Incidental Mutation 'R5547:Cryz'
| ID |
436335 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cryz
|
| Ensembl Gene |
ENSMUSG00000028199 |
| Gene Name |
crystallin, zeta |
| Synonyms |
SEZ9, Sez9, quinone reductase |
| MMRRC Submission |
043105-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.199)
|
| Stock # |
R5547 (G1)
|
| Quality Score |
223 |
|
Status
|
Not validated
|
| Chromosome |
3 |
| Chromosomal Location |
154302348-154328819 bp(+) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
C to T
at 154317194 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Stop codon
at position 138
(R138*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000142101
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000029850]
[ENSMUST00000135723]
[ENSMUST00000140644]
[ENSMUST00000144764]
[ENSMUST00000155232]
[ENSMUST00000155385]
[ENSMUST00000184537]
[ENSMUST00000192462]
[ENSMUST00000194876]
|
| AlphaFold |
P47199 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000029850
AA Change: R138*
|
| SMART Domains |
Protein: ENSMUSP00000029850
Gene: ENSMUSG00000028199
AA Change: R138*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ADH_N
|
35 |
131 |
3.3e-14 |
PFAM |
|
Pfam:ADH_zinc_N
|
160 |
290 |
1.3e-30 |
PFAM |
|
Pfam:ADH_zinc_N_2
|
192 |
329 |
1.7e-20 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000135723
|
| SMART Domains |
Protein: ENSMUSP00000143311
Gene: ENSMUSG00000028199
| Domain | Start | End | E-Value | Type |
|---|
|
PDB:1YB5|B
|
1 |
38 |
5e-17 |
PDB |
|
SCOP:d1qora1
|
9 |
38 |
9e-5 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000140644
|
| SMART Domains |
Protein: ENSMUSP00000115146
Gene: ENSMUSG00000028199
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ADH_N
|
35 |
98 |
1.5e-16 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000144764
AA Change: R138*
|
| SMART Domains |
Protein: ENSMUSP00000121269
Gene: ENSMUSG00000028199
AA Change: R138*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ADH_N
|
35 |
132 |
2.6e-17 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000155232
AA Change: R138*
|
| SMART Domains |
Protein: ENSMUSP00000118449
Gene: ENSMUSG00000028199
AA Change: R138*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ADH_N
|
35 |
135 |
3.5e-17 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000155385
|
| SMART Domains |
Protein: ENSMUSP00000122619
Gene: ENSMUSG00000028199
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ADH_N
|
35 |
130 |
2.1e-17 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000184537
AA Change: R138*
|
| SMART Domains |
Protein: ENSMUSP00000139387
Gene: ENSMUSG00000028199
AA Change: R138*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ADH_N
|
35 |
180 |
4.7e-17 |
PFAM |
|
Pfam:ADH_zinc_N
|
160 |
218 |
5.4e-13 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000192462
AA Change: R138*
|
| SMART Domains |
Protein: ENSMUSP00000142105
Gene: ENSMUSG00000028199
AA Change: R138*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ADH_N
|
35 |
131 |
2.8e-16 |
PFAM |
|
Pfam:ADH_zinc_N
|
160 |
290 |
1.8e-29 |
PFAM |
|
Pfam:ADH_zinc_N_2
|
192 |
329 |
4.3e-17 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000194876
AA Change: R138*
|
| SMART Domains |
Protein: ENSMUSP00000142101
Gene: ENSMUSG00000028199
AA Change: R138*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ADH_N
|
35 |
139 |
2.2e-14 |
PFAM |
|
Pfam:ADH_zinc_N
|
160 |
290 |
1.4e-27 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000195292
