Mutagenetix > Incidental Mutation

Incidental Mutation 'R5126:Dchs1'

393550

Institutional Source

Beutler Lab

Gene Symbol

Dchs1

Ensembl Gene

ENSMUSG00000036862

Gene Name

dachsous cadherin related 1

Synonyms

3110041P15Rik, C130033F22Rik

MMRRC Submission

042714-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R5126 (G1)

Quality Score

125

Status

Not validated

Chromosome

Chromosomal Location

105752990-105787654 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 105753517 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 3273 (S3273P)

Ref Sequence

ENSEMBL: ENSMUSP00000077574 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000033184] [ENSMUST00000078482] [ENSMUST00000210066]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000033184

SMART Domains

Protein: ENSMUSP00000033184
Gene: ENSMUSG00000030894

Domain	Start	End	E-Value	Type
low complexity region	2	17	N/A	INTRINSIC
Pro-kuma_activ	32	176	4.53e-50	SMART
low complexity region	177	189	N/A	INTRINSIC
Pfam:Peptidase_S8	251	492	1.1e-9	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000078482
AA Change: S3273P

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000077574
Gene: ENSMUSG00000036862
AA Change: S3273P

Domain	Start	End	E-Value	Type
signal peptide	1	36	N/A	INTRINSIC
CA	58	135	5.2e-11	SMART
CA	159	247	6.1e-17	SMART
CA	271	354	2.6e-30	SMART
CA	382	464	7.8e-26	SMART
CA	489	570	1.2e-34	SMART
CA	594	677	1.9e-27	SMART
CA	701	782	5.3e-11	SMART
CA	806	886	1e-12	SMART
CA	910	990	3.3e-14	SMART
CA	1016	1097	3.6e-18	SMART
CA	1121	1203	3.1e-34	SMART
CA	1233	1307	8.8e-16	SMART
low complexity region	1323	1335	N/A	INTRINSIC
CA	1344	1427	9.9e-9	SMART
CA	1451	1537	1.5e-23	SMART
CA	1560	1640	7.2e-32	SMART
CA	1664	1742	1.8e-31	SMART
CA	1765	1846	7.8e-30	SMART
CA	1870	1951	3.7e-26	SMART
low complexity region	1957	1965	N/A	INTRINSIC
CA	1979	2059	1.1e-6	SMART
CA	2083	2162	2.7e-18	SMART
CA	2186	2268	2.2e-26	SMART
CA	2291	2367	1e-18	SMART
CA	2391	2473	1.8e-23	SMART
CA	2497	2593	3.5e-21	SMART
CA	2617	2697	1.2e-25	SMART
CA	2721	2804	1.9e-18	SMART
CA	2828	2919	3e-3	SMART
transmembrane domain	2932	2954	N/A	INTRINSIC
low complexity region	3001	3017	N/A	INTRINSIC
low complexity region	3046	3055	N/A	INTRINSIC
low complexity region	3088	3097	N/A	INTRINSIC
low complexity region	3185	3196	N/A	INTRINSIC
low complexity region	3237	3259	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000140959

