Incidental Mutation 'R3946:Pcdhga9'
ID |
474801 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Pcdhga9
|
Ensembl Gene |
ENSMUSG00000102440 |
Gene Name |
protocadherin gamma subfamily A, 9 |
Synonyms |
|
MMRRC Submission |
040827-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.133)
|
Stock # |
R3946 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
18 |
Chromosomal Location |
37736936-37841870 bp(+) (GRCm38) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 37737844 bp (GRCm38)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Aspartic acid
at position 242
(V242D)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000089555
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000003599]
[ENSMUST00000066149]
[ENSMUST00000073447]
[ENSMUST00000091935]
[ENSMUST00000115661]
[ENSMUST00000192511]
[ENSMUST00000192535]
[ENSMUST00000192931]
[ENSMUST00000193414]
[ENSMUST00000193869]
[ENSMUST00000194190]
[ENSMUST00000194418]
[ENSMUST00000195112]
[ENSMUST00000194544]
[ENSMUST00000195823]
[ENSMUST00000195363]
|
AlphaFold |
Q91XX9 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000003599
|
SMART Domains |
Protein: ENSMUSP00000003599 Gene: ENSMUSG00000103088
Domain | Start | End | E-Value | Type |
CA
|
47 |
131 |
8.06e-6 |
SMART |
CA
|
155 |
240 |
2.29e-19 |
SMART |
CA
|
264 |
345 |
3.36e-26 |
SMART |
CA
|
369 |
450 |
4.94e-24 |
SMART |
CA
|
474 |
560 |
7.6e-25 |
SMART |
CA
|
591 |
672 |
9.18e-10 |
SMART |
Pfam:Cadherin_C_2
|
687 |
768 |
3.5e-20 |
PFAM |
Pfam:Cadherin_tail
|
807 |
930 |
8.1e-38 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000066149
|
SMART Domains |
Protein: ENSMUSP00000067728 Gene: ENSMUSG00000103897
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
29 |
N/A |
INTRINSIC |
CA
|
31 |
131 |
4.84e-2 |
SMART |
CA
|
155 |
240 |
1.48e-22 |
SMART |
CA
|
264 |
345 |
1.14e-23 |
SMART |
CA
|
369 |
450 |
9.44e-21 |
SMART |
CA
|
474 |
560 |
1.03e-26 |
SMART |
CA
|
591 |
669 |
3.64e-13 |
SMART |
Pfam:Cadherin_C_2
|
688 |
772 |
3e-25 |
PFAM |
Pfam:Cadherin_tail
|
809 |
932 |
8.1e-38 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000073447
|
SMART Domains |
Protein: ENSMUSP00000073150 Gene: ENSMUSG00000104346
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
CA
|
42 |
128 |
2.15e-2 |
SMART |
CA
|
152 |
237 |
4.8e-13 |
SMART |
CA
|
261 |
342 |
9.36e-25 |
SMART |
CA
|
366 |
447 |
6.62e-25 |
SMART |
CA
|
471 |
557 |
6.72e-26 |
SMART |
CA
|
588 |
666 |
2.15e-15 |
SMART |
Pfam:Cadherin_C_2
|
685 |
768 |
4.8e-24 |
PFAM |
Pfam:Cadherin_tail
|
805 |
928 |
8.1e-38 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000091935
AA Change: V242D
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000089555 Gene: ENSMUSG00000102440 AA Change: V242D
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
29 |
N/A |
INTRINSIC |
CA
|
32 |
132 |
8.37e-3 |
SMART |
CA
|
156 |
241 |
5.51e-22 |
SMART |
CA
|
265 |
346 |
8.27e-26 |
SMART |
CA
|
370 |
451 |
1.4e-23 |
SMART |
CA
|
475 |
561 |
2.97e-27 |
SMART |
CA
|
592 |
670 |
1.18e-12 |
SMART |
Pfam:Cadherin_C_2
|
688 |
772 |
3.9e-24 |
PFAM |
Pfam:Cadherin_tail
|
809 |
932 |
8.1e-38 |
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: ENSMUST00000192511
