Incidental Mutation 'R5271:Gm14548'
ID400300
Institutional Source Beutler Lab
Gene Symbol Gm14548
Ensembl Gene ENSMUSG00000074417
Gene Namepredicted gene 14548
Synonyms
MMRRC Submission 042861-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.050) question?
Stock #R5271 (G1)
Quality Score225
Status Validated
Chromosome7
Chromosomal Location3884242-3898120 bp(-) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) A to T at 3897567 bp
ZygosityHeterozygous
Amino Acid Change Tyrosine to Stop codon at position 61 (Y61*)
Ref Sequence ENSEMBL: ENSMUSP00000070073 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000070639]
Predicted Effect probably null
Transcript: ENSMUST00000070639
AA Change: Y61*
SMART Domains Protein: ENSMUSP00000070073
Gene: ENSMUSG00000074417
AA Change: Y61*

DomainStartEndE-ValueType
IG 34 118 6.41e-2 SMART
IG 129 315 8.59e-3 SMART
IG_like 237 302 1.91e-1 SMART
IG 328 415 3.36e0 SMART
IG_like 435 502 3.11e0 SMART
IG 529 618 8.59e-3 SMART
low complexity region 627 636 N/A INTRINSIC
low complexity region 654 663 N/A INTRINSIC
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.6%
  • 20x: 93.6%
Validation Efficiency 97% (65/67)
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700003H04Rik T C 3: 124,579,847 K33R possibly damaging Het
4632415L05Rik C T 3: 19,895,147 noncoding transcript Het
4930542C16Rik A C 14: 24,615,530 noncoding transcript Het
Adprh A T 16: 38,446,054 L242* probably null Het
Anapc1 G A 2: 128,685,985 Q18* probably null Het
Bfar T C 16: 13,692,397 probably benign Het
Bmp1 T C 14: 70,508,128 I206V probably benign Het
Cc2d1b T A 4: 108,623,629 probably benign Het
Clock A G 5: 76,241,954 I349T probably damaging Het
Cox11 A G 11: 90,643,732 Y60C probably damaging Het
Cyp1a1 G A 9: 57,702,838 V512M probably benign Het
Dcdc2a T C 13: 25,187,688 F311S probably benign Het
Dnase1l3 T C 14: 7,993,843 D48G probably damaging Het
Engase G T 11: 118,481,397 A172S probably damaging Het
F2 T C 2: 91,635,121 probably benign Het
Gcc2 T C 10: 58,269,695 V215A possibly damaging Het
Gm11677 C T 11: 111,724,711 noncoding transcript Het
Gm20388 A G 8: 122,271,133 probably benign Het
Gm20671 T C 5: 32,819,959 K1817R possibly damaging Het
Gm20939 T A 17: 94,877,155 Y410* probably null Het
Gm27013 T C 6: 130,676,915 Y528C probably damaging Het
Gm9992 T C 17: 7,369,682 N149S possibly damaging Het
Il23r T C 6: 67,423,696 H550R probably benign Het
Iqgap1 A T 7: 80,734,148 V1056E probably damaging Het
Lrit3 T A 3: 129,788,301 Y679F probably damaging Het
Megf8 A T 7: 25,341,706 E1120V probably damaging Het
Mta1 A G 12: 113,131,957 E518G probably damaging Het
Myo9a A G 9: 59,907,382 I2200M probably damaging Het
Ncoa7 T C 10: 30,722,729 H66R probably benign Het
Ncor1 A G 11: 62,340,545 V812A probably damaging Het
Ndnf T C 6: 65,703,666 Y310H possibly damaging Het
Ndst1 G A 18: 60,705,132 T347I probably benign Het
Olfr1229 A T 2: 89,282,953 F60Y probably benign Het
Olfr512 T C 7: 108,714,217 L276S probably damaging Het
Pcdhb10 C A 18: 37,413,169 Q433K probably benign Het
Pcdhb18 G A 18: 37,491,596 V660M possibly damaging Het
Pds5b T A 5: 150,723,353 N202K possibly damaging Het
Polk T C 13: 96,483,539 S718G probably benign Het