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000195103
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.2%
- 20x: 94.8%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Crystallins are separated into two classes: taxon-specific, or enzyme, and ubiquitous. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. The former class is also called phylogenetically-restricted crystallins. This gene encodes a taxon-specific crystallin protein which has NADPH-dependent quinone reductase activity distinct from other known quinone reductases. It lacks alcohol dehydrogenase activity although by similarity it is considered a member of the zinc-containing alcohol dehydrogenase family. Unlike other mammalian species, in humans, lens expression is low. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. One pseudogene is known to exist. [provided by RefSeq, Sep 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 47 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aldh7a1 |
A |
G |
18: 56,661,356 (GRCm39) |
S492P |
probably damaging |
Het |
| Arfgef1 |
A |
T |
1: 10,231,201 (GRCm39) |
D1133E |
probably damaging |
Het |
| Avpi1 |
T |
C |
19: 42,113,382 (GRCm39) |
K25R |
probably damaging |
Het |
| Bank1 |
T |
C |
3: 135,772,110 (GRCm39) |
S708G |
probably damaging |
Het |
| C1qtnf2 |
A |
G |
11: 43,381,794 (GRCm39) |
E202G |
probably damaging |
Het |
| C6 |
T |
A |
15: 4,837,970 (GRCm39) |
V860E |
probably benign |
Het |
| Cbr1 |
T |
A |
16: 93,406,698 (GRCm39) |
V138E |
probably damaging |
Het |
| Cdip1 |
A |
G |
16: 4,587,988 (GRCm39) |
S2P |
probably damaging |
Het |
| Cep126 |
T |
C |
9: 8,100,428 (GRCm39) |
N702S |
probably damaging |
Het |
| Chek1 |
T |
C |
9: 36,623,400 (GRCm39) |
I381V |
probably benign |
Het |
| Clock |
G |
A |
5: 76,378,185 (GRCm39) |
P572S |
probably benign |
Het |
| Ctsll3 |
T |
A |
13: 60,948,551 (GRCm39) |
M103L |
probably benign |
Het |
| Daxx |
TGATGATGACGATGATGACGATGATGA |
TGATGATGACGATGATGA |
17: 34,131,615 (GRCm39) |
|
probably benign |
Het |
| Daxx |
CGATGATGATGA |
CGA |
17: 34,131,633 (GRCm39) |
|
probably benign |
Het |
| Dsg1a |
T |
G |
18: 20,469,097 (GRCm39) |
|
probably null |
Het |
| Eya4 |
T |
C |
10: 22,985,753 (GRCm39) |
E583G |
possibly damaging |
Het |
| Flt1 |
T |
A |
5: 147,591,948 (GRCm39) |
S505C |
probably damaging |
Het |
| Gpr161 |
C |
A |
1: 165,133,982 (GRCm39) |
F81L |
possibly damaging |
Het |
| H2-T15 |
G |
A |
17: 36,368,796 (GRCm39) |
H95Y |
possibly damaging |
Het |
| Hmcn1 |
A |
G |
1: 150,613,257 (GRCm39) |
V1390A |
possibly damaging |
Het |
| Ifi44l |
C |
T |
3: 151,467,142 (GRCm39) |
V63I |
unknown |
Het |
| Klhl3 |
C |
T |
13: 58,250,243 (GRCm39) |
|
probably null |
Het |
| Lekr1 |
T |
A |
3: 65,576,601 (GRCm39) |
|
probably null |
Het |
| Lhx5 |
A |
G |
5: 120,572,675 (GRCm39) |
Q98R |
probably benign |
Het |
| Nuggc |
A |
G |
14: 65,879,330 (GRCm39) |
K681E |
possibly damaging |
Het |
| Numa1 |
G |
T |
7: 101,663,137 (GRCm39) |
A735S |
probably damaging |
Het |
| Oog3 |
A |
T |
4: 143,884,598 (GRCm39) |
L446Q |
probably benign |
Het |
| Or5ac19 |
G |
A |
16: 59,089,479 (GRCm39) |
L184F |
probably benign |
Het |
| Otogl |
C |
T |
10: 107,617,909 (GRCm39) |
E1735K |
possibly damaging |
Het |
| Pcsk5 |
T |
C |
19: 17,729,488 (GRCm39) |
D119G |
probably benign |
Het |
| Pgpep1 |
T |
C |
8: 71,105,069 (GRCm39) |
K64E |
probably benign |
Het |
| Prr19 |
A |
C |
7: 25,003,388 (GRCm39) |
D334A |
probably damaging |
Het |
| Ptprh |
G |
T |
7: 4,557,221 (GRCm39) |
