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Imported Disease Annotations - OMIMTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Progressive Familial Intrahepatic Cholestasis 9 | | IAGP | | 7240710 | | OMIM | | |
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Imported Disease Annotations - OMIMTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Progressive Familial Intrahepatic Cholestasis 9 | | IAGP | | 7240710 | | OMIM | | |
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# | Reference Title | Reference Citation |
1. | GOAs Human GO annotations | GOA_HUMAN data from the GO Consortium |
2. | ClinVar Automated Import and Annotation Pipeline | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
3. | Data Import for Chemical-Gene Interactions | RGD automated import pipeline for gene-chemical interactions |
PMID:8125298 | PMID:12477932 | PMID:12618766 | PMID:14702039 | PMID:15489334 | PMID:16344560 | PMID:16751776 | PMID:17081983 | PMID:17500595 | PMID:21873635 | PMID:22863883 | PMID:22939629 |
PMID:23275563 | PMID:24705354 | PMID:24814515 | PMID:25416956 | PMID:26186194 | PMID:26344197 | PMID:26871637 | PMID:28514442 | PMID:31391242 | PMID:31515488 | PMID:32296183 | PMID:32513696 |
PMID:32687490 | PMID:32737136 | PMID:32814053 | PMID:33961781 | PMID:34048709 | PMID:35271311 |
ZFYVE19 (Homo sapiens - human) |
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Zfyve19 (Mus musculus - house mouse) |
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Zfyve19 (Rattus norvegicus - Norway rat) |
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Zfyve19 (Chinchilla lanigera - long-tailed chinchilla) |
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ZFYVE19 (Pan paniscus - bonobo/pygmy chimpanzee) |
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ZFYVE19 (Canis lupus familiaris - dog) |
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Zfyve19 (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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ZFYVE19 (Sus scrofa - pig) |
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ZFYVE19 (Chlorocebus sabaeus - green monkey) |
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Zfyve19 (Heterocephalus glaber - naked mole-rat) |
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Variants in ZFYVE19
8 total Variants ![]() |
Name | Type | Condition(s) | Position(s) | Clinical significance |
NM_001077268.1(ZFYVE19):c.1338-34C>T | single nucleotide variant | Malignant melanoma [RCV000062857] | Chr15:40814114 [GRCh38] Chr15:41106312 [GRCh37] Chr15:38893604 [NCBI36] Chr15:15q15.1 |
not provided |
GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)x3 | copy number gain | See cases [RCV000510717] | Chr15:22770422..102429112 [GRCh37] Chr15:15q11.2-26.3 |
pathogenic |
GRCh37/hg19 15q11.2-26.3(chr15:20733395-102511616)x4 | copy number gain | See cases [RCV000447765] | Chr15:20733395..102511616 [GRCh37] Chr15:15q11.2-26.3 |
pathogenic |
GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112) | copy number gain | See cases [RCV000512019] | Chr15:22770422..102429112 [GRCh37] Chr15:15q11.2-26.3 |
pathogenic |
Single allele | duplication | not provided [RCV000677926] | Chr15:31115047..102354857 [GRCh37] Chr15:15q13.2-26.3 |
pathogenic |
GRCh37/hg19 15q14-15.1 chr15:34638237..42057083 complex variant | complex | Spindle cell sarcoma [RCV000714282] | Chr15:34640169..42054561 [GRCh37] Chr15:15q14-15.1 |
pathogenic |
GRCh37/hg19 15q11.1-26.3(chr15:20071673-102461162)x3 | copy number gain | not provided [RCV000751156] | Chr15:20071673..102461162 [GRCh37] Chr15:15q11.1-26.3 |
pathogenic |
GRCh37/hg19 15q11.1-26.3(chr15:20016811-102493540)x3 | copy number gain | not provided [RCV000751155] | Chr15:20016811..102493540 [GRCh37] Chr15:15q11.1-26.3 |
pathogenic |
