Mutagenetix > Incidental Mutation

Incidental Mutation 'R9287:Cad'

703986

Institutional Source

Beutler Lab

Gene Symbol

Cad

Ensembl Gene

ENSMUSG00000013629

Gene Name

carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase

Synonyms

2410008J01Rik

MMRRC Submission

Accession Numbers

Essential gene?

Probably essential (E-score: 0.968) question?

Stock #

R9287 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

31212124-31235823 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 31230000 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Lysine at position 1499 (M1499K)

Ref Sequence

ENSEMBL: ENSMUSP00000013773 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000013773] [ENSMUST00000200953] [ENSMUST00000201182] [ENSMUST00000201838] [ENSMUST00000202795] [ENSMUST00000202973]

AlphaFold

B2RQC6

Predicted Effect

possibly damaging
Transcript: ENSMUST00000013773
AA Change: M1499K

PolyPhen 2 Score 0.670 (Sensitivity: 0.86; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000013773
Gene: ENSMUSG00000013629
AA Change: M1499K

Domain	Start	End	E-Value	Type
CPSase_sm_chain	1	139	8.81e-80	SMART
Pfam:GATase	179	356	4.7e-47	PFAM
low complexity region	397	407	N/A	INTRINSIC
Pfam:ATP-grasp_4	511	692	1.2e-15	PFAM
Pfam:CPSase_L_D2	514	718	1.8e-85	PFAM
Pfam:ATP-grasp	522	690	1.5e-9	PFAM
Pfam:Dala_Dala_lig_C	527	687	2.2e-10	PFAM
CPSase_L_D3	798	921	9.7e-59	SMART
Pfam:ATP-grasp_4	1044	1223	1.8e-23	PFAM
Pfam:CPSase_L_D2	1047	1250	3.1e-28	PFAM
Pfam:Dala_Dala_lig_C	1054	1242	2.3e-7	PFAM
Pfam:ATP-grasp	1055	1222	2.1e-12	PFAM
MGS	1327	1428	1.35e-7	SMART
Pfam:Amidohydro_1	1462	1730	7.4e-12	PFAM
low complexity region	1820	1839	N/A	INTRINSIC
low complexity region	1864	1880	N/A	INTRINSIC
Pfam:OTCace_N	1924	2065	1.9e-44	PFAM
Pfam:OTCace	2071	2221	7.6e-37	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000200953
AA Change: M1436K

PolyPhen 2 Score 0.869 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000144307
Gene: ENSMUSG00000013629
AA Change: M1436K

Domain	Start	End	E-Value	Type
CPSase_sm_chain	1	139	8.81e-80	SMART
Pfam:GATase	179	356	4.5e-47	PFAM
low complexity region	397	407	N/A	INTRINSIC
Pfam:CPSase_L_D2	514	616	1.5e-34	PFAM
Pfam:Dala_Dala_lig_C	527	625	2.4e-7	PFAM
Pfam:CPSase_L_D2	614	655	4.9e-15	PFAM
CPSase_L_D3	735	858	9.7e-59	SMART
Pfam:ATP-grasp_4	981	1160	1.7e-23	PFAM
Pfam:CPSase_L_D2	984	1187	3e-28	PFAM
Pfam:Dala_Dala_lig_C	991	1179	2.3e-7	PFAM
Pfam:ATP-grasp	992	1159	2.1e-12	PFAM
MGS	1264	1365	1.35e-7	SMART
Pfam:Amidohydro_1	1399	1667	7.1e-12	PFAM
low complexity region	1757	1776	N/A	INTRINSIC
low complexity region	1801	1817	N/A	INTRINSIC
Pfam:OTCace_N	1861	2002	1.8e-44	PFAM
Pfam:OTCace	2008	2158	7.3e-37	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000201182
AA Change: M1499K

PolyPhen 2 Score 0.831 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000144684
Gene: ENSMUSG00000013629
AA Change: M1499K

