Incidental Mutation 'R1966:Wnk2'
ID 218987
Institutional Source Beutler Lab
Gene Symbol Wnk2
Ensembl Gene ENSMUSG00000037989
Gene Name WNK lysine deficient protein kinase 2
Synonyms X83337, ESTM15, 1810073P09Rik
MMRRC Submission 039979-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.287) question?
Stock # R1966 (G1)
Quality Score 225
Status Not validated
Chromosome 13
Chromosomal Location 49189779-49301490 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 49192487 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 664 (S664P)
Ref Sequence ENSEMBL: ENSMUSP00000124598 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035538] [ENSMUST00000049265] [ENSMUST00000091623] [ENSMUST00000110096] [ENSMUST00000110097] [ENSMUST00000159196] [ENSMUST00000162581] [ENSMUST00000162403] [ENSMUST00000159559] [ENSMUST00000160087]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000035538
SMART Domains Protein: ENSMUSP00000047231
Gene: ENSMUSG00000037989

DomainStartEndE-ValueType
low complexity region 2 9 N/A INTRINSIC
low complexity region 66 78 N/A INTRINSIC
low complexity region 88 116 N/A INTRINSIC
low complexity region 124 136 N/A INTRINSIC
low complexity region 171 182 N/A INTRINSIC
Pfam:Pkinase_Tyr 195 451 4.5e-42 PFAM
Pfam:Pkinase 195 453 1.7e-56 PFAM
Pfam:OSR1_C 474 511 5.6e-22 PFAM
low complexity region 582 593 N/A INTRINSIC
low complexity region 626 642 N/A INTRINSIC
low complexity region 678 693 N/A INTRINSIC
low complexity region 707 724 N/A INTRINSIC
low complexity region 771 803 N/A INTRINSIC
low complexity region 821 831 N/A INTRINSIC
low complexity region 840 854 N/A INTRINSIC
low complexity region 875 890 N/A INTRINSIC
low complexity region 938 954 N/A INTRINSIC
low complexity region 983 1014 N/A INTRINSIC
low complexity region 1021 1048 N/A INTRINSIC
low complexity region 1113 1136 N/A INTRINSIC
internal_repeat_1 1162 1185 6.72e-6 PROSPERO
low complexity region 1275 1292 N/A INTRINSIC
low complexity region 1317 1353 N/A INTRINSIC
low complexity region 1429 1441 N/A INTRINSIC
low complexity region 1449 1457 N/A INTRINSIC
low complexity region 1464 1489 N/A INTRINSIC
low complexity region 1587 1597 N/A INTRINSIC
low complexity region 1820 1831 N/A INTRINSIC
coiled coil region 1836 1867 N/A INTRINSIC
low complexity region 2033 2053 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000049265
SMART Domains Protein: ENSMUSP00000049327
Gene: ENSMUSG00000037989

DomainStartEndE-ValueType
low complexity region 2 9 N/A INTRINSIC
low complexity region 66 78 N/A INTRINSIC
low complexity region 88 116 N/A INTRINSIC
low complexity region 124 136 N/A INTRINSIC
low complexity region 171 182 N/A INTRINSIC
S_TKc 195 453 3.3e-19 SMART
Pfam:OSR1_C 474 511 5.6e-19 PFAM
low complexity region 582 593 N/A INTRINSIC
low complexity region 626 642 N/A INTRINSIC
low complexity region 678 693 N/A INTRINSIC
low complexity region 707 724 N/A INTRINSIC
low complexity region 771 803 N/A INTRINSIC
low complexity region 821 831 N/A INTRINSIC
low complexity region 840 854 N/A INTRINSIC
low complexity region 875 890 N/A INTRINSIC
low complexity region 938 954 N/A INTRINSIC
low complexity region 983 1014 N/A INTRINSIC
low complexity region 1021 1048 N/A INTRINSIC
low complexity region 1113 1136 N/A INTRINSIC
internal_repeat_1 1162 1185 9.51e-6 PROSPERO
low complexity region 1275 1292 N/A INTRINSIC
low complexity region 1317 1353 N/A INTRINSIC
low complexity region 1429 1441 N/A INTRINSIC
low complexity region 1449 1457 N/A INTRINSIC
