Mutagenetix > Incidental Mutation

Incidental Mutation 'R6155:Dock2'

489531

Institutional Source

Beutler Lab

Gene Symbol

Dock2

Ensembl Gene

ENSMUSG00000020143

Gene Name

dedicator of cyto-kinesis 2

Synonyms

CED-5, MBC, Hch

MMRRC Submission

044302-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6155 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

34226815-34783892 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to G at 34294123 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Isoleucine at position 1072 (M1072I)

Ref Sequence

ENSEMBL: ENSMUSP00000090884 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000093193] [ENSMUST00000101365]

AlphaFold

Q8C3J5

Predicted Effect

probably benign
Transcript: ENSMUST00000093193
AA Change: M1072I

PolyPhen 2 Score 0.063 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000090884
Gene: ENSMUSG00000020143
AA Change: M1072I

Domain	Start	End	E-Value	Type
SH3	11	68	1.22e-11	SMART
Pfam:DOCK_N	71	414	2e-113	PFAM
Pfam:DOCK-C2	419	616	1e-60	PFAM
Pfam:DHR-2	1114	1614	6.3e-96	PFAM
low complexity region	1691	1706	N/A	INTRINSIC
low complexity region	1793	1800	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000101365
AA Change: M1072I

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)

SMART Domains

Protein: ENSMUSP00000098916
Gene: ENSMUSG00000020143
AA Change: M1072I

Domain	Start	End	E-Value	Type
SH3	11	68	1.22e-11	SMART
Pfam:DOCK_N	71	414	1.4e-113	PFAM
Pfam:DOCK-C2	419	616	5.5e-61	PFAM
low complexity region	1163	1171	N/A	INTRINSIC

