Mutagenetix > Incidental Mutation

Incidental Mutation 'R0731:Celsr1'

67591

Institutional Source

Beutler Lab

Gene Symbol

Celsr1

Ensembl Gene

ENSMUSG00000016028

Gene Name

cadherin, EGF LAG seven-pass G-type receptor 1

Synonyms

crash, Crsh, Scy

MMRRC Submission

038912-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.630) question?

Stock #

R0731 (G1)

Quality Score

165

Status

Validated

Chromosome

Chromosomal Location

85898929-86033777 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 85901597 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 2892 (D2892G)

Ref Sequence

ENSEMBL: ENSMUSP00000016172 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000016172] [ENSMUST00000023019]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000016172
AA Change: D2892G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000016172
Gene: ENSMUSG00000016028
AA Change: D2892G

Domain	Start	End	E-Value	Type
signal peptide	1	29	N/A	INTRINSIC
low complexity region	65	93	N/A	INTRINSIC
low complexity region	221	240	N/A	INTRINSIC
low complexity region	243	257	N/A	INTRINSIC
CA	282	366	9.51e-26	SMART
CA	390	472	1.59e-27	SMART
CA	496	578	3.8e-25	SMART
CA	602	700	2.25e-27	SMART
CA	724	802	3.14e-17	SMART
CA	826	905	2.67e-29	SMART
CA	929	1012	3.23e-28	SMART
CA	1036	1114	4.17e-22	SMART
CA	1142	1218	6.89e-1	SMART
EGF	1321	1376	3.38e-3	SMART
EGF	1381	1414	5.49e-3	SMART
EGF	1421	1456	9.7e-4	SMART
LamG	1477	1644	2.53e-33	SMART
EGF	1667	1700	6.4e-4	SMART
LamG	1726	1864	1.13e-21	SMART
EGF	1890	1923	1.84e-4	SMART
EGF	1925	1961	5.49e-3	SMART
EGF_Lam	2018	2063	7.12e-11	SMART
HormR	2066	2128	2.55e-20	SMART
Pfam:GAIN	2140	2396	1.1e-64	PFAM
GPS	2422	2475	5.03e-22	SMART
Pfam:7tm_2	2480	2712	2.6e-60	PFAM
low complexity region	2738	2753	N/A	INTRINSIC
low complexity region	2819	2852	N/A	INTRINSIC
low complexity region	2976	2988	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000023019

SMART Domains

Protein: ENSMUSP00000023019
Gene: ENSMUSG00000022386

Domain	Start	End	E-Value	Type
Pfam:NAD_synthase	1	133	7.7e-7	PFAM
Pfam:ThiI	3	79	7.7e-8	PFAM
Pfam:tRNA_Me_trans	5	383	3.4e-142	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000159362

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000159730

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000162010

Predicted Effect

unknown
Transcript: ENSMUST00000226204
AA Change: D154G

Predicted Effect

unknown
Transcript: ENSMUST00000226840
AA Change: D1524G

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.4%
3x: 98.9%
10x: 97.6%
20x: 95.5%

