Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | genetic disease | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | |
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Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | genetic disease | | IAGP | (Homo sapiens) more ... | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | |
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# | Reference Title | Reference Citation |
1. | Imbalanced Host Response to SARS-CoV-2 Drives Development of COVID-19. | Blanco-Melo D, etal., Cell. 2020 May 28;181(5):1036-1045.e9. doi: 10.1016/j.cell.2020.04.026. Epub 2020 May 15. |
2. | GOAs Human GO annotations | GOA_HUMAN data from the GO Consortium |
3. | Dysregulated expression of MIG/CXCL9, IP-10/CXCL10 and CXCL16 and their receptors in systemic sclerosis. | Rabquer BJ, etal., Arthritis Res Ther. 2011 Feb 8;13(1):R18. |
4. | ClinVar Automated Import and Annotation Pipeline | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
5. | Data Import for Chemical-Gene Interactions | RGD automated import pipeline for gene-chemical interactions |
6. | Heightened Innate Immune Responses in the Respiratory Tract of COVID-19 Patients. | Zhou Z, etal., Cell Host Microbe. 2020 Jun 10;27(6):883-890.e2. doi: 10.1016/j.chom.2020.04.017. Epub 2020 May 4. |
PMID:11017100 | PMID:11060282 | PMID:11290797 | PMID:12477932 | PMID:12902461 | PMID:12975309 | PMID:14625285 | PMID:14634054 | PMID:14699018 | PMID:14702039 | PMID:14988089 | PMID:15128827 |
PMID:15489334 | PMID:15555552 | PMID:15634930 | PMID:15836657 | PMID:15883016 | PMID:15934948 | PMID:16142401 | PMID:16200580 | PMID:16431903 | PMID:16849465 | PMID:17207965 | PMID:17300746 |
PMID:17363916 | PMID:17703412 | PMID:17803654 | PMID:17855433 | PMID:18194461 | PMID:18195710 | PMID:18240029 | PMID:18248772 | PMID:18250446 | PMID:18279707 | PMID:18293410 | PMID:18339644 |
PMID:18344492 | PMID:18373975 | PMID:18480749 | PMID:18514099 | PMID:18565283 | PMID:18577758 | PMID:18636150 | PMID:18760678 | PMID:19070478 | PMID:19258923 | PMID:19322201 | PMID:19415545 |
PMID:19426159 | PMID:19435795 | PMID:19490893 | PMID:19494317 | PMID:19528340 | PMID:19575365 | PMID:19578796 | PMID:19605674 | PMID:19674076 | PMID:19690611 | PMID:19729872 | PMID:19913121 |
PMID:19919988 | PMID:19954776 | PMID:20334513 | PMID:20503287 | PMID:20621591 | PMID:20628086 | PMID:20646641 | PMID:20848509 | PMID:20960183 | PMID:21233446 | PMID:21467783 | PMID:21468586 |
PMID:21471570 | PMID:21492481 | PMID:21505717 | PMID:21527066 | PMID:21612780 | PMID:21638128 | PMID:21773780 | PMID:21832049 | PMID:21845497 | PMID:21873635 | PMID:22055341 | PMID:22113484 |
PMID:22278019 | PMID:22378888 | PMID:22454615 | PMID:22627199 | PMID:22863086 | PMID:23009930 | PMID:23229614 | PMID:23398954 | PMID:23428418 | PMID:23628207 | PMID:23633118 | PMID:23743627 |
PMID:24064021 | PMID:24069377 | PMID:24162774 | PMID:24284794 | PMID:24302814 | PMID:24460887 | PMID:24489966 | PMID:24507753 | PMID:24513807 | PMID:24518602 | PMID:24623722 | PMID:24854635 |
PMID:24861945 | PMID:24897301 | PMID:25015061 | PMID:25142184 | PMID:25223819 | PMID:25372401 | PMID:25391425 | PMID:25416956 | PMID:25661686 | PMID:25904061 | PMID:26021984 | PMID:26045830 |
PMID:26058873 | PMID:26272362 | PMID:26345917 | PMID:26499307 | PMID:26621504 | PMID:26707275 | PMID:26708384 | PMID:26796342 | PMID:26799186 | PMID:27098626 | PMID:27355560 | PMID:27665581 |
