Mutagenetix > Incidental Mutation

Incidental Mutation 'R0055:Gm12887'

16116

Institutional Source

Beutler Lab

Gene Symbol

Gm12887

Ensembl Gene

ENSMUSG00000078575

Gene Name

predicted gene 12887

Synonyms

MMRRC Submission

038349-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.070) question?

Stock #

R0055 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

121471468-121479300 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 121473666 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Asparagine at position 61 (K61N)

Ref Sequence

ENSEMBL: ENSMUSP00000101872 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000106265]

AlphaFold

B1AVM1

Predicted Effect

probably damaging
Transcript: ENSMUST00000106265
AA Change: K61N

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000101872
Gene: ENSMUSG00000078575
AA Change: K61N

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
Pfam:Palm_thioest	37	119	2.4e-10	PFAM

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 89.7%
3x: 87.2%
10x: 80.9%
20x: 71.2%

Validation Efficiency

85% (52/61)

Allele List at MGI

Other mutations in this stock

Total: 37 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A2ml1	T	C	6: 128,547,057 (GRCm39)		probably benign	Het
Atp6v1h	A	T	1: 5,154,677 (GRCm39)	T2S	probably benign	Het
BC034090	A	T	1: 155,117,404 (GRCm39)	L238Q	probably damaging	Het
Ccdc61	T	C	7: 18,626,461 (GRCm39)	D128G	probably damaging	Het
Cfap96	A	T	8: 46,421,198 (GRCm39)	S108R	probably damaging	Het
Dennd5a	A	G	7: 109,498,998 (GRCm39)	I955T	possibly damaging	Het
Ephx4	T	C	5: 107,560,944 (GRCm39)	L32S	probably damaging	Het
Fbxo21	T	A	5: 118,138,555 (GRCm39)	D493E	probably benign	Het
Frmd4b	A	T	6: 97,300,610 (GRCm39)		probably benign	Het
Fzd1	A	T	5: 4,806,037 (GRCm39)	M515K	possibly damaging	Het
Gli2	A	G	1: 118,818,138 (GRCm39)		probably benign	Het
Grin2a	A	T	16: 9,487,671 (GRCm39)	V409D	probably damaging	Het
Grin2b	T	C	6: 135,900,201 (GRCm39)	I227V	probably benign	Het
Helz2	T	G	2: 180,870,614 (GRCm39)	D2879A	possibly damaging	Het
Itpr2	T	C	6: 146,224,631 (GRCm39)	N1453S	probably benign	Het
Lin7c	T	A	2: 109,726,798 (GRCm39)		probably benign	Het
Ly75	T	C	2: 60,152,262 (GRCm39)	E1097G	probably benign	Het
Mcm10	T	C	2: 4,996,218 (GRCm39)	N882D	probably damaging	Het
Mybph	G	T	1: 134,121,590 (GRCm39)	V88L	probably damaging	Het
Nefm	T	A	14: 68,358,648 (GRCm39)		probably benign	Het
Nf1	A	G	11: 79,362,377 (GRCm39)	E1497G	probably damaging	Het
Or2j3	T	C	17: 38,615,702 (GRCm39)	S217G	possibly damaging	Het
Or51ah3	A	G	7: 103,210,244 (GRCm39)	K187E	probably damaging	Het
Or52e18	T	A	7: 104,609,703 (GRCm39)	T79S	possibly damaging	Het
Phf8-ps	A	T	17: 33,285,696 (GRCm39)	W369R	probably damaging	Het
Plcd3	C	G	11: 102,968,411 (GRCm39)	W382S	probably damaging	Het
Plxna1	T	A	6: 89,306,721 (GRCm39)	I1370F	possibly damaging	Het
Qng1	T	C	13: 58,531,980 (GRCm39)	D192G	probably damaging	Het
Rarb	G	A	14: 16,509,066 (GRCm38)	R106C	probably damaging	Het
Rps6ka5	G	A	12: 100,644,839 (GRCm39)	T37I	probably damaging	Het
Scube1	A	G	15: 83,518,937 (GRCm39)	V301A	probably damaging	Het
Slc25a45	T	C	19: 5,930,495 (GRCm39)	F3L	probably damaging	Het
Slfn10-ps	A	G	11: 82,921,126 (GRCm39)		noncoding transcript	Het
Slit2	C	A	5: 48,439,068 (GRCm39)	C1077*	probably null	Het
Ucp1	G	T	8: 84,017,233 (GRCm39)	E8*	probably null	Het
Zdhhc11	C	T	13: 74,130,805 (GRCm39)	Q295*	probably null	Het
Zfp457	T	A	13: 67,442,098 (GRCm39)	H63L	probably damaging	Het

Other mutations in Gm12887

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01060:Gm12887	APN	4	121,473,610 (GRCm39)	splice site	probably benign
IGL02113:Gm12887	APN	4	121,473,692 (GRCm39)	missense	probably benign	0.32
R0055:Gm12887	UTSW	4	121,473,666 (GRCm39)	missense	probably damaging	0.98
R1673:Gm12887	UTSW	4	121,473,655 (GRCm39)	missense	probably damaging	0.98
R1784:Gm12887	UTSW	4	121,473,715 (GRCm39)	missense	probably benign	0.44
R1843:Gm12887	UTSW	4	121,479,227 (GRCm39)	missense	probably damaging	0.98
R4231:Gm12887	UTSW	4	121,479,299 (GRCm39)	start codon destroyed	probably null	0.53
R5258:Gm12887	UTSW	4	121,472,897 (GRCm39)	missense	probably benign
R6528:Gm12887	UTSW	4	121,472,834 (GRCm39)	missense	probably damaging	1.00
R8037:Gm12887	UTSW	4	121,472,887 (GRCm39)	missense	probably damaging	1.00
R9038:Gm12887	UTSW	4	121,473,616 (GRCm39)	critical splice donor site	probably null
R9073:Gm12887	UTSW	4	121,479,238 (GRCm39)	splice site	probably null
R9157:Gm12887	UTSW	4	121,473,701 (GRCm39)	missense	probably benign	0.06
R9313:Gm12887	UTSW	4	121,473,701 (GRCm39)	missense	probably benign	0.06

Posted On

2013-01-08