Incidental Mutation 'R1727:Slc9c1'
ID |
198278 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Slc9c1
|
Ensembl Gene |
ENSMUSG00000033210 |
Gene Name |
solute carrier family 9, subfamily C (Na+-transporting carboxylic acid decarboxylase), member 1 |
Synonyms |
LOC208169, spermNHE, Slc9a10 |
MMRRC Submission |
039759-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.398)
|
Stock # |
R1727 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
16 |
Chromosomal Location |
45355672-45427364 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 45422324 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Phenylalanine
at position 1130
(I1130F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000124969
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000159945]
|
AlphaFold |
Q6UJY2 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000159945
AA Change: I1130F
PolyPhen 2
Score 0.267 (Sensitivity: 0.91; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000124969 Gene: ENSMUSG00000033210 AA Change: I1130F
Domain | Start | End | E-Value | Type |
Pfam:Na_H_Exchanger
|
40 |
445 |
2.3e-31 |
PFAM |
low complexity region
|
588 |
602 |
N/A |
INTRINSIC |
transmembrane domain
|
635 |
654 |
N/A |
INTRINSIC |
transmembrane domain
|
669 |
686 |
N/A |
INTRINSIC |
transmembrane domain
|
691 |
713 |
N/A |
INTRINSIC |
low complexity region
|
734 |
743 |
N/A |
INTRINSIC |
cNMP
|
890 |
1026 |
4.99e-1 |
SMART |
low complexity region
|
1161 |
1175 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000162151
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000162774
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 97.5%
- 3x: 96.9%
- 10x: 95.3%
- 20x: 92.3%
|
Validation Efficiency |
96% (98/102) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] SLC9A10 is a member of the sodium-hydrogen exchanger (NHE) family (see SLC9A1, MIM 107310) and is required for male fertility and sperm motility (Wang et al., 2003 [PubMed 14634667]).[supplied by OMIM, Apr 2009] PHENOTYPE: Homozygous null mice display male infertility and asthenozoospermia. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts6 |
T |
C |
13: 104,565,472 (GRCm39) |
|
probably benign |
Het |
Ak2 |
C |
T |
4: 128,901,556 (GRCm39) |
P159L |
probably damaging |
Het |
Akap8l |
C |
T |
17: 32,551,457 (GRCm39) |
R511H |
probably damaging |
Het |
Akr1a1 |
A |
G |
4: 116,498,248 (GRCm39) |
L99P |
probably damaging |
Het |
Anxa8 |
T |
A |
14: 33,811,547 (GRCm39) |
M34K |
probably damaging |
Het |
Axl |
T |
G |
7: 25,460,191 (GRCm39) |
D767A |
possibly damaging |
Het |
B430305J03Rik |
A |
G |
3: 61,271,299 (GRCm39) |
|
probably benign |
Het |
Cdh24 |
A |
T |
14: 54,876,095 (GRCm39) |
Y182* |
probably null |
Het |
Cdk5rap2 |
T |
C |
4: 70,190,916 (GRCm39) |
D1043G |
probably benign |
Het |
Cdk5rap2 |
A |
T |
4: 70,208,209 (GRCm39) |
S746T |
possibly damaging |
Het |
Cep120 |
T |
C |
18: 53,860,801 (GRCm39) |
M210V |
probably benign |
Het |
Chga |
C |
T |
12: 102,527,696 (GRCm39) |
H117Y |
possibly damaging |
Het |
Cnga4 |
T |
C |
7: 105,054,961 (GRCm39) |
W79R |
probably damaging |
Het |
Cntnap5b |
C |
T |
1: 100,141,469 (GRCm39) |
T575I |
possibly damaging |
Het |
Col6a3 |
T |
A |
1: 90,724,296 (GRCm39) |
|
probably null |
Het |
Copz2 |
T |
C |
11: 96,744,301 (GRCm39) |
V71A |
probably benign |
Het |
Dennd3 |
G |
T |
15: 73,436,977 (GRCm39) |
R1068L |
possibly damaging |
