Incidental Mutation 'R9128:Zmynd8'
| ID |
693386 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zmynd8
|
| Ensembl Gene |
ENSMUSG00000039671 |
| Gene Name |
zinc finger, MYND-type containing 8 |
| Synonyms |
ZMYND8, RACK7, 1110013E22Rik, 2010005I16Rik, Prkcbp1, 3632413B07Rik |
| MMRRC Submission |
068927-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R9128 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
165626072-165740896 bp(-) (GRCm39) |
| Type of Mutation |
start codon destroyed |
| DNA Base Change (assembly) |
A to T
at 165700058 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Lysine
at position 1
(M1K)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000104889
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000018050]
[ENSMUST00000088113]
[ENSMUST00000099084]
[ENSMUST00000109262]
[ENSMUST00000109266]
[ENSMUST00000109269]
[ENSMUST00000136842]
[ENSMUST00000144530]
[ENSMUST00000153655]
[ENSMUST00000170272]
[ENSMUST00000177633]
|
| AlphaFold |
A2A484 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000018050
|
| SMART Domains |
Protein: ENSMUSP00000018050
Gene: ENSMUSG00000039671
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
23 |
34 |
N/A |
INTRINSIC |
|
low complexity region
|
37 |
56 |
N/A |
INTRINSIC |
|
PHD
|
90 |
131 |
2.23e-11 |
SMART |
|
BROMO
|
147 |
254 |
1.77e-17 |
SMART |
|
Pfam:PWWP
|
275 |
349 |
4e-12 |
PFAM |
|
Pfam:DUF3544
|
412 |
624 |
9.8e-112 |
PFAM |
|
internal_repeat_2
|
640 |
701 |
9.06e-5 |
PROSPERO |
|
low complexity region
|
770 |
805 |
N/A |
INTRINSIC |
|
low complexity region
|
853 |
868 |
N/A |
INTRINSIC |
|
low complexity region
|
875 |
887 |
N/A |
INTRINSIC |
|
coiled coil region
|
916 |
978 |
N/A |
INTRINSIC |
|
Pfam:zf-MYND
|
988 |
1022 |
2.2e-7 |
PFAM |
|
low complexity region
|
1055 |
1075 |
N/A |
INTRINSIC |
|
low complexity region
|
1142 |
1156 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000088113
|
| SMART Domains |
Protein: ENSMUSP00000085436
Gene: ENSMUSG00000039671
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
8 |
19 |
N/A |
INTRINSIC |
|
low complexity region
|
43 |
54 |
N/A |
INTRINSIC |
|
low complexity region
|
57 |
76 |
N/A |
INTRINSIC |
|
PHD
|
85 |
126 |
2.23e-11 |
SMART |
|
BROMO
|
142 |
249 |
1.77e-17 |
SMART |
|
Pfam:PWWP
|
271 |
346 |
2.7e-11 |
PFAM |
|
Pfam:DUF3544
|
408 |
617 |
2.1e-102 |
PFAM |
|
internal_repeat_2
|
635 |
696 |
4.2e-5 |
PROSPERO |
|
low complexity region
|
765 |
800 |
N/A |
INTRINSIC |
|
low complexity region
|
848 |
863 |
N/A |
INTRINSIC |
|
low complexity region
|
870 |
882 |
N/A |
INTRINSIC |
|
coiled coil region
|
911 |
973 |
N/A |
INTRINSIC |
|
low complexity region
|
1050 |
1070 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000099084
|
| SMART Domains |
Protein: ENSMUSP00000096683
Gene: ENSMUSG00000039671
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
23 |
34 |
N/A |
INTRINSIC |
|
low complexity region
|
37 |
56 |
N/A |
INTRINSIC |
|
PHD
|
65 |
106 |
2.23e-11 |
SMART |
|
BROMO
|
122 |
229 |
1.77e-17 |
SMART |
|
Pfam:PWWP
|
250 |
324 |
4.1e-12 |
PFAM |
|
Pfam:DUF3544
|
387 |
599 |
1e-111 |
PFAM |
|
internal_repeat_2
|
615 |
676 |
4.95e-5 |
PROSPERO |
|
low complexity region