GRCh37/hg19 15q15.1(chr15:40464942-41196807)x4 | copy number gain | not provided [RCV001259208] | Chr15:40464942..41196807 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NC_000015.9:g.(?_32964879)_(91358519_?)dup | duplication | Bloom syndrome [RCV001343104]|Familial colorectal cancer [RCV001325176] | Chr15:32964879..91358519 [GRCh37] Chr15:15q13.3-26.1 |
uncertain significance |
NM_001077268.2(ZFYVE19):c.314C>G (p.Ser105Ter) | single nucleotide variant | Cholestasis, progressive familial intrahepatic, 9 [RCV002248324] | Chr15:40809153 [GRCh38] Chr15:41101351 [GRCh37] Chr15:15q15.1 |
pathogenic |
NM_001077268.2(ZFYVE19):c.667C>T (p.Arg223Ter) | single nucleotide variant | Cholestasis, progressive familial intrahepatic, 9 [RCV002248329] | Chr15:40810166 [GRCh38] Chr15:41102364 [GRCh37] Chr15:15q15.1 |
pathogenic |
NM_018163.3(DNAJC17):c.45G>A (p.Leu15=) | single nucleotide variant | not provided [RCV002090959] | Chr15:40807402 [GRCh38] Chr15:41099600 [GRCh37] Chr15:15q15.1 |
likely benign |
NM_001077268.2(ZFYVE19):c.226A>G (p.Met76Val) | single nucleotide variant | Cholestasis, progressive familial intrahepatic, 9 [RCV002248325] | Chr15:40807815 [GRCh38] Chr15:41100013 [GRCh37] Chr15:15q15.1 |
pathogenic |
NC_000015.9:g.(?_40987528)_(41230232_?)dup | duplication | not provided [RCV003113134] | Chr15:40987528..41230232 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NC_000015.9:g.(?_41099547)_(41099644_?)del | deletion | not provided [RCV003119892] | Chr15:41099547..41099644 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NM_001077268.2(ZFYVE19):c.514C>T (p.Arg172Ter) | single nucleotide variant | Cholestasis, progressive familial intrahepatic, 9 [RCV002248326] | Chr15:40809913 [GRCh38] Chr15:41102111 [GRCh37] Chr15:15q15.1 |
pathogenic |
NM_001077268.2(ZFYVE19):c.547C>T (p.Arg183Ter) | single nucleotide variant | Cholestasis, progressive familial intrahepatic, 9 [RCV002248327] | Chr15:40809946 [GRCh38] Chr15:41102144 [GRCh37] Chr15:15q15.1 |
pathogenic |
NM_001077268.2(ZFYVE19):c.379C>T (p.Gln127Ter) | single nucleotide variant | Cholestasis, progressive familial intrahepatic, 9 [RCV002248328] | Chr15:40809218 [GRCh38] Chr15:41101416 [GRCh37] Chr15:15q15.1 |
pathogenic |
NM_001077268.2(ZFYVE19):c.203A>T (p.Asp68Val) | single nucleotide variant | Inborn genetic diseases [RCV002733050] | Chr15:40807792 [GRCh38] Chr15:41099990 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NM_018163.3(DNAJC17):c.54T>G (p.Ile18Met) | single nucleotide variant | not provided [RCV003033567] | Chr15:40807393 [GRCh38] Chr15:41099591 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NM_001077268.2(ZFYVE19):c.659T>G (p.Met220Arg) | single nucleotide variant | Inborn genetic diseases [RCV002883586] | Chr15:40810158 [GRCh38] Chr15:41102356 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NM_001077268.2(ZFYVE19):c.1175G>A (p.Arg392Gln) | single nucleotide variant | Inborn genetic diseases [RCV002981351] | Chr15:40813777 [GRCh38] Chr15:41105975 [GRCh37] Chr15:15q15.1 |
likely benign |
NM_018163.3(DNAJC17):c.18G>C (p.Glu6Asp) | single nucleotide variant | not provided [RCV002638323] | Chr15:40807429 [GRCh38] Chr15:41099627 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NM_018163.3(DNAJC17):c.43C>T (p.Leu15_Leu16=) | single nucleotide variant | not provided [RCV002658487] | Chr15:40807404 [GRCh38] Chr15:41099602 [GRCh37] Chr15:15q15.1 |
likely benign |