Het |
Dhrs7 |
T |
C |
12: 72,706,238 (GRCm39) |
T56A |
probably damaging |
Het |
Dnah17 |
G |
A |
11: 117,961,315 (GRCm39) |
T2557I |
probably damaging |
Het |
Dnah17 |
A |
T |
11: 117,987,362 (GRCm39) |
L1320* |
probably null |
Het |
Dynlt2b |
T |
A |
16: 32,241,751 (GRCm39) |
M78K |
probably benign |
Het |
Eif3b |
T |
C |
5: 140,411,077 (GRCm39) |
I176T |
probably damaging |
Het |
Eif4b |
T |
A |
15: 101,998,497 (GRCm39) |
D392E |
possibly damaging |
Het |
Eif4h |
T |
C |
5: 134,668,134 (GRCm39) |
Y7C |
probably damaging |
Het |
Enam |
A |
T |
5: 88,651,853 (GRCm39) |
S1046C |
probably damaging |
Het |
Epg5 |
T |
A |
18: 78,059,030 (GRCm39) |
V1928E |
possibly damaging |
Het |
Erbin |
T |
A |
13: 103,964,476 (GRCm39) |
E1222V |
probably benign |
Het |
Fhdc1 |
T |
A |
3: 84,353,483 (GRCm39) |
I581F |
possibly damaging |
Het |
Fhip2b |
C |
A |
14: 70,831,438 (GRCm39) |
G32V |
probably damaging |
Het |
Fstl4 |
A |
C |
11: 52,959,478 (GRCm39) |
Q173P |
probably damaging |
Het |
Gm266 |
A |
G |
12: 111,451,913 (GRCm39) |
F98L |
possibly damaging |
Het |
Gsdmc2 |
T |
C |
15: 63,721,628 (GRCm39) |
|
probably benign |
Het |
Gtf2h3 |
A |
G |
5: 124,728,419 (GRCm39) |
Q156R |
probably benign |
Het |
H2-T23 |
T |
C |
17: 36,342,545 (GRCm39) |
T198A |
possibly damaging |
Het |
Il1r1 |
C |
A |
1: 40,332,424 (GRCm39) |
A68E |
probably benign |
Het |
Kcna7 |
A |
T |
7: 45,058,930 (GRCm39) |
I406F |
possibly damaging |
Het |
Lbr |
A |
G |
1: 181,647,481 (GRCm39) |
I432T |
probably benign |
Het |
Lnx1 |
A |
T |
5: 74,768,577 (GRCm39) |
|
probably null |
Het |
Lrrcc1 |
T |
A |
3: 14,602,423 (GRCm39) |
I50N |
probably damaging |
Het |
Lss |
T |
C |
10: 76,375,678 (GRCm39) |
V237A |
possibly damaging |
Het |
Mcm10 |
A |
G |
2: 5,011,336 (GRCm39) |
F212L |
probably benign |
Het |
Methig1 |
A |
C |
15: 100,251,130 (GRCm39) |
I14L |
probably benign |
Het |
Mrpl41 |
A |
T |
2: 24,864,636 (GRCm39) |
V55E |
probably damaging |
Het |
Mtfp1 |
C |
A |
11: 4,043,982 (GRCm39) |
D83Y |
probably damaging |
Het |
Myh1 |
T |
A |
11: 67,101,292 (GRCm39) |
|
probably benign |
Het |
Myo1e |
T |
C |
9: 70,283,806 (GRCm39) |
F834S |
possibly damaging |
Het |
Ndufs7 |
A |
T |
10: 80,091,853 (GRCm39) |
|
probably benign |
Het |
Nlrp4e |
T |
A |
7: 23,020,420 (GRCm39) |
N302K |
probably benign |
Het |
Nt5e |
T |
A |
9: 88,210,082 (GRCm39) |
M115K |
possibly damaging |
Het |
Nup153 |
A |
T |
13: 46,847,261 (GRCm39) |
C723S |
probably damaging |
Het |
Obox6 |
G |
A |
7: 15,568,502 (GRCm39) |
P125S |
probably benign |
Het |
Or1n2 |
G |
A |
2: 36,797,405 (GRCm39) |
C149Y |
probably benign |
Het |
Or2t48 |
A |
T |
11: 58,420,342 (GRCm39) |
S157T |
possibly damaging |
Het |
Or52n3 |
C |
T |
7: 104,530,721 (GRCm39) |
T269I |
probably benign |
Het |
Or5an11 |
T |
G |
19: 12,246,365 (GRCm39) |
I257S |
possibly damaging |
Het |
Or8i2 |
A |
G |
2: 86,852,607 (GRCm39) |
F94L |
probably damaging |
Het |
Pcdh1 |
A |
C |
18: 38,336,085 (GRCm39) |
Y44* |
probably null |
Het |
Pcdhb6 |
A |
T |
18: 37,467,640 (GRCm39) |
D187V |
probably damaging |
Het |
Pclo |
A |
G |
5: 14,727,001 (GRCm39) |
|
probably benign |
Het |
Pdcl3 |
T |
A |
1: 39,034,836 (GRCm39) |
I80K |
possibly damaging |
Het |
Pde12 |
A |
T |
14: 26,390,022 (GRCm39) |
V229E |
probably benign |
Het |
Plcg1 |
A |
G |
2: 160,590,008 (GRCm39) |
E142G |
probably benign |
Het |
Plxnb1 |
A |
G |
9: 108,930,125 (GRCm39) |