Ptpdc1 T C 13: 48,590,698 D149G probably damaging Het
Rb1cc1 T A 1: 6,249,193 C35* probably null Het
Samd9l C T 6: 3,376,156 M368I probably benign Het
Shroom3 T C 5: 92,962,248 M1739T probably damaging Het
Slc18a3 A G 14: 32,463,748 L226P probably damaging Het
St7l A T 3: 104,868,060 Y84F probably damaging Het
Svil A T 18: 5,062,329 N392I probably benign Het
Syngr1 T A 15: 80,098,039 M9K probably benign Het
Taar2 T C 10: 23,941,032 S157P probably damaging Het
Tagap1 G T 17: 6,956,096 Y400* probably null Het
Tbc1d8 T A 1: 39,373,767 E976V probably damaging Het
Tmem163 G A 1: 127,491,552 probably benign Het
Tnfaip2 A G 12: 111,448,460 probably benign Het
Ttn C T 2: 76,706,517 S34988N possibly damaging Het
Tubg1 T G 11: 101,120,238 N15K probably damaging Het
Vmn2r-ps159 G T 4: 156,334,397 noncoding transcript Het
Zap70 T A 1: 36,781,365 V547D probably damaging Het
Zfp146 G T 7: 30,162,475 N47K probably benign Het
Znrf1 T G 8: 111,609,344 M159R probably benign Het
Other mutations in Gm14548
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00541:Gm14548 APN 7 3897386 splice site probably benign
IGL01358:Gm14548 APN 7 3895687 missense probably benign 0.41
IGL01868:Gm14548 APN 7 3897175 nonsense probably null
IGL02421:Gm14548 APN 7 3896995 missense possibly damaging 0.87
IGL02544:Gm14548 APN 7 3897186 missense probably damaging 0.96
IGL02960:Gm14548 APN 7 3897079 missense possibly damaging 0.88
IGL02973:Gm14548 APN 7 3897240 missense probably damaging 1.00
PIT4495001:Gm14548 UTSW 7 3897458 missense probably damaging 1.00
R0761:Gm14548 UTSW 7 3893979 critical splice donor site probably null
R1917:Gm14548 UTSW 7 3897638 missense probably damaging 1.00
R1920:Gm14548 UTSW 7 3897872 missense probably damaging 0.98
R2219:Gm14548 UTSW 7 3897489 missense probably benign 0.10
R2220:Gm14548 UTSW 7 3897489 missense probably benign 0.10
R4991:Gm14548 UTSW 7 3895572 missense probably benign 0.37
R5909:Gm14548 UTSW 7 3897622 missense probably damaging 1.00
R6008:Gm14548 UTSW 7 3894600 missense probably damaging 1.00
R6193:Gm14548 UTSW 7 3898050 critical splice donor site probably null
R6218:Gm14548 UTSW 7 3894032 missense possibly damaging 0.65
R6219:Gm14548 UTSW 7 3894641 missense probably damaging 1.00
R6650:Gm14548 UTSW 7 3895633 missense probably benign 0.15
R6879:Gm14548 UTSW 7 3896962 missense probably benign 0.40
R6987:Gm14548 UTSW 7 3897661 missense probably damaging 0.99
R7082:Gm14548 UTSW 7 3895511 missense probably damaging 1.00
R7087:Gm14548 UTSW 7 3897219 missense probably benign 0.08
R7144:Gm14548 UTSW 7 3897616 missense probably damaging 1.00
R7298:Gm14548 UTSW 7 3895265 missense possibly damaging 0.92
R7359:Gm14548 UTSW 7 3898104 start gained probably benign
R7751:Gm14548 UTSW 7 3895604 missense probably damaging 1.00
R7810:Gm14548 UTSW 7 3894205 missense probably damaging 1.00
R8344:Gm14548 UTSW 7 3896955 missense possibly damaging 0.93
R8428:Gm14548 UTSW 7 3895258 missense probably benign 0.02
Predicted Primers PCR Primer
(F):5'- TAACAGAGCCAAGTCTGGACAG -3'
(R):5'- AGGACTGCAATCTGAGTGTG -3'

Sequencing Primer
(F):5'- GTCTGGACAGTTATAACCTGAGTCC -3'
(R):5'- ACTGCAATCTGAGTGTGTTTGTCC -3'
Posted On2016-07-06