Incidental Mutation 'R9349:Gm9736'
ID 707969
Institutional Source Beutler Lab
Gene Symbol Gm9736
Ensembl Gene ENSMUSG00000112380
Gene Name predicted gene 9736
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # R9349 (G1)
Quality Score 225.009
Status Not validated
Chromosome 10
Chromosomal Location 77586355-77587188 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 77586393 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Alanine at position 266 (S266A)
Ref Sequence ENSEMBL: ENSMUSP00000151736 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092366] [ENSMUST00000219969]
AlphaFold A0A1W2P7N1
Predicted Effect probably benign
Transcript: ENSMUST00000092366
SMART Domains Protein: ENSMUSP00000090020
Gene: ENSMUSG00000069581

DomainStartEndE-ValueType
Blast:TSPN 1 71 8e-40 BLAST
SCOP:d1c4ra_ 2 67 2e-7 SMART
low complexity region 190 200 N/A INTRINSIC
Pfam:EPTP 208 255 2.6e-22 PFAM
Pfam:EPTP 260 307 1.4e-21 PFAM
Pfam:EPTP 312 359 8.9e-14 PFAM
Pfam:EPTP 362 417 6.2e-13 PFAM
Pfam:EPTP 422 469 1.3e-20 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000219969
AA Change: S266A
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A230072I06Rik A G 8: 12,329,665 (GRCm39) Q40R unknown Het
A730015C16Rik C T 4: 108,705,053 (GRCm39) V89I unknown Het
Adam19 G T 11: 46,022,570 (GRCm39) E508* probably null Het
Arhgef33 C T 17: 80,644,736 (GRCm39) Q22* probably null Het
Arih2 C G 9: 108,488,938 (GRCm39) R260P probably damaging Het
Astn2 T A 4: 66,184,492 (GRCm39) T202S unknown Het
Bpifb5 T A 2: 154,067,005 (GRCm39) L86Q possibly damaging Het
Brpf3 G A 17: 29,040,276 (GRCm39) S899N probably benign Het
Ccl20 T C 1: 83,095,586 (GRCm39) F49S Het
Ctse A G 1: 131,592,111 (GRCm39) T146A probably benign Het
Dhx35 T C 2: 158,671,444 (GRCm39) S292P possibly damaging Het
Fut7 C T 2: 25,314,993 (GRCm39) P84S possibly damaging Het
Gsdma T A 11: 98,566,771 (GRCm39) L366Q probably benign Het
Ifna15 T A 4: 88,476,283 (GRCm39) D67V probably benign Het
Igkv2-112 G A 6: 68,197,678 (GRCm39) V117I probably benign Het
Kcnh2 C T 5: 24,538,003 (GRCm39) G120E probably damaging Het
Kcnip1 T G 11: 33,601,548 (GRCm39) Y29S probably benign Het
Lrrc37a T G 11: 103,388,454 (GRCm39) M2324L unknown Het
Mettl5 T A 2: 69,702,113 (GRCm39) D185V possibly damaging Het
Mmp1b T A 9: 7,369,271 (GRCm39) M359L probably benign Het
Ndufa5 G A 6: 24,522,749 (GRCm39) T31I probably benign Het
Ngly1 T A 14: 16,281,801 (GRCm38) C352* probably null Het
Or14c45 A G 7: 86,176,373 (GRCm39) H136R probably benign Het
Or51a39 A T 7: 102,362,875 (GRCm39) C248* probably null Het
Pcdhac1 C T 18: 37,224,021 (GRCm39) A278V possibly damaging Het
Ppp2r3c T A 12: 55,345,268 (GRCm39) K73N probably benign Het
Rasgrf1 T C 9: 89,884,460 (GRCm39) V975A probably damaging Het
Rps27rt C T 9: 114,811,673 (GRCm39) V35M probably benign Het
Slc22a8 A G 19: 8,571,469 (GRCm39) N67D probably benign Het
Slc39a6 C A 18: 24,718,493 (GRCm39) M521I probably benign Het
Snx31 C T 15: 36,555,430 (GRCm39) S39N probably damaging Het
Speer1b C T 5: 11,823,221 (GRCm39) T130I possibly damaging Het
Sv2a T C 3: 96,096,795 (GRCm39) probably null Het
Thg1l G A 11: 45,846,273 (GRCm39) A7V probably benign Het
Ttc39c C T 18: 12,822,932 (GRCm39) Q147* probably null Het
Ube2u A G 4: 100,407,194 (GRCm39) N352D unknown Het
Uhrf1 T C 17: 56,617,737 (GRCm39) V153A possibly damaging Het
Wdfy4 A G 14: 32,875,996 (GRCm39) S143P Het
Other mutations in Gm9736
AlleleSourceChrCoordTypePredicted EffectPPH Score
R7101:Gm9736 UTSW 10 77,587,167 (GRCm39) missense unknown
R8422:Gm9736 UTSW 10 77,586,714 (GRCm39) missense unknown
R9142:Gm9736 UTSW 10 77,586,849 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- TTCAGGCAGCCTCAGAGAAG -3'
(R):5'- AAGCCTGTTTGCTGCACAC -3'

Sequencing Primer
(F):5'- AGCCTCAGAGAAGGGCTC -3'
(R):5'- GCACACCCATCTGCTCTGG -3'
Posted On 2022-04-18