Imported Disease Annotations - CTDTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | basal cell carcinoma | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:26950094 | |
|
Imported Disease Annotations - CTDTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | basal cell carcinoma | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:26950094 | |
|
|
|
|
|
|
|
|
# | Reference Title | Reference Citation |
1. | GOAs Human GO annotations | GOA_HUMAN data from the GO Consortium |
2. | ClinVar Automated Import and Annotation Pipeline | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
3. | Data Import for Chemical-Gene Interactions | RGD automated import pipeline for gene-chemical interactions |
PMID:1988494 | PMID:8012361 | PMID:8132574 | PMID:8575831 | PMID:9799600 | PMID:9812991 | PMID:12477932 | PMID:14574404 | PMID:14656967 | PMID:14667819 | PMID:15986447 | PMID:19423540 |
PMID:19851445 | PMID:19913121 | PMID:20205591 | PMID:20406964 | PMID:20438785 | PMID:20628086 | PMID:21323541 | PMID:21873635 | PMID:23263863 | PMID:23535732 | PMID:23577725 | PMID:25416956 |
PMID:28514442 | PMID:30712867 | PMID:31452512 | PMID:32296183 | PMID:32587355 | PMID:32707033 | PMID:33961781 | PMID:34315543 | PMID:35545034 | PMID:35944360 | PMID:38252411 |
STK19 (Homo sapiens - human) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Stk19 (Mus musculus - house mouse) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Stk19 (Rattus norvegicus - Norway rat) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Stk19 (Chinchilla lanigera - long-tailed chinchilla) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
STK19 (Pan paniscus - bonobo/pygmy chimpanzee) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
LOC488436 (Canis lupus familiaris - dog) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Stk19 (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
STK19 (Sus scrofa - pig) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
STK19 (Chlorocebus sabaeus - green monkey) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Stk19 (Heterocephalus glaber - naked mole-rat) |
|
.
Variants in STK19
44 total Variants |
Name | Type | Condition(s) | Position(s) | Clinical significance |
NM_004197.1(STK19):c.265G>A (p.Asp89Asn) | single nucleotide variant | Malignant melanoma of skin [RCV000425183]|Squamous cell carcinoma of the skin [RCV000437661] | Chr6:31972346 [GRCh38] Chr6:31940123 [GRCh37] Chr6:32048102 [NCBI36] Chr6:6p21.33 |
likely pathogenic|not provided |
NM_004197.1(STK19):c.854G>A (p.Trp285Ter) | single nucleotide variant | Malignant melanoma [RCV000067303] | Chr6:31980501 [GRCh38] Chr6:31948278 [GRCh37] Chr6:32056257 [NCBI36] Chr6:6p21.33 |
not provided |
GRCh38/hg38 6p21.33(chr6:31980353-32041234)x3 | copy number gain | See cases [RCV000139532] | Chr6:31980353..32041234 [GRCh38] Chr6:31948130..32009011 [GRCh37] Chr6:32056109..32116990 [NCBI36] Chr6:6p21.33 |
likely benign |
GRCh38/hg38 6p21.33(chr6:31971993-32012974)x1 | copy number loss | See cases [RCV000141578] | Chr6:31971993..32012974 [GRCh38] Chr6:31939770..31980751 [GRCh37] Chr6:32047749..32088729 [NCBI36] Chr6:6p21.33 |
benign |
GRCh38/hg38 6p21.33(chr6:31980422-32041505)x1 | copy number loss | See cases [RCV000141496] | Chr6:31980422..32041505 [GRCh38] Chr6:31948199..32009282 [GRCh37] Chr6:32056178..32117261 [NCBI36] Chr6:6p21.33 |
benign |
GRCh38/hg38 6p25.3-12.3(chr6:156974-46789291)x3 | copy number gain | See cases [RCV000143497] | Chr6:156974..46789291 [GRCh38] Chr6:156974..46757028 [GRCh37] Chr6:101974..46864987 [NCBI36] Chr6:6p25.3-12.3 |
pathogenic |
