Mutagenetix > Incidental Mutation

Incidental Mutation 'R7644:Abl2'

590392

Institutional Source

Beutler Lab

Gene Symbol

Abl2

Ensembl Gene

ENSMUSG00000026596

Gene Name

ABL proto-oncogene 2, non-receptor tyrosine kinase

Synonyms

Abll, Arg

MMRRC Submission

045723-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.565) question?

Stock #

R7644 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

156386356-156477138 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 156443563 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 24 (D24G)

Ref Sequence

ENSEMBL: ENSMUSP00000140125 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000027888] [ENSMUST00000166172] [ENSMUST00000173929] [ENSMUST00000190749]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000027888

SMART Domains

Protein: ENSMUSP00000027888
Gene: ENSMUSG00000026596

Domain	Start	End	E-Value	Type
low complexity region	20	40	N/A	INTRINSIC
SH3	110	166	9.83e-16	SMART
SH2	171	254	1.34e-33	SMART
TyrKc	288	539	2.53e-148	SMART
low complexity region	561	577	N/A	INTRINSIC
low complexity region	598	609	N/A	INTRINSIC
low complexity region	734	752	N/A	INTRINSIC
low complexity region	877	891	N/A	INTRINSIC
low complexity region	974	991	N/A	INTRINSIC
low complexity region	1036	1049	N/A	INTRINSIC
FABD	1061	1182	5.24e-65	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000166172

SMART Domains

Protein: ENSMUSP00000126181
Gene: ENSMUSG00000026596

Domain	Start	End	E-Value	Type
low complexity region	20	40	N/A	INTRINSIC
SH3	110	166	9.83e-16	SMART
SH2	171	254	1.34e-33	SMART
TyrKc	288	539	2.53e-148	SMART
low complexity region	561	577	N/A	INTRINSIC
low complexity region	598	609	N/A	INTRINSIC
low complexity region	773	787	N/A	INTRINSIC
low complexity region	870	887	N/A	INTRINSIC
low complexity region	932	945	N/A	INTRINSIC
FABD	957	1078	5.24e-65	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000173929

SMART Domains

Protein: ENSMUSP00000133381
Gene: ENSMUSG00000026596

Domain	Start	End	E-Value	Type
low complexity region	20	40	N/A	INTRINSIC
SH3	89	139	4.35e-8	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000190749
AA Change: D24G

PolyPhen 2 Score 0.080 (Sensitivity: 0.93; Specificity: 0.85)

SMART Domains

Protein: ENSMUSP00000140125
Gene: ENSMUSG00000026596
AA Change: D24G

Domain	Start	End	E-Value	Type
SH3	103	159	6.2e-18	SMART
SH2	164	247	8.4e-36	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.9%

Validation Efficiency

100% (86/86)

