Mutagenetix > Incidental Mutation

Incidental Mutation 'R1733:Dpp4'

199448

Institutional Source

Beutler Lab

Gene Symbol

Dpp4

Ensembl Gene

ENSMUSG00000035000

Gene Name

dipeptidylpeptidase 4

Synonyms

Dpp-4, THAM, Cd26

MMRRC Submission

039765-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1733 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

62330073-62412231 bp(-) (GRCm38)

Type of Mutation

critical splice acceptor site

DNA Base Change (assembly)

T to A at 62372869 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000044050 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000047812] [ENSMUST00000047812]

AlphaFold

P28843

Predicted Effect

probably null
Transcript: ENSMUST00000047812

SMART Domains

Protein: ENSMUSP00000044050
Gene: ENSMUSG00000035000

Domain	Start	End	E-Value	Type
transmembrane domain	7	29	N/A	INTRINSIC
Pfam:DPPIV_N	102	473	5.7e-110	PFAM
Pfam:Abhydrolase_5	545	752	1e-11	PFAM
Pfam:DLH	546	754	4e-7	PFAM
Pfam:Peptidase_S9	551	760	3.4e-61	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000047812

SMART Domains

Protein: ENSMUSP00000044050
Gene: ENSMUSG00000035000

Domain	Start	End	E-Value	Type
transmembrane domain	7	29	N/A	INTRINSIC
Pfam:DPPIV_N	102	473	5.7e-110	PFAM
Pfam:Abhydrolase_5	545	752	1e-11	PFAM
Pfam:DLH	546	754	4e-7	PFAM
Pfam:Peptidase_S9	551	760	3.4e-61	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000136879

