Mutagenetix > Incidental Mutation

Incidental Mutation 'R5022:Pcdhb14'

389304

Institutional Source

Beutler Lab

Gene Symbol

Pcdhb14

Ensembl Gene

ENSMUSG00000044043

Gene Name

protocadherin beta 14

Synonyms

PcdhbN, 2210006M07Rik, Pcdhb17

MMRRC Submission

042613-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.057) question?

Stock #

R5022 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

37447656-37456350 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 37450170 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Lysine at position 776 (N776K)

Ref Sequence

ENSEMBL: ENSMUSP00000054111 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000052387] [ENSMUST00000056915] [ENSMUST00000115661] [ENSMUST00000194544]

AlphaFold

Q6PB90

PDB Structure

Solution structure of mouse protocadherin beta 14 (26-137) [SOLUTION NMR]

Predicted Effect

probably benign
Transcript: ENSMUST00000052387
AA Change: N776K

PolyPhen 2 Score 0.027 (Sensitivity: 0.95; Specificity: 0.81)

SMART Domains

Protein: ENSMUSP00000054111
Gene: ENSMUSG00000044043
AA Change: N776K

Domain	Start	End	E-Value	Type
Pfam:Cadherin_2	30	112	1.4e-35	PFAM
CA	155	240	1.53e-20	SMART
CA	264	345	3.52e-29	SMART
CA	368	449	2.24e-22	SMART
CA	473	559	2.38e-26	SMART
CA	589	670	4.12e-12	SMART
Pfam:Cadherin_C_2	685	768	4.9e-27	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000056915

SMART Domains

Protein: ENSMUSP00000061087
Gene: ENSMUSG00000047307

Domain	Start	End	E-Value	Type
signal peptide	1	28	N/A	INTRINSIC
CA	58	130	5.5e-1	SMART
CA	154	239	8.55e-19	SMART
CA	263	343	3.36e-26	SMART
CA	366	447	2.24e-22	SMART
CA	471	557	1.08e-24	SMART
CA	587	668	1.25e-11	SMART
Pfam:Cadherin_C_2	685	768	2.4e-23	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

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.4%
20x: 92.6%

Validation Efficiency

99% (110/111)

