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Gene: CIMIP2C (ciliary microtubule inner protein 2C) Homo sapiens

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Symbol:

CIMIP2C

Name:

ciliary microtubule inner protein 2C

RGD ID:

2298820

HGNC Page

HGNC:27938

Description:

Predicted to be involved in flagellated sperm motility. Located in axonemal microtubule.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

C2orf70; chromosome 2 open reading frame 70; FAM166C; family with sequence similarity 166 member C; hypothetical protein LOC339778; UPF0573 protein C2orf70

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	2	26,562,587 - 26,579,524 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	26,562,585 - 26,579,532 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	26,785,455 - 26,802,392 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	26,638,985 - 26,655,899 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	2	26,629,117 - 26,646,026 (+)	NCBI		Celera
Cytogenetic Map	2	p23.3	NCBI
HuRef	2	26,524,922 - 26,541,831 (+)	NCBI		HuRef
CHM1_1	2	26,715,533 - 26,732,444 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	2	26,601,745 - 26,618,672 (+)	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

Tatton-Brown-Rahman syndrome (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

4,4'-sulfonyldiphenol (EXP)

6-propyl-2-thiouracil (ISO)

aflatoxin B1 (EXP)

Aflatoxin B2 alpha (EXP)

benzo[a]pyrene (EXP)

benzo[e]pyrene (EXP)

bisphenol A (ISO)

copper atom (ISO)

copper(0) (ISO)

Cuprizon (ISO)

diiodine (ISO)

fulvestrant (EXP)

methapyrilene (EXP)

silicon dioxide (EXP)

temozolomide (EXP)

zoledronic acid (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

flagellated sperm motility (IEA,ISS)

Cellular Component

axonemal A tubule inner sheath (IEA,ISS)

axonemal microtubule (IDA)

cilium (IEA)

cytoplasm (IEA)

cytoskeleton (IEA)

microtubule cytoskeleton (IEA)

motile cilium (IEA)

nucleus (HDA)

sperm flagellum (IEA,ISS)

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:14702039	PMID:21630459	PMID:36191189	PMID:37327785

Genomics

Comparative Map Data

CIMIP2C
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	2	26,562,587 - 26,579,524 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	2	26,562,585 - 26,579,532 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	2	26,785,455 - 26,802,392 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	2	26,638,985 - 26,655,899 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	2	26,629,117 - 26,646,026 (+)	NCBI		Celera
Cytogenetic Map	2	p23.3	NCBI
HuRef	2	26,524,922 - 26,541,831 (+)	NCBI		HuRef
CHM1_1	2	26,715,533 - 26,732,444 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	2	26,601,745 - 26,618,672 (+)	NCBI		T2T-CHM13v2.0

Cimip2c
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	5	30,623,395 - 30,641,433 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	5	30,623,391 - 30,641,432 (+)	Ensembl		GRCm39 Ensembl
GRCm38	5	30,466,029 - 30,484,089 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	5	30,466,047 - 30,484,088 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	5	30,768,450 - 30,786,460 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	5	30,742,658 - 30,760,668 (+)	NCBI		MGSCv36	mm8
Celera	5	27,944,260 - 27,962,270 (+)	NCBI		Celera
Cytogenetic Map	5	B1	NCBI
cM Map	5	16.57	NCBI

Cimip2c
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	6	31,625,187 - 31,643,500 (-)	NCBI		GRCr8
mRatBN7.2	6	25,905,294 - 25,923,615 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	6	25,905,294 - 25,923,615 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	6	26,197,967 - 26,216,277 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	6	26,513,848 - 26,532,158 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	6	25,992,822 - 26,011,126 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	6	27,305,402 - 27,323,992 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	6	27,305,402 - 27,323,992 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	6	37,117,774 - 37,136,364 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	6	25,889,215 - 25,908,084 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	6	25,383,869 - 25,401,938 (-)	NCBI		Celera
Cytogenetic Map	6	q14	NCBI

Cimip2c
(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_004955469	8,588,900 - 8,604,337 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955469	8,588,820 - 8,603,333 (+)	NCBI	ChiLan1.0	ChiLan1.0

CIMIP2C
(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	12	99,936,109 - 99,956,927 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	2A	99,940,080 - 99,960,894 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	2A	26,558,826 - 26,578,005 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	2A	26,651,265 - 26,668,192 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	2A	26,651,283 - 26,668,192 (+)	Ensembl	panpan1.1		panPan2

CIMIP2C
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	17	20,618,642 - 20,633,418 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	17	20,618,329 - 20,633,403 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	17	20,512,905 - 20,527,668 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	17	20,940,005 - 20,954,785 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	17	20,939,689 - 20,954,785 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	17	20,626,951 - 20,641,726 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	17	20,638,105 - 20,652,860 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	17	20,684,449 - 20,699,207 (+)	NCBI		UU_Cfam_GSD_1.0

Cimip2c
(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_024406292	64,927,300 - 64,943,438 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936493	5,896,206 - 5,912,182 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936493	5,896,206 - 5,912,182 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

CIMIP2C
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	3	112,458,916 - 112,474,437 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	3	112,458,914 - 112,474,431 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	3	119,458,324 - 119,473,737 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

