Imported Disease Annotations - OMIMTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | FUCOSYLTRANSFERASE 6 DEFICIENCY | | IAGP | | 7240710 | | OMIM | | |
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Imported Disease Annotations - OMIMTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | FUCOSYLTRANSFERASE 6 DEFICIENCY | | IAGP | | 7240710 | | OMIM | | |
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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. | ClinVar Automated Import and Annotation Pipeline | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
4. | Data Import for Chemical-Gene Interactions | RGD automated import pipeline for gene-chemical interactions |
PMID:1339443 | PMID:1520296 | PMID:7650030 | PMID:7656588 | PMID:7782074 | PMID:8125298 | PMID:8175676 | PMID:9363434 | PMID:9451035 | PMID:10536043 | PMID:10900002 | PMID:11530205 |
PMID:11698403 | PMID:12477932 | PMID:12670495 | PMID:14514715 | PMID:14702039 | PMID:16344560 | PMID:17054948 | PMID:17604274 | PMID:18274891 | PMID:19199708 | PMID:19349624 | PMID:19913121 |
PMID:20179215 | PMID:20628086 | PMID:20965272 | PMID:21203500 | PMID:21873635 | PMID:22155250 | PMID:22367966 | PMID:23300138 | PMID:23376485 | PMID:24232099 | PMID:24941225 | PMID:24953560 |
PMID:25962326 | PMID:27374856 | PMID:27519168 | PMID:28334792 | PMID:28771224 | PMID:29593094 | PMID:30307499 | PMID:30742932 | PMID:30808544 | PMID:32901486 | PMID:34215830 | PMID:36151332 |
FUT6 (Homo sapiens - human) |
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Fut4-ps1 (Rattus norvegicus - Norway rat) |
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FUT6 (Pan paniscus - bonobo/pygmy chimpanzee) |
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FUT5 (Canis lupus familiaris - dog) |
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LOC100513844 (Sus scrofa - pig) |
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Variants in FUT6
40 total Variants |
Name | Type | Condition(s) | Position(s) | Clinical significance |
NM_000150.4(FUT6):c.739G>A (p.Glu247Lys) | single nucleotide variant | Fucosyltransferase 6 deficiency [RCV000017626] | Chr19:5831829 [GRCh38] Chr19:5831840 [GRCh37] Chr19:19p13.3 |
pathogenic|conflicting interpretations of pathogenicity|uncertain significance |
GRCh38/hg38 19p13.3-13.2(chr19:1972245-9648879)x3 | copy number gain | See cases [RCV000052879] | Chr19:1972245..9648879 [GRCh38] Chr19:1972244..9759555 [GRCh37] Chr19:1923244..9620555 [NCBI36] Chr19:19p13.3-13.2 |
pathogenic |
GRCh38/hg38 19p13.3-13.2(chr19:4039158-9176125)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052881]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052881]|See cases [RCV000052881] | Chr19:4039158..9176125 [GRCh38] Chr19:4039156..9286801 [GRCh37] Chr19:3990156..9147801 [NCBI36] Chr19:19p13.3-13.2 |
pathogenic |
GRCh38/hg38 19p13.3(chr19:4934885-6501642)x3 | copy number gain | See cases [RCV000052882] | Chr19:4934885..6501642 [GRCh38] Chr19:4934897..6501653 [GRCh37] Chr19:4885897..6452653 [NCBI36] Chr19:19p13.3 |
pathogenic |
GRCh38/hg38 19p13.3-13.2(chr19:265917-8564134)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052876]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052876]|See cases [RCV000052876] | Chr19:265917..8564134 [GRCh38] Chr19:265917..8629018 [GRCh37] Chr19:216917..8535018 [NCBI36] Chr19:19p13.3-13.2 |
pathogenic |
NM_000150.2(FUT6):c.958C>T (p.Arg320Cys) | single nucleotide variant | Malignant melanoma [RCV000072316] | Chr19:5831610 [GRCh38] Chr19:5831621 [GRCh37] Chr19:5782621 [NCBI36] Chr19:19p13.3 |
not provided |
NM_000149.3(FUT3):c.177C>T (p.Thr59=) | single nucleotide variant | Malignant melanoma [RCV000072318] | Chr19:5844663 [GRCh38] Chr19:5844674 [GRCh37] Chr19:5795674 [NCBI36] Chr19:19p13.3 |
not provided |
NM_000149.3(FUT3):c.961C>T (p.Arg321Cys) | single nucleotide variant | Malignant melanoma [RCV000072317] | Chr19:5843879 [GRCh38] Chr19:5843890 [GRCh37] Chr19:5794890 [NCBI36] Chr19:19p13.3 |
not provided |
NM_001040701.2(FUT6):c.501dup (p.Tyr168fs) | duplication | Fucosyltransferase 6 deficiency [RCV001292763] | Chr19:5832066..5832067 [GRCh38] Chr19:5832077..5832078 [GRCh37] Chr19:19p13.3 |
pathogenic |
GRCh38/hg38 19p13.3(chr19:259395-6795611)x3 | copy number gain | See cases [RCV000142627] | Chr19:259395..6795611 [GRCh38] Chr19:259395..6795622 [GRCh37] Chr19:210395..6746622 [NCBI36] Chr19:19p13.3 |
pathogenic |
NM_000150.4(FUT6):c.945C>A (p.Tyr315Ter) | single nucleotide variant | Fucosyltransferase 6 deficiency [RCV000490274]|not provided [RCV000437989] | Chr19:5831623 [GRCh38] Chr19:5831634 [GRCh37] Chr19:19p13.3 |
