Incidental Mutation 'R8015:Tmem150b'
ID617126
Institutional Source Beutler Lab
Gene Symbol Tmem150b
Ensembl Gene ENSMUSG00000046456
Gene Nametransmembrane protein 150B
SynonymsTmem224
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.115) question?
Stock #R8015 (G1)
Quality Score225.009
Status Not validated
Chromosome7
Chromosomal Location4706832-4725249 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 4716328 bp
ZygosityHeterozygous
Amino Acid Change Glycine to Serine at position 198 (G198S)
Ref Sequence ENSEMBL: ENSMUSP00000083549 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000048248] [ENSMUST00000086363] [ENSMUST00000086364] [ENSMUST00000120836]
Predicted Effect probably benign
Transcript: ENSMUST00000048248
SMART Domains Protein: ENSMUSP00000039517
Gene: ENSMUSG00000035390

DomainStartEndE-ValueType
low complexity region 2 12 N/A INTRINSIC
low complexity region 13 30 N/A INTRINSIC
S_TKc 34 285 6.75e-103 SMART
low complexity region 330 344 N/A INTRINSIC
low complexity region 430 457 N/A INTRINSIC
low complexity region 492 517 N/A INTRINSIC
low complexity region 523 552 N/A INTRINSIC
low complexity region 668 686 N/A INTRINSIC
low complexity region 746 764 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000086363
AA Change: G198S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000083549
Gene: ENSMUSG00000046456
AA Change: G198S

DomainStartEndE-ValueType
Pfam:Frag1 4 207 7.1e-52 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000086364
SMART Domains Protein: ENSMUSP00000083550
Gene: ENSMUSG00000046456

DomainStartEndE-ValueType
Pfam:Frag1 4 114 1.5e-28 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000120836
SMART Domains Protein: ENSMUSP00000113448
Gene: ENSMUSG00000035390

DomainStartEndE-ValueType
S_TKc 1 210 1.19e-71 SMART
low complexity region 255 269 N/A INTRINSIC
low complexity region 355 382 N/A INTRINSIC
low complexity region 417 442 N/A INTRINSIC
low complexity region 448 477 N/A INTRINSIC
low complexity region 593 611 N/A INTRINSIC
low complexity region 671 689 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.2%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that belongs to the DRAM (damage-regulated autophagy modulator) family of membrane-spanning proteins. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Alad A G 4: 62,511,922 V121A probably damaging Het
Anapc2 T A 2: 25,284,676 Y684N probably benign Het
Arntl2 T C 6: 146,820,590 S220P probably damaging Het
Atp10a G T 7: 58,803,497 R808L probably benign Het
Best2 A G 8: 85,009,354 V317A probably damaging Het
Cacnb4 A G 2: 52,464,643 L241P probably damaging Het
Col6a5 T C 9: 105,881,741 T2089A possibly damaging Het
Cttnbp2 G C 6: 18,426,093 A762G possibly damaging Het
Defb13 G T 8: 21,946,812 V8F possibly damaging Het
Fam126b A G 1: 58,535,482 V300A possibly damaging Het
Fat4 A G 3: 38,981,916 D3239G possibly damaging Het
Gm16486 C T 8: 70,716,792 S1177L probably benign Het
Gm5615 A G 9: 36,534,954 V54A probably benign Het
Hmcn1 T G 1: 150,598,311 R4793S possibly damaging Het
Hspa1a T A 17: 34,970,649 Q426L probably damaging Het
Il20rb T A 9: 100,474,894 Y61F probably damaging Het
Itgb1 T A 8: 128,722,401 V496D possibly damaging Het
Jakmip1 T C 5: 37,159,765 S102P unknown Het
Jmjd8 T A 17: 25,829,328 F108I probably damaging Het
Krtap15 A G 16: 88,829,209 T55A possibly damaging Het
Lnpep C A 17: 17,546,499 V702F probably damaging Het
Lox G A 18: 52,528,348 A218V probably benign Het
Mcrs1 T A 15: 99,248,854 K99* probably null Het
Mfsd8 G A 3: 40,846,835 probably benign Het
Msto1 G T 3: 88,911,556 P264Q probably damaging Het
Nrp2 C T 1: 62,745,408 R239C probably damaging Het
Olfr1002 G T 2: 85,647,792 H176Q probably damaging Het
Olfr1368 T C 13: 21,142,133 D308G probably benign Het
Pate2 A T 9: 35,670,518 H36L probably damaging Het
Phf20l1 T G 15: 66,639,948 N925K possibly damaging Het
Pnliprp2 G T 19: 58,766,282 V253F probably damaging Het
Polr2b A G 5: 77,336,506 D745G probably damaging Het
Ptdss1 T A 13: 66,963,343 W158R possibly damaging Het
Rcn3 T A 7: 45,084,907 I226F probably damaging Het
Rhbdl1 C G 17: 25,835,851 V157L probably damaging Het
Slc30a2 A G 4: 134,347,450 T173A probably benign Het
Spata16 A G 3: 26,667,659 T110A probably benign Het
Specc1l A G 10: 75,241,068 K53E probably benign Het
Spta1 T A 1: 174,240,171 C2055S probably damaging Het
Tex14 G A 11: 87,509,600 R406Q probably benign Het
Tnfrsf14 T G 4: 154,926,661 Q81P probably damaging Het
Txndc17 A G 11: 72,207,742 K40R probably benign Het
Ube3a T A 7: 59,284,756 V560E probably damaging Het
Vmn1r14 A G 6: 57,234,030 M198V probably damaging Het
Vmn2r23 G A 6: 123,704,541 S136N probably benign Het
Vmn2r31 C T 7: 7,384,200 V791I probably damaging Het
Wdfy4 T C 14: 33,107,747 Y984C Het
Zfp386 T G 12: 116,059,407 D248E probably damaging Het
Other mutations in Tmem150b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00590:Tmem150b APN 7 4723897 missense probably benign 0.01
R1769:Tmem150b UTSW 7 4724366 missense probably damaging 1.00
R1888:Tmem150b UTSW 7 4709045 missense probably benign 0.31
R1888:Tmem150b UTSW 7 4709045 missense probably benign 0.31
R2197:Tmem150b UTSW 7 4716354 missense probably benign 0.07
R3408:Tmem150b UTSW 7 4724340 missense probably damaging 1.00
R3872:Tmem150b UTSW 7 4724361 nonsense probably null
R4820:Tmem150b UTSW 7 4723872 missense probably damaging 1.00
R5412:Tmem150b UTSW 7 4716369 missense probably null 0.54
R6280:Tmem150b UTSW 7 4724374 missense probably benign 0.00
R7427:Tmem150b UTSW 7 4716210 missense probably benign 0.29
R7658:Tmem150b UTSW 7 4720759 missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- CACAAGTCCACTTTGCCGTG -3'
(R):5'- ATTGATCCCAGCCTGAAGTG -3'

Sequencing Primer
(F):5'- TTCTCCAGAATGTCCACATCAG -3'
(R):5'- CGTGAAGTGATTGTCCTG -3'
Posted On2020-01-23