Imported Disease Annotations - CTDTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | intellectual disability | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:21937992 | |
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Imported Disease Annotations - CTDTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | intellectual disability | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:21937992 | |
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# | Reference Title | Reference Citation |
1. | GOAs Human GO annotations | GOA_HUMAN data from the GO Consortium |
2. | The isolation and characterization of cDNA encoding human and rat brain inositol polyphosphate 4-phosphatase. | Norris FA, etal., J Biol Chem 1995 Jul 7;270(27):16128-33. |
3. | The cDNA cloning and characterization of inositol polyphosphate 4-phosphatase type II. Evidence for conserved alternative splicing in the 4-phosphatase family. | Norris FA, etal., J Biol Chem 1997 Sep 19;272(38):23859-64. |
4. | KEGG Annotation Import Pipeline | Pipeline to import KEGG annotations from KEGG into RGD |
5. | SMPDB Annotation Import Pipeline | Pipeline to import SMPDB annotations from SMPDB into RGD |
6. | ClinVar Automated Import and Annotation Pipeline | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
7. | Data Import for Chemical-Gene Interactions | RGD automated import pipeline for gene-chemical interactions |
PMID:9110986 | PMID:9599410 | PMID:10097090 | PMID:10702694 | PMID:11485317 | PMID:12477932 | PMID:14702039 | PMID:15231748 | PMID:15489334 | PMID:15716355 | PMID:15815621 | PMID:18187694 |
PMID:18562305 | PMID:19264973 | PMID:20463662 | PMID:21873635 | PMID:23092984 | PMID:23463506 | PMID:25338135 | PMID:25869668 | PMID:25921289 | PMID:26344197 | PMID:26463840 | PMID:28514442 |
PMID:28611215 | PMID:29507755 | PMID:30071275 | PMID:30335467 | PMID:31253590 | PMID:31524145 | PMID:31978615 | PMID:32457219 | PMID:32694731 | PMID:33109548 | PMID:33961781 | PMID:35256949 |
PMID:35563538 | PMID:36215168 | PMID:38363325 |
INPP4A (Homo sapiens - human) |
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Inpp4a (Mus musculus - house mouse) |
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Inpp4a (Rattus norvegicus - Norway rat) |
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Inpp4a (Chinchilla lanigera - long-tailed chinchilla) |
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INPP4A (Pan paniscus - bonobo/pygmy chimpanzee) |
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INPP4A (Canis lupus familiaris - dog) |
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Inpp4a (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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INPP4A (Sus scrofa - pig) |
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INPP4A (Chlorocebus sabaeus - green monkey) |
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Inpp4a (Heterocephalus glaber - naked mole-rat) |
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Variants in INPP4A
45 total Variants |
Name | Type | Condition(s) | Position(s) | Clinical significance |
GRCh38/hg38 2q11.1-12.1(chr2:94817406-103252396)x3 | copy number gain | See cases [RCV000052946] | Chr2:94817406..103252396 [GRCh38] Chr2:95618109..103868854 [GRCh37] Chr2:94846878..103235286 [NCBI36] Chr2:2q11.1-12.1 |
pathogenic |
GRCh38/hg38 2q11.2-13(chr2:97672522-110211318)x3 | copy number gain | See cases [RCV000052947] | Chr2:97672522..110211318 [GRCh38] Chr2:98288985..110968895 [GRCh37] Chr2:97655417..110326184 [NCBI36] Chr2:2q11.2-13 |
pathogenic |
GRCh38/hg38 2p11.2-q11.2(chr2:91443218-102334856)x3 | copy number gain | See cases [RCV000052945] | Chr2:91443218..102334856 [GRCh38] Chr2:91617683..102951316 [GRCh37] Chr2:90981410..102317748 [NCBI36] Chr2:2p11.2-q11.2 |
pathogenic |
NM_001134224.1(INPP4A):c.2293C>T (p.Arg765Cys) | single nucleotide variant | Malignant melanoma [RCV000065732] | Chr2:98565765 [GRCh38] Chr2:99182228 [GRCh37] Chr2:98548660 [NCBI36] Chr2:2q11.2 |
not provided |
GRCh38/hg38 2q11.1-11.2(chr2:95337458-99072953)x3 | copy number gain | See cases [RCV000138012] | Chr2:95337458..99072953 [GRCh38] Chr2:96003206..99689416 [GRCh37] Chr2:95366933..99055848 [NCBI36] Chr2:2q11.1-11.2 |
uncertain significance |
GRCh38/hg38 2q11.2(chr2:98411773-101636907)x1 | copy number loss | See cases [RCV000139206] | Chr2:98411773..101636907 [GRCh38] Chr2:99028236..102253369 [GRCh37] Chr2:98394668..101619801 [NCBI36] Chr2:2q11.2 |
likely pathogenic |
GRCh38/hg38 2q11.1-13(chr2:94678532-110602409)x3 | copy number gain | See cases [RCV000141075] | Chr2:94678532..110602409 [GRCh38] Chr2:95344257..111359986 [GRCh37] Chr2:94707984..111076455 [NCBI36] Chr2:2q11.1-13 |
pathogenic |
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3 | copy number gain | not provided [RCV000752802] | Chr2:14238..243048760 [GRCh37] Chr2:2p25.3-q37.3 |
pathogenic |
GRCh37/hg19 2q11.1-12.3(chr2:95529039-108518266) | copy number gain | See cases [RCV000449270] | Chr2:95529039..108518266 [GRCh37] Chr2:2q11.1-12.3 |
pathogenic |
GRCh37/hg19 2q11.1-13(chr2:95327499-111370025)x4 | copy number gain | See cases [RCV000446842] | Chr2:95327499..111370025 [GRCh37] Chr2:2q11.1-13 |
pathogenic |
GRCh37/hg19 2q11.1-11.2(chr2:95691600-100587394) | copy number gain | See cases [RCV000447723] | Chr2:95691600..100587394 [GRCh37] Chr2:2q11.1-11.2 |
pathogenic |
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384) | copy number gain | See cases [RCV000512056] | Chr2:12771..242783384 [GRCh37] Chr2:2p25.3-q37.3 |
pathogenic |
GRCh37/hg19 2q11.1-12.2(chr2:95518497-107186127) | copy number gain | See cases [RCV000511158] | Chr2:95518497..107186127 [GRCh37] Chr2:2q11.1-12.2 |
uncertain significance |