|
probably null |
Het |
Pnpla1 |
A |
G |
17: 29,097,508 (GRCm39) |
I225V |
probably benign |
Het |
Polr2f |
A |
G |
15: 79,028,805 (GRCm39) |
|
probably benign |
Het |
Prob1 |
A |
G |
18: 35,787,364 (GRCm39) |
S297P |
possibly damaging |
Het |
Qsox2 |
A |
C |
2: 26,110,970 (GRCm39) |
S132A |
probably benign |
Het |
Rab19 |
T |
A |
6: 39,365,095 (GRCm39) |
Y118* |
probably null |
Het |
Rfwd3 |
C |
T |
8: 112,014,874 (GRCm39) |
R326Q |
probably damaging |
Het |
Rptn |
T |
C |
3: 93,304,445 (GRCm39) |
S593P |
possibly damaging |
Het |
Septin11 |
T |
C |
5: 93,304,783 (GRCm39) |
I200T |
probably damaging |
Het |
Slc10a4 |
T |
A |
5: 73,173,491 (GRCm39) |
|
probably benign |
Het |
Slit3 |
C |
T |
11: 35,520,659 (GRCm39) |
R599C |
probably damaging |
Het |
Snx19 |
C |
T |
9: 30,344,662 (GRCm39) |
P622L |
probably damaging |
Het |
Sspo |
T |
C |
6: 48,471,782 (GRCm39) |
L50P |
probably damaging |
Het |
St8sia1 |
A |
T |
6: 142,822,453 (GRCm39) |
C137S |
probably damaging |
Het |
Syt11 |
G |
C |
3: 88,669,259 (GRCm39) |
T211S |
possibly damaging |
Het |
Tanc1 |
A |
C |
2: 59,621,153 (GRCm39) |
Y324S |
probably damaging |
Het |
Tas2r136 |
T |
C |
6: 132,754,753 (GRCm39) |
I125V |
possibly damaging |
Het |
Tbc1d15 |
A |
T |
10: 115,046,130 (GRCm39) |
W458R |
probably damaging |
Het |
Tecta |
G |
T |
9: 42,270,597 (GRCm39) |
T1237N |
probably damaging |
Het |
Tet2 |
T |
A |
3: 133,193,051 (GRCm39) |
D461V |
probably damaging |
Het |
Tmco3 |
G |
A |
8: 13,368,866 (GRCm39) |
V573M |
possibly damaging |
Het |
Tmem212 |
A |
T |
3: 27,938,961 (GRCm39) |
M175K |
probably benign |
Het |
Traf6 |
A |
G |
2: 101,527,084 (GRCm39) |
H278R |
probably benign |
Het |
Trerf1 |
T |
A |
17: 47,652,092 (GRCm39) |
|
noncoding transcript |
Het |
Ttn |
A |
C |
2: 76,576,988 (GRCm39) |
V24635G |
probably damaging |
Het |
Ush1c |
A |
T |
7: 45,858,655 (GRCm39) |
D544E |
probably damaging |
Het |
Usp47 |
C |
T |
7: 111,685,307 (GRCm39) |
T586M |
probably damaging |
Het |
Vmn2r1 |
T |
A |
3: 63,989,163 (GRCm39) |
M34K |
probably benign |
Het |
Vmn2r102 |
T |
A |
17: 19,897,770 (GRCm39) |
W262R |
probably damaging |
Het |
Wasf3 |
C |
T |
5: 146,403,769 (GRCm39) |
A293V |
probably benign |
Het |
Xrn2 |
A |
G |
2: 146,903,436 (GRCm39) |
Q812R |
probably benign |
Het |
Zc3h7b |
T |
C |
15: 81,652,230 (GRCm39) |
I10T |
probably damaging |
Het |
Zfp747 |
A |
T |
7: 126,973,249 (GRCm39) |
L307Q |
probably damaging |
Het |
Zfp777 |
A |
T |
6: 48,020,824 (GRCm39) |
F266Y |
probably damaging |
Het |
|
Other mutations in Slc9c1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00230:Slc9c1
|
APN |
16 |
45,393,752 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL00510:Slc9c1
|
APN |
16 |
45,360,002 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00949:Slc9c1
|
APN |
16 |
45,413,721 (GRCm39) |
missense |
probably benign |
|
IGL01287:Slc9c1
|
APN |
16 |
45,404,811 (GRCm39) |
nonsense |
probably null |
|
IGL01536:Slc9c1
|
APN |
16 |
45,409,992 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01655:Slc9c1
|
APN |
16 |
45,403,335 (GRCm39) |
missense |
probably benign |
|
IGL01671:Slc9c1
|
APN |
16 |
45,380,678 (GRCm39) |
missense |
probably benign |
|
IGL01720:Slc9c1
|
APN |
16 |
45,376,132 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01758:Slc9c1
|
APN |
16 |
45,361,824 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02031:Slc9c1
|
APN |