Validation Efficiency

97% (73/75)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the flamingo subfamily, part of the cadherin superfamily. The flamingo subfamily consists of nonclassic-type cadherins; a subpopulation that does not interact with catenins. The flamingo cadherins are located at the plasma membrane and have nine cadherin domains, seven epidermal growth factor-like repeats and two laminin A G-type repeats in their ectodomain. They also have seven transmembrane domains, a characteristic unique to this subfamily. It is postulated that these proteins are receptors involved in contact-mediated communication, with cadherin domains acting as homophilic binding regions and the EGF-like domains involved in cell adhesion and receptor-ligand interactions. This particular member is a developmentally regulated, neural-specific gene which plays an unspecified role in early embryogenesis. [provided by RefSeq, Jul 2008]
PHENOTYPE: Nullizygous mice exhibit kinky tails, variable neural tube defects, abnormal hair follicle orientation, whorl-like hair patterns, and partial prenatal lethality. ENU-induced mutants show defects in planar polarity of inner ear hair cells and complete perinatal lethality due to craniorachischisis. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 73 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930430F08Rik	T	C	10: 100,586,203 (GRCm38)	T66A	probably damaging	Het
4933406M09Rik	A	C	1: 134,389,975 (GRCm38)	M162L	probably benign	Het
Acsm3	A	T	7: 119,768,024 (GRCm38)	R27*	probably null	Het
Actg1	A	G	11: 120,346,949 (GRCm38)	F255S	probably damaging	Het
Ahdc1	T	A	4: 133,062,951 (GRCm38)	V501E	possibly damaging	Het
Alpk2	A	T	18: 65,305,390 (GRCm38)	D1444E	probably damaging	Het
Btaf1	T	G	19: 36,997,495 (GRCm38)		probably null	Het
Cacnb2	A	G	2: 14,985,706 (GRCm38)	H489R	possibly damaging	Het
Ccdc162	C	A	10: 41,579,143 (GRCm38)	K398N	probably damaging	Het
Cd79b	G	T	11: 106,312,433 (GRCm38)	S145R	probably damaging	Het
Cdh11	T	A	8: 102,668,019 (GRCm38)	N264Y	probably damaging	Het
Chuk	A	G	19: 44,103,766 (GRCm38)		probably benign	Het
Clk3	T	C	9: 57,751,126 (GRCm38)		probably benign	Het
Dcaf8	A	T	1: 172,172,509 (GRCm38)	D78V	possibly damaging	Het
Dctn1	A	G	6: 83,183,089 (GRCm38)	T87A	probably damaging	Het
Ddx50	T	C	10: 62,616,249 (GRCm38)	N732D	unknown	Het
Dnah5	A	T	15: 28,311,143 (GRCm38)	Y1756F	possibly damaging	Het
Dock3	A	T	9: 106,969,856 (GRCm38)	V858E	probably damaging	Het
Fer1l4	A	G	2: 156,024,070 (GRCm38)	F1566S	probably benign	Het
Fpr-rs7	T	C	17: 20,113,854 (GRCm38)	I125V	probably benign	Het
Fuca2	C	T	10: 13,506,027 (GRCm38)	P228L	probably benign	Het
Galntl6	A	G	8: 58,535,984 (GRCm38)	F57L	probably benign	Het
Gigyf2	T	A	1: 87,407,727 (GRCm38)		probably benign	Het
Gm16505	A	T	13: 3,361,329 (GRCm38)		noncoding transcript	Het
Gm4781	T	C	10: 100,396,777 (GRCm38)		noncoding transcript	Het
