Mutagenetix > Incidental Mutation

Incidental Mutation 'R8347:Dennd2c'

645280

Institutional Source

Beutler Lab

Gene Symbol

Dennd2c

Ensembl Gene

ENSMUSG00000007379

Gene Name

DENN/MADD domain containing 2C

Synonyms

MMRRC Submission

067867-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R8347 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

103102604-103169769 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 103157709 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 716 (Y716C)

Ref Sequence

ENSEMBL: ENSMUSP00000127187 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000172288] [ENSMUST00000173206]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000172288
AA Change: Y716C

PolyPhen 2 Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000127187
Gene: ENSMUSG00000007379
AA Change: Y716C

Domain	Start	End	E-Value	Type
uDENN	481	571	1.01e-25	SMART
DENN	578	762	3.36e-77	SMART
dDENN	806	873	1.15e-20	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000173206
AA Change: Y659C

PolyPhen 2 Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000134008
Gene: ENSMUSG00000007379
AA Change: Y659C

Domain	Start	End	E-Value	Type
uDENN	424	514	1.01e-25	SMART
DENN	521	705	3.36e-77	SMART
dDENN	749	816	1.15e-20	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 98.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 69 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700014D04Rik	T	A	13: 59,742,236 (GRCm38)	D590V	possibly damaging	Het
1700123K08Rik	T	A	5: 138,562,891 (GRCm38)	I170L	probably benign	Het
Adamts15	C	T	9: 30,902,550 (GRCm38)	R773Q	probably benign	Het
Ankib1	A	G	5: 3,747,065 (GRCm38)	L249P	probably damaging	Het
Cabin1	A	G	10: 75,742,367 (GRCm38)	F499L	probably damaging	Het
Clec12b	C	T	6: 129,380,487 (GRCm38)		probably null	Het
Col23a1	G	A	11: 51,571,256 (GRCm38)	G373D	probably damaging	Het
Cse1l	C	T	2: 166,927,585 (GRCm38)	T304I	possibly damaging	Het
D6Wsu163e	T	A	6: 126,955,288 (GRCm38)	L330*	probably null	Het
Dbi	A	C	1: 120,120,820 (GRCm38)	L32R	possibly damaging	Het
Dnah5	G	A	15: 28,236,666 (GRCm38)	M379I	possibly damaging	Het
Dpys	T	C	15: 39,857,313 (GRCm38)	D17G	probably benign	Het
Dync2h1	C	T	9: 7,116,578 (GRCm38)	S2319N	possibly damaging	Het
Dyrk2	T	C	10: 118,859,983 (GRCm38)	K457E	probably damaging	Het
Efs	A	G	14: 54,919,784 (GRCm38)	C357R	probably benign	Het
Egfr	T	A	11: 16,878,174 (GRCm38)	W516R	probably damaging	Het
Folh1	T	A	7: 86,729,118 (GRCm38)	R529*	probably null	Het
Fsip2	A	C	2: 82,987,854 (GRCm38)	I4644L	probably benign	Het
Garnl3	T	C	2: 33,085,891 (GRCm38)	Y66C	probably damaging	Het
Gli3	T	C	13: 15,723,525 (GRCm38)	L730P	probably damaging	Het
Gm19668	T	C	10: 77,798,387 (GRCm38)	*249W	probably null	Het
Gm28710	G	A	5: 16,801,574 (GRCm38)	M96I	probably benign	Het
Ighv2-6-8	T	C	12: 113,796,327 (GRCm38)	D54G	probably benign	Het