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3 | copy number gain | See cases [RCV000511212] | Chr2:12771..242783384 [GRCh37] Chr2:2p25.3-q37.3 |
pathogenic |
Single allele | deletion | not provided [RCV000714264] | Chr2:40608411..146900718 [GRCh37] Chr2:2p22.1-q22.3 |
likely pathogenic |
GRCh37/hg19 2q11.1-13(chr2:96353030-114045463)x3 | copy number gain | not provided [RCV000682168] | Chr2:96353030..114045463 [GRCh37] Chr2:2q11.1-13 |
pathogenic |
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3 | copy number gain | not provided [RCV000752804] | Chr2:15672..243101834 [GRCh37] Chr2:2p25.3-q37.3 |
pathogenic |
NM_001134225.2(INPP4A):c.36C>T (p.Ala12=) | single nucleotide variant | Dyskeratosis congenita, autosomal dominant 1 [RCV000761361] | Chr2:98520084 [GRCh38] Chr2:99136547 [GRCh37] Chr2:2q11.2 |
likely pathogenic |
NM_001134225.2(INPP4A):c.352_353del (p.Ser118fs) | microsatellite | Pectus excavatum [RCV000991365] | Chr2:98535807..98535808 [GRCh38] Chr2:99152270..99152271 [GRCh37] Chr2:2q11.2 |
likely pathogenic |
NM_001134225.2(INPP4A):c.2152+8G>A | single nucleotide variant | not provided [RCV000885123] | Chr2:98564771 [GRCh38] Chr2:99181234 [GRCh37] Chr2:2q11.2 |
benign |
NM_001134225.2(INPP4A):c.1965C>T (p.Ser655=) | single nucleotide variant | not provided [RCV000972377] | Chr2:98563574 [GRCh38] Chr2:99180037 [GRCh37] Chr2:2q11.2 |
benign |
NM_001134225.2(INPP4A):c.678T>C (p.Gly226=) | single nucleotide variant | not provided [RCV000964868] | Chr2:98539535 [GRCh38] Chr2:99155998 [GRCh37] Chr2:2q11.2 |
benign |
NM_001134225.2(INPP4A):c.115C>T (p.Gln39Ter) | single nucleotide variant | Intellectual disability [RCV000986112] | Chr2:98520695 [GRCh38] Chr2:99137158 [GRCh37] Chr2:2q11.2 |
pathogenic |
NM_001134225.2(INPP4A):c.1458T>C (p.Thr486=) | single nucleotide variant | not provided [RCV000892054] | Chr2:98554381 [GRCh38] Chr2:99170844 [GRCh37] Chr2:2q11.2 |
benign |
NM_001134225.2(INPP4A):c.2034C>T (p.Thr678=) | single nucleotide variant | not provided [RCV000885380] | Chr2:98564645 [GRCh38] Chr2:99181108 [GRCh37] Chr2:2q11.2 |
benign |
NM_001134225.2(INPP4A):c.930C>T (p.Thr310=) | single nucleotide variant | not provided [RCV000892263] | Chr2:98543988 [GRCh38] Chr2:99160451 [GRCh37] Chr2:2q11.2 |
benign |
NM_001134225.2(INPP4A):c.246G>A (p.Lys82=) | single nucleotide variant | not provided [RCV000975964] | Chr2:98533471 [GRCh38] Chr2:99149934 [GRCh37] Chr2:2q11.2 |
likely benign |
NM_001134225.2(INPP4A):c.324T>A (p.Leu108=) | single nucleotide variant | not provided [RCV000933281] | Chr2:98535782 [GRCh38] Chr2:99152245 [GRCh37] Chr2:2q11.2 |
likely benign |
NM_001134225.2(INPP4A):c.2571G>C (p.Leu857=) | single nucleotide variant | not provided [RCV000955291] | Chr2:98572867 [GRCh38] Chr2:99189330 [GRCh37] Chr2:2q11.2 |
benign |
NM_001134225.2(INPP4A):c.1526G>A (p.Ser509Asn) | single nucleotide variant | not provided [RCV000879790] | Chr2:98554449 [GRCh38] Chr2:99170912 [GRCh37] Chr2:2q11.2 |
likely benign |
NM_001134225.2(INPP4A):c.1968G>C (p.Ala656=) | single nucleotide variant | not provided [RCV000879930] | Chr2:98563577 [GRCh38] Chr2:99180040 [GRCh37] Chr2:2q11.2 |
benign |
NM_001134225.2(INPP4A):c.2029-10G>C | single nucleotide variant | not provided [RCV001665407] | Chr2:98564630 [GRCh38] Chr2:99181093 [GRCh37] Chr2:2q11.2 |
likely benign |
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373) | copy number gain | Mosaic trisomy 2 [RCV002280628] | Chr2:1..243199373 [GRCh37] Chr2:2p25.3-q37.3 |
pathogenic |
GRCh37/hg19 2p25.1-q13(chr2:11504318-111365996)x1 | copy number loss | See cases [RCV002287563] | Chr2:11504318..111365996 [GRCh37] Chr2:2p25.1-q13 |
pathogenic |
NM_001134225.2(INPP4A):c.1429A>G (p.Ile477Val) | single nucleotide variant | Inborn genetic diseases [RCV003281137] | Chr2:98554352 [GRCh38] Chr2:99170815 [GRCh37] Chr2:2q11.2 |
uncertain significance |
GRCh37/hg19 2q11.1-11.2(chr2:95341388-100340514)x3 | copy number gain | not provided [RCV002473932] | Chr2:95341388..100340514 [GRCh37] Chr2:2q11.1-11.2 |
likely pathogenic |
GRCh37/hg19 2q11.2(chr2:98958721-99205212)x3 | copy number gain | not provided [RCV002472708] | Chr2:98958721..99205212 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.1623C>G (p.Asp541Glu) | single nucleotide variant | Inborn genetic diseases [RCV002683215] | Chr2:98555609 [GRCh38] Chr2:99172072 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.851C>A (p.Ser284Tyr) | single nucleotide variant | Inborn genetic diseases [RCV002887619] | Chr2:98543909 [GRCh38] Chr2:99160372 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.2410C>G (p.Leu804Val) | single nucleotide variant | Inborn genetic diseases [RCV002887508] | Chr2:98566159 [GRCh38] Chr2:99182622 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.668C>T (p.Ser223Leu) | single nucleotide variant | Inborn genetic diseases [RCV002980841] | Chr2:98538979 [GRCh38] Chr2:99155442 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.1546G>A (p.Asp516Asn) | single nucleotide variant | Inborn genetic diseases [RCV002950045] | Chr2:98554469 [GRCh38] Chr2:99170932 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.679G>A (p.Gly227Ser) | single nucleotide variant | Inborn genetic diseases [RCV003001557] | Chr2:98539536 [GRCh38] Chr2:99155999 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.1327C>T (p.Leu443Phe) | single nucleotide variant | Inborn genetic diseases [RCV002919548] | Chr2:98552949 [GRCh38] Chr2:99169412 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.44G>A (p.Arg15His) | single nucleotide variant | Inborn genetic diseases [RCV002788901] | Chr2:98520092 [GRCh38] Chr2:99136555 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.820G>A (p.Val274Met) | single nucleotide variant | Inborn genetic diseases [RCV002641807] | Chr2:98543878 [GRCh38] Chr2:99160341 