|
745 |
780 |
N/A |
INTRINSIC |
|
low complexity region
|
819 |
844 |
N/A |
INTRINSIC |
|
low complexity region
|
880 |
895 |
N/A |
INTRINSIC |
|
low complexity region
|
902 |
914 |
N/A |
INTRINSIC |
|
coiled coil region
|
943 |
1005 |
N/A |
INTRINSIC |
|
Pfam:zf-MYND
|
1015 |
1049 |
2.3e-7 |
PFAM |
|
low complexity region
|
1082 |
1102 |
N/A |
INTRINSIC |
|
low complexity region
|
1169 |
1183 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000109262
|
| SMART Domains |
Protein: ENSMUSP00000104885
Gene: ENSMUSG00000039671
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
23 |
34 |
N/A |
INTRINSIC |
|
low complexity region
|
37 |
56 |
N/A |
INTRINSIC |
|
PHD
|
65 |
106 |
2.23e-11 |
SMART |
|
BROMO
|
122 |
229 |
1.77e-17 |
SMART |
|
Pfam:PWWP
|
250 |
324 |
1.2e-12 |
PFAM |
|
Pfam:DUF3544
|
387 |
460 |
3.1e-29 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000109266
AA Change: M1K
|
| SMART Domains |
Protein: ENSMUSP00000104889
Gene: ENSMUSG00000039671
AA Change: M1K
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
6 |
11 |
N/A |
INTRINSIC |
|
low complexity region
|
43 |
54 |
N/A |
INTRINSIC |
|
low complexity region
|
57 |
76 |
N/A |
INTRINSIC |
|
PHD
|
110 |
151 |
2.23e-11 |
SMART |
|
BROMO
|
167 |
274 |
1.77e-17 |
SMART |
|
Pfam:PWWP
|
295 |
369 |
4.1e-12 |
PFAM |
|
Pfam:DUF3544
|
432 |
644 |
1e-111 |
PFAM |
|
internal_repeat_2
|
660 |
721 |
8.36e-5 |
PROSPERO |
|
low complexity region
|
790 |
825 |
N/A |
INTRINSIC |
|
low complexity region
|
873 |
888 |
N/A |
INTRINSIC |
|
low complexity region
|
895 |
907 |
N/A |
INTRINSIC |
|
coiled coil region
|
936 |
998 |
N/A |
INTRINSIC |
|
Pfam:zf-MYND
|
1008 |
1042 |
2.3e-7 |
PFAM |
|
low complexity region
|
1075 |
1095 |
N/A |
INTRINSIC |
|
low complexity region
|
1162 |
1176 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000109269
|
| SMART Domains |
Protein: ENSMUSP00000104892
Gene: ENSMUSG00000039671
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
27 |
38 |
N/A |
INTRINSIC |
|
low complexity region
|
41 |
60 |
N/A |
INTRINSIC |
|
PHD
|
94 |
135 |
2.23e-11 |
SMART |
|
BROMO
|
151 |
258 |
1.77e-17 |
SMART |
|
Pfam:PWWP
|
280 |
355 |
6.6e-11 |
PFAM |
|
Pfam:DUF3544
|
417 |
626 |
2.6e-102 |
PFAM |
|
internal_repeat_2
|
644 |
705 |
6.15e-5 |
PROSPERO |
|
low complexity region
|
774 |
809 |
N/A |
INTRINSIC |
|
low complexity region
|
848 |
873 |
N/A |
INTRINSIC |
|
low complexity region
|
909 |
924 |
N/A |
INTRINSIC |
|
low complexity region
|
931 |
943 |
N/A |
INTRINSIC |
|
coiled coil region
|
972 |
1034 |
N/A |
INTRINSIC |
|
low complexity region
|
1111 |
1131 |
N/A |
INTRINSIC |
|
low complexity region
|
1198 |
1212 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000136842
|
| SMART Domains |
Protein: ENSMUSP00000120631
Gene: ENSMUSG00000039671
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
19 |
30 |
N/A |
INTRINSIC |
|
low complexity region
|
54 |
65 |
N/A |
INTRINSIC |
|
low complexity region
|
68 |
87 |
N/A |
INTRINSIC |
|
PHD
|
96 |
137 |
2.23e-11 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000144530
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000153655
|
| SMART Domains |
Protein: ENSMUSP00000120932
Gene: ENSMUSG00000039671