PMID:27725631 | PMID:27784296 | PMID:27826097 | PMID:27869573 | PMID:27877078 | PMID:28286356 | PMID:28628472 | PMID:28633141 | PMID:28647282 | PMID:28698473 | PMID:28722105 | PMID:28759013 |
PMID:28816285 | PMID:28856928 | PMID:28886489 | PMID:28942364 | PMID:29353287 | PMID:29588487 | PMID:29779473 | PMID:29800106 | PMID:29909746 | PMID:29981574 | PMID:30049511 | PMID:30053055 |
PMID:30542347 | PMID:30792527 | PMID:30974114 | PMID:31033093 | PMID:31199046 | PMID:31270884 | PMID:31379980 | PMID:31527616 | PMID:31598726 | PMID:31752131 | PMID:31753588 | PMID:32012403 |
PMID:32163231 | PMID:32171552 | PMID:32296183 | PMID:32346064 | PMID:32365786 | PMID:32393512 | PMID:32535333 | PMID:32974919 | PMID:33306334 | PMID:33549109 | PMID:33637127 | PMID:33800554 |
PMID:33961781 | PMID:34275795 | PMID:34345211 | PMID:34353074 | PMID:34487815 | PMID:34882892 | PMID:34943917 | PMID:35120907 | PMID:35784287 | PMID:36216188 | PMID:36232370 | PMID:36373877 |
PMID:36670424 | PMID:36949045 | PMID:36950218 | PMID:37086937 | PMID:37499664 | PMID:37848726 | PMID:38044363 | PMID:38146125 |
CXCL16 (Homo sapiens - human) |
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Cxcl16 (Mus musculus - house mouse) |
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Cxcl16 (Rattus norvegicus - Norway rat) |
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Cxcl16 (Chinchilla lanigera - long-tailed chinchilla) |
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CXCL16 (Pan paniscus - bonobo/pygmy chimpanzee) |
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CXCL16 (Canis lupus familiaris - dog) |
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Cxcl16 (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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CXCL16 (Sus scrofa - pig) |
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CXCL16 (Chlorocebus sabaeus - green monkey) |
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Cxcl16 (Heterocephalus glaber - naked mole-rat) |
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Variants in CXCL16
13 total Variants |
Name | Type | Condition(s) | Position(s) | Clinical significance |
GRCh38/hg38 17p13.3-13.2(chr17:193307-5652222)x1 | copy number loss | See cases [RCV000053384] | Chr17:193307..5652222 [GRCh38] Chr17:45835..5555542 [GRCh37] Chr17:43098..5496266 [NCBI36] Chr17:17p13.3-13.2 |
pathogenic |
GRCh38/hg38 17p13.2-13.1(chr17:3601515-7178024)x1 | copy number loss | See cases [RCV000053406] | Chr17:3601515..7178024 [GRCh38] Chr17:3504809..7081343 [GRCh37] Chr17:3451558..7022067 [NCBI36] Chr17:17p13.2-13.1 |
pathogenic |
GRCh38/hg38 17p13.2(chr17:4141725-4841701)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054003]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054003]|See cases [RCV000054003] | Chr17:4141725..4841701 [GRCh38] Chr17:4045019..4744996 [GRCh37] Chr17:3991768..4691654 [NCBI36] Chr17:17p13.2 |
uncertain significance |
NM_001136046.2(ZMYND15):c.1360C>T (p.Pro454Ser) | single nucleotide variant | Malignant melanoma [RCV000071563] | Chr17:4743829 [GRCh38] Chr17:4647124 [GRCh37] Chr17:4593873 [NCBI36] Chr17:17p13.2 |
not provided |
NM_001100812.1(CXCL16):c.358+177C>T | single nucleotide variant | Lung cancer [RCV000100487] | Chr17:4738231 [GRCh38] Chr17:4641526 [GRCh37] Chr17:17p13.2 |
