Mutagenetix > Incidental Mutation

Incidental Mutation 'R7424:Unc13b'

575904

Institutional Source

Beutler Lab

Gene Symbol

Unc13b

Ensembl Gene

ENSMUSG00000028456

Gene Name

unc-13 homolog B (C. elegans)

Synonyms

Unc13h2, Munc13-2

MMRRC Submission

045502-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.317) question?

Stock #

R7424 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

43058953-43264871 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 43172235 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Isoleucine at position 1021 (T1021I)

Ref Sequence

ENSEMBL: ENSMUSP00000147100 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000079978] [ENSMUST00000107952] [ENSMUST00000107953] [ENSMUST00000163653] [ENSMUST00000207569]

AlphaFold

Q9Z1N9

Predicted Effect

probably benign
Transcript: ENSMUST00000079978

SMART Domains

Protein: ENSMUSP00000078894
Gene: ENSMUSG00000028456

Domain	Start	End	E-Value	Type
C2	3	94	1.2e-9	SMART
low complexity region	179	193	N/A	INTRINSIC
low complexity region	292	303	N/A	INTRINSIC
low complexity region	322	333	N/A	INTRINSIC
C1	478	527	4.21e-18	SMART
C2	601	708	2.07e-22	SMART
DUF1041	917	1021	2.02e-53	SMART
Pfam:Membr_traf_MHD	1262	1404	4.8e-60	PFAM
C2	1438	1544	7.56e-16	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000107952

SMART Domains

Protein: ENSMUSP00000103586
Gene: ENSMUSG00000028456

Domain	Start	End	E-Value	Type
C2	3	94	1.2e-9	SMART
low complexity region	191	205	N/A	INTRINSIC
low complexity region	304	315	N/A	INTRINSIC
low complexity region	334	345	N/A	INTRINSIC
C1	490	539	4.21e-18	SMART
C2	613	720	2.07e-22	SMART
DUF1041	929	1033	2.02e-53	SMART
Pfam:Membr_traf_MHD	1274	1416	4.8e-60	PFAM
C2	1450	1556	7.56e-16	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000107953

SMART Domains

Protein: ENSMUSP00000103587
Gene: ENSMUSG00000028456

Domain	Start	End	E-Value	Type
C2	3	94	1.2e-9	SMART
low complexity region	179	193	N/A	INTRINSIC
low complexity region	292	303	N/A	INTRINSIC
low complexity region	322	333	N/A	INTRINSIC
C1	478	527	4.21e-18	SMART
C2	601	708	2.07e-22	SMART
DUF1041	917	1021	2.02e-53	SMART
Pfam:Membr_traf_MHD	1263	1403	2.3e-56	PFAM
C2	1457	1563	7.56e-16	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000163653

SMART Domains

Protein: ENSMUSP00000128608
Gene: ENSMUSG00000028456

Domain	Start	End	E-Value	Type
C2	3	94	1.2e-9	SMART
low complexity region	191	205	N/A	INTRINSIC
low complexity region	304	315	N/A	INTRINSIC
low complexity region	334	345	N/A	INTRINSIC
C1	490	539	4.21e-18	SMART
C2	613	720	2.07e-22	SMART
DUF1041	929	1032	4.64e-53	SMART
Pfam:Membr_traf_MHD	1273	1415	4.8e-60	PFAM
C2	1449	1555	7.56e-16	SMART

