Imported Disease Annotations - CTDTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | atrial fibrillation | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:22544366 | |
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Imported Disease Annotations - CTDTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | atrial fibrillation | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:22544366 | |
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# | Reference Title | Reference Citation |
1. | GOAs Human GO annotations | GOA_HUMAN data from the GO Consortium |
2. | KEGG Annotation Import Pipeline | Pipeline to import KEGG annotations from KEGG into RGD |
3. | ClinVar Automated Import and Annotation Pipeline | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
4. | Data Import for Chemical-Gene Interactions | RGD automated import pipeline for gene-chemical interactions |
5. | The Wnt Homepage | Roel Nusse - Howard Hughes Medical Institute and the Department of Developmental Biology at Stanford University, California, USA |
6. | Alternative wnt signaling is initiated by distinct receptors. | van Amerongen R, etal., Sci Signal. 2008 Sep 2;1(35):re9. |
PMID:8167409 | PMID:11408932 | PMID:11956596 | PMID:12477932 | PMID:18413325 | PMID:20559569 | PMID:20890934 | PMID:21873635 | PMID:22544366 | PMID:22889411 | PMID:23836442 | PMID:27634302 |
PMID:28733458 | PMID:30060804 | PMID:33357447 | PMID:33961781 |
WNT8A (Homo sapiens - human) |
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Wnt8a (Mus musculus - house mouse) |
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Wnt8a (Rattus norvegicus - Norway rat) |
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Wnt8a (Chinchilla lanigera - long-tailed chinchilla) |
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WNT8A (Pan paniscus - bonobo/pygmy chimpanzee) |
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WNT8A (Canis lupus familiaris - dog) |
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Wnt8a (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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WNT8A (Sus scrofa - pig) |
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WNT8A (Chlorocebus sabaeus - green monkey) |
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Wnt8a (Heterocephalus glaber - naked mole-rat) |
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.
Variants in WNT8A
21 total Variants |
Name | Type | Condition(s) | Position(s) | Clinical significance |
GRCh38/hg38 5q23.3-33.2(chr5:130860928-155321811)x3 | copy number gain | See cases [RCV000051193] | Chr5:130860928..155321811 [GRCh38] Chr5:130196621..154701371 [GRCh37] Chr5:130224520..154681564 [NCBI36] Chr5:5q23.3-33.2 |
pathogenic |
GRCh38/hg38 5q31.1-31.2(chr5:133401565-138437038)x1 | copy number loss | See cases [RCV000052114] | Chr5:133401565..138437038 [GRCh38] Chr5:132737257..137772727 [GRCh37] Chr5:132765156..137800626 [NCBI36] Chr5:5q31.1-31.2 |
pathogenic |
GRCh38/hg38 5q21.3-33.2(chr5:106619588-156124387)x1 | copy number loss | See cases [RCV000053524] | Chr5:106619588..156124387 [GRCh38] Chr5:105955289..155551397 [GRCh37] Chr5:105983188..155483975 [NCBI36] Chr5:5q21.3-33.2 |
pathogenic |
NM_058244.3(WNT8A):c.801C>T (p.Ile267=) | single nucleotide variant | Malignant melanoma [RCV000066638] | Chr5:138090818 [GRCh38] Chr5:137426507 [GRCh37] Chr5:137454406 [NCBI36] Chr5:5q31.2 |
not provided |
NM_058244.3(WNT8A):c.1044G>A (p.Lys348=) | single nucleotide variant | Malignant melanoma [RCV000061111] | Chr5:138091061 [GRCh38] Chr5:137426750 [GRCh37] Chr5:137454649 [NCBI36] Chr5:5q31.2 |
not provided |
GRCh38/hg38 5q31.1-31.3(chr5:135297294-140106003)x3 | copy number gain | See cases [RCV000133750] | Chr5:135297294..140106003 [GRCh38] Chr5:134632984..139485588 [GRCh37] Chr5:134660883..139465772 [NCBI36] Chr5:5q31.1-31.3 |
pathogenic |
GRCh38/hg38 5q31.2-31.3(chr5:137836682-140696361)x3 | copy number gain | See cases [RCV000134725] | Chr5:137836682..140696361 [GRCh38] Chr5:137172371..140075946 [GRCh37] Chr5:137200270..140056130 [NCBI36] Chr5:5q31.2-31.3 |
pathogenic |
GRCh38/hg38 5q23.3-33.2(chr5:129847794-153353546)x3 | copy number gain | See cases [RCV000138808] | Chr5:129847794..153353546 [GRCh38] Chr5:129183487..152733106 [GRCh37] Chr5:129211386..152713299 [NCBI36] Chr5:5q23.3-33.2 |
pathogenic |
GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3 | copy number gain | not provided [RCV000487658] | Chr5:94844077..178830410 [GRCh37] Chr5:5q15-35.3 |
likely benign |
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910)x3 | copy number gain | See cases [RCV000449349] | Chr5:130125085..157574910 [GRCh37] Chr5:5q23.3-33.3 |
