Mutagenetix > Incidental Mutation

Incidental Mutation 'R4729:Pcdhb11'

358726

Institutional Source

Beutler Lab

Gene Symbol

Pcdhb11

Ensembl Gene

ENSMUSG00000051486

Gene Name

protocadherin beta 11

Synonyms

PcdhbK, Pcdhb5E

MMRRC Submission

041603-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.079) question?

Stock #

R4729 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

37554471-37558085 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

C to T at 37555419 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Stop codon at position 250 (Q250*)

Ref Sequence

ENSEMBL: ENSMUSP00000056148 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000053073] [ENSMUST00000115661] [ENSMUST00000194544]

AlphaFold

Q91UZ8

Predicted Effect

probably null
Transcript: ENSMUST00000053073
AA Change: Q250*

SMART Domains

Protein: ENSMUSP00000056148
Gene: ENSMUSG00000051486
AA Change: Q250*

Domain	Start	End	E-Value	Type
CA	54	131	3.51e-1	SMART
CA	155	240	4.11e-21	SMART
CA	264	344	6.37e-27	SMART
CA	367	448	4.79e-22	SMART
CA	472	558	7.31e-27	SMART
CA	588	669	2.46e-10	SMART
Pfam:Cadherin_C_2	686	769	3.4e-26	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000115661

SMART Domains

Protein: ENSMUSP00000111325
Gene: ENSMUSG00000103458

Domain	Start	End	E-Value	Type
CA	20	131	5.3e-2	SMART
CA	155	240	1.51e-19	SMART
CA	264	348	7.6e-25	SMART
CA	372	453	1.42e-24	SMART
CA	477	563	1.42e-24	SMART
CA	594	674	4.12e-12	SMART
low complexity region	706	721	N/A	INTRINSIC
Pfam:Cadherin_tail	796	930	3.9e-58	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000193984

