Incidental Mutation 'IGL01736:Grxcr2'
ID 105699
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Grxcr2
Ensembl Gene ENSMUSG00000073574
Gene Name glutaredoxin, cysteine rich 2
Synonyms LOC332309
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01736
Quality Score
Status
Chromosome 18
Chromosomal Location 42118388-42132114 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 42132047 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Asparagine at position 7 (K7N)
Ref Sequence ENSEMBL: ENSMUSP00000095198 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000097591]
AlphaFold Q3TYR5
Predicted Effect probably damaging
Transcript: ENSMUST00000097591
AA Change: K7N

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein containing a glutaredoxin domain, which functions in protein S-glutathionylation. A mutation in this gene was found in a family with autoosomal recessive nonsyndromic sensorineural deafness-101. [provided by RefSeq, Jun 2014]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit severe hearing loss. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acacb A G 5: 114,326,503 (GRCm39) T290A possibly damaging Het
Apip G A 2: 102,917,486 (GRCm39) V62M probably damaging Het
Appbp2 T C 11: 85,105,143 (GRCm39) K141R possibly damaging Het
Arhgef18 T A 8: 3,501,624 (GRCm39) probably benign Het
B3galt2 A G 1: 143,522,583 (GRCm39) T240A probably benign Het
Bivm A T 1: 44,180,973 (GRCm39) N385I probably damaging Het
Brd4 A T 17: 32,417,649 (GRCm39) probably benign Het
Cage1 T C 13: 38,206,789 (GRCm39) D352G possibly damaging Het
Ceacam10 A G 7: 24,480,535 (GRCm39) Y102C probably damaging Het
Diaph3 T C 14: 87,156,282 (GRCm39) D677G probably benign Het
Dis3l T C 9: 64,226,536 (GRCm39) probably null Het
Dnah6 C T 6: 73,165,360 (GRCm39) V582M probably benign Het
Fndc3b A G 3: 27,521,552 (GRCm39) L541P probably damaging Het
Folh1 T C 7: 86,391,444 (GRCm39) T384A possibly damaging Het
Gdpd3 T C 7: 126,365,695 (GRCm39) L18P probably damaging Het
Gulo A G 14: 66,234,325 (GRCm39) F246L probably benign Het
Inpp4b A T 8: 82,723,968 (GRCm39) D500V probably benign Het
Ints4 C T 7: 97,175,849 (GRCm39) L647F probably benign Het
Kif17 T A 4: 138,013,876 (GRCm39) L264Q possibly damaging Het
Kif21a T C 15: 90,843,948 (GRCm39) N1104S possibly damaging Het
Ly6e T G 15: 74,830,546 (GRCm39) L132R probably benign Het
Mis18bp1 T A 12: 65,185,452 (GRCm39) H905L probably damaging Het
Nr2f2 A G 7: 70,004,446 (GRCm39) S269P probably damaging Het
Or2b2b C A 13: 21,858,787 (GRCm39) C109F probably benign Het
Or2o1 G A 11: 49,051,354 (GRCm39) C171Y probably damaging Het
Or5d46 T A 2: 88,170,771 (GRCm39) N287K probably damaging Het
Pde8b T C 13: 95,166,910 (GRCm39) I757V probably damaging Het
Psg23 A T 7: 18,346,122 (GRCm39) I191N possibly damaging Het
Slc12a4 A T 8: 106,672,475 (GRCm39) probably null Het
Snph A T 2: 151,436,093 (GRCm39) Y209* probably null Het
Tnfaip3 T C 10: 18,882,649 (GRCm39) H256R probably damaging Het
Tnip3 T A 6: 65,573,107 (GRCm39) probably benign Het
Ttc3 T A 16: 94,243,386 (GRCm39) F1130Y probably damaging Het
Twnk T G 19: 44,998,627 (GRCm39) V515G probably damaging Het
Usp24 T A 4: 106,280,658 (GRCm39) I2324K probably benign Het
Vwa7 T C 17: 35,238,827 (GRCm39) F305S probably damaging Het
Ythdc2 A T 18: 44,983,735 (GRCm39) Q567L probably damaging Het
Zbtb11 T A 16: 55,818,523 (GRCm39) I649K probably damaging Het
Zbtb49 T C 5: 38,358,204 (GRCm39) Y683C probably damaging Het
Zfhx4 A T 3: 5,309,152 (GRCm39) M793L possibly damaging Het
Zmym6 T G 4: 127,002,437 (GRCm39) I556R probably damaging Het
Zswim8 C T 14: 20,764,780 (GRCm39) P717S probably benign Het
Other mutations in Grxcr2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02823:Grxcr2 APN 18 42,125,046 (GRCm39) missense probably damaging 1.00
R3625:Grxcr2 UTSW 18 42,131,883 (GRCm39) missense probably damaging 0.97
R4452:Grxcr2 UTSW 18 42,119,609 (GRCm39) missense probably damaging 1.00
R5317:Grxcr2 UTSW 18 42,131,916 (GRCm39) missense probably damaging 0.99
R6054:Grxcr2 UTSW 18 42,119,743 (GRCm39) missense probably benign 0.01
R6483:Grxcr2 UTSW 18 42,124,955 (GRCm39) missense probably benign
R6493:Grxcr2 UTSW 18 42,131,766 (GRCm39) missense possibly damaging 0.52
R8702:Grxcr2 UTSW 18 42,131,754 (GRCm39) missense possibly damaging 0.92
R9666:Grxcr2 UTSW 18 42,131,956 (GRCm39) missense probably damaging 1.00
R9703:Grxcr2 UTSW 18 42,124,988 (GRCm39) missense possibly damaging 0.94
Posted On 2014-01-21