Mutagenetix > Incidental Mutation

Incidental Mutation 'R2226:Gm11555'

239739

Institutional Source

Beutler Lab

Gene Symbol

Gm11555

Ensembl Gene

ENSMUSG00000078130

Gene Name

predicted gene 11555

Synonyms

MMRRC Submission

040227-MU

Accession Numbers

Essential gene?

Not available question?

Stock #

R2226 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

99540480-99541044 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 99540585 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Serine at position 141 (R141S)

Ref Sequence

ENSEMBL: ENSMUSP00000100533 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000073126] [ENSMUST00000104929]

AlphaFold

B1AQ89

Predicted Effect

unknown
Transcript: ENSMUST00000073126
AA Change: R131S

SMART Domains

Protein: ENSMUSP00000131822
Gene: ENSMUSG00000078130
AA Change: R131S

Domain	Start	End	E-Value	Type
Pfam:Keratin_B2_2	1	43	1.4e-7	PFAM
Pfam:Keratin_B2	1	79	1.9e-9	PFAM
Pfam:Keratin_B2_2	14	58	6.4e-14	PFAM
Pfam:Keratin_B2_2	39	88	2.1e-11	PFAM
Pfam:Keratin_B2_2	79	123	1.7e-12	PFAM
Pfam:Keratin_B2_2	89	134	4.6e-8	PFAM
Pfam:Keratin_B2_2	123	164	3.3e-4	PFAM

Predicted Effect

unknown
Transcript: ENSMUST00000104929
AA Change: R141S

SMART Domains

Protein: ENSMUSP00000100533
Gene: ENSMUSG00000078130
AA Change: R141S

Domain	Start	End	E-Value	Type
Pfam:Keratin_B2_2	1	58	2.8e-9	PFAM
Pfam:Keratin_B2	1	74	4.2e-11	PFAM
Pfam:Keratin_B2_2	49	96	2.1e-11	PFAM
Pfam:Keratin_B2_2	59	117	2.6e-6	PFAM
Pfam:Keratin_B2_2	89	133	5.7e-13	PFAM

