Imported Annotations - OMIM | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Porokeratosis, Disseminated Superficial Actinic, 8 | IAGP | 7240710 | OMIM |



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Imported Annotations - OMIM | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Porokeratosis, Disseminated Superficial Actinic, 8 | IAGP | 7240710 | OMIM |
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1. | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
2. | RGD automated import pipeline for gene-chemical interactions |
3. | RGD automated import pipeline for human HPO-to-gene-to-disease annotations |
PubMed | 11780052 12477932 12693554 14702039 15489334 16344560 18375752 20382737 21613220 21873635 21988832 23467297 24292772 24912190 24962569 25180256 29363573 30236596 30365528 |
SLC17A9 (Homo sapiens - human) |
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Slc17a9 (Mus musculus - house mouse) |
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Slc17a9 (Rattus norvegicus - Norway rat) |
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Slc17a9 (Chinchilla lanigera - long-tailed chinchilla) |
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SLC17A9 (Pan paniscus - bonobo/pygmy chimpanzee) |
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SLC17A9 (Canis lupus familiaris - dog) |
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Slc17a9 (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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SLC17A9 (Sus scrofa - pig) |
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RH78178 |
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RH67463 |
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G32772 |
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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. |
RefSeq Transcripts | NG_041785 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
NM_001302643 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_022082 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_011528978 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XR_936601 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GenBank Nucleotide | AK027065 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AK074107 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK095473 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK125597 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK298503 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AL121673 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC025312 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC027447 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC038593 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH471077 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
DB153870 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | NM_001302643 ⟹ NP_001289572 | ||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||
Type: | CODING | ||||||||||||||
Position: |
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Sequence: |
CCCGCCCTGCCCCGCCTGCCCGCCCTGGTGGCCGTCTGGGGGCGACAAGTCCTGAGAGAACCAGhide sequence |
RefSeq Acc Id: | NM_022082 ⟹ NP_071365 | ||||||||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||||||||
Position: |
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Sequence: |
CCCGCCCTGCCCCGCCTGCCCGCCCTGGTGGCCGTCTGGGGGCGACAAGTCCTGAGAGAACCAGhide sequence |
RefSeq Acc Id: | XM_011528978 ⟹ XP_011527280 | |||||||||
RefSeq Status: | ||||||||||
Type: | CODING | |||||||||
Position: |
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Sequence: |
