Mutagenetix > Incidental Mutation

Incidental Mutation 'R5386:Slc4a10'

425171

Institutional Source

Beutler Lab

Gene Symbol

Slc4a10

Ensembl Gene

ENSMUSG00000026904

Gene Name

solute carrier family 4, sodium bicarbonate cotransporter-like, member 10

Synonyms

NCBE

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5386 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

62046462-62326730 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 62290058 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Valine at position 843 (E843V)

Ref Sequence

ENSEMBL: ENSMUSP00000108099 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000054484] [ENSMUST00000102735] [ENSMUST00000112480]

AlphaFold

Q5DTL9

Predicted Effect

probably damaging
Transcript: ENSMUST00000054484
AA Change: E813V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000061411
Gene: ENSMUSG00000026904
AA Change: E813V

Domain	Start	End	E-Value	Type
low complexity region	57	79	N/A	INTRINSIC
low complexity region	106	111	N/A	INTRINSIC
Pfam:Band_3_cyto	146	405	9e-107	PFAM
Pfam:HCO3_cotransp	445	959	1e-246	PFAM
transmembrane domain	967	989	N/A	INTRINSIC
low complexity region	1011	1025	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000102735
AA Change: E813V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000099796
Gene: ENSMUSG00000026904
AA Change: E813V

Domain	Start	End	E-Value	Type
low complexity region	57	79	N/A	INTRINSIC
low complexity region	106	111	N/A	INTRINSIC
Pfam:Band_3_cyto	146	405	2e-106	PFAM
Pfam:HCO3_cotransp	445	959	2.4e-246	PFAM
transmembrane domain	967	989	N/A	INTRINSIC
low complexity region	1011	1025	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000112480
AA Change: E843V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000108099
Gene: ENSMUSG00000026904
AA Change: E843V

Domain	Start	End	E-Value	Type
low complexity region	57	79	N/A	INTRINSIC
low complexity region	106	111	N/A	INTRINSIC
Pfam:Band_3_cyto	146	435	9.6e-108	PFAM
Pfam:HCO3_cotransp	476	989	1.5e-245	PFAM
transmembrane domain	997	1019	N/A	INTRINSIC
low complexity region	1041	1055	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000155219

