Incidental Mutation 'R1639:Tcaim'
ID173382
Institutional Source Beutler Lab
Gene Symbol Tcaim
Ensembl Gene ENSMUSG00000046603
Gene NameT cell activation inhibitor, mitochondrial
SynonymsLOC382117, D9Ertd402e
MMRRC Submission 039675-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.116) question?
Stock #R1639 (G1)
Quality Score225
Status Validated
Chromosome9
Chromosomal Location122805539-122836334 bp(+) (GRCm38)
Type of Mutationcritical splice acceptor site
DNA Base Change (assembly) G to A at 122818773 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000049759 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000052740] [ENSMUST00000136274]
Predicted Effect probably null
Transcript: ENSMUST00000052740
SMART Domains Protein: ENSMUSP00000049759
Gene: ENSMUSG00000046603

DomainStartEndE-ValueType
Pfam:DUF4460 33 144 4.2e-40 PFAM
Pfam:DUF4461 199 503 4.1e-124 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000136274
SMART Domains Protein: ENSMUSP00000120948
Gene: ENSMUSG00000046603

DomainStartEndE-ValueType
Pfam:DUF4460 31 125 2.7e-32 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000207349
Meta Mutation Damage Score 0.574 question?
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.1%
  • 10x: 95.5%
  • 20x: 89.7%
Validation Efficiency 96% (66/69)
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933417A18Rik T C 13: 34,944,250 I150T possibly damaging Het
Acss2 C A 2: 155,556,908 T425N probably benign Het
Adam18 T A 8: 24,652,152 I203L probably benign Het
Amigo2 A G 15: 97,245,998 M181T probably benign Het
Anks1 T A 17: 28,058,306 I1045N probably damaging Het
Ap3d1 C T 10: 80,730,010 V108I probably damaging Het
Arl8a C T 1: 135,152,823 R57* probably null Het
Atp12a A T 14: 56,384,068 D720V possibly damaging Het
Brpf3 T C 17: 28,824,068 probably null Het
C2 T C 17: 34,872,403 K95E probably benign Het
Cdk19 T C 10: 40,476,969 probably null Het
Cebpz T A 17: 78,934,606 I540L possibly damaging Het
Cep128 A G 12: 91,366,368 V41A probably damaging Het
Cog7 T C 7: 121,981,419 E56G probably damaging Het
Cylc2 T C 4: 51,228,310 V127A probably benign Het
Cyp2b23 A G 7: 26,686,417 V5A possibly damaging Het
Cyp8b1 A G 9: 121,914,890 Y459H probably benign Het
Dbpht2 A G 12: 74,299,158 noncoding transcript Het
Ddx24 T C 12: 103,411,319 probably null Het
Dgki C T 6: 36,937,364 C757Y probably damaging Het
Eef2k T A 7: 120,885,828 L306H probably damaging Het
Ephb2 T C 4: 136,693,905 N378S probably benign Het
Espl1 C T 15: 102,320,714 T1767I probably damaging Het
Fbn2 C A 18: 58,058,462 A1530S probably benign Het
Fndc11 A G 2: 181,221,581 S60G possibly damaging Het
Glb1l G T 1: 75,199,601 Q612K probably benign Het
Gpsm1 A G 2: 26,345,187 E371G probably damaging Het
Gtpbp2 G A 17: 46,165,771 probably null Het
Itch A G 2: 155,179,025 probably null Het
Itga2 T C 13: 114,857,296 T774A probably benign Het
Kit A G 5: 75,652,807 I881V probably damaging Het
Lpar5 T C 6: 125,081,601 L95P probably damaging Het
Lrp6 T C 6: 134,453,566 T1511A possibly damaging Het
Mgat4c T C 10: 102,378,281 Y42H probably damaging Het
Mpp3 G T 11: 102,023,442 T109K probably damaging Het
Msantd4 A G 9: 4,385,199 E308G probably damaging Het
Mug1 T C 6: 121,880,571 S1085P probably damaging Het
Myo5b A G 18: 74,707,916 H956R probably benign Het
Ncoa7 A C 10: 30,701,992 L132R probably damaging Het
Ndufc1 T C 3: 51,408,243 T25A probably benign Het
Olfr1254 T C 2: 89,789,245 T36A probably damaging Het
Pkhd1l1 G A 15: 44,540,955 V2327M probably damaging Het
Ppp1r9b T C 11: 94,996,610 Y59H probably damaging Het
Sema4c A T 1: 36,553,534 F152I probably benign Het
Slit2 A T 5: 48,259,654 Y1016F probably damaging Het
Spata31d1c T A 13: 65,036,039 V465D probably benign Het
Ssc5d T C 7: 4,928,417 C208R probably damaging Het
Stambpl1 T G 19: 34,236,307 V312G probably benign Het
Stim1 T A 7: 102,354,541 D60E probably benign Het
Syt13 T A 2: 92,945,971 V201D probably benign Het
Tex15 T C 8: 33,570,817 S366P possibly damaging Het
Tpte G A 8: 22,320,897 R190H probably benign Het
Vmn1r4 T C 6: 56,957,075 V188A probably damaging Het
Vmn2r88 A G 14: 51,416,787 D542G probably damaging Het
Vps33b T A 7: 80,284,353 I257N probably damaging Het
Wwox G T 8: 114,445,378 G71* probably null Het
Zc3h11a G T 1: 133,624,708 Q554K probably benign Het
Zfp947 T C 17: 22,146,093 K200R probably benign Het
Zscan12 T A 13: 21,368,986 C327S probably damaging Het
Other mutations in Tcaim
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01389:Tcaim APN 9 122814562 missense possibly damaging 0.69
IGL01775:Tcaim APN 9 122818825 missense probably damaging 1.00
R1193:Tcaim UTSW 9 122818830 missense probably damaging 0.96
R1487:Tcaim UTSW 9 122818832 nonsense probably null
R1592:Tcaim UTSW 9 122818773 critical splice acceptor site probably null
R1642:Tcaim UTSW 9 122818773 critical splice acceptor site probably null
R1853:Tcaim UTSW 9 122826206 missense probably damaging 1.00
R4204:Tcaim UTSW 9 122833618 missense probably benign 0.01
R4427:Tcaim UTSW 9 122814496 missense probably benign 0.01
R6547:Tcaim UTSW 9 122814466 missense probably benign 0.22
R6599:Tcaim UTSW 9 122834779 nonsense probably null
R6906:Tcaim UTSW 9 122834774 missense probably benign 0.01
Z1088:Tcaim UTSW 9 122833657 missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TGACAAGATTCATCACAGGCAGAACTG -3'
(R):5'- GAGACGTGTGTGAGGTCTTCATCAG -3'

Sequencing Primer
(F):5'- TTAGCTGGGATGGCACCTAC -3'
(R):5'- GGGTCCTTGAACCCAGTAAAG -3'
Posted On2014-04-24