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000149306

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150979

Coding Region Coverage

1x: 97.5%
3x: 96.9%
10x: 95.2%
20x: 91.9%

Validation Efficiency

95% (95/100)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is identical to adenosine deaminase complexing protein-2, and to the T-cell activation antigen CD26. It is an intrinsic membrane glycoprotein and a serine exopeptidase that cleaves X-proline dipeptides from the N-terminus of polypeptides. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous mutants show hypoglycemia, hyperinsulinemia, and increased plasma glucagon-like peptide 1 in glucose tolerance tests. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 93 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts19	T	G	18: 59,031,929	C1034W	probably damaging	Het
Agbl2	G	T	2: 90,810,745	K737N	probably damaging	Het
Aqp9	T	A	9: 71,112,342	I279F	possibly damaging	Het
Aspm	T	A	1: 139,457,117	N166K	probably benign	Het
Atp13a3	A	T	16: 30,357,266	I186N	probably benign	Het
Btaf1	A	T	19: 36,994,962	I1366L	probably benign	Het
Camk4	A	C	18: 33,078,021	K60Q	possibly damaging	Het
Card11	G	T	5: 140,906,633	Q226K	possibly damaging	Het
Ccdc187	T	C	2: 26,293,658	D110G	possibly damaging	Het
Col5a2	C	T	1: 45,407,032	R462Q	possibly damaging	Het
Cp	A	T	3: 19,968,219		probably benign	Het
Cpz	A	T	5: 35,517,758	V38E	probably damaging	Het
Cxcr6	G	A	9: 123,810,116	V68I	probably damaging	Het
Cyp2a22	C	A	7: 26,934,762	E322D	possibly damaging	Het
D130052B06Rik	C	T	11: 33,623,784	T127I	probably benign	Het
Daam2	T	A	17: 49,490,203	M185L	possibly damaging	Het
Dnaja3	G	A	16: 4,684,165	R11K	probably null	Het
Dnttip2	T	A	3: 122,276,748	S537R	probably benign	Het
Dock9	G	T	14: 121,626,880	H572Q	probably benign	Het
Enc1	T	G	13: 97,245,042	I20S	possibly damaging	Het
Ephb6	T	A	6: 41,619,720	H900Q	probably benign	Het
Ercc3	T	C	18: 32,267,165	V690A	possibly damaging	Het
Fam90a1a	C	T	8: 21,963,369	Q247*	probably null	Het
Fkbp10	G	A	11: 100,423,931	R423H	probably benign	Het
Fus	A	G	7: 127,981,545	M265V	probably benign	Het
Gas2l3	T	A	10: 89,414,265	K330N	probably damaging	Het
Gpam	T	G	19: 55,081,469	L410F	probably damaging	Het
Gpr37l1	A	T	1: 135,161,535	V264E	possibly damaging	Het
Grk6	A	T	13: 55,453,166		probably benign	Het
Gsto1	G	T	19: 47,855,235	V19F	probably damaging	Het
H1fnt	G	T	15: 98,256,135	Q378K	unknown	Het
Hgfac	G	A	5: 35,043,674	C194Y	probably damaging	Het
Hivep1	A	G	13: 42,157,931	N1216D	probably damaging	Het
Hrg	C	T	16: 22,951,247	A42V	probably damaging	Het
Irx4	A	G	13: 73,266,705	D136G	probably benign	Het
Kcnn3	G	T	3: 89,652,090	V556L	probably benign	Het
Klk8	T	C	7: 43,802,121	Y179H	possibly damaging	Het
Klrb1f	T	A	6: 129,054,359	L173*	probably null	Het
Kremen2	A	T	17: 23,743,399		probably null	Het
Krt25	A	T	11: 99,316,552	Y400*	probably null	Het
Lingo4	A	T	3: 94,403,178	R474S	probably benign	Het
Lnpep	T	C	17: 17,553,313	K599E	probably benign	Het
Mapk8ip3	A	T	17: 24,936,850	M2K	possibly damaging	Het
Mat2b	A	T	11: 40,680,077	S307T	probably benign	Het
Mcph1	C	A	8: 18,631,963	A372D	probably benign	Het
Mfsd6	T	A	1: 52,709,365	I114F	probably damaging	Het
Mlkl	A	G	8: 111,322,748	S248P	probably damaging	Het
Mmrn1	A	T	6: 60,977,101	T789S	probably benign	Het
Mphosph8	A	G	14: 56,693,459	Y735C	probably damaging	Het
Mrc1	T	A	2: 14,257,099	Y300N	probably damaging	Het
Mrps11	A	G	7: 78,792,712	H180R	probably damaging	Het
Msh4	T	C	3: 153,867,767	D556G	probably damaging	Het
Myh10	C	A	11: 68,802,296	D1472E	probably benign	Het
Myo16	T	C	8: 10,442,283	S742P	probably damaging	Het
Nlrp5-ps	C	T	7: 14,583,053		noncoding transcript	Het
Nrp1	C	T	8: 128,468,493	P477S	probably benign	Het
Olfr1278	T	C	2: 111,292,865	V199A	probably damaging	Het
Olfr1307	T	A	2: 111,945,280	M59L	probably benign	Het
Olfr64	T	C	7: 103,892,911	S275G	probably benign	Het
Olfr936	G	T	9: 39,047,382	H57N	unknown	Het
Oplah	G	T	15: 76,302,483	C665*	probably null	Het
Otogl	T	C	10: 107,783,712	T1696A	possibly damaging	Het
Pdzrn4	A	G	15: 92,401,974	I242V	probably benign	Het
Phgdh	G	A	3: 98,328,135	T141I	probably benign	Het
Pigv	T	C	4: 133,664,926	Y311C	probably damaging	Het
Pik3c2a	T	G	7: 116,418,520	M1L	possibly damaging	Het
Pitpnm1	A	T	19: 4,109,960	K760*	probably null	Het
Pnrc1	G	A	4: 33,246,438	H174Y	probably damaging	Het
Ptgis	A	G	2: 167,191,968		probably benign	Het
Ptpn4	T	C	1: 119,716,043		probably null	Het
Rin3	T	A	12: 102,369,330	L420*	probably null	Het
Sacs	T	G	14: 61,205,454	F1650V	probably damaging	Het
Sbno2	T	A	10: 80,058,508	N1081Y	possibly damaging	Het
Sema5b	C	T	16: 35,646,367	P213L	probably damaging	Het
Sharpin	T	C	15: 76,347,936	K240R	probably benign	Het
Skint6	T	A	4: 113,177,037		probably benign	Het
Slc4a2	A	G	5: 24,429,567	E68G	probably damaging	Het
Srcin1	C	T	11: 97,533,501	V634I	probably benign	Het
Srsf10	T	A	4: 135,863,165	F134I	possibly damaging	Het
Stab1	C	A	14: 31,145,303	G1700V	probably damaging	Het
Sun1	T	G	5: 139,230,789	C290W	possibly damaging	Het
Svs6	T	A	2: 164,317,657		probably benign	Het
Tmem8b	G	A	4: 43,690,228		probably null	Het
Usp49	A	G	17: 47,672,313	D81G	probably damaging	Het
Vmn1r215	T	A	13: 23,076,678	V296D	probably benign	Het
Vmn1r6	T	A	6: 57,002,622	S90T	probably damaging	Het
Wbp2	A	G	11: 116,083,883	F42L	probably benign	Het
Wdr20rt	C	T	12: 65,227,281	T333I	possibly damaging	Het
Zfp341	C	T	2: 154,641,378	A552V	probably benign	Het
Zfp607b	A	T	7: 27,692,524	H8L	possibly damaging	Het
Zfp758	G	T	17: 22,375,849	D439Y	probably damaging	Het
Zfp946	T	C	17: 22,453,557	Y46H	probably damaging	Het
Zic2	G	A	14: 122,478,947	E432K	probably damaging	Het