Meta Mutation Damage Score

0.1025

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 97.9%
20x: 94.1%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the CDM protein family. It is specifically expressed in hematopoietic cells and is predominantly expressed in peripheral blood leukocytes. The protein is involved in remodeling of the actin cytoskeleton required for lymphocyte migration in response to chemokine signaling. It activates members of the Rho family of GTPases, for example RAC1 and RAC2, by acting as a guanine nucleotide exchange factor (GEF) to exchange bound GDP for free GTP. [provided by RefSeq, Oct 2016]
PHENOTYPE: Homozygous mutants are defective in the migration of T and B lympohcytes in response to chemokines, and thus display immune defects such as lymphocytopenia, atrophy of lymphoid follicles and loss of marginal-zone B cells. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcg3	T	C	5: 104,963,644 (GRCm38)	Y319C	probably benign	Het
Actn4	A	C	7: 28,896,141 (GRCm38)	I763S	probably damaging	Het
Actr8	G	A	14: 29,978,589 (GRCm38)		probably null	Het
Adrb1	T	C	19: 56,722,904 (GRCm38)	L178P	probably damaging	Het
Afap1	A	G	5: 35,935,609 (GRCm38)	Y19C	unknown	Het
Ankrd36	A	G	11: 5,687,442 (GRCm38)	E1337G	probably benign	Het
Arl4a	A	C	12: 40,036,520 (GRCm38)	V76G	probably damaging	Het
B230118H07Rik	A	T	2: 101,576,010 (GRCm38)		probably null	Het
Bmp1	A	T	14: 70,508,007 (GRCm38)	I246K	probably damaging	Het
Camk4	A	T	18: 32,939,447 (GRCm38)	T18S	unknown	Het
Cep152	T	C	2: 125,581,700 (GRCm38)	H927R	probably benign	Het
Clca3a2	A	G	3: 144,819,357 (GRCm38)	I38T	probably damaging	Het
Clec2g	A	C	6: 128,980,273 (GRCm38)	T54P	probably damaging	Het
Cox20	A	G	1: 178,321,797 (GRCm38)	E31G	possibly damaging	Het
Crispld1	T	A	1: 17,753,017 (GRCm38)	H407Q	probably benign	Het
Csmd1	T	C	8: 15,903,231 (GRCm38)	I3417V	probably benign	Het
Dhtkd1	A	C	2: 5,910,359 (GRCm38)	H700Q	probably null	Het
Dnah10	A	G	5: 124,785,175 (GRCm38)	T2165A	probably damaging	Het
Dnah10	G	A	5: 124,770,599 (GRCm38)	V1516M	probably damaging	Het
F11	T	A	8: 45,252,082 (GRCm38)	T141S	probably damaging	Het
Gabra6	T	A	11: 42,316,523 (GRCm38)	I245F	probably damaging	Het
Gm13101	T	A	4: 143,965,142 (GRCm38)	H337L	probably benign	Het
Gm8909	G	A	17: 36,167,507 (GRCm38)	A211V	possibly damaging	Het
Herc1	T	A	9: 66,433,423 (GRCm38)	C1685S	possibly damaging	Het
Il20	G	T	1: 130,910,740 (GRCm38)	D73E	probably damaging	Het
Ireb2	C	A	9: 54,886,527 (GRCm38)	P247Q	probably damaging	Het
Kcng3	T	C	17: 83,588,378 (GRCm38)	I220V	probably benign	Het
Lce1j	T	G	3: 92,789,072 (GRCm38)	Q133P	unknown	Het
Lgals9	C	T	11: 78,963,505 (GRCm38)	A287T	probably benign	Het
Lrrc52	A	G	1: 167,466,727 (GRCm38)		probably benign	Het
Map3k5	A	T	10: 20,118,441 (GRCm38)	H1027L	probably benign	Het
Morc3	A	G	16: 93,862,425 (GRCm38)	D407G	possibly damaging	Het
Myom1	T	C	17: 71,108,695 (GRCm38)		probably null	Het
Ncapg2	T	C	12: 116,438,011 (GRCm38)	F673S	possibly damaging	Het
Ncoa6	T	C	2: 155,407,448 (GRCm38)	D1312G	probably damaging	Het
Nkx1-1	A	T	5: 33,431,051 (GRCm38)	F298I	probably damaging	Het
Npas2	G	A	1: 39,287,476 (GRCm38)	R14Q	probably damaging	Het
Npas4	C	T	19: 4,986,870 (GRCm38)	C422Y	probably damaging	Het
Olfr1230	A	G	2: 89,296,421 (GRCm38)	L283S	probably damaging	Het
Olfr1381	T	A	11: 49,552,584 (GRCm38)	I279N	possibly damaging	Het
Olfr481	T	C	7: 108,081,286 (GRCm38)	V164A	probably benign	Het
Olfr749	T	C	14: 50,736,619 (GRCm38)	D181G	probably benign	Het
Pcdhga4	T	C	18: 37,686,493 (GRCm38)	I365T	probably damaging	Het
Pear1	T	A	3: 87,759,568 (GRCm38)	T37S	probably damaging	Het
Pkn2	A	T	3: 142,853,693 (GRCm38)	F24I	probably benign	Het
Plcb3	G	A	19: 6,966,165 (GRCm38)	A122V	probably damaging	Het
Pnliprp1	T	C	19: 58,730,133 (GRCm38)		probably null	Het
Psmb3	T	A	11: 97,712,452 (GRCm38)	F164I	probably damaging	Het
Ptch2	T	A	4: 117,096,908 (GRCm38)	F45Y	probably damaging	Het
Ptpn23	C	A	9: 110,387,781 (GRCm38)		probably benign	Het
Pusl1	A	G	4: 155,890,548 (GRCm38)	S199P	probably damaging	Het
Rasgrp2	C	A	19: 6,402,501 (GRCm38)	L35I	probably damaging	Het
Rictor	T	C	15: 6,793,977 (GRCm38)	L1545P	probably benign	Het
Rtn4r	A	T	16: 18,151,394 (GRCm38)	M229L	probably benign	Het
Ruvbl1	A	T	6: 88,479,125 (GRCm38)		probably null	Het
Slc35b3	A	T	13: 38,944,596 (GRCm38)	S30T	probably damaging	Het
Sorcs3	T	C	19: 48,398,697 (GRCm38)	V207A	possibly damaging	Het
Sox13	A	G	1: 133,393,267 (GRCm38)	S2P	probably damaging	Het
Sptbn1	A	C	11: 30,137,403 (GRCm38)	L999R	probably damaging	Het
Taf4	A	G	2: 179,913,524 (GRCm38)	V1015A	probably damaging	Het
Top3b	T	C	16: 16,891,509 (GRCm38)	L687P	probably damaging	Het
Tpp2	T	A	1: 43,956,489 (GRCm38)	V268E	probably damaging	Het
Ttc6	T	C	12: 57,737,616 (GRCm38)	Y1824H	possibly damaging	Het
Txk	A	G	5: 72,700,726 (GRCm38)	Y360H	probably damaging	Het
Vmn2r57	T	C	7: 41,428,690 (GRCm38)	I115V	probably benign	Het
Vmn2r98	T	C	17: 19,065,881 (GRCm38)	S214P	possibly damaging	Het
Zbtb48	T	C	4: 152,022,038 (GRCm38)		probably null	Het
Zzz3	A	G	3: 152,427,682 (GRCm38)	I126V	possibly damaging	Het

