Incidental Mutation 'R0038:Ggt7'
ID 32797
Institutional Source Beutler Lab
Gene Symbol Ggt7
Ensembl Gene ENSMUSG00000027603
Gene Name gamma-glutamyltransferase 7
Synonyms 6330563L03Rik, 1110017C11Rik, Ggtl3
MMRRC Submission 038332-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.341) question?
Stock # R0038 (G1)
Quality Score 225
Status Validated (trace)
Chromosome 2
Chromosomal Location 155332299-155356921 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 155344701 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 214 (D214G)
Ref Sequence ENSEMBL: ENSMUSP00000135314 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000029131] [ENSMUST00000147601] [ENSMUST00000176117]
AlphaFold Q99JP7
Predicted Effect probably benign
Transcript: ENSMUST00000029131
AA Change: D290G

PolyPhen 2 Score 0.031 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000029131
Gene: ENSMUSG00000027603
AA Change: D290G

DomainStartEndE-ValueType
low complexity region 28 42 N/A INTRINSIC
low complexity region 72 83 N/A INTRINSIC
transmembrane domain 109 131 N/A INTRINSIC
Pfam:G_glu_transpept 154 655 1.4e-143 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000138033
Predicted Effect probably benign
Transcript: ENSMUST00000147601
SMART Domains Protein: ENSMUSP00000120560
Gene: ENSMUSG00000027603

DomainStartEndE-ValueType
low complexity region 28 42 N/A INTRINSIC
low complexity region 72 83 N/A INTRINSIC
transmembrane domain 109 131 N/A INTRINSIC
Pfam:G_glu_transpept 154 202 6.6e-18 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000148296
Predicted Effect probably benign
Transcript: ENSMUST00000176117
AA Change: D214G

PolyPhen 2 Score 0.082 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000135314
Gene: ENSMUSG00000027603
AA Change: D214G

