Imported Disease Annotations - CTDTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | high grade glioma | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:19578367 | |
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Imported Disease Annotations - CTDTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | high grade glioma | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:19578367 | |
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# | Reference Title | Reference Citation |
1. | ClinVar Automated Import and Annotation Pipeline | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
2. | Data Import for Chemical-Gene Interactions | RGD automated import pipeline for gene-chemical interactions |
PMID:9734811 | PMID:11001876 | PMID:12168954 | PMID:12477932 | PMID:14532993 | PMID:14702039 | PMID:15489334 | PMID:15491607 | PMID:17081983 | PMID:19531213 | PMID:19578367 | PMID:20462933 |
PMID:20513769 | PMID:20847058 | PMID:21350045 | PMID:21531791 | PMID:21653829 | PMID:21873635 | PMID:22951725 | PMID:23300798 | PMID:23400010 | PMID:23940118 | PMID:24001599 | PMID:24097068 |
PMID:24711643 | PMID:24935770 | PMID:24982445 | PMID:25036637 | PMID:25921289 | PMID:26156397 | PMID:26167880 | PMID:26460568 | PMID:26496610 | PMID:26610392 | PMID:26673895 | PMID:26972000 |
PMID:28611215 | PMID:28886307 | PMID:29298432 | PMID:29348417 | PMID:29395067 | PMID:29467282 | PMID:30021884 | PMID:30194290 | PMID:30639242 | PMID:30868356 | PMID:30928649 | PMID:31182584 |
PMID:31215377 | PMID:31586073 | PMID:31721021 | PMID:32513696 | PMID:34079125 | PMID:35188604 | PMID:35271311 | PMID:35384245 | PMID:35748872 | PMID:35906200 | PMID:36215168 | PMID:36543534 |
PMID:36774506 | PMID:36931259 | PMID:37689310 | PMID:38117590 |
PHLDB1 (Homo sapiens - human) |
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Phldb1 (Mus musculus - house mouse) |
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Phldb1 (Rattus norvegicus - Norway rat) |
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Phldb1 (Chinchilla lanigera - long-tailed chinchilla) |
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PHLDB1 (Pan paniscus - bonobo/pygmy chimpanzee) |
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PHLDB1 (Canis lupus familiaris - dog) |
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Phldb1 (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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PHLDB1 (Sus scrofa - pig) |
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PHLDB1 (Chlorocebus sabaeus - green monkey) |
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Phldb1 (Heterocephalus glaber - naked mole-rat) |
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Variants in PHLDB1
71 total Variants |
Name | Type | Condition(s) | Position(s) | Clinical significance |
GRCh38/hg38 11q23.3-25(chr11:116851395-134998513)x3 | copy number gain | See cases [RCV000050331] | Chr11:116851395..134998513 [GRCh38] Chr11:116722111..134868407 [GRCh37] Chr11:116227321..134373617 [NCBI36] Chr11:11q23.3-25 |
pathogenic |
GRCh38/hg38 11q23.2-23.3(chr11:113444446-120648921)x3 | copy number gain | See cases [RCV000050627] | Chr11:113444446..120648921 [GRCh38] Chr11:113315168..120519630 [GRCh37] Chr11:112820378..120024840 [NCBI36] Chr11:11q23.2-23.3 |
pathogenic |
GRCh38/hg38 11q22.1-25(chr11:100348599-135040246)x3 | copy number gain | See cases [RCV000053638] | Chr11:100348599..135040246 [GRCh38] Chr11:100219331..134910140 [GRCh37] Chr11:99724541..134415350 [NCBI36] Chr11:11q22.1-25 |
pathogenic |
NM_001144758.2(PHLDB1):c.460C>T (p.Pro154Ser) | single nucleotide variant | Malignant melanoma [RCV000069184] | Chr11:118625038 [GRCh38] Chr11:118495754 [GRCh37] Chr11:118000964 [NCBI36] Chr11:11q23.3 |
not provided |
NM_001144758.2(PHLDB1):c.1471C>T (p.Arg491Trp) | single nucleotide variant | Malignant melanoma [RCV000069185] | Chr11:118628294 [GRCh38] Chr11:118499010 [GRCh37] Chr11:118004220 [NCBI36] Chr11:11q23.3 |
not provided |
GRCh38/hg38 11q23.3-25(chr11:116851372-134998526)x3 | copy number gain | See cases [RCV000134064] | Chr11:116851372..134998526 [GRCh38] Chr11:116722088..134868420 [GRCh37] Chr11:116227298..134373630 [NCBI36] Chr11:11q23.3-25 |
pathogenic |
GRCh38/hg38 11q23.2-25(chr11:112864326-131189315)x3 | copy number gain | See cases [RCV000137582] | Chr11:112864326..131189315 [GRCh38] Chr11:112832130..131059210 [GRCh37] Chr11:112240259..130564420 [NCBI36] Chr11:11q23.2-25 |
pathogenic |
GRCh38/hg38 11q23.3-25(chr11:116868935-135075271)x3 | copy number gain | See cases [RCV000137453] | Chr11:116868935..135075271 [GRCh38] Chr11:116739651..134945165 [GRCh37] Chr11:116244861..134450377 [NCBI36] Chr11:11q23.3-25 |
pathogenic|conflicting data from submitters |
GRCh38/hg38 11q23.3-25(chr11:116806268-135075271)x3 | copy number gain | See cases [RCV000138307] | Chr11:116806268..135075271 [GRCh38] Chr11:116676984..134945165 [GRCh37] Chr11:116182194..134450377 [NCBI36] Chr11:11q23.3-25 |
pathogenic |
GRCh38/hg38 11q23.3-24.2(chr11:117333952-127709156)x3 | copy number gain | See cases [RCV000139362] | Chr11:117333952..127709156 [GRCh38] Chr11:117204668..127579051 [GRCh37] Chr11:116709878..127084261 [NCBI36] Chr11:11q23.3-24.2 |
pathogenic |
GRCh38/hg38 11q23.3-25(chr11:116851395-134998513)x3 | copy number gain | See cases [RCV000148276] | Chr11:116851395..134998513 [GRCh38] Chr11:116722111..134868407 [GRCh37] Chr11:116227321..134373617 [NCBI36] Chr11:11q23.3-25 |
pathogenic |
GRCh37/hg19 11q23.3(chr11:115215434-120559928)x3 | copy number gain | See cases [RCV000240308] | Chr11:115215434..120559928 [GRCh37] Chr11:11q23.3 |
pathogenic |
GRCh37/hg19 11q23.3-25(chr11:116700253-134904063) | copy number gain | not provided [RCV000767816] | Chr11:116700253..134904063 [GRCh37] Chr11:11q23.3-25 |
pathogenic |
GRCh37/hg19 11q23.3-25(chr11:116681007-134938470)x3 | copy number gain | See cases [RCV000449449] | Chr11:116681007..134938470 [GRCh37] Chr11:11q23.3-25 |
pathogenic |
GRCh37/hg19 11q23.3-25(chr11:116684163-134938470)x3 | copy number gain | See cases [RCV000447848] | Chr11:116684163..134938470 [GRCh37] Chr11:11q23.3-25 |
pathogenic |
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) | copy number gain | See cases [RCV000511729] | Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25 |
pathogenic |
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 | copy number gain | See cases [RCV000510881] | Chr11:230616..134938470 [GRCh37] Chr11:11p15.5-q25 |
pathogenic |
GRCh37/hg19 11q23.3-25(chr11:116691675-134889485) | copy number gain | not provided [RCV000767667] | Chr11:116691675..134889485 [GRCh37] Chr11:11q23.3-25 |
pathogenic |
NM_001144758.3(PHLDB1):c.1981T>G (p.Ser661Ala) | single nucleotide variant | Inborn genetic diseases [RCV003288580] | Chr11:118631360 [GRCh38] Chr11:118502077 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.920G>A (p.Arg307His) | single nucleotide variant | Inborn genetic diseases [RCV003304362] | Chr11:118627743 [GRCh38] Chr11:118498459 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.991C>G (p.Leu331Val) | single nucleotide variant | Inborn genetic diseases [RCV003259997] | Chr11:118627814 [GRCh38] Chr11:118498530 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.1343G>A (p.Arg448Gln) | single nucleotide variant | Inborn genetic diseases [RCV003297991] | Chr11:118628166 [GRCh38] Chr11:118498882 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.4018T>G (p.Cys1340Gly) | single nucleotide variant | Inborn genetic diseases [RCV003256084] | Chr11:118656707 [GRCh38] Chr11:118527417 [GRCh37] Chr11:11q23.3 |
uncertain significance |
GRCh37/hg19 11q23.3-25(chr11:116681007-134938470)x3 | copy number gain | See cases [RCV000512291] | Chr11:116681007..134938470 [GRCh37] Chr11:11q23.3-25 |
pathogenic |
GRCh37/hg19 11q23.3-25(chr11:116681007-134938470)x3 | copy number gain | not provided [RCV000683373] | Chr11:116681007..134938470 [GRCh37] Chr11:11q23.3-25 |
pathogenic |
GRCh37/hg19 11q23.3(chr11:116669751-120979377)x3 | copy number gain | not provided [RCV000683365] | Chr11:116669751..120979377 [GRCh37] Chr11:11q23.3 |
likely pathogenic |
