Q9NP85 · PODO_HUMAN
- ProteinPodocin
- GeneNPHS2
- StatusUniProtKB reviewed (Swiss-Prot)
- Organism
- Amino acids383 (go to sequence)
- Protein existenceEvidence at protein level
- Annotation score5/5
Function
function
Plays a role in the regulation of glomerular permeability, acting probably as a linker between the plasma membrane and the cytoskeleton.
GO annotations
all annotations | all molecular function | virus receptor activity | dna binding | rna binding | cytoskeletal motor activity | catalytic activity | gtpase activity | structural molecule activity | transporter activity | cytoskeletal protein binding | lipid binding | cyclase activity | antioxidant activity | oxidoreductase activity | transferase activity | hydrolase activity | lyase activity | isomerase activity | ligase activity | protein tag activity | cargo receptor activity | histone binding | protein folding chaperone | translation regulator activity | nutrient reservoir activity | receptor ligand activity | molecular transducer activity | molecular adaptor activity | toxin activity | cell adhesion mediator activity | molecular function regulator activity | virus coreceptor activity | catalytic activity, acting on a protein | catalytic activity, acting on dna | catalytic activity, acting on rna | molecular carrier activity | transcription regulator activity | general transcription initiation factor activity | molecular sensor activity | molecular sequestering activity | atp-dependent activity | other molecular function | all biological process | mitotic cell cycle | cytokinesis | cytoplasmic translation | immune system process | muscle system process | circulatory system process | renal system process | respiratory system process | carbohydrate metabolic process | generation of precursor metabolites and energy | dna replication | dna repair | dna recombination | chromatin organization | dna-templated transcription | regulation of dna-templated transcription | trna metabolic process | protein folding | protein glycosylation | amino acid metabolic process | modified amino acid metabolic process | lipid metabolic process | vitamin metabolic process | sulfur compound metabolic process | intracellular protein transport | nucleocytoplasmic transport | autophagy | inflammatory response | mitochondrion organization | cytoskeleton organization | microtubule-based movement | peroxisome organization | lysosome organization | chromosome segregation | cell adhesion | establishment or maintenance of cell polarity | programmed cell death | photosynthesis | mrna metabolic process | snrna metabolic process | vesicle-mediated transport | reproductive process | digestive system process | signaling | cell differentiation | protein catabolic process | extracellular matrix organization | regulatory ncrna-mediated gene silencing | telomere organization | cell junction organization | wound healing | ribosome biogenesis | cilium organization | anatomical structure development | cell motility | nervous system process | endocrine process | protein maturation | transmembrane transport | nucleobase-containing small molecule metabolic process | hepaticobiliary system process | membrane organization | protein-containing complex assembly | cell wall organization or biogenesis | nitrogen cycle metabolic process | protein localization to plasma membrane | defense response to other organism | detoxification | meiotic nuclear division | mitotic nuclear division | mitochondrial gene expression | carbohydrate derivative metabolic process | other biological process | all cellular component | nuclear chromosome | extracellular region | extracellular space | cell wall | nucleus | nuclear envelope | nucleoplasm | chromosome | nucleolus | mitochondrion | lysosome | endosome | vacuole | peroxisome | endoplasmic reticulum | golgi apparatus | lipid droplet | microtubule organizing center | cytosol | ribosome | cytoskeleton | plasma membrane | cilium | plastid | thylakoid | external encapsulating structure | extracellular matrix | cytoplasmic vesicle | organelle | other cellular component | |||
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Aspect | Term | |
---|---|---|
Cellular Component | cell-cell junction | |
Cellular Component | cytoplasmic side of plasma membrane | |
Cellular Component | endoplasmic reticulum | |
Cellular Component | extracellular exosome | |
Cellular Component | membrane raft | |
Cellular Component | plasma membrane | |
Cellular Component | protein-containing complex | |
Cellular Component | slit diaphragm | |
Biological Process | actin cytoskeleton organization | |
Biological Process | gene expression | |
Biological Process | glomerular filtration | |
Biological Process | metanephric podocyte development |
Enzyme and pathway databases
Protein family/group databases
Names & Taxonomy
Protein names
- Recommended namePodocin
Gene names
Organism names
- Organism
- Taxonomic lineageEukaryota > Metazoa > Chordata > Craniata > Vertebrata > Euteleostomi > Mammalia > Eutheria > Euarchontoglires > Primates > Haplorrhini > Catarrhini > Hominidae > Homo
Accessions
- Primary accessionQ9NP85
- Secondary accessions
Proteomes
Organism-specific databases
Subcellular Location
UniProt Annotation
GO Annotation
Isoform 1
Cell membrane ; Peripheral membrane protein
Isoform 2
Features
Showing features for topological domain, intramembrane.