Other mutations in Dpp4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00492:Dpp4	APN	2	62379302	missense	probably damaging	1.00
IGL02205:Dpp4	APN	2	62352257	missense	probably damaging	1.00
IGL02276:Dpp4	APN	2	62356951	splice site	probably benign
IGL02335:Dpp4	APN	2	62334644	missense	probably benign	0.03
IGL02615:Dpp4	APN	2	62359328	missense	probably damaging	1.00
IGL02639:Dpp4	APN	2	62352240	missense	probably benign
IGL02972:Dpp4	APN	2	62352225	missense	probably damaging	1.00
IGL03366:Dpp4	APN	2	62356957	splice site	probably null
caribou	UTSW	2	62347901	missense	possibly damaging	0.69
PIT4449001:Dpp4	UTSW	2	62356644	missense	probably benign	0.00
R0502:Dpp4	UTSW	2	62364988	missense	probably damaging	0.99
R0581:Dpp4	UTSW	2	62356676	missense	probably benign
R1004:Dpp4	UTSW	2	62332640	missense	probably benign	0.08
R1075:Dpp4	UTSW	2	62352286	missense	probably benign	0.39
R1476:Dpp4	UTSW	2	62347901	missense	possibly damaging	0.69
R1702:Dpp4	UTSW	2	62386429	critical splice donor site	probably null
R1707:Dpp4	UTSW	2	62359335	splice site	probably benign
R1899:Dpp4	UTSW	2	62345050	splice site	probably benign
R2264:Dpp4	UTSW	2	62378239	missense	possibly damaging	0.71
R2496:Dpp4	UTSW	2	62387133	missense	possibly damaging	0.90
R3765:Dpp4	UTSW	2	62386436	missense	probably benign	0.17
R4278:Dpp4	UTSW	2	62379323	missense	probably damaging	1.00
R4413:Dpp4	UTSW	2	62387140	missense	possibly damaging	0.89
R4432:Dpp4	UTSW	2	62345112	missense	probably damaging	1.00
R4647:Dpp4	UTSW	2	62334605	missense	probably damaging	1.00
R4710:Dpp4	UTSW	2	62360315	missense	probably benign	0.04
R4914:Dpp4	UTSW	2	62347892	missense	probably benign	0.20
R5173:Dpp4	UTSW	2	62387130	missense	probably damaging	1.00
R5283:Dpp4	UTSW	2	62360336	missense	probably damaging	1.00
R5698:Dpp4	UTSW	2	62334311	missense	probably damaging	1.00
R6621:Dpp4	UTSW	2	62352140	missense	probably damaging	1.00
R6681:Dpp4	UTSW	2	62348549	missense	probably benign	0.01
R6739:Dpp4	UTSW	2	62387095	missense	probably benign
R6962:Dpp4	UTSW	2	62372830	missense	probably benign	0.11
R7249:Dpp4	UTSW	2	62385203	missense	probably benign	0.14
R7268:Dpp4	UTSW	2	62347842	missense	probably damaging	1.00
R7343:Dpp4	UTSW	2	62358901	nonsense	probably null
R7357:Dpp4	UTSW	2	62387077	missense	probably benign
R7366:Dpp4	UTSW	2	62354599	missense	probably damaging	1.00
R7413:Dpp4	UTSW	2	62356989	missense	probably damaging	1.00
R7431:Dpp4	UTSW	2	62352238	missense	probably benign	0.01
R7642:Dpp4	UTSW	2	62360283	critical splice donor site	probably null
R8004:Dpp4	UTSW	2	62358828	missense	probably benign	0.00
R8197:Dpp4	UTSW	2	62372827	missense	probably benign	0.31
R8341:Dpp4	UTSW	2	62347890	missense	probably benign	0.10
R8706:Dpp4	UTSW	2	62378303	missense	probably benign	0.00
R8977:Dpp4	UTSW	2	62374403	missense	probably benign	0.29
R8997:Dpp4	UTSW	2	62334614	missense	probably damaging	0.99
R9100:Dpp4	UTSW	2	62374389	missense	possibly damaging	0.51
R9616:Dpp4	UTSW	2	62387085	missense	probably damaging	1.00
R9777:Dpp4	UTSW	2	62364996	missense	probably benign	0.04

Predicted Primers

PCR Primer
(F):5'- AGGTAGTGGAAAGCGATCTACACCC -3'
(R):5'- CGGCACAAAGCACACAGATTCTGAG -3'

Sequencing Primer
(F):5'- CAAGCACTCAGGTAGAGCATC -3'
(R):5'- CCATAATTCAGATAGTTTAATGCAGC -3'

Posted On

2014-05-23