Mutagenetix > Incidental Mutation

Incidental Mutation 'R9563:Bsn'

721244

Institutional Source

Beutler Lab

Gene Symbol

Bsn

Ensembl Gene

ENSMUSG00000032589

Gene Name

bassoon

Synonyms

presynaptic cytomatrix protein

MMRRC Submission

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.295) question?

Stock #

R9563 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

107973221-108067583 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 107984616 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 374 (D374G)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000035208]

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000035208
AA Change: D3146G

SMART Domains

Protein: ENSMUSP00000035208
Gene: ENSMUSG00000032589
AA Change: D3146G

Domain	Start	End	E-Value	Type
low complexity region	4	40	N/A	INTRINSIC
low complexity region	42	77	N/A	INTRINSIC
Pfam:zf-piccolo	165	223	6.1e-30	PFAM
low complexity region	394	409	N/A	INTRINSIC
low complexity region	445	454	N/A	INTRINSIC
Pfam:zf-piccolo	462	520	5.2e-31	PFAM
low complexity region	527	540	N/A	INTRINSIC
low complexity region	627	643	N/A	INTRINSIC
low complexity region	664	681	N/A	INTRINSIC
low complexity region	694	708	N/A	INTRINSIC
low complexity region	788	803	N/A	INTRINSIC
low complexity region	994	1021	N/A	INTRINSIC
coiled coil region	1047	1101	N/A	INTRINSIC
low complexity region	1131	1145	N/A	INTRINSIC
low complexity region	1173	1190	N/A	INTRINSIC
low complexity region	1209	1220	N/A	INTRINSIC
low complexity region	1333	1343	N/A	INTRINSIC
low complexity region	1443	1455	N/A	INTRINSIC
low complexity region	1481	1498	N/A	INTRINSIC
low complexity region	1790	1800	N/A	INTRINSIC
low complexity region	2117	2126	N/A	INTRINSIC
low complexity region	2287	2303	N/A	INTRINSIC
low complexity region	2326	2356	N/A	INTRINSIC
SCOP:d1eq1a_	2362	2477	2e-7	SMART
low complexity region	2607	2614	N/A	INTRINSIC
low complexity region	2635	2651	N/A	INTRINSIC
low complexity region	2655	2672	N/A	INTRINSIC
coiled coil region	2949	2990	N/A	INTRINSIC
low complexity region	3057	3071	N/A	INTRINSIC
low complexity region	3089	3114	N/A	INTRINSIC
low complexity region	3446	3461	N/A	INTRINSIC
low complexity region	3520	3534	N/A	INTRINSIC
low complexity region	3653	3666	N/A	INTRINSIC
low complexity region	3750	3820	N/A	INTRINSIC
low complexity region	3831	3852	N/A	INTRINSIC
low complexity region	3856	3901	N/A	INTRINSIC

Predicted Effect

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.9%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Neurotransmitters are released from a specific site in the axon terminal called the active zone, which is composed of synaptic vesicles and a meshwork of cytoskeleton underlying the plasma membrane. The protein encoded by this gene is thought to be a scaffolding protein involved in organizing the presynaptic cytoskeleton. The gene is expressed primarily in neurons in the brain. A similar gene product in rodents is concentrated in the active zone of axon terminals and tightly associated with cytoskeletal structures, and is essential for regulating neurotransmitter release from a subset of synapses. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mutants lacking functional protein exhibit impaired hippocampal and photoreceptor synaptic transmission, aberrant photoreceptor ribbon synapse formation, and spontaneous epileptic seizures. [provided by MGI curators]

Allele List at MGI

All alleles(9) : Targeted, other(1) Gene trapped(8)

