Incidental Mutation 'IGL02545:Tcl1b5'
ID 297801
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tcl1b5
Ensembl Gene ENSMUSG00000000701
Gene Name T cell leukemia/lymphoma 1B, 5
Synonyms D12Ertd644e
Accession Numbers
Essential gene? Probably non essential (E-score: 0.083) question?
Stock # IGL02545
Quality Score
Status
Chromosome 12
Chromosomal Location 105142603-105147404 bp(+) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) T to A at 105146296 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000000717 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000000717]
AlphaFold P56845
Predicted Effect probably benign
Transcript: ENSMUST00000000717
SMART Domains Protein: ENSMUSP00000000717
Gene: ENSMUSG00000000701

DomainStartEndE-ValueType
Pfam:TCL1_MTCP1 1 117 1e-41 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930523C07Rik T C 1: 159,902,994 (GRCm39) L88P probably damaging Het
Adamtsl4 G A 3: 95,590,684 (GRCm39) Q354* probably null Het
Aox3 A C 1: 58,222,645 (GRCm39) D1146A probably damaging Het
Ap2a1 T A 7: 44,555,850 (GRCm39) H340L probably damaging Het
Ccni G T 5: 93,335,636 (GRCm39) F167L probably benign Het
Ctcf A G 8: 106,391,013 (GRCm39) T207A probably benign Het
D930020B18Rik A G 10: 121,525,838 (GRCm39) H580R possibly damaging Het
Dnaaf6rt A G 1: 31,262,177 (GRCm39) D53G probably damaging Het
Dock3 A T 9: 106,939,271 (GRCm39) L159Q probably damaging Het
Dync1i2 T C 2: 71,093,095 (GRCm39) I630T possibly damaging Het
Fchsd2 A G 7: 100,847,715 (GRCm39) T202A probably benign Het
Gdi2 A G 13: 3,607,009 (GRCm39) Y214C probably damaging Het
Gna14 T A 19: 16,511,090 (GRCm39) S46R probably damaging Het
Hfm1 A G 5: 107,043,153 (GRCm39) I627T probably damaging Het
Ighv1-19 G A 12: 114,672,359 (GRCm39) A87V probably damaging Het
Itch G A 2: 155,014,506 (GRCm39) probably null Het
Klrb1b T C 6: 128,797,272 (GRCm39) Q72R possibly damaging Het
Lrpprc A G 17: 85,082,853 (GRCm39) F144L probably benign Het
Lrrc7 A G 3: 157,891,011 (GRCm39) probably benign Het
Ndufa11 T A 17: 57,028,338 (GRCm39) F72L probably damaging Het
Neu1 T A 17: 35,150,477 (GRCm39) V32E probably benign Het
Or5k17 T A 16: 58,746,833 (GRCm39) I34F possibly damaging Het
Osmr T C 15: 6,853,060 (GRCm39) K611E probably damaging Het
Pcdh20 A G 14: 88,706,280 (GRCm39) V340A possibly damaging Het
Plxna2 T A 1: 194,468,998 (GRCm39) probably benign Het
Pou6f1 C T 15: 100,481,306 (GRCm39) W210* probably null Het
Ppat A G 5: 77,063,079 (GRCm39) Y511H probably damaging Het
Psme4 T G 11: 30,791,586 (GRCm39) V1147G possibly damaging Het
Scap C T 9: 110,207,758 (GRCm39) T489I probably benign Het
Sptb A G 12: 76,654,754 (GRCm39) probably null Het
Trim54 T A 5: 31,289,509 (GRCm39) probably benign Het
Unc13c C T 9: 73,388,357 (GRCm39) R2143Q probably damaging Het
Vmn1r56 A T 7: 5,199,113 (GRCm39) V168D probably benign Het
Vmn2r66 A T 7: 84,655,798 (GRCm39) M406K possibly damaging Het
Other mutations in Tcl1b5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00932:Tcl1b5 APN 12 105,142,759 (GRCm39) missense probably benign 0.39
IGL01734:Tcl1b5 APN 12 105,145,214 (GRCm39) missense probably benign 0.08
IGL02948:Tcl1b5 APN 12 105,145,273 (GRCm39) missense probably benign 0.15
IGL03037:Tcl1b5 APN 12 105,145,273 (GRCm39) missense probably benign 0.15
R0378:Tcl1b5 UTSW 12 105,145,326 (GRCm39) missense probably damaging 1.00
R5424:Tcl1b5 UTSW 12 105,146,275 (GRCm39) missense possibly damaging 0.45
R6528:Tcl1b5 UTSW 12 105,145,258 (GRCm39) missense probably benign 0.43
R7033:Tcl1b5 UTSW 12 105,142,750 (GRCm39) missense probably damaging 1.00
R7651:Tcl1b5 UTSW 12 105,142,694 (GRCm39) missense possibly damaging 0.84
R7844:Tcl1b5 UTSW 12 105,142,815 (GRCm39) critical splice donor site probably null
R8127:Tcl1b5 UTSW 12 105,146,262 (GRCm39) missense probably benign 0.43
R8200:Tcl1b5 UTSW 12 105,145,212 (GRCm39) missense probably benign
Posted On 2015-04-16