Mutagenetix > Incidental Mutation

Incidental Mutation 'R9150:Gm8267'

694985

Institutional Source

Beutler Lab

Gene Symbol

Gm8267

Ensembl Gene

ENSMUSG00000091923

Gene Name

predicted gene 8267

Synonyms

MMRRC Submission

068938-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.108) question?

Stock #

R9150 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

44954624-44962444 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 44955362 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Threonine at position 220 (S220T)

Ref Sequence

ENSEMBL: ENSMUSP00000129187 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000165003] [ENSMUST00000169062] [ENSMUST00000226900]

AlphaFold

E9Q207

Predicted Effect

probably benign
Transcript: ENSMUST00000165003
AA Change: S220T

PolyPhen 2 Score 0.177 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000129187
Gene: ENSMUSG00000091923
AA Change: S220T

Domain	Start	End	E-Value	Type
Pfam:Takusan	48	128	1.4e-28	PFAM
coiled coil region	144	175	N/A	INTRINSIC
transmembrane domain	238	260	N/A	INTRINSIC

Predicted Effect

SMART Domains

Protein: ENSMUSP00000129402
Gene: ENSMUSG00000091923
AA Change: V159D

Domain	Start	End	E-Value	Type
Pfam:Takusan	46	129	4.9e-37	PFAM
low complexity region	187	199	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000226900
AA Change: S220T

PolyPhen 2 Score 0.177 (Sensitivity: 0.92; Specificity: 0.87)

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.2%

Validation Efficiency

98% (56/57)

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Actl6b	CTCCGGTGAGTGCCTCATCC	CTCC	5: 137,553,354 (GRCm39)		probably null	Het
Ampd1	A	T	3: 102,988,359 (GRCm39)	I101F	possibly damaging	Het
Arhgap11a	A	G	2: 113,673,614 (GRCm39)	V92A	possibly damaging	Het
Arih1	C	A	9: 59,344,069 (GRCm39)	L189F	possibly damaging	Het
B4galt3	A	G	1: 171,103,899 (GRCm39)	R379G	probably benign	Het
Capn12	A	G	7: 28,590,378 (GRCm39)	N642D	probably benign	Het
Cdc42ep3	T	C	17: 79,642,299 (GRCm39)	H207R	probably benign	Het
Dcps	A	T	9: 35,035,938 (GRCm39)	L316H	probably damaging	Het
Dmgdh	A	G	13: 93,825,103 (GRCm39)	Y142C	probably damaging	Het
Elmo2	A	G	2: 165,140,607 (GRCm39)	V300A	probably damaging	Het
Eml6	A	T	11: 29,755,791 (GRCm39)	V821E	probably benign	Het
Fam181a	A	T	12: 103,282,139 (GRCm39)	N15Y	probably damaging	Het
Gm26657	G	T	4: 56,740,835 (GRCm39)	E7*	probably null	Het
Gpld1	A	T	13: 25,146,305 (GRCm39)	Y183F	probably damaging	Het
Gpr158	G	A	2: 21,831,251 (GRCm39)	G784R	probably benign	Het
Grm2	A	G	9: 106,524,657 (GRCm39)	L215P		Het
Gtpbp1	A	G	15: 79,592,165 (GRCm39)	D252G	probably damaging	Het
Heatr5b	A	G	17: 79,103,448 (GRCm39)	V1135A	probably benign	Het
Irag1	T	C	7: 110,498,205 (GRCm39)	T397A	probably benign	Het
Lrrc8e	A	C	8: 4,286,030 (GRCm39)	K752Q	probably benign	Het
Ltbp2	G	A	12: 84,837,864 (GRCm39)	P1192L	probably benign	Het
Mapre2	A	G	18: 23,991,208 (GRCm39)	T201A	probably benign	Het
Mcm9	A	T	10: 53,502,110 (GRCm39)	N85K		Het
Mdga1	T	C	17: 30,057,420 (GRCm39)	T92A	probably damaging	Het
Nemf	A	C	12: 69,387,820 (GRCm39)	D421E	probably benign	Het
Oga	A	T	19: 45,771,421 (GRCm39)	V50E	probably benign	Het
Or13g1	G	C	7: 85,955,942 (GRCm39)	F126L	probably damaging	Het
Or5k14	G	T	16: 58,693,005 (GRCm39)	C169*	probably null	Het
Or5m3	A	T	2: 85,838,626 (GRCm39)	K169*	probably null	Het
Or8k53	A	T	2: 86,177,336 (GRCm39)	M258K	probably damaging	Het
Pcdhga5	A	C	18: 37,827,933 (GRCm39)	N127T	probably damaging	Het
Phyhipl	A	T	10: 70,404,887 (GRCm39)	V107E	probably damaging	Het
Pkd1l1	G	A	11: 8,786,256 (GRCm39)	R2383C		Het
Ppp1r16a	G	A	15: 76,575,054 (GRCm39)		probably benign	Het
Pramel20	A	G	4: 143,298,531 (GRCm39)	Y158C	probably benign	Het
Rnf41	T	C	10: 128,272,399 (GRCm39)	V142A		Het
Sgcd	C	T	11: 46,870,170 (GRCm39)	V264I	probably damaging	Het
Six2	A	G	17: 85,992,763 (GRCm39)	S247P	probably benign	Het
Slc17a7	T	G	7: 44,820,167 (GRCm39)	Y241D	probably damaging	Het
Slc30a5	T	A	13: 100,939,915 (GRCm39)	K724*	probably null	Het
Slitrk1	T	A	14: 109,149,101 (GRCm39)	I537F	possibly damaging	Het
Sp140l2	T	A	1: 85,091,359 (GRCm39)	Q33L	probably damaging	Het
Spen	C	T	4: 141,244,468 (GRCm39)	R189Q	unknown	Het
Srd5a3	T	A	5: 76,297,615 (GRCm39)	L139Q	probably damaging	Het
Tgfbrap1	A	T	1: 43,114,985 (GRCm39)	Y38*	probably null	Het
Tln2	A	T	9: 67,128,778 (GRCm39)	M1437K	probably damaging	Het
Tmem87b	T	C	2: 128,687,401 (GRCm39)	I467T	probably damaging	Het
Tnfrsf21	T	A	17: 43,398,691 (GRCm39)	I599N	probably damaging	Het
Trmt112	T	A	19: 6,887,620 (GRCm39)	L23Q	probably damaging	Het
Tsc22d1	T	A	14: 76,654,056 (GRCm39)	N178K	probably damaging	Het
Ttc23	A	G	7: 67,375,850 (GRCm39)	Y476C	probably damaging	Het
Twf1	A	T	15: 94,484,274 (GRCm39)	W83R	probably damaging	Het
Vmn2r14	T	A	5: 109,367,783 (GRCm39)	H403L	probably damaging	Het
Wiz	A	T	17: 32,586,809 (GRCm39)	I167N	probably benign	Het
Zdhhc22	G	A	12: 87,035,192 (GRCm39)	P87S	probably benign	Het
Zfp618	C	T	4: 63,039,603 (GRCm39)	Q401*	probably null	Het
Zfp715	T	A	7: 42,948,713 (GRCm39)	I416F	possibly damaging	Het