Type | ID | Position(s) | Description | |||
---|---|---|---|---|---|---|
Topological domain | 1-102 | Cytoplasmic | ||||
Sequence: MERRARSSSRESRGRGGRTPHKENKRAKAERSGGGRGRQEAGPEPSGSGRAGTPGEPRAPAATVVDVDEVRGSGEEGTEVVALLESERPEEGTKSSGLGACE | ||||||
Intramembrane | 103-123 | |||||
Sequence: WLLVLISLLFIIMTFPFSIWF | ||||||
Topological domain | 124-383 | Cytoplasmic | ||||
Sequence: CVKVVQEYERVIIFRLGHLLPGRAKGPGLFFFLPCLDTYHKVDLRLQTLEIPFHEIVTKDMFIMEIDAICYYRMENASLLLSSLAHVSKAVQFLVQTTMKRLLAHRSLTEILLERKSIAQDAKVALDSVTCIWGIKVERIEIKDVRLPAGLQHSLAVEAEAQRQAKVRMIAAEAEKAASESLRMAAEILSGTPAAVQLRYLHTLQSLSTEKPSTVVLPLPFDLLNCLSSPSNRTQGSLPFPSPSKPVEPLNPKKKDSPML |
Keywords
- Cellular component
Disease & Variants
Involvement in disease
Nephrotic syndrome 2 (NPHS2)
- Note
- DescriptionA form of nephrotic syndrome, a renal disease clinically characterized by severe proteinuria, resulting in complications such as hypoalbuminemia, hyperlipidemia and edema. Kidney biopsies show non-specific histologic changes such as focal segmental glomerulosclerosis and diffuse mesangial proliferation. The disorder is resistant to steroid treatment and progresses to end-stage renal failure in the first or second decades. Some patients show later onset of the disorder.
- See alsoMIM:600995
Natural variants in NPHS2
Variant ID | Position(s) | Change | Description | |
---|---|---|---|---|
VAR_072134 | 3 | R>G | in NPHS2 | |
VAR_072135 | 18 | R>T | in NPHS2 | |
VAR_072136 | 26 | R>M | in NPHS2 | |
VAR_072137 | 28 | K>M | in NPHS2; dbSNP:rs1340195940 | |
VAR_071212 | 29 | A>T | in NPHS2; dbSNP:rs561887984 | |
VAR_072138 | 30 | E>K | in NPHS2; dbSNP:rs1477180313 | |
VAR_072139 | 30 | E>Q | in NPHS2 | |
VAR_072140 | 39 | Q>L | in NPHS2 | |
VAR_087597 | 39-383 | missing | in NPHS2 | |
VAR_072141 | 89 | P>T | in NPHS2 | |
VAR_010232 | 92 | G>C | in NPHS2; dbSNP:rs74315345 | |
VAR_071216 | 97 | G>S | in NPHS2; uncertain significance; dbSNP:rs200913299 | |
VAR_071217 | 107 | L>P | in NPHS2 | |
VAR_072142 | 115 | M>T | in NPHS2 | |
VAR_071218 | 116 | T>P | in NPHS2 | |
VAR_071219 | 118 | P>L | in NPHS2; dbSNP:rs869025495 | |
VAR_072143 | 122 | W>L | in NPHS2; dbSNP:rs750332447 | |
VAR_071220 | 122 | W>S | in NPHS2; dbSNP:rs750332447 | |
VAR_072144 | 124 | C>W | in NPHS2; dbSNP:rs139290621 | |
VAR_072145 | 126 | K>N | in NPHS2; dbSNP:rs267598208 | |
VAR_087598 | 138 | R>P | in NPHS2 | |
VAR_010233 | 138 | R>Q | in NPHS2; dbSNP:rs74315342 | |