Gm9956	T	A	10: 56,745,543 (GRCm38)	Y100*	probably null	Het
Gpr137c	T	A	14: 45,246,349 (GRCm38)	C178S	probably damaging	Het
Gpr83	A	G	9: 14,868,644 (GRCm38)	R331G	probably benign	Het
Hlcs	T	A	16: 94,131,852 (GRCm38)	H851L	probably damaging	Het
Kbtbd6	C	A	14: 79,451,884 (GRCm38)	Y6*	probably null	Het
Kif23	T	C	9: 61,925,032 (GRCm38)	R610G	possibly damaging	Het
Kifc3	G	A	8: 95,105,733 (GRCm38)	T487I	probably damaging	Het
Klra5	A	C	6: 129,908,796 (GRCm38)	D133E	possibly damaging	Het
Klra6	T	C	6: 130,022,705 (GRCm38)	E100G	probably damaging	Het
Klre1	T	A	6: 129,585,568 (GRCm38)		probably benign	Het
Lancl1	C	T	1: 67,009,910 (GRCm38)		probably null	Het
Lgr6	C	T	1: 134,994,010 (GRCm38)	A199T	probably damaging	Het
Man1b1	A	G	2: 25,338,155 (GRCm38)	I146V	possibly damaging	Het
Map4k5	T	A	12: 69,874,264 (GRCm38)		probably benign	Het
Mast3	A	G	8: 70,781,321 (GRCm38)	S178P	probably damaging	Het
Mau2	A	G	8: 70,023,612 (GRCm38)		probably null	Het
Mkrn2	A	T	6: 115,614,651 (GRCm38)	N312Y	probably damaging	Het
Mrvi1	T	C	7: 110,876,900 (GRCm38)	S615G	probably benign	Het
Myh1	A	G	11: 67,202,533 (GRCm38)	E150G	probably damaging	Het
Myo7b	T	A	18: 31,961,825 (GRCm38)		probably null	Het
Nyap1	A	G	5: 137,735,298 (GRCm38)	V491A	probably damaging	Het
Olfr1284	A	G	2: 111,379,293 (GRCm38)	M98V	probably damaging	Het
Olfr484	T	C	7: 108,124,734 (GRCm38)	I176M	probably benign	Het
Olfr518	A	T	7: 108,881,533 (GRCm38)	N24K	probably damaging	Het
Olfr954	T	C	9: 39,461,532 (GRCm38)	F34L	probably damaging	Het
Oxsm	A	T	14: 16,240,893 (GRCm38)	H385Q	probably damaging	Het
Pbld2	T	C	10: 63,056,811 (GRCm38)	S242P	probably damaging	Het
Pdzd7	T	C	19: 45,029,305 (GRCm38)	Y675C	probably damaging	Het
Pnkd	T	A	1: 74,351,541 (GRCm38)	H266Q	probably damaging	Het
Rbfox2	A	G	15: 77,099,279 (GRCm38)	S141P	probably benign	Het
Rdx	A	G	9: 52,068,218 (GRCm38)	T214A	probably benign	Het
Ripor2	A	T	13: 24,680,644 (GRCm38)	E219V	probably damaging	Het
Rufy2	G	A	10: 63,011,844 (GRCm38)		probably benign	Het
Slf2	T	A	19: 44,975,726 (GRCm38)		probably benign	Het
Snrnp200	G	T	2: 127,226,145 (GRCm38)		probably benign	Het
Snx7	T	A	3: 117,829,671 (GRCm38)		probably benign	Het
Stt3a	T	C	9: 36,735,512 (GRCm38)	I602V	probably damaging	Het
Tacr3	G	A	3: 134,855,000 (GRCm38)		probably null	Het
Tcerg1	C	T	18: 42,571,840 (GRCm38)	T978M	probably damaging	Het
Tcf7l1	G	T	6: 72,788,269 (GRCm38)	P126Q	possibly damaging	Het
Trank1	A	G	9: 111,365,488 (GRCm38)	D860G	probably damaging	Het
Try4	T	C	6: 41,304,367 (GRCm38)	L81P	probably benign	Het
Ucp1	T	C	8: 83,297,847 (GRCm38)		probably benign	Het
Ugt2b38	G	A	5: 87,420,452 (GRCm38)	A328V	probably damaging	Het
Wfikkn1	T	A	17: 25,878,017 (GRCm38)	R444S	probably damaging	Het
Zfc3h1	A	G	10: 115,410,632 (GRCm38)	T875A	probably benign	Het
Zfp11	A	G	5: 129,657,264 (GRCm38)	S378P	probably damaging	Het
Zfp984	T	A	4: 147,756,232 (GRCm38)	N54I	probably damaging	Het