Domain	Start	End	E-Value	Type
CPSase_sm_chain	1	139	8.81e-80	SMART
Pfam:GATase	179	356	4.5e-47	PFAM
low complexity region	397	407	N/A	INTRINSIC
Pfam:ATP-grasp_4	511	692	1.1e-15	PFAM
Pfam:CPSase_L_D2	514	718	1.7e-85	PFAM
Pfam:ATP-grasp	522	690	1.4e-9	PFAM
Pfam:Dala_Dala_lig_C	527	687	2.1e-10	PFAM
CPSase_L_D3	798	921	9.7e-59	SMART
Pfam:ATP-grasp_4	1044	1223	1.7e-23	PFAM
Pfam:CPSase_L_D2	1047	1250	3e-28	PFAM
Pfam:Dala_Dala_lig_C	1054	1242	2.3e-7	PFAM
Pfam:ATP-grasp	1055	1222	2.1e-12	PFAM
MGS	1327	1428	1.35e-7	SMART
Pfam:Amidohydro_1	1462	1730	7.1e-12	PFAM
low complexity region	1820	1839	N/A	INTRINSIC
low complexity region	1864	1880	N/A	INTRINSIC
Pfam:OTCace_N	1949	1994	1.4e-11	PFAM
Pfam:OTCace	2000	2150	7.3e-37	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000201838

SMART Domains

Protein: ENSMUSP00000144127
Gene: ENSMUSG00000013629

Domain	Start	End	E-Value	Type
CPSase_sm_chain	1	139	8.81e-80	SMART
Pfam:GATase	179	356	6.3e-48	PFAM
low complexity region	397	407	N/A	INTRINSIC
Pfam:ATP-grasp_4	511	692	1.9e-16	PFAM
Pfam:CPSase_L_D2	514	718	3.7e-86	PFAM
Pfam:ATP-grasp	522	690	2.5e-10	PFAM
Pfam:Dala_Dala_lig_C	526	687	4.2e-11	PFAM
CPSase_L_D3	798	921	9.7e-59	SMART
SCOP:d1a9xa3	935	964	1e-7	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000202795
AA Change: M1499K

PolyPhen 2 Score 0.805 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000144009
Gene: ENSMUSG00000013629
AA Change: M1499K

Domain	Start	End	E-Value	Type
CPSase_sm_chain	1	139	8.81e-80	SMART
Pfam:GATase	179	356	1.9e-47	PFAM
low complexity region	397	407	N/A	INTRINSIC
Pfam:ATP-grasp_4	511	692	5.9e-16	PFAM
Pfam:CPSase_L_D2	514	718	1.2e-85	PFAM
Pfam:ATP-grasp	522	690	7.3e-10	PFAM
Pfam:Dala_Dala_lig_C	527	687	1.3e-10	PFAM
CPSase_L_D3	798	921	9.7e-59	SMART
Pfam:ATP-grasp_4	1044	1223	8.9e-24	PFAM
Pfam:CPSase_L_D2	1047	1250	2.1e-28	PFAM
Pfam:Dala_Dala_lig_C	1054	1242	1.3e-7	PFAM
Pfam:ATP-grasp	1055	1222	1.1e-12	PFAM
MGS	1327	1428	1.35e-7	SMART
Pfam:Amidohydro_1	1462	1730	2.5e-11	PFAM
low complexity region	1820	1839	N/A	INTRINSIC
low complexity region	1864	1880	N/A	INTRINSIC
Pfam:OTCace_N	1970	2004	4.6e-11	PFAM
Pfam:OTCace	2010	2160	9.9e-37	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000202973

SMART Domains

Protein: ENSMUSP00000144679
Gene: ENSMUSG00000013629

Domain	Start	End	E-Value	Type
SCOP:d1gkra1	1	84	4e-28	SMART
PDB:4C6N\|A	1	119	4e-58	PDB
low complexity region	156	170	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