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3 | copy number gain | See cases [RCV000512067] | Chr6:156975..170919482 [GRCh37] Chr6:6p25.3-q27 |
pathogenic |
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482) | copy number gain | See cases [RCV000510595] | Chr6:156975..170919482 [GRCh37] Chr6:6p25.3-q27 |
pathogenic |
GRCh37/hg19 6p25.3-q27(chr6:60107-171054786)x3 | copy number gain | not provided [RCV000745400] | Chr6:60107..171054786 [GRCh37] Chr6:6p25.3-q27 |
pathogenic |
GRCh37/hg19 6p25.3-q27(chr6:165632-170919470)x3 | copy number gain | not provided [RCV000745404] | Chr6:165632..170919470 [GRCh37] Chr6:6p25.3-q27 |
pathogenic |
GRCh37/hg19 6p25.3-q27(chr6:108666-170980171)x3 | copy number gain | not provided [RCV000745403] | Chr6:108666..170980171 [GRCh37] Chr6:6p25.3-q27 |
pathogenic |
GRCh37/hg19 6p22.1-21.32(chr6:28130359-32108367)x3 | copy number gain | not provided [RCV000745592] | Chr6:28130359..32108367 [GRCh37] Chr6:6p22.1-21.32 |
uncertain significance |
GRCh37/hg19 6p22.1-q14.1(chr6:29455465-81447367) | copy number gain | not provided [RCV000767714] | Chr6:29455465..81447367 [GRCh37] Chr6:6p22.1-q14.1 |
pathogenic |
GRCh37/hg19 6p21.33-21.32(chr6:31916915-32278000)x3 | copy number gain | not provided [RCV001005792] | Chr6:31916915..32278000 [GRCh37] Chr6:6p21.33-21.32 |
uncertain significance |
GRCh37/hg19 6p21.33-21.31(chr6:31036397-34088832)x3 | copy number gain | not provided [RCV001005791] | Chr6:31036397..34088832 [GRCh37] Chr6:6p21.33-21.31 |
likely pathogenic |
NM_005510.4(DXO):c.308T>C (p.Leu103Pro) | single nucleotide variant | Inborn genetic diseases [RCV003198544] | Chr6:31971368 [GRCh38] Chr6:31939145 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NC_000006.11:g.(?_30695893)_(36953949_?)dup | duplication | Proteasome-associated autoinflammatory syndrome 1 [RCV003113679] | Chr6:30695893..36953949 [GRCh37] Chr6:6p21.33-21.2 |
uncertain significance |
NM_004197.2(STK19):c.665G>A (p.Arg222Gln) | single nucleotide variant | Inborn genetic diseases [RCV002727669] | Chr6:31980747 [GRCh38] Chr6:31948524 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_005510.4(DXO):c.191C>A (p.Ala64Asp) | single nucleotide variant | Inborn genetic diseases [RCV002840702] | Chr6:31971485 [GRCh38] Chr6:31939262 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_004197.2(STK19):c.614G>A (p.Arg205Gln) | single nucleotide variant | Inborn genetic diseases [RCV002749970] | Chr6:31980696 [GRCh38] Chr6:31948473 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_004197.2(STK19):c.438G>A (p.Met146Ile) | single nucleotide variant | Inborn genetic diseases [RCV002693078] | Chr6:31979518 [GRCh38] Chr6:31947295 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_004197.2(STK19):c.-5G>T | single nucleotide variant | Inborn genetic diseases [RCV002845024] | Chr6:31972407 [GRCh38] Chr6:31940184 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_004197.2(STK19):c.317A>G (p.Glu106Gly) | single nucleotide variant | Inborn genetic diseases [RCV002713051] | Chr6:31978982 [GRCh38] Chr6:31946759 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_005510.4(DXO):c.-186C>T | single nucleotide variant | Inborn genetic diseases [RCV002665344] | Chr6:31972108 [GRCh38] Chr6:31939885 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_004197.2(STK19):c.698T>C (p.Ile233Thr) | single nucleotide variant | Inborn genetic diseases [RCV002956177] | Chr6:31980780 [GRCh38] Chr6:31948557 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_005510.4(DXO):c.59A>G (p.Asn20Ser) | single nucleotide variant | Inborn genetic diseases [RCV002891720] | Chr6:31971617 [GRCh38] Chr6:31939394 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_004197.2(STK19):c.343G>T (p.Ala115Ser) | single nucleotide variant | Inborn genetic diseases [RCV002963962] | Chr6:31979423 [GRCh38] Chr6:31947200 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_032454.1(STK19):c.238A>T (p.Thr80Ser) | single nucleotide variant | Inborn genetic diseases [RCV002792969] | Chr6:31972319 [GRCh38] Chr6:31940096 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_005510.4(DXO):c.165T>G (p.Asp55Glu) | single nucleotide variant | Inborn genetic diseases [RCV002669852] | Chr6:31971511 [GRCh38] Chr6:31939288 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_004197.2(STK19):c.38T>C (p.Phe13Ser) | single nucleotide variant | Inborn genetic diseases [RCV002669587] | Chr6:31972449 [GRCh38] Chr6:31940226 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_004197.2(STK19):c.646C>T (p.Arg216Trp) | single nucleotide variant | Inborn genetic diseases [RCV003191813] | Chr6:31980728 [GRCh38] Chr6:31948505 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_004197.2(STK19):c.-3G>A | single nucleotide variant | Inborn genetic diseases [RCV003190066] | Chr6:31972409 [GRCh38] Chr6:31940186 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_005510.4(DXO):c.236G>A (p.Gly79Asp) | single nucleotide variant | Inborn genetic diseases [RCV003198955] | Chr6:31971440 [GRCh38] Chr6:31939217 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_004197.2(STK19):c.104C>G (p.Ser35Trp) | single nucleotide variant | Inborn genetic diseases [RCV003215269] | Chr6:31972624 [GRCh38] Chr6:31940401 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_004197.2(STK19):c.397C>T (p.Leu133Phe) | single nucleotide variant | Inborn genetic diseases [RCV003303854] | Chr6:31979477 [GRCh38] Chr6:31947254 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_004197.2(STK19):c.356G>A (p.Arg119Gln) | single nucleotide variant | Inborn genetic diseases [RCV003349142] | Chr6:31979436 [GRCh38] Chr6:31947213 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_004197.2(STK19):c.323A>G (p.Tyr108Cys) | single nucleotide variant | Inborn genetic diseases [RCV003367408] | Chr6:31978988 [GRCh38] Chr6:31946765 [GRCh37] Chr6:6p21.33 |
uncertain significance |
NM_005510.4(DXO):c.-199G>A | single nucleotide variant | not provided [RCV003428811] | Chr6:31972121 [GRCh38] Chr6:31939898 [GRCh37] Chr6:6p21.33 |
likely benign |
The detailed report is available here: | Full Report | CSV | TAB | Printer | ||||
miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/). For more information about miRGate, see PMID:25858286 or access the full paper here. |
RH36425 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||
RH11436 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||
AL035178 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||
CYP21A2_2362 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||
STK19__5340 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||
SHGC-12566 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||
WI-7720 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||
WI-16314 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||
DOM3Z |
|
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 | 2112 | 1668 | 1488 | 371 | 862 | 238 | 3402 | 973 | 2300 | 276 | 1371 | 1529 | 147 | 1180 | 2000 | 2 | ||
Low | 327 | 1322 | 238 | 253 | 1088 | 227 | 955 | 1224 | 1434 | 143 | 89 | 84 | 28 | 1 | 24 | 788 | 4 | 2 |
Below cutoff | 1 | 1 |
