Incidental Mutation 'R3837:Mid1ip1'
ID 275726
Institutional Source Beutler Lab
Gene Symbol Mid1ip1
Ensembl Gene ENSMUSG00000008035
Gene Name Mid1 interacting protein 1 (gastrulation specific G12-like (zebrafish))
Synonyms Mig12, 3110038L01Rik
MMRRC Submission 040778-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R3837 (G1)
Quality Score 222
Status Validated
Chromosome X
Chromosomal Location 10583604-10585941 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 10584620 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 51 (V51A)
Ref Sequence ENSEMBL: ENSMUSP00000120996 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000008179] [ENSMUST00000115524] [ENSMUST00000144356] [ENSMUST00000156321]
AlphaFold Q9CQ20
Predicted Effect probably benign
Transcript: ENSMUST00000008179
AA Change: V51A

PolyPhen 2 Score 0.010 (Sensitivity: 0.96; Specificity: 0.77)
SMART Domains Protein: ENSMUSP00000008179
Gene: ENSMUSG00000008035
AA Change: V51A

DomainStartEndE-ValueType
Pfam:Spot_14 2 182 1.4e-79 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000115524
AA Change: V51A

PolyPhen 2 Score 0.010 (Sensitivity: 0.96; Specificity: 0.77)
SMART Domains Protein: ENSMUSP00000111186
Gene: ENSMUSG00000008035
AA Change: V51A

DomainStartEndE-ValueType
Pfam:Spot_14 2 178 2.8e-69 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000125623
Predicted Effect noncoding transcript
Transcript: ENSMUST00000141174
Predicted Effect possibly damaging
Transcript: ENSMUST00000144356
AA Change: V51A

PolyPhen 2 Score 0.922 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000122463
Gene: ENSMUSG00000008035
AA Change: V51A

DomainStartEndE-ValueType
Pfam:Spot_14 2 51 6.6e-30 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000156321
AA Change: V51A

PolyPhen 2 Score 0.922 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000120996
Gene: ENSMUSG00000008035
AA Change: V51A

DomainStartEndE-ValueType
Pfam:Spot_14 2 51 6.6e-30 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000180511
Meta Mutation Damage Score 0.0841 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.5%
Validation Efficiency 98% (52/53)
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700028I16Rik A G 10: 82,648,219 (GRCm39) noncoding transcript Het
4930474N05Rik G A 14: 35,817,435 (GRCm39) G112S probably benign Het
Adam24 T C 8: 41,133,584 (GRCm39) S351P probably benign Het
Amigo2 T C 15: 97,143,196 (GRCm39) I409V probably damaging Het
Arhgef25 T C 10: 127,025,605 (GRCm39) T12A probably benign Het
Atg10 A T 13: 91,085,499 (GRCm39) I150K probably damaging Het
AW551984 T C 9: 39,509,204 (GRCm39) probably benign Het
Cdc20b T C 13: 113,220,542 (GRCm39) W432R probably damaging Het
Cdh9 G T 15: 16,823,524 (GRCm39) E169* probably null Het
Col28a1 C T 6: 8,014,601 (GRCm39) V935M possibly damaging Het
Col6a3 T C 1: 90,707,803 (GRCm39) N1948D unknown Het
Dnajb2 G A 1: 75,218,124 (GRCm39) probably null Het
Fam13c C T 10: 70,378,478 (GRCm39) S336L probably damaging Het
Fn1 A T 1: 71,692,314 (GRCm39) probably null Het
Fryl T C 5: 73,228,608 (GRCm39) T1708A probably benign Het
Gcnt4 A T 13: 97,083,522 (GRCm39) R273* probably null Het
Gldc T A 19: 30,096,075 (GRCm39) probably benign Het
Glra2 C T X: 164,072,612 (GRCm39) V85I probably benign Het
Gm11562 A G 11: 99,511,026 (GRCm39) I58T possibly damaging Het
Gpam T C 19: 55,068,890 (GRCm39) N450S probably benign Het
Hivep2 C A 10: 14,004,713 (GRCm39) T437K probably benign Het
Hmcn2 T C 2: 31,303,419 (GRCm39) L3020P probably damaging Het
Hmgcr A G 13: 96,795,597 (GRCm39) I324T probably benign Het
Itih1 T A 14: 30,657,785 (GRCm39) N429Y probably damaging Het
Lamtor1 T C 7: 101,559,315 (GRCm39) probably null Het
Lrrd1 A T 5: 3,900,204 (GRCm39) I170L possibly damaging Het
Magi2 G A 5: 20,420,466 (GRCm39) D301N probably benign Het
Mmrn1 G A 6: 60,921,831 (GRCm39) S96N probably benign Het
Mrc2 G A 11: 105,239,257 (GRCm39) probably null Het
Msh3 C A 13: 92,491,366 (GRCm39) G15C probably damaging Het
Myl12b C A 17: 71,281,480 (GRCm39) E120* probably null Het
Myo3a T G 2: 22,455,121 (GRCm39) probably benign Het
Nagk A T 6: 83,778,139 (GRCm39) H245L possibly damaging Het
Nap1l1 T A 10: 111,331,183 (GRCm39) probably null Het
Nlrc5 A G 8: 95,237,929 (GRCm39) probably benign Het
Ogfrl1 G A 1: 23,409,041 (GRCm39) T395I probably benign Het
Polr1b T A 2: 128,961,027 (GRCm39) F662Y possibly damaging Het
Rrbp1 T C 2: 143,831,478 (GRCm39) K230E probably damaging Het
Shld2 A G 14: 33,971,142 (GRCm39) V581A probably damaging Het
Skap2 C T 6: 51,886,279 (GRCm39) probably null Het
Skint5 A T 4: 113,797,938 (GRCm39) M215K probably damaging Het
Slc17a4 C T 13: 24,085,752 (GRCm39) R387H probably benign Het
Tdp1 A G 12: 99,860,967 (GRCm39) probably null Het
Tlr3 G A 8: 45,849,976 (GRCm39) L898F probably damaging Het
Tmem210 A G 2: 25,178,444 (GRCm39) E35G possibly damaging Het
Tpbg T C 9: 85,725,167 (GRCm39) probably benign Het
Tubb2a G T 13: 34,259,294 (GRCm39) N165K probably benign Het
Usp14 A G 18: 10,024,532 (GRCm39) probably null Het
Vmn1r33 A T 6: 66,588,701 (GRCm39) D284E possibly damaging Het
Wnk1 T C 6: 119,927,004 (GRCm39) E1265G probably damaging Het
Yme1l1 A T 2: 23,081,092 (GRCm39) T455S possibly damaging Het
Zfp111 T C 7: 23,898,891 (GRCm39) N241S possibly damaging Het
Other mutations in Mid1ip1
AlleleSourceChrCoordTypePredicted EffectPPH Score
R3836:Mid1ip1 UTSW X 10,584,620 (GRCm39) missense possibly damaging 0.92
R3838:Mid1ip1 UTSW X 10,584,620 (GRCm39) missense possibly damaging 0.92
R3839:Mid1ip1 UTSW X 10,584,620 (GRCm39) missense possibly damaging 0.92
Predicted Primers PCR Primer
(F):5'- TCTATCTCCGTGTACCAGCG -3'
(R):5'- GAACTGCTGCTCCAGATCTTCC -3'

Sequencing Primer
(F):5'- TGTACCAGCGTCCCTGTG -3'
(R):5'- ACCAGGATGTCCTTGGGCTTC -3'
Posted On 2015-04-06