100% (109/109)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The de novo synthesis of pyrimidine nucleotides is required for mammalian cells to proliferate. This gene encodes a trifunctional protein which is associated with the enzymatic activities of the first 3 enzymes in the 6-step pathway of pyrimidine biosynthesis: carbamoylphosphate synthetase (CPS II), aspartate transcarbamoylase, and dihydroorotase. This protein is regulated by the mitogen-activated protein kinase (MAPK) cascade, which indicates a direct link between activation of the MAPK cascade and de novo biosynthesis of pyrimidine nucleotides. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]

Allele List at MGI

Other mutations in this stock

Total: 108 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9430097D07Rik	T	A	2: 32,465,178 (GRCm39)		probably benign	Het
Aadacl2	C	A	3: 59,932,573 (GRCm39)	H363N	probably damaging	Het
Ace3	T	G	11: 105,888,246 (GRCm39)	S319A	probably damaging	Het
Amer3	C	T	1: 34,627,900 (GRCm39)	P713L	possibly damaging	Het
Aoah	T	C	13: 21,186,879 (GRCm39)	L453P	probably damaging	Het
Asz1	A	T	6: 18,051,290 (GRCm39)	L463Q	possibly damaging	Het
Bpifb6	T	A	2: 153,746,535 (GRCm39)	V143D	probably damaging	Het
Casp9	T	A	4: 141,534,471 (GRCm39)	C294S	probably benign	Het
Ccdc7b	T	A	8: 129,890,321 (GRCm39)	S65T	probably benign	Het
Cdh23	G	A	10: 60,143,306 (GRCm39)	A3005V	possibly damaging	Het
Cfap54	T	C	10: 92,805,565 (GRCm39)	Y1515C	possibly damaging	Het
Chrm5	A	C	2: 112,309,610 (GRCm39)	F502C	probably damaging	Het
Cnst	A	T	1: 179,407,108 (GRCm39)	T52S	possibly damaging	Het
Cntn6	T	C	6: 104,809,471 (GRCm39)	I502T	possibly damaging	Het
Col7a1	G	A	9: 108,787,457 (GRCm39)	V617M	unknown	Het
Ctsb	A	G	14: 63,370,875 (GRCm39)	D29G	probably benign	Het
Cyp3a44	T	A	5: 145,725,202 (GRCm39)	Q333L	possibly damaging	Het
Dnajc27	T	C	12: 4,146,256 (GRCm39)	V95A	possibly damaging	Het
Eea1	T	A	10: 95,831,445 (GRCm39)	Y179N	probably damaging	Het
Erbb2	T	C	11: 98,326,107 (GRCm39)	M961T	probably damaging	Het
Fat4	G	A	3: 38,945,781 (GRCm39)	G1558D	probably damaging	Het
Foxh1	T	C	15: 76,553,126 (GRCm39)	E196G	probably damaging	Het
Gcc2	T	A	10: 58,105,217 (GRCm39)	L151*	probably null	Het
Gcdh	C	T	8: 85,616,313 (GRCm39)	G294D	probably damaging	Het
Gcnt3	A	T	9: 69,941,693 (GRCm39)	F292I	probably damaging	Het
Glod4	T	C	11: 76,128,510 (GRCm39)	S131G	probably benign	Het
Gpc2	G	A	5: 138,272,586 (GRCm39)	L576F	unknown	Het
Gphn	G	A	12: 78,609,646 (GRCm39)	S330N	possibly damaging	Het
