Incidental Mutation 'R4415:Lad1'
ID326778
Institutional Source Beutler Lab
Gene Symbol Lad1
Ensembl Gene ENSMUSG00000041782
Gene Nameladinin
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.059) question?
Stock #R4415 (G1)
Quality Score225
Status Not validated
Chromosome1
Chromosomal Location135818598-135833342 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 135828746 bp
ZygosityHeterozygous
Amino Acid Change Aspartic acid to Glycine at position 364 (D364G)
Ref Sequence ENSEMBL: ENSMUSP00000044630 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000038760]
Predicted Effect probably benign
Transcript: ENSMUST00000038760
AA Change: D364G

PolyPhen 2 Score 0.056 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000044630
Gene: ENSMUSG00000041782
AA Change: D364G

DomainStartEndE-ValueType
low complexity region 16 35 N/A INTRINSIC
low complexity region 88 110 N/A INTRINSIC
low complexity region 365 377 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185756
Predicted Effect noncoding transcript
Transcript: ENSMUST00000190773
Meta Mutation Damage Score 0.0946 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.3%
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 may be an anchoring filament that is a component of basement membranes. It may contribute to the stability of the association of the epithelial layers with the underlying mesenchyme. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110017D15Rik T C 4: 41,505,574 T183A possibly damaging Het
Ace3 A T 11: 106,005,121 D631V probably benign Het
Adam17 T C 12: 21,345,701 I274V possibly damaging Het
Aebp1 A G 11: 5,865,451 D303G probably damaging Het
B020004C17Rik T C 14: 57,017,417 *233R probably null Het
Bcl9l C T 9: 44,501,879 P127S possibly damaging Het
Bdp1 T C 13: 100,030,861 D2215G probably damaging Het
Caly T C 7: 140,072,680 T52A probably damaging Het
Ccdc125 T C 13: 100,696,309 S465P possibly damaging Het
Cdc23 ACC AC 18: 34,637,318 probably null Het
Colq T C 14: 31,535,688 K231E probably damaging Het
Fam32a T A 8: 72,221,941 I77N probably damaging Het
Gm597 T A 1: 28,777,133 Q606L probably benign Het
Impdh1 C T 6: 29,209,222 V49M probably damaging Het
Kcnh7 A G 2: 62,706,073 I1055T probably damaging Het
Lama2 G T 10: 26,989,344 Y947* probably null Het
Myo5b T A 18: 74,580,408 I108N probably damaging Het
Nvl T C 1: 181,105,114 T713A probably benign Het
Oit3 T C 10: 59,428,103 Y403C probably damaging Het
Olfr814 T C 10: 129,873,957 T267A probably benign Het
Pappa A G 4: 65,305,295 T1236A probably benign Het
Rcl1 G A 19: 29,118,362 V116I probably benign Het
Rdh14 G A 12: 10,391,231 probably null Het
Rfx2 T A 17: 56,787,733 T204S possibly damaging Het
Rin2 C T 2: 145,860,446 T354I probably benign Het
Ripor1 T C 8: 105,617,976 S581P probably benign Het
Rnf213 T A 11: 119,483,964 V5084E probably damaging Het
Scn9a A T 2: 66,526,693 V1077E probably damaging Het
Slc15a5 A G 6: 138,079,756 V54A probably benign Het
Slc35b2 G A 17: 45,566,429 V161M probably benign Het
Snx19 T A 9: 30,437,483 L804Q probably damaging Het
Specc1l C A 10: 75,246,328 N519K possibly damaging Het
Stambp A T 6: 83,557,482 N274K probably damaging Het
Stox1 T C 10: 62,659,569 N975S probably benign Het
Tacc3 T G 5: 33,666,684 probably null Het
Tmem55a C T 4: 14,912,463 R191C probably damaging Het
Tubb1 G A 2: 174,457,673 E383K probably benign Het
Ube3b A T 5: 114,412,444 D844V probably damaging Het
Other mutations in Lad1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03259:Lad1 APN 1 135827656 missense probably benign 0.07
IGL03323:Lad1 APN 1 135830974 critical splice donor site probably null
R1728:Lad1 UTSW 1 135827381 missense possibly damaging 0.90
R1728:Lad1 UTSW 1 135828023 missense probably damaging 1.00
R1729:Lad1 UTSW 1 135827381 missense possibly damaging 0.90
R1729:Lad1 UTSW 1 135828023 missense probably damaging 1.00
R1730:Lad1 UTSW 1 135827381 missense possibly damaging 0.90
R1730:Lad1 UTSW 1 135828023 missense probably damaging 1.00
R1739:Lad1 UTSW 1 135827381 missense possibly damaging 0.90
R1739:Lad1 UTSW 1 135828023 missense probably damaging 1.00
R1762:Lad1 UTSW 1 135827381 missense possibly damaging 0.90
R1762:Lad1 UTSW 1 135828023 missense probably damaging 1.00
R1783:Lad1 UTSW 1 135827381 missense possibly damaging 0.90
R1783:Lad1 UTSW 1 135828023 missense probably damaging 1.00
R1784:Lad1 UTSW 1 135827381 missense possibly damaging 0.90
R1784:Lad1 UTSW 1 135828023 missense probably damaging 1.00
R1785:Lad1 UTSW 1 135827381 missense possibly damaging 0.90
R1785:Lad1 UTSW 1 135828023 missense probably damaging 1.00
R1837:Lad1 UTSW 1 135829706 missense probably benign 0.00
R1854:Lad1 UTSW 1 135827730 missense probably damaging 0.99
R4066:Lad1 UTSW 1 135827427 missense probably damaging 1.00
R4240:Lad1 UTSW 1 135827295 missense possibly damaging 0.84
R4414:Lad1 UTSW 1 135828746 missense probably benign 0.06
R4417:Lad1 UTSW 1 135828746 missense probably benign 0.06
R4770:Lad1 UTSW 1 135825793 missense probably damaging 1.00
R6419:Lad1 UTSW 1 135831892 missense possibly damaging 0.86
R6824:Lad1 UTSW 1 135827741 missense probably benign 0.04
R6905:Lad1 UTSW 1 135827880 missense probably benign 0.40
R7353:Lad1 UTSW 1 135827775 missense probably damaging 0.96
R7427:Lad1 UTSW 1 135825838 missense probably damaging 1.00
R7918:Lad1 UTSW 1 135829716 missense probably benign 0.00
R8261:Lad1 UTSW 1 135827762 missense probably damaging 0.96
R8368:Lad1 UTSW 1 135831526 missense probably damaging 1.00
R8743:Lad1 UTSW 1 135831195 missense probably benign 0.10
X0024:Lad1 UTSW 1 135830933 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ACTAAAGCTCTGCCTGGTGG -3'
(R):5'- AAGAAGACCCTTCCTATTGTCTAAC -3'

Sequencing Primer
(F):5'- CTGGGCTACATGAGACTATATAGCC -3'
(R):5'- GACCCTTCCTATTGTCTAACATACAG -3'
Posted On2015-07-07