Incidental Mutation 'IGL01593:Bnc2'
ID |
91657 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Bnc2
|
Ensembl Gene |
ENSMUSG00000028487 |
Gene Name |
basonuclin zinc finger protein 2 |
Synonyms |
8430420F16Rik, 5031434M05Rik |
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
IGL01593
|
Quality Score |
|
Status
|
|
Chromosome |
4 |
Chromosomal Location |
84193332-84593512 bp(-) (GRCm39) |
Type of Mutation |
splice site (4 bp from exon) |
DNA Base Change (assembly) |
T to C
at 84194478 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000102820]
[ENSMUST00000107198]
[ENSMUST00000176601]
[ENSMUST00000176612]
[ENSMUST00000176691]
[ENSMUST00000176971]
[ENSMUST00000176998]
|
AlphaFold |
Q8BMQ3 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000102820
AA Change: Y977C
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000099884 Gene: ENSMUSG00000028487 AA Change: Y977C
Domain | Start | End | E-Value | Type |
low complexity region
|
362 |
378 |
N/A |
INTRINSIC |
low complexity region
|
389 |
400 |
N/A |
INTRINSIC |
ZnF_C2H2
|
469 |
492 |
4.72e-2 |
SMART |
ZnF_C2H2
|
497 |
526 |
7.11e0 |
SMART |
low complexity region
|
612 |
629 |
N/A |
INTRINSIC |
low complexity region
|
633 |
642 |
N/A |
INTRINSIC |
low complexity region
|
676 |
690 |
N/A |
INTRINSIC |
ZnF_C2H2
|
861 |
884 |
1.62e0 |
SMART |
ZnF_C2H2
|
889 |
916 |
4.81e0 |
SMART |
low complexity region
|
991 |
1008 |
N/A |
INTRINSIC |
low complexity region
|
1048 |
1062 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1063 |
1086 |
1.03e-2 |
SMART |
ZnF_C2H2
|
1091 |
1118 |
3.78e-1 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000107198
AA Change: Y949C
PolyPhen 2
Score 0.986 (Sensitivity: 0.74; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000102816 Gene: ENSMUSG00000028487 AA Change: Y949C
Domain | Start | End | E-Value | Type |
low complexity region
|
334 |
350 |
N/A |
INTRINSIC |
low complexity region
|
361 |
372 |
N/A |
INTRINSIC |
ZnF_C2H2
|
441 |
464 |
4.72e-2 |
SMART |
ZnF_C2H2
|
469 |
498 |
7.11e0 |
SMART |
low complexity region
|
584 |
601 |
N/A |
INTRINSIC |
low complexity region
|
605 |
614 |
N/A |
INTRINSIC |
low complexity region
|
648 |
662 |
N/A |
INTRINSIC |
ZnF_C2H2
|
833 |
856 |
1.62e0 |
SMART |
ZnF_C2H2
|
861 |
888 |
4.81e0 |
SMART |
low complexity region
|
963 |
980 |
N/A |
INTRINSIC |
low complexity region
|
1020 |
1034 |
N/A |
INTRINSIC |
ZnF_C2H2
|
1035 |
1058 |
1.03e-2 |
SMART |
ZnF_C2H2
|
1063 |
1090 |
3.78e-1 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000176601
|
SMART Domains |
Protein: ENSMUSP00000135480 Gene: ENSMUSG00000028487
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
12 |
35 |
1.62e0 |
SMART |
low complexity region
|
53 |
67 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000176612
|
SMART Domains |
Protein: ENSMUSP00000135778 Gene: ENSMUSG00000028487
Domain | Start | End | E-Value | Type |
low complexity region
|
292 |
308 |
N/A |
INTRINSIC |
low complexity region
|
319 |
330 |
N/A |
INTRINSIC |
ZnF_C2H2
|
399 |
422 |
4.72e-2 |
SMART |
ZnF_C2H2
|
