Imported Disease Annotations - CTDObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | ZFYVE16 | Human | Experimental Liver Cirrhosis | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:25380136 | |
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Imported Disease Annotations - CTDObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | ZFYVE16 | Human | Experimental Liver Cirrhosis | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:25380136 | |
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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. | PID Annotation Import Pipeline | Pipeline to import Pathway Interaction Database annotations from NCI into RGD |
4. | Data Import for Chemical-Gene Interactions | RGD automated import pipeline for gene-chemical interactions |
PMID:8889548 | PMID:9205841 | PMID:11433298 | PMID:11546807 | PMID:12477932 | PMID:14613930 | PMID:14702039 | PMID:15144186 | PMID:15231748 | PMID:15489334 | PMID:15592455 | PMID:15621726 |
PMID:15657082 | PMID:16344560 | PMID:16775010 | PMID:17272273 | PMID:17356069 | PMID:17570516 | PMID:18029348 | PMID:19887107 | PMID:21832049 | PMID:21873635 | PMID:22939629 | PMID:25281560 |
PMID:25468996 | PMID:26186194 | PMID:26496610 | PMID:26944198 | PMID:26972000 | PMID:27880917 | PMID:28514442 | PMID:28675297 | PMID:29229926 | PMID:29467281 | PMID:29568061 | PMID:29653964 |
PMID:30021884 | PMID:31452512 | PMID:31732153 | PMID:31871319 | PMID:33417871 | PMID:33545068 | PMID:33916271 | PMID:33961781 | PMID:34079125 | PMID:34369648 | PMID:34432599 | PMID:34597346 |
PMID:34672947 | PMID:34672954 | PMID:34702444 | PMID:34709266 | PMID:34709727 | PMID:34761192 | PMID:35384245 | PMID:35439318 | PMID:36114006 | PMID:36215168 | PMID:37223481 | PMID:37232246 |
PMID:37827155 | PMID:38113892 | PMID:38803224 | PMID:38943005 | PMID:39098523 | PMID:39231216 |
ZFYVE16 (Homo sapiens - human) |
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Zfyve16 (Mus musculus - house mouse) |
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Zfyve16 (Rattus norvegicus - Norway rat) |
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Zfyve16 (Chinchilla lanigera - long-tailed chinchilla) |
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ZFYVE16 (Pan paniscus - bonobo/pygmy chimpanzee) |
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ZFYVE16 (Canis lupus familiaris - dog) |
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Zfyve16 (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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ZFYVE16 (Sus scrofa - pig) |
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ZFYVE16 (Chlorocebus sabaeus - green monkey) |
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Zfyve16 (Heterocephalus glaber - naked mole-rat) |
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Variants in ZFYVE16
75 total Variants |
Name | Type | Condition(s) | Position(s) | Clinical significance |
GRCh38/hg38 5q13.3-22.1(chr5:74163186-110809453)x3 | copy number gain | See cases [RCV000051839] | Chr5:74163186..110809453 [GRCh38] Chr5:73459011..110145153 [GRCh37] Chr5:73494767..110173052 [NCBI36] Chr5:5q13.3-22.1 |
pathogenic |
GRCh38/hg38 5q14.1(chr5:79665668-81197686)x1 | copy number loss | See cases [RCV000052576] | Chr5:79665668..81197686 [GRCh38] Chr5:78961491..80493505 [GRCh37] Chr5:78997247..80529261 [NCBI36] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.3442G>T (p.Asp1148Tyr) | single nucleotide variant | Cerebral arteriovenous malformation [RCV000656334] | Chr5:80451544 [GRCh38] Chr5:79747363 [GRCh37] Chr5:5q14.1 |
likely pathogenic |
GRCh37/hg19 5q14.1(chr5:79678575-80868550)x3 | copy number gain | See cases [RCV000448914] | Chr5:79678575..80868550 [GRCh37] Chr5:5q14.1 |
uncertain significance |
GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1 | copy number loss | See cases [RCV000511978] | Chr5:17628741..176575720 [GRCh37] Chr5:5p15.1-q35.2 |
pathogenic |
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3 | copy number gain | See cases [RCV000512039] | Chr5:113577..180719789 [GRCh37] Chr5:5p15.33-q35.3 |
pathogenic |
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789) | copy number gain | See cases [RCV000510723] | Chr5:113577..180719789 [GRCh37] Chr5:5p15.33-q35.3 |
pathogenic |
NM_001284236.3(ZFYVE16):c.1948A>G (p.Lys650Glu) | single nucleotide variant | not specified [RCV004317934] | Chr5:80438633 [GRCh38] Chr5:79734452 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.218A>G (p.Tyr73Cys) | single nucleotide variant | not specified [RCV004320745] | Chr5:80436903 [GRCh38] Chr5:79732722 [GRCh37] Chr5:5q14.1 |
likely benign |
GRCh37/hg19 5q14.1(chr5:79625636-80884586)x3 | copy number gain | not provided [RCV000682570] | Chr5:79625636..80884586 [GRCh37] Chr5:5q14.1 |
uncertain significance |
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3 | copy number gain | not provided [RCV000744323] | Chr5:25328..180693344 [GRCh37] Chr5:5p15.33-q35.3 |
pathogenic |
