Incidental Mutation 'R6292:Apip'
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ID508482
Institutional Source Beutler Lab
Gene Symbol Apip
Ensembl Gene ENSMUSG00000010911
Gene NameAPAF1 interacting protein
SynonymsCGI-29, APIP2, Mmrp19
MMRRC Submission
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #R6292 (G1)
Quality Score225.009
Status Validated
Chromosome2
Chromosomal Location103073675-103092644 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to T at 103092467 bp
ZygosityHeterozygous
Amino Acid Change Cysteine to Phenylalanine at position 210 (C210F)
Ref Sequence ENSEMBL: ENSMUSP00000011055 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000011055]
Predicted Effect probably benign
Transcript: ENSMUST00000011055
AA Change: C210F

PolyPhen 2 Score 0.416 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000011055
Gene: ENSMUSG00000010911
AA Change: C210F

DomainStartEndE-ValueType
Aldolase_II 25 221 1.64e-47 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000124540
Predicted Effect noncoding transcript
Transcript: ENSMUST00000147131
Predicted Effect noncoding transcript
Transcript: ENSMUST00000155004
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.2%
  • 20x: 94.5%
Validation Efficiency 100% (50/50)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] APIP is an APAF1 (MIM 602233)-interacting protein that acts as a negative regulator of ischemic/hypoxic injury (Cho et al., 2004 [PubMed 15262985]).[supplied by OMIM, Dec 2008]
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acacb T A 5: 114,200,251 V709E probably damaging Het
Ankrd33b C T 15: 31,325,085 probably null Het
Apaf1 T C 10: 90,991,563 T1202A possibly damaging Het
Chd9 A T 8: 90,932,922 H170L probably benign Het
Clec16a T C 16: 10,560,151 probably null Het
Ep300 T A 15: 81,616,734 probably benign Het
Etl4 C T 2: 20,743,573 H39Y probably damaging Het
Gdap1l1 A T 2: 163,451,507 I218F probably damaging Het
Gm5141 A T 13: 62,774,438 C306S probably damaging Het
Gm9961 C T 16: 11,930,472 noncoding transcript Het
Gpr27 C T 6: 99,693,658 S327L possibly damaging Het
Hectd3 A C 4: 116,998,808 T435P probably damaging Het
Hs3st1 T A 5: 39,614,790 Q170L possibly damaging Het
Hykk T C 9: 54,920,826 probably null Het
Lilra5 T C 7: 4,238,339 S92P possibly damaging Het
Lrig1 A T 6: 94,616,445 N418K probably damaging Het
Miga1 A G 3: 152,317,719 F232L probably benign Het
Mkrn2 T A 6: 115,613,334 M217K probably damaging Het
Myh7b A T 2: 155,632,396 Q1677L probably damaging Het
N4bp1 T C 8: 86,853,239 E645G probably damaging Het
Nckap5 T C 1: 125,915,015 K1752E probably damaging Het
Nek1 A G 8: 61,054,736 probably null Het
Ntng1 T C 3: 110,143,886 probably benign Het
Nup133 A G 8: 123,917,437 V730A probably benign Het
Olfr314 T A 11: 58,786,237 M1K probably null Het
Olfr620 T A 7: 103,612,179 H58L probably damaging Het
Paqr6 C T 3: 88,367,898 P213S probably damaging Het
Pign A T 1: 105,585,077 V627D possibly damaging Het
Rasal1 T A 5: 120,659,620 V139E probably damaging Het
Scgb1b24 G T 7: 33,744,152 A79S possibly damaging Het
Slc25a28 T C 19: 43,664,592 D210G probably benign Het
Slc38a3 A T 9: 107,655,154 I393N possibly damaging Het
Slc41a2 T C 10: 83,254,926 N465D probably damaging Het
Slc5a5 G A 8: 70,891,178 T160I probably damaging Het
Smarca2 C T 19: 26,630,892 A117V probably damaging Het
Sorcs2 C T 5: 36,062,587 R371H probably damaging Het
Taf4 A G 2: 179,923,987 S872P probably damaging Het
Tdrd3 G T 14: 87,506,254 C540F probably benign Het
Thumpd1 A T 7: 119,720,674 L23Q probably benign Het
Top1 A T 2: 160,698,141 Y213F probably benign Het
Txndc5 T C 13: 38,528,184 probably null Het
Unc79 C A 12: 103,142,732 A2005D possibly damaging Het
Upb1 T C 10: 75,438,171 L344P probably damaging Het
Vmn1r72 T A 7: 11,669,652 S290C probably benign Het
Vmn2r103 A G 17: 19,793,604 I219M possibly damaging Het
Wapl A G 14: 34,729,195 T729A probably damaging Het
Washc5 C T 15: 59,355,934 R393H probably damaging Het
Other mutations in Apip
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00337:Apip APN 2 103091912 missense probably benign 0.02
IGL01631:Apip APN 2 103073849 unclassified probably benign
IGL01736:Apip APN 2 103087141 missense probably damaging 0.98
IGL02734:Apip APN 2 103089544 splice site probably benign
BB006:Apip UTSW 2 103083021 missense probably benign 0.00
BB016:Apip UTSW 2 103083021 missense probably benign 0.00
R0256:Apip UTSW 2 103088571 missense possibly damaging 0.68
R1518:Apip UTSW 2 103089493 missense probably damaging 1.00
R1829:Apip UTSW 2 103088662 missense probably benign 0.09
R4930:Apip UTSW 2 103091881 nonsense probably null
R6300:Apip UTSW 2 103087153 missense possibly damaging 0.92
R6725:Apip UTSW 2 103092525 missense possibly damaging 0.79
R6759:Apip UTSW 2 103091846 missense probably benign 0.02
R6843:Apip UTSW 2 103092489 missense probably benign 0.14
R6968:Apip UTSW 2 103089453 missense possibly damaging 0.94
R7168:Apip UTSW 2 103092468 nonsense probably null
R7494:Apip UTSW 2 103092551 missense probably benign 0.00
R7929:Apip UTSW 2 103083021 missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TCCCTTGCAGGTTTGAAAATTG -3'
(R):5'- ACCATCGGTAGTATTCTGTGACAG -3'

Sequencing Primer
(F):5'- GGTTTGAAAATTGTTGGGGTCAAAAC -3'
(R):5'- CTGTGACAGATTAGTGACATCAAG -3'
Posted On2018-03-15