Mutagenetix > Incidental Mutation

Incidental Mutation 'R8682:Bsn'

661821

Institutional Source

Beutler Lab

Gene Symbol

Bsn

Ensembl Gene

ENSMUSG00000032589

Gene Name

bassoon

Synonyms

presynaptic cytomatrix protein

MMRRC Submission

068537-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.364) question?

Stock #

R8682 (G1)

Quality Score

134.008

Status

Not validated

Chromosome

Chromosomal Location

108096022-108190384 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 108106169 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 790 (Y790C)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000035208
AA Change: Y3562C

SMART Domains

Protein: ENSMUSP00000035208
Gene: ENSMUSG00000032589
AA Change: Y3562C

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: 99.9%
3x: 99.8%
10x: 98.9%
20x: 95.7%

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: 71 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1810065E05Rik	T	A	11: 58,423,899 (GRCm38)	L141Q	probably null	Het
Abtb2	A	T	2: 103,567,375 (GRCm38)	T217S	probably benign	Het
Adcy1	T	C	11: 7,161,328 (GRCm38)	I873T	probably damaging	Het
Angpt4	A	G	2: 151,927,085 (GRCm38)	M172V	probably benign	Het
Apaf1	A	T	10: 90,995,670 (GRCm38)	V1194D	probably damaging	Het
Arhgap30	T	C	1: 171,407,402 (GRCm38)	S479P	probably benign	Het
Asah2	C	T	19: 32,052,877 (GRCm38)	V132M	probably damaging	Het
Bmp10	A	G	6: 87,433,559 (GRCm38)		probably null	Het
Cacna2d1	C	A	5: 16,353,839 (GRCm38)	R732S	possibly damaging	Het
Casr	A	T	16: 36,495,422 (GRCm38)	F762Y	possibly damaging	Het
Cbln1	T	C	8: 87,472,107 (GRCm38)	D45G	possibly damaging	Het
Cd177	A	T	7: 24,760,013 (GRCm38)	M61K	possibly damaging	Het
Cdh11	T	C	8: 102,650,716 (GRCm38)	I433V	probably benign	Het
Cdhr5	A	G	7: 141,275,986 (GRCm38)		probably null	Het
Col12a1	T	A	9: 79,661,076 (GRCm38)	K1622I	probably benign	Het
Cyp2d9	A	G	15: 82,453,716 (GRCm38)	D103G	probably damaging	Het
Fem1b	A	T	9: 62,797,150 (GRCm38)	L276*	probably null	Het
Fggy	T	A	4: 95,812,121 (GRCm38)	V343E	probably damaging	Het
Flt3	A	G	5: 147,383,455 (GRCm38)	V33A	probably benign	Het
Gm6904	G	A	14: 59,258,584 (GRCm38)	T27I	probably benign	Het
Gm8994	A	G	6: 136,329,029 (GRCm38)	T163A	possibly damaging	Het
Grn	T	C	11: 102,434,820 (GRCm38)	Y288H	probably benign	Het
Grtp1	G	A	8: 13,179,499 (GRCm38)	R272W	probably damaging	Het
H2-Aa	A	G	17: 34,283,760 (GRCm38)	I144T	possibly damaging	Het
Herc1	A	G	9: 66,462,848 (GRCm38)	D469G		Het
Hsf2	G	A	10: 57,505,171 (GRCm38)	E286K	possibly damaging	Het
Hydin	A	G	8: 110,309,166 (GRCm38)	E163G	probably damaging	Het
Il6ra	A	G	3: 89,886,669 (GRCm38)	I224T	possibly damaging	Het