uncertain significance |
GRCh38/hg38 17p13.3-13.2(chr17:2062380-5258340)x1 | copy number loss | See cases [RCV000133721] | Chr17:2062380..5258340 [GRCh38] Chr17:1965674..5161635 [GRCh37] Chr17:1912424..5102359 [NCBI36] Chr17:17p13.3-13.2 |
pathogenic |
GRCh38/hg38 17p13.3-13.1(chr17:162088-6959050)x1 | copy number loss | See cases [RCV000134135] | Chr17:162088..6959050 [GRCh38] Chr17:45835..6862369 [GRCh37] Chr17:11879..6803093 [NCBI36] Chr17:17p13.3-13.1 |
pathogenic |
GRCh38/hg38 17p13.3-13.1(chr17:198748-7491129)x3 | copy number gain | See cases [RCV000134970] | Chr17:198748..7491129 [GRCh38] Chr17:50690..7394448 [GRCh37] Chr17:48539..7335172 [NCBI36] Chr17:17p13.3-13.1 |
pathogenic |
GRCh38/hg38 17p13.2(chr17:4044302-5943772)x1 | copy number loss | See cases [RCV000135548] | Chr17:4044302..5943772 [GRCh38] Chr17:3947596..5847092 [GRCh37] Chr17:3894345..5787816 [NCBI36] Chr17:17p13.2 |
likely pathogenic |
GRCh38/hg38 17p13.2(chr17:4141725-4778120)x1 | copy number loss | See cases [RCV000137514] | Chr17:4141725..4778120 [GRCh38] Chr17:4045019..4681415 [GRCh37] Chr17:3991768..4628164 [NCBI36] Chr17:17p13.2 |
uncertain significance |
GRCh38/hg38 17p13.3-13.1(chr17:162016-7697012)x1 | copy number loss | See cases [RCV000138214] | Chr17:162016..7697012 [GRCh38] Chr17:45835..7600330 [GRCh37] Chr17:11807..7541055 [NCBI36] Chr17:17p13.3-13.1 |
pathogenic |
GRCh38/hg38 17p13.3-12(chr17:162016-12343901)x3 | copy number gain | See cases [RCV000138531] | Chr17:162016..12343901 [GRCh38] Chr17:45835..12247218 [GRCh37] Chr17:11807..12187943 [NCBI36] Chr17:17p13.3-12 |
pathogenic |
GRCh38/hg38 17p13.2(chr17:4092608-5354473)x3 | copy number gain | See cases [RCV000139650] | Chr17:4092608..5354473 [GRCh38] Chr17:3995902..5257768 [GRCh37] Chr17:3942651..5198492 [NCBI36] Chr17:17p13.2 |
likely benign |
GRCh38/hg38 17p13.3-13.2(chr17:150732-5935377)x1 | copy number loss | See cases [RCV000141658] | Chr17:150732..5935377 [GRCh38] Chr17:525..5838697 [GRCh37] Chr17:525..5779421 [NCBI36] Chr17:17p13.3-13.2 |
pathogenic |
GRCh38/hg38 17p13.3-13.2(chr17:237248-4735533)x1 | copy number loss | See cases [RCV000141559] | Chr17:237248..4735533 [GRCh38] Chr17:396627..4638828 [GRCh37] Chr17:87039..4585577 [NCBI36] Chr17:17p13.3-13.2 |
pathogenic |
GRCh38/hg38 17p13.3-12(chr17:150732-14764202)x3 | copy number gain | See cases [RCV000142236] | Chr17:150732..14764202 [GRCh38] Chr17:525..14667519 [GRCh37] Chr17:525..14608244 [NCBI36] Chr17:17p13.3-12 |
pathogenic |
GRCh38/hg38 17p13.2(chr17:4141725-4873241)x3 | copy number gain | See cases [RCV000143014] | Chr17:4141725..4873241 [GRCh38] Chr17:4045019..4776536 [GRCh37] Chr17:3991768..4722711 [NCBI36] Chr17:17p13.2 |
uncertain significance |
GRCh37/hg19 17p13.2(chr17:4475016-4648525)x1 | copy number loss | See cases [RCV000449426] | Chr17:4475016..4648525 [GRCh37] Chr17:17p13.2 |
uncertain significance |
GRCh37/hg19 17p13.3-13.2(chr17:1751557-5378509)x1 | copy number loss | See cases [RCV000445994] | Chr17:1751557..5378509 [GRCh37] Chr17:17p13.3-13.2 |
pathogenic |
GRCh37/hg19 17p13.3-13.1(chr17:1113102-6742486) | copy number gain | See cases [RCV000445679] | Chr17:1113102..6742486 [GRCh37] Chr17:17p13.3-13.1 |
pathogenic |
GRCh37/hg19 17p13.2(chr17:4389607-4829150)x3 | copy number gain | See cases [RCV000448511] | Chr17:4389607..4829150 [GRCh37] Chr17:17p13.2 |