Predicted Effect

unknown
Transcript: ENSMUST00000207569
AA Change: T1021I

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.4%

Validation Efficiency

99% (76/77)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is expressed in the kidney cortical epithelial cells and is upregulated by hyperglycemia. The encoded protein shares a high level of similarity to the rat homolog, and contains 3 C2 domains and a diacylglycerol-binding C1 domain. Hyperglycemia increases the levels of diacylglycerol, which has been shown to induce apoptosis in cells transfected with this gene and thus contribute to the renal cell complications of hyperglycemia. Studies in other species also indicate a role for this protein in the priming step of synaptic vesicle exocytosis. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous mutant mice are grossly phenotypically normal. Mice older than 12 months will exhibit sporadic seizures. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
6430548M08Rik	C	T	8: 120,145,545 (GRCm38)	R71C	probably damaging	Het
Aanat	A	T	11: 116,595,629 (GRCm38)		probably benign	Het
Ahrr	G	T	13: 74,257,545 (GRCm38)	S91*	probably null	Het
Ampd1	A	T	3: 103,088,442 (GRCm38)	N223Y	probably benign	Het
Ankar	T	G	1: 72,680,058 (GRCm38)	N544T	probably damaging	Het
Ankk1	A	G	9: 49,418,750 (GRCm38)	S302P	possibly damaging	Het
Bcr	T	C	10: 75,157,100 (GRCm38)	V809A	probably benign	Het
Bpifb2	A	G	2: 153,890,540 (GRCm38)	N353S	possibly damaging	Het
Cyth1	A	T	11: 118,184,009 (GRCm38)		probably null	Het
Ddx5	A	T	11: 106,782,180 (GRCm38)	N506K	probably benign	Het
Dnaja1	A	T	4: 40,730,244 (GRCm38)	I239F	probably benign	Het
Ethe1	C	T	7: 24,606,251 (GRCm38)	T141I	probably damaging	Het
Fam160b2	T	C	14: 70,594,007 (GRCm38)	H29R	probably damaging	Het
Gdap2	A	T	3: 100,202,066 (GRCm38)	I36F	unknown	Het
Gm13030	A	T	4: 138,871,266 (GRCm38)	D115E	unknown	Het
Gm13103	C	T	4: 143,853,209 (GRCm38)	P455S	probably benign	Het
Gm17019	A	T	5: 15,029,372 (GRCm38)	L227Q	probably damaging	Het
Gm9195	T	A	14: 72,435,777 (GRCm38)	E2517D	possibly damaging	Het
Gramd2	T	A	9: 59,708,071 (GRCm38)	V39D	possibly damaging	Het
Hmcn1	C	T	1: 150,630,266 (GRCm38)	W3836*	probably null	Het
Hspa14	C	T	2: 3,489,041 (GRCm38)	D494N	possibly damaging	Het
Ifit2	A	G	19: 34,573,198 (GRCm38)	N46S	probably benign	Het
Ifna6	A	T	4: 88,827,807 (GRCm38)	E131V	possibly damaging	Het
Ift140	T	C	17: 25,037,036 (GRCm38)	V504A	possibly damaging	Het
Irgc1	T	C	7: 24,432,228 (GRCm38)	N388S	probably damaging	Het
Itgal	T	A	7: 127,317,365 (GRCm38)	V743E	probably benign	Het
Itih5	T	C	2: 10,245,637 (GRCm38)	S716P	probably damaging	Het
Kcnab1	A	T	3: 65,266,503 (GRCm38)	K78N	possibly damaging	Het
Kif1a	A	T	1: 93,054,317 (GRCm38)	V787E	possibly damaging	Het
Krt15	A	T	11: 100,135,560 (GRCm38)	V100E	possibly damaging	Het
Krt39	A	T	11: 99,518,091 (GRCm38)	V293E	probably damaging	Het
Lrrn4	A	G	2: 132,869,743 (GRCm38)	F720S	possibly damaging	Het