DomainStartEndE-ValueType
transmembrane domain 33 55 N/A INTRINSIC
Pfam:G_glu_transpept 78 271 1.4e-63 PFAM
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.8%
  • 20x: 94.2%
Validation Efficiency 100% (72/72)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of a gene family that encodes enzymes involved in both the metabolism of glutathione and in the transpeptidation of amino acids. Changes in the activity of gamma-glutamyltransferase may signal preneoplastic or toxic conditions in the liver or kidney. The protein encoded by this gene consists of a heavy and a light chain, and it can interact with CT120, a plasma membrane-associated protein that is possibly involved in lung carcinogenesis. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agfg1 T C 1: 82,863,823 (GRCm39) probably benign Het
Ankrd28 A T 14: 31,429,992 (GRCm39) M892K probably damaging Het
Arhgef25 T C 10: 127,022,734 (GRCm39) probably benign Het
Arl9 G A 5: 77,154,322 (GRCm39) E17K probably benign Het
Bbs9 G A 9: 22,415,390 (GRCm39) V105I probably benign Het
Celsr1 A T 15: 85,813,620 (GRCm39) N1997K possibly damaging Het
Cic T A 7: 24,986,565 (GRCm39) S1299T probably damaging Het
Cic C A 7: 24,986,566 (GRCm39) S1299Y probably damaging Het
Cldn8 A G 16: 88,359,922 (GRCm39) M1T probably null Het
Clec11a A G 7: 43,955,906 (GRCm39) probably benign Het
Clstn1 G A 4: 149,719,253 (GRCm39) V361M probably damaging Het
Col19a1 A T 1: 24,598,825 (GRCm39) L56Q unknown Het
Col1a2 G A 6: 4,518,822 (GRCm39) probably benign Het
Cyp2b10 G A 7: 25,614,287 (GRCm39) A254T probably benign Het
Ddx39a T C 8: 84,449,127 (GRCm39) L305P probably damaging Het
Depdc5 A G 5: 33,026,197 (GRCm39) E60G probably benign Het
Eif2ak2 T A 17: 79,171,384 (GRCm39) M340L probably benign Het
Etl4 A T 2: 20,748,385 (GRCm39) H39L probably damaging Het
Fat3 T C 9: 15,826,306 (GRCm39) T4549A probably damaging Het
Fbxw28 A T 9: 109,167,608 (GRCm39) W50R probably damaging Het
Gramd1b G A 9: 40,228,822 (GRCm39) T252M probably damaging Het
Grin1 T C 2: 25,187,471 (GRCm39) N613S probably null Het
Hcrtr2 A T 9: 76,166,963 (GRCm39) S125T probably benign Het
Hr T C 14: 70,805,525 (GRCm39) L1091P probably damaging Het
Htr2a T G 14: 74,943,687 (GRCm39) S422R probably benign Het
Ighmbp2 A G 19: 3,312,097 (GRCm39) S886P probably damaging Het
Iqcg C A 16: 32,866,012 (GRCm39) L110F probably benign Het
Kirrel3 T A 9: 34,823,066 (GRCm39) probably null Het
Kremen1 A C 11: 5,157,703 (GRCm39) probably benign Het
Lama2 T C 10: 26,862,793 (GRCm39) D2990G probably benign Het
Lin52 C G 12: 84,576,499 (GRCm39) L111V probably damaging Het
Myh15 T C 16: 48,891,504 (GRCm39) probably benign Het
Ncor1 A G 11: 62,283,377 (GRCm39) F437L probably damaging Het
Nlrp1b A G 11: 71,062,997 (GRCm39) S685P possibly damaging Het
Oog4 T C 4: 143,165,514 (GRCm39) D211G probably benign Het
Oscar A G 7: 3,619,072 (GRCm39) V2A probably benign Het
Pdzd8 A G 19: 59,288,028 (GRCm39) I1124T possibly damaging Het
Pgm3 A T 9: 86,446,726 (GRCm39) probably benign Het
Pnpla5 A G 15: 84,006,714 (GRCm39) Y90H probably damaging Het
Polr1b C T 2: 128,957,588 (GRCm39) R548* probably null Het
Ptprg T A 14: 12,213,710 (GRCm38) M1026K probably damaging Het
Rab5b C T 10: 128,518,772 (GRCm39) R120Q probably benign Het
Rapgef2 T C 3: 78,976,703 (GRCm39) I1368V probably benign Het
Rnf168 T C 16: 32,117,813 (GRCm39) V458A probably benign Het
Rnf32 T C 5: 29,410,652 (GRCm39) probably benign Het
Sclt1 T C 3: 41,583,943 (GRCm39) probably benign Het
Serpina12 A G 12: 104,004,216 (GRCm39) F139L probably damaging Het
Sos2 T G 12: 69,643,467 (GRCm39) Q971P probably damaging Het
Stag3 T A 5: 138,299,298 (GRCm39) probably null Het
Stard5 T C 7: 83,285,951 (GRCm39) probably benign Het
Stard9 T A 2: 120,526,313 (GRCm39) C857S probably benign Het
Suclg1 A G 6: 73,237,486 (GRCm39) E77G probably benign Het
Trpm7 A G 2: 126,637,388 (GRCm39) S204P probably damaging Het
Ush2a G T 1: 188,358,809 (GRCm39) G2112C probably benign Het
Vmn2r15 T A 5: 109,441,010 (GRCm39) T283S possibly damaging Het
Wdr6 A T 9: 108,450,168 (GRCm39) V1120D probably damaging Het
Zfp644 T G 5: 106,782,909 (GRCm39) E1155A probably benign Het
Other mutations in Ggt7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01285:Ggt7 APN 2 155,342,691 (GRCm39) missense probably damaging 0.99
IGL02523:Ggt7 APN 2 155,356,623 (GRCm39) missense probably damaging 1.00
IGL02999:Ggt7 APN 2 155,344,633 (GRCm39) missense probably benign 0.00
R0030:Ggt7 UTSW 2 155,348,408 (GRCm39) missense probably benign 0.00
R0106:Ggt7 UTSW 2 155,336,813 (GRCm39) missense possibly damaging 0.63
R0106:Ggt7 UTSW 2 155,336,813 (GRCm39) missense possibly damaging 0.63
R0683:Ggt7 UTSW 2 155,348,428 (GRCm39) missense probably benign 0.08
R1035:Ggt7 UTSW 2 155,348,347 (GRCm39) missense probably damaging 1.00
R1500:Ggt7 UTSW 2 155,340,966 (GRCm39) missense probably benign 0.00
R1633:Ggt7 UTSW 2 155,344,608 (GRCm39) missense probably damaging 1.00
R1693:Ggt7 UTSW 2 155,348,395 (GRCm39) missense probably damaging 0.99
R1696:Ggt7 UTSW 2 155,336,899 (GRCm39) missense possibly damaging 0.89
R1879:Ggt7 UTSW 2 155,356,707 (GRCm39) missense possibly damaging 0.91
R2219:Ggt7 UTSW 2 155,337,639 (GRCm39) missense probably damaging 1.00
R2220:Ggt7 UTSW 2 155,337,639 (GRCm39) missense probably damaging 1.00
R4010:Ggt7 UTSW 2 155,342,652 (GRCm39) missense probably benign 0.00
R5602:Ggt7 UTSW 2 155,332,919 (GRCm39) missense possibly damaging 0.82
R5680:Ggt7 UTSW 2 155,348,353 (GRCm39) missense probably damaging 1.00
R6092:Ggt7 UTSW 2 155,359,959 (GRCm39) critical splice donor site probably null
R6440:Ggt7 UTSW 2 155,340,731 (GRCm39) missense probably damaging 1.00
R6989:Ggt7 UTSW 2 155,345,380 (GRCm39) missense probably benign 0.25
R7050:Ggt7 UTSW 2 155,348,295 (GRCm39) missense probably benign 0.10
R7058:Ggt7 UTSW 2 155,345,015 (GRCm39) splice site probably null
R7395:Ggt7 UTSW 2 155,337,800 (GRCm39) missense probably benign 0.26
R7768:Ggt7 UTSW 2 155,348,421 (GRCm39) missense possibly damaging 0.60
R7946:Ggt7 UTSW 2 155,347,892 (GRCm39) missense probably damaging 0.98
X0065:Ggt7 UTSW 2 155,337,615 (GRCm39) missense probably benign 0.37
Z1176:Ggt7 UTSW 2 155,340,983 (GRCm39) missense probably damaging 1.00
Z1176:Ggt7 UTSW 2 155,332,998 (GRCm39) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- ACTGGTCTGATGTCTAGCACCAGAG -3'
(R):5'- TGTGGCCCAAGATGGCTTCAAC -3'

Sequencing Primer
(F):5'- attttgtttACAAAGTACACAACCAG -3'
(R):5'- AGATGGCTTCAACGTGACC -3'
Posted On 2013-05-09