Other mutations in Dock2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00334:Dock2	APN	11	34,704,661 (GRCm38)	missense	probably damaging	1.00
IGL00469:Dock2	APN	11	34,229,603 (GRCm38)	splice site	probably benign
IGL01061:Dock2	APN	11	34,705,826 (GRCm38)	missense	probably damaging	1.00
IGL01319:Dock2	APN	11	34,698,790 (GRCm38)	missense	possibly damaging	0.61
IGL01451:Dock2	APN	11	34,310,390 (GRCm38)	missense	probably damaging	1.00
IGL01490:Dock2	APN	11	34,705,781 (GRCm38)	missense	probably damaging	0.97
IGL01601:Dock2	APN	11	34,239,528 (GRCm38)	critical splice donor site	probably null
IGL01800:Dock2	APN	11	34,756,273 (GRCm38)	missense	probably damaging	1.00
IGL01804:Dock2	APN	11	34,262,433 (GRCm38)	missense	probably benign	0.01
IGL01823:Dock2	APN	11	34,262,391 (GRCm38)	missense	probably damaging	1.00
IGL01829:Dock2	APN	11	34,705,841 (GRCm38)	missense	probably damaging	0.98
IGL01830:Dock2	APN	11	34,691,917 (GRCm38)	nonsense	probably null
IGL01835:Dock2	APN	11	34,310,435 (GRCm38)	missense	possibly damaging	0.51
IGL01845:Dock2	APN	11	34,708,865 (GRCm38)	missense	probably benign	0.02
IGL01953:Dock2	APN	11	34,732,356 (GRCm38)	missense	probably benign	0.28
IGL01989:Dock2	APN	11	34,268,053 (GRCm38)	missense	probably benign
IGL02081:Dock2	APN	11	34,254,355 (GRCm38)	missense	probably benign
IGL02105:Dock2	APN	11	34,714,525 (GRCm38)	missense	probably damaging	1.00
IGL02153:Dock2	APN	11	34,230,670 (GRCm38)	missense	probably benign	0.01
IGL02170:Dock2	APN	11	34,267,949 (GRCm38)	missense	probably damaging	1.00
IGL02344:Dock2	APN	11	34,731,510 (GRCm38)	missense	probably damaging	0.98
IGL02389:Dock2	APN	11	34,698,740 (GRCm38)	splice site	probably benign
IGL02409:Dock2	APN	11	34,501,204 (GRCm38)	missense	probably benign	0.00
IGL02472:Dock2	APN	11	34,249,801 (GRCm38)	missense	probably benign	0.00
IGL02625:Dock2	APN	11	34,501,168 (GRCm38)	critical splice donor site	probably null
IGL02929:Dock2	APN	11	34,268,048 (GRCm38)	missense	probably damaging	1.00
IGL02951:Dock2	APN	11	34,310,448 (GRCm38)	unclassified	probably benign
IGL02999:Dock2	APN	11	34,692,259 (GRCm38)	missense	probably damaging	0.99
IGL03165:Dock2	APN	11	34,687,533 (GRCm38)	missense	probably damaging	0.99
Arches	UTSW	11	34,689,760 (GRCm38)	missense	probably damaging	1.00
capitol_reef	UTSW	11	34,294,170 (GRCm38)	critical splice acceptor site	probably null
Croesus	UTSW	11	34,721,027 (GRCm38)	missense	probably damaging	1.00
denali	UTSW	11	34,229,472 (GRCm38)	critical splice donor site	probably null
dew	UTSW	11	34,248,636 (GRCm38)	nonsense	probably null
Dinghy	UTSW	11	34,262,460 (GRCm38)	missense	possibly damaging	0.70
Dry	UTSW	11	34,231,652 (GRCm38)	missense	possibly damaging	0.79
frazz	UTSW	11	34,248,572 (GRCm38)	critical splice donor site	probably benign
frizz	UTSW	11	34,258,184 (GRCm38)	splice site	probably benign
gildenstern	UTSW	11	34,732,339 (GRCm38)	critical splice donor site	probably null
