Mutagenetix > Incidental Mutation

Incidental Mutation 'R7452:Dock3'

577815

Institutional Source

Beutler Lab

Gene Symbol

Dock3

Ensembl Gene

ENSMUSG00000039716

Gene Name

dedicator of cyto-kinesis 3

Synonyms

Moca, PBP

MMRRC Submission

045526-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.549) question?

Stock #

R7452 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

106770024-107109108 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 106866664 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Serine at position 682 (F682S)

Ref Sequence

ENSEMBL: ENSMUSP00000047652 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000044532]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000044532
AA Change: F682S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000047652
Gene: ENSMUSG00000039716
AA Change: F682S

Domain	Start	End	E-Value	Type
SH3	9	66	3.85e-9	SMART
Pfam:DOCK_N	69	412	1.4e-120	PFAM
Pfam:DOCK-C2	417	608	7.7e-56	PFAM
low complexity region	854	867	N/A	INTRINSIC
low complexity region	892	916	N/A	INTRINSIC
Pfam:DHR-2	1121	1628	9e-133	PFAM
low complexity region	1679	1690	N/A	INTRINSIC
low complexity region	1693	1704	N/A	INTRINSIC
low complexity region	1730	1754	N/A	INTRINSIC
low complexity region	1880	1902	N/A	INTRINSIC
low complexity region	1963	1977	N/A	INTRINSIC