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
15 |
N/A |
INTRINSIC |
|
low complexity region
|
43 |
54 |
N/A |
INTRINSIC |
|
low complexity region
|
57 |
76 |
N/A |
INTRINSIC |
|
PHD
|
85 |
126 |
2.23e-11 |
SMART |
|
BROMO
|
142 |
249 |
1.77e-17 |
SMART |
|
Pfam:PWWP
|
270 |
344 |
3.5e-12 |
PFAM |
|
Pfam:DUF3544
|
407 |
480 |
6.7e-29 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000170272
|
| SMART Domains |
Protein: ENSMUSP00000128680
Gene: ENSMUSG00000039671
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
23 |
34 |
N/A |
INTRINSIC |
|
low complexity region
|
37 |
56 |
N/A |
INTRINSIC |
|
PHD
|
65 |
106 |
2.23e-11 |
SMART |
|
BROMO
|
122 |
229 |
1.77e-17 |
SMART |
|
Pfam:PWWP
|
250 |
324 |
1.1e-11 |
PFAM |
|
Pfam:DUF3544
|
387 |
599 |
1.9e-111 |
PFAM |
|
internal_repeat_2
|
615 |
676 |
7.92e-5 |
PROSPERO |
|
low complexity region
|
745 |
780 |
N/A |
INTRINSIC |
|
low complexity region
|
828 |
843 |
N/A |
INTRINSIC |
|
low complexity region
|
850 |
862 |
N/A |
INTRINSIC |
|
coiled coil region
|
891 |
953 |
N/A |
INTRINSIC |
|
Pfam:zf-MYND
|
963 |
997 |
1.1e-6 |
PFAM |
|
low complexity region
|
1030 |
1050 |
N/A |
INTRINSIC |
|
low complexity region
|
1117 |
1131 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000177633
|
| SMART Domains |
Protein: ENSMUSP00000136211
Gene: ENSMUSG00000039671
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
8 |
19 |
N/A |
INTRINSIC |
|
low complexity region
|
43 |
54 |
N/A |
INTRINSIC |
|
low complexity region
|
57 |
76 |
N/A |
INTRINSIC |
|
PHD
|
85 |
126 |
2.23e-11 |
SMART |
|
BROMO
|
142 |
249 |
1.77e-17 |
SMART |
|
Pfam:PWWP
|
270 |
344 |
9.6e-12 |
PFAM |
|
Pfam:DUF3544
|
407 |
619 |
1.8e-111 |
PFAM |
|
internal_repeat_2
|
635 |
696 |
6.45e-5 |
PROSPERO |
|
low complexity region
|
765 |
800 |
N/A |
INTRINSIC |
|
low complexity region
|
848 |
863 |
N/A |
INTRINSIC |
|
low complexity region
|
870 |
882 |
N/A |
INTRINSIC |
|
coiled coil region
|
911 |
973 |
N/A |
INTRINSIC |
|
Pfam:zf-MYND
|
983 |
1017 |
6.7e-7 |
PFAM |
|
low complexity region
|
1050 |
1070 |
N/A |
INTRINSIC |
|
low complexity region
|
1137 |
1151 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.3%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a receptor for activated C-kinase (RACK) protein. The encoded protein has been shown to bind in vitro to activated protein kinase C beta I. In addition, this protein is a cutaneous T-cell lymphoma-associated antigen. Finally, the protein contains a bromodomain and two zinc fingers, and is thought to be a transcriptional regulator. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 66 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca7 |
T |
C |
10: 79,838,352 (GRCm39) |
V542A |
possibly damaging |
Het |
| Abhd8 |
G |
T |
8: 71,914,389 (GRCm39) |
R80S |
probably benign |
Het |
| Actc1 |
T |
C |
2: 113,880,946 (GRCm39) |
Y93C |
possibly damaging |
Het |
| Actn4 |
G |
T |
7: 28,593,929 (GRCm39) |
D859E |
possibly damaging |
Het |
| Adcy2 |
C |
T |
13: 68,773,927 (GRCm39) |
G1039R |
probably damaging |
Het |
| Als2 |
A |
G |
1: 59,219,709 (GRCm39) |
M1202T |
probably benign |
Het |
| Aste1 |
T |
A |
9: 105,273,908 (GRCm39) |
