Mutagenetix > Incidental Mutation

Incidental Mutation 'R1908:Btnl10'

210080

Institutional Source

Beutler Lab

Gene Symbol

Btnl10

Ensembl Gene

ENSMUSG00000020490

Gene Name

butyrophilin-like 10

Synonyms

BUTR-1, Butr1

MMRRC Submission

039927-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.079) question?

Stock #

R1908 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

58808703-58817791 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 58811367 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Proline to Glutamine at position 230 (P230Q)

Ref Sequence

ENSEMBL: ENSMUSP00000104446 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000020792] [ENSMUST00000069941] [ENSMUST00000108818] [ENSMUST00000142499]

AlphaFold

Q9JK39

Predicted Effect

possibly damaging
Transcript: ENSMUST00000020792
AA Change: P230Q

PolyPhen 2 Score 0.546 (Sensitivity: 0.88; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000020792
Gene: ENSMUSG00000020490
AA Change: P230Q

Domain	Start	End	E-Value	Type
IGv	49	130	2.62e-7	SMART
Pfam:C2-set_2	150	233	3.6e-9	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000069941
AA Change: P230Q

PolyPhen 2 Score 0.546 (Sensitivity: 0.88; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000063279
Gene: ENSMUSG00000020490
AA Change: P230Q

Domain	Start	End	E-Value	Type
IGv	49	130	2.62e-7	SMART
Pfam:C2-set_2	150	233	5.5e-7	PFAM
PRY	300	352	1.11e-11	SMART
SPRY	353	474	6.55e-24	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000108818
AA Change: P230Q

PolyPhen 2 Score 0.736 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000104446
Gene: ENSMUSG00000020490
AA Change: P230Q

Domain	Start	End	E-Value	Type
IGv	49	130	2.62e-7	SMART
Pfam:C2-set_2	150	233	3.6e-9	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000142499
AA Change: P230Q

PolyPhen 2 Score 0.546 (Sensitivity: 0.88; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000124234
Gene: ENSMUSG00000020490
AA Change: P230Q

Domain	Start	End	E-Value	Type
IGv	49	130	2.62e-7	SMART
Pfam:C2-set_2	151	233	1e-8	PFAM
PRY	300	352	1.11e-11	SMART
SPRY	353	474	6.55e-24	SMART

