Incidental Mutation 'R2195:Kalrn'
ID |
238329 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Kalrn
|
Ensembl Gene |
ENSMUSG00000061751 |
Gene Name |
kalirin, RhoGEF kinase |
Synonyms |
2210407G14Rik, Hapip, E530005C20Rik, LOC224126 |
MMRRC Submission |
040197-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.934)
|
Stock # |
R2195 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
16 |
Chromosomal Location |
33969073-34573532 bp(-) (GRCm38) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 33989810 bp (GRCm38)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Asparagine
at position 2525
(D2525N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000076088
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000076810]
[ENSMUST00000114973]
|
AlphaFold |
no structure available at present |
PDB Structure |
Solution structure of SH3 domain of mouse Kalirin-9a protein [SOLUTION NMR]
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000076810
AA Change: D2525N
PolyPhen 2
Score 0.722 (Sensitivity: 0.86; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000076088 Gene: ENSMUSG00000061751 AA Change: D2525N
Domain | Start | End | E-Value | Type |
SEC14
|
20 |
159 |
2.22e-30 |
SMART |
SPEC
|
173 |
289 |
5.32e-9 |
SMART |
SPEC
|
295 |
397 |
1.19e-11 |
SMART |
SPEC
|
400 |
515 |
1.83e0 |
SMART |
SPEC
|
521 |
623 |
9.84e-13 |
SMART |
SPEC
|
626 |
748 |
2.74e-2 |
SMART |
SPEC
|
875 |
976 |
8.11e-14 |
SMART |
SPEC
|
1106 |
1208 |
4.7e-10 |
SMART |
RhoGEF
|
1258 |
1428 |
3.6e-56 |
SMART |
PH
|
1442 |
1555 |
5.24e-8 |
SMART |
SH3
|
1622 |
1683 |
1.23e-7 |
SMART |
RhoGEF
|
1904 |
2074 |
1.47e-52 |
SMART |
PH
|
2094 |
2199 |
9.87e-4 |
SMART |
SH3
|
2295 |
2356 |
2.78e-2 |
SMART |
IGc2
|
2455 |
2527 |
4.28e-12 |
SMART |
FN3
|
2541 |
2623 |
3.07e-11 |
SMART |
S_TKc
|
2656 |
2910 |
1.28e-71 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000114973
AA Change: D856N
PolyPhen 2
Score 0.617 (Sensitivity: 0.87; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000110624 Gene: ENSMUSG00000061751 AA Change: D856N
Domain | Start | End | E-Value | Type |
RhoGEF
|
235 |
405 |
1.47e-52 |
SMART |
PH
|
425 |
530 |
9.87e-4 |
SMART |
SH3
|
626 |
687 |
2.78e-2 |
SMART |
IGc2
|
786 |
858 |
4.28e-12 |
SMART |
FN3
|
872 |
954 |
3.07e-11 |
SMART |
S_TKc
|
987 |
1241 |
1.28e-71 |
SMART |
|
Meta Mutation Damage Score |
0.0910  |
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.6%
- 20x: 96.1%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with the huntingtin-associated protein 1, which is a huntingtin binding protein that may function in vesicle trafficking. [provided by RefSeq, Apr 2016] PHENOTYPE: Mice homozygous for a knock-out allele specific for isoform 7 exhibit decreased anxiety-related behavior, contextual conditioning, and synapse formation. Mice homozygous for another knock-out allele exhibit impaired AMPA-mediated synaptic currents and abnormal behavior. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 15 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ago2 |