16 |
45,419,833 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02321:Slc9c1
|
APN |
16 |
45,376,977 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02472:Slc9c1
|
APN |
16 |
45,400,505 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02516:Slc9c1
|
APN |
16 |
45,398,238 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02732:Slc9c1
|
APN |
16 |
45,370,548 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02741:Slc9c1
|
APN |
16 |
45,401,961 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL02795:Slc9c1
|
APN |
16 |
45,395,782 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03032:Slc9c1
|
APN |
16 |
45,363,624 (GRCm39) |
splice site |
probably benign |
|
IGL03062:Slc9c1
|
APN |
16 |
45,420,121 (GRCm39) |
missense |
probably benign |
0.20 |
IGL03184:Slc9c1
|
APN |
16 |
45,368,003 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03351:Slc9c1
|
APN |
16 |
45,363,531 (GRCm39) |
missense |
probably benign |
0.01 |
P0041:Slc9c1
|
UTSW |
16 |
45,370,524 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0052:Slc9c1
|
UTSW |
16 |
45,427,219 (GRCm39) |
utr 3 prime |
probably benign |
|
R0107:Slc9c1
|
UTSW |
16 |
45,395,783 (GRCm39) |
missense |
probably benign |
0.00 |
R0255:Slc9c1
|
UTSW |
16 |
45,374,663 (GRCm39) |
missense |
probably benign |
0.25 |
R0316:Slc9c1
|
UTSW |
16 |
45,400,595 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0437:Slc9c1
|
UTSW |
16 |
45,420,250 (GRCm39) |
splice site |
probably benign |
|
R0611:Slc9c1
|
UTSW |
16 |
45,401,965 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0624:Slc9c1
|
UTSW |
16 |
45,393,719 (GRCm39) |
missense |
probably benign |
0.00 |
R0630:Slc9c1
|
UTSW |
16 |
45,363,483 (GRCm39) |
splice site |
probably benign |
|
R1106:Slc9c1
|
UTSW |
16 |
45,376,170 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1396:Slc9c1
|
UTSW |
16 |
45,393,710 (GRCm39) |
missense |
probably benign |
0.43 |
R1732:Slc9c1
|
UTSW |
16 |
45,373,291 (GRCm39) |
missense |
probably benign |
0.21 |
R1754:Slc9c1
|
UTSW |
16 |
45,409,872 (GRCm39) |
missense |
probably benign |
0.11 |
R1799:Slc9c1
|
UTSW |
16 |
45,374,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R1802:Slc9c1
|
UTSW |
16 |
45,378,644 (GRCm39) |
missense |
probably benign |
|
R1813:Slc9c1
|
UTSW |
16 |
45,393,710 (GRCm39) |
missense |
probably benign |
0.43 |
R1972:Slc9c1
|
UTSW |
16 |
45,413,835 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1985:Slc9c1
|
UTSW |
16 |
45,370,469 (GRCm39) |
missense |
probably benign |
0.01 |
R1995:Slc9c1
|
UTSW |
16 |
45,374,618 (GRCm39) |
missense |
probably damaging |
0.99 |
R2045:Slc9c1
|
UTSW |
16 |
45,400,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R2146:Slc9c1
|
UTSW |
16 |
45,413,827 (GRCm39) |
missense |
probably benign |
0.19 |
R2511:Slc9c1
|
UTSW |
16 |
45,365,099 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3716:Slc9c1
|
UTSW |
16 |
45,400,582 (GRCm39) |
missense |
probably benign |
|
R3765:Slc9c1
|
UTSW |
16 |
45,411,244 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3936:Slc9c1
|
UTSW |
16 |
45,427,193 (GRCm39) |
utr 3 prime |
probably benign |
|
R4051:Slc9c1
|
UTSW |
16 |
45,363,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R4302:Slc9c1
|
UTSW |
16 |
45,365,154 (GRCm39) |
missense |
probably benign |
0.35 |
R4433:Slc9c1
|
UTSW |
16 |
45,419,829 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4651:Slc9c1
