Incidental Mutation 'IGL01932:Gm4222'
ID 180474
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm4222
Ensembl Gene ENSMUSG00000091703
Gene Name predicted gene 4222
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL01932
Quality Score
Status
Chromosome 2
Chromosomal Location 89978763-89979232 bp(+) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) A to G at 89978801 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000150561 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099754] [ENSMUST00000213946] [ENSMUST00000215578] [ENSMUST00000215975] [ENSMUST00000216354] [ENSMUST00000217139]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000099754
SMART Domains Protein: ENSMUSP00000097343
Gene: ENSMUSG00000075065

DomainStartEndE-ValueType
Pfam:7tm_4 29 303 2.3e-54 PFAM
Pfam:7TM_GPCR_Srsx 33 300 7.5e-6 PFAM
Pfam:7tm_1 39 285 2e-24 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000165784
SMART Domains Protein: ENSMUSP00000126140
Gene: ENSMUSG00000091703

DomainStartEndE-ValueType
HOX 19 81 1.29e-3 SMART
low complexity region 118 128 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000213946
Predicted Effect probably benign
Transcript: ENSMUST00000215578
Predicted Effect probably benign
Transcript: ENSMUST00000215975
Predicted Effect probably benign
Transcript: ENSMUST00000216354
Predicted Effect probably benign
Transcript: ENSMUST00000217139
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy1 T A 11: 7,050,565 (GRCm39) probably benign Het
Adipor2 G A 6: 119,338,825 (GRCm39) H143Y probably damaging Het
Ankar A G 1: 72,738,146 (GRCm39) I12T probably benign Het
Ankdd1a C T 9: 65,414,893 (GRCm39) probably benign Het
Cadps A G 14: 12,373,609 (GRCm38) probably benign Het
Cdh22 G A 2: 165,012,728 (GRCm39) T119M probably benign Het
Col6a6 T A 9: 105,566,825 (GRCm39) K2223N probably benign Het
Dnah11 G A 12: 118,156,005 (GRCm39) probably benign Het
Ezh2 T C 6: 47,508,982 (GRCm39) T674A probably damaging Het
Ffar4 A G 19: 38,085,978 (GRCm39) E135G probably damaging Het
Fsip2 G A 2: 82,824,349 (GRCm39) R6694Q possibly damaging Het
Gm10717 A T 9: 3,026,287 (GRCm39) Y195F probably damaging Het
Gm10718 A T 9: 3,025,118 (GRCm39) Y194F probably benign Het
Gm21738 G A 14: 19,416,979 (GRCm38) S144L probably benign Het
Hipk3 T A 2: 104,301,326 (GRCm39) N289Y probably damaging Het
Kndc1 T C 7: 139,503,705 (GRCm39) L1003P probably damaging Het
Mdk T C 2: 91,761,461 (GRCm39) N72S probably damaging Het
Or2at4 T A 7: 99,384,707 (GRCm39) I119N probably damaging Het
Or52n2 T A 7: 104,542,425 (GRCm39) I137F probably damaging Het
Pafah1b3 A T 7: 24,996,516 (GRCm39) C56S probably benign Het
Pdzrn4 A G 15: 92,644,159 (GRCm39) I189V probably damaging Het
Plekhh2 A G 17: 84,884,689 (GRCm39) N801S probably benign Het
Pramel7 A T 2: 87,321,457 (GRCm39) S193T possibly damaging Het
Prkag1 A G 15: 98,712,412 (GRCm39) I171T probably damaging Het
Prorp A G 12: 55,350,910 (GRCm39) N73S probably benign Het
Rap1b A T 10: 117,658,765 (GRCm39) F23I probably damaging Het
Scamp2 A G 9: 57,468,399 (GRCm39) probably benign Het
Ttn A T 2: 76,714,818 (GRCm39) probably benign Het
Vmn2r129 C T 4: 156,690,549 (GRCm39) noncoding transcript Het
Vmn2r17 A T 5: 109,574,916 (GRCm39) R74S probably benign Het
Wif1 G T 10: 120,931,940 (GRCm39) C288F probably damaging Het
Other mutations in Gm4222
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01139:Gm4222 APN 2 89,978,889 (GRCm39) utr 3 prime probably benign
Posted On 2014-05-07