Other mutations in this stock

Total: 127 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A2m	T	A	6: 121,645,009 (GRCm39)	D953E	probably damaging	Het
Acod1	A	C	14: 103,287,109 (GRCm39)	Y80S	probably damaging	Het
Actr5	A	G	2: 158,470,135 (GRCm39)	D255G	probably damaging	Het
Akna	A	G	4: 63,312,944 (GRCm39)	V393A	probably damaging	Het
Amotl1	T	C	9: 14,473,513 (GRCm39)	K562R	possibly damaging	Het
Amz1	T	A	5: 140,738,133 (GRCm39)	D464E	probably damaging	Het
Anapc1	G	A	2: 128,505,980 (GRCm39)	Q619*	probably null	Het
Arfgef3	C	T	10: 18,522,275 (GRCm39)	G584R	probably damaging	Het
Armt1	AC	A	10: 4,400,848 (GRCm39)		probably null	Het
Atr	G	C	9: 95,802,833 (GRCm39)	V1832L	probably damaging	Het
Cap1	A	G	4: 122,758,505 (GRCm39)	V225A	probably benign	Het
Cc2d1a	A	G	8: 84,863,758 (GRCm39)	S562P	probably benign	Het
Ccdc30	T	C	4: 119,250,821 (GRCm39)	N141S	possibly damaging	Het
Cdc42bpb	A	G	12: 111,265,762 (GRCm39)	V1390A	possibly damaging	Het
Cdc42ep1	A	T	15: 78,733,782 (GRCm39)	H294L	probably benign	Het
Col6a6	C	A	9: 105,572,952 (GRCm39)	G2185C	probably benign	Het
Col7a1	T	C	9: 108,791,809 (GRCm39)	V1232A	unknown	Het
Copb1	A	G	7: 113,836,034 (GRCm39)	I449T	possibly damaging	Het
Cplane1	T	G	15: 8,216,563 (GRCm39)	L594V	probably benign	Het
Ctdsp2	A	G	10: 126,832,040 (GRCm39)	D216G	probably damaging	Het
Cttnbp2	T	A	6: 18,367,382 (GRCm39)	K1645N	probably benign	Het
Cttnbp2	A	T	6: 18,427,467 (GRCm39)	L738*	probably null	Het
Cul9	T	A	17: 46,820,897 (GRCm39)	T1927S	probably benign	Het
Cyfip2	A	G	11: 46,151,707 (GRCm39)	C531R	probably benign	Het
Cyp2j6	A	G	4: 96,414,245 (GRCm39)	I340T	probably damaging	Het
Daam1	A	G	12: 71,992,251 (GRCm39)	E322G	unknown	Het
Dab2ip	T	A	2: 35,609,915 (GRCm39)	L710*	probably null	Het
Degs1l	G	T	1: 180,882,810 (GRCm39)	V191F	possibly damaging	Het
Dph1	T	C	11: 75,076,825 (GRCm39)	T60A	possibly damaging	Het
Eme1	T	C	11: 94,541,339 (GRCm39)	D161G	probably benign	Het
Epha3	C	T	16: 63,366,510 (GRCm39)	G980D	possibly damaging	Het
Eri3	T	A	4: 117,422,013 (GRCm39)	V136E	probably benign	Het
Espl1	T	A	15: 102,228,233 (GRCm39)	I1669N	possibly damaging	Het
Exoc6	T	C	19: 37,588,071 (GRCm39)	I568T	probably damaging	Het
F3	T	A	3: 121,527,822 (GRCm39)	L85H		Het
Fam186b	G	A	15: 99,177,616 (GRCm39)	A570V	probably damaging	Het
Fbxw14	T	C	9: 109,106,335 (GRCm39)	Y234C	probably benign	Het
Fbxw25	T	A	9: 109,483,676 (GRCm39)	N179Y		Het
Foxr1	T	A	9: 44,352,199 (GRCm39)		probably benign	Het
Gas8	T	A	8: 124,263,179 (GRCm39)	V452E	possibly damaging	Het
Gdpd4	T	C	7: 97,649,369 (GRCm39)	V450A	probably damaging	Het
