Incidental Mutation 'IGL03325:Abi1'
ID 416616
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Abi1
Ensembl Gene ENSMUSG00000058835
Gene Name abl interactor 1
Synonyms Ssh3bp1, E3B1
Accession Numbers
Essential gene? Probably essential (E-score: 0.753) question?
Stock # IGL03325
Quality Score
Status
Chromosome 2
Chromosomal Location 22830085-22930207 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 22861240 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Glutamine at position 106 (R106Q)
Ref Sequence ENSEMBL: ENSMUSP00000120769 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078977] [ENSMUST00000091394] [ENSMUST00000093171] [ENSMUST00000114544] [ENSMUST00000123948] [ENSMUST00000126112] [ENSMUST00000139038] [ENSMUST00000140164] [ENSMUST00000149719] [ENSMUST00000178908] [ENSMUST00000153931]
AlphaFold Q8CBW3
Predicted Effect possibly damaging
Transcript: ENSMUST00000078977
AA Change: R106Q

PolyPhen 2 Score 0.846 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000077997
Gene: ENSMUSG00000058835
AA Change: R106Q

DomainStartEndE-ValueType
Pfam:Abi_HHR 93 171 3.7e-38 PFAM
low complexity region 176 185 N/A INTRINSIC
low complexity region 240 258 N/A INTRINSIC
low complexity region 264 282 N/A INTRINSIC
low complexity region 296 303 N/A INTRINSIC
low complexity region 337 364 N/A INTRINSIC
SH3 393 448 2.38e-23 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000091394
AA Change: R106Q

PolyPhen 2 Score 0.931 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000088957
Gene: ENSMUSG00000058835
AA Change: R106Q

DomainStartEndE-ValueType
Pfam:Abi_HHR 93 171 4.1e-38 PFAM
low complexity region 176 185 N/A INTRINSIC
low complexity region 240 258 N/A INTRINSIC
low complexity region 264 281 N/A INTRINSIC
low complexity region 295 302 N/A INTRINSIC
low complexity region 336 351 N/A INTRINSIC
low complexity region 365 392 N/A INTRINSIC
SH3 421 476 2.38e-23 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000093171
AA Change: R106Q

PolyPhen 2 Score 0.455 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000090860
Gene: ENSMUSG00000058835
AA Change: R106Q

DomainStartEndE-ValueType
Pfam:Abi_HHR 93 171 3.7e-38 PFAM
low complexity region 176 185 N/A INTRINSIC
low complexity region 240 258 N/A INTRINSIC
low complexity region 264 281 N/A INTRINSIC
low complexity region 295 302 N/A INTRINSIC
low complexity region 336 363 N/A INTRINSIC
SH3 392 447 2.38e-23 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000114544
AA Change: R106Q

PolyPhen 2 Score 0.709 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000110191
Gene: ENSMUSG00000058835
AA Change: R106Q

DomainStartEndE-ValueType
Pfam:Abi_HHR 93 170 4.4e-37 PFAM
low complexity region 171 180 N/A INTRINSIC
low complexity region 235 253 N/A INTRINSIC
low complexity region 268 300 N/A INTRINSIC
SH3 329 384 2.38e-23 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000123948
AA Change: R106Q

PolyPhen 2 Score 0.709 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000118491
Gene: ENSMUSG00000058835
AA Change: R106Q

DomainStartEndE-ValueType
Pfam:Abi_HHR 93 170 5.1e-39 PFAM
low complexity region 176 185 N/A INTRINSIC
low complexity region 240 258 N/A INTRINSIC
low complexity region 264 282 N/A INTRINSIC
low complexity region 296 303 N/A INTRINSIC
low complexity region 337 352 N/A INTRINSIC
low complexity region 366 393 N/A INTRINSIC
SH3 422 477 2.38e-23 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000126112
AA Change: R106Q

PolyPhen 2 Score 0.709 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000117335
Gene: ENSMUSG00000058835
AA Change: R106Q

DomainStartEndE-ValueType
Pfam:Abi_HHR 93 170 8.6e-37 PFAM
low complexity region 171 180 N/A INTRINSIC
low complexity region 235 253 N/A INTRINSIC
low complexity region 259 277 N/A INTRINSIC
low complexity region 291 298 N/A INTRINSIC
low complexity region 332 347 N/A INTRINSIC
low complexity region 361 388 N/A INTRINSIC
SH3 417 472 2.38e-23 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000139038
AA Change: R106Q

