Mutagenetix > Incidental Mutation

Incidental Mutation 'R7455:Gm13941'

578053

Institutional Source

Beutler Lab

Gene Symbol

Gm13941

Ensembl Gene

ENSMUSG00000079170

Gene Name

predicted gene 13941

Synonyms

MMRRC Submission

045529-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.084) question?

Stock #

R7455 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

110885009-110935204 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 110925085 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Leucine at position 173 (F173L)

Ref Sequence

ENSEMBL: ENSMUSP00000115383 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000127918]

AlphaFold

A2AJ38

Predicted Effect

unknown
Transcript: ENSMUST00000127918
AA Change: F173L

SMART Domains

Protein: ENSMUSP00000115383
Gene: ENSMUSG00000079170
AA Change: F173L

Domain	Start	End	E-Value	Type
low complexity region	225	244	N/A	INTRINSIC

Meta Mutation Damage Score

0.0852

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.0%

Validation Efficiency

98% (62/63)

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Agbl1	C	T	7: 76,074,503 (GRCm39)	H646Y	unknown	Het
Ak5	C	T	3: 152,187,209 (GRCm39)	R426H	probably damaging	Het
Akap9	T	C	5: 4,022,792 (GRCm39)	V1207A	probably benign	Het
Asph	A	T	4: 9,531,732 (GRCm39)		probably null	Het
Avpr1a	T	G	10: 122,285,169 (GRCm39)	C154G	probably damaging	Het
Boll	T	C	1: 55,339,262 (GRCm39)	Q283R	probably benign	Het
Cad	C	T	5: 31,231,506 (GRCm39)	P1743S	probably damaging	Het
Ccdc137	T	G	11: 120,350,985 (GRCm39)	M129R	probably damaging	Het
Cdh23	A	G	10: 60,142,003 (GRCm39)	I3028T	possibly damaging	Het
Cep68	T	A	11: 20,180,571 (GRCm39)	I687F	probably damaging	Het
Ces2a	T	A	8: 105,464,154 (GRCm39)	I262N	probably damaging	Het
Cfap44	A	G	16: 44,225,147 (GRCm39)		probably benign	Het
Cfap69	T	G	5: 5,675,873 (GRCm39)	H247P	possibly damaging	Het
Cideb	T	C	14: 55,992,292 (GRCm39)	T134A	probably damaging	Het
Cilp2	A	T	8: 70,333,721 (GRCm39)	D1092E	probably damaging	Het
Cptp	G	A	4: 155,950,957 (GRCm39)	R170C	probably damaging	Het
Cysrt1	A	G	2: 25,129,422 (GRCm39)	L30S	probably benign	Het
Dcc	A	G	18: 71,553,394 (GRCm39)	V754A	probably benign	Het
Entrep2	A	G	7: 64,409,161 (GRCm39)	V411A	probably benign	Het
Fer1l5	A	T	1: 36,428,064 (GRCm39)	T453S	probably benign	Het
Fnbp4	ACCACCTCCACCTCCACCTCC	ACCACCTCCACCTCCACCTCCACCTCC	2: 90,608,159 (GRCm39)		probably benign	Het
Frem2	C	T	3: 53,479,701 (GRCm39)		probably null	Het
Greb1l	G	A	18: 10,554,915 (GRCm39)	A1654T	probably damaging	Het
Inpp4b	T	A	8: 82,798,332 (GRCm39)	I840N	probably damaging	Het
Kdm4b	T	A	17: 56,703,657 (GRCm39)	I746N	probably damaging	Het
Lins1	C	A	7: 66,361,692 (GRCm39)	H448N	probably benign	Het
Ly9	A	T	1: 171,421,507 (GRCm39)	Y581*	probably null	Het
Mark1	T	A	1: 184,651,947 (GRCm39)	E186V	probably damaging	Het
Mcph1	T	A	8: 18,681,775 (GRCm39)	V304E	probably benign	Het
Mical3	T	C	6: 120,935,705 (GRCm39)	D1607G	probably damaging	Het
Mup18	A	G	4: 61,592,171 (GRCm39)	V31A	probably benign	Het
Nectin3	A	T	16: 46,317,105 (GRCm39)	C11*	probably null	Het
Nedd1	A	T	10: 92,536,787 (GRCm39)	L172M	probably benign	Het
Nim1k	G	A	13: 120,173,995 (GRCm39)	R300W	probably damaging	Het
Oprm1	T	C	10: 6,780,204 (GRCm39)	F289L	probably damaging	Het
Or4c115	G	T	2: 88,927,434 (GRCm39)	P279Q	probably damaging	Het
Or7g12	A	G	9: 18,900,150 (GRCm39)	I289V	possibly damaging	Het
Or8c8	T	C	9: 38,165,550 (GRCm39)	V276A	probably damaging	Het
Parg	T	C	14: 31,931,432 (GRCm39)	Y351H	probably benign	Het
Phf3	A	C	1: 30,876,239 (GRCm39)	V118G	probably damaging	Het
Pik3c2g	T	C	6: 139,913,643 (GRCm39)	Y1014H	unknown	Het
Pmp22	A	G	11: 63,025,339 (GRCm39)		probably null	Het
Ppfibp1	T	A	6: 146,917,848 (GRCm39)	F501L	probably damaging	Het
Rgl2	G	A	17: 34,151,657 (GRCm39)	A234T	probably benign	Het
Rhpn2	G	A	7: 35,070,669 (GRCm39)		probably null	Het
Ryr3	T	C	2: 112,559,211 (GRCm39)	K3058E	probably damaging	Het
Sbsn	A	T	7: 30,452,602 (GRCm39)	Q539L	possibly damaging	Het
Scgn	G	A	13: 24,150,848 (GRCm39)	R168C	probably benign	Het
Serpinb10	A	G	1: 107,463,832 (GRCm39)	Y38C	probably damaging	Het
Sfmbt2	G	A	2: 10,582,766 (GRCm39)	V709I	probably benign	Het
Slc1a2	A	T	2: 102,566,299 (GRCm39)	M10L	probably benign	Het
Sox6	T	G	7: 115,088,904 (GRCm39)	I653L	probably benign	Het
Tespa1	A	G	10: 130,196,559 (GRCm39)	I166V	probably benign	Het
Tex15	T	C	8: 34,067,025 (GRCm39)	Y2152H	possibly damaging	Het
Tlr9	A	G	9: 106,101,729 (GRCm39)	N340S	probably benign	Het
Tmem198	G	A	1: 75,456,430 (GRCm39)	R28Q	unknown	Het
Tut7	T	C	13: 59,969,871 (GRCm39)	Y8C	probably benign	Het
Vmn2r7	T	C	3: 64,624,014 (GRCm39)	D102G	probably benign	Het
Wdr93	A	G	7: 79,425,267 (GRCm39)	M529V	probably benign	Het
Zfp110	A	G	7: 12,581,984 (GRCm39)	H310R	probably benign	Het
Zfp36l2	A	G	17: 84,494,575 (GRCm39)	S21P	probably damaging	Het
Zfp534	G	A	4: 147,759,212 (GRCm39)	H486Y	probably damaging	Het
Zfp638	G	A	6: 83,907,127 (GRCm39)	V431I	probably damaging	Het