low complexity region 1464 1489 N/A INTRINSIC
low complexity region 1587 1597 N/A INTRINSIC
internal_repeat_2 1611 1703 2.12e-5 PROSPERO
low complexity region 1820 1831 N/A INTRINSIC
coiled coil region 1836 1867 N/A INTRINSIC
internal_repeat_2 1923 2023 2.12e-5 PROSPERO
low complexity region 2069 2089 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000091623
AA Change: S2169P
SMART Domains Protein: ENSMUSP00000089212
Gene: ENSMUSG00000037989
AA Change: S2169P

DomainStartEndE-ValueType
low complexity region 2 9 N/A INTRINSIC
low complexity region 66 78 N/A INTRINSIC
low complexity region 88 116 N/A INTRINSIC
low complexity region 124 136 N/A INTRINSIC
low complexity region 171 182 N/A INTRINSIC
Pfam:Pkinase_Tyr 195 451 1.6e-41 PFAM
Pfam:Pkinase 195 453 1e-54 PFAM
Pfam:OSR1_C 474 511 4e-22 PFAM
low complexity region 582 593 N/A INTRINSIC
low complexity region 626 642 N/A INTRINSIC
low complexity region 678 693 N/A INTRINSIC
low complexity region 707 724 N/A INTRINSIC
low complexity region 771 803 N/A INTRINSIC
low complexity region 821 831 N/A INTRINSIC
low complexity region 840 854 N/A INTRINSIC
low complexity region 875 890 N/A INTRINSIC
low complexity region 938 954 N/A INTRINSIC
low complexity region 983 1014 N/A INTRINSIC
low complexity region 1021 1048 N/A INTRINSIC
low complexity region 1113 1136 N/A INTRINSIC
internal_repeat_1 1162 1185 1.52e-5 PROSPERO
low complexity region 1275 1292 N/A INTRINSIC
low complexity region 1317 1353 N/A INTRINSIC
low complexity region 1429 1441 N/A INTRINSIC
low complexity region 1449 1457 N/A INTRINSIC
low complexity region 1464 1489 N/A INTRINSIC
low complexity region 1587 1597 N/A INTRINSIC
internal_repeat_2 1611 1713 7.41e-5 PROSPERO
low complexity region 1820 1831 N/A INTRINSIC
coiled coil region 1836 1867 N/A INTRINSIC
internal_repeat_2 1923 2027 7.41e-5 PROSPERO
low complexity region 2117 2137 N/A INTRINSIC
low complexity region 2191 2202 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000110096
SMART Domains Protein: ENSMUSP00000105723
Gene: ENSMUSG00000037989

DomainStartEndE-ValueType
low complexity region 2 9 N/A INTRINSIC
low complexity region 66 78 N/A INTRINSIC
low complexity region 88 116 N/A INTRINSIC
low complexity region 124 136 N/A INTRINSIC
low complexity region 171 182 N/A INTRINSIC
Pfam:Pkinase_Tyr 195 451 4.6e-42 PFAM
Pfam:Pkinase 195 453 1.7e-56 PFAM
Pfam:OSR1_C 474 511 5.6e-22 PFAM
low complexity region 582 593 N/A INTRINSIC
low complexity region 626 642 N/A INTRINSIC
low complexity region 678 693 N/A INTRINSIC
low complexity region 707 724 N/A INTRINSIC
low complexity region 771 803 N/A INTRINSIC
low complexity region 821 831 N/A INTRINSIC
low complexity region 840 854 N/A INTRINSIC
low complexity region 875 890 N/A INTRINSIC
low complexity region 938 954 N/A INTRINSIC
low complexity region 1015 1038 N/A INTRINSIC
internal_repeat_1 1064 1087 2.89e-5 PROSPERO
low complexity region 1177 1194 N/A INTRINSIC
low complexity region 1219 1255 N/A INTRINSIC
low complexity region 1331 1343 N/A INTRINSIC
low complexity region 1351 1359 N/A INTRINSIC
low complexity region 1366 1391 N/A INTRINSIC
low complexity region 1489 1498 N/A INTRINSIC
low complexity region 1721 1732 N/A INTRINSIC
coiled coil region 1737 1768 N/A INTRINSIC
low complexity region 2018 2038 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000110097
SMART Domains Protein: ENSMUSP00000105724
Gene: ENSMUSG00000037989

DomainStartEndE-ValueType
low complexity region 2 9 N/A INTRINSIC