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 | copy number gain | not provided [RCV000737348] | Chr11:198510..134934063 [GRCh37] Chr11:11p15.5-q25 |
pathogenic |
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 | copy number gain | not provided [RCV000749874] | Chr11:70864..134938470 [GRCh37] Chr11:11p15.5-q25 |
pathogenic |
GRCh37/hg19 11q23.3-25(chr11:116697066-134934063)x3 | copy number gain | not provided [RCV000737686] | Chr11:116697066..134934063 [GRCh37] Chr11:11q23.3-25 |
pathogenic |
NM_001144758.3(PHLDB1):c.1724G>A (p.Arg575Gln) | single nucleotide variant | Inborn genetic diseases [RCV003270836] | Chr11:118628547 [GRCh38] Chr11:118499263 [GRCh37] Chr11:11q23.3 |
uncertain significance |
GRCh37/hg19 11q23.3-25(chr11:117830263-134938470)x3 | copy number gain | not provided [RCV000848151] | Chr11:117830263..134938470 [GRCh37] Chr11:11q23.3-25 |
pathogenic |
NC_000011.9:g.(?_118007722)_(119170511_?)del | deletion | Long QT syndrome 10 [RCV000816632] | Chr11:118007722..119170511 [GRCh37] Chr11:11q23.3 |
uncertain significance |
GRCh37/hg19 11q23.3(chr11:118280670-119650105)x3 | copy number gain | not provided [RCV001006451] | Chr11:118280670..119650105 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NC_000011.9:g.(?_117856768)_(118972385_?)del | deletion | Combined immunodeficiency due to CD3gamma deficiency [RCV001382626]|Immunodeficiency 18 [RCV001389243]|Immunodeficiency 19 [RCV001031688]|Inflammatory bowel disease 28 [RCV001386823] | Chr11:117856768..118972385 [GRCh37] Chr11:11q23.3 |
pathogenic |
NM_001144758.3(PHLDB1):c.3559C>T (p.Arg1187Cys) | single nucleotide variant | Inborn genetic diseases [RCV003240572] | Chr11:118647981 [GRCh38] Chr11:118518697 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NC_000011.9:g.(?_117856768)_(118972385_?)dup | duplication | Glucose-6-phosphate transport defect [RCV001031254]|Immunodeficiency 18 [RCV001338286] | Chr11:117856768..118972385 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.118C>G (p.Pro40Ala) | single nucleotide variant | Inborn genetic diseases [RCV003294777] | Chr11:118614616 [GRCh38] Chr11:118485331 [GRCh37] Chr11:11q23.3 |
uncertain significance |
Single allele | deletion | Short stature [RCV001003892] | Chr11:114433313..131230466 [GRCh37] Chr11:11q23.2-25 |
likely pathogenic |
NC_000011.9:g.(?_117856768)_(118972385_?)dup | duplication | Combined immunodeficiency due to CD3gamma deficiency [RCV001313154]|Glucose-6-phosphate transport defect [RCV001031254]|Immunodeficiency 18 [RCV001338286]|Immunodeficiency 19 [RCV001322413]|Inflammatory bowel disease 28 [RCV001304384] | Chr11:117856768..118972385 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NC_000011.9:g.(?_118007722)_(119170511_?)del | deletion | Long QT syndrome 10 [RCV001309948] | Chr11:118007722..119170511 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NC_000011.9:g.104288964_134937416dup | duplication | Distal trisomy 11q [RCV001250234] | Chr11:104288964..134937416 [GRCh37] Chr11:11q22.3-25 |
pathogenic |
NC_000011.9:g.(?_116691583)_(121500272_?)dup | duplication | Combined immunodeficiency due to CD3gamma deficiency [RCV003119252]|Immunodeficiency 18 [RCV003109226]|Immunodeficiency 19 [RCV003109224]|Inflammatory bowel disease 28 [RCV003109225]|Isolated microphthalmia 5 [RCV003119251]|RASopathy [RCV003119250] | Chr11:116691583..121500272 [GRCh37] Chr11:11q23.3-24.1 |
uncertain significance |
GRCh37/hg19 11q23.1-24.3(chr11:112375478-128785742)x3 | copy number gain | not provided [RCV001829187] | Chr11:112375478..128785742 [GRCh37] Chr11:11q23.1-24.3 |
pathogenic |
NC_000011.9:g.(?_116660844)_(121500272_?)dup | duplication | not provided [RCV003107886] | Chr11:116660844..121500272 [GRCh37] Chr11:11q23.3-24.1 |
uncertain significance |
NC_000011.9:g.(?_118007742)_(119170491_?)dup | duplication | DPAGT1-congenital disorder of glycosylation [RCV001975773] | Chr11:118007742..119170491 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NC_000011.9:g.(?_118390313)_(118550336_?)del | deletion | not provided [RCV001940057] | Chr11:118390313..118550336 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NC_000011.9:g.(?_117209303)_(120133495_?)dup | duplication | not provided [RCV003122151] | Chr11:117209303..120133495 [GRCh37] Chr11:11q23.3 |
uncertain significance |
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3 | copy number gain | MISSED ABORTION [RCV002282973] | Chr11:32799481..134938470 [GRCh37] Chr11:11p13-q25 |
pathogenic |
NM_001144758.3(PHLDB1):c.2741A>C (p.Glu914Ala) | single nucleotide variant | Inborn genetic diseases [RCV003257950] | Chr11:118642258 [GRCh38] Chr11:118512976 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.173C>T (p.Pro58Leu) | single nucleotide variant | Inborn genetic diseases [RCV002841025] | Chr11:118614671 [GRCh38] Chr11:118485386 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.81C>G (p.Ile27Met) | single nucleotide variant | Inborn genetic diseases [RCV002729078] | Chr11:118614579 [GRCh38] Chr11:118485294 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.1613T>A (p.Leu538Gln) | single nucleotide variant | Inborn genetic diseases [RCV002882993] | Chr11:118628436 [GRCh38] Chr11:118499152 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.710C>G (p.Thr237Ser) | single nucleotide variant | Inborn genetic diseases [RCV002968440] | Chr11:118627533 [GRCh38] Chr11:118498249 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.1190C>G (p.Thr397Arg) | single nucleotide variant | Inborn genetic diseases [RCV002728313] | Chr11:118628013 [GRCh38] Chr11:118498729 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.3995G>C (p.Ser1332Thr) | single nucleotide variant | Inborn genetic diseases [RCV002682196] | Chr11:118656684 [GRCh38] Chr11:118527394 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.328G>C (p.Val110Leu) | single nucleotide variant | Inborn genetic diseases [RCV002733890] | Chr11:118616184 [GRCh38] Chr11:118486899 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.1031G>A (p.Arg344Gln) | single nucleotide variant | Inborn genetic diseases [RCV002946688] | Chr11:118627854 [GRCh38] Chr11:118498570 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.3149G>A (p.Arg1050Gln) | single nucleotide variant | Inborn genetic diseases [RCV002976916] | Chr11:118645383 [GRCh38] Chr11:118516101 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.1804C>T (p.Arg602Trp) | single nucleotide variant | Inborn genetic diseases [RCV002980766] | Chr11:118628627 [GRCh38] Chr11:118499343 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.2233G>A (p.Ala745Thr) | single nucleotide variant | Inborn genetic diseases [RCV002781729] | Chr11:118632045 [GRCh38] Chr11:118502762 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.2200G>A (p.Val734Met) | single nucleotide variant | Inborn genetic diseases [RCV002759282] | Chr11:118632012 [GRCh38] Chr11:118502729 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.983G>A (p.Arg328Gln) | single nucleotide variant | Inborn genetic diseases [RCV002925647] | Chr11:118627806 [GRCh38] Chr11:118498522 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.2137G>T (p.Val713Leu) | single nucleotide variant | Inborn genetic diseases [RCV002869337] | Chr11:118631949 [GRCh38] Chr11:118502666 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.1364G>A (p.Arg455Gln) | single nucleotide variant | Inborn genetic diseases [RCV002888280] | Chr11:118628187 [GRCh38] Chr11:118498903 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.3598C>T (p.Arg1200Trp) | single nucleotide variant | Inborn genetic diseases [RCV002955406] | Chr11:118648020 [GRCh38] Chr11:118518736 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.1376C>T (p.Pro459Leu) | single nucleotide variant | Inborn genetic diseases [RCV002665969] | Chr11:118628199 [GRCh38] Chr11:118498915 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.893C>T (p.Pro298Leu) | single nucleotide variant | Inborn genetic diseases [RCV002764181] | Chr11:118627716 [GRCh38] Chr11:118498432 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.2085G>C (p.Glu695Asp) | single nucleotide variant | Inborn genetic diseases [RCV002763825] | Chr11:118631464 [GRCh38] Chr11:118502181 