427 |
456 |
7.11e0 |
SMART |
low complexity region
|
542 |
559 |
N/A |
INTRINSIC |
low complexity region
|
563 |
572 |
N/A |
INTRINSIC |
low complexity region
|
606 |
620 |
N/A |
INTRINSIC |
ZnF_C2H2
|
791 |
814 |
1.62e0 |
SMART |
low complexity region
|
832 |
846 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000176691
AA Change: Y882C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000135375 Gene: ENSMUSG00000028487 AA Change: Y882C
Domain | Start | End | E-Value | Type |
low complexity region
|
267 |
283 |
N/A |
INTRINSIC |
low complexity region
|
294 |
305 |
N/A |
INTRINSIC |
ZnF_C2H2
|
374 |
397 |
4.72e-2 |
SMART |
ZnF_C2H2
|
402 |
431 |
7.11e0 |
SMART |
low complexity region
|
517 |
534 |
N/A |
INTRINSIC |
low complexity region
|
538 |
547 |
N/A |
INTRINSIC |
low complexity region
|
581 |
595 |
N/A |
INTRINSIC |
ZnF_C2H2
|
766 |
789 |
1.62e0 |
SMART |
ZnF_C2H2
|
794 |
821 |
4.81e0 |
SMART |
low complexity region
|
896 |
913 |
N/A |
INTRINSIC |
low complexity region
|
953 |
967 |
N/A |
INTRINSIC |
ZnF_C2H2
|
968 |
991 |
1.03e-2 |
SMART |
ZnF_C2H2
|
996 |
1023 |
3.78e-1 |
SMART |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000176702
|
SMART Domains |
Protein: ENSMUSP00000134774 Gene: ENSMUSG00000028487
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
105 |
128 |
1.62e0 |
SMART |
low complexity region
|
146 |
160 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000176971
AA Change: Y89C
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000135607 Gene: ENSMUSG00000028487 AA Change: Y89C
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
3 |
28 |
1.98e2 |
SMART |
low complexity region
|
103 |
120 |
N/A |
INTRINSIC |
low complexity region
|
160 |
174 |
N/A |
INTRINSIC |
ZnF_C2H2
|
175 |
198 |
1.03e-2 |
SMART |
ZnF_C2H2
|
203 |
230 |
3.78e-1 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000177277
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000176998
|
SMART Domains |
Protein: ENSMUSP00000135283 Gene: ENSMUSG00000028487
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
12 |
35 |
1.62e0 |
SMART |
low complexity region
|
53 |
67 |
N/A |
INTRINSIC |
|
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 conserved zinc finger protein. The encoded protein functions in skin color saturation. Mutations in this gene are associated with facial pigmented spots. This gene is also associated with susceptibility to adolescent idiopathic scoliosis. [provided by RefSeq, Jul 2016] PHENOTYPE: Mice homozygous for a gene trap insertion die within 24 hrs of birth and display cleft palate, an overall size reduction of the head and tongue, and abnormal craniofacial bone development due to impaired multiplication of embryonic craniofacial mesenchymal cells. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc12 |
A |
T |
8: 87,284,279 (GRCm39) |
I310N |
probably damaging |
Het |
Abtb3 |
T |
A |
10: 85,490,339 (GRCm39) |
|
probably benign |
Het |
Ackr4 |
C |
T |
9: 103,963,130 (GRCm39) |
|
probably benign |
Het |
Ankib1 |
A |
T |
5: 3,782,590 (GRCm39) |
D346E |