low complexity region 66 78 N/A INTRINSIC
low complexity region 88 116 N/A INTRINSIC
low complexity region 124 136 N/A INTRINSIC
low complexity region 171 182 N/A INTRINSIC
Pfam:Pkinase_Tyr 195 451 4.7e-42 PFAM
Pfam:Pkinase 195 453 1.7e-56 PFAM
Pfam:OSR1_C 474 511 5.8e-22 PFAM
low complexity region 582 593 N/A INTRINSIC
low complexity region 626 642 N/A INTRINSIC
low complexity region 678 693 N/A INTRINSIC
low complexity region 707 724 N/A INTRINSIC
low complexity region 771 803 N/A INTRINSIC
low complexity region 821 831 N/A INTRINSIC
low complexity region 840 854 N/A INTRINSIC
low complexity region 875 890 N/A INTRINSIC
low complexity region 938 954 N/A INTRINSIC
low complexity region 983 1014 N/A INTRINSIC
low complexity region 1021 1048 N/A INTRINSIC
low complexity region 1113 1136 N/A INTRINSIC
internal_repeat_1 1162 1185 1.16e-5 PROSPERO
low complexity region 1275 1292 N/A INTRINSIC
low complexity region 1317 1353 N/A INTRINSIC
low complexity region 1429 1441 N/A INTRINSIC
low complexity region 1449 1457 N/A INTRINSIC
low complexity region 1464 1489 N/A INTRINSIC
low complexity region 1587 1597 N/A INTRINSIC
internal_repeat_2 1611 1713 5.74e-5 PROSPERO
low complexity region 1820 1831 N/A INTRINSIC
coiled coil region 1836 1867 N/A INTRINSIC
internal_repeat_2 1923 2027 5.74e-5 PROSPERO
low complexity region 2117 2137 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000159196
AA Change: S664P

PolyPhen 2 Score 0.958 (Sensitivity: 0.78; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000124598
Gene: ENSMUSG00000037989
AA Change: S664P

DomainStartEndE-ValueType
low complexity region 82 92 N/A INTRINSIC
low complexity region 315 326 N/A INTRINSIC
coiled coil region 331 362 N/A INTRINSIC
low complexity region 612 632 N/A INTRINSIC
low complexity region 686 697 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000162581
SMART Domains Protein: ENSMUSP00000125448
Gene: ENSMUSG00000037989

DomainStartEndE-ValueType
low complexity region 2 9 N/A INTRINSIC
low complexity region 66 78 N/A INTRINSIC
low complexity region 88 116 N/A INTRINSIC
low complexity region 124 136 N/A INTRINSIC
low complexity region 171 182 N/A INTRINSIC
Pfam:Pkinase_Tyr 195 451 4.5e-42 PFAM
Pfam:Pkinase 195 453 1.7e-56 PFAM
Pfam:OSR1_C 474 511 5.6e-22 PFAM
low complexity region 582 593 N/A INTRINSIC
low complexity region 626 642 N/A INTRINSIC
low complexity region 678 693 N/A INTRINSIC
low complexity region 707 724 N/A INTRINSIC
low complexity region 771 803 N/A INTRINSIC
low complexity region 821 831 N/A INTRINSIC
low complexity region 840 854 N/A INTRINSIC
low complexity region 875 890 N/A INTRINSIC
low complexity region 938 954 N/A INTRINSIC
low complexity region 983 1014 N/A INTRINSIC
low complexity region 1021 1048 N/A INTRINSIC
low complexity region 1113 1136 N/A INTRINSIC
internal_repeat_1 1162 1185 6.72e-6 PROSPERO
low complexity region 1275 1292 N/A INTRINSIC
low complexity region 1317 1353 N/A INTRINSIC
low complexity region 1429 1441 N/A INTRINSIC
low complexity region 1449 1457 N/A INTRINSIC
low complexity region 1464 1489 N/A INTRINSIC
low complexity region 1587 1597 N/A INTRINSIC
low complexity region 1820 1831 N/A INTRINSIC
coiled coil region 1836 1867 N/A INTRINSIC
low complexity region 2033 2053 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000162403
SMART Domains Protein: ENSMUSP00000125539
Gene: ENSMUSG00000037989

DomainStartEndE-ValueType
low complexity region 2 9 N/A INTRINSIC
