Incidental Mutation 'IGL00157:Gm10735'
ID 306554
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm10735
Ensembl Gene ENSMUSG00000074650
Gene Name predicted gene 10735
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.061) question?
Stock # IGL00157
Quality Score
Status
Chromosome 13
Chromosomal Location 113175835-113178777 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 113178018 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000156385 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022282] [ENSMUST00000099162] [ENSMUST00000109244] [ENSMUST00000180543] [ENSMUST00000181117] [ENSMUST00000181568] [ENSMUST00000231962]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000022282
SMART Domains Protein: ENSMUSP00000022282
Gene: ENSMUSG00000021760

DomainStartEndE-ValueType
Pfam:AhpC-TSA 44 143 1.3e-8 PFAM
Pfam:GSHPx 47 155 5.3e-36 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000083641
Predicted Effect noncoding transcript
Transcript: ENSMUST00000099162
SMART Domains Protein: ENSMUSP00000096766
Gene: ENSMUSG00000074650

DomainStartEndE-ValueType
low complexity region 3 12 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000104833
Predicted Effect probably benign
Transcript: ENSMUST00000109244
SMART Domains Protein: ENSMUSP00000104867
Gene: ENSMUSG00000078926

DomainStartEndE-ValueType
low complexity region 85 97 N/A INTRINSIC
WD40 218 257 6.6e1 SMART
WD40 266 301 5.75e-1 SMART
WD40 304 341 9.24e-1 SMART
WD40 345 383 9.02e-7 SMART
WD40 391 432 3.55e1 SMART
WD40 473 517 2.01e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000180543
Predicted Effect probably benign
Transcript: ENSMUST00000181117
SMART Domains Protein: ENSMUSP00000137915
Gene: ENSMUSG00000078926

DomainStartEndE-ValueType
low complexity region 85 97 N/A INTRINSIC
WD40 218 257 6.6e1 SMART
WD40 266 301 5.75e-1 SMART
WD40 304 341 9.24e-1 SMART
WD40 345 383 9.02e-7 SMART
WD40 391 432 3.55e1 SMART
WD40 473 513 1.78e-5 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000181568
SMART Domains Protein: ENSMUSP00000137849
Gene: ENSMUSG00000078926

DomainStartEndE-ValueType
low complexity region 85 97 N/A INTRINSIC
WD40 218 257 6.6e1 SMART
WD40 266 301 5.75e-1 SMART
WD40 304 341 9.24e-1 SMART
WD40 345 383 9.02e-7 SMART
WD40 431 475 2.01e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000231962
Predicted Effect probably benign
Transcript: ENSMUST00000181741
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acp4 A G 7: 43,902,875 (GRCm39) V331A possibly damaging Het
Casr C A 16: 36,316,172 (GRCm39) V633F probably damaging Het
Cblb T G 16: 52,003,670 (GRCm39) V716G probably benign Het
Cbln2 C T 18: 86,734,509 (GRCm39) Q156* probably null Het
Cnn1 G T 9: 22,010,693 (GRCm39) L14F possibly damaging Het
D830013O20Rik T C 12: 73,411,021 (GRCm39) noncoding transcript Het
Drd1 A G 13: 54,207,897 (GRCm39) S99P probably damaging Het
Fat1 T C 8: 45,404,707 (GRCm39) V486A possibly damaging Het
Galnt7 T C 8: 57,993,073 (GRCm39) N416S probably damaging Het
H2-T5 A T 17: 36,476,246 (GRCm39) probably null Het
Jag2 T C 12: 112,876,338 (GRCm39) T790A probably benign Het
Klhdc1 T A 12: 69,288,782 (GRCm39) Y31N possibly damaging Het
Lama1 A T 17: 68,122,923 (GRCm39) M2769L probably benign Het
Mms19 A G 19: 41,933,896 (GRCm39) probably null Het
Msrb2 C A 2: 19,399,152 (GRCm39) P172T probably damaging Het
Or8g35 A G 9: 39,381,539 (GRCm39) V161A probably benign Het
Or8k41 T C 2: 86,313,562 (GRCm39) S175G probably benign Het
Pcdhb9 T A 18: 37,536,332 (GRCm39) D775E possibly damaging Het
Pkhd1 T C 1: 20,637,098 (GRCm39) probably null Het
Preb A T 5: 31,113,308 (GRCm39) D375E probably damaging Het
Prkdc T C 16: 15,515,090 (GRCm39) I1010T probably damaging Het
Rbp2 A G 9: 98,380,950 (GRCm39) probably null Het
Septin9 A G 11: 117,243,010 (GRCm39) T66A probably damaging Het
Serpinb9b A T 13: 33,219,608 (GRCm39) E178D probably benign Het
Shld2 A G 14: 33,990,582 (GRCm39) V108A probably benign Het
Tg A G 15: 66,719,015 (GRCm39) Y258C probably damaging Het
Tmprss7 T C 16: 45,483,731 (GRCm39) R548G probably benign Het
Uba7 G A 9: 107,856,310 (GRCm39) A536T probably benign Het
Vmn2r114 G A 17: 23,510,639 (GRCm39) P614S probably damaging Het
Xpc A G 6: 91,469,246 (GRCm39) probably benign Het
Yrdc T C 4: 124,747,754 (GRCm39) S86P probably damaging Het
Zbed6 G T 1: 133,585,114 (GRCm39) A741D probably damaging Het
Other mutations in Gm10735
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4229:Gm10735 UTSW 13 113,177,743 (GRCm39) unclassified probably benign
R4230:Gm10735 UTSW 13 113,177,743 (GRCm39) unclassified probably benign
R6220:Gm10735 UTSW 13 113,178,030 (GRCm39) unclassified probably benign
Posted On 2015-04-16