TRAPPC9

Protein-coding gene in the species Homo sapiens
TRAPPC9
Identifiers
AliasesTRAPPC9, IBP, IKBKBBP, MRT13, NIBP, TRS120, T1, trafficking protein particle complex 9, trafficking protein particle complex subunit 9
External IDsOMIM: 611966; MGI: 1923760; HomoloGene: 81931; GeneCards: TRAPPC9; OMA:TRAPPC9 - orthologs
Gene location (Human)
Chromosome 8 (human)
Chr.Chromosome 8 (human)[1]
Chromosome 8 (human)
Genomic location for TRAPPC9
Genomic location for TRAPPC9
Band8q24.3Start139,727,725 bp[1]
End140,458,579 bp[1]
Gene location (Mouse)
Chromosome 15 (mouse)
Chr.Chromosome 15 (mouse)[2]
Chromosome 15 (mouse)
Genomic location for TRAPPC9
Genomic location for TRAPPC9
Band15|15 D3Start72,461,469 bp[2]
End72,933,053 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • muscle of thigh

  • gastrocnemius muscle

  • apex of heart

  • pancreatic ductal cell

  • ganglionic eminence

  • right uterine tube

  • prefrontal cortex

  • anterior pituitary

  • islet of Langerhans

  • tendon of biceps brachii
Top expressed in
  • neural layer of retina

  • muscle of thigh

  • dentate gyrus of hippocampal formation granule cell

  • primary visual cortex

  • right kidney

  • spermatocyte

  • cerebellar cortex

  • habenula

  • central gray substance of midbrain

  • seminiferous tubule
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
  • protein binding
Cellular component
  • cytoplasm
  • cytosol
  • trans-Golgi network
  • Golgi apparatus
  • endoplasmic reticulum
  • Golgi membrane
  • TRAPP complex
Biological process
  • cell differentiation
  • COPII vesicle coating
  • positive regulation of NF-kappaB transcription factor activity
  • neuron differentiation
  • cerebral cortex development
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

83696

76510

Ensembl

ENSG00000167632

ENSMUSG00000047921

UniProt

Q96Q05

Q3U0M1

RefSeq (mRNA)
NM_001160372
NM_031466
NM_001321646
NM_001374682
NM_001374683

NM_001374684

NM_001164641
NM_001164642
NM_001164643
NM_029640
NM_180662

RefSeq (protein)
NP_001153844
NP_001308575
NP_113654
NP_001361611
NP_001361612

NP_001361613

NP_001158113
NP_001158115
NP_083916
NP_850993

Location (UCSC)Chr 8: 139.73 – 140.46 MbChr 15: 72.46 – 72.93 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Trafficking protein particle complex 9 is a protein that in humans is encoded by the TRAPPC9 gene.[5]

Function

This gene encodes a protein that likely plays a role in NF-kappa-B signaling. Mutations in this gene have been associated with autosomal-recessive mental retardation. Alternatively spliced transcript variants have been described.

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000167632 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000047921 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: Trafficking protein particle complex 9". Retrieved 2017-06-10.

Further reading

  • Hu WH, Pendergast JS, Mo XM, Brambilla R, Bracchi-Ricard V, Li F, Walters WM, Blits B, He L, Schaal SM, Bethea JR (2005). "NIBP, a novel NIK and IKK(beta)-binding protein that enhances NF-(kappa)B activation". J. Biol. Chem. 280 (32): 29233–41. doi:10.1074/jbc.M501670200. PMC 3707486. PMID 15951441.
  • Yoshida T, Kato K, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y (2009). "Association of gene polymorphisms with chronic kidney disease in Japanese individuals". Int. J. Mol. Med. 24 (4): 539–47. doi:10.3892/ijmm_00000263. PMID 19724895.
  • Oguri M, Kato K, Yokoi K, Yoshida T, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y (2010). "Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals". Am. J. Hypertens. 23 (1): 70–7. doi:10.1038/ajh.2009.190. PMID 19851296.
  • Mochida GH, Mahajnah M, Hill AD, Basel-Vanagaite L, Gleason D, Hill RS, Bodell A, Crosier M, Straussberg R, Walsh CA (2009). "A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly". Am. J. Hum. Genet. 85 (6): 897–902. doi:10.1016/j.ajhg.2009.10.027. PMC 2790576. PMID 20004763.
  • Mir A, Kaufman L, Noor A, Motazacker MM, Jamil T, Azam M, Kahrizi K, Rafiq MA, Weksberg R, Nasr T, Naeem F, Tzschach A, Kuss AW, Ishak GE, Doherty D, Ropers HH, Barkovich AJ, Najmabadi H, Ayub M, Vincent JB (2009). "Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardation". Am. J. Hum. Genet. 85 (6): 909–15. doi:10.1016/j.ajhg.2009.11.009. PMC 2790571. PMID 20004765.
  • Yoshida T, Kato K, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y (2010). "Association of genetic variants with hemorrhagic stroke in Japanese individuals". Int. J. Mol. Med. 25 (4): 649–56. doi:10.3892/ijmm_00000388. PMID 20198315.
  • Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR (2010). "Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score". Mol. Med. 16 (7–8): 247–53. doi:10.2119/molmed.2009.00159. PMC 2896464. PMID 20379614.
  • Barrowman J, Bhandari D, Reinisch K, Ferro-Novick S (2010). "TRAPP complexes in membrane traffic: convergence through a common Rab". Nat. Rev. Mol. Cell Biol. 11 (11): 759–63. doi:10.1038/nrm2999. PMID 20966969. S2CID 20099084.
  • Zong M, Wu XG, Chan CW, Choi MY, Chan HC, Tanner JA, Yu S (2011). "The adaptor function of TRAPPC2 in mammalian TRAPPs explains TRAPPC2-associated SEDT and TRAPPC9-associated congenital intellectual disability". PLOS ONE. 6 (8): e23350. Bibcode:2011PLoSO...623350Z. doi:10.1371/journal.pone.0023350. PMC 3156116. PMID 21858081.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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