Coding Region Coverage

1x: 97.3%
3x: 96.8%
10x: 95.4%
20x: 93.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 83 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca8b	C	A	11: 109,847,924 (GRCm39)	L852F	possibly damaging	Het
Abcc6	T	C	7: 45,669,558 (GRCm39)		probably null	Het
Alg11	T	G	8: 22,555,584 (GRCm39)	C240G	probably damaging	Het
Aox1	A	G	1: 58,141,783 (GRCm39)	I1190V	probably damaging	Het
Apc2	T	G	10: 80,150,678 (GRCm39)	S1911A	probably benign	Het
Arfgef3	T	C	10: 18,528,511 (GRCm39)	D292G	possibly damaging	Het
Arhgef4	C	A	1: 34,763,340 (GRCm39)	S865R	probably benign	Het
Ass1	T	A	2: 31,383,160 (GRCm39)	Y190*	probably null	Het
B4galnt3	A	T	6: 120,187,051 (GRCm39)		probably null	Het
C3	A	G	17: 57,516,489 (GRCm39)	Y1348H	probably damaging	Het
Ccdc198	G	T	14: 49,464,032 (GRCm39)	D292E	probably damaging	Het
Cebpz	A	T	17: 79,242,336 (GRCm39)	Y439*	probably null	Het
Cic	C	A	7: 24,986,265 (GRCm39)	T1229K	probably damaging	Het
Clip4	T	C	17: 72,144,744 (GRCm39)	S524P	probably damaging	Het
Col6a3	A	C	1: 90,739,421 (GRCm39)	I269R	probably damaging	Het
Dbh	C	T	2: 27,071,506 (GRCm39)	T533I	possibly damaging	Het
Dcaf17	A	T	2: 70,890,713 (GRCm39)	R83*	probably null	Het
Dennd2b	G	A	7: 109,124,533 (GRCm39)	Q686*	probably null	Het
Dnah1	A	G	14: 30,984,515 (GRCm39)	L3923P	probably damaging	Het
Dnah7a	A	T	1: 53,670,721 (GRCm39)	D510E	probably benign	Het
Dock6	A	G	9: 21,752,925 (GRCm39)	F296S	probably damaging	Het
Eif4enif1	T	C	11: 3,177,455 (GRCm39)	S341P	probably damaging	Het
Epb41l1	G	T	2: 156,352,737 (GRCm39)	G461V	possibly damaging	Het
Epg5	T	A	18: 78,002,247 (GRCm39)	D555E	probably benign	Het
Fes	T	C	7: 80,036,609 (GRCm39)	R113G	probably damaging	Het
Garre1	T	A	7: 33,957,461 (GRCm39)	I59L	probably benign	Het
Gm10684	A	G	9: 45,021,511 (GRCm39)		probably benign	Het
Gm12185	T	C	11: 48,806,231 (GRCm39)	E320G	probably benign	Het
Gm14412	G	T	2: 177,007,269 (GRCm39)	H209N	probably damaging	Het
Gm14412	A	C	2: 177,007,630 (GRCm39)	S88R	probably benign	Het
Grhl1	T	A	12: 24,658,555 (GRCm39)	L400Q	probably damaging	Het
Havcr1	T	A	11: 46,664,511 (GRCm39)	Y216*	probably null	Het
Hephl1	A	C	9: 14,985,420 (GRCm39)	Y745*	probably null	Het
Hmcn2	T	G	2: 31,301,922 (GRCm39)		probably null	Het
Hs3st6	A	G	17: 24,977,110 (GRCm39)	K197E	possibly damaging	Het
Ifi214	C	T	1: 173,357,077 (GRCm39)	V9I	probably benign	Het
Jakmip2	T	C	18: 43,700,209 (GRCm39)	T450A	probably benign	Het
Lrp4	T	A	2: 91,328,753 (GRCm39)	V1551D	possibly damaging	Het
Macf1	A	T	4: 123,351,634 (GRCm39)	H1634Q	possibly damaging	Het
Mcpt8	T	A	14: 56,321,291 (GRCm39)	I58F	probably benign	Het