uncertain significance |
GRCh37/hg19 17p13.2(chr17:4633847-4856516)x1 | copy number loss | See cases [RCV000510443] | Chr17:4633847..4856516 [GRCh37] Chr17:17p13.2 |
uncertain significance |
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) | copy number gain | See cases [RCV000511439] | Chr17:526..81041938 [GRCh37] Chr17:17p13.3-q25.3 |
pathogenic |
GRCh37/hg19 17p13.3-12(chr17:525-15027737)x3 | copy number gain | See cases [RCV000511786] | Chr17:525..15027737 [GRCh37] Chr17:17p13.3-12 |
pathogenic |
NM_001386809.1(CXCL16):c.17G>T (p.Arg6Leu) | single nucleotide variant | Inborn genetic diseases [RCV003256900] | Chr17:4739323 [GRCh38] Chr17:4642618 [GRCh37] Chr17:17p13.2 |
uncertain significance |
NM_001386809.1(CXCL16):c.388G>A (p.Ala130Thr) | single nucleotide variant | Inborn genetic diseases [RCV003295159] | Chr17:4735422 [GRCh38] Chr17:4638717 [GRCh37] Chr17:17p13.2 |
uncertain significance |
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 | copy number gain | See cases [RCV000512441] | Chr17:526..81041938 [GRCh37] Chr17:17p13.3-q25.3 |
pathogenic |
GRCh37/hg19 17p13.3-12(chr17:525-11186432)x3 | copy number gain | not provided [RCV000683866] | Chr17:525..11186432 [GRCh37] Chr17:17p13.3-12 |
pathogenic |
GRCh37/hg19 17p13.2(chr17:4475016-4884701)x3 | copy number gain | not provided [RCV000683882] | Chr17:4475016..4884701 [GRCh37] Chr17:17p13.2 |
uncertain significance |
GRCh37/hg19 17p13.2(chr17:4633847-4926646)x3 | copy number gain | not provided [RCV000683883] | Chr17:4633847..4926646 [GRCh37] Chr17:17p13.2 |
uncertain significance |
GRCh37/hg19 17p13.2(chr17:4036861-5174346)x3 | copy number gain | not provided [RCV000683881] | Chr17:4036861..5174346 [GRCh37] Chr17:17p13.2 |
uncertain significance |
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 | copy number gain | not provided [RCV000739324] | Chr17:8547..81060040 [GRCh37] Chr17:17p13.3-q25.3 |
pathogenic |
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 | copy number gain | not provided [RCV000739320] | Chr17:7214..81058310 [GRCh37] Chr17:17p13.3-q25.3 |
pathogenic |
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 | copy number gain | not provided [RCV000739325] | Chr17:12344..81057996 [GRCh37] Chr17:17p13.3-q25.3 |
pathogenic |
GRCh37/hg19 17p13.2(chr17:3336162-4918458)x1 | copy number loss | not provided [RCV000739374] | Chr17:3336162..4918458 [GRCh37] Chr17:17p13.2 |
likely pathogenic |
GRCh37/hg19 17p13.3-13.2(chr17:47546-6287620) | copy number gain | Chromosome 17P13.3, telomeric, duplication syndrome [RCV000767586] | Chr17:47546..6287620 [GRCh37] Chr17:17p13.3-13.2 |
pathogenic |
GRCh37/hg19 17p13.2(chr17:3759126-6128911)x1 | copy number loss | not provided [RCV000849625] | Chr17:3759126..6128911 [GRCh37] Chr17:17p13.2 |
uncertain significance |
NM_001386809.1(CXCL16):c.575C>T (p.Pro192Leu) | single nucleotide variant | not provided [RCV000957512] | Chr17:4735235 [GRCh38] Chr17:4638530 [GRCh37] Chr17:17p13.2 |
benign |
NM_001386809.1(CXCL16):c.-49G>A | single nucleotide variant | not provided [RCV000957513] | Chr17:4739388 [GRCh38] Chr17:4642683 [GRCh37] Chr17:17p13.2 |
benign |
GRCh37/hg19 17p13.3-13.2(chr17:8547-5627408)x1 | copy number loss | See cases [RCV001007429] | Chr17:8547..5627408 [GRCh37] Chr17:17p13.3-13.2 |
pathogenic |
GRCh37/hg19 17p13.2(chr17:4113551-5023913) | copy number loss | not specified [RCV002052580] | Chr17:4113551..5023913 [GRCh37] Chr17:17p13.2 |