Allele List at MGI

Other mutations in this stock

Total: 105 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca1	TCGACTGC	T	4: 53,041,570		probably null	Het
Abca15	T	C	7: 120,346,096	I465T	probably damaging	Het
Abca3	C	T	17: 24,374,300	R224C	probably damaging	Het
Abcb4	T	A	5: 8,909,054		probably null	Het
Acan	T	C	7: 79,092,808		probably null	Het
Aebp2	G	A	6: 140,637,730	R109Q	possibly damaging	Het
Agfg2	A	T	5: 137,660,160		probably null	Het
Ankib1	T	A	5: 3,734,011	I322F	possibly damaging	Het
AW551984	A	T	9: 39,597,965	N293K	probably benign	Het
BC028528	T	A	3: 95,888,823		probably benign	Het
Bicc1	A	G	10: 70,947,883	S393P	possibly damaging	Het
Birc6	A	G	17: 74,692,332	Y4656C	probably damaging	Het
Bmp3	A	G	5: 98,872,824	R369G	probably damaging	Het
C1d	T	A	11: 17,266,674	N135K	probably benign	Het
Ccdc148	G	A	2: 58,827,632	A453V	probably damaging	Het
Cd163	C	T	6: 124,325,288	T937I	probably damaging	Het
Celf2	C	T	2: 6,607,847		probably benign	Het
Chga	T	C	12: 102,562,837	W358R	probably damaging	Het
Clec4b2	A	T	6: 123,200,956	S77C	probably null	Het
Crim1	T	C	17: 78,280,129	V221A	possibly damaging	Het
D630003M21Rik	A	T	2: 158,217,633	S116T	probably damaging	Het
Dlg5	T	C	14: 24,136,622	E1847G	probably damaging	Het
Dmxl1	T	A	18: 49,895,127	I2206K	probably damaging	Het
Dusp7	T	A	9: 106,373,741	L355Q	probably damaging	Het
Exd2	T	A	12: 80,496,790	N582K	probably damaging	Het
Fbln1	G	A	15: 85,237,626	S316N	probably damaging	Het
Fchsd1	A	G	18: 37,964,810	I340T	possibly damaging	Het
Fn1	T	C	1: 71,624,179	Y1050C	probably damaging	Het
Fsip2	A	G	2: 82,979,429	I2031V	probably benign	Het
Gm10803	A	C	2: 93,564,172	L96F	probably damaging	Het
Gm12169	T	A	11: 46,528,532	D58E	probably damaging	Het
Gm14569	T	C	X: 36,430,817	D1413G	probably benign	Het
Gm15455	T	C	1: 33,837,351		noncoding transcript	Het
Gm1818	G	C	12: 48,555,535		noncoding transcript	Het
Gm4907	G	A	X: 23,907,241	G327E	probably damaging	Het
Gm5039	T	C	12: 88,321,301	I61V	probably benign	Het
Gm5420	A	T	10: 21,691,727		noncoding transcript	Het
Gm6803	A	T	12: 88,018,711	S21T	unknown	Het
Gm7104	A	T	12: 88,285,759		noncoding transcript	Het
Gp2	A	G	7: 119,449,114	I427T	probably damaging	Het
Gpc4	G	A	X: 52,074,563	R148C	probably damaging	Het
Gpr142	A	C	11: 114,804,388	S60R	probably benign	Het
Helz2	T	C	2: 181,240,569	R144G	probably benign	Het
Herc1	A	T	9: 66,470,326	K3458M	possibly damaging	Het
Hnf4g	G	T	3: 3,644,587	A144S	probably damaging	Het
Irs2	A	C	8: 10,987,012	*1322G	probably null	Het
Keg1	A	G	19: 12,719,157	N288S	probably damaging	Het
Kif19a	G	A	11: 114,767,227	M37I	probably benign	Het
Klhl1	G	A	14: 96,136,706	P635S	probably benign	Het
Klk14	G	A	7: 43,692,077	C51Y	probably damaging	Het
Lsm11	T	C	11: 45,944,839	D25G	probably damaging	Het
Manea	A	T	4: 26,336,630	Y215*	probably null	Het
