Incidental Mutation 'R1389:Kalrn'
ID 162562
Institutional Source Beutler Lab
Gene Symbol Kalrn
Ensembl Gene ENSMUSG00000061751
Gene Name kalirin, RhoGEF kinase
Synonyms 2210407G14Rik, Hapip, E530005C20Rik, LOC224126
MMRRC Submission 039451-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.922) question?
Stock # R1389 (G1)
Quality Score 225
Status Not validated
Chromosome 16
Chromosomal Location 33969073-34573532 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 33988803 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Valine at position 903 (I903V)
Ref Sequence ENSEMBL: ENSMUSP00000110624 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000076810] [ENSMUST00000114973]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000076810
AA Change: I2572V

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000076088
Gene: ENSMUSG00000061751
AA Change: I2572V

DomainStartEndE-ValueType
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 probably benign
Transcript: ENSMUST00000114973
AA Change: I903V

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)
SMART Domains Protein: ENSMUSP00000110624
Gene: ENSMUSG00000061751
AA Change: I903V

DomainStartEndE-ValueType
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
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.1%
  • 10x: 95.7%
  • 20x: 90.6%
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: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsl3 A C 1: 78,688,282 (GRCm38) I142L probably benign Het
Adgra2 C T 8: 27,111,088 (GRCm38) P252L probably damaging Het
Akap6 A G 12: 53,139,520 (GRCm38) E1239G probably benign Het
Arhgef17 TGGAGGAGGAGGAGGAGG TGGAGGAGGAGGAGG 7: 100,931,037 (GRCm38) probably benign Het
Btbd11 A G 10: 85,640,596 (GRCm38) T914A possibly damaging Het
Calml4 A T 9: 62,871,266 (GRCm38) D12V probably damaging Het
Car9 G T 4: 43,512,439 (GRCm38) probably null Het
Ccar2 C A 14: 70,140,109 (GRCm38) V699L possibly damaging Het
Ccdc27 T C 4: 154,041,769 (GRCm38) M88V unknown Het
Ceacam15 T C 7: 16,672,063 (GRCm38) R188G probably damaging Het
Dcaf8 G A 1: 172,174,052 (GRCm38) R272H probably benign Het
Dchs1 A G 7: 105,755,571 (GRCm38) V2588A probably benign Het
Dst G A 1: 34,211,232 (GRCm38) R1749H probably damaging Het
Exog A G 9: 119,462,506 (GRCm38) Q283R probably benign Het
Fmnl1 A T 11: 103,186,709 (GRCm38) probably null Het
Gramd1c T C 16: 43,990,722 (GRCm38) D213G probably damaging Het
Iqgap1 A G 7: 80,759,756 (GRCm38) probably null Het
Itgae A G 11: 73,125,362 (GRCm38) Y799C probably damaging Het
Kcnh1 A G 1: 192,505,763 (GRCm38) E844G probably benign Het
Khdc1a A T 1: 21,350,027 (GRCm38) D3V probably damaging Het
Ly6g T C 15: 75,156,766 (GRCm38) F25S probably benign Het
Mapk1ip1 G A 7: 138,836,727 (GRCm38) probably benign Het
Mfsd3 A G 15: 76,702,689 (GRCm38) H243R probably benign Het
Mms22l T A 4: 24,591,076 (GRCm38) Y1016N probably damaging Het
Mrgprb5 A T 7: 48,168,330 (GRCm38) V219E probably damaging Het