Greb1	T	C	12: 16,774,824 (GRCm39)	Y191C	probably benign	Het
H3c11	T	C	13: 21,967,221 (GRCm39)	D107G	probably damaging	Het
Haus3	G	A	5: 34,325,300 (GRCm39)	R120W	probably benign	Het
Herc1	G	T	9: 66,294,193 (GRCm39)		probably null	Het
Hyal2	T	C	9: 107,447,844 (GRCm39)	W166R	probably damaging	Het
Inka1	T	A	9: 107,861,488 (GRCm39)	Y276F	probably benign	Het
Itga7	C	T	10: 128,789,669 (GRCm39)	A1003V	probably damaging	Het
Itga8	T	A	2: 12,165,219 (GRCm39)	I797F	possibly damaging	Het
Kank2	T	C	9: 21,705,852 (GRCm39)	T389A	possibly damaging	Het
Kcnb2	T	A	1: 15,779,737 (GRCm39)	I203N	probably damaging	Het
Kif21b	T	A	1: 136,077,166 (GRCm39)	L396Q	probably damaging	Het
Kng1	T	G	16: 22,879,170 (GRCm39)	I78S	probably damaging	Het
Ldlrad4	T	C	18: 68,387,551 (GRCm39)	S288P	probably benign	Het
Lmntd2	A	G	7: 140,790,701 (GRCm39)	S516P		Het
Lrp1b	T	A	2: 41,185,711 (GRCm39)	I1449F		Het
Lrrk2	T	A	15: 91,634,043 (GRCm39)	I1380K	possibly damaging	Het
Lvrn	T	G	18: 47,017,506 (GRCm39)	I612S	probably damaging	Het
Lyst	T	C	13: 13,812,408 (GRCm39)	L940P	probably benign	Het
Man2a2	T	A	7: 80,006,101 (GRCm39)	M996L	probably benign	Het
Map3k3	T	A	11: 106,041,860 (GRCm39)	I413N	probably damaging	Het
Map4k5	A	G	12: 69,863,167 (GRCm39)	V629A	probably benign	Het
Mapre2	A	G	18: 24,023,981 (GRCm39)	E325G	unknown	Het
Mbnl1	A	G	3: 60,520,715 (GRCm39)	N101S	probably benign	Het
Meltf	T	A	16: 31,703,869 (GRCm39)	C199S	probably damaging	Het
Mmab	T	C	5: 114,574,850 (GRCm39)	E141G	probably benign	Het
Mtcl2	G	A	2: 156,902,182 (GRCm39)	R278C	probably damaging	Het
Mtus2	T	C	5: 148,250,217 (GRCm39)	L1317P		Het
Muc6	T	A	7: 141,217,783 (GRCm39)	T2297S	possibly damaging	Het
Myom2	A	T	8: 15,158,399 (GRCm39)	K784*	probably null	Het
Nek1	A	G	8: 61,577,157 (GRCm39)	E1118G	probably benign	Het
Nrtn	A	G	17: 57,058,416 (GRCm39)	V195A	probably damaging	Het
Nsd3	G	A	8: 26,204,230 (GRCm39)	V420I		Het
Or52e4	T	C	7: 104,706,281 (GRCm39)	L276P	possibly damaging	Het
Or52z13	A	T	7: 103,247,225 (GRCm39)	Q234L	probably benign	Het
Or5ac23	T	C	16: 59,149,765 (GRCm39)	I36V	probably benign	Het
Or5b99	T	A	19: 12,976,983 (GRCm39)	I211N	probably damaging	Het
Or5t9	A	G	2: 86,659,098 (GRCm39)	M1V	probably null	Het
Or6ae1	G	A	7: 139,742,233 (GRCm39)	T210I	probably damaging	Het
Or6c33	T	C	10: 129,853,287 (GRCm39)	I19T	probably benign	Het
Or8b56	A	T	9: 38,739,014 (GRCm39)	H3L	probably benign	Het
Pde10a	G	T	17: 9,020,710 (GRCm39)	A216S	unknown	Het
Phldb2	T	C	16: 45,645,247 (GRCm39)	T400A	possibly damaging	Het
Pkd1l1	T	A	11: 8,815,502 (GRCm39)	T1920S		Het
