Mutagenetix > Incidental Mutation

Incidental Mutation 'R3833:Pja2'

275510

Institutional Source

Beutler Lab

Gene Symbol

Pja2

Ensembl Gene

ENSMUSG00000024083

Gene Name

praja ring finger ubiquitin ligase 2

Synonyms

Neurodap1

MMRRC Submission

040888-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R3833 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

64588001-64638878 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 64616397 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 166 (D166G)

Ref Sequence

ENSEMBL: ENSMUSP00000134380 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000024888] [ENSMUST00000024889] [ENSMUST00000172733] [ENSMUST00000172818]

AlphaFold

Q80U04

Predicted Effect

probably benign
Transcript: ENSMUST00000024888
AA Change: D166G

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

SMART Domains

Protein: ENSMUSP00000024888
Gene: ENSMUSG00000024083
AA Change: D166G

Domain	Start	End	E-Value	Type
low complexity region	532	548	N/A	INTRINSIC
RING	633	673	3.84e-6	SMART
low complexity region	678	703	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000024889
AA Change: D166G

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

SMART Domains

Protein: ENSMUSP00000024889
Gene: ENSMUSG00000024083
AA Change: D166G

Domain	Start	End	E-Value	Type
low complexity region	470	486	N/A	INTRINSIC
RING	571	611	3.84e-6	SMART
low complexity region	616	641	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000172733
AA Change: D166G

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

SMART Domains

Protein: ENSMUSP00000133730
Gene: ENSMUSG00000024083
AA Change: D166G

Domain	Start	End	E-Value	Type
low complexity region	470	486	N/A	INTRINSIC
RING	571	611	3.84e-6	SMART
low complexity region	616	641	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000172818
AA Change: D166G

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

SMART Domains

Protein: ENSMUSP00000134380
Gene: ENSMUSG00000024083
AA Change: D166G

Domain	Start	End	E-Value	Type
low complexity region	532	548	N/A	INTRINSIC
RING	633	673	3.84e-6	SMART
low complexity region	678	703	N/A	INTRINSIC

Meta Mutation Damage Score

0.5191

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.7%
20x: 96.4%

Validation Efficiency

97% (70/72)