CIMIP2C
(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	14	81,059,408 - 81,077,554 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	14	81,057,764 - 81,076,400 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666045	31,071,037 - 31,089,094 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Cimip2c
(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_004624738	8,702,652 - 8,716,962 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in CIMIP2C
6 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 2p25.3-23.1(chr2:30141-31766749)x3	copy number gain	See cases [RCV000052929]	Chr2:30141..31766749 [GRCh38] Chr2:30141..31991818 [GRCh37] Chr2:20141..31845322 [NCBI36] Chr2:2p25.3-23.1	pathogenic
GRCh38/hg38 2p25.3-16.1(chr2:66097-55570637)x3	copy number gain	See cases [RCV000052933]	Chr2:66097..55570637 [GRCh38] Chr2:66097..55797773 [GRCh37] Chr2:56097..55651277 [NCBI36] Chr2:2p25.3-16.1	pathogenic
GRCh38/hg38 2p23.3(chr2:25759602-27297636)x3	copy number gain	See cases [RCV000052629]	Chr2:25759602..27297636 [GRCh38] Chr2:25982471..27520504 [GRCh37] Chr2:25835975..27374008 [NCBI36] Chr2:2p23.3	uncertain significance
NM_001105519.1(C2orf70):c.408C>T (p.Pro136=)	single nucleotide variant	Malignant melanoma [RCV000060537]	Chr2:26577575 [GRCh38] Chr2:26800443 [GRCh37] Chr2:26653947 [NCBI36] Chr2:2p23.3	not provided
GRCh38/hg38 2p25.3-23.2(chr2:30341-28419664)x3	copy number gain	See cases [RCV000135398]	Chr2:30341..28419664 [GRCh38] Chr2:30341..28642531 [GRCh37] Chr2:20341..28496035 [NCBI36] Chr2:2p25.3-23.2	pathogenic
GRCh38/hg38 2p23.3(chr2:25064306-27154398)x1	copy number loss	See cases [RCV000137065]	Chr2:25064306..27154398 [GRCh38] Chr2:25287175..27377266 [GRCh37] Chr2:25140679..27230770 [NCBI36] Chr2:2p23.3	uncertain significance
GRCh38/hg38 2p25.3-22.3(chr2:12770-33711509)x3	copy number gain	See cases [RCV000141829]	Chr2:12770..33711509 [GRCh38] Chr2:12770..33936576 [GRCh37] Chr2:2770..33790080 [NCBI36] Chr2:2p25.3-22.3	pathogenic
GRCh38/hg38 2p25.1-11.2(chr2:7495123-87705899)x3	copy number gain	See cases [RCV000141494]	Chr2:7495123..87705899 [GRCh38] Chr2:7635254..88005418 [GRCh37] Chr2:7552705..87786533 [NCBI36] Chr2:2p25.1-11.2	benign
GRCh38/hg38 2p24.1-23.2(chr2:22579652-28525186)x1	copy number loss	See cases [RCV000142071]	Chr2:22579652..28525186 [GRCh38] Chr2:22802524..28748053 [GRCh37] Chr2:22656029..28601557 [NCBI36] Chr2:2p24.1-23.2	pathogenic
GRCh38/hg38 2p25.3-21(chr2:236816-45983232)x3	copy number gain	See cases [RCV000143682]	Chr2:236816..45983232 [GRCh38] Chr2:236816..46210371 [GRCh37] Chr2:226816..46063875 [NCBI36] Chr2:2p25.3-21	pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3	copy number gain	not provided [RCV000752802]	Chr2:14238..243048760 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2p23.3(chr2:26592685-27262646)x3	copy number gain	See cases [RCV000448086]	Chr2:26592685..27262646 [GRCh37] Chr2:2p23.3	uncertain significance
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)	copy number gain	See cases [RCV000512056]	Chr2:12771..242783384 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3	copy number gain	See cases [RCV000511212]	Chr2:12771..242783384 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2p24.1-16.3(chr2:22665048-52850368)x3	copy number gain	not provided [RCV000752875]	Chr2:22665048..52850368 [GRCh37] Chr2:2p24.1-16.3	pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3	copy number gain	not provided [RCV000752804]	Chr2:15672..243101834 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2p23.3(chr2:26796310-26804143)x3	copy number gain	not provided [RCV000740356]	Chr2:26796310..26804143 [GRCh37] Chr2:2p23.3	benign
GRCh37/hg19 2p23.3(chr2:26669414-26803419)x1	copy number loss	not provided [RCV000848846]	Chr2:26669414..26803419 [GRCh37] Chr2:2p23.3	uncertain significance
GRCh37/hg19 2p23.3-21(chr2:24601818-43466284)x3	copy number gain	See cases [RCV001581099]	Chr2:24601818..43466284 [GRCh37] Chr2:2p23.3-21	pathogenic
GRCh37/hg19 2p23.3-21(chr2:24881528-43460021)x3	copy number gain	not provided [RCV001532444]	Chr2:24881528..43460021 [GRCh37] Chr2:2p23.3-21	likely pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373)	copy number gain	Mosaic trisomy 2 [RCV002280628]	Chr2:1..243199373 [GRCh37] Chr2:2p25.3-q37.3	pathogenic
GRCh37/hg19 2p23.3(chr2:26592685-27262646)	copy number gain	not specified [RCV002053078]	Chr2:26592685..27262646 [GRCh37] Chr2:2p23.3	uncertain significance
NC_000002.11:g.(?_24443763)_(27746306_?)dup	duplication	Short-rib thoracic dysplasia 10 with or without polydactyly [RCV001911738]	Chr2:24443763..27746306 [GRCh37] Chr2:2p23.3	uncertain significance
NC_000002.11:g.(?_24443763)_(29022169_?)dup	duplication	Tatton-Brown-Rahman overgrowth syndrome [RCV003113871]\|not provided [RCV003113870]	Chr2:24443763..29022169 [GRCh37] Chr2:2p23.3-23.2	uncertain significance\|no classifications from unflagged records
NC_000002.11:g.(?_24443763)_(30143525_?)dup	duplication	not provided [RCV003113441]	Chr2:24443763..30143525 [GRCh37] Chr2:2p23.3-23.1	uncertain significance
GRCh37/hg19 2p25.1-q13(chr2:11504318-111365996)x1	copy number loss	See cases [RCV002287563]	Chr2:11504318..111365996 [GRCh37] Chr2:2p25.1-q13	pathogenic
GRCh37/hg19 2p25.3-22.3(chr2:706460-35523639)x3	copy number gain	not provided [RCV002473946]	Chr2:706460..35523639 [GRCh37] Chr2:2p25.3-22.3	pathogenic
GRCh37/hg19 2p25.3-22.3(chr2:12771-35541353)x3	copy number gain	See cases [RCV004442780]	Chr2:12771..35541353 [GRCh37] Chr2:2p25.3-22.3	pathogenic
NM_001105519.3(CIMIP2C):c.124G>A (p.Gly42Ser)	single nucleotide variant	not specified [RCV004551065]	Chr2:26575951 [GRCh38] Chr2:26798819 [GRCh37] Chr2:2p23.3	uncertain significance
NM_001105519.3(CIMIP2C):c.134C>A (p.Thr45Asn)	single nucleotide variant	not specified [RCV004551066]	Chr2:26575961 [GRCh38] Chr2:26798829 [GRCh37] Chr2:2p23.3	uncertain significance
NM_001105519.3(CIMIP2C):c.151G>T (p.Asp51Tyr)	single nucleotide variant	not specified [RCV004551067]	Chr2:26575978 [GRCh38] Chr2:26798846 [GRCh37] Chr2:2p23.3	uncertain significance
NM_001105519.3(CIMIP2C):c.335C>T (p.Thr112Met)	single nucleotide variant	not specified [RCV004551068]	Chr2:26576162 [GRCh38] Chr2:26799030 [GRCh37] Chr2:2p23.3	uncertain significance
NM_001105519.3(CIMIP2C):c.406C>T (p.Pro136Ser)	single nucleotide variant	not specified [RCV004551069]	Chr2:26577573 [GRCh38] Chr2:26800441 [GRCh37] Chr2:2p23.3	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	768
Count of miRNA genes:	406
Interacting mature miRNAs:	428
Transcripts:	ENST00000329615, ENST00000409392, ENST00000453368, ENST00000479453
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

RH99278

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	2	26,798,829 - 26,799,014	UniSTS	GRCh37
Build 36	2	26,652,333 - 26,652,518	RGD	NCBI36
Celera	2	26,642,460 - 26,642,645	RGD
Cytogenetic Map	2	p23.3	UniSTS
HuRef	2	26,538,265 - 26,538,450	UniSTS
GeneMap99-GB4 RH Map	2	89.82	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
827	2232	2085	1824	4514	1430	1918	1	340	541	187	1660	4701	4231	20	3602	1	732	1509	1477	166	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001105519	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001322426	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011532810	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011532811	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017003962	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017003963	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017003964	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017003965	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017003966	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047444117	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047444118	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054341714	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054341715	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054341716	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054341717	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054341718	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054341719	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054341720	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054341721	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054341722	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_007073116	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_008486355	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AA725022	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AA758869	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC015977	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC108070	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK091483	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX114846	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471053	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068276	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY021315	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000329615 ⟹ ENSP00000332875

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	26,562,587 - 26,579,524 (+)	Ensembl

Ensembl Acc Id:

ENST00000409392 ⟹ ENSP00000386615

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	26,562,585 - 26,579,532 (+)	Ensembl

Ensembl Acc Id:

ENST00000453368 ⟹ ENSP00000395924

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	26,576,126 - 26,579,524 (+)	Ensembl

Ensembl Acc Id:

ENST00000479453

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	2	26,563,035 - 26,579,529 (+)	Ensembl

RefSeq Acc Id:

NM_001105519 ⟹ NP_001098989

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	26,562,587 - 26,579,524 (+)	NCBI
GRCh37	2	26,785,427 - 26,802,395 (+)	NCBI
Build 36	2	26,638,985 - 26,655,899 (+)	NCBI Archive
Celera	2	26,629,117 - 26,646,026 (+)	RGD
HuRef	2	26,524,922 - 26,541,831 (+)	RGD
CHM1_1	2	26,715,479 - 26,732,449 (+)	NCBI
T2T-CHM13v2.0	2	26,601,745 - 26,618,672 (+)	NCBI

