SEC31A (SEC31 homolog A, COPII coat complex component) - Rat Genome Database

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Gene: SEC31A (SEC31 homolog A, COPII coat complex component) Homo sapiens
Analyze
Symbol: SEC31A
Name: SEC31 homolog A, COPII coat complex component
RGD ID: 1350188
HGNC Page HGNC:17052
Description: Enables calcium-dependent protein binding activity. Involved in COPII-coated vesicle cargo loading and response to calcium ion. Located in several cellular components, including COPII-coated ER to Golgi transport vesicle; endoplasmic reticulum exit site; and perinuclear region of cytoplasm. Part of COPII vesicle coat. Implicated in Halperin-Birk syndrome.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: ABP125; ABP130; DKFZp686N07171; HPBKS; HSPC275; HSPC334; KIAA0905; MGC90305; NEDSOSB; protein transport protein Sec31A; protein-transport protein SEC31; Sec31 homolog A; SEC31 homolog A, COPII coating complex component; SEC31-like 1; sec31-like 1 (s. cerevisiae); SEC31-like protein 1; SEC31-related protein A; SEC31L1; web1-like protein; yeast Sec31p homolog
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38482,818,509 - 82,900,569 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl482,818,509 - 82,901,166 (-)EnsemblGRCh38hg38GRCh38
GRCh37483,739,662 - 83,821,722 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36483,958,838 - 84,031,424 (-)NCBINCBI36Build 36hg18NCBI36
Build 34484,096,993 - 84,169,579NCBI
Celera481,030,957 - 81,102,991 (-)NCBICelera
Cytogenetic Map4q21.22NCBI
HuRef479,479,736 - 79,553,039 (-)NCBIHuRef
CHM1_1483,716,332 - 83,788,863 (-)NCBICHM1_1
T2T-CHM13v2.0486,147,772 - 86,229,788 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
1,2-dichloroethane  (ISO)
1,2-dimethylhydrazine  (ISO)
17alpha-ethynylestradiol  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,6-dimethoxyphenol  (EXP)
2,6-dinitrotoluene  (ISO)
2-hydroxypropanoic acid  (EXP)
3,4-methylenedioxymethamphetamine  (ISO)
3H-1,2-dithiole-3-thione  (ISO)
4,4'-sulfonyldiphenol  (EXP)
5-fluorouracil  (EXP)
6-propyl-2-thiouracil  (ISO)
actinomycin D  (EXP)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (EXP)
amitrole  (ISO)
ammonium chloride  (ISO)
amphetamine  (ISO)
aristolochic acid A  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
arsenite(3-)  (EXP)
benzo[a]pyrene  (EXP)
benzo[a]pyrene diol epoxide I  (EXP)
beta-lapachone  (EXP)
bisphenol A  (EXP,ISO)
bisphenol AF  (EXP)
bisphenol F  (EXP)
cadmium dichloride  (ISO)
caffeine  (EXP)
carbamazepine  (EXP)
carbon nanotube  (ISO)
CGP 52608  (EXP)
chlorpyrifos  (ISO)
cisplatin  (EXP)
clofibrate  (ISO)
clozapine  (EXP)
cobalt dichloride  (EXP)
coumarin  (EXP)
cyclosporin A  (EXP)
dicrotophos  (EXP)
dorsomorphin  (EXP)
doxorubicin  (EXP)
elemental selenium  (EXP)
endosulfan  (ISO)
enzyme inhibitor  (EXP)
ethyl methanesulfonate  (EXP)
flavonoids  (ISO)
folic acid  (ISO)
FR900359  (EXP)
furfural  (EXP)
gamma-hexachlorocyclohexane  (ISO)
hydralazine  (EXP)
hydrogen peroxide  (EXP)
inulin  (ISO)
irinotecan  (EXP)
ivermectin  (EXP)
lead(0)  (EXP)
Mesaconitine  (ISO)
methimazole  (ISO)
methyl methanesulfonate  (EXP)
mitoxantrone  (EXP)
N,N-diethyl-m-toluamide  (ISO)
N-acetyl-L-cysteine  (ISO)
nitrates  (ISO)
Nutlin-3  (EXP)
ozone  (EXP)
paracetamol  (ISO)
paraquat  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (EXP)
permethrin  (ISO)
phenylmercury acetate  (EXP)
piroxicam  (EXP)
propiconazole  (ISO)
Propiverine  (ISO)
quercetin  (EXP)
rac-lactic acid  (EXP)
resveratrol  (ISO)
SB 431542  (EXP)
selenium atom  (EXP)
silicon dioxide  (EXP)
sodium arsenite  (EXP,ISO)
tamibarotene  (EXP)
tamoxifen  (ISO)
testosterone  (ISO)
thapsigargin  (EXP,ISO)
thiram  (EXP)
tolcapone  (ISO)
triphenyl phosphate  (EXP)
tungsten  (ISO)
tunicamycin  (EXP)
valproic acid  (EXP)
vitamin E  (EXP)
zearalenone  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# 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. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8125298   PMID:8889548   PMID:10048485   PMID:10737800   PMID:10788476   PMID:11031247   PMID:11252894   PMID:11269867   PMID:12107410   PMID:12477932   PMID:12665801   PMID:14702039  
PMID:15146057   PMID:16161041   PMID:16344560   PMID:16407955   PMID:16957052   PMID:17196169   PMID:17214967   PMID:17499046   PMID:17981133   PMID:18029348   PMID:18692470   PMID:18713835  
PMID:18843296   PMID:19054391   PMID:19401338   PMID:19738201   PMID:19822759   PMID:20379614   PMID:20691033   PMID:20696395   PMID:20834162   PMID:20936779   PMID:21109691   PMID:21145461  
PMID:21301993   PMID:21325169   PMID:21653829   PMID:21873635   PMID:21900206   PMID:22331354   PMID:22358839   PMID:22623428   PMID:22658674   PMID:22792322   PMID:22802641   PMID:22939629  
PMID:23349870   PMID:23414517   PMID:24069399   PMID:24825317   PMID:25006245   PMID:25201882   PMID:25416956   PMID:25540196   PMID:25667979   PMID:25921289   PMID:26186194   PMID:26344197  
PMID:26496610   PMID:26638075   PMID:26673895   PMID:26831064   PMID:27337956   PMID:27565346   PMID:27716508   PMID:28319085   PMID:28442536   PMID:28514442   PMID:28515276   PMID:28581483  
PMID:28986522   PMID:29467282   PMID:29507755   PMID:29509190   PMID:29540532   PMID:29568061   PMID:29604273   PMID:29653964   PMID:29669786   PMID:29704455   PMID:29955894   PMID:30021884  
PMID:30464055   PMID:30596474   PMID:30948266   PMID:31073040   PMID:31091453   PMID:31586073   PMID:31732153   PMID:31995728   PMID:32296183   PMID:32552912   PMID:32687490   PMID:32694731  
PMID:32707033   PMID:32807901   PMID:32878247   PMID:33022573   PMID:33239621   PMID:33545068   PMID:33845483   PMID:33961781   PMID:34079125   PMID:34349018   PMID:34578187   PMID:34591612  
PMID:34597346   PMID:34709727   PMID:35013218   PMID:35013556   PMID:35032548   PMID:35120648   PMID:35241646   PMID:35256949   PMID:35271311   PMID:35337019   PMID:35384245   PMID:35446349  
PMID:35509820   PMID:35659652   PMID:35831314   PMID:35844135   PMID:35906200   PMID:35914814   PMID:35944360   PMID:35987950   PMID:36114006   PMID:36215168   PMID:36232890   PMID:36305789  
PMID:36543142   PMID:36652337   PMID:36861887   PMID:36976175   PMID:37223481   PMID:37506885   PMID:37827155   PMID:37848033   PMID:38400880   PMID:38569033   PMID:38697112   PMID:38943005  
PMID:39231216  


Genomics

Comparative Map Data
SEC31A
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38482,818,509 - 82,900,569 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl482,818,509 - 82,901,166 (-)EnsemblGRCh38hg38GRCh38
GRCh37483,739,662 - 83,821,722 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36483,958,838 - 84,031,424 (-)NCBINCBI36Build 36hg18NCBI36
Build 34484,096,993 - 84,169,579NCBI
Celera481,030,957 - 81,102,991 (-)NCBICelera
Cytogenetic Map4q21.22NCBI
HuRef479,479,736 - 79,553,039 (-)NCBIHuRef
CHM1_1483,716,332 - 83,788,863 (-)NCBICHM1_1
T2T-CHM13v2.0486,147,772 - 86,229,788 (-)NCBIT2T-CHM13v2.0
Sec31a
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm395100,509,508 - 100,564,132 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl5100,509,508 - 100,564,093 (-)EnsemblGRCm39 Ensembl
GRCm385100,361,649 - 100,416,273 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl5100,361,649 - 100,416,234 (-)EnsemblGRCm38mm10GRCm38
MGSCv375100,790,668 - 100,845,253 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv365100,601,947 - 100,662,097 (-)NCBIMGSCv36mm8
Celera597,687,421 - 97,742,015 (-)NCBICelera
Cytogenetic Map5E4NCBI
cM Map548.48NCBI
Sec31a
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8149,518,655 - 9,573,579 (+)NCBIGRCr8
mRatBN7.2149,214,324 - 9,269,281 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl149,214,349 - 9,269,273 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx149,186,187 - 9,240,986 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01410,486,059 - 10,540,858 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0149,182,662 - 9,237,463 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01410,854,713 - 10,909,579 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1410,854,682 - 10,909,612 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01410,801,850 - 10,856,889 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41410,466,582 - 10,522,655 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11410,466,581 - 10,522,655 (+)NCBI
Celera149,321,723 - 9,376,348 (+)NCBICelera
Cytogenetic Map14p22NCBI
Sec31a
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554336,830,540 - 6,891,258 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554336,830,732 - 6,891,259 (-)NCBIChiLan1.0ChiLan1.0
SEC31A
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2347,179,928 - 47,252,488 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1447,369,105 - 47,447,681 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0441,312,389 - 41,384,924 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1447,164,207 - 47,236,223 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl447,173,348 - 47,235,812 (+)Ensemblpanpan1.1panPan2
SEC31A
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1326,761,018 - 6,840,802 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl326,761,289 - 6,840,709 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha3235,044,306 - 35,123,841 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0326,782,111 - 6,862,117 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl326,782,111 - 6,862,121 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1326,852,892 - 6,933,085 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0326,722,105 - 6,801,751 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.03233,164,400 - 33,244,629 (+)NCBIUU_Cfam_GSD_1.0
Sec31a
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244052855,503,050 - 5,580,731 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049367381,676,436 - 1,744,896 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049367381,664,916 - 1,741,739 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SEC31A
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl8135,426,403 - 135,495,121 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.18135,431,965 - 135,495,124 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.28144,727,204 - 144,774,058 (+)NCBISscrofa10.2Sscrofa10.2susScr3
