Advanced Search (OLGA)

Gene: SEC24C (SEC24 homolog C, COPII coat complex component) Homo sapiens

Subscribe to Updates

Analyze

Symbol:

SEC24C

Name:

SEC24 homolog C, COPII coat complex component

RGD ID:

1321602

HGNC Page

HGNC:10705

Description:

Enables SNARE binding activity and zinc ion binding activity. Involved in COPII-coated vesicle cargo loading. Located in cytosol. Part of COPII vesicle coat.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

KIAA0079; protein transport protein Sec24C; SEC24 family member C; SEC24 family, member C; SEC24 related gene family, member C; SEC24-related protein C

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	10	73,744,372 - 73,772,161 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	10	73,744,372 - 73,772,161 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	10	75,504,130 - 75,531,919 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	10	75,174,138 - 75,201,925 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	10	75,174,137 - 75,201,923	NCBI
Celera	10	68,787,456 - 68,815,097 (+)	NCBI		Celera
Cytogenetic Map	10	q22.2	NCBI
HuRef	10	69,499,590 - 69,527,108 (+)	NCBI		HuRef
CHM1_1	10	75,785,879 - 75,813,704 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	10	74,615,788 - 74,643,577 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
SEC24C	Human	microcephaly		IAGP	RGD:38597102	8554872	ClinVar Annotator: match by term: Microcephaly	ClinVar	PMID:25741868

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
SEC24C	Human	(1->4)-beta-D-glucan	multiple interactions	ISO	RGD:1551587	6480464	[perfluorooctane sulfonic acid co-treated with Cellulose] results in decreased expression of SEC24C mRNA	CTD	PMID:36331819
SEC24C	Human	1,2-dimethylhydrazine	increases expression	ISO	RGD:1551587	6480464	1,2-Dimethylhydrazine results in increased expression of SEC24C mRNA	CTD	PMID:22206623
SEC24C	Human	17beta-estradiol	increases expression	ISO	RGD:1551587	6480464	Estradiol results in increased expression of SEC24C mRNA	CTD	PMID:39298647
SEC24C	Human	17beta-hydroxy-5alpha-androstan-3-one	increases expression	EXP		6480464	Dihydrotestosterone results in increased expression of SEC24C mRNA	CTD	PMID:29581250
SEC24C	Human	2,3,7,8-tetrachlorodibenzodioxine	decreases expression	ISO	RGD:1551587	6480464	Tetrachlorodibenzodioxin results in decreased expression of SEC24C mRNA	CTD	PMID:26290441
SEC24C	Human	2,3,7,8-tetrachlorodibenzodioxine	decreases expression	ISO	RGD:1597739	6480464	Tetrachlorodibenzodioxin results in decreased expression of SEC24C mRNA	CTD	PMID:33387578
SEC24C	Human	2,6-dimethoxyphenol	multiple interactions	EXP		6480464	[Sodium Chloride co-treated with pyrogallol 1,3-dimethyl ether] results in decreased expression of SEC24C protein; [Sodium more ...	CTD	PMID:38598786
SEC24C	Human	2-hydroxypropanoic acid	decreases expression	EXP		6480464	Lactic Acid results in decreased expression of SEC24C mRNA	CTD	PMID:30851411
SEC24C	Human	3,4-methylenedioxymethamphetamine	increases expression	ISO	RGD:1551587	6480464	N-Methyl-3,4-methylenedioxyamphetamine results in increased expression of SEC24C mRNA	CTD	PMID:20188158
SEC24C	Human	acrolein	multiple interactions	EXP		6480464	[Acrolein co-treated with methacrylaldehyde co-treated with alpha-pinene co-treated with Ozone] results in increased oxidation of more ...	CTD	PMID:32699268
SEC24C	Human	actinomycin D	multiple interactions	EXP		6480464	[Dactinomycin co-treated with nutlin 3] results in increased secretion of SEC24C protein	CTD	PMID:38460933
SEC24C	Human	aflatoxin B1	increases methylation	EXP		6480464	Aflatoxin B1 results in increased methylation of SEC24C gene; Aflatoxin B1 results in increased methylation more ...	CTD	PMID:27153756\|PMID:30157460
SEC24C	Human	alachlor	affects expression	ISO	RGD:1597739	6480464	alachlor affects the expression of SEC24C mRNA	CTD	PMID:19425180
SEC24C	Human	alpha-pinene	multiple interactions	EXP		6480464	[Acrolein co-treated with methacrylaldehyde co-treated with alpha-pinene co-treated with Ozone] results in increased oxidation of more ...	CTD	PMID:32699268
SEC24C	Human	antirheumatic drug	decreases expression	EXP		6480464	Antirheumatic Agents results in decreased expression of SEC24C mRNA	CTD	PMID:24449571
SEC24C	Human	arsane	multiple interactions	EXP		6480464	[sodium arsenite results in increased abundance of Arsenic] which results in decreased expression of SEC24C more ...	CTD	PMID:39836092
SEC24C	Human	arsenic atom	multiple interactions	EXP		6480464	[sodium arsenite results in increased abundance of Arsenic] which results in decreased expression of SEC24C more ...	CTD	PMID:39836092
SEC24C	Human	bisphenol A	increases expression	ISO	RGD:1597739	6480464	bisphenol A results in increased expression of SEC24C mRNA	CTD	PMID:25181051\|PMID:34947998
SEC24C	Human	bisphenol A	increases expression	EXP		6480464	bisphenol A results in increased expression of SEC24C protein	CTD	PMID:34186270\|PMID:37567409
SEC24C	Human	bisphenol A	increases expression	ISO	RGD:1551587	6480464	bisphenol A results in increased expression of SEC24C mRNA	CTD	PMID:33221593
SEC24C	Human	bisphenol A	decreases expression	ISO	RGD:1597739	6480464	bisphenol A results in decreased expression of SEC24C mRNA	CTD	PMID:30816183
SEC24C	Human	bisphenol A	decreases expression	EXP		6480464	bisphenol A results in decreased expression of SEC24C mRNA; bisphenol A results in decreased expression more ...	CTD	PMID:29275510\|PMID:31675489
SEC24C	Human	bisphenol A	increases methylation	ISO	RGD:1597739	6480464	bisphenol A results in increased methylation of SEC24C gene	CTD	PMID:28505145
SEC24C	Human	cadmium dichloride	increases expression	EXP		6480464	Cadmium Chloride results in increased expression of SEC24C protein	CTD	PMID:24527689
SEC24C	Human	cisplatin	decreases expression	EXP		6480464	Cisplatin results in decreased expression of SEC24C mRNA	CTD	PMID:27594783
SEC24C	Human	cobalt dichloride	increases expression	ISO	RGD:1551587	6480464	cobaltous chloride results in increased expression of SEC24C mRNA	CTD	PMID:21139344
SEC24C	Human	cyclosporin A	increases expression	EXP		6480464	Cyclosporine results in increased expression of SEC24C mRNA	CTD	PMID:25562108
SEC24C	Human	Dibutyl phosphate	affects expression	EXP		6480464	di-n-butylphosphoric acid affects the expression of SEC24C mRNA	CTD	PMID:37042841
SEC24C	Human	dicrotophos	increases expression	EXP		6480464	dicrotophos results in increased expression of SEC24C mRNA	CTD	PMID:28302478
SEC24C	Human	diethylstilbestrol	increases expression	ISO	RGD:1597739	6480464	Diethylstilbestrol results in increased expression of SEC24C mRNA	CTD	PMID:21658437
SEC24C	Human	doxorubicin	decreases expression	EXP		6480464	Doxorubicin results in decreased expression of SEC24C mRNA	CTD	PMID:29803840
SEC24C	Human	endosulfan	increases expression	ISO	RGD:1597739	6480464	Endosulfan results in increased expression of SEC24C mRNA	CTD	PMID:31464424
SEC24C	Human	enzyme inhibitor	multiple interactions	EXP		6480464	[Enzyme Inhibitors results in decreased activity of OGA protein] which results in increased O-linked glycosylation more ...	CTD	PMID:23301498
SEC24C	Human	ethanol	affects splicing	ISO	RGD:1551587	6480464	Ethanol affects the splicing of SEC24C mRNA	CTD	PMID:30319688
SEC24C	Human	furfural	multiple interactions	EXP		6480464	[Sodium Chloride co-treated with Furaldehyde] results in decreased expression of and affects the localization of more ...	CTD	PMID:38598786
SEC24C	Human	ivermectin	decreases expression	EXP		6480464	Ivermectin results in decreased expression of SEC24C protein	CTD	PMID:32959892
SEC24C	Human	mercury atom	increases expression	EXP		6480464	Mercury results in increased expression of SEC24C mRNA	CTD	PMID:16823088
SEC24C	Human	mercury(0)	increases expression	EXP		6480464	Mercury results in increased expression of SEC24C mRNA	CTD	PMID:16823088
SEC24C	Human	methapyrilene	decreases expression	ISO	RGD:1597739	6480464	Methapyrilene results in decreased expression of SEC24C mRNA	CTD	PMID:30467583
SEC24C	Human	nitrates	multiple interactions	ISO	RGD:1551587	6480464	[Particulate Matter results in increased abundance of Nitrates] which results in increased expression of SEC24C more ...	CTD	PMID:35964746
SEC24C	Human	Nutlin-3	multiple interactions	EXP		6480464	[Dactinomycin co-treated with nutlin 3] results in increased secretion of SEC24C protein	CTD	PMID:38460933
SEC24C	Human	ozone	multiple interactions	EXP		6480464	[Acrolein co-treated with methacrylaldehyde co-treated with alpha-pinene co-treated with Ozone] results in increased oxidation of more ...	CTD	PMID:32699268
SEC24C	Human	paracetamol	affects expression	ISO	RGD:1551587	6480464	Acetaminophen affects the expression of SEC24C mRNA	CTD	PMID:17562736
SEC24C	Human	paracetamol	decreases expression	ISO	RGD:1597739	6480464	Acetaminophen results in decreased expression of SEC24C mRNA	CTD	PMID:33387578
SEC24C	Human	paracetamol	decreases expression	EXP		6480464	Acetaminophen results in decreased expression of SEC24C mRNA	CTD	PMID:21420995
SEC24C	Human	perfluorooctane-1-sulfonic acid	multiple interactions	ISO	RGD:1551587	6480464	[perfluorooctane sulfonic acid co-treated with Cellulose] results in decreased expression of SEC24C mRNA	CTD	PMID:36331819
SEC24C	Human	pirinixic acid	decreases expression	ISO	RGD:1551587	6480464	pirinixic acid results in decreased expression of SEC24C mRNA	CTD	PMID:18445702
SEC24C	Human	rac-lactic acid	decreases expression	EXP		6480464	Lactic Acid results in decreased expression of SEC24C mRNA	CTD	PMID:30851411
SEC24C	Human	SB 431542	multiple interactions	EXP		6480464	[LDN 193189 co-treated with 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide co-treated with FGF2 protein] results in increased expression of SEC24C more ...	CTD	PMID:37664457
SEC24C	Human	sodium arsenite	multiple interactions	EXP		6480464	[sodium arsenite results in increased abundance of Arsenic] which results in decreased expression of SEC24C more ...	CTD	PMID:33939924\|PMID:39836092
SEC24C	Human	sodium chloride	multiple interactions	EXP		6480464	[Sodium Chloride co-treated with Furaldehyde] results in decreased expression of and affects the localization of more ...	CTD	PMID:38598786
SEC24C	Human	thioacetamide	decreases expression	ISO	RGD:1597739	6480464	Thioacetamide results in decreased expression of SEC24C mRNA	CTD	PMID:34492290
SEC24C	Human	titanium dioxide	decreases methylation	ISO	RGD:1551587	6480464	titanium dioxide results in decreased methylation of SEC24C gene; titanium dioxide results in decreased methylation more ...	CTD	PMID:35295148
SEC24C	Human	vinclozolin	increases expression	ISO	RGD:1597739	6480464	vinclozolin results in increased expression of SEC24C mRNA	CTD	PMID:23034163

Biological Process

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
SEC24C	Human	COPII-coated vesicle cargo loading	involved_in	IDA		150520179	PMID:17499046, PMID:18843296	UniProt	PMID:17499046\|PMID:18843296
SEC24C	Human	COPII-coated vesicle cargo loading	involved_in	IBA	PANTHER:PTN000351470\|SGD:S000001140\|SGD:S000001371\|SGD:S000004994\|UniProtKB:O94855\|UniProtKB:O95486\|UniProtKB:O95487\|UniProtKB:P53992	150520179		GO_Central	GO_REF:0000033
SEC24C	Human	endoplasmic reticulum to Golgi vesicle-mediated transport	involved_in	NAS		150520179	PMID:10329445	UniProt	PMID:10329445
SEC24C	Human	endoplasmic reticulum to Golgi vesicle-mediated transport	involved_in	IEA	InterPro:IPR006895\|InterPro:IPR006896\|InterPro:IPR006900\|InterPro:IPR036174\|InterPro:IPR036175\|InterPro:IPR041742	150520179		InterPro	GO_REF:0000002
SEC24C	Human	endoplasmic reticulum to Golgi vesicle-mediated transport	involved_in	IMP		150520179	PMID:20427317	UniProt	PMID:20427317
SEC24C	Human	in utero embryonic development	acts_upstream_of_or_within	IEA	UniProtKB:G3X972\|ensembl:ENSMUSP00000045955	150520179		Ensembl	GO_REF:0000107
SEC24C	Human	intracellular protein transport	involved_in	IEA	InterPro:IPR006895\|InterPro:IPR006896\|InterPro:IPR006900\|InterPro:IPR036174\|InterPro:IPR036175\|InterPro:IPR041742	150520179		InterPro	GO_REF:0000002
SEC24C	Human	protein transport	involved_in	IEA	UniProtKB-KW:KW-0653	150520179		UniProt	GO_REF:0000043
SEC24C	Human	vesicle-mediated transport	involved_in	IEA	UniProtKB-KW:KW-0931	150520179		UniProt	GO_REF:0000043