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 |
GRCh37/hg19 5q21.3-35.3(chr5:106716357-180687338)x3 | copy number gain | See cases [RCV000448245] | Chr5:106716357..180687338 [GRCh37] Chr5:5q21.3-35.3 |
pathogenic |
NC_000005.9:g.(?_86400000)_(154000000_?)del | deletion | Familial adenomatous polyposis 1 [RCV002231249]|Hereditary cancer-predisposing syndrome [RCV000554476] | Chr5:86400000..154000000 [GRCh37] Chr5:5q14.3-33.2 |
pathogenic |
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 |
NM_001300939.2(WNT8A):c.698C>T (p.Ala233Val) | single nucleotide variant | Inborn genetic diseases [RCV003273764] | Chr5:138090661 [GRCh38] Chr5:137426350 [GRCh37] Chr5:5q31.2 |
uncertain significance |
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 |
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 |
Single allele | deletion | Neurodevelopmental disorder [RCV000787436] | Chr5:14685137..149511942 [GRCh37] Chr5:5p15.2-q32 |
uncertain significance |
NC_000005.9:g.(?_136633338)_(140998481_?)dup | duplication | PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome [RCV001339088] | Chr5:136633338..140998481 [GRCh37] Chr5:5q31.2-31.3 |
uncertain significance |
GRCh37/hg19 5q31.2(chr5:136409875-137739167) | copy number loss | Microcephaly [RCV001352638] | Chr5:136409875..137739167 [GRCh37] Chr5:5q31.2 |
pathogenic |
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910) | copy number gain | not specified [RCV002053526] | Chr5:130125085..157574910 [GRCh37] Chr5:5q23.3-33.3 |
pathogenic |
NM_001300939.2(WNT8A):c.142A>G (p.Ile48Val) | single nucleotide variant | Hypospadias [RCV001824103] | Chr5:138084269 [GRCh38] Chr5:137419958 [GRCh37] Chr5:5q31.2 |
uncertain significance |
GRCh37/hg19 5q31.1-31.2(chr5:132031902-137623639) | copy number loss | not specified [RCV002053530] | Chr5:132031902..137623639 [GRCh37] Chr5:5q31.1-31.2 |
pathogenic |
NC_000005.9:g.(?_136957787)_(140078137_?)dup | duplication | PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome [RCV003116437] | Chr5:136957787..140078137 [GRCh37] Chr5:5q31.2-31.3 |
uncertain significance |
NC_000005.9:g.(?_136957787)_(138861289_?)del | deletion | STING-associated vasculopathy with onset in infancy [RCV003113978] | Chr5:136957787..138861289 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_001300939.2(WNT8A):c.1052A>G (p.Lys351Arg) | single nucleotide variant | Inborn genetic diseases [RCV003259733] | Chr5:138091015 [GRCh38] Chr5:137426704 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_001300939.2(WNT8A):c.239G>T (p.Arg80Leu) | single nucleotide variant | Inborn genetic diseases [RCV002945480] | Chr5:138084580 [GRCh38] Chr5:137420269 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_001300939.2(WNT8A):c.152C>A (p.Pro51His) | single nucleotide variant | Inborn genetic diseases [RCV002777523] | Chr5:138084279 [GRCh38] Chr5:137419968 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_001300939.2(WNT8A):c.772G>A (p.Ala258Thr) | single nucleotide variant | Inborn genetic diseases [RCV002799281] | Chr5:138090735 [GRCh38] Chr5:137426424 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_001300939.2(WNT8A):c.592T>G (p.Cys198Gly) | single nucleotide variant | Inborn genetic diseases [RCV002951716] | Chr5:138090555 [GRCh38] Chr5:137426244 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_001300939.2(WNT8A):c.173C>T (p.Thr58Met) | single nucleotide variant | Inborn genetic diseases [RCV002951638] | Chr5:138084514 [GRCh38] Chr5:137420203 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_001300939.2(WNT8A):c.197A>C (p.Gln66Pro) | single nucleotide variant | Inborn genetic diseases [RCV002930446] | Chr5:138084538 [GRCh38] Chr5:137420227 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_001300939.2(WNT8A):c.799C>A (p.Leu267Met) | single nucleotide variant | Inborn genetic diseases [RCV002767952] | Chr5:138090762 [GRCh38] Chr5:137426451 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_001300939.2(WNT8A):c.757T>C (p.Trp253Arg) | single nucleotide variant | Inborn genetic diseases [RCV002742060] | Chr5:138090720 [GRCh38] Chr5:137426409 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_001300939.2(WNT8A):c.872G>A (p.Arg291His) | single nucleotide variant | Inborn genetic diseases [RCV002916928] | Chr5:138090835 [GRCh38] Chr5:137426524 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_001300939.2(WNT8A):c.748G>A (p.Glu250Lys) | single nucleotide variant | Inborn genetic diseases [RCV003004135] | Chr5:138090711 [GRCh38] Chr5:137426400 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_001300939.2(WNT8A):c.886A>T (p.Asn296Tyr) | single nucleotide variant | Inborn genetic diseases [RCV002789534] | Chr5:138090849 [GRCh38] Chr5:137426538 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_001300939.2(WNT8A):c.384A>T (p.Glu128Asp) | single nucleotide variant | Inborn genetic diseases [RCV002764007] | Chr5:138087894 [GRCh38] Chr5:137423583 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_001300939.2(WNT8A):c.536A>C (p.Asn179Thr) | single nucleotide variant | Inborn genetic diseases [RCV002679273] | Chr5:138089041 [GRCh38] Chr5:137424730 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_001300939.2(WNT8A):c.929G>A (p.Arg310His) | single nucleotide variant | Inborn genetic diseases [RCV003283728] | Chr5:138090892 [GRCh38] Chr5:137426581 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_001300939.2(WNT8A):c.-32A>G | single nucleotide variant | Inborn genetic diseases [RCV003173110] | Chr5:138084096 [GRCh38] Chr5:137419785 [GRCh37] Chr5:5q31.2 |
likely benign |
NM_001300939.2(WNT8A):c.-5G>A | single nucleotide variant | Inborn genetic diseases [RCV003365873] | Chr5:138084123 [GRCh38] Chr5:137419812 [GRCh37] Chr5:5q31.2 |
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. |
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 | |
High | |||||||||||||||
Medium | 3 | 20 | 1 | ||||||||||||
Low | 3 | 2 | 2 | 1 | 15 | 1 | 89 | 1 | 662 | 4 | 385 | 2 | |||
Below cutoff | 645 | 638 | 636 | 87 | 465 | 34 | 1453 | 554 | 2287 | 76 | 472 | 546 | 53 | 302 | 1001 |
RefSeq Transcripts | NM_001300938 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
NM_001300939 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_058244 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NR_125351 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011543625 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017009824 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017009825 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017009826 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047417692 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047417693 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054353426 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054353427 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054353428 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GenBank Nucleotide | AB057725 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AC113382 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AY009402 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC144001 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC144497 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH471062 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CP068273 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CQ970126 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | ENST00000361560 ⟹ ENSP00000354726 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000398754 ⟹ ENSP00000381739 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000504809 ⟹ ENSP00000424809 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000506684 ⟹ ENSP00000426653 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | NM_001300938 ⟹ NP_001287867 | ||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||
Type: | CODING | ||||||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_001300939 ⟹ NP_001287868 | ||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||
Type: | CODING | ||||||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NM_058244 ⟹ NP_490645 | ||||||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | NR_125351 | ||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||
Type: | NON-CODING | ||||||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | XM_017009826 ⟹ XP_016865315 | ||||||||
Type: | CODING | ||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | XM_047417692 ⟹ XP_047273648 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_047417693 ⟹ XP_047273649 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054353426 ⟹ XP_054209401 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054353427 ⟹ XP_054209402 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | XM_054353428 ⟹ XP_054209403 | ||||||||
Type: | CODING | ||||||||
Position: |
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Protein RefSeqs | NP_001287867 | (Get FASTA) | NCBI Sequence Viewer |
NP_001287868 | (Get FASTA) | NCBI Sequence Viewer | |
NP_490645 | (Get FASTA) | NCBI Sequence Viewer | |
XP_016865315 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047273648 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047273649 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054209401 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054209402 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054209403 | (Get FASTA) | NCBI Sequence Viewer | |
