Mutagenetix > Incidental Mutation

Incidental Mutation 'R7820:Ptch1'

601836

Institutional Source

Beutler Lab

Gene Symbol

Ptch1

Ensembl Gene

ENSMUSG00000021466

Gene Name

patched 1

Synonyms

A230106A15Rik, Patched 1, Ptc1, Ptc

MMRRC Submission

045874-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R7820 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

63508328-63573598 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 63523061 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Glutamine at position 885 (L885Q)

Ref Sequence

ENSEMBL: ENSMUSP00000141489 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000021921] [ENSMUST00000192155] [ENSMUST00000194663] [ENSMUST00000195258]

AlphaFold

Q61115

Predicted Effect

probably damaging
Transcript: ENSMUST00000021921
AA Change: L1022Q

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000021921
Gene: ENSMUSG00000021466
AA Change: L1022Q

Domain	Start	End	E-Value	Type
low complexity region	4	30	N/A	INTRINSIC
Pfam:Patched	351	871	7.6e-47	PFAM
Pfam:Sterol-sensing	448	602	1.5e-45	PFAM
Pfam:Patched	952	1166	9.8e-33	PFAM
low complexity region	1180	1189	N/A	INTRINSIC
low complexity region	1204	1213	N/A	INTRINSIC
low complexity region	1281	1296	N/A	INTRINSIC
low complexity region	1355	1367	N/A	INTRINSIC
low complexity region	1369	1384	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000192155
AA Change: L885Q

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000141489
Gene: ENSMUSG00000021466
AA Change: L885Q

Domain	Start	End	E-Value	Type
Pfam:Patched	214	733	3.1e-44	PFAM
Pfam:Sterol-sensing	311	465	2.8e-46	PFAM
Pfam:Patched	814	1029	3.1e-30	PFAM
low complexity region	1043	1052	N/A	INTRINSIC
low complexity region	1067	1076	N/A	INTRINSIC
low complexity region	1144	1159	N/A	INTRINSIC
low complexity region	1218	1230	N/A	INTRINSIC
low complexity region	1232	1247	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000194663

SMART Domains

Protein: ENSMUSP00000141766
Gene: ENSMUSG00000021466

Domain	Start	End	E-Value	Type
Pfam:Patched	298	569	4.7e-34	PFAM
Pfam:Sterol-sensing	396	550	7.9e-47	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000195258

SMART Domains

Protein: ENSMUSP00000141309
Gene: ENSMUSG00000021466

Domain	Start	End	E-Value	Type
Pfam:Patched	212	426	7.8e-28	PFAM
Pfam:Sterol-sensing	311	426	8e-33	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