Allele List at MGI

Other mutations in this stock

Total: 73 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9630041A04Rik	G	A	9: 101,820,062 (GRCm39)	G161S	probably damaging	Het
Acp7	T	C	7: 28,314,519 (GRCm39)	D282G	probably benign	Het
Atp10d	T	A	5: 72,396,568 (GRCm39)	C258S	possibly damaging	Het
Atp6ap1	T	C	X: 73,340,813 (GRCm39)	I10T	possibly damaging	Het
Atp6v0d2	T	G	4: 19,922,395 (GRCm39)	N35H	probably damaging	Het
Bcat1	T	A	6: 144,955,834 (GRCm39)	D349V	probably damaging	Het
Cacnb2	A	T	2: 14,986,236 (GRCm39)	I338F	probably damaging	Het
Ccn6	T	C	10: 39,030,945 (GRCm39)	K193E	probably benign	Het
Ccr1	T	C	9: 123,764,324 (GRCm39)	T69A	possibly damaging	Het
Cenpe	T	G	3: 134,928,083 (GRCm39)		probably benign	Het
Cps1	G	A	1: 67,178,946 (GRCm39)	G53R	probably damaging	Het
Cstb	T	C	10: 78,263,184 (GRCm39)	F70L	probably benign	Het
Cyb5d2	G	T	11: 72,686,349 (GRCm39)	S80R	possibly damaging	Het
Cyfip2	T	C	11: 46,152,333 (GRCm39)	D485G	probably benign	Het
Cyp27b1	G	T	10: 126,886,929 (GRCm39)	V382L	probably damaging	Het
Cyp8b1	C	A	9: 121,745,109 (GRCm39)	Q74H	probably benign	Het
Dennd2a	G	A	6: 39,483,651 (GRCm39)	P403L	probably damaging	Het
Dennd2a	G	T	6: 39,483,657 (GRCm39)	S401Y	probably damaging	Het
Dnaaf5	T	C	5: 139,167,320 (GRCm39)	V447A	possibly damaging	Het
Dpp9	A	T	17: 56,506,113 (GRCm39)	F429I	possibly damaging	Het
Gcn1	A	T	5: 115,730,191 (GRCm39)	Q835L	probably benign	Het
Gtf2b	T	A	3: 142,477,153 (GRCm39)	D8E	probably benign	Het
Hao1	A	T	2: 134,364,925 (GRCm39)	V234D	probably damaging	Het
Hephl1	T	C	9: 14,981,044 (GRCm39)	E796G	probably damaging	Het
Herc4	A	G	10: 63,081,739 (GRCm39)	I21V	probably benign	Het
Htt	T	A	5: 34,979,062 (GRCm39)	V815D	probably benign	Het
Iglv2	A	T	16: 19,079,593 (GRCm39)	M1K	probably null	Het
Igsf8	G	T	1: 172,145,837 (GRCm39)	A315S	probably benign	Het
Il1a	T	C	2: 129,148,599 (GRCm39)	D37G	possibly damaging	Het
Iqcb1	T	A	16: 36,652,276 (GRCm39)	C62*	probably null	Het
Itgad	A	T	7: 127,785,405 (GRCm39)	T381S	probably damaging	Het
Itpkb	T	C	1: 180,161,260 (GRCm39)	V462A	probably benign	Het
Kalrn	T	A	16: 33,860,259 (GRCm39)	R199*	probably null	Het
Kif24	G	T	4: 41,395,064 (GRCm39)	A603D	probably damaging	Het
Kif26b	GAAA	GAA	1: 178,744,181 (GRCm39)		probably null	Het
Klrc3	A	G	6: 129,620,181 (GRCm39)	L24P	probably damaging	Het
Lmnb1	A	C	18: 56,861,598 (GRCm39)	D163A	probably benign	Het
Lrrc9	T	C	12: 72,529,765 (GRCm39)	L912P	probably damaging	Het
Mageh1	A	T	X: 151,820,004 (GRCm39)	W111R	probably damaging	Het
Mapk7	A	G	11: 61,380,680 (GRCm39)	S641P	possibly damaging	Het
Mapt	A	T	11: 104,177,961 (GRCm39)	Q38L	possibly damaging	Het
Med12	C	A	X: 100,339,498 (GRCm39)	P2037Q	possibly damaging	Het
Med22	A	G	2: 26,800,379 (GRCm39)	S17P	probably damaging	Het
Mep1b	C	T	18: 21,219,296 (GRCm39)	T150I	possibly damaging	Het
Mroh1	C	T	15: 76,285,819 (GRCm39)	T71I	probably benign	Het
Nap1l3	A	G	X: 121,305,995 (GRCm39)	V241A	possibly damaging	Het
Pcdhga6	A	T	18: 37,841,479 (GRCm39)	N400Y	probably damaging	Het
Pdgfd	T	C	9: 6,359,762 (GRCm39)	S278P	probably damaging	Het
Pgap1	A	G	1: 54,596,624 (GRCm39)	M39T	probably damaging	Het
Pgc	C	A	17: 48,040,236 (GRCm39)	F93L	probably null	Het
Phf14	A	G	6: 11,933,873 (GRCm39)		probably null	Het
Piezo2	A	G	18: 63,214,733 (GRCm39)		probably null	Het
Ppp1r12c	T	A	7: 4,485,785 (GRCm39)		probably benign	Het
Pus3	G	C	9: 35,477,874 (GRCm39)	G369R	probably benign	Het
Rhbdf2	T	A	11: 116,495,250 (GRCm39)	D251V	probably damaging	Het
Rsad1	A	G	11: 94,434,130 (GRCm39)	V366A	probably benign	Het
S100a10	T	C	3: 93,471,680 (GRCm39)	V88A	probably damaging	Het
Scarf1	T	C	11: 75,406,078 (GRCm39)	C121R	probably damaging	Het
Scn7a	A	G	2: 66,528,028 (GRCm39)	S821P	probably damaging	Het
Sco1	T	C	11: 66,944,605 (GRCm39)	V76A	probably damaging	Het
Sdsl	C	A	5: 120,601,183 (GRCm39)	A30S	probably benign	Het
Slc26a6	C	T	9: 108,733,117 (GRCm39)	T32I	possibly damaging	Het
Slit3	A	T	11: 35,579,509 (GRCm39)	S1229C	probably null	Het
Snd1	G	T	6: 28,531,403 (GRCm39)		probably benign	Het
Tdrd3	A	G	14: 87,718,221 (GRCm39)	T201A	probably damaging	Het
Tekt1	T	C	11: 72,245,645 (GRCm39)	N170S	probably benign	Het
Thsd1	T	G	8: 22,733,132 (GRCm39)	S60A	possibly damaging	Het
Tmem121b	C	T	6: 120,469,841 (GRCm39)	G292E	probably damaging	Het
Trim63	A	G	4: 134,048,507 (GRCm39)	N172S	probably benign	Het
Usp24	T	C	4: 106,219,209 (GRCm39)		probably null	Het
Zdhhc16	T	A	19: 41,926,553 (GRCm39)		probably null	Het
Zfp1010	T	C	2: 176,956,998 (GRCm39)	S167G	possibly damaging	Het
Zfp709	G	A	8: 72,642,906 (GRCm39)	V112M	probably benign	Het