A |
T |
15: 73,119,469 |
V540E |
probably benign |
Het |
Cep295 |
T |
A |
9: 15,332,321 |
Q1613L |
probably damaging |
Het |
Cib3 |
A |
T |
8: 72,204,413 |
I160N |
probably damaging |
Het |
Col1a2 |
G |
A |
6: 4,518,822 |
|
probably benign |
Het |
Coq10b |
T |
A |
1: 55,061,298 |
L47Q |
probably damaging |
Het |
Impg2 |
T |
C |
16: 56,260,134 |
V767A |
probably benign |
Het |
Kmt2e |
T |
C |
5: 23,502,196 |
|
probably null |
Het |
Marf1 |
T |
C |
16: 14,111,699 |
D1681G |
probably benign |
Het |
Nid1 |
G |
T |
13: 13,476,203 |
V442L |
probably damaging |
Het |
Olfr1079 |
T |
C |
2: 86,538,903 |
E2G |
probably benign |
Het |
Olfr532 |
T |
C |
7: 140,419,225 |
T183A |
possibly damaging |
Het |
Ppfia1 |
T |
C |
7: 144,516,107 |
N363S |
probably damaging |
Het |
Stxbp2 |
A |
G |
8: 3,634,615 |
|
probably null |
Het |
Tnf |
A |
G |
17: 35,201,113 |
|
probably null |
Het |
Zkscan7 |
T |
C |
9: 122,895,621 |
F552L |
possibly damaging |
Het |
|
Other mutations in Kalrn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01361:Kalrn
|
APN |
16 |
34175722 |
splice site |
probably benign |
|
IGL01364:Kalrn
|
APN |
16 |
34262629 |
missense |
probably damaging |
1.00 |
IGL01510:Kalrn
|
APN |
16 |
34235330 |
missense |
possibly damaging |
0.52 |
IGL01664:Kalrn
|
APN |
16 |
34294161 |
missense |
probably damaging |
1.00 |
IGL01934:Kalrn
|
APN |
16 |
34198512 |
splice site |
probably null |
|
IGL02059:Kalrn
|
APN |
16 |
34252341 |
missense |
possibly damaging |
0.95 |
IGL02102:Kalrn
|
APN |
16 |
34220222 |
missense |
probably damaging |
1.00 |
IGL02306:Kalrn
|
APN |
16 |
34310527 |
missense |
probably damaging |
0.97 |
IGL02328:Kalrn
|
APN |
16 |
34332224 |
missense |
probably damaging |
0.98 |
IGL02532:Kalrn
|
APN |
16 |
34360846 |
missense |
probably damaging |
1.00 |
IGL02685:Kalrn
|
APN |
16 |
34513959 |
nonsense |
probably null |
|
IGL02696:Kalrn
|
APN |
16 |
34220114 |
missense |
probably damaging |
1.00 |
IGL02708:Kalrn
|
APN |
16 |
34392050 |
missense |
probably damaging |
1.00 |
IGL02937:Kalrn
|
APN |
16 |
34220130 |
nonsense |
probably null |
|
IGL03188:Kalrn
|
APN |
16 |
34314192 |
missense |
probably benign |
0.01 |
IGL03289:Kalrn
|
APN |
16 |
34385297 |
missense |
possibly damaging |
0.90 |
IGL03408:Kalrn
|
APN |
16 |
34314176 |
missense |
probably damaging |
0.99 |
breeze
|
UTSW |
16 |
34013675 |
missense |
|
|
ethereal
|
UTSW |
16 |
33975435 |
utr 3 prime |
probably benign |
|
Feather
|
UTSW |
16 |
34314209 |
missense |
probably damaging |
0.99 |
Hidden
|
UTSW |
16 |
34027976 |
missense |
probably damaging |
1.00 |
Soulful
|
UTSW |
16 |
34187484 |
nonsense |
probably null |
|
G1Funyon:Kalrn
|
UTSW |
16 |
34357100 |
missense |
probably benign |
0.05 |
PIT4498001:Kalrn
|
UTSW |
16 |
34031582 |
missense |
possibly damaging |
0.81 |
R0019:Kalrn
|
UTSW |
16 |
34198514 |
splice site |
probably benign |
|
R0043:Kalrn
|
UTSW |
16 |
34054906 |
missense |
probably damaging |
1.00 |
R0052:Kalrn
|
UTSW |
16 |
34357171 |
missense |
probably damaging |
1.00 |
R0066:Kalrn
|
