Incidental Mutation 'IGL01982:Tmem106b'
ID 182790
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tmem106b
Ensembl Gene ENSMUSG00000029571
Gene Name transmembrane protein 106B
Synonyms 2310036D22Rik, 5830455K21Rik, 6430519M21Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01982
Quality Score
Status
Chromosome 6
Chromosomal Location 13069758-13089268 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 13071968 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000122392 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031556] [ENSMUST00000122916] [ENSMUST00000124234] [ENSMUST00000142211]
AlphaFold Q80X71
Predicted Effect probably benign
Transcript: ENSMUST00000031556
SMART Domains Protein: ENSMUSP00000031556
Gene: ENSMUSG00000029571

DomainStartEndE-ValueType
Pfam:DUF1356 28 259 1.6e-120 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000122916
SMART Domains Protein: ENSMUSP00000122107
Gene: ENSMUSG00000029571

DomainStartEndE-ValueType
Pfam:DUF1356 14 186 5.8e-86 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000124234
SMART Domains Protein: ENSMUSP00000123208
Gene: ENSMUSG00000029571

DomainStartEndE-ValueType
Pfam:DUF1356 14 93 1.7e-35 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000136742
Predicted Effect probably benign
Transcript: ENSMUST00000142211
SMART Domains Protein: ENSMUSP00000122392
Gene: ENSMUSG00000029571

