.Ala190Thr)	single nucleotide variant	not specified [RCV004315940]	Chr4:77055272 [GRCh38] Chr4:77976425 [GRCh37] Chr4:4q21.1	uncertain significance
GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)x3	copy number gain	See cases [RCV000512241]	Chr4:68346..190957473 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:49450-190915650)x3	copy number gain	not provided [RCV000743155]	Chr4:49450..190915650 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:49450-190963766)x3	copy number gain	not provided [RCV000743156]	Chr4:49450..190963766 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:11525-191028879)x3	copy number gain	not provided [RCV000743147]	Chr4:11525..191028879 [GRCh37] Chr4:4p16.3-q35.2	pathogenic
GRCh37/hg19 4q13.2-21.21(chr4:68950363-79738598)x1	copy number loss	not provided [RCV001005553]	Chr4:68950363..79738598 [GRCh37] Chr4:4q13.2-21.21	pathogenic
GRCh37/hg19 4q13.3-21.23(chr4:72680879-86426232)x1	copy number loss	not provided [RCV001005556]	Chr4:72680879..86426232 [GRCh37] Chr4:4q13.3-21.23	pathogenic
GRCh37/hg19 4q21.1(chr4:77242490-78093831)x1	copy number loss	not provided [RCV001005561]	Chr4:77242490..78093831 [GRCh37] Chr4:4q21.1	uncertain significance
NM_006835.3(CCNI):c.899T>C (p.Val300Ala)	single nucleotide variant	not specified [RCV004285856]	Chr4:77048454 [GRCh38] Chr4:77969607 [GRCh37] Chr4:4q21.1	uncertain significance
GRCh37/hg19 4q13.2-21.22(chr4:68242784-82991431)x3	copy number gain	not provided [RCV000845944]	Chr4:68242784..82991431 [GRCh37] Chr4:4q13.2-21.22	pathogenic
GRCh37/hg19 4q21.1(chr4:77278194-78393601)x3	copy number gain	not provided [RCV000848750]	Chr4:77278194..78393601 [GRCh37] Chr4:4q21.1	uncertain significance
GRCh37/hg19 4q21.1(chr4:77278194-78393601)x3	copy number gain	not provided [RCV000846115]	Chr4:77278194..78393601 [GRCh37] Chr4:4q21.1	uncertain significance
GRCh37/hg19 4q13.3-21.1(chr4:71561780-78304341)x1	copy number loss	not provided [RCV000846231]	Chr4:71561780..78304341 [GRCh37] Chr4:4q13.3-21.1	pathogenic
GRCh37/hg19 4q13.3-21.3(chr4:71412409-87920784)x1	copy number loss	See cases [RCV001263040]	Chr4:71412409..87920784 [GRCh37] Chr4:4q13.3-21.3	pathogenic
GRCh37/hg19 4q13.3-22.1(chr4:75737340-91131156)	copy number gain	not specified [RCV002053429]	Chr4:75737340..91131156 [GRCh37] Chr4:4q13.3-22.1	pathogenic
GRCh37/hg19 4q12-31.21(chr4:52866944-143582507)x3	copy number gain	not provided [RCV001827738]	Chr4:52866944..143582507 [GRCh37] Chr4:4q12-31.21	pathogenic
GRCh37/hg19 4q13.3-21.21(chr4:73055313-80083154)	copy number loss	not specified [RCV002053427]	Chr4:73055313..80083154 [GRCh37] Chr4:4q13.3-21.21	pathogenic
NC_000004.12:g.67833055_82716065del	deletion	See cases [RCV003313802]	Chr4:67833055..82716065 [GRCh38] Chr4:4q13.2-21.22	pathogenic
NM_006835.3(CCNI):c.733C>T (p.His245Tyr)	single nucleotide variant	not specified [RCV004121037]	Chr4:77048620 [GRCh38] Chr4:77969773 [GRCh37] Chr4:4q21.1	uncertain significance
NM_006835.3(CCNI):c.179A>G (p.Asn60Ser)	single nucleotide variant	not specified [RCV004089892]	Chr4:77058571 [GRCh38] Chr4:77979724 [GRCh37] Chr4:4q21.1	uncertain significance
GRCh37/hg19 4q13.3-21.21(chr4:74822261-79345650)x1	copy number loss	not specified [RCV003986507]	Chr4:74822261..79345650 [GRCh37] Chr4:4q13.3-21.21	uncertain significance
GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3	copy number gain	not provided [RCV003885507]	Chr4:45455621..191003541 [GRCh37] Chr4:4p12-q35.2	pathogenic
NM_006835.3(CCNI):c.616A>G (p.Met206Val)	single nucleotide variant	not specified [RCV004430762]	Chr4:77055224 [GRCh38] Chr4:77976377 [GRCh37] Chr4:4q21.1	uncertain significance
NM_006835.3(CCNI):c.238G>A (p.Val80Ile)	single nucleotide variant	not specified [RCV004430761]	Chr4:77058512 [GRCh38] Chr4:77979665 [GRCh37] Chr4:4q21.1	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1198
Count of miRNA genes:	705
Interacting mature miRNAs:	800
Transcripts:	ENST00000237654, ENST00000504697, ENST00000505609, ENST00000506614, ENST00000507788, ENST00000511943, ENST00000513774, ENST00000515468, ENST00000515790, ENST00000537948
Prediction methods:	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

SHGC-59775

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	77,969,307 - 77,969,453	UniSTS	GRCh37
Build 36	4	78,188,331 - 78,188,477	RGD	NCBI36
Celera	4	75,270,695 - 75,270,841	RGD
Cytogenetic Map	4	q21.1	UniSTS
HuRef	4	73,721,136 - 73,721,282	UniSTS
GeneMap99-GB4 RH Map	4	443.86	UniSTS

SHGC-80948

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	77,977,118 - 77,977,429	UniSTS	GRCh37
Build 36	4	78,196,142 - 78,196,453	RGD	NCBI36
Celera	4	75,278,506 - 75,278,817	RGD
Cytogenetic Map	4	q21.1	UniSTS
HuRef	4	73,728,947 - 73,729,258	UniSTS
TNG Radiation Hybrid Map	4	44931.0	UniSTS

SHGC-85345

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	77,977,251 - 77,977,586	UniSTS	GRCh37
Build 36	4	78,196,275 - 78,196,610	RGD	NCBI36
Celera	4	75,278,639 - 75,278,974	RGD
Cytogenetic Map	4	q21.1	UniSTS
HuRef	4	73,729,080 - 73,729,415	UniSTS
TNG Radiation Hybrid Map	4	44925.0	UniSTS

SHGC-132958

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	77,991,746 - 77,992,075	UniSTS	GRCh37
Build 36	4	78,210,770 - 78,211,099	RGD	NCBI36
Celera	4	75,293,126 - 75,293,455	RGD
Cytogenetic Map	4	q21.1	UniSTS
HuRef	4	73,743,572 - 73,743,901	UniSTS
TNG Radiation Hybrid Map	4	44904.0	UniSTS

D4S494

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	77,985,436 - 77,985,603	UniSTS	GRCh37
Build 36	4	78,204,460 - 78,204,627	RGD	NCBI36
Celera	4	75,286,823 - 75,286,990	RGD
Cytogenetic Map	4	q21.1	UniSTS
HuRef	4	73,737,265 - 73,737,432	UniSTS
TNG Radiation Hybrid Map	4	44994.0	UniSTS

D4S3098

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	77,969,256 - 77,969,448	UniSTS	GRCh37
Build 36	4	78,188,280 - 78,188,472	RGD	NCBI36
Celera	4	75,270,644 - 75,270,836	RGD
Cytogenetic Map	4	q21.1	UniSTS
HuRef	4	73,721,085 - 73,721,277	UniSTS
Whitehead-YAC Contig Map	4		UniSTS

SHGC-64017

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	77,970,151 - 77,970,267	UniSTS	GRCh37
Build 36	4	78,189,175 - 78,189,291	RGD	NCBI36
Celera	4	75,271,539 - 75,271,655	RGD
Cytogenetic Map	4	q21.1	UniSTS
HuRef	4	73,721,980 - 73,722,096	UniSTS
TNG Radiation Hybrid Map	4	44976.0	UniSTS

STS-N58372

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	77,970,152 - 77,970,424	UniSTS	GRCh37
Build 36	4	78,189,176 - 78,189,448	RGD	NCBI36
Celera	4	75,271,540 - 75,271,812	RGD
Cytogenetic Map	4	q21.1	UniSTS
HuRef	4	73,721,981 - 73,722,253	UniSTS
TNG Radiation Hybrid Map	4	44976.0	UniSTS
GeneMap99-GB4 RH Map	4	437.81	UniSTS
NCBI RH Map	4	903.2	UniSTS

SHGC-58048

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	77,991,760 - 77,991,995	UniSTS	GRCh37
Build 36	4	78,210,784 - 78,211,019	RGD	NCBI36
Celera	4	75,293,140 - 75,293,375	RGD
Cytogenetic Map	4	q21.1	UniSTS
HuRef	4	73,743,586 - 73,743,821	UniSTS

SHGC-67650

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	4	77,970,283 - 77,970,423	UniSTS	GRCh37
Build 36	4	78,189,307 - 78,189,447	RGD	NCBI36
Celera	4	75,271,671 - 75,271,811	RGD
Cytogenetic Map	4	q21.1	UniSTS
HuRef	4	73,722,112 - 73,722,252	UniSTS
GeneMap99-GB4 RH Map	4	443.86	UniSTS

Expression

RNA-SEQ Expression

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2437	2788	2253	4973	1726	2351	6	624	1951	465	2269	7305	6471	53	3734	1	852	1744	1617	175	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001348132	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001348133	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001348134	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001348135	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001348136	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001348137	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001348138	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001348139	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001348140	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_006835	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB209766	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC104771	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC111196	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF135162	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK222931	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK301111	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK312632	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY207372	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC000420	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC004975	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BT020019	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471057	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068274	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CR541783	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	D50310	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000237654 ⟹ ENSP00000237654

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	77,047,155 - 77,075,989 (-)	Ensembl

Ensembl Acc Id:

ENST00000504697

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	77,056,065 - 77,065,080 (-)	Ensembl

Ensembl Acc Id:

ENST00000505609 ⟹ ENSP00000426467

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	77,056,044 - 77,074,910 (-)	Ensembl

Ensembl Acc Id:

ENST00000506614

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	77,055,234 - 77,056,485 (-)	Ensembl

Ensembl Acc Id:

ENST00000507788 ⟹ ENSP00000421594

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	77,047,155 - 77,076,309 (-)	Ensembl

Ensembl Acc Id:

ENST00000511943 ⟹ ENSP00000425360

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	77,055,323 - 77,075,693 (-)	Ensembl

Ensembl Acc Id:

ENST00000513774 ⟹ ENSP00000426235

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	77,058,510 - 77,075,332 (-)	Ensembl

Ensembl Acc Id:

ENST00000515468 ⟹ ENSP00000425935

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	77,048,115 - 77,056,049 (-)	Ensembl