VAR_079808 | 138-383 | missing | in NPHS2 | |
VAR_072146 | 139 | L>R | in NPHS2; dbSNP:rs1345260812 | |
VAR_072147 | 142 | L>P | in NPHS2; dbSNP:rs12240233 | |
VAR_010234 | 160 | D>G | in NPHS2; dbSNP:rs74315346 | |
VAR_071221 | 168 | R>C | in NPHS2; dbSNP:rs786204583 | |
VAR_071222 | 168 | R>H | in NPHS2; dbSNP:rs530318579 | |
VAR_071223 | 168 | R>S | in NPHS2 | |
VAR_071224 | 172 | L>V | in NPHS2; uncertain significance | |
VAR_071225 | 175 | P>V | in NPHS2; requires 2 nucleotide substitutions | |
VAR_010235 | 180 | V>M | in NPHS2; dbSNP:rs74315347 | |
VAR_071226 | 183 | D>Y | in NPHS2; dbSNP:rs2125784628 | |
VAR_071227 | 187 | M>I | in NPHS2; uncertain significance; dbSNP:rs1673966819 | |
VAR_072148 | 192 | I>V | in NPHS2 | |
VAR_071228 | 208 | A>T | in NPHS2; dbSNP:rs200587413 | |
VAR_072149 | 211 | S>A | in NPHS2 | |
VAR_072150 | 213 | A>T | in NPHS2 | |
VAR_072151 | 218 | V>G | in NPHS2 | |
VAR_071229 | 221 | T>I | in NPHS2 | |
VAR_072152 | 228 | H>D | in NPHS2 | |
VAR_072153 | 229 | R>L | in NPHS2 | |
VAR_071230 | 229 | R>Q | in NPHS2; uncertain significance; dbSNP:rs61747728 | |
VAR_071231 | 236-238 | missing | in NPHS2 | |
VAR_071233 | 238 | R>S | in NPHS2; dbSNP:rs748812981 | |
VAR_087599 | 254 | C>F | in NPHS2; uncertain significance | |
VAR_071235 | 260 | V>E | in NPHS2; dbSNP:rs775006954 | |
VAR_072154 | 267 | D>N | in NPHS2 | |
VAR_072155 | 268 | V>L | in NPHS2 | |
VAR_072156 | 276 | H>L | in NPHS2 | |
VAR_071237 | 281 | E>A | in NPHS2 | |
VAR_071238 | 281 | E>K | in NPHS2 | |
VAR_075617 | 284 | A>V | in NPHS2; uncertain significance; dbSNP:rs780761368 | |
VAR_071239 | 290 | V>M | in NPHS2; dbSNP:rs200482683 | |
VAR_010236 | 291 | R>W | in NPHS2; dbSNP:rs74315348 | |
VAR_071240 | 296 | E>K | in NPHS2 | |
VAR_072157 | 301 | missing | in NPHS2 | |
VAR_071241 | 309 | A>V | in NPHS2 | |
VAR_075618 | 310 | E>K | in NPHS2; uncertain significance; dbSNP:rs1673254835 | |
VAR_079810 | 310 | E>V | in NPHS2; uncertain significance; dbSNP:rs1572255744 | |
VAR_071242 | 315 | T>I | in NPHS2; uncertain significance | |
VAR_072158 | 322 | R>Q | in NPHS2; dbSNP:rs776859868 | |
VAR_079811 | 328 | Q>R | in NPHS2; uncertain significance; dbSNP:rs1673239865 | |
VAR_071243 | 333 | E>G | in NPHS2; uncertain significance; dbSNP:rs866921812 | |
VAR_072159 | 341 | P>S | in NPHS2; dbSNP:rs1214047676 | |
VAR_072160 | 370 | V>G | in NPHS2 |
Features
Showing features for natural variant.
