Incidental Mutation 'R7627:Gm5145'
ID589520
Institutional Source Beutler Lab
Gene Symbol Gm5145
Ensembl Gene ENSMUSG00000071273
Gene Namepredicted pseudogene 5145
Synonyms
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.913) question?
Stock #R7627 (G1)
Quality Score225.009
Status Not validated
Chromosome17
Chromosomal Location20570362-20571198 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) G to T at 20570392 bp
ZygosityHeterozygous
Amino Acid Change Glutamic Acid to Stop codon at position 11 (E11*)
Ref Sequence ENSEMBL: ENSMUSP00000093293 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095633] [ENSMUST00000169559]
Predicted Effect probably null
Transcript: ENSMUST00000095633
AA Change: E11*
SMART Domains Protein: ENSMUSP00000093293
Gene: ENSMUSG00000071273
AA Change: E11*

DomainStartEndE-ValueType
RRM 17 84 5.29e-5 SMART
low complexity region 101 113 N/A INTRINSIC
low complexity region 119 130 N/A INTRINSIC
low complexity region 160 175 N/A INTRINSIC
low complexity region 179 199 N/A INTRINSIC
RRM 207 274 1.55e-11 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000169559
SMART Domains Protein: ENSMUSP00000129347
Gene: ENSMUSG00000091259

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:ANF_receptor 83 467 3.1e-33 PFAM
Pfam:NCD3G 510 563 5.2e-22 PFAM
Pfam:7tm_3 594 831 4.2e-51 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9230112D13Rik T A 14: 34,512,098 I79L unknown Het
Acta2 G A 19: 34,252,531 T8I probably benign Het
Acvrl1 G A 15: 101,135,866 R143Q probably benign Het
Adam22 A G 5: 8,367,933 S8P probably benign Het
Ankrd11 A G 8: 122,890,951 I2054T possibly damaging Het
Cactin CCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAG CCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAG 10: 81,321,318 probably benign Het
Cad T A 5: 31,060,164 L354Q probably damaging Het
Ccdc15 A T 9: 37,342,402 C184S unknown Het
Ccl8 A G 11: 82,116,039 D26G probably benign Het
Ccsap T C 8: 123,842,358 Y248C probably damaging Het
Col5a1 T G 2: 27,950,653 Y271* probably null Het
Dnmt3b A G 2: 153,677,580 N695S probably benign Het
Dync1li2 A G 8: 104,429,508 C234R probably benign Het
Dync2h1 A T 9: 7,101,111 D2758E probably benign Het
Eif2ak3 A T 6: 70,892,935 T869S probably benign Het
Foxn4 G T 5: 114,260,434 P175H possibly damaging Het
Gbp5 T G 3: 142,500,558 M1R probably null Het
Glp2r G T 11: 67,746,763 L30I unknown Het
Gls A T 1: 52,166,266 D639E probably benign Het
Gm5724 C T 6: 141,744,545 V161I probably damaging Het
Gm9772 T A 17: 22,007,179 K41N probably damaging Het
Gnat3 A T 5: 17,999,748 D133V Het
Gse1 C A 8: 120,572,777 P849T unknown Het
Hist1h2ak C A 13: 21,753,746 V28L probably benign Het
Hoxb9 A G 11: 96,274,695 T197A probably damaging Het
Krt39 A G 11: 99,514,749 S442P possibly damaging Het
Leng9 A G 7: 4,148,618 L353P probably damaging Het
Mamdc2 A T 19: 23,310,991 M561K probably damaging Het
Mamdc4 A G 2: 25,568,213 V395A probably damaging Het
Mrpl32 G A 13: 14,612,913 R36C probably benign Het
Olfr1415 A T 1: 92,491,385 Y123* probably null Het
Olfr859 A G 9: 19,808,651 D111G probably damaging Het
Papss1 T A 3: 131,585,112 D205E probably benign Het
Pdlim2 T C 14: 70,171,475 D151G probably benign Het
Pdxp T C 15: 78,914,139 V57A probably damaging Het
Plec T A 15: 76,177,394 E2781V probably damaging Het
Prr7 GCGCCGCCGCACGCGCACCCGCACCCACACCATCACGCACTGCCGCACCCACCGCCGCCGCAC GCGCCGCCGCAC 13: 55,472,334 probably benign Het
Rnf32 G A 5: 29,197,950 probably benign Het
Ryr2 A G 13: 11,761,327 V1108A possibly damaging Het
Slc4a8 A G 15: 100,788,223 H276R probably benign Het
Spta1 T A 1: 174,205,378 D1000E probably damaging Het
Sva C A 6: 42,042,664 Q153K unknown Het
Tmprss11d T C 5: 86,309,506 Y236C possibly damaging Het
Zfp160 T C 17: 21,027,008 S607P probably damaging Het
Zfp82 C A 7: 30,056,722 G312W probably damaging Het
Other mutations in Gm5145
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02350:Gm5145 APN 17 20570440 missense probably damaging 1.00
IGL02357:Gm5145 APN 17 20570440 missense probably damaging 1.00
IGL02587:Gm5145 APN 17 20571190 missense probably damaging 1.00
R3159:Gm5145 UTSW 17 20570893 missense probably benign 0.00
R3885:Gm5145 UTSW 17 20571010 missense probably benign 0.30
R4151:Gm5145 UTSW 17 20571098 missense probably damaging 1.00
R4583:Gm5145 UTSW 17 20570453 missense probably benign 0.02
R4798:Gm5145 UTSW 17 20570548 missense probably damaging 1.00
R7147:Gm5145 UTSW 17 20571061 missense probably damaging 1.00
R7297:Gm5145 UTSW 17 20570731 missense probably benign 0.00
R7670:Gm5145 UTSW 17 20570384 missense probably benign 0.09
R7897:Gm5145 UTSW 17 20570705 missense probably benign
R7901:Gm5145 UTSW 17 20570638 missense possibly damaging 0.86
R8336:Gm5145 UTSW 17 20570425 missense probably damaging 1.00
Z1177:Gm5145 UTSW 17 20571052 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GCTTTGTTGCTAATCTGTGACATC -3'
(R):5'- GCTTGTAGAAAGGGAAGCCC -3'

Sequencing Primer
(F):5'- GCTAATCTGTGACATCCTCCC -3'
(R):5'- ATGGGCTTCATGACCTCCTTG -3'
Posted On2019-10-24