Incidental Mutation 'R8956:Adam22'
ID |
682002 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Adam22
|
Ensembl Gene |
ENSMUSG00000040537 |
Gene Name |
a disintegrin and metallopeptidase domain 22 |
Synonyms |
MDC2, 2900022I03Rik |
MMRRC Submission |
068792-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R8956 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
5 |
Chromosomal Location |
8122352-8418160 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 8142343 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Isoleucine
at position 814
(T814I)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000111046
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000046838]
[ENSMUST00000050166]
[ENSMUST00000088744]
[ENSMUST00000088761]
[ENSMUST00000115386]
[ENSMUST00000115388]
[ENSMUST00000123168]
[ENSMUST00000126384]
[ENSMUST00000130315]
[ENSMUST00000136524]
[ENSMUST00000136808]
[ENSMUST00000139048]
[ENSMUST00000139841]
[ENSMUST00000144241]
[ENSMUST00000153427]
[ENSMUST00000153889]
[ENSMUST00000154935]
[ENSMUST00000197700]
[ENSMUST00000199853]
|
AlphaFold |
Q9R1V6 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000046838
AA Change: T856I
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000049120 Gene: ENSMUSG00000040537 AA Change: T856I
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
Pfam:Pep_M12B_propep
|
44 |
186 |
7e-27 |
PFAM |
low complexity region
|
214 |
230 |
N/A |
INTRINSIC |
Pfam:Reprolysin_5
|
235 |
405 |
9.3e-9 |
PFAM |
Pfam:Reprolysin
|
237 |
436 |
1.1e-58 |
PFAM |
Pfam:Reprolysin_3
|
261 |
379 |
3e-12 |
PFAM |
DISIN
|
451 |
527 |
3.38e-31 |
SMART |
ACR
|
528 |
669 |
3.05e-58 |
SMART |
EGF
|
676 |
710 |
1.28e1 |
SMART |
transmembrane domain
|
735 |
757 |
N/A |
INTRINSIC |
low complexity region
|
789 |
808 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000050166
AA Change: T820I
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000055000 Gene: ENSMUSG00000040537 AA Change: T820I
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
Pfam:Pep_M12B_propep
|
44 |
186 |
7.6e-27 |
PFAM |
low complexity region
|
214 |
230 |
N/A |
INTRINSIC |
Pfam:Reprolysin_5
|
235 |
405 |
1.1e-8 |
PFAM |
Pfam:Reprolysin
|
237 |
436 |
1.1e-58 |
PFAM |
Pfam:Reprolysin_3
|
261 |
379 |
3.4e-12 |
PFAM |
DISIN
|
451 |
527 |
3.38e-31 |
SMART |
ACR
|
528 |
669 |
3.05e-58 |
SMART |
EGF
|
676 |
710 |
1.28e1 |
SMART |
transmembrane domain
|
735 |
757 |
N/A |
INTRINSIC |
low complexity region
|
824 |
839 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000088744
AA Change: T879I
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000086122 Gene: ENSMUSG00000040537 AA Change: T879I
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
Pfam:Pep_M12B_propep
|
41 |
186 |
4.2e-29 |
PFAM |
low complexity region
|
214 |
230 |
N/A |
INTRINSIC |
Pfam:Reprolysin_5
|
235 |
405 |
1.2e-8 |
PFAM |
Pfam:Reprolysin
|
237 |
436 |
2.9e-65 |
PFAM |
Pfam:Reprolysin_3
|
261 |
378 |
9.2e-13 |
PFAM |
DISIN
|
451 |
527 |
3.38e-31 |
SMART |
ACR
|
528 |
669 |
3.05e-58 |
SMART |
EGF
|
676 |
710 |
1.28e1 |
SMART |
transmembrane domain
|
736 |
758 |
N/A |
INTRINSIC |
low complexity region
|
785 |
800 |
N/A |
INTRINSIC |
low complexity region
|
883 |