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.2812A>G (p.Met938Val) | single nucleotide variant | Inborn genetic diseases [RCV002929347] | Chr2:98587501 [GRCh38] Chr2:99203964 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.114A>G (p.Ile38Met) | single nucleotide variant | Inborn genetic diseases [RCV002826274] | Chr2:98520694 [GRCh38] Chr2:99137157 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.1507C>T (p.Arg503Trp) | single nucleotide variant | Inborn genetic diseases [RCV002813359] | Chr2:98554430 [GRCh38] Chr2:99170893 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.1642C>T (p.Arg548Trp) | single nucleotide variant | Inborn genetic diseases [RCV002670662] | Chr2:98555628 [GRCh38] Chr2:99172091 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.1355A>G (p.Gln452Arg) | single nucleotide variant | Inborn genetic diseases [RCV002673368] | Chr2:98554278 [GRCh38] Chr2:99170741 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.673T>C (p.Phe225Leu) | single nucleotide variant | Inborn genetic diseases [RCV002921040] | Chr2:98539530 [GRCh38] Chr2:99155993 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.1837C>T (p.Pro613Ser) | single nucleotide variant | Inborn genetic diseases [RCV002936351] | Chr2:98559477 [GRCh38] Chr2:99175940 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.355G>A (p.Val119Met) | single nucleotide variant | Inborn genetic diseases [RCV002896712] | Chr2:98535813 [GRCh38] Chr2:99152276 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.1072G>A (p.Val358Ile) | single nucleotide variant | Inborn genetic diseases [RCV003196970] | Chr2:98546603 [GRCh38] Chr2:99163066 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.2528G>A (p.Arg843Gln) | single nucleotide variant | Inborn genetic diseases [RCV003204494] | Chr2:98572824 [GRCh38] Chr2:99189287 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.182A>G (p.Asp61Gly) | single nucleotide variant | Inborn genetic diseases [RCV003373536] | Chr2:98533407 [GRCh38] Chr2:99149870 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.779G>A (p.Arg260Gln) | single nucleotide variant | Inborn genetic diseases [RCV003362446] | Chr2:98539636 [GRCh38] Chr2:99156099 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.887C>T (p.Thr296Ile) | single nucleotide variant | Inborn genetic diseases [RCV003386231] | Chr2:98543945 [GRCh38] Chr2:99160408 [GRCh37] Chr2:2q11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.2195T>C (p.Met732Thr) | single nucleotide variant | Inborn genetic diseases [RCV003366061] | Chr2:98565682 [GRCh38] Chr2:99182145 [GRCh37] Chr2:2q11.2 |
uncertain significance |
GRCh37/hg19 2q11.1-11.2(chr2:95773428-102550061)x3 | copy number gain | not provided [RCV003484069] | Chr2:95773428..102550061 [GRCh37] Chr2:2q11.1-11.2 |
likely pathogenic |
GRCh37/hg19 2q11.1-11.2(chr2:96732520-99142320)x3 | copy number gain | not provided [RCV003484071] | Chr2:96732520..99142320 [GRCh37] Chr2:2q11.1-11.2 |
uncertain significance |
NM_001134225.2(INPP4A):c.1635_1649del (p.Gln545_Leu549del) | deletion | not provided [RCV003885580] | Chr2:98555615..98555629 [GRCh38] Chr2:99172078..99172092 [GRCh37] Chr2:2q11.2 |
likely benign |
NM_001134225.2(INPP4A):c.1870G>A (p.Ala624Thr) | single nucleotide variant | Inborn genetic diseases [RCV003361748] | Chr2:98563479 [GRCh38] Chr2:99179942 [GRCh37] Chr2:2q11.2 |
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. |
D2S2187 |
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RH98872 |
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RH102815 |
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RH119794 |
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RH119291 |
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DYS418 |
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D2S1315 |
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D2S2002 |
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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 | 1298 | 699 | 359 | 19 | 1199 | 23 | 905 | 678 | 2028 | 88 | 450 | 682 | 7 | 1 | 191 | 559 | 4 | 2 |
Low | 1141 | 2292 | 1366 | 604 | 752 | 441 | 3451 | 1519 | 1706 | 331 | 1010 | 931 | 168 | 1013 | 2229 | 2 | ||
Below cutoff | 1 | 1 | 1 |
RefSeq Transcripts | NG_029890 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
NM_001134224 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001134225 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001351424 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001351425 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001351426 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001351427 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001351428 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001351429 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001566 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_004027 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006712499 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006712500 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006712501 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006712502 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006712503 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006712504 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006712505 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006712506 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_006712508 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011511122 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011511123 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011511124 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011511125 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011511127 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017003994 