Sequence:

show sequence

AGGCTCGCTGTACTCGCGCACCCACCATGGCCTCCCGCAGCGCGGGCACCCTACTGACCGAGTT
CAATGCCGCCTACGTGCCCCCTGGACTCATGCCCGGGTACCAGGGCCACGTCCCCACTGTGGCC
TTCTCCTTTGGCGCTCCCTACGGCACCACCACCCTCAAGTACTTCCAGGACCACCGCAACAGAG
CCATGGAGAAGAGCCACACTCCCTTCAGCCAAGGCGGCCATTTCCCCACCATCTTCTCCACCAA
CCCCAACCTCCTGCTGATGGAGCGCGCCAGCACCCGGGACCGCTGGCTGCACAAGCCCAGCTAC
ACTCGCTTCAACCTGGACAGCCATCGCTCCACAGAGCTTACGAATTTCTACCAGATGGTCCAGC
AGCATCGGAAGTACTATCAAGACAAGACGGGCACAGTGCCTCGAGTCCCCTACTTTGCGATGCC
CGTGAGGGAGCCGGAACGGTACCCCCTCCCCACCGTCCTGCCTCCTCTGTGCCCAAAGAAGAAG
TGGCACCTTTTAAGACTAGCCCCCGAGAACCTGAAGACCTACCAGACCTTCCCATCAGGGAAGA
GGGTCTCTCCACAGGAGCGGAAAAAGAGAGACTGCTACTTTGAGTTCAGAGCATGAGACTTTTA
GTTCAGAGCAGAGCCTGATGCCTGAGATCCTGGGTCGTGACCAGCCTGGCTTGCTTGGAATAAA
ATCTTTAGCCATGA

hide sequence

RefSeq Acc Id:

NM_001322426 ⟹ NP_001309355

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	26,562,587 - 26,579,524 (+)	NCBI
CHM1_1	2	26,715,479 - 26,732,449 (+)	NCBI
T2T-CHM13v2.0	2	26,601,745 - 26,618,672 (+)	NCBI

Sequence:

show sequence

AGGCTCGCTGTACTCGCGCACCCACCATGGCCTCCCGCAGCGCGGGCACCCTACTGACCGAGTT
CAATGCCGCCTACGTGCCCCCTGGACTCATGCCCGGATGCCATGGGTTGACTCTGATTTAAAGA
GATTCTTAGTACCAGGGCCACGTCCCCACTGTGGCCTTCTCCTTTGGCGCTCCCTACGGCACCA
CCACCCTCAAGTACTTCCAGGACCACCGCAACAGAGCCATGGAGAAGAGCCACACTCCCTTCAG
CCAAGGCGGCCATTTCCCCACCATCTTCTCCACCAACCCCAACCTCCTGCTGATGGAGCGCGCC
AGCACCCGGGACCGCTGGCTGCACAAGCCCAGCTACACTCGCTTCAACCTGGACAGCCATCGCT
CCACAGAGCTTACGAATTTCTACCAGATGGTCCAGCAGCATCGGAAGTACTATCAAGACAAGAC
GGGCACAGTGCCTCGAGTCCCCTACTTTGCGATGCCCGTGAGGGAGCCGGAACGGTACCCCCTC
CCCACCGTCCTGCCTCCTCTGTGCCCAAAGAAGAAGTGGCACCTTTTAAGACTAGCCCCCGAGA
ACCTGAAGACCTACCAGACCTTCCCATCAGGGAAGAGGGTCTCTCCACAGGAGCGGAAAAAGAG
AGACTGCTACTTTGAGTTCAGAGCATGAGACTTTTAGTTCAGAGCAGAGCCTGATGCCTGAGAT
CCTGGGTCGTGACCAGCCTGGCTTGCTTGGAATAAAATCTTTAGCCATGA

hide sequence

RefSeq Acc Id:

XM_011532810 ⟹ XP_011531112

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	26,562,587 - 26,579,524 (+)	NCBI

Sequence:

show sequence

CTCGCGCACCCACCATGGCCTCCCGCAGCGCGGGCACCCTACTGACCGAGTTCAATGCCGCCTA
CGTGCCCCCTGGACTCATGCCCGGGCAGCGCCCGTTCTGTTGGTGAGGAGACCGAGGCCCAAGG
CACAGGGAAAGACCCCAGAAGAGGAGGTGGCTACGGCCATGGCATGGCTGCCATCACCCAAGAC
AGACCCCGGAGGTTCACCAGTGTTTAAGAGGCGGGCAGAGGAGAAGGCTCATGAAGGTGTGGTC
AGAGATGTTGGCAAAAGCAACAGAAAGGAGCAAAGGTGTCATCCAAACCAACAGCAGCGTTTCA
GGAAGGGAGAGGTACCAGGGCCACGTCCCCACTGTGGCCTTCTCCTTTGGCGCTCCCTACGGCA
CCACCACCCTCAAGTACTTCCAGGACCACCGCAACAGAGCCATGGAGAAGAGCCACACTCCCTT
CAGCCAAGGCGGCCATTTCCCCACCATCTTCTCCACCAACCCCAACCTCCTGCTGATGGAGCGC
GCCAGCACCCGGGACCGCTGGCTGCACAAGCCCAGCTACACTCGCTTCAACCTGGACAGCCATC
GCTCCACAGAGCTTACGAATTTCTACCAGATGGTCCAGCAGCATCGGAAGTACTATCAAGACAA
GACGGGCACAGTGCCTCGAGTCCCCTACTTTGCGATGCCCGTGAGGGAGCCGGAACGGTACCCC
CTCCCCACCGTCCTGCCTCCTCTGTGCCCAAAGAAGAAGTGGCACCTTTTAAGACTAGCCCCCG
AGAACCTGAAGACCTACCAGACCTTCCCATCAGGGAAGAGGGTCTCTCCACAGGAGCGGAAAAA
GAGAGACTGCTACTTTGAGTTCAGAGCATGAGACTTTTAGTTCAGAGCAGAGCCTGATGCCTGA
GATCCTGGGTCGTGACCAGCCTGGCTTGCTTGGAATAAAATCTTTAGCCATGACCATGCTACCC
ATCTCTCCTCTGGATCCCAGGGACACTCGGCCACAGCAGGAAATGCCCCCTGAAGGTCACACAG
CATTGTGTCCTGAGGGCCTGCGGAAAGCTCTGTCCCAGGGACTCAAGCCAAGGAAAAGTGGTGT
CCGGCTACCTGGCAGGTCCAGCTACCTTCTCCCCAAGGTGGGGCAAATGGAGTTGAGGAATGTA
GGGTTCCCTAGTCTTAGTGGCAGGTCACTCAGGTACAGAGACCTCCCACCAGATTCCACTGGTA
TAAGCAAGGAAGTCCAATTGCGCCGGTCTAAGAATGAAGGGGAAATGACCCCAGAATAATTGCA
CTGGGTGTGATTGGAAAGGAATTTTCATCAGAGCCCTGACTTGGCGTCGTTTTGTCCACACGAT
CACTTGTGAGGGAAGAGGTGTTATTATCCCCACTTTACTGATAAAGATATTGAGGCTCAGAGAA
GGTGAGAAAGTTGCCCAAGCTTACATAGTTGGGAAGTAACACAGCCAGAATTTGAATTCAGGTC
TTTCTGACTCCCAAGCCCTGGTTTTTCCACGACACAGCCTGCTTGTGGTCCATGTGGAGACTGA
GGGGCGGGGAAGACATAAACCTGGGGATCCTGAAGGAGTCTGTGGAGGGCGGAGCCTGGGAGAA
GAAGCTGTGTGCAGCAGGCACCTTCTGCATTCTGCCTAGGCTGGCTTGGTAGGGTGGATGCAGC
ATCTACCCCTGAAGCTGTTTCTAGAAGACGATGGGAGGGAATGACCTAGGACCAGACAACTCTT
CCAGGAATCCCTATGTTTCGGGGCCCCAGGCCGGAAGTGGATGCTGGGCATGGGTGCTGAAGCC
ACATGCCTGGGGTGGTCTTTGAGGGTCTGGAGGGTCTGCTCCCACAAGGCTGCTGCTTCCTACC
TCCCAGGAGGCTCCTGCCTGCTGGGGCAGGGGTGGGACGGGGGTGAGAGCCCCTCAGTGACAGG
ATCTGGGATGGGGACCTTAGACCAAGGCGGGGACCTTCTCCAACATTCCAGCACCTCTTAGATT
TGATCAAGGGCCCTCCATTAAGGGACAAGGCCCTTATTGTCCTTCAATGGGTGAATCAGGACCT
AACTGCAAGGGGAACACAGCCCGGTTCAAGTACACCTGGGGCTGAAGCAGCCCCTCCTCTGTAG
CCAGCGATTAGACACCTCCCCCAGGACAGTGTAAATAAGAAAAACCCAATGGGGGGCTTCTTCT
GTGTCTCAAAGTCCCTGAGGAGCTGGACCCCAAAGGCTGTCTGTGGTGGCCAAATTCATTCCAG
GGCTTGGCTGAATAGCAAAGCAAATAAACTCTAATTGCTGGTCCCACAATCAGGGCCAAGATGC
CTTCTCCCTCAGAAGGGGAGTGGGGAGCCGGGCACCGGCTGGAATGGCTGCTATGTGCACGTCT
CTGTGCAGCTGTGAACTGTGAGGTGCTGGGGGTCGGGGGTTTTGATGAAGGGAGGGAAGGACAT
GTATCTTGCTAGGGACCTTCATCCCATTTGGCTTGGCCCCCTGCTATGACATGGGTTGAGATTT
GAACTATTCCCTCAGAAAGATTGCCACCCCAGCCTGCTTGACATCGCTGGCACACTGAAGCCCT
GGAAAGGGCAGTTCTTAATAAAAAGTACCAT