UTSW |
16 |
34203957 |
missense |
probably damaging |
1.00 |
R0098:Kalrn
|
UTSW |
16 |
33975619 |
missense |
possibly damaging |
0.89 |
R0098:Kalrn
|
UTSW |
16 |
33975619 |
missense |
possibly damaging |
0.89 |
R0111:Kalrn
|
UTSW |
16 |
34031590 |
missense |
probably damaging |
1.00 |
R0113:Kalrn
|
UTSW |
16 |
34049936 |
intron |
probably benign |
|
R0183:Kalrn
|
UTSW |
16 |
34171379 |
splice site |
probably null |
|
R0422:Kalrn
|
UTSW |
16 |
34314273 |
missense |
probably damaging |
0.99 |
R0498:Kalrn
|
UTSW |
16 |
34054891 |
missense |
possibly damaging |
0.61 |
R0614:Kalrn
|
UTSW |
16 |
33993670 |
splice site |
probably benign |
|
R0656:Kalrn
|
UTSW |
16 |
34032467 |
missense |
probably damaging |
1.00 |
R0671:Kalrn
|
UTSW |
16 |
34116408 |
missense |
probably benign |
0.04 |
R0707:Kalrn
|
UTSW |
16 |
34010581 |
missense |
possibly damaging |
0.88 |
R0709:Kalrn
|
UTSW |
16 |
34035554 |
missense |
probably damaging |
1.00 |
R0834:Kalrn
|
UTSW |
16 |
34049919 |
missense |
possibly damaging |
0.94 |
R0976:Kalrn
|
UTSW |
16 |
34385390 |
missense |
probably damaging |
1.00 |
R1297:Kalrn
|
UTSW |
16 |
34016498 |
missense |
probably damaging |
0.99 |
R1355:Kalrn
|
UTSW |
16 |
33975584 |
missense |
possibly damaging |
0.74 |
R1370:Kalrn
|
UTSW |
16 |
33975584 |
missense |
possibly damaging |
0.74 |
R1389:Kalrn
|
UTSW |
16 |
33988803 |
missense |
probably benign |
0.01 |
R1398:Kalrn
|
UTSW |
16 |
34212820 |
missense |
probably damaging |
1.00 |
R1427:Kalrn
|
UTSW |
16 |
33975754 |
missense |
probably damaging |
1.00 |
R1458:Kalrn
|
UTSW |
16 |
34174487 |
missense |
probably damaging |
1.00 |
R1470:Kalrn
|
UTSW |
16 |
34187471 |
missense |
probably damaging |
1.00 |
R1470:Kalrn
|
UTSW |
16 |
34187471 |
missense |
probably damaging |
1.00 |
R1557:Kalrn
|
UTSW |
16 |
34314278 |
missense |
possibly damaging |
0.92 |
R1559:Kalrn
|
UTSW |
16 |
34010548 |
missense |
possibly damaging |
0.92 |
R1654:Kalrn
|
UTSW |
16 |
33975738 |
missense |
probably damaging |
1.00 |
R1703:Kalrn
|
UTSW |
16 |
34205326 |
missense |
probably damaging |
1.00 |
R1759:Kalrn
|
UTSW |
16 |
34360950 |
missense |
probably damaging |
0.97 |
R1764:Kalrn
|
UTSW |
16 |
34212873 |
missense |
probably damaging |
1.00 |
R1824:Kalrn
|
UTSW |
16 |
34294215 |
missense |
probably damaging |
1.00 |
R1845:Kalrn
|
UTSW |
16 |
34356961 |
missense |
probably damaging |
0.99 |
R1850:Kalrn
|
UTSW |
16 |
33975923 |
missense |
probably damaging |
0.98 |
R1921:Kalrn
|
UTSW |
16 |
34392093 |
missense |
probably benign |
0.02 |
R1922:Kalrn
|
UTSW |
16 |
34392093 |
missense |
probably benign |
0.02 |
R1970:Kalrn
|
UTSW |
16 |
33977524 |
critical splice donor site |
probably null |
|
R1991:Kalrn
|
UTSW |
16 |
33975738 |
missense |
probably damaging |
1.00 |
R1992:Kalrn
|
UTSW |
16 |
33975738 |
missense |
probably damaging |
1.00 |
R2001:Kalrn
|
UTSW |
16 |
34028045 |
missense |
probably damaging |
1.00 |
R2025:Kalrn
|
UTSW |
16 |
34189736 |
missense |
probably damaging |
0.96 |
R2048:Kalrn
|
UTSW |
16 |
34252310 |
missense |