96% (49/51)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the patched gene family. The encoded protein is the receptor for sonic hedgehog, a secreted molecule implicated in the formation of embryonic structures and in tumorigenesis, as well as the desert hedgehog and indian hedgehog proteins. This gene functions as a tumor suppressor. Mutations of this gene have been associated with basal cell nevus syndrome, esophageal squamous cell carcinoma, trichoepitheliomas, transitional cell carcinomas of the bladder, as well as holoprosencephaly. Alternative splicing results in multiple transcript variants encoding different isoforms. Additional splice variants have been described, but their full length sequences and biological validity cannot be determined currently. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous null embryos die by day 10 with neural tube defects. Heterozygotes are large with excess cerebellar granule cell proliferation and sometimes, hindlimb defects and medulloblastomas. Hypomorphic and spontaneous mutants have reproductive defects. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 51 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933405O20Rik	T	A	7: 50,599,623 (GRCm38)	I135N	probably benign	Het
Abca14	A	T	7: 120,212,721 (GRCm38)	N175I	probably benign	Het
Adam12	A	G	7: 133,998,188 (GRCm38)	V99A	probably benign	Het
Ankfn1	G	T	11: 89,421,130 (GRCm38)	P730T	probably damaging	Het
Arhgap21	A	G	2: 20,863,172 (GRCm38)	S847P	probably damaging	Het
Cacna1i	C	T	15: 80,372,372 (GRCm38)	A989V	probably benign	Het
Cacnb2	T	A	2: 14,960,666 (GRCm38)	N152K	probably damaging	Het
Chd3	A	T	11: 69,353,238 (GRCm38)	Y1334N	probably damaging	Het
Clca4a	A	T	3: 144,960,671 (GRCm38)	D473E	probably damaging	Het
Crhr2	A	C	6: 55,102,779 (GRCm38)	I191S	probably damaging	Het
E430018J23Rik	A	T	7: 127,391,436 (GRCm38)	W460R	possibly damaging	Het
Eef1akmt3	T	C	10: 127,033,194 (GRCm38)	Q137R	possibly damaging	Het
Eml1	T	C	12: 108,515,174 (GRCm38)	I432T	possibly damaging	Het
Fcgbp	A	G	7: 28,120,359 (GRCm38)	T2504A	probably benign	Het
Hmgxb4	G	T	8: 75,000,946 (GRCm38)	E186*	probably null	Het
Ighv16-1	T	C	12: 114,068,969 (GRCm38)	N71S	probably benign	Het
Kif2b	A	G	11: 91,577,274 (GRCm38)	V61A	probably benign	Het
Map1b	C	T	13: 99,431,177 (GRCm38)	G1679R	unknown	Het
Mast4	G	A	13: 102,754,088 (GRCm38)	S1086L	probably damaging	Het
Mcm8	A	G	2: 132,840,772 (GRCm38)	E724G	possibly damaging	Het
Mfap5	C	A	6: 122,520,921 (GRCm38)	D51E	probably damaging	Het
Mon1a	T	C	9: 107,901,312 (GRCm38)	L245P	probably damaging	Het
Mtx1	G	T	3: 89,214,008 (GRCm38)	H106Q	probably benign	Het
Naip1	G	A	13: 100,423,070 (GRCm38)	S1142F	probably benign	Het
Ngp	A	G	9: 110,420,864 (GRCm38)	T77A	probably benign	Het
Oca2	A	T	7: 56,331,965 (GRCm38)	I612F	probably damaging	Het
Odf3	A	C	7: 140,849,263 (GRCm38)	T128P	probably benign	Het
Olfr1224-ps1	T	A	2: 89,156,248 (GRCm38)	D309V	probably benign	Het
Olfr147	A	T	9: 38,403,566 (GRCm38)	I228F	probably damaging	Het
Olfr96	A	T	17: 37,225,895 (GRCm38)	M257L	probably benign	Het
Otop3	T	A	11: 115,339,588 (GRCm38)	V97D	probably damaging	Het
Ovgp1	A	G	3: 105,986,521 (GRCm38)		probably benign	Het
Pdc	T	C	1: 150,333,270 (GRCm38)	I168T	probably damaging	Het
Peg10	CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG	CCACATCAGGATCCACATCAGGATGCACATCAG	6: 4,756,398 (GRCm38)		probably benign	Het
Plekha7	A	T	7: 116,237,480 (GRCm38)	F18I	probably benign	Het
Plppr4	A	G	3: 117,321,949 (GRCm38)	I753T	possibly damaging	Het
Pms2	T	G	5: 143,914,633 (GRCm38)	S123A	possibly damaging	Het
Pou4f2	T	A	8: 78,436,502 (GRCm38)		probably benign	Het
Repin1	G	T	6: 48,597,345 (GRCm38)	E403*	probably null	Het
Rgs11	T	A	17: 26,205,195 (GRCm38)		probably null	Het
Samd3	T	A	10: 26,233,518 (GRCm38)		probably null	Het
Slit3	A	G	11: 35,700,408 (GRCm38)	D1349G	probably benign	Het
Sorbs2	A	T	8: 45,796,556 (GRCm38)	Q868L	probably null	Het
Speer4f1	T	A	5: 17,479,530 (GRCm38)	S185R	probably damaging	Het
Spin2f	A	G	X: 31,254,699 (GRCm38)	K28R	probably benign	Het
Tas2r125	T	G	6: 132,909,878 (GRCm38)	I76M	probably benign	Het
Tex15	A	T	8: 33,575,062 (GRCm38)	I1507F	probably damaging	Het
Tmem2	C	T	19: 21,807,461 (GRCm38)	A436V	probably damaging	Het
Vmn1r215	A	T	13: 23,076,545 (GRCm38)	I252F	probably damaging	Het
Vmn1r71	A	G	7: 10,748,725 (GRCm38)	F12S	possibly damaging	Het
Zfp128	A	G	7: 12,891,022 (GRCm38)	Y439C	probably benign	Het