NM_001077268.2(ZFYVE19):c.107G>A (p.Gly36Asp) | single nucleotide variant | Inborn genetic diseases [RCV002980787] | Chr15:40807696 [GRCh38] Chr15:41099894 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NM_001077268.2(ZFYVE19):c.1297G>A (p.Ala433Thr) | single nucleotide variant | Inborn genetic diseases [RCV002783355] | Chr15:40814030 [GRCh38] Chr15:41106228 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NM_018163.3(DNAJC17):c.17A>C (p.Glu6Ala) | single nucleotide variant | not provided [RCV002912487] | Chr15:40807430 [GRCh38] Chr15:41099628 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NM_018163.3(DNAJC17):c.23T>C (p.Leu8Ser) | single nucleotide variant | not provided [RCV002785235] | Chr15:40807424 [GRCh38] Chr15:41099622 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NM_018163.3(DNAJC17):c.59A>C (p.Glu20Ala) | single nucleotide variant | not provided [RCV002663254] | Chr15:40807388 [GRCh38] Chr15:41099586 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NM_001077268.2(ZFYVE19):c.1127C>A (p.Ser376Tyr) | single nucleotide variant | Inborn genetic diseases [RCV002807834] | Chr15:40813729 [GRCh38] Chr15:41105927 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NM_018163.3(DNAJC17):c.78+8C>T | single nucleotide variant | not provided [RCV002600314] | Chr15:40807361 [GRCh38] Chr15:41099559 [GRCh37] Chr15:15q15.1 |
likely benign |
NM_001077268.2(ZFYVE19):c.718G>A (p.Ala240Thr) | single nucleotide variant | Inborn genetic diseases [RCV002936479] | Chr15:40810649 [GRCh38] Chr15:41102847 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NM_001077268.2(ZFYVE19):c.763G>A (p.Asp255Asn) | single nucleotide variant | Inborn genetic diseases [RCV002835618] | Chr15:40810694 [GRCh38] Chr15:41102892 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NM_018163.3(DNAJC17):c.68C>A (p.Ala23Glu) | single nucleotide variant | not provided [RCV002650263] | Chr15:40807379 [GRCh38] Chr15:41099577 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NM_001077268.2(ZFYVE19):c.962C>T (p.Thr321Met) | single nucleotide variant | Inborn genetic diseases [RCV002919911] | Chr15:40812834 [GRCh38] Chr15:41105032 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NM_001077268.2(ZFYVE19):c.1166A>T (p.Gln389Leu) | single nucleotide variant | Inborn genetic diseases [RCV002944601] | Chr15:40813768 [GRCh38] Chr15:41105966 [GRCh37] Chr15:15q15.1 |
uncertain significance |
NM_018163.3(DNAJC17):c.78+13G>T | single nucleotide variant | not provided [RCV002584375] | Chr15:40807356 [GRCh38] Chr15:41099554 [GRCh37] Chr15:15q15.1 |
likely benign |
The detailed report is available here: | ![]() | Full Report | ![]() | CSV | ![]() | TAB | ![]() | Printer |
miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/). For more information about miRGate, see PMID:25858286 or access the full paper here. |
WI-21808 |
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D11S3114 |
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D8S2279 |
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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 | visual system | adipose tissue | appendage | entire extraembryonic component | pharyngeal arch | |
High | ||||||||||||||||||
Medium | 2037 | 1149 | 1417 | 499 | 1230 | 346 | 2964 | 861 | 2523 | 344 | 1371 | 1457 | 164 | 854 | 1741 | 1 | 1 | |
Low | 402 | 1842 | 309 | 125 | 721 | 119 | 1393 | 1336 | 1211 | 75 | 89 | 156 | 10 | 1 | 350 | 1047 | 5 | 1 |
Below cutoff |
RefSeq Acc Id: | ENST00000299173 ⟹ ENSP00000299173 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000336455 ⟹ ENSP00000337824 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000355341 ⟹ ENSP00000347498 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000560078 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000561617 ⟹ ENSP00000454704 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000561768 ⟹ ENSP00000456485 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000563497 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000563530 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000564258 ⟹ ENSP00000457617 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000566407 ⟹ ENSP00000456304 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000566767 ⟹ ENSP00000457839 