SEC31A
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1731,207,349 - 31,288,484 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl731,207,089 - 31,288,574 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660379,776,537 - 9,857,889 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Sec31a
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247578,040,894 - 8,122,785 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in SEC31A
92 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 4q21.1-21.23(chr4:75453111-84094295)x1 copy number loss See cases [RCV000050786] Chr4:75453111..84094295 [GRCh38]
Chr4:76378321..85015448 [GRCh37]
Chr4:76597345..85234472 [NCBI36]
Chr4:4q21.1-21.23
pathogenic
GRCh38/hg38 4q12-22.3(chr4:51831622-97505618)x3 copy number gain See cases [RCV000051772] Chr4:51831622..97505618 [GRCh38]
Chr4:52697788..98426769 [GRCh37]
Chr4:52392545..98645792 [NCBI36]
Chr4:4q12-22.3
pathogenic
GRCh38/hg38 4q13.2-21.23(chr4:67869564-85517308)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053294]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053294]|See cases [RCV000053294] Chr4:67869564..85517308 [GRCh38]
Chr4:68735282..86438461 [GRCh37]
Chr4:68417877..86657485 [NCBI36]
Chr4:4q13.2-21.23
pathogenic
GRCh38/hg38 4q13.3-22.1(chr4:74031395-90421127)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053296]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053296]|See cases [RCV000053296] Chr4:74031395..90421127 [GRCh38]
Chr4:74897112..91342278 [GRCh37]
Chr4:75115976..91561301 [NCBI36]
Chr4:4q13.3-22.1
pathogenic
GRCh38/hg38 4q21.21-22.1(chr4:79575748-92412449)x1 copy number loss See cases [RCV000053297] Chr4:79575748..92412449 [GRCh38]
Chr4:80496902..93333600 [GRCh37]
Chr4:80715926..93552623 [NCBI36]
Chr4:4q21.21-22.1
pathogenic
GRCh38/hg38 4q21.21-21.23(chr4:81061483-83332595)x1 copy number loss See cases [RCV000053298] Chr4:81061483..83332595 [GRCh38]
Chr4:81982637..84253748 [GRCh37]
Chr4:82201661..84472772 [NCBI36]
Chr4:4q21.21-21.23
pathogenic
GRCh38/hg38 4q21.22-21.23(chr4:81733333-83448842)x1 copy number loss See cases [RCV000053299] Chr4:81733333..83448842 [GRCh38]
Chr4:82654487..84369995 [GRCh37]
Chr4:82873511..84589019 [NCBI36]
Chr4:4q21.22-21.23
pathogenic
GRCh38/hg38 4q21.22-21.23(chr4:81802008-83437114)x1 copy number loss See cases [RCV000053300] Chr4:81802008..83437114 [GRCh38]
Chr4:82723161..84358267 [GRCh37]
Chr4:82942185..84577291 [NCBI36]
Chr4:4q21.22-21.23
pathogenic
GRCh38/hg38 4q21.22-21.3(chr4:82248692-86778340)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053319]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053319]|See cases [RCV000053319] Chr4:82248692..86778340 [GRCh38]
Chr4:83169845..87699493 [GRCh37]
Chr4:83388869..87918517 [NCBI36]
Chr4:4q21.22-21.3
pathogenic
GRCh38/hg38 4q21.21-22.3(chr4:80879777-94809447)x1 copy number loss See cases [RCV000134977] Chr4:80879777..94809447 [GRCh38]
Chr4:81800931..95730598 [GRCh37]
Chr4:82019955..95949621 [NCBI36]
Chr4:4q21.21-22.3
pathogenic
GRCh38/hg38 4q21.21-21.22(chr4:79742612-83153725)x1 copy number loss See cases [RCV000135797] Chr4:79742612..83153725 [GRCh38]
Chr4:80663766..84074878 [GRCh37]
Chr4:80882790..84293902 [NCBI36]
Chr4:4q21.21-21.22
uncertain significance
GRCh38/hg38 4q21.21-21.23(chr4:79786514-85832807)x1 copy number loss See cases [RCV000136865] Chr4:79786514..85832807 [GRCh38]
Chr4:80707668..86753960 [GRCh37]
Chr4:80926692..86972984 [NCBI36]
Chr4:4q21.21-21.23
pathogenic
GRCh38/hg38 4q21.21-24(chr4:80427023-100855441)x1 copy number loss See cases [RCV000137269] Chr4:80427023..100855441 [GRCh38]
Chr4:81348177..101776598 [GRCh37]
Chr4:81567201..101995621 [NCBI36]
Chr4:4q21.21-24
pathogenic
GRCh38/hg38 4q21.21-21.23(chr4:80908016-84329610)x1 copy number loss See cases [RCV000137863] Chr4:80908016..84329610 [GRCh38]
Chr4:81829170..85250763 [GRCh37]
Chr4:82048194..85469787 [NCBI36]
Chr4:4q21.21-21.23
likely pathogenic
GRCh38/hg38 4q13.3-21.3(chr4:72262258-86002147)x3 copy number gain See cases [RCV000138312] Chr4:72262258..86002147 [GRCh38]
Chr4:73127975..86923300 [GRCh37]
Chr4:73346839..87142324 [NCBI36]
Chr4:4q13.3-21.3
pathogenic
GRCh38/hg38 4q21.21-21.3(chr4:80043949-86948317)x1 copy number loss See cases [RCV000140416] Chr4:80043949..86948317 [GRCh38]
Chr4:80965103..87869469 [GRCh37]
Chr4:81184127..88088493 [NCBI36]
Chr4:4q21.21-21.3
pathogenic
GRCh38/hg38 4q21.22-21.23(chr4:81675848-83970410)x1 copy number loss See cases [RCV000143321] Chr4:81675848..83970410 [GRCh38]
Chr4:82597002..84891563 [GRCh37]
Chr4:82816026..85110587 [NCBI36]
Chr4:4q21.22-21.23
likely pathogenic
GRCh38/hg38 4q13.2-22.3(chr4:68686088-95294456)x3 copy number gain See cases [RCV000143458] Chr4:68686088..95294456 [GRCh38]
Chr4:69551806..96215607 [GRCh37]
Chr4:69234401..96434630 [NCBI36]
Chr4:4q13.2-22.3
pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:12440-190904441)x3 copy number gain See cases [RCV000446653] Chr4:12440..190904441 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
GRCh37/hg19 4q21.21-22.1(chr4:82283358-90341831)x1 copy number loss See cases [RCV000447691] Chr4:82283358..90341831 [GRCh37]
Chr4:4q21.21-22.1
pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473) copy number gain See cases [RCV000510453] Chr4:68346..190957473 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
GRCh37/hg19 4q21.21-21.23(chr4:82359656-84155605)x1 copy number loss See cases [RCV000511583] Chr4:82359656..84155605 [GRCh37]
Chr4:4q21.21-21.23
likely pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)x3 copy number gain See cases [RCV000512241] Chr4:68346..190957473 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
GRCh37/hg19 4q21.21-22.3(chr4:81314915-96636651)x1 copy number loss not provided [RCV000682426] Chr4:81314915..96636651 [GRCh37]
Chr4:4q21.21-22.3
pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:49450-190915650)x3 copy number gain not provided [RCV000743155] Chr4:49450..190915650 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:49450-190963766)x3 copy number gain not provided [RCV000743156] Chr4:49450..190963766 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:11525-191028879)x3 copy number gain not provided [RCV000743147] Chr4:11525..191028879 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
NM_001077207.4(SEC31A):c.787A>G (p.Ile263Val) single nucleotide variant not provided [RCV000896633] Chr4:82870420 [GRCh38]
Chr4:83791573 [GRCh37]
Chr4:4q21.22
benign
NM_001077207.4(SEC31A):c.2141C>T (p.Pro714Leu) single nucleotide variant not specified [RCV004296261] Chr4:82853583 [GRCh38]
Chr4:83774736 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.583G>T (p.Val195Leu) single nucleotide variant not specified [RCV004286492] Chr4:82874667 [GRCh38]
Chr4:83795820 [GRCh37]
Chr4:4q21.22
uncertain significance
GRCh37/hg19 4q21.21-22.1(chr4:80482400-92572499)x1 copy number loss See cases [RCV000790579] Chr4:80482400..92572499 [GRCh37]
Chr4:4q21.21-22.1
pathogenic
GRCh37/hg19 4q21.21-22.1(chr4:82043901-88334228) copy number loss not provided [RCV000767792] Chr4:82043901..88334228 [GRCh37]
Chr4:4q21.21-22.1
pathogenic
NM_001077207.4(SEC31A):c.2522C>T (p.Pro841Leu) single nucleotide variant not provided [RCV000962091] Chr4:82844490 [GRCh38]
Chr4:83765643 [GRCh37]
Chr4:4q21.22
benign
NM_001077207.4(SEC31A):c.251A>G (p.Asp84Gly) single nucleotide variant not provided [RCV002280289]|not specified [RCV004047545] Chr4:82878881 [GRCh38]
Chr4:83800034 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1457G>A (p.Arg486His) single nucleotide variant not provided [RCV002280291] Chr4:82863370 [GRCh38]
Chr4:83784523 [GRCh37]
Chr4:4q21.22
uncertain significance
GRCh37/hg19 4q21.22-21.23(chr4:82593140-85651685)x1 copy number loss not provided [RCV001005566] Chr4:82593140..85651685 [GRCh37]
Chr4:4q21.22-21.23
pathogenic
NM_001077207.4(SEC31A):c.2776_2777dup (p.Ala927fs) duplication Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies [RCV000855664] Chr4:82842330..82842331 [GRCh38]
Chr4:83763483..83763484 [GRCh37]
Chr4:4q21.22
pathogenic
GRCh37/hg19 4q21.1-21.23(chr4:78769297-84968832)x1 copy number loss not provided [RCV000846933] Chr4:78769297..84968832 [GRCh37]
Chr4:4q21.1-21.23
pathogenic
GRCh37/hg19 4q21.21-21.22(chr4:80199183-84074906)x1 copy number loss not provided [RCV000848187] Chr4:80199183..84074906 [GRCh37]
Chr4:4q21.21-21.22
pathogenic
NM_001077207.4(SEC31A):c.3246C>T (p.Pro1082=) single nucleotide variant not provided [RCV000935846] Chr4:82827414 [GRCh38]
Chr4:83748567 [GRCh37]
Chr4:4q21.22
likely benign
NM_001077207.4(SEC31A):c.3092C>T (p.Pro1031Leu) single nucleotide variant not provided [RCV000956227] Chr4:82827568 [GRCh38]
Chr4:83748721 [GRCh37]
Chr4:4q21.22
benign
NM_001077207.4(SEC31A):c.1977T>C (p.Tyr659=) single nucleotide variant not provided [RCV000956228] Chr4:82854934 [GRCh38]
Chr4:83776087 [GRCh37]
Chr4:4q21.22
benign
NM_001077207.4(SEC31A):c.2126A>G (p.Gln709Arg) single nucleotide variant not specified [RCV004313523] Chr4:82853598 [GRCh38]
Chr4:83774751 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1844A>G (p.Lys615Arg) single nucleotide variant not specified [RCV004298757] Chr4:82856989 [GRCh38]
Chr4:83778142 [GRCh37]
Chr4:4q21.22
uncertain significance
GRCh37/hg19 4q13.3-21.23(chr4:72680879-86426232)x1 copy number loss not provided [RCV001005556] Chr4:72680879..86426232 [GRCh37]
Chr4:4q13.3-21.23
pathogenic
Single allele deletion Chromosome 4q21 deletion syndrome [RCV001172266] Chr4:83196931..85540706 [GRCh37]
Chr4:4q21.22-21.23
pathogenic
GRCh37/hg19 4q13.3-21.3(chr4:71412409-87920784)x1 copy number loss See cases [RCV001263040] Chr4:71412409..87920784 [GRCh37]
Chr4:4q13.3-21.3
pathogenic
NM_001077207.4(SEC31A):c.1374C>G (p.Cys458Trp) single nucleotide variant Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies [RCV001329558] Chr4:82864422 [GRCh38]
Chr4:83785575 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2503-29C>A single nucleotide variant Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies [RCV001807568]|not provided [RCV004716831] Chr4:82844538 [GRCh38]
Chr4:83765691 [GRCh37]
Chr4:4q21.22
benign