Cellular Component

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
SEC24C	Human	COPII vesicle coat	part_of	IDA		150520179	PMID:10075675, PMID:10329445, PMID:17499046	UniProt	PMID:10075675\|PMID:10329445\|PMID:17499046
SEC24C	Human	COPII vesicle coat	part_of	IBA	FB:FBgn0262126\|MGI:2139764\|PANTHER:PTN000351470\|SGD:S000001140\|SGD:S000001371\|SGD:S000004994\|UniProtKB:C0H5J6\|UniProtKB:O94855\|UniProtKB:O95486\|UniProtKB:O95487\|UniProtKB:P53992\|UniProtKB:Q57XV4\|UniProtKB:Q580T3	150520179		GO_Central	GO_REF:0000033
SEC24C	Human	COPII vesicle coat	part_of	IEA	InterPro:IPR006895\|InterPro:IPR006896\|InterPro:IPR006900\|InterPro:IPR036174\|InterPro:IPR036175\|InterPro:IPR041742	150520179		InterPro	GO_REF:0000002
SEC24C	Human	COPII vesicle coat	part_of	NAS		150520179	PMID:10214955	UniProt	PMID:10214955
SEC24C	Human	cytoplasm	located_in	IEA	UniProtKB-KW:KW-0963	150520179		UniProt	GO_REF:0000043
SEC24C	Human	cytoplasmic vesicle	located_in	IEA	UniProtKB-KW:KW-0968	150520179		UniProt	GO_REF:0000043
SEC24C	Human	cytosol	located_in	TAS		150520179		Reactome	Reactome:R-HSA-203973\|Reactome:R-HSA-203979\|Reactome:R-HSA-204008\|Reactome:R-HSA-5694409\|Reactome:R-HSA-5694413\|Reactome:R-HSA-5694417\|Reactome:R-HSA-5694418\|Reactome:R-HSA-5694421\|Reactome:R-HSA-5694435\|Reactome:R-HSA-5694439\|Reactome:R-HSA-5694441\|Reactome:R-HSA-5694446\|Reactome:R-HSA-5694522\|Reactome:R-HSA-5694527\|Reactome:R-HSA-983422
SEC24C	Human	cytosol	located_in	IDA		150520179	PMID:10075675	UniProt	PMID:10075675
SEC24C	Human	cytosol	located_in	IEA	UniProtKB-SubCell:SL-0091	150520179		UniProt	GO_REF:0000044
SEC24C	Human	endoplasmic reticulum	located_in	IEA	UniProtKB-KW:KW-0256	150520179		UniProt	GO_REF:0000043
SEC24C	Human	endoplasmic reticulum exit site	is_active_in	IBA	FB:FBgn0262126\|PANTHER:PTN000351470\|PomBase:SPAC22F8.08\|TAIR:locus:2038633	150520179		GO_Central	GO_REF:0000033
SEC24C	Human	endoplasmic reticulum membrane	located_in	TAS		150520179		Reactome	Reactome:R-HSA-203973\|Reactome:R-HSA-203979\|Reactome:R-HSA-204008\|Reactome:R-HSA-2130731\|Reactome:R-HSA-2213243\|Reactome:R-HSA-5694417\|Reactome:R-HSA-5694435\|Reactome:R-HSA-5694436\|Reactome:R-HSA-5694522\|Reactome:R-HSA-5694527\|Reactome:R-HSA-983424\|Reactome:R-HSA-983425\|Reactome:R-HSA-983426\|Reactome:R-NUL-1655838\|Reactome:R-NUL-1655840
SEC24C	Human	endoplasmic reticulum membrane	located_in	IEA	UniProtKB-SubCell:SL-0097	150520179		UniProt	GO_REF:0000044
SEC24C	Human	ER to Golgi transport vesicle membrane	located_in	IEA	UniProtKB-SubCell:SL-0078	150520179		UniProt	GO_REF:0000044
SEC24C	Human	ER to Golgi transport vesicle membrane	located_in	TAS		150520179		Reactome	Reactome:R-HSA-203973\|Reactome:R-HSA-5694409\|Reactome:R-HSA-5694418\|Reactome:R-HSA-5694439\|Reactome:R-HSA-5694441\|Reactome:R-HSA-5694446\|Reactome:R-HSA-983422\|Reactome:R-HSA-983424
SEC24C	Human	membrane	located_in	IEA	UniProtKB-KW:KW-0472	150520179		UniProt	GO_REF:0000043

Molecular Function

Only show annotations with direct experimental evidence (0 objects hidden)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
SEC24C	Human	metal ion binding	enables	IEA	UniProtKB-KW:KW-0479	150520179		UniProt	GO_REF:0000043
SEC24C	Human	protein binding	enables	IPI	UniProtKB:P00540\|UniProtKB:Q15437	150520179	PMID:31515488	IntAct	PMID:31515488
SEC24C	Human	protein binding	enables	IPI	UniProtKB:Q8NEL9	150520179	PMID:17428803	UniProt	PMID:17428803
SEC24C	Human	protein binding	enables	IPI	UniProtKB:Q15436	150520179	PMID:10075675, PMID:18692470	IntAct	PMID:10075675\|PMID:18692470
SEC24C	Human	protein binding	enables	IPI	UniProtKB:Q86WV6	150520179	PMID:30842662	UniProt	PMID:30842662
SEC24C	Human	protein binding	enables	IPI	UniProtKB:O43516\|UniProtKB:P00540	150520179	PMID:25416956	IntAct	PMID:25416956
SEC24C	Human	protein binding	enables	IPI	UniProtKB:Q9QVY3	150520179	PMID:15899885	UniProt	PMID:15899885
SEC24C	Human	protein binding	enables	IPI	UniProtKB:Q15437	150520179	PMID:16189514	IntAct	PMID:16189514
SEC24C	Human	protein binding	enables	IPI	UniProtKB:Q15436\|UniProtKB:Q15437	150520179	PMID:33961781, PMID:35271311	IntAct	PMID:33961781\|PMID:35271311
SEC24C	Human	SNARE binding	enables	IPI	UniProtKB:O14653\|UniProtKB:Q13190	150520179	PMID:18843296	UniProt	PMID:18843296
SEC24C	Human	SNARE binding	enables	IBA	PANTHER:PTN000351470\|UniProtKB:O94855\|UniProtKB:P53992	150520179		GO_Central	GO_REF:0000033
SEC24C	Human	zinc ion binding	enables	IEA	InterPro:IPR006895\|InterPro:IPR036174	150520179		InterPro	GO_REF:0000002
SEC24C	Human	zinc ion binding	enables	IDA		150520179	PMID:18843296	UniProt	PMID:18843296
SEC24C	Human	zinc ion binding	enables	IBA	PANTHER:PTN000351470\|UniProtKB:O94855\|UniProtKB:O95486\|UniProtKB:O95487\|UniProtKB:P53992	150520179		GO_Central	GO_REF:0000033

Imported Annotations - KEGG (archival)

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
SEC24C	Human	Endoplasmic Reticulum-associated degradation pathway		IEA		6907045		KEGG	hsa:04141

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
SEC24C	Human	Abnormal aortic arch morphology		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Abnormal aortic valve morphology		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Abnormal cardiovascular system morphology		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Abnormal dental enamel morphology		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Abnormal eyelid morphology		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Abnormal facial shape		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Abnormal lung lobation		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Abnormal pulmonary valve morphology		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Abnormal skull morphology		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Abnormal thorax morphology		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Abnormality of the dentition		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Abnormality of the pharynx		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Abnormality of the tonsils		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Abnormality of the uterus		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Abnormality of thrombocytes		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Acne		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Aganglionic megacolon		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Anal atresia		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Anorectal anomaly		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Anxiety		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Aphasia		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Arachnodactyly		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Arrhinencephaly		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Arthritis		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Asthma		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Atelectasis		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Atrial septal defect		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Attention deficit hyperactivity disorder		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Atypical behavior		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Autism		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Autoimmunity		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Bipolar affective disorder		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Bowel incontinence		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Bulbous nose		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Carious teeth		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Cataract		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Choanal atresia		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Cholelithiasis		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Chronic otitis media		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Chronic pulmonary obstruction		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Cleft palate		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Conductive hearing impairment		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Constipation		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Corneal neovascularization		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Cryptorchidism		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Depression		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Downslanted palpebral fissures		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Epicanthus		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Failure to thrive		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Feeding difficulties in infancy		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Foot polydactyly		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Gastroesophageal reflux		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Gastrointestinal hemorrhage		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Glaucoma		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Global developmental delay		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Hand polydactyly		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Hearing impairment		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Hydrocephalus		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Hypernasal speech		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Hypertelorism		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Hypertensive crisis		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Hyperthyroidism		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Hypocalcemia		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Hypoparathyroidism		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Hypopigmented skin patches		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Hypoplasia of the thymus		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Hypospadias		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Hypothyroidism		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Hypotonia		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Immunodeficiency		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Impaired T cell function		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Inguinal hernia		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Intellectual disability		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Intellectual disability, mild		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Intestinal malrotation		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Intrauterine growth retardation		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Joint hypermobility		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Laryngomalacia		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Long face		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Long philtrum		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Low-set ears		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Malar flattening		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Meningocele		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Microcephaly		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Micrognathia		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Microphthalmia		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Multiple renal cysts		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Multiple suture craniosynostosis		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Myalgia		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Narrow mouth		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Obesity		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Optic atrophy		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Overfolded helix		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Parkinsonism		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Patellar dislocation		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Patent ductus arteriosus		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Platybasia		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Polycystic kidney dysplasia		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Polyhydramnios		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Posterior embryotoxon		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Prominent nasal bridge		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Ptosis		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Purpura		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Renal hypoplasia		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Retinal arteriolar tortuosity		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Schizophrenia		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Scoliosis		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Seborrheic dermatitis		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Seizure		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Short neck		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Short philtrum		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Short stature		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Small earlobe		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Specific learning disability		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Spina bifida		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Splenomegaly		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Strabismus		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Talipes equinovarus		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Telecanthus		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Tetany		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Tetralogy of Fallot		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Thrombocytopenia		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Tricuspid atresia		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Truncus arteriosus		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Turricephaly		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Umbilical hernia		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Upslanted palpebral fissure		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Varicose veins		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Ventricular septal defect		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Vesicoureteral reflux		IAGP		8699517		HPO	ORPHA:567
SEC24C	Human	Wide nasal bridge		IAGP		8699517		HPO	ORPHA:567

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
SEC24C	Human	Microcephaly		IAGP	RGD:38597102	8554872	ClinVar Annotator: match by term: Microcephaly	ClinVar	PMID:25741868

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	KEGG Annotation Import Pipeline	Pipeline to import KEGG annotations from KEGG into RGD
3.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

PMID:7584044	PMID:10075675	PMID:10214955	PMID:10329445	PMID:11031247	PMID:11252894	PMID:12477932	PMID:14744259	PMID:15013749	PMID:15302935	PMID:15489334	PMID:15899885
PMID:16189514	PMID:16751776	PMID:17373700	PMID:17428803	PMID:17499046	PMID:18029348	PMID:18329616	PMID:18692470	PMID:18843296	PMID:19269366	PMID:19738201	PMID:19786618
PMID:20085233	PMID:20427317	PMID:20467437	PMID:21145461	PMID:21454670	PMID:21525241	PMID:21832049	PMID:21873635	PMID:21988832	PMID:22404651	PMID:22586326	PMID:22623428
PMID:22658674	PMID:22779921	PMID:22863883	PMID:22939629	PMID:23288844	PMID:23658022	PMID:24453475	PMID:24550385	PMID:24711643	PMID:24999758	PMID:25036637	PMID:25416956
PMID:25921289	PMID:26344197	PMID:26496610	PMID:26618866	PMID:26638075	PMID:26673895	PMID:26777405	PMID:26831064	PMID:27107014	PMID:27248496	PMID:27684187	PMID:27716508
PMID:28298439	PMID:28319085	PMID:28515276	PMID:28679754	PMID:29229926	PMID:29467282	PMID:29509190	PMID:29778605	PMID:29844126	PMID:29939162	PMID:29955894	PMID:30021884
PMID:30463901	PMID:30596474	PMID:30842662	PMID:30884312	PMID:30979931	PMID:31048545	PMID:31091453	PMID:31515488	PMID:31536960	PMID:31586073	PMID:31995728	PMID:32058034
PMID:32129710	PMID:32513696	PMID:32807901	PMID:33144569	PMID:33239621	PMID:33277362	PMID:33545068	PMID:33649557	PMID:33957083	PMID:33961781	PMID:34079125	PMID:34504087
PMID:34591612	PMID:34638806	PMID:34709727	PMID:34728620	PMID:35013218	PMID:35013556	PMID:35256949	PMID:35271311	PMID:35509820	PMID:35563538	PMID:35696571	PMID:35777956
PMID:35831314	PMID:35844135	PMID:35906200	PMID:35944360	PMID:36114006	PMID:36215168	PMID:36225252	PMID:36244648	PMID:36424410	PMID:36634849	PMID:37059091	PMID:37223481
PMID:37827155	PMID:37848033	PMID:38113892	PMID:38569033	PMID:38697112	PMID:39098523	PMID:39231216

SEC24C
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	10	73,744,372 - 73,772,161 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	10	73,744,372 - 73,772,161 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	10	75,504,130 - 75,531,919 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	10	75,174,138 - 75,201,925 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	10	75,174,137 - 75,201,923	NCBI
Celera	10	68,787,456 - 68,815,097 (+)	NCBI		Celera
Cytogenetic Map	10	q22.2	NCBI
HuRef	10	69,499,590 - 69,527,108 (+)	NCBI		HuRef
CHM1_1	10	75,785,879 - 75,813,704 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	10	74,615,788 - 74,643,577 (+)	NCBI		T2T-CHM13v2.0

Sec24c
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	14	20,722,709 - 20,744,920 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	14	20,724,376 - 20,744,920 (+)	Ensembl		GRCm39 Ensembl
GRCm38	14	20,674,285 - 20,694,852 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	14	20,674,308 - 20,694,852 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	14	21,493,543 - 21,514,072 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	14	19,462,895 - 19,483,402 (+)	NCBI		MGSCv36	mm8
Celera	14	17,057,076 - 17,077,620 (+)	NCBI		Celera
Cytogenetic Map	14	A3	NCBI
cM Map	14	11.53	NCBI

Sec24c
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	15	3,651,714 - 3,674,420 (-)	NCBI		GRCr8
mRatBN7.2	15	3,602,460 - 3,624,524 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	15	3,602,460 - 3,624,422 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	15	3,612,651 - 3,634,612 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	15	4,999,127 - 5,021,088 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	15	3,611,460 - 3,633,423 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	15	4,035,196 - 4,057,209 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	15	4,035,196 - 4,057,157 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	15	8,136,414 - 8,158,441 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	15	3,827,910 - 3,849,871 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	15	969,764 - 991,725 (+)	NCBI		Celera
Cytogenetic Map	15	p16	NCBI

Sec24c
(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	NW_004955437	18,132,969 - 18,161,167 (-)	NCBI	ChiLan1.0	ChiLan1.0

SEC24C
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	8	85,895,130 - 85,923,080 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	10	85,900,407 - 85,928,404 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	10	70,267,194 - 70,295,116 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	10	72,940,855 - 72,968,027 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	10	72,943,116 - 72,968,027 (+)	Ensembl	panpan1.1		panPan2