898 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000088761
AA Change: T856I
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000086139 Gene: ENSMUSG00000040537 AA Change: T856I
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
Pfam:Pep_M12B_propep
|
44 |
186 |
8.1e-27 |
PFAM |
low complexity region
|
214 |
230 |
N/A |
INTRINSIC |
Pfam:Reprolysin_5
|
235 |
405 |
1.2e-8 |
PFAM |
Pfam:Reprolysin
|
237 |
436 |
1.1e-58 |
PFAM |
Pfam:Reprolysin_3
|
261 |
379 |
3.6e-12 |
PFAM |
DISIN
|
451 |
527 |
3.38e-31 |
SMART |
ACR
|
528 |
669 |
3.05e-58 |
SMART |
EGF
|
676 |
710 |
1.28e1 |
SMART |
transmembrane domain
|
735 |
757 |
N/A |
INTRINSIC |
low complexity region
|
789 |
808 |
N/A |
INTRINSIC |
low complexity region
|
860 |
875 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000115386
AA Change: T820I
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000111044 Gene: ENSMUSG00000040537 AA Change: T820I
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
Pfam:Pep_M12B_propep
|
44 |
186 |
3.4e-27 |
PFAM |
low complexity region
|
214 |
230 |
N/A |
INTRINSIC |
Pfam:Reprolysin_5
|
235 |
405 |
5.1e-9 |
PFAM |
Pfam:Reprolysin
|
237 |
436 |
5e-59 |
PFAM |
Pfam:Reprolysin_3
|
261 |
379 |
1.6e-12 |
PFAM |
DISIN
|
451 |
527 |
3.38e-31 |
SMART |
ACR
|
528 |
669 |
3.05e-58 |
SMART |
EGF
|
676 |
710 |
1.28e1 |
SMART |
transmembrane domain
|
735 |
757 |
N/A |
INTRINSIC |
low complexity region
|
850 |
870 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000115388
AA Change: T814I
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000111046 Gene: ENSMUSG00000040537 AA Change: T814I
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
Pfam:Pep_M12B_propep
|
44 |
186 |
8e-27 |
PFAM |
low complexity region
|
214 |
230 |
N/A |
INTRINSIC |
Pfam:Reprolysin_5
|
235 |
405 |
1.1e-8 |
PFAM |
Pfam:Reprolysin
|
237 |
436 |
1.1e-58 |
PFAM |
Pfam:Reprolysin_3
|
261 |
379 |
3.5e-12 |
PFAM |
DISIN
|
451 |
527 |
3.38e-31 |
SMART |
ACR
|
528 |
669 |
3.05e-58 |
SMART |
EGF
|
676 |
710 |
1.28e1 |
SMART |
transmembrane domain
|
735 |
757 |
N/A |
INTRINSIC |
low complexity region
|
852 |
872 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000123168
AA Change: T112I
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000122758 Gene: ENSMUSG00000040537 AA Change: T112I
Domain | Start | End | E-Value | Type |
transmembrane domain
|
27 |
49 |
N/A |
INTRINSIC |
low complexity region
|
123 |
143 |
N/A |
INTRINSIC |
|
Predicted Effect |
|
SMART Domains |
Protein: ENSMUSP00000122652 Gene: ENSMUSG00000040537 AA Change: T202I
Domain | Start | End | E-Value | Type |
Blast:ACR
|
2 |
52 |
5e-28 |
BLAST |
EGF
|
59 |
93 |
1.28e1 |
SMART |
transmembrane domain
|
118 |
140 |
N/A |
INTRINSIC |
low complexity region
|
207 |
222 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000126384
AA Change: T177I
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000118571 Gene: ENSMUSG00000040537 AA Change: T177I
Domain | Start | End | E-Value | Type |
transmembrane domain
|
27 |
49 |
N/A |
INTRINSIC |
low complexity region
|
83 |
98 |
N/A |
INTRINSIC |
low complexity region
|
181 |
196 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000130315
AA Change: T112I
PolyPhen 2