probably benign |
0.18 |
R2076:Kalrn
|
UTSW |
16 |
34332143 |
missense |
probably benign |
0.15 |
R2118:Kalrn
|
UTSW |
16 |
34332230 |
missense |
possibly damaging |
0.84 |
R2136:Kalrn
|
UTSW |
16 |
34307724 |
missense |
possibly damaging |
0.82 |
R2145:Kalrn
|
UTSW |
16 |
34009262 |
unclassified |
probably benign |
|
R2193:Kalrn
|
UTSW |
16 |
33989810 |
missense |
possibly damaging |
0.72 |
R2234:Kalrn
|
UTSW |
16 |
34176262 |
splice site |
probably null |
|
R2404:Kalrn
|
UTSW |
16 |
33989810 |
missense |
possibly damaging |
0.72 |
R2405:Kalrn
|
UTSW |
16 |
33989810 |
missense |
possibly damaging |
0.72 |
R2408:Kalrn
|
UTSW |
16 |
33989810 |
missense |
possibly damaging |
0.72 |
R2411:Kalrn
|
UTSW |
16 |
33989810 |
missense |
possibly damaging |
0.72 |
R2570:Kalrn
|
UTSW |
16 |
34310495 |
missense |
probably damaging |
1.00 |
R2903:Kalrn
|
UTSW |
16 |
33989810 |
missense |
possibly damaging |
0.72 |
R2904:Kalrn
|
UTSW |
16 |
33989810 |
missense |
possibly damaging |
0.72 |
R2924:Kalrn
|
UTSW |
16 |
33989810 |
missense |
possibly damaging |
0.72 |
R3411:Kalrn
|
UTSW |
16 |
34212272 |
missense |
probably benign |
0.07 |
R3693:Kalrn
|
UTSW |
16 |
34357315 |
missense |
probably damaging |
1.00 |
R3709:Kalrn
|
UTSW |
16 |
34392030 |
splice site |
probably null |
|
R3788:Kalrn
|
UTSW |
16 |
34220240 |
missense |
probably damaging |
1.00 |
R3833:Kalrn
|
UTSW |
16 |
34039889 |
nonsense |
probably null |
|
R3871:Kalrn
|
UTSW |
16 |
34203856 |
splice site |
probably null |
|
R3934:Kalrn
|
UTSW |
16 |
34310531 |
missense |
probably benign |
0.34 |
R4033:Kalrn
|
UTSW |
16 |
33989810 |
missense |
possibly damaging |
0.72 |
R4056:Kalrn
|
UTSW |
16 |
34314209 |
missense |
probably damaging |
0.99 |
R4057:Kalrn
|
UTSW |
16 |
34314209 |
missense |
probably damaging |
0.99 |
R4303:Kalrn
|
UTSW |
16 |
34235391 |
missense |
probably damaging |
1.00 |
R4402:Kalrn
|
UTSW |
16 |
33989810 |
missense |
possibly damaging |
0.72 |
R4444:Kalrn
|
UTSW |
16 |
33989810 |
missense |
possibly damaging |
0.72 |
R4482:Kalrn
|
UTSW |
16 |
33989810 |
missense |
possibly damaging |
0.72 |
R4487:Kalrn
|
UTSW |
16 |
33989810 |
missense |
possibly damaging |
0.72 |
R4558:Kalrn
|
UTSW |
16 |
33987208 |
missense |
possibly damaging |
0.46 |
R4572:Kalrn
|
UTSW |
16 |
34392042 |
missense |
probably damaging |
0.98 |
R4583:Kalrn
|
UTSW |
16 |
34235267 |
missense |
probably damaging |
1.00 |
R4604:Kalrn
|
UTSW |
16 |
34513926 |
missense |
possibly damaging |
0.46 |
R4620:Kalrn
|
UTSW |
16 |
34028705 |
missense |
probably damaging |
0.99 |
R4651:Kalrn
|
UTSW |
16 |
34176391 |
missense |
probably damaging |
1.00 |
R4703:Kalrn
|
UTSW |
16 |
34203957 |
missense |
probably damaging |
1.00 |
R4704:Kalrn
|
UTSW |
16 |
34203957 |
missense |
probably damaging |
1.00 |
R4705:Kalrn
|
UTSW |
16 |
34203957 |
missense |
probably damaging |
1.00 |
R4760:Kalrn
|
UTSW |
16 |
34198487 |
missense |
probably damaging |
1.00 |
R4793:Kalrn
|
UTSW |
16 |
33989810 |
missense |
possibly damaging |
0.72 |
R4794:Kalrn
|
UTSW |
16 |
33989810 |