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000210018

Predicted Effect

probably benign
Transcript: ENSMUST00000210066

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000210395

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000210730

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000210840

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000211204

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000211226

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000211560

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000211659

Coding Region Coverage

1x: 98.9%
3x: 98.0%
10x: 95.1%
20x: 88.0%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the cadherin superfamily whose members encode calcium-dependent cell-cell adhesion molecules. The encoded protein has a signal peptide, 27 cadherin repeat domains and a unique cytoplasmic region. This particular cadherin family member is expressed in fibroblasts but not in melanocytes or keratinocytes. The cell-cell adhesion of fibroblasts is thought to be necessary for wound healing. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit postnatal lethality, growth retardation, small lungs, abnormal cochlea morphology, abnormal kidney morphology, cardiovascular abnormalities and skeletal abnormalities. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 48 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts13	G	A	2: 26,996,915 (GRCm38)		probably null	Het
Ahdc1	T	A	4: 133,063,522 (GRCm38)	F691L	probably benign	Het
Ahsa2	T	A	11: 23,491,036 (GRCm38)	I202F	possibly damaging	Het
Akap10	C	T	11: 61,916,189 (GRCm38)	A72T	probably damaging	Het
Ccnb1	C	G	13: 100,781,775 (GRCm38)	Q121H	possibly damaging	Het
Cep164	A	G	9: 45,787,424 (GRCm38)		probably null	Het
Cltc	A	G	11: 86,712,669 (GRCm38)	V781A	probably damaging	Het
Dnajc16	C	A	4: 141,774,509 (GRCm38)	V337L	probably benign	Het
E130309D02Rik	G	T	5: 143,307,946 (GRCm38)	P259T	probably benign	Het
Fstl4	T	C	11: 53,186,561 (GRCm38)	V715A	possibly damaging	Het
Grik1	C	T	16: 87,947,859 (GRCm38)	G502S	probably damaging	Het
Ifi213	A	G	1: 173,590,015 (GRCm38)	V277A	possibly damaging	Het
Jph3	T	C	8: 121,753,048 (GRCm38)	V155A	possibly damaging	Het
Katnal2	T	C	18: 77,017,598 (GRCm38)	E51G	probably benign	Het
Kcna2	T	A	3: 107,104,234 (GRCm38)	F44I	probably damaging	Het
Kcna6	T	C	6: 126,738,732 (GRCm38)	E398G	probably damaging	Het
Kif15	A	T	9: 122,975,758 (GRCm38)	H190L	probably damaging	Het
Lmbrd2	A	G	15: 9,194,701 (GRCm38)	R597G	possibly damaging	Het
Lrtm2	T	A	6: 119,317,439 (GRCm38)	M244L	probably benign	Het
Ly6c2	A	C	15: 75,111,643 (GRCm38)	S9A	possibly damaging	Het
Mbd4	T	A	6: 115,848,968 (GRCm38)		probably null	Het
Mfsd2b	A	G	12: 4,866,183 (GRCm38)	I269T	probably benign	Het
Muc6	A	T	7: 141,651,299 (GRCm38)	C218S	probably damaging	Het
Nlrc5	G	T	8: 94,474,671 (GRCm38)	R131L	possibly damaging	Het
Nlrp1b	A	T	11: 71,181,533 (GRCm38)	C495S	possibly damaging	Het
Nsf	C	A	11: 103,882,792 (GRCm38)	E299*	probably null	Het
Obscn	T	A	11: 59,077,063 (GRCm38)	E336D	probably damaging	Het
Olfr112	G	T	17: 37,563,828 (GRCm38)	T161K	probably benign	Het
Pan3	A	G	5: 147,527,198 (GRCm38)	N587S	probably benign	Het
Plch2	T	C	4: 155,000,519 (GRCm38)	D321G	probably damaging	Het
Plscr4	G	A	9: 92,488,741 (GRCm38)	D254N	probably damaging	Het
Pnmal1	A	C	7: 16,961,317 (GRCm38)	M366L	probably benign	Het
Pnpla7	G	T	2: 24,980,044 (GRCm38)	C12F	possibly damaging	Het
Pqlc2	T	C	4: 139,302,532 (GRCm38)	T63A	probably benign	Het
Ptprk	G	T	10: 28,575,644 (GRCm38)		probably null	Het
Rgs22	A	G	15: 36,040,644 (GRCm38)	V899A	probably damaging	Het
Ruvbl1	T	A	6: 88,485,901 (GRCm38)	C336S	probably benign	Het
Slc27a5	T	A	7: 12,991,320 (GRCm38)	H400L	probably damaging	Het
Slco1a4	A	T	6: 141,815,582 (GRCm38)	V435D	possibly damaging	Het
Snx14	A	T	9: 88,382,099 (GRCm38)	Y818N	probably damaging	Het
Tln2	A	G	9: 67,258,535 (GRCm38)	I2098T	probably damaging	Het
Tlr11	T	C	14: 50,360,830 (GRCm38)	L91P	probably damaging	Het
Tmem208	T	A	8: 105,334,650 (GRCm38)	F103I	probably benign	Het
Tmem8	T	C	17: 26,121,640 (GRCm38)	I666T	probably damaging	Het
Vmn2r3	C	T	3: 64,259,319 (GRCm38)	C797Y	probably damaging	Het
Vwde	T	A	6: 13,187,260 (GRCm38)	M743L	probably benign	Het
Wdcp	C	A	12: 4,850,617 (GRCm38)	R158S	probably damaging	Het
Zfp773	T	C	7: 7,136,624 (GRCm38)	T9A	unknown	Het

