Incidental Mutation 'R3149:Gm7137'
ID 264357
Institutional Source Beutler Lab
Gene Symbol Gm7137
Ensembl Gene ENSMUSG00000095721
Gene Name predicted gene 7137
Synonyms
MMRRC Submission 040601-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.118) question?
Stock # R3149 (G1)
Quality Score 177
Status Not validated
Chromosome 10
Chromosomal Location 77623324-77624034 bp(-) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to C at 77623839 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000090020 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092366] [ENSMUST00000180161]
AlphaFold J3QMW1
Predicted Effect probably benign
Transcript: ENSMUST00000092366
SMART Domains Protein: ENSMUSP00000090020
Gene: ENSMUSG00000069581

DomainStartEndE-ValueType
Blast:TSPN 1 71 8e-40 BLAST
SCOP:d1c4ra_ 2 67 2e-7 SMART
low complexity region 190 200 N/A INTRINSIC
Pfam:EPTP 208 255 2.6e-22 PFAM
Pfam:EPTP 260 307 1.4e-21 PFAM
Pfam:EPTP 312 359 8.9e-14 PFAM
Pfam:EPTP 362 417 6.2e-13 PFAM
Pfam:EPTP 422 469 1.3e-20 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000180161
AA Change: T66A
SMART Domains Protein: ENSMUSP00000136480
Gene: ENSMUSG00000095721
AA Change: T66A

DomainStartEndE-ValueType
low complexity region 23 64 N/A INTRINSIC
Pfam:Keratin_B2_2 114 162 5.3e-8 PFAM
Pfam:Keratin_B2_2 189 236 2.4e-3 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.5%
  • 20x: 95.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsbg3 G A 17: 57,183,348 (GRCm39) A30T probably benign Het
Atox1 A G 11: 55,341,379 (GRCm39) L52P possibly damaging Het
Cel T C 2: 28,446,143 (GRCm39) D576G probably benign Het
Csf2ra C A 19: 61,215,758 (GRCm39) A16S possibly damaging Het
Cyp4f18 T C 8: 72,747,044 (GRCm39) D317G possibly damaging Het
Dus1l T C 11: 120,683,930 (GRCm39) T173A possibly damaging Het
Dzip1 T C 14: 119,148,780 (GRCm39) T300A probably benign Het
Ggta1 A T 2: 35,292,635 (GRCm39) I224N probably damaging Het
Gm5150 A G 3: 16,060,479 (GRCm39) L3P probably damaging Het
Gm5592 A G 7: 40,937,804 (GRCm39) E362G probably benign Het
Gpatch2l A G 12: 86,291,089 (GRCm39) T91A possibly damaging Het
Hoxa13 G T 6: 52,237,284 (GRCm39) probably benign Het
Ift46 A G 9: 44,695,045 (GRCm39) D65G probably damaging Het
Kirrel1 C T 3: 86,996,458 (GRCm39) M380I probably null Het
Mapk11 T C 15: 89,029,653 (GRCm39) probably null Het
Mettl25 T C 10: 105,662,214 (GRCm39) D252G probably benign Het
Mrc2 G A 11: 105,239,257 (GRCm39) probably null Het
Or10ab4 C T 7: 107,654,989 (GRCm39) R267C probably benign Het
Pecam1 A G 11: 106,575,107 (GRCm39) V601A possibly damaging Het
Prkx A T X: 76,814,881 (GRCm39) F260I probably damaging Het
Rassf9 A T 10: 102,380,687 (GRCm39) D21V possibly damaging Het
Rmnd5a T A 6: 71,406,085 (GRCm39) I68L probably benign Het
Rock2 T C 12: 17,015,092 (GRCm39) S762P probably damaging Het
Septin4 T C 11: 87,458,070 (GRCm39) V148A possibly damaging Het
Srgap2 T C 1: 131,220,327 (GRCm39) T216A probably benign Het
Tasor2 G A 13: 3,624,359 (GRCm39) P1182S probably damaging Het
Vmn1r86 T A 7: 12,836,358 (GRCm39) K123* probably null Het
Vmn2r68 A C 7: 84,886,875 (GRCm39) V13G probably benign Het
Vps13d G C 4: 144,853,147 (GRCm39) N2322K possibly damaging Het
Xpo5 A G 17: 46,553,173 (GRCm39) probably null Het
Zswim9 T C 7: 13,011,196 (GRCm39) T51A possibly damaging Het
Other mutations in Gm7137
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0415:Gm7137 UTSW 10 77,624,007 (GRCm39) intron probably benign
R5058:Gm7137 UTSW 10 77,623,905 (GRCm39) intron probably benign
R6354:Gm7137 UTSW 10 77,623,481 (GRCm39) intron probably benign
R8220:Gm7137 UTSW 10 77,623,785 (GRCm39) missense unknown
R9384:Gm7137 UTSW 10 77,623,614 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- TTGACAGCATGAGGACTGG -3'
(R):5'- ATGTCTGTCTGCTCTGATGC -3'

Sequencing Primer
(F):5'- TCCAGAGCAGATGGGTGTGC -3'
(R):5'- GCTCTGATGCTCTCACCAAC -3'
Posted On 2015-02-05