Score 0.986 (Sensitivity: 0.74; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000121156 Gene: ENSMUSG00000040537 AA Change: T112I
Domain | Start | End | E-Value | Type |
transmembrane domain
|
27 |
49 |
N/A |
INTRINSIC |
low complexity region
|
150 |
170 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000136524
AA Change: T112I
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000116422 Gene: ENSMUSG00000040537 AA Change: T112I
Domain | Start | End | E-Value | Type |
transmembrane domain
|
27 |
49 |
N/A |
INTRINSIC |
low complexity region
|
152 |
172 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000136808
AA Change: T177I
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000122426 Gene: ENSMUSG00000040537 AA Change: T177I
Domain | Start | End | E-Value | Type |
transmembrane domain
|
27 |
49 |
N/A |
INTRINSIC |
low complexity region
|
83 |
98 |
N/A |
INTRINSIC |
low complexity region
|
207 |
227 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000139048
AA Change: T148I
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000116736 Gene: ENSMUSG00000040537 AA Change: T148I
Domain | Start | End | E-Value | Type |
transmembrane domain
|
27 |
49 |
N/A |
INTRINSIC |
low complexity region
|
81 |
100 |
N/A |
INTRINSIC |
low complexity region
|
186 |
206 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000139841
AA Change: T106I
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000115775 Gene: ENSMUSG00000040537 AA Change: T106I
Domain | Start | End | E-Value | Type |
transmembrane domain
|
27 |
49 |
N/A |
INTRINSIC |
low complexity region
|
144 |
164 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000144241
AA Change: T142I
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000138353 Gene: ENSMUSG00000040537 AA Change: T142I
Domain | Start | End | E-Value | Type |
transmembrane domain
|
27 |
49 |
N/A |
INTRINSIC |
low complexity region
|
75 |
94 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000153427
AA Change: T142I
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000120995 Gene: ENSMUSG00000040537 AA Change: T142I
Domain | Start | End | E-Value | Type |
transmembrane domain
|
27 |
49 |
N/A |
INTRINSIC |
low complexity region
|
75 |
94 |
N/A |
INTRINSIC |
low complexity region
|
209 |
229 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000153889
AA Change: T148I
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000123196 Gene: ENSMUSG00000040537 AA Change: T148I
Domain | Start | End | E-Value | Type |
transmembrane domain
|
27 |
49 |
N/A |
INTRINSIC |
low complexity region
|
81 |
100 |
N/A |
INTRINSIC |
low complexity region
|
152 |
167 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000154935
AA Change: T177I
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000119409 Gene: ENSMUSG00000040537 AA Change: T177I
Domain | Start | End | E-Value | Type |
transmembrane domain
|
27 |
49 |
N/A |
INTRINSIC |
low complexity region
|
83 |
98 |
N/A |
INTRINSIC |
low complexity region
|
225 |
245 |
N/A |
INTRINSIC |
|
Predicted Effect |
silent
Transcript: ENSMUST00000197700
|
SMART Domains |
Protein: ENSMUSP00000142580 Gene: ENSMUSG00000040537
Domain | Start | End | E-Value | Type |
transmembrane domain
|
27 |
49 |
N/A |
INTRINSIC |