low complexity region 66 78 N/A INTRINSIC
low complexity region 88 116 N/A INTRINSIC
low complexity region 124 136 N/A INTRINSIC
low complexity region 171 182 N/A INTRINSIC
Pfam:Pkinase_Tyr 195 451 4.3e-42 PFAM
Pfam:Pkinase 195 453 1.6e-56 PFAM
Pfam:OSR1_C 474 511 5.3e-22 PFAM
low complexity region 582 593 N/A INTRINSIC
low complexity region 626 642 N/A INTRINSIC
low complexity region 678 693 N/A INTRINSIC
low complexity region 707 736 N/A INTRINSIC
low complexity region 759 791 N/A INTRINSIC
low complexity region 809 819 N/A INTRINSIC
low complexity region 828 842 N/A INTRINSIC
low complexity region 863 878 N/A INTRINSIC
low complexity region 926 942 N/A INTRINSIC
low complexity region 1003 1026 N/A INTRINSIC
internal_repeat_1 1052 1075 1.05e-5 PROSPERO
low complexity region 1165 1182 N/A INTRINSIC
low complexity region 1207 1243 N/A INTRINSIC
low complexity region 1319 1331 N/A INTRINSIC
low complexity region 1339 1347 N/A INTRINSIC
low complexity region 1354 1379 N/A INTRINSIC
low complexity region 1477 1487 N/A INTRINSIC
internal_repeat_2 1501 1593 2.32e-5 PROSPERO
low complexity region 1710 1721 N/A INTRINSIC
coiled coil region 1726 1757 N/A INTRINSIC
internal_repeat_2 1813 1913 2.32e-5 PROSPERO
low complexity region 1959 1979 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000159559
SMART Domains Protein: ENSMUSP00000123915
Gene: ENSMUSG00000037989

DomainStartEndE-ValueType
low complexity region 2 9 N/A INTRINSIC
low complexity region 66 78 N/A INTRINSIC
low complexity region 88 116 N/A INTRINSIC
low complexity region 124 136 N/A INTRINSIC
low complexity region 171 182 N/A INTRINSIC
Pfam:Pkinase_Tyr 195 451 4.7e-42 PFAM
Pfam:Pkinase 195 453 1.7e-56 PFAM
Pfam:OSR1_C 474 511 5.8e-22 PFAM
low complexity region 582 593 N/A INTRINSIC
low complexity region 626 642 N/A INTRINSIC
low complexity region 678 693 N/A INTRINSIC
low complexity region 707 736 N/A INTRINSIC
low complexity region 759 791 N/A INTRINSIC
low complexity region 809 819 N/A INTRINSIC
low complexity region 828 842 N/A INTRINSIC
low complexity region 863 878 N/A INTRINSIC
low complexity region 926 942 N/A INTRINSIC
low complexity region 971 1002 N/A INTRINSIC
low complexity region 1009 1036 N/A INTRINSIC
low complexity region 1101 1124 N/A INTRINSIC
internal_repeat_1 1150 1173 7.19e-6 PROSPERO
low complexity region 1263 1280 N/A INTRINSIC
low complexity region 1305 1341 N/A INTRINSIC
low complexity region 1417 1429 N/A INTRINSIC
low complexity region 1437 1445 N/A INTRINSIC
low complexity region 1452 1477 N/A INTRINSIC
low complexity region 1575 1585 N/A INTRINSIC
internal_repeat_2 1599 1701 3.66e-5 PROSPERO
low complexity region 1808 1819 N/A INTRINSIC
coiled coil region 1824 1855 N/A INTRINSIC
internal_repeat_2 1911 2015 3.66e-5 PROSPERO
low complexity region 2105 2125 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000160087
SMART Domains Protein: ENSMUSP00000124614
Gene: ENSMUSG00000037989

DomainStartEndE-ValueType
low complexity region 61 71 N/A INTRINSIC
low complexity region 80 94 N/A INTRINSIC
low complexity region 115 130 N/A INTRINSIC
low complexity region 178 194 N/A INTRINSIC
low complexity region 255 278 N/A INTRINSIC
low complexity region 417 434 N/A INTRINSIC
low complexity region 459 495 N/A INTRINSIC
low complexity region 571 583 N/A INTRINSIC
low complexity region 591 599 N/A INTRINSIC
low complexity region 606 631 N/A INTRINSIC
low complexity region 729 738 N/A INTRINSIC
low complexity region 961 972 N/A INTRINSIC