Type | ID | Position(s) | Description | |||
---|---|---|---|---|---|---|
Natural variant | VAR_072134 | 3 | in NPHS2 | |||
Sequence: R → G | ||||||
Natural variant | VAR_072135 | 18 | in NPHS2 | |||
Sequence: R → T | ||||||
Natural variant | VAR_010231 | 20 | in dbSNP:rs74315344 | |||
Sequence: P → L | ||||||
Natural variant | VAR_072136 | 26 | in NPHS2 | |||
Sequence: R → M | ||||||
Natural variant | VAR_072137 | 28 | in NPHS2; dbSNP:rs1340195940 | |||
Sequence: K → M | ||||||
Natural variant | VAR_071212 | 29 | in NPHS2; dbSNP:rs561887984 | |||
Sequence: A → T | ||||||
Natural variant | VAR_072138 | 30 | in NPHS2; dbSNP:rs1477180313 | |||
Sequence: E → K | ||||||
Natural variant | VAR_072139 | 30 | in NPHS2 | |||
Sequence: E → Q | ||||||
Natural variant | VAR_071213 | 34 | in dbSNP:rs1674742844 | |||
Sequence: G → E | ||||||
Natural variant | VAR_072140 | 39 | in NPHS2 | |||
Sequence: Q → L | ||||||
Natural variant | VAR_087597 | 39-383 | in NPHS2 | |||
Sequence: Missing | ||||||
Natural variant | VAR_071214 | 44 | ||||
Sequence: E → A | ||||||
Natural variant | VAR_071215 | 61 | in dbSNP:rs201050491 | |||
Sequence: A → V | ||||||
Natural variant | VAR_072141 | 89 | in NPHS2 | |||
Sequence: P → T | ||||||
Natural variant | VAR_010232 | 92 | in NPHS2; dbSNP:rs74315345 | |||
Sequence: G → C | ||||||
Natural variant | VAR_071216 | 97 | in NPHS2; uncertain significance; dbSNP:rs200913299 | |||
Sequence: G → S | ||||||
Natural variant | VAR_071217 | 107 | in NPHS2 | |||
Sequence: L → P | ||||||
Natural variant | VAR_072142 | 115 | in NPHS2 | |||
Sequence: M → T | ||||||
Natural variant | VAR_071218 | 116 | in NPHS2 | |||
Sequence: T → P | ||||||
Natural variant | VAR_071219 | 118 | in NPHS2; dbSNP:rs869025495 | |||
Sequence: P → L | ||||||
Natural variant | VAR_072143 | 122 | in NPHS2; dbSNP:rs750332447 | |||
Sequence: W → L | ||||||
Natural variant | VAR_071220 | 122 | in NPHS2; dbSNP:rs750332447 | |||
Sequence: W → S | ||||||
Natural variant | VAR_072144 | 124 | in NPHS2; dbSNP:rs139290621 | |||
Sequence: C → W | ||||||
Natural variant | VAR_072145 | 126 | in NPHS2; dbSNP:rs267598208 | |||
Sequence: K → N | ||||||
Natural variant | VAR_087598 | 138 | in NPHS2 | |||
Sequence: R → P | ||||||
Natural variant | VAR_010233 | 138 | in NPHS2; dbSNP:rs74315342 | |||
Sequence: R → Q | ||||||
Natural variant | VAR_079808 | 138-383 | in NPHS2 | |||
Sequence: Missing | ||||||
Natural variant | VAR_072146 | 139 | in NPHS2; dbSNP:rs1345260812 | |||
Sequence: L → R | ||||||
Natural variant | VAR_072147 | 142 | in NPHS2; dbSNP:rs12240233 | |||
Sequence: L → P | ||||||
Natural variant | VAR_010234 | 160 | in NPHS2; dbSNP:rs74315346 | |||
Sequence: D → G | ||||||
Natural variant | VAR_071221 | 168 | in NPHS2; dbSNP:rs786204583 | |||
Sequence: R → C | ||||||
Natural variant | VAR_071222 | 168 | in NPHS2; dbSNP:rs530318579 | |||
Sequence: R → H | ||||||
Natural variant | VAR_071223 | 168 | in NPHS2 | |||
Sequence: R → S | ||||||
Natural variant | VAR_071224 | 172 | in NPHS2; uncertain significance | |||
Sequence: L → V | ||||||
Natural variant | VAR_071225 | 175 | in NPHS2; requires 2 nucleotide substitutions | |||
Sequence: P → V | ||||||
Natural variant | VAR_010235 | 180 | in NPHS2; dbSNP:rs74315347 | |||
Sequence: V → M | ||||||
Natural variant | VAR_071226 | 183 | in NPHS2; dbSNP:rs2125784628 | |||
Sequence: D → Y | ||||||
Natural variant | VAR_071227 | 187 | in NPHS2; uncertain significance; dbSNP:rs1673966819 | |||
Sequence: M → I | ||||||
Natural variant | VAR_072148 | 192 | in NPHS2 | |||