uncertain significance |
GRCh37/hg19 17p13.2(chr17:4475016-4648525) | copy number loss | not specified [RCV002052581] | Chr17:4475016..4648525 [GRCh37] Chr17:17p13.2 |
uncertain significance |
NM_001386809.1(CXCL16):c.662C>T (p.Ala221Val) | single nucleotide variant | Inborn genetic diseases [RCV002734643] | Chr17:4735148 [GRCh38] Chr17:4638443 [GRCh37] Chr17:17p13.2 |
likely benign |
NM_001386809.1(CXCL16):c.-29C>T | single nucleotide variant | Inborn genetic diseases [RCV002817035] | Chr17:4739368 [GRCh38] Chr17:4642663 [GRCh37] Chr17:17p13.2 |
uncertain significance |
NM_001386809.1(CXCL16):c.421C>T (p.Leu141Phe) | single nucleotide variant | Inborn genetic diseases [RCV002645440] | Chr17:4735389 [GRCh38] Chr17:4638684 [GRCh37] Chr17:17p13.2 |
uncertain significance |
NM_001386809.1(CXCL16):c.428C>G (p.Ser143Cys) | single nucleotide variant | Inborn genetic diseases [RCV002893357] | Chr17:4735382 [GRCh38] Chr17:4638677 [GRCh37] Chr17:17p13.2 |
uncertain significance |
NM_001386809.1(CXCL16):c.5G>A (p.Gly2Glu) | single nucleotide variant | Inborn genetic diseases [RCV002641908] | Chr17:4739335 [GRCh38] Chr17:4642630 [GRCh37] Chr17:17p13.2 |
uncertain significance |
NM_001386809.1(CXCL16):c.610G>A (p.Ala204Thr) | single nucleotide variant | Inborn genetic diseases [RCV003193402] | Chr17:4735200 [GRCh38] Chr17:4638495 [GRCh37] Chr17:17p13.2 |
uncertain significance |
GRCh38/hg38 17p13.3-12(chr17:165730-11404096)x3 | copy number gain | Chromosome 17p13.3 duplication syndrome [RCV003327726] | Chr17:165730..11404096 [GRCh38] Chr17:17p13.3-12 |
pathogenic |
GRCh37/hg19 17p13.3-13.2(chr17:9474-6017500)x1 | copy number loss | not specified [RCV003987214] | Chr17:9474..6017500 [GRCh37] Chr17:17p13.3-13.2 |
pathogenic |
GRCh37/hg19 17p13.3-11.2(chr17:525-21510992)x3 | copy number gain | not specified [RCV003987215] | Chr17:525..21510992 [GRCh37] Chr17:17p13.3-11.2 |
pathogenic |
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. |
RH102488 |
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RH103349 |
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STS-W86753 |
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D15S1477 |
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D11S2921 |
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alimentary part of gastrointestinal system | circulatory system | endocrine system | exocrine system | hemolymphoid system | hepatobiliary system | integumental system | musculoskeletal system | nervous system | renal system | reproductive system | respiratory system | sensory system | adipose tissue | appendage | entire extraembryonic component | pharyngeal arch | |
High | 5 | ||||||||||||||||
Medium | 1684 | 2048 | 1556 | 514 | 1366 | 357 | 3144 | 485 | 1770 | 322 | 1319 | 1466 | 170 | 1119 | 1870 | 1 | |
Low | 750 | 932 | 164 | 110 | 423 | 108 | 1131 | 1619 | 1919 | 95 | 120 | 136 | 2 | 85 | 839 | 3 | 2 |
Below cutoff | 1 | 6 | 6 | 150 | 80 | 90 | 38 | 2 | 11 | 10 | 1 | 79 | 1 |
RefSeq Transcripts | NM_001100812 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
