Mutagenetix > Incidental Mutation

Incidental Mutation 'R7372:Bsn'

572166

Institutional Source

Beutler Lab

Gene Symbol

Bsn

Ensembl Gene

ENSMUSG00000032589

Gene Name

bassoon

Synonyms

presynaptic cytomatrix protein

MMRRC Submission

045455-MU

Accession Numbers

Essential gene?

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

Stock #

R7372 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

107973221-108067583 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 107987718 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Asparagine at position 2678 (I2678N)

Ref Sequence

ENSEMBL: ENSMUSP00000035208 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000035208
AA Change: I2678N

SMART Domains

Protein: ENSMUSP00000035208
Gene: ENSMUSG00000032589
AA Change: I2678N

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

probably benign
Transcript: ENSMUST00000124763

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.2%

Validation Efficiency

99% (68/69)

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: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abl2	G	A	1: 156,450,189 (GRCm39)	V119M	probably damaging	Het
Acss2	T	C	2: 155,399,100 (GRCm39)	V454A	probably damaging	Het
Adam6b	T	A	12: 113,453,784 (GRCm39)	D200E	probably benign	Het
Adarb1	T	A	10: 77,131,712 (GRCm39)		probably null	Het
Aqp12	C	T	1: 92,934,088 (GRCm39)		probably benign	Het
Atrnl1	T	C	19: 57,924,078 (GRCm39)	V1281A	possibly damaging	Het
Brdt	A	G	5: 107,518,160 (GRCm39)	E761G	possibly damaging	Het
C2cd2	A	T	16: 97,676,580 (GRCm39)	C136S		Het
Camk4	A	G	18: 33,318,178 (GRCm39)	D445G	probably benign	Het
Cckar	T	C	5: 53,864,624 (GRCm39)	T26A	probably damaging	Het
Cd209a	T	A	8: 3,798,857 (GRCm39)		probably null	Het
Cept1	A	G	3: 106,411,056 (GRCm39)	F379S	probably benign	Het
Crhr1	A	G	11: 104,054,719 (GRCm39)		probably null	Het
Cryzl1	T	C	16: 91,509,085 (GRCm39)	E72G	probably benign	Het
Ctnnal1	T	A	4: 56,826,285 (GRCm39)	E526V	possibly damaging	Het
Cyp3a41a	T	C	5: 145,650,374 (GRCm39)	I90V	possibly damaging	Het
Dek	T	C	13: 47,259,053 (GRCm39)	E51G	unknown	Het
Dnaaf6rt	A	T	1: 31,262,432 (GRCm39)	D138V	probably damaging	Het
Evc2	T	A	5: 37,544,477 (GRCm39)	V742E	probably damaging	Het
Fat4	G	A	3: 38,944,358 (GRCm39)	V1084M	probably damaging	Het
Fscb	G	A	12: 64,518,598 (GRCm39)	T956I	unknown	Het
Glipr2	T	C	4: 43,968,184 (GRCm39)	L29P	probably damaging	Het
Gm19402	A	T	10: 77,526,261 (GRCm39)	S111T	unknown	Het
Gm4553	ACCCTTGCAGCCACCACAGGAGCCACAGCCCCCACAGGAGCTACAGCCTCCCTTGCAGCCACCACAGGAGCCACAGCCCCCACAGGAGCTACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCC	ACCCTTGCAGCCACCACAGGAGCCACAGCCCCCACAGGAGCTACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCC	7: 141,719,157 (GRCm39)		probably benign	Het
Gnl3	T	C	14: 30,738,843 (GRCm39)	K115E	probably benign	Het
Gpn1	T	A	5: 31,658,465 (GRCm39)	F147I	probably damaging	Het