coiled coil region 977 1008 N/A INTRINSIC
low complexity region 1258 1278 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.6%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a cytoplasmic serine-threonine kinase that belongs to the protein kinase superfamily. The protein plays an important role in the regulation of electrolyte homeostasis, cell signaling survival, and proliferation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]
Allele List at MGI
Other mutations in this stock
Total: 100 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2410002F23Rik T A 7: 43,900,650 (GRCm39) V185E probably benign Het
Abca1 A C 4: 53,050,409 (GRCm39) V1608G probably damaging Het
Ap2b1 T C 11: 83,237,721 (GRCm39) I557T probably benign Het
Arhgef15 G T 11: 68,845,501 (GRCm39) P117Q probably damaging Het
Arhgef39 T C 4: 43,496,710 (GRCm39) S335G probably benign Het
Blm A T 7: 80,162,934 (GRCm39) F139Y possibly damaging Het
Cacna2d1 C T 5: 16,538,783 (GRCm39) R581* probably null Het
Cadps C A 14: 12,822,450 (GRCm38) E97* probably null Het
Cavin2 T A 1: 51,328,801 (GRCm39) L86Q probably damaging Het
Ccdc136 A G 6: 29,418,091 (GRCm39) E787G probably damaging Het
Ccdc39 T C 3: 33,880,629 (GRCm39) K446R probably damaging Het
Cdh23 T C 10: 60,159,361 (GRCm39) Y2138C probably damaging Het
Cdk12 T A 11: 98,094,916 (GRCm39) Y241* probably null Het
Clcn4 T A 7: 7,287,184 (GRCm39) *688L probably null Het
Cntnap1 T C 11: 101,071,212 (GRCm39) V375A possibly damaging Het
Coq5 T A 5: 115,432,890 (GRCm39) probably null Het
Cyp4b1 A G 4: 115,483,076 (GRCm39) I405T probably benign Het
Det1 T C 7: 78,492,966 (GRCm39) Y346C probably damaging Het
Enpp3 A T 10: 24,683,389 (GRCm39) V276E probably damaging Het
Epb41l2 G A 10: 25,317,666 (GRCm39) R61Q probably benign Het
Fam76b G A 9: 13,739,362 (GRCm39) probably null Het
Fbxo45 A T 16: 32,052,048 (GRCm39) D238E probably benign Het
Fnip2 G A 3: 79,400,779 (GRCm39) T314I probably benign Het
Fsip2 T C 2: 82,823,124 (GRCm39) S6286P possibly damaging Het
Gbf1 T C 19: 46,260,003 (GRCm39) F999L probably damaging Het
Gnao1 C A 8: 94,670,827 (GRCm39) T102K probably benign Het
Gpatch2 T A 1: 187,054,498 (GRCm39) D76E probably damaging Het
Gpd1l A G 9: 114,743,462 (GRCm39) I146T probably benign Het
Grik2 A T 10: 49,232,005 (GRCm39) H508Q probably damaging Het
Hapstr1 A G 16: 8,648,445 (GRCm39) E41G possibly damaging Het
Hk3 A T 13: 55,162,268 (GRCm39) F112Y probably damaging Het
Hmcn2 T G 2: 31,279,341 (GRCm39) I1781S probably damaging Het
Inhba A T 13: 16,201,221 (GRCm39) K261M probably damaging Het
Jarid2 T A 13: 45,059,752 (GRCm39) N661K probably damaging Het
Kcna2 T C 3: 107,011,946 (GRCm39) S176P probably damaging Het
Kcnj3 A T 2: 55,327,343 (GRCm39) Q44L probably damaging Het
Kcns1 G T 2: 164,010,455 (GRCm39) F101L probably damaging Het
Kdm5b T A 1: 134,541,611 (GRCm39) probably null Het
Klhl14 C T 18: 21,687,730 (GRCm39) G564D probably damaging Het
Klhl18 A T 9: 110,305,658 (GRCm39) V2E probably benign Het
Klhl6 T C 16: 19,801,572 (GRCm39) E61G probably damaging Het
Krt1 T C 15: 101,757,427 (GRCm39) D261G probably benign Het
Lama5 C A 2: 179,830,145 (GRCm39) C1896F probably damaging Het
Lrba A G 3: 86,513,175 (GRCm39) probably null Het
Lrch3 A G 16: 32,734,755 (GRCm39) T82A possibly damaging Het
Maml3 C G 3: 52,011,560 (GRCm39) G2A unknown Het
Mapkap1 T A 2: 34,408,691 (GRCm39) N34K probably damaging Het
Muc13 A T 16: 33,634,909 (GRCm39) I488F probably damaging Het