AGACGGAAGCGCGCTGGGACTGACACGTGGACTTGGGCGGTGCTGCCCGGGTGGGTCAGCCTGGhide sequence |
RefSeq Acc Id: | XR_936601 | |||||||||
RefSeq Status: | ||||||||||
Type: | NON-CODING | |||||||||
Position: |
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Sequence: |
GACAAGTCCTGAGAGAACCAGACGGAAGCGCGCTGGGACTGACACGTGGACTTGGGCGGTGCTGhide sequence |
Protein RefSeqs | NP_001289572 | (Get FASTA) | NCBI Sequence Viewer |
NP_071365 | (Get FASTA) | NCBI Sequence Viewer | |
XP_011527280 | (Get FASTA) | NCBI Sequence Viewer | |
GenBank Protein | AAH25312 | (Get FASTA) | NCBI Sequence Viewer |
AAH27447 | (Get FASTA) | NCBI Sequence Viewer | |
BAB15644 | (Get FASTA) | NCBI Sequence Viewer | |
BAB84933 | (Get FASTA) | NCBI Sequence Viewer | |
BAG53064 | (Get FASTA) | NCBI Sequence Viewer | |
BAG60710 | (Get FASTA) | NCBI Sequence Viewer | |
EAW75313 | (Get FASTA) | NCBI Sequence Viewer | |
EAW75314 | (Get FASTA) | NCBI Sequence Viewer | |
EAW75315 | (Get FASTA) | NCBI Sequence Viewer | |
EAW75316 | (Get FASTA) | NCBI Sequence Viewer | |
EAW75317 | (Get FASTA) | NCBI Sequence Viewer | |
Q9BYT1 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_071365 ⟸ NM_022082 |
- Peptide Label: | isoform 1 |
- Sequence: |
MQPPPDEARRDMAGDTQWSRPECQAWTGTLLLGTCLLYCARSSMPICTVSMSQDFGWNKKEAGIhide sequence |
RefSeq Acc Id: | NP_001289572 ⟸ NM_001302643 |
- Peptide Label: | isoform 2 |
- Sequence: |
MTLTSRRQDSQEARPECQAWTGTLLLGTCLLYCARSSMPICTVSMSQDFGWNKKEAGIVLSSFFhide sequence |
RefSeq Acc Id: | XP_011527280 ⟸ XM_011528978 |
- Peptide Label: | isoform X1 |
- Sequence: |
MTFSRILMGLLQGVYFPALTSLLSQKVRESERAFTYSIVGAGSQFGTLLTGAVGSLLLEWYGWQhide sequence |
RGD ID: | 6799080 | |||||||||
Promoter ID: | HG_KWN:40136 | |||||||||
Type: | CpG-Island | |||||||||
SO ACC ID: | SO:0000170 | |||||||||
Source: | MPROMDB | |||||||||
Tissues & Cell Lines: | K562, Lymphoblastoid, NB4 | |||||||||
Transcripts: | NM_022082, OTTHUMT00000080101, OTTHUMT00000080104, UC002YDZ.2 | |||||||||
Position: |
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RGD ID: | 6799062 | |||||||||
Promoter ID: | HG_KWN:40138 | |||||||||
Type: | CpG-Island | |||||||||
SO ACC ID: | SO:0000170 | |||||||||
Source: | MPROMDB | |||||||||
Tissues & Cell Lines: | Lymphoblastoid | |||||||||
Transcripts: | OTTHUMT00000080102 | |||||||||
Position: |
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RGD ID: | 6799064 | |||||||||
Promoter ID: | HG_KWN:40139 | |||||||||
Type: | CpG-Island | |||||||||
SO ACC ID: | SO:0000170 | |||||||||
Source: | MPROMDB | |||||||||
Tissues & Cell Lines: | Lymphoblastoid, NB4 | |||||||||
Transcripts: | OTTHUMT00000080105 | |||||||||
Position: |
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RGD ID: | 13602364 | |||||||||
Promoter ID: | EPDNEW_H27366 | |||||||||
Type: | initiation region | |||||||||
Name: | SLC17A9_1 | |||||||||
Description: | solute carrier family 17 member 9 | |||||||||
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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RGD ID: | 13602370 | |||||||||
Promoter ID: | EPDNEW_H27367 | |||||||||
Type: | initiation region | |||||||||
Name: | SLC17A9_2 | |||||||||
Description: | solute carrier family 17 member 9 | |||||||||
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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Name | Type | Condition(s) | Position(s) | Clinical significance |
GRCh38/hg38 20q13.33(chr20:62455231-63839491)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052768]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052768]|See cases [RCV000052768] | Chr20:62455231..63839491 [GRCh38] Chr20:61030287..62470844 [GRCh37] Chr20:60463682..61941288 [NCBI36] Chr20:20q13.33 |