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3 | copy number gain | not provided [RCV000744317] | Chr5:13648..180905029 [GRCh37] Chr5:5p15.33-q35.3 |
pathogenic |
NM_001284236.3(ZFYVE16):c.3755G>C (p.Gly1252Ala) | single nucleotide variant | Dextrocardia [RCV000754895] | Chr5:80456525 [GRCh38] Chr5:79752344 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.1798G>A (p.Asp600Asn) | single nucleotide variant | Dextrocardia [RCV000754894] | Chr5:80438483 [GRCh38] Chr5:79734302 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.127G>A (p.Val43Ile) | single nucleotide variant | not provided [RCV000886537] | Chr5:80436812 [GRCh38] Chr5:79732631 [GRCh37] Chr5:5q14.1 |
benign |
Single allele | deletion | Neurodevelopmental disorder [RCV000787436] | Chr5:14685137..149511942 [GRCh37] Chr5:5p15.2-q32 |
uncertain significance |
GRCh37/hg19 5q14.1(chr5:79528733-80545287)x3 | copy number gain | not provided [RCV001005691] | Chr5:79528733..80545287 [GRCh37] Chr5:5q14.1 |
uncertain significance |
GRCh37/hg19 5q14.1(chr5:79664621-80767791)x3 | copy number gain | not provided [RCV000845611] | Chr5:79664621..80767791 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.3617C>T (p.Ala1206Val) | single nucleotide variant | not specified [RCV004316673] | Chr5:80455701 [GRCh38] Chr5:79751520 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.4383G>A (p.Ala1461=) | single nucleotide variant | not provided [RCV000886538] | Chr5:80474752 [GRCh38] Chr5:79770571 [GRCh37] Chr5:5q14.1 |
benign |
NM_001284236.3(ZFYVE16):c.749G>A (p.Arg250Gln) | single nucleotide variant | not provided [RCV000946855] | Chr5:80437434 [GRCh38] Chr5:79733253 [GRCh37] Chr5:5q14.1 |
benign |
NM_001284236.3(ZFYVE16):c.1181G>A (p.Arg394Gln) | single nucleotide variant | not provided [RCV000946856] | Chr5:80437866 [GRCh38] Chr5:79733685 [GRCh37] Chr5:5q14.1 |
benign |
GRCh37/hg19 5q13.2-15(chr5:72790061-97478870)x3 | copy number gain | not provided [RCV001005683] | Chr5:72790061..97478870 [GRCh37] Chr5:5q13.2-15 |
pathogenic |
GRCh37/hg19 5q14.1(chr5:79705427-80237350)x3 | copy number gain | not provided [RCV001005692] | Chr5:79705427..80237350 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.1780A>G (p.Ile594Val) | single nucleotide variant | not specified [RCV004271692] | Chr5:80438465 [GRCh38] Chr5:79734284 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.1058A>G (p.Asp353Gly) | single nucleotide variant | not specified [RCV004139657] | Chr5:80437743 [GRCh38] Chr5:79733562 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.3047C>G (p.Pro1016Arg) | single nucleotide variant | not specified [RCV004188913] | Chr5:80448348 [GRCh38] Chr5:79744167 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.1079C>G (p.Ser360Cys) | single nucleotide variant | not specified [RCV004209325] | Chr5:80437764 [GRCh38] Chr5:79733583 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2020A>G (p.Ile674Val) | single nucleotide variant | not specified [RCV004086171] | Chr5:80438705 [GRCh38] Chr5:79734524 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.920C>T (p.Pro307Leu) | single nucleotide variant | not specified [RCV004216274] | Chr5:80437605 [GRCh38] Chr5:79733424 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2591C>G (p.Ser864Cys) | single nucleotide variant | not specified [RCV004083156] | Chr5:80445272 [GRCh38] Chr5:79741091 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.197G>T (p.Cys66Phe) | single nucleotide variant | not specified [RCV004188874] | Chr5:80436882 [GRCh38] Chr5:79732701 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.1382C>G (p.Thr461Arg) | single nucleotide variant | not specified [RCV004195857] | Chr5:80438067 [GRCh38] Chr5:79733886 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2185A>G (p.Asn729Asp) | single nucleotide variant | not specified [RCV004239935] | Chr5:80438870 [GRCh38] Chr5:79734689 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.922A>G (p.Lys308Glu) | single nucleotide variant | not specified [RCV004076114] | Chr5:80437607 [GRCh38] Chr5:79733426 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.3274T>G (p.Leu1092Val) | single nucleotide variant | not specified [RCV004141825] | Chr5:80450478 [GRCh38] Chr5:79746297 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.764T>C (p.Met255Thr) | single nucleotide variant | not specified [RCV004154390] | Chr5:80437449 [GRCh38] Chr5:79733268 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.1364A>G (p.Lys455Arg) | single nucleotide variant | not specified [RCV004214638] | Chr5:80438049 [GRCh38] Chr5:79733868 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.3580A>G (p.Met1194Val) | single nucleotide variant | not specified [RCV004118203] | Chr5:80451682 [GRCh38] Chr5:79747501 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2423A>G (p.Gln808Arg) | single nucleotide variant | not specified [RCV004237393] | Chr5:80443126 [GRCh38] Chr5:79738945 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2962A>G (p.Ser988Gly) | single nucleotide