low complexity region
|
129 |
145 |
N/A |
INTRINSIC |
|
Predicted Effect |
silent
Transcript: ENSMUST00000199853
|
SMART Domains |
Protein: ENSMUSP00000143097 Gene: ENSMUSG00000040537
Domain | Start | End | E-Value | Type |
transmembrane domain
|
27 |
49 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.7%
|
Validation Efficiency |
98% (87/89) |
MGI Phenotype |
FUNCTION: This gene encodes a member of a disintegrin and metalloprotease (ADAM) family of endoproteases that play important roles in various biological processes including cell signaling, adhesion and migration. The encoded preproprotein undergoes proteolytic processing to generate a mature, functional protein. The protein encoded by this gene is believed to lack metalloproteinase activity due to the lack of a critical catalytic motif. Mice lacking the encoded protein exhibit severe ataxia, hypomyelination and premature death. Alternative splicing results in multiple transcript variants encoding different isoforms, some of which may undergo similar processing. [provided by RefSeq, May 2016] PHENOTYPE: Homozygous mutant mice exhibit severe ataxia, die before weaning and have marked hypomyelination of the peripheral nerves. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acan |
C |
T |
7: 78,750,713 (GRCm39) |
T1828I |
probably benign |
Het |
Acsf2 |
A |
G |
11: 94,461,211 (GRCm39) |
S322P |
probably benign |
Het |
Acss2 |
T |
A |
2: 155,391,438 (GRCm39) |
I170N |
probably damaging |
Het |
Agrn |
G |
T |
4: 156,250,995 (GRCm39) |
D1914E |
probably damaging |
Het |
Akap6 |
T |
C |
12: 53,187,127 (GRCm39) |
S1514P |
probably benign |
Het |
Akap9 |
T |
C |
5: 3,998,805 (GRCm39) |
L58P |
possibly damaging |
Het |
Apof |
A |
G |
10: 128,105,712 (GRCm39) |
I289V |
probably benign |
Het |
Arhgap35 |
G |
A |
7: 16,348,404 (GRCm39) |
|
probably benign |
Het |
Atad3a |
A |
C |
4: 155,838,054 (GRCm39) |
F239L |
probably damaging |
Het |
Atf6 |
T |
C |
1: 170,621,576 (GRCm39) |
T482A |
probably damaging |
Het |
Atg9b |
T |
C |
5: 24,591,850 (GRCm39) |
|
probably benign |
Het |
Atp8b4 |
T |
A |
2: 126,167,327 (GRCm39) |
|
probably null |
Het |
B4galt5 |
T |
C |
2: 167,143,260 (GRCm39) |
Y388C |
probably damaging |
Het |
Bahd1 |
T |
C |
2: 118,749,689 (GRCm39) |
L495P |
probably damaging |
Het |
Bcl6 |
T |
C |
16: 23,793,716 (GRCm39) |
E77G |
probably damaging |
Het |
Bst1 |
C |
A |
5: 43,982,716 (GRCm39) |
S187* |
probably null |
Het |
Car4 |
A |
G |
11: 84,855,377 (GRCm39) |
N170S |
probably null |
Het |
Cdk14 |
A |
T |
5: 5,277,182 (GRCm39) |
V131E |
probably damaging |
Het |
Cdk4 |
T |
A |
10: 126,900,546 (GRCm39) |
|
probably benign |
Het |
Cebpe |
T |
C |
14: 54,949,121 (GRCm39) |
R99G |
probably damaging |
Het |
Col9a1 |
G |
A |
1: 24,276,300 (GRCm39) |
G736D |
probably damaging |
Het |
Copa |
T |
A |
1: 171,937,480 (GRCm39) |
V477D |
possibly damaging |
Het |
Coq9 |
G |
A |
8: 95,576,886 (GRCm39) |
G166D |
probably benign |
Het |
Cttnbp2 |
A |
T |
6: 18,434,165 (GRCm39) |
N564K |
possibly damaging |
Het |
Dgkq |
T |
C |
5: 108,798,095 (GRCm39) |
N721S |
probably benign |
Het |
Dnhd1 |
A |
T |
7: 105,341,852 (GRCm39) |
Y1217F |
probably damaging |
Het |
Eef1akmt4 |
G |
T |
16: 20,437,398 (GRCm39) |
E247* |