probably benign |
Het |
Asap2 |
G |
T |
12: 21,263,203 (GRCm39) |
A273S |
probably null |
Het |
Atp6v0d2 |
C |
A |
4: 19,881,436 (GRCm39) |
R219L |
probably damaging |
Het |
Atp6v1e2 |
A |
T |
17: 87,251,727 (GRCm39) |
F224I |
probably damaging |
Het |
Cd33 |
A |
G |
7: 43,179,705 (GRCm39) |
L241P |
possibly damaging |
Het |
Clec4g |
A |
T |
8: 3,769,474 (GRCm39) |
|
probably null |
Het |
Dym |
C |
T |
18: 75,247,852 (GRCm39) |
|
probably benign |
Het |
Enpp5 |
A |
G |
17: 44,391,612 (GRCm39) |
T14A |
probably benign |
Het |
Ggt1 |
T |
C |
10: 75,421,121 (GRCm39) |
|
probably null |
Het |
Gm17541 |
T |
A |
12: 4,739,868 (GRCm39) |
|
probably benign |
Het |
Gpr39 |
A |
T |
1: 125,605,188 (GRCm39) |
I39F |
probably benign |
Het |
Kcnb1 |
G |
T |
2: 166,948,127 (GRCm39) |
F240L |
probably damaging |
Het |
Kcnt1 |
T |
A |
2: 25,788,766 (GRCm39) |
V400E |
probably damaging |
Het |
Klhdc7a |
A |
G |
4: 139,694,125 (GRCm39) |
I274T |
probably damaging |
Het |
Lrwd1 |
A |
T |
5: 136,163,483 (GRCm39) |
L71Q |
probably damaging |
Het |
Mycbp2 |
A |
T |
14: 103,528,723 (GRCm39) |
|
probably null |
Het |
Nckap1 |
A |
T |
2: 80,350,914 (GRCm39) |
M725K |
probably benign |
Het |
Odad2 |
T |
C |
18: 7,127,345 (GRCm39) |
K956R |
probably benign |
Het |
Or2b7 |
T |
A |
13: 21,739,389 (GRCm39) |
I268F |
probably damaging |
Het |
Pole2 |
C |
T |
12: 69,269,873 (GRCm39) |
|
probably null |
Het |
Prss32 |
A |
G |
17: 24,074,982 (GRCm39) |
T111A |
probably benign |
Het |
Rgs9 |
A |
G |
11: 109,139,875 (GRCm39) |
|
probably benign |
Het |
Slc2a4 |
A |
G |
11: 69,835,654 (GRCm39) |
C361R |
probably damaging |
Het |
Ston1 |
G |
A |
17: 88,944,438 (GRCm39) |
G615R |
probably null |
Het |
Tas2r139 |
T |
G |
6: 42,117,891 (GRCm39) |
W8G |
probably benign |
Het |
Tmem101 |
A |
T |
11: 102,046,704 (GRCm39) |
L55Q |
probably damaging |
Het |
Tnni3k |
T |
C |
3: 154,646,666 (GRCm39) |
|
probably null |
Het |
Uba2 |
A |
G |
7: 33,845,689 (GRCm39) |
V478A |
probably damaging |
Het |
Vps13a |
T |
C |
19: 16,739,545 (GRCm39) |
D52G |
probably damaging |
Het |
|
Other mutations in Bnc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01902:Bnc2
|
APN |
4 |
84,309,181 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02228:Bnc2
|
APN |
4 |
84,211,313 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02396:Bnc2
|
APN |
4 |
84,194,246 (GRCm39) |
missense |
probably benign |
0.16 |
R0125:Bnc2
|
UTSW |
4 |
84,211,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R0650:Bnc2
|
UTSW |
4 |
84,211,433 (GRCm39) |
missense |
probably benign |
0.04 |
R1082:Bnc2
|
UTSW |
4 |
84,464,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R1334:Bnc2
|
UTSW |
4 |
84,194,526 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1439:Bnc2
|
UTSW |
4 |
84,194,305 (GRCm39) |
missense |
probably benign |
0.38 |
R1447:Bnc2
|
UTSW |
4 |
84,211,457 (GRCm39) |
missense |
probably benign |
0.13 |
R1515:Bnc2
|
UTSW |
4 |
84,332,563 (GRCm39) |
missense |
probably null |
0.99 |
R1548:Bnc2
|
UTSW |
4 |
84,194,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R1818:Bnc2
