Mutagenetix > Incidental Mutation

Incidental Mutation 'R4558:Pcdhb4'

342961

Institutional Source

Beutler Lab

Gene Symbol

Pcdhb4

Ensembl Gene

ENSMUSG00000045689

Gene Name

protocadherin beta 4

Synonyms

PcdhbD, Pcdhb5A

MMRRC Submission

042005-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.063) question?

Stock #

R4558 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

37440508-37444225 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 37443017 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Valine at position 776 (I776V)

Ref Sequence

ENSEMBL: ENSMUSP00000059770 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000056712] [ENSMUST00000115661] [ENSMUST00000194544]

AlphaFold

Q91XZ6

Predicted Effect

probably benign
Transcript: ENSMUST00000056712
AA Change: I776V

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

SMART Domains

Protein: ENSMUSP00000059770
Gene: ENSMUSG00000045689
AA Change: I776V

Domain	Start	End	E-Value	Type
CA	54	131	1.66e0	SMART
CA	155	240	1.07e-19	SMART
CA	264	344	6.03e-28	SMART
CA	367	448	2.57e-22	SMART
CA	472	558	3.36e-26	SMART
CA	588	669	3.48e-10	SMART
Pfam:Cadherin_C_2	685	768	1e-25	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

noncoding transcript
Transcript: ENSMUST00000193025

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

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 95.1%

Validation Efficiency

100% (36/36)

Allele List at MGI

Other mutations in this stock

Total: 32 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700017G19Rik	A	G	3: 40,567,240 (GRCm39)		noncoding transcript	Het
A830018L16Rik	C	A	1: 12,042,300 (GRCm39)	S440*	probably null	Het
Acot11	T	C	4: 106,605,563 (GRCm39)	N583S	probably damaging	Het
Alox12	T	G	11: 70,143,889 (GRCm39)	M164L	probably benign	Het
Atad2b	A	G	12: 4,993,223 (GRCm39)	I247M	probably benign	Het
Bmpr2	T	A	1: 59,884,851 (GRCm39)	M279K	probably damaging	Het
Cacna2d3	T	C	14: 28,825,670 (GRCm39)	T502A	possibly damaging	Het
Casp12	A	T	9: 5,352,742 (GRCm39)	Y188F	probably damaging	Het
Catsperb	A	G	12: 101,557,799 (GRCm39)	Y790C	possibly damaging	Het
Cnbd1	G	T	4: 19,055,095 (GRCm39)	N110K	possibly damaging	Het
Entrep1	G	A	19: 24,007,913 (GRCm39)	S130L	probably damaging	Het
Fam227b	C	T	2: 125,968,963 (GRCm39)	S37N	probably benign	Het
Fsip2	T	C	2: 82,815,297 (GRCm39)	S3677P	possibly damaging	Het
Gm10764	A	G	10: 87,126,682 (GRCm39)		noncoding transcript	Het
H2-Q6	T	C	17: 35,647,291 (GRCm39)	V312A	probably benign	Het
Hecw1	T	A	13: 14,422,190 (GRCm39)	D972V	probably damaging	Het
Kalrn	G	A	16: 33,807,578 (GRCm39)	T2597I	possibly damaging	Het
Kng1	C	A	16: 22,896,168 (GRCm39)		probably null	Het
Med13	T	C	11: 86,189,880 (GRCm39)	T1010A	probably damaging	Het
Nbeal1	C	T	1: 60,320,469 (GRCm39)	R2021*	probably null	Het
Ncapg	A	T	5: 45,833,986 (GRCm39)	T341S	probably benign	Het
Obscn	T	C	11: 59,022,472 (GRCm39)	R758G	possibly damaging	Het
Pabir2	G	A	X: 52,349,554 (GRCm39)		probably benign	Het
Ppp4r4	T	C	12: 103,573,192 (GRCm39)	V697A	probably benign	Het
Pramel13	T	C	4: 144,122,542 (GRCm39)	M1V	probably null	Het
Psd4	G	A	2: 24,294,806 (GRCm39)	V789M	probably damaging	Het
Rasa3	T	C	8: 13,648,259 (GRCm39)	E135G	probably damaging	Het
Serpinb9c	T	A	13: 33,338,482 (GRCm39)	E139V	probably benign	Het
Sgsm1	G	A	5: 113,405,977 (GRCm39)		probably benign	Het
Tmem161b	A	G	13: 84,399,363 (GRCm39)	I6M	possibly damaging	Het
Upf2	A	G	2: 5,978,404 (GRCm39)	M423V	unknown	Het
Vmn1r207	A	G	13: 22,910,581 (GRCm39)		noncoding transcript	Het