Other mutations in Dchs1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00235:Dchs1	APN	7	105,758,743 (GRCm38)	missense	probably damaging	1.00
IGL00422:Dchs1	APN	7	105,758,029 (GRCm38)	missense	possibly damaging	0.88
IGL00427:Dchs1	APN	7	105,758,424 (GRCm38)	missense	probably damaging	0.98
IGL00469:Dchs1	APN	7	105,755,261 (GRCm38)	missense	probably damaging	1.00
IGL00470:Dchs1	APN	7	105,758,207 (GRCm38)	missense	probably damaging	1.00
IGL00534:Dchs1	APN	7	105,757,943 (GRCm38)	missense	probably benign
IGL01292:Dchs1	APN	7	105,760,891 (GRCm38)	missense	probably damaging	0.98
IGL01380:Dchs1	APN	7	105,762,211 (GRCm38)	missense	probably damaging	1.00
IGL01396:Dchs1	APN	7	105,772,283 (GRCm38)	missense	probably damaging	1.00
IGL01448:Dchs1	APN	7	105,771,927 (GRCm38)	missense	probably damaging	0.98
IGL01759:Dchs1	APN	7	105,755,302 (GRCm38)	missense	probably benign	0.00
IGL01829:Dchs1	APN	7	105,755,397 (GRCm38)	missense	probably damaging	0.99
IGL01946:Dchs1	APN	7	105,759,105 (GRCm38)	missense	probably damaging	1.00
IGL01955:Dchs1	APN	7	105,757,591 (GRCm38)	missense	probably benign	0.00
IGL02012:Dchs1	APN	7	105,764,297 (GRCm38)	missense	probably damaging	0.98
IGL02222:Dchs1	APN	7	105,764,887 (GRCm38)	missense	probably damaging	1.00
IGL02261:Dchs1	APN	7	105,772,569 (GRCm38)	missense	probably damaging	1.00
IGL02365:Dchs1	APN	7	105,755,188 (GRCm38)	missense	probably benign	0.22
IGL02430:Dchs1	APN	7	105,771,971 (GRCm38)	missense	probably benign	0.34
IGL02500:Dchs1	APN	7	105,755,806 (GRCm38)	missense	probably benign
IGL02741:Dchs1	APN	7	105,757,323 (GRCm38)	missense	probably damaging	1.00
IGL02890:Dchs1	APN	7	105,756,491 (GRCm38)	missense	probably damaging	1.00
IGL03213:Dchs1	APN	7	105,755,072 (GRCm38)	missense	probably damaging	1.00
G1patch:Dchs1	UTSW	7	105,758,793 (GRCm38)	missense	probably damaging	0.99
P0026:Dchs1	UTSW	7	105,758,405 (GRCm38)	missense	probably damaging	0.99
PIT4377001:Dchs1	UTSW	7	105,757,588 (GRCm38)	missense	probably damaging	1.00
PIT4791001:Dchs1	UTSW	7	105,758,971 (GRCm38)	missense	probably damaging	1.00
R0013:Dchs1	UTSW	7	105,755,836 (GRCm38)	missense	possibly damaging	0.90
R0090:Dchs1	UTSW	7	105,755,932 (GRCm38)	missense	probably benign	0.18
R0091:Dchs1	UTSW	7	105,766,094 (GRCm38)	splice site	probably benign
R0193:Dchs1	UTSW	7	105,764,983 (GRCm38)	missense	probably benign	0.40
R0395:Dchs1	UTSW	7	105,758,538 (GRCm38)	missense	probably damaging	1.00
R0448:Dchs1	UTSW	7	105,765,927 (GRCm38)	missense	probably benign	0.00