Gsdmd	T	A	15: 75,737,618 (GRCm39)	L232H	probably benign	Het
Helz2	A	G	2: 180,880,216 (GRCm39)	V500A	possibly damaging	Het
Hemk1	T	C	9: 107,214,267 (GRCm39)	E55G	probably benign	Het
Hs2st1	A	T	3: 144,141,221 (GRCm39)		probably null	Het
Ighv1-63	A	G	12: 115,459,486 (GRCm39)	V37A	probably damaging	Het
Iqsec3	C	A	6: 121,360,991 (GRCm39)	E956*	probably null	Het
Kcnh8	T	A	17: 53,201,129 (GRCm39)	I521K	probably damaging	Het
Kif3c	T	A	12: 3,437,592 (GRCm39)	M531K	probably benign	Het
Kif5c	T	A	2: 49,648,671 (GRCm39)		probably null	Het
Krt15	A	T	11: 100,026,386 (GRCm39)	V100E	possibly damaging	Het
Lcor	T	C	19: 41,573,945 (GRCm39)	L900P	probably damaging	Het
Lrrc32	A	G	7: 98,149,014 (GRCm39)	D598G	probably benign	Het
Mug2	T	C	6: 122,060,425 (GRCm39)	V1387A	possibly damaging	Het
Nin	T	A	12: 70,102,803 (GRCm39)	E275V		Het
Or5p68	A	G	7: 107,945,703 (GRCm39)	F162L	probably benign	Het
Papolg	A	G	11: 23,816,439 (GRCm39)	I698T	probably benign	Het
Pcdhb20	A	G	18: 37,639,840 (GRCm39)	N789D	probably benign	Het
Pik3cg	C	T	12: 32,247,196 (GRCm39)	M842I	probably damaging	Het
Pnn	T	A	12: 59,115,765 (GRCm39)	D135E	probably damaging	Het
Pold1	C	A	7: 44,192,847 (GRCm39)	R5L	possibly damaging	Het
Prl8a1	A	T	13: 27,758,089 (GRCm39)	F207I	probably damaging	Het
Prr11	A	G	11: 86,989,600 (GRCm39)	V257A	probably benign	Het
Prtg	C	T	9: 72,758,848 (GRCm39)	R401*	probably null	Het
Rasgrp1	A	G	2: 117,115,635 (GRCm39)	M651T	probably benign	Het
Ryr2	T	A	13: 11,695,885 (GRCm39)	H2994L	probably damaging	Het
Snx13	A	T	12: 35,128,950 (GRCm39)	I23L	probably benign	Het
Snx7	A	G	3: 117,576,000 (GRCm39)	L429P	probably damaging	Het
Spta1	C	T	1: 174,025,201 (GRCm39)	Q689*	probably null	Het
Spty2d1	T	C	7: 46,648,692 (GRCm39)	D79G	probably damaging	Het
Tbc1d9b	A	G	11: 50,059,515 (GRCm39)		probably null	Het
Tnxb	T	C	17: 34,936,228 (GRCm39)	F2722L	possibly damaging	Het
Tppp2	C	T	14: 52,156,865 (GRCm39)	R81C	probably benign	Het
Trim6	G	T	7: 103,881,843 (GRCm39)	A391S	probably benign	Het
Trim69	A	C	2: 122,009,064 (GRCm39)	T375P	possibly damaging	Het
Trim72	A	G	7: 127,603,858 (GRCm39)	N68S	possibly damaging	Het
Trrap	G	A	5: 144,726,208 (GRCm39)	V386I	probably benign	Het
Ttn	T	C	2: 76,778,275 (GRCm39)	I1371V	unknown	Het
Usp17lb	A	T	7: 104,490,913 (GRCm39)		probably null	Het
Vmn2r20	A	T	6: 123,362,468 (GRCm39)	L772Q	probably damaging	Het
Ypel3	A	G	7: 126,379,200 (GRCm39)	E91G	probably benign	Het
Zbtb21	C	T	16: 97,751,569 (GRCm39)	E905K	possibly damaging	Het
Zfp189	T	A	4: 49,530,417 (GRCm39)	C507S	possibly 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
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
R9563:Bsn	UTSW	9	107,984,616 (GRCm39)	missense
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'- GCAGTTGGTCCTATGAGCTG -3'
(R):5'- GCAGACAGCAGTGTTCAGAC -3'

Sequencing Primer
(F):5'- TCCTATGAGCTGTGGCCCAG -3'
(R):5'- TACCTTGTGACTCGCAGGC -3'

Posted On

2019-09-13