Nars2 G A 7: 97,002,829 (GRCm38) S209N probably benign Het
Nckap5 T C 1: 126,026,710 (GRCm38) T702A probably damaging Het
Olfr385 T C 11: 73,589,543 (GRCm38) N65S possibly damaging Het
Paf1 A G 7: 28,398,832 (GRCm38) probably benign Het
Prl3d1 A T 13: 27,098,710 (GRCm38) R145* probably null Het
Rasl10b G A 11: 83,417,839 (GRCm38) probably null Het
Rnf13 T A 3: 57,779,496 (GRCm38) N103K probably damaging Het
Senp1 T C 15: 98,075,853 (GRCm38) S170G probably benign Het
Slc46a2 A G 4: 59,914,620 (GRCm38) L101P probably damaging Het
Tmem123 C T 9: 7,791,106 (GRCm38) T136M probably damaging Het
Tpo T A 12: 30,103,110 (GRCm38) H415L probably damaging Het
Vipr2 A G 12: 116,137,330 (GRCm38) I255V probably benign Het
Zc3h11a A T 1: 133,633,803 (GRCm38) V310E probably damaging Het
Zfp3 T A 11: 70,772,636 (GRCm38) C474S probably damaging Het
Zfp707 T A 15: 75,974,616 (GRCm38) C99S probably damaging Het
Zranb1 C T 7: 132,971,333 (GRCm38) P410S probably damaging Het
Zswim8 G T 14: 20,710,748 (GRCm38) R30L probably damaging Het
Other mutations in Kalrn
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01361:Kalrn APN 16 34,175,722 (GRCm38) splice site probably benign
IGL01364:Kalrn APN 16 34,262,629 (GRCm38) missense probably damaging 1.00
IGL01510:Kalrn APN 16 34,235,330 (GRCm38) missense possibly damaging 0.52
IGL01664:Kalrn APN 16 34,294,161 (GRCm38) missense probably damaging 1.00
IGL01934:Kalrn APN 16 34,198,512 (GRCm38) splice site probably null
IGL02059:Kalrn APN 16 34,252,341 (GRCm38) missense possibly damaging 0.95
IGL02102:Kalrn APN 16 34,220,222 (GRCm38) missense probably damaging 1.00
IGL02306:Kalrn APN 16 34,310,527 (GRCm38) missense probably damaging 0.97
IGL02328:Kalrn APN 16 34,332,224 (GRCm38) missense probably damaging 0.98
IGL02532:Kalrn APN 16 34,360,846 (GRCm38) missense probably damaging 1.00
IGL02685:Kalrn APN 16 34,513,959 (GRCm38) nonsense probably null
IGL02696:Kalrn APN 16 34,220,114 (GRCm38) missense probably damaging 1.00
IGL02708:Kalrn APN 16 34,392,050 (GRCm38) missense probably damaging 1.00
IGL02937:Kalrn APN 16 34,220,130 (GRCm38) nonsense probably null
IGL03188:Kalrn APN 16 34,314,192 (GRCm38) missense probably benign 0.01
IGL03289:Kalrn APN 16 34,385,297 (GRCm38) missense possibly damaging 0.90
IGL03408:Kalrn APN 16 34,314,176 (GRCm38) missense probably damaging 0.99
breeze UTSW 16 34,013,675 (GRCm38) missense
ethereal UTSW 16 33,975,435 (GRCm38) utr 3 prime probably benign
Feather UTSW 16 34,314,209 (GRCm38) missense probably damaging 0.99
Hidden UTSW 16 34,027,976 (GRCm38) missense probably damaging 1.00
Soulful UTSW 16 34,187,484 (GRCm38) nonsense probably null
G1Funyon:Kalrn UTSW 16 34,357,100 (GRCm38) missense probably benign 0.05
PIT4498001:Kalrn UTSW 16 34,031,582 (GRCm38) missense possibly damaging 0.81
R0019:Kalrn UTSW 16 34,198,514 (GRCm38) splice site probably benign
R0043:Kalrn UTSW 16 34,054,906 (GRCm38) missense probably damaging 1.00
