Incidental Mutation 'IGL01835:Zbtb17'
ID |
154943 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Zbtb17
|
Ensembl Gene |
ENSMUSG00000006215 |
Gene Name |
zinc finger and BTB domain containing 17 |
Synonyms |
mZ13, Zfp100, Miz1 |
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
IGL01835
|
Quality Score |
|
Status
|
|
Chromosome |
4 |
Chromosomal Location |
141171984-141195248 bp(+) (GRCm39) |
Type of Mutation |
critical splice donor site (2 bp from exon) |
DNA Base Change (assembly) |
T to C
at 141192749 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000006377
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000006377]
[ENSMUST00000078886]
[ENSMUST00000105786]
|
AlphaFold |
Q60821 |
Predicted Effect |
probably null
Transcript: ENSMUST00000006377
|
SMART Domains |
Protein: ENSMUSP00000006377 Gene: ENSMUSG00000006215
Domain | Start | End | E-Value | Type |
BTB
|
24 |
116 |
1.38e-27 |
SMART |
low complexity region
|
203 |
222 |
N/A |
INTRINSIC |
ZnF_C2H2
|
297 |
319 |
6.42e-4 |
SMART |
ZnF_C2H2
|
325 |
347 |
3.11e-2 |
SMART |
ZnF_C2H2
|
353 |
375 |
2.49e-1 |
SMART |
ZnF_C2H2
|
381 |
403 |
8.47e-4 |
SMART |
ZnF_C2H2
|
409 |
431 |
8.47e-4 |
SMART |
ZnF_C2H2
|
437 |
459 |
1.22e-4 |
SMART |
ZnF_C2H2
|
465 |
487 |
4.94e-5 |
SMART |
ZnF_C2H2
|
493 |
515 |
3.26e-5 |
SMART |
ZnF_C2H2
|
521 |
543 |
7.26e-3 |
SMART |
ZnF_C2H2
|
549 |
571 |
4.79e-3 |
SMART |
ZnF_C2H2
|
577 |
599 |
1.58e-3 |
SMART |
ZnF_C2H2
|
605 |
628 |
2.57e-3 |
SMART |
low complexity region
|
654 |
674 |
N/A |
INTRINSIC |
ZnF_C2H2
|
708 |
730 |
4.4e-2 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000078886
|
SMART Domains |
Protein: ENSMUSP00000077925 Gene: ENSMUSG00000040761
Domain | Start | End | E-Value | Type |
RRM
|
7 |
77 |
7.77e-12 |
SMART |
low complexity region
|
109 |
121 |
N/A |
INTRINSIC |
low complexity region
|
235 |
257 |
N/A |
INTRINSIC |
low complexity region
|
262 |
311 |
N/A |
INTRINSIC |
RRM
|
338 |
411 |
8.6e-5 |
SMART |
RRM
|
441 |
511 |
1.56e-16 |
SMART |
RRM
|
520 |
587 |
1.84e-13 |
SMART |
low complexity region
|
617 |
632 |
N/A |
INTRINSIC |
low complexity region
|
669 |
691 |
N/A |
INTRINSIC |
low complexity region
|
695 |
720 |
N/A |
INTRINSIC |
low complexity region
|
749 |
773 |
N/A |
INTRINSIC |
coiled coil region
|
800 |
825 |
N/A |
INTRINSIC |
low complexity region
|
830 |
841 |
N/A |
INTRINSIC |
internal_repeat_2
|
844 |
954 |
6.27e-5 |
PROSPERO |
coiled coil region
|
1494 |
1522 |
N/A |
INTRINSIC |
low complexity region
|
1587 |
1627 |
N/A |
INTRINSIC |
low complexity region
|
1635 |
1641 |
N/A |
INTRINSIC |
low complexity region
|
1642 |
1671 |
N/A |
INTRINSIC |
low complexity region
|
1747 |
1758 |
N/A |
INTRINSIC |
low complexity region
|
1810 |
1823 |
N/A |
INTRINSIC |
low complexity region
|
1888 |
1903 |
N/A |
INTRINSIC |
low complexity region
|
1940 |
1955 |
N/A |
INTRINSIC |
low complexity region
|
2003 |
2012 |
N/A |
INTRINSIC |
internal_repeat_2
|
2015 |
2115 |
6.27e-5 |
PROSPERO |
low complexity region
|
2127 |
2147 |
N/A |
INTRINSIC |
low complexity region
|
2169 |
2191 |
N/A |
INTRINSIC |
low complexity region
|
2207 |
2219 |
N/A |
INTRINSIC |
low complexity region
|
2304 |
2323 |
N/A |
INTRINSIC |
low complexity region
|
2332 |
2371 |
N/A |
INTRINSIC |
low complexity region
|
2396 |
2413 |
N/A |
INTRINSIC |
low complexity region
|
2518 |