Irs2	C	A	8: 11,008,000 (GRCm38)	S144I	possibly damaging	Het
Itgb5	T	C	16: 33,940,678 (GRCm38)	C628R	probably damaging	Het
Kcnh4	A	T	11: 100,757,749 (GRCm38)	V43D	probably damaging	Het
Krtap16-3	A	T	16: 88,962,619 (GRCm38)	Y69N	unknown	Het
Lcn12	A	C	2: 25,492,033 (GRCm38)	D176E	possibly damaging	Het
Lilr4b	T	A	10: 51,481,754 (GRCm38)	F181L	probably damaging	Het
Med13l	T	A	5: 118,742,597 (GRCm38)	H1251Q	probably benign	Het
Nppb	C	A	4: 147,986,299 (GRCm38)	L44M	probably damaging	Het
Nutm2	T	C	13: 50,472,337 (GRCm38)	V320A	probably benign	Het
Olfr1272	A	T	2: 90,281,676 (GRCm38)	W300R	probably benign	Het
Olfr291	C	T	7: 84,856,755 (GRCm38)	P131S	probably damaging	Het
Olfr628	A	G	7: 103,731,943 (GRCm38)	S6G	probably benign	Het
Olfr987	T	A	2: 85,331,703 (GRCm38)	H65L	probably damaging	Het
Padi6	T	C	4: 140,735,408 (GRCm38)	M301V	probably benign	Het
Pappa	G	A	4: 65,327,065 (GRCm38)	R1530Q	probably damaging	Het
Pcgf6	C	T	19: 47,045,838 (GRCm38)	D255N	possibly damaging	Het
Pgap3	TCAGCAGCAGCAGCAGCAG	TCAGCAGCAGCAGCAG	11: 98,390,749 (GRCm38)		probably benign	Het
Phip	A	G	9: 82,908,763 (GRCm38)	I710T	probably benign	Het
Pla2r1	A	T	2: 60,534,903 (GRCm38)	Y108N	probably damaging	Het
Plat	G	T	8: 22,772,232 (GRCm38)	G91W	probably damaging	Het
Rint1	C	G	5: 23,811,772 (GRCm38)	L512V	probably damaging	Het
Sdad1	A	C	5: 92,298,229 (GRCm38)	F282L	probably benign	Het
Sirt5	G	T	13: 43,380,501 (GRCm38)	A189S	probably benign	Het
Slc14a1	T	C	18: 78,111,431 (GRCm38)	T247A	probably benign	Het
Slc22a6	C	G	19: 8,621,805 (GRCm38)	R267G	probably damaging	Het
Slfn3	A	G	11: 83,213,589 (GRCm38)	K429E	possibly damaging	Het
Spag17	T	C	3: 100,027,641 (GRCm38)	F721S	probably benign	Het
St3gal1	G	A	15: 67,113,662 (GRCm38)	R48C	probably damaging	Het
Sult2a6	A	G	7: 14,225,958 (GRCm38)	Y217H	probably benign	Het
Synj2	A	G	17: 6,009,785 (GRCm38)	N394S	probably damaging	Het
Telo2	A	T	17: 25,104,637 (GRCm38)	Y605*	probably null	Het
Trank1	T	A	9: 111,367,249 (GRCm38)	L1447Q	probably damaging	Het
Trim56	A	G	5: 137,112,592 (GRCm38)	L690P	probably damaging	Het
Trmt13	T	C	3: 116,582,768 (GRCm38)	T325A	probably benign	Het
Ttn	T	A	2: 76,709,467 (GRCm38)	T34392S	probably benign	Het
Uncx	A	G	5: 139,546,816 (GRCm38)	E212G	probably damaging	Het
Ush2a	A	G	1: 188,947,084 (GRCm38)	T4830A	probably benign	Het
Usp34	C	A	11: 23,412,345 (GRCm38)	T1616N		Het
Vars	C	T	17: 35,015,977 (GRCm38)	L1261F	possibly damaging	Het
Vmn1r223	T	C	13: 23,249,850 (GRCm38)	S205P	probably damaging	Het
Vmn2r118	A	T	17: 55,610,423 (GRCm38)	I363K	possibly damaging	Het
Vmn2r69	A	T	7: 85,415,630 (GRCm38)	M16K	probably benign	Het
Wdr62	G	A	7: 30,262,703 (GRCm38)	T428I	possibly damaging	Het
Yeats4	A	T	10: 117,217,469 (GRCm38)	L129Q	probably benign	Het
Zfp423	T	C	8: 87,783,156 (GRCm38)	R187G	probably damaging	Het
Zfp853	A	T	5: 143,288,947 (GRCm38)	L321Q	unknown	Het