variant | not specified [RCV004177933] | Chr5:80448263 [GRCh38] Chr5:79744082 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2683T>C (p.Cys895Arg) | single nucleotide variant | not specified [RCV004241710] | Chr5:80445364 [GRCh38] Chr5:79741183 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.4207G>A (p.Gly1403Arg) | single nucleotide variant | not specified [RCV004170634] | Chr5:80473773 [GRCh38] Chr5:79769592 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.3124C>T (p.Pro1042Ser) | single nucleotide variant | not specified [RCV004243630] | Chr5:80449611 [GRCh38] Chr5:79745430 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.1508T>C (p.Phe503Ser) | single nucleotide variant | not specified [RCV004168314] | Chr5:80438193 [GRCh38] Chr5:79734012 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.972C>A (p.Phe324Leu) | single nucleotide variant | not specified [RCV004193238] | Chr5:80437657 [GRCh38] Chr5:79733476 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.455A>G (p.Asp152Gly) | single nucleotide variant | not specified [RCV004180653] | Chr5:80437140 [GRCh38] Chr5:79732959 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.502T>C (p.Ser168Pro) | single nucleotide variant | not specified [RCV004103526] | Chr5:80437187 [GRCh38] Chr5:79733006 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.4382C>T (p.Ala1461Val) | single nucleotide variant | not specified [RCV004081653] | Chr5:80474751 [GRCh38] Chr5:79770570 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2050G>A (p.Val684Ile) | single nucleotide variant | not specified [RCV004181389] | Chr5:80438735 [GRCh38] Chr5:79734554 [GRCh37] Chr5:5q14.1 |
likely benign |
NM_001284236.3(ZFYVE16):c.3440A>G (p.Lys1147Arg) | single nucleotide variant | not specified [RCV004177701] | Chr5:80451542 [GRCh38] Chr5:79747361 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2668T>C (p.Ser890Pro) | single nucleotide variant | not specified [RCV004221521] | Chr5:80445349 [GRCh38] Chr5:79741168 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.1060A>G (p.Asn354Asp) | single nucleotide variant | not specified [RCV004167556] | Chr5:80437745 [GRCh38] Chr5:79733564 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2546T>G (p.Leu849Trp) | single nucleotide variant | not specified [RCV004105122] | Chr5:80443249 [GRCh38] Chr5:79739068 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.3463A>G (p.Ile1155Val) | single nucleotide variant | not specified [RCV004073737] | Chr5:80451565 [GRCh38] Chr5:79747384 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.187G>A (p.Val63Ile) | single nucleotide variant | not specified [RCV004185549] | Chr5:80436872 [GRCh38] Chr5:79732691 [GRCh37] Chr5:5q14.1 |
likely benign |
NM_001284236.3(ZFYVE16):c.1408G>T (p.Gly470Cys) | single nucleotide variant | not specified [RCV004260380] | Chr5:80438093 [GRCh38] Chr5:79733912 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.1631C>T (p.Thr544Ile) | single nucleotide variant | not specified [RCV004286908] | Chr5:80438316 [GRCh38] Chr5:79734135 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.3832A>C (p.Ile1278Leu) | single nucleotide variant | not specified [RCV004262626] | Chr5:80456981 [GRCh38] Chr5:79752800 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.1985C>T (p.Ser662Leu) | single nucleotide variant | not specified [RCV004268148] | Chr5:80438670 [GRCh38] Chr5:79734489 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.1840A>G (p.Lys614Glu) | single nucleotide variant | not specified [RCV004277670] | Chr5:80438525 [GRCh38] Chr5:79734344 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.3361A>G (p.Ile1121Val) | single nucleotide variant | not specified [RCV004263637] | Chr5:80450565 [GRCh38] Chr5:79746384 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.250A>G (p.Thr84Ala) | single nucleotide variant | not specified [RCV004337685] | Chr5:80436935 [GRCh38] Chr5:79732754 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.1790A>G (p.Glu597Gly) | single nucleotide variant | not specified [RCV004351911] | Chr5:80438475 [GRCh38] Chr5:79734294 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.3119A>T (p.Glu1040Val) | single nucleotide variant | not specified [RCV004345714] | Chr5:80449606 [GRCh38] Chr5:79745425 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.3933T>G (p.His1311Gln) | single nucleotide variant | not specified [RCV004352130] | Chr5:80457082 [GRCh38] Chr5:79752901 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.858C>T (p.Val286=) | single nucleotide variant | not provided [RCV003429692] | Chr5:80437543 [GRCh38] Chr5:79733362 [GRCh37] Chr5:5q14.1 |
likely benign |
NM_001284236.3(ZFYVE16):c.1033G>T (p.Asp345Tyr) | single nucleotide variant | not specified [RCV004486264] | Chr5:80437718 [GRCh38] Chr5:79733537 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.1180C>T (p.Arg394Trp) | single nucleotide variant | not specified [RCV004486265] | Chr5:80437865 [GRCh38] Chr5:79733684 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2224C>G (p.Pro742Ala) | single nucleotide variant | not specified [RCV004486269] | Chr5:80438909 [GRCh38] Chr5:79734728 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2488A>G (p.Thr830Ala) | single nucleotide variant | not specified [RCV004486270] | Chr5:80443191 [GRCh38] Chr5:79739010 [GRCh37] Chr5:5q14.1 |
