Mutagenetix > Incidental Mutation

Incidental Mutation 'R4518:Pacs2'

334086

Institutional Source

Beutler Lab

Gene Symbol

Pacs2

Ensembl Gene

ENSMUSG00000021143

Gene Name

phosphofurin acidic cluster sorting protein 2

Synonyms

6720425G15Rik, Pacs1l

MMRRC Submission

041762-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4518 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

112978128-113038021 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 113024289 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 360 (D360G)

Ref Sequence

ENSEMBL: ENSMUSP00000152145 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000084891] [ENSMUST00000220541] [ENSMUST00000223502]

AlphaFold

Q3V3Q7

Predicted Effect

probably benign
Transcript: ENSMUST00000084891
AA Change: D390G

PolyPhen 2 Score 0.315 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000081953
Gene: ENSMUSG00000021143
AA Change: D390G

Domain	Start	End	E-Value	Type
low complexity region	4	16	N/A	INTRINSIC
low complexity region	199	213	N/A	INTRINSIC
low complexity region	281	296	N/A	INTRINSIC
low complexity region	299	313	N/A	INTRINSIC
Pfam:Pacs-1	474	888	1.4e-208	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000197963

Predicted Effect

probably benign
Transcript: ENSMUST00000220541
AA Change: D360G

PolyPhen 2 Score 0.315 (Sensitivity: 0.90; Specificity: 0.89)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000220715

Predicted Effect

probably benign
Transcript: ENSMUST00000223502
AA Change: D390G

PolyPhen 2 Score 0.038 (Sensitivity: 0.94; Specificity: 0.82)

Meta Mutation Damage Score

0.0754

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.1%
20x: 94.9%

Validation Efficiency

98% (60/61)

MGI Phenotype

PHENOTYPE: Mice homozygous for a gene trap allele exhibit decreased sensitivity to TRAIL-induced spleen apoptosis. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 54 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3110082J24Rik	T	A	5: 30,311,006 (GRCm39)		probably null	Het
Abr	A	G	11: 76,363,344 (GRCm39)	S167P	possibly damaging	Het
Adamtsl2	T	C	2: 26,985,559 (GRCm39)	L481P	probably benign	Het
Atp8b3	C	T	10: 80,359,681 (GRCm39)	M984I	probably benign	Het
Brip1	G	A	11: 85,968,704 (GRCm39)	A827V	possibly damaging	Het
Carns1	T	G	19: 4,220,069 (GRCm39)	T389P	probably benign	Het
Ccdc88a	T	C	11: 29,432,651 (GRCm39)	I1219T	probably benign	Het
Cckar	T	C	5: 53,857,264 (GRCm39)	N311S	probably damaging	Het
Cenpc1	A	G	5: 86,195,446 (GRCm39)	S108P	possibly damaging	Het
Chpf	G	T	1: 75,451,689 (GRCm39)	S588R	probably damaging	Het
Clca3a2	T	A	3: 144,514,466 (GRCm39)	T414S	probably damaging	Het
Cntrl	A	G	2: 35,038,986 (GRCm39)	E1092G	probably damaging	Het
Crb2	C	A	2: 37,680,401 (GRCm39)	T443K	probably damaging	Het
Crppa	G	A	12: 36,523,179 (GRCm39)	V203I	possibly damaging	Het
Cwf19l1	A	G	19: 44,121,473 (GRCm39)	V25A	probably damaging	Het
Cyb561d1	T	C	3: 108,106,887 (GRCm39)	I111V	possibly damaging	Het
Dbn1	A	T	13: 55,624,042 (GRCm39)	I350N	possibly damaging	Het
Dnajb4	T	C	3: 151,890,813 (GRCm39)	I329V	probably benign	Het
Dnmt1	G	T	9: 20,823,274 (GRCm39)	D1055E	probably benign	Het
Fam168a	C	T	7: 100,483,247 (GRCm39)	A176V	probably damaging	Het
Farp2	A	G	1: 93,548,363 (GRCm39)	E1016G	probably benign	Het
Fibcd1	A	T	2: 31,707,207 (GRCm39)	V350E	probably damaging	Het
Galnt3	C	A	2: 65,923,954 (GRCm39)	R438L	probably damaging	Het
Golga4	T	A	9: 118,388,076 (GRCm39)	S1733T	probably benign	Het
Golgb1	G	A	16: 36,749,625 (GRCm39)	E3076K	probably damaging	Het
Grm7	A	G	6: 110,891,507 (GRCm39)		probably null	Het
Hcn2	T	C	10: 79,560,536 (GRCm39)	V289A	probably benign	Het
Hipk1	G	T	3: 103,657,688 (GRCm39)	H799N	probably damaging	Het
Klf14	A	G	6: 30,934,867 (GRCm39)	S256P	possibly damaging	Het
Muc6	T	A	7: 141,230,489 (GRCm39)	T1214S	probably benign	Het
Nlrp2	T	A	7: 5,328,055 (GRCm39)	D666V	possibly damaging	Het
Ntng1	A	G	3: 109,842,329 (GRCm39)	I148T	probably damaging	Het
Or4k35	T	C	2: 111,100,263 (GRCm39)	M150V	probably benign	Het
Or7d9	A	G	9: 20,197,546 (GRCm39)	I184V	probably benign	Het
Or7g27	T	A	9: 19,250,556 (GRCm39)	S267T	possibly damaging	Het
Orc4	G	A	2: 48,827,501 (GRCm39)	P31S	probably benign	Het
Pabir3	G	A	X: 52,382,376 (GRCm39)	R94H	possibly damaging	Het
Parp8	C	A	13: 117,032,209 (GRCm39)	L321F	possibly damaging	Het
Pdss2	T	A	10: 43,248,146 (GRCm39)	S217T	probably damaging	Het
Plekhn1	T	C	4: 156,309,988 (GRCm39)	S109G	probably damaging	Het
Prlr	C	A	15: 10,329,085 (GRCm39)	T520K	possibly damaging	Het
Prokr2	T	A	2: 132,216,012 (GRCm39)		probably null	Het
Rab3gap2	G	A	1: 184,999,265 (GRCm39)	V991I	probably benign	Het
Reln	T	C	5: 22,106,741 (GRCm39)	I3210V	probably benign	Het
Rims2	T	C	15: 39,300,922 (GRCm39)	Y218H	probably damaging	Het
Slc41a1	T	C	1: 131,766,863 (GRCm39)	V127A	probably damaging	Het
St8sia6	T	A	2: 13,797,562 (GRCm39)		probably null	Het
Tlr6	A	G	5: 65,112,247 (GRCm39)	F220S	possibly damaging	Het
Trmt1l	C	T	1: 151,324,094 (GRCm39)	Q314*	probably null	Het
Ubqlnl	C	T	7: 103,798,925 (GRCm39)	V191M	probably benign	Het
Vnn3	G	A	10: 23,743,124 (GRCm39)	V445M	possibly damaging	Het
Ypel1	A	T	16: 16,913,905 (GRCm39)	F173I	possibly damaging	Het
Zfhx4	T	C	3: 5,477,578 (GRCm39)	C3398R	probably damaging	Het
Zfyve16	T	C	13: 92,657,820 (GRCm39)	E697G	possibly damaging	Het