Meta Mutation Damage Score

0.7544

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 98.8%

Validation Efficiency

100% (75/75)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is specifically expressed in the central nervous system (CNS). It encodes a member of the DOCK (dedicator of cytokinesis) family of guanine nucleotide exchange factors (GEFs). This protein, dedicator of cytokinesis 3 (DOCK3), is also known as modifier of cell adhesion (MOCA) and presenilin-binding protein (PBP). The DOCK3 and DOCK1, -2 and -4 share several conserved amino acids in their DHR-2 (DOCK homology region 2) domains that are required for GEF activity, and bind directly to WAVE proteins [Wiskott-Aldrich syndrome protein (WASP) family Verprolin-homologous proteins] via their DHR-1 domains. The DOCK3 induces axonal outgrowth in CNS by stimulating membrane recruitment of the WAVE complex and activating the small G protein Rac1. This gene is associated with an attention deficit hyperactivity disorder-like phenotype by a complex chromosomal rearrangement. [provided by RefSeq, Aug 2010]
PHENOTYPE: Mice homozygous for a null allele exhibit abnormal behaviors and muscular weakness associated with axonal dystrophy. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 74 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A2m	C	A	6: 121,618,291 (GRCm39)	Q195K	probably damaging	Het
Abcg4	C	T	9: 44,190,897 (GRCm39)	G249R	probably damaging	Het
Actn1	T	C	12: 80,230,376 (GRCm39)	T293A	probably benign	Het
Adamts5	T	A	16: 85,674,869 (GRCm39)	T432S	probably benign	Het
Adh5	A	G	3: 138,160,506 (GRCm39)	T347A	probably benign	Het
Agbl5	A	G	5: 31,050,735 (GRCm39)	D432G	probably damaging	Het
Ank3	A	G	10: 69,734,881 (GRCm39)	T797A	possibly damaging	Het
Aoc1	T	G	6: 48,885,724 (GRCm39)	V743G	probably benign	Het
Arap2	A	T	5: 62,833,892 (GRCm39)	S858R	probably benign	Het
Arid1a	A	C	4: 133,480,438 (GRCm39)	V162G	possibly damaging	Het
Armc9	A	G	1: 86,140,814 (GRCm39)	D588G	possibly damaging	Het
Art3	A	G	5: 92,540,539 (GRCm39)	Y94C	probably damaging	Het
Btaf1	T	A	19: 36,946,527 (GRCm39)	D444E	probably damaging	Het
Cav2	A	G	6: 17,282,075 (GRCm39)	H111R	probably damaging	Het
Ccdc148	A	G	2: 58,717,596 (GRCm39)	L469P	probably damaging	Het
Celsr2	T	A	3: 108,320,406 (GRCm39)	E802V	possibly damaging	Het
Cfap57	T	C	4: 118,452,981 (GRCm39)	D574G	probably damaging	Het
Chd7	A	C	4: 8,854,731 (GRCm39)	D2024A	probably benign	Het
Corin	T	A	5: 72,592,590 (GRCm39)	D269V	possibly damaging	Het
Cyp4a12a	A	T	4: 115,184,795 (GRCm39)	I359F	probably damaging	Het
Defb6	T	C	8: 19,275,540 (GRCm39)	L7P	probably damaging	Het
Dnah7c	A	T	1: 46,686,196 (GRCm39)	M1817L	possibly damaging	Het
Enpep	T	A	3: 129,065,052 (GRCm39)	Y879F	possibly damaging	Het
Enpp2	T	C	15: 54,730,132 (GRCm39)	N462S	probably damaging	Het
Ephb3	T	C	16: 21,036,107 (GRCm39)		probably null	Het
F7	C	T	8: 13,085,215 (GRCm39)	H414Y	probably benign	Het