Sequence: I → V | ||||||
Natural variant | VAR_071228 | 208 | in NPHS2; dbSNP:rs200587413 | |||
Sequence: A → T | ||||||
Natural variant | VAR_072149 | 211 | in NPHS2 | |||
Sequence: S → A | ||||||
Natural variant | VAR_072150 | 213 | in NPHS2 | |||
Sequence: A → T | ||||||
Natural variant | VAR_072151 | 218 | in NPHS2 | |||
Sequence: V → G | ||||||
Natural variant | VAR_071229 | 221 | in NPHS2 | |||
Sequence: T → I | ||||||
Natural variant | VAR_072152 | 228 | in NPHS2 | |||
Sequence: H → D | ||||||
Natural variant | VAR_072153 | 229 | in NPHS2 | |||
Sequence: R → L | ||||||
Natural variant | VAR_071230 | 229 | in NPHS2; uncertain significance; dbSNP:rs61747728 | |||
Sequence: R → Q | ||||||
Natural variant | VAR_071231 | 236-238 | in NPHS2 | |||
Sequence: Missing | ||||||
Natural variant | VAR_071232 | 237 | in dbSNP:rs146906190 | |||
Sequence: E → Q | ||||||
Natural variant | VAR_071233 | 238 | in NPHS2; dbSNP:rs748812981 | |||
Sequence: R → S | ||||||
Natural variant | VAR_071234 | 242 | in dbSNP:rs61747727 | |||
Sequence: A → V | ||||||
Natural variant | VAR_087599 | 254 | in NPHS2; uncertain significance | |||
Sequence: C → F | ||||||
Natural variant | VAR_071235 | 260 | in NPHS2; dbSNP:rs775006954 | |||
Sequence: V → E | ||||||
Natural variant | VAR_071236 | 264 | in dbSNP:rs369697947 | |||
Sequence: E → Q | ||||||
Natural variant | VAR_072154 | 267 | in NPHS2 | |||
Sequence: D → N | ||||||
Natural variant | VAR_072155 | 268 | in NPHS2 | |||
Sequence: V → L | ||||||
Natural variant | VAR_072156 | 276 | in NPHS2 | |||
Sequence: H → L | ||||||
Natural variant | VAR_071237 | 281 | in NPHS2 | |||
Sequence: E → A | ||||||
Natural variant | VAR_071238 | 281 | in NPHS2 | |||
Sequence: E → K | ||||||
Natural variant | VAR_075617 | 284 | in NPHS2; uncertain significance; dbSNP:rs780761368 | |||
Sequence: A → V | ||||||
Natural variant | VAR_071239 | 290 | in NPHS2; dbSNP:rs200482683 | |||
Sequence: V → M | ||||||
Natural variant | VAR_010236 | 291 | in NPHS2; dbSNP:rs74315348 | |||
Sequence: R → W | ||||||
Natural variant | VAR_071240 | 296 | in NPHS2 | |||
Sequence: E → K | ||||||
Natural variant | VAR_079809 | 297 | in dbSNP:rs199506378 | |||
Sequence: A → V | ||||||
Natural variant | VAR_072157 | 301 | in NPHS2 | |||
Sequence: Missing | ||||||
Natural variant | VAR_071241 | 309 | in NPHS2 | |||
Sequence: A → V | ||||||
Natural variant | VAR_075618 | 310 | in NPHS2; uncertain significance; dbSNP:rs1673254835 | |||
Sequence: E → K | ||||||
Natural variant | VAR_079810 | 310 | in NPHS2; uncertain significance; dbSNP:rs1572255744 | |||
Sequence: E → V | ||||||
Natural variant | VAR_071242 | 315 | in NPHS2; uncertain significance | |||
Sequence: T → I | ||||||
Natural variant | VAR_072158 | 322 | in NPHS2; dbSNP:rs776859868 | |||
Sequence: R → Q | ||||||
Natural variant | VAR_079811 | 328 | in NPHS2; uncertain significance; dbSNP:rs1673239865 | |||
Sequence: Q → R | ||||||
Natural variant | VAR_071243 | 333 | in NPHS2; uncertain significance; dbSNP:rs866921812 | |||
Sequence: E → G | ||||||
Natural variant | VAR_072159 | 341 | in NPHS2; dbSNP:rs1214047676 | |||
Sequence: P → S | ||||||
Natural variant | VAR_072160 | 370 | in NPHS2 | |||
Sequence: V → G |
Variants
We now provide the "Disease & Variants" viewer in its own tab.
The viewer provides 550 variants from UniProt as well as other sources including ClinVar and dbSNP.
Keywords
- Disease
Organism-specific databases
Miscellaneous
Genetic variation databases
PTM/Processing
Features
Showing features for chain, lipidation, glycosylation.