benign|conflicting interpretations of pathogenicity|uncertain significance |
GRCh37/hg19 19p13.3(chr19:5835025-5843070)x3 | copy number gain | See cases [RCV000448826] | Chr19:5835025..5843070 [GRCh37] Chr19:19p13.3 |
uncertain significance |
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) | copy number gain | See cases [RCV000512296] | Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43 |
pathogenic |
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 | copy number gain | See cases [RCV000511289] | Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43 |
pathogenic|uncertain significance |
GRCh37/hg19 19p13.3-13.2(chr19:3120160-9732820)x3 | copy number gain | not provided [RCV000684096] | Chr19:3120160..9732820 [GRCh37] Chr19:19p13.3-13.2 |
pathogenic |
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 | copy number gain | not provided [RCV000752439] | Chr19:68029..59110290 [GRCh37] Chr19:19p13.3-q13.43 |
pathogenic |
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 | copy number gain | not provided [RCV000752444] | Chr19:260912..59097160 [GRCh37] Chr19:19p13.3-q13.43 |
pathogenic |
GRCh37/hg19 19p13.3(chr19:5455422-5995450)x3 | copy number gain | not provided [RCV000740012] | Chr19:5455422..5995450 [GRCh37] Chr19:19p13.3 |
benign |
GRCh37/hg19 19p13.3(chr19:5655792-5867913)x3 | copy number gain | not provided [RCV000740016] | Chr19:5655792..5867913 [GRCh37] Chr19:19p13.3 |
benign |
GRCh37/hg19 19p13.3(chr19:5823903-6175936)x3 | copy number gain | not provided [RCV000740019] | Chr19:5823903..6175936 [GRCh37] Chr19:19p13.3 |
benign |
NM_000150.4(FUT6):c.979C>T (p.Pro327Ser) | single nucleotide variant | Inborn genetic diseases [RCV003266716] | Chr19:5831589 [GRCh38] Chr19:5831600 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.877G>T (p.Asp293Tyr) | single nucleotide variant | Inborn genetic diseases [RCV003249549] | Chr19:5831691 [GRCh38] Chr19:5831702 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.811G>A (p.Val271Met) | single nucleotide variant | Inborn genetic diseases [RCV003239899] | Chr19:5831757 [GRCh38] Chr19:5831768 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.370C>T (p.Pro124Ser) | single nucleotide variant | Fucosyltransferase 6 deficiency [RCV001258299] | Chr19:5832198 [GRCh38] Chr19:5832209 [GRCh37] Chr19:19p13.3 |
benign |
NM_000150.4(FUT6):c.907C>G (p.Arg303Gly) | single nucleotide variant | FUT6-related condition [RCV003983864]|Fucosyltransferase 6 deficiency [RCV001258298] | Chr19:5831661 [GRCh38] Chr19:5831672 [GRCh37] Chr19:19p13.3 |
benign |
NM_000150.4(FUT6):c.1023G>A (p.Trp341Ter) | single nucleotide variant | Fucosyltransferase 6 deficiency [RCV001332224] | Chr19:5831545 [GRCh38] Chr19:5831556 [GRCh37] Chr19:19p13.3 |
pathogenic |
NM_000150.4(FUT6):c.207del (p.Trp69fs) | deletion | Fucosyltransferase 6 deficiency [RCV001334265] | Chr19:5832361 [GRCh38] Chr19:5832372 [GRCh37] Chr19:19p13.3 |
pathogenic |
NM_000150.4(FUT6):c.328C>T (p.Arg110Ter) | single nucleotide variant | Fucosyltransferase 6 deficiency [RCV001334266] | Chr19:5832240 [GRCh38] Chr19:5832251 [GRCh37] Chr19:19p13.3 |
pathogenic |
NM_000150.4(FUT6):c.957T>G (p.Phe319Leu) | single nucleotide variant | not provided [RCV001355287] | Chr19:5831611 [GRCh38] Chr19:5831622 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NC_000019.9:g.(?_5678562)_(5903719_?)dup | duplication | not provided [RCV002239957] | Chr19:5678562..5903719 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NC_000019.9:g.(?_5678562)_(5897028_?)dup | duplication | not provided [RCV001918791] | Chr19:5678562..5897028 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.7C>T (p.Pro3Ser) | single nucleotide variant | Inborn genetic diseases [RCV003263442] | Chr19:5832561 [GRCh38] Chr19:5832572 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.1033G>C (p.Glu345Gln) | single nucleotide variant | Inborn genetic diseases [RCV002687729] | Chr19:5831535 [GRCh38] Chr19:5831546 [GRCh37] Chr19:19p13.3 |
likely benign |