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017003995 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017003996 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017004000 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017004001 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017004003 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_024452876 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444198 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444199 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444200 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444201 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444203 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444204 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444205 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444206 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444207 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444209 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444210 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444211 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444212 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444213 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444214 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444215 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444217 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_047444218 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341838 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341839 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341840 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341841 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341842 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341843 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341844 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341845 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341846 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341847 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341848 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341849 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341850 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341851 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341852 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341853 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341854 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341855 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341856 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341857 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341858 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341859 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341860 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341861 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341862 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341863 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341864 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341865 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341866 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341867 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341868 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341869 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341870 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_054341871 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_001738737 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_001738738 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_007074203 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_008486362 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_922915 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_922916 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GenBank Nucleotide | AB462500 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AC010134 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AF368319 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK057550 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK091533 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK307823 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC005082 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC028361 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH471127 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CP068276 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
U26398 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
U96919 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | ENST00000074304 ⟹ ENSP00000074304 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000409016 ⟹ ENSP00000386704 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000409463 ⟹ ENSP00000386329 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000409540 ⟹ ENSP00000387294 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000409851 ⟹ ENSP00000386777 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000463367 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000467042 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000468638 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000498026 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000523221 ⟹ ENSP00000427722 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000706935 ⟹ ENSP00000516656 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | NM_001134224 ⟹ NP_001127696 | ||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001134225 ⟹ NP_001127697 | ||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001351424 ⟹ NP_001338353 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001351425 ⟹ NP_001338354 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001351426 ⟹ NP_001338355 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001351427 ⟹ NP_001338356 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001351428 ⟹ NP_001338357 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001351429 ⟹ NP_001338358 | ||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
