Incidental Mutation 'R1398:Gm4922'
ID160243
Institutional Source Beutler Lab
Gene Symbol Gm4922
Ensembl Gene ENSMUSG00000044624
Gene Namepredicted gene 4922
Synonyms
MMRRC Submission 039460-MU
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #R1398 (G1)
Quality Score225
Status Validated
Chromosome10
Chromosomal Location18779725-18786793 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 18783748 bp
ZygosityHeterozygous
Amino Acid Change Serine to Cysteine at position 409 (S409C)
Ref Sequence ENSEMBL: ENSMUSP00000149756 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055107] [ENSMUST00000216654]
Predicted Effect possibly damaging
Transcript: ENSMUST00000055107
AA Change: S409C

PolyPhen 2 Score 0.650 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000055273
Gene: ENSMUSG00000044624
AA Change: S409C

DomainStartEndE-ValueType
low complexity region 3 13 N/A INTRINSIC
S_TKc 28 275 1.92e-75 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000215162
Predicted Effect possibly damaging
Transcript: ENSMUST00000216654
AA Change: S409C

PolyPhen 2 Score 0.650 (Sensitivity: 0.87; Specificity: 0.91)
Meta Mutation Damage Score 0.0912 question?
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.1%
  • 10x: 95.6%
  • 20x: 90.7%
Validation Efficiency 96% (75/78)
Allele List at MGI
Other mutations in this stock
Total: 74 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931408C20Rik G T 1: 26,685,341 Q253K possibly damaging Het
9330182L06Rik A G 5: 9,380,297 Y69C probably damaging Het
Abca17 T C 17: 24,328,537 K288E probably damaging Het
Aldh3a2 T C 11: 61,256,736 probably null Het
Anks1b A G 10: 90,050,029 T196A probably damaging Het
Anks6 T A 4: 47,044,926 T327S possibly damaging Het
Bdh2 T C 3: 135,295,296 probably benign Het
C4b T A 17: 34,730,719 probably benign Het
Cacna2d1 G A 5: 16,357,766 V847I possibly damaging Het
Cadps G T 14: 12,449,822 T1129K probably damaging Het
Cdc45 A G 16: 18,781,971 probably benign Het
Cep63 A T 9: 102,603,086 probably benign Het
Chil4 T A 3: 106,219,509 probably null Het
Cnot11 A G 1: 39,545,180 R478G probably damaging Het
Cyp2c67 A G 19: 39,638,625 S254P probably damaging Het
Dnah11 T A 12: 118,057,106 K87* probably null Het
Dpy19l2 T A 9: 24,581,263 probably benign Het
Dsc1 A T 18: 20,088,336 I694N probably damaging Het
Ehd4 A T 2: 120,127,600 I168K probably benign Het
Eif4e A T 3: 138,546,375 N25Y probably damaging Het
Eme2 G A 17: 24,892,918 S263F probably damaging Het
Fam160b1 T A 19: 57,372,926 probably benign Het
Fgfrl1 T A 5: 108,706,281 probably benign Het
Gm3159 T A 14: 4,398,586 Y92* probably null Het
Gmcl1 G A 6: 86,714,262 probably benign Het
Grsf1 A G 5: 88,665,847 Y231H probably benign Het
Heatr4 T A 12: 83,967,621 H614L possibly damaging Het
Hoxa13 C G 6: 52,260,647 probably benign Het
Hoxa13 G C 6: 52,260,648 probably benign Het
Isg20l2 C A 3: 87,938,754 L325I probably benign Het
Kalrn A G 16: 34,212,820 Y879H probably damaging Het
Kcnk10 C A 12: 98,436,226 W318L probably damaging Het
Kctd1 T C 18: 15,062,597 E323G possibly damaging Het
Kif4 G T X: 100,689,097 A492S probably benign Het
Krtap4-1 T C 11: 99,627,732 T151A unknown Het
Ldlr A T 9: 21,739,542 Q449L probably benign Het
Lepr T A 4: 101,792,019 D872E probably damaging Het
Lgals12 C T 19: 7,603,957 probably benign Het
Lrig3 C T 10: 126,003,088 P488L probably benign Het
Lrrc4b A C 7: 44,462,452 I583L probably benign Het
Lyst T C 13: 13,740,536 S3272P possibly damaging Het
March2 T C 17: 33,696,122 H166R probably damaging Het
Mtbp C A 15: 55,577,537 Y373* probably null Het
