Q8IVL1 (NAV2_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 74.
History...
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Neuron navigator 2 EC=3.6.4.12 Alternative name(s): Helicase APC down-regulated 1 Pore membrane and/or filament-interacting-like protein 2 Retinoic acid inducible in neuroblastoma 1 Steerin-2 Unc-53 homolog 2 Short name=unc53H2 | ||||
| Gene names |
| ||||
| Organism | Homo sapiens (Human) | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 2488 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | Possesses 3' to 5' helicase activity and exonuclease activity. Involved in neuronal development, specifically in the development of different sensory organs. Ref.2 Ref.3 |
| Catalytic activity | ATP + H2O = ADP + phosphate. |
| Subcellular location | |
| Tissue specificity | Highly expressed in the brain, kidney and liver. Also expressed in the thyroid, mammary gland, spinal cord, heart, placenta and lung. Abundantly expressed in colon cancers. Ref.1 Ref.2 Ref.10 Ref.11 |
| Developmental stage | Highly expressed in the nervous system of developing embryos. Also expressed in fetal heart, liver and kidney. Ref.1 |
| Induction | By all-trans retinoic acid (ATRA). Up-regulated in colorectal carcinomas. Ref.1 Ref.2 |
| Sequence similarities | Belongs to the Nav/unc-53 family. Contains 1 CH (calponin-homology) domain. |
| Caution | Ref.3 experiments have been carried out in mouse. |
| Sequence caution | The sequence BAA92657.3 differs from that shown. Reason: Erroneous initiation. Translation N-terminally shortened. The sequence BAB85038.1 differs from that shown. Reason: Frameshift at position 2074. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Nucleus |
| Coding sequence diversity | Alternative splicing Polymorphism |
| Domain | Coiled coil |
| Ligand | ATP-binding Nucleotide-binding |
| Molecular function | Helicase Hydrolase |
| PTM | Phosphoprotein |
| Technical term | 3D-structure Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Cellular component | nucleus Inferred from electronic annotation. Source: UniProtKB-SubCell |
| Molecular function | ATP binding Inferred from electronic annotation. Source: UniProtKB-KW helicase activityInferred from electronic annotation. Source: UniProtKB-KW |
| Complete GO annotation... | |
Alternative products
| This entry describes 13 isoforms produced by alternative splicing. [Align] [Select] Note: Additional isoforms may exist. | ||||||
| Isoform 1 (identifier: Q8IVL1-1) 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. | ||||||
| Isoform 2 (identifier: Q8IVL1-2) Also known as: RAINB1d; The sequence of this isoform differs from the canonical sequence as follows: 256-278: Missing. 1634-1666: Missing. | ||||||
| Isoform 3 (identifier: Q8IVL1-3) Also known as: HELAD1L; The sequence of this isoform differs from the canonical sequence as follows: 256-278: Missing. 1634-1666: Missing. 1832-1834: Missing. | ||||||
| Isoform 4 (identifier: Q8IVL1-4) Also known as: HELAD1S; The sequence of this isoform differs from the canonical sequence as follows: 1-89: MPAILVASKM...GSVENGFDTQ → MESVSESSQQQKRKPVIHGLEDQKR 256-278: Missing. 1634-1666: Missing. 1832-1834: Missing. | ||||||
| Isoform 5 (identifier: Q8IVL1-5) The sequence of this isoform differs from the canonical sequence as follows: 1-937: Missing. 938-945: SLGLGDAD → MLWPRNLT 1480-1501: Missing. 1634-1666: Missing. 1832-1834: Missing. | ||||||