Heatr5a	C	T	12: 51,967,260 (GRCm39)	C872Y	probably damaging	Het
Hephl1	G	A	9: 14,995,775 (GRCm39)	S449L	probably benign	Het
Hrh2	G	T	13: 54,368,358 (GRCm39)	M111I	probably benign	Het
Igfn1	A	G	1: 135,925,544 (GRCm39)	V70A	probably benign	Het
Il2	G	A	3: 37,179,988 (GRCm39)	T23I	probably damaging	Het
Irak4	A	G	15: 94,460,917 (GRCm39)	T382A	possibly damaging	Het
Itih2	A	G	2: 10,128,297 (GRCm39)	S135P	possibly damaging	Het
Kansl3	C	T	1: 36,388,497 (GRCm39)	D457N	probably damaging	Het
Kcns3	A	G	12: 11,141,601 (GRCm39)	I366T	probably damaging	Het
Kif26a	C	A	12: 112,145,719 (GRCm39)	Y1743*	probably null	Het
Lama4	A	T	10: 38,981,960 (GRCm39)	I1730F	probably damaging	Het
Lax1	T	C	1: 133,607,931 (GRCm39)	N270S	probably benign	Het
Lrp1	G	T	10: 127,403,233 (GRCm39)	D2113E	probably damaging	Het
Lrp6	A	G	6: 134,483,259 (GRCm39)	V482A	probably benign	Het
Luzp2	A	G	7: 54,914,108 (GRCm39)		probably benign	Het
Mc5r	C	A	18: 68,472,200 (GRCm39)	D186E	probably damaging	Het
Mcph1	A	T	8: 18,657,293 (GRCm39)		probably null	Het
Mgam	A	G	6: 40,705,905 (GRCm39)		probably benign	Het
Mmrn1	A	C	6: 60,952,939 (GRCm39)	T407P	probably damaging	Het
Mrpl1	T	C	5: 96,386,806 (GRCm39)	V265A	probably benign	Het
Mrpl15	C	T	1: 4,846,856 (GRCm39)	G240D	probably damaging	Het
Msx1	A	T	5: 37,978,795 (GRCm39)	M240K	probably damaging	Het
Mtf1	T	C	4: 124,724,934 (GRCm39)	L337P	probably damaging	Het
Muc5ac	T	A	7: 141,361,626 (GRCm39)	C1646S	probably damaging	Het
Mvb12a	C	A	8: 71,999,638 (GRCm39)	T219N	probably damaging	Het
Myo16	G	A	8: 10,526,114 (GRCm39)	V885M	unknown	Het
N4bp2	T	A	5: 65,960,855 (GRCm39)	S509T	probably benign	Het
Nckap1	A	G	2: 80,383,750 (GRCm39)	V144A	possibly damaging	Het
Nkx2-6	G	T	14: 69,412,404 (GRCm39)	G191C	possibly damaging	Het
Nmnat2	T	C	1: 152,962,138 (GRCm39)	I126T	probably damaging	Het
Nrp2	C	T	1: 62,835,014 (GRCm39)	R863W	probably damaging	Het
Nup188	C	T	2: 30,226,726 (GRCm39)	R1168C	probably damaging	Het
Oas3	T	A	5: 120,892,754 (GRCm39)	D1091V	probably damaging	Het
Optn	T	A	2: 5,036,126 (GRCm39)	Q452L	probably damaging	Het
Or8b47	C	T	9: 38,435,082 (GRCm39)	T18I	probably damaging	Het
Pcca	G	A	14: 122,854,178 (GRCm39)	V157I	probably benign	Het
Pcdha9	A	G	18: 37,132,281 (GRCm39)	D450G	probably benign	Het
Pcnx1	T	A	12: 82,042,323 (GRCm39)	S38T	probably benign	Het
Phrf1	C	G	7: 140,840,055 (GRCm39)	D1083E	probably benign	Het
Plaat5	T	A	19: 7,596,691 (GRCm39)	Y159*	probably null	Het
Plcb4	G	A	2: 135,829,817 (GRCm39)	A947T	probably benign	Het