Other mutations in Pcdhb4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00490:Pcdhb4	APN	18	37,442,969 (GRCm39)	missense	possibly damaging	0.68
IGL01319:Pcdhb4	APN	18	37,441,566 (GRCm39)	missense	probably benign
IGL01325:Pcdhb4	APN	18	37,442,676 (GRCm39)	missense	probably damaging	1.00
IGL01608:Pcdhb4	APN	18	37,441,803 (GRCm39)	missense	probably damaging	1.00
IGL01808:Pcdhb4	APN	18	37,442,067 (GRCm39)	missense	probably damaging	1.00
IGL01962:Pcdhb4	APN	18	37,442,057 (GRCm39)	missense	possibly damaging	0.90
IGL02280:Pcdhb4	APN	18	37,440,735 (GRCm39)	missense	probably benign	0.00
IGL02622:Pcdhb4	APN	18	37,442,721 (GRCm39)	missense	probably benign	0.00
IGL03025:Pcdhb4	APN	18	37,443,030 (GRCm39)	missense	possibly damaging	0.62
IGL03137:Pcdhb4	APN	18	37,441,569 (GRCm39)	missense	probably damaging	0.98
P0031:Pcdhb4	UTSW	18	37,441,938 (GRCm39)	missense	probably damaging	1.00
R0385:Pcdhb4	UTSW	18	37,442,268 (GRCm39)	missense	probably damaging	1.00
R0611:Pcdhb4	UTSW	18	37,441,263 (GRCm39)	missense	probably damaging	1.00
R0671:Pcdhb4	UTSW	18	37,440,795 (GRCm39)	missense	probably benign	0.01
R0738:Pcdhb4	UTSW	18	37,441,764 (GRCm39)	missense	probably damaging	1.00
R0853:Pcdhb4	UTSW	18	37,442,938 (GRCm39)	nonsense	probably null
R0893:Pcdhb4	UTSW	18	37,442,423 (GRCm39)	splice site	probably null
R1932:Pcdhb4	UTSW	18	37,442,594 (GRCm39)	missense	probably benign	0.33
R1945:Pcdhb4	UTSW	18	37,441,921 (GRCm39)	missense	probably damaging	1.00
R2194:Pcdhb4	UTSW	18	37,441,788 (GRCm39)	missense	probably damaging	1.00
R2273:Pcdhb4	UTSW	18	37,441,979 (GRCm39)	missense	probably damaging	1.00
R3807:Pcdhb4	UTSW	18	37,442,367 (GRCm39)	missense	probably damaging	0.98
R3815:Pcdhb4	UTSW	18	37,441,065 (GRCm39)	missense	probably damaging	1.00
R3816:Pcdhb4	UTSW	18	37,441,065 (GRCm39)	missense	probably damaging	1.00
R3974:Pcdhb4	UTSW	18	37,441,901 (GRCm39)	missense	possibly damaging	0.55
R4606:Pcdhb4	UTSW	18	37,441,705 (GRCm39)	missense	probably damaging	1.00
R4615:Pcdhb4	UTSW	18	37,441,553 (GRCm39)	missense	probably benign	0.02
R4840:Pcdhb4	UTSW	18	37,441,452 (GRCm39)	missense	possibly damaging	0.60
R5240:Pcdhb4	UTSW	18	37,442,979 (GRCm39)	missense	possibly damaging	0.78
R5272:Pcdhb4	UTSW	18	37,440,819 (GRCm39)	missense	probably benign	0.04
