Incidental Mutation 'IGL02898:Gm9956'
ID363479
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm9956
Ensembl Gene ENSMUSG00000054758
Gene Namepredicted gene 9956
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL02898
Quality Score
Status
Chromosome10
Chromosomal Location56745134-56748254 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 56745254 bp
ZygosityHeterozygous
Amino Acid Change Serine to Leucine at position 4 (S4L)
Ref Sequence ENSEMBL: ENSMUSP00000071080 (fasta)
Gene Model predicted gene model for transcript(s):
Predicted Effect unknown
Transcript: ENSMUST00000067972
AA Change: S4L
SMART Domains Protein: ENSMUSP00000071080
Gene: ENSMUSG00000054758
AA Change: S4L

DomainStartEndE-ValueType
transmembrane domain 94 116 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamtsl5 A G 10: 80,342,231 probably benign Het
Brd3 A G 2: 27,459,741 S267P possibly damaging Het
Btaf1 A G 19: 36,969,068 T425A probably benign Het
Caskin1 A T 17: 24,502,409 E544D probably benign Het
Col20a1 C T 2: 180,989,112 Q58* probably null Het
Eif2ak1 G A 5: 143,889,452 V428I probably damaging Het
Fez2 A G 17: 78,384,755 I345T probably benign Het
Focad A T 4: 88,391,997 M1388L probably benign Het
Gfer T C 17: 24,695,947 R41G probably benign Het
Gm6614 T A 6: 141,994,297 Y160F probably benign Het
Krtap6-1 G A 16: 89,031,755 G13D unknown Het
Megf8 A G 7: 25,346,508 E1492G possibly damaging Het
Myh7 T C 14: 54,983,740 I909V probably damaging Het
Olfr380 T A 11: 73,453,735 H159L probably damaging Het
Olfr741 T A 14: 50,486,186 S243T probably damaging Het
Otog A G 7: 46,310,138 E2902G probably damaging Het
Pik3r4 A G 9: 105,650,406 I319M probably benign Het
Piwil4 A T 9: 14,706,287 probably benign Het
Plekho1 T A 3: 95,992,181 H100L probably damaging Het
Prr30 T G 14: 101,198,481 D215A probably benign Het
Prss52 C T 14: 64,113,666 A300V possibly damaging Het
Ralgps2 C A 1: 156,817,744 K514N probably benign Het
Robo4 T C 9: 37,408,176 I463T probably damaging Het
Sars A T 3: 108,429,263 F268Y probably damaging Het
Sidt1 C T 16: 44,282,495 R289Q possibly damaging Het
Slco2a1 T C 9: 103,079,606 V539A probably damaging Het
Snrnp200 A G 2: 127,216,756 probably benign Het
Spag17 A G 3: 100,101,386 D1944G probably benign Het
Spata1 C T 3: 146,475,339 R288Q possibly damaging Het
Tatdn3 T C 1: 191,046,310 *233W probably null Het
Ttc3 T A 16: 94,419,426 V555E probably damaging Het
V1rd19 A C 7: 24,003,429 T107P probably damaging Het
Other mutations in Gm9956
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01702:Gm9956 APN 10 56745239 start gained 0.00
IGL02411:Gm9956 APN 10 56745292 missense unknown
R0513:Gm9956 UTSW 10 56745195 start gained unknown
R0731:Gm9956 UTSW 10 56745543 nonsense probably null
R0841:Gm9956 UTSW 10 56745328 missense unknown
R0841:Gm9956 UTSW 10 56745329 missense unknown
R1289:Gm9956 UTSW 10 56745580 missense probably damaging 0.99
Posted OnDec 18, 2015