Ppp1r3g	G	A	13: 36,152,834 (GRCm39)	D85N	possibly damaging	Het
Pramel34	G	A	5: 93,785,969 (GRCm39)	H104Y	possibly damaging	Het
Prom2	A	C	2: 127,380,185 (GRCm39)	V349G	probably damaging	Het
Prrc2c	C	T	1: 162,541,843 (GRCm39)	S382N	probably benign	Het
Rai14	A	T	15: 10,592,204 (GRCm39)	N230K	probably benign	Het
Rexo5	A	T	7: 119,402,025 (GRCm39)	K142I	probably damaging	Het
Rgs22	T	C	15: 36,098,409 (GRCm39)	H484R	probably damaging	Het
Rims2	C	T	15: 39,543,086 (GRCm39)	A1440V	probably damaging	Het
Serpinb1a	T	C	13: 33,026,946 (GRCm39)	E332G	probably damaging	Het
Sh2b1	TGGGGACCAGCTCAGCCACGGGGACCAGCTC	TGGGGACCAGCTCAGCCACGGGGACCAGCTCAGCCACGGGGACCAGCTC	7: 126,066,742 (GRCm39)		probably benign	Het
Slc26a7	C	T	4: 14,516,165 (GRCm39)	G555S	possibly damaging	Het
Slc4a2	A	T	5: 24,639,123 (GRCm39)	D386V	probably damaging	Het
Slc6a17	C	T	3: 107,384,551 (GRCm39)	V350M	probably damaging	Het
Smc2	A	G	4: 52,449,361 (GRCm39)	Y174C	probably damaging	Het
Smoc2	A	G	17: 14,619,686 (GRCm39)	Y355C	probably damaging	Het
Smpd1	T	A	7: 105,204,442 (GRCm39)	V107E	probably benign	Het
Snapc1	T	C	12: 74,018,773 (GRCm39)		probably benign	Het
Spata31e2	T	C	1: 26,722,426 (GRCm39)	D918G	possibly damaging	Het
Steap4	T	G	5: 8,026,683 (GRCm39)	F215L	probably benign	Het
Tbc1d1	T	A	5: 64,435,364 (GRCm39)	S501T	probably damaging	Het
Tec	A	G	5: 72,926,117 (GRCm39)	Y312H	probably damaging	Het
Ticrr	C	A	7: 79,343,516 (GRCm39)	T1127K	possibly damaging	Het
Tlk2	A	G	11: 105,147,722 (GRCm39)	D438G	probably benign	Het
Tln2	C	A	9: 67,277,980 (GRCm39)	V343L	probably benign	Het
Tmem156	T	A	5: 65,231,148 (GRCm39)	I241F	probably damaging	Het
Tmtc1	G	T	6: 148,186,390 (GRCm39)	N559K	probably benign	Het
Trbv4	A	T	6: 41,036,696 (GRCm39)	I74F	probably benign	Het
Trmt1l	C	T	1: 151,328,899 (GRCm39)	P524S	probably damaging	Het
Trpa1	A	T	1: 14,956,040 (GRCm39)	C776*	probably null	Het
Ttc41	T	A	10: 86,599,830 (GRCm39)	S1043R	probably benign	Het
Ttn	A	G	2: 76,576,646 (GRCm39)	L24749S	probably damaging	Het
Ube2o	C	T	11: 116,471,942 (GRCm39)	G100R	probably damaging	Het
Unc5b	T	C	10: 60,609,532 (GRCm39)	E588G	possibly damaging	Het
Usp43	G	T	11: 67,770,922 (GRCm39)	Q571K	probably damaging	Het
Vmn1r127	G	A	7: 21,052,927 (GRCm39)	P287L	possibly damaging	Het
Wasf3	T	A	5: 146,397,857 (GRCm39)	M208K	possibly damaging	Het
Xab2	A	G	8: 3,663,000 (GRCm39)	F527S	possibly damaging	Het
Zfp644	T	G	5: 106,785,774 (GRCm39)	N258H	possibly damaging	Het
Zfp947	A	C	17: 22,364,594 (GRCm39)	F360C	probably damaging	Het

