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Imported Disease Annotations - CTDObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | SEC31A | Human | diffuse large B-cell lymphoma | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:22474449 | |
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Imported Disease Annotations - CTDObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | SEC31A | Human | diffuse large B-cell lymphoma | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:22474449 | |
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# | 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 |
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 |
SEC31A (Homo sapiens - human) |
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Sec31a (Mus musculus - house mouse) |
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Sec31a (Rattus norvegicus - Norway rat) |
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Sec31a (Chinchilla lanigera - long-tailed chinchilla) |
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SEC31A (Pan paniscus - bonobo/pygmy chimpanzee) |
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SEC31A (Canis lupus familiaris - dog) |
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Sec31a (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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SEC31A (Sus scrofa - pig) |
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SEC31A (Chlorocebus sabaeus - green monkey) |
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Sec31a (Heterocephalus glaber - naked mole-rat) |
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Variants in SEC31A
92 total 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 |
The detailed report is available here: | ![]() | Full Report | ![]() | CSV | ![]() | TAB | ![]() | Printer |
miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/). For more information about miRGate, see PMID:25858286 or access the full paper here. |
The following QTLs overlap with this region. | ![]() | Full Report | ![]() | CSV | ![]() | TAB | ![]() | Printer | ![]() | Gviewer |
SHGC-19008 |
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G33437 |
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RH98310 |
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RH123704 |
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||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
SHGC-24814 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
SEC31L1__5379 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
SHGC-57474 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
A009A37 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
RH36083 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
D4S2523E |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
SHGC-50327 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
SHGC-59763 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
SHGC-67285 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
L18426 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
SEC31A |
|
adipose tissue
|
alimentary part of gastrointestinal system
|
appendage
|
circulatory system
|
ectoderm
|
endocrine system
|
endoderm
|
entire extraembryonic component
|
exocrine system
|
hemolymphoid system
|
hepatobiliary system
|
integumental system
|
mesenchyme
|
mesoderm
|
musculoskeletal system
|
nervous system
|
pharyngeal arch
|
renal system
|
reproductive system
|
respiratory system
|
sensory system
|
visual system
|
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1204 | 2439 | 2788 | 2253 | 4974 | 1726 | 2351 | 6 | 624 | 1951 | 465 | 2270 | 7306 | 6472 | 53 | 3734 | 1 | 852 | 1744 | 1617 | 175 | 1 |
RefSeq Transcripts | 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: |
|
Ensembl Acc Id: | ENST00000311785 ⟹ ENSP00000309070 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000348405 ⟹ ENSP00000337602 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000355196 ⟹ ENSP00000347329 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000395310 ⟹ ENSP00000378721 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000436790 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000443462 ⟹ ENSP00000408027 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000448323 ⟹ ENSP00000400926 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000500777 ⟹ ENSP00000421464 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000503058 ⟹ ENSP00000425056 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000503210 ⟹ ENSP00000422563 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000503226 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000503937 ⟹ ENSP00000422371 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000505434 ⟹ ENSP00000425095 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000505472 ⟹ ENSP00000421633 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000505479 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000505984 ⟹ ENSP00000424451 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000506495 ⟹ ENSP00000425064 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000506497 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000507051 ⟹ ENSP00000476156 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000507340 ⟹ ENSP00000422797 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000507676 ⟹ ENSP00000475765 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000507816 ⟹ ENSP00000421001 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000507828 ⟹ ENSP00000426562 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000507867 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000508479 ⟹ ENSP00000425999 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000508502 ⟹ ENSP00000424635 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000509142 ⟹ ENSP00000426569 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000509691 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000510167 ⟹ ENSP00000422267 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000510310 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000511338 ⟹ ENSP00000425140 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000511975 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000512664 ⟹ ENSP00000424336 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000512732 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000513323 ⟹ ENSP00000426950 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000513858 ⟹ ENSP00000426886 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000514326 ⟹ ENSP00000425555 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000514362 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000515062 ⟹ ENSP00000426943 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000515749 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | NM_001077206 ⟹ NP_001070674 | ||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001077207 ⟹ NP_001070675 | ||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001077208 ⟹ NP_001070676 | ||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001191049 ⟹ NP_001177978 | ||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001300744 ⟹ NP_001287673 | ||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||
Type: | CODING | ||||||||||||||||
Position: |
|
||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001300745 ⟹ NP_001287674 | ||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||
Type: | CODING | ||||||||||||||||
Position: |
|
||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001318119 ⟹ NP_001305048 | ||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||
Type: | CODING | ||||||||||||||||
Position: |
|
||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001318120 ⟹ NP_001305049 | ||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||
Type: | CODING | ||||||||||||||||
Position: |
|
||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001400154 ⟹ NP_001387083 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400155 ⟹ NP_001387084 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400156 ⟹ NP_001387085 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400157 ⟹ NP_001387086 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400158 ⟹ NP_001387087 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400159 ⟹ NP_001387088 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400160 ⟹ NP_001387089 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400161 ⟹ NP_001387090 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400162 ⟹ NP_001387091 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400164 ⟹ NP_001387093 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400165 ⟹ NP_001387094 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400166 ⟹ NP_001387095 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400167 ⟹ NP_001387096 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400168 ⟹ NP_001387097 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400180 ⟹ NP_001387109 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400184 ⟹ NP_001387113 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400186 ⟹ NP_001387115 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400188 ⟹ NP_001387117 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400190 ⟹ NP_001387119 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400191 ⟹ NP_001387120 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400193 ⟹ NP_001387122 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400194 ⟹ NP_001387123 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400197 ⟹ NP_001387126 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400198 ⟹ NP_001387127 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400200 ⟹ NP_001387129 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400202 ⟹ NP_001387131 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400203 ⟹ NP_001387132 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400204 ⟹ NP_001387133 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400205 ⟹ NP_001387134 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400206 ⟹ NP_001387135 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400207 ⟹ NP_001387136 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400208 ⟹ NP_001387137 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400209 ⟹ NP_001387138 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400210 ⟹ NP_001387139 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400211 ⟹ NP_001387140 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400212 ⟹ NP_001387141 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400213 ⟹ NP_001387142 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400214 ⟹ NP_001387143 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400215 ⟹ NP_001387144 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400216 ⟹ NP_001387145 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400217 ⟹ NP_001387146 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400218 ⟹ NP_001387147 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400219 ⟹ NP_001387148 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400220 ⟹ NP_001387149 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400221 ⟹ NP_001387150 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400222 ⟹ NP_001387151 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400223 ⟹ NP_001387152 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_001400224 ⟹ NP_001387153 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
RefSeq Acc Id: | NM_016211 ⟹ NP_057295 | ||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||
Sequence: |
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 |
Name | Modeler | Protein Id | AA Range | Protein Structure |
AF-O94979-F1-model_v2 | AlphaFold | O94979 | 1-1220 | view protein structure |
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: |
|
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: |
|
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: |
|
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: |
|
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: |
|
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 |
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 |