| Isoform 6 (identifier: Q8IVL1-6) The sequence of this isoform differs from the canonical sequence as follows: 1-1578: Missing. 1634-1666: Missing. 1832-1834: Missing. | ||||||
| Isoform 7 (identifier: Q8IVL1-7) The sequence of this isoform differs from the canonical sequence as follows: 1-1896: Missing. | ||||||
| Isoform 8 (identifier: Q8IVL1-8) The sequence of this isoform differs from the canonical sequence as follows: 1-88: MPAILVASKM...SGSVENGFDT → MLWPRNLT | ||||||
| Isoform 9 (identifier: Q8IVL1-9) The sequence of this isoform differs from the canonical sequence as follows: 1-88: MPAILVASKM...SGSVENGFDT → MAGTSAASSWGGGK | ||||||
| Isoform 10 (identifier: Q8IVL1-10) The sequence of this isoform differs from the canonical sequence as follows: 1-88: MPAILVASKM...SGSVENGFDT → MSVMLWRWEQNNTTMKL | ||||||
| Isoform 11 (identifier: Q8IVL1-11) The sequence of this isoform differs from the canonical sequence as follows: 1-88: MPAILVASKM...SGSVENGFDT → MESVSESSQQQKRKPVIHGLEDQKR | ||||||
| Isoform 12 (identifier: Q8IVL1-12) The sequence of this isoform differs from the canonical sequence as follows: 1-88: MPAILVASKM...SGSVENGFDT → MQECDSKFFLPSGSNSGFTLLSNQ | ||||||
| Isoform 13 (identifier: Q8IVL1-13) The sequence of this isoform differs from the canonical sequence as follows: 1-88: MPAILVASKM...SGSVENGFDT → MAIDLYCGLACLWGIHEPR |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||||||||||||||||
Molecule processing | |||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 2488 | 2488 | Neuron navigator 2 | PRO_0000267198 | |||||||||||||||||||
Regions | |||||||||||||||||||||||
| Domain | 85 – 192 | 108 | CH | ||||||||||||||||||||
| Nucleotide binding | 2157 – 2164 | 8 | ATP Potential | ||||||||||||||||||||
| Coiled coil | 498 – 531 | 34 | Potential | ||||||||||||||||||||
| Coiled coil | 743 – 771 | 29 | Potential | ||||||||||||||||||||
| Coiled coil | 1686 – 1773 | 88 | Potential | ||||||||||||||||||||
| Coiled coil | 1897 – 1964 | 68 | Potential | ||||||||||||||||||||
| Compositional bias | 192 – 255 | 64 | Gln-rich | ||||||||||||||||||||
| Compositional bias | 324 – 328 | 5 | Poly-Pro | ||||||||||||||||||||
| Compositional bias | 633 – 638 | 6 | Poly-Ser | ||||||||||||||||||||
| Compositional bias | 1363 – 1683 | 321 | Ser-rich | ||||||||||||||||||||
| Compositional bias | 1824 – 1829 | 6 | Poly-Lys | ||||||||||||||||||||
Amino acid modifications | |||||||||||||||||||||||
| Modified residue | 1480 | 1 | Phosphoserine Ref.15 | ||||||||||||||||||||
| Modified residue | 1484 | 1 | Phosphoserine Ref.15 | ||||||||||||||||||||
| Modified residue | 1488 | 1 | Phosphoserine Ref.15 | ||||||||||||||||||||
| Modified residue | 1703 | 1 | Phosphoserine Ref.12 | ||||||||||||||||||||
| Modified residue | 1977 | 1 | Phosphoserine Ref.13 Ref.14 Ref.15 | ||||||||||||||||||||
Natural variations | |||||||||||||||||||||||
| Alternative sequence | 1 – 1896 | 1896 | Missing in isoform 7. | VSP_021924 | |||||||||||||||||||
| Alternative sequence | 1 – 1578 | 1578 | Missing in isoform 6. | VSP_021925 | |||||||||||||||||||
| Alternative sequence | 1 – 937 | 937 | Missing in isoform 5. | VSP_021926 | |||||||||||||||||||
| Alternative sequence | 1 – 89 | 89 | MPAIL…GFDTQ → MESVSESSQQQKRKPVIHGL EDQKR in isoform 4. | VSP_021927 | |||||||||||||||||||
| Alternative sequence | 1 – 88 | 88 | MPAIL…NGFDT → MSVMLWRWEQNNTTMKL in isoform 10. | VSP_021928 | |||||||||||||||||||