Other mutations in Gm8267

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01345:Gm8267	APN	14	44,962,412 (GRCm39)	missense	probably damaging	0.98
IGL02031:Gm8267	APN	14	44,955,374 (GRCm39)	missense	possibly damaging	0.85
R3619:Gm8267	UTSW	14	44,961,513 (GRCm39)	missense	possibly damaging	0.95
R4715:Gm8267	UTSW	14	44,955,292 (GRCm39)	missense	probably benign	0.33
R6599:Gm8267	UTSW	14	44,955,367 (GRCm39)	missense	possibly damaging	0.86
R7001:Gm8267	UTSW	14	44,960,385 (GRCm39)	missense	possibly damaging	0.94
R7057:Gm8267	UTSW	14	44,959,481 (GRCm39)	missense	probably damaging	0.99
R7439:Gm8267	UTSW	14	44,960,397 (GRCm39)	missense	probably damaging	1.00
R7441:Gm8267	UTSW	14	44,960,397 (GRCm39)	missense	probably damaging	1.00
R8053:Gm8267	UTSW	14	44,962,307 (GRCm39)	missense	possibly damaging	0.82
R8313:Gm8267	UTSW	14	44,961,515 (GRCm39)	missense	probably damaging	0.97
R8721:Gm8267	UTSW	14	44,959,507 (GRCm39)	missense	possibly damaging	0.94
R9464:Gm8267	UTSW	14	44,960,346 (GRCm39)	missense	probably damaging	0.99
Z1088:Gm8267	UTSW	14	44,962,322 (GRCm39)	missense	probably benign	0.28

Predicted Primers

PCR Primer
(F):5'- TAGCTCTTGATGTGCCTCAGC -3'
(R):5'- ATGACACTTGGGGATGCAGG -3'

Sequencing Primer
(F):5'- AGCACATGTCTGAATTCCTCTACATG -3'
(R):5'- ATGCAGGGAATGACCTCAGCC -3'

Posted On

2022-01-20