godsgrace	UTSW	11	34,695,453 (GRCm38)	missense	probably damaging	1.00
Harborside	UTSW	11	34,262,445 (GRCm38)	missense	probably benign
Landing	UTSW	11	34,714,501 (GRCm38)	missense	possibly damaging	0.83
latest	UTSW	11	34,756,222 (GRCm38)	missense	probably damaging	1.00
Launch	UTSW	11	34,256,562 (GRCm38)	missense	probably damaging	1.00
liaoning	UTSW	11	34,708,793 (GRCm38)	missense	probably damaging	1.00
lucre	UTSW	11	34,704,609 (GRCm38)	frame shift	probably null
midas	UTSW	11	34,294,323 (GRCm38)	missense	probably damaging	0.99
muelle	UTSW	11	34,687,538 (GRCm38)	missense	probably damaging	1.00
narrowest	UTSW	11	34,282,652 (GRCm38)	missense	probably damaging	0.98
pier	UTSW	11	34,689,766 (GRCm38)	missense	probably damaging	1.00
Plank	UTSW	11	34,783,795 (GRCm38)	missense	possibly damaging	0.51
resplendent	UTSW	11	34,727,460 (GRCm38)	nonsense	probably null
riches	UTSW	11	34,688,452 (GRCm38)	critical splice donor site	probably null
skiff	UTSW	11	34,262,388 (GRCm38)	missense	probably null	0.80
Slip	UTSW	11	34,294,286 (GRCm38)	missense	probably benign	0.25
toothskin	UTSW	11	34,464,922 (GRCm38)	missense	probably damaging	1.00
Touch	UTSW	11	34,273,750 (GRCm38)	missense	possibly damaging	0.95
wassup	UTSW	11	34,503,413 (GRCm38)	missense	probably damaging	1.00
Wharf	UTSW	11	34,732,371 (GRCm38)	missense	possibly damaging	0.81
BB009:Dock2	UTSW	11	34,267,998 (GRCm38)	missense	probably benign	0.00
BB019:Dock2	UTSW	11	34,267,998 (GRCm38)	missense	probably benign	0.00
IGL03052:Dock2	UTSW	11	34,232,853 (GRCm38)	missense	probably benign	0.01
PIT4377001:Dock2	UTSW	11	34,721,008 (GRCm38)	missense	probably benign	0.02
R0006:Dock2	UTSW	11	34,312,453 (GRCm38)	unclassified	probably benign
R0012:Dock2	UTSW	11	34,783,795 (GRCm38)	missense	possibly damaging	0.51
R0063:Dock2	UTSW	11	34,756,284 (GRCm38)	critical splice acceptor site	probably null
R0063:Dock2	UTSW	11	34,756,284 (GRCm38)	critical splice acceptor site	probably null
R0116:Dock2	UTSW	11	34,688,565 (GRCm38)	intron	probably benign
R0149:Dock2	UTSW	11	34,438,327 (GRCm38)	missense	probably damaging	1.00
R0361:Dock2	UTSW	11	34,438,327 (GRCm38)	missense	probably damaging	1.00
R0462:Dock2	UTSW	11	34,268,052 (GRCm38)	missense	possibly damaging	0.74
R0471:Dock2	UTSW	11	34,688,553 (GRCm38)	missense	probably benign	0.30
R0538:Dock2	UTSW	11	34,704,718 (GRCm38)	splice site	probably benign
R0543:Dock2	UTSW	11	34,294,325 (GRCm38)	missense	probably damaging	1.00
R0660:Dock2	UTSW	11	34,248,621 (GRCm38)	missense	probably damaging	1.00
R0676:Dock2	UTSW	11	34,695,236 (GRCm38)	missense	probably damaging	0.99
R0722:Dock2	UTSW	11	34,464,970 (GRCm38)	splice site	probably benign
R0801:Dock2	UTSW	11	34,708,793 (GRCm38)	missense	probably damaging	1.00
R1110:Dock2	UTSW	11	34,256,535 (GRCm38)	missense	possibly damaging	0.78
R1171:Dock2	UTSW	11	34,695,241 (GRCm38)	missense	probably damaging	1.00