| Alternative sequence | 1 – 88 | 88 | MPAIL…NGFDT → MESVSESSQQQKRKPVIHGL EDQKR in isoform 11. | VSP_021929 | |||||||||||||||||||
| Alternative sequence | 1 – 88 | 88 | MPAIL…NGFDT → MQECDSKFFLPSGSNSGFTL LSNQ in isoform 12. | VSP_021930 | |||||||||||||||||||
| Alternative sequence | 1 – 88 | 88 | MPAIL…NGFDT → MAIDLYCGLACLWGIHEPR in isoform 13. | VSP_021931 | |||||||||||||||||||
| Alternative sequence | 1 – 88 | 88 | MPAIL…NGFDT → MLWPRNLT in isoform 8. | VSP_021932 | |||||||||||||||||||
| Alternative sequence | 1 – 88 | 88 | MPAIL…NGFDT → MAGTSAASSWGGGK in isoform 9. | VSP_021933 | |||||||||||||||||||
| Alternative sequence | 256 – 278 | 23 | Missing in isoform 2, isoform 3 and isoform 4. | VSP_021934 | |||||||||||||||||||
| Alternative sequence | 938 – 945 | 8 | SLGLGDAD → MLWPRNLT in isoform 5. | VSP_021935 | |||||||||||||||||||
| Alternative sequence | 1480 – 1501 | 22 | Missing in isoform 5. | VSP_021936 | |||||||||||||||||||
| Alternative sequence | 1634 – 1666 | 33 | Missing in isoform 2, isoform 3, isoform 4, isoform 5 and isoform 6. | VSP_021937 | |||||||||||||||||||
| Alternative sequence | 1832 – 1834 | 3 | Missing in isoform 3, isoform 4, isoform 5 and isoform 6. | VSP_021938 | |||||||||||||||||||
| Natural variant | 109 | 1 | R → K. Ref.2 Ref.3 Corresponds to variant rs6483617 [ dbSNP | Ensembl ]. | VAR_029640 | |||||||||||||||||||
| Natural variant | 491 | 1 | Q → H. Corresponds to variant rs16937251 [ dbSNP | Ensembl ]. | VAR_029641 | |||||||||||||||||||
| Natural variant | 1041 | 1 | E → D. Ref.7 Corresponds to variant rs3802799 [ dbSNP | Ensembl ]. | VAR_029642 | |||||||||||||||||||
| Natural variant | 1077 | 1 | P → A. Ref.1 Ref.2 Ref.3 Ref.4 Ref.7 Ref.9 Corresponds to variant rs3802800 [ dbSNP | Ensembl ]. | VAR_029643 | |||||||||||||||||||
| Natural variant | 2374 | 1 | V → I. Ref.7 Corresponds to variant rs35891966 [ dbSNP | Ensembl ]. | VAR_032252 | |||||||||||||||||||
Experimental info | |||||||||||||||||||||||
| Sequence conflict | 100 | 1 | A → T in BAC00854. Ref.2 | ||||||||||||||||||||
| Sequence conflict | 100 | 1 | A → T in CAD32471. Ref.3 | ||||||||||||||||||||
| Sequence conflict | 259 | 1 | S → P in AAL96479. Ref.1 | ||||||||||||||||||||
| Sequence conflict | 259 | 1 | S → P in AAL96480. Ref.1 | ||||||||||||||||||||
| Sequence conflict | 259 | 1 | S → P in BAA92657. Ref.4 | ||||||||||||||||||||
| Sequence conflict | 282 | 1 | P → S in CAD32471. Ref.3 | ||||||||||||||||||||
| Sequence conflict | 1046 | 1 | T → M in BAB85038. Ref.7 | ||||||||||||||||||||
| Sequence conflict | 1173 | 1 | G → D in BAB85038. Ref.7 | ||||||||||||||||||||
| Sequence conflict | 1845 | 1 | Missing in AAH16054. Ref.8 | ||||||||||||||||||||
| Sequence conflict | 1939 | 1 | M → V in BAB85038. Ref.7 | ||||||||||||||||||||
| Sequence conflict | 2012 | 1 | E → G in BAA91965. Ref.7 | ||||||||||||||||||||
| Sequence conflict | 2053 | 1 | V → A in BAA91723. Ref.7 | ||||||||||||||||||||
| Sequence conflict | 2075 | 1 | L → V in BAB85038. Ref.7 | ||||||||||||||||||||
| Sequence conflict | 2296 | 1 | K → E in BAA91965. Ref.7 | ||||||||||||||||||||
| Sequence conflict | 2299 | 1 | E → K in BAB85038. Ref.7 | ||||||||||||||||||||
| Sequence conflict | 2395 | 1 | M → V in BAA91723. Ref.7 | ||||||||||||||||||||
Secondary structure | |||||||||||||||||||||||
Helix Strand Turn | |||||||||||||||||||||||
| Helix | 90 – 101 | 12 | |||||||||||||||||||||
