Mutagenetix > Incidental Mutations

Incidental Mutation 'R0046:Dpp3'

15821

Institutional Source

Beutler Lab

Gene Symbol

Dpp3

Ensembl Gene

ENSMUSG00000063904

Gene Name

dipeptidylpeptidase 3

Synonyms

4930533O14Rik

MMRRC Submission

038340-MU

Accession Numbers

Is this an essential gene?

Possibly non essential (E-score: 0.311) question?

Stock #

R0046 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

4907229-4928287 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 4914643 bp

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Lysine at position 545 (N545K)

Ref Sequence

ENSEMBL: ENSMUSP00000025851 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000025851]

Predicted Effect

probably damaging
Transcript: ENSMUST00000025851
AA Change: N545K

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000025851
Gene: ENSMUSG00000063904
AA Change: N545K

Domain	Start	End	E-Value	Type
Pfam:Peptidase_M49	143	704	1.3e-236	PFAM

Meta Mutation Damage Score

0.1535

Coding Region Coverage

1x: 89.2%
3x: 86.2%
10x: 78.3%
20x: 64.0%

Validation Efficiency

98% (86/88)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that is a member of the M49 family of metallopeptidases. This cytoplasmic protein binds a single zinc ion with its zinc-binding motif (HELLGH) and has post-proline dipeptidyl aminopeptidase activity, cleaving Xaa-Pro dipeptides from the N-termini of proteins. Increased activity of this protein is associated with endometrial and ovarian cancers. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Feb 2012]

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Actl7a	A	T	4: 56,743,877	K135*	probably null	Het
Adamts16	A	G	13: 70,763,460	S871P	probably benign	Het
Adcy10	A	T	1: 165,539,834	I558F	probably damaging	Het
Adsl	T	G	15: 80,962,788		probably null	Het
Aldob	T	C	4: 49,543,842	I47V	possibly damaging	Het
Alkbh8	A	G	9: 3,343,247	E46G	probably damaging	Het
Atp1a4	A	T	1: 172,240,097	L533Q	probably benign	Het
Auts2	T	C	5: 131,770,785		noncoding transcript	Het
B3gnt3	T	C	8: 71,692,923	Y267C	probably damaging	Het
BC051142	T	C	17: 34,460,121		probably null	Het
Ccdc39	A	G	3: 33,844,152	F15L	possibly damaging	Het
Cntnap5c	T	G	17: 58,359,300	D1108E	probably benign	Het
Col14a1	G	A	15: 55,408,963		probably benign	Het
Col9a3	G	A	2: 180,609,487	A317T	possibly damaging	Het
Cpt1c	A	T	7: 44,959,832		probably benign	Het
Cpt2	A	G	4: 107,904,362		probably null	Het
Crebrf	T	A	17: 26,763,334	L565M	probably damaging	Het
Dmxl1	T	A	18: 49,878,082	V1102E	probably benign	Het
Dock4	G	A	12: 40,737,360		probably benign	Het
Elmo2	T	A	2: 165,298,726	N275I	probably damaging	Het
Farp1	A	G	14: 121,255,513	K509R	probably benign	Het
Flg	T	A	3: 93,277,721		probably benign	Het
Gas2l2	A	T	11: 83,421,910	W859R	probably damaging	Het
Gatm	T	C	2: 122,600,744	D254G	probably damaging	Het
Gjd4	T	A	18: 9,280,998	I27F	probably damaging	Het
Gm19410	A	G	8: 35,802,645	E1148G	probably benign	Het
Haus5	C	T	7: 30,654,180	V591I	probably benign	Het
Kcnab3	G	A	11: 69,330,227		probably null	Het
Limk1	T	C	5: 134,672,761	Y96C	probably damaging	Het
Lrp2bp	T	A	8: 46,013,155	Y100*	probably null	Het
Ly75	A	T	2: 60,339,457		probably benign	Het
Mamstr	T	G	7: 45,641,770		probably benign	Het
Man1a	A	G	10: 53,919,187	Y657H	probably damaging	Het
Marf1	G	A	16: 14,111,727	P1672S	possibly damaging	Het
Mboat7	T	C	7: 3,683,818	Y341C	probably damaging	Het
Nhsl1	A	T	10: 18,525,669	N881I	probably damaging	Het
Nox3	T	C	17: 3,682,961	Y225C	probably benign	Het
Olfr1214	C	T	2: 88,987,349	M284I	probably benign	Het
Olfr1260	C	T	2: 89,978,507	T243I	probably damaging	Het
Pclo	C	T	5: 14,540,479	T931M	unknown	Het
Pfas	G	T	11: 68,990,467	R1025S	probably benign	Het
Prg4	T	C	1: 150,456,086	T279A	possibly damaging	Het
Psma1	A	T	7: 114,267,205		probably benign	Het
Rab11fip1	A	G	8: 27,153,121	L550P	probably damaging	Het
Rgs12	T	A	5: 34,965,320	I149N	probably damaging	Het
Rmnd5a	T	C	6: 71,399,231	H195R	probably damaging	Het
Rnf17	T	C	14: 56,471,373	L750P	probably damaging	Het
Rtcb	T	C	10: 85,957,656	N18D	probably benign	Het
Seh1l	T	C	18: 67,792,016		probably null	Het
Sptbn2	T	C	19: 4,745,377		probably benign	Het
Stag3	C	T	5: 138,283,023		probably benign	Het
Taar2	G	A	10: 23,941,495	R311H	probably benign	Het
Taok3	C	T	5: 117,272,229	Q829*	probably null	Het
Ttn	A	G	2: 76,951,542		probably benign	Het
Unc79	A	G	12: 103,125,681	E1756G	probably damaging	Het
Usp35	A	T	7: 97,313,597		probably null	Het
Zbtb40	A	G	4: 136,987,278	C1067R	probably damaging	Het

