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|---|---|
| Accession Number: | Q96H72 |
| Protein Name: | Zinc transporter ZIP13 |
| Length: | 371 |
| Molecular Weight: | 39011.00 |
| Species: | Homo sapiens (Human) [9606] |
| Number of TMSs: | 7 |
| Location1 / Topology2 / Orientation3: | Membrane1 / Multi-pass membrane protein2 |
| Substrate | zinc(2+) |
Cross database links:
| Entrez Gene ID: | 91252 |
|---|---|
| Pfam: | PF02535 |
| KEGG: | hsa:91252 hsa:91252 |
Gene Ontology
GO:0016021
C:integral to membrane
GO:0046873
F:metal ion transmembrane transporter activity
GO:0006829
P:zinc ion transport
GO:0030173
C:integral to Golgi membrane
GO:0048471
C:perinuclear region of cytoplasm
GO:0005385
F:zinc ion transmembrane transporter activity
GO:0006882
P:cellular zinc ion homeostasis
GO:0061448
P:connective tissue development
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References (11)[1] “Complete sequencing and characterization of 21,243 full-length human cDNAs.” Ota T.et.al. 14702039 [2] “Human chromosome 11 DNA sequence and analysis including novel gene identification.” Taylor T.D.et.al. 16554811 [3] “The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).” The MGC Project Teamet.al. 15489334 [4] “The full-ORF clone resource of the German cDNA consortium.” Bechtel S.et.al. 17974005 [5] “Spondylocheiro dysplastic form of the Ehlers-Danlos syndrome -- an autosomal-recessive entity caused by mutations in the zinc transporter gene SLC39A13.” Giunta C.et.al. 18513683 [6] “Complete sequencing and characterization of 21,243 full-length human cDNAs.” Ota T.et.al. 14702039 [7] “Human chromosome 11 DNA sequence and analysis including novel gene identification.” Taylor T.D.et.al. 16554811 [8] “The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).” The MGC Project Teamet.al. 15489334 [9] “The full-ORF clone resource of the German cDNA consortium.” Bechtel S.et.al. 17974005 [10] “Biochemical characterization of human ZIP13 protein: a homo-dimerized zinc transporter involved in the spondylocheiro dysplastic Ehlers-Danlos syndrome.” Bin B.H.et.al. 21917916 [11] “Spondylocheiro dysplastic form of the Ehlers-Danlos syndrome -- an autosomal-recessive entity caused by mutations in the zinc transporter gene SLC39A13.” Giunta C.et.al. 18513683
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External Searches:
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Analyze:
| Predict TMSs (Predict number of transmembrane segments) | ||||
| FASTA formatted sequence |
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1: MPGCPCPGCG MAGPRLLFLT ALALELLERA GGSQPALRSR GTATACRLDN KESESWGALL 61: SGERLDTWIC SLLGSLMVGL SGVFPLLVIP LEMGTMLRSE AGAWRLKQLL SFALGGLLGN 121: VFLHLLPEAW AYTCSASPGG EGQSLQQQQQ LGLWVIAGIL TFLALEKMFL DSKEEGTSQA 181: PNKDPTAAAA ALNGGHCLAQ PAAEPGLGAV VRSIKVSGYL NLLANTIDNF THGLAVAASF 241: LVSKKIGLLT TMAILLHEIP HEVGDFAILL RAGFDRWSAA KLQLSTALGG LLGAGFAICT 301: QSPKGVVGCS PAAEETAAWV LPFTSGGFLY IALVNVLPDL LEEEDPWRSL QQLLLLCAGI 361: VVMVLFSLFV D