| Helix | 111 – 114 | 4 | |||||||||||||||||||||
| Helix | 122 – 128 | 7 | |||||||||||||||||||||
| Helix | 145 – 159 | 15 | |||||||||||||||||||||
| Helix | 169 – 173 | 5 | |||||||||||||||||||||
| Helix | 177 – 180 | 4 | |||||||||||||||||||||
| Helix | 184 – 191 | 8 | |||||||||||||||||||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "A mammalian homolog of unc-53 is regulated by all-trans retinoic acid in neuroblastoma cells and embryos." Merrill R.A., Plum L.A., Kaiser M.E., Clagett-Dame M. Proc. Natl. Acad. Sci. U.S.A. 99:3422-3427(2002) [PubMed: 11904404] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS 2 AND 3), INDUCTION BY ATRA, TISSUE SPECIFICITY, DEVELOPMENTAL STAGE, VARIANT ALA-1077. |
| [2] | "Isolation of HELAD1, a novel human helicase gene up-regulated in colorectal carcinomas." Ishiguro H., Shimokawa T., Tsunoda T., Tanaka T., Fujii Y., Nakamura Y., Furukawa Y. Oncogene 21:6387-6394(2002) [PubMed: 12214280] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS 3 AND 4), SUBCELLULAR LOCATION, FUNCTION AS A HELICASE, INDUCTION, TISSUE SPECIFICITY, VARIANTS LYS-109 AND ALA-1077. |
| [3] | "Sensory deficits in mice hypomorphic for a mammalian homologue of unc-53." Peeters P.J., Baker A., Goris I., Daneels G., Verhasselt P., Luyten W.H.M.L., Geysen J.J.G.H., Kass S.U., Moechars D.W.E. Brain Res. Dev. Brain Res. 150:89-101(2004) [PubMed: 15158073] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS 1; 8; 9; 10; 11; 12 AND 13), FUNCTION, VARIANTS LYS-109 AND ALA-1077. |
| [4] | "Prediction of the coding sequences of unidentified human genes. XVI. The complete sequences of 150 new cDNA clones from brain which code for large proteins in vitro." Nagase T., Kikuno R., Ishikawa K., Hirosawa M., Ohara O. DNA Res. 7:65-73(2000) [PubMed: 10718198] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2), VARIANT ALA-1077. Tissue: Brain. |
| [5] | "Construction of expression-ready cDNA clones for KIAA genes: manual curation of 330 KIAA cDNA clones." Nakajima D., Okazaki N., Yamakawa H., Kikuno R., Ohara O., Nagase T. DNA Res. 9:99-106(2002) [PubMed: 12168954] [Abstract] Cited for: SEQUENCE REVISION. |
| [6] | Ohara O. Submitted (JAN-2005) to the EMBL/GenBank/DDBJ databases Cited for: SEQUENCE REVISION. |
| [7] | "Complete sequencing and characterization of 21,243 full-length human cDNAs." Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. Sugano S.Nat. Genet. 36:40-45(2004) [PubMed: 14702039] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 5; 6 AND 7), VARIANTS ASP-1041; ALA-1077 AND ILE-2374. Tissue: Placenta. |
| [8] | "Human chromosome 11 DNA sequence and analysis including novel gene identification." Taylor T.D., Noguchi H., Totoki Y., Toyoda A., Kuroki Y., Dewar K., Lloyd C., Itoh T., Takeda T., Kim D.-W., She X., Barlow K.F., Bloom T., Bruford E., Chang J.L., Cuomo C.A., Eichler E., FitzGerald M.G. Sakaki Y.Nature 440:497-500(2006) [PubMed: 16554811] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [9] | "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)." The MGC Project Team Genome Res. 14:2121-2127(2004) [PubMed: 15489334] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 6), VARIANT ALA-1077. Tissue: Skin. |
| [10] | "Pore membrane and/or filament interacting like protein 1 (POMFIL1) is predominantly expressed in the nervous system and encodes different protein isoforms." Coy J.F., Wiemann S., Bechmann I., Baechner D., Nitsch R., Kretz O., Christiansen H., Poustka A. Gene 290:73-94(2002) [PubMed: 12062803] [Abstract] Cited for: IDENTIFICATION, TISSUE SPECIFICITY. |