NM_001077207.4(SEC31A):c.1045-26G>T single nucleotide variant Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies [RCV001807570]|not provided [RCV004716833] Chr4:82866986 [GRCh38]
Chr4:83788139 [GRCh37]
Chr4:4q21.22
benign
NM_001077207.4(SEC31A):c.2154+36G>C single nucleotide variant Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies [RCV001807569]|not provided [RCV004716832] Chr4:82853534 [GRCh38]
Chr4:83774687 [GRCh37]
Chr4:4q21.22
benign
NM_001077207.4(SEC31A):c.1008T>A (p.Gly336=) single nucleotide variant Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies [RCV001807571]|not provided [RCV004716834] Chr4:82867191 [GRCh38]
Chr4:83788344 [GRCh37]
Chr4:4q21.22
benign
NM_001077207.4(SEC31A):c.597A>G (p.Arg199=) single nucleotide variant Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies [RCV001807573]|not provided [RCV004717852] Chr4:82874653 [GRCh38]
Chr4:83795806 [GRCh37]
Chr4:4q21.22
benign
NM_001077207.4(SEC31A):c.640-4T>G single nucleotide variant Neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies [RCV001807572]|not provided [RCV004716835] Chr4:82872090 [GRCh38]
Chr4:83793243 [GRCh37]
Chr4:4q21.22
benign
GRCh37/hg19 4q21.21-22.1(chr4:80467886-93362064)x1 copy number loss not provided [RCV001829208] Chr4:80467886..93362064 [GRCh37]
Chr4:4q21.21-22.1
pathogenic
GRCh37/hg19 4q21.22(chr4:83402855-83847970)x3 copy number gain not provided [RCV001832953] Chr4:83402855..83847970 [GRCh37]
Chr4:4q21.22
uncertain significance
GRCh37/hg19 4q12-31.21(chr4:52866944-143582507)x3 copy number gain not provided [RCV001827738] Chr4:52866944..143582507 [GRCh37]
Chr4:4q12-31.21
pathogenic
GRCh37/hg19 4q13.3-22.1(chr4:75737340-91131156) copy number gain not specified [RCV002053429] Chr4:75737340..91131156 [GRCh37]
Chr4:4q13.3-22.1
pathogenic
GRCh37/hg19 4q21.21-22.2(chr4:79780152-94873225) copy number loss not specified [RCV002053432] Chr4:79780152..94873225 [GRCh37]
Chr4:4q21.21-22.2
pathogenic
GRCh37/hg19 4q21.21-22.1(chr4:81054789-90667421) copy number loss not specified [RCV002053435] Chr4:81054789..90667421 [GRCh37]
Chr4:4q21.21-22.1
pathogenic
GRCh37/hg19 4q21.22(chr4:83506831-83776627)x3 copy number gain not provided [RCV001834477] Chr4:83506831..83776627 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2432A>G (p.Lys811Arg) single nucleotide variant not specified [RCV004329370] Chr4:82848874 [GRCh38]
Chr4:83770027 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2656G>A (p.Gly886Arg) single nucleotide variant not specified [RCV004194322] Chr4:82842452 [GRCh38]
Chr4:83763605 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2909C>G (p.Pro970Arg) single nucleotide variant not specified [RCV004236339] Chr4:82842199 [GRCh38]
Chr4:83763352 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.3376C>G (p.Leu1126Val) single nucleotide variant not specified [RCV004233657] Chr4:82824590 [GRCh38]
Chr4:83745743 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1609G>C (p.Glu537Gln) single nucleotide variant not specified [RCV004121850] Chr4:82861648 [GRCh38]
Chr4:83782801 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1804G>A (p.Ala602Thr) single nucleotide variant not specified [RCV004192154] Chr4:82857029 [GRCh38]
Chr4:83778182 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1010G>A (p.Ser337Asn) single nucleotide variant not specified [RCV004192153] Chr4:82867189 [GRCh38]
Chr4:83788342 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.603T>G (p.Asn201Lys) single nucleotide variant not specified [RCV004217146] Chr4:82874647 [GRCh38]
Chr4:83795800 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.3311C>T (p.Thr1104Ile) single nucleotide variant not specified [RCV004151917] Chr4:82824655 [GRCh38]
Chr4:83745808 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.973G>A (p.Asp325Asn) single nucleotide variant not specified [RCV004227344] Chr4:82867226 [GRCh38]
Chr4:83788379 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.3308C>T (p.Pro1103Leu) single nucleotide variant not specified [RCV004113517] Chr4:82824658 [GRCh38]
Chr4:83745811 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1877C>G (p.Thr626Ser) single nucleotide variant not specified [RCV004120298] Chr4:82856956 [GRCh38]
Chr4:83778109 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2518C>T (p.Pro840Ser) single nucleotide variant not specified [RCV004226759] Chr4:82844494 [GRCh38]
Chr4:83765647 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2389C>T (p.His797Tyr) single nucleotide variant not specified [RCV004119427] Chr4:82848917 [GRCh38]
Chr4:83770070 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2513C>G (p.Pro838Arg) single nucleotide variant not specified [RCV004136384] Chr4:82844499 [GRCh38]
Chr4:83765652 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.20A>G (p.Asp7Gly) single nucleotide variant not specified [RCV004227032] Chr4:82881917 [GRCh38]
Chr4:83803070 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2917A>G (p.Thr973Ala) single nucleotide variant not specified [RCV004088499] Chr4:82842191 [GRCh38]
Chr4:83763344 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.957A>T (p.Leu319Phe) single nucleotide variant not specified [RCV004122113] Chr4:82867242 [GRCh38]
Chr4:83788395 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.292A>G (p.Ile98Val) single nucleotide variant not specified [RCV004172009] Chr4:82878840 [GRCh38]
Chr4:83799993 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1985C>T (p.Pro662Leu) single nucleotide variant not specified [RCV004219719] Chr4:82854926 [GRCh38]
Chr4:83776079 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2533A>G (p.Met845Val) single nucleotide variant not specified [RCV004219707] Chr4:82844479 [GRCh38]
Chr4:83765632 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1322G>A (p.Arg441Gln) single nucleotide variant not specified [RCV004290528] Chr4:82864474 [GRCh38]
Chr4:83785627 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1349A>G (p.Gln450Arg) single nucleotide variant not specified [RCV004267156] Chr4:82864447 [GRCh38]
Chr4:83785600 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.3647A>G (p.Asn1216Ser) single nucleotide variant not specified [RCV004278172] Chr4:82819090 [GRCh38]
Chr4:83740243 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1742A>G (p.Asn581Ser) single nucleotide variant not specified [RCV004264424] Chr4:82857091 [GRCh38]
Chr4:83778244 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1189T>G (p.Ser397Ala) single nucleotide variant not specified [RCV004311266] Chr4:82866816 [GRCh38]
Chr4:83787969 [GRCh37]
Chr4:4q21.22
uncertain significance
GRCh38/hg38 4q21.21-23(chr4:79123548-99457773)x1 copy number loss Chromosome 4q21 deletion syndrome [RCV003327709] Chr4:79123548..99457773 [GRCh38]
Chr4:4q21.21-23
pathogenic
NM_001077207.4(SEC31A):c.1136T>C (p.Ile379Thr) single nucleotide variant not specified [RCV004341628] Chr4:82866869 [GRCh38]
Chr4:83788022 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.3255A>C (p.Glu1085Asp) single nucleotide variant not specified [RCV004352290] Chr4:82827405 [GRCh38]
Chr4:83748558 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.823T>A (p.Leu275Met) single nucleotide variant not specified [RCV004362156] Chr4:82870384 [GRCh38]
Chr4:83791537 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.3329A>C (p.Lys1110Thr) single nucleotide variant not specified [RCV004344978] Chr4:82824637 [GRCh38]
Chr4:83745790 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1890T>C (p.Thr630=) single nucleotide variant not provided [RCV003439369] Chr4:82855021 [GRCh38]
Chr4:83776174 [GRCh37]
Chr4:4q21.22
likely benign
NM_001077207.4(SEC31A):c.2833C>T (p.Pro945Ser) single nucleotide variant not specified [RCV003404842] Chr4:82842275 [GRCh38]
Chr4:83763428 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.511A>G (p.Ile171Val) single nucleotide variant not specified [RCV003404814] Chr4:82874739 [GRCh38]
Chr4:83795892 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1986G>A (p.Pro662=) single nucleotide variant not provided [RCV003439368] Chr4:82854925 [GRCh38]
Chr4:83776078 [GRCh37]
Chr4:4q21.22
likely benign
NM_001077207.4(SEC31A):c.1368T>G (p.Asn456Lys) single nucleotide variant not provided [RCV003439370] Chr4:82864428 [GRCh38]
Chr4:83785581 [GRCh37]
Chr4:4q21.22
likely benign
NM_001077207.4(SEC31A):c.2874A>G (p.Pro958=) single nucleotide variant not provided [RCV003439365] Chr4:82842234 [GRCh38]
Chr4:83763387 [GRCh37]
Chr4:4q21.22
likely benign
NM_001077207.4(SEC31A):c.2265T>C (p.Asn755=) single nucleotide variant not provided [RCV003439367] Chr4:82851494 [GRCh38]
Chr4:83772647 [GRCh37]
Chr4:4q21.22
likely benign
NM_001077207.4(SEC31A):c.501G>A (p.Pro167=) single nucleotide variant not provided [RCV003435052] Chr4:82874749 [GRCh38]
Chr4:83795902 [GRCh37]
Chr4:4q21.22
likely benign
NM_001077207.4(SEC31A):c.2868C>T (p.Gly956=) single nucleotide variant not provided [RCV003439366] Chr4:82842240 [GRCh38]
Chr4:83763393 [GRCh37]
Chr4:4q21.22
likely benign
NM_001077207.4(SEC31A):c.699C>T (p.Ser233=) single nucleotide variant not provided [RCV003439371] Chr4:82872027 [GRCh38]
Chr4:83793180 [GRCh37]
Chr4:4q21.22
likely benign
NM_001077207.4(SEC31A):c.2968+1G>T single nucleotide variant SEC31A-related disorder [RCV003939501] Chr4:82842139 [GRCh38]
Chr4:83763292 [GRCh37]
Chr4:4q21.22
likely benign
GRCh37/hg19 4q21.21-22.3(chr4:81558759-95965995)x1 copy number loss not specified [RCV003986493] Chr4:81558759..95965995 [GRCh37]
Chr4:4q21.21-22.3
pathogenic
NM_001077207.4(SEC31A):c.402+3T>G single nucleotide variant SEC31A-related disorder [RCV003968997] Chr4:82878727 [GRCh38]
Chr4:83799880 [GRCh37]
Chr4:4q21.22
likely benign
NM_001077207.4(SEC31A):c.112A>G (p.Ser38Gly) single nucleotide variant not specified [RCV004447694] Chr4:82880890 [GRCh38]
Chr4:83802043 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2332A>T (p.Asn778Tyr) single nucleotide variant not specified [RCV004447703] Chr4:82848974 [GRCh38]
Chr4:83770127 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2347C>T (p.Arg783Cys) single nucleotide variant not specified [RCV004447704] Chr4:82848959 [GRCh38]
Chr4:83770112 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2375A>G (p.Glu792Gly) single nucleotide variant not specified [RCV004447705] Chr4:82848931 [GRCh38]