Ptgs2	T	A	1: 149,981,419 (GRCm39)	N567K	probably benign	Het
Pwp1	T	A	10: 85,712,370 (GRCm39)	D141E	probably damaging	Het
Rab3ip	T	C	10: 116,754,668 (GRCm39)	E296G	probably null	Het
Rb1cc1	A	G	1: 6,314,339 (GRCm39)	K337R	probably benign	Het
Rbp3	A	G	14: 33,677,477 (GRCm39)	D475G	probably damaging	Het
Ric3	T	C	7: 108,637,997 (GRCm39)	E253G	possibly damaging	Het
Rictor	A	T	15: 6,797,562 (GRCm39)	N306I	possibly damaging	Het
Rnf214	A	T	9: 45,811,141 (GRCm39)	V174E	possibly damaging	Het
Robo3	A	G	9: 37,340,900 (GRCm39)	F124S	probably damaging	Het
Rrad	A	G	8: 105,355,324 (GRCm39)	F228S	probably damaging	Het
Scn3a	A	T	2: 65,291,595 (GRCm39)	M1717K	probably damaging	Het
Scn3b	A	G	9: 40,193,729 (GRCm39)	D152G	probably benign	Het
Scn5a	C	A	9: 119,315,803 (GRCm39)	R1635L	probably damaging	Het
Sec61b	A	G	4: 47,483,049 (GRCm39)	Y93C	probably damaging	Het
Shprh	T	A	10: 11,042,235 (GRCm39)	Y739*	probably null	Het
Skor2	C	T	18: 76,946,376 (GRCm39)	H33Y	unknown	Het
Slc26a7	T	C	4: 14,519,496 (GRCm39)	N508S	probably benign	Het
Slc7a12	A	G	3: 14,564,360 (GRCm39)	I349V	possibly damaging	Het
Slit1	T	C	19: 41,596,874 (GRCm39)	Y1075C	probably damaging	Het
Sltm	C	T	9: 70,480,841 (GRCm39)	A231V	unknown	Het
Smg1	A	G	7: 117,812,208 (GRCm39)	S52P	unknown	Het
Sorl1	A	G	9: 41,957,893 (GRCm39)	Y584H	probably damaging	Het
Spmip2	A	T	3: 79,356,616 (GRCm39)	M140L	probably benign	Het
Ssbp1	T	A	6: 40,454,968 (GRCm39)	S142R	probably benign	Het
Stard3	A	G	11: 98,270,797 (GRCm39)		probably null	Het
Strn3	G	T	12: 51,674,300 (GRCm39)	H531N	possibly damaging	Het
Stx17	A	G	4: 48,180,739 (GRCm39)	T195A	probably damaging	Het
Tekt2	C	T	4: 126,217,444 (GRCm39)	R207H	probably damaging	Het
Tmed5	A	C	5: 108,280,100 (GRCm39)		probably null	Het
Tmem132a	C	T	19: 10,838,960 (GRCm39)	R494H	probably benign	Het
Tom1	A	G	8: 75,787,177 (GRCm39)	K406E	probably benign	Het
Trav5d-4	A	T	14: 53,239,473 (GRCm39)	N43Y	probably damaging	Het
Trbv19	G	T	6: 41,155,945 (GRCm39)	K105N	possibly damaging	Het
Trim34a	C	T	7: 103,910,328 (GRCm39)	Q377*	probably null	Het
Trp53bp2	T	A	1: 182,276,378 (GRCm39)	N786K	probably benign	Het
Trpc3	A	G	3: 36,705,683 (GRCm39)	M504T	probably benign	Het
Ttc28	A	T	5: 111,371,092 (GRCm39)	M545L	probably benign	Het
Uggt1	A	C	1: 36,204,627 (GRCm39)	V996G	possibly damaging	Het
Vmn2r65	G	A	7: 84,589,880 (GRCm39)	Q679*	probably null	Het
Wdfy4	T	C	14: 32,692,833 (GRCm39)	I2958V		Het
Zbtb37	C	T	1: 160,847,840 (GRCm39)	S389N	possibly damaging	Het
Zfp235	T	C	7: 23,841,669 (GRCm39)	V696A	possibly damaging	Het
Zzef1	T	A	11: 72,765,732 (GRCm39)	C1420S	probably damaging	Het

