Mutagenetix > Incidental Mutation

Incidental Mutation 'R1221:Gm136'

100062

Institutional Source

Beutler Lab

Gene Symbol

Gm136

Ensembl Gene

ENSMUSG00000071015

Gene Name

predicted gene 136

Synonyms

LOC214568

MMRRC Submission

039290-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.064) question?

Stock #

R1221 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

34743788-34756259 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 34744127 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Glutamic Acid at position 239 (A239E)

Ref Sequence

ENSEMBL: ENSMUSP00000092748 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000095129]

AlphaFold

Q3V037

Predicted Effect

possibly damaging
Transcript: ENSMUST00000095129
AA Change: A239E

PolyPhen 2 Score 0.711 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000092748
Gene: ENSMUSG00000071015
AA Change: A239E

Domain	Start	End	E-Value	Type
low complexity region	72	83	N/A	INTRINSIC
coiled coil region	119	189	N/A	INTRINSIC
coiled coil region	223	251	N/A	INTRINSIC

Coding Region Coverage

1x: 99.2%
3x: 98.4%
10x: 96.7%
20x: 94.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 49 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aak1	T	C	6: 86,942,460 (GRCm39)	S668P	unknown	Het
Anks1	A	G	17: 28,269,616 (GRCm39)	Q770R	possibly damaging	Het
Apc2	G	A	10: 80,142,214 (GRCm39)	V378I	probably damaging	Het
Apeh	A	G	9: 107,969,808 (GRCm39)	V184A	probably benign	Het
AU018091	A	G	7: 3,208,717 (GRCm39)	F404S	probably damaging	Het
Bap1	T	C	14: 30,979,608 (GRCm39)	L537P	probably damaging	Het
Bhlha15	A	G	5: 144,128,341 (GRCm39)	Y151C	probably damaging	Het
Bmp8b	A	T	4: 123,008,504 (GRCm39)	T157S	probably damaging	Het
Btbd1	G	T	7: 81,468,005 (GRCm39)	H172N	possibly damaging	Het
C1rl	A	G	6: 124,470,940 (GRCm39)	R83G	probably benign	Het
Cep104	A	G	4: 154,072,902 (GRCm39)	T387A	probably benign	Het
Cfi	A	T	3: 129,666,618 (GRCm39)	Q447L	probably damaging	Het
Cimap1a	G	T	7: 140,428,296 (GRCm39)	W10L	probably damaging	Het
Coq6	A	G	12: 84,418,301 (GRCm39)	E295G	possibly damaging	Het
Dclre1a	T	C	19: 56,519,700 (GRCm39)	T978A	possibly damaging	Het
Dlc1	T	C	8: 37,051,985 (GRCm39)	D582G	probably benign	Het
Dlgap2	A	G	8: 14,776,952 (GRCm39)	T65A	probably benign	Het
Dock5	G	A	14: 67,996,610 (GRCm39)	S1711L	probably benign	Het
Drc3	A	C	11: 60,275,052 (GRCm39)	I338L	probably benign	Het
Dsc1	A	T	18: 20,247,599 (GRCm39)	C5*	probably null	Het
F5	A	G	1: 163,989,368 (GRCm39)	Y90C	probably damaging	Het
Gdf10	G	A	14: 33,654,710 (GRCm39)	A406T	probably benign	Het
Gm4952	A	T	19: 12,601,059 (GRCm39)	D93V	possibly damaging	Het
Gramd1c	T	C	16: 43,810,227 (GRCm39)	T454A	possibly damaging	Het
Gstm6	A	G	3: 107,848,418 (GRCm39)	I58T	probably damaging	Het
Kdm3b	C	T	18: 34,941,298 (GRCm39)	S263L	possibly damaging	Het
Kdm5b	G	C	1: 134,526,829 (GRCm39)	S317T	probably damaging	Het
Myo15b	A	G	11: 115,777,546 (GRCm39)	R71G	possibly damaging	Het
Nlrp1b	G	A	11: 71,072,290 (GRCm39)	P518S	probably benign	Het
Nme5	A	T	18: 34,704,575 (GRCm39)	I90N	probably damaging	Het
Nrxn1	T	A	17: 90,950,722 (GRCm39)	T478S	probably damaging	Het
Or8g22	A	C	9: 38,958,483 (GRCm39)	D77E	probably damaging	Het
Osmr	G	A	15: 6,853,042 (GRCm39)	Q617*	probably null	Het
Pcsk5	T	C	19: 17,814,512 (GRCm39)	D2G	possibly damaging	Het
Pdpn	G	A	4: 143,000,608 (GRCm39)	R75C	probably damaging	Het
Pidd1	A	T	7: 141,018,725 (GRCm39)	F842Y	probably damaging	Het
Resf1	T	A	6: 149,227,719 (GRCm39)	V255E	probably benign	Het
Sema3a	A	G	5: 13,566,190 (GRCm39)	Q158R	probably benign	Het
Setbp1	T	A	18: 78,899,798 (GRCm39)	R1290W	probably damaging	Het
Slc20a1	G	A	2: 129,050,324 (GRCm39)	G494D	probably benign	Het
Spag17	A	G	3: 99,889,584 (GRCm39)	E151G	possibly damaging	Het
Stt3b	A	G	9: 115,086,567 (GRCm39)	F351L	probably benign	Het
Tas1r2	A	G	4: 139,396,436 (GRCm39)	M592V	probably benign	Het
Tbcd	A	G	11: 121,387,909 (GRCm39)	T347A	probably benign	Het
Tmem109	C	A	19: 10,851,733 (GRCm39)	R37L	possibly damaging	Het
Tmem67	G	A	4: 12,045,871 (GRCm39)	S862L	possibly damaging	Het
Ttn	T	A	2: 76,781,857 (GRCm39)	D1017V	probably damaging	Het
Zfp646	G	A	7: 127,482,292 (GRCm39)	G1490S	probably benign	Het
Zfyve16	T	C	13: 92,644,813 (GRCm39)	S1130G	possibly damaging	Het