Y49* |
probably null |
Het |
| Atp8b4 |
T |
C |
2: 126,234,750 (GRCm39) |
D422G |
probably benign |
Het |
| Bag6 |
T |
A |
17: 35,363,688 (GRCm39) |
S791T |
probably damaging |
Het |
| Bivm |
T |
A |
1: 44,167,949 (GRCm39) |
W222R |
probably null |
Het |
| Bod1l |
A |
C |
5: 41,946,266 (GRCm39) |
V3003G |
probably benign |
Het |
| Bsn |
T |
C |
9: 107,993,349 (GRCm39) |
D801G |
probably benign |
Het |
| Ccdc14 |
G |
A |
16: 34,527,159 (GRCm39) |
D403N |
probably damaging |
Het |
| Cenpj |
T |
A |
14: 56,780,319 (GRCm39) |
E964V |
probably damaging |
Het |
| Cep250 |
C |
T |
2: 155,812,042 (GRCm39) |
A446V |
unknown |
Het |
| Clca3a1 |
G |
A |
3: 144,463,795 (GRCm39) |
R161W |
probably damaging |
Het |
| Dcxr |
A |
T |
11: 120,617,372 (GRCm39) |
V57E |
|
Het |
| Dnah17 |
T |
G |
11: 117,937,004 (GRCm39) |
N3400T |
possibly damaging |
Het |
| Dnaja3 |
C |
T |
16: 4,520,164 (GRCm39) |
T444I |
possibly damaging |
Het |
| Dop1a |
T |
C |
9: 86,395,208 (GRCm39) |
S772P |
probably benign |
Het |
| Ednrb |
T |
C |
14: 104,080,528 (GRCm39) |
N129D |
probably damaging |
Het |
| Ep300 |
T |
A |
15: 81,533,946 (GRCm39) |
M2001K |
unknown |
Het |
| Fam3b |
A |
G |
16: 97,302,200 (GRCm39) |
I8T |
probably benign |
Het |
| Fam98c |
A |
T |
7: 28,854,115 (GRCm39) |
S85T |
|
Het |
| Fat1 |
G |
A |
8: 45,462,878 (GRCm39) |
V1232I |
probably benign |
Het |
| Fzd3 |
T |
A |
14: 65,449,626 (GRCm39) |
Y484F |
probably damaging |
Het |
| H3f3a |
T |
C |
1: 180,630,660 (GRCm39) |
I131M |
possibly damaging |
Het |
| Ifi206 |
A |
T |
1: 173,299,022 (GRCm39) |
D861E |
unknown |
Het |
| Ihh |
T |
C |
1: 74,985,498 (GRCm39) |
Y329C |
probably damaging |
Het |
| Jak2 |
A |
G |
19: 29,278,462 (GRCm39) |
N909D |
probably damaging |
Het |
| Krtap12-1 |
C |
A |
10: 77,556,623 (GRCm39) |
C55* |
probably null |
Het |
| Mical2 |
A |
C |
7: 111,870,589 (GRCm39) |
K26T |
possibly damaging |
Het |
| Mreg |
T |
C |
1: 72,231,216 (GRCm39) |
T81A |
probably benign |
Het |
| Muc16 |
T |
C |
9: 18,558,878 (GRCm39) |
T2472A |
unknown |
Het |
| Nanos3 |
A |
T |
8: 84,903,080 (GRCm39) |
D27E |
probably benign |
Het |
| Nox3 |
T |
G |
17: 3,720,136 (GRCm39) |
S350R |
probably damaging |
Het |
| Or4m1 |
A |
G |
14: 50,558,214 (GRCm39) |
V26A |
probably benign |
Het |
| Or8k18 |
T |
A |
2: 86,086,022 (GRCm39) |
N5I |
probably damaging |
Het |
| Pafah2 |
C |
T |
4: 134,147,281 (GRCm39) |
T310M |
probably damaging |
Het |
| Pals1 |
A |
G |
12: 78,843,832 (GRCm39) |
E12G |
probably benign |
Het |
| Pianp |
A |
G |
6: 124,977,658 (GRCm39) |
I185V |
probably benign |
Het |
| Pja2 |
T |
C |
17: 64,616,470 (GRCm39) |
T142A |
probably benign |
Het |
| Poln |
G |
A |
5: 34,171,658 (GRCm39) |
P747L |
probably damaging |
Het |
| Pramel25 |
T |
A |
4: 143,520,178 (GRCm39) |
S141T |
probably benign |
Het |
| Rdx |
T |
A |
9: 51,976,179 (GRCm39) |
L39* |
probably null |
Het |
| Rnf146 |
A |
G |
10: 29,223,539 (GRCm39) |
W116R |
probably damaging |
Het |
| Rsf1 |
G |
GACGGCGGCT |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
| Sec24d |
A |
G |
3: 123,087,810 (GRCm39) |
T224A |
probably benign |
Het |
| Serpinb9 |
T |
A |
13: 33,190,686 (GRCm39) |
I54K |
possibly damaging |
Het |