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadacl3	A	T	4: 144,190,295 (GRCm39)	V2E	possibly damaging	Het
Aen	C	A	7: 78,552,199 (GRCm39)	T15K	probably benign	Het
Aggf1	A	G	13: 95,507,354 (GRCm39)	S144P	probably damaging	Het
Ar	T	A	X: 97,194,937 (GRCm39)	M517K	probably benign	Het
Ascc3	A	G	10: 50,630,148 (GRCm39)	T1746A	probably benign	Het
Atg9b	A	G	5: 24,591,393 (GRCm39)	V735A	possibly damaging	Het
Atp1b3	A	G	9: 96,225,329 (GRCm39)	F113S	probably damaging	Het
Cacna1h	T	C	17: 25,604,917 (GRCm39)	N1132S	probably benign	Het
Ccdc150	A	G	1: 54,404,084 (GRCm39)	I943V	probably null	Het
Cntnap4	A	G	8: 113,542,120 (GRCm39)	D751G	probably damaging	Het
Dgkk	T	A	X: 6,741,487 (GRCm39)	D102E	probably damaging	Het
Efhb	A	T	17: 53,769,457 (GRCm39)		probably null	Het
Elfn2	A	G	15: 78,558,443 (GRCm39)	W35R	probably damaging	Het
Emcn	T	C	3: 137,109,778 (GRCm39)	I140T	possibly damaging	Het
Epha2	G	A	4: 141,048,548 (GRCm39)	R569H	probably damaging	Het
Gabrg2	A	T	11: 41,862,735 (GRCm39)	F116L	probably damaging	Het
Hectd3	T	C	4: 116,852,886 (GRCm39)	I96T	possibly damaging	Het
Hnrnpul2	T	A	19: 8,802,349 (GRCm39)	N405K	probably damaging	Het
Iigp1	A	T	18: 60,522,960 (GRCm39)	K26I	possibly damaging	Het
Kirrel2	T	C	7: 30,153,579 (GRCm39)	K260R	probably damaging	Het
Kpna1	G	A	16: 35,851,591 (GRCm39)	A392T	probably damaging	Het
Krt19	T	C	11: 100,032,401 (GRCm39)	E260G	probably damaging	Het
Marchf7	A	G	2: 60,060,190 (GRCm39)	R106G	probably benign	Het
Mthfd2l	G	T	5: 91,096,693 (GRCm39)	E105*	probably null	Het
Mtus1	C	T	8: 41,535,812 (GRCm39)	V635M	probably damaging	Het
Ndufaf5	T	C	2: 140,030,780 (GRCm39)	V222A	probably benign	Het
Nkpd1	A	T	7: 19,253,745 (GRCm39)	Y37F	probably benign	Het
Nsun7	T	A	5: 66,418,562 (GRCm39)	Y97*	probably null	Het
Nxph3	T	C	11: 95,404,990 (GRCm39)	Y17C	probably benign	Het
Or2l5	T	C	16: 19,333,996 (GRCm39)	H130R	probably benign	Het
Or4k1	A	G	14: 50,378,076 (GRCm39)	S7P	probably damaging	Het
Or51a5	A	G	7: 102,771,115 (GRCm39)	M292T	probably benign	Het
Or5aq1	A	C	2: 86,966,590 (GRCm39)	V25G	possibly damaging	Het
Or7g19	A	T	9: 18,856,177 (GRCm39)	I78F	probably damaging	Het
P2rx2	A	G	5: 110,490,745 (GRCm39)	F26S	probably damaging	Het
Pank1	A	T	19: 34,804,763 (GRCm39)	L131Q	probably damaging	Het
Pcx	T	C	19: 4,668,026 (GRCm39)	I516T	possibly damaging	Het
Pkhd1l1	T	C	15: 44,376,188 (GRCm39)	I950T	possibly damaging	Het
Ppwd1	A	G	13: 104,353,753 (GRCm39)	L335P	probably damaging	Het
Ptch1	A	G	13: 63,661,485 (GRCm39)	S1218P	probably damaging	Het
Ptpn4	C	T	1: 119,610,515 (GRCm39)	R664Q	probably damaging	Het
Semp2l1	A	T	1: 32,584,934 (GRCm39)	H325Q	probably damaging	Het
Sfxn1	A	G	13: 54,239,536 (GRCm39)	T20A	possibly damaging	Het
Sgsm3	A	G	15: 80,888,069 (GRCm39)	E53G	probably damaging	Het
Slc22a19	C	T	19: 7,661,215 (GRCm39)	V320M	possibly damaging	Het
Slc25a33	A	T	4: 149,838,306 (GRCm39)	I122N	probably benign	Het
Spata31d1a	T	A	13: 59,851,529 (GRCm39)	I200L	probably benign	Het
Spin2g	A	T	X: 33,656,599 (GRCm39)	I171N	possibly damaging	Het
Srsf6	G	A	2: 162,773,619 (GRCm39)	S10N	probably damaging	Het
Tesl2	T	A	X: 23,825,173 (GRCm39)	M1L	probably null	Het
Thoc2l	T	A	5: 104,667,286 (GRCm39)	Y603N	probably damaging	Het
Ttc12	A	G	9: 49,353,135 (GRCm39)		probably null	Het
Vmn2r100	A	G	17: 19,742,634 (GRCm39)	K336R	probably benign	Het
Vmn2r108	A	T	17: 20,701,295 (GRCm39)	Y68*	probably null	Het
Zfp738	A	G	13: 67,818,431 (GRCm39)	F520S	probably damaging	Het

Other mutations in Gm11555

Allele	Source	Chr	Coord	Type	Predicted Effect
R0486:Gm11555	UTSW	11	99,540,986 (GRCm39)	missense	unknown
R0531:Gm11555	UTSW	11	99,540,844 (GRCm39)	splice site	probably benign
R3870:Gm11555	UTSW	11	99,540,816 (GRCm39)	nonsense	probably null
R7759:Gm11555	UTSW	11	99,540,568 (GRCm39)	missense	unknown
R9075:Gm11555	UTSW	11	99,540,694 (GRCm39)	missense

Predicted Primers

PCR Primer
(F):5'- GGCTTCTCATCAGACTCATAAAGCTG -3'
(R):5'- TCTGTGTGCTGCCAGTCAAG -3'

Sequencing Primer
(F):5'- GACTCATAAAGCTGAATTATGCAGC -3'
(R):5'- TGCCAGTCAAGCTGCTG -3'

Posted On

2014-10-15