Map2	G	A	1: 66,414,824 (GRCm38)	A958T	possibly damaging	Het
Map3k9	A	G	12: 81,724,097 (GRCm38)	S906P	probably benign	Het
Mdc1	T	C	17: 35,853,309 (GRCm38)	S1250P	probably benign	Het
Meltf	G	A	16: 31,884,946 (GRCm38)	V164I	probably damaging	Het
Mtap	T	G	4: 89,179,462 (GRCm38)		probably null	Het
Mtus1	C	A	8: 41,022,406 (GRCm38)	V184F	probably damaging	Het
Myh1	A	T	11: 67,213,663 (GRCm38)	D1015V	probably damaging	Het
Ndrg1	T	C	15: 66,944,938 (GRCm38)		probably null	Het
Nkd1	G	T	8: 88,585,175 (GRCm38)	V130L	probably benign	Het
Nsfl1c	A	G	2: 151,500,753 (GRCm38)	D81G	probably benign	Het
Nt5c1b	T	A	12: 10,381,391 (GRCm38)		probably null	Het
Nucb1	T	C	7: 45,498,778 (GRCm38)	K204E	possibly damaging	Het
Nwd1	T	G	8: 72,675,173 (GRCm38)	M774R	possibly damaging	Het
Olfr165	A	T	16: 19,407,194 (GRCm38)	V274E	probably damaging	Het
Olfr262	A	T	19: 12,240,954 (GRCm38)	S236T	possibly damaging	Het
Olfr654	G	C	7: 104,588,700 (GRCm38)	E299Q	probably damaging	Het
Pan3	T	A	5: 147,536,272 (GRCm38)		probably null	Het
Pcdh15	A	T	10: 74,506,485 (GRCm38)	T1135S	probably benign	Het
Pfas	A	G	11: 69,000,092 (GRCm38)	I331T	probably damaging	Het
Plxna2	T	A	1: 194,806,339 (GRCm38)	I1641N	probably damaging	Het
Ptar1	A	T	19: 23,718,101 (GRCm38)	R311W	probably damaging	Het
Ranbp2	T	G	10: 58,479,194 (GRCm38)	M1912R	probably damaging	Het
Rbm12	A	G	2: 156,097,303 (GRCm38)	F350L	possibly damaging	Het
Sdhaf1	T	C	7: 30,322,043 (GRCm38)	D96G	probably benign	Het
Serpinb6b	T	A	13: 32,968,667 (GRCm38)	M53K	probably damaging	Het
Sh2d6	A	T	6: 72,517,164 (GRCm38)	L147Q	probably benign	Het
Slc19a2	T	A	1: 164,260,876 (GRCm38)	C298S	probably benign	Het
Son	AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG	AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG	16: 91,660,334 (GRCm38)		probably benign	Het
St8sia2	T	A	7: 73,960,902 (GRCm38)	Q211L	possibly damaging	Het
Sult2a2	T	C	7: 13,734,897 (GRCm38)	I96T	possibly damaging	Het
Tab2	G	T	10: 7,907,483 (GRCm38)	H678Q	probably damaging	Het
Tnfaip6	A	G	2: 52,038,216 (GRCm38)	E14G	probably benign	Het
Trip11	A	T	12: 101,885,198 (GRCm38)	L869H	probably damaging	Het
Tslp	T	C	18: 32,819,080 (GRCm38)	Y133H	not run	Het
Ttn	A	G	2: 76,932,143 (GRCm38)	V3374A	unknown	Het
Ttn	T	C	2: 76,740,990 (GRCm38)	I26520V	probably damaging	Het
Tubgcp2	T	A	7: 140,007,924 (GRCm38)	I263F	possibly damaging	Het
Uaca	A	G	9: 60,870,110 (GRCm38)	E593G	probably damaging	Het
Ush1c	T	A	7: 46,225,555 (GRCm38)	I131F	probably benign	Het
Usp24	C	A	4: 106,379,107 (GRCm38)	D997E	probably benign	Het
Usp54	T	C	14: 20,577,040 (GRCm38)	T517A	probably benign	Het
Vmn1r151	A	T	7: 22,499,080 (GRCm38)	M200K	possibly damaging	Het
Vmn2r43	T	C	7: 8,255,329 (GRCm38)	D295G	probably damaging	Het
Vmn2r70	G	A	7: 85,563,868 (GRCm38)	P444S	probably damaging	Het
Vmn2r85	G	T	10: 130,418,980 (GRCm38)	P612T	probably damaging	Het
Vps13d	A	T	4: 145,148,747 (GRCm38)	V1736D		Het
Zbtb11	A	T	16: 55,990,487 (GRCm38)	H336L	probably benign	Het