missense |
possibly damaging |
0.72 |
R4811:Kalrn
|
UTSW |
16 |
34356969 |
missense |
probably damaging |
1.00 |
R4816:Kalrn
|
UTSW |
16 |
34514019 |
unclassified |
probably benign |
|
R4888:Kalrn
|
UTSW |
16 |
34171330 |
missense |
probably damaging |
1.00 |
R4952:Kalrn
|
UTSW |
16 |
34357415 |
splice site |
probably null |
|
R5030:Kalrn
|
UTSW |
16 |
33975742 |
missense |
probably benign |
0.00 |
R5045:Kalrn
|
UTSW |
16 |
34314352 |
nonsense |
probably null |
|
R5117:Kalrn
|
UTSW |
16 |
34033601 |
critical splice acceptor site |
probably null |
|
R5289:Kalrn
|
UTSW |
16 |
34252341 |
missense |
possibly damaging |
0.95 |
R5426:Kalrn
|
UTSW |
16 |
34262653 |
missense |
probably damaging |
1.00 |
R5432:Kalrn
|
UTSW |
16 |
34053622 |
missense |
probably damaging |
1.00 |
R5611:Kalrn
|
UTSW |
16 |
34175780 |
missense |
probably damaging |
1.00 |
R5629:Kalrn
|
UTSW |
16 |
34039934 |
missense |
possibly damaging |
0.77 |
R5635:Kalrn
|
UTSW |
16 |
34014084 |
missense |
probably damaging |
1.00 |
R5713:Kalrn
|
UTSW |
16 |
34016579 |
missense |
probably benign |
|
R5716:Kalrn
|
UTSW |
16 |
33987176 |
missense |
probably benign |
0.01 |
R5772:Kalrn
|
UTSW |
16 |
33975820 |
missense |
probably damaging |
1.00 |
R5797:Kalrn
|
UTSW |
16 |
34212249 |
missense |
probably damaging |
0.98 |
R5835:Kalrn
|
UTSW |
16 |
33987091 |
missense |
probably benign |
0.28 |
R5895:Kalrn
|
UTSW |
16 |
33975435 |
utr 3 prime |
probably benign |
|
R5924:Kalrn
|
UTSW |
16 |
34243833 |
missense |
probably damaging |
1.00 |
R5999:Kalrn
|
UTSW |
16 |
34357343 |
missense |
probably damaging |
1.00 |
R6010:Kalrn
|
UTSW |
16 |
34010580 |
missense |
probably benign |
0.06 |
R6052:Kalrn
|
UTSW |
16 |
34360885 |
missense |
probably damaging |
1.00 |
R6122:Kalrn
|
UTSW |
16 |
33985191 |
missense |
possibly damaging |
0.82 |
R6128:Kalrn
|
UTSW |
16 |
34212885 |
missense |
probably damaging |
0.99 |
R6136:Kalrn
|
UTSW |
16 |
34357111 |
missense |
probably damaging |
1.00 |
R6178:Kalrn
|
UTSW |
16 |
34053639 |
missense |
possibly damaging |
0.88 |
R6229:Kalrn
|
UTSW |
16 |
34055071 |
missense |
probably damaging |
1.00 |
R6376:Kalrn
|
UTSW |
16 |
33975991 |
missense |
probably benign |
|
R6397:Kalrn
|
UTSW |
16 |
33992985 |
missense |
probably damaging |
1.00 |
R6429:Kalrn
|
UTSW |
16 |
34332164 |
missense |
possibly damaging |
0.85 |
R6473:Kalrn
|
UTSW |
16 |
34205302 |
missense |
probably damaging |
1.00 |
R6481:Kalrn
|
UTSW |
16 |
34360984 |
missense |
probably damaging |
1.00 |
R6597:Kalrn
|
UTSW |
16 |
34182747 |
missense |
probably damaging |
1.00 |
R6736:Kalrn
|
UTSW |
16 |
34217923 |
missense |
probably damaging |
1.00 |
R6808:Kalrn
|
UTSW |
16 |
34027976 |
missense |
probably damaging |
1.00 |
R6897:Kalrn
|
UTSW |
16 |
33975703 |
missense |
probably damaging |
0.99 |
R6955:Kalrn
|
UTSW |
16 |
34220136 |
missense |
probably damaging |
1.00 |
R7060:Kalrn
|
UTSW |
16 |
34357048 |
missense |
probably damaging |
0.99 |
R7064:Kalrn
|
UTSW |
16 |
34217891 |
missense |
probably damaging |
1.00 |
R7132:Kalrn
|