R0480:Dchs1	UTSW	7	105,771,489 (GRCm38)	missense	probably benign	0.14
R0485:Dchs1	UTSW	7	105,772,727 (GRCm38)	missense	probably benign	0.00
R0566:Dchs1	UTSW	7	105,759,195 (GRCm38)	missense	probably benign	0.00
R0571:Dchs1	UTSW	7	105,771,996 (GRCm38)	missense	probably damaging	1.00
R0573:Dchs1	UTSW	7	105,758,778 (GRCm38)	missense	probably damaging	0.98
R0577:Dchs1	UTSW	7	105,764,255 (GRCm38)	missense	possibly damaging	0.78
R0622:Dchs1	UTSW	7	105,763,449 (GRCm38)	missense	probably damaging	1.00
R0654:Dchs1	UTSW	7	105,772,349 (GRCm38)	missense	probably damaging	1.00
R0677:Dchs1	UTSW	7	105,764,984 (GRCm38)	missense	probably damaging	1.00
R1171:Dchs1	UTSW	7	105,757,714 (GRCm38)	missense	probably benign
R1241:Dchs1	UTSW	7	105,758,178 (GRCm38)	missense	probably damaging	1.00
R1389:Dchs1	UTSW	7	105,755,571 (GRCm38)	missense	probably benign	0.40
R1427:Dchs1	UTSW	7	105,766,191 (GRCm38)	missense	probably benign	0.06
R1458:Dchs1	UTSW	7	105,755,244 (GRCm38)	missense	probably damaging	1.00
R1513:Dchs1	UTSW	7	105,772,071 (GRCm38)	nonsense	probably null
R1524:Dchs1	UTSW	7	105,764,525 (GRCm38)	missense	probably damaging	1.00
R1525:Dchs1	UTSW	7	105,758,931 (GRCm38)	missense	probably damaging	1.00
R1534:Dchs1	UTSW	7	105,772,040 (GRCm38)	missense	probably damaging	0.98
R1567:Dchs1	UTSW	7	105,771,861 (GRCm38)	missense	probably benign	0.01
R1577:Dchs1	UTSW	7	105,765,955 (GRCm38)	missense	probably damaging	1.00
R1603:Dchs1	UTSW	7	105,762,770 (GRCm38)	missense	probably benign	0.24
R1676:Dchs1	UTSW	7	105,754,921 (GRCm38)	missense	probably benign	0.40
R1794:Dchs1	UTSW	7	105,771,720 (GRCm38)	missense	probably benign	0.02
R1826:Dchs1	UTSW	7	105,757,627 (GRCm38)	missense	probably damaging	1.00
R1892:Dchs1	UTSW	7	105,764,156 (GRCm38)	missense	probably benign	0.00
R1924:Dchs1	UTSW	7	105,772,280 (GRCm38)	missense	possibly damaging	0.81
R1932:Dchs1	UTSW	7	105,765,902 (GRCm38)	missense	probably damaging	1.00
R1962:Dchs1	UTSW	7	105,764,201 (GRCm38)	missense	probably damaging	1.00
R1985:Dchs1	UTSW	7	105,772,398 (GRCm38)	missense	possibly damaging	0.72
R1993:Dchs1	UTSW	7	105,762,548 (GRCm38)	missense	probably benign	0.00
R2007:Dchs1	UTSW	7	105,755,325 (GRCm38)	missense	probably damaging	1.00
R2316:Dchs1	UTSW	7	105,764,204 (GRCm38)	missense	possibly damaging	0.71
R2351:Dchs1	UTSW	7	105,754,094 (GRCm38)	missense	probably benign
R2474:Dchs1	UTSW	7	105,755,074 (GRCm38)	missense	probably benign	0.37
R2474:Dchs1	UTSW	7	105,772,838 (GRCm38)	missense	probably damaging	1.00