R0052:Kalrn UTSW 16 34,357,171 (GRCm38) missense probably damaging 1.00
R0066:Kalrn UTSW 16 34,203,957 (GRCm38) missense probably damaging 1.00
R0098:Kalrn UTSW 16 33,975,619 (GRCm38) missense possibly damaging 0.89
R0098:Kalrn UTSW 16 33,975,619 (GRCm38) missense possibly damaging 0.89
R0111:Kalrn UTSW 16 34,031,590 (GRCm38) missense probably damaging 1.00
R0113:Kalrn UTSW 16 34,049,936 (GRCm38) intron probably benign
R0183:Kalrn UTSW 16 34,171,379 (GRCm38) splice site probably null
R0422:Kalrn UTSW 16 34,314,273 (GRCm38) missense probably damaging 0.99
R0498:Kalrn UTSW 16 34,054,891 (GRCm38) missense possibly damaging 0.61
R0614:Kalrn UTSW 16 33,993,670 (GRCm38) splice site probably benign
R0656:Kalrn UTSW 16 34,032,467 (GRCm38) missense probably damaging 1.00
R0671:Kalrn UTSW 16 34,116,408 (GRCm38) missense probably benign 0.04
R0707:Kalrn UTSW 16 34,010,581 (GRCm38) missense possibly damaging 0.88
R0709:Kalrn UTSW 16 34,035,554 (GRCm38) missense probably damaging 1.00
R0834:Kalrn UTSW 16 34,049,919 (GRCm38) missense possibly damaging 0.94
R0976:Kalrn UTSW 16 34,385,390 (GRCm38) missense probably damaging 1.00
R1297:Kalrn UTSW 16 34,016,498 (GRCm38) missense probably damaging 0.99
R1355:Kalrn UTSW 16 33,975,584 (GRCm38) missense possibly damaging 0.74
R1370:Kalrn UTSW 16 33,975,584 (GRCm38) missense possibly damaging 0.74
R1398:Kalrn UTSW 16 34,212,820 (GRCm38) missense probably damaging 1.00
R1427:Kalrn UTSW 16 33,975,754 (GRCm38) missense probably damaging 1.00
R1458:Kalrn UTSW 16 34,174,487 (GRCm38) missense probably damaging 1.00
R1470:Kalrn UTSW 16 34,187,471 (GRCm38) missense probably damaging 1.00
R1470:Kalrn UTSW 16 34,187,471 (GRCm38) missense probably damaging 1.00
R1557:Kalrn UTSW 16 34,314,278 (GRCm38) missense possibly damaging 0.92
R1559:Kalrn UTSW 16 34,010,548 (GRCm38) missense possibly damaging 0.92
R1654:Kalrn UTSW 16 33,975,738 (GRCm38) missense probably damaging 1.00
R1703:Kalrn UTSW 16 34,205,326 (GRCm38) missense probably damaging 1.00
R1759:Kalrn UTSW 16 34,360,950 (GRCm38) missense probably damaging 0.97
R1764:Kalrn UTSW 16 34,212,873 (GRCm38) missense probably damaging 1.00
R1824:Kalrn UTSW 16 34,294,215 (GRCm38) missense probably damaging 1.00
R1845:Kalrn UTSW 16 34,356,961 (GRCm38) missense probably damaging 0.99
R1850:Kalrn UTSW 16 33,975,923 (GRCm38) missense probably damaging 0.98
R1921:Kalrn UTSW 16 34,392,093 (GRCm38) missense probably benign 0.02
R1922:Kalrn UTSW 16 34,392,093 (GRCm38) missense probably benign 0.02
R1970:Kalrn UTSW 16 33,977,524 (GRCm38) critical splice donor site probably null
R1991:Kalrn UTSW 16 33,975,738 (GRCm38) missense probably damaging 1.00
R1992:Kalrn UTSW 16 33,975,738 (GRCm38) missense probably damaging 1.00
R2001:Kalrn UTSW 16 34,028,045 (GRCm38) missense probably damaging 1.00
R2025:Kalrn UTSW 16 34,189,736 (GRCm38) missense probably damaging 0.96
R2048:Kalrn UTSW 16 34,252,310 (GRCm38) missense probably benign 0.18