Fbn1	T	C	2: 125,347,375 (GRCm39)	H50R	possibly damaging	Het
Fig4	T	C	10: 41,116,633 (GRCm39)	D586G	possibly damaging	Het
Fryl	A	G	5: 73,181,331 (GRCm39)	L2825P	probably damaging	Het
Gal3st2	T	A	1: 93,800,240 (GRCm39)	H30Q	possibly damaging	Het
Garre1	A	G	7: 33,945,096 (GRCm39)	S595P	probably benign	Het
Gm12886	G	A	4: 121,274,671 (GRCm39)	Q70*	probably null	Het
Gm8104	A	C	14: 42,967,501 (GRCm39)	T190P	probably benign	Het
Hps3	A	T	3: 20,065,592 (GRCm39)	N749K	probably damaging	Het
Hr	A	G	14: 70,808,926 (GRCm39)	T1101A	probably damaging	Het
Htatip2	T	A	7: 49,423,074 (GRCm39)	S210T	probably benign	Het
Ift80	T	C	3: 68,901,615 (GRCm39)		probably null	Het
Iqgap1	A	G	7: 80,410,577 (GRCm39)	V212A	possibly damaging	Het
Itih5	A	G	2: 10,243,607 (GRCm39)	E448G	probably damaging	Het
Kdm5b	T	C	1: 134,552,686 (GRCm39)	C1221R	probably damaging	Het
Lrrc72	T	C	12: 36,262,692 (GRCm39)	Y52C	probably benign	Het
Map1b	C	T	13: 99,644,648 (GRCm39)	R85Q	probably damaging	Het
Mdn1	T	C	4: 32,739,030 (GRCm39)	I3617T	possibly damaging	Het
Mtpap	T	A	18: 4,379,705 (GRCm39)	H98Q	possibly damaging	Het
Nemf	A	T	12: 69,384,733 (GRCm39)		probably null	Het
Neto1	A	T	18: 86,517,056 (GRCm39)	I458L	probably benign	Het
Nfam1	T	A	15: 82,899,163 (GRCm39)	M128L	probably benign	Het
Or2y13	C	A	11: 49,415,208 (GRCm39)	H219Q	probably benign	Het
Or4g16	A	G	2: 111,137,266 (GRCm39)	T239A	probably damaging	Het
Or5p75-ps1	C	T	7: 108,107,800 (GRCm39)	T179I	unknown	Het
Or8b50	A	T	9: 38,518,384 (GRCm39)	I208F	probably benign	Het
P2ry14	C	T	3: 59,023,466 (GRCm39)	G7D	probably benign	Het
Pde11a	A	G	2: 75,966,758 (GRCm39)	Y564H	probably damaging	Het
Pex5l	C	T	3: 33,058,467 (GRCm39)	V262I	probably benign	Het
Poli	A	G	18: 70,642,049 (GRCm39)	V717A	possibly damaging	Het
Prdm14	A	T	1: 13,195,783 (GRCm39)	W93R	probably damaging	Het
Rbm46	T	C	3: 82,771,428 (GRCm39)	M396V	probably benign	Het
Rcor2	T	C	19: 7,248,587 (GRCm39)	V212A	probably benign	Het
Rcor3	C	A	1: 191,822,173 (GRCm39)	G8V	probably damaging	Het
Rhox4d	G	A	X: 36,700,645 (GRCm39)	G191E	unknown	Het
Rictor	C	T	15: 6,801,635 (GRCm39)	S441L	probably benign	Het
Skp2	T	A	15: 9,113,920 (GRCm39)	Q366L	probably damaging	Het
Slc13a3	A	T	2: 165,269,034 (GRCm39)	S312T	probably benign	Het
Sstr1	T	C	12: 58,260,142 (GRCm39)	L255P	probably damaging	Het
Steap3	T	C	1: 120,155,585 (GRCm39)	E458G	possibly damaging	Het
Sv2b	T	A	7: 74,797,461 (GRCm39)	D311V	probably damaging	Het
Tmem132b	A	G	5: 125,715,332 (GRCm39)	D347G	probably benign	Het
Tmem161a	A	G	8: 70,630,138 (GRCm39)	D108G	probably damaging	Het
Traf5	T	A	1: 191,731,792 (GRCm39)	I47F		Het
Trp53bp2	C	T	1: 182,274,133 (GRCm39)	Q95*	probably null	Het
Ttn	G	T	2: 76,707,487 (GRCm39)		probably null	Het
Usf3	T	C	16: 44,040,397 (GRCm39)	S1626P	probably benign	Het
Usp3	T	C	9: 66,474,180 (GRCm39)	R33G	probably benign	Het
Zbtb20	G	T	16: 43,431,039 (GRCm39)	A517S	probably damaging	Het