probably null |
Het |
Elovl7 |
A |
T |
13: 108,393,320 (GRCm39) |
I18F |
probably benign |
Het |
Eml5 |
T |
C |
12: 98,818,952 (GRCm39) |
K785E |
possibly damaging |
Het |
Faap100 |
C |
A |
11: 120,268,185 (GRCm39) |
C196F |
probably damaging |
Het |
Fat2 |
G |
A |
11: 55,173,729 (GRCm39) |
T2328M |
probably damaging |
Het |
Gcnt2 |
T |
A |
13: 41,041,204 (GRCm39) |
I121N |
probably benign |
Het |
Gm12253 |
A |
G |
11: 58,327,605 (GRCm39) |
K152E |
probably benign |
Het |
Gm16440 |
T |
A |
14: 17,574,527 (GRCm39) |
R167* |
probably null |
Het |
Gm43302 |
T |
A |
5: 105,425,602 (GRCm39) |
I276F |
possibly damaging |
Het |
Gys2 |
A |
G |
6: 142,374,267 (GRCm39) |
S593P |
probably damaging |
Het |
H2-M10.4 |
T |
A |
17: 36,772,245 (GRCm39) |
N168Y |
probably benign |
Het |
Hpca |
C |
A |
4: 129,012,287 (GRCm39) |
R83L |
probably damaging |
Het |
Igkv8-28 |
A |
G |
6: 70,121,109 (GRCm39) |
F13L |
probably benign |
Het |
Il17ra |
A |
T |
6: 120,458,465 (GRCm39) |
I539F |
probably damaging |
Het |
Kdm4a |
A |
G |
4: 118,019,013 (GRCm39) |
V401A |
possibly damaging |
Het |
Krt86 |
A |
T |
15: 101,375,157 (GRCm39) |
T351S |
probably benign |
Het |
Lig4 |
A |
G |
8: 10,021,378 (GRCm39) |
C801R |
probably benign |
Het |
Lrrn4 |
G |
A |
2: 132,714,011 (GRCm39) |
P312S |
probably damaging |
Het |
Macf1 |
T |
A |
4: 123,368,641 (GRCm39) |
H2040L |
probably benign |
Het |
Madcam1 |
A |
G |
10: 79,502,466 (GRCm39) |
K317E |
possibly damaging |
Het |
Maip1 |
T |
C |
1: 57,450,961 (GRCm39) |
I201T |
probably damaging |
Het |
Map4k4 |
C |
A |
1: 40,039,840 (GRCm39) |
D513E |
probably benign |
Het |
Mideas |
T |
A |
12: 84,209,102 (GRCm39) |
I667L |
probably benign |
Het |
Mpped1 |
G |
A |
15: 83,740,469 (GRCm39) |
G137R |
probably damaging |
Het |
Mrgprd |
T |
G |
7: 144,875,923 (GRCm39) |
F265V |
probably benign |
Het |
Myct1 |
C |
T |
10: 5,554,208 (GRCm39) |
T25I |
probably damaging |
Het |
Mylk |
A |
G |
16: 34,791,779 (GRCm39) |
T1484A |
probably benign |
Het |
Nbas |
C |
T |
12: 13,482,923 (GRCm39) |
S1400L |
possibly damaging |
Het |
Nedd4 |
T |
A |
9: 72,633,708 (GRCm39) |
S405T |
probably benign |
Het |
Neil2 |
A |
G |
14: 63,429,227 (GRCm39) |
V22A |
probably damaging |
Het |
Nrip1 |
G |
C |
16: 76,089,193 (GRCm39) |
A788G |
probably benign |
Het |
Ogfr |
AGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGAGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAAGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGGGGCCAGAG |
AGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGAGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAAGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCAAAAGGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGGGGCCAGAG |
2: 180,236,850 (GRCm39) |
|
probably benign |
Het |
Or10ab4 |
A |
G |
7: 107,655,160 (GRCm39) |
T324A |
probably benign |
Het |
Or10d4c |
C |
T |
9: 39,558,496 (GRCm39) |
T158I |
probably damaging |
Het |
Or2b7 |
T |
C |
13: 21,740,169 (GRCm39) |
I8V |
probably benign |
Het |
Or2bd2 |
G |
A |
7: 6,442,020 (GRCm39) |
|
probably benign |
Het |
Or2r2 |
T |
A |
6: 42,463,830 (GRCm39) |
Q99L |
probably damaging |
Het |
Or6c215 |
C |
T |
10: 129,638,222 (GRCm39) |
M57I |
possibly damaging |
Het |
Orc2 |
T |
