si:dkey-24l11.1

Ensembl ID:

ENSDARG00000060879

ZFIN ID:

ZDB-GENE-050419-117

Description:

hypothetical protein LOC571287 [Source:RefSeq peptide;Acc:NP_001074966]

Human Orthologues:

SLC28A1, SLC28A2

Human Descriptions:

solute carrier family 28 (sodium-coupled nucleoside transporter), member 1 [Source:HGNC Symbol;Acc:1
solute carrier family 28 (sodium-coupled nucleoside transporter), member 2 [Source:HGNC Symbol;Acc:1

Mouse Orthologues:

Gm14085, Slc28a1, Slc28a2

Mouse Descriptions:

predicted gene 14085 Gene [Source:MGI Symbol;Acc:MGI:3702173]
solute carrier family 28 (sodium-coupled nucleoside transporter), member 1 Gene [Source:MGI Symbol;A
solute carrier family 28 (sodium-coupled nucleoside transporter), member 2 Gene [Source:MGI Symbol;A

Allele Name	Consequence	Status	Availability
sa23315	Nonsense	Available for shipment	Available now
sa17349	Nonsense	Available for shipment	Available now
sa36664	Essential Splice Site	Available for shipment	Available now
sa23316	Nonsense	Available for shipment	Available now
sa36665	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Allele Name:

sa23315

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000086215	Nonsense	5	654	2	18
ENSDART00000098356	Nonsense	5	589	2	17
ENSDART00000132728	None	None	632	None	17

Genomic Location (Zv9):

Chromosome 18 (position 26773697)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	26846952
GRCz11	18	26829330

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCATTTAAGCTGGTAAAGCCCTTTTGGTTACTTTTCTTGCAGAGGACAAA[G/T]AAGATTTGCAGTTGACGGACGTCTCGTATGGGAACGAACAAGGCGTGGAT

Long Flanking Sequence:

CCCTTCTTCACGTTACATTTTTCAGTTCCTGATAGTTTGTTTTCTTCCACACTTAGTATCTTGTAGCCGCTGGAAATAAGGAGGAGCTTCATTGTAATAAATGATAACAAGATGCTGTTTCATTGACATCACTGACCAGCAATCTGATAGCAGCATGCATGTGTCTTAAACAAAAACACATTAGTATGTAGTTAGTTAATGATAAGATTTCCAAGTGGGCAGAGTATATATCCCAGCTCAAGGTTCAGAACCCAGCACTTGTCACAGAGAACGCAGAATGAGTAAGCCATTTATTTACCTCTCTATTCTTTACACATTTTTTCAAACAAGTATTTTAAACCACTGCATAAAGGAGGTGTCGGTTTCGTATTTGTTGGTAGTAGTTAATGATTATTTTGGATGAGATTTGAAAACGGTCTTGTTTAGAAACTTTAATAGTTGGATCAAGGTTCATTTAAGCTGGTAAAGCCCTTTTGGTTACTTTTCTTGCAGAGGACAAA[G/T]AAGATTTGCAGTTGACGGACGTCTCGTATGGGAACGAACAAGGCGTGGATAATCCAGTCTTTGTGAAGGTATGTTTGAGAAGAAGTGAGGGAGTTTTAGAAGATTTAAAGGTATAGTTCACGCAGAAATGAAGATCTACTCGGCATATTTGTTTTAAACAAAAAAAGAAGATATTTTGAGAAATGTTGGAAACTAGTAGCTAATGAGAATCAGTATACACTGTTAAAATTACATTAATAGTTTCCATTTATTTATGGTGGAATTGCATTATGAGACCTTGATCTCTGCTCTGTCGACTTCTGATATTGAAAATTCAAGTGGCTTTTATTGACATTTTAGTAGTTTGAAATAATAATGTATAAGAAATAATATGTAGAGAAATAAGTCTGTAAATTAACAGAAAAAATACTGGCAGTTTTGGTACTGTATATACAACACTAACCCAGACAATGTATCACTTCAAACTATTAACAATGTTAATAAAAGTCACTTTAACTCTC

Associated Phenotype:

Not determined

Allele Name:

sa17349

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000086215	Nonsense	126	654	5	18
ENSDART00000098356	Nonsense	126	589	5	17
ENSDART00000132728	Nonsense	112	632	4	17

Genomic Location (Zv9):

Chromosome 18 (position 26775379)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	26848634
GRCz11	18	26831012

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CTCACTTGTCTGGGRGTTTTCATCCTCGTGTGCGAACTAGTGTTTCGGTA[C/A]AAGGKTGACAGCATCAAGAGGTGCYTCAAGCCTGTGCAGMGATGTTTTAG

Long Flanking Sequence:

AGCAATTTAATGATCTGATAATTTTACTTATCAAAATTACATTTCTAGCCATTGTTAAGAAAATGTAAAATTACCATCCGACTGACAAGTAACCCTGTTTCTTATGTTTTCCAACACCAACTTTTATTCGCATTTAGTCCTACTTTACAATTCACATATACAAAGTTATTCTCCATTGTTTGTTACAGCAAAGCATGTCTACCCATCACAGTCACAGAGACCTTCTTCAAGACTCACTCCAAAATAATCAAATATATTGTGTTGGCAATCCTTGCTGCAGGTTATATATCTTCATCCTCCCAGTTTAATATCTATAATTGCATTAATGCATTGGTGATCCTTCTCTCAAAGTGATCATGTATTTTGTGTTTATTTCCTATTGTAGGTTATCTGGCGTACTTCATTTATGCCTGTTATTTAAGCTTCCAGAGGGCTCTTGCATTGGTGGTCCTCACTTGTCTGGGAGTTTTCATCCTCGTGTGCGAACTAGTGTTTCGGTA[C/A]AAGGGTGACAGCATCAAGAGGTGCTTCAAGCCTGTGCAGAGATGTTTTAGATCCAATATGAAATGGATGAAATGGTGAGTAGGACTTTAATACACTATACCCTTAAATCTTTAATGTTTTTTGAAAGAAGTCTTTTTTGTTAGCATTATTTTAAGTAGTATTTAAATATTGTAAAACAATATTAAATAAATAAAACCTATTTTGTATGTTAAGGTATTTTAAAATGAAATAGATTTCTGTCACGGTACTCCAGTCTTTATCGTCACATGATCTTTCAGAAATCTAGTAGTAATTCTAATAAGCTAAATCCTTATCCTTATTAATATTGTTATTAATCTTTTTGCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCT

Associated Phenotype:

Not determined

Allele Name:

sa36664

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

G > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000086215	Essential Splice Site	151	654	5	18
ENSDART00000098356	Essential Splice Site	151	589	5	17
ENSDART00000132728	Essential Splice Site	137	632	4	17

Genomic Location (Zv9):

Chromosome 18 (position 26775454)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	26848709
GRCz11	18	26831087

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTCAAGCCTGTGCAGAGATGTTTTAGATCCAATATGAAATGGATGAAATG[G/T]TGAGTAGGACTTTAATACACTATACCCTTAAATCTTTAATGTTTTTTGAA

Long Flanking Sequence:

ATCCGACTGACAAGTAACCCTGTTTCTTATGTTTTCCAACACCAACTTTTATTCGCATTTAGTCCTACTTTACAATTCACATATACAAAGTTATTCTCCATTGTTTGTTACAGCAAAGCATGTCTACCCATCACAGTCACAGAGACCTTCTTCAAGACTCACTCCAAAATAATCAAATATATTGTGTTGGCAATCCTTGCTGCAGGTTATATATCTTCATCCTCCCAGTTTAATATCTATAATTGCATTAATGCATTGGTGATCCTTCTCTCAAAGTGATCATGTATTTTGTGTTTATTTCCTATTGTAGGTTATCTGGCGTACTTCATTTATGCCTGTTATTTAAGCTTCCAGAGGGCTCTTGCATTGGTGGTCCTCACTTGTCTGGGAGTTTTCATCCTCGTGTGCGAACTAGTGTTTCGGTACAAGGGTGACAGCATCAAGAGGTGCTTCAAGCCTGTGCAGAGATGTTTTAGATCCAATATGAAATGGATGAAATG[G/T]TGAGTAGGACTTTAATACACTATACCCTTAAATCTTTAATGTTTTTTGAAAGAAGTCTTTTTTGTTAGCATTATTTTAAGTAGTATTTAAATATTGTAAAACAATATTAAATAAATAAAACCTATTTTGTATGTTAAGGTATTTTAAAATGAAATAGATTTCTGTCACGGTACTCCAGTCTTTATCGTCACATGATCTTTCAGAAATCTAGTAGTAATTCTAATAAGCTAAATCCTTATCCTTATTAATATTGTTATTAATCTTTTTGCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCCATCCATCCATCCATCCATCCATCCATC

Associated Phenotype:

Not determined

Allele Name:

sa23316

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000086215	Nonsense	397	654	12	18
ENSDART00000098356	Nonsense	397	589	12	17
ENSDART00000132728	Nonsense	383	632	11	17

Genomic Location (Zv9):

Chromosome 18 (position 26788715)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	26861970
GRCz11	18	26844348

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTCCTACCCTGAAACGGAAAAGAGCAAGTTCACATCTAAAAGTCAAATT[A/T]AAGTGGACAGTGGGTGGGTTTACCTCTCACATATGAGTTAAGGTGTCTTT

Long Flanking Sequence:

ATCCTGTAATTTGCTAAACAATTTAGCACAGTAGTTTTGAACAGGACTGAGGTTGATTAACAGATTTATGCAAATAATTTGAAAAAAATCTTCATCTGATGCATTTTTACAGCAGTTTAATTCAGTGGATGTTATGATCCCTGACATAACAAAAGTGTAGTAAAATTGAACAGTGCACAAGGGTTAACAGAATGCTTATTGTTTTTAGCATGATTCCAGTGATGCTAGTTCAGTAGCCATTAATTGTTACCTTTAACTTTACCAAGGCAATAAAATCAACTATGTAAAAAAAAAAAAAAACATTTACCCATTTAACTTAAAAATGATCAGGTTTGGTTATTACTACAGTATGTTTTGGGATAATGAATGTCTTTTGTATACAGATTGATGCCTCGTCTTTGATTTCTGCTTCAGTGATGGCTGCTCCATGTGCTTTAGCCATCTCCAAACTGTCCTACCCTGAAACGGAAAAGAGCAAGTTCACATCTAAAAGTCAAATT[A/T]AAGTGGACAGTGGGTGGGTTTACCTCTCACATATGAGTTAAGGTGTCTTTCTCATGTGTGTCATGTAGAAATATCTTTATGTAATGCCATGTTGTTTGTTCTCAGAGGTGAGCAGAACGTGTTGGAAGCTGTTAGCGGCGGTGCGTCTGCTTCTATAGGGCTTGTGGCCAACATTGCTGCTAACCTGATTGCTTTTCTTGCCATCTTGGGCTTCATTAATGCAACTCTAAGATGGTTGGGGGGCATGGTGGGATACCCAGATGTCACCTTTGAGGTGTGTAGCATAATCTTTTTTCATTTGAAGAGAAAATTATTAGTCCTCCTGCATGTGAAATTTTAGTTCTGTTTCAAATATTTCCAAAGTGATGATGAACAGAGCAATGACATTTTCACAGTGAGTAGGTTAACATGGACAACAATACTCAGATTTTTGTACAAATCACTGTTTACATACCATGTAAACAGTGATTTTTTATTAATTTAATCCAATTAAAGTCATA

Associated Phenotype:

Not determined

Allele Name:

sa36665

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000086215	Essential Splice Site	522	654	14	18
ENSDART00000098356	None	None	589	None	17
ENSDART00000132728	Essential Splice Site	508	632	13	17

Genomic Location (Zv9):

Chromosome 18 (position 26791359)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	26864614
GRCz11	18	26846992

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGGCTTAATGGCATTTTAGATGACAACGGAGATCCAAATTGGATCTCAG[T/A]AAGTATTTGTGTGGGCTCATCAAAATATGCATAAATTTGCCATTAACATA

Long Flanking Sequence:

AGTATAAAAATCACAGGGAGTTGTAACAGATATTTTAATCCCAGTTTCCTTGCAAAAAAAGGCAATAAAGGTGCCCTTTAATATATTATATAGTAAGATATTTATTTTGAAGAAGGTTATATTTATTTAACAAAAATCATTAGTGGAAAAAACAGCACAATTGTAAAATGCTATTAGAAATGACAATAACTGTTTTTAAATTTTATTTTATTTTAACATGTAGTTCAGACTTGTGATTCACAGCTATATTTTTGGCTTTATATTTAAAAGTGTTCTAAAAGCATGTTCATCTTCAATCCCTTAGCTGATCTGCTCTTTTGTCTTCATGCCGGTGGCCTTCATGATGGGAATTCCATACGATGAGTCTTTCAAAGTGGCTGAACTCATCGGCACTAAACTCTTCCTCAATGAGTTTATAGCCTACGAGAAGCTGTCAGAGCTCAAAAACAACAGGCTTAATGGCATTTTAGATGACAACGGAGATCCAAATTGGATCTCAG[T/A]AAGTATTTGTGTGGGCTCATCAAAATATGCATAAATTTGCCATTAACATACATAATTAGTGGTTTGTGGGGTGCATTAAATGGATACTTCACCTCAAAAACAATACTTGCTCACCCACAAAGAGCTCCAAACTTTTATGAGATTATTTTTTCTTTTGAATACAAAAAGAGGATATTTTGAAGAATGTTGCAAACCTGAAACAACAACTACATCCGTAGTTGGAAAAAATAAATCTCTTTAAATGTGTTTTGTCCAAACTTTTTGCAGGTTCGGTCAGAAATCATCTGCACTTATGCCCTGTGTGGCTTTGCTAATTTCAGCTCTCTTGGAATTGTGATTGGAGGCCTGTGTGAGTATCTGTTCAAATTTTTATAGTCCTGACAATGCATCTTATGACATTTTTTTGGGCATTTTTTTCAGTAGATATTTATATAACATCACTGACTGATACTTTTTAAAAATGGTTTTGTTTCACAGCCTCTATTTGTCCACCAAAGAAG

Associated Phenotype:

Not determined

ZMP

Alleles

Mutation Details

Mutation Details

Mutation Details

Mutation Details

Mutation Details