pathogenic |
GRCh38/hg38 20q13.33(chr20:62545370-64241486)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052769]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052769]|See cases [RCV000052769] | Chr20:62545370..64241486 [GRCh38] Chr20:61142577..62872839 [GRCh37] Chr20:60553022..62343283 [NCBI36] Chr20:20q13.33 |
pathogenic |
GRCh38/hg38 20q13.33(chr20:62561794-63331723)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052770]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052770]|See cases [RCV000052770] | Chr20:62561794..63331723 [GRCh38] Chr20:61211869..61963075 [GRCh37] Chr20:60569446..61433519 [NCBI36] Chr20:20q13.33 |
pathogenic |
GRCh38/hg38 20q13.12-13.33(chr20:44787704-64277321)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053035]|Abnormality of the heart [RCV000053036]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053035]|See cases [RCV000053035] | Chr20:44787704..64277321 [GRCh38] Chr20:43416345..62908674 [GRCh37] Chr20:42849759..62379118 [NCBI36] Chr20:20q13.12-13.33 |
pathogenic |
NM_022082.3(SLC17A9):c.1139C>T (p.Ala380Val) | single nucleotide variant | Malignant melanoma [RCV000063795] | Chr20:62966724 [GRCh38] Chr20:61598076 [GRCh37] Chr20:61068521 [NCBI36] Chr20:20q13.33 |
not provided |
NM_022082.4(SLC17A9):c.932G>A (p.Arg311Gln) | single nucleotide variant | POROKERATOSIS 8, DISSEMINATED SUPERFICIAL ACTINIC TYPE [RCV000144721]|Porokeratosis 8, disseminated superficial actinic type [RCV000144721] | Chr20:62965153 [GRCh38] Chr20:61596505 [GRCh37] Chr20:20q13.33 |
pathogenic |
NM_022082.4(SLC17A9):c.25C>T (p.Arg9Cys) | single nucleotide variant | POROKERATOSIS 8, DISSEMINATED SUPERFICIAL ACTINIC TYPE [RCV000144722]|Porokeratosis 8, disseminated superficial actinic type [RCV000144722] | Chr20:62952855 [GRCh38] Chr20:61584207 [GRCh37] Chr20:20q13.33 |
pathogenic |
GRCh38/hg38 20q13.33(chr20:62561794-64277321)x1 | copy number loss | See cases [RCV000133842] | Chr20:62561794..64277321 [GRCh38] Chr20:61211869..62908674 [GRCh37] Chr20:60569446..62379118 [NCBI36] Chr20:20q13.33 |
pathogenic |
GRCh38/hg38 20q13.32-13.33(chr20:59041966-64277321)x3 | copy number gain | See cases [RCV000135805] | Chr20:59041966..64277321 [GRCh38] Chr20:57617021..62908674 [GRCh37] Chr20:57050416..62379118 [NCBI36] Chr20:20q13.32-13.33 |
pathogenic |
GRCh38/hg38 20p13-q13.33(chr20:99557-64277321)x3 | copy number gain | See cases [RCV000135859] | Chr20:99557..64277321 [GRCh38] Chr20:80198..62908674 [GRCh37] Chr20:28198..62379118 [NCBI36] Chr20:20p13-q13.33 |
pathogenic |
GRCh38/hg38 20q13.2-13.33(chr20:56198032-64277321)x3 | copy number gain | See cases [RCV000138035] | Chr20:56198032..64277321 [GRCh38] Chr20:54773088..62908674 [GRCh37] Chr20:54206495..62379118 [NCBI36] Chr20:20q13.2-13.33 |
pathogenic |
GRCh38/hg38 20q13.33(chr20:61326549-64277326)x3 | copy number gain | See cases [RCV000139100] | Chr20:61326549..64277326 [GRCh38] Chr20:59901605..62908679 [GRCh37] Chr20:59335000..62379123 [NCBI36] Chr20:20q13.33 |
pathogenic |
GRCh38/hg38 20q13.33(chr20:62939140-63198970)x3 | copy number gain | See cases [RCV000139758] | Chr20:62939140..63198970 [GRCh38] Chr20:61570492..61830322 [GRCh37] Chr20:61040937..61300767 [NCBI36] Chr20:20q13.33 |
likely benign |
GRCh38/hg38 20q13.31-13.33(chr20:57229415-64273089)x3 | copy number gain | See cases [RCV000141347] | Chr20:57229415..64273089 [GRCh38] Chr20:55804471..62904442 [GRCh37] Chr20:55237878..62374886 [NCBI36] Chr20:20q13.31-13.33 |
pathogenic |