Other mutations in Dock3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00940:Dock3	APN	9	106,788,576 (GRCm39)	splice site	probably benign
IGL01067:Dock3	APN	9	106,959,572 (GRCm39)	critical splice donor site	probably null
IGL01160:Dock3	APN	9	106,783,887 (GRCm39)	missense	probably damaging	1.00
IGL01290:Dock3	APN	9	106,835,599 (GRCm39)	splice site	probably benign
IGL01291:Dock3	APN	9	106,835,599 (GRCm39)	splice site	probably benign
IGL01391:Dock3	APN	9	106,784,433 (GRCm39)	missense	possibly damaging	0.55
IGL01399:Dock3	APN	9	106,870,670 (GRCm39)	missense	probably benign	0.06
IGL01660:Dock3	APN	9	106,909,563 (GRCm39)	splice site	probably benign
IGL01752:Dock3	APN	9	106,902,512 (GRCm39)	splice site	probably benign
IGL01820:Dock3	APN	9	106,773,092 (GRCm39)	missense	probably damaging	1.00
IGL01908:Dock3	APN	9	106,783,861 (GRCm39)	missense	possibly damaging	0.81
IGL02191:Dock3	APN	9	106,815,340 (GRCm39)	missense	probably benign
IGL02227:Dock3	APN	9	106,939,254 (GRCm39)	missense	probably damaging	0.98
IGL02309:Dock3	APN	9	106,790,351 (GRCm39)	missense	probably damaging	1.00
IGL02408:Dock3	APN	9	106,790,298 (GRCm39)	splice site	probably benign
IGL02469:Dock3	APN	9	106,863,215 (GRCm39)	missense	probably damaging	0.98
IGL02545:Dock3	APN	9	106,939,271 (GRCm39)	missense	probably damaging	1.00
IGL02894:Dock3	APN	9	106,807,298 (GRCm39)	missense	probably benign	0.00
IGL02934:Dock3	APN	9	106,900,944 (GRCm39)	missense	probably benign	0.01
IGL03027:Dock3	APN	9	106,870,677 (GRCm39)	missense	probably damaging	0.98
IGL03068:Dock3	APN	9	106,841,958 (GRCm39)	missense	possibly damaging	0.82
IGL03128:Dock3	APN	9	106,909,491 (GRCm39)	missense	probably benign	0.05
IGL03161:Dock3	APN	9	106,900,987 (GRCm39)	missense	probably damaging	0.99
IGL03263:Dock3	APN	9	106,807,330 (GRCm39)	splice site	probably benign
IGL03279:Dock3	APN	9	106,788,447 (GRCm39)	splice site	probably benign
IGL03366:Dock3	APN	9	106,882,632 (GRCm39)	missense	probably benign	0.01
Implosion	UTSW	9	106,815,125 (GRCm39)	missense	probably benign	0.00
Squeeze	UTSW	9	106,807,242 (GRCm39)	missense	probably damaging	1.00
Tight	UTSW	9	106,872,080 (GRCm39)	missense	probably damaging	1.00
ANU05:Dock3	UTSW	9	106,772,862 (GRCm39)	missense	probably benign
R0025:Dock3	UTSW	9	106,790,467 (GRCm39)	missense	possibly damaging	0.90
R0025:Dock3	UTSW	9	106,790,467 (GRCm39)	missense	possibly damaging	0.90
R0030:Dock3	UTSW	9	106,789,512 (GRCm39)	missense	possibly damaging	0.64
R0076:Dock3	UTSW	9	106,788,685 (GRCm39)	splice site	probably benign
R0076:Dock3	UTSW	9	106,788,685 (GRCm39)	splice site	probably benign
R0206:Dock3	UTSW	9	106,874,195 (GRCm39)	nonsense	probably null
R0208:Dock3	UTSW	9	106,874,195 (GRCm39)	nonsense	probably null
R0384:Dock3	UTSW	9	106,779,094 (GRCm39)	splice site	probably benign
R0610:Dock3	UTSW	9	106,900,987 (GRCm39)	missense	probably damaging	0.99
R0731:Dock3	UTSW	9	106,847,055 (GRCm39)	missense	probably damaging	1.00
R1184:Dock3	UTSW	9	106,846,999 (GRCm39)	missense	probably damaging	1.00
R1350:Dock3	UTSW	9	106,791,831 (GRCm39)	missense	possibly damaging	0.52