2533 |
N/A |
INTRINSIC |
low complexity region
|
2545 |
2555 |
N/A |
INTRINSIC |
low complexity region
|
2696 |
2722 |
N/A |
INTRINSIC |
low complexity region
|
2931 |
2942 |
N/A |
INTRINSIC |
low complexity region
|
2994 |
3006 |
N/A |
INTRINSIC |
low complexity region
|
3192 |
3212 |
N/A |
INTRINSIC |
low complexity region
|
3299 |
3337 |
N/A |
INTRINSIC |
Pfam:SPOC
|
3465 |
3586 |
2.7e-29 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000105786
|
SMART Domains |
Protein: ENSMUSP00000101412 Gene: ENSMUSG00000040761
Domain | Start | End | E-Value | Type |
RRM
|
7 |
77 |
7.77e-12 |
SMART |
low complexity region
|
109 |
121 |
N/A |
INTRINSIC |
low complexity region
|
235 |
257 |
N/A |
INTRINSIC |
low complexity region
|
262 |
311 |
N/A |
INTRINSIC |
RRM
|
338 |
411 |
8.6e-5 |
SMART |
RRM
|
441 |
511 |
1.56e-16 |
SMART |
RRM
|
520 |
587 |
1.84e-13 |
SMART |
low complexity region
|
692 |
714 |
N/A |
INTRINSIC |
low complexity region
|
718 |
743 |
N/A |
INTRINSIC |
low complexity region
|
772 |
796 |
N/A |
INTRINSIC |
coiled coil region
|
823 |
848 |
N/A |
INTRINSIC |
low complexity region
|
853 |
864 |
N/A |
INTRINSIC |
internal_repeat_2
|
867 |
977 |
8.58e-5 |
PROSPERO |
coiled coil region
|
1517 |
1545 |
N/A |
INTRINSIC |
low complexity region
|
1610 |
1650 |
N/A |
INTRINSIC |
low complexity region
|
1658 |
1664 |
N/A |
INTRINSIC |
low complexity region
|
1665 |
1694 |
N/A |
INTRINSIC |
low complexity region
|
1770 |
1781 |
N/A |
INTRINSIC |
low complexity region
|
1833 |
1846 |
N/A |
INTRINSIC |
low complexity region
|
1911 |
1926 |
N/A |
INTRINSIC |
low complexity region
|
1963 |
1978 |
N/A |
INTRINSIC |
low complexity region
|
2026 |
2035 |
N/A |
INTRINSIC |
internal_repeat_2
|
2038 |
2138 |
8.58e-5 |
PROSPERO |
low complexity region
|
2150 |
2170 |
N/A |
INTRINSIC |
low complexity region
|
2192 |
2214 |
N/A |
INTRINSIC |
low complexity region
|
2230 |
2242 |
N/A |
INTRINSIC |
low complexity region
|
2327 |
2346 |
N/A |
INTRINSIC |
low complexity region
|
2355 |
2394 |
N/A |
INTRINSIC |
low complexity region
|
2419 |
2436 |
N/A |
INTRINSIC |
low complexity region
|
2541 |
2556 |
N/A |
INTRINSIC |
low complexity region
|
2568 |
2578 |
N/A |
INTRINSIC |
low complexity region
|
2719 |
2745 |
N/A |
INTRINSIC |
low complexity region
|
2954 |
2965 |
N/A |
INTRINSIC |
low complexity region
|
3017 |
3029 |
N/A |
INTRINSIC |
low complexity region
|
3215 |
3235 |
N/A |
INTRINSIC |
low complexity region
|
3322 |
3360 |
N/A |
INTRINSIC |
Pfam:SPOC
|
3488 |
3609 |
2.7e-29 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000123477
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000130482
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000142020
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000142438
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000147227
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000142695
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a zinc finger protein involved in the regulation of c-myc. The symbol MIZ1 has also been associated with PIAS2 which is a different gene located on chromosome 18. [provided by RefSeq, Jul 2008] PHENOTYPE: Embryonic development of homozygous null mice is severely impaired and death occurs prior to E8.5. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
A |
12: 71,213,957 (GRCm39) |