R1387:Dock2	UTSW	11	34,273,309 (GRCm38)	splice site	probably benign
R1445:Dock2	UTSW	11	34,239,705 (GRCm38)	missense	probably benign
R1494:Dock2	UTSW	11	34,282,761 (GRCm38)	nonsense	probably null
R1589:Dock2	UTSW	11	34,706,461 (GRCm38)	missense	probably damaging	0.99
R1597:Dock2	UTSW	11	34,704,647 (GRCm38)	missense	probably benign	0.00
R1629:Dock2	UTSW	11	34,262,480 (GRCm38)	splice site	probably null
R1749:Dock2	UTSW	11	34,232,767 (GRCm38)	critical splice donor site	probably null
R1888:Dock2	UTSW	11	34,707,342 (GRCm38)	missense	probably damaging	1.00
R1888:Dock2	UTSW	11	34,707,342 (GRCm38)	missense	probably damaging	1.00
R1899:Dock2	UTSW	11	34,294,286 (GRCm38)	missense	probably benign	0.25
R1924:Dock2	UTSW	11	34,464,934 (GRCm38)	missense	possibly damaging	0.69
R2031:Dock2	UTSW	11	34,727,470 (GRCm38)	splice site	probably benign
R2045:Dock2	UTSW	11	34,294,106 (GRCm38)	splice site	probably null
R2098:Dock2	UTSW	11	34,719,005 (GRCm38)	missense	probably damaging	0.99
R2098:Dock2	UTSW	11	34,266,279 (GRCm38)	missense	probably benign	0.16
R2129:Dock2	UTSW	11	34,727,415 (GRCm38)	missense	probably damaging	1.00
R2147:Dock2	UTSW	11	34,229,472 (GRCm38)	critical splice donor site	probably null
R2149:Dock2	UTSW	11	34,229,472 (GRCm38)	critical splice donor site	probably null
R2150:Dock2	UTSW	11	34,229,472 (GRCm38)	critical splice donor site	probably null
R2176:Dock2	UTSW	11	34,695,217 (GRCm38)	missense	probably benign	0.00
R2230:Dock2	UTSW	11	34,294,323 (GRCm38)	missense	probably damaging	0.99
R2508:Dock2	UTSW	11	34,312,485 (GRCm38)	missense	probably benign	0.04
R2875:Dock2	UTSW	11	34,718,885 (GRCm38)	missense	probably damaging	1.00
R2885:Dock2	UTSW	11	34,689,766 (GRCm38)	missense	probably damaging	1.00
R2910:Dock2	UTSW	11	34,232,910 (GRCm38)	splice site	probably benign
R3081:Dock2	UTSW	11	34,231,610 (GRCm38)	missense	probably benign
R3418:Dock2	UTSW	11	34,689,760 (GRCm38)	missense	probably damaging	1.00
R3552:Dock2	UTSW	11	34,720,960 (GRCm38)	missense	probably benign	0.22
R3731:Dock2	UTSW	11	34,708,895 (GRCm38)	missense	probably damaging	1.00
R3846:Dock2	UTSW	11	34,732,371 (GRCm38)	missense	possibly damaging	0.81
R4135:Dock2	UTSW	11	34,714,501 (GRCm38)	missense	possibly damaging	0.83
R4598:Dock2	UTSW	11	34,239,536 (GRCm38)	missense	probably damaging	1.00
R4599:Dock2	UTSW	11	34,239,536 (GRCm38)	missense	probably damaging	1.00
R4715:Dock2	UTSW	11	34,294,118 (GRCm38)	missense	probably damaging	1.00
R4722:Dock2	UTSW	11	34,695,471 (GRCm38)	missense	probably damaging	1.00
R4742:Dock2	UTSW	11	34,294,170 (GRCm38)	critical splice acceptor site	probably null
R4830:Dock2	UTSW	11	34,273,767 (GRCm38)	splice site	probably null
R4884:Dock2	UTSW	11	34,266,248 (GRCm38)	missense	probably damaging	1.00
R4990:Dock2	UTSW	11	34,695,251 (GRCm38)	missense	probably damaging	1.00
R5334:Dock2	UTSW	11	34,228,643 (GRCm38)	missense	probably benign	0.00