NM_000150.4(FUT6):c.560C>G (p.Ala187Gly) | single nucleotide variant | Inborn genetic diseases [RCV002753178] | Chr19:5832008 [GRCh38] Chr19:5832019 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.130T>A (p.Tyr44Asn) | single nucleotide variant | Inborn genetic diseases [RCV002778002] | Chr19:5832438 [GRCh38] Chr19:5832449 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.448G>A (p.Gly150Arg) | single nucleotide variant | Inborn genetic diseases [RCV002688284] | Chr19:5832120 [GRCh38] Chr19:5832131 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.964C>T (p.Arg322Trp) | single nucleotide variant | Inborn genetic diseases [RCV002749128] | Chr19:5831604 [GRCh38] Chr19:5831615 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.754C>T (p.Pro252Ser) | single nucleotide variant | Inborn genetic diseases [RCV002778298] | Chr19:5831814 [GRCh38] Chr19:5831825 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.468G>C (p.Met156Ile) | single nucleotide variant | Inborn genetic diseases [RCV002969707] | Chr19:5832100 [GRCh38] Chr19:5832111 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.310G>A (p.Ala104Thr) | single nucleotide variant | Inborn genetic diseases [RCV002694046] | Chr19:5832258 [GRCh38] Chr19:5832269 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.118G>A (p.Asp40Asn) | single nucleotide variant | Inborn genetic diseases [RCV002783023] | Chr19:5832450 [GRCh38] Chr19:5832461 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.236G>A (p.Arg79His) | single nucleotide variant | Inborn genetic diseases [RCV002758812] | Chr19:5832332 [GRCh38] Chr19:5832343 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.103C>T (p.Arg35Cys) | single nucleotide variant | Inborn genetic diseases [RCV002706935] | Chr19:5832465 [GRCh38] Chr19:5832476 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.518C>T (p.Pro173Leu) | single nucleotide variant | Inborn genetic diseases [RCV002744001] | Chr19:5832050 [GRCh38] Chr19:5832061 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.568G>C (p.Glu190Gln) | single nucleotide variant | Inborn genetic diseases [RCV002665991] | Chr19:5832000 [GRCh38] Chr19:5832011 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.323A>G (p.His108Arg) | single nucleotide variant | Inborn genetic diseases [RCV002747926] | Chr19:5832245 [GRCh38] Chr19:5832256 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.982C>T (p.Arg328Cys) | single nucleotide variant | Inborn genetic diseases [RCV002724206] | Chr19:5831586 [GRCh38] Chr19:5831597 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.287G>A (p.Arg96His) | single nucleotide variant | Inborn genetic diseases [RCV002724985] | Chr19:5832281 [GRCh38] Chr19:5832292 [GRCh37] Chr19:19p13.3 |
uncertain significance |
NM_000150.4(FUT6):c.1057G>A (p.Gly353Ser) | single nucleotide variant | Inborn genetic diseases [RCV003178537] | Chr19:5831511 [GRCh38] Chr19:5831522 [GRCh37] Chr19:19p13.3 |
likely benign |
NM_000150.4(FUT6):c.526G>A (p.Gly176Ser) | single nucleotide variant | Inborn genetic diseases [RCV003383790] | Chr19:5832042 [GRCh38] Chr19:5832053 [GRCh37] Chr19:19p13.3 |
uncertain significance |
GRCh37/hg19 19p13.3-13.2(chr19:260912-7246777)x3 | copy number gain | not provided [RCV003485190] | Chr19:260912..7246777 [GRCh37] Chr19:19p13.3-13.2 |
pathogenic |
NM_000150.4(FUT6):c.585A>G (p.Ala195=) | single nucleotide variant | not provided [RCV003406806] | Chr19:5831983 [GRCh38] Chr19:5831994 [GRCh37] Chr19:19p13.3 |
likely benign |
NM_000150.4(FUT6):c.138T>C (p.Asn46=) | single nucleotide variant | FUT6-related condition [RCV003964200] | Chr19:5832430 [GRCh38] Chr19:5832441 [GRCh37] Chr19:19p13.3 |
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. |
RH80293 |
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SGC35572 |
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FUT6_663 |
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D11S3114 |
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D8S2279 |
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D11S3316 |
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alimentary part of gastrointestinal system | circulatory system | endocrine system | exocrine system | hemolymphoid system | hepatobiliary system | integumental system | musculoskeletal system | nervous system | renal system | reproductive system | respiratory system | sensory system | adipose tissue | appendage | entire extraembryonic component | pharyngeal arch | |
High | |||||||||||||||||
Medium | 402 | 1 | 52 | 212 | 97 | 54 | 2 | 183 | 107 | 18 | 158 | 2 | |||||
Low | 336 | 7 | 388 | 383 | 106 | 379 | 14 | 67 | 12 | 109 | 178 | 156 | 7 | 7 | 8 | 1 | |
Below cutoff | 1370 | 1602 | 880 | 23 | 1020 | 26 | 2783 | 1218 | 2178 | 80 | 998 | 1091 | 6 | 664 | 1659 | 2 |
RefSeq Transcripts | NG_007505 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