GRCh38/hg38 20q13.33(chr20:62582073-64284202)x1 | copy number loss | See cases [RCV000141744] | Chr20:62582073..64284202 [GRCh38] Chr20:61179280..62915555 [GRCh37] Chr20:60589725..62385999 [NCBI36] Chr20:20q13.33 |
pathogenic |
GRCh38/hg38 20q13.33(chr20:62663307-64284202)x1 | copy number loss | See cases [RCV000141676] | Chr20:62663307..64284202 [GRCh38] Chr20:61294659..62915555 [GRCh37] Chr20:60765104..62385999 [NCBI36] Chr20:20q13.33 |
pathogenic |
GRCh38/hg38 20q13.2-13.33(chr20:53236165-64284202)x3 | copy number gain | See cases [RCV000143584] | Chr20:53236165..64284202 [GRCh38] Chr20:51852704..62915555 [GRCh37] Chr20:51286111..62385999 [NCBI36] Chr20:20q13.2-13.33 |
likely pathogenic |
GRCh37/hg19 20q13.33(chr20:60882468-62045494)x1 | copy number loss | Ductal breast carcinoma [RCV000207130] | Chr20:60882468..62045494 [GRCh37] Chr20:20q13.33 |
uncertain significance |
chr20:60885242-61929348 complex variant | complex | Ductal breast carcinoma [RCV000207152] | Chr20:60885242..61929348 [GRCh37] Chr20:20q13.33 |
uncertain significance |
GRCh37/hg19 20q13.33(chr20:61429900-62293991)x1 | copy number loss | See cases [RCV000240573] | Chr20:61429900..62293991 [GRCh37] Chr20:20q13.33 |
pathogenic |
GRCh37/hg19 20q13.33(chr20:61337529-62904501)x1 | copy number loss | not provided [RCV000488148] | Chr20:61337529..62904501 [GRCh37] Chr20:20q13.33 |
likely pathogenic |
GRCh37/hg19 20q13.33(chr20:61595624-61637326)x3 | copy number gain | See cases [RCV000445922] | Chr20:61595624..61637326 [GRCh37] Chr20:20q13.33 |
benign |
GRCh37/hg19 20q13.33(chr20:60473339-62915555)x3 | copy number gain | See cases [RCV000446009] | Chr20:60473339..62915555 [GRCh37] Chr20:20q13.33 |
uncertain significance |
GRCh37/hg19 20q13.2-13.33(chr20:51542616-62915555)x3 | copy number gain | See cases [RCV000511980] | Chr20:51542616..62915555 [GRCh37] Chr20:20q13.2-13.33 |
likely pathogenic |
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)x3 | copy number gain | See cases [RCV000510832] | Chr20:61569..62915555 [GRCh37] Chr20:20p13-q13.33 |
pathogenic |
GRCh37/hg19 20p13-q13.33(chr20:61569-62915555) | copy number gain | See cases [RCV000512450] | Chr20:61569..62915555 [GRCh37] Chr20:20p13-q13.33 |
pathogenic |
GRCh37/hg19 20q13.33(chr20:61530581-61911114)x1 | copy number loss | See cases [RCV000512342] | Chr20:61530581..61911114 [GRCh37] Chr20:20q13.33 |
likely benign |
GRCh37/hg19 20q13.33(chr20:61022397-61738592)x1 | copy number loss | not provided [RCV000684122] | Chr20:61022397..61738592 [GRCh37] Chr20:20q13.33 |
uncertain significance |
NM_022082.4(SLC17A9):c.931C>T (p.Arg311Trp) | single nucleotide variant | Porokeratosis 8, disseminated superficial actinic type [RCV000714806] | Chr20:62965152 [GRCh38] Chr20:61596504 [GRCh37] Chr20:20q13.33 |
uncertain significance |
GRCh37/hg19 20p13-q13.33(chr20:63244-62948788)x3 | copy number gain | not provided [RCV000741058] | Chr20:63244..62948788 [GRCh37] Chr20:20p13-q13.33 |
pathogenic |
GRCh37/hg19 20p13-q13.33(chr20:63244-62961294)x3 | copy number gain | not provided [RCV000741059] | Chr20:63244..62961294 [GRCh37] Chr20:20p13-q13.33 |
pathogenic |
GRCh37/hg19 20q13.33(chr20:60053234-62961294)x3 | copy number gain | not provided [RCV000741328] | Chr20:60053234..62961294 [GRCh37] Chr20:20q13.33 |
pathogenic |
GRCh37/hg19 20q13.33(chr20:60063645-62961294)x3 | copy number gain | not provided [RCV000741329] | Chr20:60063645..62961294 [GRCh37] Chr20:20q13.33 |
pathogenic |
GRCh37/hg19 20q13.33(chr20:61576777-61604147)x3 | copy number gain | not provided [RCV000741361] | Chr20:61576777..61604147 [GRCh37] Chr20:20q13.33 |
benign |
GRCh37/hg19 20q13.33(chr20:61585706-61604147)x3 | copy number gain | not provided [RCV000741362] | Chr20:61585706..61604147 [GRCh37] Chr20:20q13.33 |