|
UTSW |
4 |
84,210,111 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1819:Bnc2
|
UTSW |
4 |
84,210,111 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2345:Bnc2
|
UTSW |
4 |
84,210,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R2897:Bnc2
|
UTSW |
4 |
84,211,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R2898:Bnc2
|
UTSW |
4 |
84,211,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R2966:Bnc2
|
UTSW |
4 |
84,211,754 (GRCm39) |
missense |
probably benign |
0.14 |
R3404:Bnc2
|
UTSW |
4 |
84,464,478 (GRCm39) |
missense |
probably damaging |
0.98 |
R4235:Bnc2
|
UTSW |
4 |
84,211,751 (GRCm39) |
missense |
probably damaging |
0.96 |
R4546:Bnc2
|
UTSW |
4 |
84,210,213 (GRCm39) |
missense |
probably benign |
0.34 |
R4676:Bnc2
|
UTSW |
4 |
84,211,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R4926:Bnc2
|
UTSW |
4 |
84,194,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R5060:Bnc2
|
UTSW |
4 |
84,449,872 (GRCm39) |
missense |
probably benign |
0.02 |
R5365:Bnc2
|
UTSW |
4 |
84,329,666 (GRCm39) |
intron |
probably benign |
|
R5735:Bnc2
|
UTSW |
4 |
84,210,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R5872:Bnc2
|
UTSW |
4 |
84,211,007 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5921:Bnc2
|
UTSW |
4 |
84,211,292 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5999:Bnc2
|
UTSW |
4 |
84,474,137 (GRCm39) |
missense |
probably benign |
0.20 |
R6351:Bnc2
|
UTSW |
4 |
84,211,380 (GRCm39) |
missense |
probably benign |
0.16 |
R6869:Bnc2
|
UTSW |
4 |
84,211,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R7236:Bnc2
|
UTSW |
4 |
84,474,101 (GRCm39) |
missense |
probably benign |
0.31 |
R7363:Bnc2
|
UTSW |
4 |
84,210,308 (GRCm39) |
missense |
probably benign |
0.02 |
R7643:Bnc2
|
UTSW |
4 |
84,424,811 (GRCm39) |
missense |
probably benign |
0.01 |
R8017:Bnc2
|
UTSW |
4 |
84,329,662 (GRCm39) |
missense |
|
|
R8019:Bnc2
|
UTSW |
4 |
84,329,662 (GRCm39) |
missense |
|
|
R8050:Bnc2
|
UTSW |
4 |
84,210,573 (GRCm39) |
missense |
probably benign |
0.00 |
R8311:Bnc2
|
UTSW |
4 |
84,194,582 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8463:Bnc2
|
UTSW |
4 |
84,211,608 (GRCm39) |
missense |
probably damaging |
0.99 |
R8676:Bnc2
|
UTSW |
4 |
84,194,550 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8722:Bnc2
|
UTSW |
4 |
84,211,883 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8845:Bnc2
|
UTSW |
4 |
84,194,338 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8887:Bnc2
|
UTSW |
4 |
84,209,707 (GRCm39) |
intron |
probably benign |
|
R9051:Bnc2
|
UTSW |
4 |
84,210,138 (GRCm39) |
missense |
probably benign |
0.00 |
R9142:Bnc2
|
UTSW |
4 |
84,474,111 (GRCm39) |
missense |
probably benign |
0.03 |
R9165:Bnc2
|
UTSW |
4 |
84,329,731 (GRCm39) |
missense |
|
|
R9297:Bnc2
|
UTSW |
4 |
84,474,136 (GRCm39) |
intron |
probably benign |
|
R9638:Bnc2
|
UTSW |
4 |
84,332,492 (GRCm39) |
missense |
probably damaging |
1.00 |
X0021:Bnc2
|
UTSW |
4 |
84,211,377 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2013-12-09 |