ZMP

LOC570283

Ensembl ID:

ENSDARG00000079873

Human Orthologue:

SLC29A4

Human Description:

solute carrier family 29 (nucleoside transporters), member 4 [Source:HGNC Symbol;Acc:23097]

Mouse Orthologue:

Slc29a4

Mouse Description:

solute carrier family 29 (nucleoside transporters), member 4 Gene [Source:MGI Symbol;Acc:MGI:2385330

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa1968	Nonsense	F2 line generated	Not yet available
sa19419	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa1968

Status:

F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110932	Nonsense	79	521	2	10

Genomic Location (Zv9):

Chromosome 1 (position 7680045)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	7919850
GRCz11	1	8603961

KASP Assay ID:

554-2504.1 (used for ordering genotyping assays)

KASP Sequence:

GGTGTGGGCTTTCTACTGCCATACAACAGCTTTATCACTGATGTGGATTA[T/A]CTCCATCGTAAATTCAAAGGNNNNNTGCAACCAACCTGTGTCATGAAGTCATCAC

Long Flanking Sequence:

CACACTCTCGATTTCTGGTTTGGTTTTGATATGATAAAACTTGCATGTACTGTAGCTTTCATATAAACTGTTGATGTAAAATATTGCATAGAATAGTGCAAACCTATTTTTGTCCGCCAAAGTCATAAAATATTAACAATAATTCAACAAAACATACAGTATGTTCACAGTTCTGTGTTGTCACACATGACATAGGTGAAGAGAAGTATTATTTATTTAGTAGTATTAAATGTTTTAAATATTACATTTTAAGTGCTTTATTTAGATAGTAGTTATTACTTAAATGTATTTATGATTTAATAAATGATTAAATGAATGATTAATTAAATTAATTAAAATTAGCCATTTTTTAGGAGGTATTCATTTATGTTTTATGCTTTAATTTCAGACTCTGACGAATCCATTCCAGATGATCGATACCATAGCATCTACTTTGCCATGCTGCTGGCTGGTGTGGGCTTTCTACTGCCATACAACAGCTTTATCACTGATGTGGATTA[T/A]CTCCATCGTAAATTCAAAGGTGCAACCAACCTGTGTCATGAAGTCATCACACAAAAAATTAAACGTACCTAGTGCTGTATAACAAACTATTGCATGTACAGTAAACAAAAAAAGTTGTGCTTATCAATTCCTCTTTTCTGTTCCTCTGTCAGGCACCTCTATTGTGTTCGACATGAGTTTGACGTACATACTGGTGGCTCTCAGCGCTGTCATCGTGAACAACGCGCTGGTGGAGAGACTGAGTTTACATACTCGCATCTGTGTGGGTGAGAACATGCAAAAGCTGTCAATGTAAGATCTAAGACAAGCTCAGGAGCTCCTCATGAGTTTTCAGTCATTGTTAAAAAAAATGCAACGCCATTAAAAAATTTGTTGCATTTACAGGATACCTGTTTGCGTTGGGACCTTTGGTGTGTGTGAGTGTATTTGACGTCTGGTTGGAGCTGTTCAACACTCAGCAGTCCTATGCTGTTACTCTGGCTGCGGTTGCCATTGTTGCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa19419

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110932	Nonsense	467	521	9	10

Genomic Location (Zv9):

Chromosome 1 (position 7684481)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	7924286
GRCz11	1	8608397

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTGGCTCTGTACCAATGATACAGGCAGCTGGCAAAGTGCCACTTCAGCAG[C/T]GAGAGGTGGCAGGTGAGTATGGCACACACATGAAGTGGGATGTGTAGACA

Long Flanking Sequence:

ATATTTCATCACTCTGTGTCTGTTCCCTGGTTTGGAGTCAGAGTTGCACAACGATACACTGGGAGAATGGCTGCCTATCCTCACCATGGCTCTGTTCAACATGGCTGACTTTGTGGGCAAGGTAAAATGAATCTTTTTTTGTAGTCATATATGTTAGGAATGATTGATGATGGGGCAGCACGGTCGCTCACCTCACAGCAAGAAGTAGTATAGTATCTATTGTAATCAATGTAAAATGGTAACAGTTCAAATCTCTTTGCTTTACTCTTTAGATCTTGGCGGCGTGCCCATACGAGTGGGGTGGTGTGCAGCTGCTGGTGTGTTCGTGTTTGCGCGTTCTCTTCTTGCCCCTGTTTGTGATGTGTGTGTCGCCTGTGCAGCGCCCCCTGCTGGCACACCCTGCCTGGCCCTGCGGCCTGTCTGTGATGCTAGGTATCAGTAACGGATATCTTGGCTCTGTACCAATGATACAGGCAGCTGGCAAAGTGCCACTTCAGCAG[C/T]GAGAGGTGGCAGGTGAGTATGGCACACACATGAAGTGGGATGTGTAGACATTTCTGATAAGGAGCTAAAGTACAGATCTGCATTAGTTTTAAATGCATTATTAAATTTGCATTAGTTTAGTTAACATTGAAATTTGTCAGAGATTATCTCTAGAATGGGTTTAATTTAGATGCACTCTTTTGTTTGATGATTGTGTTATAAAGTCAATTTAGTGAACGTTTTCTTCGCTTTGTTTCACCTGTTTTGAGTTCAGCAAACTGCTGTTTAATCATTGTAAATAAAGTGATCATCCTGACTCAAATGTAAACACATTGACTTGGCAAAAGAAAAGCTGCAGGTTAGATTTAAGGAAATCTTGAAGCATCTATGACTTGATCTTTATTACATGATTATTATGTTCTTTCTTTTTTTTTACTATTTTAACCTTAAATGATGCAATGTGGAACTTTTTAGTAAAAAAAATAACCACGTTGGAAGATGCTTCCCTTGCAGAAATATTC

Associated Phenotype:

Not determined