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 family of nonreceptor tyrosine protein kinases. The protein is highly similar to the c-abl oncogene 1 protein, including the tyrosine kinase, SH2 and SH3 domains, and it plays a role in cytoskeletal rearrangements through its C-terminal F-actin- and microtubule-binding sequences. This gene is expressed in both normal and tumor cells, and is involved in translocation with the ets variant 6 gene in leukemia. Multiple alternatively spliced transcript variants encoding different protein isoforms have been found for this gene. [provided by RefSeq, Nov 2009]
PHENOTYPE: Mice homozygous for targeted mutations that inactivate the gene display multiple behavioral abnormalities indicating neuronal defects. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 86 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700001O22Rik	C	T	2: 30,687,966 (GRCm39)	R209Q	possibly damaging	Het
Adar	C	T	3: 89,652,826 (GRCm39)	A754V	probably benign	Het
Adcy8	C	T	15: 64,571,218 (GRCm39)	V1172I	possibly damaging	Het
Adgrl2	C	T	3: 148,544,789 (GRCm39)	V769M	probably damaging	Het
Akna	T	A	4: 63,313,634 (GRCm39)	Q163L	possibly damaging	Het
Alox15	C	T	11: 70,236,368 (GRCm39)	A511T	probably null	Het
Ano8	C	T	8: 71,937,474 (GRCm39)	G90D	probably damaging	Het
Aqp5	G	A	15: 99,492,107 (GRCm39)	R235H	probably damaging	Het
B3galt4	A	T	17: 34,169,419 (GRCm39)	V273E	probably damaging	Het
Ccdc125	C	T	13: 100,814,884 (GRCm39)		probably null	Het
Ccdc90b	A	G	7: 92,216,868 (GRCm39)	R47G	possibly damaging	Het
Celsr2	G	T	3: 108,320,806 (GRCm39)	L669I	probably damaging	Het
Clasp1	T	G	1: 118,440,480 (GRCm39)		probably null	Het
Clec4a2	C	T	6: 123,101,974 (GRCm39)	P43L	probably benign	Het
Cntn1	T	C	15: 92,207,890 (GRCm39)	I827T	probably benign	Het
Col9a1	G	T	1: 24,224,243 (GRCm39)	V142F	unknown	Het
Cplane1	T	A	15: 8,252,611 (GRCm39)	D1944E	probably benign	Het
Cts7	G	T	13: 61,504,782 (GRCm39)	Y23*	probably null	Het
Dcdc2a	T	A	13: 25,291,674 (GRCm39)	Y220N	probably damaging	Het
Dennd2b	A	T	7: 109,156,000 (GRCm39)	L250*	probably null	Het
Dmxl1	T	G	18: 50,026,619 (GRCm39)	V1909G	probably benign	Het
Ehd2	G	A	7: 15,691,474 (GRCm39)	P286L	possibly damaging	Het
Elf3	G	T	1: 135,184,244 (GRCm39)	A208E	possibly damaging	Het
Eml5	A	G	12: 98,822,203 (GRCm39)	I775T	probably benign	Het
Ephb1	T	C	9: 101,813,393 (GRCm39)	T791A	probably damaging	Het
Fanci	C	A	7: 79,094,219 (GRCm39)	S1105*	probably null	Het
Fastkd1	T	A	2: 69,527,184 (GRCm39)		probably null	Het
Fat4	A	G	3: 39,064,390 (GRCm39)	E4782G	possibly damaging	Het
Fnta	T	C	8: 26,503,516 (GRCm39)	I90V	probably damaging	Het
Fosl1	C	T	19: 5,500,332 (GRCm39)	R84*	probably null	Het
Gdf2	T	C	14: 33,666,847 (GRCm39)	F190L	probably benign	Het
Gzmn	T	A	14: 56,404,776 (GRCm39)	Q88L	probably damaging	Het
Hat1	T	A	2: 71,240,525 (GRCm39)	L73Q	probably damaging	Het
Hdhd2	G	A	18: 77,031,871 (GRCm39)	G109E	possibly damaging	Het
Il22ra1	A	G	4: 135,460,346 (GRCm39)	N34S	probably damaging	Het
Ino80d	T	C	1: 63,097,930 (GRCm39)	T760A	probably benign	Het
