Incidental Mutation 'R4515:Pcdhac1'
| ID |
332888 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Pcdhac1
|
| Ensembl Gene |
ENSMUSG00000103255 |
| Gene Name |
protocadherin alpha subfamily C, 1 |
| Synonyms |
CNRc1 |
| MMRRC Submission |
041589-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R4515 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
18 |
| Chromosomal Location |
37090013-37187657 bp(+) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 37091379 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Asparagine
at position 415
(I415N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000007584
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000007584]
[ENSMUST00000047614]
[ENSMUST00000070797]
[ENSMUST00000115657]
[ENSMUST00000115658]
[ENSMUST00000115659]
[ENSMUST00000115661]
[ENSMUST00000115662]
[ENSMUST00000192168]
[ENSMUST00000192295]
[ENSMUST00000192447]
[ENSMUST00000195590]
[ENSMUST00000193777]
[ENSMUST00000193389]
[ENSMUST00000193839]
[ENSMUST00000194751]
[ENSMUST00000194544]
[ENSMUST00000194038]
[ENSMUST00000192503]
[ENSMUST00000192512]
[ENSMUST00000192631]
|
| AlphaFold |
Q91Y10 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000007584
AA Change: I415N
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000007584
Gene: ENSMUSG00000103255
AA Change: I415N
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
|
CA
|
45 |
122 |
3.59e-1 |
SMART |
|
CA
|
146 |
231 |
6.32e-22 |
SMART |
|
CA
|
255 |
338 |
5.18e-18 |
SMART |
|
CA
|
362 |
443 |
9.73e-23 |
SMART |
|
CA
|
467 |
554 |
4.24e-23 |
SMART |
|
CA
|
584 |
662 |
1.11e-8 |
SMART |
|
Pfam:Cadherin_C_2
|
682 |
773 |
1.1e-12 |
PFAM |
|
Pfam:Cadherin_tail
|
813 |
947 |
5.4e-58 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000047614
|
| SMART Domains |
Protein: ENSMUSP00000047609
Gene: ENSMUSG00000103310
| Domain | Start | End | E-Value | Type |
|---|
|
CA
|
19 |
131 |
3.78e-2 |
SMART |
|
CA
|
155 |
240 |
3.26e-24 |
SMART |
|
CA
|
264 |
348 |
6.37e-27 |
SMART |
|
CA
|
372 |
453 |
3.31e-25 |
SMART |
|
CA
|
477 |
563 |
6.18e-25 |
SMART |
|
CA
|
594 |
676 |
5.6e-14 |
SMART |
|
low complexity region
|
679 |
696 |
N/A |
INTRINSIC |
|
transmembrane domain
|
699 |
721 |
N/A |
INTRINSIC |
|
Pfam:Cadherin_tail
|
799 |
933 |
5.3e-58 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000070797
|
| SMART Domains |
Protein: ENSMUSP00000068828
Gene: ENSMUSG00000103442
| Domain | Start | End | E-Value | Type |
|---|
|
CA
|
22 |
132 |
3.09e-2 |
SMART |
|
CA
|
156 |
241 |
6.14e-20 |
SMART |
|
CA
|
265 |
349 |
3.92e-27 |
SMART |
|
CA
|
373 |
454 |
4.94e-24 |
SMART |
|
CA
|
478 |
564 |
1e-24 |
SMART |
|
CA
|
592 |
672 |
4.55e-14 |
SMART |
|
transmembrane domain
|
694 |
716 |
N/A |
INTRINSIC |
|
Pfam:Cadherin_tail
|
797 |
931 |
5.3e-58 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000115657
|
| SMART Domains |
Protein: ENSMUSP00000111321
Gene: ENSMUSG00000102206
| Domain | Start | End | E-Value | Type |
|---|
|
CA
|
21 |
131 |
2.95e-2 |
SMART |
|
CA
|
155 |
240 |
7.44e-19 |
SMART |
|
CA
|
264 |
347 |