R1393:Dock3	UTSW	9	106,788,548 (GRCm39)	missense	probably damaging	1.00
R1424:Dock3	UTSW	9	106,790,392 (GRCm39)	missense	probably damaging	1.00
R1469:Dock3	UTSW	9	106,832,908 (GRCm39)	missense	probably benign	0.37
R1469:Dock3	UTSW	9	106,832,908 (GRCm39)	missense	probably benign	0.37
R1539:Dock3	UTSW	9	106,874,112 (GRCm39)	missense	probably benign	0.23
R1539:Dock3	UTSW	9	106,829,563 (GRCm39)	missense	probably damaging	1.00
R1571:Dock3	UTSW	9	106,815,158 (GRCm39)	missense	possibly damaging	0.92
R1682:Dock3	UTSW	9	106,851,040 (GRCm39)	missense	probably damaging	0.98
R1795:Dock3	UTSW	9	106,902,534 (GRCm39)	missense	probably damaging	0.99
R1987:Dock3	UTSW	9	106,985,620 (GRCm39)	missense	probably benign	0.01
R2000:Dock3	UTSW	9	106,870,160 (GRCm39)	splice site	probably benign
R2074:Dock3	UTSW	9	106,870,662 (GRCm39)	missense	possibly damaging	0.46
R2114:Dock3	UTSW	9	106,870,743 (GRCm39)	missense	probably benign	0.00
R2265:Dock3	UTSW	9	106,818,525 (GRCm39)	missense	probably damaging	1.00
R2269:Dock3	UTSW	9	106,818,525 (GRCm39)	missense	probably damaging	1.00
R2370:Dock3	UTSW	9	106,829,554 (GRCm39)	missense	probably damaging	1.00
R2377:Dock3	UTSW	9	106,773,090 (GRCm39)	missense	probably damaging	0.98
R2385:Dock3	UTSW	9	106,868,324 (GRCm39)	missense	probably damaging	1.00
R2426:Dock3	UTSW	9	106,791,740 (GRCm39)	missense	possibly damaging	0.76
R3076:Dock3	UTSW	9	106,818,725 (GRCm39)	critical splice acceptor site	probably null
R3122:Dock3	UTSW	9	106,788,542 (GRCm39)	missense	probably damaging	0.99
R4052:Dock3	UTSW	9	106,850,995 (GRCm39)	missense	probably damaging	0.99
R4294:Dock3	UTSW	9	106,807,242 (GRCm39)	missense	probably damaging	1.00
R4623:Dock3	UTSW	9	106,939,244 (GRCm39)	missense	possibly damaging	0.61
R4664:Dock3	UTSW	9	106,870,743 (GRCm39)	missense	possibly damaging	0.71
R4705:Dock3	UTSW	9	106,902,535 (GRCm39)	missense	probably damaging	1.00
R4771:Dock3	UTSW	9	106,829,557 (GRCm39)	missense	possibly damaging	0.89
R4898:Dock3	UTSW	9	106,870,171 (GRCm39)	missense	possibly damaging	0.75
R4898:Dock3	UTSW	9	106,807,266 (GRCm39)	missense	probably damaging	1.00
R4948:Dock3	UTSW	9	106,868,354 (GRCm39)	missense	probably damaging	0.96
R4961:Dock3	UTSW	9	106,818,515 (GRCm39)	missense	probably damaging	1.00
R4986:Dock3	UTSW	9	106,809,182 (GRCm39)	missense	probably damaging	1.00
R5054:Dock3	UTSW	9	106,815,105 (GRCm39)	missense	probably damaging	1.00
R5065:Dock3	UTSW	9	106,832,883 (GRCm39)	missense	probably damaging	1.00
R5081:Dock3	UTSW	9	106,868,292 (GRCm39)	missense	probably damaging	1.00
R5101:Dock3	UTSW	9	106,846,980 (GRCm39)	missense	probably damaging	1.00
R5135:Dock3	UTSW	9	106,810,196 (GRCm39)	missense	probably damaging	1.00
R5227:Dock3	UTSW	9	106,863,269 (GRCm39)	missense	probably damaging	1.00
R5257:Dock3	UTSW	9	106,874,124 (GRCm39)	missense	probably damaging	1.00
R5258:Dock3	UTSW	9	106,874,124 (GRCm39)	missense	probably damaging	1.00
R5273:Dock3	UTSW	9	106,777,904 (GRCm39)	critical splice donor site	probably null
R5322:Dock3	UTSW	9	106,779,028 (GRCm39)	missense	probably benign	0.14
R5482:Dock3	UTSW	9	106,855,937 (GRCm39)	nonsense	probably null