Other mutations in Dennd2c

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01763:Dennd2c	APN	3	103,156,908 (GRCm38)	missense	probably damaging	1.00
IGL01791:Dennd2c	APN	3	103,166,425 (GRCm38)	missense	probably benign	0.19
IGL02100:Dennd2c	APN	3	103,153,675 (GRCm38)	missense	probably damaging	0.98
IGL02119:Dennd2c	APN	3	103,137,243 (GRCm38)	missense	probably damaging	0.99
IGL02395:Dennd2c	APN	3	103,157,765 (GRCm38)	missense	probably benign	0.00
IGL02631:Dennd2c	APN	3	103,156,071 (GRCm38)	missense	possibly damaging	0.56
IGL02895:Dennd2c	APN	3	103,137,203 (GRCm38)	missense	possibly damaging	0.76
convolution	UTSW	3	103,156,107 (GRCm38)	missense	probably damaging	1.00
Resolution	UTSW	3	103,133,345 (GRCm38)	missense	possibly damaging	0.51
R1749:Dennd2c	UTSW	3	103,132,036 (GRCm38)	missense	possibly damaging	0.92
R1931:Dennd2c	UTSW	3	103,133,252 (GRCm38)	missense	probably benign	0.32
R1964:Dennd2c	UTSW	3	103,166,491 (GRCm38)	missense	probably damaging	1.00
R1972:Dennd2c	UTSW	3	103,131,698 (GRCm38)	missense	probably benign	0.01
R1973:Dennd2c	UTSW	3	103,131,698 (GRCm38)	missense	probably benign	0.01
R2025:Dennd2c	UTSW	3	103,131,689 (GRCm38)	missense	possibly damaging	0.71
R2350:Dennd2c	UTSW	3	103,132,001 (GRCm38)	missense	probably benign	0.00
R2373:Dennd2c	UTSW	3	103,156,842 (GRCm38)	missense	probably damaging	0.99
R4555:Dennd2c	UTSW	3	103,131,886 (GRCm38)	missense	probably benign	0.00
R4916:Dennd2c	UTSW	3	103,131,824 (GRCm38)	missense	probably benign	0.00
R5560:Dennd2c	UTSW	3	103,161,555 (GRCm38)	missense	probably damaging	1.00
R6291:Dennd2c	UTSW	3	103,131,609 (GRCm38)	nonsense	probably null
R6395:Dennd2c	UTSW	3	103,149,224 (GRCm38)	critical splice donor site	probably null
R6567:Dennd2c	UTSW	3	103,132,019 (GRCm38)	missense	probably benign	0.02
R6681:Dennd2c	UTSW	3	103,131,661 (GRCm38)	missense	probably benign	0.01
R7106:Dennd2c	UTSW	3	103,131,577 (GRCm38)	missense	possibly damaging	0.82
R7162:Dennd2c	UTSW	3	103,156,107 (GRCm38)	missense	probably damaging	1.00
R7514:Dennd2c	UTSW	3	103,163,062 (GRCm38)	missense	probably benign	0.00
R7591:Dennd2c	UTSW	3	103,133,345 (GRCm38)	missense	possibly damaging	0.51
R7698:Dennd2c	UTSW	3	103,165,043 (GRCm38)	missense	possibly damaging	0.65
R8069:Dennd2c	UTSW	3	103,165,130 (GRCm38)	missense	probably damaging	1.00
R8086:Dennd2c	UTSW	3	103,133,345 (GRCm38)	missense	possibly damaging	0.51
R8247:Dennd2c	UTSW	3	103,152,321 (GRCm38)	missense	probably damaging	0.99
R8829:Dennd2c	UTSW	3	103,152,404 (GRCm38)	critical splice donor site	probably null
R8832:Dennd2c	UTSW	3	103,152,404 (GRCm38)	critical splice donor site	probably null
R9131:Dennd2c	UTSW	3	103,157,715 (GRCm38)	missense	probably damaging	1.00
R9332:Dennd2c	UTSW	3	103,131,561 (GRCm38)	missense	probably benign	0.01
R9350:Dennd2c	UTSW	3	103,131,992 (GRCm38)	missense	possibly damaging	0.79
R9520:Dennd2c	UTSW	3	103,137,168 (GRCm38)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- TAGTGAACCAGACTGAGATGACTG -3'
(R):5'- AAGATCATTTGATTCCGTTGCC -3'

Sequencing Primer
(F):5'- CCAGACTGAGATGACTGTTAAAATG -3'
(R):5'- GCCAATACTCTAGTGTTCCCCATAGG -3'

Posted On

2020-09-02