Ensembl Acc Id:

ENST00000515790

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	77,066,165 - 77,075,620 (-)	Ensembl

Ensembl Acc Id:

ENST00000718433 ⟹ ENSP00000520818

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	4	77,047,155 - 77,075,989 (-)	Ensembl

RefSeq Acc Id:

NM_001348132 ⟹ NP_001335061

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	77,047,155 - 77,075,989 (-)	NCBI
T2T-CHM13v2.0	4	80,387,967 - 80,416,780 (-)	NCBI

Sequence:

show sequence

CTCCCTCCCCAGCCTTCCCCGCGAGCGGACGCGGCAGCGCCTCTGTCTCGCTTTTTCTTATTTT
TCCCCCCTTTCCCCTTTCTTTTTTTTTTTTTCTTTTCTTTTCTCCCCTCCCCCCCTTTCACCAT
TTCCCCTCGGAGGCGCTTTCCCCGGGCAGGGGCAGAGCCGGTCTCACCCCCCGCCTCTCCCCGG
CCCCCGCCGCCCTATGGCGAGAGGGAGCCCCCTCCCAACCCGGGCTCGAGCGGCGGCGGCCTCA
GGCCGGGGGTCATCATGGAACTAATTCGCTGACCGACCCAGCGGCCGCAGCCGTGCGTCCCGCT
CGAGCGCCAGCGCCCGCGCCCGCGCCCCCCGATCCGCTTCCCCTTTCTCCCTCCTCAGTTGGCC
GAGTCGTCCCGCGCGCACCGCCTCCGCGCGCCTATGAGAATGAGGTGGTAACGGGCCCCCGGAT
GACCCCGCGTCACCACTGTGAGGCCTACAGCTCTGCCGGGGAGGAGGAGGAGGAGGAAGAGGAG
GAGAAGCTACAGCAAGCTGGGTAGCAGGCAGATCCAAAGGATATCATGAAGTTTCCAGGGCCTT
TGGAAAACCAGAGATTGTCTTTCCTGTTGGAAAAGGCAATCACTAGGGAAGCACAGATGTGGAA
AGTGAATGTGCGGAAAATGCCTTCAAATCAGAATGTTTCTCCATCCCAGAGAGATGAAGTAATT
CAATGGCTGGCCAAACTCAAGTACCAATTCAACCTTTACCCAGAAACATTTGCTCTGGCTAGCA
GTCTTTTGGATAGGTTTTTAGCTACCGTAAAGGCTCATCCAAAATACTTGAGTTGTATTGCAAT
CAGCTGTTTTTTCCTAGCTGCCAAGACTGTTGAGGAAGATGAGAGAATTCCAGTACTAAAGGTA
TTGGCAAGAGACAGTTTCTGTGGATGTTCCTCATCTGAAATTTTGAGAATGGAGAGAATTATTC
TGGATAAGTTGAATTGGGATCTTCACACAGCCACACCATTGGATTTTCTTCATATTTTCCATGC
CATTGCAGTGTCAACTAGGCCTCAGTTACTTTTCAGTTTGCCCAAATTGAGCCCATCTCAACAT
TTGGCAGTCCTTACCAAGCAACTACTTCACTGTATGGCCTGCAACCAACTTCTGCAATTCAGAG
GATCCATGCTTGCTCTGGCCATGGTTAGTCTGGAAATGGAGAAACTCATTCCTGATTGGCTTTC
TCTTACAATTGAACTGCTTCAGAAAGCACAGATGGATAGCTCCCAGTTGATCCATTGTCGGGAG
CTTGTGGCACATCACCTTTCTACTCTGCAGTCTTCCCTGCCTCTGAATTCCGTTTATGTCTACC
GTCCCCTCAAGCACACCCTGGTGACCTGTGACAAAGGAGTGTTCAGATTACATCCCTCCTCTGT
CCCAGGCCCAGACTTCTCCAAGGACAACAGCAAGCCAGAAGTGCCAGTCAGAGGTACAGCAGCC
TTTTACCATCATCTCCCAGCTGCCAGTGGGTGCAAGCAGACCTCTACTAAACGCAAAGTAGAGG
AAATGGAAGTGGATGACTTCTATGATGGAATCAAACGGCTCTATAATGAAGATAATGTCTCAGA
AAATGTGGGTTCTGTGTGTGGCACTGATTTATCAAGACAAGAGGGACATGCTTCCCCTTGTCCA
CCTTTGCAGCCTGTTTCTGTCATGTAGTTTCAACAAGTGCTACCTTTGAGTGTAAACTAAGGTA
GACTACTTTGGGAATGAGAACATGCAAAATCAGGAAAGGCTGTAGAAGGAAATATACCTTAACA
GGCTGATTTGGAGTGAGCCAGAAAAAAAAAATAAAACTCTCATTATTTGTGTGGCTAATTATAA
TTCAGCGTTATTTAAGCACATAAAGACCAAAAAAAAAAAAAAGAAATCCAAAAGATCCAAACTT
TTTTTAAACTTAAAAAATCTCTTTGTAGTATGTCAGTTGCACTTTTTTTCTGCCATAATGTAAC
GTAGCTTGCCCCGTCAAAAATTCAATTAAAATTCATGGCCAGCAATCCTGTTCCCCCTCAGCAT
CCTGATTTAATTTTCCTGTTGCTTTTGCTTGCTTCTCCATTTAATAGTTACTGAACTTTATGCA
TGTTGATCTATATTGATTTTCACTGCAGTTGAATGAACAAATTATTTCAGTGTGACAGCCATGA
CTCAAGTTCCAATTAGTCTGAAAAGGGTACTTTGGAATTGTCCCATATTAATCAGAGATGGCAA
AAGAAAAAGTTCTCATATTACCAGGTTGATTTTGTGTCTCATTTCAAATTTTAATTTAAAATTA
TGGTTTTCATTTTTGTTTACCTTAAAGTGATGCTTAAAAGTGGCATGTAATTAGGACACTTAGG
TTTGTTGAAAGCATTTTCGACATTTGTATAAAAGAATTTGTGATAAATATATCCAGGTGCTCAC
CAAAGAAACATGTATTAACAACTTAAATTAGATTTTTCTAACTGATAGTTTTCACTCATTTATA
ATCAGTAGGAGAGACTGTCTAGATGTTGGGGCAGCTCTATGATTTAAGTCTGTAACATGTTATA
ACTGAATTTAGTACCCTAGTTTTGTTAAGCTATTAGGATTTTCTAATAGAACTTACTCCCCCTG
CCTCCCCAGCCTTATGTTTCTTTTAATGACTTCTGGATCCTGAGCTCCCTTTGCAGTCTGAAAA
AGGTATTGCAGTCAGAACTGTGTACTGATGATAAAAGCCTCTGGTAGCAATAAAAAGTTGTCCT
TAA

hide sequence

RefSeq Acc Id:

NM_001348133 ⟹ NP_001335062

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	77,047,155 - 77,074,910 (-)	NCBI
T2T-CHM13v2.0	4	80,387,967 - 80,415,701 (-)	NCBI

Sequence:

show sequence

AAATAACTGGAATTTGAAAGGAGGACAGAGGAGCCTCCGCTGGAGCTAGGGGGCTCCGTTACAG
ATCCTTTTGGCAGAAGTTGACAATTGGGTATCAAAACAGTGGAAGGTGTTTCGGGAGGTAGCTA
CAGCAAGCTGGGTAGCAGGCAGATCCAAAGGATATCATGAAGTTTCCAGGGCCTTTGGAAAACC
AGAGATTGTCTTTCCTGTTGGAAAAGGCAATCACTAGGGAAGCACAGATGTGGAAAGTGAATGT
GCGGAAAATGCCTTCAAATCAGAATGTTTCTCCATCCCAGAGAGATGAAGTAATTCAATGGCTG
GCCAAACTCAAGTACCAATTCAACCTTTACCCAGAAACATTTGCTCTGGCTAGCAGTCTTTTGG
ATAGGTTTTTAGCTACCGTAAAGGCTCATCCAAAATACTTGAGTTGTATTGCAATCAGCTGTTT
TTTCCTAGCTGCCAAGACTGTTGAGGAAGATGAGAGAATTCCAGTACTAAAGGTATTGGCAAGA
GACAGTTTCTGTGGATGTTCCTCATCTGAAATTTTGAGAATGGAGAGAATTATTCTGGATAAGT
TGAATTGGGATCTTCACACAGCCACACCATTGGATTTTCTTCATATTTTCCATGCCATTGCAGT
GTCAACTAGGCCTCAGTTACTTTTCAGTTTGCCCAAATTGAGCCCATCTCAACATTTGGCAGTC
CTTACCAAGCAACTACTTCACTGTATGGCCTGCAACCAACTTCTGCAATTCAGAGGATCCATGC
TTGCTCTGGCCATGGTTAGTCTGGAAATGGAGAAACTCATTCCTGATTGGCTTTCTCTTACAAT
TGAACTGCTTCAGAAAGCACAGATGGATAGCTCCCAGTTGATCCATTGTCGGGAGCTTGTGGCA
CATCACCTTTCTACTCTGCAGTCTTCCCTGCCTCTGAATTCCGTTTATGTCTACCGTCCCCTCA
AGCACACCCTGGTGACCTGTGACAAAGGAGTGTTCAGATTACATCCCTCCTCTGTCCCAGGCCC
AGACTTCTCCAAGGACAACAGCAAGCCAGAAGTGCCAGTCAGAGGTACAGCAGCCTTTTACCAT
CATCTCCCAGCTGCCAGTGGGTGCAAGCAGACCTCTACTAAACGCAAAGTAGAGGAAATGGAAG
TGGATGACTTCTATGATGGAATCAAACGGCTCTATAATGAAGATAATGTCTCAGAAAATGTGGG
TTCTGTGTGTGGCACTGATTTATCAAGACAAGAGGGACATGCTTCCCCTTGTCCACCTTTGCAG
CCTGTTTCTGTCATGTAGTTTCAACAAGTGCTACCTTTGAGTGTAAACTAAGGTAGACTACTTT
GGGAATGAGAACATGCAAAATCAGGAAAGGCTGTAGAAGGAAATATACCTTAACAGGCTGATTT
GGAGTGAGCCAGAAAAAAAAAATAAAACTCTCATTATTTGTGTGGCTAATTATAATTCAGCGTT
ATTTAAGCACATAAAGACCAAAAAAAAAAAAAAGAAATCCAAAAGATCCAAACTTTTTTTAAAC
TTAAAAAATCTCTTTGTAGTATGTCAGTTGCACTTTTTTTCTGCCATAATGTAACGTAGCTTGC
CCCGTCAAAAATTCAATTAAAATTCATGGCCAGCAATCCTGTTCCCCCTCAGCATCCTGATTTA
ATTTTCCTGTTGCTTTTGCTTGCTTCTCCATTTAATAGTTACTGAACTTTATGCATGTTGATCT
ATATTGATTTTCACTGCAGTTGAATGAACAAATTATTTCAGTGTGACAGCCATGACTCAAGTTC
CAATTAGTCTGAAAAGGGTACTTTGGAATTGTCCCATATTAATCAGAGATGGCAAAAGAAAAAG
TTCTCATATTACCAGGTTGATTTTGTGTCTCATTTCAAATTTTAATTTAAAATTATGGTTTTCA
TTTTTGTTTACCTTAAAGTGATGCTTAAAAGTGGCATGTAATTAGGACACTTAGGTTTGTTGAA
AGCATTTTCGACATTTGTATAAAAGAATTTGTGATAAATATATCCAGGTGCTCACCAAAGAAAC
ATGTATTAACAACTTAAATTAGATTTTTCTAACTGATAGTTTTCACTCATTTATAATCAGTAGG
AGAGACTGTCTAGATGTTGGGGCAGCTCTATGATTTAAGTCTGTAACATGTTATAACTGAATTT
AGTACCCTAGTTTTGTTAAGCTATTAGGATTTTCTAATAGAACTTACTCCCCCTGCCTCCCCAG
CCTTATGTTTCTTTTAATGACTTCTGGATCCTGAGCTCCCTTTGCAGTCTGAAAAAGGTATTGC
AGTCAGAACTGTGTACTGATGATAAAAGCCTCTGGTAGCAATAAAAAGTTGTCCTTAA

hide sequence

RefSeq Acc Id:

NM_001348134 ⟹ NP_001335063

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	77,047,155 - 77,075,989 (-)	NCBI
T2T-CHM13v2.0	4	80,387,967 - 80,416,780 (-)	NCBI

Sequence:

show sequence

CTCCCTCCCCAGCCTTCCCCGCGAGCGGACGCGGCAGCGCCTCTGTCTCGCTTTTTCTTATTTT
TCCCCCCTTTCCCCTTTCTTTTTTTTTTTTTCTTTTCTTTTCTCCCCTCCCCCCCTTTCACCAT
TTCCCCTCGGAGGCGCTTTCCCCGGGCAGGGGCAGAGCCGGTCTCACCCCCCGCCTCTCCCCGG
CCCCCGCCGCCCTATGGCGAGAGGGAGCCCCCTCCCAACCCGGGCTCGAGCGGCGGCGGCCTCA
GGCCGGGGGTCATCATGGAACTAATTCGCTGACCGACCCAGCGGCCGCAGCCGTGCGTCCCGCT
CGAGCGCCAGCGCCCGCGCCCGCGCCCCCCGATCCGCTTCCCCTTTCTCCCTCCTCAGTTGGCC
GAGTCGTCCCGCGCGCACCGCCTCCGCGCGCCTATGAGAATGAGGTGGTAACGGGCCCCCGGAT
GACCCCGCGTCACCACTGTGAGGCCTACAGCTCTGCCGGGGAGGAGGAGGAGGAGGAAGAGGAG
GAGAAGAATGTTTCTCCATCCCAGAGAGATGAAGTAATTCAATGGCTGGCCAAACTCAAGTACC
AATTCAACCTTTACCCAGAAACATTTGCTCTGGCTAGCAGTCTTTTGGATAGGTTTTTAGCTAC
CGTAAAGGCTCATCCAAAATACTTGAGTTGTATTGCAATCAGCTGTTTTTTCCTAGCTGCCAAG
ACTGTTGAGGAAGATGAGAGAATTCCAGTACTAAAGGTATTGGCAAGAGACAGTTTCTGTGGAT
GTTCCTCATCTGAAATTTTGAGAATGGAGAGAATTATTCTGGATAAGTTGAATTGGGATCTTCA
CACAGCCACACCATTGGATTTTCTTCATATTTTCCATGCCATTGCAGTGTCAACTAGGCCTCAG
TTACTTTTCAGTTTGCCCAAATTGAGCCCATCTCAACATTTGGCAGTCCTTACCAAGCAACTAC
TTCACTGTATGGCCTGCAACCAACTTCTGCAATTCAGAGGATCCATGCTTGCTCTGGCCATGGT
TAGTCTGGAAATGGAGAAACTCATTCCTGATTGGCTTTCTCTTACAATTGAACTGCTTCAGAAA
GCACAGATGGATAGCTCCCAGTTGATCCATTGTCGGGAGCTTGTGGCACATCACCTTTCTACTC
TGCAGTCTTCCCTGCCTCTGAATTCCGTTTATGTCTACCGTCCCCTCAAGCACACCCTGGTGAC
CTGTGACAAAGGAGTGTTCAGATTACATCCCTCCTCTGTCCCAGGCCCAGACTTCTCCAAGGAC
AACAGCAAGCCAGAAGTGCCAGTCAGAGGTACAGCAGCCTTTTACCATCATCTCCCAGCTGCCA
GTGGGTGCAAGCAGACCTCTACTAAACGCAAAGTAGAGGAAATGGAAGTGGATGACTTCTATGA
TGGAATCAAACGGCTCTATAATGAAGATAATGTCTCAGAAAATGTGGGTTCTGTGTGTGGCACT
GATTTATCAAGACAAGAGGGACATGCTTCCCCTTGTCCACCTTTGCAGCCTGTTTCTGTCATGT
AGTTTCAACAAGTGCTACCTTTGAGTGTAAACTAAGGTAGACTACTTTGGGAATGAGAACATGC
AAAATCAGGAAAGGCTGTAGAAGGAAATATACCTTAACAGGCTGATTTGGAGTGAGCCAGAAAA
AAAAAATAAAACTCTCATTATTTGTGTGGCTAATTATAATTCAGCGTTATTTAAGCACATAAAG
ACCAAAAAAAAAAAAAAGAAATCCAAAAGATCCAAACTTTTTTTAAACTTAAAAAATCTCTTTG
TAGTATGTCAGTTGCACTTTTTTTCTGCCATAATGTAACGTAGCTTGCCCCGTCAAAAATTCAA
TTAAAATTCATGGCCAGCAATCCTGTTCCCCCTCAGCATCCTGATTTAATTTTCCTGTTGCTTT
TGCTTGCTTCTCCATTTAATAGTTACTGAACTTTATGCATGTTGATCTATATTGATTTTCACTG
CAGTTGAATGAACAAATTATTTCAGTGTGACAGCCATGACTCAAGTTCCAATTAGTCTGAAAAG
GGTACTTTGGAATTGTCCCATATTAATCAGAGATGGCAAAAGAAAAAGTTCTCATATTACCAGG
TTGATTTTGTGTCTCATTTCAAATTTTAATTTAAAATTATGGTTTTCATTTTTGTTTACCTTAA
AGTGATGCTTAAAAGTGGCATGTAATTAGGACACTTAGGTTTGTTGAAAGCATTTTCGACATTT
GTATAAAAGAATTTGTGATAAATATATCCAGGTGCTCACCAAAGAAACATGTATTAACAACTTA
AATTAGATTTTTCTAACTGATAGTTTTCACTCATTTATAATCAGTAGGAGAGACTGTCTAGATG
TTGGGGCAGCTCTATGATTTAAGTCTGTAACATGTTATAACTGAATTTAGTACCCTAGTTTTGT
TAAGCTATTAGGATTTTCTAATAGAACTTACTCCCCCTGCCTCCCCAGCCTTATGTTTCTTTTA
ATGACTTCTGGATCCTGAGCTCCCTTTGCAGTCTGAAAAAGGTATTGCAGTCAGAACTGTGTAC
TGATGATAAAAGCCTCTGGTAGCAATAAAAAGTTGTCCTTAA

hide sequence

RefSeq Acc Id:

NM_001348135 ⟹ NP_001335064

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	77,047,155 - 77,075,989 (-)	NCBI
T2T-CHM13v2.0	4	80,387,967 - 80,416,780 (-)	NCBI

Sequence:

show sequence

CTCCCTCCCCAGCCTTCCCCGCGAGCGGACGCGGCAGCGCCTCTGTCTCGCTTTTTCTTATTTT
TCCCCCCTTTCCCCTTTCTTTTTTTTTTTTTCTTTTCTTTTCTCCCCTCCCCCCCTTTCACCAT
TTCCCCTCGGAGGCGCTTTCCCCGGGCAGGGGCAGAGCCGGTCTCACCCCCCGCCTCTCCCCGG
CCCCCGCCGCCCTATGGCGAGAGGGAGCCCCCTCCCAACCCGGGCTCGAGCGGCGGCGGCCTCA
GGCCGGGGGTCATCATGGAACTAATTCGCTGACCGACCCAGCGGCCGCAGCCGTGCGTCCCGCT
CGAGCGCCAGCGCCCGCGCCCGCGCCCCCCGATCCGCTTCCCCTTTCTCCCTCCTCAGTTGGCC
GAGTCGTCCCGCGCGCACCGCCTCCGCGCGCCTATGAGAATGAGGTGGTAACGGGCCCCCGGAT
GACCCCGCGTCACCACTGTGAGGCCTACAGCTCTGCCGGGGAGGAGGAGGAGGAGGAAGAGGAG
GAGAAGGTAGCTACAGCAAGCTGGGTAGCAGGCAGATCCAAAGGATATCATGAAGTTTCCAGGG
CCTTTGGAAAACCAGAGATTGTCTTTCCTGTTGGAAAAGGCAATCACTAGGGAAGCACAGATGT
GGAAAGTGAATGTGCGGAAAATGCCTTCAAATCAGAATGTTTCTCCATCCCAGAGAGATGAAGT
AATTCAATGGCTGGCCAAACTCAAGTACCAATTCAACCTTTACCCAGAAACATTTGCTCTGGCT
AGCAGTCTTTTGGATAGGTTTTTAGCTACCGTAAAGGCTCATCCAAAATACTTGAGTTGTATTG
CAATCAGCTGTTTTTTCCTAGCTGCCAAGACTGTTGAGGAAGATGAGAGAATTCCAGTACTAAA
GTTCCATGCCATTGCAGTGTCAACTAGGCCTCAGTTACTTTTCAGTTTGCCCAAATTGAGCCCA
TCTCAACATTTGGCAGTCCTTACCAAGCAACTACTTCACTGTATGGCCTGCAACCAACTTCTGC
AATTCAGAGGATCCATGCTTGCTCTGGCCATGGTTAGTCTGGAAATGGAGAAACTCATTCCTGA
TTGGCTTTCTCTTACAATTGAACTGCTTCAGAAAGCACAGATGGATAGCTCCCAGTTGATCCAT
TGTCGGGAGCTTGTGGCACATCACCTTTCTACTCTGCAGTCTTCCCTGCCTCTGAATTCCGTTT
ATGTCTACCGTCCCCTCAAGCACACCCTGGTGACCTGTGACAAAGGAGTGTTCAGATTACATCC
CTCCTCTGTCCCAGGCCCAGACTTCTCCAAGGACAACAGCAAGCCAGAAGTGCCAGTCAGAGGT
ACAGCAGCCTTTTACCATCATCTCCCAGCTGCCAGTGGGTGCAAGCAGACCTCTACTAAACGCA
AAGTAGAGGAAATGGAAGTGGATGACTTCTATGATGGAATCAAACGGCTCTATAATGAAGATAA
TGTCTCAGAAAATGTGGGTTCTGTGTGTGGCACTGATTTATCAAGACAAGAGGGACATGCTTCC
CCTTGTCCACCTTTGCAGCCTGTTTCTGTCATGTAGTTTCAACAAGTGCTACCTTTGAGTGTAA
ACTAAGGTAGACTACTTTGGGAATGAGAACATGCAAAATCAGGAAAGGCTGTAGAAGGAAATAT
ACCTTAACAGGCTGATTTGGAGTGAGCCAGAAAAAAAAAATAAAACTCTCATTATTTGTGTGGC
TAATTATAATTCAGCGTTATTTAAGCACATAAAGACCAAAAAAAAAAAAAAGAAATCCAAAAGA
TCCAAACTTTTTTTAAACTTAAAAAATCTCTTTGTAGTATGTCAGTTGCACTTTTTTTCTGCCA
TAATGTAACGTAGCTTGCCCCGTCAAAAATTCAATTAAAATTCATGGCCAGCAATCCTGTTCCC
CCTCAGCATCCTGATTTAATTTTCCTGTTGCTTTTGCTTGCTTCTCCATTTAATAGTTACTGAA
CTTTATGCATGTTGATCTATATTGATTTTCACTGCAGTTGAATGAACAAATTATTTCAGTGTGA
CAGCCATGACTCAAGTTCCAATTAGTCTGAAAAGGGTACTTTGGAATTGTCCCATATTAATCAG
AGATGGCAAAAGAAAAAGTTCTCATATTACCAGGTTGATTTTGTGTCTCATTTCAAATTTTAAT
TTAAAATTATGGTTTTCATTTTTGTTTACCTTAAAGTGATGCTTAAAAGTGGCATGTAATTAGG
ACACTTAGGTTTGTTGAAAGCATTTTCGACATTTGTATAAAAGAATTTGTGATAAATATATCCA
GGTGCTCACCAAAGAAACATGTATTAACAACTTAAATTAGATTTTTCTAACTGATAGTTTTCAC
TCATTTATAATCAGTAGGAGAGACTGTCTAGATGTTGGGGCAGCTCTATGATTTAAGTCTGTAA
CATGTTATAACTGAATTTAGTACCCTAGTTTTGTTAAGCTATTAGGATTTTCTAATAGAACTTA
CTCCCCCTGCCTCCCCAGCCTTATGTTTCTTTTAATGACTTCTGGATCCTGAGCTCCCTTTGCA
GTCTGAAAAAGGTATTGCAGTCAGAACTGTGTACTGATGATAAAAGCCTCTGGTAGCAATAAAA
AGTTGTCCTTAA