|
UTSW |
16 |
45,367,756 (GRCm39) |
makesense |
probably null |
|
R4928:Slc9c1
|
UTSW |
16 |
45,395,772 (GRCm39) |
missense |
probably benign |
0.42 |
R4957:Slc9c1
|
UTSW |
16 |
45,365,194 (GRCm39) |
missense |
probably benign |
0.45 |
R4989:Slc9c1
|
UTSW |
16 |
45,413,800 (GRCm39) |
missense |
probably benign |
0.03 |
R5478:Slc9c1
|
UTSW |
16 |
45,374,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R5534:Slc9c1
|
UTSW |
16 |
45,376,977 (GRCm39) |
missense |
probably benign |
0.00 |
R5898:Slc9c1
|
UTSW |
16 |
45,365,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R5939:Slc9c1
|
UTSW |
16 |
45,368,031 (GRCm39) |
missense |
probably benign |
0.00 |
R6110:Slc9c1
|
UTSW |
16 |
45,395,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R6115:Slc9c1
|
UTSW |
16 |
45,376,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R6277:Slc9c1
|
UTSW |
16 |
45,427,204 (GRCm39) |
utr 3 prime |
probably benign |
|
R6286:Slc9c1
|
UTSW |
16 |
45,398,194 (GRCm39) |
missense |
probably benign |
0.14 |
R7268:Slc9c1
|
UTSW |
16 |
45,370,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R7272:Slc9c1
|
UTSW |
16 |
45,401,878 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7431:Slc9c1
|
UTSW |
16 |
45,413,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R7573:Slc9c1
|
UTSW |
16 |
45,398,256 (GRCm39) |
missense |
probably benign |
0.00 |
R7881:Slc9c1
|
UTSW |
16 |
45,403,332 (GRCm39) |
missense |
probably benign |
0.00 |
R8207:Slc9c1
|
UTSW |
16 |
45,360,076 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8289:Slc9c1
|
UTSW |
16 |
45,403,344 (GRCm39) |
missense |
probably benign |
0.09 |
R8302:Slc9c1
|
UTSW |
16 |
45,368,058 (GRCm39) |
missense |
probably benign |
|
R8328:Slc9c1
|
UTSW |
16 |
45,398,227 (GRCm39) |
missense |
probably damaging |
0.97 |
R8421:Slc9c1
|
UTSW |
16 |
45,413,734 (GRCm39) |
missense |
probably damaging |
0.97 |
R8691:Slc9c1
|
UTSW |
16 |
45,427,182 (GRCm39) |
missense |
probably benign |
0.00 |
R8712:Slc9c1
|
UTSW |
16 |
45,380,646 (GRCm39) |
missense |
probably benign |
0.00 |
R9128:Slc9c1
|
UTSW |
16 |
45,400,490 (GRCm39) |
missense |
probably benign |
0.25 |
R9191:Slc9c1
|
UTSW |
16 |
45,420,144 (GRCm39) |
missense |
possibly damaging |
0.57 |
R9230:Slc9c1
|
UTSW |
16 |
45,398,275 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9248:Slc9c1
|
UTSW |
16 |
45,370,551 (GRCm39) |
missense |
probably benign |
0.01 |
R9417:Slc9c1
|
UTSW |
16 |
45,413,848 (GRCm39) |
missense |
probably benign |
0.45 |
R9519:Slc9c1
|
UTSW |
16 |
45,395,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R9570:Slc9c1
|
UTSW |
16 |
45,380,705 (GRCm39) |
missense |
probably benign |
0.13 |
R9686:Slc9c1
|
UTSW |
16 |
45,400,577 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9695:Slc9c1
|
UTSW |
16 |
45,368,026 (GRCm39) |
missense |
probably benign |
0.00 |
R9742:Slc9c1
|
UTSW |
16 |
45,400,616 (GRCm39) |
missense |
probably damaging |
1.00 |
V8831:Slc9c1
|
UTSW |
16 |
45,398,262 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1176:Slc9c1
|
UTSW |
16 |
45,378,601 (GRCm39) |
missense |
possibly damaging |
0.48 |
Z1177:Slc9c1
|
UTSW |
16 |
45,393,782 (GRCm39) |
frame shift |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- TGGTCATTCCAGCAGTCAGCAAG -3'
(R):5'- TGCCTCCTAGATACCATGAGGAGC -3'
Sequencing Primer
(F):5'- GCAAGCTGAAGACCTAGTATACCAG -3'
(R):5'- gcaagaaaactcgcaccc -3'
|
Posted On |
2014-05-23 |