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000567756 ⟹ ENSP00000458096 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000568062 ⟹ ENSP00000455157 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000569057 ⟹ ENSP00000456679 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000570108 ⟹ ENSP00000456223 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000570162 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | NM_001077268 ⟹ NP_001070736 | ||||||||||||||||||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_001258420 ⟹ NP_001245349 | ||||||||||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_001258421 ⟹ NP_001245350 | ||||||||||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_032850 ⟹ NP_116239 | ||||||||||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | XM_017022684 ⟹ XP_016878173 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | XM_024450092 ⟹ XP_024305860 | ||||||||
RefSeq Status: | |||||||||
Type: | CODING | ||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | XR_931925 | ||||||||
RefSeq Status: | |||||||||
Type: | NON-CODING | ||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NP_001070736 ⟸ NM_001077268 |
- Peptide Label: | isoform 1 |
- UniProtKB: | Q8WU96 (UniProtKB/Swiss-Prot), Q96K21 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | NP_001245349 ⟸ NM_001258420 |
- Peptide Label: | isoform 2 |
- UniProtKB: | Q96K21 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | NP_001245350 ⟸ NM_001258421 |
- Peptide Label: | isoform 4 |
- UniProtKB: | Q96K21 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | NP_116239 ⟸ NM_032850 |
- Peptide Label: | isoform 3 |
- UniProtKB: | Q96K21 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | XP_016878173 ⟸ XM_017022684 |
- Peptide Label: | isoform X2 |
- Sequence: |
RefSeq Acc Id: | XP_024305860 ⟸ XM_024450092 |
- Peptide Label: | isoform X1 |
- Sequence: |
RefSeq Acc Id: | ENSP00000456223 ⟸ ENST00000570108 |
RefSeq Acc Id: | ENSP00000337824 ⟸ ENST00000336455 |
RefSeq Acc Id: | ENSP00000299173 ⟸ ENST00000299173 |
RefSeq Acc Id: | ENSP00000456485 ⟸ ENST00000561768 |
RefSeq Acc Id: | ENSP00000454704 ⟸ ENST00000561617 |
RefSeq Acc Id: | ENSP00000457617 ⟸ ENST00000564258 |
RefSeq Acc Id: | ENSP00000347498 ⟸ ENST00000355341 |
RefSeq Acc Id: | ENSP00000456304 ⟸ ENST00000566407 |
RefSeq Acc Id: | ENSP00000457839 ⟸ ENST00000566767 |
RefSeq Acc Id: | ENSP00000458096 ⟸ ENST00000567756 |
RefSeq Acc Id: | ENSP00000455157 ⟸ ENST00000568062 |
RefSeq Acc Id: | ENSP00000456679 ⟸ ENST00000569057 |
Name | Modeler | Protein Id | AA Range | Protein Structure |
AF-Q96K21-F1-model_v2 | AlphaFold | Q96K21 | 1-471 | view protein structure |
RGD ID: | 6792263 | ||||||||
Promoter ID: | HG_KWN:21062 | ||||||||
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: | ENST00000336455, NM_001077268, UC001ZMU.1, UC001ZMV.1, UC001ZMW.1, UC001ZMX.1, UC010BCC.1 | ||||||||
Position: |
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RGD ID: | 7229129 | ||||||||
Promoter ID: | EPDNEW_H20310 | ||||||||
Type: | initiation region | ||||||||
Name: | ZFYVE19_1 | ||||||||
Description: | zinc finger FYVE-type containing 19 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H20311 EPDNEW_H20313 | ||||||||
Experiment Methods: | Single-end sequencing.; Paired-end sequencing. | ||||||||
Position: |
|
RGD ID: | 7229131 | ||||||||
Promoter ID: | EPDNEW_H20311 | ||||||||
Type: | multiple initiation site | ||||||||
Name: | ZFYVE19_2 | ||||||||
Description: | zinc finger FYVE-type containing 19 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H20310 EPDNEW_H20313 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
|
RGD ID: | 7229133 | ||||||||
Promoter ID: | EPDNEW_H20313 | ||||||||
Type: | initiation region | ||||||||
Name: | ZFYVE19_3 | ||||||||