benign |
GRCh37/hg19 20p13-q13.33(chr20:63244-62912463)x3 | copy number gain | not provided [RCV000741057] | Chr20:63244..62912463 [GRCh37] Chr20:20p13-q13.33 |
pathogenic |
GRCh37/hg19 20q13.2-13.33(chr20:54143747-62194881) | copy number gain | not provided [RCV000767669] | Chr20:54143747..62194881 [GRCh37] Chr20:20q13.2-13.33 |
pathogenic |
GRCh37/hg19 20q13.33(chr20:61548147-61619208)x1 | copy number loss | not provided [RCV000849776] | Chr20:61548147..61619208 [GRCh37] Chr20:20q13.33 |
uncertain significance |
GRCh37/hg19 20q13.33(chr20:60946209-61975606)x3 | copy number gain | not provided [RCV000847979] | Chr20:60946209..61975606 [GRCh37] Chr20:20q13.33 |
uncertain significance |
Database | Acc Id | Source(s) |
AGR Gene | HGNC:16192 | AgrOrtholog |
COSMIC | SLC17A9 | COSMIC |
Ensembl Genes | ENSG00000101194 | ENTREZGENE, UniProtKB/Swiss-Prot |
Ensembl Protein | ENSP00000359374 | ENTREZGENE, UniProtKB/Swiss-Prot |
ENSP00000359376 | ENTREZGENE, UniProtKB/Swiss-Prot | |
ENSP00000388215 | UniProtKB/TrEMBL | |
Ensembl Transcript | ENST00000370349 | ENTREZGENE, UniProtKB/Swiss-Prot |
ENST00000370351 | ENTREZGENE, UniProtKB/Swiss-Prot | |
ENST00000411611 | UniProtKB/TrEMBL | |
GTEx | ENSG00000101194 | GTEx |
HGNC ID | HGNC:16192 | ENTREZGENE |
Human Proteome Map | SLC17A9 | Human Proteome Map |
InterPro | MFS | UniProtKB/Swiss-Prot |
MFS_dom | UniProtKB/Swiss-Prot | |
MFS_trans_sf | UniProtKB/Swiss-Prot | |
Sugar_transporter_CS | UniProtKB/Swiss-Prot | |
KEGG Report | hsa:63910 | UniProtKB/Swiss-Prot |
NCBI Gene | 63910 | ENTREZGENE |
OMIM | 612107 | OMIM |
616063 | OMIM | |
Pfam | MFS_1 | UniProtKB/Swiss-Prot |
PharmGKB | PA164725806 | PharmGKB |
PROSITE | MFS | UniProtKB/Swiss-Prot |
SUGAR_TRANSPORT_2 | UniProtKB/Swiss-Prot | |
Superfamily-SCOP | SSF103473 | UniProtKB/Swiss-Prot |
UniGene | Hs.512686 | ENTREZGENE |
UniProt | H0UI90_HUMAN | UniProtKB/TrEMBL |
Q5W197_HUMAN | UniProtKB/TrEMBL | |
Q9BYT1 | ENTREZGENE, UniProtKB/Swiss-Prot | |
UniProt Secondary | B3KTF2 | UniProtKB/Swiss-Prot |
Q5W198 | UniProtKB/Swiss-Prot | |
Q8TB07 | UniProtKB/Swiss-Prot | |
Q8TBP4 | UniProtKB/Swiss-Prot | |
Q8TEL5 | UniProtKB/Swiss-Prot | |
Q9BYT0 | UniProtKB/Swiss-Prot | |
Q9BYT2 | UniProtKB/Swiss-Prot |
Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
---|---|---|---|---|---|---|---|
2016-02-23 | SLC17A9 | solute carrier family 17 member 9 | solute carrier family 17 (vesicular nucleotide transporter), member 9 | Symbol and/or name change | 5135510 | APPROVED | |
2013-07-23 | SLC17A9 | solute carrier family 17 (vesicular nucleotide transporter), member 9 | solute carrier family 17, member 9 | Symbol and/or name change | 5135510 | APPROVED | |
2011-07-27 | SLC17A9 | solute carrier family 17, member 9 | C20orf59 | chromosome 20 open reading frame 59 | Symbol and/or name change | 5135510 | APPROVED |
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More on SLC17A9 | |
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Alliance Gene |
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NCBI Gene |
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Ensembl Gene |
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JBrowse: hg19 hg38 |
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HGNC Report |
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NCBI Genome Data Viewer |
CRRD Object Information | |
CRRD ID: | 1323655 |
Created: | 2005-01-12 |
Species: | Homo sapiens |
Last Modified: | 2019-11-26 |
Status: | ACTIVE |
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.