Mutagenetix > Incidental Mutation

Incidental Mutation 'R8111:Gm10800'

630849

Institutional Source

Beutler Lab

Gene Symbol

Gm10800

Ensembl Gene

ENSMUSG00000075014

Gene Name

predicted gene 10800

Synonyms

MMRRC Submission

067540-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.285) question?

Stock #

R8111 (G1)

Quality Score

126.457

Status

Not validated

Chromosome

Chromosomal Location

98496892-98497646 bp(-) (GRCm39)

Type of Mutation

frame shift

DNA Base Change (assembly)

CAAGAAAACTGAAAATCAAAGAAAACTGAAAATCA to CAAGAAAACTGAAAATCA at 98497361 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000097275 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000099683] [ENSMUST00000099684]

AlphaFold

D3Z496

Predicted Effect

probably null
Transcript: ENSMUST00000099683

SMART Domains

Protein: ENSMUSP00000097275
Gene: ENSMUSG00000075014

Domain	Start	End	E-Value	Type
internal_repeat_1	1	41	1.13e-5	PROSPERO
internal_repeat_2	26	49	4.11e-5	PROSPERO
transmembrane domain	78	96	N/A	INTRINSIC
internal_repeat_1	114	174	1.13e-5	PROSPERO
low complexity region	177	188	N/A	INTRINSIC
internal_repeat_2	197	219	4.11e-5	PROSPERO

Predicted Effect

probably benign
Transcript: ENSMUST00000099684

SMART Domains

Protein: ENSMUSP00000097276
Gene: ENSMUSG00000075015

Domain	Start	End	E-Value	Type
internal_repeat_1	2	73	1.19e-13	PROSPERO
internal_repeat_1	80	167	1.19e-13	PROSPERO

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.7%
20x: 93.2%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3425401B19Rik	C	T	14: 32,382,266 (GRCm39)	W1233*	probably null	Het
4930590J08Rik	A	G	6: 91,894,691 (GRCm39)	I247V	probably benign	Het
8030423J24Rik	T	A	13: 71,032,077 (GRCm39)	C50S	unknown	Het
Adam29	T	G	8: 56,324,585 (GRCm39)	H623P	probably benign	Het
Adamts5	A	G	16: 85,696,203 (GRCm39)	V318A	probably damaging	Het
Ano3	T	C	2: 110,614,058 (GRCm39)	D215G	possibly damaging	Het
Ap3b2	A	G	7: 81,113,530 (GRCm39)	I893T	unknown	Het
Apob	G	A	12: 8,058,801 (GRCm39)	A2428T	probably benign	Het
Armc3	T	C	2: 19,301,674 (GRCm39)	V660A	probably benign	Het
Atf7	G	T	15: 102,471,769 (GRCm39)	T42K	probably damaging	Het
Atg9a	A	T	1: 75,164,366 (GRCm39)	I160N	probably damaging	Het
Atp2b1	T	C	10: 98,832,786 (GRCm39)	V429A	possibly damaging	Het
Bpifb3	A	C	2: 153,764,609 (GRCm39)	H167P	probably benign	Het
Cacna1f	G	T	X: 7,487,326 (GRCm39)	E921D	probably damaging	Het
Ccdc57	T	A	11: 120,769,713 (GRCm39)	L713F	probably damaging	Het
Chd1l	C	T	3: 97,494,526 (GRCm39)	E385K	possibly damaging	Het
Csmd1	C	T	8: 15,967,306 (GRCm39)	V3186I	probably benign	Het
Dclre1c	T	A	2: 3,448,185 (GRCm39)	D349E	probably benign	Het
Dlg1	C	T	16: 31,661,620 (GRCm39)	T657M	possibly damaging	Het
Dync2h1	T	C	9: 7,148,688 (GRCm39)	I919V	probably benign	Het
Dync2i2	C	A	2: 29,921,859 (GRCm39)	A501S	possibly damaging	Het
Eml5	A	G	12: 98,758,773 (GRCm39)		probably null	Het
Epas1	C	A	17: 87,125,860 (GRCm39)	S286*	probably null	Het
Fat1	G	A	8: 45,479,095 (GRCm39)	V2714I	possibly damaging	Het
Fuca2	T	C	10: 13,390,545 (GRCm39)	M447T	probably benign	Het
Gm11110	A	C	17: 57,410,427 (GRCm39)	C24G	probably null	Het
Gm6176	T	A	7: 21,750,593 (GRCm39)	I113F	probably benign	Het
Gmcl1	G	T	6: 86,698,408 (GRCm39)	A163E	probably damaging	Het
Gpat2	G	T	2: 127,275,777 (GRCm39)	L518F	probably damaging	Het
Gpr137b	T	C	13: 13,533,991 (GRCm39)	Y355C		Het
Hgsnat	C	T	8: 26,458,440 (GRCm39)	V195I	probably benign	Het
Hivep3	T	A	4: 119,955,583 (GRCm39)	S1300T	probably damaging	Het
Hs3st2	A	T	7: 120,992,362 (GRCm39)	H137L	probably damaging	Het
Iffo1	T	C	6: 125,122,781 (GRCm39)	S188P	possibly damaging	Het
Itih1	T	C	14: 30,654,225 (GRCm39)	D684G	probably damaging	Het
Lrba	C	A	3: 86,235,012 (GRCm39)	N852K	probably damaging	Het
Lrriq4	T	C	3: 30,709,930 (GRCm39)	S425P	possibly damaging	Het
Mdn1	T	A	4: 32,674,003 (GRCm39)	S562T	possibly damaging	Het
Mex3a	T	C	3: 88,444,064 (GRCm39)	V380A	probably benign	Het
Mgat4d	A	T	8: 84,094,776 (GRCm39)	N271I	probably damaging	Het
Mmp24	T	A	2: 155,649,345 (GRCm39)	V254E	possibly damaging	Het
Muc16	T	A	9: 18,503,925 (GRCm39)	R6455S	possibly damaging	Het
Npffr1	T	A	10: 61,459,128 (GRCm39)	V127E	probably damaging	Het
Obox5	T	A	7: 15,492,541 (GRCm39)	N165K	probably damaging	Het
Or10g3b	G	A	14: 52,587,344 (GRCm39)	T53M	possibly damaging	Het
Otulin	A	C	15: 27,606,381 (GRCm39)	V344G	probably damaging	Het
Pappa	A	G	4: 65,180,229 (GRCm39)	D1030G	probably damaging	Het
Pdzd2	G	A	15: 12,373,592 (GRCm39)	S2181L	probably benign	Het
Ppp2r3c	C	A	12: 55,344,634 (GRCm39)	M111I	probably benign	Het
Prss37	T	C	6: 40,494,747 (GRCm39)	T13A	probably benign	Het
Sfi1	TCGC	TC	11: 3,096,254 (GRCm39)		probably null	Het
Sgo2b	T	A	8: 64,396,138 (GRCm39)	K39N	probably damaging	Het
Sike1	T	C	3: 102,909,123 (GRCm39)	*208Q	probably null	Het
Spire1	A	G	18: 67,652,391 (GRCm39)	S229P	probably damaging	Het
Tmem132b	A	G	5: 125,699,857 (GRCm39)	I132V	probably benign	Het
Umodl1	T	C	17: 31,190,792 (GRCm39)	V213A	probably damaging	Het
Washc1	C	G	17: 66,423,033 (GRCm39)	Q116E	probably benign	Het
Zfp553	T	A	7: 126,836,093 (GRCm39)	C549*	probably null	Het
Zfp9	G	A	6: 118,441,561 (GRCm39)	P367L	probably damaging	Het