Other mutations in Dpp3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01487:Dpp3	APN	19	4913892	missense	probably benign	0.00
IGL01657:Dpp3	APN	19	4918304	missense	possibly damaging	0.72
IGL02105:Dpp3	APN	19	4916771	missense	probably damaging	1.00
IGL02251:Dpp3	APN	19	4918315	missense	probably benign
IGL02669:Dpp3	APN	19	4923682	critical splice donor site	probably null
IGL02739:Dpp3	APN	19	4923728	missense	probably damaging	1.00
IGL02851:Dpp3	APN	19	4923131	missense	probably benign	0.06
R0046:Dpp3	UTSW	19	4914643	missense	probably damaging	0.99
R0053:Dpp3	UTSW	19	4923126	missense	probably damaging	0.99
R0505:Dpp3	UTSW	19	4914654	missense	probably damaging	1.00
R0681:Dpp3	UTSW	19	4914654	missense	probably damaging	1.00
R1163:Dpp3	UTSW	19	4914923	nonsense	probably null
R1200:Dpp3	UTSW	19	4923129	missense	probably benign
R1761:Dpp3	UTSW	19	4921149	missense	probably benign	0.37
R1931:Dpp3	UTSW	19	4917860	splice site	probably benign
R2255:Dpp3	UTSW	19	4918319	missense	probably benign
R2424:Dpp3	UTSW	19	4907707	nonsense	probably null
R3718:Dpp3	UTSW	19	4923065	critical splice donor site	probably null
R3727:Dpp3	UTSW	19	4923185	missense	probably benign	0.30
R5080:Dpp3	UTSW	19	4915080	missense	probably benign	0.00
R5587:Dpp3	UTSW	19	4918267	missense	probably damaging	0.98
R5786:Dpp3	UTSW	19	4918322	missense	possibly damaging	0.53
R5986:Dpp3	UTSW	19	4918357	missense	probably benign	0.18
R6128:Dpp3	UTSW	19	4922392	missense	probably benign	0.05
R6989:Dpp3	UTSW	19	4921167	missense	probably damaging	1.00
R7019:Dpp3	UTSW	19	4916789	missense	possibly damaging	0.83
R7070:Dpp3	UTSW	19	4918328	missense	probably benign	0.24
R7100:Dpp3	UTSW	19	4918041	missense	probably damaging	1.00
R7265:Dpp3	UTSW	19	4923769	missense	probably damaging	1.00
R7495:Dpp3	UTSW	19	4917913	missense	probably damaging	1.00

Posted On

2013-01-08