SEC24C
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	4	24,183,768 - 24,209,062 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	4	24,184,225 - 24,209,060 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	4	24,321,736 - 24,346,654 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	4	24,464,258 - 24,489,180 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	4	24,464,359 - 24,489,181 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	4	24,361,452 - 24,386,365 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	4	24,562,030 - 24,586,984 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	4	24,917,128 - 24,942,052 (+)	NCBI		UU_Cfam_GSD_1.0

Sec24c
(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_024407213	56,881,827 - 56,909,455 (-)	NCBI		HiC_Itri_2
SpeTri2.0	NW_004936521	5,374,555 - 5,402,123 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

SEC24C
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	14	76,473,776 - 76,499,125 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	14	76,473,706 - 76,499,127 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	14	82,600,366 - 82,625,765 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

SEC24C
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	9	57,600,783 - 57,628,501 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	9	57,601,863 - 57,626,038 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666048	18,177,900 - 18,206,162 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Sec24c
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624754	7,261,511 - 7,288,869 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624754	7,261,770 - 7,288,874 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants in SEC24C
92 total Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 10q21.2-22.2(chr10:62229688-74468143)x1	copy number loss	See cases [RCV000052530]	Chr10:62229688..74468143 [GRCh38] Chr10:63989447..76227901 [GRCh37] Chr10:63659453..75897907 [NCBI36] Chr10:10q21.2-22.2	pathogenic
GRCh38/hg38 10q22.1-22.2(chr10:72720628-75612374)x1	copy number loss	See cases [RCV000052531]	Chr10:72720628..75612374 [GRCh38] Chr10:74480386..77372132 [GRCh37] Chr10:74150392..77042138 [NCBI36] Chr10:10q22.1-22.2	pathogenic
GRCh38/hg38 10q21.1-22.2(chr10:58436466-74415216)x1	copy number loss	See cases [RCV000052511]	Chr10:58436466..74415216 [GRCh38] Chr10:60196226..76174974 [GRCh37] Chr10:59866232..75844980 [NCBI36] Chr10:10q21.1-22.2	pathogenic
NM_004922.3(SEC24C):c.1030C>T (p.Pro344Ser)	single nucleotide variant	Malignant melanoma [RCV000062074]	Chr10:73763532 [GRCh38] Chr10:75523290 [GRCh37] Chr10:75193296 [NCBI36] Chr10:10q22.2	not provided
NM_004922.3(SEC24C):c.1143C>T (p.Ile381=)	single nucleotide variant	Malignant melanoma [RCV000062075]	Chr10:73763899 [GRCh38] Chr10:75523657 [GRCh37] Chr10:75193663 [NCBI36] Chr10:10q22.2	not provided
GRCh38/hg38 10q21.3-22.3(chr10:67196567-79422057)x3	copy number gain	See cases [RCV000135438]	Chr10:67196567..79422057 [GRCh38] Chr10:68956325..81181813 [GRCh37] Chr10:68626331..80851819 [NCBI36] Chr10:10q21.3-22.3	pathogenic
GRCh38/hg38 10q21.3-22.2(chr10:63402579-75296099)x1	copy number loss	See cases [RCV000136658]	Chr10:63402579..75296099 [GRCh38] Chr10:65162339..77055857 [GRCh37] Chr10:64832345..76725863 [NCBI36] Chr10:10q21.3-22.2	pathogenic\|likely benign
GRCh38/hg38 10q11.23-23.2(chr10:50729367-87147204)x3	copy number gain	See cases [RCV000138007]	Chr10:50729367..87147204 [GRCh38] Chr10:52489127..88906961 [GRCh37] Chr10:52159133..88896941 [NCBI36] Chr10:10q11.23-23.2	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3	copy number gain	See cases [RCV000448750]	Chr10:93297..135378918 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)	copy number gain	See cases [RCV000511389]	Chr10:100027..135427143 [GRCh37] Chr10:10p15.3-q26.3	pathogenic\|uncertain significance
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3	copy number gain	See cases [RCV000510861]	Chr10:100027..135427143 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
GRCh37/hg19 10q22.2(chr10:75179409-76009153)x3	copy number gain	See cases [RCV000511191]	Chr10:75179409..76009153 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.463T>C (p.Ser155Pro)	single nucleotide variant	not specified [RCV004291960]	Chr10:73759776 [GRCh38] Chr10:75519534 [GRCh37] Chr10:10q22.2	likely benign
GRCh37/hg19 10q11.21-26.3(chr10:42347406-135534747)x1	copy number loss	Poly (ADP-Ribose) polymerase inhibitor response [RCV000626438]	Chr10:42347406..135534747 [GRCh37] Chr10:10q11.21-26.3	drug response
GRCh37/hg19 10q21.3-23.32(chr10:69040366-93194993)x3	copy number gain	not provided [RCV000683289]	Chr10:69040366..93194993 [GRCh37] Chr10:10q21.3-23.32	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:73232-135524321)x3	copy number gain	not provided [RCV000749464]	Chr10:73232..135524321 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:98087-135477883)x3	copy number gain	not provided [RCV000749465]	Chr10:98087..135477883 [GRCh37] Chr10:10p15.3-q26.3	pathogenic
NM_198597.3(SEC24C):c.2610G>A (p.Thr870=)	single nucleotide variant	not provided [RCV001532606]	Chr10:73769661 [GRCh38] Chr10:75529419 [GRCh37] Chr10:10q22.2	likely benign
NM_198597.3(SEC24C):c.2874C>T (p.Pro958=)	single nucleotide variant	not provided [RCV000927557]	Chr10:73770291 [GRCh38] Chr10:75530049 [GRCh37] Chr10:10q22.2	likely benign
NM_198597.3(SEC24C):c.1800-7T>C	single nucleotide variant	not provided [RCV000894019]	Chr10:73766753 [GRCh38] Chr10:75526511 [GRCh37] Chr10:10q22.2	benign
NM_198597.3(SEC24C):c.1698C>T (p.Ala566=)	single nucleotide variant	not provided [RCV000953631]	Chr10:73766440 [GRCh38] Chr10:75526198 [GRCh37] Chr10:10q22.2	benign
NM_198597.3(SEC24C):c.850+10T>G	single nucleotide variant	not provided [RCV000963662]	Chr10:73760396 [GRCh38] Chr10:75520154 [GRCh37] Chr10:10q22.2	benign
NM_198597.3(SEC24C):c.2988C>T (p.Ser996=)	single nucleotide variant	not provided [RCV000959878]	Chr10:73770405 [GRCh38] Chr10:75530163 [GRCh37] Chr10:10q22.2	likely benign
GRCh37/hg19 10q22.2(chr10:75251395-75763287)x1	copy number loss	not provided [RCV000849346]	Chr10:75251395..75763287 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2201G>A (p.Arg734Gln)	single nucleotide variant	not specified [RCV004304069]	Chr10:73768829 [GRCh38] Chr10:75528587 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.3145-4G>A	single nucleotide variant	not provided [RCV000888299]	Chr10:73770951 [GRCh38] Chr10:75530709 [GRCh37] Chr10:10q22.2	benign
NM_198597.3(SEC24C):c.771C>G (p.Gly257=)	single nucleotide variant	not provided [RCV000951110]	Chr10:73760307 [GRCh38] Chr10:75520065 [GRCh37] Chr10:10q22.2	benign
NM_198597.3(SEC24C):c.763C>G (p.Pro255Ala)	single nucleotide variant	not provided [RCV000891462]	Chr10:73760299 [GRCh38] Chr10:75520057 [GRCh37] Chr10:10q22.2	benign
NM_198597.3(SEC24C):c.1500C>A (p.Ser500Arg)	single nucleotide variant	Microcephaly [RCV001252937]	Chr10:73766103 [GRCh38] Chr10:75525861 [GRCh37] Chr10:10q22.2	uncertain significance
GRCh37/hg19 10q21.3-22.3(chr10:68735254-78885714)	copy number loss	not specified [RCV002052875]	Chr10:68735254..78885714 [GRCh37] Chr10:10q21.3-22.3	pathogenic
NM_198597.3(SEC24C):c.542C>G (p.Ser181Cys)	single nucleotide variant	not specified [RCV004215388]	Chr10:73760078 [GRCh38] Chr10:75519836 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.1529T>C (p.Val510Ala)	single nucleotide variant	not specified [RCV004098067]	Chr10:73766132 [GRCh38] Chr10:75525890 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.3168C>G (p.Asp1056Glu)	single nucleotide variant	not specified [RCV004141960]	Chr10:73770978 [GRCh38] Chr10:75530736 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.526T>A (p.Ser176Thr)	single nucleotide variant	not specified [RCV004189770]	Chr10:73760062 [GRCh38] Chr10:75519820 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2379C>A (p.Phe793Leu)	single nucleotide variant	not specified [RCV004140578]	Chr10:73769107 [GRCh38] Chr10:75528865 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2398A>G (p.Asn800Asp)	single nucleotide variant	not specified [RCV004120380]	Chr10:73769126 [GRCh38] Chr10:75528884 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2602C>A (p.Arg868Ser)	single nucleotide variant	not specified [RCV004126645]	Chr10:73769653 [GRCh38] Chr10:75529411 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2219G>A (p.Arg740His)	single nucleotide variant	not specified [RCV004227705]	Chr10:73768847 [GRCh38] Chr10:75528605 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.872G>T (p.Gly291Val)	single nucleotide variant	not specified [RCV004111409]	Chr10:73760734 [GRCh38] Chr10:75520492 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.284C>G (p.Pro95Arg)	single nucleotide variant	not specified [RCV004132246]	Chr10:73751219 [GRCh38] Chr10:75510977 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2257A>G (p.Met753Val)	single nucleotide variant	not specified [RCV004160707]	Chr10:73768885 [GRCh38] Chr10:75528643 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.317G>A (p.Gly106Glu)	single nucleotide variant	not specified [RCV004233985]	Chr10:73759630 [GRCh38] Chr10:75519388 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.1327A>G (p.Arg443Gly)	single nucleotide variant	not specified [RCV004210521]	Chr10:73765550 [GRCh38] Chr10:75525308 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.1655A>G (p.Tyr552Cys)	single nucleotide variant	not specified [RCV004121619]	Chr10:73766397 [GRCh38] Chr10:75526155 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.3220G>T (p.Gly1074Trp)	single nucleotide variant	not specified [RCV004162259]	Chr10:73771030 [GRCh38] Chr10:75530788 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.1637G>A (p.Arg546His)	single nucleotide variant	not specified [RCV004082770]	Chr10:73766379 [GRCh38] Chr10:75526137 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.1486A>G (p.Asn496Asp)	single nucleotide variant	not specified [RCV004213717]	Chr10:73766089 [GRCh38] Chr10:75525847 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.439G>A (p.Gly147Ser)	single nucleotide variant	not specified [RCV004223229]	Chr10:73759752 [GRCh38] Chr10:75519510 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.1330C>T (p.Arg444Cys)	single nucleotide variant	not specified [RCV004250317]	Chr10:73765553 [GRCh38] Chr10:75525311 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.941A>C (p.Gln314Pro)	single nucleotide variant	not specified [RCV004253039]	Chr10:73760803 [GRCh38] Chr10:75520561 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2494T>G (p.Cys832Gly)	single nucleotide variant	not specified [RCV004297337]	Chr10:73769416 [GRCh38] Chr10:75529174 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.3154G>T (p.Val1052Leu)	single nucleotide variant	not specified [RCV004257344]	Chr10:73770964 [GRCh38] Chr10:75530722 [GRCh37] Chr10:10q22.2	uncertain significance
GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143)	copy number gain	Distal trisomy 10q [RCV003319593]	Chr10:11138692..135427143 [GRCh37] Chr10:10p14-q26.3	pathogenic
NM_198597.3(SEC24C):c.2494T>C (p.Cys832Arg)	single nucleotide variant	not specified [RCV004328748]	Chr10:73769416 [GRCh38] Chr10:75529174 [GRCh37] Chr10:10q22.2	uncertain significance
GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143)	copy number loss	Distal 10q deletion syndrome [RCV003319583]	Chr10:12829206..135427143 [GRCh37] Chr10:10p13-q26.3	pathogenic
NM_198597.3(SEC24C):c.2587C>T (p.Pro863Ser)	single nucleotide variant	not specified [RCV004337652]	Chr10:73769638 [GRCh38] Chr10:75529396 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.1960A>G (p.Lys654Glu)	single nucleotide variant	not specified [RCV004348432]	Chr10:73767120 [GRCh38] Chr10:75526878 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.3026C>G (p.Ser1009Cys)	single nucleotide variant	not specified [RCV004364994]	Chr10:73770443 [GRCh38] Chr10:75530201 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.40G>C (p.Gly14Arg)	single nucleotide variant	not specified [RCV004360650]	Chr10:73746872 [GRCh38] Chr10:75506630 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.430C>G (p.Gln144Glu)	single nucleotide variant	not specified [RCV004362357]	Chr10:73759743 [GRCh38] Chr10:75519501 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2393G>A (p.Arg798Gln)	single nucleotide variant	not specified [RCV004365406]	Chr10:73769121 [GRCh38] Chr10:75528879 [GRCh37] Chr10:10q22.2	uncertain significance
GRCh37/hg19 10q11.21-24.2(chr10:42709645-100834951)x3	copy number gain	not provided [RCV003484798]	Chr10:42709645..100834951 [GRCh37] Chr10:10q11.21-24.2	pathogenic
NM_198597.3(SEC24C):c.2392C>T (p.Arg798Trp)	single nucleotide variant	not specified [RCV004447668]	Chr10:73769120 [GRCh38] Chr10:75528878 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2602C>T (p.Arg868Cys)	single nucleotide variant	not specified [RCV004447669]	Chr10:73769653 [GRCh38] Chr10:75529411 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.1616G>A (p.Gly539Glu)	single nucleotide variant	not specified [RCV004447664]	Chr10:73766358 [GRCh38] Chr10:75526116 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.491C>T (p.Thr164Ile)	single nucleotide variant	not specified [RCV004447679]	Chr10:73760027 [GRCh38] Chr10:75519785 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.611G>A (p.Arg204Gln)	single nucleotide variant	not specified [RCV004447680]	Chr10:73760147 [GRCh38] Chr10:75519905 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.131A>G (p.Tyr44Cys)	single nucleotide variant	not specified [RCV004447660]	Chr10:73746963 [GRCh38] Chr10:75506721 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.1469T>C (p.Val490Ala)	single nucleotide variant	not specified [RCV004447662]	Chr10:73765902 [GRCh38] Chr10:75525660 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.1563G>C (p.Arg521Ser)	single nucleotide variant	not specified [RCV004447663]	Chr10:73766166 [GRCh38] Chr10:75525924 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.1771G>A (p.Val591Ile)	single nucleotide variant	not specified [RCV004447666]	Chr10:73766513 [GRCh38] Chr10:75526271 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2191G>A (p.Asp731Asn)	single nucleotide variant	not specified [RCV004447667]	Chr10:73768819 [GRCh38] Chr10:75528577 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2614A>T (p.Ile872Phe)	single nucleotide variant	not specified [RCV004447670]	Chr10:73769665 [GRCh38] Chr10:75529423 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2836T>G (p.Phe946Val)	single nucleotide variant	not specified [RCV004447671]	Chr10:73769989 [GRCh38] Chr10:75529747 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.292A>G (p.Thr98Ala)	single nucleotide variant	not specified [RCV004447673]	Chr10:73751227 [GRCh38] Chr10:75510985 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2930A>T (p.Asn977Ile)	single nucleotide variant	not specified [RCV004447674]	Chr10:73770347 [GRCh38] Chr10:75530105 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.3068T>G (p.Val1023Gly)	single nucleotide variant	not specified [RCV004447675]	Chr10:73770722 [GRCh38] Chr10:75530480 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.3196C>G (p.Leu1066Val)	single nucleotide variant	not specified [RCV004447676]	Chr10:73771006 [GRCh38] Chr10:75530764 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.422C>A (p.Ser141Tyr)	single nucleotide variant	not specified [RCV004447678]	Chr10:73759735 [GRCh38] Chr10:75519493 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.1321G>A (p.Gly441Arg)	single nucleotide variant	not specified [RCV004447661]	Chr10:73765544 [GRCh38] Chr10:75525302 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2769C>G (p.Val923=)	single nucleotide variant	not provided [RCV004585617]	Chr10:73769922 [GRCh38] Chr10:75529680 [GRCh37] Chr10:10q22.2	likely benign
NM_198597.3(SEC24C):c.1024A>G (p.Thr342Ala)	single nucleotide variant	not specified [RCV004667030]	Chr10:73763526 [GRCh38] Chr10:75523284 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.128C>T (p.Ala43Val)	single nucleotide variant	not specified [RCV004663651]	Chr10:73746960 [GRCh38] Chr10:75506718 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2126T>A (p.Leu709His)	single nucleotide variant	not specified [RCV004663652]	Chr10:73767952 [GRCh38] Chr10:75527710 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2602C>G (p.Arg868Gly)	single nucleotide variant	not specified [RCV004663653]	Chr10:73769653 [GRCh38] Chr10:75529411 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.986C>T (p.Pro329Leu)	single nucleotide variant	not specified [RCV004663656]	Chr10:73760848 [GRCh38] Chr10:75520606 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.184G>A (p.Ala62Thr)	single nucleotide variant	not specified [RCV004663649]	Chr10:73751119 [GRCh38] Chr10:75510877 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2994A>C (p.Gln998His)	single nucleotide variant	not specified [RCV004663650]	Chr10:73770411 [GRCh38] Chr10:75530169 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2385T>G (p.His795Gln)	single nucleotide variant	not specified [RCV004663655]	Chr10:73769113 [GRCh38] Chr10:75528871 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2371G>T (p.Val791Leu)	single nucleotide variant	not specified [RCV004663648]	Chr10:73769099 [GRCh38] Chr10:75528857 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2281A>G (p.Ile761Val)	single nucleotide variant	not specified [RCV004663654]	Chr10:73769009 [GRCh38] Chr10:75528767 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2930A>G (p.Asn977Ser)	single nucleotide variant	not specified [RCV004663658]	Chr10:73770347 [GRCh38] Chr10:75530105 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.164C>T (p.Pro55Leu)	single nucleotide variant	not specified [RCV004861572]	Chr10:73746996 [GRCh38] Chr10:75506754 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.664C>T (p.Arg222Trp)	single nucleotide variant	not specified [RCV004861578]	Chr10:73760200 [GRCh38] Chr10:75519958 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2447G>C (p.Cys816Ser)	single nucleotide variant	not specified [RCV004861580]	Chr10:73769369 [GRCh38] Chr10:75529127 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.868C>T (p.Arg290Trp)	single nucleotide variant	not specified [RCV004861575]	Chr10:73760730 [GRCh38] Chr10:75520488 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2440A>T (p.Thr814Ser)	single nucleotide variant	not specified [RCV004861576]	Chr10:73769362 [GRCh38] Chr10:75529120 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.1928A>G (p.His643Arg)	single nucleotide variant	not specified [RCV004861577]	Chr10:73767088 [GRCh38] Chr10:75526846 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.623C>T (p.Ser208Leu)	single nucleotide variant	not specified [RCV004861582]	Chr10:73760159 [GRCh38] Chr10:75519917 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.370C>T (p.Leu124Phe)	single nucleotide variant	not specified [RCV004861583]	Chr10:73759683 [GRCh38] Chr10:75519441 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.293C>G (p.Thr98Ser)	single nucleotide variant	not specified [RCV004861579]	Chr10:73751228 [GRCh38] Chr10:75510986 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.748C>A (p.Pro250Thr)	single nucleotide variant	not specified [RCV004861574]	Chr10:73760284 [GRCh38] Chr10:75520042 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.304C>G (p.Gln102Glu)	single nucleotide variant	not specified [RCV004861584]	Chr10:73751239 [GRCh38] Chr10:75510997 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.1550C>T (p.Thr517Ile)	single nucleotide variant	not specified [RCV004861585]	Chr10:73766153 [GRCh38] Chr10:75525911 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.859G>A (p.Gly287Arg)	single nucleotide variant	not specified [RCV004861573]	Chr10:73760721 [GRCh38] Chr10:75520479 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.971A>G (p.Asp324Gly)	single nucleotide variant	not specified [RCV004861581]	Chr10:73760833 [GRCh38] Chr10:75520591 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.2410G>A (p.Gly804Arg)	single nucleotide variant	not specified [RCV004861586]	Chr10:73769138 [GRCh38] Chr10:75528896 [GRCh37] Chr10:10q22.2	uncertain significance
NM_198597.3(SEC24C):c.38T>C (p.Phe13Ser)	single nucleotide variant	not specified [RCV004861587]	Chr10:73746870 [GRCh38] Chr10:75506628 [GRCh37] Chr10:10q22.2	uncertain significance