|
||||||||||||
Sequence: |
RefSeq Acc Id: | NM_001566 ⟹ NP_001557 | ||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_004027 ⟹ NP_004018 | ||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | XM_006712499 ⟹ XP_006712562 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_006712500 ⟹ XP_006712563 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_006712501 ⟹ XP_006712564 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_006712502 ⟹ XP_006712565 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_006712503 ⟹ XP_006712566 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_006712505 ⟹ XP_006712568 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_006712506 ⟹ XP_006712569 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011511122 ⟹ XP_011509424 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011511123 ⟹ XP_011509425 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011511124 ⟹ XP_011509426 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011511125 ⟹ XP_011509427 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_011511127 ⟹ XP_011509429 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_017003994 ⟹ XP_016859483 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_017004000 ⟹ XP_016859489 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_017004001 ⟹ XP_016859490 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_024452876 ⟹ XP_024308644 | ||||||||
Type: | CODING | ||||||||
Position: |
|
||||||||
Sequence: |
RefSeq Acc Id: | XM_047444198 ⟹ XP_047300154 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047444199 ⟹ XP_047300155 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047444200 ⟹ XP_047300156 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047444201 ⟹ XP_047300157 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047444203 ⟹ XP_047300159 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047444204 ⟹ XP_047300160 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047444205 ⟹ XP_047300161 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047444206 ⟹ XP_047300162 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047444207 ⟹ XP_047300163 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047444209 ⟹ XP_047300165 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047444210 ⟹ XP_047300166 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047444211 ⟹ XP_047300167 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047444212 ⟹ XP_047300168 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047444213 ⟹ XP_047300169 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047444214 ⟹ XP_047300170 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047444215 ⟹ XP_047300171 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047444217 ⟹ XP_047300173 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_047444218 ⟹ XP_047300174 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341838 ⟹ XP_054197813 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341839 ⟹ XP_054197814 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341840 ⟹ XP_054197815 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341841 ⟹ XP_054197816 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341842 ⟹ XP_054197817 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341843 ⟹ XP_054197818 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341844 ⟹ XP_054197819 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341845 ⟹ XP_054197820 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341846 ⟹ XP_054197821 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341847 ⟹ XP_054197822 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341848 ⟹ XP_054197823 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341849 ⟹ XP_054197824 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341850 ⟹ XP_054197825 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341851 ⟹ XP_054197826 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341852 ⟹ XP_054197827 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341853 ⟹ XP_054197828 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341854 ⟹ XP_054197829 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341855 ⟹ XP_054197830 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341856 ⟹ XP_054197831 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341857 ⟹ XP_054197832 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341858 ⟹ XP_054197833 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341859 ⟹ XP_054197834 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341860 ⟹ XP_054197835 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341861 ⟹ XP_054197836 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341862 ⟹ XP_054197837 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341863 ⟹ XP_054197838 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341864 ⟹ XP_054197839 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341865 ⟹ XP_054197840 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341866 ⟹ XP_054197841 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341867 ⟹ XP_054197842 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341868 ⟹ XP_054197843 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341869 ⟹ XP_054197844 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341870 ⟹ XP_054197845 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XM_054341871 ⟹ XP_054197846 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XR_007074203 | ||||||||