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.2866C>T (p.Arg956Cys) | single nucleotide variant | Inborn genetic diseases [RCV002708909] | Chr11:118642383 [GRCh38] Chr11:118513101 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.2897A>G (p.Asp966Gly) | single nucleotide variant | Inborn genetic diseases [RCV002874415] | Chr11:118643819 [GRCh38] Chr11:118514537 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.208G>C (p.Ala70Pro) | single nucleotide variant | Inborn genetic diseases [RCV002744131] | Chr11:118616064 [GRCh38] Chr11:118486779 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.911G>A (p.Ser304Asn) | single nucleotide variant | Inborn genetic diseases [RCV002803595] | Chr11:118627734 [GRCh38] Chr11:118498450 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.3574C>T (p.Arg1192Trp) | single nucleotide variant | Inborn genetic diseases [RCV003010932] | Chr11:118647996 [GRCh38] Chr11:118518712 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.2021G>A (p.Arg674His) | single nucleotide variant | Inborn genetic diseases [RCV002963669] | Chr11:118631400 [GRCh38] Chr11:118502117 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.3367A>G (p.Ser1123Gly) | single nucleotide variant | Inborn genetic diseases [RCV002702790] | Chr11:118645601 [GRCh38] Chr11:118516319 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.3242C>T (p.Ser1081Leu) | single nucleotide variant | Inborn genetic diseases [RCV002717847] | Chr11:118645476 [GRCh38] Chr11:118516194 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.271C>T (p.Arg91Trp) | single nucleotide variant | Inborn genetic diseases [RCV002657324] | Chr11:118616127 [GRCh38] Chr11:118486842 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.1397G>A (p.Arg466Gln) | single nucleotide variant | Inborn genetic diseases [RCV002944766] | Chr11:118628220 [GRCh38] Chr11:118498936 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.2191A>C (p.Lys731Gln) | single nucleotide variant | Inborn genetic diseases [RCV003197588] | Chr11:118632003 [GRCh38] Chr11:118502720 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.616C>A (p.Leu206Ile) | single nucleotide variant | Inborn genetic diseases [RCV003179485] | Chr11:118627439 [GRCh38] Chr11:118498155 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.344G>A (p.Arg115Gln) | single nucleotide variant | Inborn genetic diseases [RCV003212740] | Chr11:118616200 [GRCh38] Chr11:118486915 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.2603G>A (p.Arg868His) | single nucleotide variant | Bardet-Biedl syndrome [RCV003224788] | Chr11:118638958 [GRCh38] Chr11:118509676 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.2902G>A (p.Glu968Lys) | single nucleotide variant | Inborn genetic diseases [RCV003207919] | Chr11:118643824 [GRCh38] Chr11:118514542 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.3743C>T (p.Thr1248Ile) | single nucleotide variant | Inborn genetic diseases [RCV003179609] | Chr11:118650165 [GRCh38] Chr11:118520870 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.3340C>A (p.Leu1114Met) | single nucleotide variant | Inborn genetic diseases [RCV003208573] | Chr11:118645574 [GRCh38] Chr11:118516292 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.3844C>T (p.Arg1282Trp) | single nucleotide variant | Inborn genetic diseases [RCV003212115] | Chr11:118650517 [GRCh38] Chr11:118521222 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.3146G>A (p.Arg1049Gln) | single nucleotide variant | Inborn genetic diseases [RCV003262092] | Chr11:118645380 [GRCh38] Chr11:118516098 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.3059G>A (p.Arg1020His) | single nucleotide variant | Inborn genetic diseases [RCV003306809] | Chr11:118644112 [GRCh38] Chr11:118514830 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.2837C>T (p.Ser946Phe) | single nucleotide variant | Inborn genetic diseases [RCV003378649] | Chr11:118642354 [GRCh38] Chr11:118513072 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.1613T>C (p.Leu538Pro) | single nucleotide variant | Inborn genetic diseases [RCV003345120] | Chr11:118628436 [GRCh38] Chr11:118499152 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.1748G>A (p.Ser583Asn) | single nucleotide variant | Inborn genetic diseases [RCV003345802] | Chr11:118628571 [GRCh38] Chr11:118499287 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.2690_2693del (p.Leu897fs) | microsatellite | Osteogenesis imperfecta, type 23 [RCV003444536] | Chr11:118639198..118639201 [GRCh38] Chr11:118509916..118509919 [GRCh37] Chr11:11q23.3 |
pathogenic |
NM_001144758.3(PHLDB1):c.517C>T (p.Pro173Ser) | single nucleotide variant | Inborn genetic diseases [RCV003356162] | Chr11:118627340 [GRCh38] Chr11:118498056 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.1376C>G (p.Pro459Arg) | single nucleotide variant | Inborn genetic diseases [RCV003386003] | Chr11:118628199 [GRCh38] Chr11:118498915 [GRCh37] Chr11:11q23.3 |
uncertain significance |
NM_001144758.3(PHLDB1):c.1346G>A (p.Arg449Gln) | single nucleotide variant | Inborn genetic diseases [RCV003350888] | Chr11:118628169 [GRCh38] Chr11:118498885 [GRCh37] Chr11:11q23.3 |
uncertain significance |
Single allele | duplication | not provided [RCV003448710] | Chr11:102134973..134945611 [GRCh37] Chr11:11q22.2-25 |
pathogenic |
NM_001144758.3(PHLDB1):c.3974G>A (p.Arg1325His) | single nucleotide variant | not provided [RCV003424829] | Chr11:118655873 [GRCh38] Chr11:118526583 [GRCh37] Chr11:11q23.3 |
likely benign |
NM_001144758.3(PHLDB1):c.1538G>A (p.Gly513Asp) | single nucleotide variant | not provided [RCV003424824] | Chr11:118628361 [GRCh38] Chr11:118499077 [GRCh37] Chr11:11q23.3 |
likely benign |
NM_001144758.3(PHLDB1):c.3615C>T (p.Val1205=) | single nucleotide variant | not provided [RCV003424827] | Chr11:118648037 [GRCh38] Chr11:118518753 [GRCh37] Chr11:11q23.3 |
benign |
NM_001144758.3(PHLDB1):c.2392dup (p.Leu798fs) | duplication | Osteogenesis imperfecta, type 23 [RCV003444535] | Chr11:118635402..118635403 [GRCh38] Chr11:118506120..118506121 [GRCh37] Chr11:11q23.3 |
pathogenic |
NM_001144758.3(PHLDB1):c.2586C>T (p.Ala862=) | single nucleotide variant | not provided [RCV003424826] | Chr11:118638941 [GRCh38] Chr11:118509659 [GRCh37] Chr11:11q23.3 |
likely benign |
NM_001144758.3(PHLDB1):c.1761C>T (p.Asp587=) | single nucleotide variant | not provided [RCV003424825] | Chr11:118628584 [GRCh38] Chr11:118499300 [GRCh37] Chr11:11q23.3 |
likely benign |
NM_001144758.3(PHLDB1):c.3654+5A>G | single nucleotide variant | not provided [RCV003424828] | Chr11:118648081 [GRCh38] Chr11:118518797 [GRCh37] Chr11:11q23.3 |
likely benign |
NM_001144758.3(PHLDB1):c.3322G>A (p.Ala1108Thr) | single nucleotide variant | not provided [RCV003885659] | Chr11:118645556 [GRCh38] Chr11:118516274 [GRCh37] Chr11:11q23.3 |
likely benign |
NM_001144758.3(PHLDB1):c.3389C>T (p.Ser1130Leu) | single nucleotide variant | Inborn genetic diseases [RCV003381145] | Chr11:118645623 [GRCh38] Chr11:118516341 [GRCh37] Chr11:11q23.3 |
uncertain significance |
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. |
D11S1364 |
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G62130 |
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D11S614 |
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PHLDB1__6986 |
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D11S2065 |
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RH11874 |
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D11S2274E |
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D10S16 | No map positions available. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
D1S1423 |
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D11S2921 |
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D1S1425 |
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||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
D10S16 |
|
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 | visual system | adipose tissue | appendage | entire extraembryonic component | pharyngeal arch | |
High | ||||||||||||||||||
Medium | 2224 | 2181 | 1243 | 181 | 428 | 39 | 3937 | 1807 | 3511 | 216 | 1282 | 1389 | 151 | 1204 | 2471 | 1 | ||