likely benign |
NM_001284236.3(ZFYVE16):c.4120G>T (p.Asp1374Tyr) | single nucleotide variant | not specified [RCV004486281] | Chr5:80472856 [GRCh38] Chr5:79768675 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.4277T>C (p.Ile1426Thr) | single nucleotide variant | not specified [RCV004486283] | Chr5:80473843 [GRCh38] Chr5:79769662 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.806G>A (p.Cys269Tyr) | single nucleotide variant | not specified [RCV004486286] | Chr5:80437491 [GRCh38] Chr5:79733310 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.889G>A (p.Gly297Ser) | single nucleotide variant | not specified [RCV004486288] | Chr5:80437574 [GRCh38] Chr5:79733393 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2924C>G (p.Thr975Ser) | single nucleotide variant | not specified [RCV004486274] | Chr5:80448225 [GRCh38] Chr5:79744044 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.3743A>T (p.His1248Leu) | single nucleotide variant | not specified [RCV004486279] | Chr5:80456513 [GRCh38] Chr5:79752332 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.868G>A (p.Ala290Thr) | single nucleotide variant | not specified [RCV004486287] | Chr5:80437553 [GRCh38] Chr5:79733372 [GRCh37] Chr5:5q14.1 |
likely benign |
NM_001284236.3(ZFYVE16):c.2121T>A (p.Asp707Glu) | single nucleotide variant | not specified [RCV004486268] | Chr5:80438806 [GRCh38] Chr5:79734625 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.4270G>C (p.Glu1424Gln) | single nucleotide variant | not specified [RCV004486282] | Chr5:80473836 [GRCh38] Chr5:79769655 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.3424A>G (p.Ser1142Gly) | single nucleotide variant | not specified [RCV004486277] | Chr5:80451526 [GRCh38] Chr5:79747345 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.362G>A (p.Arg121Gln) | single nucleotide variant | not specified [RCV004486278] | Chr5:80437047 [GRCh38] Chr5:79732866 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.4015A>G (p.Ile1339Val) | single nucleotide variant | not specified [RCV004486280] | Chr5:80459485 [GRCh38] Chr5:79755304 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2518A>T (p.Thr840Ser) | single nucleotide variant | not specified [RCV004486271] | Chr5:80443221 [GRCh38] Chr5:79739040 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2608G>T (p.Val870Leu) | single nucleotide variant | not specified [RCV004486272] | Chr5:80445289 [GRCh38] Chr5:79741108 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2986T>A (p.Ser996Thr) | single nucleotide variant | not specified [RCV004486276] | Chr5:80448287 [GRCh38] Chr5:79744106 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.155G>A (p.Arg52Gln) | single nucleotide variant | not specified [RCV004486267] | Chr5:80436840 [GRCh38] Chr5:79732659 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2753C>T (p.Ser918Phe) | single nucleotide variant | not specified [RCV004486273] | Chr5:80448054 [GRCh38] Chr5:79743873 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.656A>G (p.Tyr219Cys) | single nucleotide variant | not specified [RCV004486285] | Chr5:80437341 [GRCh38] Chr5:79733160 [GRCh37] Chr5:5q14.1 |
likely benign |
NM_001284236.3(ZFYVE16):c.1526A>G (p.Asp509Gly) | single nucleotide variant | not specified [RCV004687103] | Chr5:80438211 [GRCh38] Chr5:79734030 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2071A>G (p.Ile691Val) | single nucleotide variant | not specified [RCV004687106] | Chr5:80438756 [GRCh38] Chr5:79734575 [GRCh37] Chr5:5q14.1 |
likely benign |
NM_001284236.3(ZFYVE16):c.2620G>C (p.Asp874His) | single nucleotide variant | not specified [RCV004687100] | Chr5:80445301 [GRCh38] Chr5:79741120 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.932A>T (p.Asp311Val) | single nucleotide variant | not specified [RCV004687101] | Chr5:80437617 [GRCh38] Chr5:79733436 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2041G>A (p.Ala681Thr) | single nucleotide variant | not specified [RCV004687102] | Chr5:80438726 [GRCh38] Chr5:79734545 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.4583T>C (p.Ile1528Thr) | single nucleotide variant | not specified [RCV004687105] | Chr5:80477340 [GRCh38] Chr5:79773159 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.2881A>G (p.Thr961Ala) | single nucleotide variant | not specified [RCV004687099] | Chr5:80448182 [GRCh38] Chr5:79744001 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.62A>G (p.Gln21Arg) | single nucleotide variant | not specified [RCV004687097] | Chr5:80434209 [GRCh38] Chr5:79730028 [GRCh37] Chr5:5q14.1 |
uncertain significance |