R5553:Dock3	UTSW	9	106,868,309 (GRCm39)	missense	possibly damaging	0.81
R5631:Dock3	UTSW	9	106,832,898 (GRCm39)	missense	probably benign	0.01
R5739:Dock3	UTSW	9	106,850,995 (GRCm39)	missense	possibly damaging	0.92
R5838:Dock3	UTSW	9	106,772,687 (GRCm39)	missense	possibly damaging	0.51
R5888:Dock3	UTSW	9	106,901,002 (GRCm39)	missense	probably benign	0.12
R5960:Dock3	UTSW	9	106,788,554 (GRCm39)	nonsense	probably null
R5974:Dock3	UTSW	9	106,871,261 (GRCm39)	missense	probably damaging	1.00
R6116:Dock3	UTSW	9	106,809,161 (GRCm39)	missense	probably damaging	1.00
R6162:Dock3	UTSW	9	106,841,998 (GRCm39)	missense	possibly damaging	0.88
R6176:Dock3	UTSW	9	106,790,147 (GRCm39)	missense	probably benign	0.05
R6219:Dock3	UTSW	9	106,872,080 (GRCm39)	missense	probably damaging	1.00
R6238:Dock3	UTSW	9	106,790,147 (GRCm39)	missense	probably benign	0.05
R6266:Dock3	UTSW	9	106,841,952 (GRCm39)	missense	probably damaging	0.99
R6291:Dock3	UTSW	9	106,785,631 (GRCm39)	missense	probably benign
R6531:Dock3	UTSW	9	106,844,415 (GRCm39)	missense	probably benign
R6567:Dock3	UTSW	9	106,773,946 (GRCm39)	missense	probably benign	0.13
R6572:Dock3	UTSW	9	106,866,674 (GRCm39)	missense	probably damaging	0.99
R6620:Dock3	UTSW	9	106,815,125 (GRCm39)	missense	probably benign	0.00
R6726:Dock3	UTSW	9	107,036,651 (GRCm39)	nonsense	probably null
R7085:Dock3	UTSW	9	106,779,086 (GRCm39)	missense	probably damaging	1.00
R7151:Dock3	UTSW	9	106,841,916 (GRCm39)	missense	possibly damaging	0.68
R7320:Dock3	UTSW	9	106,772,723 (GRCm39)	missense	probably benign	0.20
R7357:Dock3	UTSW	9	106,882,568 (GRCm39)	missense	probably benign	0.34
R7423:Dock3	UTSW	9	106,844,370 (GRCm39)	missense	probably damaging	0.98
R7426:Dock3	UTSW	9	106,772,782 (GRCm39)	missense	probably benign
R7439:Dock3	UTSW	9	106,900,931 (GRCm39)	missense	probably damaging	1.00
R7470:Dock3	UTSW	9	106,882,644 (GRCm39)	missense	probably damaging	1.00
R7879:Dock3	UTSW	9	106,785,700 (GRCm39)	missense	probably benign	0.05
R8047:Dock3	UTSW	9	106,870,208 (GRCm39)	missense	possibly damaging	0.93
R8308:Dock3	UTSW	9	106,790,371 (GRCm39)	missense	probably benign	0.00
R8837:Dock3	UTSW	9	106,774,539 (GRCm39)	missense	probably benign
R8862:Dock3	UTSW	9	106,855,927 (GRCm39)	missense	probably damaging	1.00
R8952:Dock3	UTSW	9	106,850,958 (GRCm39)	missense	probably benign	0.03
R9230:Dock3	UTSW	9	106,807,223 (GRCm39)	missense	probably damaging	1.00
R9269:Dock3	UTSW	9	106,818,522 (GRCm39)	missense	probably benign	0.01
R9272:Dock3	UTSW	9	106,774,569 (GRCm39)	missense	probably benign	0.00
R9344:Dock3	UTSW	9	106,870,763 (GRCm39)	missense	probably damaging	1.00
R9757:Dock3	UTSW	9	106,901,035 (GRCm39)	missense	possibly damaging	0.48
R9764:Dock3	UTSW	9	106,959,713 (GRCm39)	missense	probably benign	0.00
R9766:Dock3	UTSW	9	106,788,483 (GRCm39)	missense	probably benign	0.01
X0023:Dock3	UTSW	9	106,863,197 (GRCm39)	missense	possibly damaging	0.95

Predicted Primers

PCR Primer
(F):5'- GCATGGTAAGTTTTAGCTACATGG -3'
(R):5'- CTCAGTAACATAGGGTACAGATCTGG -3'

Sequencing Primer
(F):5'- GCTACATGGAATCAAACTTGAAAAC -3'
(R):5'- CATAGGGTACAGATCTGGATTGG -3'

Posted On

2019-10-07