Mdga2	C	T	12: 66,470,760	C100Y	possibly damaging	Het
Mthfd1	T	G	12: 76,294,374	V480G	probably damaging	Het
Mthfd1	T	A	12: 76,301,328	M582K	probably damaging	Het
Myh7b	G	C	2: 155,632,373	R1669S	possibly damaging	Het
Nanos1	T	C	19: 60,756,980	Y239H	probably damaging	Het
Nat8	G	A	6: 85,830,857	T98I	possibly damaging	Het
Ndufs3	C	A	2: 90,898,660	A161S	probably benign	Het
Nexmif	A	T	X: 104,087,350	N320K	probably damaging	Het
Olfr1216	A	G	2: 89,014,043	V7A	probably damaging	Het
Olfr1228	C	T	2: 89,249,417	M92I	probably benign	Het
Olfr164	A	T	16: 19,286,059	V228D	probably damaging	Het
Olfr239	T	C	17: 33,199,777	F239S	probably damaging	Het
Olfr457	A	T	6: 42,471,287	V297E	possibly damaging	Het
Olfr589	G	A	7: 103,155,735	P4L	probably benign	Het
Olfr727	T	C	14: 50,127,012	V145A	possibly damaging	Het
Olfr822	T	C	10: 130,074,593	L61P	probably damaging	Het
Pip5k1c	G	A	10: 81,310,889		probably null	Het
Plk4	G	A	3: 40,802,077		probably null	Het
Prmt8	A	G	6: 127,711,163	Y231H	possibly damaging	Het
Prpf4b	T	C	13: 34,883,599		probably benign	Het
Ptpn21	G	A	12: 98,679,407	R1091C	probably damaging	Het
Pwwp2b	C	T	7: 139,255,578	P312S	possibly damaging	Het
Rad21	A	T	15: 51,966,706	I503K	probably benign	Het
Rai14	A	G	15: 10,574,506	S789P	probably damaging	Het
Rbm26	C	T	14: 105,144,252	D486N	probably damaging	Het
Rnf20	A	G	4: 49,642,016		probably benign	Het
Ros1	A	G	10: 52,124,075	V1118A	possibly damaging	Het
Sema3d	A	C	5: 12,584,956	Y663S	probably damaging	Het
Serpina6	A	G	12: 103,651,712	W281R	probably damaging	Het
Slc8a3	A	G	12: 81,199,558	V900A	probably damaging	Het
Spats2l	G	T	1: 57,879,556	V30L	probably damaging	Het
Spg21	A	G	9: 65,475,949	D139G	probably damaging	Het
Sun3	T	C	11: 9,038,314	T3A	probably damaging	Het
Tcrg-V1	T	A	13: 19,340,231	S42T	probably benign	Het
Tep1	A	G	14: 50,828,999	Y2335H	probably benign	Het
Timm21	C	A	18: 84,949,414	V112L	possibly damaging	Het
Tlk1	A	T	2: 70,742,065	N386K	probably benign	Het
Trappc10	G	T	10: 78,217,160	F260L	possibly damaging	Het
Trmt112	T	C	19: 6,910,753	V91A	probably benign	Het
Ucp2	A	T	7: 100,498,372	N186I	possibly damaging	Het
Vmn1r119	A	G	7: 21,012,320	S46P	probably benign	Het
Vmn2r101	A	T	17: 19,611,387		probably null	Het
Vmn2r105	T	A	17: 20,208,414	H800L	probably damaging	Het
Vmn2r69	T	C	7: 85,411,159	M406V	possibly damaging	Het
Vmn2r84	A	G	10: 130,386,548	L601P	probably damaging	Het
Vps16	A	G	2: 130,439,452	S235G	probably benign	Het
Wap	T	C	11: 6,637,339		probably benign	Het
Wdr11	A	G	7: 129,624,711	I744M	probably benign	Het
Xiap	T	C	X: 42,094,465	F23L	probably benign	Het
Xkr7	A	G	2: 153,054,380	T385A	probably benign	Het
Zfp524	A	T	7: 5,018,417	I315F	probably benign	Het
Zfp62	T	A	11: 49,215,729	S216T	probably damaging	Het
Znfx1	T	C	2: 167,039,826	Y217C	probably damaging	Het