Low | 206 | 193 | 467 | 428 | 360 | 412 | 419 | 386 | 220 | 203 | 177 | 222 | 24 | 1 | 317 | 3 | 1 | |
Below cutoff | 7 | 617 | 16 | 14 | 867 | 14 | 4 | 3 | 2 |
RefSeq Transcripts | NM_001144758 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
NM_001144759 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_015157 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_005271468 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_005271469 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_005271470 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_005271471 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_005271472 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_005271473 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_005271474 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_005271475 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_005277680 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006718796 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006718797 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006718798 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006718799 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006718800 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006718801 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006718802 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006718803 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011542703 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011542704 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011542705 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011542706 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011542707 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011542708 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011542709 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011542710 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011542711 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011542713 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011542714 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011542715 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017017407 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017017408 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017017409 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017017410 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017017411 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047426632 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047426633 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047426634 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047426635 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047426636 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047426637 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047426638 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047426639 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047426640 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047426641 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047426642 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047426643 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047426644 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047426645 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047426646 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047426647 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047426648 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368141 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368142 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368143 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368144 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368145 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368146 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368147 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368148 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368149 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368150 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368151 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368152 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368153 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368154 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368155 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368156 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368157 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368158 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368159 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368160 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368161 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368162 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368163 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368164 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368165 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368166 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368167 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368168 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368169 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368170 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368171 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368172 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368173 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368174 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368175 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368176 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368177 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368178 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368179 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368180 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368181 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368182 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368183 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368184 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368185 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368186 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368187 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054368188 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_001747797 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_001747798 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_001747799 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_007062463 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_008488367 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_008488368 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_947813 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GenBank Nucleotide | AB014538 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AB094090 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AB177859 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AI917888 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK021690 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK027510 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK074070 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK074747 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK074918 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK125783 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK294550 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK295819 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK296345 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AL080230 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AL832373 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AP000941 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AP002954 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC013031 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC014510 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC098586 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BX489377 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BX648176 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH471065 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CP068267 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CR749783 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