Chr4:83770084 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.3028A>G (p.Met1010Val) single nucleotide variant not specified [RCV004447709] Chr4:82827632 [GRCh38]
Chr4:83748785 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.3128C>T (p.Pro1043Leu) single nucleotide variant not specified [RCV004447710] Chr4:82827532 [GRCh38]
Chr4:83748685 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.3390C>G (p.Cys1130Trp) single nucleotide variant not specified [RCV004447711] Chr4:82824576 [GRCh38]
Chr4:83745729 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.3502A>G (p.Ser1168Gly) single nucleotide variant not specified [RCV004447712] Chr4:82819235 [GRCh38]
Chr4:83740388 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1033C>G (p.Gln345Glu) single nucleotide variant not specified [RCV004447693] Chr4:82867166 [GRCh38]
Chr4:83788319 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1997C>T (p.Ser666Leu) single nucleotide variant not specified [RCV004447700] Chr4:82854914 [GRCh38]
Chr4:83776067 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2606C>T (p.Pro869Leu) single nucleotide variant not specified [RCV004447707] Chr4:82844406 [GRCh38]
Chr4:83765559 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.997A>G (p.Ile333Val) single nucleotide variant not specified [RCV004447713] Chr4:82867202 [GRCh38]
Chr4:83788355 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1423T>G (p.Ser475Ala) single nucleotide variant not specified [RCV004447696] Chr4:82864373 [GRCh38]
Chr4:83785526 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1830G>T (p.Leu610Phe) single nucleotide variant not specified [RCV004447698] Chr4:82857003 [GRCh38]
Chr4:83778156 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1135A>G (p.Ile379Val) single nucleotide variant not specified [RCV004447695] Chr4:82866870 [GRCh38]
Chr4:83788023 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.143T>C (p.Leu48Ser) single nucleotide variant not specified [RCV004447697] Chr4:82880859 [GRCh38]
Chr4:83802012 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1850A>G (p.Tyr617Cys) single nucleotide variant not specified [RCV004447699] Chr4:82856983 [GRCh38]
Chr4:83778136 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2155G>T (p.Asp719Tyr) single nucleotide variant not specified [RCV004447701] Chr4:82851604 [GRCh38]
Chr4:83772757 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.944del (p.Asn315fs) deletion not specified [RCV003988260] Chr4:82867255 [GRCh38]
Chr4:83788408 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.908C>A (p.Thr303Lys) single nucleotide variant SEC31A-related disorder [RCV003943986] Chr4:82867291 [GRCh38]
Chr4:83788444 [GRCh37]
Chr4:4q21.22
likely benign
GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3 copy number gain not provided [RCV003885507] Chr4:45455621..191003541 [GRCh37]
Chr4:4p12-q35.2
pathogenic
NM_001077207.4(SEC31A):c.2216C>G (p.Thr739Ser) single nucleotide variant not specified [RCV004447702] Chr4:82851543 [GRCh38]
Chr4:83772696 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2413G>A (p.Glu805Lys) single nucleotide variant not specified [RCV004447706] Chr4:82848893 [GRCh38]
Chr4:83770046 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2653T>G (p.Phe885Val) single nucleotide variant not specified [RCV004447708] Chr4:82842455 [GRCh38]
Chr4:83763608 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.3196G>A (p.Val1066Ile) single nucleotide variant not provided [RCV003886244] Chr4:82827464 [GRCh38]
Chr4:83748617 [GRCh37]
Chr4:4q21.22
likely benign
NM_001077207.4(SEC31A):c.708C>A (p.Asp236Glu) single nucleotide variant not specified [RCV004663666] Chr4:82872018 [GRCh38]
Chr4:83793171 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2348G>A (p.Arg783His) single nucleotide variant not specified [RCV004663664] Chr4:82848958 [GRCh38]
Chr4:83770111 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1639G>A (p.Glu547Lys) single nucleotide variant not specified [RCV004663668] Chr4:82857752 [GRCh38]
Chr4:83778905 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2428C>T (p.Pro810Ser) single nucleotide variant not specified [RCV004667033] Chr4:82848878 [GRCh38]
Chr4:83770031 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.581C>T (p.Thr194Ile) single nucleotide variant not specified [RCV004663665] Chr4:82874669 [GRCh38]
Chr4:83795822 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.458A>T (p.Asn153Ile) single nucleotide variant not specified [RCV004663667] Chr4:82875767 [GRCh38]
Chr4:83796920 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.1082C>T (p.Thr361Ile) single nucleotide variant not specified [RCV004663663] Chr4:82866923 [GRCh38]
Chr4:83788076 [GRCh37]
Chr4:4q21.22
uncertain significance
NM_001077207.4(SEC31A):c.2154+8C>T single nucleotide variant not provided [RCV004810939] Chr4:82853562 [GRCh38]
Chr4:83774715 [GRCh37]
Chr4:4q21.22
likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:5868
Count of miRNA genes:1154
Interacting mature miRNAs:1429
Transcripts:ENST00000264405, ENST00000311785, ENST00000326950, ENST00000348405, ENST00000355196, ENST00000395310, ENST00000432794, ENST00000436790, ENST00000443462, ENST00000448323, ENST00000500777, ENST00000503058, ENST00000503210, ENST00000503226, ENST00000503937, ENST00000505434, ENST00000505472, ENST00000505479, ENST00000505984, ENST00000506495, ENST00000506497, ENST00000507051, ENST00000507340, ENST00000507676, ENST00000507816, ENST00000507828, ENST00000507867, ENST00000508479, ENST00000508502, ENST00000509142, ENST00000509691, ENST00000510167, ENST00000510310, ENST00000511338, ENST00000511975, ENST00000512664, ENST00000512732, ENST00000513323, ENST00000513858, ENST00000514326, ENST00000514362, ENST00000515062, ENST00000515749
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
597365386GWAS1461460_Heosinophil count QTL GWAS1461460 (human)2e-09eosinophil quantity (VT:0002602)blood eosinophil count (CMO:0000033)48289901782899018Human
597216298GWAS1312372_Hbody height QTL GWAS1312372 (human)8e-12body height (VT:0001253)body height (CMO:0000106)48283767482837675Human
597074896GWAS1170970_Hasthma QTL GWAS1170970 (human)0.000003asthma48287276882872769Human
406893388GWAS542364_Hneutrophil percentage of leukocytes QTL GWAS542364 (human)8e-09neutrophil percentage of leukocytesblood neutrophil count to total leukocyte count ratio (CMO:0000370)48288605682886057Human
597224629GWAS1320703_Hurate measurement, bone density QTL GWAS1320703 (human)9e-09bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)48283277382832774Human

Markers in Region
SHGC-19008  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37483,740,257 - 83,740,390UniSTSGRCh37
Build 36483,959,281 - 83,959,414RGDNCBI36
Celera481,031,400 - 81,031,533RGD
Cytogenetic Map4q21.22UniSTS
HuRef479,480,179 - 79,480,312UniSTS
G33437  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37483,748,532 - 83,748,750UniSTSGRCh37
Build 36483,967,556 - 83,967,774RGDNCBI36
Celera481,039,680 - 81,039,898RGD
Cytogenetic Map4q21.22UniSTS
HuRef479,488,459 - 79,488,677UniSTS
RH98310  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37483,748,532 - 83,748,697UniSTSGRCh37
Build 36483,967,556 - 83,967,721RGDNCBI36
Celera481,039,680 - 81,039,845RGD
Cytogenetic Map4q21.22UniSTS
HuRef479,488,459 - 79,488,624UniSTS
GeneMap99-GB4 RH Map4449.12UniSTS
RH123704  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37483,766,105 - 83,766,413UniSTSGRCh37
Build 36483,985,129 - 83,985,437RGDNCBI36
Celera481,056,626 - 81,056,934RGD
Cytogenetic Map4q21.22UniSTS
HuRef479,506,065 - 79,506,373UniSTS
TNG Radiation Hybrid Map449561.0UniSTS
SHGC-24814  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37483,764,854 - 83,764,996UniSTSGRCh37
Build 36483,983,878 - 83,984,020RGDNCBI36
Celera481,055,375 - 81,055,517RGD
Cytogenetic Map4q21.22UniSTS
HuRef479,504,814 - 79,504,956UniSTS
TNG Radiation Hybrid Map449572.0UniSTS
GeneMap99-GB4 RH Map4449.12UniSTS
Whitehead-RH Map4494.8UniSTS
GeneMap99-G3 RH Map44553.0UniSTS
SEC31L1__5379  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37483,739,690 - 83,740,350UniSTSGRCh37
Build 36483,958,714 - 83,959,374RGDNCBI36
Celera481,030,833 - 81,031,493RGD
HuRef479,479,612 - 79,480,272UniSTS
SHGC-57474  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37483,758,789 - 83,758,931UniSTSGRCh37
Build 36483,977,813 - 83,977,955RGDNCBI36
Celera481,049,249 - 81,049,391RGD
Cytogenetic Map4q21.22UniSTS
HuRef479,498,724 - 79,498,866UniSTS
TNG Radiation Hybrid Map449558.0UniSTS
A009A37  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37483,776,754 - 83,776,895UniSTSGRCh37
Build 36483,995,778 - 83,995,919RGDNCBI36
Celera481,067,286 - 81,067,427RGD
Cytogenetic Map4q21.22UniSTS
HuRef479,516,726 - 79,516,867UniSTS
GeneMap99-GB4 RH Map4449.65UniSTS
RH36083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37483,790,866 - 83,791,014UniSTSGRCh37
Build 36484,009,890 - 84,010,038RGDNCBI36
Celera481,081,394 - 81,081,542RGD
Cytogenetic Map4q21.22UniSTS
HuRef479,531,082 - 79,531,230UniSTS
GeneMap99-GB4 RH Map4448.81UniSTS
D4S2523E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37483,748,686 - 83,748,761UniSTSGRCh37
Build 36483,967,710 - 83,967,785RGDNCBI36
Celera481,039,834 - 81,039,909RGD
Cytogenetic Map4q21.22UniSTS
HuRef479,488,613 - 79,488,688UniSTS
TNG Radiation Hybrid Map449534.0UniSTS
Stanford-G3 RH Map44562.0UniSTS
NCBI RH Map41028.0UniSTS
GeneMap99-G3 RH Map44546.0UniSTS
SHGC-50327  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37483,740,273 - 83,740,383UniSTSGRCh37
Build 36483,959,297 - 83,959,407RGDNCBI36
Celera481,031,416 - 81,031,526RGD
Cytogenetic Map4q21.22UniSTS
HuRef479,480,195 - 79,480,305UniSTS
TNG Radiation Hybrid Map449530.0UniSTS
SHGC-59763  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37483,776,037 - 83,776,145UniSTSGRCh37
Build 36483,995,061 - 83,995,169RGDNCBI36
Celera481,066,569 - 81,066,677RGD
Cytogenetic Map4q21.22UniSTS
HuRef479,516,009 - 79,516,117UniSTS
GeneMap99-GB4 RH Map4449.12UniSTS
SHGC-67285  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37483,739,891 - 83,740,073UniSTSGRCh37
Build 36483,958,915 - 83,959,097RGDNCBI36
