Incidental Mutation 'R6758:Gm10801'
ID 531103
Institutional Source Beutler Lab
Gene Symbol Gm10801
Ensembl Gene ENSMUSG00000075015
Gene Name predicted gene 10801
Synonyms
MMRRC Submission 044874-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.366) question?
Stock # R6758 (G1)
Quality Score 142.467
Status Not validated
Chromosome 2
Chromosomal Location 98492582-98494428 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to CGTG 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: 99.7%
  • 10x: 98.4%
  • 20x: 95.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 21 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ankrd17 A T 5: 90,411,172 (GRCm39) D1374E probably damaging Het
Cd96 C A 16: 45,938,367 (GRCm39) V33L possibly damaging Het
Drd1 T C 13: 54,207,308 (GRCm39) E295G probably benign Het
Fzd8 T A 18: 9,213,238 (GRCm39) C107S possibly damaging Het
Gm11595 C A 11: 99,663,366 (GRCm39) V105L unknown Het
Gm11595 A T 11: 99,663,367 (GRCm39) C104* probably null Het
Igsf3 T C 3: 101,332,814 (GRCm39) Y31H probably damaging Het
Ikzf2 A T 1: 69,578,059 (GRCm39) H483Q probably damaging Het
Itgbl1 A G 14: 124,094,901 (GRCm39) K309E probably benign Het
Myt1l T G 12: 29,892,599 (GRCm39) Y79D possibly damaging Het
Nid2 T A 14: 19,852,551 (GRCm39) S1086R probably damaging Het
Or1o1 A G 17: 37,716,586 (GRCm39) D49G probably damaging Het
Or5h24 T C 16: 58,919,328 (GRCm39) E9G probably damaging Het
Or6c65 T C 10: 129,603,920 (GRCm39) I185T probably damaging Het
Rorc A G 3: 94,294,825 (GRCm39) N51S possibly damaging Het
Sanbr T C 11: 23,538,475 (GRCm39) probably null Het
Simc1 C T 13: 54,673,361 (GRCm39) P570S possibly damaging Het
Smn1 T A 13: 100,268,946 (GRCm39) M264K possibly damaging Het
Tiam2 A G 17: 3,568,678 (GRCm39) D1608G probably benign Het
Tll1 C A 8: 64,494,439 (GRCm39) probably null Het
Trim15 A G 17: 37,173,233 (GRCm39) L284P probably benign 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
R6684: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'- ATCTGTGTAGAAAGCTGTTGCTC -3'
(R):5'- ACTTTCTCTAGCCCCGGAAAC -3'

Sequencing Primer
(F):5'- TGGCTCAATGGCAGAGTGC -3'
(R):5'- ATGCACACTGTAAGACCTGG -3'
Posted On 2018-08-01