Mutagenetix > Incidental Mutation

Incidental Mutation 'RF002:Gm14025'

602543

Institutional Source

Beutler Lab

Gene Symbol

Gm14025

Ensembl Gene

ENSMUSG00000079051

Gene Name

predicted gene 14025

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.080) question?

Stock #

RF002 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

129025073-129048172 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 129038794 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Serine at position 404 (F404S)

Ref Sequence

ENSEMBL: ENSMUSP00000123404 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000145798]

AlphaFold

A2AP89

Predicted Effect

SMART Domains

Protein: ENSMUSP00000123404
Gene: ENSMUSG00000079051
AA Change: F404S

Domain	Start	End	E-Value	Type
Pfam:Vinculin	14	248	5.8e-18	PFAM
Pfam:Vinculin	281	619	2.1e-20	PFAM

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 99.4%
20x: 98.7%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
AI837181	CGG	CGGTGG	19: 5,425,234		probably benign	Het
AI837181	GGC	GGCTGC	19: 5,425,235		probably benign	Het
Angptl1	A	T	1: 156,857,224	Q321L	possibly damaging	Het
AY358078	T	TAGGATAATGC	14: 51,805,593		probably null	Het
Blm	CCTCCTCCTCCTCCTCCTCCTCCT	CCTCCTCCTCCTGCTCCTCCTCCTCCTCCTCCTCCT	7: 80,512,905		probably benign	Het
Blm	CTC	CTCATCCTCCTCATC	7: 80,512,927		probably benign	Het
Car13	T	C	3: 14,654,914	Y129H	probably damaging	Het
Cd109	TTATTTATTTAT	TTATTTATTTATGTATTTATTTAT	9: 78,712,523		probably benign	Het
Cd109	TATTTAT	TATTTATTTATTCATTTAT	9: 78,712,528		probably benign	Het
Cdh26	T	C	2: 178,466,631	C341R	probably damaging	Het
Chga	GCA	GCACCA	12: 102,561,421		probably benign	Het
Col11a1	A	T	3: 114,217,001	I1689L	unknown	Het
Dnah6	T	G	6: 73,101,889	S2364R	probably benign	Het
E4f1	CCG	CCGACG	17: 24,455,186		probably benign	Het
Fah	A	C	7: 84,589,628	N336K	probably damaging	Het
Fam71e1	CCTGGGTCTGAGGGAGGA	CCTGGGTCTGAGGGAGGAAGGCTGGATCCTGGATAACTGGGTCTGAGGGAGGA	7: 44,500,520		probably null	Het
Fbxo11	A	T	17: 87,996,053	I664K		Het
Fcgbp	A	G	7: 28,089,755	D582G	probably benign	Het
Gabre	C	CCGGCTA	X: 72,270,057		probably null	Het
Gm1110	A	G	9: 26,920,640	Y72H	probably damaging	Het
Inpp5e	C	T	2: 26,408,377	A71T	possibly damaging	Het
Iqcm	C	T	8: 75,577,899	T96I	probably benign	Het
Lce1m	TGCCACCGCTGC	TGCCACCGCTGCCGCCACCGCTGC	3: 93,018,283		probably benign	Het
Lce1m	AC	ACCGCCGCTGCCCC	3: 93,018,299		probably benign	Het
Lrch1	TTGGTGGTGCTGGTGG	TTGGTGG	14: 74,947,574		probably benign	Het
Lyst	A	G	13: 13,634,363	D206G	probably benign	Het
Map4k5	A	T	12: 69,856,856	D58E	probably damaging	Het
Mapkapk2	A	G	1: 131,056,513	S251P	probably damaging	Het
Mcph1	CCTG	CCTGCTG	8: 18,652,529		probably benign	Het
Men1	T	C	19: 6,340,116	S600P	probably damaging	Het
Mllt1	C	T	17: 56,896,300	V394M	probably benign	Het
Mllt1	C	A	17: 56,896,301	M393I	possibly damaging	Het
Nacc1	T	C	8: 84,676,219	E315G	possibly damaging	Het
Nefh	GGGGACTTGGCCTC	GGGGACTTGGCCTCACCTAGGGACTTGGCCTC	11: 4,941,047		probably benign	Het
Nefh	GACTTGGCCTC	GACTTGGCCTCACCTGGGGACTTGGCCTC	11: 4,941,050		probably benign	Het
Nid2	TAACACCGCCA	TA	14: 19,751,366		probably benign	Het
Olfr1484	T	A	19: 13,586,051	I206N	probably damaging	Het
Parp2	A	G	14: 50,817,386	E262G	probably damaging	Het
Pdik1l	TTT	TTTGTTTTTGTGTT	4: 134,279,375		probably null	Het
Pop1	G	A	15: 34,502,437	G90D	probably damaging	Het
Ppp3cc	T	C	14: 70,267,339	T73A	possibly damaging	Het
Prdm15	C	T	16: 97,799,629	D810N	probably damaging	Het
Prpf4b	T	A	13: 34,884,236	S349R	unknown	Het
Rassf6	TCCTGTAGAGCAATGGGGATTC	TCCTGTAGAGCAATGGGGATTCTGCCTCACTCATGGGCCTGTAGAGCAATGGGGATTC	5: 90,608,921		probably benign	Het
Rassf6	GTAGAGCAATGGGGATTC	GTAGAGCAATGGGGATTCTGCCTCACTCATGGTCCTTTAGAGCAATGGGGATTC	5: 90,608,925		probably null	Het
Sdk2	T	C	11: 113,885,252	E208G	probably benign	Het
Smurf2	G	T	11: 106,852,587	P211Q	probably benign	Het
Snx25	C	A	8: 46,116,181		probably null	Het
Spata6	T	A	4: 111,828,305	M469K	probably benign	Het
Spta1	G	T	1: 174,231,360	A1954S	possibly damaging	Het
Sry	CTGGTCGTGGAACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGGTGGTGGTCATGGAACTGCTG	CTGGTCATGGAACTGCTG	Y: 2,662,564		probably benign	Het
Stard8	GAG	GAGTAG	X: 99,066,515		probably null	Het
Tfeb	AGC	AGCGGC	17: 47,786,102		probably benign	Het
Tlcd1	T	A	11: 78,180,194	L203Q	probably benign	Het
Tlr11	T	C	14: 50,361,225	F223L	possibly damaging	Het
Usp48	T	A	4: 137,605,795	V100D	probably damaging	Het
Vmn2r56	G	A	7: 12,694,830	T503I	probably benign	Het
Vps18	T	C	2: 119,297,390	L898P	probably damaging	Het
Zfp384	GCCCAGGCCCAGGCCCAGGCCCAG	GCCCAGGCCCAGTCCCAGGCCCAGGCCCAGGCCCAG	6: 125,036,471		probably benign	Het
Zfp706	T	A	15: 37,003,705	Y39F	probably benign	Het
Zhx3	T	A	2: 160,781,806	N147I	probably damaging	Het