Muc5ac A G 7: 141,357,113 (GRCm39) D1129G possibly damaging Het
Nacc1 A T 8: 85,403,010 (GRCm39) N288K probably damaging Het
Nek1 T G 8: 61,469,330 (GRCm39) I129R probably damaging Het
Nf1 T A 11: 79,302,390 (GRCm39) S319R possibly damaging Het
Nle1 C T 11: 82,792,614 (GRCm39) G432D probably damaging Het
Nol4l A G 2: 153,371,375 (GRCm39) V103A probably benign Het
Oca2 A G 7: 56,064,215 (GRCm39) I737V probably damaging Het
Or12k5 A T 2: 36,894,960 (GRCm39) F222Y possibly damaging Het
Or1j17 G A 2: 36,578,796 (GRCm39) V261I probably benign Het
Or4b1 T C 2: 89,979,748 (GRCm39) S201G probably damaging Het
Or51l4 G T 7: 103,404,375 (GRCm39) T139K probably damaging Het
Or52ac1 A G 7: 104,246,008 (GRCm39) C127R probably damaging Het
Or6k6 G T 1: 173,944,817 (GRCm39) S255* probably null Het
Or6s1 T A 14: 51,308,614 (GRCm39) I79F probably damaging Het
Orc1 T A 4: 108,469,414 (GRCm39) I746N probably damaging Het
Pbxip1 A G 3: 89,352,795 (GRCm39) D147G probably damaging Het
Pirb A T 7: 3,720,637 (GRCm39) L287Q probably benign Het
Plin5 T A 17: 56,419,186 (GRCm39) D412V probably damaging Het
Plxna2 A T 1: 194,327,008 (GRCm39) Y314F possibly damaging Het
Ppid A T 3: 79,509,606 (GRCm39) K308* probably null Het
Prss38 T C 11: 59,264,310 (GRCm39) Y219C probably damaging Het
Ptx3 C T 3: 66,132,042 (GRCm39) R188C probably damaging Het
Ralgds T A 2: 28,435,887 (GRCm39) V504E probably damaging Het
Rere T C 4: 150,701,330 (GRCm39) Y1237H probably damaging Het
Rpp30 C T 19: 36,066,549 (GRCm39) S94L probably damaging Het
Rrp15 C T 1: 186,468,402 (GRCm39) V205I possibly damaging Het
Scpep1 A G 11: 88,843,240 (GRCm39) W73R probably damaging Het
Sec23ip A G 7: 128,357,077 (GRCm39) H376R probably damaging Het
Serping1 G T 2: 84,596,072 (GRCm39) T454K probably damaging Het
Shtn1 T G 19: 58,963,470 (GRCm39) Y615S probably benign Het
Slc20a2 C A 8: 23,035,553 (GRCm39) P184T probably damaging Het
Slc22a29 C A 19: 8,195,772 (GRCm39) R89L probably damaging Het
Slc2a2 A G 3: 28,773,634 (GRCm39) Q313R probably damaging Het
Tas2r122 A T 6: 132,688,157 (GRCm39) Y245* probably null Het
Ticrr C A 7: 79,344,483 (GRCm39) C1449* probably null Het
Tmem181a T C 17: 6,353,501 (GRCm39) V412A probably benign Het
Tmtc4 T A 14: 123,165,011 (GRCm39) E616V probably benign Het
Tnrc6b A G 15: 80,764,640 (GRCm39) K714R probably damaging Het
Trpm8 T A 1: 88,260,470 (GRCm39) probably null Het
Ubr2 T C 17: 47,265,845 (GRCm39) T1163A probably benign Het
Ubr4 A G 4: 139,178,555 (GRCm39) probably null Het
Ulk2 A T 11: 61,710,297 (GRCm39) probably null Het
Ulk4 T A 9: 121,086,182 (GRCm39) M350L probably benign Het
Vmn1r185 T C 7: 26,310,956 (GRCm39) E183G probably benign Het
Vmn1r76 T A 7: 11,664,441 (GRCm39) I223F probably damaging Het
Wdr27 T C 17: 15,154,861 (GRCm39) T19A possibly damaging Het
Wdr59 T G 8: 112,177,535 (GRCm39) T973P possibly damaging Het
Zfp1004 T A 2: 150,033,827 (GRCm39) D49E probably benign Het
Zfp120 A T 2: 149,959,318 (GRCm39) C335S probably damaging Het
Zfp30 C A 7: 29,491,877 (GRCm39) Q44K probably benign Het
Zfp541 T C 7: 15,812,996 (GRCm39) S550P probably benign Het
Zw10 C A 9: 48,980,133 (GRCm39) N421K probably damaging Het
Other mutations in Wnk2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01518:Wnk2 APN 13 49,221,668 (GRCm39) missense possibly damaging 0.89
IGL01575:Wnk2 APN 13 49,300,152 (GRCm39) missense probably damaging 1.00
IGL01601:Wnk2 APN 13 49,230,038 (GRCm39) missense probably damaging 1.00
IGL01775:Wnk2 APN 13 49,224,586 (GRCm39) missense probably damaging 1.00