NM_000150 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001040701 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001369502 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001369504 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001369505 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001381955 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001381956 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001381957 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001381958 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001381959 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011527872 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011527875 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047438553 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047438554 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047438555 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047438556 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047438557 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047438558 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047438559 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047438560 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047438561 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054320430 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054320431 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054320432 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054320433 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054320434 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054320435 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054320436 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054320437 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054320438 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054320439 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054320440 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054320441 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054320442 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054320443 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054320444 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054333258 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054333259 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054333260 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054333261 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GenBank Nucleotide | AC024592 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AF131211 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK098073 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK225795 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK313130 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC040472 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC061700 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH471139 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CP068259 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
DA426469 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
DA622182 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
DA628976 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
DA761223 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
DA761273 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
L01698 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
M98825 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NTIA01000094 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
U27331 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
U27332 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
U27333 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
U27334 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
U27335 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
U27336 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
U27337 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | ENST00000286955 ⟹ ENSP00000286955 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000318336 ⟹ ENSP00000313398 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000524754 ⟹ ENSP00000431708 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000526499 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000527106 ⟹ ENSP00000432954 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000528505 ⟹ ENSP00000433811 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000531085 ⟹ ENSP00000432161 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000531199 ⟹ ENSP00000436413 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000532464 ⟹ ENSP00000431880 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000591079 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000592563 ⟹ ENSP00000466016 