Other mutations in Pcdhb14

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02260:Pcdhb14	APN	18	37450033	missense	probably benign	0.28
IGL02314:Pcdhb14	APN	18	37450195	missense	probably benign	0.03
IGL02411:Pcdhb14	APN	18	37449770	missense	possibly damaging	0.78
IGL02553:Pcdhb14	APN	18	37448018	nonsense	probably null
IGL02797:Pcdhb14	APN	18	37449851	missense	probably damaging	1.00
IGL03184:Pcdhb14	APN	18	37449032	missense	probably benign	0.00
IGL03352:Pcdhb14	APN	18	37449004	missense	possibly damaging	0.67
R0166:Pcdhb14	UTSW	18	37448489	splice site	probably null
R0467:Pcdhb14	UTSW	18	37449224	missense	probably damaging	0.98
R0675:Pcdhb14	UTSW	18	37448339	missense	possibly damaging	0.91
R0730:Pcdhb14	UTSW	18	37448868	missense	probably damaging	1.00
R1119:Pcdhb14	UTSW	18	37448587	missense	probably damaging	0.99
R1121:Pcdhb14	UTSW	18	37449592	missense	probably damaging	1.00
R1338:Pcdhb14	UTSW	18	37449890	missense	probably benign	0.00
R1726:Pcdhb14	UTSW	18	37449594	nonsense	probably null
R1743:Pcdhb14	UTSW	18	37448178	missense	probably benign	0.01
R1779:Pcdhb14	UTSW	18	37449482	missense	probably damaging	1.00
R1795:Pcdhb14	UTSW	18	37449535	missense	probably benign
R2131:Pcdhb14	UTSW	18	37447870	missense	probably benign	0.00
R2133:Pcdhb14	UTSW	18	37447870	missense	probably benign	0.00
R3792:Pcdhb14	UTSW	18	37449662	missense	probably damaging	1.00
R3916:Pcdhb14	UTSW	18	37448545	missense	possibly damaging	0.48
R4197:Pcdhb14	UTSW	18	37448305	missense	probably benign	0.01
R4282:Pcdhb14	UTSW	18	37450142	missense	probably damaging	1.00
R4657:Pcdhb14	UTSW	18	37448847	missense	possibly damaging	0.92
R4801:Pcdhb14	UTSW	18	37448278	missense	probably benign	0.28
R4802:Pcdhb14	UTSW	18	37448278	missense	probably benign	0.28
R5034:Pcdhb14	UTSW	18	37448806	missense	probably damaging	0.98
R5664:Pcdhb14	UTSW	18	37448996	missense	possibly damaging	0.54
R5840:Pcdhb14	UTSW	18	37448750	missense	probably benign	0.23
R5966:Pcdhb14	UTSW	18	37448242	missense	probably benign
R6090:Pcdhb14	UTSW	18	37448606	missense	probably benign	0.45
R6148:Pcdhb14	UTSW	18	37449230	missense	probably damaging	1.00
R6187:Pcdhb14	UTSW	18	37448444	missense	probably damaging	1.00
R6972:Pcdhb14	UTSW	18	37449692	missense	probably damaging	1.00
R7394:Pcdhb14	UTSW	18	37448908	missense	probably benign	0.29
R7510:Pcdhb14	UTSW	18	37449592	missense	probably damaging	0.97
R7724:Pcdhb14	UTSW	18	37448884	missense	possibly damaging	0.62
R7757:Pcdhb14	UTSW	18	37449834	missense	possibly damaging	0.95
R8305:Pcdhb14	UTSW	18	37450022	missense	possibly damaging	0.48
R8338:Pcdhb14	UTSW	18	37449122	missense	probably damaging	1.00
R8497:Pcdhb14	UTSW	18	37449296	missense	probably benign	0.02
R8700:Pcdhb14	UTSW	18	37449599	missense	probably damaging	1.00
R8792:Pcdhb14	UTSW	18	37449488	missense	probably damaging	0.99
R8891:Pcdhb14	UTSW	18	37449639	missense	probably damaging	1.00
R8992:Pcdhb14	UTSW	18	37449178	missense	probably damaging	1.00
R9043:Pcdhb14	UTSW	18	37448798	missense	probably damaging	0.98
R9069:Pcdhb14	UTSW	18	37450104	nonsense	probably null
R9127:Pcdhb14	UTSW	18	37449038	missense	probably damaging	0.99
R9345:Pcdhb14	UTSW	18	37448228	missense	probably damaging	0.98
R9470:Pcdhb14	UTSW	18	37448023	missense	probably benign
R9626:Pcdhb14	UTSW	18	37448734	missense	probably damaging	1.00
R9758:Pcdhb14	UTSW	18	37448987	missense	probably benign	0.08
X0065:Pcdhb14	UTSW	18	37449421	missense	possibly damaging	0.95
X0065:Pcdhb14	UTSW	18	37449984	nonsense	probably null
Z1177:Pcdhb14	UTSW	18	37449854	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TACCTGGTCATTGCCTTGGC -3'
(R):5'- TGACTACCAGTATCATGCTAGTG -3'

Sequencing Primer
(F):5'- AAGGCTGGGGAGACTTCTC -3'
(R):5'- AGTGCAGACCTCTTTCCACGAG -3'

Posted On

2016-06-06