Predicted Target Of

	Summary Value
Count of predictions:	3482
Count of miRNA genes:	914
Interacting mature miRNAs:	1111
Transcripts:	ENST00000339365, ENST00000345254, ENST00000411652, ENST00000465076, ENST00000477008, ENST00000496827, ENST00000535742, ENST00000540668, ENST00000546025
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.

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
597346456	GWAS1442530_H	forced expiratory volume QTL GWAS1442530 (human)		2e-25	forced expiratory volume	forced expiratory volume (CMO:0000254)	10	73752694	73752695	Human
597103906	GWAS1199980_H	self rated health QTL GWAS1199980 (human)		4e-08	self rated health		10	73759933	73759934	Human
597260128	GWAS1356202_H	forced expiratory volume QTL GWAS1356202 (human)		5e-12	forced expiratory volume	forced expiratory volume (CMO:0000254)	10	73766241	73766242	Human

RH44836

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	11	59,192,676 - 59,192,781	UniSTS	GRCh37
GRCh37	10	75,502,799 - 75,502,905	UniSTS	GRCh37
Build 36	10	75,172,805 - 75,172,911	RGD	NCBI36
Celera	10	68,786,123 - 68,786,229	RGD
Celera	11	56,553,956 - 56,554,061	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
HuRef	11	55,540,430 - 55,540,535	UniSTS
HuRef	10	69,498,258 - 69,498,364	UniSTS
GeneMap99-GB4 RH Map	10	380.97	UniSTS

WI-18926

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	75,531,173 - 75,531,320	UniSTS	GRCh37
Build 36	10	75,201,179 - 75,201,326	RGD	NCBI36
Celera	10	68,814,351 - 68,814,498	RGD
Cytogenetic Map	10	q22.3	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
HuRef	10	69,526,348 - 69,526,495	UniSTS
GeneMap99-GB4 RH Map	10	381.17	UniSTS
Whitehead-RH Map	10	458.1	UniSTS

RH25307

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	75,531,376 - 75,531,854	UniSTS	GRCh37
Build 36	10	75,201,382 - 75,201,860	RGD	NCBI36
Celera	10	68,814,554 - 68,815,032	RGD
Cytogenetic Map	10	q22.3	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
HuRef	10	69,526,551 - 69,527,029	UniSTS

SEC24C_392

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	75,531,091 - 75,531,928	UniSTS	GRCh37
Build 36	10	75,201,097 - 75,201,934	RGD	NCBI36
Celera	10	68,814,269 - 68,815,106	RGD
HuRef	10	69,526,266 - 69,527,103	UniSTS

D10S2187

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	75,531,492 - 75,531,608	UniSTS	GRCh37
Build 36	10	75,201,498 - 75,201,614	RGD	NCBI36
Celera	10	68,814,670 - 68,814,786	RGD
Cytogenetic Map	10	q22.3	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
HuRef	10	69,526,667 - 69,526,783	UniSTS
Whitehead-YAC Contig Map	10		UniSTS

RH44071

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	10	75,531,630 - 75,531,797	UniSTS	GRCh37
Build 36	10	75,201,636 - 75,201,803	RGD	NCBI36
Celera	10	68,814,808 - 68,814,975	RGD
Cytogenetic Map	10	q22.3	UniSTS
Cytogenetic Map	10	q22.2	UniSTS
HuRef	10	69,526,805 - 69,526,972	UniSTS
GeneMap99-GB4 RH Map	10	380.97	UniSTS

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	2439	2788	2253	4974	1726	2351	6	624	1951	465	2270	7306	6472	53	3734	1	852	1744	1617	175	1


RefSeq Transcripts	NM_004922	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_198597	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011540380	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011540381	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017016967	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017016968	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047426031	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047426032	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047426033	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047426034	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047426035	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367226	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367227	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367228	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367229	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367230	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054367231	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC022400	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK098512	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK298598	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK299826	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK303085	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK309918	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK316451	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL596994	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL832110	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC018928	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BQ710971	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CA419040	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471083	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068268	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	D38555	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DQ574455	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000339365 ⟹ ENSP00000343405

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	73,744,391 - 73,772,161 (+)	Ensembl

Ensembl Acc Id:

ENST00000345254 ⟹ ENSP00000321845

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	73,744,372 - 73,772,161 (+)	Ensembl

Ensembl Acc Id:

ENST00000465076 ⟹ ENSP00000437000

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	73,744,384 - 73,772,159 (+)	Ensembl

Ensembl Acc Id:

ENST00000477008

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	73,746,867 - 73,752,102 (+)	Ensembl

Ensembl Acc Id:

ENST00000496827

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	73,767,894 - 73,770,379 (+)	Ensembl

Ensembl Acc Id:

ENST00000634508 ⟹ ENSP00000489340

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	73,760,110 - 73,763,555 (+)	Ensembl

Ensembl Acc Id:

ENST00000635550 ⟹ ENSP00000489351

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	10	73,744,400 - 73,771,235 (+)	Ensembl

RefSeq Acc Id:

NM_004922 ⟹ NP_004913

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	73,744,372 - 73,772,161 (+)	NCBI
GRCh37	10	75,504,039 - 75,531,933 (+)	NCBI
Build 36	10	75,174,138 - 75,201,925 (+)	NCBI Archive
Celera	10	68,787,456 - 68,815,097 (+)	RGD
HuRef	10	69,499,590 - 69,527,108 (+)	ENTREZGENE
CHM1_1	10	75,785,879 - 75,813,704 (+)	NCBI
T2T-CHM13v2.0	10	74,615,788 - 74,643,577 (+)	NCBI

Sequence:

show sequence

GGAACCGGAAGTGGAGCCTGGGAGCCTTGACGTTAGGAACGAAGTCTAACCTGGATCTGGAGCCGGGAGATAATCTGAATGCTGGCTGGGGCAGAAAATTACTAAGATCCTGTGGAAGTGTGAGGATT
ATTAAACTGATCACTGTCTGATAAGGTGAGATCAAATTGGGAATGCTTTCATAATGAACGTCAACCAGTCAGTTCCACCTGTGCCACCATTTGGGCAGCCCCAGCCCATCTACCCAGGGTATCATCAG
TCCAGCTATGGTGGGCAATCAGGGTCCACAGCCCCCGCCATTCCCTATGGAGCCTACAATGGCCCAGTACCAGGCTATCAGCAAACACCTCCCCAAGGTATGTCAAGAGCCCCACCTTCCTCGGGGGC
ACCTCCAGCCTCAACAGCACAGGCTCCTTGTGGCCAGGCTGCATATGGCCAGTTTGGCCAAGGAGATGTACAGAATGGGCCAAGCTCCACTGTTCAGATGCAAAGGCTGCCTGGGTCTCAGCCATTTG
GGTCCCCATTGGCCCCTGTGGGCAACCAGCCACCTGTGCTTCAGCCCTATGGCCCTCCCCCGACAAGTGCACAGGTGGCTACGCAGCTGTCTGGAATGCAGATCAGCGGTGCTGTGGCCCCAGCCCCT
CCTTCTTCAGGGCTGGGCTTTGGCCCACCAACATCGCTGGCTTCAGCCTCAGGAAGTTTCCCTAACTCTGGTCTGTATGGCTCCTATCCTCAGGGCCAGGCTCCTCCCCTTAGCCAGGCCCAAGGTCA
TCCTGGGATCCAGACTCCCCAGCGATCTGCCCCATCACAGGCCTCCAGCTTCACACCCCCAGCTTCAGGGGGTCCTCGGCTGCCTTCGATGACTGGTCCACTCCTGCCTGGACAGAGTTTTGGAGGGC
CCTCAGTGAGCCAGCCCAACCATGTGTCTTCACCTCCTCAAGCTCTGCCCCCTGGCACCCAGATGACTGGGCCCCTGGGACCACTGCCACCTATGCACTCCCCGCAGCAGCCAGGCTATCAGCCCCAA
CAAAATGGTTCCTTCGGACCAGCCCGGGGCCCTCAGTCTAATTATGGAGGCCCCTACCCAGCAGCACCCACCTTTGGCAGTCAGCCTGGGCCTCCTCAGCCACTGCCTCCTAAGCGCCTGGACCCTGA
TGCCATCCCAAGCCCTATTCAGGTCATTGAAGATGACAGGAACAACCGGGGTACAGAGCCATTTGTTACTGGAGTACGGGGCCAGGTGCCACCCTTAGTCACTACCAACTTCCTGGTGAAAGACCAAG
GGAATGCAAGTCCCCGATACATCCGATGTACATCCTATAATATCCCTTGCACATCTGACATGGCTAAGCAGGCTCAGGTGCCCCTGGCAGCAGTCATCAAACCGCTGGCAAGGCTGCCCCCAGAGGAG
GCTTCACCGTATGTTGTGGACCATGGGGAATCTGGCCCTTTGCGCTGCAACCGCTGCAAAGCATACATGTGTCCCTTCATGCAGTTCATTGAAGGAGGGAGGCGTTTCCAGTGCTGTTTTTGCAGCTG
TATCAATGATGTTCCCCCCCAGTATTTTCAGCACCTGGATCATACCGGCAAACGTGTGGATGCTTATGACCGCCCTGAGCTATCCCTGGGCTCTTATGAATTCTTGGCCACTGTAGATTACTGCAAGA
ACAATAAGTTCCCCAGCCCTCCTGCCTTTATCTTCATGATTGACGTCTCCTACAATGCCATCAGGACTGGTCTTGTTAGGCTCCTCTGTGAGGAGCTCAAGTCACTGTTAGACTTTCTACCTAGGGAG
GGTGGGGCAGAAGAGTCAGCAATCCGCGTTGGCTTTGTCACCTACAATAAGGTGCTCCACTTCTATAATGTGAAGAGCTCATTGGCCCAGCCACAGATGATGGTTGTGTCTGATGTGGCTGACATGTT
TGTGCCACTGCTGGATGGCTTCCTGGTCAACGTCAATGAGTCTCGGGCAGTTATCACCAGCTTATTGGATCAGATTCCAGAAATGTTTGCAGACACAAGGGAAACAGAGACAGTATTTGTACCAGTTA
TCCAGGCTGGAATGGAGGCTCTGAAGGCTGCTGAGTGTGCAGGGAAGCTCTTTCTATTCCATACATCCCTGCCCATTGCAGAGGCCCCAGGGAAACTGAAGAACAGAGATGACAGGAAGCTGATCAAT
ACAGACAAGGAGAAGACTCTGTTCCAGCCTCAGACAGGTGCCTATCAGACCCTGGCCAAAGAGTGTGTGGCCCAAGGCTGCTGTGTAGATCTCTTTCTCTTCCCTAACCAGTATGTGGATGTGGCCAC
ACTCTCTGTTGTGCCCCAGCTCACTGGTGGCTCTGTCTACAAATATGCTTCCTTTCAGGTGGAGAACGACCAGGAGCGGTTCCTGAGTGACCTGCGTCGTGATGTCCAGAAGGTTGTTGGCTTTGATG
CTGTGATGCGGGTCCGGACAAGCACTGGTATCCGTGCTGTAGATTTCTTTGGAGCTTTCTACATGAGCAACACGACAGATGTGGAGCTGGCTGGGCTAGATGGGGACAAAACAGTGACTGTGGAGTTC
AAGCATGACGATCGGCTCAATGAAGAGAGCGGAGCTCTCCTGCAGTGTGCCCTGCTTTACACCAGCTGTGCAGGGCAGCGTCGGCTCCGCATCCATAATCTGGCCCTGAACTGCTGCACCCAGCTGGC
TGATCTATATCGAAACTGTGAGACTGACACGCTCATCAACTACATGGCCAAGTTTGCATATCGGGGAGTCCTGAATAGCCCTGTGAAGGCTGTTCGTGACACGCTCATCACCCAGTGTGCCCAGATCC
TGGCCTGTTACAGAAAGAACTGTGCTAGCCCCTCCTCTGCAGGACAGTTGATCCTTCCTGAGTGCATGAAGCTACTCCCAGTTTACCTGAACTGTGTGTTGAAGAGTGATGTCCTGCAGCCTGGAGCT
GAAGTCACTACTGATGACCGTGCCTATGTCCGACAGCTAGTTACCTCCATGGATGTGACTGAGACCAATGTCTTCTTCTACCCTCGGCTCTTACCTTTGACAAAGTCTCCCGTTGAGAGTACTACCGA
ACCACCAGCAGTTCGAGCCTCTGAAGAGCGTCTAAGCAATGGGGATATATATTTACTGGAGAATGGGCTCAACCTCTTCCTCTGGGTGGGAGCAAGCGTCCAACAGGGTGTTGTCCAGAGCCTTTTCA
GCGTCTCCTCCTTCAGTCAGATCACCAGTGGTTTGAGTGTTCTGCCAGTTCTGGATAATCCACTGTCCAAGAAGGTTCGAGGCCTCATTGATAGCTTACGGGCACAGAGATCCCGGTACATGAAGCTT
ACCGTGGTGAAACAGGAAGACAAGATGGAGATGCTGTTCAAGCACTTCCTGGTGGAAGACAAGAGTCTGAGTGGGGGAGCATCTTATGTGGACTTTCTCTGTCATATGCACAAGGAGATTCGGCAGCT
ACTGAGCTAAAGCAAGTGGGTAAATGGCATAGGGCCCAGGCTAGCTTCCAGAAAGCACCCCAGGATGTCAGAGAAATTGGGACAGTAACATATCTTATGTAAGCTGACCTCAGTCTCTCTGGGGGGAG
GGGGAGATATAAGGAGACACCTTCTTTCTGGGCTCAAGTATCCTGCCACTCTGTCATGTCCTGCTGATGGAAGGTGCCCCTGTTCCCTCATTCTACCCTCTTTTTCCTGCTAATCCTGTCATAATGAA
TGTAGCTTCTCAGTTCACTGTATATGATTCGGTATTGGGGGTTTGGAGGCACCCAGACCCTGGCAATATTATGTGTCCCTTTGGACCAGTCTCCCAAGAGGAGAGGGGCAGGCAGGAAAGAGTGGGGA
TCCTAAGGTTACTACAGGGGGCTCAGTGTCATCCACAACTTCCTATATTAGGGATAAAACATATAGGTGCACAAGAGCTGGGGTATAGCCCATAGGTGGTGGAGAGAAAAGTGGTCAGTCCTTCTTGG
GCCTGGAGGTTAGCAGTCAAGTTTCTCTGCTTTCACTGCTCGCTCGCTCTCTCCTGCAATGATTGATGATCACTCCGTGGATAGAGAGGCACACTGTCAGAGGTGACCGGAGAACTGAGTTGCAAAAT
ATATTAAGATCTGGTAGAGGTACCAGCTTCCTTTCCAGCTGGAGAGGCCCCAACACTGGATGGTTCTGTAGGGAGCCTAGGGAGCCTGGTCATCAACTTGCAATACCTCACAGAGCCAGTTCACATCC
CACTCTGAGCTCCCACGAGAAACACTGCTTCTCCAGGCCCGGGGTTGTTGGGGAGAGAGGCAGAGGCAGCTGGAGCGCCGTTCTCTCCTGCTGGGACACCGCTTGGGCTTTGGTATTGACTGAGTGGC
TGACAGTTATCTTCCAACCCCAACTGGCTTGGGGGCAGGACAAGGGCTAGGCTTGATGGTGGCCAGGCTTGCCTGCTCCCCACCTGGGATGCCCCTGCTCTGGACCTCTCATTTCTCTTCATTGGTTT
ATTTTTCAATGCATCTTTAATTTGTAAAGAAATAAAATAAATTAAGATGTAA

hide sequence

RefSeq Acc Id:

NM_198597 ⟹ NP_940999

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	73,744,372 - 73,772,161 (+)	NCBI
GRCh37	10	75,504,039 - 75,531,933 (+)	NCBI
Build 36	10	75,174,138 - 75,201,925 (+)	NCBI Archive
Celera	10	68,787,456 - 68,815,097 (+)	RGD
HuRef	10	69,499,590 - 69,527,108 (+)	ENTREZGENE
CHM1_1	10	75,785,879 - 75,813,704 (+)	NCBI
T2T-CHM13v2.0	10	74,615,788 - 74,643,577 (+)	NCBI

Sequence:

show sequence

GGAACCGGAAGTGGAGCCTGGGAGCCTTGACGTTAGGAACGAAGTCTAACCTGGATCTGGAGCC
GGGTGAGATCAAATTGGGAATGCTTTCATAATGAACGTCAACCAGTCAGTTCCACCTGTGCCACCATTTGGGCAGCCCCAGCCCATCTACCCAGGGTATCATCAGTCCAGCTATGGTGGGCAATCAGG
GTCCACAGCCCCCGCCATTCCCTATGGAGCCTACAATGGCCCAGTACCAGGCTATCAGCAAACACCTCCCCAAGGTATGTCAAGAGCCCCACCTTCCTCGGGGGCACCTCCAGCCTCAACAGCACAGG
CTCCTTGTGGCCAGGCTGCATATGGCCAGTTTGGCCAAGGAGATGTACAGAATGGGCCAAGCTCCACTGTTCAGATGCAAAGGCTGCCTGGGTCTCAGCCATTTGGGTCCCCATTGGCCCCTGTGGGC
AACCAGCCACCTGTGCTTCAGCCCTATGGCCCTCCCCCGACAAGTGCACAGGTGGCTACGCAGCTGTCTGGAATGCAGATCAGCGGTGCTGTGGCCCCAGCCCCTCCTTCTTCAGGGCTGGGCTTTGG
CCCACCAACATCGCTGGCTTCAGCCTCAGGAAGTTTCCCTAACTCTGGTCTGTATGGCTCCTATCCTCAGGGCCAGGCTCCTCCCCTTAGCCAGGCCCAAGGTCATCCTGGGATCCAGACTCCCCAGC
GATCTGCCCCATCACAGGCCTCCAGCTTCACACCCCCAGCTTCAGGGGGTCCTCGGCTGCCTTCGATGACTGGTCCACTCCTGCCTGGACAGAGTTTTGGAGGGCCCTCAGTGAGCCAGCCCAACCAT
GTGTCTTCACCTCCTCAAGCTCTGCCCCCTGGCACCCAGATGACTGGGCCCCTGGGACCACTGCCACCTATGCACTCCCCGCAGCAGCCAGGCTATCAGCCCCAACAAAATGGTTCCTTCGGACCAGC
CCGGGGCCCTCAGTCTAATTATGGAGGCCCCTACCCAGCAGCACCCACCTTTGGCAGTCAGCCTGGGCCTCCTCAGCCACTGCCTCCTAAGCGCCTGGACCCTGATGCCATCCCAAGCCCTATTCAGG
TCATTGAAGATGACAGGAACAACCGGGGTACAGAGCCATTTGTTACTGGAGTACGGGGCCAGGTGCCACCCTTAGTCACTACCAACTTCCTGGTGAAAGACCAAGGGAATGCAAGTCCCCGATACATC
CGATGTACATCCTATAATATCCCTTGCACATCTGACATGGCTAAGCAGGCTCAGGTGCCCCTGGCAGCAGTCATCAAACCGCTGGCAAGGCTGCCCCCAGAGGAGGCTTCACCGTATGTTGTGGACCA
TGGGGAATCTGGCCCTTTGCGCTGCAACCGCTGCAAAGCATACATGTGTCCCTTCATGCAGTTCATTGAAGGAGGGAGGCGTTTCCAGTGCTGTTTTTGCAGCTGTATCAATGATGTTCCCCCCCAGT
ATTTTCAGCACCTGGATCATACCGGCAAACGTGTGGATGCTTATGACCGCCCTGAGCTATCCCTGGGCTCTTATGAATTCTTGGCCACTGTAGATTACTGCAAGAACAATAAGTTCCCCAGCCCTCCT
GCCTTTATCTTCATGATTGACGTCTCCTACAATGCCATCAGGACTGGTCTTGTTAGGCTCCTCTGTGAGGAGCTCAAGTCACTGTTAGACTTTCTACCTAGGGAGGGTGGGGCAGAAGAGTCAGCAAT
CCGCGTTGGCTTTGTCACCTACAATAAGGTGCTCCACTTCTATAATGTGAAGAGCTCATTGGCCCAGCCACAGATGATGGTTGTGTCTGATGTGGCTGACATGTTTGTGCCACTGCTGGATGGCTTCC
TGGTCAACGTCAATGAGTCTCGGGCAGTTATCACCAGCTTATTGGATCAGATTCCAGAAATGTTTGCAGACACAAGGGAAACAGAGACAGTATTTGTACCAGTTATCCAGGCTGGAATGGAGGCTCTG
AAGGCTGCTGAGTGTGCAGGGAAGCTCTTTCTATTCCATACATCCCTGCCCATTGCAGAGGCCCCAGGGAAACTGAAGAACAGAGATGACAGGAAGCTGATCAATACAGACAAGGAGAAGACTCTGTT
CCAGCCTCAGACAGGTGCCTATCAGACCCTGGCCAAAGAGTGTGTGGCCCAAGGCTGCTGTGTAGATCTCTTTCTCTTCCCTAACCAGTATGTGGATGTGGCCACACTCTCTGTTGTGCCCCAGCTCA
CTGGTGGCTCTGTCTACAAATATGCTTCCTTTCAGGTGGAGAACGACCAGGAGCGGTTCCTGAGTGACCTGCGTCGTGATGTCCAGAAGGTTGTTGGCTTTGATGCTGTGATGCGGGTCCGGACAAGC
ACTGGTATCCGTGCTGTAGATTTCTTTGGAGCTTTCTACATGAGCAACACGACAGATGTGGAGCTGGCTGGGCTAGATGGGGACAAAACAGTGACTGTGGAGTTCAAGCATGACGATCGGCTCAATGA
AGAGAGCGGAGCTCTCCTGCAGTGTGCCCTGCTTTACACCAGCTGTGCAGGGCAGCGTCGGCTCCGCATCCATAATCTGGCCCTGAACTGCTGCACCCAGCTGGCTGATCTATATCGAAACTGTGAGA
CTGACACGCTCATCAACTACATGGCCAAGTTTGCATATCGGGGAGTCCTGAATAGCCCTGTGAAGGCTGTTCGTGACACGCTCATCACCCAGTGTGCCCAGATCCTGGCCTGTTACAGAAAGAACTGT
GCTAGCCCCTCCTCTGCAGGACAGTTGATCCTTCCTGAGTGCATGAAGCTACTCCCAGTTTACCTGAACTGTGTGTTGAAGAGTGATGTCCTGCAGCCTGGAGCTGAAGTCACTACTGATGACCGTGC
CTATGTCCGACAGCTAGTTACCTCCATGGATGTGACTGAGACCAATGTCTTCTTCTACCCTCGGCTCTTACCTTTGACAAAGTCTCCCGTTGAGAGTACTACCGAACCACCAGCAGTTCGAGCCTCTG
AAGAGCGTCTAAGCAATGGGGATATATATTTACTGGAGAATGGGCTCAACCTCTTCCTCTGGGTGGGAGCAAGCGTCCAACAGGGTGTTGTCCAGAGCCTTTTCAGCGTCTCCTCCTTCAGTCAGATC
ACCAGTGGTTTGAGTGTTCTGCCAGTTCTGGATAATCCACTGTCCAAGAAGGTTCGAGGCCTCATTGATAGCTTACGGGCACAGAGATCCCGGTACATGAAGCTTACCGTGGTGAAACAGGAAGACAA
GATGGAGATGCTGTTCAAGCACTTCCTGGTGGAAGACAAGAGTCTGAGTGGGGGAGCATCTTATGTGGACTTTCTCTGTCATATGCACAAGGAGATTCGGCAGCTACTGAGCTAAAGCAAGTGGGTAA
ATGGCATAGGGCCCAGGCTAGCTTCCAGAAAGCACCCCAGGATGTCAGAGAAATTGGGACAGTAACATATCTTATGTAAGCTGACCTCAGTCTCTCTGGGGGGAGGGGGAGATATAAGGAGACACCTT
CTTTCTGGGCTCAAGTATCCTGCCACTCTGTCATGTCCTGCTGATGGAAGGTGCCCCTGTTCCCTCATTCTACCCTCTTTTTCCTGCTAATCCTGTCATAATGAATGTAGCTTCTCAGTTCACTGTAT
ATGATTCGGTATTGGGGGTTTGGAGGCACCCAGACCCTGGCAATATTATGTGTCCCTTTGGACCAGTCTCCCAAGAGGAGAGGGGCAGGCAGGAAAGAGTGGGGATCCTAAGGTTACTACAGGGGGCT
CAGTGTCATCCACAACTTCCTATATTAGGGATAAAACATATAGGTGCACAAGAGCTGGGGTATAGCCCATAGGTGGTGGAGAGAAAAGTGGTCAGTCCTTCTTGGGCCTGGAGGTTAGCAGTCAAGTT
TCTCTGCTTTCACTGCTCGCTCGCTCTCTCCTGCAATGATTGATGATCACTCCGTGGATAGAGAGGCACACTGTCAGAGGTGACCGGAGAACTGAGTTGCAAAATATATTAAGATCTGGTAGAGGTAC
CAGCTTCCTTTCCAGCTGGAGAGGCCCCAACACTGGATGGTTCTGTAGGGAGCCTAGGGAGCCTGGTCATCAACTTGCAATACCTCACAGAGCCAGTTCACATCCCACTCTGAGCTCCCACGAGAAAC
ACTGCTTCTCCAGGCCCGGGGTTGTTGGGGAGAGAGGCAGAGGCAGCTGGAGCGCCGTTCTCTCCTGCTGGGACACCGCTTGGGCTTTGGTATTGACTGAGTGGCTGACAGTTATCTTCCAACCCCAA
CTGGCTTGGGGGCAGGACAAGGGCTAGGCTTGATGGTGGCCAGGCTTGCCTGCTCCCCACCTGGGATGCCCCTGCTCTGGACCTCTCATTTCTCTTCATTGGTTTATTTTTCAATGCATCTTTAATTT
GTAAAGAAATAAAATAAATTAAGATGTAA

