Incidental Mutation 'R4651:Slc9c1'
| ID |
351330 |
| 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 |
041911-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.398)
|
| Stock # |
R4651 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
16 |
| Chromosomal Location |
45355672-45427364 bp(+) (GRCm39) |
| Type of Mutation |
makesense |
| DNA Base Change (assembly) |
A to T
at 45367756 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Stop codon to Leucine
at position 163
(*163L)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000159945]
|
| AlphaFold |
Q6UJY2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000159945
|
| SMART Domains |
Protein: ENSMUSP00000124969
Gene: ENSMUSG00000033210
| 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 null
Transcript: ENSMUST00000162774
AA Change: *163L
|
| Meta Mutation Damage Score |
0.9755 |
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.3%
|
| Validation Efficiency |
97% (98/101) |
| 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: 91 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
| 2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
| 4933409G03Rik |
G |
A |
2: 68,436,559 (GRCm39) |
E168K |
unknown |
Het |
| Ahnak2 |
T |
G |
12: 112,741,271 (GRCm39) |
S128R |
possibly damaging |
Het |
| Ankrd26 |
T |
C |
6: 118,492,787 (GRCm39) |
D1319G |
probably benign |
Het |
| Ankrd35 |
T |
C |
3: 96,591,343 (GRCm39) |
V543A |
probably benign |
Het |
| Ano10 |
A |
T |
9: 122,090,181 (GRCm39) |
Y377* |
probably null |
Het |
| Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
| Atp10b |
G |
A |
11: 43,085,472 (GRCm39) |
G284S |
probably damaging |
Het |
| Atp5f1c |
A |
G |
2: 10,068,287 (GRCm39) |
F180S |
probably damaging |
Het |
| Btnl4 |
A |
G |
17: 34,691,602 (GRCm39) |
S296P |
probably benign |
Het |
| Cast |
A |
G |
13: 74,894,133 (GRCm39) |
S171P |
probably benign |
Het |
| Catsperb |
G |
A |
12: 101,507,771 (GRCm39) |
A513T |
probably benign |
Het |
| Ccnf |
C |
A |
17: 24,450,760 (GRCm39) |
R406L |
probably damaging |
Het |
| Ceacam12 |
A |
G |
7: 17,801,359 (GRCm39) |
T113A |
probably damaging |
Het |
| Cipc |
T |
C |
12: 87,008,864 (GRCm39) |
V241A |
probably benign |
Het |
| Col12a1 |
A |
T |
9: 79,520,228 (GRCm39) |
D2815E |
probably damaging |
Het |
| Cpox |
G |
T |
16: 58,491,050 (GRCm39) |
R87L |
possibly damaging |
Het |
| Cttnbp2 |
A |
G |
6: 18,434,037 (GRCm39) |
I607T |
possibly damaging |
Het |
| Cux1 |
A |
T |
5: 136,596,083 (GRCm39) |
N4K |
probably damaging |
Het |
| Cyp3a25 |
T |
C |
5: 145,931,701 (GRCm39) |
T136A |
probably benign |
Het |
| Dhx58 |
T |
A |
11: 100,592,185 (GRCm39) |
N288Y |
probably damaging |
Het |
| Dnah10 |
T |
C |
5: 124,806,207 (GRCm39) |
Y127H |
probably benign |
Het |
| Dnd1 |
G |
A |
18: 36,898,114 (GRCm39) |