5.63e-28 |
SMART |
|
CA
|
371 |
452 |
3.14e-26 |
SMART |
|
CA
|
476 |
562 |
1.42e-24 |
SMART |
|
CA
|
593 |
675 |
1.03e-12 |
SMART |
|
transmembrane domain
|
697 |
719 |
N/A |
INTRINSIC |
|
low complexity region
|
783 |
794 |
N/A |
INTRINSIC |
|
low complexity region
|
918 |
942 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000115658
|
| SMART Domains |
Protein: ENSMUSP00000111322
Gene: ENSMUSG00000007440
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
15 |
21 |
N/A |
INTRINSIC |
|
CA
|
46 |
132 |
6.34e-2 |
SMART |
|
CA
|
156 |
241 |
4.65e-20 |
SMART |
|
CA
|
265 |
349 |
1.25e-25 |
SMART |
|
CA
|
373 |
454 |
9.22e-24 |
SMART |
|
CA
|
478 |
564 |
4.3e-24 |
SMART |
|
CA
|
595 |
678 |
5.07e-12 |
SMART |
|
low complexity region
|
706 |
721 |
N/A |
INTRINSIC |
|
Pfam:Cadherin_tail
|
795 |
929 |
5.3e-58 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000115659
|
| SMART Domains |
Protein: ENSMUSP00000111323
Gene: ENSMUSG00000103770
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
44 |
51 |
N/A |
INTRINSIC |
|
CA
|
75 |
161 |
2.46e-2 |
SMART |
|
CA
|
185 |
270 |
8.1e-20 |
SMART |
|
CA
|
294 |
378 |
1.69e-22 |
SMART |
|
CA
|
402 |
483 |
1.52e-24 |
SMART |
|
CA
|
507 |
593 |
5.68e-24 |
SMART |
|
CA
|
624 |
705 |
6.69e-12 |
SMART |
|
transmembrane domain
|
727 |
749 |
N/A |
INTRINSIC |
|
Pfam:Cadherin_tail
|
828 |
962 |
5.6e-58 |
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: ENSMUST00000115662
|
| SMART Domains |
Protein: ENSMUSP00000111326
Gene: ENSMUSG00000104148
| Domain | Start | End | E-Value | Type |
|---|
|
CA
|
45 |
131 |
6.34e-2 |
SMART |
|
CA
|
155 |
240 |
2.98e-18 |
SMART |
|
CA
|
264 |
348 |
2.17e-29 |
SMART |
|
CA
|
372 |
453 |
2.84e-24 |
SMART |
|
CA
|
477 |
563 |
5.02e-25 |
SMART |
|
CA
|
594 |
675 |
8.16e-16 |
SMART |
|
transmembrane domain
|
695 |
717 |
N/A |
INTRINSIC |
|
low complexity region
|
916 |
940 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000192168
|
| SMART Domains |
Protein: ENSMUSP00000142293
Gene: ENSMUSG00000103092
| Domain | Start | End | E-Value | Type |
|---|
|
CA
|
21 |
131 |
2.2e-2 |
SMART |
|
CA
|
155 |
240 |
2.05e-21 |
SMART |
|
CA
|
264 |
348 |
8.81e-21 |
SMART |
|
CA
|
372 |
453 |
2.01e-24 |
SMART |
|
CA
|
477 |
563 |
1.42e-24 |
SMART |
|
CA
|
591 |
673 |
1.63e-15 |
SMART |
|
transmembrane domain
|
693 |
715 |
N/A |
INTRINSIC |
|
low complexity region
|
902 |
926 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000192295
|
| SMART Domains |
Protein: ENSMUSP00000142103
Gene: ENSMUSG00000104252
| 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 |
568 |
5.38e-1 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000192447
|
| SMART Domains |
Protein: ENSMUSP00000142270
Gene: ENSMUSG00000102206
| Domain | Start | End | E-Value | Type |
|---|
|
CA
|
21 |
131 |
1.5e-4 |
SMART |
|
CA
|
155 |
240 |
3.6e-21 |
SMART |
|
CA
|
264 |
347 |
2.8e-30 |
SMART |
|
CA
|
371 |
452 |
1.5e-28 |
SMART |
|
CA
|
476 |
562 |
6.8e-27 |
SMART |
|
CA
|
593 |
675 |
4.9e-15 |
SMART |
|
transmembrane domain
|
697 |
719 |
N/A |