Celera481,031,034 - 81,031,216RGD
Cytogenetic Map4q21.22UniSTS
HuRef479,479,813 - 79,479,995UniSTS
TNG Radiation Hybrid Map449493.0UniSTS
GeneMap99-GB4 RH Map4448.81UniSTS
L18426  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map12q24.1-q24.3UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map9p24.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map21q22.1UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map20p11.21UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map16p13.13-p13.12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map14q22-q24UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map9p21.1UniSTS
SEC31A  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37483,748,679 - 83,750,214UniSTSGRCh37
Celera481,039,827 - 81,041,366UniSTS
HuRef479,488,606 - 79,490,144UniSTS


Expression

RNA-SEQ Expression

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

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_029569 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001077206 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001077207 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001077208 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001191049 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001300744 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001300745 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001318119 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001318120 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400154 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400155 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400156 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400157 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400158 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400159 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400160 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400161 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400162 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400164 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400165 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400166 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400167 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400168 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400180 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400184 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400186 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400188 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400190 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400191 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400193 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400194 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400197 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400198 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400200 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400202 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400203 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400204 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400205 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400206 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400207 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400208 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400209 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400210 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400211 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400212 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400213 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400214 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400215 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400216 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400217 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400218 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400219 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400220 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400221 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400222 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400223 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001400224 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_016211 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB018358 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB018359 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB020712 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC021105 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC108469 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF139184 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF161393 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF161452 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI802473 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK001014 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK002161 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK125897 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK225934 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295810 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL049463 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL704825 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY137583 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC031292 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC039834 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC047883 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC084583 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC117221 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC143489 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC143491 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC143492 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BE710081 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM677531 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA397330 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA428539 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471057 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR933696 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA142666 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA218900 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA508741 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA720299 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB287803 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC342364 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KX533487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OP794581 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000264405   ⟹   ENSP00000264405
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,819,022 - 82,871,950 (-)Ensembl
Ensembl Acc Id: ENST00000311785   ⟹   ENSP00000309070
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,818,662 - 82,891,259 (-)Ensembl
Ensembl Acc Id: ENST00000348405   ⟹   ENSP00000337602
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,818,661 - 82,891,136 (-)Ensembl
Ensembl Acc Id: ENST00000355196   ⟹   ENSP00000347329
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,819,011 - 82,900,538 (-)Ensembl
Ensembl Acc Id: ENST00000395310   ⟹   ENSP00000378721
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,818,509 - 82,891,153 (-)Ensembl
Ensembl Acc Id: ENST00000436790
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,863,211 - 82,891,184 (-)Ensembl
Ensembl Acc Id: ENST00000443462   ⟹   ENSP00000408027
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,818,662 - 82,891,178 (-)Ensembl
Ensembl Acc Id: ENST00000448323   ⟹   ENSP00000400926
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,818,662 - 82,891,266 (-)Ensembl
Ensembl Acc Id: ENST00000500777   ⟹   ENSP00000421464
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,818,672 - 82,881,940 (-)Ensembl
Ensembl Acc Id: ENST00000503058   ⟹   ENSP00000425056
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,871,933 - 82,891,120 (-)Ensembl
Ensembl Acc Id: ENST00000503210   ⟹   ENSP00000422563
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,878,888 - 82,901,166 (-)Ensembl
Ensembl Acc Id: ENST00000503226
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,854,906 - 82,857,998 (-)Ensembl
Ensembl Acc Id: ENST00000503937   ⟹   ENSP00000422371
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,818,661 - 82,844,460 (-)Ensembl
Ensembl Acc Id: ENST00000505434   ⟹   ENSP00000425095
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,880,804 - 82,891,102 (-)Ensembl
Ensembl Acc Id: ENST00000505472   ⟹   ENSP00000421633
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,818,672 - 82,881,937 (-)Ensembl
Ensembl Acc Id: ENST00000505479
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,819,038 - 82,821,451 (-)Ensembl
Ensembl Acc Id: ENST00000505984   ⟹   ENSP00000424451
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,819,044 - 82,891,148 (-)Ensembl
Ensembl Acc Id: ENST00000506495   ⟹   ENSP00000425064
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,881,857 - 82,900,569 (-)Ensembl
Ensembl Acc Id: ENST00000506497
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,877,557 - 82,891,133 (-)Ensembl
Ensembl Acc Id: ENST00000507051   ⟹   ENSP00000476156
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,881,902 - 82,900,569 (-)Ensembl
Ensembl Acc Id: ENST00000507340   ⟹   ENSP00000422797
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,875,785 - 82,891,240 (-)Ensembl
Ensembl Acc Id: ENST00000507676   ⟹   ENSP00000475765
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,880,807 - 82,900,538 (-)Ensembl
Ensembl Acc Id: ENST00000507816   ⟹   ENSP00000421001
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,874,698 - 82,891,205 (-)Ensembl
Ensembl Acc Id: ENST00000507828   ⟹   ENSP00000426562
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,848,826 - 82,866,931 (-)Ensembl
Ensembl Acc Id: ENST00000507867
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,877,489 - 82,891,178 (-)Ensembl