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.3%
20x: 95.4%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene belongs to a small family of sodium-coupled bicarbonate transporters (NCBTs) that regulate the intracellular pH of neurons, the secretion of bicarbonate ions across the choroid plexus, and the pH of the brain extracellular fluid. The protein encoded by this gene was initially identified as a sodium-driven chloride bicarbonate exchanger (NCBE) though there is now evidence that its sodium/bicarbonate cotransport activity is independent of any chloride ion countertransport under physiological conditions. This gene is now classified as a member A10 of the SLC4 family of transmembrane solute carriers. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, May 2010]
PHENOTYPE: Mice with homozygous disruption of this gene exhibit reduced brain ventricle volume, reduced neuronal excitability, impaired pH regulation of neurons, and increased threshold to induced seizures. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 134 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2410089E03Rik	G	A	15: 8,194,413 (GRCm38)	G887R	probably damaging	Het
4931406P16Rik	A	G	7: 34,242,388 (GRCm38)	F120L	probably damaging	Het
Abcc12	T	G	8: 86,517,489 (GRCm38)	K1012Q	possibly damaging	Het
Afmid	G	A	11: 117,828,142 (GRCm38)	G33R	probably benign	Het
Agbl3	G	T	6: 34,799,196 (GRCm38)	W207C	probably damaging	Het
Ajuba	T	C	14: 54,570,398 (GRCm38)	Y459C	probably damaging	Het
Ak2	T	C	4: 129,008,172 (GRCm38)	S213P	probably benign	Het
Alk	T	A	17: 71,875,012 (GRCm38)	N1339Y	probably damaging	Het
Angpt1	T	C	15: 42,438,365 (GRCm38)	S416G	probably damaging	Het
Ank2	C	T	3: 126,981,933 (GRCm38)	V854M	probably benign	Het
Ankrd61	G	T	5: 143,891,664 (GRCm38)	N122K	possibly damaging	Het
Armc9	T	A	1: 86,198,289 (GRCm38)	L34Q	probably null	Het
Aspg	T	A	12: 112,123,032 (GRCm38)	V418E	probably benign	Het
Baz1b	C	T	5: 135,238,059 (GRCm38)	R1241C	probably damaging	Het
Bclaf1	T	C	10: 20,325,592 (GRCm38)	V201A	possibly damaging	Het
C1ql3	A	T	2: 13,004,358 (GRCm38)	D225E	probably damaging	Het
Capn9	A	G	8: 124,605,540 (GRCm38)	T417A	possibly damaging	Het
Card14	C	T	11: 119,317,289 (GRCm38)	R62C	probably damaging	Het
Cc2d2a	A	G	5: 43,730,041 (GRCm38)	N1271S	probably benign	Het
Ccpg1	G	A	9: 73,013,044 (GRCm38)	S647N	probably benign	Het
Cdv3	T	C	9: 103,355,230 (GRCm38)	K133R	possibly damaging	Het
Cep128	A	C	12: 90,999,571 (GRCm38)	S1087R	probably benign	Het
Cep70	T	A	9: 99,281,075 (GRCm38)	L325Q	probably damaging	Het
Chit1	T	G	1: 134,149,454 (GRCm38)	F332V	probably damaging	Het
Chodl	C	A	16: 78,946,697 (GRCm38)	T219K	probably damaging	Het
Cntn4	T	C	6: 106,181,804 (GRCm38)	L10P	possibly damaging	Het
Copg1	G	T	6: 87,890,207 (GRCm38)	M87I	possibly damaging	Het
Cyp3a59	A	G	5: 146,085,768 (GRCm38)	Y28C	probably benign	Het
Dchs1	A	C	7: 105,758,029 (GRCm38)	V2119G	probably damaging	Het
Dedd	T	C	1: 171,338,383 (GRCm38)	L23P	probably damaging	Het
Dmxl2	A	G	9: 54,378,757 (GRCm38)	S2715P	probably benign	Het
Dnah9	T	C	11: 66,029,356 (GRCm38)	N2237S	probably damaging	Het