R3429:Dchs1	UTSW	7	105,756,504 (GRCm38)	missense	possibly damaging	0.85
R3430:Dchs1	UTSW	7	105,756,504 (GRCm38)	missense	possibly damaging	0.85
R3737:Dchs1	UTSW	7	105,762,316 (GRCm38)	missense	possibly damaging	0.88
R3767:Dchs1	UTSW	7	105,757,085 (GRCm38)	missense	possibly damaging	0.67
R3874:Dchs1	UTSW	7	105,761,635 (GRCm38)	missense	probably damaging	1.00
R3883:Dchs1	UTSW	7	105,762,563 (GRCm38)	missense	probably damaging	1.00
R4105:Dchs1	UTSW	7	105,765,140 (GRCm38)	missense	probably damaging	1.00
R4209:Dchs1	UTSW	7	105,766,190 (GRCm38)	missense	probably damaging	0.99
R4329:Dchs1	UTSW	7	105,753,759 (GRCm38)	missense	probably damaging	1.00
R4516:Dchs1	UTSW	7	105,754,852 (GRCm38)	missense	probably damaging	1.00
R4579:Dchs1	UTSW	7	105,758,973 (GRCm38)	missense	probably benign
R4579:Dchs1	UTSW	7	105,754,765 (GRCm38)	missense	probably damaging	1.00
R4588:Dchs1	UTSW	7	105,756,041 (GRCm38)	missense	probably benign
R4613:Dchs1	UTSW	7	105,772,724 (GRCm38)	missense	probably damaging	1.00
R4632:Dchs1	UTSW	7	105,754,355 (GRCm38)	missense	probably benign	0.02
R4696:Dchs1	UTSW	7	105,764,627 (GRCm38)	missense	probably damaging	1.00
R4725:Dchs1	UTSW	7	105,765,552 (GRCm38)	missense	probably damaging	1.00
R4725:Dchs1	UTSW	7	105,755,253 (GRCm38)	missense	probably damaging	0.98
R4738:Dchs1	UTSW	7	105,758,673 (GRCm38)	missense	probably damaging	0.96
R4768:Dchs1	UTSW	7	105,771,620 (GRCm38)	missense	possibly damaging	0.96
R4784:Dchs1	UTSW	7	105,765,926 (GRCm38)	missense	probably damaging	1.00
R4864:Dchs1	UTSW	7	105,755,253 (GRCm38)	missense	probably damaging	0.98
R4880:Dchs1	UTSW	7	105,755,730 (GRCm38)	missense	probably benign	0.00
R4909:Dchs1	UTSW	7	105,766,255 (GRCm38)	missense	probably damaging	1.00
R5102:Dchs1	UTSW	7	105,772,177 (GRCm38)	missense	probably benign	0.09
R5109:Dchs1	UTSW	7	105,765,014 (GRCm38)	missense	probably benign
R5149:Dchs1	UTSW	7	105,755,658 (GRCm38)	missense	probably damaging	0.98
R5330:Dchs1	UTSW	7	105,754,602 (GRCm38)	missense	probably damaging	1.00
R5384:Dchs1	UTSW	7	105,772,055 (GRCm38)	missense	probably damaging	1.00
R5384:Dchs1	UTSW	7	105,758,029 (GRCm38)	missense	probably damaging	1.00
R5386:Dchs1	UTSW	7	105,758,029 (GRCm38)	missense	probably damaging	1.00
R5622:Dchs1	UTSW	7	105,755,293 (GRCm38)	missense	probably benign	0.11
R5623:Dchs1	UTSW	7	105,772,769 (GRCm38)	missense	probably damaging	1.00
R5708:Dchs1	UTSW	7	105,772,809 (GRCm38)	missense	probably damaging	1.00
R5718:Dchs1	UTSW	7	105,755,748 (GRCm38)	missense	probably benign	0.01