Itga7	A	G	10: 128,789,370 (GRCm39)	D971G	probably benign	Het
Kdm6b	T	C	11: 69,291,032 (GRCm39)	N1574S	unknown	Het
Kel	T	C	6: 41,667,742 (GRCm39)	E400G	probably benign	Het
Kif22	G	A	7: 126,632,134 (GRCm39)	T350I	probably damaging	Het
Kif26b	A	G	1: 178,506,839 (GRCm39)	N305S	probably benign	Het
Klk12	A	C	7: 43,419,134 (GRCm39)	Q33P	probably damaging	Het
Klk1b24	G	A	7: 43,841,304 (GRCm39)		probably null	Het
Krtap31-1	T	A	11: 99,799,048 (GRCm39)	C84S	possibly damaging	Het
Ky	T	A	9: 102,414,972 (GRCm39)	S295T	probably benign	Het
Lpin3	T	A	2: 160,738,690 (GRCm39)	M214K	probably benign	Het
Mak	T	A	13: 41,183,586 (GRCm39)	N565Y	probably benign	Het
Mphosph6	T	C	8: 118,528,623 (GRCm39)	T7A	probably benign	Het
Muc6	G	C	7: 141,217,659 (GRCm39)	P2338R	probably damaging	Het
Myh11	T	C	16: 14,039,688 (GRCm39)	T814A		Het
Nmbr	T	C	10: 14,636,433 (GRCm39)	L134P	probably damaging	Het
Nup107	C	T	10: 117,606,375 (GRCm39)	V456M	probably damaging	Het
Or56b1b	A	G	7: 108,164,649 (GRCm39)	S118P	possibly damaging	Het
Or8g22	C	A	9: 38,958,638 (GRCm39)	D26Y	probably damaging	Het
Pink1	A	T	4: 138,044,683 (GRCm39)	H351Q	probably damaging	Het
Piwil4	A	T	9: 14,645,711 (GRCm39)		probably null	Het
Pkd1l1	C	A	11: 8,825,758 (GRCm39)	V1498F		Het
Polb	A	G	8: 23,130,443 (GRCm39)	I161T	probably benign	Het
Polg	A	T	7: 79,101,416 (GRCm39)	L1097Q	probably damaging	Het
Prelp	T	C	1: 133,842,356 (GRCm39)	N263S	probably benign	Het
Pten	T	C	19: 32,789,234 (GRCm39)	C211R	probably damaging	Het
Ptprc	G	A	1: 137,995,645 (GRCm39)	A1012V	probably benign	Het
Ptprr	T	A	10: 115,884,133 (GRCm39)	H63Q	probably benign	Het
Rapsn	A	T	2: 90,872,299 (GRCm39)	H211L	possibly damaging	Het
Reln	T	C	5: 22,183,929 (GRCm39)	N1690S	probably benign	Het
Rpap2	A	G	5: 107,768,167 (GRCm39)	E335G	probably benign	Het
Rspry1	T	A	8: 95,385,396 (GRCm39)	S567T	probably benign	Het
Sf3b1	G	A	1: 55,036,302 (GRCm39)	R924*	probably null	Het
Sftpb	G	A	6: 72,286,818 (GRCm39)	E241K	probably benign	Het
Smarca4	G	T	9: 21,566,950 (GRCm39)	A677S	probably benign	Het
Srrm2	G	A	17: 24,038,294 (GRCm39)	R1646Q	unknown	Het
Tex15	T	A	8: 34,064,445 (GRCm39)	C1292S	probably benign	Het
Tmem140	A	G	6: 34,849,708 (GRCm39)	I75V	probably benign	Het
Trhr2	T	A	8: 123,084,061 (GRCm39)	Q313L	possibly damaging	Het
Trim35	A	G	14: 66,534,546 (GRCm39)	T10A	unknown	Het
Ttn	T	C	2: 76,750,124 (GRCm39)	I3642V	probably benign	Het
Ugt1a2	T	C	1: 88,128,507 (GRCm39)	L50P	probably damaging	Het
Unc13a	C	A	8: 72,087,182 (GRCm39)	V1522L	probably benign	Het
Usp33	A	G	3: 152,063,589 (GRCm39)	D21G	possibly damaging	Het
Vmn1r90	G	A	7: 14,295,616 (GRCm39)	Q161*	probably null	Het
Vmn2r117	A	T	17: 23,696,265 (GRCm39)	W381R	probably damaging	Het
Vmn2r16	G	C	5: 109,487,837 (GRCm39)	A237P	probably damaging	Het
Vmn2r74	A	G	7: 85,606,746 (GRCm39)	V200A	probably benign	Het
Yjefn3	C	T	8: 70,340,544 (GRCm39)	V227M	probably damaging	Het
Zfp652	T	C	11: 95,640,914 (GRCm39)	F280L	probably damaging	Het
Zfp748	G	A	13: 67,689,568 (GRCm39)	T564I	probably damaging	Het