Drosha	A	G	15: 12,842,121 (GRCm38)	I337V	probably benign	Het
Duox2	A	G	2: 122,295,136 (GRCm38)	V330A	probably benign	Het
Dusp11	T	C	6: 85,947,605 (GRCm38)	*322W	probably null	Het
Dusp8	T	A	7: 142,089,993 (GRCm38)	Q61L	possibly damaging	Het
Ears2	G	C	7: 122,044,377 (GRCm38)	T426S	probably benign	Het
Elmo1	T	C	13: 20,600,210 (GRCm38)	Y646H	probably benign	Het
Eps15	T	A	4: 109,321,225 (GRCm38)	I220K	possibly damaging	Het
Faap100	T	A	11: 120,377,632 (GRCm38)	E105V	possibly damaging	Het
Fam171a2	C	A	11: 102,437,867 (GRCm38)	V689L	possibly damaging	Het
Fam213b	T	A	4: 154,899,005 (GRCm38)	M1L	probably benign	Het
Fam91a1	G	A	15: 58,448,394 (GRCm38)	S645N	probably benign	Het
Fancg	G	A	4: 43,007,076 (GRCm38)	Q234*	probably null	Het
Gid4	T	A	11: 60,432,442 (GRCm38)		probably null	Het
Gm14085	C	A	2: 122,522,778 (GRCm38)	L480I	probably benign	Het
Gm7361	A	C	5: 26,258,905 (GRCm38)	T53P	probably benign	Het
Golgb1	T	A	16: 36,912,315 (GRCm38)	C641*	probably null	Het
Gon4l	T	A	3: 88,858,496 (GRCm38)	M409K	probably benign	Het
Gpatch8	A	T	11: 102,508,227 (GRCm38)		probably null	Het
Gpr156	T	A	16: 37,948,309 (GRCm38)	V64E	possibly damaging	Het
Grid2	T	A	6: 63,931,105 (GRCm38)	I243K	probably damaging	Het
Gucy2g	G	A	19: 55,215,116 (GRCm38)	A750V	probably damaging	Het
Hdac5	T	C	11: 102,202,141 (GRCm38)	E590G	possibly damaging	Het
Herc3	T	A	6: 58,874,278 (GRCm38)	M504K	probably damaging	Het
Hif1a	A	G	12: 73,944,093 (GRCm38)	E713G	probably benign	Het
Hmx3	A	G	7: 131,544,304 (GRCm38)	D247G	probably damaging	Het
Hoxd11	G	T	2: 74,682,819 (GRCm38)	E143*	probably null	Het
Ifitm3	T	C	7: 141,010,641 (GRCm38)	N2S	probably benign	Het
Il17f	T	C	1: 20,777,957 (GRCm38)	Q99R	probably benign	Het
Itga6	T	A	2: 71,841,150 (GRCm38)	S341R	probably damaging	Het
Itgam	A	G	7: 128,107,980 (GRCm38)	N661S	probably benign	Het
Jag1	A	T	2: 137,095,544 (GRCm38)	H303Q	possibly damaging	Het
Kcnh8	T	A	17: 52,725,995 (GRCm38)	N103K	probably benign	Het
Kdm6b	T	C	11: 69,400,810 (GRCm38)		probably benign	Het
Keg1	A	C	19: 12,714,538 (GRCm38)	N63T	probably damaging	Het
Klf12	T	A	14: 99,900,159 (GRCm38)	H317L	probably damaging	Het
Lrp1	A	T	10: 127,592,114 (GRCm38)	V530E	probably damaging	Het
Mrgpra6	A	G	7: 47,188,881 (GRCm38)	C190R	probably damaging	Het
Myo1a	G	T	10: 127,705,897 (GRCm38)	E102*	probably null	Het
Napa	A	T	7: 16,116,472 (GRCm38)	E265D	probably benign	Het
Ncam1	A	C	9: 49,564,874 (GRCm38)	V305G	probably damaging	Het
Nek8	T	C	11: 78,170,437 (GRCm38)		probably null	Het
Olfr1115	C	T	2: 87,252,483 (GRCm38)	P182L	probably benign	Het
Olfr1242	G	T	2: 89,494,137 (GRCm38)	Y58*	probably null	Het
Olfr1275	T	C	2: 111,231,194 (GRCm38)	T200A	probably benign	Het
Olfr191	T	A	16: 59,085,890 (GRCm38)	M198L	probably benign	Het
Olfr243	T	C	7: 103,717,355 (GRCm38)	F254L	probably benign	Het
Olfr251	A	T	9: 38,377,985 (GRCm38)	I29F	probably benign	Het
Olfr739	T	A	14: 50,425,389 (GRCm38)	V290E	possibly damaging	Het
Olfr971	A	G	9: 39,839,830 (GRCm38)	Y132C	possibly damaging	Het
Olfr987	T	C	2: 85,331,635 (GRCm38)	T88A	probably benign	Het
Pabpc4	A	G	4: 123,294,997 (GRCm38)	Q417R	probably benign	Het