Other mutations in Cad

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00821:Cad	APN	5	31,218,828 (GRCm39)	missense	probably damaging	1.00
IGL00908:Cad	APN	5	31,216,398 (GRCm39)	missense	possibly damaging	0.93
IGL01068:Cad	APN	5	31,219,114 (GRCm39)	splice site	probably benign
IGL01638:Cad	APN	5	31,224,958 (GRCm39)	missense	probably damaging	1.00
IGL02483:Cad	APN	5	31,218,170 (GRCm39)	critical splice acceptor site	probably null
IGL02499:Cad	APN	5	31,226,948 (GRCm39)	missense	probably damaging	1.00
IGL02691:Cad	APN	5	31,212,638 (GRCm39)	missense	probably damaging	1.00
IGL03002:Cad	APN	5	31,212,330 (GRCm39)	missense	probably benign	0.00
PIT4696001:Cad	UTSW	5	31,229,438 (GRCm39)	missense	probably damaging	0.99
R0212:Cad	UTSW	5	31,235,454 (GRCm39)	missense	probably damaging	1.00
R0317:Cad	UTSW	5	31,229,665 (GRCm39)	missense	probably benign	0.01
R0335:Cad	UTSW	5	31,231,329 (GRCm39)	unclassified	probably benign
R0401:Cad	UTSW	5	31,231,330 (GRCm39)	unclassified	probably benign
R0445:Cad	UTSW	5	31,230,053 (GRCm39)	missense	probably benign	0.08
R0494:Cad	UTSW	5	31,234,856 (GRCm39)	unclassified	probably benign
R0532:Cad	UTSW	5	31,219,531 (GRCm39)	splice site	probably benign
R0539:Cad	UTSW	5	31,232,801 (GRCm39)	splice site	probably benign
R0578:Cad	UTSW	5	31,216,120 (GRCm39)	missense	probably benign	0.01
R0590:Cad	UTSW	5	31,219,575 (GRCm39)	missense	probably damaging	1.00
R0638:Cad	UTSW	5	31,235,032 (GRCm39)	missense	probably damaging	0.98
R0831:Cad	UTSW	5	31,224,944 (GRCm39)	missense	probably damaging	1.00
R1329:Cad	UTSW	5	31,216,926 (GRCm39)	missense	probably damaging	1.00
R1513:Cad	UTSW	5	31,226,106 (GRCm39)	missense	probably damaging	1.00
R1531:Cad	UTSW	5	31,233,563 (GRCm39)	missense	probably benign	0.14
R1763:Cad	UTSW	5	31,218,295 (GRCm39)	missense	probably damaging	1.00
R1785:Cad	UTSW	5	31,215,416 (GRCm39)	missense	probably damaging	1.00
R1786:Cad	UTSW	5	31,215,416 (GRCm39)	missense	probably damaging	1.00
R2131:Cad	UTSW	5	31,215,416 (GRCm39)	missense	probably damaging	1.00
R2165:Cad	UTSW	5	31,219,564 (GRCm39)	missense	probably damaging	1.00
R3103:Cad	UTSW	5	31,219,018 (GRCm39)	missense	possibly damaging	0.95
R3113:Cad	UTSW	5	31,231,481 (GRCm39)	missense	possibly damaging	0.50
R3762:Cad	UTSW	5	31,232,890 (GRCm39)	splice site	probably null
R3847:Cad	UTSW	5	31,218,994 (GRCm39)	missense	probably damaging	1.00
R3898:Cad	UTSW	5	31,231,366 (GRCm39)	missense	probably benign	0.06
R3943:Cad	UTSW	5	31,229,729 (GRCm39)	critical splice donor site	probably null
R4213:Cad	UTSW	5	31,229,688 (GRCm39)	missense	probably benign	0.01
R4458:Cad	UTSW	5	31,218,570 (GRCm39)	missense	probably damaging	1.00
R4562:Cad	UTSW	5	31,215,477 (GRCm39)	missense	possibly damaging	0.82
R4629:Cad	UTSW	5	31,227,639 (GRCm39)	missense	probably damaging	1.00
R4717:Cad	UTSW	5	31,224,030 (GRCm39)	critical splice acceptor site	probably null