C |
1: 58,505,221 (GRCm39) |
N478S |
probably damaging |
Het |
Oxct1 |
A |
G |
15: 4,064,806 (GRCm39) |
E48G |
possibly damaging |
Het |
Pcca |
A |
G |
14: 122,975,324 (GRCm39) |
I28V |
probably benign |
Het |
Pcdha8 |
T |
C |
18: 37,126,241 (GRCm39) |
V241A |
probably benign |
Het |
Pgap6 |
T |
A |
17: 26,339,374 (GRCm39) |
S563T |
possibly damaging |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Pkd2 |
T |
A |
5: 104,631,090 (GRCm39) |
W505R |
probably damaging |
Het |
Plxnc1 |
C |
T |
10: 94,746,448 (GRCm39) |
V430I |
probably benign |
Het |
Prkd3 |
A |
G |
17: 79,278,883 (GRCm39) |
M401T |
probably damaging |
Het |
Rgmb |
A |
G |
17: 16,027,748 (GRCm39) |
C324R |
probably benign |
Het |
Rsph6a |
A |
T |
7: 18,799,364 (GRCm39) |
|
probably benign |
Het |
Sclt1 |
A |
T |
3: 41,636,209 (GRCm39) |
M264K |
probably benign |
Het |
Serhl |
T |
A |
15: 82,985,899 (GRCm39) |
V30D |
possibly damaging |
Het |
Sfrp1 |
T |
C |
8: 23,902,159 (GRCm39) |
V120A |
probably damaging |
Het |
Slc22a8 |
C |
T |
19: 8,587,030 (GRCm39) |
Q408* |
probably null |
Het |
Slc35b2 |
A |
G |
17: 45,877,673 (GRCm39) |
T218A |
probably damaging |
Het |
Slco4c1 |
A |
T |
1: 96,765,242 (GRCm39) |
F403I |
probably damaging |
Het |
Sorbs1 |
T |
A |
19: 40,351,660 (GRCm39) |
H250L |
probably damaging |
Het |
Sorcs3 |
T |
A |
19: 48,737,810 (GRCm39) |
C742* |
probably null |
Het |
Tnc |
T |
C |
4: 63,918,970 (GRCm39) |
Y1151C |
probably damaging |
Het |
Tor1aip1 |
T |
A |
1: 155,909,582 (GRCm39) |
|
probably benign |
Het |
Trim9 |
T |
C |
12: 70,393,665 (GRCm39) |
Q93R |
probably damaging |
Het |
Tsnaxip1 |
A |
G |
8: 106,570,813 (GRCm39) |
Y613C |
probably damaging |
Het |
Ttc6 |
C |
T |
12: 57,775,196 (GRCm39) |
Q1631* |
probably null |
Het |
Ubr5 |
A |
G |
15: 38,015,367 (GRCm39) |
L881P |
probably damaging |
Het |
Upp2 |
C |
T |
2: 58,457,454 (GRCm39) |
|
probably benign |
Het |
Vmn1r203 |
T |
A |
13: 22,709,004 (GRCm39) |
S262T |
possibly damaging |
Het |
Vmn2r116 |
A |
T |
17: 23,605,736 (GRCm39) |
D216V |
probably damaging |
Het |
Vps52 |
A |
G |
17: 34,177,049 (GRCm39) |
Q96R |
probably benign |
Het |
|
Other mutations in Adam22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01325:Adam22
|
APN |
5 |
8,177,333 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01368:Adam22
|
APN |
5 |
8,177,411 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01406:Adam22
|
APN |
5 |
8,180,212 (GRCm39) |
nonsense |
probably null |
|
IGL01463:Adam22
|
APN |
5 |
8,142,790 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01691:Adam22
|
APN |
5 |
8,142,742 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01798:Adam22
|
APN |
5 |
8,282,604 (GRCm39) |
splice site |
probably null |
|
IGL01975:Adam22
|
APN |
5 |
8,217,396 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02076:Adam22
|
APN |
5 |
8,186,900 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02170:Adam22
|
APN |
5 |
8,184,845 (GRCm39) |
missense |
probably benign |
|
IGL02189:Adam22
|
APN |
5 |
8,380,029 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02859:Adam22
|
APN |
5 |
8,217,375 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03189:Adam22
|
APN |
5 |
8,161,897 (GRCm39) |
nonsense |
probably null |
