Incidental Mutation 'R1389:Mapk1ip1'
ID 262773
Institutional Source Beutler Lab
Gene Symbol Mapk1ip1
Ensembl Gene ENSMUSG00000041775
Gene Name mitogen-activated protein kinase 1 interacting protein 1
Synonyms Miss, 2310009E07Rik
MMRRC Submission 039451-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.171) question?
Stock # R1389 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 138437547-138447996 bp(-) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) G to A at 138438456 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000112631 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000075667] [ENSMUST00000118810] [ENSMUST00000119664]
AlphaFold Q9D7G9
Predicted Effect probably benign
Transcript: ENSMUST00000075667
SMART Domains Protein: ENSMUSP00000075090
Gene: ENSMUSG00000041775

DomainStartEndE-ValueType
low complexity region 20 35 N/A INTRINSIC
low complexity region 143 165 N/A INTRINSIC
low complexity region 200 213 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000118810
SMART Domains Protein: ENSMUSP00000113813
Gene: ENSMUSG00000041775

DomainStartEndE-ValueType
low complexity region 20 35 N/A INTRINSIC
low complexity region 143 165 N/A INTRINSIC
low complexity region 200 213 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000119664
SMART Domains Protein: ENSMUSP00000112631
Gene: ENSMUSG00000041775

DomainStartEndE-ValueType
Pfam:MISS 1 166 5.5e-52 PFAM
low complexity region 200 213 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.1%
  • 10x: 95.7%
  • 20x: 90.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abtb3 A G 10: 85,476,460 (GRCm39) T914A possibly damaging Het
Acsl3 A C 1: 78,665,999 (GRCm39) I142L probably benign Het
Adgra2 C T 8: 27,601,116 (GRCm39) P252L probably damaging Het
Akap6 A G 12: 53,186,303 (GRCm39) E1239G probably benign Het
Arhgef17 TGGAGGAGGAGGAGGAGG TGGAGGAGGAGGAGG 7: 100,580,244 (GRCm39) probably benign Het
Calml4 A T 9: 62,778,548 (GRCm39) D12V probably damaging Het
Car9 G T 4: 43,512,439 (GRCm39) probably null Het
Ccar2 C A 14: 70,377,558 (GRCm39) V699L possibly damaging Het
Ccdc27 T C 4: 154,126,226 (GRCm39) M88V unknown Het
Ceacam15 T C 7: 16,405,988 (GRCm39) R188G probably damaging Het
Dcaf8 G A 1: 172,001,619 (GRCm39) R272H probably benign Het
Dchs1 A G 7: 105,404,778 (GRCm39) V2588A probably benign Het
Dst G A 1: 34,250,313 (GRCm39) R1749H probably damaging Het
Exog A G 9: 119,291,572 (GRCm39) Q283R probably benign Het
Fmnl1 A T 11: 103,077,535 (GRCm39) probably null Het
Gramd1c T C 16: 43,811,085 (GRCm39) D213G probably damaging Het
Iqgap1 A G 7: 80,409,504 (GRCm39) probably null Het
Itgae A G 11: 73,016,188 (GRCm39) Y799C probably damaging Het
Kalrn T C 16: 33,809,173 (GRCm39) I903V probably benign Het
Kcnh1 A G 1: 192,188,071 (GRCm39) E844G probably benign Het
Khdc1a A T 1: 21,420,251 (GRCm39) D3V probably damaging Het
Ly6g T C 15: 75,028,615 (GRCm39) F25S probably benign Het
Mfsd3 A G 15: 76,586,889 (GRCm39) H243R probably benign Het
Mms22l T A 4: 24,591,076 (GRCm39) Y1016N probably damaging Het
Mrgprb5 A T 7: 47,818,078 (GRCm39) V219E probably damaging Het
Nars2 G A 7: 96,652,036 (GRCm39) S209N probably benign Het
Nckap5 T C 1: 125,954,447 (GRCm39) T702A probably damaging Het
Or1e26 T C 11: 73,480,369 (GRCm39) N65S possibly damaging Het
Paf1 A G 7: 28,098,257 (GRCm39) probably benign Het
Prl3d1 A T 13: 27,282,693 (GRCm39) R145* probably null Het
Rasl10b G A 11: 83,308,665 (GRCm39) probably null Het
Rnf13 T A 3: 57,686,917 (GRCm39) N103K probably damaging Het
Senp1 T C 15: 97,973,734 (GRCm39) S170G probably benign Het
Slc46a2 A G 4: 59,914,620 (GRCm39) L101P probably damaging Het
Tmem123 C T 9: 7,791,107 (GRCm39) T136M probably damaging Het
Tpo T A 12: 30,153,109 (GRCm39) H415L probably damaging Het
Vipr2 A G 12: 116,100,950 (GRCm39) I255V probably benign Het
Zc3h11a A T 1: 133,561,541 (GRCm39) V310E probably damaging Het
Zfp3 T A 11: 70,663,462 (GRCm39) C474S probably damaging Het
Zfp707 T A 15: 75,846,465 (GRCm39) C99S probably damaging Het
Zranb1 C T 7: 132,573,062 (GRCm39) P410S probably damaging Het
Zswim8 G T 14: 20,760,816 (GRCm39) R30L probably damaging Het
Other mutations in Mapk1ip1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01098:Mapk1ip1 APN 7 138,438,191 (GRCm39) missense probably damaging 0.97
IGL01794:Mapk1ip1 APN 7 138,438,426 (GRCm39) start codon destroyed probably null 0.02
R0631:Mapk1ip1 UTSW 7 138,437,684 (GRCm39) missense possibly damaging 0.53
R5801:Mapk1ip1 UTSW 7 138,438,239 (GRCm39) missense possibly damaging 0.71
R6083:Mapk1ip1 UTSW 7 138,438,317 (GRCm39) nonsense probably null
Predicted Primers
Posted On 2015-02-04