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | NM_000150 ⟹ NP_000141 | ||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_001040701 ⟹ NP_001035791 | ||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_001369502 ⟹ NP_001356431 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_001369504 ⟹ NP_001356433 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_001369505 ⟹ NP_001356434 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_001381955 ⟹ NP_001368884 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_001381956 ⟹ NP_001368885 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_001381957 ⟹ NP_001368886 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_001381958 ⟹ NP_001368887 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_001381959 ⟹ NP_001368888 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | XM_047438553 ⟹ XP_047294509 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_047438554 ⟹ XP_047294510 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_047438555 ⟹ XP_047294511 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_047438556 ⟹ XP_047294512 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_047438557 ⟹ XP_047294513 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_047438558 ⟹ XP_047294514 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_047438559 ⟹ XP_047294515 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_047438560 ⟹ XP_047294516 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_047438561 ⟹ XP_047294517 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054320430 ⟹ XP_054176405 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054320431 ⟹ XP_054176406 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054320432 ⟹ XP_054176407 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054320433 ⟹ XP_054176408 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054320434 ⟹ XP_054176409 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054320435 ⟹ XP_054176410 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054320436 ⟹ XP_054176411 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054320437 ⟹ XP_054176412 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054320438 ⟹ XP_054176413 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054320439 ⟹ XP_054176414 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054320440 ⟹ XP_054176415 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054320441 ⟹ XP_054176416 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054320442 ⟹ XP_054176417 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054320443 ⟹ XP_054176418 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054320444 ⟹ XP_054176419 | ||||||||
Type: | CODING | ||||||||
Position: |
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Protein RefSeqs | NP_000141 | (Get FASTA) | NCBI Sequence Viewer |
NP_001035791 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001356431 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001356433 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001356434 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001368884 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001368885 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001368886 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001368887 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001368888 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047294509 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047294510 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047294511 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047294512 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047294513 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047294514 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047294515 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047294516 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047294517 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054176405 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054176406 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054176407 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054176408 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054176409 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054176410 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054176411 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054176412 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054176413 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054176414 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054176415 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054176416 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054176417 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054176418 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054176419 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054189233 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054189234 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054189235 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054189236 | (Get FASTA) | NCBI Sequence Viewer | |