Other mutations in Unc13b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00392:Unc13b	APN	4	43,240,285 (GRCm38)	missense	probably damaging	1.00
IGL00832:Unc13b	APN	4	43,258,921 (GRCm38)	missense	probably damaging	1.00
IGL01111:Unc13b	APN	4	43,096,927 (GRCm38)	missense	possibly damaging	0.76
IGL01115:Unc13b	APN	4	43,258,492 (GRCm38)	missense	probably damaging	1.00
IGL01137:Unc13b	APN	4	43,091,291 (GRCm38)	missense	probably damaging	1.00
IGL01637:Unc13b	APN	4	43,241,066 (GRCm38)	missense	probably damaging	1.00
IGL01789:Unc13b	APN	4	43,239,462 (GRCm38)	missense	probably damaging	1.00
IGL01792:Unc13b	APN	4	43,250,218 (GRCm38)	missense	probably damaging	0.99
IGL01877:Unc13b	APN	4	43,249,583 (GRCm38)	critical splice donor site	probably null
IGL01924:Unc13b	APN	4	43,239,385 (GRCm38)	nonsense	probably null
IGL02087:Unc13b	APN	4	43,091,270 (GRCm38)	missense	probably null	1.00
IGL02197:Unc13b	APN	4	43,165,828 (GRCm38)	missense	probably damaging	0.99
IGL02504:Unc13b	APN	4	43,263,031 (GRCm38)	missense	probably damaging	1.00
IGL02659:Unc13b	APN	4	43,235,332 (GRCm38)	missense	probably damaging	1.00
IGL03031:Unc13b	APN	4	43,235,368 (GRCm38)	missense	probably damaging	1.00
IGL03036:Unc13b	APN	4	43,235,249 (GRCm38)	missense	probably damaging	1.00
IGL03209:Unc13b	APN	4	43,239,351 (GRCm38)	missense	probably damaging	0.99
IGL03352:Unc13b	APN	4	43,237,110 (GRCm38)	missense	possibly damaging	0.90
BB006:Unc13b	UTSW	4	43,174,399 (GRCm38)	missense	unknown
BB016:Unc13b	UTSW	4	43,174,399 (GRCm38)	missense	unknown
G1Funyon:Unc13b	UTSW	4	43,263,568 (GRCm38)	missense	probably benign
P0028:Unc13b	UTSW	4	43,256,225 (GRCm38)	missense	probably damaging	1.00
PIT4585001:Unc13b	UTSW	4	43,091,298 (GRCm38)	missense	probably benign	0.03
R0019:Unc13b	UTSW	4	43,096,990 (GRCm38)	missense	possibly damaging	0.58
R0019:Unc13b	UTSW	4	43,096,990 (GRCm38)	missense	possibly damaging	0.58
R0335:Unc13b	UTSW	4	43,236,983 (GRCm38)	missense	possibly damaging	0.95
R0504:Unc13b	UTSW	4	43,263,559 (GRCm38)	missense	probably damaging	0.99
R0631:Unc13b	UTSW	4	43,182,849 (GRCm38)	missense	possibly damaging	0.47
R0748:Unc13b	UTSW	4	43,241,164 (GRCm38)	splice site	probably benign
R1275:Unc13b	UTSW	4	43,235,366 (GRCm38)	missense	probably damaging	1.00
R1293:Unc13b	UTSW	4	43,235,190 (GRCm38)	missense	probably damaging	1.00
R1434:Unc13b	UTSW	4	43,239,385 (GRCm38)	nonsense	probably null
R1552:Unc13b	UTSW	4	43,237,144 (GRCm38)	missense	probably damaging	0.99
R1591:Unc13b	UTSW	4	43,244,747 (GRCm38)	missense	probably damaging	1.00