EF445008 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
KF455534 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | ENST00000356063 ⟹ ENSP00000348359 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000361417 ⟹ ENSP00000354498 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000392852 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000524713 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000525226 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000525427 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000526374 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000526537 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000526699 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000526826 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000527259 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000527500 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000527898 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000528594 ⟹ ENSP00000435520 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000528875 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000529005 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000530708 ⟹ ENSP00000481393 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000530994 ⟹ ENSP00000431508 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000531987 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000532517 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000532639 ⟹ ENSP00000478254 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000534140 ⟹ ENSP00000482728 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000600882 ⟹ ENSP00000469820 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000612681 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000614369 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000617208 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000620788 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000621027 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | NM_001144758 ⟹ NP_001138230 | ||||||||||||||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001144759 ⟹ NP_001138231 | ||||||||||||||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_015157 ⟹ NP_055972 | ||||||||||||||||||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | XM_005271468 ⟹ XP_005271525 | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | XM_005271469 ⟹ XP_005271526 | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | XM_005271470 ⟹ XP_005271527 | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | XM_005271471 ⟹ XP_005271528 | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | XM_005271472 ⟹ XP_005271529 | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | XM_005271473 ⟹ XP_005271530 | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | XM_005271474 ⟹ XP_005271531 | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | XM_005271475 ⟹ XP_005271532 | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | XM_005277680 ⟹ XP_005277737 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_006718797 ⟹ XP_006718860 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_006718798 ⟹ XP_006718861 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_006718799 ⟹ XP_006718862 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_006718800 ⟹ XP_006718863 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_006718801 ⟹ XP_006718864 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_006718802 ⟹ XP_006718865 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_006718803 ⟹ XP_006718866 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011542703 ⟹ XP_011541005 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011542704 ⟹ XP_011541006 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011542705 ⟹ XP_011541007 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011542706 ⟹ XP_011541008 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011542707 ⟹ XP_011541009 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011542708 ⟹ XP_011541010 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011542709 ⟹ XP_011541011 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011542710 ⟹ XP_011541012 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011542714 ⟹ XP_011541016 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011542715 ⟹ XP_011541017 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_017017407 ⟹ XP_016872896 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_017017408 ⟹ XP_016872897 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_017017409 ⟹ XP_016872898 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_017017410 ⟹ XP_016872899 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_017017411 ⟹ XP_016872900 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_047426632 ⟹ XP_047282588 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047426633 ⟹ XP_047282589 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047426634 ⟹ XP_047282590 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047426635 ⟹ XP_047282591 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047426636 ⟹ XP_047282592 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047426637 ⟹ XP_047282593 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047426638 ⟹ XP_047282594 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047426639 ⟹ XP_047282595 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047426640 ⟹ XP_047282596 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047426641 ⟹ XP_047282597 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047426642 ⟹ XP_047282598 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047426643 ⟹ XP_047282599 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047426644 ⟹ XP_047282600 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047426645 ⟹ XP_047282601 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047426646 ⟹ XP_047282602 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047426647 ⟹ XP_047282603 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047426648 ⟹ XP_047282604 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368141 ⟹ XP_054224116 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368142 ⟹ XP_054224117 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368143 ⟹ XP_054224118 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368144 ⟹ XP_054224119 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368145 ⟹ XP_054224120 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368146 ⟹ XP_054224121 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368147 ⟹ XP_054224122 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368148 ⟹ XP_054224123 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368149 ⟹ XP_054224124 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368150 ⟹ XP_054224125 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368151 ⟹ XP_054224126 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368152 ⟹ XP_054224127 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368153 ⟹ XP_054224128 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368154 ⟹ XP_054224129 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368155 ⟹ XP_054224130 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368156 ⟹ XP_054224131 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368157 ⟹ XP_054224132 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368158 ⟹ XP_054224133 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368159 ⟹ XP_054224134 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368160 ⟹ XP_054224135 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368161 ⟹ XP_054224136 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368162 ⟹ XP_054224137 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368163 ⟹ XP_054224138 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368164 ⟹ XP_054224139 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368165 ⟹ XP_054224140 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368166 ⟹ XP_054224141 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368167 ⟹ XP_054224142 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368168 ⟹ XP_054224143 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368169 ⟹ XP_054224144 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368170 ⟹ XP_054224145 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368171 ⟹ XP_054224146 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368172 ⟹ XP_054224147 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368173 ⟹ XP_054224148 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368174 ⟹ XP_054224149 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368175 ⟹ XP_054224150 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368176 ⟹ XP_054224151 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368177 ⟹ XP_054224152 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368178 ⟹ XP_054224153 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368179 ⟹ XP_054224154 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368180 ⟹ XP_054224155 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368181 ⟹ XP_054224156 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368182 ⟹ XP_054224157 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368183 ⟹ XP_054224158 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368184 ⟹ XP_054224159 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368185 ⟹ XP_054224160 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368186 ⟹ XP_054224161 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368187 ⟹ XP_054224162 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054368188 ⟹ XP_054224163 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XR_007062463 | ||||||||
Type: | NON-CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XR_008488367 | ||||||||
Type: | NON-CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XR_008488368 | ||||||||
Type: | NON-CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XR_947813 | ||||||||
Type: | NON-CODING | ||||||||
Position: |
|
||||||||
Sequence: |
Protein RefSeqs | NP_001138230 | (Get FASTA) | NCBI Sequence Viewer |
NP_001138231 | (Get FASTA) | NCBI Sequence Viewer | |
NP_055972 | (Get FASTA) | NCBI Sequence Viewer | |
XP_005271525 | (Get FASTA) | NCBI Sequence Viewer | |
XP_005271526 | (Get FASTA) | NCBI Sequence Viewer | |
XP_005271527 | (Get FASTA) | NCBI Sequence Viewer | |
XP_005271528 | (Get FASTA) | NCBI Sequence Viewer | |
XP_005271529 | (Get FASTA) | NCBI Sequence Viewer | |
XP_005271530 | (Get FASTA) | NCBI Sequence Viewer | |
XP_005271531 | (Get FASTA) | NCBI Sequence Viewer | |
XP_005271532 | (Get FASTA) | NCBI Sequence Viewer | |
XP_005277737 | (Get FASTA) | NCBI Sequence Viewer | |
XP_006718860 | (Get FASTA) | NCBI Sequence Viewer | |
XP_006718861 | (Get FASTA) | NCBI Sequence Viewer | |
XP_006718862 | (Get FASTA) | NCBI Sequence Viewer | |
XP_006718863 | (Get FASTA) | NCBI Sequence Viewer | |
XP_006718864 | (Get FASTA) | NCBI Sequence Viewer | |
XP_006718865 | (Get FASTA) | NCBI Sequence Viewer | |
XP_006718866 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011541005 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011541006 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011541007 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011541008 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011541009 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011541010 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011541011 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011541012 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011541016 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011541017 | (Get FASTA) | NCBI Sequence Viewer | |
XP_016872896 | (Get FASTA) | NCBI Sequence Viewer | |
XP_016872897 | (Get FASTA) | NCBI Sequence Viewer | |
XP_016872898 | (Get FASTA) | NCBI Sequence Viewer | |
XP_016872899 | (Get FASTA) | NCBI Sequence Viewer | |
XP_016872900 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047282588 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047282589 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047282590 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047282591 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047282592 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047282593 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047282594 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047282595 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047282596 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047282597 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047282598 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047282599 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047282600 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047282601 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047282602 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047282603 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047282604 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224116 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224117 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224118 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224119 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224120 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224121 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224122 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224123 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224124 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224125 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224126 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224127 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224128 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224129 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224130 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224131 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224132 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224133 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224134 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224135 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224136 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224137 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224138 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224139 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224140 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224141 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224142 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224143 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224144 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224145 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224146 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224147 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224148 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224149 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224150 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224151 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224152 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224153 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224154 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224155 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224156 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224157 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224158 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224159 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224160 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224161 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224162 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054224163 | (Get FASTA) | NCBI Sequence Viewer | |
GenBank Protein | AAH13031 | (Get FASTA) | NCBI Sequence Viewer |