|
probably benign |
Het |
| Ehmt2 |
C |
A |
17: 35,132,790 (GRCm39) |
N1171K |
probably damaging |
Het |
| Fanci |
T |
A |
7: 79,085,004 (GRCm39) |
M838K |
possibly damaging |
Het |
| Flot1 |
T |
C |
17: 36,143,436 (GRCm39) |
|
probably benign |
Het |
| Gad2 |
A |
T |
2: 22,558,374 (GRCm39) |
D364V |
probably damaging |
Het |
| Gm10375 |
C |
A |
14: 43,844,326 (GRCm39) |
|
probably null |
Het |
| Gm9996 |
T |
A |
10: 29,019,754 (GRCm39) |
|
probably benign |
Het |
| Gnat3 |
T |
A |
5: 18,220,568 (GRCm39) |
L247H |
probably damaging |
Het |
| Ip6k3 |
C |
T |
17: 27,364,265 (GRCm39) |
C261Y |
probably damaging |
Het |
| Irgc |
C |
A |
7: 24,132,238 (GRCm39) |
R193L |
probably damaging |
Het |
| Kalrn |
G |
T |
16: 33,996,761 (GRCm39) |
P1477Q |
probably damaging |
Het |
| Kyat1 |
G |
T |
2: 30,084,076 (GRCm39) |
H15N |
probably benign |
Het |
| Lamc1 |
T |
G |
1: 153,104,523 (GRCm39) |
S59R |
probably damaging |
Het |
| Llgl1 |
A |
G |
11: 60,599,477 (GRCm39) |
D486G |
possibly damaging |
Het |
| Lrrc9 |
T |
C |
12: 72,524,160 (GRCm39) |
W790R |
probably damaging |
Het |
| Lsm2 |
T |
A |
17: 35,204,571 (GRCm39) |
|
probably benign |
Het |
| Med8 |
A |
T |
4: 118,268,089 (GRCm39) |
E5V |
probably damaging |
Het |
| Mefv |
A |
G |
16: 3,535,682 (GRCm39) |
L82P |
probably damaging |
Het |
| Mettl25b |
T |
C |
3: 87,834,979 (GRCm39) |
H107R |
probably benign |
Het |
| Mettl3 |
T |
A |
14: 52,532,549 (GRCm39) |
I545F |
probably damaging |
Het |
| Naa20 |
CTCTAGA |
C |
2: 145,753,752 (GRCm39) |
|
probably benign |
Het |
| Ncapg2 |
T |
A |
12: 116,389,407 (GRCm39) |
N342K |
probably damaging |
Het |
| Ndufaf6 |
T |
A |
4: 11,062,070 (GRCm39) |
Y187F |
probably damaging |
Het |
| Nomo1 |
T |
A |
7: 45,717,866 (GRCm39) |
I799N |
probably damaging |
Het |
| Obscn |
G |
A |
11: 58,929,703 (GRCm39) |
R5824C |
probably damaging |
Het |
| Or4f6 |
G |
T |
2: 111,838,595 (GRCm39) |
S312Y |
probably damaging |
Het |
| Or6c214 |
T |
C |
10: 129,591,287 (GRCm39) |
I11V |
probably benign |
Het |
| Or6n2 |
A |
G |
1: 173,897,394 (GRCm39) |
I177V |
possibly damaging |
Het |
| Or7g30 |
T |
A |
9: 19,352,591 (GRCm39) |
C127* |
probably null |
Het |
| Pgm3 |
T |
A |
9: 86,440,523 (GRCm39) |
R389S |
probably benign |
Het |
| Pkd2l2 |
A |
T |
18: 34,542,889 (GRCm39) |
R20* |
probably null |
Het |
| Pkhd1 |
T |
A |
1: 20,451,747 (GRCm39) |
I2183F |
probably damaging |
Het |
| Ppp4r3a |
T |
A |
12: 101,049,170 (GRCm39) |
|
probably benign |
Het |
| Prpf38b |
G |
A |
3: 108,811,408 (GRCm39) |
|
probably benign |
Het |
| Prpf4b |
A |
T |
13: 35,083,954 (GRCm39) |
M908L |
probably benign |
Het |
| Prps2 |
T |
C |
X: 166,135,288 (GRCm39) |
D183G |
probably damaging |
Het |
| Prrc2c |
A |
T |
1: 162,550,843 (GRCm39) |
H40Q |
probably damaging |
Het |
| Ptprk |
T |
C |