Other mutations in Bsn

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00161:Bsn	APN	9	107,992,309 (GRCm39)	missense	probably benign	0.01
IGL00330:Bsn	APN	9	107,992,539 (GRCm39)	missense	probably damaging	1.00
IGL00863:Bsn	APN	9	107,992,521 (GRCm39)	missense	probably damaging	1.00
IGL01123:Bsn	APN	9	107,993,185 (GRCm39)	missense	probably damaging	1.00
IGL01330:Bsn	APN	9	107,988,112 (GRCm39)	unclassified	probably benign
IGL01336:Bsn	APN	9	107,988,984 (GRCm39)	missense	probably damaging	0.99
IGL01399:Bsn	APN	9	107,984,386 (GRCm39)	missense	unknown
IGL01683:Bsn	APN	9	107,992,095 (GRCm39)	missense	possibly damaging	0.71
IGL02022:Bsn	APN	9	107,987,617 (GRCm39)	unclassified	probably benign
IGL02396:Bsn	APN	9	107,993,245 (GRCm39)	missense	possibly damaging	0.90
IGL02538:Bsn	APN	9	107,982,435 (GRCm39)	missense	unknown
IGL02565:Bsn	APN	9	107,990,487 (GRCm39)	missense	probably damaging	0.99
IGL02661:Bsn	APN	9	107,984,135 (GRCm39)	nonsense	probably null
IGL02739:Bsn	APN	9	107,989,745 (GRCm39)	missense	probably benign	0.14
IGL02951:Bsn	APN	9	107,992,812 (GRCm39)	missense	probably damaging	1.00
IGL02987:Bsn	APN	9	108,003,503 (GRCm39)	missense	probably benign	0.03
IGL03033:Bsn	APN	9	107,993,192 (GRCm39)	missense	probably damaging	1.00
IGL03069:Bsn	APN	9	107,991,462 (GRCm39)	missense	probably damaging	1.00
IGL03076:Bsn	APN	9	107,982,581 (GRCm39)	missense	unknown
R0068:Bsn	UTSW	9	107,989,336 (GRCm39)	missense	probably damaging	1.00
R0068:Bsn	UTSW	9	107,989,336 (GRCm39)	missense	probably damaging	1.00
R0167:Bsn	UTSW	9	108,003,185 (GRCm39)	missense	probably benign	0.01
R0234:Bsn	UTSW	9	107,993,595 (GRCm39)	missense	possibly damaging	0.50
R0234:Bsn	UTSW	9	107,993,595 (GRCm39)	missense	possibly damaging	0.50
R0359:Bsn	UTSW	9	107,989,045 (GRCm39)	missense	possibly damaging	0.81
R0514:Bsn	UTSW	9	108,002,981 (GRCm39)	missense	probably benign	0.07
R0593:Bsn	UTSW	9	107,987,505 (GRCm39)	missense	unknown
R0617:Bsn	UTSW	9	107,984,439 (GRCm39)	missense	unknown
R0636:Bsn	UTSW	9	107,985,033 (GRCm39)	missense	unknown
R0652:Bsn	UTSW	9	107,982,941 (GRCm39)	missense	unknown
R0718:Bsn	UTSW	9	107,988,559 (GRCm39)	unclassified	probably benign
R0730:Bsn	UTSW	9	107,984,011 (GRCm39)	missense	unknown
R0905:Bsn	UTSW	9	107,982,834 (GRCm39)	missense	unknown
R0963:Bsn	UTSW	9	107,989,006 (GRCm39)	missense	possibly damaging	0.81
R0992:Bsn	UTSW	9	107,991,553 (GRCm39)	nonsense	probably null
R1101:Bsn	UTSW	9	107,993,610 (GRCm39)	missense	probably damaging	1.00
R1393:Bsn	UTSW	9	107,987,716 (GRCm39)	unclassified	probably benign
R1490:Bsn	UTSW	9	107,991,193 (GRCm39)	missense	probably benign	0.03
R1566:Bsn	UTSW	9	108,003,184 (GRCm39)	missense	probably benign	0.35
R1582:Bsn	UTSW	9	107,982,291 (GRCm39)	missense	unknown
R1738:Bsn	UTSW	9	107,984,133 (GRCm39)	missense	unknown
R1867:Bsn	UTSW	9	107,983,918 (GRCm39)	missense	unknown
R1918:Bsn	UTSW	9	107,984,772 (GRCm39)	missense	unknown
