Incidental Mutation 'IGL01791:Gm10521'
ID 155230
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm10521
Ensembl Gene ENSMUSG00000073492
Gene Name predicted gene 10521
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.101) question?
Stock # IGL01791
Quality Score
Status
Chromosome 1
Chromosomal Location 171723231-171725804 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 171723964 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 92 (S92P)
Ref Sequence ENSEMBL: ENSMUSP00000095074 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000097466]
AlphaFold E9PZK0
Predicted Effect unknown
Transcript: ENSMUST00000097466
AA Change: S92P
SMART Domains Protein: ENSMUSP00000095074
Gene: ENSMUSG00000073492
AA Change: S92P

DomainStartEndE-ValueType
low complexity region 28 98 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap32 A G 9: 32,158,486 (GRCm39) I174V probably damaging Het
Asb15 T A 6: 24,567,211 (GRCm39) C511S probably damaging Het
Atr C T 9: 95,803,834 (GRCm39) A1896V probably benign Het
B3gnt4 C T 5: 123,649,162 (GRCm39) R176C probably damaging Het
Brf1 T C 12: 112,926,095 (GRCm39) D557G probably benign Het
Catsperg2 T A 7: 29,404,090 (GRCm39) probably null Het
Cdip1 A G 16: 4,586,729 (GRCm39) I122T probably damaging Het
Ctrl C T 8: 106,659,199 (GRCm39) E147K probably benign Het
Dennd2c T C 3: 103,073,741 (GRCm39) V829A probably benign Het
Dync1h1 T A 12: 110,625,364 (GRCm39) L3874Q probably damaging Het
Dynlt4 T A 4: 116,985,794 (GRCm39) S206T probably damaging Het
Gm57858 T C 3: 36,089,416 (GRCm39) probably benign Het
Gzf1 G A 2: 148,525,981 (GRCm39) A151T probably benign Het
Hddc2 A G 10: 31,202,022 (GRCm39) Y123C probably damaging Het
Hyal4 T C 6: 24,763,894 (GRCm39) probably benign Het
Ighv16-1 T C 12: 114,032,589 (GRCm39) N71S probably benign Het
Ing2 A T 8: 48,122,070 (GRCm39) S159R probably benign Het
Itga1 A T 13: 115,124,197 (GRCm39) N698K probably benign Het
Lemd2 A T 17: 27,409,702 (GRCm39) I483N probably damaging Het
Lyst T C 13: 13,809,887 (GRCm39) L519P probably damaging Het
Mapk10 T C 5: 103,144,514 (GRCm39) N101S probably damaging Het
Nfatc4 A T 14: 56,069,695 (GRCm39) E164V probably null Het
Nfkb2 T G 19: 46,298,278 (GRCm39) probably benign Het
Nox3 A G 17: 3,733,218 (GRCm39) V231A possibly damaging Het
Nup160 G A 2: 90,534,197 (GRCm39) G674D probably damaging Het
Or1l4b A T 2: 37,036,548 (GRCm39) D108V probably damaging Het
Or56b1 C T 7: 104,285,682 (GRCm39) T267I possibly damaging Het
Otoa T G 7: 120,755,072 (GRCm39) V998G probably benign Het
Pcnx3 A T 19: 5,723,295 (GRCm39) M1300K probably benign Het
Pde4b A G 4: 102,448,127 (GRCm39) probably benign Het
Rfc1 T A 5: 65,420,488 (GRCm39) K1104I probably benign Het
Serpina1f G T 12: 103,659,761 (GRCm39) Q174K probably damaging Het
Serping1 T C 2: 84,603,721 (GRCm39) N107D possibly damaging Het
Speer4c2 C A 5: 15,861,884 (GRCm39) probably benign Het
Surf6 A G 2: 26,789,759 (GRCm39) S94P probably benign Het
Tigd4 T A 3: 84,502,052 (GRCm39) I323N probably damaging Het
Vmn2r28 T C 7: 5,491,161 (GRCm39) D362G probably benign Het
Wdfy3 A G 5: 102,085,278 (GRCm39) S739P probably damaging Het
Other mutations in Gm10521
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01124:Gm10521 APN 1 171,724,010 (GRCm39) missense unknown
R3752:Gm10521 UTSW 1 171,723,712 (GRCm39) missense unknown
R5477:Gm10521 UTSW 1 171,724,067 (GRCm39) missense unknown
R5907:Gm10521 UTSW 1 171,724,070 (GRCm39) missense unknown
R8036:Gm10521 UTSW 1 171,723,752 (GRCm39) missense unknown
R8422:Gm10521 UTSW 1 171,724,026 (GRCm39) missense unknown
R9275:Gm10521 UTSW 1 171,724,030 (GRCm39) missense unknown
RF035:Gm10521 UTSW 1 171,723,860 (GRCm39) frame shift probably null
Posted On 2014-02-04