10: 28,139,686 (GRCm39) |
I137T |
probably damaging |
Het |
| Sdr42e1 |
T |
C |
8: 118,390,360 (GRCm39) |
T94A |
probably benign |
Het |
| Setd2 |
A |
G |
9: 110,423,200 (GRCm39) |
D2085G |
possibly damaging |
Het |
| Sgce |
T |
C |
6: 4,689,560 (GRCm39) |
|
probably benign |
Het |
| Shisa3 |
A |
G |
5: 67,765,992 (GRCm39) |
D81G |
probably damaging |
Het |
| Sipa1l1 |
T |
A |
12: 82,469,245 (GRCm39) |
L1248* |
probably null |
Het |
| Skint7 |
T |
G |
4: 111,839,309 (GRCm39) |
M201R |
probably damaging |
Het |
| Slc5a3 |
T |
A |
16: 91,874,090 (GRCm39) |
V49E |
probably benign |
Het |
| Smyd3 |
A |
G |
1: 178,871,306 (GRCm39) |
Y358H |
probably benign |
Het |
| Srp68 |
A |
T |
11: 116,164,840 (GRCm39) |
S31R |
probably benign |
Het |
| Stag1 |
T |
A |
9: 100,678,769 (GRCm39) |
M230K |
probably damaging |
Het |
| Strc |
A |
T |
2: 121,204,829 (GRCm39) |
D985E |
possibly damaging |
Het |
| Syne2 |
A |
G |
12: 76,036,013 (GRCm39) |
T3767A |
probably damaging |
Het |
| Sytl2 |
C |
A |
7: 90,024,633 (GRCm39) |
P207Q |
probably damaging |
Het |
| Tbc1d2b |
A |
G |
9: 90,089,940 (GRCm39) |
F863S |
probably damaging |
Het |
| Tek |
T |
C |
4: 94,669,121 (GRCm39) |
S41P |
probably damaging |
Het |
| Top1 |
T |
C |
2: 160,554,637 (GRCm39) |
Y463H |
probably damaging |
Het |
| Trim24 |
T |
G |
6: 37,934,774 (GRCm39) |
|
probably null |
Het |
| Trim38 |
A |
T |
13: 23,966,952 (GRCm39) |
D133V |
probably damaging |
Het |
| Ttn |
A |
G |
2: 76,576,979 (GRCm39) |
V24638A |
possibly damaging |
Het |
| Ttn |
A |
G |
2: 76,701,213 (GRCm39) |
|
probably benign |
Het |
| Tyro3 |
G |
C |
2: 119,647,349 (GRCm39) |
G826A |
probably benign |
Het |
| Ube2b |
A |
G |
11: 51,886,199 (GRCm39) |
|
probably null |
Het |
| Ubxn4 |
T |
A |
1: 128,202,587 (GRCm39) |
W410R |
probably benign |
Het |
| Unc45a |
T |
C |
7: 79,982,777 (GRCm39) |
K383E |
possibly damaging |
Het |
| Usp7 |
A |
C |
16: 8,516,278 (GRCm39) |
|
probably benign |
Het |
| Vmn1r193 |
C |
T |
13: 22,403,695 (GRCm39) |
G99D |
probably damaging |
Het |
| Vrk2 |
T |
C |
11: 26,439,803 (GRCm39) |
D256G |
probably damaging |
Het |
| Wdr81 |
A |
G |
11: 75,342,066 (GRCm39) |
V1067A |
probably damaging |
Het |
| Wiz |
C |
T |
17: 32,576,655 (GRCm39) |
R624Q |
probably damaging |
Het |
| Zcwpw2 |
A |
G |
9: 117,843,119 (GRCm39) |
|
noncoding transcript |
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 |
|
R1727:Slc9c1
|
UTSW |
16 |
45,422,324 (GRCm39) |
missense |
probably benign |
0.27 |
|
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 |
|
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'- GGTTTTGCTGATAAATGAACACCC -3'
(R):5'- CTTCTAGAAAGACCTAAACATGTCGAG -3'
Sequencing Primer
(F):5'- CCAAAATGTGGTGGCTTAAAGC -3'
(R):5'- TGTCGAGGAAGATAAAGCTGCGTC -3'
|
| Posted On |
2015-10-08 |
Incidental Mutation