Incidental Mutation 'IGL02903:Anks6'
| ID |
363688 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Anks6
|
| Ensembl Gene |
ENSMUSG00000066191 |
| Gene Name |
ankyrin repeat and sterile alpha motif domain containing 6 |
| Synonyms |
b2b1801.1Clo, LOC269533, 2210417J20Rik, SamCystin, Samd6 |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL02903
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
4 |
| Chromosomal Location |
47015669-47057427 bp(-) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 47045004 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamic Acid to Lysine
at position 301
(E301K)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000155271
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000084616]
[ENSMUST00000107747]
[ENSMUST00000229609]
|
| AlphaFold |
Q6GQX6 |
| Predicted Effect |
unknown
Transcript: ENSMUST00000084616
AA Change: E301K
|
| SMART Domains |
Protein: ENSMUSP00000081665
Gene: ENSMUSG00000066191
AA Change: E301K
| Domain | Start | End | E-Value | Type |
|---|
|
ANK
|
8 |
37 |
2.39e2 |
SMART |
|
ANK
|
68 |
97 |
5.62e-4 |
SMART |
|
ANK
|
101 |
130 |
2.05e-6 |
SMART |
|
ANK
|
134 |
163 |
1.9e-1 |
SMART |
|
ANK
|
181 |
210 |
8.99e-3 |
SMART |
|
ANK
|
215 |
244 |
7.83e-3 |
SMART |
|
ANK
|
282 |
312 |
5.87e2 |
SMART |
|
ANK
|
316 |
345 |
1.22e-4 |
SMART |
|
ANK
|
350 |
379 |
3.57e-6 |
SMART |
|
ANK
|
383 |
414 |
1.23e3 |
SMART |
|
low complexity region
|
539 |
575 |
N/A |
INTRINSIC |
|
low complexity region
|
619 |
673 |
N/A |
INTRINSIC |
|
SAM
|
700 |
766 |
2.73e-10 |
SMART |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000107747
AA Change: E301K
PolyPhen 2
Score 0.899 (Sensitivity: 0.82; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000103376
Gene: ENSMUSG00000066191
AA Change: E301K
| Domain | Start | End | E-Value | Type |
|---|
|
ANK
|
8 |
37 |
2.39e2 |
SMART |
|
ANK
|
68 |
97 |
5.62e-4 |
SMART |
|
ANK
|
101 |
130 |
2.05e-6 |
SMART |
|
ANK
|
134 |
163 |
1.9e-1 |
SMART |
|
ANK
|
181 |
210 |
8.99e-3 |
SMART |
|
ANK
|
215 |
244 |
7.83e-3 |
SMART |
|
ANK
|
282 |
312 |
5.87e2 |
SMART |
|
ANK
|
316 |
345 |
1.22e-4 |
SMART |
|
ANK
|
350 |
379 |
3.57e-6 |
SMART |
|
ANK
|
383 |
414 |
1.23e3 |
SMART |
|
low complexity region
|
607 |
643 |
N/A |
INTRINSIC |
|
low complexity region
|
687 |
741 |
N/A |
INTRINSIC |
|
low complexity region
|
748 |
768 |
N/A |
INTRINSIC |
|
Blast:SAM
|
769 |
796 |
1e-9 |
BLAST |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000119580
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000154664
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000229609
AA Change: E301K
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
| 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 protein containing multiple ankyrin repeats and a SAM domain. It is thought that this protein may localize to the proximal region of the primary cilium, and may play a role in renal and cardiovascular development. Mutations in this gene have been shown to cause a form of nephronophthisis (NPHP16), a chronic tubulo-interstitial nephritis. [provided by RefSeq, Jul 2015]
PHENOTYPE: Mice homozygous for an ENU-induced mutation exhibit complex congenital heart defects including TGA, DORV and septal defects associated with heterotaxy. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 37 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2410089E03Rik |
