Mutagenetix > Incidental Mutation

Incidental Mutation 'R1897:Atf7ip2'

212077

Institutional Source

Beutler Lab

Gene Symbol

Atf7ip2

Ensembl Gene

ENSMUSG00000039200

Gene Name

activating transcription factor 7 interacting protein 2

Synonyms

4930558K11Rik, PSM2, Get-1

MMRRC Submission

039917-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.086) question?

Stock #

R1897 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

10010513-10068595 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 10028948 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Proline to Leucine at position 160 (P160L)

Ref Sequence

ENSEMBL: ENSMUSP00000113573 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000044005] [ENSMUST00000100191] [ENSMUST00000117220] [ENSMUST00000119023] [ENSMUST00000230872]

AlphaFold

Q3UL97

Predicted Effect

probably damaging
Transcript: ENSMUST00000044005
AA Change: P160L

PolyPhen 2 Score 0.966 (Sensitivity: 0.77; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000036731
Gene: ENSMUSG00000039200
AA Change: P160L

Domain	Start	End	E-Value	Type
Pfam:ATF7IP_BD	59	270	4.7e-75	PFAM
low complexity region	322	336	N/A	INTRINSIC
FN3	346	435	7.55e0	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000100191
AA Change: P160L

PolyPhen 2 Score 0.966 (Sensitivity: 0.77; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000097766
Gene: ENSMUSG00000039200
AA Change: P160L

Domain	Start	End	E-Value	Type
low complexity region	180	192	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000117220
AA Change: P160L

PolyPhen 2 Score 0.966 (Sensitivity: 0.77; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000113573
Gene: ENSMUSG00000039200
AA Change: P160L

Domain	Start	End	E-Value	Type
low complexity region	180	192	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000119023
AA Change: P160L

PolyPhen 2 Score 0.739 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000113480
Gene: ENSMUSG00000039200
AA Change: P160L

Domain	Start	End	E-Value	Type
low complexity region	180	192	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000133674

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000230210

Predicted Effect

probably benign
Transcript: ENSMUST00000230872

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 97.4%
3x: 96.8%
10x: 95.3%
20x: 92.8%

Validation Efficiency

99% (72/73)