| Slc25a13 |
A |
T |
6: 6,109,987 (GRCm39) |
L324Q |
probably null |
Het |
| Slc9c1 |
T |
C |
16: 45,400,490 (GRCm39) |
L700P |
probably benign |
Het |
| Snta1 |
T |
C |
2: 154,222,856 (GRCm39) |
K289R |
probably benign |
Het |
| Sppl2a |
A |
G |
2: 126,765,393 (GRCm39) |
F243S |
probably damaging |
Het |
| Syne1 |
T |
C |
10: 5,058,556 (GRCm39) |
E7319G |
probably benign |
Het |
| Taf5l |
G |
A |
8: 124,730,014 (GRCm39) |
P225L |
probably benign |
Het |
| Tet2 |
A |
T |
3: 133,175,374 (GRCm39) |
N1324K |
possibly damaging |
Het |
| Usp5 |
A |
T |
6: 124,800,414 (GRCm39) |
|
probably null |
Het |
| Vmn2r124 |
G |
T |
17: 18,294,439 (GRCm39) |
R842L |
probably benign |
Het |
| Vps16 |
A |
G |
2: 130,266,319 (GRCm39) |
D2G |
possibly damaging |
Het |
| Vwf |
T |
C |
6: 125,619,693 (GRCm39) |
L1457P |
|
Het |
| Xpo1 |
A |
G |
11: 23,235,058 (GRCm39) |
T576A |
probably damaging |
Het |
| Zdhhc6 |
A |
T |
19: 55,301,680 (GRCm39) |
Y100* |
probably null |
Het |
| Zfp534 |
T |
A |
4: 147,760,082 (GRCm39) |
R196* |
probably null |
Het |
| Zfp710 |
C |
T |
7: 79,731,122 (GRCm39) |
R100W |
probably damaging |
Het |
| Zfp750 |
T |
C |
11: 121,404,674 (GRCm39) |
K67R |
probably benign |
Het |
| Zmynd10 |
T |
C |
9: 107,426,326 (GRCm39) |
S158P |
|
Het |
|
| Other mutations in Zmynd8 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01288:Zmynd8
|
APN |
2 |
165,654,734 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01311:Zmynd8
|
APN |
2 |
165,647,129 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02317:Zmynd8
|
APN |
2 |
165,662,492 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
IGL02548:Zmynd8
|
APN |
2 |
165,675,325 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02798:Zmynd8
|
APN |
2 |
165,694,070 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL02933:Zmynd8
|
APN |
2 |
165,670,238 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
cain
|
UTSW |
2 |
165,699,973 (GRCm39) |
critical splice donor site |
probably null |
|
|
F5770:Zmynd8
|
UTSW |
2 |
165,654,314 (GRCm39) |
nonsense |
probably null |
|
|
I1329:Zmynd8
|
UTSW |
2 |
165,670,145 (GRCm39) |
missense |
probably damaging |
1.00 |
|
P0031:Zmynd8
|
UTSW |
2 |
165,662,618 (GRCm39) |
splice site |
probably benign |
|
|
R0267:Zmynd8
|
UTSW |
2 |
165,670,322 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0608:Zmynd8
|
UTSW |
2 |
165,629,078 (GRCm39) |
splice site |
probably null |
|
|
R1663:Zmynd8
|
UTSW |
2 |
165,649,805 (GRCm39) |
missense |
probably benign |
0.11 |
|
R2212:Zmynd8
|
UTSW |
2 |
165,657,371 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3412:Zmynd8
|
UTSW |
2 |
165,657,371 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3413:Zmynd8
|
UTSW |
2 |
165,657,371 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3749:Zmynd8
|
UTSW |
2 |
165,647,118 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3820:Zmynd8
|
UTSW |
2 |
165,657,381 (GRCm39) |
nonsense |
probably null |
|
|
R3836:Zmynd8
|
UTSW |
2 |
165,700,019 (GRCm39) |
missense |
probably benign |
0.05 |
|
R3957:Zmynd8
|
UTSW |
2 |
165,654,395 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4379:Zmynd8
|
UTSW |
2 |
165,649,858 (GRCm39) |
splice site |
probably null |