| [11] | "Neuron navigator: a human gene family with homology to unc-53, a cell guidance gene from Caenorhabditis elegans." Maes T., Barcelo A., Buesa C. Genomics 80:21-30(2002) [PubMed: 12079279] [Abstract] Cited for: ALTERNATIVE SPLICING, TISSUE SPECIFICITY. |
| [12] | "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks." Olsen J.V., Blagoev B., Gnad F., Macek B., Kumar C., Mortensen P., Mann M. Cell 127:635-648(2006) [PubMed: 17081983] [Abstract] Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-1703, MASS SPECTROMETRY. Tissue: Cervix carcinoma. |
| [13] | "A probability-based approach for high-throughput protein phosphorylation analysis and site localization." Beausoleil S.A., Villen J., Gerber S.A., Rush J., Gygi S.P. Nat. Biotechnol. 24:1285-1292(2006) [PubMed: 16964243] [Abstract] Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-1977, MASS SPECTROMETRY. Tissue: Cervix carcinoma. |
| [14] | "Combining protein-based IMAC, peptide-based IMAC, and MudPIT for efficient phosphoproteomic analysis." Cantin G.T., Yi W., Lu B., Park S.K., Xu T., Lee J.-D., Yates J.R. III J. Proteome Res. 7:1346-1351(2008) [PubMed: 18220336] [Abstract] Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-1977, MASS SPECTROMETRY. Tissue: Cervix carcinoma. |
| [15] | "A quantitative atlas of mitotic phosphorylation." Dephoure N., Zhou C., Villen J., Beausoleil S.A., Bakalarski C.E., Elledge S.J., Gygi S.P. Proc. Natl. Acad. Sci. U.S.A. 105:10762-10767(2008) [PubMed: 18669648] [Abstract] Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-1480; SER-1484; SER-1488 AND SER-1977, MASS SPECTROMETRY. Tissue: Cervix carcinoma. |
| [16] | "Solution structure of the CH domain from human neuron navigator 2." RIKEN structural genomics initiative (RSGI) Submitted (FEB-2009) to the PDB data bank Cited for: STRUCTURE BY NMR OF 90-197. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| EMBL GenBank DDBJ | AF466143 mRNA. Translation: AAL96479.1. AF466144 mRNA. Translation: AAL96480.1. AB063115 mRNA. Translation: BAC00853.1. AB063116 mRNA. Translation: BAC00854.1. AJ488102 mRNA. Translation: CAD32471.1. AJ488203 mRNA. Translation: CAD32556.1. AJ488204 mRNA. Translation: CAD32557.1. AJ488205 mRNA. Translation: CAD32558.1. AJ488206 mRNA. Translation: CAD32559.1. AJ488207 mRNA. Translation: CAD32560.1. AJ488208 mRNA. Translation: CAD32561.1. AB037840 mRNA. Translation: BAA92657.3. Different initiation. AK001495 mRNA. Translation: BAA91723.1. AK001892 mRNA. Translation: BAA91965.1. AK074287 mRNA. Translation: BAB85038.1. Frameshift. AC009549 Genomic DNA. No translation available. AC015684 Genomic DNA. No translation available. AC023950 Genomic DNA. No translation available. AC090662 Genomic DNA. No translation available. AC111163 Genomic DNA. No translation available. AC113193 Genomic DNA. No translation available. BC016054 mRNA. Translation: AAH16054.1. | ||||||||||||
| IPI | IPI00152696. IPI00217052. IPI00815697. IPI00815765. IPI00815856. IPI00816020. IPI00816099. IPI00816407. IPI00816570. IPI00816751. IPI00816806. IPI00872269. IPI00879900. | ||||||||||||
| RefSeq | NP_001104488.1. NM_001111018.1. NP_001231892.1. NM_001244963.1. NP_660093.2. NM_145117.4. NP_892009.3. NM_182964.5. | ||||||||||||