|
IGL03326:Adam22
|
APN |
5 |
8,177,421 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03329:Adam22
|
APN |
5 |
8,199,210 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL03354:Adam22
|
APN |
5 |
8,208,890 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL03394:Adam22
|
APN |
5 |
8,217,379 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03047:Adam22
|
UTSW |
5 |
8,132,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R0445:Adam22
|
UTSW |
5 |
8,230,591 (GRCm39) |
intron |
probably benign |
|
R0486:Adam22
|
UTSW |
5 |
8,380,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R0669:Adam22
|
UTSW |
5 |
8,193,036 (GRCm39) |
splice site |
probably benign |
|
R0866:Adam22
|
UTSW |
5 |
8,132,156 (GRCm39) |
missense |
probably damaging |
0.98 |
R1510:Adam22
|
UTSW |
5 |
8,202,408 (GRCm39) |
missense |
probably benign |
0.06 |
R1562:Adam22
|
UTSW |
5 |
8,145,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R1640:Adam22
|
UTSW |
5 |
8,195,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Adam22
|
UTSW |
5 |
8,184,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R1939:Adam22
|
UTSW |
5 |
8,380,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R1998:Adam22
|
UTSW |
5 |
8,379,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R2012:Adam22
|
UTSW |
5 |
8,167,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R2214:Adam22
|
UTSW |
5 |
8,186,805 (GRCm39) |
critical splice donor site |
probably null |
|
R2270:Adam22
|
UTSW |
5 |
8,171,108 (GRCm39) |
missense |
probably damaging |
0.98 |
R2271:Adam22
|
UTSW |
5 |
8,171,108 (GRCm39) |
missense |
probably damaging |
0.98 |
R2286:Adam22
|
UTSW |
5 |
8,195,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R2304:Adam22
|
UTSW |
5 |
8,142,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R2406:Adam22
|
UTSW |
5 |
8,230,064 (GRCm39) |
intron |
probably benign |
|
R2656:Adam22
|
UTSW |
5 |
8,167,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R3106:Adam22
|
UTSW |
5 |
8,167,583 (GRCm39) |
splice site |
probably null |
|
R3870:Adam22
|
UTSW |
5 |
8,182,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R3923:Adam22
|
UTSW |
5 |
8,180,514 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4092:Adam22
|
UTSW |
5 |
8,145,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R4180:Adam22
|
UTSW |
5 |
8,199,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R4247:Adam22
|
UTSW |
5 |
8,195,626 (GRCm39) |
missense |
probably benign |
|
R4486:Adam22
|
UTSW |
5 |
8,230,227 (GRCm39) |
intron |
probably benign |
|
R4629:Adam22
|
UTSW |
5 |
8,282,663 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4744:Adam22
|
UTSW |
5 |
8,128,699 (GRCm39) |
missense |
probably damaging |
0.98 |
R4839:Adam22
|
UTSW |
5 |
8,186,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R5007:Adam22
|
UTSW |
5 |
8,217,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R5030:Adam22
|
UTSW |
5 |
8,229,645 (GRCm39) |
intron |
probably benign |
|
R5061:Adam22
|
UTSW |
5 |
8,230,238 (GRCm39) |
intron |
probably benign |
|
R5312:Adam22
|
UTSW |
5 |
8,140,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R5353:Adam22
|
UTSW |
5 |
8,140,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R5354:Adam22
|
UTSW |