Type: | NON-CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XR_008486362 | ||||||||
Type: | NON-CODING | ||||||||
Position: |
|
RefSeq Acc Id: | XR_922915 | ||||||||
Type: | NON-CODING | ||||||||
Position: |
|
||||||||
Sequence: |
Protein RefSeqs | NP_001127696 | (Get FASTA) | NCBI Sequence Viewer |
NP_001127697 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001338353 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001338354 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001338355 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001338356 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001338357 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001338358 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001557 | (Get FASTA) | NCBI Sequence Viewer | |
NP_004018 | (Get FASTA) | NCBI Sequence Viewer | |
XP_006712562 | (Get FASTA) | NCBI Sequence Viewer | |
XP_006712563 | (Get FASTA) | NCBI Sequence Viewer | |
XP_006712564 | (Get FASTA) | NCBI Sequence Viewer | |
XP_006712565 | (Get FASTA) | NCBI Sequence Viewer | |
XP_006712566 | (Get FASTA) | NCBI Sequence Viewer | |
XP_006712568 | (Get FASTA) | NCBI Sequence Viewer | |
XP_006712569 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011509424 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011509425 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011509426 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011509427 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011509429 | (Get FASTA) | NCBI Sequence Viewer | |
XP_016859483 | (Get FASTA) | NCBI Sequence Viewer | |
XP_016859489 | (Get FASTA) | NCBI Sequence Viewer | |
XP_016859490 | (Get FASTA) | NCBI Sequence Viewer | |
XP_024308644 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300154 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300155 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300156 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300157 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300159 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300160 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300161 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300162 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300163 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300165 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300166 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300167 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300168 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300169 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300170 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300171 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300173 | (Get FASTA) | NCBI Sequence Viewer | |
XP_047300174 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197813 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197814 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197815 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197816 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197817 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197818 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197819 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197820 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197821 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197822 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197823 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197824 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197825 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197826 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197827 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197828 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197829 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197830 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197831 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197832 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197833 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197834 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197835 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197836 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197837 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197838 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197839 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197840 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197841 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197842 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197843 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197844 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197845 | (Get FASTA) | NCBI Sequence Viewer | |
XP_054197846 | (Get FASTA) | NCBI Sequence Viewer | |
GenBank Protein | AAB01068 | (Get FASTA) | NCBI Sequence Viewer |
AAB72150 | (Get FASTA) | NCBI Sequence Viewer | |
AAH28361 | (Get FASTA) | NCBI Sequence Viewer | |
AAK58870 | (Get FASTA) | NCBI Sequence Viewer | |
AAX93230 | (Get FASTA) | NCBI Sequence Viewer | |
EAX01904 | (Get FASTA) | NCBI Sequence Viewer | |
EAX01905 | (Get FASTA) | NCBI Sequence Viewer | |
EAX01906 | (Get FASTA) | NCBI Sequence Viewer | |
EAX01907 | (Get FASTA) | NCBI Sequence Viewer | |
EAX01908 | (Get FASTA) | NCBI Sequence Viewer | |
EAX01909 | (Get FASTA) | NCBI Sequence Viewer | |
EAX01910 | (Get FASTA) | NCBI Sequence Viewer | |
Ensembl Protein | ENSP00000386329.1 | ||
ENSP00000386704 | |||
ENSP00000386704.3 | |||
ENSP00000386777 | |||
ENSP00000386777.4 | |||
ENSP00000387294 | |||
ENSP00000387294.3 | |||