hide sequence

RefSeq Acc Id:

NM_001348136 ⟹ NP_001335065

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	77,047,155 - 77,075,989 (-)	NCBI
T2T-CHM13v2.0	4	80,387,967 - 80,416,780 (-)	NCBI

Sequence:

show sequence

CTCCCTCCCCAGCCTTCCCCGCGAGCGGACGCGGCAGCGCCTCTGTCTCGCTTTTTCTTATTTT
TCCCCCCTTTCCCCTTTCTTTTTTTTTTTTTCTTTTCTTTTCTCCCCTCCCCCCCTTTCACCAT
TTCCCCTCGGAGGCGCTTTCCCCGGGCAGGGGCAGAGCCGGTCTCACCCCCCGCCTCTCCCCGG
CCCCCGCCGCCCTATGGCGAGAGGGAGCCCCCTCCCAACCCGGGCTCGAGCGGCGGCGGCCTCA
GGCCGGGGGTCATCATGGAACTAATTCGCTGACCGACCCAGCGGCCGCAGCCGTGCGTCCCGCT
CGAGCGCCAGCGCCCGCGCCCGCGCCCCCCGATCCGCTTCCCCTTTCTCCCTCCTCAGTTGGCC
GAGTCGTCCCGCGCGCACCGCCTCCGCGCGCCTATGAGAATGAGGTGGTAACGGGCCCCCGGAT
GACCCCGCGTCACCACTGTGAGGCCTACAGCTCTGCCGGGGAGGAGGAGGAGGAGGAAGAGGAG
GAGAAGGTAGCTACAGCAAGCTGGGTAGCAGGCAGATCCAAAGGATATCATGAAGTTTCCAGGG
CCTTTGGAAAACCAGAGATTGTCTTTCCTGTTGGAAAAGGCAATCACTAGGGAAGCACAGATGT
GGAAAGTGAATGTGCGGAAAATGCCTTCAAATCAGGCTCATCCAAAATACTTGAGTTGTATTGC
AATCAGCTGTTTTTTCCTAGCTGCCAAGACTGTTGAGGAAGATGAGAGAATTCCAGTACTAAAG
GTATTGGCAAGAGACAGTTTCTGTGGATGTTCCTCATCTGAAATTTTGAGAATGGAGAGAATTA
TTCTGGATAAGTTGAATTGGGATCTTCACACAGCCACACCATTGGATTTTCTTCATATTTTCCA
TGCCATTGCAGTGTCAACTAGGCCTCAGTTACTTTTCAGTTTGCCCAAATTGAGCCCATCTCAA
CATTTGGCAGTCCTTACCAAGCAACTACTTCACTGTATGGCCTGCAACCAACTTCTGCAATTCA
GAGGATCCATGCTTGCTCTGGCCATGGTTAGTCTGGAAATGGAGAAACTCATTCCTGATTGGCT
TTCTCTTACAATTGAACTGCTTCAGAAAGCACAGATGGATAGCTCCCAGTTGATCCATTGTCGG
GAGCTTGTGGCACATCACCTTTCTACTCTGCAGTCTTCCCTGCCTCTGAATTCCGTTTATGTCT
ACCGTCCCCTCAAGCACACCCTGGTGACCTGTGACAAAGGAGTGTTCAGATTACATCCCTCCTC
TGTCCCAGGCCCAGACTTCTCCAAGGACAACAGCAAGCCAGAAGTGCCAGTCAGAGGTACAGCA
GCCTTTTACCATCATCTCCCAGCTGCCAGTGGGTGCAAGCAGACCTCTACTAAACGCAAAGTAG
AGGAAATGGAAGTGGATGACTTCTATGATGGAATCAAACGGCTCTATAATGAAGATAATGTCTC
AGAAAATGTGGGTTCTGTGTGTGGCACTGATTTATCAAGACAAGAGGGACATGCTTCCCCTTGT
CCACCTTTGCAGCCTGTTTCTGTCATGTAGTTTCAACAAGTGCTACCTTTGAGTGTAAACTAAG
GTAGACTACTTTGGGAATGAGAACATGCAAAATCAGGAAAGGCTGTAGAAGGAAATATACCTTA
ACAGGCTGATTTGGAGTGAGCCAGAAAAAAAAAATAAAACTCTCATTATTTGTGTGGCTAATTA
TAATTCAGCGTTATTTAAGCACATAAAGACCAAAAAAAAAAAAAAGAAATCCAAAAGATCCAAA
CTTTTTTTAAACTTAAAAAATCTCTTTGTAGTATGTCAGTTGCACTTTTTTTCTGCCATAATGT
AACGTAGCTTGCCCCGTCAAAAATTCAATTAAAATTCATGGCCAGCAATCCTGTTCCCCCTCAG
CATCCTGATTTAATTTTCCTGTTGCTTTTGCTTGCTTCTCCATTTAATAGTTACTGAACTTTAT
GCATGTTGATCTATATTGATTTTCACTGCAGTTGAATGAACAAATTATTTCAGTGTGACAGCCA
TGACTCAAGTTCCAATTAGTCTGAAAAGGGTACTTTGGAATTGTCCCATATTAATCAGAGATGG
CAAAAGAAAAAGTTCTCATATTACCAGGTTGATTTTGTGTCTCATTTCAAATTTTAATTTAAAA
TTATGGTTTTCATTTTTGTTTACCTTAAAGTGATGCTTAAAAGTGGCATGTAATTAGGACACTT
AGGTTTGTTGAAAGCATTTTCGACATTTGTATAAAAGAATTTGTGATAAATATATCCAGGTGCT
CACCAAAGAAACATGTATTAACAACTTAAATTAGATTTTTCTAACTGATAGTTTTCACTCATTT
ATAATCAGTAGGAGAGACTGTCTAGATGTTGGGGCAGCTCTATGATTTAAGTCTGTAACATGTT
ATAACTGAATTTAGTACCCTAGTTTTGTTAAGCTATTAGGATTTTCTAATAGAACTTACTCCCC
CTGCCTCCCCAGCCTTATGTTTCTTTTAATGACTTCTGGATCCTGAGCTCCCTTTGCAGTCTGA
AAAAGGTATTGCAGTCAGAACTGTGTACTGATGATAAAAGCCTCTGGTAGCAATAAAAAGTTGT
CCTTAA

hide sequence

RefSeq Acc Id:

NM_001348137 ⟹ NP_001335066

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	77,047,155 - 77,075,989 (-)	NCBI
T2T-CHM13v2.0	4	80,387,967 - 80,416,780 (-)	NCBI

Sequence:

show sequence

CTCCCTCCCCAGCCTTCCCCGCGAGCGGACGCGGCAGCGCCTCTGTCTCGCTTTTTCTTATTTT
TCCCCCCTTTCCCCTTTCTTTTTTTTTTTTTCTTTTCTTTTCTCCCCTCCCCCCCTTTCACCAT
TTCCCCTCGGAGGCGCTTTCCCCGGGCAGGGGCAGAGCCGGTCTCACCCCCCGCCTCTCCCCGG
CCCCCGCCGCCCTATGGCGAGAGGGAGCCCCCTCCCAACCCGGGCTCGAGCGGCGGCGGCCTCA
GGCCGGGGGTCATCATGGAACTAATTCGCTGACCGACCCAGCGGCCGCAGCCGTGCGTCCCGCT
CGAGCGCCAGCGCCCGCGCCCGCGCCCCCCGATCCGCTTCCCCTTTCTCCCTCCTCAGTTGGCC
GAGTCGTCCCGCGCGCACCGCCTCCGCGCGCCTATGAGAATGAGGTGGTAACGGGCCCCCGGAT
GACCCCGCGTCACCACTGTGAGGCCTACAGCTCTGCCGGGGAGGAGGAGGAGGAGGAAGAGGAG
GAGAAGGTAGCTACAGCAAGCTGGGTAGCAGGCAGATCCAAAGGATATCATGAAGTTTCCAGGG
CCTTTGGAAAACCAGAGATTGTCTTTCCTGTTGGAAAAGGCAATCACTAGGGAAGCACAGATGT
GGAAAGTGAATGTGCGGAAAATGCCTTCAAATCAGAATGTTTCTCCATCCCAGAGAGATGAAGT
AATTCAATGGCTGGCCAAACTCAAGTACCAATTCAACCTTTACCCAGAAACATTTGCTCTGGCT
AGCAGTCTTTTGGATAGGTTTTTAGCTACCGTAAAGTTCCATGCCATTGCAGTGTCAACTAGGC
CTCAGTTACTTTTCAGTTTGCCCAAATTGAGCCCATCTCAACATTTGGCAGTCCTTACCAAGCA
ACTACTTCACTGTATGGCCTGCAACCAACTTCTGCAATTCAGAGGATCCATGCTTGCTCTGGCC
ATGGTTAGTCTGGAAATGGAGAAACTCATTCCTGATTGGCTTTCTCTTACAATTGAACTGCTTC
AGAAAGCACAGATGGATAGCTCCCAGTTGATCCATTGTCGGGAGCTTGTGGCACATCACCTTTC
TACTCTGCAGTCTTCCCTGCCTCTGAATTCCGTTTATGTCTACCGTCCCCTCAAGCACACCCTG
GTGACCTGTGACAAAGGAGTGTTCAGATTACATCCCTCCTCTGTCCCAGGCCCAGACTTCTCCA
AGGACAACAGCAAGCCAGAAGTGCCAGTCAGAGGTACAGCAGCCTTTTACCATCATCTCCCAGC
TGCCAGTGGGTGCAAGCAGACCTCTACTAAACGCAAAGTAGAGGAAATGGAAGTGGATGACTTC
TATGATGGAATCAAACGGCTCTATAATGAAGATAATGTCTCAGAAAATGTGGGTTCTGTGTGTG
GCACTGATTTATCAAGACAAGAGGGACATGCTTCCCCTTGTCCACCTTTGCAGCCTGTTTCTGT
CATGTAGTTTCAACAAGTGCTACCTTTGAGTGTAAACTAAGGTAGACTACTTTGGGAATGAGAA
CATGCAAAATCAGGAAAGGCTGTAGAAGGAAATATACCTTAACAGGCTGATTTGGAGTGAGCCA
GAAAAAAAAAATAAAACTCTCATTATTTGTGTGGCTAATTATAATTCAGCGTTATTTAAGCACA
TAAAGACCAAAAAAAAAAAAAAGAAATCCAAAAGATCCAAACTTTTTTTAAACTTAAAAAATCT
CTTTGTAGTATGTCAGTTGCACTTTTTTTCTGCCATAATGTAACGTAGCTTGCCCCGTCAAAAA
TTCAATTAAAATTCATGGCCAGCAATCCTGTTCCCCCTCAGCATCCTGATTTAATTTTCCTGTT
GCTTTTGCTTGCTTCTCCATTTAATAGTTACTGAACTTTATGCATGTTGATCTATATTGATTTT
CACTGCAGTTGAATGAACAAATTATTTCAGTGTGACAGCCATGACTCAAGTTCCAATTAGTCTG
AAAAGGGTACTTTGGAATTGTCCCATATTAATCAGAGATGGCAAAAGAAAAAGTTCTCATATTA
CCAGGTTGATTTTGTGTCTCATTTCAAATTTTAATTTAAAATTATGGTTTTCATTTTTGTTTAC
CTTAAAGTGATGCTTAAAAGTGGCATGTAATTAGGACACTTAGGTTTGTTGAAAGCATTTTCGA
CATTTGTATAAAAGAATTTGTGATAAATATATCCAGGTGCTCACCAAAGAAACATGTATTAACA
ACTTAAATTAGATTTTTCTAACTGATAGTTTTCACTCATTTATAATCAGTAGGAGAGACTGTCT
AGATGTTGGGGCAGCTCTATGATTTAAGTCTGTAACATGTTATAACTGAATTTAGTACCCTAGT
TTTGTTAAGCTATTAGGATTTTCTAATAGAACTTACTCCCCCTGCCTCCCCAGCCTTATGTTTC
TTTTAATGACTTCTGGATCCTGAGCTCCCTTTGCAGTCTGAAAAAGGTATTGCAGTCAGAACTG
TGTACTGATGATAAAAGCCTCTGGTAGCAATAAAAAGTTGTCCTTAA

hide sequence

RefSeq Acc Id:

NM_001348138 ⟹ NP_001335067

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	77,047,155 - 77,075,989 (-)	NCBI
T2T-CHM13v2.0	4	80,387,967 - 80,416,780 (-)	NCBI

Sequence:

show sequence

CTCCCTCCCCAGCCTTCCCCGCGAGCGGACGCGGCAGCGCCTCTGTCTCGCTTTTTCTTATTTT
TCCCCCCTTTCCCCTTTCTTTTTTTTTTTTTCTTTTCTTTTCTCCCCTCCCCCCCTTTCACCAT
TTCCCCTCGGAGGCGCTTTCCCCGGGCAGGGGCAGAGCCGGTCTCACCCCCCGCCTCTCCCCGG
CCCCCGCCGCCCTATGGCGAGAGGGAGCCCCCTCCCAACCCGGGCTCGAGCGGCGGCGGCCTCA
GGCCGGGGGTCATCATGGAACTAATTCGCTGACCGACCCAGCGGCCGCAGCCGTGCGTCCCGCT
CGAGCGCCAGCGCCCGCGCCCGCGCCCCCCGATCCGCTTCCCCTTTCTCCCTCCTCAGTTGGCC
GAGTCGTCCCGCGCGCACCGCCTCCGCGCGCCTATGAGAATGAGGTGGTAACGGGCCCCCGGAT
GACCCCGCGTCACCACTGTGAGGCCTACAGCTCTGCCGGGGAGGAGGAGGAGGAGGAAGAGGAG
GAGAAGGTAGCTACAGCAAGCTGGGTAGCAGGCAGATCCAAAGGATATCATGAAGTTTCCAGGG
CCTTTGGAAAACCAGAGATTGTCTTTCCTGTTGGAAAAGGCAATCACTAGGGAAGCACAGATGT
GGAAAGTGAATGTGCGGAAAATGCCTTCAAATCAGAATGTTTCTCCATCCCAGAGAGATGAAGT
AATTCAATGGCTGGCCAAACTCAAGTACCAATTCAACCTTTACCCAGAAACATTTGCTCTGGCT
AGCAGTCTTTTGGATAGGTTTTTAGCTACCGTAAAGGCTCATCCAAAATACTTGAGTTGTATTG
CAATCAGCTGTTTTTTCCTAGCTGCCAAGACTGTTGAGGAAGATGAGAATTCCAGTACTAAAGG
TATTGGCAAGAGACAGTTTCTGTGGATGTTCCTCATCTGAAATTTTGAGAATGGAGAGAATTAT
TCTGGATAAGTTGAATTGGGATCTTCACACAGCCACACCATTGGATTTTCTTCATATTTTCCAT
GCCATTGCAGTGTCAACTAGGCCTCAGTTACTTTTCAGTTTGCCCAAATTGAGCCCATCTCAAC
ATTTGGCAGTCCTTACCAAGCAACTACTTCACTGTATGGCCTGCAACCAACTTCTGCAATTCAG
AGGATCCATGCTTGCTCTGGCCATGGTTAGTCTGGAAATGGAGAAACTCATTCCTGATTGGCTT
TCTCTTACAATTGAACTGCTTCAGAAAGCACAGATGGATAGCTCCCAGTTGATCCATTGTCGGG
AGCTTGTGGCACATCACCTTTCTACTCTGCAGTCTTCCCTGCCTCTGAATTCCGTTTATGTCTA
CCGTCCCCTCAAGCACACCCTGGTGACCTGTGACAAAGGAGTGTTCAGATTACATCCCTCCTCT
GTCCCAGGCCCAGACTTCTCCAAGGACAACAGCAAGCCAGAAGTGCCAGTCAGAGGTACAGCAG
CCTTTTACCATCATCTCCCAGCTGCCAGTGGGTGCAAGCAGACCTCTACTAAACGCAAAGTAGA
GGAAATGGAAGTGGATGACTTCTATGATGGAATCAAACGGCTCTATAATGAAGATAATGTCTCA
GAAAATGTGGGTTCTGTGTGTGGCACTGATTTATCAAGACAAGAGGGACATGCTTCCCCTTGTC
CACCTTTGCAGCCTGTTTCTGTCATGTAGTTTCAACAAGTGCTACCTTTGAGTGTAAACTAAGG
TAGACTACTTTGGGAATGAGAACATGCAAAATCAGGAAAGGCTGTAGAAGGAAATATACCTTAA
CAGGCTGATTTGGAGTGAGCCAGAAAAAAAAAATAAAACTCTCATTATTTGTGTGGCTAATTAT
AATTCAGCGTTATTTAAGCACATAAAGACCAAAAAAAAAAAAAAGAAATCCAAAAGATCCAAAC
TTTTTTTAAACTTAAAAAATCTCTTTGTAGTATGTCAGTTGCACTTTTTTTCTGCCATAATGTA
ACGTAGCTTGCCCCGTCAAAAATTCAATTAAAATTCATGGCCAGCAATCCTGTTCCCCCTCAGC
ATCCTGATTTAATTTTCCTGTTGCTTTTGCTTGCTTCTCCATTTAATAGTTACTGAACTTTATG
CATGTTGATCTATATTGATTTTCACTGCAGTTGAATGAACAAATTATTTCAGTGTGACAGCCAT
GACTCAAGTTCCAATTAGTCTGAAAAGGGTACTTTGGAATTGTCCCATATTAATCAGAGATGGC
AAAAGAAAAAGTTCTCATATTACCAGGTTGATTTTGTGTCTCATTTCAAATTTTAATTTAAAAT
TATGGTTTTCATTTTTGTTTACCTTAAAGTGATGCTTAAAAGTGGCATGTAATTAGGACACTTA
GGTTTGTTGAAAGCATTTTCGACATTTGTATAAAAGAATTTGTGATAAATATATCCAGGTGCTC
ACCAAAGAAACATGTATTAACAACTTAAATTAGATTTTTCTAACTGATAGTTTTCACTCATTTA
TAATCAGTAGGAGAGACTGTCTAGATGTTGGGGCAGCTCTATGATTTAAGTCTGTAACATGTTA
TAACTGAATTTAGTACCCTAGTTTTGTTAAGCTATTAGGATTTTCTAATAGAACTTACTCCCCC
TGCCTCCCCAGCCTTATGTTTCTTTTAATGACTTCTGGATCCTGAGCTCCCTTTGCAGTCTGAA
AAAGGTATTGCAGTCAGAACTGTGTACTGATGATAAAAGCCTCTGGTAGCAATAAAAAGTTGTC
CTTAA

hide sequence

RefSeq Acc Id:

NM_001348139 ⟹ NP_001335068

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	77,047,155 - 77,075,989 (-)	NCBI
T2T-CHM13v2.0	4	80,387,967 - 80,416,780 (-)	NCBI