R5586:Pcdhb4	UTSW	18	37,442,034 (GRCm39)	missense	probably damaging	1.00
R5683:Pcdhb4	UTSW	18	37,442,042 (GRCm39)	missense	probably benign	0.45
R5917:Pcdhb4	UTSW	18	37,442,619 (GRCm39)	missense	probably damaging	1.00
R6110:Pcdhb4	UTSW	18	37,441,482 (GRCm39)	missense	possibly damaging	0.80
R6383:Pcdhb4	UTSW	18	37,441,074 (GRCm39)	missense	probably damaging	1.00
R6877:Pcdhb4	UTSW	18	37,442,625 (GRCm39)	missense	probably damaging	1.00
R7036:Pcdhb4	UTSW	18	37,441,835 (GRCm39)	missense	possibly damaging	0.95
R7204:Pcdhb4	UTSW	18	37,442,292 (GRCm39)	missense	probably damaging	1.00
R7271:Pcdhb4	UTSW	18	37,441,222 (GRCm39)	missense	possibly damaging	0.89
R7436:Pcdhb4	UTSW	18	37,442,328 (GRCm39)	missense	probably damaging	1.00
R7444:Pcdhb4	UTSW	18	37,442,505 (GRCm39)	missense	probably damaging	1.00
R7614:Pcdhb4	UTSW	18	37,442,602 (GRCm39)	missense	probably benign	0.40
R7650:Pcdhb4	UTSW	18	37,442,667 (GRCm39)	missense	probably damaging	1.00
R7664:Pcdhb4	UTSW	18	37,442,293 (GRCm39)	missense	probably damaging	1.00
R8080:Pcdhb4	UTSW	18	37,442,349 (GRCm39)	missense	probably benign	0.42
R8087:Pcdhb4	UTSW	18	37,441,717 (GRCm39)	missense	probably damaging	1.00
R8115:Pcdhb4	UTSW	18	37,442,453 (GRCm39)	missense	probably damaging	0.99
R8697:Pcdhb4	UTSW	18	37,441,832 (GRCm39)	missense	probably benign	0.15
R8815:Pcdhb4	UTSW	18	37,442,055 (GRCm39)	missense	probably damaging	1.00
R9008:Pcdhb4	UTSW	18	37,440,714 (GRCm39)	missense	probably benign
R9225:Pcdhb4	UTSW	18	37,441,695 (GRCm39)	missense	possibly damaging	0.68
R9278:Pcdhb4	UTSW	18	37,441,925 (GRCm39)	missense	possibly damaging	0.61
R9299:Pcdhb4	UTSW	18	37,442,264 (GRCm39)	missense	probably benign	0.02
R9390:Pcdhb4	UTSW	18	37,442,781 (GRCm39)	missense	possibly damaging	0.80
R9582:Pcdhb4	UTSW	18	37,441,417 (GRCm39)	missense	probably damaging	1.00
R9686:Pcdhb4	UTSW	18	37,442,943 (GRCm39)	missense	probably damaging	0.98
R9721:Pcdhb4	UTSW	18	37,442,905 (GRCm39)	missense	possibly damaging	0.70
Z1177:Pcdhb4	UTSW	18	37,442,966 (GRCm39)	missense	probably benign	0.02

Predicted Primers

PCR Primer
(F):5'- CTGGATCCTACACGGGAAGAAG -3'
(R):5'- ACTAAGACAGCAGGCAGTTG -3'

Sequencing Primer
(F):5'- GGAAGAAGATAATCTCACGCTGTATC -3'
(R):5'- CAGCAGGCAGTTGAAGCATTAATTG -3'

Posted On

2015-09-24