Other mutations in Gm13941

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL00323:Gm13941	APN	2	110,935,198 (GRCm39)	missense	unknown
IGL00420:Gm13941	APN	2	110,922,193 (GRCm39)	splice site	probably benign
IGL01149:Gm13941	APN	2	110,931,482 (GRCm39)	missense	unknown
IGL01319:Gm13941	APN	2	110,925,150 (GRCm39)	critical splice acceptor site	probably null
IGL02557:Gm13941	APN	2	110,931,501 (GRCm39)	missense	unknown
IGL03163:Gm13941	APN	2	110,928,761 (GRCm39)	missense	unknown
R0067:Gm13941	UTSW	2	110,889,761 (GRCm39)	unclassified	noncoding transcript
R0918:Gm13941	UTSW	2	110,930,945 (GRCm39)	missense	unknown
R2315:Gm13941	UTSW	2	110,935,162 (GRCm39)	missense	unknown
R3847:Gm13941	UTSW	2	110,935,198 (GRCm39)	missense	unknown
R3848:Gm13941	UTSW	2	110,935,198 (GRCm39)	missense	unknown
R5416:Gm13941	UTSW	2	110,925,079 (GRCm39)	missense	unknown
R5574:Gm13941	UTSW	2	110,930,951 (GRCm39)	missense	unknown
R6389:Gm13941	UTSW	2	110,928,734 (GRCm39)	missense	unknown
R6616:Gm13941	UTSW	2	110,931,520 (GRCm39)	missense	unknown
R7056:Gm13941	UTSW	2	110,927,147 (GRCm39)	missense	unknown
R8197:Gm13941	UTSW	2	110,926,921 (GRCm39)	splice site	probably null
R9116:Gm13941	UTSW	2	110,935,146 (GRCm39)	missense	unknown
R9164:Gm13941	UTSW	2	110,936,324 (GRCm39)	missense	unknown
R9536:Gm13941	UTSW	2	110,918,861 (GRCm39)	missense	unknown
R9763:Gm13941	UTSW	2	110,931,518 (GRCm39)	missense	unknown
Z1177:Gm13941	UTSW	2	110,925,123 (GRCm39)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- CTTTCCTTAGACATCACTCAAACTGAC -3'
(R):5'- ACAAGAAATGTGCTCCATGTGAG -3'

Sequencing Primer
(F):5'- GACATCACTCAAACTGACATCTTTG -3'
(R):5'- CCGAATTTGTTGCTTCGA -3'

Posted On

2019-10-07