|
SMART Domains |
Protein: ENSMUSP00000141704 Gene: ENSMUSG00000103472
Domain | Start | End | E-Value | Type |
CA
|
47 |
133 |
1.57e-2 |
SMART |
CA
|
157 |
242 |
3.24e-19 |
SMART |
CA
|
266 |
347 |
3.21e-23 |
SMART |
CA
|
371 |
452 |
9.08e-23 |
SMART |
CA
|
476 |
562 |
1.32e-24 |
SMART |
CA
|
593 |
671 |
3.5e-15 |
SMART |
transmembrane domain
|
694 |
716 |
N/A |
INTRINSIC |
low complexity region
|
916 |
935 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000192535
|
SMART Domains |
Protein: ENSMUSP00000142010 Gene: ENSMUSG00000103749
Domain | Start | End | E-Value | Type |
low complexity region
|
17 |
25 |
N/A |
INTRINSIC |
CA
|
56 |
131 |
8e-3 |
SMART |
CA
|
155 |
240 |
2.49e-20 |
SMART |
CA
|
264 |
341 |
4.97e-29 |
SMART |
CA
|
365 |
446 |
1.09e-25 |
SMART |
CA
|
470 |
556 |
1.75e-24 |
SMART |
CA
|
587 |
668 |
9.18e-10 |
SMART |
transmembrane domain
|
687 |
709 |
N/A |
INTRINSIC |
low complexity region
|
907 |
926 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000192931
|
SMART Domains |
Protein: ENSMUSP00000141348 Gene: ENSMUSG00000103037
Domain | Start | End | E-Value | Type |
CA
|
36 |
119 |
8e-3 |
SMART |
CA
|
143 |
228 |
1.34e-20 |
SMART |
CA
|
252 |
333 |
1.52e-24 |
SMART |
CA
|
357 |
438 |
9.22e-24 |
SMART |
CA
|
462 |
548 |
1.24e-24 |
SMART |
CA
|
579 |
660 |
1.3e-9 |
SMART |
transmembrane domain
|
679 |
701 |
N/A |
INTRINSIC |
low complexity region
|
899 |
918 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000193006
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000193414
|
SMART Domains |
Protein: ENSMUSP00000141893 Gene: ENSMUSG00000103567
Domain | Start | End | E-Value | Type |
CA
|
45 |
131 |
2.45e-1 |
SMART |
CA
|
155 |
240 |
1.05e-18 |
SMART |
CA
|
264 |
345 |
6.52e-24 |
SMART |
CA
|
369 |
450 |
5.99e-23 |
SMART |
CA
|
474 |
560 |
6.99e-24 |
SMART |
CA
|
591 |
669 |
5.31e-15 |
SMART |
transmembrane domain
|
692 |
714 |
N/A |
INTRINSIC |
low complexity region
|
913 |
932 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000193869
|
SMART Domains |
Protein: ENSMUSP00000141482 Gene: ENSMUSG00000103332
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
28 |
N/A |
INTRINSIC |
CA
|
45 |
131 |
1.64e-2 |
SMART |
CA
|
155 |
240 |
6.42e-23 |
SMART |
CA
|
264 |
345 |
1.76e-20 |
SMART |
CA
|
369 |
450 |
2.27e-23 |
SMART |
CA
|
474 |
560 |
1.5e-23 |
SMART |
CA
|
591 |
669 |
1.17e-16 |
SMART |
transmembrane domain
|
692 |
714 |
N/A |
INTRINSIC |
low complexity region
|
912 |
931 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000193984
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000194190
|
SMART Domains |
Protein: ENSMUSP00000142062 Gene: ENSMUSG00000103144
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
28 |
N/A |
INTRINSIC |
CA
|
31 |
131 |
3.16e-2 |
SMART |
CA
|
155 |
240 |
5.39e-16 |
SMART |
CA
|
264 |
345 |
6.72e-26 |
SMART |
CA
|
369 |
450 |
1.32e-24 |
SMART |
CA
|
474 |
560 |
4.17e-22 |
SMART |
CA
|
591 |
669 |
4.48e-13 |
SMART |
transmembrane domain
|
692 |
714 |
N/A |
INTRINSIC |
low complexity region
|
912 |
931 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000194418
|
SMART Domains |
Protein: ENSMUSP00000142140 Gene: ENSMUSG00000103677