Allele List at MGI

Other mutations in this stock

Total: 70 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acbd6	A	G	1: 155,434,564 (GRCm39)	S61G	probably damaging	Het
Acot12	A	G	13: 91,932,516 (GRCm39)	N504S	probably benign	Het
Adcy3	C	T	12: 4,223,450 (GRCm39)		probably benign	Het
Adcyap1r1	A	T	6: 55,456,179 (GRCm39)	H168L	probably damaging	Het
Adgrd1	A	G	5: 129,206,065 (GRCm39)	E213G	probably benign	Het
Aldh1l2	G	T	10: 83,338,389 (GRCm39)	T510K	probably damaging	Het
Apol7e	A	T	15: 77,602,094 (GRCm39)	M231L	probably benign	Het
Asb1	C	A	1: 91,474,647 (GRCm39)		probably null	Het
Atp8a1	A	G	5: 67,895,772 (GRCm39)	L554P	probably damaging	Het
Ccdc18	A	T	5: 108,343,908 (GRCm39)	M884L	probably benign	Het
Ccdc93	A	G	1: 121,418,941 (GRCm39)	I499V	probably benign	Het
Ccl20	A	G	1: 83,095,616 (GRCm39)	D60G	probably damaging	Het
Cdhr3	T	C	12: 33,095,192 (GRCm39)	T626A	possibly damaging	Het
Cep250	A	G	2: 155,818,015 (GRCm39)	E789G	probably damaging	Het
Cmpk2	T	C	12: 26,524,046 (GRCm39)	L281P	probably damaging	Het
Col6a6	A	T	9: 105,662,943 (GRCm39)	M198K	possibly damaging	Het
Crocc	G	A	4: 140,746,047 (GRCm39)	R1691C	probably damaging	Het
Csf1	C	T	3: 107,655,595 (GRCm39)	V90M	probably damaging	Het
Cul2	T	G	18: 3,414,164 (GRCm39)	M86R	probably benign	Het
Dbndd2	T	C	2: 164,330,584 (GRCm39)	F79S	probably damaging	Het
Dkk1	G	T	19: 30,526,678 (GRCm39)	N34K	possibly damaging	Het
Dnah6	T	A	6: 73,158,745 (GRCm39)	L619F	probably benign	Het
Eif2b5	T	C	16: 20,325,787 (GRCm39)	V588A	probably damaging	Het
Elf3	A	T	1: 135,184,875 (GRCm39)	Y104N	probably damaging	Het
Fahd2a	T	C	2: 127,278,530 (GRCm39)	D272G	probably damaging	Het
Fbxw15	A	T	9: 109,387,271 (GRCm39)	C188*	probably null	Het
Fbxw8	T	C	5: 118,266,941 (GRCm39)	Y174C	probably benign	Het
Gnl1	C	A	17: 36,299,584 (GRCm39)	P585Q	possibly damaging	Het
Greb1l	T	C	18: 10,498,992 (GRCm39)	S292P	probably benign	Het
Gsk3b	G	A	16: 38,037,446 (GRCm39)		probably null	Het
Hcls1	C	T	16: 36,783,005 (GRCm39)	P452L	probably damaging	Het
Hdlbp	A	T	1: 93,350,007 (GRCm39)		probably benign	Het
Hecw1	A	G	13: 14,552,525 (GRCm39)	S25P	probably damaging	Het
Hells	T	C	19: 38,928,928 (GRCm39)	V100A	probably benign	Het
Isl1	C	T	13: 116,439,866 (GRCm39)	E161K	probably benign	Het
Klra9	G	T	6: 130,162,555 (GRCm39)	N160K	possibly damaging	Het
Lama4	T	C	10: 38,936,182 (GRCm39)	V619A	probably damaging	Het
Mpc1	G	A	17: 8,515,710 (GRCm39)	R134Q	possibly damaging	Het
Myo5c	A	T	9: 75,199,523 (GRCm39)	N1377I	probably benign	Het
Myrf	T	C	19: 10,195,596 (GRCm39)	I607V	probably benign	Het
Or2g1	T	G	17: 38,107,075 (GRCm39)	S247A	probably benign	Het
Or8g53	A	T	9: 39,683,361 (GRCm39)	I245K	probably damaging	Het
Pik3c2b	A	G	1: 132,994,654 (GRCm39)	D206G	possibly damaging	Het
Pipox	A	G	11: 77,773,568 (GRCm39)	Y228H	probably damaging	Het
Pitrm1	T	A	13: 6,610,131 (GRCm39)	V401D	possibly damaging	Het
Plod1	C	T	4: 148,010,657 (GRCm39)	E265K	probably damaging	Het
Ptpn21	A	T	12: 98,646,664 (GRCm39)		probably null	Het
Qars1	C	T	9: 108,391,282 (GRCm39)	Q7*	probably null	Het
Rpap2	T	A	5: 107,780,961 (GRCm39)	V479E	possibly damaging	Het
Rsf1	G	A	7: 97,229,117 (GRCm39)		probably benign	Het
Rusc2	A	G	4: 43,421,749 (GRCm39)	Y723C	probably damaging	Het
Ryr2	A	T	13: 11,765,818 (GRCm39)	M1306K	probably benign	Het
Sesn3	A	C	9: 14,219,941 (GRCm39)	Y110S	probably damaging	Het
Sgce	C	T	6: 4,691,511 (GRCm39)	V319I	probably benign	Het
Slc15a5	G	T	6: 138,056,762 (GRCm39)	F51L	possibly damaging	Het
Slit2	T	A	5: 48,395,765 (GRCm39)	C723S	probably damaging	Het
Sncaip	A	G	18: 53,027,862 (GRCm39)		probably null	Het
Snx2	T	A	18: 53,330,950 (GRCm39)	D138E	probably damaging	Het
Spef2	A	T	15: 9,729,740 (GRCm39)	L126*	probably null	Het
Stam	T	C	2: 14,133,837 (GRCm39)	S195P	probably damaging	Het
Strn	T	C	17: 78,990,271 (GRCm39)	I82V	probably benign	Het
Synj2	T	A	17: 6,072,412 (GRCm39)	C202*	probably null	Het
Tecpr2	A	G	12: 110,899,681 (GRCm39)	D683G	probably benign	Het
Tfec	A	G	6: 16,835,307 (GRCm39)	V157A	probably damaging	Het
Tff1	T	G	17: 31,383,912 (GRCm39)	Q28P	probably benign	Het
Vmn2r86	A	G	10: 130,288,314 (GRCm39)	Y396H	probably damaging	Het
Vmn2r87	A	T	10: 130,307,829 (GRCm39)	M803K	probably damaging	Het
Vmn2r90	A	G	17: 17,953,566 (GRCm39)	K577E	probably damaging	Het
Vrk1	T	C	12: 106,002,799 (GRCm39)		probably benign	Het
Wdr20	A	G	12: 110,760,157 (GRCm39)	T348A	probably benign	Het