ENSP00000427722 | |||
ENSP00000427722.1 | |||
ENSP00000516656.1 | |||
GenBank Protein | Q96PE3 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_001127696 ⟸ NM_001134224 |
- Peptide Label: | isoform d |
- UniProtKB: | Q53TD8 (UniProtKB/Swiss-Prot), Q13187 (UniProtKB/Swiss-Prot), O15326 (UniProtKB/Swiss-Prot), Q8TC02 (UniProtKB/Swiss-Prot), Q96PE3 (UniProtKB/Swiss-Prot), A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_004018 ⟸ NM_004027 |
- Peptide Label: | isoform a |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001127697 ⟸ NM_001134225 |
- Peptide Label: | isoform c |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001557 ⟸ NM_001566 |
- Peptide Label: | isoform b |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_006712566 ⟸ XM_006712503 |
- Peptide Label: | isoform X6 |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_006712568 ⟸ XM_006712505 |
- Peptide Label: | isoform X14 |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_006712562 ⟸ XM_006712499 |
- Peptide Label: | isoform X1 |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_006712565 ⟸ XM_006712502 |
- Peptide Label: | isoform X4 |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_006712569 ⟸ XM_006712506 |
- Peptide Label: | isoform X16 |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_006712563 ⟸ XM_006712500 |
- Peptide Label: | isoform X2 |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_006712564 ⟸ XM_006712501 |
- Peptide Label: | isoform X3 |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_011509426 ⟸ XM_011511124 |
- Peptide Label: | isoform X19 |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_011509425 ⟸ XM_011511123 |
- Peptide Label: | isoform X12 |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_011509424 ⟸ XM_011511122 |
- Peptide Label: | isoform X5 |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_011509427 ⟸ XM_011511125 |
- Peptide Label: | isoform X28 |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_011509429 ⟸ XM_011511127 |
- Peptide Label: | isoform X30 |
- Sequence: |
RefSeq Acc Id: | XP_016859489 ⟸ XM_017004000 |
- Peptide Label: | isoform X21 |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_016859483 ⟸ XM_017003994 |
- Peptide Label: | isoform X13 |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_016859490 ⟸ XM_017004001 |
- Peptide Label: | isoform X22 |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | XP_024308644 ⟸ XM_024452876 |
- Peptide Label: | isoform X1 |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001338353 ⟸ NM_001351424 |
- Peptide Label: | isoform e |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001338354 ⟸ NM_001351425 |
- Peptide Label: | isoform f |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001338355 ⟸ NM_001351426 |
- Peptide Label: | isoform f |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001338356 ⟸ NM_001351427 |
- Peptide Label: | isoform a |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001338357 ⟸ NM_001351428 |
- Peptide Label: | isoform g |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_001338358 ⟸ NM_001351429 |
- Peptide Label: | isoform h |
- UniProtKB: | A0A9L9PY55 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | ENSP00000074304 ⟸ ENST00000074304 |
RefSeq Acc Id: | ENSP00000427722 ⟸ ENST00000523221 |
RefSeq Acc Id: | ENSP00000386777 ⟸ ENST00000409851 |
RefSeq Acc Id: | ENSP00000387294 ⟸ ENST00000409540 |
RefSeq Acc Id: | ENSP00000386704 ⟸ ENST00000409016 |
RefSeq Acc Id: | ENSP00000386329 ⟸ ENST00000409463 |
RefSeq Acc Id: | XP_047300155 ⟸ XM_047444199 |
- Peptide Label: | isoform X8 |
RefSeq Acc Id: | XP_047300165 ⟸ XM_047444209 |
- Peptide Label: | isoform X19 |
RefSeq Acc Id: | XP_047300160 ⟸ XM_047444204 |
- Peptide Label: | isoform X11 |
RefSeq Acc Id: | XP_047300156 ⟸ XM_047444200 |
- Peptide Label: | isoform X9 |
RefSeq Acc Id: | XP_047300157 ⟸ XM_047444201 |
- Peptide Label: | isoform X10 |
RefSeq Acc Id: | XP_047300159 ⟸ XM_047444203 |
- Peptide Label: | isoform X11 |
RefSeq Acc Id: | XP_047300167 ⟸ XM_047444211 |
- Peptide Label: | isoform X23 |
RefSeq Acc Id: | XP_047300162 ⟸ XM_047444206 |
- Peptide Label: | isoform X17 |
RefSeq Acc Id: | XP_047300166 ⟸ XM_047444210 |
- Peptide Label: | isoform X20 |
RefSeq Acc Id: | XP_047300170 ⟸ XM_047444214 |
- Peptide Label: | isoform X26 |
RefSeq Acc Id: | XP_047300161 ⟸ XM_047444205 |
- Peptide Label: | isoform X15 |
RefSeq Acc Id: | XP_047300154 ⟸ XM_047444198 |
- Peptide Label: | isoform X7 |
RefSeq Acc Id: | XP_047300163 ⟸ XM_047444207 |
- Peptide Label: | isoform X18 |
RefSeq Acc Id: | XP_047300168 ⟸ XM_047444212 |
- Peptide Label: | isoform X24 |
RefSeq Acc Id: | XP_047300169 ⟸ XM_047444213 |
- Peptide Label: | isoform X25 |
RefSeq Acc Id: | XP_047300171 ⟸ XM_047444215 |
- Peptide Label: | isoform X27 |
RefSeq Acc Id: | XP_047300173 ⟸ XM_047444217 |
- Peptide Label: | isoform X29 |
RefSeq Acc Id: | XP_047300174 ⟸ XM_047444218 |
- Peptide Label: | isoform X31 |
RefSeq Acc Id: | ENSP00000516656 ⟸ ENST00000706935 |
RefSeq Acc Id: | XP_054197821 ⟸ XM_054341846 |
- Peptide Label: | isoform X8 |
RefSeq Acc Id: | XP_054197825 ⟸ XM_054341850 |
- Peptide Label: | isoform X11 |
RefSeq Acc Id: | XP_054197814 ⟸ XM_054341839 |
- Peptide Label: | isoform X1 |
RefSeq Acc Id: | XP_054197819 ⟸ XM_054341844 |
- Peptide Label: | isoform X6 |
RefSeq Acc Id: | XP_054197822 ⟸ XM_054341847 |
- Peptide Label: | isoform X9 |
RefSeq Acc Id: | XP_054197836 ⟸ XM_054341861 |
- Peptide Label: | isoform X21 |
RefSeq Acc Id: | XP_054197823 ⟸ XM_054341848 |
- Peptide Label: | isoform X10 |
RefSeq Acc Id: | XP_054197834 ⟸ XM_054341859 |
- Peptide Label: | isoform X19 |
RefSeq Acc Id: | XP_054197837 ⟸ XM_054341862 |
- Peptide Label: | isoform X22 |
RefSeq Acc Id: | XP_054197824 ⟸ XM_054341849 |