Other mutations in Ptch1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00567:Ptch1	APN	13	63,527,175 (GRCm38)	missense	probably benign	0.00
IGL01084:Ptch1	APN	13	63,543,637 (GRCm38)	missense	probably damaging	0.99
IGL01369:Ptch1	APN	13	63,511,681 (GRCm38)	missense	probably benign
IGL02260:Ptch1	APN	13	63,565,352 (GRCm38)	unclassified	probably benign
IGL02439:Ptch1	APN	13	63,545,096 (GRCm38)	missense	probably damaging	1.00
IGL02588:Ptch1	APN	13	63,511,918 (GRCm38)	missense	probably benign	0.13
IGL02797:Ptch1	APN	13	63,533,607 (GRCm38)	missense	probably benign
R0463:Ptch1	UTSW	13	63,520,307 (GRCm38)	missense	probably damaging	0.98
R0539:Ptch1	UTSW	13	63,543,480 (GRCm38)	splice site	probably benign
R0657:Ptch1	UTSW	13	63,513,751 (GRCm38)	missense	possibly damaging	0.90
R0971:Ptch1	UTSW	13	63,539,843 (GRCm38)	missense	probably benign	0.23
R1466:Ptch1	UTSW	13	63,524,969 (GRCm38)	missense	probably benign	0.02
R1466:Ptch1	UTSW	13	63,524,969 (GRCm38)	missense	probably benign	0.02
R1539:Ptch1	UTSW	13	63,541,287 (GRCm38)	missense	probably benign	0.00
R1616:Ptch1	UTSW	13	63,539,842 (GRCm38)	missense	possibly damaging	0.96
R1883:Ptch1	UTSW	13	63,512,027 (GRCm38)	nonsense	probably null
R1985:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R1986:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R2024:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R2025:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R2026:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R2027:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R2096:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R2097:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R2100:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R2105:Ptch1	UTSW	13	63,545,245 (GRCm38)	missense	probably benign
R2165:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R2166:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R2167:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R2168:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R2226:Ptch1	UTSW	13	63,513,671 (GRCm38)	missense	probably damaging	1.00
R2437:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R2504:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R2507:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R2696:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R2698:Ptch1	UTSW	13	63,542,224 (GRCm38)	missense	probably damaging	1.00
R2698:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R2971:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R3410:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R3708:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R3744:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R3745:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R3783:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R3784:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R3785:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R3807:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R3950:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R4013:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R4015:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R4016:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R4017:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R4035:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R4083:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R4084:Ptch1	UTSW	13	63,524,959 (GRCm38)	missense	probably benign	0.00