Domain | Start | End | E-Value | Type |
CA
|
44 |
130 |
1.64e-2 |
SMART |
CA
|
154 |
239 |
3.93e-18 |
SMART |
CA
|
263 |
344 |
5.22e-23 |
SMART |
CA
|
368 |
449 |
5.02e-25 |
SMART |
CA
|
473 |
559 |
2.07e-26 |
SMART |
CA
|
590 |
668 |
6.84e-18 |
SMART |
transmembrane domain
|
690 |
712 |
N/A |
INTRINSIC |
low complexity region
|
911 |
930 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000194814
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000195112
|
SMART Domains |
Protein: ENSMUSP00000141449 Gene: ENSMUSG00000102748
Domain | Start | End | E-Value | Type |
CA
|
24 |
130 |
8.18e-3 |
SMART |
CA
|
154 |
239 |
1.39e-18 |
SMART |
CA
|
263 |
344 |
7.91e-23 |
SMART |
CA
|
368 |
449 |
2.27e-23 |
SMART |
CA
|
473 |
559 |
1.24e-24 |
SMART |
CA
|
590 |
671 |
1.3e-9 |
SMART |
transmembrane domain
|
690 |
712 |
N/A |
INTRINSIC |
low complexity region
|
909 |
928 |
N/A |
INTRINSIC |
|
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 |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000195823
|
SMART Domains |
Protein: ENSMUSP00000141803 Gene: ENSMUSG00000103793
Domain | Start | End | E-Value | Type |
low complexity region
|
13 |
24 |
N/A |
INTRINSIC |
CA
|
45 |
131 |
2.41e-2 |
SMART |
CA
|
155 |
240 |
5.77e-16 |
SMART |
CA
|
264 |
345 |
1.1e-21 |
SMART |
CA
|
369 |
450 |
2.75e-22 |
SMART |
low complexity region
|
453 |
462 |
N/A |
INTRINSIC |
CA
|
474 |
560 |
9.22e-24 |
SMART |
CA
|
591 |
669 |
2.4e-13 |
SMART |
transmembrane domain
|
692 |
714 |
N/A |
INTRINSIC |
low complexity region
|
913 |
932 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000195363
|
SMART Domains |
Protein: ENSMUSP00000142227 Gene: ENSMUSG00000103585
Domain | Start | End | E-Value | Type |
low complexity region
|
17 |
25 |
N/A |
INTRINSIC |
CA
|
56 |
131 |
1.47e-2 |
SMART |
CA
|
155 |
240 |
1.23e-19 |
SMART |
CA
|
264 |
343 |
5.54e-27 |
SMART |
CA
|
367 |
448 |
5.09e-26 |
SMART |
CA
|
472 |
558 |
1.98e-23 |
SMART |
CA
|
589 |
670 |
1.3e-9 |
SMART |
transmembrane domain
|
689 |
711 |
N/A |
INTRINSIC |
low complexity region
|
893 |
912 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.0%
- 20x: 94.1%
|
Validation Efficiency |
98% (60/61) |
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 gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aaed1 |
T |
C |
13: 64,309,098 |
I104V |
probably damaging |
Het |
Abi2 |
A |
G |
1: 60,453,754 |
Q328R |
probably damaging |
Het |
Agr3 |
C |
A |
12: 35,947,513 |
|
probably benign |
Het |
Brca2 |
T |
A |
5: 150,536,704 |
S481R |
probably damaging |
Het |
Cabin1 |
T |
G |
10: 75,745,259 |
Q411P |
probably damaging |
Het |
Calr3 |
A |
G |
8: 72,443,620 |
Y22H |
probably damaging |
Het |
Caprin1 |
T |
A |
2: 103,796,766 |
I59F |
probably damaging |
Het |
Cdk5rap1 |
T |
C |
2: 154,348,716 |
T442A |
probably damaging |
Het |
Chn2 |
T |
C |
6: 54,269,426 |
|
probably benign |
Het |
Cic |
C |
A |
7: 25,272,346 |
R501S |
possibly damaging |
Het |
Coch |
A |
G |
12: 51,601,812 |
|
probably null |
Het |
Defa25 |
G |
A |
8: 21,084,490 |
V17I |
probably null |
Het |
Dglucy |
T |
C |
12: 100,838,700 |
|
probably null |
Het |
Dtx1 |
T |
G |
5: 120,681,286 |
T616P |
possibly damaging |
Het |
Eef1g |