- Peptide Label: | isoform X11 |
RefSeq Acc Id: | XP_054197838 ⟸ XM_054341863 |
- Peptide Label: | isoform X23 |
RefSeq Acc Id: | XP_054197828 ⟸ XM_054341853 |
- Peptide Label: | isoform X14 |
RefSeq Acc Id: | XP_054197829 ⟸ XM_054341854 |
- Peptide Label: | isoform X14 |
RefSeq Acc Id: | XP_054197832 ⟸ XM_054341857 |
- Peptide Label: | isoform X17 |
RefSeq Acc Id: | XP_054197835 ⟸ XM_054341860 |
- Peptide Label: | isoform X20 |
RefSeq Acc Id: | XP_054197841 ⟸ XM_054341866 |
- Peptide Label: | isoform X26 |
RefSeq Acc Id: | XP_054197830 ⟸ XM_054341855 |
- Peptide Label: | isoform X15 |
RefSeq Acc Id: | XP_054197813 ⟸ XM_054341838 |
- Peptide Label: | isoform X1 |
RefSeq Acc Id: | XP_054197817 ⟸ XM_054341842 |
- Peptide Label: | isoform X4 |
RefSeq Acc Id: | XP_054197831 ⟸ XM_054341856 |
- Peptide Label: | isoform X16 |
RefSeq Acc Id: | XP_054197815 ⟸ XM_054341840 |
- Peptide Label: | isoform X2 |
RefSeq Acc Id: | XP_054197816 ⟸ XM_054341841 |
- Peptide Label: | isoform X3 |
RefSeq Acc Id: | XP_054197820 ⟸ XM_054341845 |
- Peptide Label: | isoform X7 |
RefSeq Acc Id: | XP_054197827 ⟸ XM_054341852 |
- Peptide Label: | isoform X13 |
RefSeq Acc Id: | XP_054197833 ⟸ XM_054341858 |
- Peptide Label: | isoform X18 |
RefSeq Acc Id: | XP_054197818 ⟸ XM_054341843 |
- Peptide Label: | isoform X5 |
RefSeq Acc Id: | XP_054197826 ⟸ XM_054341851 |
- Peptide Label: | isoform X12 |
RefSeq Acc Id: | XP_054197839 ⟸ XM_054341864 |
- Peptide Label: | isoform X24 |
RefSeq Acc Id: | XP_054197840 ⟸ XM_054341865 |
- Peptide Label: | isoform X25 |
RefSeq Acc Id: | XP_054197842 ⟸ XM_054341867 |
- Peptide Label: | isoform X27 |
RefSeq Acc Id: | XP_054197843 ⟸ XM_054341868 |
- Peptide Label: | isoform X28 |
RefSeq Acc Id: | XP_054197844 ⟸ XM_054341869 |
- Peptide Label: | isoform X29 |
RefSeq Acc Id: | XP_054197846 ⟸ XM_054341871 |
- Peptide Label: | isoform X31 |
RefSeq Acc Id: | XP_054197845 ⟸ XM_054341870 |
- Peptide Label: | isoform X30 |
Name | Modeler | Protein Id | AA Range | Protein Structure |
AF-Q96PE3-F1-model_v2 | AlphaFold | Q96PE3 | 1-977 | view protein structure |
RGD ID: | 6861120 | ||||||||
Promoter ID: | EPDNEW_H3725 | ||||||||
Type: | initiation region | ||||||||
Name: | INPP4A_1 | ||||||||
Description: | inositol polyphosphate-4-phosphatase type I A | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H3726 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
|
RGD ID: | 6797653 | ||||||||
Promoter ID: | HG_KWN:34057 | ||||||||
Type: | Non-CpG | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | CD4+TCell, Lymphoblastoid | ||||||||
Transcripts: | OTTHUMT00000329570, UC002SYY.1 | ||||||||
Position: |
|
RGD ID: | 6861122 | ||||||||
Promoter ID: | EPDNEW_H3726 | ||||||||
Type: | multiple initiation site | ||||||||
Name: | INPP4A_2 | ||||||||
Description: | inositol polyphosphate-4-phosphatase type I A | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H3725 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
|
RGD ID: | 6797654 | ||||||||
Promoter ID: | HG_KWN:34058 | ||||||||
Type: | Non-CpG | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | Lymphoblastoid | ||||||||
Transcripts: | OTTHUMT00000329571 | ||||||||
Position: |
|
RGD ID: | 6797655 | ||||||||
Promoter ID: | HG_KWN:34059 | ||||||||
Type: | CpG-Island | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | Lymphoblastoid | ||||||||
Transcripts: | OTTHUMT00000329572 | ||||||||
Position: |
|
RGD ID: | 6797656 | ||||||||
Promoter ID: | HG_KWN:34060 | ||||||||
Type: | Non-CpG | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | Lymphoblastoid | ||||||||
Transcripts: | OTTHUMT00000329573 | ||||||||
Position: |
|
Database | Acc Id | Source(s) |
AGR Gene | HGNC:6074 | AgrOrtholog |
COSMIC | INPP4A | COSMIC |
Ensembl Genes | ENSG00000040933 | Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Ensembl Transcript | ENST00000409016 | ENTREZGENE |
ENST00000409016.8 | UniProtKB/Swiss-Prot | |
ENST00000409463.5 | UniProtKB/TrEMBL | |
ENST00000409540 | ENTREZGENE | |
ENST00000409540.7 | UniProtKB/Swiss-Prot | |
ENST00000409851 | ENTREZGENE | |
ENST00000409851.8 | UniProtKB/Swiss-Prot | |
ENST00000523221 | ENTREZGENE | |
ENST00000523221.1 | UniProtKB/Swiss-Prot | |
ENST00000706935.1 | UniProtKB/TrEMBL | |
Gene3D-CATH | 2.60.40.150 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
GTEx | ENSG00000040933 | GTEx |
HGNC ID | HGNC:6074 | ENTREZGENE |
Human Proteome Map | INPP4A | Human Proteome Map |
InterPro | C2_dom | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
C2_domain_sf | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
INPP4 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
KEGG Report | hsa:3631 | UniProtKB/Swiss-Prot |
NCBI Gene | 3631 | ENTREZGENE |
OMIM | 600916 | OMIM |
PANTHER | INOSITOL POLYPHOSPHATE-4-PHOSPHATASE TYPE I A | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
PTHR12187 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
PharmGKB | PA29882 | PharmGKB |
PROSITE | PS50004 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Superfamily-SCOP | SSF49562 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
UniProt | A0A9L9PY55 | ENTREZGENE, UniProtKB/TrEMBL |
B8ZZB2_HUMAN | UniProtKB/TrEMBL | |
INP4A_HUMAN | UniProtKB/Swiss-Prot | |
O15326 | ENTREZGENE | |
Q13187 | ENTREZGENE | |
Q53TD8 | ENTREZGENE | |
Q8TC02 | ENTREZGENE | |
Q96PE3 | ENTREZGENE | |
UniProt Secondary | O15326 | UniProtKB/Swiss-Prot |
Q13187 | UniProtKB/Swiss-Prot | |
Q53TD8 | UniProtKB/Swiss-Prot | |
Q8TC02 | UniProtKB/Swiss-Prot |
Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
---|---|---|---|---|---|---|---|
2015-08-25 | INPP4A | inositol polyphosphate-4-phosphatase type I A | INPP4A | inositol polyphosphate-4-phosphatase, type I, 107kDa | Symbol and/or name change | 5135510 | APPROVED |