PolyPhen 2 Score 0.333 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000116093
Gene: ENSMUSG00000058835
AA Change: R106Q

DomainStartEndE-ValueType
Pfam:Abi_HHR 93 171 3.4e-38 PFAM
low complexity region 176 185 N/A INTRINSIC
low complexity region 240 258 N/A INTRINSIC
low complexity region 264 293 N/A INTRINSIC
low complexity region 307 334 N/A INTRINSIC
SH3 363 418 2.38e-23 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000140164
AA Change: R106Q

PolyPhen 2 Score 0.709 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000120462
Gene: ENSMUSG00000058835
AA Change: R106Q

DomainStartEndE-ValueType
Pfam:Abi_HHR 93 170 8.6e-37 PFAM
low complexity region 171 180 N/A INTRINSIC
low complexity region 235 253 N/A INTRINSIC
low complexity region 259 276 N/A INTRINSIC
low complexity region 290 297 N/A INTRINSIC
low complexity region 331 346 N/A INTRINSIC
low complexity region 360 387 N/A INTRINSIC
SH3 416 471 2.38e-23 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000149719
AA Change: R106Q

PolyPhen 2 Score 0.709 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000120621
Gene: ENSMUSG00000058835
AA Change: R106Q

DomainStartEndE-ValueType
Pfam:Abi_HHR 93 170 7.8e-37 PFAM
low complexity region 171 180 N/A INTRINSIC
low complexity region 235 253 N/A INTRINSIC
low complexity region 259 276 N/A INTRINSIC
low complexity region 290 297 N/A INTRINSIC
low complexity region 331 358 N/A INTRINSIC
SH3 387 442 2.38e-23 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000178908
AA Change: R106Q

PolyPhen 2 Score 0.966 (Sensitivity: 0.77; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000136846
Gene: ENSMUSG00000058835
AA Change: R106Q

DomainStartEndE-ValueType
Pfam:Abi_HHR 93 171 3.9e-37 PFAM
low complexity region 176 185 N/A INTRINSIC
low complexity region 240 258 N/A INTRINSIC
low complexity region 264 282 N/A INTRINSIC
low complexity region 296 303 N/A INTRINSIC
low complexity region 337 352 N/A INTRINSIC
low complexity region 366 393 N/A INTRINSIC
SH3 422 477 2.38e-23 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000153931
AA Change: R106Q

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000120769
Gene: ENSMUSG00000058835
AA Change: R106Q