Panx3	A	T	9: 37,669,024 (GRCm38)	M11K	probably damaging	Het
Pcbp1	C	T	6: 86,525,489 (GRCm38)	E143K	probably damaging	Het
Pdcd7	G	A	9: 65,358,692 (GRCm38)	W477*	probably null	Het
Pi4k2a	G	A	19: 42,090,515 (GRCm38)	S5N	probably damaging	Het
Plag1	T	A	4: 3,904,075 (GRCm38)	Q372L	probably benign	Het
Plce1	C	A	19: 38,760,091 (GRCm38)	N1755K	probably damaging	Het
Pld4	G	T	12: 112,763,988 (GRCm38)	E102*	probably null	Het
Pnlip	A	G	19: 58,679,607 (GRCm38)	N345S	probably benign	Het
Ppm1e	A	T	11: 87,358,551 (GRCm38)	L118Q	possibly damaging	Het
Prkra	T	G	2: 76,639,278 (GRCm38)	T146P	probably damaging	Het
Prpf8	A	G	11: 75,495,799 (GRCm38)	D1038G	probably damaging	Het
Prss51	T	A	14: 64,097,094 (GRCm38)	V108E	probably damaging	Het
Ptch1	A	G	13: 63,545,043 (GRCm38)	Y181H	probably damaging	Het
Reln	A	G	5: 22,039,529 (GRCm38)	V817A	probably benign	Het
Rictor	C	A	15: 6,789,504 (GRCm38)	Q1403K	probably benign	Het
Rims1	T	A	1: 22,412,245 (GRCm38)	I882F	probably damaging	Het
Rnf19a	A	G	15: 36,242,039 (GRCm38)	V618A	probably benign	Het
Ryr1	A	T	7: 29,117,416 (GRCm38)	I65N	probably damaging	Het
S1pr2	T	C	9: 20,967,594 (GRCm38)	T313A	probably benign	Het
Serpine2	A	T	1: 79,821,287 (GRCm38)	Y83*	probably null	Het
Sfi1	A	ATCTTCCCAAAGCCAGTGC	11: 3,153,384 (GRCm38)		probably benign	Het
Sgip1	T	C	4: 102,915,059 (GRCm38)	V215A	probably benign	Het
Sgsm3	T	C	15: 81,007,999 (GRCm38)	V256A	probably benign	Het
Shroom4	T	A	X: 6,585,469 (GRCm38)	C894*	probably null	Het
Slc14a2	T	A	18: 78,185,840 (GRCm38)	D306V	possibly damaging	Het
Smyd4	T	A	11: 75,390,156 (GRCm38)	C152S	probably damaging	Het
Snx10	T	C	6: 51,575,972 (GRCm38)	Y32H	probably damaging	Het
Sorl1	T	C	9: 42,057,284 (GRCm38)	T558A	possibly damaging	Het
Spata31d1b	G	A	13: 59,719,052 (GRCm38)	C1338Y	possibly damaging	Het
Sppl2c	T	A	11: 104,187,301 (GRCm38)	I309K	possibly damaging	Het
Stard9	A	G	2: 120,700,630 (GRCm38)	E2456G	probably damaging	Het
Stx1b	A	T	7: 127,815,403 (GRCm38)	D16E	probably benign	Het
Tecpr2	T	C	12: 110,915,453 (GRCm38)	V152A	probably damaging	Het
Tedc1	T	C	12: 113,156,682 (GRCm38)	V47A	probably benign	Het
Tep1	A	T	14: 50,868,317 (GRCm38)	L82Q	probably damaging	Het
Tgm4	A	G	9: 123,056,494 (GRCm38)	Y367C	probably damaging	Het
Tle1	C	T	4: 72,141,844 (GRCm38)	V258M	probably damaging	Het
Tm9sf1	C	T	14: 55,642,844 (GRCm38)	G32D	possibly damaging	Het
Tmco2	A	G	4: 121,105,984 (GRCm38)	L106P	probably damaging	Het
Tmem131	A	T	1: 36,872,558 (GRCm38)	C103S	possibly damaging	Het
Tmprss7	T	A	16: 45,669,528 (GRCm38)	I444F	possibly damaging	Het
Trank1	T	C	9: 111,362,402 (GRCm38)	V493A	probably benign	Het
Trim80	A	T	11: 115,448,017 (GRCm38)	T558S	probably benign	Het
Trmt6	C	A	2: 132,808,783 (GRCm38)	A302S	probably benign	Het
Ttc17	A	T	2: 94,303,640 (GRCm38)	W1067R	probably damaging	Het
Tulp4	T	A	17: 6,236,293 (GRCm38)	V1532D	probably damaging	Het
Ubqlnl	T	G	7: 104,149,217 (GRCm38)	I358L	probably benign	Het
Ulk3	T	A	9: 57,590,740 (GRCm38)	I108N	possibly damaging	Het
Vps13b	A	T	15: 35,640,528 (GRCm38)		probably null	Het
Vwa3a	A	G	7: 120,790,142 (GRCm38)	K68E	possibly damaging	Het
Zfp746	G	T	6: 48,064,176 (GRCm38)	H538N	possibly damaging	Het

