Incidental Mutation 'R6684:Gm10801'
ID 527602
Institutional Source Beutler Lab
Gene Symbol Gm10801
Ensembl Gene ENSMUSG00000075015
Gene Name predicted gene 10801
Synonyms
MMRRC Submission 044803-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.366) question?
Stock # R6684 (G1)
Quality Score 157.468
Status Not validated
Chromosome 2
Chromosomal Location 98492582-98494428 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to CGTA at 98494152 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000097276 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099683] [ENSMUST00000099684]
AlphaFold F7C7Q0
Predicted Effect probably benign
Transcript: ENSMUST00000099683
SMART Domains Protein: ENSMUSP00000097275
Gene: ENSMUSG00000075014

DomainStartEndE-ValueType
internal_repeat_1 1 41 1.13e-5 PROSPERO
internal_repeat_2 26 49 4.11e-5 PROSPERO
transmembrane domain 78 96 N/A INTRINSIC
internal_repeat_1 114 174 1.13e-5 PROSPERO
low complexity region 177 188 N/A INTRINSIC
internal_repeat_2 197 219 4.11e-5 PROSPERO
Predicted Effect probably null
Transcript: ENSMUST00000099684
SMART Domains Protein: ENSMUSP00000097276
Gene: ENSMUSG00000075015

