TICAM1 S186L [cytosol]

Stable Identifier
R-HSA-5607964
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
TICAM1 S186L [cytosol] icon
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
22105173 Herpes simplex encephalitis in children with autosomal recessive and dominant TRIF deficiency

Alkhamis, N, Abel, L, Halwani, R, Ghadiri, A, Lebon, P, Al-Muhsen, S, Alangari, A, Lorenzo, L, Maluenda, J, Plancoulaine, S, Mahvelati, F, Cardon, A, Rozenberg, F, Sancho-Shimizu, V, Al-Makadma, AS, Ciancanelli, M, Chaussabel, D, Fabrega, S, Rezaei, N, AlSum, Z, PĂ©rez de Diego, R, Herman, M, Seya, T, Jouanguy, E, Matsumoto, M, Puel, A, Picard, C, Boucherit, S, Tatematsu, M, Zhang, SY, Guo, Y, Casanova, JL, Israelsson, E, Tardieu, M

J. Clin. Invest. 2011
External Reference Information
External Reference
Gene Names
TICAM1, PRVTIRB, TRIF
Chain
chain:1-712
Reference Transcript
Other Identifiers
11719258_at
148022
16867409
213191_PM_at
213191_at
35230_at
3846983
3846984
3846985
3846986
3846987
3846988
3846989
3846990
3846991
3846992
3846993
3846994
3846995
3846996
3846997
3846998
3846999
3847000
8032899
A_23_P376096
A_23_P90311
GE54626
GE803521
GO:0002224
GO:0002281
GO:0002376
GO:0002735
GO:0002756
GO:0005515
GO:0005737
GO:0005739
GO:0005768
GO:0005769
GO:0005773
GO:0005776
GO:0005829
GO:0006351
GO:0006355
GO:0006809
GO:0006914
GO:0006915
GO:0006954
GO:0007165
GO:0007249
GO:0010008
GO:0010508
GO:0010628
GO:0012501
GO:0019901
GO:0023052
GO:0030890
GO:0031398
GO:0031410
GO:0031663
GO:0032092
GO:0032481
GO:0032496
GO:0032722
GO:0032728
GO:0032755
GO:0032760
GO:0032816
GO:0035666
GO:0036211
GO:0042100
GO:0042113
GO:0043123
GO:0043226
GO:0043254
GO:0043330
GO:0045087
GO:0045429
GO:0050871
GO:0051092
GO:0051607
GO:0060090
GO:0060907
GO:0065003
GO:0071222
GO:0097027
GO:0097190
GO:0097342
GO:0098542
GO:0098772
GO:0140052
GO:1900017
HMNXSV003006219
Hs.29344.0.S1_3p_at
ILMN_1724863
ILMN_1815079
PH_hs_0002548
RNA95678|RNS_760_128
TC19001071.hg
Participates
Other forms of this molecule
Modified Residues
Name
L-serine 186 replaced with L-leucine
Coordinate
186
PsiMod
A protein modification that effectively removes or replaces an L-serine.
A protein modification that effectively converts a source amino acid residue to an L-leucine.
Disease
Name Identifier Synonyms
primary immunodeficiency disease DOID:612 immune deficiency disorder, immunodeficiency syndrome, hypoimmunity
Cross References
RefSeq
OpenTargets
GeneCards
PRO
Pharos - Targets
Orphanet
PDB
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