R1628:Unc13b	UTSW	4	43,263,371 (GRCm38)	missense	probably damaging	1.00
R1740:Unc13b	UTSW	4	43,240,285 (GRCm38)	missense	probably damaging	1.00
R1839:Unc13b	UTSW	4	43,258,308 (GRCm38)	splice site	probably benign
R2045:Unc13b	UTSW	4	43,091,266 (GRCm38)	missense	probably damaging	1.00
R2191:Unc13b	UTSW	4	43,245,566 (GRCm38)	nonsense	probably null
R2259:Unc13b	UTSW	4	43,182,780 (GRCm38)	missense	possibly damaging	0.87
R2307:Unc13b	UTSW	4	43,239,854 (GRCm38)	missense	probably damaging	0.98
R2317:Unc13b	UTSW	4	43,245,514 (GRCm38)	missense	probably damaging	1.00
R2402:Unc13b	UTSW	4	43,095,843 (GRCm38)	missense	probably benign
R2847:Unc13b	UTSW	4	43,180,404 (GRCm38)	missense	probably benign	0.04
R3414:Unc13b	UTSW	4	43,234,658 (GRCm38)	splice site	probably benign
R3436:Unc13b	UTSW	4	43,097,028 (GRCm38)	splice site	probably benign
R3955:Unc13b	UTSW	4	43,256,834 (GRCm38)	missense	probably damaging	1.00
R3957:Unc13b	UTSW	4	43,256,834 (GRCm38)	missense	probably damaging	1.00
R4015:Unc13b	UTSW	4	43,237,801 (GRCm38)	missense	probably damaging	1.00
R4650:Unc13b	UTSW	4	43,261,035 (GRCm38)	missense	probably damaging	0.97
R4836:Unc13b	UTSW	4	43,237,137 (GRCm38)	missense	probably damaging	1.00
R5041:Unc13b	UTSW	4	43,237,836 (GRCm38)	missense	probably benign	0.41
R5413:Unc13b	UTSW	4	43,257,936 (GRCm38)	critical splice donor site	probably null
R5994:Unc13b	UTSW	4	43,172,596 (GRCm38)	intron	probably benign
R6015:Unc13b	UTSW	4	43,177,995 (GRCm38)	nonsense	probably null
R6090:Unc13b	UTSW	4	43,239,306 (GRCm38)	missense	probably damaging	1.00
R6242:Unc13b	UTSW	4	43,165,800 (GRCm38)	missense	possibly damaging	0.92
R6246:Unc13b	UTSW	4	43,216,246 (GRCm38)	missense	probably benign	0.18
R6427:Unc13b	UTSW	4	43,176,966 (GRCm38)	unclassified	probably benign
R6660:Unc13b	UTSW	4	43,177,412 (GRCm38)	unclassified	probably benign
R6670:Unc13b	UTSW	4	43,255,562 (GRCm38)	missense	probably damaging	0.99
R6753:Unc13b	UTSW	4	43,239,331 (GRCm38)	missense	probably damaging	1.00
R6858:Unc13b	UTSW	4	43,165,828 (GRCm38)	missense	possibly damaging	0.85
R6886:Unc13b	UTSW	4	43,170,156 (GRCm38)	intron	probably benign
R6969:Unc13b	UTSW	4	43,263,538 (GRCm38)	missense	possibly damaging	0.94
R6994:Unc13b	UTSW	4	43,173,203 (GRCm38)	intron	probably benign
R6994:Unc13b	UTSW	4	43,171,403 (GRCm38)	intron	probably benign
R7080:Unc13b	UTSW	4	43,171,926 (GRCm38)	missense	unknown
R7117:Unc13b	UTSW	4	43,216,544 (GRCm38)	missense	probably benign	0.33
R7132:Unc13b	UTSW	4	43,215,757 (GRCm38)	missense	probably benign	0.17
R7181:Unc13b	UTSW	4	43,258,893 (GRCm38)	missense	probably damaging	0.99