R5743:Dchs1	UTSW	7	105,771,596 (GRCm38)	missense	probably benign
R5759:Dchs1	UTSW	7	105,764,176 (GRCm38)	missense	probably damaging	0.99
R5772:Dchs1	UTSW	7	105,773,040 (GRCm38)	missense	probably damaging	1.00
R5860:Dchs1	UTSW	7	105,772,035 (GRCm38)	missense	probably damaging	1.00
R5916:Dchs1	UTSW	7	105,759,166 (GRCm38)	missense	probably damaging	1.00
R5965:Dchs1	UTSW	7	105,755,925 (GRCm38)	missense	probably damaging	1.00
R5997:Dchs1	UTSW	7	105,754,095 (GRCm38)	missense	probably benign	0.08
R6065:Dchs1	UTSW	7	105,755,421 (GRCm38)	missense	probably damaging	1.00
R6136:Dchs1	UTSW	7	105,760,925 (GRCm38)	missense	probably benign
R6137:Dchs1	UTSW	7	105,765,106 (GRCm38)	missense	probably damaging	0.99
R6324:Dchs1	UTSW	7	105,764,938 (GRCm38)	missense	probably benign	0.05
R6363:Dchs1	UTSW	7	105,758,472 (GRCm38)	missense	probably benign	0.12
R6466:Dchs1	UTSW	7	105,764,541 (GRCm38)	missense	probably benign	0.09
R6544:Dchs1	UTSW	7	105,758,178 (GRCm38)	missense	probably damaging	1.00
R6572:Dchs1	UTSW	7	105,758,806 (GRCm38)	missense	possibly damaging	0.94
R6579:Dchs1	UTSW	7	105,762,913 (GRCm38)	missense	probably benign	0.17
R6632:Dchs1	UTSW	7	105,761,878 (GRCm38)	missense	probably damaging	1.00
R6725:Dchs1	UTSW	7	105,758,793 (GRCm38)	missense	probably damaging	0.99
R6789:Dchs1	UTSW	7	105,757,003 (GRCm38)	missense	possibly damaging	0.61
R6868:Dchs1	UTSW	7	105,763,503 (GRCm38)	missense	possibly damaging	0.91
R7058:Dchs1	UTSW	7	105,757,021 (GRCm38)	missense	probably benign
R7064:Dchs1	UTSW	7	105,763,185 (GRCm38)	missense	probably damaging	0.99
R7076:Dchs1	UTSW	7	105,761,871 (GRCm38)	missense	probably benign	0.04
R7191:Dchs1	UTSW	7	105,765,439 (GRCm38)	missense	possibly damaging	0.89
R7298:Dchs1	UTSW	7	105,755,131 (GRCm38)	nonsense	probably null
R7380:Dchs1	UTSW	7	105,758,628 (GRCm38)	missense	probably benign	0.35
R7438:Dchs1	UTSW	7	105,754,948 (GRCm38)	missense	probably benign	0.30
R7496:Dchs1	UTSW	7	105,761,859 (GRCm38)	missense	probably damaging	1.00
R7534:Dchs1	UTSW	7	105,772,373 (GRCm38)	missense	probably benign	0.00
R7604:Dchs1	UTSW	7	105,765,982 (GRCm38)	missense	probably damaging	1.00
R7631:Dchs1	UTSW	7	105,759,238 (GRCm38)	missense	probably benign
R7821:Dchs1	UTSW	7	105,765,145 (GRCm38)	missense	probably benign	0.00
R7834:Dchs1	UTSW	7	105,765,567 (GRCm38)	missense	probably benign	0.39
R7841:Dchs1	UTSW	7	105,762,973 (GRCm38)	missense	probably benign
R7913:Dchs1	UTSW	7	105,759,228 (GRCm38)	missense	possibly damaging	0.61