Other mutations in Abl2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01400:Abl2	APN	1	156,462,754 (GRCm39)	missense	probably damaging	1.00
IGL01679:Abl2	APN	1	156,470,035 (GRCm39)	missense	probably benign	0.01
IGL02289:Abl2	APN	1	156,457,424 (GRCm39)	missense	probably damaging	1.00
PIT4495001:Abl2	UTSW	1	156,460,755 (GRCm39)	missense	probably damaging	1.00
R0907:Abl2	UTSW	1	156,457,429 (GRCm39)	missense	probably damaging	1.00
R1232:Abl2	UTSW	1	156,469,300 (GRCm39)	missense	probably damaging	1.00
R2069:Abl2	UTSW	1	156,448,397 (GRCm39)	splice site	probably null
R4224:Abl2	UTSW	1	156,461,417 (GRCm39)	missense	probably damaging	0.98
R4305:Abl2	UTSW	1	156,469,133 (GRCm39)	missense	probably damaging	0.99
R4411:Abl2	UTSW	1	156,457,652 (GRCm39)	missense	possibly damaging	0.86
R4490:Abl2	UTSW	1	156,461,349 (GRCm39)	missense	probably damaging	1.00
R5132:Abl2	UTSW	1	156,469,402 (GRCm39)	nonsense	probably null
R5383:Abl2	UTSW	1	156,469,802 (GRCm39)	missense	possibly damaging	0.89
R5428:Abl2	UTSW	1	156,469,681 (GRCm39)	missense	probably damaging	1.00
R5436:Abl2	UTSW	1	156,457,450 (GRCm39)	missense	probably damaging	1.00
R5760:Abl2	UTSW	1	156,469,427 (GRCm39)	missense	probably benign	0.06
R6051:Abl2	UTSW	1	156,469,655 (GRCm39)	missense	probably damaging	1.00
R6955:Abl2	UTSW	1	156,450,219 (GRCm39)	missense	probably damaging	1.00
R7002:Abl2	UTSW	1	156,386,703 (GRCm39)	missense	probably damaging	1.00
R7038:Abl2	UTSW	1	156,468,979 (GRCm39)	missense	possibly damaging	0.95
R7172:Abl2	UTSW	1	156,450,157 (GRCm39)	missense	probably damaging	1.00
R7268:Abl2	UTSW	1	156,461,509 (GRCm39)	critical splice donor site	probably null
R7282:Abl2	UTSW	1	156,457,630 (GRCm39)	missense	probably damaging	1.00
R7303:Abl2	UTSW	1	156,468,820 (GRCm39)	missense	probably benign	0.00
R7372:Abl2	UTSW	1	156,450,189 (GRCm39)	missense	probably damaging	1.00
R7375:Abl2	UTSW	1	156,450,184 (GRCm39)	missense	probably damaging	1.00
R7443:Abl2	UTSW	1	156,452,951 (GRCm39)	missense	probably damaging	1.00
R7468:Abl2	UTSW	1	156,450,104 (GRCm39)	missense	possibly damaging	0.68
R7614:Abl2	UTSW	1	156,464,429 (GRCm39)	missense	possibly damaging	0.71
R7783:Abl2	UTSW	1	156,386,641 (GRCm39)	missense	probably benign
R8158:Abl2	UTSW	1	156,469,639 (GRCm39)	missense	probably benign	0.00
R8675:Abl2	UTSW	1	156,452,909 (GRCm39)	missense	probably damaging	1.00
R8930:Abl2	UTSW	1	156,461,402 (GRCm39)	missense	probably damaging	0.98
R8932:Abl2	UTSW	1	156,461,402 (GRCm39)	missense	probably damaging	0.98
R9217:Abl2	UTSW	1	156,452,902 (GRCm39)	missense	probably damaging	1.00
R9262:Abl2	UTSW	1	156,469,820 (GRCm39)	missense	possibly damaging	0.93
R9290:Abl2	UTSW	1	156,457,538 (GRCm39)	missense	probably damaging	1.00
R9571:Abl2	UTSW	1	156,469,084 (GRCm39)	missense	probably damaging	0.99
X0067:Abl2	UTSW	1	156,459,003 (GRCm39)	splice site	probably null
Z1177:Abl2	UTSW	1	156,469,123 (GRCm39)	frame shift	probably null
Z1177:Abl2	UTSW	1	156,468,676 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ACCGGATCCCTGAGGTTTTG -3'
(R):5'- ACAAGCCATGTAATCCTCACTG -3'

Sequencing Primer
(F):5'- CCCTGTGGGTTGAACTTGCAC -3'
(R):5'- TGTAATCCTCACTGAGCCCAG -3'

Posted On

2019-10-24