M728K |
probably benign |
Het |
2700049A03Rik |
T |
A |
12: 71,213,955 (GRCm39) |
Y727* |
probably null |
Het |
Adam23 |
T |
C |
1: 63,582,278 (GRCm39) |
Y309H |
probably damaging |
Het |
Ash2l |
C |
T |
8: 26,329,868 (GRCm39) |
V97M |
probably damaging |
Het |
Cyp4f13 |
A |
G |
17: 33,149,588 (GRCm39) |
F83L |
probably benign |
Het |
Dnah6 |
A |
T |
6: 73,112,784 (GRCm39) |
S1607T |
probably damaging |
Het |
Dock2 |
T |
A |
11: 34,260,435 (GRCm39) |
M969L |
possibly damaging |
Het |
Dse |
T |
A |
10: 34,036,213 (GRCm39) |
|
probably benign |
Het |
Dusp22 |
C |
T |
13: 30,892,666 (GRCm39) |
|
probably null |
Het |
F5 |
G |
A |
1: 164,021,937 (GRCm39) |
V1471I |
probably benign |
Het |
Gm14403 |
A |
T |
2: 177,199,049 (GRCm39) |
E48D |
probably damaging |
Het |
Gm6309 |
G |
A |
5: 146,105,085 (GRCm39) |
A276V |
probably damaging |
Het |
Icam4 |
A |
T |
9: 20,941,086 (GRCm39) |
T113S |
probably damaging |
Het |
Ipo5 |
T |
C |
14: 121,163,650 (GRCm39) |
V236A |
probably benign |
Het |
Mrc2 |
T |
G |
11: 105,227,503 (GRCm39) |
F579V |
probably damaging |
Het |
Myl4 |
T |
A |
11: 104,468,279 (GRCm39) |
M1K |
probably null |
Het |
Oas3 |
A |
T |
5: 120,904,193 (GRCm39) |
C560* |
probably null |
Het |
Or2w25 |
T |
C |
11: 59,504,165 (GRCm39) |
V125A |
probably damaging |
Het |
Or52e18 |
T |
C |
7: 104,609,669 (GRCm39) |
N90S |
probably benign |
Het |
Prlr |
G |
A |
15: 10,329,129 (GRCm39) |
V535I |
probably damaging |
Het |
Ptprd |
T |
C |
4: 76,165,058 (GRCm39) |
T48A |
probably benign |
Het |
Rasa4 |
A |
G |
5: 136,131,461 (GRCm39) |
H485R |
possibly damaging |
Het |
Rnf13 |
A |
T |
3: 57,728,007 (GRCm39) |
H229L |
probably damaging |
Het |
Rpap3 |
T |
C |
15: 97,601,120 (GRCm39) |
D39G |
possibly damaging |
Het |
Sec23ip |
T |
A |
7: 128,357,035 (GRCm39) |
|
probably null |
Het |
Sirpa |
T |
A |
2: 129,457,484 (GRCm39) |
F186Y |
possibly damaging |
Het |
Slc26a11 |
T |
C |
11: 119,268,040 (GRCm39) |
Y473H |
probably benign |
Het |
Slc36a2 |
T |
C |
11: 55,053,559 (GRCm39) |
I360V |
probably benign |
Het |
Spg11 |
G |
A |
2: 121,918,705 (GRCm39) |
R975C |
probably benign |
Het |
Sppl2b |
T |
A |
10: 80,701,175 (GRCm39) |
I350N |
probably damaging |
Het |
Tas2r139 |
A |
T |
6: 42,118,366 (GRCm39) |
N166I |
probably benign |
Het |
Trav14n-3 |
A |
G |
14: 53,607,786 (GRCm39) |
T39A |
possibly damaging |
Het |
Vmn2r61 |
A |
G |
7: 41,950,015 (GRCm39) |
M812V |
probably benign |
Het |
Vmn2r87 |
A |
C |
10: 130,314,978 (GRCm39) |
F203V |
probably damaging |
Het |
Vwde |
A |
C |
6: 13,186,823 (GRCm39) |
V888G |
probably benign |
Het |
|
Other mutations in Zbtb17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01137:Zbtb17
|
APN |
4 |
141,193,678 (GRCm39) |
nonsense |
probably null |
|
IGL01449:Zbtb17
|
APN |
4 |
141,190,616 (GRCm39) |
missense |
probably benign |
|
IGL02141:Zbtb17
|
APN |
4 |
141,192,264 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02142:Zbtb17
|
APN |
4 |
141,192,293 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02167:Zbtb17
|
APN |
4 |
141,189,140 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02388:Zbtb17
|
APN |
4 |
141,189,224 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02600:Zbtb17
|
APN |
4 |
141,194,196 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02617:Zbtb17
|
APN |
4 |
141,192,399 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03290:Zbtb17