Other mutations in Celsr1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00392:Celsr1	APN	15	85,931,345 (GRCm38)	missense	probably benign	0.04
IGL00519:Celsr1	APN	15	86,030,836 (GRCm38)	missense	probably damaging	1.00
IGL00909:Celsr1	APN	15	85,922,235 (GRCm38)	missense	probably damaging	1.00
IGL01303:Celsr1	APN	15	86,030,491 (GRCm38)	missense	probably damaging	0.97
IGL01726:Celsr1	APN	15	85,926,190 (GRCm38)	missense	probably benign	0.35
IGL01910:Celsr1	APN	15	85,929,895 (GRCm38)	missense	probably benign
IGL01931:Celsr1	APN	15	85,907,660 (GRCm38)	missense	probably damaging	1.00
IGL01952:Celsr1	APN	15	85,963,223 (GRCm38)	missense	probably benign	0.35
IGL02090:Celsr1	APN	15	85,907,721 (GRCm38)	missense	possibly damaging	0.49
IGL02191:Celsr1	APN	15	85,979,004 (GRCm38)	missense	possibly damaging	0.69
IGL02372:Celsr1	APN	15	85,929,907 (GRCm38)	missense	probably benign	0.01
IGL02413:Celsr1	APN	15	86,031,226 (GRCm38)	missense	possibly damaging	0.96
IGL02478:Celsr1	APN	15	85,941,136 (GRCm38)	missense	possibly damaging	0.68
IGL02507:Celsr1	APN	15	85,900,688 (GRCm38)	utr 3 prime	probably benign
IGL02508:Celsr1	APN	15	86,030,617 (GRCm38)	nonsense	probably null
IGL02899:Celsr1	APN	15	86,031,726 (GRCm38)	missense	probably damaging	0.98
IGL02939:Celsr1	APN	15	85,901,472 (GRCm38)	missense	probably benign
IGL03212:Celsr1	APN	15	85,930,677 (GRCm38)	missense	probably benign	0.04
P0028:Celsr1	UTSW	15	85,922,235 (GRCm38)	missense	probably damaging	1.00
PIT4305001:Celsr1	UTSW	15	85,900,937 (GRCm38)	missense	possibly damaging	0.87
PIT4480001:Celsr1	UTSW	15	86,032,414 (GRCm38)	missense	probably damaging	0.99
R0018:Celsr1	UTSW	15	86,031,042 (GRCm38)	missense	possibly damaging	0.47
R0018:Celsr1	UTSW	15	86,031,042 (GRCm38)	missense	possibly damaging	0.47
R0038:Celsr1	UTSW	15	85,929,419 (GRCm38)	missense	possibly damaging	0.65
R0057:Celsr1	UTSW	15	86,030,762 (GRCm38)	missense	probably benign	0.02
R0060:Celsr1	UTSW	15	85,922,198 (GRCm38)	missense	probably damaging	0.98
R0060:Celsr1	UTSW	15	85,922,198 (GRCm38)	missense	probably damaging	0.98
R0279:Celsr1	UTSW	15	85,902,864 (GRCm38)	missense	probably benign	0.00
R0570:Celsr1	UTSW	15	85,903,365 (GRCm38)	missense	probably benign	0.18
R0611:Celsr1	UTSW	15	85,932,323 (GRCm38)	missense	possibly damaging	0.91
R0792:Celsr1	UTSW	15	85,931,276 (GRCm38)	missense	probably benign	0.02
R0943:Celsr1	UTSW	15	85,903,288 (GRCm38)	missense	probably damaging	1.00
R0989:Celsr1	UTSW	15	86,031,279 (GRCm38)	missense	probably benign	0.39
R1118:Celsr1	UTSW	15	86,032,047 (GRCm38)	missense	probably damaging	1.00
R1237:Celsr1	UTSW	15	85,903,974 (GRCm38)	missense	probably benign	0.01
R1239:Celsr1	UTSW	15	85,979,146 (GRCm38)	missense	probably damaging	0.99
R1405:Celsr1	UTSW	15	85,905,434 (GRCm38)	splice site	probably null
R1405:Celsr1	UTSW	15	85,905,434 (GRCm38)	splice site	probably null
R1522:Celsr1	UTSW	15	85,931,276 (GRCm38)	missense	probably benign	0.02
R1662:Celsr1	UTSW	15	86,031,062 (GRCm38)	missense	probably damaging	1.00
R1673:Celsr1	UTSW	15	85,932,457 (GRCm38)	missense	probably benign	0.00
R1795:Celsr1	UTSW	15	86,030,323 (GRCm38)	missense	probably damaging	0.99
R1799:Celsr1	UTSW	15	86,032,685 (GRCm38)	missense	probably damaging	1.00
R1858:Celsr1	UTSW	15	86,032,759 (GRCm38)	missense	probably damaging	1.00
R2040:Celsr1	UTSW	15	86,032,887 (GRCm38)	missense	probably damaging	1.00
R2050:Celsr1	UTSW	15	86,030,547 (GRCm38)	missense	probably benign	0.02
R2131:Celsr1	UTSW	15	85,963,223 (GRCm38)	missense	probably benign	0.35
R2132:Celsr1	UTSW	15	86,031,967 (GRCm38)	missense	possibly damaging	0.91
R2189:Celsr1	UTSW	15	85,979,230 (GRCm38)	missense	possibly damaging	0.93
R2192:Celsr1	UTSW	15	85,916,723 (GRCm38)	missense	possibly damaging	0.93
R4213:Celsr1	UTSW	15	86,031,807 (GRCm38)	missense	probably damaging	1.00
R4356:Celsr1	UTSW	15	85,978,827 (GRCm38)	missense	probably damaging	1.00