Myh2 C T 11: 67,185,287 H767Y probably benign Het
Ncam1 G A 9: 49,517,589 probably benign Het
Neb T A 2: 52,289,646 N1282Y probably damaging Het
Nectin3 A G 16: 46,448,756 Y428H possibly damaging Het
Nrros A T 16: 32,143,144 I649N probably damaging Het
Nvl A T 1: 181,097,126 probably benign Het
Olfr495 T A 7: 108,395,501 V127E probably damaging Het
Pms1 A T 1: 53,207,276 V368E possibly damaging Het
Polq T A 16: 37,062,495 S1674T possibly damaging Het
Ppp1r21 T C 17: 88,542,879 V31A probably damaging Het
Rev3l T A 10: 39,821,583 V692E probably benign Het
Robo4 T C 9: 37,408,076 probably null Het
Rps6kc1 T C 1: 190,800,015 I597V probably damaging Het
Rtel1 T A 2: 181,335,865 probably null Het
Scn9a A G 2: 66,484,586 M1587T probably benign Het
Sec31b T A 19: 44,523,665 I597F probably benign Het
Skint5 T C 4: 113,779,071 N650S unknown Het
Slc22a28 G T 19: 8,130,202 S167* probably null Het
Slfn1 T A 11: 83,121,142 M28K probably damaging Het
Smc6 T C 12: 11,271,879 probably benign Het
Sox8 T C 17: 25,567,883 H282R probably benign Het
Syngr3 C A 17: 24,686,440 V161L probably benign Het
Trak1 C T 9: 121,454,359 S397F probably damaging Het
Uso1 C T 5: 92,181,468 A405V probably benign Het
Uvrag G T 7: 99,065,820 Y190* probably null Het
Vps13d A T 4: 145,099,983 L1726Q probably null Het
Vwf A T 6: 125,603,457 Q556L probably benign Het
Wdr70 T A 15: 8,035,844 M246L probably benign Het
Yipf3 T C 17: 46,251,446 F285S probably damaging Het
Zdhhc13 G A 7: 48,826,873 G579R probably damaging Het
Zdhhc18 G C 4: 133,627,297 F125L probably benign Het
Other mutations in Gm4922
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01810:Gm4922 APN 10 18784047 missense probably benign 0.20
IGL01818:Gm4922 APN 10 18784953 missense unknown
IGL01931:Gm4922 APN 10 18784294 missense probably benign 0.01
IGL02021:Gm4922 APN 10 18784477 missense probably damaging 1.00
IGL02573:Gm4922 APN 10 18783675 missense probably benign 0.05
IGL03305:Gm4922 APN 10 18783484 nonsense probably null
R0149:Gm4922 UTSW 10 18783541 missense probably benign 0.10
R0361:Gm4922 UTSW 10 18783541 missense probably benign 0.10
R0564:Gm4922 UTSW 10 18784065 missense possibly damaging 0.66
R1079:Gm4922 UTSW 10 18784338 missense probably damaging 0.97
R1163:Gm4922 UTSW 10 18783721 missense possibly damaging 0.83
R1164:Gm4922 UTSW 10 18783721 missense possibly damaging 0.83
R1458:Gm4922 UTSW 10 18783892 nonsense probably null
R1867:Gm4922 UTSW 10 18784463 missense possibly damaging 0.73
R1994:Gm4922 UTSW 10 18783640 missense probably benign 0.10
R2146:Gm4922 UTSW 10 18783516 missense probably benign
R2437:Gm4922 UTSW 10 18784081 missense probably benign 0.00
R3551:Gm4922 UTSW 10 18784496 missense probably benign 0.01
R3939:Gm4922 UTSW 10 18784614 missense probably damaging 1.00
R4580:Gm4922 UTSW 10 18783684 missense probably benign 0.00
R4602:Gm4922 UTSW 10 18784259 nonsense probably null
R4704:Gm4922 UTSW 10 18784819 missense probably benign 0.20
R4790:Gm4922 UTSW 10 18784168 missense possibly damaging 0.58
R5478:Gm4922 UTSW 10 18784137 missense probably benign
R5510:Gm4922 UTSW 10 18783997 missense probably benign 0.00
R5694:Gm4922 UTSW 10 18784287 missense possibly damaging 0.76
R6080:Gm4922 UTSW 10 18784752 missense probably damaging 1.00
R6869:Gm4922 UTSW 10 18784515 missense probably damaging 1.00
R6923:Gm4922 UTSW 10 18783868 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GGCAACGTGCAGCAACACAATG -3'
(R):5'- GCCACCTTTCCCTTCAGTAACAGAC -3'

Sequencing Primer
(F):5'- TGCAGCAACACAATGTCTGG -3'
(R):5'- GACTCTGGAGCTTTTTCTCTGC -3'
Posted On2014-03-14