GenBank Protein | AAA99222 | (Get FASTA) | NCBI Sequence Viewer |
AAB03078 | (Get FASTA) | NCBI Sequence Viewer | |
AAC50190 | (Get FASTA) | NCBI Sequence Viewer | |
AAC50191 | (Get FASTA) | NCBI Sequence Viewer | |
AAC50192 | (Get FASTA) | NCBI Sequence Viewer | |
AAC50193 | (Get FASTA) | NCBI Sequence Viewer | |
AAC50194 | (Get FASTA) | NCBI Sequence Viewer | |
AAC50195 | (Get FASTA) | NCBI Sequence Viewer | |
AAC50196 | (Get FASTA) | NCBI Sequence Viewer | |
AAD33509 | (Get FASTA) | NCBI Sequence Viewer | |
AAH61700 | (Get FASTA) | NCBI Sequence Viewer | |
BAG35950 | (Get FASTA) | NCBI Sequence Viewer | |
EAW69136 | (Get FASTA) | NCBI Sequence Viewer | |
EAW69137 | (Get FASTA) | NCBI Sequence Viewer | |
EAW69138 | (Get FASTA) | NCBI Sequence Viewer | |
EAW69139 | (Get FASTA) | NCBI Sequence Viewer | |
Ensembl Protein | ENSP00000286955 | ||
ENSP00000286955.5 | |||
ENSP00000313398 | |||
ENSP00000313398.4 | |||
ENSP00000431708.1 | |||
ENSP00000431880.1 | |||
ENSP00000432161.1 | |||
ENSP00000432954 | |||
ENSP00000432954.1 | |||
ENSP00000433811.1 | |||
ENSP00000436413.1 | |||
ENSP00000466016 | |||
ENSP00000466016.1 | |||
GenBank Protein | P51993 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_001035791 ⟸ NM_001040701 |
- Peptide Label: | isoform 1 |
- UniProtKB: | D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), P51993 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_000141 ⟸ NM_000150 |
- Peptide Label: | isoform 1 |
- UniProtKB: | D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), P51993 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001356431 ⟸ NM_001369502 |
- Peptide Label: | isoform 1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | NP_001356433 ⟸ NM_001369504 |
- Peptide Label: | isoform 1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | NP_001356434 ⟸ NM_001369505 |
- Peptide Label: | isoform 1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | NP_001368886 ⟸ NM_001381957 |
- Peptide Label: | isoform 2 |
- UniProtKB: | B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | NP_001368888 ⟸ NM_001381959 |
- Peptide Label: | isoform 2 |
- UniProtKB: | B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | NP_001368887 ⟸ NM_001381958 |
- Peptide Label: | isoform 2 |
- UniProtKB: | B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | NP_001368885 ⟸ NM_001381956 |
- Peptide Label: | isoform 1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | NP_001368884 ⟸ NM_001381955 |
- Peptide Label: | isoform 1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | ENSP00000436413 ⟸ ENST00000531199 |
RefSeq Acc Id: | ENSP00000432161 ⟸ ENST00000531085 |
RefSeq Acc Id: | ENSP00000431880 ⟸ ENST00000532464 |
RefSeq Acc Id: | ENSP00000286955 ⟸ ENST00000286955 |
RefSeq Acc Id: | ENSP00000431708 ⟸ ENST00000524754 |
RefSeq Acc Id: | ENSP00000432954 ⟸ ENST00000527106 |
RefSeq Acc Id: | ENSP00000433811 ⟸ ENST00000528505 |
RefSeq Acc Id: | ENSP00000466016 ⟸ ENST00000592563 |
RefSeq Acc Id: | ENSP00000313398 ⟸ ENST00000318336 |
RefSeq Acc Id: | XP_047294516 ⟸ XM_047438560 |
- Peptide Label: | isoform X2 |
- UniProtKB: | B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_047294513 ⟸ XM_047438557 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_047294512 ⟸ XM_047438556 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_047294509 ⟸ XM_047438553 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_047294514 ⟸ XM_047438558 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_047294517 ⟸ XM_047438561 |
- Peptide Label: | isoform X2 |
- UniProtKB: | B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_047294511 ⟸ XM_047438555 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_047294510 ⟸ XM_047438554 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_047294515 ⟸ XM_047438559 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054176417 ⟸ XM_054320442 |
- Peptide Label: | isoform X2 |