RefSeq Acc Id: | ENST00000375331 ⟹ ENSP00000364480 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000375333 ⟹ ENSP00000364482 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000460018 ⟹ ENSP00000418350 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000463823 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000466132 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000466336 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000469907 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000471028 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000473983 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000478486 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000479644 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000483801 ⟹ ENSP00000418866 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000484540 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000490822 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000491861 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000492583 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000519179 ⟹ ENSP00000454870 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | ENST00000685781 ⟹ ENSP00000509445 | ||||||||
Type: | CODING | ||||||||
Position: |
|
RefSeq Acc Id: | NM_004197 ⟹ NP_004188 | ||||||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NM_032454 ⟹ NP_115830 | ||||||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NR_026717 | ||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||
Type: | NON-CODING | ||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||
Sequence: |
RefSeq Acc Id: | NP_115830 ⟸ NM_032454 |
- Peptide Label: | isoform 2 |
- UniProtKB: | A0A1U9X8L3 (UniProtKB/TrEMBL) |
- Sequence: |
RefSeq Acc Id: | NP_004188 ⟸ NM_004197 |
- Peptide Label: | isoform 1 |
- UniProtKB: | Q5ST75 (UniProtKB/Swiss-Prot), Q5ST72 (UniProtKB/Swiss-Prot), Q5JP77 (UniProtKB/Swiss-Prot), Q31617 (UniProtKB/Swiss-Prot), Q13159 (UniProtKB/Swiss-Prot), P49842 (UniProtKB/Swiss-Prot), B0QZR5 (UniProtKB/Swiss-Prot), A6NFW8 (UniProtKB/Swiss-Prot), A6NF95 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | ENSP00000454870 ⟸ ENST00000519179 |
RefSeq Acc Id: | ENSP00000364480 ⟸ ENST00000375331 |
RefSeq Acc Id: | ENSP00000364482 ⟸ ENST00000375333 |
RefSeq Acc Id: | ENSP00000418866 ⟸ ENST00000483801 |
RefSeq Acc Id: | ENSP00000418350 ⟸ ENST00000460018 |
RefSeq Acc Id: | ENSP00000509445 ⟸ ENST00000685781 |
Name | Modeler | Protein Id | AA Range | Protein Structure |
AF-P49842-F1-model_v2 | AlphaFold | P49842 | 1-368 | view protein structure |
RGD ID: | 6872696 | ||||||||
Promoter ID: | EPDNEW_H9513 | ||||||||
Type: | initiation region | ||||||||
Name: | STK19_2 | ||||||||
Description: | serine/threonine kinase 19 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H9517 | ||||||||
Experiment Methods: | Single-end sequencing.; Paired-end sequencing. | ||||||||
Position: |
|
RGD ID: | 6872704 | ||||||||
Promoter ID: | EPDNEW_H9517 | ||||||||
Type: | initiation region | ||||||||
Name: | STK19_1 | ||||||||
Description: | serine/threonine kinase 19 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Alternative Promoters: | null; see alsoEPDNEW_H9513 | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
|
RGD ID: | 6804821 | ||||||||
Promoter ID: | HG_KWN:53035 | ||||||||
Type: | CpG-Island | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | K562, Lymphoblastoid, NB4 | ||||||||
Transcripts: | OTTHUMT00000076481, UC003NYT.1 | ||||||||
Position: |
|
RGD ID: | 6804144 | ||||||||
Promoter ID: | HG_KWN:53036 | ||||||||
Type: | CpG-Island | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | CD4+TCell, CD4+TCell_12Hour, CD4+TCell_2Hour, Jurkat, K562, Lymphoblastoid, NB4 | ||||||||
Transcripts: | ENST00000375338, NM_004197, NM_032454, OTTHUMT00000076477, OTTHUMT00000076478, OTTHUMT00000076480, OTTHUMT00000076485, OTTHUMT00000268648, OTTHUMT00000268668, OTTHUMT00000268669, UC010JTM.1 | ||||||||
