Incidental Mutation 'R0659:Tmem229b'
ID61796
Institutional Source Beutler Lab
Gene Symbol Tmem229b
Ensembl Gene ENSMUSG00000046157
Gene Nametransmembrane protein 229B
Synonyms
MMRRC Submission 038844-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.183) question?
Stock #R0659 (G1)
Quality Score90
Status Validated
Chromosome12
Chromosomal Location78961795-79007627 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 78965134 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Alanine at position 8 (T8A)
Ref Sequence ENSEMBL: ENSMUSP00000134348 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000056660] [ENSMUST00000070174] [ENSMUST00000174072] [ENSMUST00000174697] [ENSMUST00000174721]
Predicted Effect probably benign
Transcript: ENSMUST00000056660
AA Change: T8A

PolyPhen 2 Score 0.090 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000053835
Gene: ENSMUSG00000046157
AA Change: T8A

DomainStartEndE-ValueType
Pfam:DUF1113 11 147 3.7e-14 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000070174
AA Change: T8A

PolyPhen 2 Score 0.090 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000070637
Gene: ENSMUSG00000046157
AA Change: T8A

DomainStartEndE-ValueType
Pfam:DUF1113 11 147 3.7e-14 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000174072
AA Change: T8A

PolyPhen 2 Score 0.090 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000134376
Gene: ENSMUSG00000046157
AA Change: T8A

DomainStartEndE-ValueType
Pfam:ABC_trans_CmpB 12 148 1.8e-13 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000174697
AA Change: T8A

PolyPhen 2 Score 0.090 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000134348
Gene: ENSMUSG00000046157
AA Change: T8A

DomainStartEndE-ValueType
Pfam:DUF1113 11 147 3.7e-14 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000174721
AA Change: T8A

PolyPhen 2 Score 0.038 (Sensitivity: 0.94; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000134605
Gene: ENSMUSG00000046157
AA Change: T8A

DomainStartEndE-ValueType
transmembrane domain 13 35 N/A INTRINSIC
transmembrane domain 41 60 N/A INTRINSIC
transmembrane domain 73 95 N/A INTRINSIC
Meta Mutation Damage Score 0.0641 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.9%
  • 10x: 97.7%
  • 20x: 95.6%
Validation Efficiency 99% (72/73)
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts19 A G 18: 59,007,493 probably benign Het
Ahnak A G 19: 9,015,002 H4550R possibly damaging Het
Anxa6 A G 11: 54,983,347 V591A probably damaging Het
Apol7c A G 15: 77,526,273 S158P probably damaging Het
Asxl1 T A 2: 153,400,724 S1065T possibly damaging Het
Cacna2d4 A G 6: 119,345,106 probably benign Het
Cd109 T C 9: 78,680,170 probably benign Het
Cep78 C T 19: 15,956,190 V675M probably damaging Het
Ces4a T C 8: 105,144,922 probably benign Het
Chpf A G 1: 75,477,723 V137A probably damaging Het
Comp T C 8: 70,379,101 S457P possibly damaging Het
Cth A G 3: 157,920,115 probably benign Het
Cyp2a12 T C 7: 27,034,138 L314P probably damaging Het
Ets1 C T 9: 32,738,293 R309C probably damaging Het
Fam208b T C 13: 3,574,448 D1834G probably damaging Het
Foxp2 T C 6: 15,254,279 probably benign Het
Gm9875 T G 2: 13,558,184 F108V unknown Het
Golga5 G T 12: 102,476,208 V269F possibly damaging Het
Greb1 T C 12: 16,680,212 Y1738C probably damaging Het
Grin2a G T 16: 9,992,472 P21Q probably damaging Het
Hdac5 A T 11: 102,196,024 V70E probably damaging Het
Hdac9 T C 12: 34,437,222 Q60R probably damaging Het
Hsd17b3 T C 13: 64,073,936 T92A possibly damaging Het
Itpk1 C T 12: 102,606,078 probably benign Het
Lin28a T C 4: 134,008,099 probably benign Het
Mapk6 T C 9: 75,397,962 S58G probably damaging Het
Mmp21 G A 7: 133,677,667 probably benign Het
Mroh2a C A 1: 88,242,420 A685D possibly damaging Het
Mroh2a G A 1: 88,250,342 D1053N probably damaging Het
Msh3 T C 13: 92,345,096 N303D possibly damaging Het
Mto1 T A 9: 78,457,508 I343N probably damaging Het
Mto1 C T 9: 78,470,790 T638M probably damaging Het
Myo18b T C 5: 112,760,327 K2027E possibly damaging Het
Myo7a T C 7: 98,054,338 probably benign Het
Nlrp9a T C 7: 26,557,278 I107T probably damaging Het
Olfr181 C A 16: 58,926,409 R54L possibly damaging Het
Olfr970 T G 9: 39,819,816 M59R possibly damaging Het
Osbpl5 A G 7: 143,705,030 S268P probably damaging Het
Pih1d1 T A 7: 45,159,975 S289T probably benign Het
Pik3c2b A G 1: 133,071,200 D353G probably damaging Het
Ppef2 A G 5: 92,230,509 L609P probably damaging Het
Prune2 A T 19: 17,122,835 D1901V probably damaging Het
Rdh9 T C 10: 127,776,575 Y31H possibly damaging Het
Slc5a9 T A 4: 111,883,871 Y526F possibly damaging Het
Slitrk5 A G 14: 111,680,689 K582E probably benign Het
Sult1c2 A T 17: 53,831,778 M257K probably damaging Het
Tmem132d A G 5: 127,984,287 I417T possibly damaging Het
Tmem237 T C 1: 59,114,094 I89M possibly damaging Het
Tnfrsf17 A T 16: 11,319,819 D140V probably damaging Het
Tnrc6b T A 15: 80,923,446 probably benign Het
Trio A G 15: 27,831,399 L194P probably damaging Het
Vmn2r74 T C 7: 85,955,914 probably benign Het
Vps13c T A 9: 67,920,935 M1457K probably benign Het
Zfhx2 A G 14: 55,073,801 C479R possibly damaging Het
Zfp420 T A 7: 29,875,539 C395S probably damaging Het
Zfp740 A G 15: 102,212,659 T136A possibly damaging Het
Zfp82 C T 7: 30,056,329 E443K probably damaging Het
Zranb2 A G 3: 157,541,763 S193G probably benign Het
Other mutations in Tmem229b
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1531:Tmem229b UTSW 12 78964911 missense probably damaging 0.98
R5545:Tmem229b UTSW 12 78964809 missense probably damaging 1.00
R6508:Tmem229b UTSW 12 78964906 missense probably damaging 1.00
R8036:Tmem229b UTSW 12 78965088 missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- GAAGGTACATACGCTCCACGATCAG -3'
(R):5'- GACCAATGGGTCAGGACAGCTAAC -3'

Sequencing Primer
(F):5'- CTCCACGATCAGGATGGAGG -3'
(R):5'- GGTCAGGACAGCTAACTCTTCAG -3'
Posted On2013-07-30