INTRINSIC |
|
low complexity region
|
783 |
794 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000194691
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000195590
|
| SMART Domains |
Protein: ENSMUSP00000141355
Gene: ENSMUSG00000104148
| Domain | Start | End | E-Value | Type |
|---|
|
CA
|
45 |
131 |
6.34e-2 |
SMART |
|
CA
|
155 |
240 |
2.98e-18 |
SMART |
|
CA
|
264 |
348 |
2.17e-29 |
SMART |
|
CA
|
372 |
453 |
2.84e-24 |
SMART |
|
CA
|
477 |
563 |
5.02e-25 |
SMART |
|
CA
|
594 |
675 |
8.16e-16 |
SMART |
|
transmembrane domain
|
695 |
717 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000193777
|
| SMART Domains |
Protein: ENSMUSP00000141587
Gene: ENSMUSG00000103707
| Domain | Start | End | E-Value | Type |
|---|
|
CA
|
21 |
131 |
5.67e-2 |
SMART |
|
CA
|
155 |
240 |
4.72e-21 |
SMART |
|
CA
|
264 |
348 |
1.9e-25 |
SMART |
|
CA
|
372 |
453 |
3.31e-25 |
SMART |
|
CA
|
477 |
563 |
1.42e-24 |
SMART |
|
CA
|
594 |
676 |
5.91e-13 |
SMART |
|
low complexity region
|
914 |
938 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000193389
|
| SMART Domains |
Protein: ENSMUSP00000141459
Gene: ENSMUSG00000103707
| Domain | Start | End | E-Value | Type |
|---|
|
CA
|
21 |
131 |
5.67e-2 |
SMART |
|
CA
|
155 |
240 |
4.72e-21 |
SMART |
|
CA
|
264 |
348 |
1.9e-25 |
SMART |
|
CA
|
372 |
453 |
3.31e-25 |
SMART |
|
CA
|
477 |
563 |
1.42e-24 |
SMART |
|
CA
|
594 |
676 |
5.91e-13 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000193839
|
| SMART Domains |
Protein: ENSMUSP00000142308
Gene: ENSMUSG00000103442
| Domain | Start | End | E-Value | Type |
|---|
|
CA
|
22 |
132 |
3.09e-2 |
SMART |
|
CA
|
156 |
241 |
6.14e-20 |
SMART |
|
CA
|
265 |
349 |
3.92e-27 |
SMART |
|
CA
|
373 |
454 |
4.94e-24 |
SMART |
|
CA
|
478 |
564 |
1e-24 |
SMART |
|
CA
|
592 |
672 |
4.55e-14 |
SMART |
|
transmembrane domain
|
694 |
716 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000194751
|
| SMART Domains |
Protein: ENSMUSP00000142285
Gene: ENSMUSG00000103707
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
15 |
21 |
N/A |
INTRINSIC |
|
Pfam:Cadherin_2
|
29 |
112 |
4.5e-32 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000193984
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000193856
|
| 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: ENSMUST00000194038
|
| SMART Domains |
Protein: ENSMUSP00000142159
Gene: ENSMUSG00000103800
| Domain | Start | End | E-Value | Type |
|---|
|
CA
|
20 |
131 |
6.34e-2 |
SMART |
|
CA
|
155 |
240 |
4.27e-19 |
SMART |
|
CA
|
264 |
348 |
2.04e-25 |
SMART |
|
CA
|
372 |
453 |
2.84e-24 |
SMART |
|
CA
|
477 |
563 |
9.88e-24 |
SMART |
|
CA
|
594 |
676 |
8.62e-15 |
SMART |
|
transmembrane domain
|
699 |
721 |
N/A |
INTRINSIC |
|
low complexity region
|
914 |
938 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000192503
|
| SMART Domains |
Protein: ENSMUSP00000141989
Gene: ENSMUSG00000102312
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
11 |
17 |
N/A |
INTRINSIC |
|
CA
|
42 |
128 |
3.78e-2 |
SMART |
|
CA
|
152 |
237 |
8.94e-22 |
SMART |
|
CA
|