hide sequence

RefSeq Acc Id:

XM_011532811 ⟹ XP_011531113

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	26,572,827 - 26,579,524 (+)	NCBI

Sequence:

show sequence

CCCCCCAATTTTGGTTGCTTAAATTAGTTTTACTTTGACAGGTTTTATAACATTTACATTCCAT
TCTGTAACTAGCATTCACCTAGTTGCTATTCCTGGTTCTGCACTTCAATAGATTTGAAGCTCAC
CACCACTCATTCTAACAGAGGCTCTACATTACTGAGTTGGTTTTTTTTTTTTTTTCTCTTGAAT
CATCTCTTGATTGGCAGGATTTTGTCGCTGAACATGACTTTCAAGAAGAGCTTGTGGGTGCTTT
AGTTGCTGAGCCCTTTCATGCTAGGAAAGGGTGGCTTTGTACCCCTGTGACCGCCTGGCTGGTG
TGGTATTCTTGGGTTATGCTCTTTTCCCTGCGGAATGCTGTGGGTATCTTCCTTTGCCTTTCAT
TCTATCACTTCATCTTTTTGCTGGGGTTGGCAGCACCTGGAGATGAGCATCTCTTCCATTCCCT
ACATTCTGAACCACTTGAGAAAGAAGGTGAAAGAGGAATGTGGCTGTTAGAGAATGGGGTGAAC
ACAGCCTCAGAATGAGACAGGCGCTGGGGCCGGCCTCCTCCCCACGGGCAGAGCCTGTCCATCT
AACACCTAAGGCTTGGAGGGGCGGAGCAGGCTTCCTTGCTTCCGAGGAGGAGAAGGAGGGAGGG
GAGAGGTGGGCCACAGGCTGCCCGATGGTTCCAGTGTGGGAGGAACCTCCCCTCCACGTGGGAG
GAGCCCTCAGGATAGAGGAGGCAGCATCTCCCCATCACTTGTCTTTGACATCTTAATTTATTGA
ATCTATATCTTGATTAAGCTTCATCTACAGCACGAAGTGCTCTCAGGAACTTGCTTACACGTCA
CAGGTTAGGTTTTTTCCCAAACAAGTTTCTTCATCAGTGCGAATGTTGCAGCGGGACAGTGTGA
GCCGAGGACATTGGATTTGGCAACAGCAGGACCTGATATGACCTTAATTTAGATGTAGAGGTTC
ACGTTTCAATGGTGGGTCTGAAGGCAGACTGAGGGAGGTCAAGGAAAGGGTGAGAGTTGAGAAA
TCAGGCAGAAGATGCAGCGTATTCCTTAGTGAGCTCCAGAAGGAGGGAGGGAATCTGCAATCCC
GCCTTCCTCTTCGCCATCTTTAATGTCTCCTCTCTTGGCTGCTTCCCCTCTGCCTATAAACGGG
CACCAGCCTTTACTGTGGAAATGTACAATCTAGGAACCACGGCTCATGCCCACTTACAGGCAGA
GGGGAAGAGGCCGAGAGGGAGGGGGATATTAAAGATGACGGAAGAAGGGCAGAGGCTGAGAGAG
ACAGGGAGGAGTCGGATGGGACAATGAGGCCTTGGGTGAAACCAGAGCAGGAGCTCCAGACCCA
GGAGTGGCGCCCAGGCCGGGAGGAAGACTCTGTCTCCTGAAGCGGCCAAGGTGACCACACAGCC
TCACAGGAGAGAGAGCAAGGCACCCACCAATTCCTCCGTCTTCCCAGTTCCAGAGGAGACCTGG
CCTCCGCGGGGAACTCAGGGGGCCAAGGAGGAAGGGCACTGAGGTGGTGGAGAAGAGTCAGGAC
CGCCAGGGTCACGGTGTCAAGGGCGGCGCCTCTGTGGCATCCAGGGATGCAGCGCCCGTTCTGT
TGGTGAGGAGACCGAGGCCCAAGGCACAGGGAAAGACCCCAGAAGAGGAGGTGGCTACGGCCAT
GGCATGGCTGCCATCACCCAAGACAGACCCCGGAGGTTCACCAGTGTTTAAGAGGCGGGCAGAG
GAGAAGGCTCATGAAGGTGTGGTCAGAGATGTTGGCAAAAGCAACAGAAAGGAGCAAAGGTGTC
ATCCAAACCAACAGCAGCGTTTCAGGAAGGGAGAGGTACCAGGGCCACGTCCCCACTGTGGCCT
TCTCCTTTGGCGCTCCCTACGGCACCACCACCCTCAAGTACTTCCAGGACCACCGCAACAGAGC
CATGGAGAAGAGCCACACTCCCTTCAGCCAAGGCGGCCATTTCCCCACCATCTTCTCCACCAAC
CCCAACCTCCTGCTGATGGAGCGCGCCAGCACCCGGGACCGCTGGCTGCACAAGCCCAGCTACA
CTCGCTTCAACCTGGACAGCCATCGCTCCACAGAGCTTACGAATTTCTACCAGATGGTCCAGCA
GCATCGGAAGTACTATCAAGACAAGACGGGCACAGTGCCTCGAGTCCCCTACTTTGCGATGCCC
GTGAGGGAGCCGGAACGGTACCCCCTCCCCACCGTCCTGCCTCCTCTGTGCCCAAAGAAGAAGT
GGCACCTTTTAAGACTAGCCCCCGAGAACCTGAAGACCTACCAGACCTTCCCATCAGGGAAGAG
GGTCTCTCCACAGGAGCGGAAAAAGAGAGACTGCTACTTTGAGTTCAGAGCATGAGACTTTTAG
TTCAGAGCAGAGCCTGATGCCTGAGATCCTGGGTCGTGACCAGCCTGGCTTGCTTGGAATAAAA
TCTTTAGCCATGACCATGCTACCCATCTCTCCTCTGGATCCCAGGGACACTCGGCCACAGCAGG
AAATGCCCCCTGAAGGTCACACAGCATTGTGTCCTGAGGGCCTGCGGAAAGCTCTGTCCCAGGG
ACTCAAGCCAAGGAAAAGTGGTGTCCGGCTACCTGGCAGGTCCAGCTACCTTCTCCCCAAGGTG
GGGCAAATGGAGTTGAGGAATGTAGGGTTCCCTAGTCTTAGTGGCAGGTCACTCAGGTACAGAG
ACCTCCCACCAGATTCCACTGGTATAAGCAAGGAAGTCCAATTGCGCCGGTCTAAGAATGAAGG
GGAAATGACCCCAGAATAATTGCACTGGGTGTGATTGGAAAGGAATTTTCATCAGAGCCCTGAC
TTGGCGTCGTTTTGTCCACACGATCACTTGTGAGGGAAGAGGTGTTATTATCCCCACTTTACTG
ATAAAGATATTGAGGCTCAGAGAAGGTGAGAAAGTTGCCCAAGCTTACATAGTTGGGAAGTAAC
ACAGCCAGAATTTGAATTCAGGTCTTTCTGACTCCCAAGCCCTGGTTTTTCCACGACACAGCCT
GCTTGTGGTCCATGTGGAGACTGAGGGGCGGGGAAGACATAAACCTGGGGATCCTGAAGGAGTC
TGTGGAGGGCGGAGCCTGGGAGAAGAAGCTGTGTGCAGCAGGCACCTTCTGCATTCTGCCTAGG
CTGGCTTGGTAGGGTGGATGCAGCATCTACCCCTGAAGCTGTTTCTAGAAGACGATGGGAGGGA
ATGACCTAGGACCAGACAACTCTTCCAGGAATCCCTATGTTTCGGGGCCCCAGGCCGGAAGTGG
ATGCTGGGCATGGGTGCTGAAGCCACATGCCTGGGGTGGTCTTTGAGGGTCTGGAGGGTCTGCT
CCCACAAGGCTGCTGCTTCCTACCTCCCAGGAGGCTCCTGCCTGCTGGGGCAGGGGTGGGACGG
GGGTGAGAGCCCCTCAGTGACAGGATCTGGGATGGGGACCTTAGACCAAGGCGGGGACCTTCTC
CAACATTCCAGCACCTCTTAGATTTGATCAAGGGCCCTCCATTAAGGGACAAGGCCCTTATTGT
CCTTCAATGGGTGAATCAGGACCTAACTGCAAGGGGAACACAGCCCGGTTCAAGTACACCTGGG
GCTGAAGCAGCCCCTCCTCTGTAGCCAGCGATTAGACACCTCCCCCAGGACAGTGTAAATAAGA
AAAACCCAATGGGGGGCTTCTTCTGTGTCTCAAAGTCCCTGAGGAGCTGGACCCCAAAGGCTGT
CTGTGGTGGCCAAATTCATTCCAGGGCTTGGCTGAATAGCAAAGCAAATAAACTCTAATTGCTG
GTCCCACAATCAGGGCCAAGATGCCTTCTCCCTCAGAAGGGGAGTGGGGAGCCGGGCACCGGCT
GGAATGGCTGCTATGTGCACGTCTCTGTGCAGCTGTGAACTGTGAGGTGCTGGGGGTCGGGGGT
TTTGATGAAGGGAGGGAAGGACATGTATCTTGCTAGGGACCTTCATCCCATTTGGCTTGGCCCC
CTGCTATGACATGGGTTGAGATTTGAACTATTCCCTCAGAAAGATTGCCACCCCAGCCTGCTTG
ACATCGCTGGCACACTGAAGCCCTGGAAAGGGCAGTTCTTAATAAAAAGTACCAT