AAH14510 | (Get FASTA) | NCBI Sequence Viewer | |
AAH98586 | (Get FASTA) | NCBI Sequence Viewer | |
ACA06041 | (Get FASTA) | NCBI Sequence Viewer | |
ACA06042 | (Get FASTA) | NCBI Sequence Viewer | |
ACA06043 | (Get FASTA) | NCBI Sequence Viewer | |
BAA31613 | (Get FASTA) | NCBI Sequence Viewer | |
BAB55164 | (Get FASTA) | NCBI Sequence Viewer | |
BAB84896 | (Get FASTA) | NCBI Sequence Viewer | |
BAC11292 | (Get FASTA) | NCBI Sequence Viewer | |
BAC76044 | (Get FASTA) | NCBI Sequence Viewer | |
BAC86289 | (Get FASTA) | NCBI Sequence Viewer | |
BAD66837 | (Get FASTA) | NCBI Sequence Viewer | |
BAG51996 | (Get FASTA) | NCBI Sequence Viewer | |
BAG58636 | (Get FASTA) | NCBI Sequence Viewer | |
BAG59029 | (Get FASTA) | NCBI Sequence Viewer | |
BAH11805 | (Get FASTA) | NCBI Sequence Viewer | |
CAH18649 | (Get FASTA) | NCBI Sequence Viewer | |
EAW67400 | (Get FASTA) | NCBI Sequence Viewer | |
EAW67401 | (Get FASTA) | NCBI Sequence Viewer | |
EAW67402 | (Get FASTA) | NCBI Sequence Viewer | |
EAW67403 | (Get FASTA) | NCBI Sequence Viewer | |
EAW67404 | (Get FASTA) | NCBI Sequence Viewer | |
EAW67405 | (Get FASTA) | NCBI Sequence Viewer | |
EAW67406 | (Get FASTA) | NCBI Sequence Viewer | |
EAW67407 | (Get FASTA) | NCBI Sequence Viewer | |
Ensembl Protein | ENSP00000348359 | ||
ENSP00000348359.5 | |||
ENSP00000354498 | |||
ENSP00000354498.2 | |||
ENSP00000431508.1 | |||
ENSP00000435520.1 | |||
ENSP00000469820 | |||
ENSP00000469820.1 | |||
ENSP00000478254.1 | |||
ENSP00000482728.1 | |||
GenBank Protein | Q86UU1 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_055972 ⟸ NM_015157 |
- Peptide Label: | isoform a |
- UniProtKB: | Q4KMF8 (UniProtKB/Swiss-Prot), O75133 (UniProtKB/Swiss-Prot), B0YJ64 (UniProtKB/Swiss-Prot), B0YJ63 (UniProtKB/Swiss-Prot), Q8TEQ2 (UniProtKB/Swiss-Prot), Q86UU1 (UniProtKB/Swiss-Prot), Q5W9G0 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001138230 ⟸ NM_001144758 |
- Peptide Label: | isoform a |
- UniProtKB: | B0YJ63 (UniProtKB/Swiss-Prot), Q4KMF8 (UniProtKB/Swiss-Prot), O75133 (UniProtKB/Swiss-Prot), B0YJ64 (UniProtKB/Swiss-Prot), Q8TEQ2 (UniProtKB/Swiss-Prot), Q86UU1 (UniProtKB/Swiss-Prot), Q5W9G0 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001138231 ⟸ NM_001144759 |
- Peptide Label: | isoform b |
- UniProtKB: | Q5W9G0 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_005271527 ⟸ XM_005271470 |
- Peptide Label: | isoform X20 |
- Sequence: |
RefSeq Acc Id: | XP_005271525 ⟸ XM_005271468 |
- Peptide Label: | isoform X17 |
- Sequence: |
RefSeq Acc Id: | XP_005271526 ⟸ XM_005271469 |
- Peptide Label: | isoform X19 |
- Sequence: |
RefSeq Acc Id: | XP_005271528 ⟸ XM_005271471 |
- Peptide Label: | isoform X23 |
- Sequence: |
RefSeq Acc Id: | XP_005271529 ⟸ XM_005271472 |
- Peptide Label: | isoform X26 |
- Sequence: |
RefSeq Acc Id: | XP_005271530 ⟸ XM_005271473 |
- Peptide Label: | isoform X28 |
- Sequence: |
RefSeq Acc Id: | XP_005271531 ⟸ XM_005271474 |
- Peptide Label: | isoform X29 |
- Sequence: |
RefSeq Acc Id: | XP_005271532 ⟸ XM_005271475 |
- Peptide Label: | isoform X41 |
- Sequence: |
RefSeq Acc Id: | XP_006718860 ⟸ XM_006718797 |
- Peptide Label: | isoform X9 |
- Sequence: |
RefSeq Acc Id: | XP_006718861 ⟸ XM_006718798 |
- Peptide Label: | isoform X14 |
- Sequence: |
RefSeq Acc Id: | XP_006718862 ⟸ XM_006718799 |
- Peptide Label: | isoform X15 |
- Sequence: |
RefSeq Acc Id: | XP_006718863 ⟸ XM_006718800 |
- Peptide Label: | isoform X16 |
- Sequence: |
RefSeq Acc Id: | XP_006718864 ⟸ XM_006718801 |
- Peptide Label: | isoform X18 |
- Sequence: |
RefSeq Acc Id: | XP_006718865 ⟸ XM_006718802 |
- Peptide Label: | isoform X22 |
- Sequence: |
RefSeq Acc Id: | XP_006718866 ⟸ XM_006718803 |
- Peptide Label: | isoform X24 |
- Sequence: |
RefSeq Acc Id: | XP_005277737 ⟸ XM_005277680 |
- Peptide Label: | isoform X2 |
- Sequence: |
RefSeq Acc Id: | XP_011541011 ⟸ XM_011542709 |
- Peptide Label: | isoform X8 |
- Sequence: |
RefSeq Acc Id: | XP_011541010 ⟸ XM_011542708 |
- Peptide Label: | isoform X8 |
- Sequence: |
RefSeq Acc Id: | XP_011541005 ⟸ XM_011542703 |
- Peptide Label: | isoform X1 |
- Sequence: |
RefSeq Acc Id: | XP_011541006 ⟸ XM_011542704 |
- Peptide Label: | isoform X3 |
- Sequence: |
RefSeq Acc Id: | XP_011541007 ⟸ XM_011542705 |
- Peptide Label: | isoform X4 |
- Sequence: |
RefSeq Acc Id: | XP_011541008 ⟸ XM_011542706 |
- Peptide Label: | isoform X5 |
- Sequence: |
RefSeq Acc Id: | XP_011541012 ⟸ XM_011542710 |
- Peptide Label: | isoform X10 |
- Sequence: |
RefSeq Acc Id: | XP_011541009 ⟸ XM_011542707 |
- Peptide Label: | isoform X6 |
- Sequence: |
RefSeq Acc Id: | XP_011541016 ⟸ XM_011542714 |
- Peptide Label: | isoform X42 |
- Sequence: |
RefSeq Acc Id: | XP_011541017 ⟸ XM_011542715 |
- Peptide Label: | isoform X43 |
- UniProtKB: | Q96D60 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_016872898 ⟸ XM_017017409 |
- Peptide Label: | isoform X12 |
- Sequence: |
RefSeq Acc Id: | XP_016872897 ⟸ XM_017017408 |
- Peptide Label: | isoform X11 |
- Sequence: |
RefSeq Acc Id: | XP_016872899 ⟸ XM_017017410 |
- Peptide Label: | isoform X13 |
- Sequence: |
RefSeq Acc Id: | XP_016872896 ⟸ XM_017017407 |
- Peptide Label: | isoform X7 |
- Sequence: |
RefSeq Acc Id: | XP_016872900 ⟸ XM_017017411 |
- Peptide Label: | isoform X41 |
- Sequence: |
RefSeq Acc Id: | ENSP00000481393 ⟸ ENST00000530708 |
RefSeq Acc Id: | ENSP00000431508 ⟸ ENST00000530994 |
RefSeq Acc Id: | ENSP00000354498 ⟸ ENST00000361417 |
RefSeq Acc Id: | ENSP00000478254 ⟸ ENST00000532639 |
RefSeq Acc Id: | ENSP00000482728 ⟸ ENST00000534140 |
RefSeq Acc Id: | ENSP00000469820 ⟸ ENST00000600882 |
RefSeq Acc Id: | ENSP00000348359 ⟸ ENST00000356063 |
RefSeq Acc Id: | ENSP00000435520 ⟸ ENST00000528594 |
RefSeq Acc Id: | XP_047282596 ⟸ XM_047426640 |
- Peptide Label: | isoform X32 |
RefSeq Acc Id: | XP_047282593 ⟸ XM_047426637 |
- Peptide Label: | isoform X30 |
RefSeq Acc Id: | XP_047282594 ⟸ XM_047426638 |
- Peptide Label: | isoform X31 |
RefSeq Acc Id: | XP_047282595 ⟸ XM_047426639 |
- Peptide Label: | isoform X32 |
RefSeq Acc Id: | XP_047282597 ⟸ XM_047426641 |
- Peptide Label: | isoform X33 |
RefSeq Acc Id: | XP_047282588 ⟸ XM_047426632 |
- Peptide Label: | isoform X21 |
RefSeq Acc Id: | XP_047282590 ⟸ XM_047426634 |
- Peptide Label: | isoform X44 |
RefSeq Acc Id: | XP_047282589 ⟸ XM_047426633 |
- Peptide Label: | isoform X25 |
RefSeq Acc Id: | XP_047282591 ⟸ XM_047426635 |
- Peptide Label: | isoform X27 |
RefSeq Acc Id: | XP_047282592 ⟸ XM_047426636 |
- Peptide Label: | isoform X45 |
RefSeq Acc Id: | XP_047282604 ⟸ XM_047426648 |
- Peptide Label: | isoform X40 |
RefSeq Acc Id: | XP_047282601 ⟸ XM_047426645 |
- Peptide Label: | isoform X37 |
RefSeq Acc Id: | XP_047282598 ⟸ XM_047426642 |
- Peptide Label: | isoform X34 |
RefSeq Acc Id: | XP_047282603 ⟸ XM_047426647 |
- Peptide Label: | isoform X39 |
RefSeq Acc Id: | XP_047282600 ⟸ XM_047426644 |
- Peptide Label: | isoform X36 |
RefSeq Acc Id: | XP_047282602 ⟸ XM_047426646 |
- Peptide Label: | isoform X38 |
RefSeq Acc Id: | XP_047282599 ⟸ XM_047426643 |
- Peptide Label: | isoform X35 |
RefSeq Acc Id: | XP_054224124 ⟸ XM_054368149 |
- Peptide Label: | isoform X8 |
RefSeq Acc Id: | XP_054224148 ⟸ XM_054368173 |
- Peptide Label: | isoform X30 |
RefSeq Acc Id: | XP_054224149 ⟸ XM_054368174 |
- Peptide Label: | isoform X31 |
RefSeq Acc Id: | XP_054224150 ⟸ XM_054368175 |
- Peptide Label: | isoform X32 |
RefSeq Acc Id: | XP_054224152 ⟸ XM_054368177 |
- Peptide Label: | isoform X33 |
RefSeq Acc Id: | XP_054224123 ⟸ XM_054368148 |
- Peptide Label: | isoform X8 |
RefSeq Acc Id: | XP_054224151 ⟸ XM_054368176 |
- Peptide Label: | isoform X32 |
RefSeq Acc Id: | XP_054224146 ⟸ XM_054368171 |
- Peptide Label: | isoform X29 |
RefSeq Acc Id: | XP_054224116 ⟸ XM_054368141 |
- Peptide Label: | isoform X1 |
RefSeq Acc Id: | XP_054224118 ⟸ XM_054368143 |
- Peptide Label: | isoform X3 |
RefSeq Acc Id: | XP_054224119 ⟸ XM_054368144 |
- Peptide Label: | isoform X4 |
RefSeq Acc Id: | XP_054224120 ⟸ XM_054368145 |
- Peptide Label: | isoform X5 |
RefSeq Acc Id: | XP_054224126 ⟸ XM_054368151 |
- Peptide Label: | isoform X10 |
RefSeq Acc Id: | XP_054224128 ⟸ XM_054368153 |
- Peptide Label: | isoform X12 |