NM_001284236.3(ZFYVE16):c.3325A>G (p.Thr1109Ala) | single nucleotide variant | not specified [RCV004687104] | Chr5:80450529 [GRCh38] Chr5:79746348 [GRCh37] Chr5:5q14.1 |
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. |
The following QTLs overlap with this region. | Full Report | CSV | TAB | Printer | Gviewer |
WI-15051 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
RH70374 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
SHGC-84992 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
WI-17790 |
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||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
STS-R68242 |
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||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
D15S1477 |
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||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
D8S2279 |
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||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
ZFYVE16 |
|
adipose tissue
|
alimentary part of gastrointestinal system
|
appendage
|
circulatory system
|
ectoderm
|
endocrine system
|
endoderm
|
entire extraembryonic component
|
exocrine system
|
hemolymphoid system
|
hepatobiliary system
|
integumental system
|
mesenchyme
|
mesoderm
|
musculoskeletal system
|
nervous system
|
pharyngeal arch
|
renal system
|
reproductive system
|
respiratory system
|
sensory system
|
visual system
|
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1204 | 2439 | 2788 | 2253 | 4973 | 1726 | 2351 | 6 | 624 | 1951 | 465 | 2269 | 7306 | 6472 | 53 | 3734 | 1 | 852 | 1744 | 1617 | 175 | 1 |
RefSeq Transcripts | NM_001105251 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
NM_001284236 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001284237 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001349434 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_014733 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NR_146172 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NR_146173 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NR_146174 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_005248632 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017010091 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017010092 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017010096 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_024446270 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_024446271 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_024446272 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_024446273 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047417941 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047417942 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047417943 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047417944 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047417946 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047417947 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054353902 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054353903 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054353904 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054353905 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054353906 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054353907 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054353908 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054353909 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054353910 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054353911 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_001742373 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_001742375 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_001742376 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_001742377 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_001742378 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_001742379 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_001742380 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_001742381 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_001742382 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_001742384 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_002956199 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_007058663 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_008487202 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GenBank Nucleotide | AB002303 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AC008771 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AF434817 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK090896 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK127003 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AL833087 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AW952550 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC030808 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC032227 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC063868 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BX537424 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BX649172 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BX956000 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CB854699 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH471084 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CP068273 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CR933621 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