Sequence:

show sequence

CTCCCTCCCCAGCCTTCCCCGCGAGCGGACGCGGCAGCGCCTCTGTCTCGCTTTTTCTTATTTT
TCCCCCCTTTCCCCTTTCTTTTTTTTTTTTTCTTTTCTTTTCTCCCCTCCCCCCCTTTCACCAT
TTCCCCTCGGAGGCGCTTTCCCCGGGCAGGGGCAGAGCCGGTCTCACCCCCCGCCTCTCCCCGG
CCCCCGCCGCCCTATGGCGAGAGGGAGCCCCCTCCCAACCCGGGCTCGAGCGGCGGCGGCCTCA
GGCCGGGGGTCATCATGGAACTAATTCGCTGACCGACCCAGCGGCCGCAGCCGTGCGTCCCGCT
CGAGCGCCAGCGCCCGCGCCCGCGCCCCCCGATCCGCTTCCCCTTTCTCCCTCCTCAGTTGGCC
GAGTCGTCCCGCGCGCACCGCCTCCGCGCGCCTATGAGAATGAGGTGGTAACGGGCCCCCGGAT
GACCCCGCGTCACCACTGTGAGGCCTACAGCTCTGCCGGGGAGGAGGAGGAGGAGGAAGAGGAG
GAGAAGGTAGCTACAGCAAGCTGGGTAGCAGGCAGATCCAAAGGATATCATGAAGTTTCCAGGG
CCTTTGGAAAACCAGAGATTGTCTTTCCTGTTGGAAAAGGCAATCACTAGGGAAGCACAGATGT
GGAAAGTGAATGTGCGGAAAATGCCTTCAAATCAGTTCCATGCCATTGCAGTGTCAACTAGGCC
TCAGTTACTTTTCAGTTTGCCCAAATTGAGCCCATCTCAACATTTGGCAGTCCTTACCAAGCAA
CTACTTCACTGTATGGCCTGCAACCAACTTCTGCAATTCAGAGGATCCATGCTTGCTCTGGCCA
TGGTTAGTCTGGAAATGGAGAAACTCATTCCTGATTGGCTTTCTCTTACAATTGAACTGCTTCA
GAAAGCACAGATGGATAGCTCCCAGTTGATCCATTGTCGGGAGCTTGTGGCACATCACCTTTCT
ACTCTGCAGTCTTCCCTGCCTCTGAATTCCGTTTATGTCTACCGTCCCCTCAAGCACACCCTGG
TGACCTGTGACAAAGGAGTGTTCAGATTACATCCCTCCTCTGTCCCAGGCCCAGACTTCTCCAA
GGACAACAGCAAGCCAGAAGTGCCAGTCAGAGGTACAGCAGCCTTTTACCATCATCTCCCAGCT
GCCAGTGGGTGCAAGCAGACCTCTACTAAACGCAAAGTAGAGGAAATGGAAGTGGATGACTTCT
ATGATGGAATCAAACGGCTCTATAATGAAGATAATGTCTCAGAAAATGTGGGTTCTGTGTGTGG
CACTGATTTATCAAGACAAGAGGGACATGCTTCCCCTTGTCCACCTTTGCAGCCTGTTTCTGTC
ATGTAGTTTCAACAAGTGCTACCTTTGAGTGTAAACTAAGGTAGACTACTTTGGGAATGAGAAC
ATGCAAAATCAGGAAAGGCTGTAGAAGGAAATATACCTTAACAGGCTGATTTGGAGTGAGCCAG
AAAAAAAAAATAAAACTCTCATTATTTGTGTGGCTAATTATAATTCAGCGTTATTTAAGCACAT
AAAGACCAAAAAAAAAAAAAAGAAATCCAAAAGATCCAAACTTTTTTTAAACTTAAAAAATCTC
TTTGTAGTATGTCAGTTGCACTTTTTTTCTGCCATAATGTAACGTAGCTTGCCCCGTCAAAAAT
TCAATTAAAATTCATGGCCAGCAATCCTGTTCCCCCTCAGCATCCTGATTTAATTTTCCTGTTG
CTTTTGCTTGCTTCTCCATTTAATAGTTACTGAACTTTATGCATGTTGATCTATATTGATTTTC
ACTGCAGTTGAATGAACAAATTATTTCAGTGTGACAGCCATGACTCAAGTTCCAATTAGTCTGA
AAAGGGTACTTTGGAATTGTCCCATATTAATCAGAGATGGCAAAAGAAAAAGTTCTCATATTAC
CAGGTTGATTTTGTGTCTCATTTCAAATTTTAATTTAAAATTATGGTTTTCATTTTTGTTTACC
TTAAAGTGATGCTTAAAAGTGGCATGTAATTAGGACACTTAGGTTTGTTGAAAGCATTTTCGAC
ATTTGTATAAAAGAATTTGTGATAAATATATCCAGGTGCTCACCAAAGAAACATGTATTAACAA
CTTAAATTAGATTTTTCTAACTGATAGTTTTCACTCATTTATAATCAGTAGGAGAGACTGTCTA
GATGTTGGGGCAGCTCTATGATTTAAGTCTGTAACATGTTATAACTGAATTTAGTACCCTAGTT
TTGTTAAGCTATTAGGATTTTCTAATAGAACTTACTCCCCCTGCCTCCCCAGCCTTATGTTTCT
TTTAATGACTTCTGGATCCTGAGCTCCCTTTGCAGTCTGAAAAAGGTATTGCAGTCAGAACTGT
GTACTGATGATAAAAGCCTCTGGTAGCAATAAAAAGTTGTCCTTAA

hide sequence

RefSeq Acc Id:

NM_001348140 ⟹ NP_001335069

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	77,047,155 - 77,075,989 (-)	NCBI
T2T-CHM13v2.0	4	80,387,967 - 80,416,780 (-)	NCBI

Sequence:

show sequence

CTCCCTCCCCAGCCTTCCCCGCGAGCGGACGCGGCAGCGCCTCTGTCTCGCTTTTTCTTATTTT
TCCCCCCTTTCCCCTTTCTTTTTTTTTTTTTCTTTTCTTTTCTCCCCTCCCCCCCTTTCACCAT
TTCCCCTCGGAGGCGCTTTCCCCGGGCAGGGGCAGAGCCGGTCTCACCCCCCGCCTCTCCCCGG
CCCCCGCCGCCCTATGGCGAGAGGGAGCCCCCTCCCAACCCGGGCTCGAGCGGCGGCGGCCTCA
GGCCGGGGGTCATCATGGAACTAATTCGCTGACCGACCCAGCGGCCGCAGCCGTGCGTCCCGCT
CGAGCGCCAGCGCCCGCGCCCGCGCCCCCCGATCCGCTTCCCCTTTCTCCCTCCTCAGTTGGCC
GAGTCGTCCCGCGCGCACCGCCTCCGCGCGCCTATGAGAATGAGGTGGTAACGGGCCCCCGGAT
GACCCCGCGTCACCACTGTGAGGCCTACAGCTCTGCCGGGGAGGAGGAGGAGGAGGAAGAGGAG
GAGAAGGTAGCTACAGCAAGCTGGGTAGCAGGCAGATCCAAAGGATATCATGAAGTTTCCAGGG
CCTTTGGAAAACCAGAGATTGTCTTTCCTGTTGGAAAAGGCAATCACTAGGGAAGCACAGATGT
GGAAAGTGAATGTGCGGAAAATGCCTTCAAATCAGAATGTTTCTCCATCCCAGAGAGATGAAGT
AATTCAATGGCTGGCCAAACTCAAGTACCAATTCAACCTTTACCCAGAAACATTTGCTCTGGCT
AGCAGTCTTTTGGATAGGTTTTTAGCTACCGTAAAGGCTCATCCAAAATACTTGAGTTGTATTG
CAATCAGCTGTTTTTTCCTAGCTGCCAAGACTGTTGAGGAAGATGAGAGAATTCCAGTACTAAA
GGTATTGGCAAGAGACAGTTTCTGTGGATGTTCCTCATCTGAAATTTTGAGAATGGAGAGAATT
ATTCTGGATAAGTTGAATTGGGATCTTCACACAGCCACACCATTGGATTTTCTTCATATTTCCT
TACCAAGCAACTACTTCACTGTATGGCCTGCAACCAACTTCTGCAATTCAGAGGATCCATGCTT
GCTCTGGCCATGGTTAGTCTGGAAATGGAGAAACTCATTCCTGATTGGCTTTCTCTTACAATTG
AACTGCTTCAGAAAGCACAGATGGATAGCTCCCAGTTGATCCATTGTCGGGAGCTTGTGGCACA
TCACCTTTCTACTCTGCAGTCTTCCCTGCCTCTGAATTCCGTTTATGTCTACCGTCCCCTCAAG
CACACCCTGGTGACCTGTGACAAAGGAGTGTTCAGATTACATCCCTCCTCTGTCCCAGGCCCAG
ACTTCTCCAAGGACAACAGCAAGCCAGAAGTGCCAGTCAGAGGTACAGCAGCCTTTTACCATCA
TCTCCCAGCTGCCAGTGGGTGCAAGCAGACCTCTACTAAACGCAAAGTAGAGGAAATGGAAGTG
GATGACTTCTATGATGGAATCAAACGGCTCTATAATGAAGATAATGTCTCAGAAAATGTGGGTT
CTGTGTGTGGCACTGATTTATCAAGACAAGAGGGACATGCTTCCCCTTGTCCACCTTTGCAGCC
TGTTTCTGTCATGTAGTTTCAACAAGTGCTACCTTTGAGTGTAAACTAAGGTAGACTACTTTGG
GAATGAGAACATGCAAAATCAGGAAAGGCTGTAGAAGGAAATATACCTTAACAGGCTGATTTGG
AGTGAGCCAGAAAAAAAAAATAAAACTCTCATTATTTGTGTGGCTAATTATAATTCAGCGTTAT
TTAAGCACATAAAGACCAAAAAAAAAAAAAAGAAATCCAAAAGATCCAAACTTTTTTTAAACTT
AAAAAATCTCTTTGTAGTATGTCAGTTGCACTTTTTTTCTGCCATAATGTAACGTAGCTTGCCC
CGTCAAAAATTCAATTAAAATTCATGGCCAGCAATCCTGTTCCCCCTCAGCATCCTGATTTAAT
TTTCCTGTTGCTTTTGCTTGCTTCTCCATTTAATAGTTACTGAACTTTATGCATGTTGATCTAT
ATTGATTTTCACTGCAGTTGAATGAACAAATTATTTCAGTGTGACAGCCATGACTCAAGTTCCA
ATTAGTCTGAAAAGGGTACTTTGGAATTGTCCCATATTAATCAGAGATGGCAAAAGAAAAAGTT
CTCATATTACCAGGTTGATTTTGTGTCTCATTTCAAATTTTAATTTAAAATTATGGTTTTCATT
TTTGTTTACCTTAAAGTGATGCTTAAAAGTGGCATGTAATTAGGACACTTAGGTTTGTTGAAAG
CATTTTCGACATTTGTATAAAAGAATTTGTGATAAATATATCCAGGTGCTCACCAAAGAAACAT
GTATTAACAACTTAAATTAGATTTTTCTAACTGATAGTTTTCACTCATTTATAATCAGTAGGAG
AGACTGTCTAGATGTTGGGGCAGCTCTATGATTTAAGTCTGTAACATGTTATAACTGAATTTAG
TACCCTAGTTTTGTTAAGCTATTAGGATTTTCTAATAGAACTTACTCCCCCTGCCTCCCCAGCC
TTATGTTTCTTTTAATGACTTCTGGATCCTGAGCTCCCTTTGCAGTCTGAAAAAGGTATTGCAG
TCAGAACTGTGTACTGATGATAAAAGCCTCTGGTAGCAATAAAAAGTTGTCCTTAA

hide sequence

RefSeq Acc Id:

NM_006835 ⟹ NP_006826

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	4	77,047,155 - 77,075,989 (-)	NCBI
GRCh37	4	77,968,308 - 77,998,719 (-)	NCBI
Build 36	4	78,188,189 - 78,216,149 (-)	NCBI Archive
Celera	4	75,270,553 - 75,298,504 (-)	RGD
HuRef	4	73,720,994 - 73,748,951 (-)	RGD
CHM1_1	4	77,946,423 - 77,974,382 (-)	NCBI
T2T-CHM13v2.0	4	80,387,967 - 80,416,780 (-)	NCBI

Sequence:

show sequence

CTCCCTCCCCAGCCTTCCCCGCGAGCGGACGCGGCAGCGCCTCTGTCTCGCTTTTTCTTATTTT
TCCCCCCTTTCCCCTTTCTTTTTTTTTTTTTCTTTTCTTTTCTCCCCTCCCCCCCTTTCACCAT
TTCCCCTCGGAGGCGCTTTCCCCGGGCAGGGGCAGAGCCGGTCTCACCCCCCGCCTCTCCCCGG
CCCCCGCCGCCCTATGGCGAGAGGGAGCCCCCTCCCAACCCGGGCTCGAGCGGCGGCGGCCTCA
GGCCGGGGGTCATCATGGAACTAATTCGCTGACCGACCCAGCGGCCGCAGCCGTGCGTCCCGCT
CGAGCGCCAGCGCCCGCGCCCGCGCCCCCCGATCCGCTTCCCCTTTCTCCCTCCTCAGTTGGCC
GAGTCGTCCCGCGCGCACCGCCTCCGCGCGCCTATGAGAATGAGGTGGTAACGGGCCCCCGGAT
GACCCCGCGTCACCACTGTGAGGCCTACAGCTCTGCCGGGGAGGAGGAGGAGGAGGAAGAGGAG
GAGAAGGTAGCTACAGCAAGCTGGGTAGCAGGCAGATCCAAAGGATATCATGAAGTTTCCAGGG
CCTTTGGAAAACCAGAGATTGTCTTTCCTGTTGGAAAAGGCAATCACTAGGGAAGCACAGATGT
GGAAAGTGAATGTGCGGAAAATGCCTTCAAATCAGAATGTTTCTCCATCCCAGAGAGATGAAGT
AATTCAATGGCTGGCCAAACTCAAGTACCAATTCAACCTTTACCCAGAAACATTTGCTCTGGCT
AGCAGTCTTTTGGATAGGTTTTTAGCTACCGTAAAGGCTCATCCAAAATACTTGAGTTGTATTG
CAATCAGCTGTTTTTTCCTAGCTGCCAAGACTGTTGAGGAAGATGAGAGAATTCCAGTACTAAA
GGTATTGGCAAGAGACAGTTTCTGTGGATGTTCCTCATCTGAAATTTTGAGAATGGAGAGAATT
ATTCTGGATAAGTTGAATTGGGATCTTCACACAGCCACACCATTGGATTTTCTTCATATTTTCC
ATGCCATTGCAGTGTCAACTAGGCCTCAGTTACTTTTCAGTTTGCCCAAATTGAGCCCATCTCA
ACATTTGGCAGTCCTTACCAAGCAACTACTTCACTGTATGGCCTGCAACCAACTTCTGCAATTC
AGAGGATCCATGCTTGCTCTGGCCATGGTTAGTCTGGAAATGGAGAAACTCATTCCTGATTGGC
TTTCTCTTACAATTGAACTGCTTCAGAAAGCACAGATGGATAGCTCCCAGTTGATCCATTGTCG
GGAGCTTGTGGCACATCACCTTTCTACTCTGCAGTCTTCCCTGCCTCTGAATTCCGTTTATGTC
TACCGTCCCCTCAAGCACACCCTGGTGACCTGTGACAAAGGAGTGTTCAGATTACATCCCTCCT
CTGTCCCAGGCCCAGACTTCTCCAAGGACAACAGCAAGCCAGAAGTGCCAGTCAGAGGTACAGC
AGCCTTTTACCATCATCTCCCAGCTGCCAGTGGGTGCAAGCAGACCTCTACTAAACGCAAAGTA
GAGGAAATGGAAGTGGATGACTTCTATGATGGAATCAAACGGCTCTATAATGAAGATAATGTCT
CAGAAAATGTGGGTTCTGTGTGTGGCACTGATTTATCAAGACAAGAGGGACATGCTTCCCCTTG
TCCACCTTTGCAGCCTGTTTCTGTCATGTAGTTTCAACAAGTGCTACCTTTGAGTGTAAACTAA
GGTAGACTACTTTGGGAATGAGAACATGCAAAATCAGGAAAGGCTGTAGAAGGAAATATACCTT
AACAGGCTGATTTGGAGTGAGCCAGAAAAAAAAAATAAAACTCTCATTATTTGTGTGGCTAATT
ATAATTCAGCGTTATTTAAGCACATAAAGACCAAAAAAAAAAAAAAGAAATCCAAAAGATCCAA
ACTTTTTTTAAACTTAAAAAATCTCTTTGTAGTATGTCAGTTGCACTTTTTTTCTGCCATAATG
TAACGTAGCTTGCCCCGTCAAAAATTCAATTAAAATTCATGGCCAGCAATCCTGTTCCCCCTCA
GCATCCTGATTTAATTTTCCTGTTGCTTTTGCTTGCTTCTCCATTTAATAGTTACTGAACTTTA
TGCATGTTGATCTATATTGATTTTCACTGCAGTTGAATGAACAAATTATTTCAGTGTGACAGCC
ATGACTCAAGTTCCAATTAGTCTGAAAAGGGTACTTTGGAATTGTCCCATATTAATCAGAGATG
GCAAAAGAAAAAGTTCTCATATTACCAGGTTGATTTTGTGTCTCATTTCAAATTTTAATTTAAA
ATTATGGTTTTCATTTTTGTTTACCTTAAAGTGATGCTTAAAAGTGGCATGTAATTAGGACACT
TAGGTTTGTTGAAAGCATTTTCGACATTTGTATAAAAGAATTTGTGATAAATATATCCAGGTGC
TCACCAAAGAAACATGTATTAACAACTTAAATTAGATTTTTCTAACTGATAGTTTTCACTCATT
TATAATCAGTAGGAGAGACTGTCTAGATGTTGGGGCAGCTCTATGATTTAAGTCTGTAACATGT
TATAACTGAATTTAGTACCCTAGTTTTGTTAAGCTATTAGGATTTTCTAATAGAACTTACTCCC
CCTGCCTCCCCAGCCTTATGTTTCTTTTAATGACTTCTGGATCCTGAGCTCCCTTTGCAGTCTG
AAAAAGGTATTGCAGTCAGAACTGTGTACTGATGATAAAAGCCTCTGGTAGCAATAAAAAGTTG
TCCTTAA

hide sequence

Protein Sequences


Protein RefSeqs	NP_001335061	(Get FASTA)	NCBI Sequence Viewer
	NP_001335062	(Get FASTA)	NCBI Sequence Viewer
	NP_001335063	(Get FASTA)	NCBI Sequence Viewer
	NP_001335064	(Get FASTA)	NCBI Sequence Viewer
	NP_001335065	(Get FASTA)	NCBI Sequence Viewer
	NP_001335066	(Get FASTA)	NCBI Sequence Viewer
	NP_001335067	(Get FASTA)	NCBI Sequence Viewer
	NP_001335068	(Get FASTA)	NCBI Sequence Viewer
	NP_001335069	(Get FASTA)	NCBI Sequence Viewer
	NP_006826	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAF43786	(Get FASTA)	NCBI Sequence Viewer
	AAH00420	(Get FASTA)	NCBI Sequence Viewer
	AAH04975	(Get FASTA)	NCBI Sequence Viewer
	AAO13492	(Get FASTA)	NCBI Sequence Viewer
	AAV38822	(Get FASTA)	NCBI Sequence Viewer
	BAA08849	(Get FASTA)	NCBI Sequence Viewer
	BAD93003	(Get FASTA)	NCBI Sequence Viewer
	BAD96651	(Get FASTA)	NCBI Sequence Viewer
	BAG35517	(Get FASTA)	NCBI Sequence Viewer
	BAH13410	(Get FASTA)	NCBI Sequence Viewer
	CAG46582	(Get FASTA)	NCBI Sequence Viewer
	EAX05808	(Get FASTA)	NCBI Sequence Viewer
	EAX05809	(Get FASTA)	NCBI Sequence Viewer
	EAX05810	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000237654
	ENSP00000237654.4
	ENSP00000421594
	ENSP00000421594.1
	ENSP00000425360.1
	ENSP00000425935.1
	ENSP00000426235.1
	ENSP00000426467.1
	ENSP00000520818
GenBank Protein	Q14094	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_006826 ⟸ NM_006835
- Peptide Label:	isoform a
- UniProtKB:	B2R6M0 (UniProtKB/Swiss-Prot), B7Z6X4 (UniProtKB/Swiss-Prot), Q14094 (UniProtKB/Swiss-Prot), Q6FHH0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MKFPGPLENQRLSFLLEKAITREAQMWKVNVRKMPSNQNVSPSQRDEVIQWLAKLKYQFNLYPE TFALASSLLDRFLATVKAHPKYLSCIAISCFFLAAKTVEEDERIPVLKVLARDSFCGCSSSEIL RMERIILDKLNWDLHTATPLDFLHIFHAIAVSTRPQLLFSLPKLSPSQHLAVLTKQLLHCMACN QLLQFRGSMLALAMVSLEMEKLIPDWLSLTIELLQKAQMDSSQLIHCRELVAHHLSTLQSSLPL NSVYVYRPLKHTLVTCDKGVFRLHPSSVPGPDFSKDNSKPEVPVRGTAAFYHHLPAASGCKQTS TKRKVEEMEVDDFYDGIKRLYNEDNVSENVGSVCGTDLSRQEGHASPCPPLQPVSVM hide sequence

RefSeq Acc Id:	NP_001335063 ⟸ NM_001348134
- Peptide Label:	isoform b
- UniProtKB:	Q53GK0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MTPRHHCEAYSSAGEEEEEEEEEKNVSPSQRDEVIQWLAKLKYQFNLYPETFALASSLLDRFLA TVKAHPKYLSCIAISCFFLAAKTVEEDERIPVLKVLARDSFCGCSSSEILRMERIILDKLNWDL HTATPLDFLHIFHAIAVSTRPQLLFSLPKLSPSQHLAVLTKQLLHCMACNQLLQFRGSMLALAM VSLEMEKLIPDWLSLTIELLQKAQMDSSQLIHCRELVAHHLSTLQSSLPLNSVYVYRPLKHTLV TCDKGVFRLHPSSVPGPDFSKDNSKPEVPVRGTAAFYHHLPAASGCKQTSTKRKVEEMEVDDFY DGIKRLYNEDNVSENVGSVCGTDLSRQEGHASPCPPLQPVSVM hide sequence