R5570:Dock2	UTSW	11	34,727,406 (GRCm38)	missense	probably damaging	1.00
R5602:Dock2	UTSW	11	34,254,391 (GRCm38)	missense	probably benign	0.16
R5681:Dock2	UTSW	11	34,249,836 (GRCm38)	missense	probably benign	0.06
R5809:Dock2	UTSW	11	34,262,445 (GRCm38)	missense	probably benign
R5860:Dock2	UTSW	11	34,256,562 (GRCm38)	missense	probably damaging	1.00
R6111:Dock2	UTSW	11	34,708,787 (GRCm38)	missense	probably damaging	0.99
R6156:Dock2	UTSW	11	34,247,789 (GRCm38)	missense	possibly damaging	0.51
R6173:Dock2	UTSW	11	34,262,388 (GRCm38)	missense	probably null	0.80
R6182:Dock2	UTSW	11	34,229,476 (GRCm38)	missense	probably damaging	0.97
R6188:Dock2	UTSW	11	34,503,396 (GRCm38)	missense	probably damaging	0.98
R6191:Dock2	UTSW	11	34,231,652 (GRCm38)	missense	possibly damaging	0.79
R6283:Dock2	UTSW	11	34,707,325 (GRCm38)	missense	probably damaging	0.99
R6395:Dock2	UTSW	11	34,232,874 (GRCm38)	missense	probably damaging	1.00
R6465:Dock2	UTSW	11	34,503,413 (GRCm38)	missense	probably damaging	1.00
R6500:Dock2	UTSW	11	34,362,822 (GRCm38)	missense	possibly damaging	0.76
R6561:Dock2	UTSW	11	34,687,538 (GRCm38)	missense	probably damaging	1.00
R6745:Dock2	UTSW	11	34,705,843 (GRCm38)	missense	probably damaging	1.00
R6745:Dock2	UTSW	11	34,705,842 (GRCm38)	missense	probably damaging	1.00
R6880:Dock2	UTSW	11	34,688,452 (GRCm38)	critical splice donor site	probably null
R6913:Dock2	UTSW	11	34,756,222 (GRCm38)	missense	probably damaging	1.00
R6997:Dock2	UTSW	11	34,464,922 (GRCm38)	missense	probably damaging	1.00
R7057:Dock2	UTSW	11	34,695,217 (GRCm38)	missense	probably benign	0.00
R7057:Dock2	UTSW	11	34,227,684 (GRCm38)	missense	probably benign	0.10
R7134:Dock2	UTSW	11	34,310,363 (GRCm38)	missense	probably benign	0.03
R7188:Dock2	UTSW	11	34,239,675 (GRCm38)	missense	possibly damaging	0.87
R7239:Dock2	UTSW	11	34,231,677 (GRCm38)	missense	probably benign	0.00
R7247:Dock2	UTSW	11	34,714,513 (GRCm38)	nonsense	probably null
R7250:Dock2	UTSW	11	34,695,293 (GRCm38)	missense	probably damaging	1.00
R7250:Dock2	UTSW	11	34,695,205 (GRCm38)	missense	probably benign	0.01
R7271:Dock2	UTSW	11	34,273,750 (GRCm38)	missense	possibly damaging	0.95
R7284:Dock2	UTSW	11	34,230,672 (GRCm38)	missense	probably benign	0.01
R7397:Dock2	UTSW	11	34,718,989 (GRCm38)	missense	probably benign	0.00
R7464:Dock2	UTSW	11	34,695,278 (GRCm38)	missense	probably damaging	0.99
R7512:Dock2	UTSW	11	34,312,542 (GRCm38)	missense	possibly damaging	0.95
R7556:Dock2	UTSW	11	34,720,951 (GRCm38)	missense	probably benign	0.43
R7663:Dock2	UTSW	11	34,721,027 (GRCm38)	missense	probably damaging	1.00
R7779:Dock2	UTSW	11	34,714,455 (GRCm38)	missense	probably benign	0.38
R7797:Dock2	UTSW	11	34,282,652 (GRCm38)	missense	probably damaging	0.98
R7855:Dock2	UTSW	11	34,273,698 (GRCm38)	missense	probably damaging	1.00
R7922:Dock2	UTSW	11	34,707,327 (GRCm38)	missense	probably benign	0.29