Other mutations in Slc4a10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00676:Slc4a10	APN	2	62,290,001 (GRCm38)	missense	probably damaging	1.00
IGL00990:Slc4a10	APN	2	62,286,940 (GRCm38)	missense	probably damaging	1.00
IGL01294:Slc4a10	APN	2	62,253,309 (GRCm38)	critical splice acceptor site	probably null
IGL01628:Slc4a10	APN	2	62,268,666 (GRCm38)	missense	probably damaging	1.00
IGL01773:Slc4a10	APN	2	62,190,757 (GRCm38)	missense	probably damaging	0.97
IGL02119:Slc4a10	APN	2	62,228,670 (GRCm38)	missense	probably damaging	1.00
IGL02125:Slc4a10	APN	2	62,268,171 (GRCm38)	missense	probably benign	0.02
IGL02406:Slc4a10	APN	2	62,190,769 (GRCm38)	missense	probably benign	0.37
IGL02890:Slc4a10	APN	2	62,286,916 (GRCm38)	missense	probably damaging	1.00
IGL02959:Slc4a10	APN	2	62,268,143 (GRCm38)	missense	probably damaging	1.00
IGL02979:Slc4a10	APN	2	62,288,747 (GRCm38)	missense	probably null	1.00
IGL03144:Slc4a10	APN	2	62,250,466 (GRCm38)	missense	probably benign	0.00
IGL03175:Slc4a10	APN	2	62,296,960 (GRCm38)	missense	probably damaging	0.99
IGL03383:Slc4a10	APN	2	62,267,436 (GRCm38)	missense	probably damaging	1.00
IGL03412:Slc4a10	APN	2	62,250,543 (GRCm38)	splice site	probably benign
R0085:Slc4a10	UTSW	2	62,244,346 (GRCm38)	splice site	probably benign
R0401:Slc4a10	UTSW	2	62,190,848 (GRCm38)	missense	probably benign	0.27
R0433:Slc4a10	UTSW	2	62,289,983 (GRCm38)	missense	probably benign	0.01
R0482:Slc4a10	UTSW	2	62,297,017 (GRCm38)	splice site	probably benign
R0506:Slc4a10	UTSW	2	62,250,533 (GRCm38)	missense	probably benign	0.13
R0511:Slc4a10	UTSW	2	62,286,862 (GRCm38)	missense	probably damaging	0.97
R0590:Slc4a10	UTSW	2	62,190,893 (GRCm38)	splice site	probably benign
R0883:Slc4a10	UTSW	2	62,243,398 (GRCm38)	missense	probably benign	0.11
R1167:Slc4a10	UTSW	2	62,228,574 (GRCm38)	missense	probably damaging	1.00
R1276:Slc4a10	UTSW	2	62,250,443 (GRCm38)	missense	probably damaging	0.99
R1395:Slc4a10	UTSW	2	62,313,286 (GRCm38)	missense	probably benign	0.00
R1455:Slc4a10	UTSW	2	62,286,930 (GRCm38)	missense	probably damaging	1.00
R1589:Slc4a10	UTSW	2	62,257,462 (GRCm38)	missense	probably damaging	1.00
R1677:Slc4a10	UTSW	2	62,324,727 (GRCm38)	missense	probably benign
R1848:Slc4a10	UTSW	2	62,316,606 (GRCm38)	missense	probably damaging	1.00
R1987:Slc4a10	UTSW	2	62,268,204 (GRCm38)	missense	probably damaging	1.00
R1988:Slc4a10	UTSW	2	62,268,204 (GRCm38)	missense	probably damaging	1.00
R2018:Slc4a10	UTSW	2	62,234,381 (GRCm38)	missense	probably damaging	1.00
R2019:Slc4a10	UTSW	2	62,234,381 (GRCm38)	missense	probably damaging	1.00
R2407:Slc4a10	UTSW	2	62,313,343 (GRCm38)	missense	probably benign
R4067:Slc4a10	UTSW	2	62,046,645 (GRCm38)	start codon destroyed	probably benign	0.00
R4184:Slc4a10	UTSW	2	62,317,442 (GRCm38)	intron	probably benign
R4255:Slc4a10	UTSW	2	62,281,936 (GRCm38)	missense	probably benign	0.10
R4282:Slc4a10	UTSW	2	62,244,343 (GRCm38)	splice site	probably null
R4296:Slc4a10	UTSW	2	62,234,428 (GRCm38)	missense	possibly damaging	0.80
R4361:Slc4a10	UTSW	2	62,243,385 (GRCm38)	missense	probably benign	0.00
R4596:Slc4a10	UTSW	2	62,296,858 (GRCm38)	missense	probably damaging	1.00
R4709:Slc4a10	UTSW	2	62,257,517 (GRCm38)	missense	probably null	1.00