R1933:Bsn	UTSW	9	107,993,643 (GRCm39)	missense	possibly damaging	0.91
R1946:Bsn	UTSW	9	107,991,850 (GRCm39)	missense	probably damaging	0.99
R1978:Bsn	UTSW	9	107,991,748 (GRCm39)	missense	probably benign	0.35
R2068:Bsn	UTSW	9	108,003,749 (GRCm39)	missense	possibly damaging	0.95
R2068:Bsn	UTSW	9	107,987,883 (GRCm39)	unclassified	probably benign
R2113:Bsn	UTSW	9	107,992,085 (GRCm39)	missense	probably benign	0.14
R2136:Bsn	UTSW	9	107,990,430 (GRCm39)	missense	probably damaging	1.00
R2172:Bsn	UTSW	9	107,987,191 (GRCm39)	intron	probably benign
R2266:Bsn	UTSW	9	107,992,323 (GRCm39)	missense	probably damaging	1.00
R2293:Bsn	UTSW	9	107,990,266 (GRCm39)	missense	possibly damaging	0.47
R2294:Bsn	UTSW	9	107,990,266 (GRCm39)	missense	possibly damaging	0.47
R2368:Bsn	UTSW	9	107,988,229 (GRCm39)	nonsense	probably null
R2442:Bsn	UTSW	9	107,984,119 (GRCm39)	missense	unknown
R2507:Bsn	UTSW	9	107,993,313 (GRCm39)	missense	probably damaging	1.00
R2880:Bsn	UTSW	9	107,990,266 (GRCm39)	missense	possibly damaging	0.47
R2881:Bsn	UTSW	9	107,990,266 (GRCm39)	missense	possibly damaging	0.47
R2922:Bsn	UTSW	9	107,992,668 (GRCm39)	missense	probably damaging	1.00
R2922:Bsn	UTSW	9	107,985,385 (GRCm39)	missense	unknown
R3618:Bsn	UTSW	9	107,994,760 (GRCm39)	critical splice acceptor site	probably null
R3742:Bsn	UTSW	9	107,982,938 (GRCm39)	missense	unknown
R3825:Bsn	UTSW	9	107,984,055 (GRCm39)	missense	unknown
R3982:Bsn	UTSW	9	107,984,365 (GRCm39)	missense	unknown
R4094:Bsn	UTSW	9	107,991,069 (GRCm39)	missense	probably damaging	1.00
R4158:Bsn	UTSW	9	107,990,145 (GRCm39)	missense	possibly damaging	0.95
R4225:Bsn	UTSW	9	107,983,932 (GRCm39)	missense	unknown
R4261:Bsn	UTSW	9	107,987,883 (GRCm39)	unclassified	probably benign
R4482:Bsn	UTSW	9	107,991,863 (GRCm39)	missense	probably damaging	1.00
R4515:Bsn	UTSW	9	107,981,277 (GRCm39)	splice site	probably null
R4585:Bsn	UTSW	9	107,987,662 (GRCm39)	unclassified	probably benign
R4628:Bsn	UTSW	9	107,990,434 (GRCm39)	missense	probably damaging	1.00
R4636:Bsn	UTSW	9	107,992,623 (GRCm39)	missense	probably damaging	1.00
R4679:Bsn	UTSW	9	107,987,329 (GRCm39)	missense	unknown
R4723:Bsn	UTSW	9	107,989,854 (GRCm39)	missense	probably benign	0.03
R4843:Bsn	UTSW	9	107,984,388 (GRCm39)	missense	unknown
R4885:Bsn	UTSW	9	107,984,726 (GRCm39)	nonsense	probably null
R4936:Bsn	UTSW	9	107,988,960 (GRCm39)	missense	probably damaging	1.00
R4942:Bsn	UTSW	9	107,983,678 (GRCm39)	missense	unknown
R4972:Bsn	UTSW	9	107,992,377 (GRCm39)	missense	probably damaging	1.00
R4992:Bsn	UTSW	9	107,992,747 (GRCm39)	missense	probably damaging	1.00
R5067:Bsn	UTSW	9	107,989,152 (GRCm39)	missense	probably damaging	1.00
R5206:Bsn	UTSW	9	107,982,572 (GRCm39)	missense	unknown
R5286:Bsn	UTSW	9	107,988,123 (GRCm39)	unclassified	probably benign
R5492:Bsn	UTSW	9	107,989,714 (GRCm39)	missense	probably damaging	0.98
R5553:Bsn	UTSW	9	107,987,620 (GRCm39)	unclassified	probably benign
R5561:Bsn	UTSW	9	107,982,710 (GRCm39)	missense	unknown