R7932:Dock2	UTSW	11	34,267,998 (GRCm38)	missense	probably benign	0.00
R8013:Dock2	UTSW	11	34,705,850 (GRCm38)	missense	probably damaging	0.96
R8192:Dock2	UTSW	11	34,732,339 (GRCm38)	critical splice donor site	probably null
R8244:Dock2	UTSW	11	34,695,453 (GRCm38)	missense	probably damaging	1.00
R8307:Dock2	UTSW	11	34,310,362 (GRCm38)	missense	possibly damaging	0.95
R8418:Dock2	UTSW	11	34,718,968 (GRCm38)	missense	probably benign	0.01
R8460:Dock2	UTSW	11	34,230,825 (GRCm38)	critical splice acceptor site	probably null
R8495:Dock2	UTSW	11	34,231,622 (GRCm38)	missense	probably benign	0.14
R8556:Dock2	UTSW	11	34,262,457 (GRCm38)	missense	possibly damaging	0.84
R8690:Dock2	UTSW	11	34,727,460 (GRCm38)	nonsense	probably null
R8743:Dock2	UTSW	11	34,273,252 (GRCm38)	nonsense	probably null
R8757:Dock2	UTSW	11	34,695,240 (GRCm38)	missense	probably benign	0.13
R8759:Dock2	UTSW	11	34,695,240 (GRCm38)	missense	probably benign	0.13
R8793:Dock2	UTSW	11	34,501,215 (GRCm38)	missense	probably benign	0.00
R8882:Dock2	UTSW	11	34,704,609 (GRCm38)	frame shift	probably null
R8885:Dock2	UTSW	11	34,310,396 (GRCm38)	missense	probably benign	0.01
R8943:Dock2	UTSW	11	34,708,819 (GRCm38)	missense	possibly damaging	0.63
R9171:Dock2	UTSW	11	34,698,843 (GRCm38)	missense	probably benign	0.12
R9182:Dock2	UTSW	11	34,310,398 (GRCm38)	missense	possibly damaging	0.51
R9203:Dock2	UTSW	11	34,731,539 (GRCm38)	missense	possibly damaging	0.92
R9310:Dock2	UTSW	11	34,294,139 (GRCm38)	missense	possibly damaging	0.71
R9388:Dock2	UTSW	11	34,262,460 (GRCm38)	missense	possibly damaging	0.70
R9490:Dock2	UTSW	11	34,698,755 (GRCm38)	missense	possibly damaging	0.90
R9568:Dock2	UTSW	11	34,708,811 (GRCm38)	missense	possibly damaging	0.83
R9593:Dock2	UTSW	11	34,228,607 (GRCm38)	missense	probably benign	0.34
R9694:Dock2	UTSW	11	34,268,054 (GRCm38)	missense	probably benign
R9697:Dock2	UTSW	11	34,254,417 (GRCm38)	missense	probably benign
R9753:Dock2	UTSW	11	34,273,673 (GRCm38)	missense	possibly damaging	0.68
R9783:Dock2	UTSW	11	34,258,128 (GRCm38)	missense	possibly damaging	0.83
X0017:Dock2	UTSW	11	34,266,271 (GRCm38)	missense	probably benign	0.08
X0018:Dock2	UTSW	11	34,232,833 (GRCm38)	missense	possibly damaging	0.65
X0058:Dock2	UTSW	11	34,256,564 (GRCm38)	missense	probably damaging	1.00
X0066:Dock2	UTSW	11	34,310,357 (GRCm38)	missense	possibly damaging	0.95
Z1088:Dock2	UTSW	11	34,692,382 (GRCm38)	missense	probably damaging	1.00
Z1088:Dock2	UTSW	11	34,438,300 (GRCm38)	missense	probably benign	0.14
Z1088:Dock2	UTSW	11	34,695,212 (GRCm38)	nonsense	probably null
Z1176:Dock2	UTSW	11	34,718,924 (GRCm38)	missense	probably benign	0.04
Z1177:Dock2	UTSW	11	34,312,553 (GRCm38)	missense	possibly damaging	0.68

Predicted Primers

PCR Primer
(F):5'- TGCATGACAACAGTTCTCACAC -3'
(R):5'- ATCACTCAGGACTCTCTGCAGC -3'

Sequencing Primer
(F):5'- AGTTCTCACACCAGCCCTG -3'
(R):5'- AGCTGGAGCAGTTCACAC -3'

Posted On

2017-10-10