R4755:Slc4a10	UTSW	2	62,296,988 (GRCm38)	missense	probably damaging	1.00
R4836:Slc4a10	UTSW	2	62,268,187 (GRCm38)	missense	probably damaging	1.00
R4841:Slc4a10	UTSW	2	62,257,595 (GRCm38)	missense	possibly damaging	0.68
R4998:Slc4a10	UTSW	2	62,244,439 (GRCm38)	missense	probably benign	0.00
R5069:Slc4a10	UTSW	2	62,267,571 (GRCm38)	missense	probably benign	0.06
R5223:Slc4a10	UTSW	2	62,253,366 (GRCm38)	missense	probably damaging	1.00
R5244:Slc4a10	UTSW	2	62,288,725 (GRCm38)	missense	probably damaging	1.00
R5808:Slc4a10	UTSW	2	62,250,472 (GRCm38)	missense	probably damaging	1.00
R5999:Slc4a10	UTSW	2	62,243,431 (GRCm38)	missense	probably benign	0.10
R6007:Slc4a10	UTSW	2	62,268,872 (GRCm38)	missense	probably benign	0.44
R6009:Slc4a10	UTSW	2	62,046,690 (GRCm38)	missense	probably benign	0.00
R6015:Slc4a10	UTSW	2	62,228,702 (GRCm38)	missense	probably benign	0.05
R6103:Slc4a10	UTSW	2	62,234,465 (GRCm38)	missense	probably damaging	1.00
R6141:Slc4a10	UTSW	2	62,211,445 (GRCm38)	missense	probably damaging	1.00
R6193:Slc4a10	UTSW	2	62,243,357 (GRCm38)	splice site	probably null
R6217:Slc4a10	UTSW	2	62,303,951 (GRCm38)	missense	probably benign	0.27
R6280:Slc4a10	UTSW	2	62,281,966 (GRCm38)	missense	probably benign	0.05
R6523:Slc4a10	UTSW	2	62,286,961 (GRCm38)	nonsense	probably null
R6643:Slc4a10	UTSW	2	62,228,710 (GRCm38)	missense	possibly damaging	0.96
R6660:Slc4a10	UTSW	2	62,250,403 (GRCm38)	missense	possibly damaging	0.55
R7008:Slc4a10	UTSW	2	62,286,922 (GRCm38)	missense	probably benign	0.00
R7083:Slc4a10	UTSW	2	62,234,495 (GRCm38)	missense	probably benign	0.03
R7223:Slc4a10	UTSW	2	62,268,665 (GRCm38)	missense	probably damaging	0.99
R7243:Slc4a10	UTSW	2	62,303,862 (GRCm38)	missense	probably damaging	1.00
R7449:Slc4a10	UTSW	2	62,303,946 (GRCm38)	missense	probably benign
R7621:Slc4a10	UTSW	2	62,250,479 (GRCm38)	missense	probably damaging	0.98
R7692:Slc4a10	UTSW	2	62,303,964 (GRCm38)	missense	possibly damaging	0.94
R7742:Slc4a10	UTSW	2	62,296,850 (GRCm38)	missense	probably damaging	1.00
R7905:Slc4a10	UTSW	2	62,268,151 (GRCm38)	missense	probably damaging	1.00
R8179:Slc4a10	UTSW	2	62,243,448 (GRCm38)	missense	possibly damaging	0.64
R8528:Slc4a10	UTSW	2	62,296,796 (GRCm38)	missense	possibly damaging	0.79
R8531:Slc4a10	UTSW	2	62,267,507 (GRCm38)	missense	probably damaging	1.00
R8772:Slc4a10	UTSW	2	62,303,940 (GRCm38)	missense	probably damaging	1.00
R9307:Slc4a10	UTSW	2	62,253,318 (GRCm38)	missense	probably damaging	1.00
R9531:Slc4a10	UTSW	2	62,268,810 (GRCm38)	missense	probably damaging	1.00
R9732:Slc4a10	UTSW	2	62,304,742 (GRCm38)	missense	probably damaging	0.97
U24488:Slc4a10	UTSW	2	62,046,658 (GRCm38)	missense	probably benign	0.05
X0019:Slc4a10	UTSW	2	62,228,599 (GRCm38)	missense	probably damaging	1.00
Z1088:Slc4a10	UTSW	2	62,228,571 (GRCm38)	missense	probably damaging	1.00
Z1176:Slc4a10	UTSW	2	62,244,416 (GRCm38)	missense	probably benign
Z1176:Slc4a10	UTSW	2	62,211,379 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GAATGCTCAGCCAATCACTTC -3'
(R):5'- GTTCATAGCACCATAAGACAAAGTG -3'

Sequencing Primer
(F):5'- GCTCAGCCAATCACTTCATAATTAAG -3'
(R):5'- GACAGAATCTATGGCCATC -3'

Posted On

2016-08-04