Itih3	T	A	14: 30,920,716 (GRCm38)	I204F	possibly damaging	Het
Kcnj9	A	T	1: 172,326,113 (GRCm38)	M148K	possibly damaging	Het
Lepr	T	G	4: 101,792,072 (GRCm38)	V890G	probably benign	Het
Mslnl	A	G	17: 25,746,988 (GRCm38)	D612G	probably benign	Het
Myl2	T	A	5: 122,106,735 (GRCm38)	V156D	probably damaging	Het
Neb	C	A	2: 52,246,845 (GRCm38)	W3208L	probably damaging	Het
Neto2	T	C	8: 85,640,666 (GRCm38)	Y511C	probably benign	Het
Obox2	C	A	7: 15,396,987 (GRCm38)	T48K	possibly damaging	Het
Olfr1109	A	T	2: 87,093,046 (GRCm38)	M117K	possibly damaging	Het
Olfr305	C	T	7: 86,364,165 (GRCm38)	M57I	probably damaging	Het
Olfr568	T	A	7: 102,877,439 (GRCm38)	F106L	probably benign	Het
Osbpl6	C	G	2: 76,577,081 (GRCm38)	H486D	probably benign	Het
Pfkfb3	T	C	2: 11,484,333 (GRCm38)	K264E	probably benign	Het
Pla2r1	T	A	2: 60,422,776 (GRCm38)	T1324S	possibly damaging	Het
Plekhg1	A	T	10: 3,947,523 (GRCm38)	Y495F		Het
Ppp2r5d	T	C	17: 46,687,063 (GRCm38)	K225E	probably benign	Het
Ptpn11	T	C	5: 121,167,990 (GRCm38)	D64G	possibly damaging	Het
Ptprs	A	G	17: 56,435,849 (GRCm38)	I431T	probably damaging	Het
Rapgef5	T	C	12: 117,581,812 (GRCm38)	S100P	probably benign	Het
Rnf219	G	T	14: 104,480,233 (GRCm38)	R235S	probably damaging	Het
Shh	T	A	5: 28,458,060 (GRCm38)	H370L	probably benign	Het
Siah3	A	T	14: 75,525,603 (GRCm38)	H98L	possibly damaging	Het
Sim2	C	T	16: 94,123,333 (GRCm38)	H446Y	probably benign	Het
Skint4	T	C	4: 112,136,040 (GRCm38)	I320T	possibly damaging	Het
Sorcs1	A	T	19: 50,378,960 (GRCm38)	N221K	probably damaging	Het
Sox6	T	C	7: 115,476,956 (GRCm38)	S816G	probably damaging	Het
Sphkap	T	C	1: 83,279,276 (GRCm38)	T251A	probably benign	Het
Stard9	T	C	2: 120,703,315 (GRCm38)	V3351A	possibly damaging	Het
Tbc1d15	A	G	10: 115,210,290 (GRCm38)	V436A	probably benign	Het
Thsd7b	A	T	1: 129,760,274 (GRCm38)	K641*	probably null	Het
Tmc5	G	T	7: 118,670,702 (GRCm38)	V892F	possibly damaging	Het
Tpsab1	T	A	17: 25,343,711 (GRCm38)	H238L	probably benign	Het
Trank1	A	G	9: 111,365,344 (GRCm38)	N812S	probably benign	Het
Trio	T	A	15: 27,905,192 (GRCm38)	N163Y	unknown	Het
Ttc39d	A	G	17: 80,217,264 (GRCm38)	T451A	probably benign	Het
Ube3b	T	C	5: 114,412,290 (GRCm38)	L832P	probably damaging	Het
Vmn2r15	C	A	5: 109,294,072 (GRCm38)	C165F	probably damaging	Het
Vmn2r90	T	C	17: 17,712,082 (GRCm38)	F84L	possibly damaging	Het
Wdr60	A	T	12: 116,224,990 (GRCm38)	H661Q	probably damaging	Het
Wdr95	C	T	5: 149,595,287 (GRCm38)	T531I	possibly damaging	Het
Zcrb1	C	A	15: 93,386,237 (GRCm38)	G191V	probably benign	Het
Zfp111	G	A	7: 24,198,558 (GRCm38)	P544S	probably damaging	Het
Zfyve9	T	C	4: 108,719,342 (GRCm38)	S181G	probably benign	Het