DA216169 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
DA216340 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
DB208042 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
DR005686 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
KC877016 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
Ensembl Acc Id: | ENST00000338008 ⟹ ENSP00000337159 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000505560 ⟹ ENSP00000426848 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000507548 ⟹ ENSP00000421785 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000509558 ⟹ ENSP00000426536 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000509562 ⟹ ENSP00000422356 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000510158 ⟹ ENSP00000423663 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000510995 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000511050 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000511829 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000512442 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000512558 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000512907 | ||||||||
Type: | CODING | ||||||||
Position: |
|
Ensembl Acc Id: | ENST00000513789 ⟹ ENSP00000426500 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | NM_001105251 ⟹ NP_001098721 | ||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001284236 ⟹ NP_001271165 | ||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||
Position: |
|
||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001284237 ⟹ NP_001271166 | ||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||
Position: |
|
||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001349434 ⟹ NP_001336363 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | NM_014733 ⟹ NP_055548 | ||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NR_146172 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | NON-CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | NR_146173 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | NON-CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | NR_146174 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | NON-CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | XM_005248632 ⟹ XP_005248689 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_017010091 ⟹ XP_016865580 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_017010092 ⟹ XP_016865581 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_024446270 ⟹ XP_024302038 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_047417941 ⟹ XP_047273897 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047417942 ⟹ XP_047273898 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047417943 ⟹ XP_047273899 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047417944 ⟹ XP_047273900 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047417946 ⟹ XP_047273902 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047417947 ⟹ XP_047273903 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054353902 ⟹ XP_054209877 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054353903 ⟹ XP_054209878 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054353904 ⟹ XP_054209879 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054353905 ⟹ XP_054209880 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054353906 ⟹ XP_054209881 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054353907 ⟹ XP_054209882 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054353908 ⟹ XP_054209883 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054353909 ⟹ XP_054209884 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054353910 ⟹ XP_054209885 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054353911 ⟹ XP_054209886 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XR_007058663 | ||||||||
Type: | NON-CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XR_008487202 | ||||||||
Type: | NON-CODING | ||||||||
Position: |
|
Protein RefSeqs | NP_001098721 | (Get FASTA) | NCBI Sequence Viewer |
NP_001271165 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001271166 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001336363 | (Get FASTA) | NCBI Sequence Viewer | |
NP_055548 | (Get FASTA) | NCBI Sequence Viewer | |
XP_005248689 | (Get FASTA) | NCBI Sequence Viewer | |
XP_016865580 | (Get FASTA) | NCBI Sequence Viewer | |
XP_016865581 | (Get FASTA) | NCBI Sequence Viewer | |
