Incidental Mutation 'IGL02304:Gm9637'
ID287519
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm9637
Ensembl Gene ENSMUSG00000093814
Gene Namepredicted gene 9637
Synonyms
Accession Numbers
Is this an essential gene? Possibly essential (E-score: 0.636) question?
Stock #IGL02304
Quality Score
Status
Chromosome14
Chromosomal Location19401727-19402599 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) A to T at 19402545 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000179141
SMART Domains Protein: ENSMUSP00000137522
Gene: ENSMUSG00000093814

DomainStartEndE-ValueType
S_TKc 36 283 1.12e-85 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930546C10Rik G T 18: 68,950,051 H31N unknown Het
Adamts8 A G 9: 30,956,656 N592S possibly damaging Het
Atp1a2 C A 1: 172,289,353 E232D probably benign Het
Cacnb3 A T 15: 98,642,382 D323V probably damaging Het
Cdh9 A T 15: 16,848,601 T456S probably benign Het
Cep162 A T 9: 87,227,147 probably benign Het
Clvs2 T C 10: 33,528,447 M258V probably benign Het
Col6a5 T C 9: 105,928,414 T1098A unknown Het
Foxs1 T C 2: 152,932,350 D261G probably benign Het
Gas2l2 T C 11: 83,424,238 probably benign Het
Gins4 A T 8: 23,232,609 M98K probably benign Het
Gm12355 C T 11: 98,625,538 R3H probably benign Het
Herc1 A G 9: 66,476,414 D3720G probably benign Het
Kcnh5 C T 12: 74,976,697 M532I probably benign Het
Kcnk18 T C 19: 59,234,863 Y147H probably damaging Het
Kif21a A T 15: 90,965,535 F55Y probably damaging Het
Krt15 T A 11: 100,133,677 I278F possibly damaging Het
L3mbtl4 T A 17: 68,587,185 Y395* probably null Het
Mcm3ap T A 10: 76,484,738 N843K possibly damaging Het
Mpdz T C 4: 81,310,157 K1337E possibly damaging Het
Mpdz G A 4: 81,297,559 probably benign Het
Ms4a6d T C 19: 11,603,141 probably benign Het
Myo7a G T 7: 98,077,736 R922S possibly damaging Het
Nek1 G T 8: 61,012,167 G97C probably damaging Het
Obscn A G 11: 59,076,622 Y2963H probably damaging Het
Olfr1138 C T 2: 87,737,986 V113M probably benign Het
Olfr1294 T C 2: 111,537,401 N296S probably benign Het
Olfr731 T C 14: 50,238,760 N42D probably damaging Het
Prmt3 G A 7: 49,826,737 V365I probably benign Het
Prrc2c T C 1: 162,684,136 T958A probably benign Het
Ptprb T C 10: 116,331,259 Y947H probably damaging Het
Pus10 C T 11: 23,712,275 S315L probably damaging Het
Rmi1 C A 13: 58,409,476 S513* probably null Het
Sec14l3 C T 11: 4,074,768 P239L probably damaging Het
Slc44a3 T C 3: 121,527,074 T93A possibly damaging Het
Stat1 G A 1: 52,132,544 A125T probably benign Het
Tigd2 C T 6: 59,211,698 Q517* probably null Het
Trav13d-3 C T 14: 53,033,380 Q100* probably null Het
Trim67 G A 8: 124,825,952 D598N probably damaging Het
Trio A G 15: 27,735,436 L2856P probably damaging Het
Other mutations in Gm9637
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02449:Gm9637 APN 14 19402436 exon noncoding transcript
IGL02492:Gm9637 APN 14 19402182 exon noncoding transcript
IGL03060:Gm9637 APN 14 19402173 exon noncoding transcript
R0062:Gm9637 UTSW 14 19402570 exon noncoding transcript
R0621:Gm9637 UTSW 14 19402011 exon noncoding transcript
R1122:Gm9637 UTSW 14 19401879 exon noncoding transcript
R1762:Gm9637 UTSW 14 19402408 exon noncoding transcript
R1812:Gm9637 UTSW 14 19402395 exon noncoding transcript
R2880:Gm9637 UTSW 14 19401978 exon noncoding transcript
R3685:Gm9637 UTSW 14 19401950 exon noncoding transcript
R3810:Gm9637 UTSW 14 19402398 exon noncoding transcript
R3812:Gm9637 UTSW 14 19402398 exon noncoding transcript
R5415:Gm9637 UTSW 14 19402143 exon noncoding transcript
R8245:Gm9637 UTSW 14 19402598 missense noncoding transcript
Z1088:Gm9637 UTSW 14 19401731 exon noncoding transcript
Posted On2015-04-16