Ensembl Acc Id: ENST00000508479   ⟹   ENSP00000425999
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,843,685 - 82,891,153 (-)Ensembl
Ensembl Acc Id: ENST00000508502   ⟹   ENSP00000424635
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,819,011 - 82,891,203 (-)Ensembl
Ensembl Acc Id: ENST00000509142   ⟹   ENSP00000426569
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,818,662 - 82,891,214 (-)Ensembl
Ensembl Acc Id: ENST00000509691
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,827,556 - 82,829,413 (-)Ensembl
Ensembl Acc Id: ENST00000510167   ⟹   ENSP00000422267
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,853,631 - 82,864,598 (-)Ensembl
Ensembl Acc Id: ENST00000510310
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,878,776 - 82,891,261 (-)Ensembl
Ensembl Acc Id: ENST00000511338   ⟹   ENSP00000425140
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,824,598 - 82,848,843 (-)Ensembl
Ensembl Acc Id: ENST00000511975
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,875,772 - 82,891,178 (-)Ensembl
Ensembl Acc Id: ENST00000512664   ⟹   ENSP00000424336
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,851,514 - 82,864,455 (-)Ensembl
Ensembl Acc Id: ENST00000512732
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,854,950 - 82,861,846 (-)Ensembl
Ensembl Acc Id: ENST00000513323   ⟹   ENSP00000426950
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,875,731 - 82,891,018 (-)Ensembl
Ensembl Acc Id: ENST00000513858   ⟹   ENSP00000426886
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,818,661 - 82,891,153 (-)Ensembl
Ensembl Acc Id: ENST00000514326   ⟹   ENSP00000425555
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,875,727 - 82,891,095 (-)Ensembl
Ensembl Acc Id: ENST00000514362
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,827,500 - 82,831,361 (-)Ensembl
Ensembl Acc Id: ENST00000515062   ⟹   ENSP00000426943
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,819,021 - 82,827,612 (-)Ensembl
Ensembl Acc Id: ENST00000515749
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl482,827,548 - 82,842,824 (-)Ensembl
RefSeq Acc Id: NM_001077206   ⟹   NP_001070674
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,509 - 82,891,153 (-)NCBI
GRCh37483,739,814 - 83,812,419 (-)ENTREZGENE
Build 36483,958,838 - 84,031,424 (-)NCBI Archive
HuRef479,479,736 - 79,553,039 (-)ENTREZGENE
CHM1_1483,716,180 - 83,788,877 (-)NCBI
T2T-CHM13v2.0486,147,772 - 86,220,378 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001077207   ⟹   NP_001070675
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,509 - 82,891,153 (-)NCBI
GRCh37483,739,814 - 83,812,419 (-)ENTREZGENE
Build 36483,958,838 - 84,031,424 (-)NCBI Archive
HuRef479,479,736 - 79,553,039 (-)ENTREZGENE
CHM1_1483,716,180 - 83,788,877 (-)NCBI
T2T-CHM13v2.0486,147,772 - 86,220,378 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001077208   ⟹   NP_001070676
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,509 - 82,891,153 (-)NCBI
GRCh37483,739,814 - 83,812,419 (-)ENTREZGENE
Build 36483,958,838 - 84,031,424 (-)NCBI Archive
HuRef479,479,736 - 79,553,039 (-)ENTREZGENE
CHM1_1483,716,180 - 83,788,877 (-)NCBI
T2T-CHM13v2.0486,147,772 - 86,220,378 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001191049   ⟹   NP_001177978
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,509 - 82,891,280 (-)NCBI
GRCh37483,739,814 - 83,812,419 (-)ENTREZGENE
HuRef479,479,736 - 79,553,039 (-)ENTREZGENE
CHM1_1483,716,180 - 83,788,877 (-)NCBI
T2T-CHM13v2.0486,147,772 - 86,220,505 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001300744   ⟹   NP_001287673
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,509 - 82,891,153 (-)NCBI
CHM1_1483,716,180 - 83,788,877 (-)NCBI
T2T-CHM13v2.0486,147,772 - 86,220,378 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001300745   ⟹   NP_001287674
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,509 - 82,891,153 (-)NCBI
CHM1_1483,716,180 - 83,788,877 (-)NCBI
T2T-CHM13v2.0486,147,772 - 86,220,378 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001318119   ⟹   NP_001305048
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,509 - 82,891,153 (-)NCBI
CHM1_1483,716,180 - 83,788,877 (-)NCBI
T2T-CHM13v2.0486,147,772 - 86,220,378 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001318120   ⟹   NP_001305049
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,509 - 82,900,569 (-)NCBI
CHM1_1483,716,180 - 83,798,162 (-)NCBI
T2T-CHM13v2.0486,147,772 - 86,229,788 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001400154   ⟹   NP_001387083
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400155   ⟹   NP_001387084
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400156   ⟹   NP_001387085
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400157   ⟹   NP_001387086
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400158   ⟹   NP_001387087
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,065 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,290 (-)NCBI
RefSeq Acc Id: NM_001400159   ⟹   NP_001387088
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400160   ⟹   NP_001387089
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,065 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,290 (-)NCBI
RefSeq Acc Id: NM_001400161   ⟹   NP_001387090
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400162   ⟹   NP_001387091
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400164   ⟹   NP_001387093
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400165   ⟹   NP_001387094
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400166   ⟹   NP_001387095
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,065 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,290 (-)NCBI
RefSeq Acc Id: NM_001400167   ⟹   NP_001387096
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400168   ⟹   NP_001387097
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400180   ⟹   NP_001387109
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400184   ⟹   NP_001387113
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400186   ⟹   NP_001387115
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400188   ⟹   NP_001387117
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400190   ⟹   NP_001387119
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,065 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,290 (-)NCBI
RefSeq Acc Id: NM_001400191   ⟹   NP_001387120
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,065 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,290 (-)NCBI
RefSeq Acc Id: NM_001400193   ⟹   NP_001387122
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,065 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,290 (-)NCBI
RefSeq Acc Id: NM_001400194   ⟹   NP_001387123
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400197   ⟹   NP_001387126
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400198   ⟹   NP_001387127
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400200   ⟹   NP_001387129
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400202   ⟹   NP_001387131
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400203   ⟹   NP_001387132
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,065 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,290 (-)NCBI
RefSeq Acc Id: NM_001400204   ⟹   NP_001387133
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400205   ⟹   NP_001387134
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400206   ⟹   NP_001387135
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,065 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,290 (-)NCBI
RefSeq Acc Id: NM_001400207   ⟹   NP_001387136
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400208   ⟹   NP_001387137
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400209   ⟹   NP_001387138
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,065 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,290 (-)NCBI
RefSeq Acc Id: NM_001400210   ⟹   NP_001387139
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400211   ⟹   NP_001387140
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400212   ⟹   NP_001387141
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,255 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,480 (-)NCBI
RefSeq Acc Id: NM_001400213   ⟹   NP_001387142
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400214   ⟹   NP_001387143
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,255 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,480 (-)NCBI
RefSeq Acc Id: NM_001400215   ⟹   NP_001387144
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400216   ⟹   NP_001387145
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400217   ⟹   NP_001387146
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400218   ⟹   NP_001387147
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400219   ⟹   NP_001387148
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400220   ⟹   NP_001387149
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400221   ⟹   NP_001387150
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400222   ⟹   NP_001387151
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400223   ⟹   NP_001387152
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_001400224   ⟹   NP_001387153
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,661 - 82,891,153 (-)NCBI
T2T-CHM13v2.0486,147,924 - 86,220,378 (-)NCBI
RefSeq Acc Id: NM_016211   ⟹   NP_057295
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,818,509 - 82,891,153 (-)NCBI
GRCh37483,739,814 - 83,812,419 (-)ENTREZGENE
Build 36483,958,838 - 84,031,424 (-)NCBI Archive
HuRef479,479,736 - 79,553,039 (-)ENTREZGENE
CHM1_1483,716,180 - 83,788,877 (-)NCBI
T2T-CHM13v2.0486,147,772 - 86,220,378 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001070674 (Get FASTA)   NCBI Sequence Viewer  
  NP_001070675 (Get FASTA)   NCBI Sequence Viewer  
  NP_001070676 (Get FASTA)   NCBI Sequence Viewer  
  NP_001177978 (Get FASTA)   NCBI Sequence Viewer  
  NP_001287673 (Get FASTA)   NCBI Sequence Viewer  
  NP_001287674 (Get FASTA)   NCBI Sequence Viewer  
  NP_001305048 (Get FASTA)   NCBI Sequence Viewer  