hide sequence

RefSeq Acc Id:

XM_011540380 ⟹ XP_011538682

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	73,744,372 - 73,772,161 (+)	NCBI

Sequence:

show sequence

GGTGACGGGACGGCCCCCTCGGAACCGGAAGTGGAGCCTGGGAGCCTTGACGTTAGGAACGAAG
TCTAACCTGGATCTGGAGCCGGGTGAGATCAAATTGGGAATGCTTTCATAATGAACGTCAACCAGTCAGTTCCACCTGTGCCACCATTTGGGCAGCCCCAGCCCATCTACCCAGGGTATCATCAGTCC
AGCTATGGTGGGCAATCAGGGTCCACAGCCCCCGCCATTCCCTATGGAGCCTACAATGGCCCAGTACCAGGCTATCAGCAAACACCTCCCCAAGGTATGTCAAGAGCCCCACCTTCCTCGGGGGCACC
TCCAGCCTCAACAGCACAGGCTCCTTGTGGCCAGGCTGCATATGGCCAGTTTGGCCAAGGAGATGTACAGAATGGGCCAAGCTCCACTGTTCAGATGCAAAGGCTGCCTGGGTCTCAGCCATTTGGGT
CCCCATTGGCCCCTGTGGGCAACCAGCCACCTGTGCTTCAGCCCTATGGCCCTCCCCCGACAAGTGCACAGGTGGCTACGCAGCTGTCTGGAATGCAGATCAGCGGTGCTGTGGCCCCAGCCCCTCCT
TCTTCAGGGCTGGGCTTTGGCCCACCAACATCGCTGGCTTCAGCCTCAGGAAGTTTCCCTAACTCTGGTCTGTATGGCTCCTATCCTCAGGGCCAGGCTCCTCCCCTTAGCCAGGCCCAAGGTCATCC
TGGGATCCAGACTCCCCAGCGATCTGCCCCATCACAGGCCTCCAGCTTCACACCCCCAGCTTCAGGGGGTCCTCGGCTGCCTTCGATGACTGGTCCACTCCTGCCTGGACAGAGTTTTGGAGGGCCCT
CAGTGAGCCAGCCCAACCATGTGTCTTCACCTCCTCAAGCTCTGCCCCCTGGCACCCAGATGACTGGGCCCCTGGGACCACTGCCACCTATGCACTCCCCGCAGCAGCCAGGCTATCAGCCCCAACAA
AATGGTTCCTTCGGACCAGCCCGGGGCCCTCAGTCTAATTATGGAGGCCCCTACCCAGCAGCACCCACCTTTGGCAGTCAGCCTGGGCCTCCTCAGCCACTGCCTCCTAAGCGCCTGGACCCTGATGC
CATCCCAAGCCCTCAACTCAGTGAGCTGCCTCCTCAGCAGAAAACCAGGCACAGAATAGACCCCGATGCCATTCCTAGTCCAATTCAGGTCATTGAAGATGACAGGAACAACCGGGGTACAGAGCCAT
TTGTTACTGGAGTACGGGGCCAGGTGCCACCCTTAGTCACTACCAACTTCCTGGTGAAAGACCAAGGGAATGCAAGTCCCCGATACATCCGATGTACATCCTATAATATCCCTTGCACATCTGACATG
GCTAAGCAGGCTCAGGTGCCCCTGGCAGCAGTCATCAAACCGCTGGCAAGGCTGCCCCCAGAGGAGGCTTCACCGTATGTTGTGGACCATGGGGAATCTGGCCCTTTGCGCTGCAACCGCTGCAAAGC
ATACATGTGTCCCTTCATGCAGTTCATTGAAGGAGGGAGGCGTTTCCAGTGCTGTTTTTGCAGCTGTATCAATGATGTTCCCCCCCAGTATTTTCAGCACCTGGATCATACCGGCAAACGTGTGGATG
CTTATGACCGCCCTGAGCTATCCCTGGGCTCTTATGAATTCTTGGCCACTGTAGATTACTGCAAGAACAATAAGTTCCCCAGCCCTCCTGCCTTTATCTTCATGATTGACGTCTCCTACAATGCCATC
AGGACTGGTCTTGTTAGGCTCCTCTGTGAGGAGCTCAAGTCACTGTTAGACTTTCTACCTAGGGAGGGTGGGGCAGAAGAGTCAGCAATCCGCGTTGGCTTTGTCACCTACAATAAGGTGCTCCACTT
CTATAATGTGAAGAGCTCATTGGCCCAGCCACAGATGATGGTTGTGTCTGATGTGGCTGACATGTTTGTGCCACTGCTGGATGGCTTCCTGGTCAACGTCAATGAGTCTCGGGCAGTTATCACCAGCT
TATTGGATCAGATTCCAGAAATGTTTGCAGACACAAGGGAAACAGAGACAGTATTTGTACCAGTTATCCAGGCTGGAATGGAGGCTCTGAAGGCTGCTGAGTGTGCAGGGAAGCTCTTTCTATTCCAT
ACATCCCTGCCCATTGCAGAGGCCCCAGGGAAACTGAAGAACAGAGATGACAGGAAGCTGATCAATACAGACAAGGAGAAGACTCTGTTCCAGCCTCAGACAGGTGCCTATCAGACCCTGGCCAAAGA
GTGTGTGGCCCAAGGCTGCTGTGTAGATCTCTTTCTCTTCCCTAACCAGTATGTGGATGTGGCCACACTCTCTGTTGTGCCCCAGCTCACTGGTGGCTCTGTCTACAAATATGCTTCCTTTCAGGTGG
AGAACGACCAGGAGCGGTTCCTGAGTGACCTGCGTCGTGATGTCCAGAAGGTTGTTGGCTTTGATGCTGTGATGCGGGTCCGGACAAGCACTGGTATCCGTGCTGTAGATTTCTTTGGAGCTTTCTAC
ATGAGCAACACGACAGATGTGGAGCTGGCTGGGCTAGATGGGGACAAAACAGTGACTGTGGAGTTCAAGCATGACGATCGGCTCAATGAAGAGAGCGGAGCTCTCCTGCAGTGTGCCCTGCTTTACAC
CAGCTGTGCAGGGCAGCGTCGGCTCCGCATCCATAATCTGGCCCTGAACTGCTGCACCCAGCTGGCTGATCTATATCGAAACTGTGAGACTGACACGCTCATCAACTACATGGCCAAGTTTGCATATC
GGGGAGTCCTGAATAGCCCTGTGAAGGCTGTTCGTGACACGCTCATCACCCAGTGTGCCCAGATCCTGGCCTGTTACAGAAAGAACTGTGCTAGCCCCTCCTCTGCAGGACAGTTGATCCTTCCTGAG
TGCATGAAGCTACTCCCAGTTTACCTGAACTGTGTGTTGAAGAGTGATGTCCTGCAGCCTGGAGCTGAAGTCACTACTGATGACCGTGCCTATGTCCGACAGCTAGTTACCTCCATGGATGTGACTGA
GACCAATGTCTTCTTCTACCCTCGGCTCTTACCTTTGACAAAGTCTCCCGTTGAGAGTACTACCGAACCACCAGCAGTTCGAGCCTCTGAAGAGCGTCTAAGCAATGGGGATATATATTTACTGGAGA
ATGGGCTCAACCTCTTCCTCTGGGTGGGAGCAAGCGTCCAACAGGGTGTTGTCCAGAGCCTTTTCAGCGTCTCCTCCTTCAGTCAGATCACCAGTGGTTTGAGTGTTCTGCCAGTTCTGGATAATCCA
CTGTCCAAGAAGGTTCGAGGCCTCATTGATAGCTTACGGGCACAGAGATCCCGGTACATGAAGCTTACCGTGGTGAAACAGGAAGACAAGATGGAGATGCTGTTCAAGCACTTCCTGGTGGAAGACAA
GAGTCTGAGTGGGGGAGCATCTTATGTGGACTTTCTCTGTCATATGCACAAGGAGATTCGGCAGCTACTGAGCTAAAGCAAGTGGGTAAATGGCATAGGGCCCAGGCTAGCTTCCAGAAAGCACCCCA
GGATGTCAGAGAAATTGGGACAGTAACATATCTTATGTAAGCTGACCTCAGTCTCTCTGGGGGGAGGGGGAGATATAAGGAGACACCTTCTTTCTGGGCTCAAGTATCCTGCCACTCTGTCATGTCCT
GCTGATGGAAGGTGCCCCTGTTCCCTCATTCTACCCTCTTTTTCCTGCTAATCCTGTCATAATGAATGTAGCTTCTCAGTTCACTGTATATGATTCGGTATTGGGGGTTTGGAGGCACCCAGACCCTG
GCAATATTATGTGTCCCTTTGGACCAGTCTCCCAAGAGGAGAGGGGCAGGCAGGAAAGAGTGGGGATCCTAAGGTTACTACAGGGGGCTCAGTGTCATCCACAACTTCCTATATTAGGGATAAAACAT
ATAGGTGCACAAGAGCTGGGGTATAGCCCATAGGTGGTGGAGAGAAAAGTGGTCAGTCCTTCTTGGGCCTGGAGGTTAGCAGTCAAGTTTCTCTGCTTTCACTGCTCGCTCGCTCTCTCCTGCAATGA
TTGATGATCACTCCGTGGATAGAGAGGCACACTGTCAGAGGTGACCGGAGAACTGAGTTGCAAAATATATTAAGATCTGGTAGAGGTACCAGCTTCCTTTCCAGCTGGAGAGGCCCCAACACTGGATG
GTTCTGTAGGGAGCCTAGGGAGCCTGGTCATCAACTTGCAATACCTCACAGAGCCAGTTCACATCCCACTCTGAGCTCCCACGAGAAACACTGCTTCTCCAGGCCCGGGGTTGTTGGGGAGAGAGGCA
GAGGCAGCTGGAGCGCCGTTCTCTCCTGCTGGGACACCGCTTGGGCTTTGGTATTGACTGAGTGGCTGACAGTTATCTTCCAACCCCAACTGGCTTGGGGGCAGGACAAGGGCTAGGCTTGATGGTGG
CCAGGCTTGCCTGCTCCCCACCTGGGATGCCCCTGCTCTGGACCTCTCATTTCTCTTCATTGGTTTATTTTTCAATGCATCTTTAATTTGTAAAGAAATAAAATAAATTAAGATGTAACCATTA

hide sequence

RefSeq Acc Id:

XM_011540381 ⟹ XP_011538683

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	73,744,372 - 73,772,161 (+)	NCBI

