Incidental Mutation 'IGL01810:Hmgn3'
ID 155823
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Hmgn3
Ensembl Gene ENSMUSG00000066456
Gene Name high mobility group nucleosomal binding domain 3
Synonyms 1110002A15Rik, HMGN3a, TRIP7, HMGN3b, 6330514M13Rik
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.368) question?
Stock # IGL01810
Quality Score
Status
Chromosome 9
Chromosomal Location 83109948-83146685 bp(-) (GRCm38)
Type of Mutation utr 3 prime
DNA Base Change (assembly) C to A at 83110384 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000140247 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000161796] [ENSMUST00000162246] [ENSMUST00000185315] [ENSMUST00000187193] [ENSMUST00000190154]
AlphaFold Q9DCB1
Predicted Effect probably benign
Transcript: ENSMUST00000161796
SMART Domains Protein: ENSMUSP00000125616
Gene: ENSMUSG00000066456

DomainStartEndE-ValueType
HMG17 2 76 3.32e-24 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000162246
SMART Domains Protein: ENSMUSP00000124278
Gene: ENSMUSG00000066456

DomainStartEndE-ValueType
HMG17 2 94 5.21e-40 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000185315
SMART Domains Protein: ENSMUSP00000140356
Gene: ENSMUSG00000066456

DomainStartEndE-ValueType
HMG17 2 94 1.16e-37 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185359
Predicted Effect probably benign
Transcript: ENSMUST00000187193
SMART Domains Protein: ENSMUSP00000140980
Gene: ENSMUSG00000066456

DomainStartEndE-ValueType
HMG17 2 94 5.5e-40 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000189777
Predicted Effect probably benign
Transcript: ENSMUST00000190154
SMART Domains Protein: ENSMUSP00000140247
Gene: ENSMUSG00000066456

DomainStartEndE-ValueType
HMG17 2 94 1.16e-37 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000190580
Predicted Effect noncoding transcript
Transcript: ENSMUST00000191105
Predicted Effect noncoding transcript
Transcript: ENSMUST00000194697
Predicted Effect noncoding transcript
Transcript: ENSMUST00000217211
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a null allele exhibit impaired glucose tolerance with decreased insulin serum levels and increased glucose serum levels during feeding. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aarsd1 G T 11: 101,417,359 Y10* probably null Het
Aass C A 6: 23,107,634 Q383H probably damaging Het
Bag1 T C 4: 40,936,657 D333G probably damaging Het
Cap2 A G 13: 46,639,949 probably benign Het
Col27a1 G T 4: 63,225,631 A519S probably benign Het
Cr2 A G 1: 195,159,595 V726A possibly damaging Het
Csmd2 A G 4: 128,480,845 probably benign Het
Dennd4c A G 4: 86,799,551 D595G possibly damaging Het
Ercc2 G T 7: 19,393,449 R340L probably damaging Het
Espl1 A G 15: 102,298,205 T35A probably benign Het
Fndc3a A G 14: 72,566,141 Y525H probably benign Het
Gm4922 T C 10: 18,784,047 Q309R probably benign Het
Gm5263 T C 1: 146,420,554 noncoding transcript Het
Gm6563 A C 19: 23,676,387 R180S probably damaging Het
Gpr182 C A 10: 127,750,864 V73F probably damaging Het
Gramd1b C T 9: 40,315,773 R179H probably damaging Het
Hk1 C T 10: 62,353,105 A10T probably benign Het
Il1b C T 2: 129,369,729 E24K probably damaging Het
Itgb6 G T 2: 60,627,985 Q475K probably benign Het
Lrrc74b A G 16: 17,545,558 S368P probably benign Het
Mfsd2b T C 12: 4,866,469 T234A possibly damaging Het
Muc6 A T 7: 141,651,062 Y270N probably damaging Het
Naip6 A G 13: 100,288,095 probably benign Het
Olfr142 A T 2: 90,252,132 Y285* probably null Het
Pear1 G A 3: 87,752,301 T742I probably damaging Het
Peli2 G A 14: 48,256,034 V238I probably benign Het
Pira2 A G 7: 3,844,612 L26P probably damaging Het
Pot1b A G 17: 55,662,521 V549A possibly damaging Het
Prdm16 T C 4: 154,347,927 Y295C probably benign Het
Ptprd A T 4: 76,140,507 probably benign Het
Rap1gap A T 4: 137,716,155 M145L probably benign Het
Setd7 A T 3: 51,532,967 probably benign Het
Ssx2ip T C 3: 146,428,010 I258T probably benign Het
Stard9 T C 2: 120,699,084 Y1941H possibly damaging Het
Stxbp3 T C 3: 108,800,152 E420G probably benign Het
Tpra1 T C 6: 88,909,342 V101A probably damaging Het
Tpx2 G T 2: 152,884,235 Q373H probably damaging Het
Ttn C T 2: 76,727,008 R29914Q probably damaging Het
Ubr3 T C 2: 70,003,465 probably null Het
Usp18 G A 6: 121,253,771 G53D probably damaging Het
Vps13c A T 9: 67,955,780 H3026L probably benign Het
Zan T C 5: 137,463,626 E1097G unknown Het
Other mutations in Hmgn3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03142:Hmgn3 APN 9 83146429 critical splice donor site probably benign
R0519:Hmgn3 UTSW 9 83112248 missense probably damaging 1.00
R0601:Hmgn3 UTSW 9 83146429 critical splice donor site probably null
R6008:Hmgn3 UTSW 9 83112231 missense probably damaging 0.99
R8346:Hmgn3 UTSW 9 83111106 missense probably damaging 1.00
Posted On 2014-02-04