Incidental Mutation 'R7529:Pcdhb15'
| ID |
583235 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Pcdhb15
|
| Ensembl Gene |
ENSMUSG00000047033 |
| Gene Name |
protocadherin beta 15 |
| Synonyms |
Pcdhb7, PcdhbO |
| MMRRC Submission |
045601-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.065)
|
| Stock # |
R7529 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
18 |
| Chromosomal Location |
37606599-37609393 bp(+) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
G to T
at 37607526 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamic Acid to Stop codon
at position 253
(E253*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000059598
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000050034]
[ENSMUST00000051442]
[ENSMUST00000115661]
[ENSMUST00000194544]
|
| AlphaFold |
Q91Y04 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000050034
AA Change: E253*
|
| SMART Domains |
Protein: ENSMUSP00000059598
Gene: ENSMUSG00000047033
AA Change: E253*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Cadherin_2
|
30 |
112 |
2.6e-33 |
PFAM |
|
CA
|
155 |
240 |
7.79e-22 |
SMART |
|
CA
|
264 |
345 |
4.37e-25 |
SMART |
|
CA
|
368 |
449 |
4.4e-21 |
SMART |
|
CA
|
473 |
559 |
7.38e-23 |
SMART |
|
CA
|
589 |
670 |
4.48e-13 |
SMART |
|
Pfam:Cadherin_C_2
|
686 |
770 |
5.3e-25 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000051442
|
| SMART Domains |
Protein: ENSMUSP00000056347
Gene: ENSMUSG00000047910
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
28 |
N/A |
INTRINSIC |
|
CA
|
46 |
132 |
7.7e-1 |
SMART |
|
CA
|
156 |
241 |
1.93e-17 |
SMART |
|
CA
|
265 |
346 |
4.2e-27 |
SMART |
|
CA
|
369 |
450 |
1.08e-24 |
SMART |
|
CA
|
474 |
560 |
3.31e-25 |
SMART |
|
CA
|
590 |
671 |
2.87e-11 |
SMART |
|
Pfam:Cadherin_C_2
|
687 |
770 |
4.1e-27 |
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 |
0.9703 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
100% (79/79) |
| 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 protocadherin beta gene cluster, one of three related gene clusters tandemly linked on chromosome five. The gene clusters demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The beta cluster contains 16 genes and 3 pseudogenes, each encoding 6 extracellular cadherin domains and a cytoplasmic tail that deviates from others in the cadherin superfamily. The extracellular domains interact in a homophilic manner to specify differential cell-cell connections. Unlike the alpha and gamma clusters, the transcripts from these genes are made up of only one large exon, not sharing common 3' exons as expected. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins. Their specific functions are unknown but they most likely play a critical role in the establishment and function of specific cell-cell neural connections. The transcript for this particular family member uses more than one polyadenylation site. [provided by RefSeq, Jul 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 79 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 9130023H24Rik |
T |
A |
7: 127,836,336 (GRCm39) |
K86* |
probably null |
Het |
| Ablim3 |
A |
C |
18: 61,955,039 (GRCm39) |
S317A |
probably benign |
Het |
| Adcy1 |
T |
C |
11: 7,089,157 (GRCm39) |
S524P |
probably damaging |
Het |
| Agps |
C |
A |
2: 75,662,696 (GRCm39) |
A47E |
possibly damaging |
Het |
| Arhgef15 |
G |
T |
11: 68,844,848 (GRCm39) |
R250S |
probably damaging |
Het |
| Armh1 |
C |
A |
4: 117,070,938 (GRCm39) |
A396S |
probably benign |
Het |
| Atoh8 |
G |
T |
6: 72,200,825 (GRCm39) |
D288E |
probably benign |
Het |
| B3galt2 |
A |
C |
1: 143,522,274 (GRCm39) |
K137Q |
probably benign |
Het |
| Cacna2d4 |
G |
A |
6: 119,247,727 (GRCm39) |
V343I |
probably benign |
Het |
| Cage1 |
T |
C |
13: 38,209,731 (GRCm39) |
N82S |
possibly damaging |