R2076:Kalrn UTSW 16 34,332,143 (GRCm38) missense probably benign 0.15
R2118:Kalrn UTSW 16 34,332,230 (GRCm38) missense possibly damaging 0.84
R2136:Kalrn UTSW 16 34,307,724 (GRCm38) missense possibly damaging 0.82
R2145:Kalrn UTSW 16 34,009,262 (GRCm38) unclassified probably benign
R2193:Kalrn UTSW 16 33,989,810 (GRCm38) missense possibly damaging 0.72
R2195:Kalrn UTSW 16 33,989,810 (GRCm38) missense possibly damaging 0.72
R2234:Kalrn UTSW 16 34,176,262 (GRCm38) splice site probably null
R2404:Kalrn UTSW 16 33,989,810 (GRCm38) missense possibly damaging 0.72
R2405:Kalrn UTSW 16 33,989,810 (GRCm38) missense possibly damaging 0.72
R2408:Kalrn UTSW 16 33,989,810 (GRCm38) missense possibly damaging 0.72
R2411:Kalrn UTSW 16 33,989,810 (GRCm38) missense possibly damaging 0.72
R2570:Kalrn UTSW 16 34,310,495 (GRCm38) missense probably damaging 1.00
R2903:Kalrn UTSW 16 33,989,810 (GRCm38) missense possibly damaging 0.72
R2904:Kalrn UTSW 16 33,989,810 (GRCm38) missense possibly damaging 0.72
R2924:Kalrn UTSW 16 33,989,810 (GRCm38) missense possibly damaging 0.72
R3411:Kalrn UTSW 16 34,212,272 (GRCm38) missense probably benign 0.07
R3693:Kalrn UTSW 16 34,357,315 (GRCm38) missense probably damaging 1.00
R3709:Kalrn UTSW 16 34,392,030 (GRCm38) splice site probably null
R3788:Kalrn UTSW 16 34,220,240 (GRCm38) missense probably damaging 1.00
R3833:Kalrn UTSW 16 34,039,889 (GRCm38) nonsense probably null
R3871:Kalrn UTSW 16 34,203,856 (GRCm38) splice site probably null
R3934:Kalrn UTSW 16 34,310,531 (GRCm38) missense probably benign 0.34
R4033:Kalrn UTSW 16 33,989,810 (GRCm38) missense possibly damaging 0.72
R4056:Kalrn UTSW 16 34,314,209 (GRCm38) missense probably damaging 0.99
R4057:Kalrn UTSW 16 34,314,209 (GRCm38) missense probably damaging 0.99
R4303:Kalrn UTSW 16 34,235,391 (GRCm38) missense probably damaging 1.00
R4402:Kalrn UTSW 16 33,989,810 (GRCm38) missense possibly damaging 0.72
R4444:Kalrn UTSW 16 33,989,810 (GRCm38) missense possibly damaging 0.72
R4482:Kalrn UTSW 16 33,989,810 (GRCm38) missense possibly damaging 0.72
R4487:Kalrn UTSW 16 33,989,810 (GRCm38) missense possibly damaging 0.72
R4558:Kalrn UTSW 16 33,987,208 (GRCm38) missense possibly damaging 0.46
R4572:Kalrn UTSW 16 34,392,042 (GRCm38) missense probably damaging 0.98
R4583:Kalrn UTSW 16 34,235,267 (GRCm38) missense probably damaging 1.00
R4604:Kalrn UTSW 16 34,513,926 (GRCm38) missense possibly damaging 0.46
R4620:Kalrn UTSW 16 34,028,705 (GRCm38) missense probably damaging 0.99
R4651:Kalrn UTSW 16 34,176,391 (GRCm38) missense probably damaging 1.00
R4703:Kalrn UTSW 16 34,203,957 (GRCm38) missense probably damaging 1.00
R4704:Kalrn UTSW 16 34,203,957 (GRCm38) missense probably damaging 1.00
R4705:Kalrn UTSW 16 34,203,957 (GRCm38) missense probably damaging 1.00
R4760:Kalrn UTSW 16 34,198,487 (GRCm38) missense probably damaging 1.00
R4793:Kalrn UTSW 16 33,989,810 (GRCm38) missense possibly damaging 0.72
