Incidental Mutation 'IGL00336:Gpr137b'
ID 4346
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gpr137b
Ensembl Gene ENSMUSG00000021306
Gene Name G protein-coupled receptor 137B
Synonyms Tm7sf1, C80741, 2310041G17Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL00336
Quality Score
Status
Chromosome 13
Chromosomal Location 13532205-13568599 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 13549000 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000152434 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000021738] [ENSMUST00000220628] [ENSMUST00000222958] [ENSMUST00000223093]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000021738
SMART Domains Protein: ENSMUSP00000021738
Gene: ENSMUSG00000021306

DomainStartEndE-ValueType
Blast:G_alpha 19 64 9e-7 BLAST
Blast:G_alpha 80 264 2e-22 BLAST
transmembrane domain 276 298 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000220628
Predicted Effect noncoding transcript
Transcript: ENSMUST00000221340
Predicted Effect noncoding transcript
Transcript: ENSMUST00000221498
Predicted Effect probably benign
Transcript: ENSMUST00000222958
Predicted Effect probably benign
Transcript: ENSMUST00000223093
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A430033K04Rik A G 5: 138,645,366 (GRCm39) Y417C probably damaging Het
Adam28 T A 14: 68,859,569 (GRCm39) H548L possibly damaging Het
Agbl3 A T 6: 34,823,771 (GRCm39) D812V probably damaging Het
Aopep A T 13: 63,163,237 (GRCm39) D86V possibly damaging Het
Aox1 T A 1: 58,098,203 (GRCm39) L305Q probably damaging Het
Arhgef38 A G 3: 132,837,812 (GRCm39) V706A probably benign Het
Arl15 A G 13: 114,291,288 (GRCm39) I171V probably benign Het
Cacna1s C A 1: 136,012,011 (GRCm39) Y237* probably null Het
Ccnt1 T C 15: 98,462,990 (GRCm39) T61A possibly damaging Het
Col25a1 T A 3: 129,975,433 (GRCm39) probably benign Het
Col4a1 T A 8: 11,290,077 (GRCm39) probably benign Het
Dcun1d1 T C 3: 35,970,455 (GRCm39) E130G possibly damaging Het
Dnah7b G A 1: 46,181,309 (GRCm39) M1065I probably benign Het
Ephb2 T G 4: 136,384,795 (GRCm39) K872T probably damaging Het
Fga G A 3: 82,938,981 (GRCm39) G452D probably damaging Het
Flrt1 T A 19: 7,074,277 (GRCm39) N90I probably damaging Het
Fut10 T A 8: 31,685,319 (GRCm39) probably null Het
Gm4553 T C 7: 141,718,964 (GRCm39) S155G unknown Het
Gprc5d G A 6: 135,093,488 (GRCm39) Q140* probably null Het
Ifi27l2b T C 12: 103,417,476 (GRCm39) K237R unknown Het
Ipo8 A T 6: 148,684,284 (GRCm39) M836K possibly damaging Het
Kcnq4 G A 4: 120,555,213 (GRCm39) Q657* probably null Het
Lama1 A T 17: 68,120,943 (GRCm39) H2693L probably benign Het
Lrrc23 A G 6: 124,755,889 (GRCm39) W40R probably damaging Het
Minar1 T C 9: 89,485,196 (GRCm39) D67G probably damaging Het
Morn2 C A 17: 80,602,933 (GRCm39) probably benign Het
Ms4a6b T A 19: 11,506,854 (GRCm39) N214K possibly damaging Het
Nags A T 11: 102,039,892 (GRCm39) S527C probably damaging Het
Ndst1 C T 18: 60,841,028 (GRCm39) G218D probably damaging Het
Or10j5 G A 1: 172,785,045 (GRCm39) V228M probably benign Het
Or5b94 T A 19: 12,651,924 (GRCm39) Y118* probably null Het
Or8h7 C T 2: 86,720,589 (GRCm39) C310Y probably benign Het
Oxa1l G T 14: 54,600,802 (GRCm39) G92* probably null Het
Parp16 A T 9: 65,137,245 (GRCm39) E157V probably damaging Het
Pcdh17 A T 14: 84,684,984 (GRCm39) I484F probably damaging Het
Pex16 A G 2: 92,209,580 (GRCm39) R263G probably benign Het
Pkd1l3 G A 8: 110,356,869 (GRCm39) E765K possibly damaging Het
Plce1 T C 19: 38,640,350 (GRCm39) V532A probably damaging Het
Polq A G 16: 36,885,609 (GRCm39) probably benign Het
Pramel5 T C 4: 143,998,191 (GRCm39) T351A probably damaging Het
Prokr1 A T 6: 87,565,593 (GRCm39) I84N probably damaging Het
Prss30 A T 17: 24,192,695 (GRCm39) S162T probably benign Het
Ranbp2 A G 10: 58,287,806 (GRCm39) K25E probably damaging Het
Rapsn A G 2: 90,866,205 (GRCm39) T22A probably damaging Het
Rhoj G T 12: 75,355,680 (GRCm39) G9V probably damaging Het
Rnf213 A G 11: 119,340,169 (GRCm39) R3467G probably benign Het
Rreb1 C A 13: 38,113,622 (GRCm39) S327* probably null Het
Scn5a G A 9: 119,315,290 (GRCm39) P1806L probably damaging Het
Sema6a C A 18: 47,423,042 (GRCm39) probably null Het
Stag3 G A 5: 138,295,921 (GRCm39) E416K probably benign Het
Stpg1 T A 4: 135,256,856 (GRCm39) S216T possibly damaging Het
Tfeb C A 17: 48,102,589 (GRCm39) N426K probably benign Het
Trp53bp1 G T 2: 121,087,060 (GRCm39) Q199K possibly damaging Het
Ubr4 A G 4: 139,155,877 (GRCm39) D2234G probably damaging Het
Ush1c T G 7: 45,846,194 (GRCm39) Q866P probably benign Het
Vdr T A 15: 97,782,735 (GRCm39) D29V probably damaging Het
Vps13c T C 9: 67,853,224 (GRCm39) V2439A probably benign Het
Xirp2 T C 2: 67,342,942 (GRCm39) S1728P possibly damaging Het
Zfp9 A G 6: 118,441,436 (GRCm39) S409P probably damaging Het
Other mutations in Gpr137b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00969:Gpr137b APN 13 13,539,650 (GRCm39) nonsense probably null
R0276:Gpr137b UTSW 13 13,542,160 (GRCm39) splice site probably benign
R1102:Gpr137b UTSW 13 13,539,616 (GRCm39) splice site probably benign
R4012:Gpr137b UTSW 13 13,533,947 (GRCm39) missense probably benign
R4712:Gpr137b UTSW 13 13,533,974 (GRCm39) missense probably benign 0.07
R5892:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
R6269:Gpr137b UTSW 13 13,538,096 (GRCm39) missense probably damaging 1.00
R6841:Gpr137b UTSW 13 13,538,094 (GRCm39) missense probably damaging 1.00
R7165:Gpr137b UTSW 13 13,542,205 (GRCm39) missense probably damaging 1.00
R7772:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
R7996:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
R7997:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
R7998:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
R7999:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
R8049:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
R8093:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
R8108:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
R8109:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
R8111:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
R8153:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
R8154:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
R8156:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
R8358:Gpr137b UTSW 13 13,533,929 (GRCm39) missense probably benign
R8686:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
R8687:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
R8688:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
R8921:Gpr137b UTSW 13 13,533,991 (GRCm39) missense
Posted On 2012-04-20