R4811:Cad	UTSW	5	31,232,034 (GRCm39)	missense	probably benign	0.02
R5044:Cad	UTSW	5	31,212,365 (GRCm39)	missense	probably benign	0.00
R5630:Cad	UTSW	5	31,217,917 (GRCm39)	missense	probably damaging	1.00
R5660:Cad	UTSW	5	31,234,191 (GRCm39)	missense	probably damaging	1.00
R6008:Cad	UTSW	5	31,226,456 (GRCm39)	missense	probably damaging	1.00
R6029:Cad	UTSW	5	31,212,327 (GRCm39)	missense	possibly damaging	0.65
R6073:Cad	UTSW	5	31,219,906 (GRCm39)	missense	possibly damaging	0.84
R6240:Cad	UTSW	5	31,230,322 (GRCm39)	missense	probably benign	0.00
R6260:Cad	UTSW	5	31,224,144 (GRCm39)	missense	probably null
R7145:Cad	UTSW	5	31,224,956 (GRCm39)	missense	possibly damaging	0.89
R7303:Cad	UTSW	5	31,217,557 (GRCm39)	critical splice donor site	probably null
R7352:Cad	UTSW	5	31,215,422 (GRCm39)	missense	probably damaging	1.00
R7382:Cad	UTSW	5	31,233,173 (GRCm39)	missense	probably benign
R7387:Cad	UTSW	5	31,219,284 (GRCm39)	missense	probably damaging	1.00
R7455:Cad	UTSW	5	31,231,506 (GRCm39)	missense	probably damaging	0.99
R7596:Cad	UTSW	5	31,226,392 (GRCm39)	missense	probably benign
R7627:Cad	UTSW	5	31,217,508 (GRCm39)	missense	probably damaging	1.00
R7898:Cad	UTSW	5	31,218,829 (GRCm39)	missense	probably damaging	1.00
R8022:Cad	UTSW	5	31,226,150 (GRCm39)	missense	probably damaging	1.00
R8115:Cad	UTSW	5	31,218,271 (GRCm39)	missense	possibly damaging	0.82
R8511:Cad	UTSW	5	31,233,165 (GRCm39)	missense	probably benign	0.00
R8523:Cad	UTSW	5	31,215,450 (GRCm39)	missense	probably damaging	0.98
R8690:Cad	UTSW	5	31,232,500 (GRCm39)	missense	possibly damaging	0.58
R8697:Cad	UTSW	5	31,231,945 (GRCm39)	missense	probably benign	0.06
R8698:Cad	UTSW	5	31,234,819 (GRCm39)	missense	probably benign
R8699:Cad	UTSW	5	31,233,605 (GRCm39)	missense	possibly damaging	0.80
R8803:Cad	UTSW	5	31,226,908 (GRCm39)	missense	probably damaging	1.00
R9262:Cad	UTSW	5	31,225,009 (GRCm39)	missense	probably null
R9272:Cad	UTSW	5	31,218,576 (GRCm39)	missense	possibly damaging	0.91
R9314:Cad	UTSW	5	31,234,988 (GRCm39)	missense	probably damaging	1.00
R9609:Cad	UTSW	5	31,228,018 (GRCm39)	critical splice donor site	probably null
R9665:Cad	UTSW	5	31,229,703 (GRCm39)	missense	probably benign	0.28
RF001:Cad	UTSW	5	31,217,556 (GRCm39)	critical splice donor site	probably benign
RF012:Cad	UTSW	5	31,217,556 (GRCm39)	critical splice donor site	probably benign
X0021:Cad	UTSW	5	31,225,475 (GRCm39)	missense	probably null	1.00
X0022:Cad	UTSW	5	31,229,661 (GRCm39)	missense	probably damaging	0.99
Z1177:Cad	UTSW	5	31,232,472 (GRCm39)	missense	probably benign	0.25
Z1177:Cad	UTSW	5	31,225,765 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTCCATGGTGCTCTTCATTGAG -3'
(R):5'- TCTCAGATGAGGCTCCAAGG -3'

Sequencing Primer
(F):5'- CATTGAGAACTTGTATCAGTGGC -3'
(R):5'- TAAAGTCACAGCGGGCGC -3'

Posted On

2022-03-25