Other mutations in Bsn

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00161:Bsn	APN	9	108,115,110 (GRCm38)	missense	probably benign	0.01
IGL00330:Bsn	APN	9	108,115,340 (GRCm38)	missense	probably damaging	1.00
IGL00863:Bsn	APN	9	108,115,322 (GRCm38)	missense	probably damaging	1.00
IGL01123:Bsn	APN	9	108,115,986 (GRCm38)	missense	probably damaging	1.00
IGL01330:Bsn	APN	9	108,110,913 (GRCm38)	unclassified	probably benign
IGL01336:Bsn	APN	9	108,111,785 (GRCm38)	missense	probably damaging	0.99
IGL01399:Bsn	APN	9	108,107,187 (GRCm38)	missense	unknown
IGL01683:Bsn	APN	9	108,114,896 (GRCm38)	missense	possibly damaging	0.71
IGL02022:Bsn	APN	9	108,110,418 (GRCm38)	unclassified	probably benign
IGL02396:Bsn	APN	9	108,116,046 (GRCm38)	missense	possibly damaging	0.90
IGL02538:Bsn	APN	9	108,105,236 (GRCm38)	missense	unknown
IGL02565:Bsn	APN	9	108,113,288 (GRCm38)	missense	probably damaging	0.99
IGL02661:Bsn	APN	9	108,106,936 (GRCm38)	nonsense	probably null
IGL02739:Bsn	APN	9	108,112,546 (GRCm38)	missense	probably benign	0.14
IGL02951:Bsn	APN	9	108,115,613 (GRCm38)	missense	probably damaging	1.00
IGL02987:Bsn	APN	9	108,126,304 (GRCm38)	missense	probably benign	0.03
IGL03033:Bsn	APN	9	108,115,993 (GRCm38)	missense	probably damaging	1.00
IGL03069:Bsn	APN	9	108,114,263 (GRCm38)	missense	probably damaging	1.00
IGL03076:Bsn	APN	9	108,105,382 (GRCm38)	missense	unknown
R0068:Bsn	UTSW	9	108,112,137 (GRCm38)	missense	probably damaging	1.00
R0068:Bsn	UTSW	9	108,112,137 (GRCm38)	missense	probably damaging	1.00
R0167:Bsn	UTSW	9	108,125,986 (GRCm38)	missense	probably benign	0.01
R0234:Bsn	UTSW	9	108,116,396 (GRCm38)	missense	possibly damaging	0.50
R0234:Bsn	UTSW	9	108,116,396 (GRCm38)	missense	possibly damaging	0.50
R0359:Bsn	UTSW	9	108,111,846 (GRCm38)	missense	possibly damaging	0.81
R0514:Bsn	UTSW	9	108,125,782 (GRCm38)	missense	probably benign	0.07
R0593:Bsn	UTSW	9	108,110,306 (GRCm38)	missense	unknown
R0617:Bsn	UTSW	9	108,107,240 (GRCm38)	missense	unknown
R0636:Bsn	UTSW	9	108,107,834 (GRCm38)	missense	unknown
R0652:Bsn	UTSW	9	108,105,742 (GRCm38)	missense	unknown
R0718:Bsn	UTSW	9	108,111,360 (GRCm38)	unclassified	probably benign
R0730:Bsn	UTSW	9	108,106,812 (GRCm38)	missense	unknown
R0905:Bsn	UTSW	9	108,105,635 (GRCm38)	missense	unknown
R0963:Bsn	UTSW	9	108,111,807 (GRCm38)	missense	possibly damaging	0.81
R0992:Bsn	UTSW	9	108,114,354 (GRCm38)	nonsense	probably null
R1101:Bsn	UTSW	9	108,116,411 (GRCm38)	missense	probably damaging	1.00
R1393:Bsn	UTSW	9	108,110,517 (GRCm38)	unclassified	probably benign
R1490:Bsn	UTSW	9	108,113,994 (GRCm38)	missense	probably benign	0.03
R1566:Bsn	UTSW	9	108,125,985 (GRCm38)	missense	probably benign	0.35
R1582:Bsn	UTSW	9	108,105,092 (GRCm38)	missense	unknown
R1738:Bsn	UTSW	9	108,106,934 (GRCm38)	missense	unknown
R1867:Bsn	UTSW	9	108,106,719 (GRCm38)	missense	unknown
R1918:Bsn	UTSW	9	108,107,573 (GRCm38)	missense	unknown