GenBank Protein | AAG38662 | (Get FASTA) | NCBI Sequence Viewer |
BAB60960 | (Get FASTA) | NCBI Sequence Viewer | |
CAI38650 | (Get FASTA) | NCBI Sequence Viewer | |
EAW62165 | (Get FASTA) | NCBI Sequence Viewer | |
EAW62166 | (Get FASTA) | NCBI Sequence Viewer | |
EAW62167 | (Get FASTA) | NCBI Sequence Viewer | |
EAW62168 | (Get FASTA) | NCBI Sequence Viewer | |
Ensembl Protein | ENSP00000354726.2 | ||
ENSP00000381739 | |||
ENSP00000381739.1 | |||
ENSP00000424809 | |||
ENSP00000424809.1 | |||
ENSP00000426653 | |||
ENSP00000426653.1 | |||
GenBank Protein | Q9H1J5 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_490645 ⟸ NM_058244 |
- Peptide Label: | isoform 3 precursor |
- UniProtKB: | Q96S51 (UniProtKB/Swiss-Prot), Q9H1J5 (UniProtKB/Swiss-Prot), D6RF94 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001287868 ⟸ NM_001300939 |
- Peptide Label: | isoform 2 precursor |
- UniProtKB: | D6RF47 (UniProtKB/TrEMBL), D6RF94 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001287867 ⟸ NM_001300938 |
- Peptide Label: | isoform 1 precursor |
- UniProtKB: | D6RF94 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_016865315 ⟸ XM_017009826 |
- Peptide Label: | isoform X1 |
- Sequence: |
RefSeq Acc Id: | ENSP00000381739 ⟸ ENST00000398754 |
RefSeq Acc Id: | ENSP00000424809 ⟸ ENST00000504809 |
RefSeq Acc Id: | ENSP00000426653 ⟸ ENST00000506684 |
RefSeq Acc Id: | ENSP00000354726 ⟸ ENST00000361560 |
RefSeq Acc Id: | XP_047273648 ⟸ XM_047417692 |
- Peptide Label: | isoform X1 |
RefSeq Acc Id: | XP_047273649 ⟸ XM_047417693 |
- Peptide Label: | isoform X1 |
RefSeq Acc Id: | XP_054209402 ⟸ XM_054353427 |
- Peptide Label: | isoform X1 |
RefSeq Acc Id: | XP_054209401 ⟸ XM_054353426 |
- Peptide Label: | isoform X1 |
RefSeq Acc Id: | XP_054209403 ⟸ XM_054353428 |
- Peptide Label: | isoform X1 |
Name | Modeler | Protein Id | AA Range | Protein Structure |
AF-Q9H1J5-F1-model_v2 | AlphaFold | Q9H1J5 | 1-351 | view protein structure |
RGD ID: | 6870682 | ||||||||
Promoter ID: | EPDNEW_H8506 | ||||||||
Type: | initiation region | ||||||||
Name: | WNT8A_1 | ||||||||
Description: | Wnt family member 8A | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
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Database | Acc Id | Source(s) |
AGR Gene | HGNC:12788 | AgrOrtholog |
COSMIC | WNT8A | COSMIC |
Ensembl Genes | ENSG00000061492 | Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Ensembl Transcript | ENST00000361560 | ENTREZGENE |
ENST00000361560.6 | UniProtKB/Swiss-Prot | |
ENST00000398754 | ENTREZGENE | |
ENST00000398754.1 | UniProtKB/Swiss-Prot | |
ENST00000504809 | ENTREZGENE | |
ENST00000504809.5 | UniProtKB/TrEMBL | |
ENST00000506684 | ENTREZGENE | |
ENST00000506684.6 | UniProtKB/TrEMBL | |
Gene3D-CATH | 3.30.2460.20 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
GTEx | ENSG00000061492 | GTEx |
HGNC ID | HGNC:12788 | ENTREZGENE |
Human Proteome Map | WNT8A | Human Proteome Map |
InterPro | Protein_Wnt-8A/8C | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Wnt | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Wnt8 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Wnt_C | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Wnt_CS | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
KEGG Report | hsa:7478 | UniProtKB/Swiss-Prot |
NCBI Gene | 7478 | ENTREZGENE |
OMIM | 606360 | OMIM |
PANTHER | PTHR12027 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
PTHR12027:SF92 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Pfam | wnt | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
PharmGKB | PA37389 | PharmGKB |
PRINTS | WNT8PROTEIN | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
WNTPROTEIN | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
PROSITE | WNT1 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
SMART | WNT1 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
UniProt | D6RF47 | ENTREZGENE, UniProtKB/TrEMBL |
D6RF94 | ENTREZGENE, UniProtKB/TrEMBL | |
Q96S51 | ENTREZGENE | |
Q9H1J5 | ENTREZGENE, UniProtKB/Swiss-Prot | |
UniProt Secondary | Q96S51 | UniProtKB/Swiss-Prot |
Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
---|---|---|---|---|---|---|---|
2016-03-28 | WNT8A | Wnt family member 8A | WNT8A | wingless-type MMTV integration site family member 8A | Symbol and/or name change | 5135510 | APPROVED |
2015-11-24 | WNT8A | wingless-type MMTV integration site family member 8A | WNT8A | wingless-type MMTV integration site family, member 8A | Symbol and/or name change | 5135510 | APPROVED |