UTSW |
16 |
34256227 |
missense |
unknown |
|
R7154:Kalrn
|
UTSW |
16 |
34212157 |
critical splice donor site |
probably null |
|
R7181:Kalrn
|
UTSW |
16 |
34163077 |
missense |
probably benign |
0.00 |
R7234:Kalrn
|
UTSW |
16 |
34176422 |
missense |
possibly damaging |
0.63 |
R7235:Kalrn
|
UTSW |
16 |
34175761 |
missense |
probably benign |
0.18 |
R7504:Kalrn
|
UTSW |
16 |
34256233 |
missense |
unknown |
|
R7563:Kalrn
|
UTSW |
16 |
34392094 |
missense |
probably damaging |
0.97 |
R7612:Kalrn
|
UTSW |
16 |
34314212 |
missense |
possibly damaging |
0.68 |
R7772:Kalrn
|
UTSW |
16 |
34031582 |
missense |
probably benign |
0.04 |
R7796:Kalrn
|
UTSW |
16 |
34187484 |
nonsense |
probably null |
|
R7867:Kalrn
|
UTSW |
16 |
33989791 |
missense |
possibly damaging |
0.94 |
R7869:Kalrn
|
UTSW |
16 |
33988847 |
missense |
probably damaging |
0.98 |
R7914:Kalrn
|
UTSW |
16 |
34028752 |
missense |
probably benign |
|
R8080:Kalrn
|
UTSW |
16 |
33975668 |
missense |
possibly damaging |
0.83 |
R8147:Kalrn
|
UTSW |
16 |
34055044 |
missense |
probably benign |
|
R8239:Kalrn
|
UTSW |
16 |
34049783 |
missense |
noncoding transcript |
|
R8281:Kalrn
|
UTSW |
16 |
34035061 |
nonsense |
probably null |
|
R8294:Kalrn
|
UTSW |
16 |
34033584 |
missense |
probably benign |
0.12 |
R8301:Kalrn
|
UTSW |
16 |
34357100 |
missense |
probably benign |
0.05 |
R8686:Kalrn
|
UTSW |
16 |
34360935 |
missense |
probably damaging |
1.00 |
R8693:Kalrn
|
UTSW |
16 |
34034514 |
missense |
probably damaging |
1.00 |
R8798:Kalrn
|
UTSW |
16 |
33982855 |
missense |
possibly damaging |
0.65 |
R8878:Kalrn
|
UTSW |
16 |
34198460 |
missense |
probably benign |
0.05 |
R8878:Kalrn
|
UTSW |
16 |
34205326 |
missense |
probably damaging |
1.00 |
R8880:Kalrn
|
UTSW |
16 |
34217935 |
missense |
probably damaging |
1.00 |
R8883:Kalrn
|
UTSW |
16 |
33993655 |
missense |
probably damaging |
1.00 |
R8887:Kalrn
|
UTSW |
16 |
34227126 |
missense |
probably benign |
0.22 |
R9048:Kalrn
|
UTSW |
16 |
34034484 |
missense |
possibly damaging |
0.84 |
R9111:Kalrn
|
UTSW |
16 |
34361001 |
missense |
probably damaging |
0.96 |
R9317:Kalrn
|
UTSW |
16 |
34013675 |
missense |
|
|
R9424:Kalrn
|
UTSW |
16 |
33988818 |
missense |
probably benign |
0.06 |
R9442:Kalrn
|
UTSW |
16 |
34095879 |
start codon destroyed |
probably null |
0.56 |
R9445:Kalrn
|
UTSW |
16 |
33985230 |
missense |
probably benign |
0.13 |
R9515:Kalrn
|
UTSW |
16 |
34034494 |
missense |
probably damaging |
1.00 |
R9516:Kalrn
|
UTSW |
16 |
34034494 |
missense |
probably damaging |
1.00 |
R9625:Kalrn
|
UTSW |
16 |
34028827 |
critical splice acceptor site |
probably null |
|
R9645:Kalrn
|
UTSW |
16 |
34212213 |
missense |
probably benign |
0.01 |
RF014:Kalrn
|
UTSW |
16 |
34039933 |
missense |
probably benign |
0.01 |
Z1177:Kalrn
|
UTSW |
16 |
34035506 |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GGTAATGTCTTTGAGGCCATAATAG -3'
(R):5'- CAAGTTGTAGAGCTGGGCTGAG -3'
Sequencing Primer
(F):5'- CCATAAACTGATGGGTGTGTCC -3'
(R):5'- AGGCACTCCCAGCTCTG -3'
|
Posted On |
2014-10-02 |