DomainStartEndE-ValueType
Pfam:DUF1356 14 70 3.3e-18 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000142798
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 67 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca12 A C 1: 71,385,857 (GRCm39) S254A probably benign Het
Abca7 T G 10: 79,838,475 (GRCm39) L583R probably damaging Het
Acp1 A T 12: 30,961,491 (GRCm39) L14H possibly damaging Het
Adar A G 3: 89,645,397 (GRCm39) I3V probably benign Het
Adh4 C T 3: 138,134,788 (GRCm39) probably benign Het
Aldh1l1 A G 6: 90,536,845 (GRCm39) I103V probably benign Het
Asic3 C A 5: 24,622,719 (GRCm39) T523N probably benign Het
Aspm T C 1: 139,419,326 (GRCm39) V1732A probably benign Het
Atad3a C T 4: 155,838,384 (GRCm39) R211Q possibly damaging Het
Bahcc1 A G 11: 120,178,299 (GRCm39) Y2286C probably damaging Het
BC034090 T C 1: 155,099,078 (GRCm39) E569G probably damaging Het
Bpifb3 A G 2: 153,767,521 (GRCm39) N237S probably benign Het
Bysl C A 17: 47,921,996 (GRCm39) probably null Het
C2cd6 T C 1: 59,106,932 (GRCm39) probably benign Het
Ccdc141 A G 2: 76,861,003 (GRCm39) F925L probably damaging Het
Cdca2 A T 14: 67,915,168 (GRCm39) V697E probably damaging Het
Cers1 A G 8: 70,776,081 (GRCm39) D324G probably damaging Het
Ctsq T A 13: 61,186,732 (GRCm39) I91F probably benign Het
Ctsq C T 13: 61,187,335 (GRCm39) C11Y probably benign Het
Cyp11b1 T C 15: 74,711,252 (GRCm39) N142S possibly damaging Het
Cyp3a59 G T 5: 146,041,545 (GRCm39) S363I probably benign Het
Eps15l1 A T 8: 73,132,919 (GRCm39) D567E probably benign Het
Esf1 G A 2: 140,006,448 (GRCm39) A233V probably benign Het
Fras1 A T 5: 96,887,107 (GRCm39) I2630F possibly damaging Het
Fyb1 A T 15: 6,609,658 (GRCm39) E77V probably null Het
Gjb6 C A 14: 57,362,030 (GRCm39) W77L probably damaging Het
Gm21983 A G 7: 26,879,703 (GRCm39) V88A possibly damaging Het
Gm8247 A G 14: 44,823,088 (GRCm39) T52A probably damaging Het
Gpr108 T C 17: 57,544,877 (GRCm39) K329E probably damaging Het
Gpr141 T A 13: 19,935,908 (GRCm39) H289L probably benign Het
Ilvbl T C 10: 78,414,856 (GRCm39) Y240H probably damaging Het
Kntc1 G A 5: 123,947,159 (GRCm39) A1868T probably benign Het
Lrmda A C 14: 22,634,550 (GRCm39) N112T probably damaging Het
Ly75 T C 2: 60,142,108 (GRCm39) Y1334C probably damaging Het
Macc1 C A 12: 119,409,369 (GRCm39) P46T probably benign Het
Madd A T 2: 91,006,052 (GRCm39) F381Y probably damaging Het
Map3k20 C T 2: 72,128,677 (GRCm39) Q38* probably null Het
Mcm4 A T 16: 15,448,284 (GRCm39) D424E possibly damaging Het
Micu1 T A 10: 59,699,100 (GRCm39) M463K possibly damaging Het
Mkrn2os A G 6: 115,562,492 (GRCm39) L157P probably damaging Het
Nectin2 A G 7: 19,451,487 (GRCm39) S516P probably damaging Het
Nme5 T A 18: 34,702,928 (GRCm39) D120V probably damaging Het
Npy4r T C 14: 33,869,282 (GRCm39) N2S possibly damaging Het
Nup107 A T 10: 117,595,245 (GRCm39) probably benign Het
Omd T C 13: 49,742,973 (GRCm39) Y8H possibly damaging Het
Phf8-ps T G 17: 33,285,289 (GRCm39) E504D probably benign Het
Ppp1r15a T C 7: 45,173,803 (GRCm39) probably benign Het
Ppp2ca T C 11: 51,989,891 (GRCm39) F6L probably benign Het
Rab1a T C 11: 20,174,717 (GRCm39) S97P probably benign Het
Ranbp3l G A 15: 9,058,827 (GRCm39) G359R probably damaging Het
Rnf213 A T 11: 119,334,094 (GRCm39) H3101L probably damaging Het
Slc27a4 T C 2: 29,702,627 (GRCm39) F509S probably damaging Het
Slco4a1 T C 2: 180,114,946 (GRCm39) V623A probably benign Het
Spart T A 3: 55,035,911 (GRCm39) probably null Het
Sptan1 A G 2: 29,909,980 (GRCm39) D1780G probably damaging Het
Tgm7 G T 2: 120,924,106 (GRCm39) Y605* probably null Het
Trak2 G A 1: 58,965,814 (GRCm39) A120V possibly damaging Het
Trappc8 G A 18: 21,007,769 (GRCm39) probably benign Het
Trim66 T C 7: 109,057,970 (GRCm39) T973A probably benign Het
Ttyh3 C A 5: 140,621,829 (GRCm39) probably benign Het
Ugt2b37 A C 5: 87,390,291 (GRCm39) I385S probably damaging Het
Usf3 A G 16: 44,039,180 (GRCm39) N1220S possibly damaging Het
Utrn A T 10: 12,623,773 (GRCm39) I155N probably damaging Het
Vps13b C T 15: 35,439,050 (GRCm39) Q377* probably null Het
Washc2 A T 6: 116,213,150 (GRCm39) E570D probably benign Het
Wscd1 T C 11: 71,657,699 (GRCm39) V168A possibly damaging Het
Zfp386 T A 12: 116,022,788 (GRCm39) C169S probably benign Het
Other mutations in Tmem106b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01545:Tmem106b APN 6 13,071,842 (GRCm39) missense probably benign
IGL02402:Tmem106b APN 6 13,081,600 (GRCm39) missense possibly damaging 0.92
R0784:Tmem106b UTSW 6 13,084,252 (GRCm39) missense probably damaging 1.00
R1630:Tmem106b UTSW 6 13,081,540 (GRCm39) missense probably benign 0.43
R3958:Tmem106b UTSW 6 13,081,587 (GRCm39) missense probably damaging 1.00
R4516:Tmem106b UTSW 6 13,075,098 (GRCm39) missense probably damaging 1.00
R5315:Tmem106b UTSW 6 13,081,559 (GRCm39) missense probably damaging 1.00
R5759:Tmem106b UTSW 6 13,075,041 (GRCm39) missense probably damaging 1.00
R5949:Tmem106b UTSW 6 13,083,418 (GRCm39) missense probably damaging 1.00
R6179:Tmem106b UTSW 6 13,084,252 (GRCm39) missense probably damaging 1.00
R6935:Tmem106b UTSW 6 13,081,554 (GRCm39) missense possibly damaging 0.91
R6964:Tmem106b UTSW 6 13,082,422 (GRCm39) missense probably benign 0.00
R7142:Tmem106b UTSW 6 13,081,564 (GRCm39) missense probably damaging 1.00
R7380:Tmem106b UTSW 6 13,078,167 (GRCm39) missense probably damaging 0.99
R7694:Tmem106b UTSW 6 13,078,105 (GRCm39) missense probably benign 0.15
R8357:Tmem106b UTSW 6 13,084,243 (GRCm39) missense probably damaging 1.00
R8457:Tmem106b UTSW 6 13,084,243 (GRCm39) missense probably damaging 1.00
R9206:Tmem106b UTSW 6 13,082,430 (GRCm39) missense probably damaging 1.00
R9208:Tmem106b UTSW 6 13,082,430 (GRCm39) missense probably damaging 1.00
Posted On 2014-05-07