|
|
R4526:Zmynd8
|
UTSW |
2 |
165,649,527 (GRCm39) |
intron |
probably benign |
|
|
R4739:Zmynd8
|
UTSW |
2 |
165,647,249 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4838:Zmynd8
|
UTSW |
2 |
165,681,954 (GRCm39) |
nonsense |
probably null |
|
|
R4932:Zmynd8
|
UTSW |
2 |
165,676,871 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R4933:Zmynd8
|
UTSW |
2 |
165,676,871 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R4997:Zmynd8
|
UTSW |
2 |
165,634,736 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5652:Zmynd8
|
UTSW |
2 |
165,649,618 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5741:Zmynd8
|
UTSW |
2 |
165,681,937 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6008:Zmynd8
|
UTSW |
2 |
165,684,707 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R6242:Zmynd8
|
UTSW |
2 |
165,740,867 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R6332:Zmynd8
|
UTSW |
2 |
165,680,772 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6394:Zmynd8
|
UTSW |
2 |
165,687,943 (GRCm39) |
nonsense |
probably null |
|
|
R6772:Zmynd8
|
UTSW |
2 |
165,649,521 (GRCm39) |
missense |
probably benign |
0.35 |
|
R6970:Zmynd8
|
UTSW |
2 |
165,717,670 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6986:Zmynd8
|
UTSW |
2 |
165,675,335 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7229:Zmynd8
|
UTSW |
2 |
165,699,973 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7266:Zmynd8
|
UTSW |
2 |
165,649,492 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R7296:Zmynd8
|
UTSW |
2 |
165,681,929 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7642:Zmynd8
|
UTSW |
2 |
165,654,346 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7818:Zmynd8
|
UTSW |
2 |
165,684,751 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7821:Zmynd8
|
UTSW |
2 |
165,723,000 (GRCm39) |
intron |
probably benign |
|
|
R8135:Zmynd8
|
UTSW |
2 |
165,654,346 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8828:Zmynd8
|
UTSW |
2 |
165,654,466 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9200:Zmynd8
|
UTSW |
2 |
165,682,005 (GRCm39) |
missense |
probably benign |
|
|
R9345:Zmynd8
|
UTSW |
2 |
165,654,668 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R9478:Zmynd8
|
UTSW |
2 |
165,649,569 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9626:Zmynd8
|
UTSW |
2 |
165,654,268 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9649:Zmynd8
|
UTSW |
2 |
165,680,772 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9759:Zmynd8
|
UTSW |
2 |
165,680,746 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
V7580:Zmynd8
|
UTSW |
2 |
165,654,314 (GRCm39) |
nonsense |
probably null |
|
|
V7581:Zmynd8
|
UTSW |
2 |
165,654,314 (GRCm39) |
nonsense |
probably null |
|
|
V7583:Zmynd8
|
UTSW |
2 |
165,654,314 (GRCm39) |
nonsense |
probably null |
|
|
Z1088:Zmynd8
|
UTSW |
2 |
165,670,091 (GRCm39) |
missense |
probably benign |
|
|
Z1176:Zmynd8
|
UTSW |
2 |
165,670,108 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCACCCAGAACCAGGAAGTG -3'
(R):5'- ATCTAAGGCCTGTGGATACGAG -3'
Sequencing Primer
(F):5'- GAGAGGTCACACTCAGCTTG -3'
(R):5'- TGTGGATACGAGGCCGG -3'
|
| Posted On |
2022-01-20 |
Incidental Mutation