Mga	T	A	2: 119,757,075 (GRCm39)	H1018Q	possibly damaging	Het
Myo10	T	A	15: 25,801,308 (GRCm39)	V1499E	probably damaging	Het
Myom2	G	T	8: 15,131,023 (GRCm39)	D320Y	probably damaging	Het
Or11g7	T	A	14: 50,691,295 (GRCm39)	M262K	probably damaging	Het
Or13a27	T	C	7: 139,925,378 (GRCm39)	I175V	probably benign	Het
Or2r11	C	T	6: 42,437,360 (GRCm39)	V198M	probably benign	Het
Or2t26	A	C	11: 49,039,101 (GRCm39)	N6H	possibly damaging	Het
Or4c115	G	A	2: 88,927,888 (GRCm39)	P128S	probably damaging	Het
Or5d47	A	T	2: 87,804,403 (GRCm39)	V202D	possibly damaging	Het
Pabpc4	G	T	4: 123,182,861 (GRCm39)	R166L	possibly damaging	Het
Pcdhb8	A	G	18: 37,489,015 (GRCm39)	E231G	possibly damaging	Het
Pomgnt2	A	T	9: 121,811,257 (GRCm39)	I508N	possibly damaging	Het
Ppp2r5e	C	G	12: 75,516,341 (GRCm39)	A239P	probably damaging	Het
Prdm15	G	T	16: 97,638,885 (GRCm39)	D58E	probably benign	Het
Rgl2	A	G	17: 34,151,122 (GRCm39)	T117A	probably benign	Het
Rp1	A	G	1: 4,418,943 (GRCm39)	I723T	probably damaging	Het
Serpina3g	A	G	12: 104,207,536 (GRCm39)	E233G	probably damaging	Het
Skint6	T	A	4: 112,749,187 (GRCm39)	S798C	probably benign	Het
Slc35f1	T	C	10: 52,898,000 (GRCm39)	L137P	possibly damaging	Het
Slc6a20a	T	C	9: 123,485,373 (GRCm39)	N246S	probably damaging	Het
Slc7a2	T	C	8: 41,369,534 (GRCm39)	L663S	probably benign	Het
Slco1a4	A	G	6: 141,761,173 (GRCm39)		probably null	Het
Slit2	A	G	5: 48,439,330 (GRCm39)	T41A	probably damaging	Het
Smc2	T	C	4: 52,450,863 (GRCm39)	I227T	probably damaging	Het
Smg1	A	G	7: 117,753,422 (GRCm39)		probably benign	Het
Ssu2	A	T	6: 112,361,388 (GRCm39)	L23M	probably benign	Het
Syne2	A	G	12: 76,141,053 (GRCm39)		probably null	Het
Tekt1	T	C	11: 72,242,761 (GRCm39)	T249A	probably benign	Het
Tfr2	T	C	5: 137,569,954 (GRCm39)	V120A	probably benign	Het
Thsd7b	C	T	1: 129,605,846 (GRCm39)	P529L	probably damaging	Het
Tll1	C	T	8: 64,478,141 (GRCm39)	D871N	probably damaging	Het
Tlr11	A	C	14: 50,598,664 (GRCm39)	I217L	probably benign	Het
Tmem87b	T	A	2: 128,673,479 (GRCm39)	V241D	probably damaging	Het
Tshz2	T	A	2: 169,727,465 (GRCm39)	I218N	possibly damaging	Het
Vmn1r18	A	T	6: 57,367,026 (GRCm39)	I176N	possibly damaging	Het
Vmn2r68	T	A	7: 84,883,260 (GRCm39)	H164L	probably benign	Het
Vmn2r74	T	C	7: 85,601,650 (GRCm39)	T663A	probably benign	Het
Vmn2r8	T	C	5: 108,945,436 (GRCm39)	T724A	probably benign	Het
Wdr11	T	C	7: 129,206,954 (GRCm39)	V289A	possibly damaging	Het
Zfp62	T	A	11: 49,107,047 (GRCm39)	D379E	probably damaging	Het
Zfp78	C	T	7: 6,381,897 (GRCm39)	P316S	probably damaging	Het
Zfyve27	T	G	19: 42,159,987 (GRCm39)	M1R	probably null	Het
Zkscan8	G	A	13: 21,709,325 (GRCm39)	P191L	probably damaging	Het