S691* |
probably null |
Het |
| Recql4 |
G |
A |
15: 76,589,994 (GRCm39) |
R684* |
probably null |
Het |
| Rnf112 |
C |
T |
11: 61,341,854 (GRCm39) |
V317I |
possibly damaging |
Het |
| Rnf40 |
T |
C |
7: 127,188,302 (GRCm39) |
|
probably null |
Het |
| Secisbp2l |
C |
T |
2: 125,582,657 (GRCm39) |
G933D |
possibly damaging |
Het |
| Spag17 |
T |
C |
3: 99,963,468 (GRCm39) |
V1062A |
probably benign |
Het |
| Tbc1d1 |
A |
G |
5: 64,481,887 (GRCm39) |
D696G |
possibly damaging |
Het |
| Tdo2 |
T |
C |
3: 81,866,247 (GRCm39) |
R339G |
probably damaging |
Het |
| Tmem245 |
C |
T |
4: 56,910,156 (GRCm39) |
|
probably null |
Het |
| Trim24 |
A |
G |
6: 37,942,485 (GRCm39) |
E965G |
probably damaging |
Het |
| Trmt112 |
T |
C |
19: 6,888,156 (GRCm39) |
S103P |
probably damaging |
Het |
| Trpv6 |
A |
T |
6: 41,613,088 (GRCm39) |
V26D |
possibly damaging |
Het |
| Zfp850 |
A |
G |
7: 27,688,844 (GRCm39) |
C455R |
probably damaging |
Het |
| Zfp946 |
T |
C |
17: 22,673,873 (GRCm39) |
I209T |
probably benign |
Het |
| Zfp957 |
T |
C |
14: 79,451,406 (GRCm39) |
N131S |
probably benign |
Het |
|
| Other mutations in Cryz |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00499:Cryz
|
APN |
3 |
154,310,579 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL00838:Cryz
|
APN |
3 |
154,324,112 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00969:Cryz
|
APN |
3 |
154,324,163 (GRCm39) |
nonsense |
probably null |
|
|
IGL01571:Cryz
|
APN |
3 |
154,327,380 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03082:Cryz
|
APN |
3 |
154,310,563 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0049:Cryz
|
UTSW |
3 |
154,317,189 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0049:Cryz
|
UTSW |
3 |
154,317,189 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1116:Cryz
|
UTSW |
3 |
154,327,240 (GRCm39) |
splice site |
probably benign |
|
|
R1470:Cryz
|
UTSW |
3 |
154,312,113 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1470:Cryz
|
UTSW |
3 |
154,312,113 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1586:Cryz
|
UTSW |
3 |
154,317,147 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2018:Cryz
|
UTSW |
3 |
154,327,320 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2223:Cryz
|
UTSW |
3 |
154,324,191 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R2334:Cryz
|
UTSW |
3 |
154,327,828 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4488:Cryz
|
UTSW |
3 |
154,324,094 (GRCm39) |
splice site |
probably benign |
|
|
R5595:Cryz
|
UTSW |
3 |
154,312,155 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5917:Cryz
|
UTSW |
3 |
154,327,403 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7197:Cryz
|
UTSW |
3 |
154,327,205 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7473:Cryz
|
UTSW |
3 |
154,312,157 (GRCm39) |
missense |
probably benign |
|
|
R8121:Cryz
|
UTSW |
3 |
154,327,382 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9215:Cryz
|
UTSW |
3 |
154,324,446 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9222:Cryz
|
UTSW |
3 |
154,317,203 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9651:Cryz
|
UTSW |
3 |
154,327,765 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1176:Cryz
|
UTSW |
3 |
154,327,406 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGGAAGCTGGCACTGTCAAG -3'
(R):5'- CTGACTCCCATGTTTTGTGAAAATG -3'
Sequencing Primer
(F):5'- GTCAAGGTCCCAGCCATCTTAG -3'
(R):5'- CCCATGTTTTGTGAAAATGATCTTC -3'
|
| Posted On |
2016-10-24 |
Incidental Mutation