Other mutations in Pacs2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01774:Pacs2	APN	12	113,020,462 (GRCm39)	missense	probably benign	0.01
IGL01830:Pacs2	APN	12	113,020,574 (GRCm39)	nonsense	probably null
IGL02229:Pacs2	APN	12	113,020,420 (GRCm39)	splice site	probably benign
IGL02307:Pacs2	APN	12	113,034,393 (GRCm39)	missense	probably damaging	1.00
IGL02700:Pacs2	APN	12	113,025,330 (GRCm39)	missense	probably damaging	1.00
BB003:Pacs2	UTSW	12	113,024,372 (GRCm39)	missense	probably damaging	1.00
BB013:Pacs2	UTSW	12	113,024,372 (GRCm39)	missense	probably damaging	1.00
R0241:Pacs2	UTSW	12	113,032,890 (GRCm39)	splice site	probably benign
R0433:Pacs2	UTSW	12	113,020,464 (GRCm39)	missense	possibly damaging	0.77
R0512:Pacs2	UTSW	12	113,014,547 (GRCm39)	missense	probably damaging	0.99
R0761:Pacs2	UTSW	12	113,023,688 (GRCm39)	splice site	probably benign
R2017:Pacs2	UTSW	12	113,026,077 (GRCm39)	missense	probably damaging	1.00
R2070:Pacs2	UTSW	12	113,024,731 (GRCm39)	missense	probably damaging	1.00
R2162:Pacs2	UTSW	12	113,014,567 (GRCm39)	missense	probably benign
R2231:Pacs2	UTSW	12	113,026,987 (GRCm39)	missense	probably damaging	1.00
R2232:Pacs2	UTSW	12	113,026,987 (GRCm39)	missense	probably damaging	1.00
R2396:Pacs2	UTSW	12	113,026,987 (GRCm39)	missense	probably damaging	1.00
R2397:Pacs2	UTSW	12	113,026,987 (GRCm39)	missense	probably damaging	1.00
R3010:Pacs2	UTSW	12	113,024,700 (GRCm39)	missense	probably benign
R3403:Pacs2	UTSW	12	113,014,570 (GRCm39)	missense	probably damaging	1.00
R3950:Pacs2	UTSW	12	113,024,733 (GRCm39)	missense	probably damaging	1.00
R3952:Pacs2	UTSW	12	113,024,733 (GRCm39)	missense	probably damaging	1.00
R5673:Pacs2	UTSW	12	113,032,618 (GRCm39)	missense	probably damaging	1.00
R5693:Pacs2	UTSW	12	113,013,526 (GRCm39)	missense	probably damaging	1.00
R7212:Pacs2	UTSW	12	113,025,312 (GRCm39)	missense	possibly damaging	0.77
R7926:Pacs2	UTSW	12	113,024,372 (GRCm39)	missense	probably damaging	1.00
R8032:Pacs2	UTSW	12	113,025,278 (GRCm39)	missense	probably damaging	1.00
R8224:Pacs2	UTSW	12	113,023,380 (GRCm39)	missense	probably damaging	1.00
R8944:Pacs2	UTSW	12	113,020,476 (GRCm39)	missense	probably damaging	1.00
R9036:Pacs2	UTSW	12	113,026,104 (GRCm39)	missense	possibly damaging	0.93
R9253:Pacs2	UTSW	12	113,014,137 (GRCm39)	missense	probably benign	0.00
R9461:Pacs2	UTSW	12	113,010,727 (GRCm39)	missense	probably benign	0.36
Z1177:Pacs2	UTSW	12	113,034,350 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGCTGATCATAGTTGGTCCAAG -3'
(R):5'- CTAGTGACCAAGTGGCTTCC -3'

Sequencing Primer
(F):5'- CTGATCATAGTTGGTCCAAGAGTTAC -3'
(R):5'- GGCTTCCCACAACCCTG -3'

Posted On

2015-08-18