Incidental Mutation 'R3741:Tmem88b'
ID270363
Institutional Source Beutler Lab
Gene Symbol Tmem88b
Ensembl Gene ENSMUSG00000073680
Gene Nametransmembrane protein 88B
Synonyms
MMRRC Submission 040727-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.056) question?
Stock #R3741 (G1)
Quality Score225
Status Validated
Chromosome4
Chromosomal Location155781591-155785874 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 155785427 bp
ZygosityHeterozygous
Amino Acid Change Leucine to Proline at position 59 (L59P)
Ref Sequence ENSEMBL: ENSMUSP00000095349 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000097742]
Predicted Effect probably damaging
Transcript: ENSMUST00000097742
AA Change: L59P

PolyPhen 2 Score 0.963 (Sensitivity: 0.78; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000095349
Gene: ENSMUSG00000073680
AA Change: L59P

DomainStartEndE-ValueType
transmembrane domain 30 52 N/A INTRINSIC
transmembrane domain 62 84 N/A INTRINSIC
transmembrane domain 105 127 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185136
Meta Mutation Damage Score 0.2665 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.3%
Validation Efficiency 97% (37/38)
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aspm T C 1: 139,478,619 V1748A possibly damaging Het
Atp10b A T 11: 43,235,662 S1082C probably damaging Het
Atp8b2 C G 3: 89,946,031 A726P probably benign Het
B4galt3 C A 1: 171,274,043 H196N probably damaging Het
Bbip1 T C 19: 53,932,175 M1V probably null Het
Bbox1 A G 2: 110,305,577 I19T possibly damaging Het
Bclaf3 T A X: 159,551,832 H41Q probably benign Het
Ctsm T A 13: 61,539,627 Q107L probably benign Het
Ctso G A 3: 81,952,249 V288I probably benign Het
Cyp2a4 A C 7: 26,308,544 K125N probably damaging Het
Dapk1 T C 13: 60,748,200 S701P probably benign Het
Dnah1 A G 14: 31,265,467 probably benign Het
Dnah11 A G 12: 118,131,341 M718T probably benign Het
Dnah2 C A 11: 69,448,469 A3071S probably damaging Het
Epb41l4a A T 18: 33,828,102 probably null Het
Fam135a A T 1: 24,014,811 M1215K probably damaging Het
Gm6489 T A 1: 31,287,683 noncoding transcript Het
Hhipl1 A G 12: 108,318,717 Y443C probably damaging Het
Hoxc13 G A 15: 102,921,438 G84D possibly damaging Het
Ifi207 T C 1: 173,727,562 I851M probably damaging Het
Lipk T G 19: 34,021,707 L134R probably damaging Het
Mov10l1 A G 15: 89,012,142 N678D possibly damaging Het
Msrb3 A T 10: 120,784,214 F67I probably damaging Het
Myo1a A G 10: 127,714,898 D593G probably benign Het
Nsf C T 11: 103,930,752 E26K possibly damaging Het
Nup210l A T 3: 90,207,394 M1759L probably benign Het
Optn C A 2: 5,034,198 M371I possibly damaging Het
Rims1 A T 1: 22,373,443 V380D probably damaging Het
Rnf148 A G 6: 23,654,065 C311R possibly damaging Het
Rrp12 T C 19: 41,885,728 D377G probably damaging Het
Sbp T A 17: 23,945,582 probably benign Het
Sipa1 T C 19: 5,654,857 E570G probably damaging Het
Spem2 T C 11: 69,816,730 R470G possibly damaging Het
Syngr4 T C 7: 45,895,770 E5G possibly damaging Het
Ttn T A 2: 76,790,359 K13995* probably null Het
Vmn1r69 A G 7: 10,580,142 Y221H possibly damaging Het
Zfp386 T A 12: 116,059,550 L296* probably null Het
Other mutations in Tmem88b
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0598:Tmem88b UTSW 4 155784367 missense probably benign
R3740:Tmem88b UTSW 4 155785427 missense probably damaging 0.96
R3742:Tmem88b UTSW 4 155785427 missense probably damaging 0.96
R5511:Tmem88b UTSW 4 155785545 missense probably damaging 0.99
R6374:Tmem88b UTSW 4 155785764 unclassified probably benign
R6551:Tmem88b UTSW 4 155785692 unclassified probably benign
Predicted Primers PCR Primer
(F):5'- GGGTAGATTCACCTTCAACCC -3'
(R):5'- GCCTACCACTGTGATCTTGG -3'

Sequencing Primer
(F):5'- GTAGATTCACCTTCAACCCCAAGG -3'
(R):5'- ATCTTGGGGGAACATCCTTCAAGC -3'
Posted On2015-03-18