Predicted Effect

probably benign
Transcript: ENSMUST00000194544

SMART Domains

Protein: ENSMUSP00000141847
Gene: ENSMUSG00000102836

Domain	Start	End	E-Value	Type
Blast:CA	18	66	5e-20	BLAST

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.1%
20x: 94.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930562C15Rik	T	A	16: 4,667,187 (GRCm39)	L220H	unknown	Het
Amt	T	A	9: 108,177,851 (GRCm39)	L272Q	probably damaging	Het
Ank2	G	C	3: 126,770,545 (GRCm39)	Y894*	probably null	Het
Ankzf1	T	A	1: 75,170,908 (GRCm39)	F105I	probably damaging	Het
Aox4	C	A	1: 58,298,236 (GRCm39)	Y1067*	probably null	Het
BC034090	T	A	1: 155,100,836 (GRCm39)	Q476L	probably damaging	Het
Bhmt	G	T	13: 93,763,871 (GRCm39)	R57S	probably damaging	Het
Cacna1c	A	T	6: 118,633,136 (GRCm39)	F964L	probably damaging	Het
Celsr3	A	C	9: 108,724,851 (GRCm39)	S396R	probably benign	Het
Cpne4	C	A	9: 104,799,755 (GRCm39)	Q191K	probably damaging	Het
Csnk1g2	T	C	10: 80,475,038 (GRCm39)	Y352H	probably benign	Het
D630003M21Rik	A	G	2: 158,058,623 (GRCm39)	S426P	probably damaging	Het
Dennd10	T	A	19: 60,823,309 (GRCm39)	F315I	probably benign	Het
Dido1	G	T	2: 180,329,443 (GRCm39)	N326K	probably benign	Het
E2f2	T	A	4: 135,911,760 (GRCm39)	I257N	probably damaging	Het
Elfn1	T	G	5: 139,959,413 (GRCm39)	F806V	probably damaging	Het
Eml6	T	A	11: 29,783,204 (GRCm39)	Y559F	probably damaging	Het
Erich6	A	G	3: 58,543,480 (GRCm39)		probably null	Het
Fam78a	T	C	2: 31,972,617 (GRCm39)	N101S	probably damaging	Het
Fam83h	A	G	15: 75,874,185 (GRCm39)	S1051P	probably benign	Het
Galns	C	T	8: 123,330,195 (GRCm39)	G112D	probably damaging	Het
Gm9923	A	G	10: 72,145,524 (GRCm39)	K125R	probably damaging	Het
Hectd3	G	A	4: 116,854,415 (GRCm39)	V326M	probably damaging	Het
Iars2	A	G	1: 185,048,248 (GRCm39)	S495P	possibly damaging	Het
Ice1	T	C	13: 70,754,503 (GRCm39)	R528G	probably damaging	Het
Igkv12-38	T	A	6: 69,920,368 (GRCm39)	Y50F	possibly damaging	Het
Inpp5j	T	C	11: 3,445,025 (GRCm39)	S883G	probably damaging	Het
Irf8	T	C	8: 121,480,178 (GRCm39)	S139P	probably damaging	Het
Itpr2	A	G	6: 146,274,671 (GRCm39)	F837S	probably damaging	Het
Kcnq4	G	T	4: 120,570,271 (GRCm39)	D357E	possibly damaging	Het
Klhl1	A	G	14: 96,517,584 (GRCm39)	L364P	probably damaging	Het
Krt7	A	G	15: 101,318,439 (GRCm39)	I309V	probably benign	Het
Krt76	G	T	15: 101,797,516 (GRCm39)	A281D	probably damaging	Het
Lancl2	T	C	6: 57,714,697 (GRCm39)	F430L	probably damaging	Het
Llgl2	T	C	11: 115,739,125 (GRCm39)	V332A	probably damaging	Het