- UniProtKB: | B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054176413 ⟸ XM_054320438 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054176405 ⟸ XM_054320430 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054176408 ⟸ XM_054320433 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054176406 ⟸ XM_054320431 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054176415 ⟸ XM_054320440 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054176418 ⟸ XM_054320443 |
- Peptide Label: | isoform X2 |
- UniProtKB: | B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054176411 ⟸ XM_054320436 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054176419 ⟸ XM_054320444 |
- Peptide Label: | isoform X2 |
- UniProtKB: | B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054176407 ⟸ XM_054320432 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054176410 ⟸ XM_054320435 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054176409 ⟸ XM_054320434 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054176416 ⟸ XM_054320441 |
- Peptide Label: | isoform X2 |
- UniProtKB: | B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054176412 ⟸ XM_054320437 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
RefSeq Acc Id: | XP_054176414 ⟸ XM_054320439 |
- Peptide Label: | isoform X1 |
- UniProtKB: | P51993 (UniProtKB/Swiss-Prot), D6W637 (UniProtKB/Swiss-Prot), A6NEX0 (UniProtKB/Swiss-Prot), Q9UND8 (UniProtKB/Swiss-Prot), B2R7V3 (UniProtKB/TrEMBL) |
Name | Modeler | Protein Id | AA Range | Protein Structure |
AF-P51993-F1-model_v2 | AlphaFold | P51993 | 1-359 | view protein structure |
RGD ID: | 7238175 | ||||||||
Promoter ID: | EPDNEW_H24833 | ||||||||
Type: | initiation region | ||||||||
Name: | FUT6_1 | ||||||||
Description: | fucosyltransferase 6 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H24834 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
|
RGD ID: | 7238177 | ||||||||
Promoter ID: | EPDNEW_H24834 | ||||||||
Type: | initiation region | ||||||||
Name: | FUT6_2 | ||||||||
Description: | fucosyltransferase 6 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H24833 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
|
Database | Acc Id | Source(s) |
AGR Gene | HGNC:4017 | AgrOrtholog |
COSMIC | FUT6 | COSMIC |
Ensembl Genes | ENSG00000156413 | Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Ensembl Transcript | ENST00000286955 | ENTREZGENE |
ENST00000286955.5 | UniProtKB/Swiss-Prot | |
ENST00000318336 | ENTREZGENE | |
ENST00000318336.10 | UniProtKB/Swiss-Prot | |
ENST00000524754.1 | UniProtKB/Swiss-Prot | |
ENST00000527106 | ENTREZGENE | |
ENST00000527106.5 | UniProtKB/Swiss-Prot | |
ENST00000528505.1 | UniProtKB/TrEMBL | |
ENST00000531085.5 | UniProtKB/TrEMBL | |
ENST00000531199.1 | UniProtKB/TrEMBL | |
ENST00000532464.5 | UniProtKB/TrEMBL | |
ENST00000592563 | ENTREZGENE | |
ENST00000592563.1 | UniProtKB/Swiss-Prot | |
Gene3D-CATH | 3.40.50.11660 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
GTEx | ENSG00000156413 | GTEx |
HGNC ID | HGNC:4017 | ENTREZGENE |
Human Proteome Map | FUT6 | Human Proteome Map |
InterPro | Glyco_tran_10_N | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Glyco_trans_10 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
GT10-like_sf | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
KEGG Report | hsa:2528 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
NCBI Gene | 2528 | ENTREZGENE |
OMIM | 136836 | OMIM |
PANTHER | 4-GALACTOSYL-N-ACETYLGLUCOSAMINIDE 3-ALPHA-L-FUCOSYLTRANSFERASE FUT6 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
PTHR11929 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Pfam | Glyco_tran_10_N | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Glyco_transf_10 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
PharmGKB | PA28433 | PharmGKB |
Superfamily-SCOP | UDP-Glycosyltransferase/glycogen phosphorylase | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
UniProt | A6NEX0 | ENTREZGENE |
B2R7V3 | ENTREZGENE, UniProtKB/TrEMBL | |
D6W637 | ENTREZGENE | |
E9PJ18_HUMAN | UniProtKB/TrEMBL | |
E9PJB4_HUMAN | UniProtKB/TrEMBL | |
E9PP56_HUMAN | UniProtKB/TrEMBL | |
E9PS22_HUMAN | UniProtKB/TrEMBL | |
FUT6_HUMAN | UniProtKB/Swiss-Prot, ENTREZGENE | |
Q6P7E6_HUMAN | UniProtKB/TrEMBL | |
Q9UND8 | ENTREZGENE | |
UniProt Secondary | A6NEX0 | UniProtKB/Swiss-Prot |
D6W637 | UniProtKB/Swiss-Prot | |
Q9UND8 | UniProtKB/Swiss-Prot |
Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
---|---|---|---|---|---|---|---|
2015-12-01 | FUT6 | fucosyltransferase 6 | FUT6 | fucosyltransferase 6 (alpha (1,3) fucosyltransferase) | Symbol and/or name change | 5135510 | APPROVED |