R1933:Bsn	UTSW	9	108,116,444 (GRCm38)	missense	possibly damaging	0.91
R1946:Bsn	UTSW	9	108,114,651 (GRCm38)	missense	probably damaging	0.99
R1978:Bsn	UTSW	9	108,114,549 (GRCm38)	missense	probably benign	0.35
R2068:Bsn	UTSW	9	108,126,550 (GRCm38)	missense	possibly damaging	0.95
R2068:Bsn	UTSW	9	108,110,684 (GRCm38)	unclassified	probably benign
R2113:Bsn	UTSW	9	108,114,886 (GRCm38)	missense	probably benign	0.14
R2136:Bsn	UTSW	9	108,113,231 (GRCm38)	missense	probably damaging	1.00
R2172:Bsn	UTSW	9	108,109,992 (GRCm38)	intron	probably benign
R2266:Bsn	UTSW	9	108,115,124 (GRCm38)	missense	probably damaging	1.00
R2293:Bsn	UTSW	9	108,113,067 (GRCm38)	missense	possibly damaging	0.47
R2294:Bsn	UTSW	9	108,113,067 (GRCm38)	missense	possibly damaging	0.47
R2368:Bsn	UTSW	9	108,111,030 (GRCm38)	nonsense	probably null
R2442:Bsn	UTSW	9	108,106,920 (GRCm38)	missense	unknown
R2507:Bsn	UTSW	9	108,116,114 (GRCm38)	missense	probably damaging	1.00
R2880:Bsn	UTSW	9	108,113,067 (GRCm38)	missense	possibly damaging	0.47
R2881:Bsn	UTSW	9	108,113,067 (GRCm38)	missense	possibly damaging	0.47
R2922:Bsn	UTSW	9	108,115,469 (GRCm38)	missense	probably damaging	1.00
R2922:Bsn	UTSW	9	108,108,186 (GRCm38)	missense	unknown
R3618:Bsn	UTSW	9	108,117,561 (GRCm38)	critical splice acceptor site	probably null
R3742:Bsn	UTSW	9	108,105,739 (GRCm38)	missense	unknown
R3825:Bsn	UTSW	9	108,106,856 (GRCm38)	missense	unknown
R3982:Bsn	UTSW	9	108,107,166 (GRCm38)	missense	unknown
R4094:Bsn	UTSW	9	108,113,870 (GRCm38)	missense	probably damaging	1.00
R4158:Bsn	UTSW	9	108,112,946 (GRCm38)	missense	possibly damaging	0.95
R4225:Bsn	UTSW	9	108,106,733 (GRCm38)	missense	unknown
R4261:Bsn	UTSW	9	108,110,684 (GRCm38)	unclassified	probably benign
R4482:Bsn	UTSW	9	108,114,664 (GRCm38)	missense	probably damaging	1.00
R4515:Bsn	UTSW	9	108,104,078 (GRCm38)	splice site	probably null
R4585:Bsn	UTSW	9	108,110,463 (GRCm38)	unclassified	probably benign
R4628:Bsn	UTSW	9	108,113,235 (GRCm38)	missense	probably damaging	1.00
R4636:Bsn	UTSW	9	108,115,424 (GRCm38)	missense	probably damaging	1.00
R4679:Bsn	UTSW	9	108,110,130 (GRCm38)	missense	unknown
R4723:Bsn	UTSW	9	108,112,655 (GRCm38)	missense	probably benign	0.03
R4843:Bsn	UTSW	9	108,107,189 (GRCm38)	missense	unknown
R4885:Bsn	UTSW	9	108,107,527 (GRCm38)	nonsense	probably null
R4936:Bsn	UTSW	9	108,111,761 (GRCm38)	missense	probably damaging	1.00
R4942:Bsn	UTSW	9	108,106,479 (GRCm38)	missense	unknown
R4972:Bsn	UTSW	9	108,115,178 (GRCm38)	missense	probably damaging	1.00
R4992:Bsn	UTSW	9	108,115,548 (GRCm38)	missense	probably damaging	1.00
R5067:Bsn	UTSW	9	108,111,953 (GRCm38)	missense	probably damaging	1.00
R5206:Bsn	UTSW	9	108,105,373 (GRCm38)	missense	unknown
R5286:Bsn	UTSW	9	108,110,924 (GRCm38)	unclassified	probably benign
R5492:Bsn	UTSW	9	108,112,515 (GRCm38)	missense	probably damaging	0.98
R5553:Bsn	UTSW	9	108,110,421 (GRCm38)	unclassified	probably benign
R5561:Bsn	UTSW	9	108,105,511 (GRCm38)	missense	unknown