R4414:Celsr1	UTSW	15	85,927,999 (GRCm38)	missense	probably damaging	1.00
R4414:Celsr1	UTSW	15	85,963,133 (GRCm38)	missense	probably benign	0.00
R4416:Celsr1	UTSW	15	85,927,999 (GRCm38)	missense	probably damaging	1.00
R4645:Celsr1	UTSW	15	85,916,756 (GRCm38)	missense	probably benign	0.35
R4666:Celsr1	UTSW	15	86,030,494 (GRCm38)	missense	probably damaging	1.00
R4687:Celsr1	UTSW	15	85,932,460 (GRCm38)	missense	possibly damaging	0.94
R4735:Celsr1	UTSW	15	85,906,029 (GRCm38)	critical splice acceptor site	probably null
R4804:Celsr1	UTSW	15	85,937,953 (GRCm38)	missense	possibly damaging	0.49
R4995:Celsr1	UTSW	15	85,937,911 (GRCm38)	missense	probably damaging	0.99
R5070:Celsr1	UTSW	15	85,939,134 (GRCm38)	missense	possibly damaging	0.89
R5218:Celsr1	UTSW	15	85,932,384 (GRCm38)	missense	probably damaging	1.00
R5280:Celsr1	UTSW	15	85,930,546 (GRCm38)	missense	probably benign
R5310:Celsr1	UTSW	15	85,926,222 (GRCm38)	missense	possibly damaging	0.88
R5388:Celsr1	UTSW	15	85,925,518 (GRCm38)	missense	probably damaging	0.99
R5484:Celsr1	UTSW	15	85,931,282 (GRCm38)	missense	probably benign	0.00
R5639:Celsr1	UTSW	15	86,030,767 (GRCm38)	missense	probably damaging	1.00
R5758:Celsr1	UTSW	15	85,941,264 (GRCm38)	missense	probably benign	0.27
R5778:Celsr1	UTSW	15	86,032,955 (GRCm38)	missense	probably damaging	1.00
R5893:Celsr1	UTSW	15	85,904,014 (GRCm38)	missense	probably benign	0.02
R5915:Celsr1	UTSW	15	86,030,349 (GRCm38)	missense	probably damaging	0.96
R5915:Celsr1	UTSW	15	85,937,975 (GRCm38)	missense	probably benign
R5932:Celsr1	UTSW	15	86,032,704 (GRCm38)	missense	probably damaging	1.00
R5950:Celsr1	UTSW	15	86,032,500 (GRCm38)	missense	probably damaging	1.00
R5975:Celsr1	UTSW	15	85,919,038 (GRCm38)	splice site	probably null
R6050:Celsr1	UTSW	15	85,930,611 (GRCm38)	missense	probably benign	0.00
R6117:Celsr1	UTSW	15	85,932,411 (GRCm38)	missense	probably benign	0.04
R6178:Celsr1	UTSW	15	85,901,021 (GRCm38)	missense	probably benign	0.08
R6186:Celsr1	UTSW	15	85,921,193 (GRCm38)	missense	possibly damaging	0.84
R6212:Celsr1	UTSW	15	85,916,687 (GRCm38)	missense	probably benign	0.25
R6307:Celsr1	UTSW	15	85,928,330 (GRCm38)	missense	probably benign
R6320:Celsr1	UTSW	15	85,900,959 (GRCm38)	missense	probably benign	0.13
R6349:Celsr1	UTSW	15	86,031,684 (GRCm38)	missense	probably damaging	1.00
R6478:Celsr1	UTSW	15	85,925,518 (GRCm38)	missense	probably damaging	0.99
R6504:Celsr1	UTSW	15	85,978,920 (GRCm38)	missense	probably benign	0.07
R6607:Celsr1	UTSW	15	85,963,285 (GRCm38)	missense	probably benign
R6615:Celsr1	UTSW	15	85,902,114 (GRCm38)	critical splice donor site	probably null
R6661:Celsr1	UTSW	15	85,918,934 (GRCm38)	missense	probably damaging	1.00
R6722:Celsr1	UTSW	15	85,905,914 (GRCm38)	critical splice donor site	probably null
R6743:Celsr1	UTSW	15	85,907,598 (GRCm38)	missense	probably damaging	0.96
R6746:Celsr1	UTSW	15	86,031,495 (GRCm38)	missense	probably damaging	1.00
R6772:Celsr1	UTSW	15	86,030,782 (GRCm38)	missense	probably benign
R6838:Celsr1	UTSW	15	85,939,194 (GRCm38)	missense	probably benign
R6886:Celsr1	UTSW	15	86,031,654 (GRCm38)	missense	probably benign	0.00
R7030:Celsr1	UTSW	15	85,905,478 (GRCm38)	missense	probably damaging	0.99
R7060:Celsr1	UTSW	15	86,032,655 (GRCm38)	missense	probably benign	0.07
R7080:Celsr1	UTSW	15	85,932,451 (GRCm38)	missense	possibly damaging	0.87
R7325:Celsr1	UTSW	15	86,033,008 (GRCm38)	missense	probably damaging	0.99
R7357:Celsr1	UTSW	15	86,030,514 (GRCm38)	missense	probably benign	0.00
R7371:Celsr1	UTSW	15	86,030,674 (GRCm38)	missense	possibly damaging	0.91
R7446:Celsr1	UTSW	15	85,907,673 (GRCm38)	missense	possibly damaging	0.95
R7465:Celsr1	UTSW	15	86,033,392 (GRCm38)	missense	probably benign
R7491:Celsr1	UTSW	15	86,032,518 (GRCm38)	missense	possibly damaging	0.78
R7639:Celsr1	UTSW	15	85,929,872 (GRCm38)	missense	probably benign	0.00