Het |
| Cep350 |
A |
G |
1: 155,737,669 (GRCm39) |
S2725P |
probably benign |
Het |
| Cfap65 |
T |
C |
1: 74,965,769 (GRCm39) |
N414D |
probably damaging |
Het |
| Cgnl1 |
A |
C |
9: 71,539,040 (GRCm39) |
L1154R |
probably damaging |
Het |
| Cmya5 |
A |
T |
13: 93,233,942 (GRCm39) |
M382K |
probably benign |
Het |
| Dchs2 |
G |
A |
3: 83,261,705 (GRCm39) |
V2658M |
possibly damaging |
Het |
| Dlgap5 |
T |
C |
14: 47,653,876 (GRCm39) |
N51S |
probably damaging |
Het |
| Dnah17 |
A |
G |
11: 117,940,692 (GRCm39) |
|
probably null |
Het |
| Dnal1 |
A |
G |
12: 84,178,117 (GRCm39) |
I35V |
probably benign |
Het |
| Dtnbp1 |
A |
G |
13: 45,084,546 (GRCm39) |
F198S |
probably damaging |
Het |
| Edar |
A |
T |
10: 58,447,830 (GRCm39) |
S160T |
probably benign |
Het |
| Enpp3 |
A |
T |
10: 24,674,072 (GRCm39) |
N409K |
probably damaging |
Het |
| Ercc6 |
T |
A |
14: 32,282,686 (GRCm39) |
C726* |
probably null |
Het |
| Extl2 |
G |
A |
3: 115,821,055 (GRCm39) |
V301I |
possibly damaging |
Het |
| G2e3 |
A |
G |
12: 51,418,387 (GRCm39) |
Q594R |
probably damaging |
Het |
| Gal3st2c |
A |
G |
1: 93,937,039 (GRCm39) |
N328S |
probably benign |
Het |
| Galnt17 |
A |
G |
5: 131,335,218 (GRCm39) |
V74A |
probably damaging |
Het |
| Ggta1 |
A |
G |
2: 35,304,256 (GRCm39) |
W76R |
probably damaging |
Het |
| Gm9772 |
T |
A |
17: 22,226,140 (GRCm39) |
D48V |
probably benign |
Het |
| Herpud2 |
T |
C |
9: 25,020,193 (GRCm39) |
T388A |
probably damaging |
Het |
| Ighv5-9-1 |
A |
G |
12: 113,699,954 (GRCm39) |
S53P |
possibly damaging |
Het |
| Il23r |
T |
A |
6: 67,467,720 (GRCm39) |
M16L |
possibly damaging |
Het |
| Ints1 |
G |
A |
5: 139,753,481 (GRCm39) |
A717V |
possibly damaging |
Het |
| Itpr2 |
A |
T |
6: 146,096,096 (GRCm39) |
L2122Q |
probably damaging |
Het |
| Klrg2 |
A |
T |
6: 38,607,266 (GRCm39) |
V248E |
probably damaging |
Het |
| Krtap5-5 |
A |
G |
7: 141,783,429 (GRCm39) |
C74R |
unknown |
Het |
| Luzp1 |
G |
T |
4: 136,268,243 (GRCm39) |
L155F |
probably damaging |
Het |
| Mcam |
T |
C |
9: 44,050,192 (GRCm39) |
V209A |
probably benign |
Het |
| Med1 |
G |
C |
11: 98,046,791 (GRCm39) |
T1335R |
unknown |
Het |
| Mroh2b |
A |
G |
15: 4,978,491 (GRCm39) |
I1346V |
probably damaging |
Het |
| Mrpl4 |
C |
G |
9: 20,918,975 (GRCm39) |
Q201E |
probably benign |
Het |
| Muc21 |
A |
T |
17: 35,930,123 (GRCm39) |
S1354R |
unknown |
Het |
| Mylk2 |
T |
C |
2: 152,757,624 (GRCm39) |
L326P |
probably damaging |
Het |
| Myot |
A |
T |
18: 44,479,240 (GRCm39) |
R326* |
probably null |
Het |
| Nox3 |
T |
A |
17: 3,722,050 (GRCm39) |
R288S |
probably damaging |
Het |
| Nox4 |
A |
T |
7: 87,044,976 (GRCm39) |
Y572F |
unknown |
Het |
| Or2v2 |
A |
G |
11: 49,003,686 (GRCm39) |
L289P |
probably damaging |
Het |
| Or5an10 |
A |
G |
19: 12,276,086 (GRCm39) |
S137P |
probably damaging |
Het |
| Plcb2 |
T |
C |
2: 118,540,715 (GRCm39) |
H1052R |
probably damaging |
Het |
| Plpp5 |
A |
T |
8: 26,214,233 (GRCm39) |
Q250L |
probably benign |
Het |
| Plxna2 |
T |
C |
1: 194,326,179 (GRCm39) |
Y38H |
probably benign |
Het |
| Pnpla8 |
A |
G |
12: 44,329,963 (GRCm39) |
K172E |
probably benign |
Het |
| Pramel23 |
T |
C |
4: 143,429,244 (GRCm39) |
|
|
Het |
| Prl8a9 |
T |
A |
13: 27,744,511 (GRCm39) |
D110V |
probably benign |
Het |
| Prrx1 |
T |
C |
1: 163,081,533 (GRCm39) |
|
probably null |
Het |
| Prss52 |
T |
A |
14: 64,347,037 (GRCm39) |
H70Q |
probably benign |
Het |
| Rcc1 |
T |
C |
4: 132,061,874 (GRCm39) |
T300A |
probably benign |
Het |
| Rnf114 |
T |
C |
2: 167,349,014 (GRCm39) |
V64A |
possibly damaging |
Het |
| Rnf168 |
T |
C |
16: 32,117,732 (GRCm39) |
I431T |
probably damaging |
Het |
| Rnmt |
A |
G |
18: 68,444,726 (GRCm39) |
M232V |
probably benign |
Het |
| Rrs1 |
A |
C |
1: 9,616,417 (GRCm39) |
Q223H |
probably benign |
Het |