R7192:Unc13b	UTSW	4	43,258,519 (GRCm38)	missense	probably damaging	1.00
R7246:Unc13b	UTSW	4	43,172,910 (GRCm38)	missense	unknown
R7342:Unc13b	UTSW	4	43,258,703 (GRCm38)	missense	probably damaging	0.99
R7345:Unc13b	UTSW	4	43,173,966 (GRCm38)	missense	unknown
R7355:Unc13b	UTSW	4	43,237,754 (GRCm38)	missense	probably damaging	1.00
R7391:Unc13b	UTSW	4	43,216,459 (GRCm38)	missense	probably benign	0.03
R7419:Unc13b	UTSW	4	43,174,023 (GRCm38)	missense	unknown
R7517:Unc13b	UTSW	4	43,215,765 (GRCm38)	missense	probably benign
R7532:Unc13b	UTSW	4	43,249,565 (GRCm38)	missense	probably benign	0.44
R7564:Unc13b	UTSW	4	43,091,258 (GRCm38)	missense	probably damaging	1.00
R7598:Unc13b	UTSW	4	43,263,569 (GRCm38)	missense	probably benign	0.20
R7604:Unc13b	UTSW	4	43,256,776 (GRCm38)	missense	possibly damaging	0.95
R7604:Unc13b	UTSW	4	43,170,102 (GRCm38)	missense	unknown
R7643:Unc13b	UTSW	4	43,216,333 (GRCm38)	missense	probably benign
R7718:Unc13b	UTSW	4	43,173,854 (GRCm38)	missense	unknown
R7735:Unc13b	UTSW	4	43,165,791 (GRCm38)	missense	probably damaging	1.00
R7756:Unc13b	UTSW	4	43,177,312 (GRCm38)	small deletion	probably benign
R7757:Unc13b	UTSW	4	43,177,341 (GRCm38)	small insertion	probably benign
R7757:Unc13b	UTSW	4	43,177,330 (GRCm38)	small insertion	probably benign
R7757:Unc13b	UTSW	4	43,177,312 (GRCm38)	small deletion	probably benign
R7758:Unc13b	UTSW	4	43,177,344 (GRCm38)	small insertion	probably benign
R7758:Unc13b	UTSW	4	43,177,312 (GRCm38)	small insertion	probably benign
R7781:Unc13b	UTSW	4	43,259,546 (GRCm38)	missense	possibly damaging	0.87
R7793:Unc13b	UTSW	4	43,172,737 (GRCm38)	missense	unknown
R7858:Unc13b	UTSW	4	43,176,285 (GRCm38)	missense	unknown
R7867:Unc13b	UTSW	4	43,232,573 (GRCm38)	nonsense	probably null
R7897:Unc13b	UTSW	4	43,171,860 (GRCm38)	missense	unknown
R7904:Unc13b	UTSW	4	43,217,075 (GRCm38)	missense	probably benign
R7929:Unc13b	UTSW	4	43,174,399 (GRCm38)	missense	unknown
R7984:Unc13b	UTSW	4	43,173,973 (GRCm38)	missense	unknown
R8069:Unc13b	UTSW	4	43,177,597 (GRCm38)	missense	unknown
R8101:Unc13b	UTSW	4	43,239,918 (GRCm38)	missense	probably benign	0.08
R8246:Unc13b	UTSW	4	43,175,954 (GRCm38)	missense	unknown
R8289:Unc13b	UTSW	4	43,172,524 (GRCm38)	nonsense	probably null
R8301:Unc13b	UTSW	4	43,263,568 (GRCm38)	missense	probably benign
R8397:Unc13b	UTSW	4	43,217,290 (GRCm38)	missense	probably benign	0.12
R8421:Unc13b	UTSW	4	43,178,304 (GRCm38)	missense	unknown
R8738:Unc13b	UTSW	4	43,177,564 (GRCm38)	missense	unknown
R8746:Unc13b	UTSW	4	43,176,120 (GRCm38)	missense	unknown