261 |
345 |
3.74e-24 |
SMART |
|
CA
|
369 |
450 |
1.09e-25 |
SMART |
|
CA
|
474 |
560 |
1.42e-24 |
SMART |
|
CA
|
588 |
670 |
2.96e-13 |
SMART |
|
transmembrane domain
|
692 |
714 |
N/A |
INTRINSIC |
|
low complexity region
|
910 |
934 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000192512
|
| SMART Domains |
Protein: ENSMUSP00000141408
Gene: ENSMUSG00000104252
| 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 |
|
low complexity region
|
915 |
939 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000192631
|
| SMART Domains |
Protein: ENSMUSP00000142156
Gene: ENSMUSG00000104318
| Domain | Start | End | E-Value | Type |
|---|
|
CA
|
21 |
131 |
2.58e-2 |
SMART |
|
CA
|
155 |
240 |
4.27e-19 |
SMART |
|
CA
|
264 |
348 |
1.42e-24 |
SMART |
|
CA
|
372 |
453 |
9.36e-25 |
SMART |
|
CA
|
477 |
563 |
1.42e-24 |
SMART |
|
CA
|
594 |
671 |
4.03e-6 |
SMART |
|
transmembrane domain
|
696 |
718 |
N/A |
INTRINSIC |
|
low complexity region
|
905 |
929 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.5644 |
| Coding Region Coverage |
- 1x: 99.5%
- 3x: 98.7%
- 10x: 97.1%
- 20x: 94.6%
|
| Validation Efficiency |
96% (65/68) |
| 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 alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been observed and additional variants have been suggested but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a reporter allele are viable and fertile with no apparent gross phenotype. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 59 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A430033K04Rik |
G |
T |
5: 138,647,744 (GRCm38) |
K630N |
probably damaging |
Het |
| Acss2 |
C |
A |
2: 155,556,363 (GRCm38) |
L335I |
probably benign |
Het |
| Alg6 |
A |
T |
4: 99,752,786 (GRCm38) |
|
probably benign |
Het |
| Atp8b3 |
C |
T |
10: 80,523,847 (GRCm38) |
M984I |
probably benign |
Het |
| Bsn |
G |
T |
9: 108,104,078 (GRCm38) |
|
probably null |
Het |
| Ccdc88a |
T |
C |
11: 29,482,651 (GRCm38) |
I1219T |
probably benign |
Het |
| Cdhr4 |
G |
A |
9: 107,992,951 (GRCm38) |
E52K |
probably benign |
Het |
| Ces1a |
T |
A |
8: 93,020,904 (GRCm38) |
N500Y |
probably damaging |
Het |
| Chd3 |
G |
T |
11: 69,349,877 (GRCm38) |
R1579S |
probably benign |
Het |
| Chrnb3 |
T |
C |
8: 27,385,090 (GRCm38) |
L39P |
probably damaging |
Het |
| Ckm |
A |
G |
7: 19,420,284 (GRCm38) |
K319E |
probably damaging |
Het |
| Cnot6 |
C |
T |
11: 49,702,536 (GRCm38) |
|
probably null |
Het |
| Copg1 |
A |
G |
6: 87,907,546 (GRCm38) |
|
probably benign |
Het |
| Dbn1 |
A |
T |
13: 55,476,229 (GRCm38) |
I350N |
possibly damaging |
Het |
| Dnah2 |
A |
G |
11: 69,465,631 (GRCm38) |
S2135P |
possibly damaging |
Het |
| Dsg2 |
C |
A |
18: 20,601,387 (GRCm38) |
D807E |
probably benign |
Het |
| Fam122c |
G |
A |
X: 53,293,499 (GRCm38) |
R94H |
possibly damaging |
Het |
| Foxi1 |
A |
G |
11: 34,207,972 (GRCm38) |
F18L |
probably damaging |
Het |
| Galnt3 |
C |
A |
2: 66,093,610 (GRCm38) |
R438L |
probably damaging |
Het |
| Glod4 |
T |
A |
11: 76,243,571 (GRCm38) |
D25V |