R4794:Kalrn UTSW 16 33,989,810 (GRCm38) missense possibly damaging 0.72
R4811:Kalrn UTSW 16 34,356,969 (GRCm38) missense probably damaging 1.00
R4816:Kalrn UTSW 16 34,514,019 (GRCm38) unclassified probably benign
R4888:Kalrn UTSW 16 34,171,330 (GRCm38) missense probably damaging 1.00
R4952:Kalrn UTSW 16 34,357,415 (GRCm38) splice site probably null
R5030:Kalrn UTSW 16 33,975,742 (GRCm38) missense probably benign 0.00
R5045:Kalrn UTSW 16 34,314,352 (GRCm38) nonsense probably null
R5117:Kalrn UTSW 16 34,033,601 (GRCm38) critical splice acceptor site probably null
R5289:Kalrn UTSW 16 34,252,341 (GRCm38) missense possibly damaging 0.95
R5426:Kalrn UTSW 16 34,262,653 (GRCm38) missense probably damaging 1.00
R5432:Kalrn UTSW 16 34,053,622 (GRCm38) missense probably damaging 1.00
R5611:Kalrn UTSW 16 34,175,780 (GRCm38) missense probably damaging 1.00
R5629:Kalrn UTSW 16 34,039,934 (GRCm38) missense possibly damaging 0.77
R5635:Kalrn UTSW 16 34,014,084 (GRCm38) missense probably damaging 1.00
R5713:Kalrn UTSW 16 34,016,579 (GRCm38) missense probably benign
R5716:Kalrn UTSW 16 33,987,176 (GRCm38) missense probably benign 0.01
R5772:Kalrn UTSW 16 33,975,820 (GRCm38) missense probably damaging 1.00
R5797:Kalrn UTSW 16 34,212,249 (GRCm38) missense probably damaging 0.98
R5835:Kalrn UTSW 16 33,987,091 (GRCm38) missense probably benign 0.28
R5895:Kalrn UTSW 16 33,975,435 (GRCm38) utr 3 prime probably benign
R5924:Kalrn UTSW 16 34,243,833 (GRCm38) missense probably damaging 1.00
R5999:Kalrn UTSW 16 34,357,343 (GRCm38) missense probably damaging 1.00
R6010:Kalrn UTSW 16 34,010,580 (GRCm38) missense probably benign 0.06
R6052:Kalrn UTSW 16 34,360,885 (GRCm38) missense probably damaging 1.00
R6122:Kalrn UTSW 16 33,985,191 (GRCm38) missense possibly damaging 0.82
R6128:Kalrn UTSW 16 34,212,885 (GRCm38) missense probably damaging 0.99
R6136:Kalrn UTSW 16 34,357,111 (GRCm38) missense probably damaging 1.00
R6178:Kalrn UTSW 16 34,053,639 (GRCm38) missense possibly damaging 0.88
R6229:Kalrn UTSW 16 34,055,071 (GRCm38) missense probably damaging 1.00
R6376:Kalrn UTSW 16 33,975,991 (GRCm38) missense probably benign
R6397:Kalrn UTSW 16 33,992,985 (GRCm38) missense probably damaging 1.00
R6429:Kalrn UTSW 16 34,332,164 (GRCm38) missense possibly damaging 0.85
R6473:Kalrn UTSW 16 34,205,302 (GRCm38) missense probably damaging 1.00
R6481:Kalrn UTSW 16 34,360,984 (GRCm38) missense probably damaging 1.00
R6597:Kalrn UTSW 16 34,182,747 (GRCm38) missense probably damaging 1.00
R6736:Kalrn UTSW 16 34,217,923 (GRCm38) missense probably damaging 1.00
R6808:Kalrn UTSW 16 34,027,976 (GRCm38) missense probably damaging 1.00
R6897:Kalrn UTSW 16 33,975,703 (GRCm38) missense probably damaging 0.99
R6955:Kalrn UTSW 16 34,220,136 (GRCm38) missense probably damaging 1.00
R7060:Kalrn UTSW 16 34,357,048 (GRCm38) missense probably damaging 0.99
R7064:Kalrn UTSW 16 34,217,891 (GRCm38) missense probably damaging 1.00