Other mutations in Btnl10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02033:Btnl10	APN	11	58,810,141 (GRCm39)	missense	probably damaging	0.98
IGL03368:Btnl10	APN	11	58,810,212 (GRCm39)	missense	possibly damaging	0.61
FR4304:Btnl10	UTSW	11	58,814,756 (GRCm39)	small insertion	probably benign
FR4449:Btnl10	UTSW	11	58,814,754 (GRCm39)	small insertion	probably benign
FR4589:Btnl10	UTSW	11	58,814,755 (GRCm39)	small insertion	probably benign
FR4737:Btnl10	UTSW	11	58,814,757 (GRCm39)	small insertion	probably benign
FR4976:Btnl10	UTSW	11	58,814,755 (GRCm39)	small insertion	probably benign
R0420:Btnl10	UTSW	11	58,814,277 (GRCm39)	missense	probably damaging	1.00
R1875:Btnl10	UTSW	11	58,814,586 (GRCm39)	missense	probably damaging	0.97
R3176:Btnl10	UTSW	11	58,813,216 (GRCm39)	missense	probably benign	0.00
R3177:Btnl10	UTSW	11	58,813,216 (GRCm39)	missense	probably benign	0.00
R3276:Btnl10	UTSW	11	58,813,216 (GRCm39)	missense	probably benign	0.00
R3277:Btnl10	UTSW	11	58,813,216 (GRCm39)	missense	probably benign	0.00
R4600:Btnl10	UTSW	11	58,814,426 (GRCm39)	missense	probably benign	0.01
R4611:Btnl10	UTSW	11	58,811,183 (GRCm39)	missense	probably damaging	1.00
R5447:Btnl10	UTSW	11	58,813,144 (GRCm39)	missense	probably benign	0.13
R5484:Btnl10	UTSW	11	58,814,651 (GRCm39)	missense	probably damaging	0.98
R5787:Btnl10	UTSW	11	58,811,169 (GRCm39)	missense	probably damaging	1.00
R5824:Btnl10	UTSW	11	58,814,266 (GRCm39)	missense	probably benign	0.05
R5859:Btnl10	UTSW	11	58,813,138 (GRCm39)	missense	probably benign	0.10
R6109:Btnl10	UTSW	11	58,811,130 (GRCm39)	missense	probably damaging	0.98
R6123:Btnl10	UTSW	11	58,811,130 (GRCm39)	missense	probably damaging	0.98
R6318:Btnl10	UTSW	11	58,817,691 (GRCm39)	utr 3 prime	probably benign
R7064:Btnl10	UTSW	11	58,810,134 (GRCm39)	missense	possibly damaging	0.74
R7083:Btnl10	UTSW	11	58,809,963 (GRCm39)	missense	probably damaging	1.00
R7152:Btnl10	UTSW	11	58,813,223 (GRCm39)	missense	probably benign
R7393:Btnl10	UTSW	11	58,814,532 (GRCm39)	missense	probably damaging	1.00
R7507:Btnl10	UTSW	11	58,811,384 (GRCm39)	missense	probably benign	0.05
R7893:Btnl10	UTSW	11	58,814,635 (GRCm39)	missense	probably benign	0.01
R8485:Btnl10	UTSW	11	58,811,142 (GRCm39)	missense	possibly damaging	0.92
R8529:Btnl10	UTSW	11	58,813,238 (GRCm39)	missense	probably benign	0.00
R8909:Btnl10	UTSW	11	58,813,198 (GRCm39)	missense	probably benign	0.00
R9205:Btnl10	UTSW	11	58,811,345 (GRCm39)	missense	probably damaging	1.00
R9564:Btnl10	UTSW	11	58,813,189 (GRCm39)	missense	probably benign	0.13
R9565:Btnl10	UTSW	11	58,813,189 (GRCm39)	missense	probably benign	0.13
R9675:Btnl10	UTSW	11	58,814,442 (GRCm39)	missense	probably damaging	1.00
RF018:Btnl10	UTSW	11	58,814,752 (GRCm39)	small insertion	probably benign
RF043:Btnl10	UTSW	11	58,814,752 (GRCm39)	small insertion	probably benign
X0064:Btnl10	UTSW	11	58,814,436 (GRCm39)	missense	probably damaging	1.00
Z1186:Btnl10	UTSW	11	58,817,650 (GRCm39)	missense	unknown
Z1186:Btnl10	UTSW	11	58,814,753 (GRCm39)	small insertion	probably benign
Z1186:Btnl10	UTSW	11	58,810,138 (GRCm39)	missense	probably benign
Z1187:Btnl10	UTSW	11	58,814,755 (GRCm39)	small insertion	probably benign
Z1187:Btnl10	UTSW	11	58,814,753 (GRCm39)	small insertion	probably benign
Z1187:Btnl10	UTSW	11	58,810,138 (GRCm39)	missense	probably benign
Z1187:Btnl10	UTSW	11	58,817,650 (GRCm39)	missense	unknown
Z1188:Btnl10	UTSW	11	58,814,753 (GRCm39)	small insertion	probably benign
Z1188:Btnl10	UTSW	11	58,810,138 (GRCm39)	missense	probably benign
Z1188:Btnl10	UTSW	11	58,817,650 (GRCm39)	missense	unknown
Z1189:Btnl10	UTSW	11	58,817,650 (GRCm39)	missense	unknown
Z1189:Btnl10	UTSW	11	58,814,753 (GRCm39)	small insertion	probably benign
Z1189:Btnl10	UTSW	11	58,810,138 (GRCm39)	missense	probably benign
Z1190:Btnl10	UTSW	11	58,817,650 (GRCm39)	missense	unknown
Z1190:Btnl10	UTSW	11	58,814,753 (GRCm39)	small insertion	probably benign
Z1190:Btnl10	UTSW	11	58,810,138 (GRCm39)	missense	probably benign
Z1191:Btnl10	UTSW	11	58,814,755 (GRCm39)	small insertion	probably benign
Z1191:Btnl10	UTSW	11	58,814,753 (GRCm39)	small insertion	probably benign
Z1191:Btnl10	UTSW	11	58,810,138 (GRCm39)	missense	probably benign
Z1191:Btnl10	UTSW	11	58,817,650 (GRCm39)	missense	unknown
Z1192:Btnl10	UTSW	11	58,814,754 (GRCm39)	small insertion	probably benign
Z1192:Btnl10	UTSW	11	58,814,753 (GRCm39)	small insertion	probably benign
Z1192:Btnl10	UTSW	11	58,810,138 (GRCm39)	missense	probably benign
Z1192:Btnl10	UTSW	11	58,817,650 (GRCm39)	missense	unknown
Z1192:Btnl10	UTSW	11	58,814,757 (GRCm39)	small insertion	probably benign

Predicted Primers

PCR Primer
(F):5'- CCAGAATCCGTGTGACTGAC -3'
(R):5'- TTGTCTTGGAAACCAACATCCC -3'

Sequencing Primer
(F):5'- ACCTCAGCAGGCTGGTAC -3'
(R):5'- CTACGACCCTCTTGGCCAG -3'

Posted On

2014-06-30