Other mutations in Gm10800

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01022:Gm10800	APN	2	98,497,576 (GRCm39)	unclassified	probably benign
BB012:Gm10800	UTSW	2	98,497,378 (GRCm39)	frame shift	probably null
FR4976:Gm10800	UTSW	2	98,497,378 (GRCm39)	frame shift	probably null
PIT4131001:Gm10800	UTSW	2	98,497,250 (GRCm39)	missense	probably benign
PIT4131001:Gm10800	UTSW	2	98,497,163 (GRCm39)	missense	probably benign
PIT4131001:Gm10800	UTSW	2	98,496,893 (GRCm39)	missense	probably benign	0.11
PIT4142001:Gm10800	UTSW	2	98,497,250 (GRCm39)	missense	probably benign
PIT4142001:Gm10800	UTSW	2	98,497,163 (GRCm39)	missense	probably benign
PIT4142001:Gm10800	UTSW	2	98,496,893 (GRCm39)	missense	probably benign	0.11
PIT4142001:Gm10800	UTSW	2	98,497,361 (GRCm39)	frame shift	probably null
PIT4402001:Gm10800	UTSW	2	98,497,361 (GRCm39)	frame shift	probably null
PIT4498001:Gm10800	UTSW	2	98,497,361 (GRCm39)	frame shift	probably null
R0025:Gm10800	UTSW	2	98,496,925 (GRCm39)	missense	probably benign	0.05
R5077:Gm10800	UTSW	2	98,497,379 (GRCm39)	missense	probably benign	0.01
R5687:Gm10800	UTSW	2	98,496,965 (GRCm39)	missense	probably benign
R7146:Gm10800	UTSW	2	98,497,378 (GRCm39)	frame shift	probably null
R7206:Gm10800	UTSW	2	98,497,378 (GRCm39)	frame shift	probably null
R7619:Gm10800	UTSW	2	98,497,378 (GRCm39)	frame shift	probably null
R7930:Gm10800	UTSW	2	98,497,379 (GRCm39)	unclassified	probably benign
R7931:Gm10800	UTSW	2	98,497,379 (GRCm39)	unclassified	probably benign
R7998:Gm10800	UTSW	2	98,497,378 (GRCm39)	frame shift	probably null
R8019:Gm10800	UTSW	2	98,497,378 (GRCm39)	frame shift	probably null
R8110:Gm10800	UTSW	2	98,497,361 (GRCm39)	frame shift	probably null
R8488:Gm10800	UTSW	2	98,497,379 (GRCm39)	unclassified	probably benign
R8509:Gm10800	UTSW	2	98,497,379 (GRCm39)	unclassified	probably benign
R8692:Gm10800	UTSW	2	98,497,379 (GRCm39)	unclassified	probably benign
R8722:Gm10800	UTSW	2	98,497,379 (GRCm39)	unclassified	probably benign
R8789:Gm10800	UTSW	2	98,497,361 (GRCm39)	frame shift	probably null
R8902:Gm10800	UTSW	2	98,497,361 (GRCm39)	frame shift	probably null
R8903:Gm10800	UTSW	2	98,497,361 (GRCm39)	frame shift	probably null
R8935:Gm10800	UTSW	2	98,497,378 (GRCm39)	frame shift	probably null
R9104:Gm10800	UTSW	2	98,497,379 (GRCm39)	unclassified	probably benign
R9571:Gm10800	UTSW	2	98,497,378 (GRCm39)	frame shift	probably null

Predicted Primers

PCR Primer
(F):5'- TGAGAAACATCTACTTGACGACTTG -3'
(R):5'- GTGTGTACCTACTTTGGAAACAG -3'

Sequencing Primer
(F):5'- CTACTTGACGACTTGAAAAATGACG -3'
(R):5'- GCCATATTTCACGTCCTAAAGTGTG -3'

Posted On

2020-06-30