Sequence:

show sequence

GCCATAAAGTGACTGGAACATCTGAAAAAAAATGTCAGGAGGGAAATACATACGACTCAGCAGAGGCGCACAGGCGGCGGCCATGATGGGAAGATGAAAGAGGCGCATGCGCGGCATCCGGGTCCCCG
AAATGCAGACGTGGCAGAAGAAGTGGCCCGGCCCTAAAGCGTGGAGGAGGAACTTCCGGGGGTGACGGGACGGCCCCCTCGGAACCGGAAGTGGAGCCTGGGAGCCTTGACGTTAGGAACGAAGTCTA
ACCTGGATCTGGAGCCGGGAGATAATCTGAATGCTGGCTGGGGCAGAAAATTACTAAGATCCTGTGGAAGTGTGAGGATTATTAAACTGATCACTGTCTGATAAGGTGAGATCAAATTGGGAATGCTT
TCATAATGAACGTCAACCAGTCAGTTCCACCTGTGCCACCATTTGGGCAGCCCCAGCCCATCTACCCAGGGTATCATCAGTCCAGCTATGGTGGGCAATCAGGGTCCACAGCCCCCGCCATTCCCTAT
GGAGCCTACAATGGCCCAGTACCAGGCTATCAGCAAACACCTCCCCAAGGTATGTCAAGAGCCCCACCTTCCTCGGGGGCACCTCCAGCCTCAACAGCACAGGCTCCTTGTGGCCAGGCTGCATATGG
CCAGTTTGGCCAAGGAGATGTACAGAATGGGCCAAGCTCCACTGTTCAGATGCAAAGGCTGCCTGGGTCTCAGCCATTTGGGTCCCCATTGGCCCCTGTGGGCAACCAGCCACCTGTGCTTCAGCCCT
ATGGCCCTCCCCCGACAAGTGCACAGGTGGCTACGCAGCTGTCTGGAATGCAGATCAGCGGTGCTGTGGCCCCAGCCCCTCCTTCTTCAGGGCTGGGCTTTGGCCCACCAACATCGCTGGCTTCAGCC
TCAGGAAGTTTCCCTAACTCTGGTCTGTATGGCTCCTATCCTCAGGGCCAGGCTCCTCCCCTTAGCCAGGCCCAAGGTCATCCTGGGATCCAGACTCCCCAGCGATCTGCCCCATCACAGGCCTCCAG
CTTCACACCCCCAGCTTCAGGGGGTCCTCGGCTGCCTTCGATGACTGGTCCACTCCTGCCTGGACAGAGTTTTGGAGGGCCCTCAGTGAGCCAGCCCAACCATGTGTCTTCACCTCCTCAAGCTCTGC
CCCCTGGCACCCAGATGACTGGGCCCCTGGGACCACTGCCACCTATGCACTCCCCGCAGCAGCCAGGCTATCAGCCCCAACAAAATGGTTCCTTCGGACCAGCCCGGGGCCCTCAGTCTAATTATGGA
GGCCCCTACCCAGCAGCACCCACCTTTGGCAGTCAGCCTGGGCCTCCTCAGCCACTGCCTCCTAAGCGCCTGGACCCTGATGCCATCCCAAGCCCTCAACTCAGTGAGCTGCCTCCTCAGCAGAAAAC
CAGGCACAGAATAGACCCCGATGCCATTCCTAGTCCAATTCAGGTCATTGAAGATGACAGGAACAACCGGGGTACAGAGCCATTTGTTACTGGAGTACGGGGCCAGGTGCCACCCTTAGTCACTACCA
ACTTCCTGGTGAAAGACCAAGGGAATGCAAGTCCCCGATACATCCGATGTACATCCTATAATATCCCTTGCACATCTGACATGGCTAAGCAGGCTCAGGTGCCCCTGGCAGCAGTCATCAAACCGCTG
GCAAGGCTGCCCCCAGAGGAGGCTTCACCGTATGTTGTGGACCATGGGGAATCTGGCCCTTTGCGCTGCAACCGCTGCAAAGCATACATGTGTCCCTTCATGCAGTTCATTGAAGGAGGGAGGCGTTT
CCAGTGCTGTTTTTGCAGCTGTATCAATGATGTTCCCCCCCAGTATTTTCAGCACCTGGATCATACCGGCAAACGTGTGGATGCTTATGACCGCCCTGAGCTATCCCTGGGCTCTTATGAATTCTTGG
CCACTGTAGATTACTGCAAGAACAATAAGTTCCCCAGCCCTCCTGCCTTTATCTTCATGATTGACGTCTCCTACAATGCCATCAGGACTGGTCTTGTTAGGCTCCTCTGTGAGGAGCTCAAGTCACTG
TTAGACTTTCTACCTAGGGAGGGTGGGGCAGAAGAGTCAGCAATCCGCGTTGGCTTTGTCACCTACAATAAGGTGCTCCACTTCTATAATGTGAAGAGCTCATTGGCCCAGCCACAGATGATGGTTGT
GTCTGATGTGGCTGACATGTTTGTGCCACTGCTGGATGGCTTCCTGGTCAACGTCAATGAGTCTCGGGCAGTTATCACCAGCTTATTGGATCAGATTCCAGAAATGTTTGCAGACACAAGGGAAACAG
AGACAGTATTTGTACCAGTTATCCAGGCTGGAATGGAGGCTCTGAAGGCTGCTGAGTGTGCAGGGAAGCTCTTTCTATTCCATACATCCCTGCCCATTGCAGAGGCCCCAGGGAAACTGAAGAACAGA
GATGACAGGAAGCTGATCAATACAGACAAGGAGAAGACTCTGTTCCAGCCTCAGACAGGTGCCTATCAGACCCTGGCCAAAGAGTGTGTGGCCCAAGGCTGCTGTGTAGATCTCTTTCTCTTCCCTAA
CCAGTATGTGGATGTGGCCACACTCTCTGTTGTGCCCCAGCTCACTGGTGGCTCTGTCTACAAATATGCTTCCTTTCAGGTGGAGAACGACCAGGAGCGGTTCCTGAGTGACCTGCGTCGTGATGTCC
AGAAGGTTGTTGGCTTTGATGCTGTGATGCGGGTCCGGACAAGCACTGGTATCCGTGCTGTAGATTTCTTTGGAGCTTTCTACATGAGCAACACGACAGATGTGGAGCTGGCTGGGCTAGATGGGGAC
AAAACAGTGACTGTGGAGTTCAAGCATGACGATCGGCTCAATGAAGAGAGCGGAGCTCTCCTGCAGTGTGCCCTGCTTTACACCAGCTGTGCAGGGCAGCGTCGGCTCCGCATCCATAATCTGGCCCT
GAACTGCTGCACCCAGCTGGCTGATCTATATCGAAACTGTGAGACTGACACGCTCATCAACTACATGGCCAAGTTTGCATATCGGGGAGTCCTGAATAGCCCTGTGAAGGCTGTTCGTGACACGCTCA
TCACCCAGTGTGCCCAGATCCTGGCCTGTTACAGAAAGAACTGTGCTAGCCCCTCCTCTGCAGGACAGTTGATCCTTCCTGAGTGCATGAAGCTACTCCCAGTTTACCTGAACTGTGTGTTGAAGAGT
GATGTCCTGCAGCCTGGAGCTGAAGTCACTACTGATGACCGTGCCTATGTCCGACAGCTAGTTACCTCCATGGATGTGACTGAGACCAATGTCTTCTTCTACCCTCGGCTCTTACCTTTGACAAAGTC
TCCCGTTGAGAGTACTACCGAACCACCAGCAGTTCGAGCCTCTGAAGAGCGTCTAAGCAATGGGGATATATATTTACTGGAGAATGGGCTCAACCTCTTCCTCTGGGTGGGAGCAAGCGTCCAACAGG
GTGTTGTCCAGAGCCTTTTCAGCGTCTCCTCCTTCAGTCAGATCACCAGTGGTTTGAGTGTTCTGCCAGTTCTGGATAATCCACTGTCCAAGAAGGTTCGAGGCCTCATTGATAGCTTACGGGCACAG
AGATCCCGGTACATGAAGCTTACCGTGGTGAAACAGGAAGACAAGATGGAGATGCTGTTCAAGCACTTCCTGGTGGAAGACAAGAGTCTGAGTGGGGGAGCATCTTATGTGGACTTTCTCTGTCATAT
GCACAAGGAGATTCGGCAGCTACTGAGCTAAAGCAAGTGGGTAAATGGCATAGGGCCCAGGCTAGCTTCCAGAAAGCACCCCAGGATGTCAGAGAAATTGGGACAGTAACATATCTTATGTAAGCTGA
CCTCAGTCTCTCTGGGGGGAGGGGGAGATATAAGGAGACACCTTCTTTCTGGGCTCAAGTATCCTGCCACTCTGTCATGTCCTGCTGATGGAAGGTGCCCCTGTTCCCTCATTCTACCCTCTTTTTCC
TGCTAATCCTGTCATAATGAATGTAGCTTCTCAGTTCACTGTATATGATTCGGTATTGGGGGTTTGGAGGCACCCAGACCCTGGCAATATTATGTGTCCCTTTGGACCAGTCTCCCAAGAGGAGAGGG
GCAGGCAGGAAAGAGTGGGGATCCTAAGGTTACTACAGGGGGCTCAGTGTCATCCACAACTTCCTATATTAGGGATAAAACATATAGGTGCACAAGAGCTGGGGTATAGCCCATAGGTGGTGGAGAGA
AAAGTGGTCAGTCCTTCTTGGGCCTGGAGGTTAGCAGTCAAGTTTCTCTGCTTTCACTGCTCGCTCGCTCTCTCCTGCAATGATTGATGATCACTCCGTGGATAGAGAGGCACACTGTCAGAGGTGAC
CGGAGAACTGAGTTGCAAAATATATTAAGATCTGGTAGAGGTACCAGCTTCCTTTCCAGCTGGAGAGGCCCCAACACTGGATGGTTCTGTAGGGAGCCTAGGGAGCCTGGTCATCAACTTGCAATACC
TCACAGAGCCAGTTCACATCCCACTCTGAGCTCCCACGAGAAACACTGCTTCTCCAGGCCCGGGGTTGTTGGGGAGAGAGGCAGAGGCAGCTGGAGCGCCGTTCTCTCCTGCTGGGACACCGCTTGGG
CTTTGGTATTGACTGAGTGGCTGACAGTTATCTTCCAACCCCAACTGGCTTGGGGGCAGGACAAGGGCTAGGCTTGATGGTGGCCAGGCTTGCCTGCTCCCCACCTGGGATGCCCCTGCTCTGGACCT
CTCATTTCTCTTCATTGGTTTATTTTTCAATGCATCTTTAATTTGTAAAGAAATAAAATAAATTAAGATGTAA

hide sequence

RefSeq Acc Id:

XM_047426031 ⟹ XP_047281987

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	73,744,372 - 73,772,161 (+)	NCBI

RefSeq Acc Id:

XM_047426032 ⟹ XP_047281988

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	73,744,372 - 73,772,161 (+)	NCBI

RefSeq Acc Id:

XM_047426033 ⟹ XP_047281989

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	73,744,372 - 73,772,161 (+)	NCBI

RefSeq Acc Id:

XM_047426034 ⟹ XP_047281990

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	73,744,372 - 73,772,161 (+)	NCBI

RefSeq Acc Id:

XM_047426035 ⟹ XP_047281991

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	73,746,996 - 73,772,161 (+)	NCBI

RefSeq Acc Id:

XM_054367226 ⟹ XP_054223201

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	74,615,788 - 74,643,577 (+)	NCBI

RefSeq Acc Id:

XM_054367227 ⟹ XP_054223202

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	74,615,788 - 74,643,577 (+)	NCBI

RefSeq Acc Id:

XM_054367228 ⟹ XP_054223203

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	74,615,845 - 74,643,577 (+)	NCBI

RefSeq Acc Id:

XM_054367229 ⟹ XP_054223204

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	74,615,805 - 74,643,577 (+)	NCBI

RefSeq Acc Id:

XM_054367230 ⟹ XP_054223205

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	74,615,840 - 74,643,577 (+)	NCBI

RefSeq Acc Id:

XM_054367231 ⟹ XP_054223206

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	10	74,618,412 - 74,643,577 (+)	NCBI


Protein RefSeqs	NP_004913	(Get FASTA)	NCBI Sequence Viewer
	NP_940999	(Get FASTA)	NCBI Sequence Viewer
	XP_011538682	(Get FASTA)	NCBI Sequence Viewer
	XP_011538683	(Get FASTA)	NCBI Sequence Viewer
	XP_047281987	(Get FASTA)	NCBI Sequence Viewer
	XP_047281988	(Get FASTA)	NCBI Sequence Viewer
	XP_047281989	(Get FASTA)	NCBI Sequence Viewer
	XP_047281990	(Get FASTA)	NCBI Sequence Viewer
	XP_047281991	(Get FASTA)	NCBI Sequence Viewer
	XP_054223201	(Get FASTA)	NCBI Sequence Viewer
	XP_054223202	(Get FASTA)	NCBI Sequence Viewer
	XP_054223203	(Get FASTA)	NCBI Sequence Viewer
	XP_054223204	(Get FASTA)	NCBI Sequence Viewer
	XP_054223205	(Get FASTA)	NCBI Sequence Viewer
	XP_054223206	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH18928	(Get FASTA)	NCBI Sequence Viewer
	BAA07558	(Get FASTA)	NCBI Sequence Viewer
	BAG60784	(Get FASTA)	NCBI Sequence Viewer
	BAG61695	(Get FASTA)	NCBI Sequence Viewer
	BAG64196	(Get FASTA)	NCBI Sequence Viewer
	BAH14822	(Get FASTA)	NCBI Sequence Viewer
	EAW54515	(Get FASTA)	NCBI Sequence Viewer
	EAW54516	(Get FASTA)	NCBI Sequence Viewer
	EAW54517	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000321845
	ENSP00000321845.6
	ENSP00000343405
	ENSP00000343405.2
GenBank Protein	P53992	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:

NP_004913 ⟸ NM_004922

- UniProtKB:

B4DZT4 (UniProtKB/Swiss-Prot), Q8WV25 (UniProtKB/Swiss-Prot), P53992 (UniProtKB/Swiss-Prot), G5EA31 (UniProtKB/TrEMBL)

- Sequence:

show sequence

MNVNQSVPPVPPFGQPQPIYPGYHQSSYGGQSGSTAPAIPYGAYNGPVPGYQQTPPQGMSRAPPSSGAPPASTAQAPCGQAAYGQFGQGDVQNGPSSTVQMQRLPGSQPFGSPLAPVGNQPPVLQPYG
PPPTSAQVATQLSGMQISGAVAPAPPSSGLGFGPPTSLASASGSFPNSGLYGSYPQGQAPPLSQAQGHPGIQTPQRSAPSQASSFTPPASGGPRLPSMTGPLLPGQSFGGPSVSQPNHVSSPPQALPP
GTQMTGPLGPLPPMHSPQQPGYQPQQNGSFGPARGPQSNYGGPYPAAPTFGSQPGPPQPLPPKRLDPDAIPSPIQVIEDDRNNRGTEPFVTGVRGQVPPLVTTNFLVKDQGNASPRYIRCTSYNIPCT
SDMAKQAQVPLAAVIKPLARLPPEEASPYVVDHGESGPLRCNRCKAYMCPFMQFIEGGRRFQCCFCSCINDVPPQYFQHLDHTGKRVDAYDRPELSLGSYEFLATVDYCKNNKFPSPPAFIFMIDVSY
NAIRTGLVRLLCEELKSLLDFLPREGGAEESAIRVGFVTYNKVLHFYNVKSSLAQPQMMVVSDVADMFVPLLDGFLVNVNESRAVITSLLDQIPEMFADTRETETVFVPVIQAGMEALKAAECAGKLF
LFHTSLPIAEAPGKLKNRDDRKLINTDKEKTLFQPQTGAYQTLAKECVAQGCCVDLFLFPNQYVDVATLSVVPQLTGGSVYKYASFQVENDQERFLSDLRRDVQKVVGFDAVMRVRTSTGIRAVDFFG
AFYMSNTTDVELAGLDGDKTVTVEFKHDDRLNEESGALLQCALLYTSCAGQRRLRIHNLALNCCTQLADLYRNCETDTLINYMAKFAYRGVLNSPVKAVRDTLITQCAQILACYRKNCASPSSAGQLI
LPECMKLLPVYLNCVLKSDVLQPGAEVTTDDRAYVRQLVTSMDVTETNVFFYPRLLPLTKSPVESTTEPPAVRASEERLSNGDIYLLENGLNLFLWVGASVQQGVVQSLFSVSSFSQITSGLSVLPVL
DNPLSKKVRGLIDSLRAQRSRYMKLTVVKQEDKMEMLFKHFLVEDKSLSGGASYVDFLCHMHKEIRQLLS

hide sequence

RefSeq Acc Id:

NP_940999 ⟸ NM_198597

- UniProtKB:

B4DZT4 (UniProtKB/Swiss-Prot), Q8WV25 (UniProtKB/Swiss-Prot), P53992 (UniProtKB/Swiss-Prot), G5EA31 (UniProtKB/TrEMBL)

- Sequence:

show sequence

MNVNQSVPPVPPFGQPQPIYPGYHQSSYGGQSGSTAPAIPYGAYNGPVPGYQQTPPQGMSRAPPSSGAPPASTAQAPCGQAAYGQFGQGDVQNGPSSTVQMQRLPGSQPFGSPLAPVGNQPPVLQPYG
PPPTSAQVATQLSGMQISGAVAPAPPSSGLGFGPPTSLASASGSFPNSGLYGSYPQGQAPPLSQAQGHPGIQTPQRSAPSQASSFTPPASGGPRLPSMTGPLLPGQSFGGPSVSQPNHVSSPPQALPP
GTQMTGPLGPLPPMHSPQQPGYQPQQNGSFGPARGPQSNYGGPYPAAPTFGSQPGPPQPLPPKRLDPDAIPSPIQVIEDDRNNRGTEPFVTGVRGQVPPLVTTNFLVKDQGNASPRYIRCTSYNIPCT
SDMAKQAQVPLAAVIKPLARLPPEEASPYVVDHGESGPLRCNRCKAYMCPFMQFIEGGRRFQCCFCSCINDVPPQYFQHLDHTGKRVDAYDRPELSLGSYEFLATVDYCKNNKFPSPPAFIFMIDVSY
NAIRTGLVRLLCEELKSLLDFLPREGGAEESAIRVGFVTYNKVLHFYNVKSSLAQPQMMVVSDVADMFVPLLDGFLVNVNESRAVITSLLDQIPEMFADTRETETVFVPVIQAGMEALKAAECAGKLF
LFHTSLPIAEAPGKLKNRDDRKLINTDKEKTLFQPQTGAYQTLAKECVAQGCCVDLFLFPNQYVDVATLSVVPQLTGGSVYKYASFQVENDQERFLSDLRRDVQKVVGFDAVMRVRTSTGIRAVDFFG
AFYMSNTTDVELAGLDGDKTVTVEFKHDDRLNEESGALLQCALLYTSCAGQRRLRIHNLALNCCTQLADLYRNCETDTLINYMAKFAYRGVLNSPVKAVRDTLITQCAQILACYRKNCASPSSAGQLI
LPECMKLLPVYLNCVLKSDVLQPGAEVTTDDRAYVRQLVTSMDVTETNVFFYPRLLPLTKSPVESTTEPPAVRASEERLSNGDIYLLENGLNLFLWVGASVQQGVVQSLFSVSSFSQITSGLSVLPVL
DNPLSKKVRGLIDSLRAQRSRYMKLTVVKQEDKMEMLFKHFLVEDKSLSGGASYVDFLCHMHKEIRQLLS

hide sequence

RefSeq Acc Id:	XP_011538682 ⟸ XM_011540380
- Peptide Label:	isoform X1
- UniProtKB:	G5EA31 (UniProtKB/TrEMBL)
- Sequence:	show sequence MNVNQSVPPVPPFGQPQPIYPGYHQSSYGGQSGSTAPAIPYGAYNGPVPGYQQTPPQGMSRAPPSSGAPPASTAQAPCGQAAYGQFGQGDVQNGPSSTVQMQRLPGSQPFGSPLAPVGNQPPVLQPYG PPPTSAQVATQLSGMQISGAVAPAPPSSGLGFGPPTSLASASGSFPNSGLYGSYPQGQAPPLSQAQGHPGIQTPQRSAPSQASSFTPPASGGPRLPSMTGPLLPGQSFGGPSVSQPNHVSSPPQALPP GTQMTGPLGPLPPMHSPQQPGYQPQQNGSFGPARGPQSNYGGPYPAAPTFGSQPGPPQPLPPKRLDPDAIPSPQLSELPPQQKTRHRIDPDAIPSPIQVIEDDRNNRGTEPFVTGVRGQVPPLVTTNF LVKDQGNASPRYIRCTSYNIPCTSDMAKQAQVPLAAVIKPLARLPPEEASPYVVDHGESGPLRCNRCKAYMCPFMQFIEGGRRFQCCFCSCINDVPPQYFQHLDHTGKRVDAYDRPELSLGSYEFLAT VDYCKNNKFPSPPAFIFMIDVSYNAIRTGLVRLLCEELKSLLDFLPREGGAEESAIRVGFVTYNKVLHFYNVKSSLAQPQMMVVSDVADMFVPLLDGFLVNVNESRAVITSLLDQIPEMFADTRETET VFVPVIQAGMEALKAAECAGKLFLFHTSLPIAEAPGKLKNRDDRKLINTDKEKTLFQPQTGAYQTLAKECVAQGCCVDLFLFPNQYVDVATLSVVPQLTGGSVYKYASFQVENDQERFLSDLRRDVQK VVGFDAVMRVRTSTGIRAVDFFGAFYMSNTTDVELAGLDGDKTVTVEFKHDDRLNEESGALLQCALLYTSCAGQRRLRIHNLALNCCTQLADLYRNCETDTLINYMAKFAYRGVLNSPVKAVRDTLIT QCAQILACYRKNCASPSSAGQLILPECMKLLPVYLNCVLKSDVLQPGAEVTTDDRAYVRQLVTSMDVTETNVFFYPRLLPLTKSPVESTTEPPAVRASEERLSNGDIYLLENGLNLFLWVGASVQQGV VQSLFSVSSFSQITSGLSVLPVLDNPLSKKVRGLIDSLRAQRSRYMKLTVVKQEDKMEMLFKHFLVEDKSLSGGASYVDFLCHMHKEIRQLLS hide sequence

RefSeq Acc Id:	XP_011538683 ⟸ XM_011540381
- Peptide Label:	isoform X1
- UniProtKB:	G5EA31 (UniProtKB/TrEMBL)
- Sequence:	show sequence MNVNQSVPPVPPFGQPQPIYPGYHQSSYGGQSGSTAPAIPYGAYNGPVPGYQQTPPQGMSRAPPSSGAPPASTAQAPCGQAAYGQFGQGDVQNGPSSTVQMQRLPGSQPFGSPLAPVGNQPPVLQPYG PPPTSAQVATQLSGMQISGAVAPAPPSSGLGFGPPTSLASASGSFPNSGLYGSYPQGQAPPLSQAQGHPGIQTPQRSAPSQASSFTPPASGGPRLPSMTGPLLPGQSFGGPSVSQPNHVSSPPQALPP GTQMTGPLGPLPPMHSPQQPGYQPQQNGSFGPARGPQSNYGGPYPAAPTFGSQPGPPQPLPPKRLDPDAIPSPQLSELPPQQKTRHRIDPDAIPSPIQVIEDDRNNRGTEPFVTGVRGQVPPLVTTNF LVKDQGNASPRYIRCTSYNIPCTSDMAKQAQVPLAAVIKPLARLPPEEASPYVVDHGESGPLRCNRCKAYMCPFMQFIEGGRRFQCCFCSCINDVPPQYFQHLDHTGKRVDAYDRPELSLGSYEFLAT VDYCKNNKFPSPPAFIFMIDVSYNAIRTGLVRLLCEELKSLLDFLPREGGAEESAIRVGFVTYNKVLHFYNVKSSLAQPQMMVVSDVADMFVPLLDGFLVNVNESRAVITSLLDQIPEMFADTRETET VFVPVIQAGMEALKAAECAGKLFLFHTSLPIAEAPGKLKNRDDRKLINTDKEKTLFQPQTGAYQTLAKECVAQGCCVDLFLFPNQYVDVATLSVVPQLTGGSVYKYASFQVENDQERFLSDLRRDVQK VVGFDAVMRVRTSTGIRAVDFFGAFYMSNTTDVELAGLDGDKTVTVEFKHDDRLNEESGALLQCALLYTSCAGQRRLRIHNLALNCCTQLADLYRNCETDTLINYMAKFAYRGVLNSPVKAVRDTLIT QCAQILACYRKNCASPSSAGQLILPECMKLLPVYLNCVLKSDVLQPGAEVTTDDRAYVRQLVTSMDVTETNVFFYPRLLPLTKSPVESTTEPPAVRASEERLSNGDIYLLENGLNLFLWVGASVQQGV VQSLFSVSSFSQITSGLSVLPVLDNPLSKKVRGLIDSLRAQRSRYMKLTVVKQEDKMEMLFKHFLVEDKSLSGGASYVDFLCHMHKEIRQLLS hide sequence

Ensembl Acc Id:

ENSP00000321845 ⟸ ENST00000345254

Protein Domains

Gelsolin-like Sec23/Sec24 beta-sandwich Sec23/Sec24 helical Sec23/Sec24 trunk Zinc finger Sec23/Sec24-type

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-P53992-F1-model_v2	AlphaFold	P53992	1-1094	view protein structure

RGD ID:

7217867

Promoter ID:

EPDNEW_H14679

Type:

initiation region

Name:

SEC24C_1

Description:

SEC24 homolog C, COPII coat complex component

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	10	73,744,372 - 73,744,432	EPDNEW

RGD ID:

6788243

Promoter ID:

HG_KWN:10074

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

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

Transcripts:

NM_004922, NM_198597, OTTHUMT00000048680, UC009XRJ.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	10	75,173,651 - 75,174,227 (+)	MPROMDB

RGD ID:

6809880

Promoter ID:

HG_ACW:8579

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

SEC24CANDFUT11.OAPR07

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	10	75,189,111 - 75,189,611 (+)	MPROMDB

RGD ID:

6788242

Promoter ID:

HG_KWN:10076

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

HeLa_S3

Transcripts:

OTTHUMT00000048682

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	10	75,196,676 - 75,197,176 (+)	MPROMDB

RGD ID:

6809881

Promoter ID:

HG_ACW:8583

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

SEC24CANDFUT11.UAPR07-UNSPLICED

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	10	75,209,426 - 75,209,926 (+)	MPROMDB

Database	Acc Id	Source(s)
COSMIC	SEC24C	COSMIC
Ensembl Genes	ENSG00000176986	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000339365	ENTREZGENE
	ENST00000339365.2	UniProtKB/Swiss-Prot
	ENST00000345254	ENTREZGENE
	ENST00000345254.9	UniProtKB/Swiss-Prot
Gene3D-CATH	3.40.20.10	UniProtKB/Swiss-Prot
	3.40.50.410	UniProtKB/Swiss-Prot
	beta-sandwich domain of Sec23/24	UniProtKB/Swiss-Prot
	Sec23/Sec24 helical domain	UniProtKB/Swiss-Prot
	Zn-finger domain of Sec23/24	UniProtKB/Swiss-Prot
GTEx	ENSG00000176986	GTEx
HGNC ID	HGNC:10705	ENTREZGENE
Human Proteome Map	SEC24C	Human Proteome Map
InterPro	ADF-H/Gelsolin-like_dom_sf	UniProtKB/Swiss-Prot
	Gelsolin-like_dom	UniProtKB/Swiss-Prot
	Gelsolin-like_dom_sf	UniProtKB/Swiss-Prot
	Sec23/24_helical_dom	UniProtKB/Swiss-Prot
	Sec23/24_helical_dom_sf	UniProtKB/Swiss-Prot
	Sec23/24_trunk_dom	UniProtKB/Swiss-Prot
	Sec23_24_beta_S	UniProtKB/Swiss-Prot
	SEC23_SEC24_subfamily	UniProtKB/Swiss-Prot
	Sec24-like_trunk_dom	UniProtKB/Swiss-Prot
	vWFA_dom_sf	UniProtKB/Swiss-Prot
	Znf_Sec23_Sec24	UniProtKB/Swiss-Prot
	Znf_Sec23_Sec24_sf	UniProtKB/Swiss-Prot
KEGG Report	hsa:9632	UniProtKB/Swiss-Prot
NCBI Gene	9632	ENTREZGENE
OMIM	607185	OMIM
PANTHER	PROTEIN TRANSPORT PROTEIN SEC24C	UniProtKB/Swiss-Prot
	SEC24-RELATED PROTEIN	UniProtKB/Swiss-Prot
Pfam	Gelsolin	UniProtKB/Swiss-Prot
	Sec23_BS	UniProtKB/Swiss-Prot
	Sec23_helical	UniProtKB/Swiss-Prot
	Sec23_trunk	UniProtKB/Swiss-Prot
	zf-Sec23_Sec24	UniProtKB/Swiss-Prot
PharmGKB	PA35628	PharmGKB
Superfamily-SCOP	beta-sandwich domain of Sec23/24	UniProtKB/Swiss-Prot
	SSF53300	UniProtKB/Swiss-Prot
	SSF81811	UniProtKB/Swiss-Prot
	SSF82754	UniProtKB/Swiss-Prot
	SSF82919	UniProtKB/Swiss-Prot
UniProt	A0A0U1RR49_HUMAN	UniProtKB/TrEMBL
	A0A0U1RR58_HUMAN	UniProtKB/TrEMBL
	B4DSN3	ENTREZGENE, UniProtKB/TrEMBL
	B4DZT4	ENTREZGENE
	G5EA31	ENTREZGENE, UniProtKB/TrEMBL
	P53992	ENTREZGENE
	Q8WV25	ENTREZGENE
	SC24C_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	B4DZT4	UniProtKB/Swiss-Prot
	Q8WV25	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2015-08-11	SEC24C	SEC24 homolog C, COPII coat complex component	SEC24C	SEC24 family member C	Symbol and/or name change	5135510	APPROVED
2013-10-29	SEC24C	SEC24 family member C	SEC24C	SEC24 family, member C (S. cerevisiae)	Symbol and/or name change	5135510	APPROVED

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


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


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

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

Imported Disease Annotations - ClinVar

Imported Annotations - KEGG (archival)

Imported Human Phenotype Annotations - HPO

Imported Human Phenotype Annotations - ClinVar

Send us a Message

Imported Disease Annotations - ClinVar

Imported Annotations - KEGG (archival)

Imported Human Phenotype Annotations - HPO

Imported Human Phenotype Annotations - ClinVar