Mutagenetix > Incidental Mutation

Incidental Mutation 'R1763:Gm436'

193183

Institutional Source

Beutler Lab

Gene Symbol

Gm436

Ensembl Gene

ENSMUSG00000078505

Gene Name

predicted gene 436

Synonyms

LOC230890

MMRRC Submission

039795-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.048) question?

Stock #

R1763 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

144669937-144686368 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 144669959 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 401 (V401A)

Ref Sequence

ENSEMBL: ENSMUSP00000101373 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000105747]

AlphaFold

B1AVU6

Predicted Effect

probably benign
Transcript: ENSMUST00000105747
AA Change: V401A

PolyPhen 2 Score 0.244 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000101373
Gene: ENSMUSG00000078505
AA Change: V401A

Domain	Start	End	E-Value	Type
transmembrane domain	2	24	N/A	INTRINSIC
Pfam:Abhydrolase_3	115	285	1.6e-29	PFAM
Pfam:Abhydrolase_3	292	381	9e-12	PFAM

Meta Mutation Damage Score

0.1754

Coding Region Coverage

1x: 97.4%
3x: 96.8%
10x: 95.1%
20x: 92.0%

Validation Efficiency

98% (85/87)

Allele List at MGI

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca4	G	A	3: 122,110,681	V794M	probably benign	Het
Abca4	A	T	3: 122,163,830	T772S	probably damaging	Het
Acox3	G	A	5: 35,608,339		probably null	Het
Adamts17	A	G	7: 67,147,715	N1060S	probably damaging	Het
Akap8l	C	T	17: 32,332,483	R511H	probably damaging	Het
Als2	T	C	1: 59,174,991	Y1346C	probably benign	Het
Apol10b	A	T	15: 77,585,015	F321I	probably benign	Het
Atp5f1	A	G	3: 105,951,589		probably null	Het
Bloc1s5	A	G	13: 38,619,084		probably benign	Het
Btbd9	T	C	17: 30,334,297	N397S	possibly damaging	Het
Cacna1d	A	G	14: 30,099,196	V1121A	probably benign	Het
Cad	G	A	5: 31,060,951	V460I	probably damaging	Het
Caprin2	A	T	6: 148,843,121	D935E	probably damaging	Het
Ccdc150	A	T	1: 54,354,636	K686N	probably benign	Het
Ccnt2	T	C	1: 127,799,406	F186L	possibly damaging	Het
Cd5l	G	A	3: 87,367,880		probably null	Het
Chrna7	A	G	7: 63,099,252	V494A	probably benign	Het
Clec2i	T	G	6: 128,895,425	Y198*	probably null	Het
Col22a1	A	G	15: 72,007,176	V44A	probably damaging	Het
Cspg4	T	A	9: 56,886,979	I666N	probably damaging	Het
Cyp3a16	A	T	5: 145,465,031		probably null	Het
Dlk1	G	T	12: 109,458,119	C102F	probably damaging	Het
Dscc1	T	A	15: 55,084,139	H215L	probably damaging	Het
Dscc1	CTGAATGAAT	CTGAAT	15: 55,080,176		probably benign	Het
Dus1l	C	G	11: 120,795,671	G15R	probably benign	Het
Eps8l1	G	T	7: 4,471,823	V268L	probably benign	Het
F2	A	C	2: 91,634,906	C104W	probably damaging	Het
F5	C	A	1: 164,192,535	Q860K	probably benign	Het
Fmn2	T	C	1: 174,502,266	L74P	unknown	Het
Frmd6	G	A	12: 70,893,622	R347Q	possibly damaging	Het
Gabbr1	T	G	17: 37,054,767	S158A	probably damaging	Het
Galc	T	C	12: 98,234,266	N295S	probably damaging	Het
Gm6408	A	T	5: 146,482,322	N49I	probably damaging	Het
Grm1	T	A	10: 11,079,866	T225S	possibly damaging	Het
Grm8	C	T	6: 27,285,867	V849I	possibly damaging	Het
Hmcn2	A	G	2: 31,314,590	D59G	probably damaging	Het
Iars	G	A	13: 49,723,077		probably null	Het
Ifi27	C	T	12: 103,437,682	A127V	possibly damaging	Het
Ikbip	A	G	10: 91,096,481	N329S	probably damaging	Het
Ikbke	T	C	1: 131,265,877	T479A	probably benign	Het
Krt12	T	A	11: 99,416,060	N472I	probably damaging	Het
Lmnb2	A	T	10: 80,907,191	L193Q	probably damaging	Het
Lrriq4	T	C	3: 30,650,252	V128A	probably benign	Het
Map4k4	C	A	1: 40,000,757		probably benign	Het
Mtmr7	T	C	8: 40,551,811	T575A	probably benign	Het
Myh13	G	A	11: 67,334,576	A256T	probably benign	Het
Napepld	A	G	5: 21,683,410	Y14H	probably benign	Het
Npr1	T	C	3: 90,459,337	T552A	probably damaging	Het
Nudt15	A	G	14: 73,521,647	F127S	probably benign	Het
Nwd2	T	A	5: 63,808,271	S1733T	probably benign	Het
Olfr1189	A	G	2: 88,592,436	I211V	probably benign	Het
Olfr1257	G	A	2: 89,881,129	G101E	probably damaging	Het
Olfr1348	T	G	7: 6,501,441	I262L	probably benign	Het
Olfr907	A	G	9: 38,499,038	Y123C	probably damaging	Het
Olfr96	T	C	17: 37,225,430	F102L	probably benign	Het
Paqr7	A	T	4: 134,507,098	I89F	probably benign	Het
Pidd1	C	A	7: 141,439,630	V706L	probably benign	Het
Polr3c	A	T	3: 96,713,595	I469N	probably damaging	Het
Ppip5k1	A	G	2: 121,348,547	Y233H	probably damaging	Het
Psmc3	A	G	2: 91,055,995	T166A	possibly damaging	Het
Ptchd3	A	T	11: 121,842,542	I753L	probably benign	Het
Rad21	T	C	15: 51,978,170	K50R	probably damaging	Het
Rad54b	A	G	4: 11,604,989	E479G	possibly damaging	Het
Rfwd3	C	T	8: 111,288,242	R326Q	probably damaging	Het
Rgs20	C	T	1: 4,910,640	R154Q	probably damaging	Het
Sbf1	T	C	15: 89,294,425	D1449G	probably damaging	Het
Sema4g	C	T	19: 45,001,605	R708*	probably null	Het
Sept9	T	C	11: 117,290,428	I18T	probably benign	Het
Serpinb6b	A	G	13: 32,978,058	E280G	probably damaging	Het
Slamf6	T	C	1: 171,942,587		probably benign	Het
Slc6a21	G	A	7: 45,287,734	W554*	probably null	Het
Slco1a4	A	C	6: 141,812,731	I518R	probably benign	Het
Stab1	T	A	14: 31,168,416	Q26L	probably benign	Het
Stox1	A	G	10: 62,667,965	F104L	probably damaging	Het
Suco	T	C	1: 161,834,949	K638E	possibly damaging	Het
Synpo	T	C	18: 60,602,784	K458E	probably damaging	Het
Szt2	A	T	4: 118,372,368	W2820R	unknown	Het
Tmtc1	C	A	6: 148,294,618	G499W	probably damaging	Het
Tonsl	A	C	15: 76,638,066	S242R	probably damaging	Het
Trpc4	G	T	3: 54,194,822	S47I	possibly damaging	Het
Zfp106	G	A	2: 120,520,428	R1581C	probably benign	Het
Zfp27	A	G	7: 29,895,376	L388P	possibly damaging	Het