|
APN |
4 |
141,194,244 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03391:Zbtb17
|
APN |
4 |
141,194,069 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02799:Zbtb17
|
UTSW |
4 |
141,190,691 (GRCm39) |
missense |
probably benign |
0.20 |
R0698:Zbtb17
|
UTSW |
4 |
141,193,407 (GRCm39) |
splice site |
probably null |
|
R0736:Zbtb17
|
UTSW |
4 |
141,189,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R1924:Zbtb17
|
UTSW |
4 |
141,191,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R1940:Zbtb17
|
UTSW |
4 |
141,192,859 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2164:Zbtb17
|
UTSW |
4 |
141,191,557 (GRCm39) |
missense |
probably benign |
|
R2517:Zbtb17
|
UTSW |
4 |
141,191,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R3424:Zbtb17
|
UTSW |
4 |
141,192,299 (GRCm39) |
missense |
probably damaging |
0.99 |
R3884:Zbtb17
|
UTSW |
4 |
141,191,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R4609:Zbtb17
|
UTSW |
4 |
141,193,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R5055:Zbtb17
|
UTSW |
4 |
141,193,860 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5327:Zbtb17
|
UTSW |
4 |
141,192,942 (GRCm39) |
missense |
probably benign |
0.22 |
R5363:Zbtb17
|
UTSW |
4 |
141,194,072 (GRCm39) |
missense |
probably benign |
0.02 |
R5987:Zbtb17
|
UTSW |
4 |
141,192,128 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6038:Zbtb17
|
UTSW |
4 |
141,191,752 (GRCm39) |
missense |
probably benign |
0.05 |
R6038:Zbtb17
|
UTSW |
4 |
141,191,752 (GRCm39) |
missense |
probably benign |
0.05 |
R6311:Zbtb17
|
UTSW |
4 |
141,190,694 (GRCm39) |
missense |
probably benign |
0.00 |
R6320:Zbtb17
|
UTSW |
4 |
141,190,694 (GRCm39) |
missense |
probably benign |
0.00 |
R6321:Zbtb17
|
UTSW |
4 |
141,190,694 (GRCm39) |
missense |
probably benign |
0.00 |
R6322:Zbtb17
|
UTSW |
4 |
141,190,694 (GRCm39) |
missense |
probably benign |
0.00 |
R6337:Zbtb17
|
UTSW |
4 |
141,190,694 (GRCm39) |
missense |
probably benign |
0.00 |
R6365:Zbtb17
|
UTSW |
4 |
141,190,694 (GRCm39) |
missense |
probably benign |
0.00 |
R6492:Zbtb17
|
UTSW |
4 |
141,190,694 (GRCm39) |
missense |
probably benign |
0.00 |
R6605:Zbtb17
|
UTSW |
4 |
141,192,261 (GRCm39) |
missense |
probably damaging |
0.99 |
R6695:Zbtb17
|
UTSW |
4 |
141,189,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R7717:Zbtb17
|
UTSW |
4 |
141,193,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R7999:Zbtb17
|
UTSW |
4 |
141,189,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R8542:Zbtb17
|
UTSW |
4 |
141,194,139 (GRCm39) |
unclassified |
probably benign |
|
R8544:Zbtb17
|
UTSW |
4 |
141,194,139 (GRCm39) |
unclassified |
probably benign |
|
R8545:Zbtb17
|
UTSW |
4 |
141,194,139 (GRCm39) |
unclassified |
probably benign |
|
R8836:Zbtb17
|
UTSW |
4 |
141,189,233 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9072:Zbtb17
|
UTSW |
4 |
141,193,676 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9073:Zbtb17
|
UTSW |
4 |
141,193,676 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9389:Zbtb17
|
UTSW |
4 |
141,193,131 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9785:Zbtb17
|
UTSW |
4 |
141,194,271 (GRCm39) |
missense |
possibly damaging |
0.64 |
Z1176:Zbtb17
|
UTSW |
4 |
141,190,990 (GRCm39) |
missense |
probably benign |
0.00 |
|
Posted On |
2014-02-04 |