NM_001386809 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GenBank Nucleotide | AC091153 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AF275260 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AF301016 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AF337812 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK027389 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK292114 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK315017 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AW264069 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AY358909 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC017588 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC044930 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CA307348 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH471108 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CP068261 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
DC373874 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
EF064742 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
JC209418 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
JC209420 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | ENST00000293778 ⟹ ENSP00000293778 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000573123 ⟹ ENSP00000460145 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000574412 ⟹ ENSP00000459592 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000575168 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000576153 ⟹ ENSP00000501470 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000674482 ⟹ ENSP00000501455 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | NM_001100812 ⟹ NP_001094282 | ||||||||||||||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_001386809 ⟹ NP_001373738 | ||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
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Sequence: |
Protein RefSeqs | NP_001094282 | (Get FASTA) | NCBI Sequence Viewer |
NP_001373738 | (Get FASTA) | NCBI Sequence Viewer | |
GenBank Protein | AAG31750 | (Get FASTA) | NCBI Sequence Viewer |
AAG34365 | (Get FASTA) | NCBI Sequence Viewer | |
AAH17588 | (Get FASTA) | NCBI Sequence Viewer | |
AAH44930 | (Get FASTA) | NCBI Sequence Viewer | |
AAK38275 | (Get FASTA) | NCBI Sequence Viewer | |
AAQ89268 | (Get FASTA) | NCBI Sequence Viewer | |
ABK41925 | (Get FASTA) | NCBI Sequence Viewer | |
BAB55078 | (Get FASTA) | NCBI Sequence Viewer | |
BAF84803 | (Get FASTA) | NCBI Sequence Viewer | |
BAG37507 | (Get FASTA) | NCBI Sequence Viewer | |
CDM22050 | (Get FASTA) | NCBI Sequence Viewer | |
CDM22051 | (Get FASTA) | NCBI Sequence Viewer | |
EAW90416 | (Get FASTA) | NCBI Sequence Viewer | |
Ensembl Protein | ENSP00000293778 | ||
ENSP00000293778.7 | |||
ENSP00000459592 | |||
ENSP00000459592.2 | |||
ENSP00000460145.1 | |||
ENSP00000501470.1 | |||
GenBank Protein | Q9H2A7 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_001094282 ⟸ NM_001100812 |
- Peptide Label: | isoform 1 precursor |
- UniProtKB: | Q9H2A7 (UniProtKB/Swiss-Prot), Q9BXD6 (UniProtKB/Swiss-Prot), Q96K63 (UniProtKB/Swiss-Prot), Q8TC80 (UniProtKB/Swiss-Prot), B2RCB0 (UniProtKB/Swiss-Prot), A8K7U9 (UniProtKB/Swiss-Prot), A0N0N4 (UniProtKB/Swiss-Prot), Q9H2F6 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | ENSP00000501455 ⟸ ENST00000674482 |
RefSeq Acc Id: | ENSP00000293778 ⟸ ENST00000293778 |
RefSeq Acc Id: | ENSP00000460145 ⟸ ENST00000573123 |
RefSeq Acc Id: | ENSP00000459592 ⟸ ENST00000574412 |
RefSeq Acc Id: | ENSP00000501470 ⟸ ENST00000576153 |
RefSeq Acc Id: | NP_001373738 ⟸ NM_001386809 |