Other mutations in Gm136

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00585:Gm136	APN	4	34,752,322 (GRCm39)	missense	probably damaging	1.00
R0104:Gm136	UTSW	4	34,746,593 (GRCm39)	missense	possibly damaging	0.65
R0108:Gm136	UTSW	4	34,746,593 (GRCm39)	missense	possibly damaging	0.65
R1635:Gm136	UTSW	4	34,750,919 (GRCm39)	critical splice donor site	probably null
R1674:Gm136	UTSW	4	34,746,662 (GRCm39)	splice site	probably benign
R1971:Gm136	UTSW	4	34,755,986 (GRCm39)	missense	probably benign	0.00
R2496:Gm136	UTSW	4	34,746,541 (GRCm39)	missense	probably damaging	1.00
R4441:Gm136	UTSW	4	34,755,911 (GRCm39)	missense	probably benign	0.35
R4901:Gm136	UTSW	4	34,746,580 (GRCm39)	nonsense	probably null
R5300:Gm136	UTSW	4	34,750,930 (GRCm39)	missense	probably damaging	0.98
R6609:Gm136	UTSW	4	34,746,526 (GRCm39)	missense	probably benign
R6709:Gm136	UTSW	4	34,755,884 (GRCm39)	missense	probably damaging	1.00
R6824:Gm136	UTSW	4	34,746,591 (GRCm39)	missense	probably benign	0.15
R7098:Gm136	UTSW	4	34,746,628 (GRCm39)	missense	probably benign	0.08
R7689:Gm136	UTSW	4	34,743,875 (GRCm39)	missense	probably null	0.00
R8249:Gm136	UTSW	4	34,750,955 (GRCm39)	missense	probably benign
R9068:Gm136	UTSW	4	34,750,928 (GRCm39)	missense	possibly damaging	0.47

Predicted Primers

PCR Primer
(F):5'- TGGTGACATTTCAGCCGATGAGC -3'
(R):5'- TGGAGGAATTTGTAACCACTGGCG -3'

Sequencing Primer
(F):5'- CTTTCGGGCAGAATGAAGTC -3'
(R):5'- CTGGCGTAACCGTCATTAAAG -3'

Posted On

2014-01-15