R4179:Ptch1	UTSW	13	63,534,329 (GRCm38)	missense	probably damaging	1.00
R4222:Ptch1	UTSW	13	63,534,329 (GRCm38)	missense	probably damaging	1.00
R4348:Ptch1	UTSW	13	63,534,329 (GRCm38)	missense	probably damaging	1.00
R4349:Ptch1	UTSW	13	63,534,329 (GRCm38)	missense	probably damaging	1.00
R4350:Ptch1	UTSW	13	63,534,329 (GRCm38)	missense	probably damaging	1.00
R4351:Ptch1	UTSW	13	63,534,329 (GRCm38)	missense	probably damaging	1.00
R4353:Ptch1	UTSW	13	63,534,329 (GRCm38)	missense	probably damaging	1.00
R4485:Ptch1	UTSW	13	63,534,329 (GRCm38)	missense	probably damaging	1.00
R4595:Ptch1	UTSW	13	63,543,608 (GRCm38)	missense	possibly damaging	0.68
R4625:Ptch1	UTSW	13	63,523,164 (GRCm38)	missense	probably benign	0.02
R4809:Ptch1	UTSW	13	63,513,708 (GRCm38)	missense	probably damaging	0.98
R4904:Ptch1	UTSW	13	63,523,004 (GRCm38)	missense	probably damaging	1.00
R4911:Ptch1	UTSW	13	63,523,052 (GRCm38)	missense	probably damaging	1.00
R4942:Ptch1	UTSW	13	63,525,070 (GRCm38)	missense	probably benign	0.02
R5386:Ptch1	UTSW	13	63,545,043 (GRCm38)	missense	probably damaging	0.98
R5447:Ptch1	UTSW	13	63,527,245 (GRCm38)	missense	probably benign
R5604:Ptch1	UTSW	13	63,525,122 (GRCm38)	missense	probably benign	0.01
R5846:Ptch1	UTSW	13	63,565,454 (GRCm38)	unclassified	probably benign
R5926:Ptch1	UTSW	13	63,545,055 (GRCm38)	missense	probably benign	0.01
R5945:Ptch1	UTSW	13	63,573,419 (GRCm38)	utr 5 prime	probably benign
R5957:Ptch1	UTSW	13	63,525,115 (GRCm38)	missense	probably damaging	1.00
R6326:Ptch1	UTSW	13	63,543,545 (GRCm38)	missense	probably damaging	1.00
R6358:Ptch1	UTSW	13	63,513,689 (GRCm38)	missense	probably damaging	0.96
R6376:Ptch1	UTSW	13	63,543,608 (GRCm38)	missense	possibly damaging	0.68
R6599:Ptch1	UTSW	13	63,523,104 (GRCm38)	missense	probably damaging	0.98
R6615:Ptch1	UTSW	13	63,539,830 (GRCm38)	missense	possibly damaging	0.46
R6965:Ptch1	UTSW	13	63,525,067 (GRCm38)	missense	possibly damaging	0.63
R7149:Ptch1	UTSW	13	63,511,736 (GRCm38)	missense	probably benign	0.23
R7168:Ptch1	UTSW	13	63,512,060 (GRCm38)	missense	probably benign
R7257:Ptch1	UTSW	13	63,573,294 (GRCm38)	missense	not run
R7258:Ptch1	UTSW	13	63,573,294 (GRCm38)	missense	not run
R7259:Ptch1	UTSW	13	63,573,294 (GRCm38)	missense	not run
R7368:Ptch1	UTSW	13	63,511,984 (GRCm38)	missense	probably benign	0.06
R7525:Ptch1	UTSW	13	63,511,714 (GRCm38)	missense	probably benign	0.00
R7528:Ptch1	UTSW	13	63,511,714 (GRCm38)	missense	probably benign	0.00
R8077:Ptch1	UTSW	13	63,540,812 (GRCm38)	missense	probably damaging	0.98
R8373:Ptch1	UTSW	13	63,541,168 (GRCm38)	missense	probably damaging	1.00
R8398:Ptch1	UTSW	13	63,525,125 (GRCm38)	missense	probably benign	0.06
R8407:Ptch1	UTSW	13	63,514,243 (GRCm38)	missense	probably null	1.00
R8839:Ptch1	UTSW	13	63,541,224 (GRCm38)	missense	probably damaging	1.00
R9075:Ptch1	UTSW	13	63,533,521 (GRCm38)	missense	possibly damaging	0.87
R9476:Ptch1	UTSW	13	63,533,634 (GRCm38)	missense	probably benign	0.05
R9514:Ptch1	UTSW	13	63,527,257 (GRCm38)	missense	probably benign
R9528:Ptch1	UTSW	13	63,513,801 (GRCm38)	missense	probably benign	0.00
R9568:Ptch1	UTSW	13	63,542,173 (GRCm38)	missense	probably damaging	0.99
Z1177:Ptch1	UTSW	13	63,520,279 (GRCm38)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- GCGTTAGAAGGATCCCCATG -3'
(R):5'- ATCGAGTACGCTCAGTTCCC -3'

Sequencing Primer
(F):5'- GTTAGAAGGATCCCCATGAACCTC -3'
(R):5'- GAGTACGCTCAGTTCCCTTTCTAC -3'

Posted On

2019-12-03