hide sequence

RefSeq Acc Id:

XM_017003962 ⟹ XP_016859451

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	26,562,587 - 26,579,524 (+)	NCBI

Sequence:

show sequence

GCACCCACCATGGCCTCCCGCAGCGCGGGCACCCTACTGACCGAGTTCAATGCCGCCTACGTGC
CCCCTGGACTCATGCCCGGATGCCATGGGTTGACTCTGATTTAAAGAGATTCTTAGCAGCGCCC
GTTCTGTTGGTGAGGAGACCGAGGCCCAAGGCACAGGGAAAGACCCCAGAAGAGGTACCAGGGC
CACGTCCCCACTGTGGCCTTCTCCTTTGGCGCTCCCTACGGCACCACCACCCTCAAGTACTTCC
AGGACCACCGCAACAGAGCCATGGAGAAGAGCCACACTCCCTTCAGCCAAGGCGGCCATTTCCC
CACCATCTTCTCCACCAACCCCAACCTCCTGCTGATGGAGCGCGCCAGCACCCGGGACCGCTGG
CTGCACAAGCCCAGCTACACTCGCTTCAACCTGGACAGCCATCGCTCCACAGAGCTTACGAATT
TCTACCAGATGGTCCAGCAGCATCGGAAGTACTATCAAGACAAGACGGGCACAGTGCCTCGAGT
CCCCTACTTTGCGATGCCCGTGAGGGAGCCGGAACGGTACCCCCTCCCCACCGTCCTGTTGCCT
GGCCACTTGCACTGCTGCTGACAGTTTCACAACGAACGCAAAGGGCCAACCAGGTGGTTGGGAG
AAGAGGGCCTCCTCTGTGCCCAAAGAAGAAGTGGCACCTTTTAAGACTAGCCCCCGAGAACCTG
AAGACCTACCAGACCTTCCCATCAGGGAAGAGGGTCTCTCCACAGGAGCGGAAAAAGAGAGACT
GCTACTTTGAGTTCAGAGCATGAGACTTTTAGTTCAGAGCAGAGCCTGATGCCTGAGATCCTGG
GTCGTGACCAGCCTGGCTTGCTTGGAATAAAATCTTTAGCCATGACCATG

hide sequence

RefSeq Acc Id:

XM_017003963 ⟹ XP_016859452

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	26,562,587 - 26,579,524 (+)	NCBI

Sequence:

show sequence

TGGCCTCCCGCAGCGCGGGCACCCTACTGACCGAGTTCAATGCCGCCTACGTGCCCCCTGGACT
CATGCCCGGGCCTGGGGCCCTTCACTGATCTGTGGCTCCACCACCCCCACCGTGATCGGCAGGT
ACCAGGGCCACGTCCCCACTGTGGCCTTCTCCTTTGGCGCTCCCTACGGCACCACCACCCTCAA
GTACTTCCAGGACCACCGCAACAGAGCCATGGAGAAGAGCCACACTCCCTTCAGCCAAGGCGGC
CATTTCCCCACCATCTTCTCCACCAACCCCAACCTCCTGCTGATGGAGCGCGCCAGCACCCGGG
ACCGCTGGCTGCACAAGCCCAGCTACACTCGCTTCAACCTGGACAGCCATCGCTCCACAGAGCT
TACGAATTTCTACCAGATGGTCCAGCAGCATCGGAAGTACTATCAAGACAAGACGGGCACAGTG
CCTCGAGTCCCCTACTTTGCGATGCCCGTGAGGGAGCCGGAACGGTACCCCCTCCCCACCGTCC
TGTTGCCTGGCCACTTGCACTGCTGCTGACAGTTTCACAACGAACGCAAAGGGCCAACCAGGTG
GTTGGGAGAAGAGGGCCTCCTCTGTGCCCAAAGAAGAAGTGGCACCTTTTAAGACTAGCCCCCG
AGAACCTGAAGACCTACCAGACCTTCCCATCAGGGAAGAGGGTCTCTCCACAGGAGCGGAAAAA
GAGAGACTGCTACTTTGAGTTCAGAGCATGAGACTTTTAGTTCAGAGCAGAGCCTGATGCCTGA
GATCCTGGGTCGTGACCAGCCTGGCTTGCTTGGAATAAAATCTTTAGCCATGACCATG

hide sequence

RefSeq Acc Id:

XM_017003964 ⟹ XP_016859453

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	26,562,587 - 26,579,524 (+)	NCBI

Sequence:

show sequence

CCGTGGGGCGGAGCGGAGCGCCAGGCTCGCTGTACTCGCGCACCCACCATGGCCTCCCGCAGCG
CGGGCACCCTACTGACCGAGTTCAATGCCGCCTACGTGCCCCCTGGACTCATGCCCGGATGCCA
TGGGTTGACTCTGATTTAAAGAGATTCTTAGTACCAGGGCCACGTCCCCACTGTGGCCTTCTCC
TTTGGCGCTCCCTACGGCACCACCACCCTCAAGTACTTCCAGGACCACCGCAACAGAGCCATGG
AGAAGAGCCACACTCCCTTCAGCCAAGGCGGCCATTTCCCCACCATCTTCTCCACCAACCCCAA
CCTCCTGCTGATGGAGCGCGCCAGCACCCGGGACCGCTGGCTGCACAAGCCCAGCTACACTCGC
TTCAACCTGGACAGCCATCGCTCCACAGAGCTTACGAATTTCTACCAGATGGTCCAGCAGCATC
GGAAGTACTATCAAGACAAGACGGGCACAGTGCCTCGAGTCCCCTACTTTGCGATGCCCGTGAG
GGAGCCGGAACGGTACCCCCTCCCCACCGTCCTGTTGCCTGGCCACTTGCACTGCTGCTGACAG
TTTCACAACGAACGCAAAGGGCCAACCAGGTGGTTGGGAGAAGAGGGCCTCCTCTGTGCCCAAA
GAAGAAGTGGCACCTTTTAAGACTAGCCCCCGAGAACCTGAAGACCTACCAGACCTTCCCATCA
GGGAAGAGGGTCTCTCCACAGGAGCGGAAAAAGAGAGACTGCTACTTTGAGTTCAGAGCATGAG
ACTTTTAGTTCAGAGCAGAGCCTGATGCCTGAGATCCTGGGTCGTGACCAGCCTGGCTTGCTTG
GAATAAAATCTTTAGCCATGACCATG

hide sequence

RefSeq Acc Id:

XM_017003965 ⟹ XP_016859454

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	26,562,587 - 26,579,524 (+)	NCBI

Sequence:

show sequence

GCACCCACCATGGCCTCCCGCAGCGCGGGCACCCTACTGACCGAGTTCAATGCCGCCTACGTGC
CCCCTGGACTCATGCCCGGATGCCATGGGTTGACTCTGATTTAAAGAGATTCTTAGCAGCGCCC
GTTCTGTTGGTGAGGAGACCGAGGCCCAAGGCACAGGGAAAGACCCCAGAAGAGGTACCAGGGC
CACGTCCCCACTGTGGCCTTCTCCTTTGGCGCTCCCTACGGCACCACCACCCTCAAGTACTTCC
AGGACCACCGCAACAGAGCCATGGAGAAGAGCCACACTCCCTTCAGCCAAGGCGGCCATTTCCC
CACCATCTTCTCCACCAACCCCAACCTCCTGCTGATGGAGCGCGCCAGCACCCGGGACCGCTGG
CTGCACAAGCCCAGCTACACTCGCTTCAACCTGGACAGCCATCGCTCCACAGAGCTTACGAATT
TCTACCAGATGGTCCAGCAGCATCGGAAGTACTATCAAGACAAGACGGGCACAGTGCCTCGAGT
CCCCTACTTTGCGATGCCCGTGAGGGAGCCGGAACGGTACCCCCTCCCCACCGTCCTGCCTCCT
CTGTGCCCAAAGAAGAAGTGGCACCTTTTAAGACTAGCCCCCGAGAACCTGAAGACCTACCAGA
CCTTCCCATCAGGGAAGAGGGTCTCTCCACAGGAGCGGAAAAAGAGAGACTGCTACTTTGAGTT
CAGAGCATGAGACTTTTAGTTCAGAGCAGAGCCTGATGCCTGAGATCCTGGGTCGTGACCAGCC
TGGCTTGCTTGGAATAAAATCTTTAGCCATGACCATGCTACCCATCTCTCCTCTGGATCCCAGG
GACACTCGGCCACAGCAGGAAATGCCCCCTGAAGGTCACACAGCATTGTGTCCTGAGGGCCTGC
GGAAAGCTCTGTCCCAGGGACTCAAGCCAAGGAAAAGTGGTGTCCGGCTACCTGGCAGGTCCAG
CTACCTTCTCCCCAAGGTGGGGCAAATGGAGTTGAGGAATGTAGGGTTCCCTAGTCTTAGTGGC
AGGTCACTCAGGTACAGAGACCTCCCACCAGATTCCACTGGTATAAGCAAGGAAGTCCAATTGC
GCCGGTCTAAGAATGAAGGGGAAATGACCCCAGAATAATTGCACTGGGTGTGATTGGAAAGGAA
TTTTCATCAGAGCCCTGACTTGGCGTCGTTTTGTCCACACGATCACTTGTGAGGGAAGAGGTGT
TATTATCCCCACTTTACTGATAAAGATATTGAGGCTCAGAGAAGGTGAGAAAGTTGCCCAAGCT
TACATAGTTGGGAAGTAACACAGCCAGAATTTGAATTCAGGTCTTTCTGACTCCCAAGCCCTGG
TTTTTCCACGACACAGCCTGCTTGTGGTCCATGTGGAGACTGAGGGGCGGGGAAGACATAAACC
TGGGGATCCTGAAGGAGTCTGTGGAGGGCGGAGCCTGGGAGAAGAAGCTGTGTGCAGCAGGCAC
CTTCTGCATTCTGCCTAGGCTGGCTTGGTAGGGTGGATGCAGCATCTACCCCTGAAGCTGTTTC
TAGAAGACGATGGGAGGGAATGACCTAGGACCAGACAACTCTTCCAGGAATCCCTATGTTTCGG
GGCCCCAGGCCGGAAGTGGATGCTGGGCATGGGTGCTGAAGCCACATGCCTGGGGTGGTCTTTG
AGGGTCTGGAGGGTCTGCTCCCACAAGGCTGCTGCTTCCTACCTCCCAGGAGGCTCCTGCCTGC
TGGGGCAGGGGTGGGACGGGGGTGAGAGCCCCTCAGTGACAGGATCTGGGATGGGGACCTTAGA
CCAAGGCGGGGACCTTCTCCAACATTCCAGCACCTCTTAGATTTGATCAAGGGCCCTCCATTAA
GGGACAAGGCCCTTATTGTCCTTCAATGGGTGAATCAGGACCTAACTGCAAGGGGAACACAGCC
CGGTTCAAGTACACCTGGGGCTGAAGCAGCCCCTCCTCTGTAGCCAGCGATTAGACACCTCCCC
CAGGACAGTGTAAATAAGAAAAACCCAATGGGGGGCTTCTTCTGTGTCTCAAAGTCCCTGAGGA
GCTGGACCCCAAAGGCTGTCTGTGGTGGCCAAATTCATTCCAGGGCTTGGCTGAATAGCAAAGC
AAATAAACTCTAATTGCTGGTCCCACAATCAGGGCCAAGATGCCTTCTCCCTCAGAAGGGGAGT
GGGGAGCCGGGCACCGGCTGGAATGGCTGCTATGTGCACGTCTCTGTGCAGCTGTGAACTGTGA
GGTGCTGGGGGTCGGGGGTTTTGATGAAGGGAGGGAAGGACATGTATCTTGCTAGGGACCTTCA
TCCCATTTGGCTTGGCCCCCTGCTATGACATGGGTTGAGATTTGAACTATTCCCTCAGAAAGAT
TGCCACCCCAGCCTGCTTGACATCGCTGGCACACTGAAGCCCTGGAAAGGGCAGTTCTTAATAA
AAAGTACCAT

hide sequence

RefSeq Acc Id:

XM_017003966 ⟹ XP_016859455

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	26,562,587 - 26,579,524 (+)	NCBI

Sequence:

show sequence

CTCGCGCACCCACCATGGCCTCCCGCAGCGCGGGCACCCTACTGACCGAGTTCAATGCCGCCTA
CGTGCCCCCTGGACTCATGCCCGGGCAGCGCCCGTTCTGTTGGTGAGGAGACCGAGGCCCAAGG
CACAGGGAAAGACCCCAGAAGAGGAGGTGGCTACGGCCATGGCATGGCTGCCATCACCCAAGAC
AGACCCCGGAGGTTCACCAGTGTTTAAGAGGCGGGCAGAGGAGAAGGCTCATGAAGGTGTGGTC
AGAGATGTTGGCAAAAGCAACAGAAAGGAGCAAAGGTGTCATCCAAACCAACAGCAGCGTTTCA
GGAAGGGAGAGGTACCAGGGCCACGTCCCCACTGTGGCCTTCTCCTTTGGCGCTCCCTACGGCA
CCACCACCCTCAAGTACTTCCAGGACCACCGCAACAGAGCCATGGAGAAGAGCCACACTCCCTT
CAGCCAAGGCGGCCATTTCCCCACCATCTTCTCCACCAACCCCAACCTCCTGCTGATGGAGCGC
GCCAGCACCCGGGACCGCTGGCTGCACAAGCCCAGCTACACTCGCTTCAACCTGGACAGCCATC
GCTCCACAGAGCTTACGAATTTCTACCAGATGGTCCAGCAGCATCGGAAGTACTATCAAGACAA
GACGGGCACAGTGCCTCGAGTCCCCTACTTTGCGATGCCCGTGAGGGAGCCGGAACGGTACCCC
CTCCCCACCGTCCTGTTGCCTGGCCACTTGCACTGCTGCTGACAGTTTCACAACGAACGCAAAG
GGCCAACCAGGTGGTTGGGAGAAGAGGGCCTCCTCTGTGCCCAAAGAAGAAGTGGCACCTTTTA
AGACTAGCCCCCGAGAACCTGAAGACCTACCAGACCTTCCCATCAGGGAAGAGGGTCTCTCCAC
AGGAGCGGAAAAAGAGAGACTGCTACTTTGAGTTCAGAGCATGAGACTTTTAGTTCAGAGCAGA
GCCTGATGCCTGAGATCCTGGGTCGTGACCAGCCTGGCTTGCTTGGAATAAAATCTTTAGCCAT
GACCATG

hide sequence

RefSeq Acc Id:

XM_047444117 ⟹ XP_047300073

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	26,562,587 - 26,579,524 (+)	NCBI

RefSeq Acc Id:

XM_047444118 ⟹ XP_047300074

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	26,572,832 - 26,579,524 (+)	NCBI

RefSeq Acc Id:

XM_054341714 ⟹ XP_054197689

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	26,601,745 - 26,618,672 (+)	NCBI

RefSeq Acc Id:

XM_054341715 ⟹ XP_054197690

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	26,601,745 - 26,618,672 (+)	NCBI

RefSeq Acc Id:

XM_054341716 ⟹ XP_054197691

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	26,601,745 - 26,618,672 (+)	NCBI

RefSeq Acc Id:

XM_054341717 ⟹ XP_054197692

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	26,601,745 - 26,618,672 (+)	NCBI

RefSeq Acc Id:

XM_054341718 ⟹ XP_054197693

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	26,611,975 - 26,618,672 (+)	NCBI

RefSeq Acc Id:

XM_054341719 ⟹ XP_054197694

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	26,601,745 - 26,618,672 (+)	NCBI

RefSeq Acc Id:

XM_054341720 ⟹ XP_054197695

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	26,613,274 - 26,618,672 (+)	NCBI

RefSeq Acc Id:

XM_054341721 ⟹ XP_054197696

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	26,601,745 - 26,618,672 (+)	NCBI

RefSeq Acc Id:

XM_054341722 ⟹ XP_054197697

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	26,611,980 - 26,618,672 (+)	NCBI

RefSeq Acc Id:

XR_007073116

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	2	26,562,587 - 26,579,524 (+)	NCBI

RefSeq Acc Id:

XR_008486355

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	2	26,601,745 - 26,618,672 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_001098989	(Get FASTA)	NCBI Sequence Viewer
	NP_001309355	(Get FASTA)	NCBI Sequence Viewer
	XP_011531112	(Get FASTA)	NCBI Sequence Viewer
	XP_011531113	(Get FASTA)	NCBI Sequence Viewer
	XP_016859451	(Get FASTA)	NCBI Sequence Viewer
	XP_016859452	(Get FASTA)	NCBI Sequence Viewer
	XP_016859453	(Get FASTA)	NCBI Sequence Viewer
	XP_016859454	(Get FASTA)	NCBI Sequence Viewer
	XP_016859455	(Get FASTA)	NCBI Sequence Viewer
	XP_047300073	(Get FASTA)	NCBI Sequence Viewer
	XP_047300074	(Get FASTA)	NCBI Sequence Viewer
	XP_054197689	(Get FASTA)	NCBI Sequence Viewer
	XP_054197690	(Get FASTA)	NCBI Sequence Viewer
	XP_054197691	(Get FASTA)	NCBI Sequence Viewer
	XP_054197692	(Get FASTA)	NCBI Sequence Viewer
	XP_054197693	(Get FASTA)	NCBI Sequence Viewer
	XP_054197694	(Get FASTA)	NCBI Sequence Viewer
	XP_054197695	(Get FASTA)	NCBI Sequence Viewer
	XP_054197696	(Get FASTA)	NCBI Sequence Viewer
	XP_054197697	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	A6NJV1	(Get FASTA)	NCBI Sequence Viewer
	EAX00681	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000332875
	ENSP00000332875.3
	ENSP00000386615
	ENSP00000386615.1
	ENSP00000395924.1

RefSeq Acc Id:	NP_001098989 ⟸ NM_001105519
- Peptide Label:	isoform 1
- UniProtKB:	A6NJV1 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MASRSAGTLLTEFNAAYVPPGLMPGYQGHVPTVAFSFGAPYGTTTLKYFQDHRNRAMEKSHTPF SQGGHFPTIFSTNPNLLLMERASTRDRWLHKPSYTRFNLDSHRSTELTNFYQMVQQHRKYYQDK TGTVPRVPYFAMPVREPERYPLPTVLPPLCPKKKWHLLRLAPENLKTYQTFPSGKRVSPQERKK RDCYFEFRA hide sequence

RefSeq Acc Id:

XP_011531112 ⟸ XM_011532810

- Peptide Label:

isoform X4

- Sequence:

show sequence

MKVWSEMLAKATERSKGVIQTNSSVSGRERYQGHVPTVAFSFGAPYGTTTLKYFQDHRNRAMEK
SHTPFSQGGHFPTIFSTNPNLLLMERASTRDRWLHKPSYTRFNLDSHRSTELTNFYQMVQQHRK
YYQDKTGTVPRVPYFAMPVREPERYPLPTVLPPLCPKKKWHLLRLAPENLKTYQTFPSGKRVSP
QERKKRDCYFEFRA

hide sequence

RefSeq Acc Id:

XP_011531113 ⟸ XM_011532811

- Peptide Label:

isoform X4

- Sequence:

show sequence

MKVWSEMLAKATERSKGVIQTNSSVSGRERYQGHVPTVAFSFGAPYGTTTLKYFQDHRNRAMEK
SHTPFSQGGHFPTIFSTNPNLLLMERASTRDRWLHKPSYTRFNLDSHRSTELTNFYQMVQQHRK
YYQDKTGTVPRVPYFAMPVREPERYPLPTVLPPLCPKKKWHLLRLAPENLKTYQTFPSGKRVSP
QERKKRDCYFEFRA

hide sequence

RefSeq Acc Id:	NP_001309355 ⟸ NM_001322426
- Peptide Label:	isoform 2
- UniProtKB:	B8ZZ55 (UniProtKB/TrEMBL)
- Sequence:	show sequence MPWVDSDLKRFLVPGPRPHCGLLLWRSLRHHHPQVLPGPPQQSHGEEPHSLQPRRPFPHHLLHQ PQPPADGARQHPGPLAAQAQLHSLQPGQPSLHRAYEFLPDGPAASEVLSRQDGHSASSPLLCDA REGAGTVPPPHRPASSVPKEEVAPFKTSPREPEDLPDLPIREEGLSTGAEKERLLL hide sequence

RefSeq Acc Id:

XP_016859453 ⟸ XM_017003964

- Peptide Label:

isoform X3

- Sequence:

show sequence

MPWVDSDLKRFLVPGPRPHCGLLLWRSLRHHHPQVLPGPPQQSHGEEPHSLQPRRPFPHHLLHQ
PQPPADGARQHPGPLAAQAQLHSLQPGQPSLHRAYEFLPDGPAASEVLSRQDGHSASSPLLCDA
REGAGTVPPPHRPVAWPLALLLTVSQRTQRANQVVGRRGPPLCPKKKWHLLRLAPENLKTYQTF
PSGKRVSPQERKKRDCYFEFRA

hide sequence

RefSeq Acc Id:	XP_016859455 ⟸ XM_017003966
- Peptide Label:	isoform X6
- Sequence:	show sequence MKVWSEMLAKATERSKGVIQTNSSVSGRERYQGHVPTVAFSFGAPYGTTTLKYFQDHRNRAMEK SHTPFSQGGHFPTIFSTNPNLLLMERASTRDRWLHKPSYTRFNLDSHRSTELTNFYQMVQQHRK YYQDKTGTVPRVPYFAMPVREPERYPLPTVLLPGHLHCC hide sequence

RefSeq Acc Id:

XP_016859454 ⟸ XM_017003965

- Peptide Label:

isoform X5

- Sequence:

show sequence

MPWVDSDLKRFLAAPVLLVRRPRPKAQGKTPEEVPGPRPHCGLLLWRSLRHHHPQVLPGPPQQS
HGEEPHSLQPRRPFPHHLLHQPQPPADGARQHPGPLAAQAQLHSLQPGQPSLHRAYEFLPDGPA
ASEVLSRQDGHSASSPLLCDAREGAGTVPPPHRPASSVPKEEVAPFKTSPREPEDLPDLPIREE
GLSTGAEKERLLL

hide sequence

RefSeq Acc Id:

XP_016859451 ⟸ XM_017003962

- Peptide Label:

isoform X1

- Sequence:

show sequence

MPWVDSDLKRFLAAPVLLVRRPRPKAQGKTPEEVPGPRPHCGLLLWRSLRHHHPQVLPGPPQQS
HGEEPHSLQPRRPFPHHLLHQPQPPADGARQHPGPLAAQAQLHSLQPGQPSLHRAYEFLPDGPA
ASEVLSRQDGHSASSPLLCDAREGAGTVPPPHRPVAWPLALLLTVSQRTQRANQVVGRRGPPLC
PKKKWHLLRLAPENLKTYQTFPSGKRVSPQERKKRDCYFEFRA

hide sequence

RefSeq Acc Id:

XP_016859452 ⟸ XM_017003963

- Peptide Label:

isoform X2

- Sequence:

show sequence

MPPTCPLDSCPGLGPFTDLWLHHPHRDRQVPGPRPHCGLLLWRSLRHHHPQVLPGPPQQSHGEE
PHSLQPRRPFPHHLLHQPQPPADGARQHPGPLAAQAQLHSLQPGQPSLHRAYEFLPDGPAASEV
LSRQDGHSASSPLLCDAREGAGTVPPPHRPVAWPLALLLTVSQRTQRANQVVGRRGPPLCPKKK
WHLLRLAPENLKTYQTFPSGKRVSPQERKKRDCYFEFRA

hide sequence

Ensembl Acc Id:

ENSP00000395924 ⟸ ENST00000453368

Ensembl Acc Id:

ENSP00000332875 ⟸ ENST00000329615

Ensembl Acc Id:

ENSP00000386615 ⟸ ENST00000409392

RefSeq Acc Id:	XP_047300073 ⟸ XM_047444117
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_047300074 ⟸ XM_047444118
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_054197689 ⟸ XM_054341714
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054197694 ⟸ XM_054341719
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054197691 ⟸ XM_054341716
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054197692 ⟸ XM_054341717
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054197696 ⟸ XM_054341721
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_054197690 ⟸ XM_054341715
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054197693 ⟸ XM_054341718
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054197697 ⟸ XM_054341722
- Peptide Label:	isoform X7

RefSeq Acc Id:	XP_054197695 ⟸ XM_054341720
- Peptide Label:	isoform X6

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-A6NJV1-F1-model_v2	AlphaFold	A6NJV1	1-201	view protein structure

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:27938	AgrOrtholog
COSMIC	CIMIP2C	COSMIC
Ensembl Genes	ENSG00000173557	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000329615	ENTREZGENE
	ENST00000329615.4	UniProtKB/Swiss-Prot
	ENST00000409392	ENTREZGENE
	ENST00000409392.5	UniProtKB/TrEMBL
	ENST00000453368.1	UniProtKB/TrEMBL
GTEx	ENSG00000173557	GTEx
HGNC ID	HGNC:27938	ENTREZGENE
Human Proteome Map	CIMIP2C	Human Proteome Map
InterPro	CIMIP2C	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	UPF0573/UPF0605	UniProtKB/Swiss-Prot
KEGG Report	hsa:339778	UniProtKB/Swiss-Prot
NCBI Gene	339778	ENTREZGENE
PANTHER	PROTEIN FAM166C	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	UPF0573 PROTEIN C2ORF70	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	DUF2475	UniProtKB/Swiss-Prot
PharmGKB	PA166352422	PharmGKB
UniProt	A6NJV1	ENTREZGENE
	B8ZZ55	ENTREZGENE, UniProtKB/TrEMBL
	CB070_HUMAN	UniProtKB/Swiss-Prot
	H7C0N2_HUMAN	UniProtKB/TrEMBL

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2023-05-01	CIMIP2C	ciliary microtubule inner protein 2C	FAM166C	family with sequence similarity 166 member C	Symbol and/or name change	19259463	PROVISIONAL
2019-09-12	FAM166C	family with sequence similarity 166 member C	C2orf70	chromosome 2 open reading frame 70	Symbol and/or name change	5135510	APPROVED

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

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

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

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

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Imported Disease Annotations - ClinVar