G |
T |
15: 8,269,778 (GRCm38) |
R3150M |
unknown |
Het |
| 2410089E03Rik |
G |
T |
15: 8,269,779 (GRCm38) |
R3150S |
unknown |
Het |
| 4931417E11Rik |
A |
G |
6: 73,469,120 (GRCm38) |
Y149H |
probably damaging |
Het |
| Alox5 |
T |
G |
6: 116,420,335 (GRCm38) |
N296T |
probably damaging |
Het |
| Astn1 |
A |
G |
1: 158,688,550 (GRCm38) |
S1237G |
probably damaging |
Het |
| Atf6 |
G |
A |
1: 170,799,714 (GRCm38) |
P394S |
probably benign |
Het |
| Atp4a |
G |
A |
7: 30,715,919 (GRCm38) |
M321I |
probably benign |
Het |
| C4bp |
G |
A |
1: 130,655,985 (GRCm38) |
T82I |
probably damaging |
Het |
| Cask |
A |
T |
X: 13,552,447 (GRCm38) |
|
probably benign |
Het |
| Cenpf |
A |
T |
1: 189,646,876 (GRCm38) |
S2906T |
probably damaging |
Het |
| Cfl1 |
T |
C |
19: 5,492,800 (GRCm38) |
F103L |
probably benign |
Het |
| Chrnb3 |
A |
T |
8: 27,386,806 (GRCm38) |
T83S |
probably damaging |
Het |
| Cmtr2 |
A |
G |
8: 110,222,878 (GRCm38) |
T607A |
probably benign |
Het |
| Cts7 |
A |
T |
13: 61,356,626 (GRCm38) |
|
probably benign |
Het |
| Dgkz |
A |
T |
2: 91,939,962 (GRCm38) |
Y514N |
possibly damaging |
Het |
| Dmrtc1b |
T |
A |
X: 102,713,567 (GRCm38) |
L206Q |
probably benign |
Het |
| Dus3l |
C |
T |
17: 56,768,363 (GRCm38) |
L397F |
probably damaging |
Het |
| Fam159b |
T |
A |
13: 104,863,610 (GRCm38) |
Y35F |
probably benign |
Het |
| Gm13089 |
A |
T |
4: 143,699,166 (GRCm38) |
M69K |
probably benign |
Het |
| Gm6356 |
C |
T |
14: 6,973,735 (GRCm38) |
G27E |
probably damaging |
Het |
| Hkdc1 |
C |
T |
10: 62,400,191 (GRCm38) |
|
probably null |
Het |
| Kcmf1 |
A |
T |
6: 72,858,883 (GRCm38) |
V21E |
possibly damaging |
Het |
| Kcnh4 |
T |
A |
11: 100,757,654 (GRCm38) |
T75S |
possibly damaging |
Het |
| Lemd2 |
A |
G |
17: 27,193,210 (GRCm38) |
|
probably benign |
Het |
| Magee1 |
G |
T |
X: 105,123,339 (GRCm38) |
R910L |
probably damaging |
Het |
| Mcm3ap |
T |
C |
10: 76,471,258 (GRCm38) |
|
probably benign |
Het |
| Mfsd4b3 |
T |
A |
10: 39,947,643 (GRCm38) |
E207V |
possibly damaging |
Het |
| Olfr1354 |
A |
G |
10: 78,917,416 (GRCm38) |
D192G |
probably damaging |
Het |
| Olfr697 |
A |
G |
7: 106,741,710 (GRCm38) |
S75P |
probably damaging |
Het |
| Pappa |
T |
C |
4: 65,261,980 (GRCm38) |
V1026A |
probably damaging |
Het |
| Paxip1 |
A |
G |
5: 27,748,872 (GRCm38) |
L942P |
probably damaging |
Het |
| Ppp1r12b |
A |
T |
1: 134,955,649 (GRCm38) |
L45Q |
probably benign |
Het |
| Ptprq |
T |
C |
10: 107,666,586 (GRCm38) |
T824A |
possibly damaging |
Het |
| Rfwd3 |
T |
C |
8: 111,278,229 (GRCm38) |
T574A |
probably benign |
Het |
| Rsbn1 |
T |
C |
3: 103,928,569 (GRCm38) |
S308P |
probably damaging |
Het |
| Smr2 |
A |
T |
5: 88,108,630 (GRCm38) |
I56F |
probably benign |
Het |
| Wdfy4 |
C |
T |
14: 33,109,650 (GRCm38) |
R873H |
probably damaging |
Het |
|
| Other mutations in Anks6 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00465:Anks6
|
APN |
4 |
47,046,054 (GRCm38) |
missense |
probably damaging |
0.98 |
|
IGL01886:Anks6
|
APN |
4 |
47,044,850 (GRCm38) |
missense |
probably damaging |
1.00 |
|
PIT4131001:Anks6
|
UTSW |
4 |
47,027,109 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0632:Anks6