R5597:Bsn	UTSW	9	107,992,131 (GRCm39)	missense	probably benign	0.06
R5646:Bsn	UTSW	9	107,987,631 (GRCm39)	unclassified	probably benign
R5796:Bsn	UTSW	9	108,003,223 (GRCm39)	missense	probably damaging	1.00
R5801:Bsn	UTSW	9	107,990,208 (GRCm39)	missense	possibly damaging	0.81
R5802:Bsn	UTSW	9	107,990,208 (GRCm39)	missense	possibly damaging	0.81
R5850:Bsn	UTSW	9	107,992,149 (GRCm39)	missense	probably damaging	0.99
R5938:Bsn	UTSW	9	107,990,208 (GRCm39)	missense	possibly damaging	0.81
R6221:Bsn	UTSW	9	107,982,765 (GRCm39)	missense	unknown
R6243:Bsn	UTSW	9	107,984,760 (GRCm39)	missense	unknown
R6254:Bsn	UTSW	9	107,989,065 (GRCm39)	missense	probably damaging	0.96
R6263:Bsn	UTSW	9	107,990,453 (GRCm39)	missense	probably damaging	1.00
R6345:Bsn	UTSW	9	107,984,554 (GRCm39)	missense	unknown
R6368:Bsn	UTSW	9	107,988,513 (GRCm39)	unclassified	probably benign
R6574:Bsn	UTSW	9	107,991,153 (GRCm39)	missense	possibly damaging	0.95
R6793:Bsn	UTSW	9	107,991,814 (GRCm39)	nonsense	probably null
R6802:Bsn	UTSW	9	107,987,823 (GRCm39)	unclassified	probably benign
R6943:Bsn	UTSW	9	107,985,016 (GRCm39)	missense	unknown
R6999:Bsn	UTSW	9	107,990,632 (GRCm39)	missense	probably benign	0.00
R7149:Bsn	UTSW	9	107,993,520 (GRCm39)	nonsense	probably null
R7199:Bsn	UTSW	9	107,992,533 (GRCm39)	missense	probably damaging	1.00
R7322:Bsn	UTSW	9	108,003,620 (GRCm39)	nonsense	probably null
R7349:Bsn	UTSW	9	107,987,982 (GRCm39)	missense	unknown
R7372:Bsn	UTSW	9	107,987,718 (GRCm39)	missense	unknown
R7373:Bsn	UTSW	9	107,990,683 (GRCm39)	missense	probably damaging	1.00
R7413:Bsn	UTSW	9	108,016,690 (GRCm39)	missense	possibly damaging	0.61
R7473:Bsn	UTSW	9	107,989,449 (GRCm39)	missense	probably damaging	1.00
R7482:Bsn	UTSW	9	107,990,728 (GRCm39)	missense	probably damaging	0.98
R7530:Bsn	UTSW	9	107,989,155 (GRCm39)	missense	probably damaging	1.00
R7549:Bsn	UTSW	9	107,992,014 (GRCm39)	missense	probably benign	0.05
R7570:Bsn	UTSW	9	107,990,742 (GRCm39)	missense	probably damaging	1.00
R7635:Bsn	UTSW	9	107,988,189 (GRCm39)	missense	unknown
R7696:Bsn	UTSW	9	107,991,700 (GRCm39)	missense	probably damaging	1.00
R7757:Bsn	UTSW	9	107,991,939 (GRCm39)	missense	possibly damaging	0.90
R7868:Bsn	UTSW	9	107,992,098 (GRCm39)	missense	possibly damaging	0.95
R7897:Bsn	UTSW	9	107,989,065 (GRCm39)	missense	probably damaging	0.98
R7960:Bsn	UTSW	9	107,992,747 (GRCm39)	missense	probably damaging	1.00
R8022:Bsn	UTSW	9	107,991,603 (GRCm39)	missense	probably benign	0.01
R8056:Bsn	UTSW	9	107,982,506 (GRCm39)	missense
R8158:Bsn	UTSW	9	107,987,232 (GRCm39)	missense	unknown
R8161:Bsn	UTSW	9	108,016,729 (GRCm39)	missense	probably benign	0.20
R8225:Bsn	UTSW	9	107,984,305 (GRCm39)	missense
R8282:Bsn	UTSW	9	107,984,890 (GRCm39)	missense	possibly damaging	0.73
R8296:Bsn	UTSW	9	107,994,578 (GRCm39)	missense	probably benign	0.00
R8415:Bsn	UTSW	9	107,988,651 (GRCm39)	missense	probably benign	0.00
R8417:Bsn	UTSW	9	107,988,651 (GRCm39)	missense	probably benign	0.00