  NP_001305049 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387083 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387084 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387085 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387086 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387087 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387088 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387089 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387090 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387091 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387093 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387094 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387095 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387096 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387097 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387109 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387113 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387115 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387117 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387119 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387120 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387122 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387123 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387126 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387127 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387129 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387131 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387132 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387133 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387134 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387135 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387136 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387137 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387138 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387139 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387140 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387141 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387142 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387143 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387144 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387145 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387146 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387147 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387148 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387149 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387150 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387151 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387152 (Get FASTA)   NCBI Sequence Viewer  
  NP_001387153 (Get FASTA)   NCBI Sequence Viewer  
  NP_057295 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAF28953 (Get FASTA)   NCBI Sequence Viewer  
  AAF29012 (Get FASTA)   NCBI Sequence Viewer  
  AAF67836 (Get FASTA)   NCBI Sequence Viewer  
  AAH47883 (Get FASTA)   NCBI Sequence Viewer  
  AAH84583 (Get FASTA)   NCBI Sequence Viewer  
  AAI17222 (Get FASTA)   NCBI Sequence Viewer  
  AAI43490 (Get FASTA)   NCBI Sequence Viewer  
  AAI43492 (Get FASTA)   NCBI Sequence Viewer  
  AAI43493 (Get FASTA)   NCBI Sequence Viewer  
  AAN15221 (Get FASTA)   NCBI Sequence Viewer  
  AQN67640 (Get FASTA)   NCBI Sequence Viewer  
  BAA74928 (Get FASTA)   NCBI Sequence Viewer  
  BAA84923 (Get FASTA)   NCBI Sequence Viewer  
  BAA84924 (Get FASTA)   NCBI Sequence Viewer  
  BAC86336 (Get FASTA)   NCBI Sequence Viewer  
  BAG58628 (Get FASTA)   NCBI Sequence Viewer  
  CAH56418 (Get FASTA)   NCBI Sequence Viewer  
  CAI45995 (Get FASTA)   NCBI Sequence Viewer  
  EAX05906 (Get FASTA)   NCBI Sequence Viewer  
  EAX05907 (Get FASTA)   NCBI Sequence Viewer  
  EAX05908 (Get FASTA)   NCBI Sequence Viewer  
  EAX05909 (Get FASTA)   NCBI Sequence Viewer  
  EAX05910 (Get FASTA)   NCBI Sequence Viewer  
  EAX05911 (Get FASTA)   NCBI Sequence Viewer  
  EAX05912 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000264405
  ENSP00000264405.5
  ENSP00000309070
  ENSP00000309070.7
  ENSP00000337602
  ENSP00000337602.5
  ENSP00000347329
  ENSP00000347329.2
  ENSP00000378721
  ENSP00000378721.2
  ENSP00000400926
  ENSP00000400926.1
  ENSP00000408027
  ENSP00000408027.2
  ENSP00000421001.1
  ENSP00000421464
  ENSP00000421464.1
  ENSP00000421633
  ENSP00000421633.1
  ENSP00000422267.1
  ENSP00000422371.1
  ENSP00000422563.1
  ENSP00000422797.1
  ENSP00000424336.1
  ENSP00000424451
  ENSP00000424451.1
  ENSP00000424635
  ENSP00000424635.1
  ENSP00000425056.1
  ENSP00000425064.1
  ENSP00000425095.1
  ENSP00000425140.1
  ENSP00000425555.1
  ENSP00000425999
  ENSP00000425999.1
  ENSP00000426562.1
  ENSP00000426569
  ENSP00000426569.1
  ENSP00000426886
  ENSP00000426886.1
  ENSP00000426943.1
  ENSP00000426950.1
  ENSP00000475765.1
  ENSP00000476156.1
GenBank Protein O94979 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_057295   ⟸   NM_016211
- Peptide Label: isoform 2
- Sequence:
RefSeq Acc Id: NP_001070674   ⟸   NM_001077206
- Peptide Label: isoform 4
- UniProtKB: O94979 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001070676   ⟸   NM_001077208
- Peptide Label: isoform 3
- UniProtKB: O94979 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001070675   ⟸   NM_001077207
- Peptide Label: isoform 1
- UniProtKB: O94979 (UniProtKB/Swiss-Prot),   Q9UM05 (UniProtKB/Swiss-Prot),   Q9P0A6 (UniProtKB/Swiss-Prot),   Q9P048 (UniProtKB/Swiss-Prot),   Q8IZH4 (UniProtKB/Swiss-Prot),   Q86TJ0 (UniProtKB/Swiss-Prot),   Q7LCX9 (UniProtKB/Swiss-Prot),   Q6ZU90 (UniProtKB/Swiss-Prot),   Q659G7 (UniProtKB/Swiss-Prot),   Q5XG74 (UniProtKB/Swiss-Prot),   Q5H9P6 (UniProtKB/Swiss-Prot),   Q17RR5 (UniProtKB/Swiss-Prot),   H7C2W3 (UniProtKB/Swiss-Prot),   B7ZL00 (UniProtKB/Swiss-Prot),   B7ZKZ7 (UniProtKB/Swiss-Prot),   B4DIW6 (UniProtKB/Swiss-Prot),   Q9UM06 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001177978   ⟸   NM_001191049
- Peptide Label: isoform 5
- UniProtKB: O94979 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001287673   ⟸   NM_001300744
- Peptide Label: isoform 6
- UniProtKB: O94979 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001287674   ⟸   NM_001300745
- Peptide Label: isoform 7
- UniProtKB: O94979 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001305049   ⟸   NM_001318120
- Peptide Label: isoform 1
- UniProtKB: O94979 (UniProtKB/Swiss-Prot),   Q9UM05 (UniProtKB/Swiss-Prot),   Q9P0A6 (UniProtKB/Swiss-Prot),   Q9P048 (UniProtKB/Swiss-Prot),   Q8IZH4 (UniProtKB/Swiss-Prot),   Q86TJ0 (UniProtKB/Swiss-Prot),   Q7LCX9 (UniProtKB/Swiss-Prot),   Q6ZU90 (UniProtKB/Swiss-Prot),   Q659G7 (UniProtKB/Swiss-Prot),   Q5XG74 (UniProtKB/Swiss-Prot),   Q5H9P6 (UniProtKB/Swiss-Prot),   Q17RR5 (UniProtKB/Swiss-Prot),   H7C2W3 (UniProtKB/Swiss-Prot),   B7ZL00 (UniProtKB/Swiss-Prot),   B7ZKZ7 (UniProtKB/Swiss-Prot),   B4DIW6 (UniProtKB/Swiss-Prot),   Q9UM06 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001305048   ⟸   NM_001318119
- Peptide Label: isoform 3
- UniProtKB: O94979 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSP00000425056   ⟸   ENST00000503058
Ensembl Acc Id: ENSP00000422563   ⟸   ENST00000503210
Ensembl Acc Id: ENSP00000422371   ⟸   ENST00000503937
Ensembl Acc Id: ENSP00000337602   ⟸   ENST00000348405
Ensembl Acc Id: ENSP00000425095   ⟸   ENST00000505434
Ensembl Acc Id: ENSP00000421633   ⟸   ENST00000505472
Ensembl Acc Id: ENSP00000424451   ⟸   ENST00000505984
Ensembl Acc Id: ENSP00000425064   ⟸   ENST00000506495
Ensembl Acc Id: ENSP00000476156   ⟸   ENST00000507051
Ensembl Acc Id: ENSP00000422797   ⟸   ENST00000507340
Ensembl Acc Id: ENSP00000421001   ⟸   ENST00000507816
Ensembl Acc Id: ENSP00000426562   ⟸   ENST00000507828
Ensembl Acc Id: ENSP00000475765   ⟸   ENST00000507676
Ensembl Acc Id: ENSP00000424635   ⟸   ENST00000508502
Ensembl Acc Id: ENSP00000425999   ⟸   ENST00000508479
Ensembl Acc Id: ENSP00000426569   ⟸   ENST00000509142
Ensembl Acc Id: ENSP00000408027   ⟸   ENST00000443462
Ensembl Acc Id: ENSP00000309070   ⟸   ENST00000311785
Ensembl Acc Id: ENSP00000422267   ⟸   ENST00000510167
Ensembl Acc Id: ENSP00000425140   ⟸   ENST00000511338
Ensembl Acc Id: ENSP00000424336   ⟸   ENST00000512664
Ensembl Acc Id: ENSP00000347329   ⟸   ENST00000355196
Ensembl Acc Id: ENSP00000400926   ⟸   ENST00000448323
Ensembl Acc Id: ENSP00000426886   ⟸   ENST00000513858
Ensembl Acc Id: ENSP00000426950   ⟸   ENST00000513323
Ensembl Acc Id: ENSP00000378721   ⟸   ENST00000395310
Ensembl Acc Id: ENSP00000264405   ⟸   ENST00000264405
Ensembl Acc Id: ENSP00000421464   ⟸   ENST00000500777
Ensembl Acc Id: ENSP00000425555   ⟸   ENST00000514326
Ensembl Acc Id: ENSP00000426943   ⟸   ENST00000515062
RefSeq Acc Id: NP_001387141   ⟸   NM_001400212
- Peptide Label: isoform 24
RefSeq Acc Id: NP_001387143   ⟸   NM_001400214
- Peptide Label: isoform 25
RefSeq Acc Id: NP_001387152   ⟸   NM_001400223
- Peptide Label: isoform 6
RefSeq Acc Id: NP_001387142   ⟸   NM_001400213
- Peptide Label: isoform 7
RefSeq Acc Id: NP_001387136   ⟸   NM_001400207
- Peptide Label: isoform 2
RefSeq Acc Id: NP_001387131   ⟸   NM_001400202
- Peptide Label: isoform 20
RefSeq Acc Id: NP_001387147   ⟸   NM_001400218
- Peptide Label: isoform 28
RefSeq Acc Id: NP_001387097   ⟸   NM_001400168
- Peptide Label: isoform 15
RefSeq Acc Id: NP_001387134   ⟸   NM_001400205
- Peptide Label: isoform 21
RefSeq Acc Id: NP_001387113   ⟸   NM_001400184
- Peptide Label: isoform 17
RefSeq Acc Id: NP_001387150   ⟸   NM_001400221
- Peptide Label: isoform 30
- UniProtKB: A0A1S5UZ19 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001387139   ⟸   NM_001400210
- Peptide Label: isoform 23
RefSeq Acc Id: NP_001387126   ⟸   NM_001400197
- Peptide Label: isoform 19
RefSeq Acc Id: NP_001387109   ⟸   NM_001400180
- Peptide Label: isoform 16
RefSeq Acc Id: NP_001387148   ⟸   NM_001400219
- Peptide Label: isoform 29
- UniProtKB: D6RHZ5 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001387146   ⟸   NM_001400217