|
UTSW |
4 |
47,033,167 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
R1220:Anks6
|
UTSW |
4 |
47,025,767 (GRCm38) |
splice site |
probably benign |
|
|
R1398:Anks6
|
UTSW |
4 |
47,044,926 (GRCm38) |
missense |
possibly damaging |
0.75 |
|
R1479:Anks6
|
UTSW |
4 |
47,044,874 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1519:Anks6
|
UTSW |
4 |
47,027,152 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R1713:Anks6
|
UTSW |
4 |
47,039,726 (GRCm38) |
missense |
probably benign |
0.00 |
|
R1781:Anks6
|
UTSW |
4 |
47,043,639 (GRCm38) |
missense |
possibly damaging |
0.87 |
|
R1853:Anks6
|
UTSW |
4 |
47,049,387 (GRCm38) |
missense |
probably benign |
0.00 |
|
R2364:Anks6
|
UTSW |
4 |
47,027,248 (GRCm38) |
missense |
possibly damaging |
0.93 |
|
R3790:Anks6
|
UTSW |
4 |
47,049,212 (GRCm38) |
missense |
probably damaging |
0.97 |
|
R4432:Anks6
|
UTSW |
4 |
47,044,905 (GRCm38) |
nonsense |
probably null |
|
|
R4700:Anks6
|
UTSW |
4 |
47,033,127 (GRCm38) |
missense |
possibly damaging |
0.86 |
|
R4847:Anks6
|
UTSW |
4 |
47,033,266 (GRCm38) |
missense |
probably benign |
|
|
R4876:Anks6
|
UTSW |
4 |
47,030,795 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4877:Anks6
|
UTSW |
4 |
47,030,795 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4878:Anks6
|
UTSW |
4 |
47,030,795 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4879:Anks6
|
UTSW |
4 |
47,030,795 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4961:Anks6
|
UTSW |
4 |
47,030,795 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4962:Anks6
|
UTSW |
4 |
47,030,795 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4968:Anks6
|
UTSW |
4 |
47,030,795 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4970:Anks6
|
UTSW |
4 |
47,030,795 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4971:Anks6
|
UTSW |
4 |
47,030,795 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5092:Anks6
|
UTSW |
4 |
47,030,795 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5113:Anks6
|
UTSW |
4 |
47,030,795 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5389:Anks6
|
UTSW |
4 |
47,038,900 (GRCm38) |
splice site |
probably benign |
|
|
R5569:Anks6
|
UTSW |
4 |
47,045,007 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5857:Anks6
|
UTSW |
4 |
47,039,736 (GRCm38) |
missense |
possibly damaging |
0.92 |
|
R5977:Anks6
|
UTSW |
4 |
47,035,748 (GRCm38) |
missense |
probably benign |
0.11 |
|
R5978:Anks6
|
UTSW |
4 |
47,049,252 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6933:Anks6
|
UTSW |
4 |
47,049,164 (GRCm38) |
missense |
probably benign |
0.25 |
|
R7175:Anks6
|
UTSW |
4 |
47,046,268 (GRCm38) |
splice site |
probably null |
|
|
R7454:Anks6
|
UTSW |
4 |
47,038,919 (GRCm38) |
missense |
unknown |
|
|
R7874:Anks6
|
UTSW |
4 |
47,049,275 (GRCm38) |
missense |
unknown |
|
|
R8146:Anks6
|
UTSW |
4 |
47,043,605 (GRCm38) |
missense |
unknown |
|
|
R8437:Anks6
|
UTSW |
4 |
47,030,705 (GRCm38) |
missense |
probably benign |
0.00 |
|
R9454:Anks6
|
UTSW |
4 |
47,016,789 (GRCm38) |
missense |
possibly damaging |
0.86 |
|
R9462:Anks6
|
UTSW |
4 |
47,033,142 (GRCm38) |
missense |
unknown |
|
|
R9567:Anks6
|
UTSW |
4 |
47,044,880 (GRCm38) |
missense |
unknown |
|
|
| Posted On |
2015-12-18 |
Incidental Mutation