RefSeq Acc Id: | XP_054224125 ⟸ XM_054368150 |
- Peptide Label: | isoform X9 |
RefSeq Acc Id: | XP_054224127 ⟸ XM_054368152 |
- Peptide Label: | isoform X11 |
RefSeq Acc Id: | XP_054224130 ⟸ XM_054368155 |
- Peptide Label: | isoform X14 |
RefSeq Acc Id: | XP_054224131 ⟸ XM_054368156 |
- Peptide Label: | isoform X15 |
RefSeq Acc Id: | XP_054224132 ⟸ XM_054368157 |
- Peptide Label: | isoform X16 |
RefSeq Acc Id: | XP_054224134 ⟸ XM_054368159 |
- Peptide Label: | isoform X18 |
RefSeq Acc Id: | XP_054224137 ⟸ XM_054368162 |
- Peptide Label: | isoform X21 |
RefSeq Acc Id: | XP_054224138 ⟸ XM_054368163 |
- Peptide Label: | isoform X22 |
RefSeq Acc Id: | XP_054224140 ⟸ XM_054368165 |
- Peptide Label: | isoform X24 |
RefSeq Acc Id: | XP_054224121 ⟸ XM_054368146 |
- Peptide Label: | isoform X6 |
RefSeq Acc Id: | XP_054224129 ⟸ XM_054368154 |
- Peptide Label: | isoform X13 |
RefSeq Acc Id: | XP_054224133 ⟸ XM_054368158 |
- Peptide Label: | isoform X17 |
RefSeq Acc Id: | XP_054224135 ⟸ XM_054368160 |
- Peptide Label: | isoform X19 |
RefSeq Acc Id: | XP_054224136 ⟸ XM_054368161 |
- Peptide Label: | isoform X20 |
RefSeq Acc Id: | XP_054224139 ⟸ XM_054368164 |
- Peptide Label: | isoform X23 |
RefSeq Acc Id: | XP_054224142 ⟸ XM_054368167 |
- Peptide Label: | isoform X26 |
RefSeq Acc Id: | XP_054224145 ⟸ XM_054368170 |
- Peptide Label: | isoform X28 |
RefSeq Acc Id: | XP_054224117 ⟸ XM_054368142 |
- Peptide Label: | isoform X2 |
RefSeq Acc Id: | XP_054224141 ⟸ XM_054368166 |
- Peptide Label: | isoform X25 |
RefSeq Acc Id: | XP_054224122 ⟸ XM_054368147 |
- Peptide Label: | isoform X7 |
RefSeq Acc Id: | XP_054224144 ⟸ XM_054368169 |
- Peptide Label: | isoform X27 |
RefSeq Acc Id: | XP_054224159 ⟸ XM_054368184 |
- Peptide Label: | isoform X40 |
RefSeq Acc Id: | XP_054224161 ⟸ XM_054368186 |
- Peptide Label: | isoform X41 |
RefSeq Acc Id: | XP_054224160 ⟸ XM_054368185 |
- Peptide Label: | isoform X41 |
RefSeq Acc Id: | XP_054224162 ⟸ XM_054368187 |
- Peptide Label: | isoform X42 |
RefSeq Acc Id: | XP_054224143 ⟸ XM_054368168 |
- Peptide Label: | isoform X46 |
RefSeq Acc Id: | XP_054224147 ⟸ XM_054368172 |
- Peptide Label: | isoform X47 |
RefSeq Acc Id: | XP_054224156 ⟸ XM_054368181 |
- Peptide Label: | isoform X37 |
RefSeq Acc Id: | XP_054224153 ⟸ XM_054368178 |
- Peptide Label: | isoform X34 |
RefSeq Acc Id: | XP_054224158 ⟸ XM_054368183 |
- Peptide Label: | isoform X39 |
RefSeq Acc Id: | XP_054224155 ⟸ XM_054368180 |
- Peptide Label: | isoform X36 |
RefSeq Acc Id: | XP_054224157 ⟸ XM_054368182 |
- Peptide Label: | isoform X38 |
RefSeq Acc Id: | XP_054224154 ⟸ XM_054368179 |
- Peptide Label: | isoform X35 |
RefSeq Acc Id: | XP_054224163 ⟸ XM_054368188 |
- Peptide Label: | isoform X43 |
Name | Modeler | Protein Id | AA Range | Protein Structure |
AF-Q86UU1-F1-model_v2 | AlphaFold | Q86UU1 | 1-1377 | view protein structure |
RGD ID: | 6789243 | ||||||||
Promoter ID: | HG_KWN:14335 | ||||||||
Type: | CpG-Island | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | CD4+TCell_2Hour, K562, NB4 | ||||||||
Transcripts: | ENST00000392852, NM_001144758, NM_001144759, UC001PTU.1 | ||||||||
Position: |
|
RGD ID: | 6810096 | ||||||||
Promoter ID: | HG_ACW:14510 | ||||||||
Type: | CpG-Island | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | HeLa_S3, K562 | ||||||||
Transcripts: | PHLDB1.QAPR07, PHLDB1.SAPR07 | ||||||||
Position: |
|
RGD ID: | 6810101 | ||||||||
Promoter ID: | HG_ACW:14511 | ||||||||
Type: | CpG-Island | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | HeLa_S3 | ||||||||
Transcripts: | PHLDB1.KAPR07, PHLDB1.TAPR07, PHLDB1.UAPR07, PHLDB1.VCAPR07, SERLEYBY.AAPR07-UNSPLICED | ||||||||
Position: |
|
RGD ID: | 7222321 | ||||||||
Promoter ID: | EPDNEW_H16906 | ||||||||
Type: | initiation region | ||||||||
Name: | PHLDB1_4 | ||||||||
Description: | pleckstrin homology like domain family B member 1 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H16907 EPDNEW_H16908 EPDNEW_H16909 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
|
RGD ID: | 7222323 | ||||||||
Promoter ID: | EPDNEW_H16907 | ||||||||
Type: | initiation region | ||||||||
Name: | PHLDB1_1 | ||||||||
Description: | pleckstrin homology like domain family B member 1 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H16906 EPDNEW_H16908 EPDNEW_H16909 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
|
RGD ID: | 7222325 | ||||||||
Promoter ID: | EPDNEW_H16908 | ||||||||
Type: | initiation region | ||||||||
Name: | PHLDB1_2 | ||||||||
Description: | pleckstrin homology like domain family B member 1 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H16906 EPDNEW_H16907 EPDNEW_H16909 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
|
RGD ID: | 7222329 | ||||||||
Promoter ID: | EPDNEW_H16909 | ||||||||
Type: | initiation region | ||||||||
Name: | PHLDB1_3 | ||||||||
Description: | pleckstrin homology like domain family B member 1 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H16906 EPDNEW_H16907 EPDNEW_H16908 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
|
Database | Acc Id | Source(s) |
AGR Gene | HGNC:23697 | AgrOrtholog |
COSMIC | PHLDB1 | COSMIC |
Ensembl Genes | ENSG00000019144 | Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Ensembl Transcript | ENST00000356063 | ENTREZGENE |
ENST00000356063.9 | UniProtKB/Swiss-Prot | |
ENST00000361417 | ENTREZGENE | |
ENST00000361417.6 | UniProtKB/Swiss-Prot | |
ENST00000528594.5 | UniProtKB/Swiss-Prot | |
ENST00000530994.5 | UniProtKB/Swiss-Prot | |
ENST00000532517 | ENTREZGENE | |
ENST00000532639.3 | UniProtKB/TrEMBL | |
ENST00000534140.2 | UniProtKB/TrEMBL | |
ENST00000600882 | ENTREZGENE | |
ENST00000600882.6 | UniProtKB/Swiss-Prot | |
ENST00000614369 | ENTREZGENE | |
Gene3D-CATH | 2.30.29.30 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
2.60.200.20 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
GTEx | ENSG00000019144 | GTEx |
HGNC ID | HGNC:23697 | ENTREZGENE |
Human Proteome Map | PHLDB1 | Human Proteome Map |
InterPro | Aconitase_4Fe-4S_BS | UniProtKB/TrEMBL |
FHA_dom | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
PH-like_dom_sf | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
PH_domain | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
PHLDB1/2/3_PH | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
SMAD_FHA_dom_sf | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
KEGG Report | hsa:23187 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
NCBI Gene | 23187 | ENTREZGENE |
OMIM | 612834 | OMIM |
PANTHER | PLECKSTRIN HOMOLOGY-LIKE DOMAIN FAMILY B MEMBER 1 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
PLECKSTRIN HOMOLOGY-LIKE DOMAIN, FAMILY B, MEMBER 3 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Pfam | FHA | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
PF00169 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
PharmGKB | PA134917952 | PharmGKB |
PROSITE | ACONITASE_2 | UniProtKB/TrEMBL |
PH_DOMAIN | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
SMART | SM00233 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Superfamily-SCOP | PH domain-like | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
SSF49879 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
UniProt | A0A087WTZ7_HUMAN | UniProtKB/TrEMBL |
A0A087WZL0_HUMAN | UniProtKB/TrEMBL | |
B0YJ63 | ENTREZGENE | |
B0YJ64 | ENTREZGENE | |
B0YJ65_HUMAN | UniProtKB/TrEMBL | |
O75133 | ENTREZGENE | |
PHLB1_HUMAN | UniProtKB/Swiss-Prot | |
Q4KMF8 | ENTREZGENE | |
Q5W9G0 | ENTREZGENE, UniProtKB/TrEMBL | |
Q6ZUD6_HUMAN | UniProtKB/TrEMBL | |
Q86UU1 | ENTREZGENE | |
Q8NC75_HUMAN | UniProtKB/TrEMBL | |
Q8TEQ2 | ENTREZGENE | |
Q96C94_HUMAN | UniProtKB/TrEMBL | |
Q96D60 | ENTREZGENE, UniProtKB/TrEMBL | |
UniProt Secondary | B0YJ63 | UniProtKB/Swiss-Prot |
B0YJ64 | UniProtKB/Swiss-Prot | |
O75133 | UniProtKB/Swiss-Prot | |
Q4KMF8 | UniProtKB/Swiss-Prot | |
Q8TEQ2 | UniProtKB/Swiss-Prot |
Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
---|---|---|---|---|---|---|---|
2016-02-02 | PHLDB1 | pleckstrin homology like domain family B member 1 | pleckstrin homology-like domain, family B, member 1 | Symbol and/or name change | 5135510 | APPROVED |