- Peptide Label: | isoform 1 precursor |
- UniProtKB: | Q9H2A7 (UniProtKB/Swiss-Prot), Q9BXD6 (UniProtKB/Swiss-Prot), Q96K63 (UniProtKB/Swiss-Prot), Q8TC80 (UniProtKB/Swiss-Prot), B2RCB0 (UniProtKB/Swiss-Prot), A8K7U9 (UniProtKB/Swiss-Prot), A0N0N4 (UniProtKB/Swiss-Prot), Q9H2F6 (UniProtKB/Swiss-Prot) |
Name | Modeler | Protein Id | AA Range | Protein Structure |
AF-Q9H2A7-F1-model_v2 | AlphaFold | Q9H2A7 | 1-254 | view protein structure |
RGD ID: | 6794751 | ||||||||
Promoter ID: | HG_KWN:24745 | ||||||||
Type: | CpG-Island | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | CD4+TCell_12Hour, HeLa_S3 | ||||||||
Transcripts: | NM_001100812, NM_001136046, NM_022059, NM_032265, OTTHUMT00000207505, UC002FYU.1, UC002FYV.1 | ||||||||
Position: |
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RGD ID: | 7233441 | ||||||||
Promoter ID: | EPDNEW_H22466 | ||||||||
Type: | initiation region | ||||||||
Name: | CXCL16_2 | ||||||||
Description: | C-X-C motif chemokine ligand 16 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H22467 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
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RGD ID: | 7233443 | ||||||||
Promoter ID: | EPDNEW_H22467 | ||||||||
Type: | initiation region | ||||||||
Name: | CXCL16_1 | ||||||||
Description: | C-X-C motif chemokine ligand 16 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H22466 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
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Database | Acc Id | Source(s) |
AGR Gene | HGNC:16642 | AgrOrtholog |
COSMIC | CXCL16 | COSMIC |
Ensembl Genes | ENSG00000161921 | Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Ensembl Transcript | ENST00000293778 | ENTREZGENE |
ENST00000293778.12 | UniProtKB/Swiss-Prot | |
ENST00000573123.1 | UniProtKB/TrEMBL | |
ENST00000574412 | ENTREZGENE | |
ENST00000574412.6 | UniProtKB/Swiss-Prot | |
ENST00000576153.5 | UniProtKB/TrEMBL | |
GTEx | ENSG00000161921 | GTEx |
HGNC ID | HGNC:16642 | ENTREZGENE |
Human Proteome Map | CXCL16 | Human Proteome Map |
InterPro | CXCL16 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
CXCL16_dom | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
KEGG Report | hsa:58191 | UniProtKB/Swiss-Prot |
NCBI Gene | 58191 | ENTREZGENE |
OMIM | 605398 | OMIM |
PANTHER | C-X-C MOTIF CHEMOKINE 16 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
PTHR14385 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Pfam | CXCL16 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
PharmGKB | PA27057 | PharmGKB |
UniProt | A0A6I8PIU7_HUMAN | UniProtKB/TrEMBL |
A0N0N4 | ENTREZGENE | |
A8K7U9 | ENTREZGENE | |
B2RCB0 | ENTREZGENE | |
CXL16_HUMAN | UniProtKB/Swiss-Prot | |
I3L333_HUMAN | UniProtKB/TrEMBL | |
Q8TC80 | ENTREZGENE | |
Q96K63 | ENTREZGENE | |
Q9BXD6 | ENTREZGENE | |
Q9H2A7 | ENTREZGENE | |
Q9H2F6 | ENTREZGENE | |
UniProt Secondary | A0N0N4 | UniProtKB/Swiss-Prot |
A8K7U9 | UniProtKB/Swiss-Prot | |
B2RCB0 | UniProtKB/Swiss-Prot | |
Q8TC80 | UniProtKB/Swiss-Prot | |
Q96K63 | UniProtKB/Swiss-Prot | |
Q9BXD6 | UniProtKB/Swiss-Prot | |
Q9H2F6 | UniProtKB/Swiss-Prot |
Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
---|---|---|---|---|---|---|---|
2016-03-07 | CXCL16 | C-X-C motif chemokine ligand 16 | chemokine (C-X-C motif) ligand 16 | Symbol and/or name change | 5135510 | APPROVED |