ZMP

LOC556849

Ensembl ID:

ENSDARG00000053481

Human Orthologue:

ENTPD5

Human Description:

ectonucleoside triphosphate diphosphohydrolase 5 [Source:HGNC Symbol;Acc:3367]

Mouse Orthologue:

Entpd5

Mouse Description:

ectonucleoside triphosphate diphosphohydrolase 5 Gene [Source:MGI Symbol;Acc:MGI:1321385]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23171	Nonsense	Available for shipment	Available now
sa42994	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa23171

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000075514	Nonsense	105	450	2	13

Genomic Location (Zv9):

Chromosome 17 (position 45205489)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	44925362
GRCz11	17	45039127

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTCTGTCTGTGTCCCACAGTTGAGCTTCCAGTGCTTGACAATGAGATGTA[C/A]CATGCAGTGAAGCCCGGACTGTCAGCATATGCAGATATGCCTGAAAAGGT

Long Flanking Sequence:

TTTCTTACCGCATCCCTCTCAGGAGCCTGTGGCTCATAGCAAGTCTGCTCACTGTGTTTGTGTTTGCCCTGGTTTATTCGCTGAATAGTGAGAAAACAAACGGAAACACAGGGGTGGGAAGGAAAAAGAGAGATGGAGAAATAGTTCTAGTTGCTCTTAAAAAATTCATCCTCAAGCAATGTTAAAAATTATGGGTTGGAACTGATAACTCAGTAATAGGTTTGCCAAAATATCCATTAAATGGAGACATGGCATCATTCTTGATGAGGTAAACTCTTAATTGCCTGTCTGGAAAAATCCTGGTGGTCGCCATTTGTGATAAACATACAATAACCAAATGTCTCTGCACGTGCACAGTAACTTTTAAAGAGATTGGAATAGAGTTGCCCGCAATCCACTGCTAAAGTGCACCTTCTAATAACATCGTTTATGGTTCCTTCTGACATTTCTGTCTGTCTGTGTCCCACAGTTGAGCTTCCAGTGCTTGACAATGAGATGTA[C/A]CATGCAGTGAAGCCCGGACTGTCAGCATATGCAGATATGCCTGAAAAGGTAAGCCACTAAATTTTTTATAGGAACATCAAGGAATGAGATTTCTACATTCTAATAGCTTTTGCTTTTCCCAGTTTACTTGTACAGCCAGAAAACCGACTATTTATATTTTTGGTTTCCATTAAGATTATCAAAAAAACTCCAGGTTTGAACATTTCGCCAGTATGAGATTTGATTTCAAGACCGCTCAAAGATTTTTTTGCTTTAATTTGTGGCCACGCAGCAAATAAAATATATGTACATGCACTTCAAAGTTTGCAGATATTCTAGAATAAATCAATTTGGTTCAAGAGAGTATTCTACCAGTGGTTTAGTTTCCCTTTTTGAACCAAGAAGCTAAGGACATTGAAAAAGTAAATATTTATCCCCTTAGTCCTGCTAGACAGGAAAAGATGCTAATCCAGGTTTGTATAGATCACACTAATGTTCTTTTATTCACTTTGATGAATATG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42994

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000075514	Nonsense	331	450	10	13

Genomic Location (Zv9):

Chromosome 17 (position 45201171)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	44921044
GRCz11	17	45034809

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTTATTTCTAGGTTATGCAGGGTATAAACTGTGCTACCAAGAGGTGCTG[C/T]AGGTGGTGAAAGGGATTGTGCATCAGCCATTTGAGGTCAAAGGAAGCAGC

Long Flanking Sequence:

GCTTCCTGTGAGGAAACCTCTCCCTGAAGAGTTTGTGGCAAACCCTCAAACTGACCTCATTATGTTGTAAGGAGGCACTTTCCTTGAAATGCACACTCCTCATTCAAGATACCTCAAATATTTTGCTTTCCTGTAGGAGACTAGTAGTTTCCTTAATATACATATAAATAGAACAGAGGGTCTTAGCATCACAACTGTGGACTTGCTACAGAAGGCTTAAAATCTGTTTTTACACAGATTCCAGGTGTTTACAAGGTATTGTGCACTGTAAATATGGGAAGGACCCTGGATAATAGAAAATTGCTTTGGCTGGCAGTTCCTGTCTAAATCTACAACTCCAGGGAGAATAACCACACTTTATTCTCAGTCAAAGAGTTTACCACATGGGACAGGATAAAGTTTACAGTATTGGAGAGTGGGGTACAATTTCTAAAGACATTTTTTATTTTATTTTATTTCTAGGTTATGCAGGGTATAAACTGTGCTACCAAGAGGTGCTG[C/T]AGGTGGTGAAAGGGATTGTGCATCAGCCATTTGAGGTCAAAGGAAGCAGCATCTTCTACGCCTTCTCCTATTACTACGACAGAGCTGTGGAGTCGGGTCTCATCGGTGAGTGGAATTGCATTAGGTCAATGCTACAGTTAGTGATGAATCATCTTCATGATTTATGACAATTGTCTCGATGTTTCAGATGGATCCCGTGGCGGTACTGTGGAAGTCAGGGACTTCAAAAAGAAAGCCAAAGAAGGTAAGATTTGGGATACTCTCCCATTCTCCAAAGAACACTCGGGTCAAAGTCCTGCCGCACACATTGCACAAACATAAACCCTTGGTGCTTATTTGCATTTGAGGTTCTCGACAATCACACTGGCTTCACAAAATGATAGCTCTGCCACCACATAAACATAGGCTGCACCTCTCCCACACAAATACTTCTGCTTGCGTGTGTTCACCTTCTTTTGTAACTGTCTAACCTGCTATCTCAGCTTTTCCATGCCCTTTGA

Associated Phenotype:

Not determined