Other mutations in Gm14025

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01318:Gm14025	APN	2	129038702	missense	probably benign	0.01
IGL02423:Gm14025	APN	2	129048048	missense	probably benign	0.03
IGL02730:Gm14025	APN	2	129038726	missense	possibly damaging	0.57
PIT4677001:Gm14025	UTSW	2	129038716	missense
R0019:Gm14025	UTSW	2	129039026	missense	probably benign	0.26
R3946:Gm14025	UTSW	2	129039601	missense	probably damaging	1.00
R4666:Gm14025	UTSW	2	129038230	missense	probably benign	0.02
R4819:Gm14025	UTSW	2	129040801	missense	probably damaging	0.96
R5634:Gm14025	UTSW	2	129039486	missense	probably benign
R6019:Gm14025	UTSW	2	129037690	missense	probably benign
R6241:Gm14025	UTSW	2	129037381	missense	possibly damaging	0.87
R6285:Gm14025	UTSW	2	129037799	missense	possibly damaging	0.82
R6377:Gm14025	UTSW	2	129036811	missense	unknown
R6464:Gm14025	UTSW	2	129039545	missense	possibly damaging	0.85
R6724:Gm14025	UTSW	2	129038056	missense	probably benign	0.23
R7050:Gm14025	UTSW	2	129027971	splice site	probably null
R7130:Gm14025	UTSW	2	129039181	missense
R7199:Gm14025	UTSW	2	129038318	missense
R7324:Gm14025	UTSW	2	129037852	missense	unknown
R7355:Gm14025	UTSW	2	129037229	missense	unknown
R7407:Gm14025	UTSW	2	129038809	missense
R7634:Gm14025	UTSW	2	129038272	missense
R7688:Gm14025	UTSW	2	129039044	nonsense	probably null
R7889:Gm14025	UTSW	2	129036994	missense	unknown
R7894:Gm14025	UTSW	2	129037129	missense	unknown
R8242:Gm14025	UTSW	2	129039393	nonsense	probably null
R8373:Gm14025	UTSW	2	129038171	missense
R8927:Gm14025	UTSW	2	129040869	missense
R8928:Gm14025	UTSW	2	129040869	missense
R9231:Gm14025	UTSW	2	129037420	missense	unknown
R9504:Gm14025	UTSW	2	129039269	missense
R9505:Gm14025	UTSW	2	129036918	missense	unknown
R9608:Gm14025	UTSW	2	129036630	nonsense	probably null
R9682:Gm14025	UTSW	2	129033609	missense	unknown
R9760:Gm14025	UTSW	2	129038579	missense
X0066:Gm14025	UTSW	2	129039067	missense	probably benign	0.33

Predicted Primers

PCR Primer
(F):5'- CAAAGCATGACAGGAGGTGTTC -3'
(R):5'- GACTGATGCGCTCTTTCGAG -3'

Sequencing Primer
(F):5'- ACAGGAGGTGTTCGGATTCCC -3'
(R):5'- GCAGTTCGCGCTGGGTTAC -3'

Posted On

2019-12-04