IGL02013:Wnk2 APN 13 49,235,510 (GRCm39) missense possibly damaging 0.46
IGL02016:Wnk2 APN 13 49,210,381 (GRCm39) missense probably damaging 1.00
IGL02167:Wnk2 APN 13 49,224,601 (GRCm39) critical splice acceptor site probably null
IGL02174:Wnk2 APN 13 49,210,643 (GRCm39) missense probably damaging 1.00
IGL02210:Wnk2 APN 13 49,244,345 (GRCm39) missense probably damaging 0.98
IGL02228:Wnk2 APN 13 49,210,416 (GRCm39) missense probably damaging 1.00
IGL02282:Wnk2 APN 13 49,221,601 (GRCm39) missense probably damaging 1.00
IGL02319:Wnk2 APN 13 49,214,914 (GRCm39) missense possibly damaging 0.73
IGL02394:Wnk2 APN 13 49,235,375 (GRCm39) splice site probably null
IGL02624:Wnk2 APN 13 49,256,278 (GRCm39) missense probably damaging 1.00
IGL02743:Wnk2 APN 13 49,248,920 (GRCm39) missense probably damaging 1.00
IGL03012:Wnk2 APN 13 49,197,865 (GRCm39) missense probably damaging 0.99
IGL03166:Wnk2 APN 13 49,224,520 (GRCm39) nonsense probably null
R0034:Wnk2 UTSW 13 49,221,556 (GRCm39) missense possibly damaging 0.64
R0385:Wnk2 UTSW 13 49,221,604 (GRCm39) missense probably damaging 1.00
R0423:Wnk2 UTSW 13 49,248,894 (GRCm39) missense possibly damaging 0.91
R0504:Wnk2 UTSW 13 49,238,872 (GRCm39) missense probably damaging 1.00
R0504:Wnk2 UTSW 13 49,238,870 (GRCm39) missense possibly damaging 0.92
R0653:Wnk2 UTSW 13 49,210,492 (GRCm39) missense possibly damaging 0.85
R1135:Wnk2 UTSW 13 49,230,034 (GRCm39) missense probably damaging 1.00
R1445:Wnk2 UTSW 13 49,224,586 (GRCm39) missense probably damaging 1.00
R1464:Wnk2 UTSW 13 49,235,451 (GRCm39) missense probably damaging 1.00
R1464:Wnk2 UTSW 13 49,235,451 (GRCm39) missense probably damaging 1.00
R1468:Wnk2 UTSW 13 49,235,571 (GRCm39) missense probably damaging 0.99
R1468:Wnk2 UTSW 13 49,235,571 (GRCm39) missense probably damaging 0.99
R1480:Wnk2 UTSW 13 49,210,708 (GRCm39) missense probably damaging 1.00
R1605:Wnk2 UTSW 13 49,214,370 (GRCm39) missense probably damaging 1.00
R1719:Wnk2 UTSW 13 49,214,202 (GRCm39) missense possibly damaging 0.76
R1891:Wnk2 UTSW 13 49,206,200 (GRCm39) nonsense probably null
R2001:Wnk2 UTSW 13 49,232,158 (GRCm39) missense possibly damaging 0.61
R2310:Wnk2 UTSW 13 49,204,053 (GRCm39) missense probably damaging 0.97
R2356:Wnk2 UTSW 13 49,192,644 (GRCm39) nonsense probably null
R2406:Wnk2 UTSW 13 49,214,964 (GRCm39) missense possibly damaging 0.86
R2519:Wnk2 UTSW 13 49,224,505 (GRCm39) missense probably damaging 0.99
R3962:Wnk2 UTSW 13 49,224,453 (GRCm39) missense probably damaging 1.00
R4160:Wnk2 UTSW 13 49,244,313 (GRCm39) missense probably damaging 1.00
R4161:Wnk2 UTSW 13 49,244,313 (GRCm39) missense probably damaging 1.00
R4226:Wnk2 UTSW 13 49,244,313 (GRCm39) missense probably damaging 1.00
R4227:Wnk2 UTSW 13 49,244,313 (GRCm39) missense probably damaging 1.00
R4234:Wnk2 UTSW 13 49,214,604 (GRCm39) missense probably benign 0.33
R4304:Wnk2 UTSW 13 49,244,313 (GRCm39) missense probably damaging 1.00
R4308:Wnk2 UTSW 13 49,244,313 (GRCm39) missense probably damaging 1.00
R4584:Wnk2 UTSW 13 49,244,313 (GRCm39) missense probably damaging 1.00
R4655:Wnk2 UTSW 13 49,210,359 (GRCm39) missense probably damaging 1.00
R4715:Wnk2 UTSW 13 49,300,708 (GRCm39) start codon destroyed unknown
R4887:Wnk2 UTSW 13 49,224,478 (GRCm39) missense probably damaging 1.00
R4888:Wnk2 UTSW 13 49,224,478 (GRCm39) missense probably damaging 1.00
R4945:Wnk2 UTSW 13 49,210,722 (GRCm39) missense probably damaging 1.00
