Incidental Mutation 'R3811:Gm9602'
ID356361
Institutional Source Beutler Lab
Gene Symbol Gm9602
Ensembl Gene ENSMUSG00000090539
Gene Namepredicted gene 9602
Synonyms
MMRRC Submission 040767-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.072) question?
Stock #R3811 (G1)
Quality Score53
Status Validated
Chromosome14
Chromosomal Location4776337-4785002 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 4776499 bp
ZygosityHeterozygous
Amino Acid Change Isoleucine to Asparagine at position 28 (I28N)
Ref Sequence ENSEMBL: ENSMUSP00000126151 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000163325] [ENSMUST00000177973]
Predicted Effect probably damaging
Transcript: ENSMUST00000163325
AA Change: I28N

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000126151
Gene: ENSMUSG00000090539
AA Change: I28N

DomainStartEndE-ValueType
Pfam:Takusan 48 128 1.9e-26 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000177973
AA Change: I29N

PolyPhen 2 Score 0.734 (Sensitivity: 0.85; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000137206
Gene: ENSMUSG00000090539
AA Change: I29N

DomainStartEndE-ValueType
Pfam:Takusan 47 130 1.9e-36 PFAM
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.6%
  • 20x: 95.9%
Validation Efficiency 97% (36/37)
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agbl3 G T 6: 34,799,729 S385I probably damaging Het
Arhgap28 G A 17: 67,896,093 P122S probably benign Het
Arid2 T C 15: 96,289,086 V73A probably benign Het
Atp1b1 C T 1: 164,443,305 R35H probably benign Het
Cacybp T C 1: 160,203,652 D202G probably benign Het
Chsy3 C G 18: 59,176,170 P165R probably benign Het
Creb3 C T 4: 43,565,501 Q227* probably null Het
Crnkl1 C A 2: 145,931,306 R140L probably damaging Het
Cyth4 A G 15: 78,604,649 E39G probably damaging Het
Dnah6 T C 6: 73,191,498 T481A probably benign Het
Dock4 T A 12: 40,779,124 I1003N possibly damaging Het
Galntl5 T C 5: 25,186,180 F26L probably benign Het
Glrx5 C G 12: 105,032,888 C63W probably damaging Het
Hivep2 A G 10: 14,130,357 T900A probably benign Het
Hmcn1 A G 1: 150,649,577 probably null Het
Ighv1-24 G T 12: 114,773,065 L72I probably benign Het
Ilvbl G A 10: 78,579,035 C244Y probably benign Het
Kat7 A G 11: 95,291,615 probably benign Het
Kcnd3 C T 3: 105,658,766 A421V probably damaging Het
Lamc1 A T 1: 153,262,708 probably null Het
Mall T A 2: 127,708,854 I129F probably damaging Het
Mdn1 A T 4: 32,693,506 K1044* probably null Het
Med23 A T 10: 24,892,592 R77* probably null Het
Med23 G A 10: 24,892,593 probably null Het
Metap2 A T 10: 93,870,164 L252* probably null Het
Olfr1066 A T 2: 86,455,347 V308E probably benign Het
Psmd1 T A 1: 86,132,715 V828D probably damaging Het
Psmd9 C T 5: 123,234,590 probably benign Het
Rbbp5 T C 1: 132,492,587 V59A probably damaging Het
Sco2 T C 15: 89,373,679 probably benign Het
Slc32a1 G T 2: 158,614,736 C437F possibly damaging Het
Spem2 T C 11: 69,817,164 E325G possibly damaging Het
Steap4 A G 5: 7,977,017 T327A probably benign Het
Tsc2 T C 17: 24,629,037 D70G probably benign Het
Txndc5 T C 13: 38,523,405 K99E probably benign Het
Other mutations in Gm9602
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02718:Gm9602 APN 14 4776474 nonsense probably null
R1317:Gm9602 UTSW 14 4776499 missense probably damaging 1.00
R7172:Gm9602 UTSW 14 4777282 missense possibly damaging 0.62
Predicted Primers PCR Primer
(F):5'- AACTAGAATCTTCTGTGTTGTCACC -3'
(R):5'- CCCAGAAAAGTAGCTGCAGG -3'

Sequencing Primer
(F):5'- CCTGTGTTGTGGTGACAGCAAC -3'
(R):5'- AAGTAGCTGCAGGTTTGTCAATTCC -3'
Posted On2015-11-09