probably damaging |
Het |
| Gm11492 |
A |
G |
11: 87,568,057 (GRCm38) |
H419R |
probably benign |
Het |
| Gm9008 |
C |
T |
6: 76,496,809 (GRCm38) |
V275I |
probably benign |
Het |
| Golga4 |
T |
A |
9: 118,559,008 (GRCm38) |
S1733T |
probably benign |
Het |
| H2-M10.3 |
C |
T |
17: 36,367,830 (GRCm38) |
|
probably null |
Het |
| Hemgn |
T |
C |
4: 46,396,477 (GRCm38) |
E253G |
probably damaging |
Het |
| Itsn1 |
G |
A |
16: 91,899,649 (GRCm38) |
V47M |
probably damaging |
Het |
| Kif5b |
A |
G |
18: 6,208,257 (GRCm38) |
V947A |
probably benign |
Het |
| Kif9 |
A |
G |
9: 110,489,867 (GRCm38) |
H133R |
probably benign |
Het |
| Lce1l |
T |
C |
3: 92,850,474 (GRCm38) |
T26A |
unknown |
Het |
| Macf1 |
T |
C |
4: 123,493,988 (GRCm38) |
E1172G |
probably damaging |
Het |
| Nkx3-2 |
C |
T |
5: 41,763,938 (GRCm38) |
V3M |
probably damaging |
Het |
| Nr2e1 |
G |
A |
10: 42,578,191 (GRCm38) |
T49I |
probably benign |
Het |
| Oc90 |
A |
G |
15: 65,892,393 (GRCm38) |
L138P |
probably damaging |
Het |
| Olfr834 |
T |
G |
9: 18,987,982 (GRCm38) |
|
probably null |
Het |
| Olfr954 |
C |
T |
9: 39,462,231 (GRCm38) |
R264* |
probably null |
Het |
| Orc4 |
G |
A |
2: 48,937,489 (GRCm38) |
P31S |
probably benign |
Het |
| Paqr3 |
T |
A |
5: 97,103,361 (GRCm38) |
N168I |
possibly damaging |
Het |
| Pdik1l |
T |
C |
4: 134,278,896 (GRCm38) |
N75S |
probably damaging |
Het |
| Pik3r4 |
A |
G |
9: 105,672,725 (GRCm38) |
H1005R |
probably damaging |
Het |
| Plekhn1 |
T |
C |
4: 156,225,531 (GRCm38) |
S109G |
probably damaging |
Het |
| Prkch |
A |
G |
12: 73,702,838 (GRCm38) |
T402A |
possibly damaging |
Het |
| Ptger4 |
C |
A |
15: 5,242,379 (GRCm38) |
R253L |
probably damaging |
Het |
| Rabac1 |
A |
T |
7: 24,970,160 (GRCm38) |
Y173* |
probably null |
Het |
| Rapsn |
G |
A |
2: 91,043,212 (GRCm38) |
V288M |
possibly damaging |
Het |
| Sec31a |
A |
G |
5: 100,365,958 (GRCm38) |
S993P |
probably damaging |
Het |
| Serpina9 |
T |
A |
12: 104,001,294 (GRCm38) |
M281L |
probably benign |
Het |
| Serpine1 |
G |
A |
5: 137,069,468 (GRCm38) |
A117V |
probably damaging |
Het |
| Sh3tc2 |
A |
G |
18: 61,987,693 (GRCm38) |
|
probably null |
Het |
| Sipa1l2 |
T |
C |
8: 125,492,226 (GRCm38) |
D124G |
probably benign |
Het |
| Slc6a12 |
T |
A |
6: 121,353,530 (GRCm38) |
|
probably null |
Het |
| Stk11 |
A |
G |
10: 80,116,601 (GRCm38) |
|
probably benign |
Het |
| Tcaf3 |
A |
G |
6: 42,589,996 (GRCm38) |
Y720H |
probably damaging |
Het |
| Tmem38a |
C |
T |
8: 72,572,161 (GRCm38) |
P20S |
possibly damaging |
Het |
| Tmprss11a |
C |
T |
5: 86,420,196 (GRCm38) |
R224K |
probably damaging |
Het |
| Tmprss15 |
C |
T |
16: 78,957,356 (GRCm38) |
S988N |
probably benign |
Het |
| Txn2 |
A |
T |
15: 77,915,443 (GRCm38) |
|
probably null |
Het |
| Ugt1a10 |
T |
A |
1: 88,056,197 (GRCm38) |
V239E |
probably damaging |
Het |
| Vmn2r102 |
A |
G |
17: 19,681,213 (GRCm38) |
Y534C |
probably damaging |
Het |
| Vmn2r78 |
A |
T |
7: 86,954,258 (GRCm38) |
D548V |
probably damaging |
Het |
|
| Other mutations in Pcdhac1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