DomainStartEndE-ValueType
internal_repeat_1 2 73 1.19e-13 PROSPERO
internal_repeat_1 80 167 1.19e-13 PROSPERO
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.0%
  • 20x: 94.1%
Validation Efficiency 94% (33/35)
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcf2 G A 5: 24,774,137 (GRCm39) R322W probably damaging Het
Capns1 C A 7: 29,893,324 (GRCm39) G63V probably damaging Het
Carmil1 G A 13: 24,206,525 (GRCm39) T5M unknown Het
Cr2 T A 1: 194,853,329 (GRCm39) K70* probably null Het
Dapk1 T A 13: 60,908,708 (GRCm39) I1107N probably damaging Het
Ehd4 A G 2: 119,984,815 (GRCm39) F48L probably damaging Het
Fam221a G T 6: 49,349,542 (GRCm39) E36* probably null Het
Fam81b G A 13: 76,350,157 (GRCm39) Q423* probably null Het
Galnt7 C T 8: 57,991,143 (GRCm39) V456I probably benign Het
Hrc A G 7: 44,985,956 (GRCm39) H369R possibly damaging Het
Impg2 T G 16: 56,080,292 (GRCm39) S590A probably benign Het
Lcn3 A T 2: 25,656,170 (GRCm39) H75L probably benign Het
Lims1 T A 10: 58,234,835 (GRCm39) probably null Het
Lkaaear1 TCTCCAGCTCCAGCTCCAGCTCCAGCTCCAGCTCCAGCTCCAG TCTCCAGCTCCAGCTCCAGCTCCAGCTCCAGCTCCAGCTCCAGCTCCAG 2: 181,339,354 (GRCm39) probably benign Het
Or5p79 A G 7: 108,221,141 (GRCm39) T41A probably damaging Het
Orai3 A G 7: 127,372,892 (GRCm39) N131S probably damaging Het
Pcdhga7 T C 18: 37,849,103 (GRCm39) L370P probably damaging Het
Phtf2 A G 5: 21,017,937 (GRCm39) probably benign Het
Plcg2 T C 8: 118,323,071 (GRCm39) Y709H probably damaging Het
Pmfbp1 T C 8: 110,262,462 (GRCm39) S719P probably benign Het
Polr3g A T 13: 81,847,650 (GRCm39) probably null Het
Ppp4r1 G A 17: 66,131,337 (GRCm39) A360T probably benign Het
Pramel6 T C 2: 87,339,748 (GRCm39) W171R probably damaging Het
Rad54b T C 4: 11,583,689 (GRCm39) probably benign Het
Rasl10a G A 11: 5,008,396 (GRCm39) E31K possibly damaging Het
Ryr3 T C 2: 112,583,433 (GRCm39) R2813G probably damaging Het
Tmem71 A G 15: 66,413,539 (GRCm39) S178P possibly damaging Het
Trim58 A G 11: 58,542,446 (GRCm39) T469A probably benign Het
Vash1 A G 12: 86,735,683 (GRCm39) T190A probably damaging Het
Ythdc2 T C 18: 45,006,136 (GRCm39) S1210P possibly damaging Het
Zfp42 G A 8: 43,749,093 (GRCm39) T136M possibly damaging Het
Zfp595 T C 13: 67,468,341 (GRCm39) Y72C probably damaging Het
Other mutations in Gm10801
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01100:Gm10801 APN 2 98,494,328 (GRCm39) missense probably benign
IGL01154:Gm10801 APN 2 98,494,328 (GRCm39) missense probably benign
Haplo UTSW 2 98,494,252 (GRCm39) splice site probably benign
Ladder UTSW 2 98,494,246 (GRCm39) splice site probably null
PIT4131001:Gm10801 UTSW 2 98,492,648 (GRCm39) missense probably benign
PIT4142001:Gm10801 UTSW 2 98,492,648 (GRCm39) missense probably benign
R0026:Gm10801 UTSW 2 98,494,254 (GRCm39) splice site probably benign
R0063:Gm10801 UTSW 2 98,494,185 (GRCm39) missense probably benign 0.30
R0334:Gm10801 UTSW 2 98,494,352 (GRCm39) missense possibly damaging 0.66
R0335:Gm10801 UTSW 2 98,494,352 (GRCm39) missense possibly damaging 0.66
R1172:Gm10801 UTSW 2 98,494,252 (GRCm39) splice site probably benign
R1321:Gm10801 UTSW 2 98,494,252 (GRCm39) splice site probably benign
R1871:Gm10801 UTSW 2 98,494,185 (GRCm39) missense probably benign 0.30
R1924:Gm10801 UTSW 2 98,494,197 (GRCm39) missense probably damaging 1.00
R2163:Gm10801 UTSW 2 98,494,352 (GRCm39) missense possibly damaging 0.66
R2306:Gm10801 UTSW 2 98,494,352 (GRCm39) missense possibly damaging 0.66
R2379:Gm10801 UTSW 2 98,494,185 (GRCm39) missense probably benign 0.30
R3078:Gm10801 UTSW 2 98,494,197 (GRCm39) missense probably damaging 1.00
R3605:Gm10801 UTSW 2 98,494,352 (GRCm39) missense possibly damaging 0.66
R3892:Gm10801 UTSW 2 98,494,246 (GRCm39) splice site probably null
R3930:Gm10801 UTSW 2 98,494,361 (GRCm39) missense possibly damaging 0.48
R4638:Gm10801 UTSW 2 98,494,352 (GRCm39) missense possibly damaging 0.66
R4709:Gm10801 UTSW 2 98,494,246 (GRCm39) splice site probably null
R5390:Gm10801 UTSW 2 98,494,151 (GRCm39) small insertion probably benign
R5405:Gm10801 UTSW 2 98,494,151 (GRCm39) small insertion probably benign
R5535:Gm10801 UTSW 2 98,492,844 (GRCm39) frame shift probably null
R5653:Gm10801 UTSW 2 98,494,396 (GRCm39) missense probably damaging 1.00
R5747:Gm10801 UTSW 2 98,494,352 (GRCm39) missense possibly damaging 0.66
R5987:Gm10801 UTSW 2 98,494,152 (GRCm39) nonsense probably null
R6086:Gm10801 UTSW 2 98,494,148 (GRCm39) nonsense probably null
R6090:Gm10801 UTSW 2 98,494,151 (GRCm39) small insertion probably benign
R6093:Gm10801 UTSW 2 98,494,152 (GRCm39) nonsense probably null
R6112:Gm10801 UTSW 2 98,494,409 (GRCm39) missense probably benign 0.00
R6184:Gm10801 UTSW 2 98,494,151 (GRCm39) small insertion probably benign
R6352:Gm10801 UTSW 2 98,494,151 (GRCm39) small insertion probably benign
R6357:Gm10801 UTSW 2 98,494,152 (GRCm39) frame shift probably null
R6395:Gm10801 UTSW 2 98,494,152 (GRCm39) small insertion probably benign
R6514:Gm10801 UTSW 2 98,494,214 (GRCm39) missense probably benign 0.19
R6547:Gm10801 UTSW 2 98,494,148 (GRCm39) nonsense probably null
R6560:Gm10801 UTSW 2 98,494,152 (GRCm39) nonsense probably null
R6640:Gm10801 UTSW 2 98,494,152 (GRCm39) nonsense probably null
R6675:Gm10801 UTSW 2 98,494,151 (GRCm39) small insertion probably benign
R6679:Gm10801 UTSW 2 98,494,151 (GRCm39) small insertion probably benign
R6758:Gm10801 UTSW 2 98,494,152 (GRCm39) nonsense probably null
R6786:Gm10801 UTSW 2 98,494,148 (GRCm39) nonsense probably null
R6886:Gm10801 UTSW 2 98,494,151 (GRCm39) small insertion probably benign
R7783:Gm10801 UTSW 2 98,494,152 (GRCm39) nonsense probably null
R8032:Gm10801 UTSW 2 98,494,152 (GRCm39) nonsense probably null
R8684:Gm10801 UTSW 2 98,492,669 (GRCm39) frame shift probably null
R8831:Gm10801 UTSW 2 98,494,334 (GRCm39) missense probably damaging 0.96
R8843:Gm10801 UTSW 2 98,494,151 (GRCm39) small insertion probably benign
R8946:Gm10801 UTSW 2 98,492,669 (GRCm39) frame shift probably null
R9135:Gm10801 UTSW 2 98,494,152 (GRCm39) nonsense probably null
R9136:Gm10801 UTSW 2 98,494,152 (GRCm39) nonsense probably null
R9423:Gm10801 UTSW 2 98,494,148 (GRCm39) nonsense probably null
R9773:Gm10801 UTSW 2 98,494,345 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- CATCTGTGTAGAAAGCTGTTGC -3'
(R):5'- CTTTCTCTAGCCCCGGAAAC -3'

Sequencing Primer
(F):5'- TGGCTCAATGGCAGAGTGC -3'
(R):5'- ATGCACACTGTAAGACCTGG -3'
Posted On 2018-07-23