Other mutations in Pja2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00904:Pja2	APN	17	64,590,526 (GRCm39)	missense	probably damaging	1.00
IGL00945:Pja2	APN	17	64,616,391 (GRCm39)	missense	probably benign	0.00
IGL01347:Pja2	APN	17	64,620,023 (GRCm39)	missense	probably benign	0.34
IGL01831:Pja2	APN	17	64,616,402 (GRCm39)	missense	probably benign	0.02
IGL01977:Pja2	APN	17	64,604,821 (GRCm39)	missense	probably benign	0.02
IGL02812:Pja2	APN	17	64,604,789 (GRCm39)	missense	probably damaging	1.00
G1patch:Pja2	UTSW	17	64,596,962 (GRCm39)	missense	probably damaging	1.00
H8441:Pja2	UTSW	17	64,618,192 (GRCm39)	missense	probably damaging	1.00
R0062:Pja2	UTSW	17	64,615,966 (GRCm39)	missense	probably damaging	1.00
R0062:Pja2	UTSW	17	64,615,966 (GRCm39)	missense	probably damaging	1.00
R0411:Pja2	UTSW	17	64,594,516 (GRCm39)	splice site	probably benign
R1240:Pja2	UTSW	17	64,616,613 (GRCm39)	missense	probably benign	0.00
R1528:Pja2	UTSW	17	64,616,217 (GRCm39)	missense	possibly damaging	0.75
R1996:Pja2	UTSW	17	64,594,639 (GRCm39)	critical splice acceptor site	probably null
R2111:Pja2	UTSW	17	64,597,031 (GRCm39)	missense	probably damaging	1.00
R2162:Pja2	UTSW	17	64,616,397 (GRCm39)	missense	probably benign	0.00
R2201:Pja2	UTSW	17	64,618,162 (GRCm39)	splice site	probably benign
R2276:Pja2	UTSW	17	64,599,865 (GRCm39)	missense	probably damaging	1.00
R2278:Pja2	UTSW	17	64,599,865 (GRCm39)	missense	probably damaging	1.00
R3831:Pja2	UTSW	17	64,616,397 (GRCm39)	missense	probably benign	0.00
R4598:Pja2	UTSW	17	64,620,025 (GRCm39)	start codon destroyed	probably null	0.69
R4801:Pja2	UTSW	17	64,599,857 (GRCm39)	missense	probably damaging	1.00
R4802:Pja2	UTSW	17	64,599,857 (GRCm39)	missense	probably damaging	1.00
R4983:Pja2	UTSW	17	64,616,053 (GRCm39)	missense	probably benign	0.00
R5634:Pja2	UTSW	17	64,599,862 (GRCm39)	missense	probably damaging	1.00
R5862:Pja2	UTSW	17	64,604,821 (GRCm39)	missense	probably benign	0.02
R5905:Pja2	UTSW	17	64,616,085 (GRCm39)	missense	probably benign	0.26
R6028:Pja2	UTSW	17	64,616,085 (GRCm39)	missense	probably benign	0.26
R6382:Pja2	UTSW	17	64,616,610 (GRCm39)	missense	probably benign	0.07
R6650:Pja2	UTSW	17	64,599,936 (GRCm39)	missense	probably damaging	1.00
R6725:Pja2	UTSW	17	64,596,962 (GRCm39)	missense	probably damaging	1.00
R6976:Pja2	UTSW	17	64,615,954 (GRCm39)	missense	probably damaging	1.00
R7250:Pja2	UTSW	17	64,616,451 (GRCm39)	missense	probably benign	0.01
R7389:Pja2	UTSW	17	64,604,722 (GRCm39)	missense	probably damaging	1.00
R7477:Pja2	UTSW	17	64,616,640 (GRCm39)	missense	possibly damaging	0.87
R7549:Pja2	UTSW	17	64,616,410 (GRCm39)	missense	probably damaging	0.98
R8405:Pja2	UTSW	17	64,616,505 (GRCm39)	missense	possibly damaging	0.87
R8458:Pja2	UTSW	17	64,599,843 (GRCm39)	missense	probably damaging	1.00
R8700:Pja2	UTSW	17	64,599,949 (GRCm39)	missense	probably damaging	1.00
R9128:Pja2	UTSW	17	64,616,470 (GRCm39)	missense	probably benign
R9336:Pja2	UTSW	17	64,590,432 (GRCm39)	missense	unknown
R9356:Pja2	UTSW	17	64,618,204 (GRCm39)	missense	probably damaging	1.00
R9658:Pja2	UTSW	17	64,599,868 (GRCm39)	missense	probably damaging	1.00
Z1176:Pja2	UTSW	17	64,599,864 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AAAGGTGCTGAATCTAGCTCTTC -3'
(R):5'- CTTGTGGTCCAGCACTGAATC -3'

Sequencing Primer
(F):5'- GGTGCTGAATCTAGCTCTTCAAACG -3'
(R):5'- GTGGTCCAGCACTGAATCAAAGC -3'

Posted On

2015-04-06