| UniGene | Hs.502116. Hs.639427. Hs.639428. Hs.64341. | ||||||||||||
3D structure databases | |||||||||||||
| PDBe RCSB PDB PDBj |
| ||||||||||||
| ProteinModelPortal | Q8IVL1. | ||||||||||||
| SMR | Q8IVL1. Positions 78-197, 2139-2244. | ||||||||||||
| ModBase | Search... | ||||||||||||
Protein-protein interaction databases | |||||||||||||
| IntAct | Q8IVL1. 4 interactions. | ||||||||||||
| MINT | MINT-1455352. | ||||||||||||
| STRING | Q8IVL1. | ||||||||||||
PTM databases | |||||||||||||
| PhosphoSite | Q8IVL1. | ||||||||||||
Polymorphism databases | |||||||||||||
| DMDM | 308153582. | ||||||||||||
Proteomic databases | |||||||||||||
| PRIDE | Q8IVL1. | ||||||||||||
Protocols and materials databases | |||||||||||||
| StructuralBiologyKnowledgebase | Search... | ||||||||||||
Genome annotation databases | |||||||||||||
| Ensembl | ENST00000396087; ENSP00000379396; ENSG00000166833. | ||||||||||||
| GeneID | 89797. | ||||||||||||
| KEGG | hsa:89797. | ||||||||||||
| UCSC | uc001mpp.1. human. uc001mpr.2. human. uc001mpu.1. human. uc009yhw.1. human. uc009yhx.1. human. | ||||||||||||
Organism-specific databases | |||||||||||||
| CTD | 89797. | ||||||||||||
| GeneCards | GC11P019372. | ||||||||||||
| H-InvDB | HIX0009501. | ||||||||||||
| HGNC | HGNC:15997. NAV2. | ||||||||||||
| HPA | HPA011755. HPA011891. | ||||||||||||
| MIM | 607026. gene. | ||||||||||||
| neXtProt | NX_Q8IVL1. | ||||||||||||
| PharmGKB | PA31452. | ||||||||||||
| HUGE | Search... | ||||||||||||
| GenAtlas | Search... | ||||||||||||
Phylogenomic databases | |||||||||||||
| eggNOG | prNOG18183. | ||||||||||||
| GeneTree | ENSGT00530000063334. | ||||||||||||
| HOVERGEN | HBG058814. | ||||||||||||
| OMA | ENMKNSV. | ||||||||||||
| PhylomeDB | Q8IVL1. | ||||||||||||
Gene expression databases | |||||||||||||
| ArrayExpress | Q8IVL1. | ||||||||||||
| Bgee | Q8IVL1. | ||||||||||||
| Genevestigator | Q8IVL1. | ||||||||||||
| GermOnline | ENSG00000166833. Homo sapiens. | ||||||||||||
Family and domain databases | |||||||||||||
| InterPro | IPR003593. ATPase_AAA+_core. IPR001715. CH-domain. [Graphical view] | ||||||||||||
| Gene3D | G3DSA:1.10.418.10. Calponin-homology. 1 hit. | ||||||||||||
| Pfam | PF00307. CH. 1 hit. [Graphical view] | ||||||||||||
| SMART | SM00382. AAA. 1 hit. SM00033. CH. 1 hit. [Graphical view] | ||||||||||||
| SUPFAM | SSF47576. Calponin-homology. 1 hit. | ||||||||||||
| PROSITE | PS50021. CH. 1 hit. [Graphical view] | ||||||||||||
| ProtoNet | Search... | ||||||||||||
Other | |||||||||||||
| NextBio | 76293. | ||||||||||||
| SOURCE | Search... | ||||||||||||
Entry information
| Entry name | NAV2_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q8IVL1 Secondary accession number(s): A6NEC1 Q9P2C8 | ||||||||
| Entry history |
| ||||||||
| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. | ||||||||
Relevant documents
| Human chromosome 11 Human chromosome 11: entries, gene names and cross-references to MIM |
| Human entries with polymorphisms or disease mutations List of human entries with polymorphisms or disease mutations |
| Human polymorphisms and disease mutations Index of human polymorphisms and disease mutations |
| MIM cross-references Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot |
| PDB cross-references Index of Protein Data Bank (PDB) cross-references |
| SIMILARITY comments Index of protein domains and families |

Clusters with