G1patch:Pcdhac1
|
UTSW |
18 |
37,090,328 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2418:Pcdhac1
|
UTSW |
18 |
37,091,328 (GRCm38) |
missense |
probably benign |
0.12 |
|
R2419:Pcdhac1
|
UTSW |
18 |
37,091,328 (GRCm38) |
missense |
probably benign |
0.12 |
|
R3876:Pcdhac1
|
UTSW |
18 |
37,091,892 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4234:Pcdhac1
|
UTSW |
18 |
37,090,958 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4722:Pcdhac1
|
UTSW |
18 |
37,091,880 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4804:Pcdhac1
|
UTSW |
18 |
37,091,178 (GRCm38) |
missense |
possibly damaging |
0.67 |
|
R4996:Pcdhac1
|
UTSW |
18 |
37,092,527 (GRCm38) |
nonsense |
probably null |
|
|
R5093:Pcdhac1
|
UTSW |
18 |
37,090,542 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5111:Pcdhac1
|
UTSW |
18 |
37,091,505 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5116:Pcdhac1
|
UTSW |
18 |
37,091,447 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5203:Pcdhac1
|
UTSW |
18 |
37,091,190 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5659:Pcdhac1
|
UTSW |
18 |
37,092,417 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5679:Pcdhac1
|
UTSW |
18 |
37,092,477 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5765:Pcdhac1
|
UTSW |
18 |
37,090,319 (GRCm38) |
nonsense |
probably null |
|
|
R6536:Pcdhac1
|
UTSW |
18 |
37,090,314 (GRCm38) |
missense |
probably benign |
0.00 |
|
R6725:Pcdhac1
|
UTSW |
18 |
37,090,328 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6764:Pcdhac1
|
UTSW |
18 |
37,090,679 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6772:Pcdhac1
|
UTSW |
18 |
37,090,236 (GRCm38) |
missense |
probably benign |
0.05 |
|
R6870:Pcdhac1
|
UTSW |
18 |
37,092,087 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7426:Pcdhac1
|
UTSW |
18 |
37,092,497 (GRCm38) |
missense |
probably benign |
|
|
R7809:Pcdhac1
|
UTSW |
18 |
37,090,956 (GRCm38) |
missense |
possibly damaging |
0.55 |
|
R8088:Pcdhac1
|
UTSW |
18 |
37,091,754 (GRCm38) |
missense |
possibly damaging |
0.74 |
|
R8201:Pcdhac1
|
UTSW |
18 |
37,090,839 (GRCm38) |
missense |
probably benign |
0.16 |
|
R8400:Pcdhac1
|
UTSW |
18 |
37,092,400 (GRCm38) |
nonsense |
probably null |
|
|
R8787:Pcdhac1
|
UTSW |
18 |
37,091,889 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9349:Pcdhac1
|
UTSW |
18 |
37,090,968 (GRCm38) |
missense |
possibly damaging |
0.50 |
|
R9733:Pcdhac1
|
UTSW |
18 |
37,092,453 (GRCm38) |
missense |
probably benign |
|
|
Z1088:Pcdhac1
|
UTSW |
18 |
37,092,566 (GRCm38) |
missense |
probably damaging |
0.97 |
|
Z1088:Pcdhac1
|
UTSW |
18 |
37,092,190 (GRCm38) |
missense |
probably damaging |
1.00 |
|
Z1177:Pcdhac1
|
UTSW |
18 |
37,092,423 (GRCm38) |
missense |
possibly damaging |
0.90 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGATGGACTTCATGACCTTCTCC -3'
(R):5'- TGGGTCCTGAGCAAACACAC -3'
Sequencing Primer
(F):5'- AATACTCGAGGATGCAGCTCCTG -3'
(R):5'- CCGCCTAAGGAAACTCCAGGG -3'
|
| Posted On |
2015-08-18 |
Incidental Mutation