XP_024302038 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047273897 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047273898 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047273899 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047273900 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047273902 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047273903 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054209877 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054209878 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054209879 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054209880 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054209881 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054209882 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054209883 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054209884 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054209885 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054209886 | (Get FASTA) | NCBI Sequence Viewer | |
GenBank Protein | AAH30808 | (Get FASTA) | NCBI Sequence Viewer |
AAL30772 | (Get FASTA) | NCBI Sequence Viewer | |
BAA20764 | (Get FASTA) | NCBI Sequence Viewer | |
BAG54419 | (Get FASTA) | NCBI Sequence Viewer | |
CAD89968 | (Get FASTA) | NCBI Sequence Viewer | |
CAD97666 | (Get FASTA) | NCBI Sequence Viewer | |
CAI45932 | (Get FASTA) | NCBI Sequence Viewer | |
EAW95850 | (Get FASTA) | NCBI Sequence Viewer | |
EAW95851 | (Get FASTA) | NCBI Sequence Viewer | |
Ensembl Protein | ENSP00000337159 | ||
ENSP00000337159.5 | |||
ENSP00000421785.1 | |||
ENSP00000422356.2 | |||
ENSP00000423663 | |||
ENSP00000423663.1 | |||
ENSP00000426500.1 | |||
ENSP00000426536.1 | |||
ENSP00000426848 | |||
ENSP00000426848.1 | |||
GenBank Protein | Q7Z3T8 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_001098721 ⟸ NM_001105251 |
- Peptide Label: | isoform a |
- UniProtKB: | Q8N5L3 (UniProtKB/Swiss-Prot), Q86T69 (UniProtKB/Swiss-Prot), Q7Z3T8 (UniProtKB/Swiss-Prot), Q7LAU7 (UniProtKB/Swiss-Prot), Q5H9U2 (UniProtKB/Swiss-Prot), O15023 (UniProtKB/Swiss-Prot), Q8NEK3 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | NP_055548 ⟸ NM_014733 |
- Peptide Label: | isoform a |
- UniProtKB: | Q8N5L3 (UniProtKB/Swiss-Prot), Q86T69 (UniProtKB/Swiss-Prot), Q7Z3T8 (UniProtKB/Swiss-Prot), Q7LAU7 (UniProtKB/Swiss-Prot), Q5H9U2 (UniProtKB/Swiss-Prot), O15023 (UniProtKB/Swiss-Prot), Q8NEK3 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | XP_005248689 ⟸ XM_005248632 |
- Peptide Label: | isoform X1 |
- UniProtKB: | Q8N5L3 (UniProtKB/Swiss-Prot), Q86T69 (UniProtKB/Swiss-Prot), Q7LAU7 (UniProtKB/Swiss-Prot), Q5H9U2 (UniProtKB/Swiss-Prot), O15023 (UniProtKB/Swiss-Prot), Q8NEK3 (UniProtKB/Swiss-Prot), Q7Z3T8 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | NP_001271165 ⟸ NM_001284236 |
- Peptide Label: | isoform a |
- UniProtKB: | Q8N5L3 (UniProtKB/Swiss-Prot), Q86T69 (UniProtKB/Swiss-Prot), Q7Z3T8 (UniProtKB/Swiss-Prot), Q7LAU7 (UniProtKB/Swiss-Prot), Q5H9U2 (UniProtKB/Swiss-Prot), O15023 (UniProtKB/Swiss-Prot), Q8NEK3 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | NP_001271166 ⟸ NM_001284237 |
- Peptide Label: | isoform b |
- Sequence: |
RefSeq Acc Id: | XP_016865581 ⟸ XM_017010092 |
- Peptide Label: | isoform X1 |
- UniProtKB: | Q8N5L3 (UniProtKB/Swiss-Prot), Q86T69 (UniProtKB/Swiss-Prot), Q7LAU7 (UniProtKB/Swiss-Prot), Q5H9U2 (UniProtKB/Swiss-Prot), O15023 (UniProtKB/Swiss-Prot), Q8NEK3 (UniProtKB/Swiss-Prot), Q7Z3T8 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | XP_016865580 ⟸ XM_017010091 |
- Peptide Label: | isoform X1 |
- UniProtKB: | Q8N5L3 (UniProtKB/Swiss-Prot), Q86T69 (UniProtKB/Swiss-Prot), Q7LAU7 (UniProtKB/Swiss-Prot), Q5H9U2 (UniProtKB/Swiss-Prot), O15023 (UniProtKB/Swiss-Prot), Q8NEK3 (UniProtKB/Swiss-Prot), Q7Z3T8 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | XP_024302038 ⟸ XM_024446270 |
- Peptide Label: | isoform X1 |
- UniProtKB: | Q8N5L3 (UniProtKB/Swiss-Prot), Q86T69 (UniProtKB/Swiss-Prot), Q7Z3T8 (UniProtKB/Swiss-Prot), Q7LAU7 (UniProtKB/Swiss-Prot), Q5H9U2 (UniProtKB/Swiss-Prot), O15023 (UniProtKB/Swiss-Prot), Q8NEK3 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | NP_001336363 ⟸ NM_001349434 |
- Peptide Label: | isoform a |
- UniProtKB: | Q8N5L3 (UniProtKB/Swiss-Prot), Q86T69 (UniProtKB/Swiss-Prot), Q7Z3T8 (UniProtKB/Swiss-Prot), Q7LAU7 (UniProtKB/Swiss-Prot), Q5H9U2 (UniProtKB/Swiss-Prot), O15023 (UniProtKB/Swiss-Prot), Q8NEK3 (UniProtKB/Swiss-Prot) |
- Sequence: |
Ensembl Acc Id: | ENSP00000426848 ⟸ ENST00000505560 |
Ensembl Acc Id: | ENSP00000421785 ⟸ ENST00000507548 |
Ensembl Acc Id: | ENSP00000426536 ⟸ ENST00000509558 |
Ensembl Acc Id: | ENSP00000422356 ⟸ ENST00000509562 |
Ensembl Acc Id: | ENSP00000337159 ⟸ ENST00000338008 |
Ensembl Acc Id: | ENSP00000423663 ⟸ ENST00000510158 |
Ensembl Acc Id: | ENSP00000426500 ⟸ ENST00000513789 |
RefSeq Acc Id: | XP_047273897 ⟸ XM_047417941 |
- Peptide Label: | isoform X1 |
