Incidental Mutation 'R9413:Gm6619'
ID 711898
Institutional Source Beutler Lab
Gene Symbol Gm6619
Ensembl Gene ENSMUSG00000095577
Gene Name predicted gene 6619
Synonyms
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.097) question?
Stock # R9413 (G1)
Quality Score 104.008
Status Not validated
Chromosome 6
Chromosomal Location 131486400-131491493 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 131491407 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Valine at position 167 (D167V)
Ref Sequence ENSEMBL: ENSMUSP00000123949 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000075020] [ENSMUST00000159229]
AlphaFold F6URP1
Predicted Effect probably benign
Transcript: ENSMUST00000075020
SMART Domains Protein: ENSMUSP00000074539
Gene: ENSMUSG00000094113

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
low complexity region 100 116 N/A INTRINSIC
low complexity region 118 166 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000159229
AA Change: D167V
SMART Domains Protein: ENSMUSP00000123949
Gene: ENSMUSG00000095577
AA Change: D167V

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
low complexity region 99 166 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 97% (35/36)
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 A T 7: 120,527,199 T1194S probably benign Het
Akr7a5 A T 4: 139,310,748 probably benign Het
Ap3b2 G T 7: 81,478,009 P140T possibly damaging Het
Ap3s1 T C 18: 46,754,464 probably null Het
Arrdc2 C T 8: 70,836,248 R381H probably damaging Het
Atg13 T C 2: 91,681,625 D286G probably benign Het
C1qtnf4 T C 2: 90,890,304 F307S probably damaging Het
Cdk5rap1 A T 2: 154,365,960 probably null Het
Chsy3 C T 18: 59,176,098 A141V possibly damaging Het
Creb3l1 C T 2: 91,991,886 probably null Het
D5Ertd579e A G 5: 36,614,934 S706P probably damaging Het
Ell2 A G 13: 75,769,586 D545G Het
Ephb6 T C 6: 41,614,575 L222P Het
Flnc G A 6: 29,441,485 R422Q probably benign Het
Gucy2c T C 6: 136,723,773 D581G possibly damaging Het
Hectd1 G A 12: 51,746,097 R2471* probably null Het
Kif1a A T 1: 93,021,297 M1501K probably benign Het
Mycbpap A G 11: 94,501,495 V390A probably damaging Het
Olfr136 A T 17: 38,335,429 T91S possibly damaging Het
Pex3 A G 10: 13,534,710 Y236H probably damaging Het
Pglyrp3 G T 3: 92,022,799 A91S probably damaging Het
Ppp1ca T C 19: 4,194,898 S292P probably damaging Het
Prkci T C 3: 31,043,766 V455A probably damaging Het
Prrx1 A G 1: 163,312,613 V8A probably benign Het
Psd4 C T 2: 24,397,460 T468I probably benign Het
Rnf213 A G 11: 119,466,233 E4203G Het
Snrnp27 T C 6: 86,676,273 D121G possibly damaging Het
Spag6 A T 2: 18,734,218 M320L probably benign Het
Spata16 T A 3: 26,924,337 M484K possibly damaging Het
Trim69 G A 2: 122,178,602 W381* probably null Het
Tubgcp3 A C 8: 12,624,885 I745S probably damaging Het
Ubxn2b A G 4: 6,204,607 D156G probably damaging Het
Vmn2r103 A G 17: 19,811,896 N644S possibly damaging Het
Other mutations in Gm6619
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01099:Gm6619 APN 6 131490430 missense possibly damaging 0.66
IGL02438:Gm6619 APN 6 131490435 missense possibly damaging 0.83
IGL02511:Gm6619 APN 6 131490367 missense possibly damaging 0.49
IGL03333:Gm6619 APN 6 131490508 intron probably benign
R0744:Gm6619 UTSW 6 131490334 missense probably damaging 0.97
R2150:Gm6619 UTSW 6 131489058 missense probably benign 0.03
R5817:Gm6619 UTSW 6 131486437 missense unknown
R6869:Gm6619 UTSW 6 131486438 missense unknown
R7439:Gm6619 UTSW 6 131490391 missense possibly damaging 0.66
R7441:Gm6619 UTSW 6 131490391 missense possibly damaging 0.66
Predicted Primers PCR Primer
(F):5'- AGCAAGTGTTTCCTCTGCCC -3'
(R):5'- TGTGAAGCCACTATCAATTCCC -3'

Sequencing Primer
(F):5'- TGAAATTCACCGTGCAGTCCATG -3'
(R):5'- TATCAATTCCCTAACATCTCCAGGG -3'
Posted On 2022-05-16