R8426:Bsn	UTSW	9	108,003,772 (GRCm39)	missense	probably damaging	1.00
R8437:Bsn	UTSW	9	107,988,651 (GRCm39)	missense	probably benign	0.00
R8438:Bsn	UTSW	9	107,988,651 (GRCm39)	missense	probably benign	0.00
R8439:Bsn	UTSW	9	107,988,651 (GRCm39)	missense	probably benign	0.00
R8440:Bsn	UTSW	9	107,988,651 (GRCm39)	missense	probably benign	0.00
R8441:Bsn	UTSW	9	107,988,651 (GRCm39)	missense	probably benign	0.00
R8442:Bsn	UTSW	9	107,988,651 (GRCm39)	missense	probably benign	0.00
R8513:Bsn	UTSW	9	107,991,709 (GRCm39)	missense	possibly damaging	0.65
R8529:Bsn	UTSW	9	107,988,651 (GRCm39)	missense	probably benign	0.00
R8535:Bsn	UTSW	9	107,988,651 (GRCm39)	missense	probably benign	0.00
R8546:Bsn	UTSW	9	107,988,651 (GRCm39)	missense	probably benign	0.00
R8548:Bsn	UTSW	9	107,988,651 (GRCm39)	missense	probably benign	0.00
R8549:Bsn	UTSW	9	107,988,651 (GRCm39)	missense	probably benign	0.00
R8682:Bsn	UTSW	9	107,983,368 (GRCm39)	missense
R8773:Bsn	UTSW	9	107,987,704 (GRCm39)	missense	unknown
R8883:Bsn	UTSW	9	107,990,227 (GRCm39)	missense	probably damaging	0.98
R8906:Bsn	UTSW	9	107,984,752 (GRCm39)	missense	unknown
R9018:Bsn	UTSW	9	107,994,488 (GRCm39)	missense	probably benign	0.06
R9070:Bsn	UTSW	9	107,987,295 (GRCm39)	missense
R9094:Bsn	UTSW	9	107,988,052 (GRCm39)	missense	unknown
R9098:Bsn	UTSW	9	107,990,173 (GRCm39)	missense	possibly damaging	0.65
R9128:Bsn	UTSW	9	107,993,349 (GRCm39)	missense	probably benign	0.21
R9162:Bsn	UTSW	9	107,987,883 (GRCm39)	missense	unknown
R9224:Bsn	UTSW	9	107,982,686 (GRCm39)	missense
R9230:Bsn	UTSW	9	107,989,459 (GRCm39)	missense	probably damaging	1.00
R9233:Bsn	UTSW	9	107,994,289 (GRCm39)	missense	probably benign	0.28
R9245:Bsn	UTSW	9	107,993,292 (GRCm39)	missense	probably damaging	1.00
R9275:Bsn	UTSW	9	107,988,819 (GRCm39)	missense	probably damaging	1.00
R9307:Bsn	UTSW	9	107,992,993 (GRCm39)	missense	probably benign	0.01
R9343:Bsn	UTSW	9	107,992,701 (GRCm39)	missense	probably damaging	1.00
R9377:Bsn	UTSW	9	107,993,361 (GRCm39)	missense	probably damaging	1.00
R9377:Bsn	UTSW	9	107,990,800 (GRCm39)	missense	probably damaging	1.00
R9378:Bsn	UTSW	9	107,984,854 (GRCm39)	missense	possibly damaging	0.85
R9408:Bsn	UTSW	9	108,016,652 (GRCm39)	nonsense	probably null
R9455:Bsn	UTSW	9	107,988,531 (GRCm39)	missense	unknown
R9615:Bsn	UTSW	9	107,984,430 (GRCm39)	missense
R9656:Bsn	UTSW	9	107,994,407 (GRCm39)	missense	probably benign	0.09
R9698:Bsn	UTSW	9	107,993,170 (GRCm39)	missense	probably damaging	1.00
X0028:Bsn	UTSW	9	107,990,703 (GRCm39)	missense	probably damaging	1.00
X0066:Bsn	UTSW	9	108,016,409 (GRCm39)	missense	probably damaging	1.00
Z1177:Bsn	UTSW	9	108,016,394 (GRCm39)	missense	probably damaging	1.00
Z1177:Bsn	UTSW	9	107,982,698 (GRCm39)	missense

Predicted Primers

PCR Primer
(F):5'- TCACGCTGCTTCGATCACTG -3'
(R):5'- GTGGACCAACTCAAAATGGATTTC -3'

Sequencing Primer
(F):5'- TTCGATCACTGCCCCGG -3'
(R):5'- TGGATTTCCAGCCCACCAG -3'

Posted On

2022-08-09