RefSeq Acc Id:	NP_001335061 ⟸ NM_001348132
- Peptide Label:	isoform a
- UniProtKB:	B2R6M0 (UniProtKB/Swiss-Prot), B7Z6X4 (UniProtKB/Swiss-Prot), Q14094 (UniProtKB/Swiss-Prot), Q6FHH0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MKFPGPLENQRLSFLLEKAITREAQMWKVNVRKMPSNQNVSPSQRDEVIQWLAKLKYQFNLYPE TFALASSLLDRFLATVKAHPKYLSCIAISCFFLAAKTVEEDERIPVLKVLARDSFCGCSSSEIL RMERIILDKLNWDLHTATPLDFLHIFHAIAVSTRPQLLFSLPKLSPSQHLAVLTKQLLHCMACN QLLQFRGSMLALAMVSLEMEKLIPDWLSLTIELLQKAQMDSSQLIHCRELVAHHLSTLQSSLPL NSVYVYRPLKHTLVTCDKGVFRLHPSSVPGPDFSKDNSKPEVPVRGTAAFYHHLPAASGCKQTS TKRKVEEMEVDDFYDGIKRLYNEDNVSENVGSVCGTDLSRQEGHASPCPPLQPVSVM hide sequence

RefSeq Acc Id:

NP_001335068 ⟸ NM_001348139

- Peptide Label:

isoform g

- Sequence:

show sequence

MKFPGPLENQRLSFLLEKAITREAQMWKVNVRKMPSNQFHAIAVSTRPQLLFSLPKLSPSQHLA
VLTKQLLHCMACNQLLQFRGSMLALAMVSLEMEKLIPDWLSLTIELLQKAQMDSSQLIHCRELV
AHHLSTLQSSLPLNSVYVYRPLKHTLVTCDKGVFRLHPSSVPGPDFSKDNSKPEVPVRGTAAFY
HHLPAASGCKQTSTKRKVEEMEVDDFYDGIKRLYNEDNVSENVGSVCGTDLSRQEGHASPCPPL
QPVSVM

hide sequence

RefSeq Acc Id:	NP_001335065 ⟸ NM_001348136
- Peptide Label:	isoform d
- UniProtKB:	Q6FHH0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MKFPGPLENQRLSFLLEKAITREAQMWKVNVRKMPSNQAHPKYLSCIAISCFFLAAKTVEEDER IPVLKVLARDSFCGCSSSEILRMERIILDKLNWDLHTATPLDFLHIFHAIAVSTRPQLLFSLPK LSPSQHLAVLTKQLLHCMACNQLLQFRGSMLALAMVSLEMEKLIPDWLSLTIELLQKAQMDSSQ LIHCRELVAHHLSTLQSSLPLNSVYVYRPLKHTLVTCDKGVFRLHPSSVPGPDFSKDNSKPEVP VRGTAAFYHHLPAASGCKQTSTKRKVEEMEVDDFYDGIKRLYNEDNVSENVGSVCGTDLSRQEG HASPCPPLQPVSVM hide sequence

RefSeq Acc Id:	NP_001335066 ⟸ NM_001348137
- Peptide Label:	isoform e
- UniProtKB:	Q6FHH0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MKFPGPLENQRLSFLLEKAITREAQMWKVNVRKMPSNQNVSPSQRDEVIQWLAKLKYQFNLYPE TFALASSLLDRFLATVKFHAIAVSTRPQLLFSLPKLSPSQHLAVLTKQLLHCMACNQLLQFRGS MLALAMVSLEMEKLIPDWLSLTIELLQKAQMDSSQLIHCRELVAHHLSTLQSSLPLNSVYVYRP LKHTLVTCDKGVFRLHPSSVPGPDFSKDNSKPEVPVRGTAAFYHHLPAASGCKQTSTKRKVEEM EVDDFYDGIKRLYNEDNVSENVGSVCGTDLSRQEGHASPCPPLQPVSVM hide sequence

RefSeq Acc Id:

NP_001335067 ⟸ NM_001348138

- Peptide Label:

isoform f

- Sequence:

show sequence

MRIPVLKVLARDSFCGCSSSEILRMERIILDKLNWDLHTATPLDFLHIFHAIAVSTRPQLLFSL
PKLSPSQHLAVLTKQLLHCMACNQLLQFRGSMLALAMVSLEMEKLIPDWLSLTIELLQKAQMDS
SQLIHCRELVAHHLSTLQSSLPLNSVYVYRPLKHTLVTCDKGVFRLHPSSVPGPDFSKDNSKPE
VPVRGTAAFYHHLPAASGCKQTSTKRKVEEMEVDDFYDGIKRLYNEDNVSENVGSVCGTDLSRQ
EGHASPCPPLQPVSVM

hide sequence

RefSeq Acc Id:	NP_001335064 ⟸ NM_001348135
- Peptide Label:	isoform c
- UniProtKB:	Q6FHH0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MKFPGPLENQRLSFLLEKAITREAQMWKVNVRKMPSNQNVSPSQRDEVIQWLAKLKYQFNLYPE TFALASSLLDRFLATVKAHPKYLSCIAISCFFLAAKTVEEDERIPVLKFHAIAVSTRPQLLFSL PKLSPSQHLAVLTKQLLHCMACNQLLQFRGSMLALAMVSLEMEKLIPDWLSLTIELLQKAQMDS SQLIHCRELVAHHLSTLQSSLPLNSVYVYRPLKHTLVTCDKGVFRLHPSSVPGPDFSKDNSKPE VPVRGTAAFYHHLPAASGCKQTSTKRKVEEMEVDDFYDGIKRLYNEDNVSENVGSVCGTDLSRQ EGHASPCPPLQPVSVM hide sequence

RefSeq Acc Id:

NP_001335069 ⟸ NM_001348140

- Peptide Label:

isoform h

- Sequence:

show sequence

MKFPGPLENQRLSFLLEKAITREAQMWKVNVRKMPSNQNVSPSQRDEVIQWLAKLKYQFNLYPE
TFALASSLLDRFLATVKAHPKYLSCIAISCFFLAAKTVEEDERIPVLKVLARDSFCGCSSSEIL
RMERIILDKLNWDLHTATPLDFLHISLPSNYFTVWPATNFCNSEDPCLLWPWLVWKWRNSFLIG
FLLQLNCFRKHRWIAPS

hide sequence

RefSeq Acc Id:	NP_001335062 ⟸ NM_001348133
- Peptide Label:	isoform a
- UniProtKB:	B2R6M0 (UniProtKB/Swiss-Prot), B7Z6X4 (UniProtKB/Swiss-Prot), Q14094 (UniProtKB/Swiss-Prot), Q6FHH0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MKFPGPLENQRLSFLLEKAITREAQMWKVNVRKMPSNQNVSPSQRDEVIQWLAKLKYQFNLYPE TFALASSLLDRFLATVKAHPKYLSCIAISCFFLAAKTVEEDERIPVLKVLARDSFCGCSSSEIL RMERIILDKLNWDLHTATPLDFLHIFHAIAVSTRPQLLFSLPKLSPSQHLAVLTKQLLHCMACN QLLQFRGSMLALAMVSLEMEKLIPDWLSLTIELLQKAQMDSSQLIHCRELVAHHLSTLQSSLPL NSVYVYRPLKHTLVTCDKGVFRLHPSSVPGPDFSKDNSKPEVPVRGTAAFYHHLPAASGCKQTS TKRKVEEMEVDDFYDGIKRLYNEDNVSENVGSVCGTDLSRQEGHASPCPPLQPVSVM hide sequence

Ensembl Acc Id:

ENSP00000426467 ⟸ ENST00000505609

Ensembl Acc Id:

ENSP00000421594 ⟸ ENST00000507788

Ensembl Acc Id:

ENSP00000425360 ⟸ ENST00000511943

Ensembl Acc Id:

ENSP00000237654 ⟸ ENST00000237654

Ensembl Acc Id:

ENSP00000426235 ⟸ ENST00000513774

Ensembl Acc Id:

ENSP00000425935 ⟸ ENST00000515468

Ensembl Acc Id:

ENSP00000520818 ⟸ ENST00000718433

Protein Domains

Cyclin N-terminal Cyclin-like

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q14094-F1-model_v2	AlphaFold	Q14094	1-377	view protein structure

Promoters

RGD ID:

6867792

Promoter ID:

EPDNEW_H7061

Type:

initiation region

Name:

CCNI_1

Description:

cyclin I

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	4	77,075,989 - 77,076,049	EPDNEW

RGD ID:

6802111

Promoter ID:

HG_KWN:48550

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

OTTHUMT00000252412

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	4	78,215,656 - 78,216,572 (-)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:1595	AgrOrtholog
COSMIC	CCNI	COSMIC
Ensembl Genes	ENSG00000118816	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000237654	ENTREZGENE
	ENST00000237654.9	UniProtKB/Swiss-Prot
	ENST00000505609.5	UniProtKB/TrEMBL
	ENST00000507788	ENTREZGENE
	ENST00000507788.2	UniProtKB/TrEMBL
	ENST00000511943.5	UniProtKB/TrEMBL
	ENST00000513774.1	UniProtKB/TrEMBL
	ENST00000515468.1	UniProtKB/TrEMBL
	ENST00000718433	ENTREZGENE
Gene3D-CATH	Cyclin-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000118816	GTEx
HGNC ID	HGNC:1595	ENTREZGENE
Human Proteome Map	CCNI	Human Proteome Map
InterPro	Cyclin	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Cyclin-like	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Cyclin-like_sf	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Cyclin_N	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:10983	UniProtKB/Swiss-Prot
NCBI Gene	10983	ENTREZGENE
OMIM	618783	OMIM
PANTHER	PTHR10177	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PTHR10177:SF187	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	Cyclin_N	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA26160	PharmGKB
SMART	CYCLIN	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP	SSF47954	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	B2R6M0	ENTREZGENE
	B7Z6X4	ENTREZGENE
	CCNI_HUMAN	UniProtKB/Swiss-Prot
	D6RDK3_HUMAN	UniProtKB/TrEMBL
	D6REZ3_HUMAN	UniProtKB/TrEMBL
	D6RG12_HUMAN	UniProtKB/TrEMBL
	D6RH01_HUMAN	UniProtKB/TrEMBL
	H0YA27_HUMAN	UniProtKB/TrEMBL
	Q14094	ENTREZGENE
	Q53GK0	ENTREZGENE, UniProtKB/TrEMBL
	Q6FHH0	ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary	B2R6M0	UniProtKB/Swiss-Prot
	B7Z6X4	UniProtKB/Swiss-Prot

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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