| Scyl3 |
A |
T |
1: 163,771,438 (GRCm39) |
L261F |
probably damaging |
Het |
| Slc24a4 |
A |
T |
12: 102,230,707 (GRCm39) |
T533S |
probably benign |
Het |
| Slc26a2 |
A |
G |
18: 61,331,430 (GRCm39) |
L667P |
probably damaging |
Het |
| Snrnp40 |
T |
A |
4: 130,278,275 (GRCm39) |
V260D |
possibly damaging |
Het |
| Snrpa |
A |
C |
7: 26,888,878 (GRCm39) |
M174R |
probably benign |
Het |
| Ss18l1 |
C |
T |
2: 179,699,950 (GRCm39) |
A270V |
possibly damaging |
Het |
| Stk19 |
G |
T |
17: 35,043,632 (GRCm39) |
Q193K |
probably benign |
Het |
| Syne1 |
T |
A |
10: 5,374,382 (GRCm39) |
I142L |
probably damaging |
Het |
| Tbx2 |
T |
C |
11: 85,731,727 (GRCm39) |
S675P |
probably benign |
Het |
| Tcaf1 |
A |
G |
6: 42,652,289 (GRCm39) |
I731T |
probably damaging |
Het |
| Tg |
G |
T |
15: 66,566,617 (GRCm39) |
G1222W |
probably damaging |
Het |
| Tsc2 |
A |
G |
17: 24,816,922 (GRCm39) |
F1581L |
probably damaging |
Het |
| Ubr4 |
G |
C |
4: 139,149,728 (GRCm39) |
V520L |
probably benign |
Het |
| Wls |
A |
T |
3: 159,578,644 (GRCm39) |
N69Y |
probably benign |
Het |
| Wnk2 |
A |
G |
13: 49,254,457 (GRCm39) |
F353L |
possibly damaging |
Het |
| Xkr6 |
G |
T |
14: 64,056,610 (GRCm39) |
V430F |
probably benign |
Het |
| Zfp64 |
C |
T |
2: 168,735,992 (GRCm39) |
G562R |
probably benign |
Het |
| Zfp663 |
T |
G |
2: 165,194,728 (GRCm39) |
E497A |
probably damaging |
Het |
| Zfp995 |
A |
T |
17: 22,099,333 (GRCm39) |
C300* |
probably null |
Het |
|
| Other mutations in Pcdhb15 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00530:Pcdhb15
|
APN |
18 |
37,608,207 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01536:Pcdhb15
|
APN |
18 |
37,608,046 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01664:Pcdhb15
|
APN |
18 |
37,607,314 (GRCm39) |
missense |
probably benign |
0.35 |
|
IGL02001:Pcdhb15
|
APN |
18 |
37,607,091 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02161:Pcdhb15
|
APN |
18 |
37,608,555 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
IGL02205:Pcdhb15
|
APN |
18 |
37,607,010 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02748:Pcdhb15
|
APN |
18 |
37,608,273 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02828:Pcdhb15
|
APN |
18 |
37,606,903 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL02974:Pcdhb15
|
APN |
18 |
37,608,067 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03119:Pcdhb15
|
APN |
18 |
37,608,067 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03136:Pcdhb15
|
APN |
18 |
37,608,067 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03150:Pcdhb15
|
APN |
18 |
37,608,067 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT1430001:Pcdhb15
|
UTSW |
18 |
37,608,724 (GRCm39) |
missense |
probably benign |
0.15 |
|
R0266:Pcdhb15
|
UTSW |
18 |
37,608,329 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0288:Pcdhb15
|
UTSW |
18 |
37,608,451 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0399:Pcdhb15
|
UTSW |
18 |
37,607,221 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R0400:Pcdhb15
|
UTSW |
18 |
37,608,948 (GRCm39) |
missense |
probably benign |
|
|
R0554:Pcdhb15
|
UTSW |
18 |
37,607,572 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0637:Pcdhb15
|
UTSW |
18 |
37,608,619 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0714:Pcdhb15
|
UTSW |
18 |
37,607,674 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1118:Pcdhb15
|
UTSW |
18 |
37,606,815 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1423:Pcdhb15
|
UTSW |
18 |
37,606,975 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1672:Pcdhb15
|
UTSW |
18 |
37,607,713 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1681:Pcdhb15
|
UTSW |
18 |
37,606,866 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1779:Pcdhb15
|
UTSW |
18 |
37,609,084 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R2206:Pcdhb15
