Incidental Mutation 'IGL03339:Igfbpl1'
ID 417166
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Igfbpl1
Ensembl Gene ENSMUSG00000035551
Gene Name insulin-like growth factor binding protein-like 1
Synonyms 2810011G06Rik, 2810453O06Rik, IGFBP-like protein
Accession Numbers
Essential gene? Probably non essential (E-score: 0.052) question?
Stock # IGL03339
Quality Score
Status
Chromosome 4
Chromosomal Location 45809507-45826827 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 45813555 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000036974 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000044297]
AlphaFold Q80W15
Predicted Effect probably benign
Transcript: ENSMUST00000044297
SMART Domains Protein: ENSMUSP00000036974
Gene: ENSMUSG00000035551

DomainStartEndE-ValueType
signal peptide 1 17 N/A INTRINSIC
IB 28 100 1.31e-3 SMART
KAZAL 82 143 6.59e-14 SMART
IGc2 159 242 5.04e-9 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000145102
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
6820408C15Rik A G 2: 152,284,376 (GRCm39) E323G probably damaging Het
A4gnt T C 9: 99,502,601 (GRCm39) S254P probably damaging Het
Actn4 A G 7: 28,601,407 (GRCm39) L447P probably damaging Het
Agbl2 C A 2: 90,627,907 (GRCm39) S237R probably damaging Het
Apc G A 18: 34,431,527 (GRCm39) D309N probably damaging Het
Arhgef3 A G 14: 27,123,814 (GRCm39) M492V probably damaging Het
Atp10b T A 11: 43,121,442 (GRCm39) M1035K probably null Het
Cfap69 T A 5: 5,636,436 (GRCm39) probably benign Het
Ctf1 A G 7: 127,313,166 (GRCm39) N24S probably benign Het
Cx3cr1 T A 9: 119,880,503 (GRCm39) K300* probably null Het
Ddx25 A T 9: 35,453,299 (GRCm39) Y484N probably damaging Het
Eif4g1 A G 16: 20,499,734 (GRCm39) E506G possibly damaging Het
Ficd G T 5: 113,876,800 (GRCm39) R325L probably benign Het
G6pc2 A G 2: 69,051,239 (GRCm39) probably benign Het
Gm11168 C A 9: 3,004,767 (GRCm39) P103T probably benign Het
Hbb-y A T 7: 103,501,976 (GRCm39) H98Q probably damaging Het
Hmcn1 A G 1: 150,577,720 (GRCm39) S2014P probably benign Het
Hoxc5 T C 15: 102,922,568 (GRCm39) Y19H probably damaging Het
Ighg2c A C 12: 113,251,614 (GRCm39) V171G unknown Het
Kctd13 A G 7: 126,544,190 (GRCm39) D296G probably benign Het
Mfsd2b A C 12: 4,924,335 (GRCm39) M1R probably null Het
Nipbl A G 15: 8,380,360 (GRCm39) S811P probably benign Het
Or10al2 G A 17: 37,983,448 (GRCm39) C178Y possibly damaging Het
Or10al3 G T 17: 38,011,682 (GRCm39) M40I probably damaging Het
Or52r1 G A 7: 102,536,989 (GRCm39) R124C probably benign Het
Or5b122 T G 19: 13,563,439 (GRCm39) M257R probably damaging Het
Pcolce2 T C 9: 95,560,393 (GRCm39) probably benign Het
Pik3c2a G T 7: 116,017,256 (GRCm39) T167K possibly damaging Het
Ppp1r18 A G 17: 36,178,938 (GRCm39) D271G probably benign Het
Rnf213 T C 11: 119,333,830 (GRCm39) I3013T probably damaging Het
Rock1 A T 18: 10,097,493 (GRCm39) M765K probably benign Het
Sec16a T C 2: 26,325,945 (GRCm39) Y1244C probably benign Het
Taar7d T C 10: 23,903,204 (GRCm39) C29R possibly damaging Het
Tlcd4 C T 3: 121,022,489 (GRCm39) probably benign Het
Ttn A C 2: 76,572,264 (GRCm39) F26210V probably damaging Het
Ube2b A T 11: 51,877,534 (GRCm39) V145D probably damaging Het
Vmn1r219 T G 13: 23,347,580 (GRCm39) S256R possibly damaging Het
Other mutations in Igfbpl1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00885:Igfbpl1 APN 4 45,826,478 (GRCm39) missense probably damaging 0.99
PIT1430001:Igfbpl1 UTSW 4 45,826,756 (GRCm39) missense unknown
PIT4504001:Igfbpl1 UTSW 4 45,813,469 (GRCm39) missense possibly damaging 0.86
R1824:Igfbpl1 UTSW 4 45,826,406 (GRCm39) missense probably benign 0.19
R2655:Igfbpl1 UTSW 4 45,816,289 (GRCm39) missense probably damaging 0.96
R3850:Igfbpl1 UTSW 4 45,826,426 (GRCm39) missense probably benign 0.02
R5431:Igfbpl1 UTSW 4 45,815,588 (GRCm39) missense probably benign 0.21
R5695:Igfbpl1 UTSW 4 45,826,374 (GRCm39) missense probably damaging 1.00
R6229:Igfbpl1 UTSW 4 45,813,517 (GRCm39) missense probably damaging 1.00
R6613:Igfbpl1 UTSW 4 45,813,447 (GRCm39) missense probably benign 0.00
R6950:Igfbpl1 UTSW 4 45,815,494 (GRCm39) missense probably damaging 1.00
R6954:Igfbpl1 UTSW 4 45,826,663 (GRCm39) missense probably damaging 1.00
R6971:Igfbpl1 UTSW 4 45,816,333 (GRCm39) missense possibly damaging 0.72
R7558:Igfbpl1 UTSW 4 45,813,497 (GRCm39) missense probably damaging 1.00
R7976:Igfbpl1 UTSW 4 45,826,786 (GRCm39) missense unknown
R8675:Igfbpl1 UTSW 4 45,813,469 (GRCm39) missense possibly damaging 0.86
R9354:Igfbpl1 UTSW 4 45,816,348 (GRCm39) missense probably damaging 1.00
R9394:Igfbpl1 UTSW 4 45,826,792 (GRCm39) start codon destroyed probably null
R9598:Igfbpl1 UTSW 4 45,815,472 (GRCm39) missense probably null 0.98
Posted On 2016-08-02