T |
C |
19: 8,969,977 |
L171P |
probably benign |
Het |
Fam135a |
A |
G |
1: 24,030,394 |
S465P |
probably damaging |
Het |
Gm14025 |
A |
G |
2: 129,039,601 |
L135P |
probably damaging |
Het |
Gm14412 |
A |
T |
2: 177,314,685 |
C472* |
probably null |
Het |
Gm7104 |
T |
C |
12: 88,286,042 |
|
noncoding transcript |
Het |
Got2 |
A |
G |
8: 95,888,230 |
S26P |
probably benign |
Het |
H2-M11 |
A |
G |
17: 36,549,231 |
I329M |
probably damaging |
Het |
Hmcn2 |
T |
A |
2: 31,382,394 |
D1295E |
possibly damaging |
Het |
Hoxd12 |
G |
T |
2: 74,675,427 |
R114L |
probably damaging |
Het |
Ilkap |
A |
C |
1: 91,387,250 |
D124E |
probably damaging |
Het |
Med6 |
T |
C |
12: 81,581,851 |
Y88C |
probably damaging |
Het |
Mep1a |
A |
T |
17: 43,475,041 |
L719* |
probably null |
Het |
Mmp23 |
T |
C |
4: 155,652,023 |
Y187C |
probably damaging |
Het |
Myo1g |
A |
G |
11: 6,520,760 |
M32T |
possibly damaging |
Het |
Ncstn |
T |
C |
1: 172,067,494 |
E614G |
probably benign |
Het |
Nr2c2 |
C |
T |
6: 92,163,138 |
R464W |
probably damaging |
Het |
Olfr1309 |
G |
A |
2: 111,983,297 |
T259M |
possibly damaging |
Het |
Otub2 |
T |
A |
12: 103,392,826 |
L58* |
probably null |
Het |
Pcdhga12 |
G |
A |
18: 37,767,629 |
V505I |
probably benign |
Het |
Pex1 |
C |
T |
5: 3,626,084 |
L891F |
probably damaging |
Het |
Pgm1 |
C |
T |
5: 64,112,061 |
T497I |
probably benign |
Het |
Pikfyve |
T |
C |
1: 65,196,681 |
F171L |
probably damaging |
Het |
Pilrb1 |
T |
G |
5: 137,857,392 |
K79T |
probably benign |
Het |
Pin1 |
C |
T |
9: 20,655,364 |
R21W |
probably damaging |
Het |
Ptprq |
A |
G |
10: 107,686,392 |
|
probably benign |
Het |
Rad17 |
G |
A |
13: 100,622,863 |
A552V |
possibly damaging |
Het |
Rbbp8 |
A |
G |
18: 11,718,868 |
T249A |
probably benign |
Het |
Rtkn |
A |
T |
6: 83,135,976 |
I10F |
probably benign |
Het |
Scube2 |
T |
A |
7: 109,857,590 |
I103F |
possibly damaging |
Het |
Sec23b |
A |
G |
2: 144,581,973 |
H514R |
probably benign |
Het |
Serbp1 |
T |
A |
6: 67,272,220 |
D223E |
probably benign |
Het |
Slc14a1 |
C |
A |
18: 78,111,392 |
V260L |
probably benign |
Het |
Slc22a23 |
A |
G |
13: 34,183,126 |
I633T |
probably damaging |
Het |
Stk19 |
A |
T |
17: 34,824,747 |
|
probably benign |
Het |
Svs2 |
T |
C |
2: 164,237,127 |
M287V |
probably benign |
Het |
Syne3 |
T |
A |
12: 104,958,066 |
Q358L |
probably damaging |
Het |
Synj1 |
A |
G |
16: 91,010,096 |
F58L |
possibly damaging |
Het |
Tg |
T |
C |
15: 66,674,023 |
V198A |
probably damaging |
Het |
Tle4 |
A |
T |
19: 14,597,388 |
Y9N |
probably damaging |
Het |
Tmem57 |
A |
G |
4: 134,804,481 |
Y626H |
probably damaging |
Het |
Tmx3 |
G |
A |
18: 90,524,335 |
A186T |
possibly damaging |
Het |
Traf3 |
G |
A |
12: 111,255,245 |
S280N |
possibly damaging |
Het |
Trmt13 |
A |
G |
3: 116,581,518 |
F447S |
probably damaging |
Het |
Trp53bp1 |
T |
A |
2: 121,228,626 |
H918L |
probably damaging |
Het |
Ush2a |
T |
G |
1: 188,728,504 |
V2654G |
probably benign |
Het |
Vmn2r25 |
A |
G |
6: 123,840,098 |
Y175H |
probably damaging |
Het |
Zfp335 |
T |
C |
2: 164,892,189 |
D1330G |
probably damaging |
Het |
|
Other mutations in Pcdhga9 |
|
Predicted Primers |
|
Posted On |
2017-04-14 |