R7132:Kalrn UTSW 16 34,256,227 (GRCm38) missense unknown
R7154:Kalrn UTSW 16 34,212,157 (GRCm38) critical splice donor site probably null
R7181:Kalrn UTSW 16 34,163,077 (GRCm38) missense probably benign 0.00
R7234:Kalrn UTSW 16 34,176,422 (GRCm38) missense possibly damaging 0.63
R7235:Kalrn UTSW 16 34,175,761 (GRCm38) missense probably benign 0.18
R7504:Kalrn UTSW 16 34,256,233 (GRCm38) missense unknown
R7563:Kalrn UTSW 16 34,392,094 (GRCm38) missense probably damaging 0.97
R7612:Kalrn UTSW 16 34,314,212 (GRCm38) missense possibly damaging 0.68
R7772:Kalrn UTSW 16 34,031,582 (GRCm38) missense probably benign 0.04
R7796:Kalrn UTSW 16 34,187,484 (GRCm38) nonsense probably null
R7867:Kalrn UTSW 16 33,989,791 (GRCm38) missense possibly damaging 0.94
R7869:Kalrn UTSW 16 33,988,847 (GRCm38) missense probably damaging 0.98
R7914:Kalrn UTSW 16 34,028,752 (GRCm38) missense probably benign
R8080:Kalrn UTSW 16 33,975,668 (GRCm38) missense possibly damaging 0.83
R8147:Kalrn UTSW 16 34,055,044 (GRCm38) missense probably benign
R8239:Kalrn UTSW 16 34,049,783 (GRCm38) missense noncoding transcript
R8281:Kalrn UTSW 16 34,035,061 (GRCm38) nonsense probably null
R8294:Kalrn UTSW 16 34,033,584 (GRCm38) missense probably benign 0.12
R8301:Kalrn UTSW 16 34,357,100 (GRCm38) missense probably benign 0.05
R8686:Kalrn UTSW 16 34,360,935 (GRCm38) missense probably damaging 1.00
R8693:Kalrn UTSW 16 34,034,514 (GRCm38) missense probably damaging 1.00
R8798:Kalrn UTSW 16 33,982,855 (GRCm38) missense possibly damaging 0.65
R8878:Kalrn UTSW 16 34,205,326 (GRCm38) missense probably damaging 1.00
R8878:Kalrn UTSW 16 34,198,460 (GRCm38) missense probably benign 0.05
R8880:Kalrn UTSW 16 34,217,935 (GRCm38) missense probably damaging 1.00
R8883:Kalrn UTSW 16 33,993,655 (GRCm38) missense probably damaging 1.00
R8887:Kalrn UTSW 16 34,227,126 (GRCm38) missense probably benign 0.22
R9048:Kalrn UTSW 16 34,034,484 (GRCm38) missense possibly damaging 0.84
R9111:Kalrn UTSW 16 34,361,001 (GRCm38) missense probably damaging 0.96
R9317:Kalrn UTSW 16 34,013,675 (GRCm38) missense
R9424:Kalrn UTSW 16 33,988,818 (GRCm38) missense probably benign 0.06
R9442:Kalrn UTSW 16 34,095,879 (GRCm38) start codon destroyed probably null 0.56
R9445:Kalrn UTSW 16 33,985,230 (GRCm38) missense probably benign 0.13
R9515:Kalrn UTSW 16 34,034,494 (GRCm38) missense probably damaging 1.00
R9516:Kalrn UTSW 16 34,034,494 (GRCm38) missense probably damaging 1.00
R9625:Kalrn UTSW 16 34,028,827 (GRCm38) critical splice acceptor site probably null
R9645:Kalrn UTSW 16 34,212,213 (GRCm38) missense probably benign 0.01
RF014:Kalrn UTSW 16 34,039,933 (GRCm38) missense probably benign 0.01
Z1177:Kalrn UTSW 16 34,035,506 (GRCm38) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CCCCAGGCTTCTGTGCTAAAACTC -3'
(R):5'- GGTTCACACAGCAGGTCCCATTTTC -3'

Sequencing Primer
(F):5'- TCTGTGCTAAAACTCCGAGG -3'
(R):5'- AGCAGGTCCCATTTTCTAGGC -3'
Posted On 2014-03-17