Lrrc26	A	T	2: 25,180,076 (GRCm39)	T26S	probably benign	Het
Lrrk1	T	A	7: 65,912,041 (GRCm39)	M1840L	probably benign	Het
Lyst	G	A	13: 13,812,486 (GRCm39)	C966Y	probably damaging	Het
Mad1l1	T	A	5: 140,247,266 (GRCm39)	S354C	possibly damaging	Het
Mbtps1	C	T	8: 120,252,159 (GRCm39)	G577D	probably damaging	Het
Mycbp2	C	T	14: 103,426,027 (GRCm39)	R2366H	probably damaging	Het
Myo18a	T	G	11: 77,668,511 (GRCm39)		probably null	Het
Naip5	G	A	13: 100,358,639 (GRCm39)	R866C	possibly damaging	Het
Nav2	T	A	7: 49,102,567 (GRCm39)	V455E	probably benign	Het
Neb	A	G	2: 52,153,674 (GRCm39)	I2417T	possibly damaging	Het
Nme5	C	T	18: 34,702,890 (GRCm39)	A133T	probably benign	Het
Nradd	T	C	9: 110,450,979 (GRCm39)	D51G	possibly damaging	Het
Pard3b	A	G	1: 62,250,843 (GRCm39)	R591G	probably damaging	Het
Pcbp4	T	C	9: 106,337,929 (GRCm39)	F73S	probably damaging	Het
Pde1c	T	A	6: 56,049,194 (GRCm39)	K766N	probably damaging	Het
Phf21b	G	A	15: 84,738,942 (GRCm39)	Q40*	probably null	Het
Prr14	A	G	7: 127,073,868 (GRCm39)	D244G	probably benign	Het
Rab11fip5	C	T	6: 85,351,249 (GRCm39)	A88T	probably damaging	Het
Rad54l2	A	T	9: 106,593,317 (GRCm39)	S428T	probably benign	Het
Rdh9	A	G	10: 127,612,621 (GRCm39)	I90V	probably benign	Het
Rhag	G	T	17: 41,139,292 (GRCm39)	G76C	probably damaging	Het
Riok3	T	A	18: 12,261,984 (GRCm39)	V6E	possibly damaging	Het
Rnf7l	A	T	10: 63,257,244 (GRCm39)	V92E	probably damaging	Het
Scn10a	A	G	9: 119,500,592 (GRCm39)	I229T	probably damaging	Het
Slco1a1	G	T	6: 141,854,695 (GRCm39)	T652K	probably benign	Het
Slit1	T	A	19: 41,635,459 (GRCm39)	I345F	probably damaging	Het
Snrnp200	A	T	2: 127,074,857 (GRCm39)	I1477F	probably damaging	Het
Snx31	G	A	15: 36,523,698 (GRCm39)	T328I	possibly damaging	Het
Strn	A	G	17: 78,965,390 (GRCm39)	F634S	probably damaging	Het
Tmem101	C	T	11: 102,047,155 (GRCm39)	G6R	probably benign	Het
Tmem199	C	G	11: 78,399,506 (GRCm39)	G131R	probably benign	Het
Trim66	A	G	7: 109,055,267 (GRCm39)		probably null	Het
Ttn	G	T	2: 76,681,929 (GRCm39)		probably benign	Het
Upk3bl	T	C	5: 136,086,247 (GRCm39)	L61P	probably benign	Het
Vmn2r108	A	G	17: 20,692,632 (GRCm39)	Y75H	probably damaging	Het
Vmn2r91	T	A	17: 18,327,906 (GRCm39)	I500K	probably damaging	Het
Vps18	C	T	2: 119,124,272 (GRCm39)	R400C	probably damaging	Het
Zeb1	C	T	18: 5,767,286 (GRCm39)	P599L	probably damaging	Het
Zfhx4	G	T	3: 5,464,557 (GRCm39)	A1572S	probably damaging	Het
Zfp677	T	A	17: 21,617,680 (GRCm39)	C246S	possibly damaging	Het
Zfp719	T	A	7: 43,239,834 (GRCm39)	I474N	probably damaging	Het