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001387137   ⟸   NM_001400208
- Peptide Label: isoform 22
RefSeq Acc Id: NP_001387093   ⟸   NM_001400164
- Peptide Label: isoform 1
- UniProtKB: Q9UM05 (UniProtKB/Swiss-Prot),   Q9P0A6 (UniProtKB/Swiss-Prot),   Q9P048 (UniProtKB/Swiss-Prot),   Q8IZH4 (UniProtKB/Swiss-Prot),   Q86TJ0 (UniProtKB/Swiss-Prot),   Q7LCX9 (UniProtKB/Swiss-Prot),   Q6ZU90 (UniProtKB/Swiss-Prot),   Q659G7 (UniProtKB/Swiss-Prot),   Q5XG74 (UniProtKB/Swiss-Prot),   Q5H9P6 (UniProtKB/Swiss-Prot),   Q17RR5 (UniProtKB/Swiss-Prot),   O94979 (UniProtKB/Swiss-Prot),   H7C2W3 (UniProtKB/Swiss-Prot),   B7ZL00 (UniProtKB/Swiss-Prot),   B7ZKZ7 (UniProtKB/Swiss-Prot),   B4DIW6 (UniProtKB/Swiss-Prot),   Q9UM06 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001387086   ⟸   NM_001400157
- Peptide Label: isoform 10
RefSeq Acc Id: NP_001387084   ⟸   NM_001400155
- Peptide Label: isoform 8
- UniProtKB: D6REX3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001387144   ⟸   NM_001400215
- Peptide Label: isoform 26
- UniProtKB: H7BXG7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001387153   ⟸   NM_001400224
- Peptide Label: isoform 31
- UniProtKB: H7BXG7 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001387127   ⟸   NM_001400198
- Peptide Label: isoform 20
RefSeq Acc Id: NP_001387096   ⟸   NM_001400167
- Peptide Label: isoform 15
RefSeq Acc Id: NP_001387090   ⟸   NM_001400161
- Peptide Label: isoform 32
RefSeq Acc Id: NP_001387145   ⟸   NM_001400216
- Peptide Label: isoform 27
RefSeq Acc Id: NP_001387133   ⟸   NM_001400204
- Peptide Label: isoform 21
RefSeq Acc Id: NP_001387115   ⟸   NM_001400186
- Peptide Label: isoform 17
RefSeq Acc Id: NP_001387094   ⟸   NM_001400165
- Peptide Label: isoform 14
RefSeq Acc Id: NP_001387091   ⟸   NM_001400162
- Peptide Label: isoform 12
RefSeq Acc Id: NP_001387151   ⟸   NM_001400222
- Peptide Label: isoform 30
- UniProtKB: A0A1S5UZ19 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001387140   ⟸   NM_001400211
- Peptide Label: isoform 23
RefSeq Acc Id: NP_001387129   ⟸   NM_001400200
- Peptide Label: isoform 19
RefSeq Acc Id: NP_001387117   ⟸   NM_001400188
- Peptide Label: isoform 16
RefSeq Acc Id: NP_001387149   ⟸   NM_001400220
- Peptide Label: isoform 29
- UniProtKB: D6RHZ5 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001387123   ⟸   NM_001400194
- Peptide Label: isoform 18
RefSeq Acc Id: NP_001387088   ⟸   NM_001400159
- Peptide Label: isoform 10
RefSeq Acc Id: NP_001387085   ⟸   NM_001400156
- Peptide Label: isoform 9
RefSeq Acc Id: NP_001387083   ⟸   NM_001400154
- Peptide Label: isoform 8
- UniProtKB: D6REX3 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001387138   ⟸   NM_001400209
- Peptide Label: isoform 2
RefSeq Acc Id: NP_001387135   ⟸   NM_001400206
- Peptide Label: isoform 21
RefSeq Acc Id: NP_001387132   ⟸   NM_001400203
- Peptide Label: isoform 19
RefSeq Acc Id: NP_001387089   ⟸   NM_001400160
- Peptide Label: isoform 11
RefSeq Acc Id: NP_001387120   ⟸   NM_001400191
- Peptide Label: isoform 3
RefSeq Acc Id: NP_001387095   ⟸   NM_001400166
- Peptide Label: isoform 1
- UniProtKB: Q9UM05 (UniProtKB/Swiss-Prot),   Q9P0A6 (UniProtKB/Swiss-Prot),   Q9P048 (UniProtKB/Swiss-Prot),   Q8IZH4 (UniProtKB/Swiss-Prot),   Q86TJ0 (UniProtKB/Swiss-Prot),   Q7LCX9 (UniProtKB/Swiss-Prot),   Q6ZU90 (UniProtKB/Swiss-Prot),   Q659G7 (UniProtKB/Swiss-Prot),   Q5XG74 (UniProtKB/Swiss-Prot),   Q5H9P6 (UniProtKB/Swiss-Prot),   Q17RR5 (UniProtKB/Swiss-Prot),   O94979 (UniProtKB/Swiss-Prot),   H7C2W3 (UniProtKB/Swiss-Prot),   B7ZL00 (UniProtKB/Swiss-Prot),   B7ZKZ7 (UniProtKB/Swiss-Prot),   B4DIW6 (UniProtKB/Swiss-Prot),   Q9UM06 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: NP_001387087   ⟸   NM_001400158
- Peptide Label: isoform 10
RefSeq Acc Id: NP_001387122   ⟸   NM_001400193
- Peptide Label: isoform 3
RefSeq Acc Id: NP_001387119   ⟸   NM_001400190
- Peptide Label: isoform 3
Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O94979-F1-model_v2 AlphaFold O94979 1-1220 view protein structure

Promoters
RGD ID:6867868
Promoter ID:EPDNEW_H7099
Type:initiation region
Name:SEC31A_2
Description:SEC31 homolog A, COPII coat complex component
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H7100  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,844,506 - 82,844,566EPDNEW
RGD ID:6867870
Promoter ID:EPDNEW_H7100
Type:initiation region
Name:SEC31A_1
Description:SEC31 homolog A, COPII coat complex component
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H7099  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38482,891,142 - 82,891,202EPDNEW
RGD ID:6802590
Promoter ID:HG_KWN:48614
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:ENST00000326950,   UC003HND.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36483,985,431 - 83,985,931 (-)MPROMDB
RGD ID:6802587
Promoter ID:HG_KWN:48616
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001077206,   NM_001077208,   NM_014933,   NM_016211,   OTTHUMT00000252640,   OTTHUMT00000252641,   UC003HNL.1,   UC003HNN.1,   UC003HNO.2
Position:
Human AssemblyChrPosition (strand)Source
Build 36484,031,326 - 84,032,337 (-)MPROMDB
RGD ID:6802400
Promoter ID:HG_KWN:48618
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_024672,   UC003HNM.1,   UC003HNP.1,   UC003HNQ.1,   UC003HNR.1,   UC003HNS.1,   UC003HNU.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36484,040,296 - 84,041,287 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:17052 AgrOrtholog
COSMIC SEC31A COSMIC
Ensembl Genes ENSG00000138674 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000264405 ENTREZGENE
  ENST00000264405.9 UniProtKB/TrEMBL
  ENST00000311785 ENTREZGENE
  ENST00000311785.11 UniProtKB/Swiss-Prot
  ENST00000348405 ENTREZGENE
  ENST00000348405.8 UniProtKB/Swiss-Prot
  ENST00000355196 ENTREZGENE
  ENST00000355196.6 UniProtKB/Swiss-Prot
  ENST00000395310 ENTREZGENE
  ENST00000395310.7 UniProtKB/Swiss-Prot
  ENST00000443462 ENTREZGENE
  ENST00000443462.6 UniProtKB/Swiss-Prot
  ENST00000448323 ENTREZGENE
  ENST00000448323.5 UniProtKB/Swiss-Prot
  ENST00000500777 ENTREZGENE
  ENST00000500777.6 UniProtKB/Swiss-Prot
  ENST00000503058.5 UniProtKB/TrEMBL
  ENST00000503210.5 UniProtKB/TrEMBL
  ENST00000503937.5 UniProtKB/TrEMBL
  ENST00000505434.5 UniProtKB/TrEMBL
  ENST00000505472 ENTREZGENE
  ENST00000505472.5 UniProtKB/TrEMBL
  ENST00000505984 ENTREZGENE
  ENST00000505984.5 UniProtKB/Swiss-Prot
  ENST00000506495.5 UniProtKB/TrEMBL
  ENST00000507051.1 UniProtKB/TrEMBL
  ENST00000507340.5 UniProtKB/TrEMBL
  ENST00000507676.5 UniProtKB/TrEMBL
  ENST00000507816.5 UniProtKB/TrEMBL
  ENST00000507828.5 UniProtKB/TrEMBL
  ENST00000508479 ENTREZGENE
  ENST00000508479.5 UniProtKB/TrEMBL
  ENST00000508502 ENTREZGENE
  ENST00000508502.5 UniProtKB/Swiss-Prot
  ENST00000509142 ENTREZGENE
  ENST00000509142.5 UniProtKB/Swiss-Prot
  ENST00000510167.1 UniProtKB/TrEMBL
  ENST00000511338.1 UniProtKB/TrEMBL
  ENST00000512664.5 UniProtKB/TrEMBL
  ENST00000513323.5 UniProtKB/TrEMBL
  ENST00000513858 ENTREZGENE
  ENST00000513858.5 UniProtKB/Swiss-Prot
  ENST00000514326.5 UniProtKB/TrEMBL
  ENST00000515062.5 UniProtKB/TrEMBL
Gene3D-CATH 1.25.40.1030 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.130.10.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Functional domain of the splicing factor Prp18 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000138674 GTEx
HGNC ID HGNC:17052 ENTREZGENE
Human Proteome Map SEC31A Human Proteome Map
InterPro ACE1_Sec16_Sec31 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SEC31-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD40/YVTN_repeat-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD40_repeat UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD40_repeat_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:22872 UniProtKB/Swiss-Prot
NCBI Gene 22872 ENTREZGENE
OMIM 610257 OMIM
PANTHER PROTEIN TRANSPORT PROTEIN SEC31A UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR13923 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Sec16_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA162402737 PharmGKB
PROSITE WD_REPEATS_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD_REPEATS_REGION UniProtKB/Swiss-Prot
SMART WD40 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF50978 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A1S5UZ19 ENTREZGENE, UniProtKB/TrEMBL
  B4DIW6 ENTREZGENE
  B7ZKZ7 ENTREZGENE
  B7ZL00 ENTREZGENE
  D6RAB3_HUMAN UniProtKB/TrEMBL
  D6RBT0_HUMAN UniProtKB/TrEMBL
  D6RCQ9_HUMAN UniProtKB/TrEMBL
  D6RE64_HUMAN UniProtKB/TrEMBL
  D6REA9_HUMAN UniProtKB/TrEMBL
  D6REC0_HUMAN UniProtKB/TrEMBL
  D6REX3 ENTREZGENE, UniProtKB/TrEMBL
  D6RHE8_HUMAN UniProtKB/TrEMBL
  D6RHZ5 ENTREZGENE, UniProtKB/TrEMBL
  H0Y8V7_HUMAN UniProtKB/TrEMBL
  H0Y8W8_HUMAN UniProtKB/TrEMBL
  H0Y9K1_HUMAN UniProtKB/TrEMBL
  H0Y9T9_HUMAN UniProtKB/TrEMBL
  H0Y9V3_HUMAN UniProtKB/TrEMBL
  H0YAB3_HUMAN UniProtKB/TrEMBL
  H0YAF5_HUMAN UniProtKB/TrEMBL
  H7BXG7 ENTREZGENE, UniProtKB/TrEMBL
  H7C2W3 ENTREZGENE
  O94979 ENTREZGENE
  Q17RR5 ENTREZGENE
  Q5H9P6 ENTREZGENE
  Q5XG74 ENTREZGENE
  Q659G7 ENTREZGENE
  Q6ZU90 ENTREZGENE
  Q7LCX9 ENTREZGENE
  Q86TJ0 ENTREZGENE
  Q8IZH4 ENTREZGENE
  Q9P048 ENTREZGENE
  Q9P0A6 ENTREZGENE
  Q9UM05 ENTREZGENE
  Q9UM06 ENTREZGENE
  SC31A_HUMAN UniProtKB/Swiss-Prot
  U3KQC9_HUMAN UniProtKB/TrEMBL
  U3KQR3_HUMAN UniProtKB/TrEMBL
UniProt Secondary B4DIW6 UniProtKB/Swiss-Prot
  B7ZKZ7 UniProtKB/Swiss-Prot
  B7ZL00 UniProtKB/Swiss-Prot
  H7C2W3 UniProtKB/Swiss-Prot
  Q17RR5 UniProtKB/Swiss-Prot
  Q5H9P6 UniProtKB/Swiss-Prot
  Q5XG74 UniProtKB/Swiss-Prot
  Q659G7 UniProtKB/Swiss-Prot
  Q6ZU90 UniProtKB/Swiss-Prot
  Q7LCX9 UniProtKB/Swiss-Prot
  Q86TJ0 UniProtKB/Swiss-Prot
  Q8IZH4 UniProtKB/Swiss-Prot
  Q9P048 UniProtKB/Swiss-Prot
  Q9P0A6 UniProtKB/Swiss-Prot
  Q9UM05 UniProtKB/Swiss-Prot
  Q9UM06 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-08-11 SEC31A  SEC31 homolog A, COPII coat complex component  SEC31A  SEC31 homolog A, COPII coating complex component  Symbol and/or name change 5135510 APPROVED
2015-07-28 SEC31A  SEC31 homolog A, COPII coating complex component  SEC31A  SEC31 homolog A (S. cerevisiae)  Symbol and/or name change 5135510 APPROVED