5 |
8,140,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R5356:Adam22
|
UTSW |
5 |
8,140,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R5423:Adam22
|
UTSW |
5 |
8,140,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R5424:Adam22
|
UTSW |
5 |
8,140,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R5719:Adam22
|
UTSW |
5 |
8,417,217 (GRCm39) |
missense |
probably benign |
|
R5763:Adam22
|
UTSW |
5 |
8,184,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R5768:Adam22
|
UTSW |
5 |
8,177,426 (GRCm39) |
missense |
probably benign |
0.35 |
R5776:Adam22
|
UTSW |
5 |
8,177,361 (GRCm39) |
missense |
probably benign |
0.26 |
R5839:Adam22
|
UTSW |
5 |
8,186,861 (GRCm39) |
missense |
probably damaging |
0.99 |
R6314:Adam22
|
UTSW |
5 |
8,177,365 (GRCm39) |
nonsense |
probably null |
|
R6520:Adam22
|
UTSW |
5 |
8,166,635 (GRCm39) |
missense |
probably damaging |
0.98 |
R6798:Adam22
|
UTSW |
5 |
8,210,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R6924:Adam22
|
UTSW |
5 |
8,417,322 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6938:Adam22
|
UTSW |
5 |
8,196,499 (GRCm39) |
missense |
probably benign |
0.01 |
R7317:Adam22
|
UTSW |
5 |
8,140,202 (GRCm39) |
missense |
probably benign |
|
R7402:Adam22
|
UTSW |
5 |
8,145,049 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7431:Adam22
|
UTSW |
5 |
8,142,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R7527:Adam22
|
UTSW |
5 |
8,132,239 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7571:Adam22
|
UTSW |
5 |
8,132,160 (GRCm39) |
nonsense |
probably null |
|
R7627:Adam22
|
UTSW |
5 |
8,417,933 (GRCm39) |
missense |
probably benign |
|
R7678:Adam22
|
UTSW |
5 |
8,137,750 (GRCm39) |
splice site |
probably null |
|
R7714:Adam22
|
UTSW |
5 |
8,167,587 (GRCm39) |
critical splice donor site |
probably null |
|
R7806:Adam22
|
UTSW |
5 |
8,142,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R7834:Adam22
|
UTSW |
5 |
8,180,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R7837:Adam22
|
UTSW |
5 |
8,199,284 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7979:Adam22
|
UTSW |
5 |
8,186,804 (GRCm39) |
critical splice donor site |
probably null |
|
R8123:Adam22
|
UTSW |
5 |
8,142,833 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8511:Adam22
|
UTSW |
5 |
8,184,558 (GRCm39) |
missense |
probably damaging |
0.98 |
R8722:Adam22
|
UTSW |
5 |
8,166,554 (GRCm39) |
missense |
probably benign |
|
R8730:Adam22
|
UTSW |
5 |
8,208,830 (GRCm39) |
missense |
probably benign |
0.00 |
R9015:Adam22
|
UTSW |
5 |
8,136,688 (GRCm39) |
intron |
probably benign |
|
R9068:Adam22
|
UTSW |
5 |
8,177,343 (GRCm39) |
missense |
probably benign |
0.01 |
R9198:Adam22
|
UTSW |
5 |
8,167,583 (GRCm39) |
splice site |
probably null |
|
R9441:Adam22
|
UTSW |
5 |
8,161,974 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9480:Adam22
|
UTSW |
5 |
8,193,077 (GRCm39) |
missense |
probably benign |
0.01 |
X0067:Adam22
|
UTSW |
5 |
8,177,329 (GRCm39) |
missense |
probably benign |
0.05 |
|
Predicted Primers |
PCR Primer
(F):5'- ACACCACAATGGCAGGTGAC -3'
(R):5'- CCGAGTTCTGAGGTAATTCTGG -3'
Sequencing Primer
(F):5'- CTATCAGTGAATATTGGTATGGGCAC -3'
(R):5'- GGTAATTCTGGCTATAAACTACGCCC -3'
|
Posted On |
2021-08-31 |