Description: | zinc finger FYVE-type containing 19 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H20310 EPDNEW_H20311 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
|
Database | Acc Id | Source(s) |
AGR Gene | HGNC:20758 | AgrOrtholog |
COSMIC | ZFYVE19 | COSMIC |
Ensembl Genes | ENSG00000166140 | Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Ensembl Protein | ENSP00000299173 | ENTREZGENE |
ENSP00000299173.10 | UniProtKB/Swiss-Prot | |
ENSP00000337824 | ENTREZGENE | |
ENSP00000337824.5 | UniProtKB/Swiss-Prot | |
ENSP00000347498 | ENTREZGENE | |
ENSP00000347498.4 | UniProtKB/Swiss-Prot | |
ENSP00000454704.1 | UniProtKB/TrEMBL | |
ENSP00000455157.1 | UniProtKB/TrEMBL | |
ENSP00000456223.1 | UniProtKB/TrEMBL | |
ENSP00000456304.1 | UniProtKB/TrEMBL | |
ENSP00000456485.1 | UniProtKB/TrEMBL | |
ENSP00000456679.1 | UniProtKB/TrEMBL | |
ENSP00000457617 | ENTREZGENE | |
ENSP00000457617.1 | UniProtKB/Swiss-Prot | |
ENSP00000457839.1 | UniProtKB/TrEMBL | |
ENSP00000458096.1 | UniProtKB/TrEMBL | |
Ensembl Transcript | ENST00000299173 | ENTREZGENE |
ENST00000299173.14 | UniProtKB/Swiss-Prot | |
ENST00000336455 | ENTREZGENE | |
ENST00000336455.9 | UniProtKB/Swiss-Prot | |
ENST00000355341 | ENTREZGENE | |
ENST00000355341.8 | UniProtKB/Swiss-Prot | |
ENST00000561617.1 | UniProtKB/TrEMBL | |
ENST00000561768.5 | UniProtKB/TrEMBL | |
ENST00000564258 | ENTREZGENE | |
ENST00000564258.5 | UniProtKB/Swiss-Prot | |
ENST00000566407.5 | UniProtKB/TrEMBL | |
ENST00000566767.1 | UniProtKB/TrEMBL | |
ENST00000567756.5 | UniProtKB/TrEMBL | |
ENST00000568062.5 | UniProtKB/TrEMBL | |
ENST00000569057.5 | UniProtKB/TrEMBL | |
ENST00000570108.5 | UniProtKB/TrEMBL | |
Gene3D-CATH | 3.30.40.10 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
GTEx | ENSG00000166140 | GTEx |
HGNC ID | HGNC:20758 | ENTREZGENE |
Human Proteome Map | ZFYVE19 | Human Proteome Map |
InterPro | Bbox1_ANCHR | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Znf_FYVE | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Znf_FYVE-rel | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Znf_FYVE_PHD | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Znf_RING/FYVE/PHD | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
KEGG Report | hsa:84936 | UniProtKB/Swiss-Prot |
NCBI Gene | 84936 | ENTREZGENE |
OMIM | 619635 | OMIM |
619849 | OMIM | |
PANTHER | ABSCISSION/NOCUT CHECKPOINT REGULATOR | UniProtKB/Swiss-Prot |
ABSCISSION/NOCUT CHECKPOINT REGULATOR | UniProtKB/Swiss-Prot | |
ABSCISSION/NOCUT CHECKPOINT REGULATOR | UniProtKB/TrEMBL | |
ABSCISSION/NOCUT CHECKPOINT REGULATOR | UniProtKB/TrEMBL | |
Pfam | FYVE | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
PharmGKB | PA134906967 | PharmGKB |
PROSITE | ZF_FYVE | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
SMART | FYVE | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Superfamily-SCOP | B-box zinc-binding domain | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
SSF57903 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
UniProt | A0A024R9K5_HUMAN | UniProtKB/TrEMBL |
ANCHR_HUMAN | UniProtKB/Swiss-Prot | |
H3BN64_HUMAN | UniProtKB/TrEMBL | |
H3BP54_HUMAN | UniProtKB/TrEMBL | |
H3BRF9_HUMAN | UniProtKB/TrEMBL | |
H3BRM1_HUMAN | UniProtKB/TrEMBL | |
H3BS07_HUMAN | UniProtKB/TrEMBL | |
H3BSF5_HUMAN | UniProtKB/TrEMBL | |
H3BUW6_HUMAN | UniProtKB/TrEMBL | |
H3BVF5_HUMAN | UniProtKB/TrEMBL | |
Q8WU96 | ENTREZGENE | |
Q96K21 | ENTREZGENE | |
UniProt Secondary | B3KVB2 | UniProtKB/Swiss-Prot |
C9JNF4 | UniProtKB/Swiss-Prot | |
H3BUF9 | UniProtKB/Swiss-Prot | |
Q86WC2 | UniProtKB/Swiss-Prot | |
Q8WU96 | UniProtKB/Swiss-Prot |
Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
---|---|---|---|---|---|---|---|
2016-02-18 | ZFYVE19 | zinc finger FYVE-type containing 19 | zinc finger, FYVE domain containing 19 | Symbol and/or name change | 5135510 | APPROVED |