Other mutations in Atf7ip2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01926:Atf7ip2	APN	16	10,059,749 (GRCm39)	missense	probably damaging	0.99
IGL01937:Atf7ip2	APN	16	10,059,401 (GRCm39)	splice site	probably null
IGL02301:Atf7ip2	APN	16	10,028,911 (GRCm39)	missense	probably benign	0.32
R0575:Atf7ip2	UTSW	16	10,055,075 (GRCm39)	missense	probably damaging	1.00
R0671:Atf7ip2	UTSW	16	10,059,743 (GRCm39)	missense	possibly damaging	0.86
R1119:Atf7ip2	UTSW	16	10,058,476 (GRCm39)	missense	possibly damaging	0.83
R1182:Atf7ip2	UTSW	16	10,059,699 (GRCm39)	missense	possibly damaging	0.93
R1302:Atf7ip2	UTSW	16	10,058,472 (GRCm39)	missense	possibly damaging	0.84
R1346:Atf7ip2	UTSW	16	10,052,195 (GRCm39)	missense	probably damaging	1.00
R1349:Atf7ip2	UTSW	16	10,052,195 (GRCm39)	missense	probably damaging	1.00
R1372:Atf7ip2	UTSW	16	10,052,195 (GRCm39)	missense	probably damaging	1.00
R1672:Atf7ip2	UTSW	16	10,027,005 (GRCm39)	missense	probably damaging	1.00
R1696:Atf7ip2	UTSW	16	10,052,195 (GRCm39)	missense	probably damaging	1.00
R1932:Atf7ip2	UTSW	16	10,059,567 (GRCm39)	missense	possibly damaging	0.86
R2143:Atf7ip2	UTSW	16	10,058,509 (GRCm39)	missense	probably null	0.68
R4612:Atf7ip2	UTSW	16	10,059,427 (GRCm39)	missense	probably benign	0.33
R4732:Atf7ip2	UTSW	16	10,059,750 (GRCm39)	missense	possibly damaging	0.92
R4733:Atf7ip2	UTSW	16	10,059,750 (GRCm39)	missense	possibly damaging	0.92
R4934:Atf7ip2	UTSW	16	10,059,447 (GRCm39)	missense	possibly damaging	0.72
R6137:Atf7ip2	UTSW	16	10,019,275 (GRCm39)	missense	probably damaging	0.99
R6432:Atf7ip2	UTSW	16	10,022,534 (GRCm39)	missense	probably damaging	1.00
R7298:Atf7ip2	UTSW	16	10,027,032 (GRCm39)	missense	possibly damaging	0.82
R7517:Atf7ip2	UTSW	16	10,059,399 (GRCm39)	splice site	probably null
R7744:Atf7ip2	UTSW	16	10,059,522 (GRCm39)	missense	possibly damaging	0.93
R8124:Atf7ip2	UTSW	16	10,026,999 (GRCm39)	missense	possibly damaging	0.67
R8245:Atf7ip2	UTSW	16	10,019,262 (GRCm39)	missense	possibly damaging	0.93
R8527:Atf7ip2	UTSW	16	10,055,129 (GRCm39)	intron	probably benign
R9329:Atf7ip2	UTSW	16	10,059,738 (GRCm39)	missense	possibly damaging	0.51
R9566:Atf7ip2	UTSW	16	10,044,893 (GRCm39)	missense	probably benign	0.01
R9670:Atf7ip2	UTSW	16	10,058,512 (GRCm39)	missense	probably benign	0.00
R9779:Atf7ip2	UTSW	16	10,055,044 (GRCm39)	missense	possibly damaging	0.85
U24488:Atf7ip2	UTSW	16	10,022,537 (GRCm39)	missense	probably damaging	0.96
X0062:Atf7ip2	UTSW	16	10,027,138 (GRCm39)	splice site	probably null
Z1177:Atf7ip2	UTSW	16	10,059,504 (GRCm39)	missense	possibly damaging	0.52

Predicted Primers

PCR Primer
(F):5'- CCTGCATTTCATAAGACTACTTGG -3'
(R):5'- AGTGGCAAATACCATGACCTTGG -3'

Sequencing Primer
(F):5'- GCATTTCATAAGACTACTTGGTCAAG -3'
(R):5'- CTCTGGATATGCTGAGAATTTCCCAG -3'

Posted On

2014-06-30