Other mutations in Gm436

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01149:Gm436	APN	4	144673779	missense	probably benign	0.12
IGL01369:Gm436	APN	4	144674645	missense	possibly damaging	0.50
IGL01503:Gm436	APN	4	144674567	missense	probably damaging	0.99
IGL01505:Gm436	APN	4	144674618	missense	probably damaging	1.00
IGL01954:Gm436	APN	4	144670171	missense	probably damaging	1.00
IGL02447:Gm436	APN	4	144674699	missense	probably benign	0.02
IGL02804:Gm436	APN	4	144670439	missense	possibly damaging	0.95
R0373:Gm436	UTSW	4	144686220	missense	possibly damaging	0.54
R1124:Gm436	UTSW	4	144670275	missense	probably benign	0.00
R1598:Gm436	UTSW	4	144670424	missense	possibly damaging	0.60
R1734:Gm436	UTSW	4	144670026	missense	probably benign	0.04
R1968:Gm436	UTSW	4	144670623	missense	possibly damaging	0.83
R3055:Gm436	UTSW	4	144674698	missense	probably benign	0.16
R3056:Gm436	UTSW	4	144674698	missense	probably benign	0.16
R3930:Gm436	UTSW	4	144670128	missense	probably damaging	1.00
R5124:Gm436	UTSW	4	144674719	missense	probably damaging	1.00
R5407:Gm436	UTSW	4	144670325	missense	probably benign	0.01
R6302:Gm436	UTSW	4	144670190	nonsense	probably null
R6814:Gm436	UTSW	4	144670646	nonsense	probably null
R6872:Gm436	UTSW	4	144670646	nonsense	probably null
R6988:Gm436	UTSW	4	144686325	missense	probably benign	0.01
R7131:Gm436	UTSW	4	144670067	missense	probably damaging	0.98
R7895:Gm436	UTSW	4	144670343	missense	possibly damaging	0.95
R8108:Gm436	UTSW	4	144670669	missense	probably benign	0.04
R8378:Gm436	UTSW	4	144670599	missense	probably benign	0.24
R8676:Gm436	UTSW	4	144670113	missense	possibly damaging	0.94
R8817:Gm436	UTSW	4	144673791	missense	probably benign	0.00
R9328:Gm436	UTSW	4	144674686	missense	probably benign	0.02
R9640:Gm436	UTSW	4	144686239	missense	possibly damaging	0.66

Predicted Primers

PCR Primer
(F):5'- TGCTGAGTTCCTTTTACTGTAAAGCCAT -3'
(R):5'- TGAGGCTGCCTATCTAGAAACAAAACAC -3'

Sequencing Primer
(F):5'- GTAAAGCCATTAGTACTTTGCTTCC -3'
(R):5'- GCAGATGATAAGACCATTGCTC -3'

Posted On

2014-05-23