R5597:Bsn	UTSW	9	108,114,932 (GRCm38)	missense	probably benign	0.06
R5646:Bsn	UTSW	9	108,110,432 (GRCm38)	unclassified	probably benign
R5796:Bsn	UTSW	9	108,126,024 (GRCm38)	missense	probably damaging	1.00
R5801:Bsn	UTSW	9	108,113,009 (GRCm38)	missense	possibly damaging	0.81
R5802:Bsn	UTSW	9	108,113,009 (GRCm38)	missense	possibly damaging	0.81
R5850:Bsn	UTSW	9	108,114,950 (GRCm38)	missense	probably damaging	0.99
R5938:Bsn	UTSW	9	108,113,009 (GRCm38)	missense	possibly damaging	0.81
R6221:Bsn	UTSW	9	108,105,566 (GRCm38)	missense	unknown
R6243:Bsn	UTSW	9	108,107,561 (GRCm38)	missense	unknown
R6254:Bsn	UTSW	9	108,111,866 (GRCm38)	missense	probably damaging	0.96
R6263:Bsn	UTSW	9	108,113,254 (GRCm38)	missense	probably damaging	1.00
R6345:Bsn	UTSW	9	108,107,355 (GRCm38)	missense	unknown
R6368:Bsn	UTSW	9	108,111,314 (GRCm38)	unclassified	probably benign
R6574:Bsn	UTSW	9	108,113,954 (GRCm38)	missense	possibly damaging	0.95
R6793:Bsn	UTSW	9	108,114,615 (GRCm38)	nonsense	probably null
R6802:Bsn	UTSW	9	108,110,624 (GRCm38)	unclassified	probably benign
R6943:Bsn	UTSW	9	108,107,817 (GRCm38)	missense	unknown
R6999:Bsn	UTSW	9	108,113,433 (GRCm38)	missense	probably benign	0.00
R7149:Bsn	UTSW	9	108,116,321 (GRCm38)	nonsense	probably null
R7199:Bsn	UTSW	9	108,115,334 (GRCm38)	missense	probably damaging	1.00
R7322:Bsn	UTSW	9	108,126,421 (GRCm38)	nonsense	probably null
R7349:Bsn	UTSW	9	108,110,783 (GRCm38)	missense	unknown
R7372:Bsn	UTSW	9	108,110,519 (GRCm38)	missense	unknown
R7373:Bsn	UTSW	9	108,113,484 (GRCm38)	missense	probably damaging	1.00
R7413:Bsn	UTSW	9	108,139,491 (GRCm38)	missense	possibly damaging	0.61
R7473:Bsn	UTSW	9	108,112,250 (GRCm38)	missense	probably damaging	1.00
R7482:Bsn	UTSW	9	108,113,529 (GRCm38)	missense	probably damaging	0.98
R7530:Bsn	UTSW	9	108,111,956 (GRCm38)	missense	probably damaging	1.00
R7549:Bsn	UTSW	9	108,114,815 (GRCm38)	missense	probably benign	0.05
R7570:Bsn	UTSW	9	108,113,543 (GRCm38)	missense	probably damaging	1.00
R7635:Bsn	UTSW	9	108,110,990 (GRCm38)	missense	unknown
R7696:Bsn	UTSW	9	108,114,501 (GRCm38)	missense	probably damaging	1.00
R7757:Bsn	UTSW	9	108,114,740 (GRCm38)	missense	possibly damaging	0.90
R7868:Bsn	UTSW	9	108,114,899 (GRCm38)	missense	possibly damaging	0.95
R7897:Bsn	UTSW	9	108,111,866 (GRCm38)	missense	probably damaging	0.98
R7960:Bsn	UTSW	9	108,115,548 (GRCm38)	missense	probably damaging	1.00
R8022:Bsn	UTSW	9	108,114,404 (GRCm38)	missense	probably benign	0.01
R8056:Bsn	UTSW	9	108,105,307 (GRCm38)	missense
R8158:Bsn	UTSW	9	108,110,033 (GRCm38)	missense	unknown
R8161:Bsn	UTSW	9	108,139,530 (GRCm38)	missense	probably benign	0.20
R8225:Bsn	UTSW	9	108,107,106 (GRCm38)	missense
R8282:Bsn	UTSW	9	108,107,691 (GRCm38)	missense	possibly damaging	0.73
R8296:Bsn	UTSW	9	108,117,379 (GRCm38)	missense	probably benign	0.00
R8415:Bsn	UTSW	9	108,111,452 (GRCm38)	missense	probably benign	0.00
R8417:Bsn	UTSW	9	108,111,452 (GRCm38)	missense	probably benign	0.00