R7685:Celsr1	UTSW	15	85,978,732 (GRCm38)	nonsense	probably null
R7741:Celsr1	UTSW	15	85,979,102 (GRCm38)	missense	possibly damaging	0.94
R7768:Celsr1	UTSW	15	85,932,409 (GRCm38)	missense	probably benign
R7974:Celsr1	UTSW	15	86,031,030 (GRCm38)	missense	probably damaging	1.00
R7977:Celsr1	UTSW	15	86,032,993 (GRCm38)	missense	probably damaging	1.00
R7987:Celsr1	UTSW	15	86,032,993 (GRCm38)	missense	probably damaging	1.00
R8073:Celsr1	UTSW	15	85,939,155 (GRCm38)	missense	probably benign	0.00
R8099:Celsr1	UTSW	15	86,031,600 (GRCm38)	missense	probably damaging	0.99
R8190:Celsr1	UTSW	15	85,902,889 (GRCm38)	missense	probably damaging	0.99
R8210:Celsr1	UTSW	15	85,979,235 (GRCm38)	missense	probably benign	0.00
R8289:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R8290:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R8292:Celsr1	UTSW	15	85,907,618 (GRCm38)	missense	possibly damaging	0.90
R8328:Celsr1	UTSW	15	85,922,244 (GRCm38)	missense	probably benign	0.00
R8330:Celsr1	UTSW	15	85,932,300 (GRCm38)	missense	probably damaging	0.99
R8333:Celsr1	UTSW	15	86,031,414 (GRCm38)	missense	possibly damaging	0.65
R8352:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R8384:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R8452:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R8463:Celsr1	UTSW	15	86,030,214 (GRCm38)	missense	probably damaging	1.00
R8479:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R8480:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R8493:Celsr1	UTSW	15	85,938,006 (GRCm38)	missense	possibly damaging	0.67
R8498:Celsr1	UTSW	15	85,939,105 (GRCm38)	missense	probably benign	0.01
R8506:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R8771:Celsr1	UTSW	15	85,903,974 (GRCm38)	missense	probably benign	0.01
R8891:Celsr1	UTSW	15	85,937,993 (GRCm38)	missense	probably benign	0.01
R8905:Celsr1	UTSW	15	85,904,068 (GRCm38)	intron	probably benign
R8924:Celsr1	UTSW	15	86,032,470 (GRCm38)	missense	possibly damaging	0.94
R8979:Celsr1	UTSW	15	85,963,139 (GRCm38)	missense	probably damaging	0.96
R9069:Celsr1	UTSW	15	86,030,571 (GRCm38)	missense	possibly damaging	0.53
R9115:Celsr1	UTSW	15	85,919,016 (GRCm38)	missense	probably damaging	1.00
R9194:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R9196:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R9198:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R9200:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R9201:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R9202:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R9203:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R9222:Celsr1	UTSW	15	85,931,270 (GRCm38)	missense	possibly damaging	0.68
R9236:Celsr1	UTSW	15	86,030,850 (GRCm38)	missense	probably damaging	1.00
R9384:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R9386:Celsr1	UTSW	15	85,979,030 (GRCm38)	missense	probably damaging	1.00
R9400:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R9401:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R9415:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R9428:Celsr1	UTSW	15	85,931,348 (GRCm38)	missense	possibly damaging	0.64
R9435:Celsr1	UTSW	15	85,922,334 (GRCm38)	splice site	probably benign
R9493:Celsr1	UTSW	15	85,901,145 (GRCm38)	missense	probably damaging	0.98
R9495:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R9499:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
R9607:Celsr1	UTSW	15	86,031,028 (GRCm38)	missense
R9673:Celsr1	UTSW	15	86,033,085 (GRCm38)	nonsense	probably null
Z1176:Celsr1	UTSW	15	85,963,100 (GRCm38)	missense	probably damaging	0.96
Z1177:Celsr1	UTSW	15	85,978,851 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGAATCCCCTCCAGTCTGCTGAAC -3'
(R):5'- TGCCAATCCTGCAAGCCAGAGATG -3'

Sequencing Primer
(F):5'- TTTGCTCCAGGGACAGACAG -3'
(R):5'- CTGCAAGCCAGAGATGAGGTC -3'

Posted On

2013-09-03