R5182:Wnk2 UTSW 13 49,214,637 (GRCm39) missense possibly damaging 0.92
R5243:Wnk2 UTSW 13 49,226,054 (GRCm39) missense possibly damaging 0.51
R5370:Wnk2 UTSW 13 49,256,437 (GRCm39) missense probably damaging 1.00
R5771:Wnk2 UTSW 13 49,256,276 (GRCm39) missense probably damaging 1.00
R5877:Wnk2 UTSW 13 49,220,782 (GRCm39) missense probably damaging 0.98
R5900:Wnk2 UTSW 13 49,256,308 (GRCm39) missense probably damaging 1.00
R5905:Wnk2 UTSW 13 49,229,821 (GRCm39) missense probably damaging 0.99
R5912:Wnk2 UTSW 13 49,214,250 (GRCm39) missense probably damaging 1.00
R5915:Wnk2 UTSW 13 49,231,561 (GRCm39) missense probably damaging 0.99
R6028:Wnk2 UTSW 13 49,229,821 (GRCm39) missense probably damaging 0.99
R6074:Wnk2 UTSW 13 49,204,875 (GRCm39) missense probably damaging 1.00
R6171:Wnk2 UTSW 13 49,214,308 (GRCm39) missense probably damaging 1.00
R6368:Wnk2 UTSW 13 49,214,814 (GRCm39) missense probably damaging 0.99
R6467:Wnk2 UTSW 13 49,300,081 (GRCm39) missense probably damaging 1.00
R6501:Wnk2 UTSW 13 49,300,159 (GRCm39) missense probably damaging 1.00
R6849:Wnk2 UTSW 13 49,220,834 (GRCm39) missense probably damaging 1.00
R6898:Wnk2 UTSW 13 49,224,557 (GRCm39) missense probably damaging 1.00
R6949:Wnk2 UTSW 13 49,254,616 (GRCm39) missense probably damaging 1.00
R7011:Wnk2 UTSW 13 49,224,567 (GRCm39) missense probably damaging 0.99
R7097:Wnk2 UTSW 13 49,256,314 (GRCm39) missense possibly damaging 0.86
R7121:Wnk2 UTSW 13 49,300,653 (GRCm39) missense probably benign 0.26
R7123:Wnk2 UTSW 13 49,235,462 (GRCm39) missense possibly damaging 0.90
R7423:Wnk2 UTSW 13 49,191,608 (GRCm39) missense probably benign 0.07
R7502:Wnk2 UTSW 13 49,300,720 (GRCm39) splice site probably null
R7529:Wnk2 UTSW 13 49,254,457 (GRCm39) missense possibly damaging 0.50
R7751:Wnk2 UTSW 13 49,231,493 (GRCm39) missense unknown
R7979:Wnk2 UTSW 13 49,248,884 (GRCm39) missense probably damaging 1.00
R8118:Wnk2 UTSW 13 49,244,459 (GRCm39) missense probably damaging 0.99
R8121:Wnk2 UTSW 13 49,214,415 (GRCm39) nonsense probably null
R8155:Wnk2 UTSW 13 49,192,577 (GRCm39) missense unknown
R8329:Wnk2 UTSW 13 49,248,914 (GRCm39) missense probably damaging 1.00
R8334:Wnk2 UTSW 13 49,203,958 (GRCm39) critical splice donor site probably null
R8872:Wnk2 UTSW 13 49,210,960 (GRCm39) missense probably benign 0.00
R8919:Wnk2 UTSW 13 49,221,711 (GRCm39) missense possibly damaging 0.86
R9091:Wnk2 UTSW 13 49,224,505 (GRCm39) missense probably benign 0.41
R9234:Wnk2 UTSW 13 49,224,274 (GRCm39) missense probably damaging 0.99
R9262:Wnk2 UTSW 13 49,221,430 (GRCm39) missense probably benign 0.12
R9268:Wnk2 UTSW 13 49,235,507 (GRCm39) missense possibly damaging 0.82
R9270:Wnk2 UTSW 13 49,224,505 (GRCm39) missense probably benign 0.41
R9386:Wnk2 UTSW 13 49,220,822 (GRCm39) missense probably damaging 0.98
R9582:Wnk2 UTSW 13 49,210,975 (GRCm39) missense probably benign 0.01
R9617:Wnk2 UTSW 13 49,192,453 (GRCm39) missense unknown
R9625:Wnk2 UTSW 13 49,254,445 (GRCm39) missense probably benign 0.20
R9794:Wnk2 UTSW 13 49,229,674 (GRCm39) missense probably benign 0.02
RF023:Wnk2 UTSW 13 49,300,255 (GRCm39) missense probably benign 0.00
X0025:Wnk2 UTSW 13 49,214,418 (GRCm39) missense probably damaging 0.99
X0063:Wnk2 UTSW 13 49,192,453 (GRCm39) missense unknown
Z1176:Wnk2 UTSW 13 49,191,537 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- CAACTGGGTTCTTCTACACGC -3'
(R):5'- TCATAGACATCTGTGCCTCGAG -3'

Sequencing Primer
(F):5'- GGGTTCTTCTACACGCTTCAGAG -3'
(R):5'- AGCAGCAGTGGGGGCATC -3'
Posted On 2014-08-25