- UniProtKB: | Q8N5L3 (UniProtKB/Swiss-Prot), Q86T69 (UniProtKB/Swiss-Prot), Q7Z3T8 (UniProtKB/Swiss-Prot), Q7LAU7 (UniProtKB/Swiss-Prot), Q5H9U2 (UniProtKB/Swiss-Prot), O15023 (UniProtKB/Swiss-Prot), Q8NEK3 (UniProtKB/Swiss-Prot) |
RefSeq Acc Id: | XP_047273898 ⟸ XM_047417942 |
- Peptide Label: | isoform X2 |
RefSeq Acc Id: | XP_047273899 ⟸ XM_047417943 |
- Peptide Label: | isoform X3 |
RefSeq Acc Id: | XP_047273903 ⟸ XM_047417947 |
- Peptide Label: | isoform X4 |
RefSeq Acc Id: | XP_047273902 ⟸ XM_047417946 |
- Peptide Label: | isoform X4 |
RefSeq Acc Id: | XP_047273900 ⟸ XM_047417944 |
- Peptide Label: | isoform X4 |
RefSeq Acc Id: | XP_054209879 ⟸ XM_054353904 |
- Peptide Label: | isoform X1 |
RefSeq Acc Id: | XP_054209877 ⟸ XM_054353902 |
- Peptide Label: | isoform X1 |
RefSeq Acc Id: | XP_054209881 ⟸ XM_054353906 |
- Peptide Label: | isoform X1 |
RefSeq Acc Id: | XP_054209878 ⟸ XM_054353903 |
- Peptide Label: | isoform X1 |
RefSeq Acc Id: | XP_054209880 ⟸ XM_054353905 |
- Peptide Label: | isoform X1 |
RefSeq Acc Id: | XP_054209882 ⟸ XM_054353907 |
- Peptide Label: | isoform X2 |
RefSeq Acc Id: | XP_054209883 ⟸ XM_054353908 |
- Peptide Label: | isoform X3 |
RefSeq Acc Id: | XP_054209886 ⟸ XM_054353911 |
- Peptide Label: | isoform X4 |
RefSeq Acc Id: | XP_054209885 ⟸ XM_054353910 |
- Peptide Label: | isoform X4 |
RefSeq Acc Id: | XP_054209884 ⟸ XM_054353909 |
- Peptide Label: | isoform X4 |
Name | Modeler | Protein Id | AA Range | Protein Structure |
AF-Q7Z3T8-F1-model_v2 | AlphaFold | Q7Z3T8 | 1-1539 | view protein structure |
RGD ID: | 6803716 | ||||||||
Promoter ID: | HG_KWN:50566 | ||||||||
Type: | CpG-Island | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, HeLa_S3, Jurkat, K562, Lymphoblastoid, NB4 | ||||||||
Transcripts: | NM_001105251, NM_014733, UC003KGP.2, UC003KGS.2, UC010JAK.1 | ||||||||
Position: |
|
RGD ID: | 6870054 | ||||||||
Promoter ID: | EPDNEW_H8164 | ||||||||
Type: | initiation region | ||||||||
Name: | ZFYVE16_2 | ||||||||
Description: | zinc finger FYVE-type containing 16 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H8165 | ||||||||
Experiment Methods: | Single-end sequencing.; Paired-end sequencing. | ||||||||
Position: |
|
RGD ID: | 6870000 | ||||||||
Promoter ID: | EPDNEW_H8165 | ||||||||
Type: | initiation region | ||||||||
Name: | ZFYVE16_1 | ||||||||
Description: | zinc finger FYVE-type containing 16 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H8164 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
|
Database | Acc Id | Source(s) |
AGR Gene | HGNC:20756 | AgrOrtholog |
COSMIC | ZFYVE16 | COSMIC |
Ensembl Genes | ENSG00000039319 | Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Ensembl Transcript | ENST00000338008 | ENTREZGENE |
ENST00000338008.9 | UniProtKB/Swiss-Prot | |
ENST00000505560 | ENTREZGENE | |
ENST00000505560.5 | UniProtKB/Swiss-Prot | |
ENST00000507548.1 | UniProtKB/TrEMBL | |
ENST00000509558.1 | UniProtKB/TrEMBL | |
ENST00000509562.2 | UniProtKB/TrEMBL | |
ENST00000510158 | ENTREZGENE | |
ENST00000510158.5 | UniProtKB/Swiss-Prot | |
ENST00000510995 | ENTREZGENE | |
ENST00000513789.1 | UniProtKB/TrEMBL | |
Gene3D-CATH | 3.30.40.10 | UniProtKB/Swiss-Prot |
3.30.500.40 | UniProtKB/Swiss-Prot | |
Domain of unknown function (DUF3480), N-terminal subdomain | UniProtKB/Swiss-Prot | |
GTEx | ENSG00000039319 | GTEx |
HGNC ID | HGNC:20756 | ENTREZGENE |
Human Proteome Map | ZFYVE16 | Human Proteome Map |
InterPro | DUF3480 | UniProtKB/Swiss-Prot |
SARA/endofin | UniProtKB/Swiss-Prot | |
Znf_FYVE | UniProtKB/Swiss-Prot | |
Znf_FYVE-rel | UniProtKB/Swiss-Prot | |
Znf_FYVE_PHD | UniProtKB/Swiss-Prot | |
Znf_RING/FYVE/PHD | UniProtKB/Swiss-Prot | |
KEGG Report | hsa:9765 | UniProtKB/Swiss-Prot |
NCBI Gene | 9765 | ENTREZGENE |
OMIM | 608880 | OMIM |
PANTHER | PTHR46319:SF1 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
ZINC FINGER FYVE DOMAIN-CONTAINING PROTEIN | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Pfam | DUF3480 | UniProtKB/Swiss-Prot |
FYVE | UniProtKB/Swiss-Prot | |
PharmGKB | PA134873366 | PharmGKB |
PIRSF | SARA/endofin | UniProtKB/Swiss-Prot |
PROSITE | ZF_FYVE | UniProtKB/Swiss-Prot |
SMART | DUF3480 | UniProtKB/Swiss-Prot |
FYVE | UniProtKB/Swiss-Prot | |
Superfamily-SCOP | SSF57903 | UniProtKB/Swiss-Prot |
UniProt | D6RC80_HUMAN | UniProtKB/TrEMBL |
H0Y8R0_HUMAN | UniProtKB/TrEMBL | |
H0YAA4_HUMAN | UniProtKB/TrEMBL | |
H0YAB1_HUMAN | UniProtKB/TrEMBL | |
O15023 | ENTREZGENE | |
Q5H9U2 | ENTREZGENE | |
Q7LAU7 | ENTREZGENE | |
Q7Z3T8 | ENTREZGENE | |
Q86T69 | ENTREZGENE | |
Q8N5L3 | ENTREZGENE | |
Q8NEK3 | ENTREZGENE | |
ZFY16_HUMAN | UniProtKB/Swiss-Prot | |
UniProt Secondary | O15023 | UniProtKB/Swiss-Prot |
Q5H9U2 | UniProtKB/Swiss-Prot | |
Q7LAU7 | UniProtKB/Swiss-Prot | |
Q86T69 | UniProtKB/Swiss-Prot | |
Q8N5L3 | UniProtKB/Swiss-Prot | |
Q8NEK3 | UniProtKB/Swiss-Prot |
Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
---|---|---|---|---|---|---|---|
2016-02-18 | ZFYVE16 | zinc finger FYVE-type containing 16 | ZFYVE16 | zinc finger, FYVE domain containing 16 | Symbol and/or name change | 5135510 | APPROVED |