DomainStartEndE-ValueType
Pfam:Abi_HHR 93 171 3e-38 PFAM
low complexity region 176 185 N/A INTRINSIC
low complexity region 240 258 N/A INTRINSIC
low complexity region 273 305 N/A INTRINSIC
SH3 334 389 2.38e-23 SMART
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the Abelson-interactor family of adaptor proteins. These proteins facilitate signal transduction as components of several multiprotein complexes, and regulate actin polymerization and cytoskeletal remodeling through interactions with Abelson tyrosine kinases. The encoded protein plays a role in macropinocytosis as a component of the WAVE2 complex, and also forms a complex with EPS8 and SOS1 that mediates signal transduction from Ras to Rac. This gene may play a role in the progression of several malignancies including melanoma, colon cancer and breast cancer, and a t(10;11) chromosomal translocation involving this gene and the MLL gene has been associated with acute myeloid leukemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 14. [provided by RefSeq, Sep 2011]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit background sensitive embryonic lethality prior during organogenesis associated with about abnormal vasculogenesis and angiogenesis. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca8b G A 11: 109,844,422 (GRCm39) R870C possibly damaging Het
Abcf2 A T 5: 24,779,210 (GRCm39) L113I probably damaging Het
Arhgef28 A G 13: 98,036,324 (GRCm39) V1645A probably benign Het
Ccdc198 A T 14: 49,481,277 (GRCm39) probably benign Het
Ceacam1 G A 7: 25,175,912 (GRCm39) A94V possibly damaging Het
Fat2 G A 11: 55,173,168 (GRCm39) T2515I probably damaging Het
Gm5800 T C 14: 51,951,983 (GRCm39) Y93C probably benign Het
Gnl1 A G 17: 36,299,548 (GRCm39) D573G probably damaging Het
Gosr1 A G 11: 76,645,229 (GRCm39) M105T probably benign Het
Gramd1c A T 16: 43,825,868 (GRCm39) Y303N probably benign Het
Heatr9 A G 11: 83,404,085 (GRCm39) probably null Het
Iigp1c T A 18: 60,378,883 (GRCm39) Y139* probably null Het
Itih2 T C 2: 10,111,546 (GRCm39) D464G probably damaging Het
Jcad T C 18: 4,673,902 (GRCm39) Y555H probably benign Het
Krtap19-3 A T 16: 88,674,609 (GRCm39) *88R probably null Het
Mrps11 T C 7: 78,440,453 (GRCm39) F114S probably damaging Het
Nat8 A T 6: 85,807,875 (GRCm39) V86E possibly damaging Het
Nek5 T C 8: 22,569,158 (GRCm39) T555A probably benign Het
Or6c3 A T 10: 129,309,474 (GRCm39) K304N probably benign Het
Pprc1 C T 19: 46,049,948 (GRCm39) T10I possibly damaging Het
Prss16 A G 13: 22,187,417 (GRCm39) V409A possibly damaging Het
Sema3d T A 5: 12,513,189 (GRCm39) L53Q probably damaging Het
Sfmbt2 T C 2: 10,582,628 (GRCm39) Y696H probably damaging Het
Sh2d3c C T 2: 32,615,270 (GRCm39) A120V probably benign Het
Smn1 A G 13: 100,264,365 (GRCm39) Y32C probably damaging Het
Sun2 C T 15: 79,622,849 (GRCm39) R110Q probably benign Het
Tcp11l2 T G 10: 84,440,764 (GRCm39) D323E possibly damaging Het
Tex55 A T 16: 38,648,355 (GRCm39) S251R probably damaging Het
Tnni3k A T 3: 154,667,451 (GRCm39) S296R probably damaging Het
Uck1 G A 2: 32,148,334 (GRCm39) R161C probably benign Het
Unc79 T A 12: 103,135,869 (GRCm39) S2435T probably damaging Het
Vmn2r114 C A 17: 23,510,652 (GRCm39) K609N probably damaging Het
Other mutations in Abi1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00904:Abi1 APN 2 22,831,942 (GRCm39) missense possibly damaging 0.71
IGL01694:Abi1 APN 2 22,850,725 (GRCm39) missense probably damaging 1.00
IGL01809:Abi1 APN 2 22,836,729 (GRCm39) missense probably benign 0.00
IGL02189:Abi1 APN 2 22,930,076 (GRCm39) start codon destroyed probably null 1.00
IGL03126:Abi1 APN 2 22,843,479 (GRCm39) missense probably benign 0.12
IGL03213:Abi1 APN 2 22,831,971 (GRCm39) missense probably damaging 1.00
R0421:Abi1 UTSW 2 22,850,839 (GRCm39) missense probably damaging 1.00
R0505:Abi1 UTSW 2 22,852,516 (GRCm39) splice site probably benign
R1265:Abi1 UTSW 2 22,836,734 (GRCm39) missense possibly damaging 0.85
R1851:Abi1 UTSW 2 22,840,276 (GRCm39) missense possibly damaging 0.78
R2975:Abi1 UTSW 2 22,847,099 (GRCm39) missense probably damaging 0.99
R3416:Abi1 UTSW 2 22,930,014 (GRCm39) missense probably damaging 1.00
R5000:Abi1 UTSW 2 22,840,211 (GRCm39) missense probably damaging 1.00
R5277:Abi1 UTSW 2 22,884,660 (GRCm39) missense probably damaging 1.00
R5945:Abi1 UTSW 2 22,929,977 (GRCm39) missense probably damaging 1.00
R6785:Abi1 UTSW 2 22,843,479 (GRCm39) missense probably benign 0.12
R7000:Abi1 UTSW 2 22,832,053 (GRCm39) missense probably damaging 1.00
R7249:Abi1 UTSW 2 22,847,101 (GRCm39) missense possibly damaging 0.82
R7565:Abi1 UTSW 2 22,836,596 (GRCm39) missense probably benign 0.00
R8052:Abi1 UTSW 2 22,843,555 (GRCm39) missense probably benign 0.04
R8252:Abi1 UTSW 2 22,861,284 (GRCm39) splice site probably benign
R8891:Abi1 UTSW 2 22,861,262 (GRCm39) missense probably damaging 0.96
R9214:Abi1 UTSW 2 22,831,989 (GRCm39) nonsense probably null
X0026:Abi1 UTSW 2 22,861,166 (GRCm39) nonsense probably null
Posted On 2016-08-02