R8041:Dchs1	UTSW	7	105,755,188 (GRCm38)	missense	probably benign	0.45
R8076:Dchs1	UTSW	7	105,761,982 (GRCm38)	missense	probably damaging	1.00
R8076:Dchs1	UTSW	7	105,755,921 (GRCm38)	missense	possibly damaging	0.52
R8087:Dchs1	UTSW	7	105,753,499 (GRCm38)	missense	probably benign	0.41
R8125:Dchs1	UTSW	7	105,764,882 (GRCm38)	missense	possibly damaging	0.91
R8223:Dchs1	UTSW	7	105,762,617 (GRCm38)	missense	possibly damaging	0.81
R8239:Dchs1	UTSW	7	105,765,511 (GRCm38)	missense	probably benign	0.22
R8476:Dchs1	UTSW	7	105,758,808 (GRCm38)	missense	probably benign	0.05
R8497:Dchs1	UTSW	7	105,758,961 (GRCm38)	missense	probably damaging	1.00
R8770:Dchs1	UTSW	7	105,771,738 (GRCm38)	missense	probably damaging	1.00
R8856:Dchs1	UTSW	7	105,760,857 (GRCm38)	missense	probably damaging	1.00
R8866:Dchs1	UTSW	7	105,755,390 (GRCm38)	missense	probably benign	0.00
R8948:Dchs1	UTSW	7	105,759,005 (GRCm38)	missense	probably benign	0.30
R8950:Dchs1	UTSW	7	105,759,005 (GRCm38)	missense	probably benign	0.30
R9029:Dchs1	UTSW	7	105,753,712 (GRCm38)	missense	probably benign	0.13
R9039:Dchs1	UTSW	7	105,756,008 (GRCm38)	missense	probably benign	0.11
R9081:Dchs1	UTSW	7	105,754,429 (GRCm38)	missense	probably benign	0.00
R9134:Dchs1	UTSW	7	105,755,703 (GRCm38)	missense	probably damaging	0.96
R9159:Dchs1	UTSW	7	105,765,919 (GRCm38)	missense	probably benign
R9162:Dchs1	UTSW	7	105,765,525 (GRCm38)	missense	probably damaging	1.00
R9169:Dchs1	UTSW	7	105,772,907 (GRCm38)	missense	probably damaging	1.00
R9262:Dchs1	UTSW	7	105,755,626 (GRCm38)	missense	probably damaging	1.00
R9292:Dchs1	UTSW	7	105,753,913 (GRCm38)	missense	probably damaging	1.00
R9325:Dchs1	UTSW	7	105,766,195 (GRCm38)	missense	possibly damaging	0.51
R9376:Dchs1	UTSW	7	105,765,774 (GRCm38)	critical splice donor site	probably null
R9392:Dchs1	UTSW	7	105,772,662 (GRCm38)	missense	probably benign	0.09
R9619:Dchs1	UTSW	7	105,764,455 (GRCm38)	missense	probably benign	0.07
R9680:Dchs1	UTSW	7	105,762,418 (GRCm38)	missense	probably damaging	1.00
R9687:Dchs1	UTSW	7	105,757,984 (GRCm38)	missense	probably damaging	0.99
R9747:Dchs1	UTSW	7	105,763,475 (GRCm38)	missense	probably damaging	1.00
Z1177:Dchs1	UTSW	7	105,757,693 (GRCm38)	missense	probably damaging	1.00
Z1177:Dchs1	UTSW	7	105,758,551 (GRCm38)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- CAGAGAAATGTGGGACCTGTC -3'
(R):5'- TGCTCGGCTCAAGGATGAAG -3'

Sequencing Primer
(F):5'- CCTGTCCCAGCTATAAGAGTTTAAGG -3'
(R):5'- GCTCAAGGATGAAGCTCGTC -3'

Posted On

2016-06-15