R8766:Unc13b	UTSW	4	43,174,722 (GRCm38)	missense	unknown
R8825:Unc13b	UTSW	4	43,237,683 (GRCm38)	splice site	probably benign
R8834:Unc13b	UTSW	4	43,175,954 (GRCm38)	missense	unknown
R8862:Unc13b	UTSW	4	43,235,207 (GRCm38)	missense	probably damaging	1.00
R8864:Unc13b	UTSW	4	43,174,724 (GRCm38)	missense	unknown
R8889:Unc13b	UTSW	4	43,176,484 (GRCm38)	missense	unknown
R8892:Unc13b	UTSW	4	43,176,484 (GRCm38)	missense	unknown
R8904:Unc13b	UTSW	4	43,178,531 (GRCm38)	intron	probably benign
R9089:Unc13b	UTSW	4	43,095,847 (GRCm38)	missense	probably damaging	1.00
R9144:Unc13b	UTSW	4	43,173,649 (GRCm38)	missense	unknown
R9149:Unc13b	UTSW	4	43,176,186 (GRCm38)	missense	unknown
R9173:Unc13b	UTSW	4	43,177,421 (GRCm38)	missense	unknown
R9200:Unc13b	UTSW	4	43,257,352 (GRCm38)	missense	possibly damaging	0.50
R9232:Unc13b	UTSW	4	43,240,321 (GRCm38)	missense	probably benign	0.03
R9269:Unc13b	UTSW	4	43,171,955 (GRCm38)	missense	unknown
R9320:Unc13b	UTSW	4	43,171,044 (GRCm38)	missense	unknown
R9335:Unc13b	UTSW	4	43,255,551 (GRCm38)	missense	probably damaging	0.99
R9335:Unc13b	UTSW	4	43,216,123 (GRCm38)	missense	possibly damaging	0.86
R9352:Unc13b	UTSW	4	43,177,313 (GRCm38)	nonsense	probably null
R9352:Unc13b	UTSW	4	43,177,312 (GRCm38)	small insertion	probably benign
R9378:Unc13b	UTSW	4	43,173,282 (GRCm38)	missense	unknown
R9382:Unc13b	UTSW	4	43,172,512 (GRCm38)	missense	unknown
R9569:Unc13b	UTSW	4	43,177,312 (GRCm38)	small deletion	probably benign
R9622:Unc13b	UTSW	4	43,172,513 (GRCm38)	missense
R9687:Unc13b	UTSW	4	43,174,920 (GRCm38)	missense	unknown
R9704:Unc13b	UTSW	4	43,237,102 (GRCm38)	missense	probably benign	0.31
R9721:Unc13b	UTSW	4	43,101,869 (GRCm38)	missense	probably benign
R9753:Unc13b	UTSW	4	43,182,842 (GRCm38)	nonsense	probably null
RF016:Unc13b	UTSW	4	43,177,350 (GRCm38)	small insertion	probably benign
RF016:Unc13b	UTSW	4	43,177,347 (GRCm38)	small insertion	probably benign
RF041:Unc13b	UTSW	4	43,177,338 (GRCm38)	small insertion	probably benign
RF056:Unc13b	UTSW	4	43,177,359 (GRCm38)	small insertion	probably benign
Z1176:Unc13b	UTSW	4	43,177,764 (GRCm38)	missense	unknown
Z1176:Unc13b	UTSW	4	43,177,191 (GRCm38)	missense	unknown
Z1176:Unc13b	UTSW	4	43,171,419 (GRCm38)	missense	unknown
Z1176:Unc13b	UTSW	4	43,261,043 (GRCm38)	missense	probably benign	0.11
Z1177:Unc13b	UTSW	4	43,173,669 (GRCm38)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- AGGAGACGTCGTCAGAATCTG -3'
(R):5'- CTATGCTGTTAAGTTTCTCTGGATC -3'

Sequencing Primer
(F):5'- GACGTCGTCAGAATCTGTAACAATTC -3'
(R):5'- CTGAATTCCTCGGTACTACC -3'

Posted On

2019-10-07