R8426:Bsn	UTSW	9	108,126,573 (GRCm38)	missense	probably damaging	1.00
R8437:Bsn	UTSW	9	108,111,452 (GRCm38)	missense	probably benign	0.00
R8438:Bsn	UTSW	9	108,111,452 (GRCm38)	missense	probably benign	0.00
R8439:Bsn	UTSW	9	108,111,452 (GRCm38)	missense	probably benign	0.00
R8440:Bsn	UTSW	9	108,111,452 (GRCm38)	missense	probably benign	0.00
R8441:Bsn	UTSW	9	108,111,452 (GRCm38)	missense	probably benign	0.00
R8442:Bsn	UTSW	9	108,111,452 (GRCm38)	missense	probably benign	0.00
R8513:Bsn	UTSW	9	108,114,510 (GRCm38)	missense	possibly damaging	0.65
R8529:Bsn	UTSW	9	108,111,452 (GRCm38)	missense	probably benign	0.00
R8535:Bsn	UTSW	9	108,111,452 (GRCm38)	missense	probably benign	0.00
R8546:Bsn	UTSW	9	108,111,452 (GRCm38)	missense	probably benign	0.00
R8548:Bsn	UTSW	9	108,111,452 (GRCm38)	missense	probably benign	0.00
R8549:Bsn	UTSW	9	108,111,452 (GRCm38)	missense	probably benign	0.00
R8773:Bsn	UTSW	9	108,110,505 (GRCm38)	missense	unknown
R8883:Bsn	UTSW	9	108,113,028 (GRCm38)	missense	probably damaging	0.98
R8906:Bsn	UTSW	9	108,107,553 (GRCm38)	missense	unknown
R9018:Bsn	UTSW	9	108,117,289 (GRCm38)	missense	probably benign	0.06
R9070:Bsn	UTSW	9	108,110,096 (GRCm38)	missense
R9094:Bsn	UTSW	9	108,110,853 (GRCm38)	missense	unknown
R9098:Bsn	UTSW	9	108,112,974 (GRCm38)	missense	possibly damaging	0.65
R9128:Bsn	UTSW	9	108,116,150 (GRCm38)	missense	probably benign	0.21
R9162:Bsn	UTSW	9	108,110,684 (GRCm38)	missense	unknown
R9224:Bsn	UTSW	9	108,105,487 (GRCm38)	missense
R9230:Bsn	UTSW	9	108,112,260 (GRCm38)	missense	probably damaging	1.00
R9233:Bsn	UTSW	9	108,117,090 (GRCm38)	missense	probably benign	0.28
R9245:Bsn	UTSW	9	108,116,093 (GRCm38)	missense	probably damaging	1.00
R9275:Bsn	UTSW	9	108,111,620 (GRCm38)	missense	probably damaging	1.00
R9307:Bsn	UTSW	9	108,115,794 (GRCm38)	missense	probably benign	0.01
R9343:Bsn	UTSW	9	108,115,502 (GRCm38)	missense	probably damaging	1.00
R9377:Bsn	UTSW	9	108,116,162 (GRCm38)	missense	probably damaging	1.00
R9377:Bsn	UTSW	9	108,113,601 (GRCm38)	missense	probably damaging	1.00
R9378:Bsn	UTSW	9	108,107,655 (GRCm38)	missense	possibly damaging	0.85
R9408:Bsn	UTSW	9	108,139,453 (GRCm38)	nonsense	probably null
R9455:Bsn	UTSW	9	108,111,332 (GRCm38)	missense	unknown
R9563:Bsn	UTSW	9	108,107,417 (GRCm38)	missense
R9615:Bsn	UTSW	9	108,107,231 (GRCm38)	missense
R9656:Bsn	UTSW	9	108,117,208 (GRCm38)	missense	probably benign	0.09
R9698:Bsn	UTSW	9	108,115,971 (GRCm38)	missense	probably damaging	1.00
X0028:Bsn	UTSW	9	108,113,504 (GRCm38)	missense	probably damaging	1.00
X0066:Bsn	UTSW	9	108,139,210 (GRCm38)	missense	probably damaging	1.00
Z1177:Bsn	UTSW	9	108,139,195 (GRCm38)	missense	probably damaging	1.00
Z1177:Bsn	UTSW	9	108,105,499 (GRCm38)	missense

Predicted Primers

PCR Primer
(F):5'- CCACTGATGAGATGCCAAGAC -3'
(R):5'- GCAGAGCGACTTCAAAAGGC -3'

Sequencing Primer
(F):5'- TGAGATGCCAAGACAGACCCTG -3'
(R):5'- ACTTCAAAAGGCGGGCTC -3'

Posted On

2021-03-08