Other mutations in Pcdhb11

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00321:Pcdhb11	APN	18	37,555,026 (GRCm39)	missense	probably benign	0.00
IGL00906:Pcdhb11	APN	18	37,555,174 (GRCm39)	missense	possibly damaging	0.67
IGL01610:Pcdhb11	APN	18	37,556,412 (GRCm39)	missense	probably benign	0.00
IGL01973:Pcdhb11	APN	18	37,556,565 (GRCm39)	missense	probably damaging	1.00
IGL01977:Pcdhb11	APN	18	37,555,344 (GRCm39)	missense	possibly damaging	0.49
IGL02164:Pcdhb11	APN	18	37,556,412 (GRCm39)	missense	probably benign	0.00
IGL02282:Pcdhb11	APN	18	37,556,881 (GRCm39)	missense	probably damaging	1.00
IGL02674:Pcdhb11	APN	18	37,556,667 (GRCm39)	missense	probably damaging	1.00
IGL02965:Pcdhb11	APN	18	37,557,021 (GRCm39)	missense	probably benign
IGL03197:Pcdhb11	APN	18	37,555,477 (GRCm39)	nonsense	probably null
1mM(1):Pcdhb11	UTSW	18	37,557,010 (GRCm39)	missense	probably benign	0.00
R0001:Pcdhb11	UTSW	18	37,557,042 (GRCm39)	missense	probably benign	0.06
R0383:Pcdhb11	UTSW	18	37,556,446 (GRCm39)	missense	probably damaging	1.00
R0421:Pcdhb11	UTSW	18	37,555,533 (GRCm39)	missense	probably benign	0.04
R0422:Pcdhb11	UTSW	18	37,554,923 (GRCm39)	missense	probably damaging	1.00
R0427:Pcdhb11	UTSW	18	37,555,818 (GRCm39)	missense	probably damaging	1.00
R0542:Pcdhb11	UTSW	18	37,556,887 (GRCm39)	missense	probably damaging	1.00
R0620:Pcdhb11	UTSW	18	37,554,864 (GRCm39)	nonsense	probably null
R1014:Pcdhb11	UTSW	18	37,556,422 (GRCm39)	missense	probably damaging	1.00
R1277:Pcdhb11	UTSW	18	37,554,769 (GRCm39)	missense	possibly damaging	0.79
R2034:Pcdhb11	UTSW	18	37,555,546 (GRCm39)	missense	probably benign	0.00
R2142:Pcdhb11	UTSW	18	37,555,176 (GRCm39)	missense	probably benign	0.28
R2496:Pcdhb11	UTSW	18	37,555,375 (GRCm39)	missense	probably benign	0.30
R3077:Pcdhb11	UTSW	18	37,555,297 (GRCm39)	missense	probably benign	0.08
R4560:Pcdhb11	UTSW	18	37,556,787 (GRCm39)	missense	possibly damaging	0.61
R4590:Pcdhb11	UTSW	18	37,555,549 (GRCm39)	missense	probably damaging	0.98
R4642:Pcdhb11	UTSW	18	37,555,021 (GRCm39)	missense	probably benign	0.01
R5012:Pcdhb11	UTSW	18	37,556,029 (GRCm39)	missense	possibly damaging	0.48
R5364:Pcdhb11	UTSW	18	37,555,232 (GRCm39)	missense	probably benign	0.06
R5910:Pcdhb11	UTSW	18	37,556,796 (GRCm39)	missense	probably benign	0.43
R6023:Pcdhb11	UTSW	18	37,555,978 (GRCm39)	missense	possibly damaging	0.94
R6106:Pcdhb11	UTSW	18	37,556,056 (GRCm39)	missense	probably damaging	1.00
R6254:Pcdhb11	UTSW	18	37,554,771 (GRCm39)	missense	probably damaging	0.99
R6276:Pcdhb11	UTSW	18	37,554,813 (GRCm39)	missense	probably benign	0.36
R6360:Pcdhb11	UTSW	18	37,555,212 (GRCm39)	missense	probably benign
R6699:Pcdhb11	UTSW	18	37,555,990 (GRCm39)	missense	probably damaging	1.00
R6732:Pcdhb11	UTSW	18	37,555,197 (GRCm39)	missense	probably benign
R6760:Pcdhb11	UTSW	18	37,554,637 (GRCm39)	intron	probably benign
R6916:Pcdhb11	UTSW	18	37,555,434 (GRCm39)	missense	possibly damaging	0.52
R7130:Pcdhb11	UTSW	18	37,556,559 (GRCm39)	missense	probably benign	0.04
R7267:Pcdhb11	UTSW	18	37,555,006 (GRCm39)	missense	possibly damaging	0.61
R7426:Pcdhb11	UTSW	18	37,556,313 (GRCm39)	missense	probably damaging	0.99
R7444:Pcdhb11	UTSW	18	37,555,672 (GRCm39)	missense	probably damaging	0.98
R7492:Pcdhb11	UTSW	18	37,556,497 (GRCm39)	missense	probably damaging	1.00
R7504:Pcdhb11	UTSW	18	37,554,852 (GRCm39)	missense	probably benign
R7537:Pcdhb11	UTSW	18	37,554,672 (GRCm39)	start codon destroyed	possibly damaging	0.88
R7728:Pcdhb11	UTSW	18	37,556,530 (GRCm39)	missense	probably damaging	1.00
R7817:Pcdhb11	UTSW	18	37,556,962 (GRCm39)	missense	probably damaging	1.00
R8071:Pcdhb11	UTSW	18	37,555,422 (GRCm39)	missense	probably benign	0.02
R8229:Pcdhb11	UTSW	18	37,555,671 (GRCm39)	missense	probably benign	0.00
R8254:Pcdhb11	UTSW	18	37,555,242 (GRCm39)	missense	probably benign	0.45
R8356:Pcdhb11	UTSW	18	37,555,252 (GRCm39)	missense	probably damaging	1.00
R8739:Pcdhb11	UTSW	18	37,555,549 (GRCm39)	missense	probably damaging	1.00
R8957:Pcdhb11	UTSW	18	37,555,872 (GRCm39)	missense	probably benign	0.09
R8957:Pcdhb11	UTSW	18	37,554,692 (GRCm39)	missense	probably benign	0.43
R8964:Pcdhb11	UTSW	18	37,556,660 (GRCm39)	missense	probably benign	0.00
R8966:Pcdhb11	UTSW	18	37,556,037 (GRCm39)	missense	possibly damaging	0.67
R9188:Pcdhb11	UTSW	18	37,556,188 (GRCm39)	missense	probably damaging	1.00
R9253:Pcdhb11	UTSW	18	37,554,529 (GRCm39)	intron	probably benign
R9632:Pcdhb11	UTSW	18	37,556,019 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCCACGTCATTACTCACAGTCG -3'
(R):5'- ATTCCCTCGAAATCCAGCTC -3'

Sequencing Primer
(F):5'- ATTACTCACAGTCGCTCAGATGG -3'
(R):5'- GCTCTTTGCTAAGACGGATTTC -3'

Posted On

2015-11-11