Type | ID | Position(s) | Description | |||
---|---|---|---|---|---|---|
Chain | PRO_0000094035 | 1-383 | Podocin | |||
Sequence: MERRARSSSRESRGRGGRTPHKENKRAKAERSGGGRGRQEAGPEPSGSGRAGTPGEPRAPAATVVDVDEVRGSGEEGTEVVALLESERPEEGTKSSGLGACEWLLVLISLLFIIMTFPFSIWFCVKVVQEYERVIIFRLGHLLPGRAKGPGLFFFLPCLDTYHKVDLRLQTLEIPFHEIVTKDMFIMEIDAICYYRMENASLLLSSLAHVSKAVQFLVQTTMKRLLAHRSLTEILLERKSIAQDAKVALDSVTCIWGIKVERIEIKDVRLPAGLQHSLAVEAEAQRQAKVRMIAAEAEKAASESLRMAAEILSGTPAAVQLRYLHTLQSLSTEKPSTVVLPLPFDLLNCLSSPSNRTQGSLPFPSPSKPVEPLNPKKKDSPML | ||||||
Lipidation | 101 | S-palmitoyl cysteine | ||||
Sequence: C | ||||||
Glycosylation | 287 | In isoform Q9NP85-2; N-linked (GlcNAc...) asparagine | ||||
Sequence: Q |
Post-translational modification
Isoform 2
Glycosylated.
Keywords
- PTM
Proteomic databases
PTM databases
Interaction
Subunit
Interacts with nephrin/NPHS1 and KIRREL1. Interacts directly with CD2AP. Interacts with DDN (By similarity).
Binary interactions
Type | Entry 1 | Entry 2 | Number of experiments | Intact | |
---|---|---|---|---|---|
BINARY | Q9NP85 | IQGAP1 P46940 | 4 | EBI-6897706, EBI-297509 |
Protein-protein interaction databases
Miscellaneous
Structure
Family & Domains
Features
Showing features for compositional bias, region.
Type | ID | Position(s) | Description | |||
---|---|---|---|---|---|---|
Compositional bias | 1-37 | Basic and acidic residues | ||||
Sequence: MERRARSSSRESRGRGGRTPHKENKRAKAERSGGGRG | ||||||
Region | 1-76 | Disordered | ||||
Sequence: MERRARSSSRESRGRGGRTPHKENKRAKAERSGGGRGRQEAGPEPSGSGRAGTPGEPRAPAATVVDVDEVRGSGEE | ||||||
Region | 355-383 | Disordered | ||||
Sequence: NRTQGSLPFPSPSKPVEPLNPKKKDSPML |
Sequence similarities
Belongs to the band 7/mec-2 family.
Phylogenomic databases
Family and domain databases
Sequence & Isoform
- Sequence statusComplete
This entry describes 2 isoforms produced by Alternative splicing.
Q9NP85-1
This isoform has been chosen as the canonical sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry.
- Name1
- Length383
- Mass (Da)42,201
- Last updated2000-10-01 v1
- ChecksumBBB57783C840F752
Q9NP85-2
- Name2
- SynonymsPod-short
- Differences from canonical
- 179-246: Missing
Features
Showing features for compositional bias, alternative sequence.
Type | ID | Position(s) | Description | |||
---|---|---|---|---|---|---|
Compositional bias | 1-37 | Basic and acidic residues | ||||
Sequence: MERRARSSSRESRGRGGRTPHKENKRAKAERSGGGRG | ||||||
Alternative sequence | VSP_000499 | 179-246 | in isoform 2 | |||
Sequence: Missing |
Keywords
- Coding sequence diversity
- Technical term
Sequence databases
Nucleotide Sequence | Protein Sequence | Molecule Type | Status | |
---|---|---|---|---|
AJ279246 EMBL· GenBank· DDBJ | CAB83272.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AJ279247 EMBL· GenBank· DDBJ | CAB83272.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AJ279248 EMBL· GenBank· DDBJ | CAB83272.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AJ279249 EMBL· GenBank· DDBJ | CAB83272.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AJ279250 EMBL· GenBank· DDBJ | CAB83272.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AJ279251 EMBL· GenBank· DDBJ | CAB83272.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AJ279252 EMBL· GenBank· DDBJ | CAB83272.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AJ279253 EMBL· GenBank· DDBJ | CAB83272.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
AJ279254 EMBL· GenBank· DDBJ | CAB83216.1 EMBL· GenBank· DDBJ | mRNA | ||
AL160286 EMBL· GenBank· DDBJ | - | Genomic DNA | No translation available. | |
CH471067 EMBL· GenBank· DDBJ | EAW91049.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
CH471067 EMBL· GenBank· DDBJ | EAW91050.1 EMBL· GenBank· DDBJ | Genomic DNA | ||
BC029141 EMBL· GenBank· DDBJ | AAH29141.1 EMBL· GenBank· DDBJ | mRNA |