|
UTSW |
18 |
37,608,075 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2207:Pcdhb15
|
UTSW |
18 |
37,608,075 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2274:Pcdhb15
|
UTSW |
18 |
37,608,496 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3406:Pcdhb15
|
UTSW |
18 |
37,608,442 (GRCm39) |
missense |
probably benign |
0.41 |
|
R3407:Pcdhb15
|
UTSW |
18 |
37,607,442 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R3417:Pcdhb15
|
UTSW |
18 |
37,608,216 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3752:Pcdhb15
|
UTSW |
18 |
37,606,810 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3773:Pcdhb15
|
UTSW |
18 |
37,608,943 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4432:Pcdhb15
|
UTSW |
18 |
37,608,565 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4433:Pcdhb15
|
UTSW |
18 |
37,608,565 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4583:Pcdhb15
|
UTSW |
18 |
37,608,628 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R4612:Pcdhb15
|
UTSW |
18 |
37,608,648 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4988:Pcdhb15
|
UTSW |
18 |
37,608,855 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5635:Pcdhb15
|
UTSW |
18 |
37,606,823 (GRCm39) |
nonsense |
probably null |
|
|
R5692:Pcdhb15
|
UTSW |
18 |
37,607,502 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5742:Pcdhb15
|
UTSW |
18 |
37,607,820 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5913:Pcdhb15
|
UTSW |
18 |
37,607,707 (GRCm39) |
missense |
probably benign |
0.07 |
|
R6350:Pcdhb15
|
UTSW |
18 |
37,608,414 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6522:Pcdhb15
|
UTSW |
18 |
37,607,314 (GRCm39) |
missense |
probably benign |
0.35 |
|
R6676:Pcdhb15
|
UTSW |
18 |
37,607,860 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R6693:Pcdhb15
|
UTSW |
18 |
37,607,394 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6905:Pcdhb15
|
UTSW |
18 |
37,607,748 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7029:Pcdhb15
|
UTSW |
18 |
37,608,621 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R7335:Pcdhb15
|
UTSW |
18 |
37,607,389 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7718:Pcdhb15
|
UTSW |
18 |
37,608,216 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7782:Pcdhb15
|
UTSW |
18 |
37,607,788 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R7967:Pcdhb15
|
UTSW |
18 |
37,607,902 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8170:Pcdhb15
|
UTSW |
18 |
37,608,637 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8323:Pcdhb15
|
UTSW |
18 |
37,608,715 (GRCm39) |
missense |
probably benign |
0.18 |
|
R8725:Pcdhb15
|
UTSW |
18 |
37,608,734 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8820:Pcdhb15
|
UTSW |
18 |
37,606,971 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9117:Pcdhb15
|
UTSW |
18 |
37,608,090 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9280:Pcdhb15
|
UTSW |
18 |
37,607,794 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9367:Pcdhb15
|
UTSW |
18 |
37,607,971 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9424:Pcdhb15
|
UTSW |
18 |
37,607,263 (GRCm39) |
missense |
|
|
|
R9432:Pcdhb15
|
UTSW |
18 |
37,608,683 (GRCm39) |
missense |
probably benign |
0.04 |
|
R9498:Pcdhb15
|
UTSW |
18 |
37,606,890 (GRCm39) |
nonsense |
probably null |
|
|
R9544:Pcdhb15
|
UTSW |
18 |
37,608,948 (GRCm39) |
missense |
probably benign |
|
|
X0062:Pcdhb15
|
UTSW |
18 |
37,609,068 (GRCm39) |
nonsense |
probably null |
|
|
X0063:Pcdhb15
|
UTSW |
18 |
37,608,137 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- CCATATTCACGTGCATGATGGAG -3'
(R):5'- CGCTTCATAGTTGAGTTCGCG -3'
Sequencing Primer
(F):5'- AGGGGCCTATCATTCCTGAACTG -3'
(R):5'- CGCGTTTAAGATAAAGTTCGCCAG -3'
|
| Posted On |
2019-10-17 |
Incidental Mutation