Position: |
|
RGD ID: | 6804819 | ||||||||
Promoter ID: | HG_KWN:53037 | ||||||||
Type: | Non-CpG | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | MPROMDB | ||||||||
Tissues & Cell Lines: | K562 | ||||||||
Transcripts: | OTTHUMT00000268670 | ||||||||
Position: |
|
Database | Acc Id | Source(s) |
AGR Gene | HGNC:11398 | AgrOrtholog |
COSMIC | STK19 | COSMIC |
Ensembl Genes | ENSG00000204344 | Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
ENSG00000206342 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
ENSG00000226033 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
ENSG00000226257 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
ENSG00000234947 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
ENSG00000236250 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
ENSG00000272295 | UniProtKB/TrEMBL | |
Ensembl Transcript | ENST00000375331.7 | UniProtKB/Swiss-Prot |
ENST00000375333.3 | UniProtKB/Swiss-Prot | |
ENST00000383327.8 | UniProtKB/Swiss-Prot | |
ENST00000383328.6 | UniProtKB/TrEMBL | |
ENST00000424104.5 | UniProtKB/Swiss-Prot | |
ENST00000425138.5 | UniProtKB/Swiss-Prot | |
ENST00000426802.5 | UniProtKB/Swiss-Prot | |
ENST00000431383.6 | UniProtKB/Swiss-Prot | |
ENST00000433397.6 | UniProtKB/Swiss-Prot | |
ENST00000438256.6 | UniProtKB/Swiss-Prot | |
ENST00000444147.5 | UniProtKB/Swiss-Prot | |
ENST00000452688.6 | UniProtKB/Swiss-Prot | |
ENST00000460018 | UniProtKB/TrEMBL | |
ENST00000466132 | ENTREZGENE | |
ENST00000481181.5 | UniProtKB/TrEMBL | |
ENST00000483801.6 | UniProtKB/TrEMBL | |
ENST00000519179.6 | UniProtKB/TrEMBL | |
ENST00000519915.1 | UniProtKB/TrEMBL | |
ENST00000520138.5 | UniProtKB/TrEMBL | |
ENST00000523972.5 | UniProtKB/TrEMBL | |
ENST00000547578.1 | UniProtKB/TrEMBL | |
ENST00000549310.1 | UniProtKB/TrEMBL | |
ENST00000550656.1 | UniProtKB/TrEMBL | |
ENST00000551718.1 | UniProtKB/TrEMBL | |
ENST00000674578.1 | UniProtKB/TrEMBL | |
ENST00000685781 | ENTREZGENE | |
ENST00000685781.1 | UniProtKB/Swiss-Prot | |
GTEx | ENSG00000204344 | GTEx |
ENSG00000206342 | GTEx | |
ENSG00000226033 | GTEx | |
ENSG00000226257 | GTEx | |
ENSG00000234947 | GTEx | |
ENSG00000236250 | GTEx | |
ENSG00000272295 | GTEx | |
HGNC ID | HGNC:11398 | ENTREZGENE |
Human Proteome Map | STK19 | Human Proteome Map |
InterPro | Ser/Thr_kinase_19 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
KEGG Report | hsa:8859 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
NCBI Gene | 8859 | ENTREZGENE |
OMIM | 604977 | OMIM |
PANTHER | PTHR15243 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
SERINE/THREONINE-PROTEIN KINASE 19 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
Pfam | Stk19 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
PharmGKB | PA36206 | PharmGKB |
UniProt | A0A0G2JKI8_HUMAN | UniProtKB/TrEMBL |
A0A0G2JLL1_HUMAN | UniProtKB/TrEMBL | |
A0A140T8X5_HUMAN | UniProtKB/TrEMBL | |
A0A140TA37_HUMAN | UniProtKB/TrEMBL | |
A0A1U9X8L3 | ENTREZGENE, UniProtKB/TrEMBL | |
A6NF95 | ENTREZGENE | |
A6NFW8 | ENTREZGENE | |
B0QZR5 | ENTREZGENE | |
B7ZLI8_HUMAN | UniProtKB/TrEMBL | |
C9J6S8_HUMAN | UniProtKB/TrEMBL | |
H0YAS4_HUMAN | UniProtKB/TrEMBL | |
P49842 | ENTREZGENE | |
Q13159 | ENTREZGENE | |
Q31617 | ENTREZGENE | |
Q5JP77 | ENTREZGENE | |
Q5ST72 | ENTREZGENE | |
Q5ST75 | ENTREZGENE | |
STK19_HUMAN | UniProtKB/Swiss-Prot | |
UniProt Secondary | A6NF95 | UniProtKB/Swiss-Prot |
A6NFW8 | UniProtKB/Swiss-Prot | |
B0QZR5 | UniProtKB/Swiss-Prot | |
Q13159 | UniProtKB/Swiss-Prot | |
Q31617 | UniProtKB/Swiss-Prot | |
Q5JP77 | UniProtKB/Swiss-Prot | |
Q5ST72 | UniProtKB/Swiss-Prot | |
Q5ST75 | UniProtKB/Swiss-Prot |