ZMP
nt5dc2
Ensembl ID:
ZFIN ID:
Description:
5'-nucleotidase domain-containing protein 2 [Source:RefSeq peptide;Acc:NP_001070611]
Human Orthologue:
NT5DC2
Human Description:
5'-nucleotidase domain containing 2 [Source:HGNC Symbol;Acc:25717]
Mouse Orthologue:
Nt5dc2
Mouse Description:
5'-nucleotidase domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1917271]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25393 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15749 | Essential Splice Site | Available for shipment | Available now |
sa41196 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25393
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083108 | Essential Splice Site | 324 | 603 | 8 | 14 |
The following transcripts of ENSDARG00000059646 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 24500251)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 23626069 |
GRCz11 | 8 | 23647308 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCAACTTTCTGCCTTTTGTGACCCTGTTTCCTTCCTTATTTGTTCTCC[A/T]GAGAAATACATTCTGCGAGGAGACGAGACGTACGCTGTGCTGCACCGGCT
Long Flanking Sequence:
GGACTTGCAATGAGTTTCTTCAGCCAGTGTTATTGAAACCTGTAGCTAATAGAAACCAGACGTGAAGATGACCCTCACAGACCCATTTTGCGCAGTGCGTTTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATAAAAGCAGAGCAGTCTTTTGTTTTCAGAGCAGCAGACTGTTGCATAATGGCATCTCTCTGGAGGATGAGATTTTAAGCAAGCCCTTCTGGCCCAATCTAATCTGTAGTTTTAATTTGTTGTATCCCTGCAAACAAGAAGGGAACATGTAAATCCTTATCACAGATGTTTCATTGCAGTATAAACACTTTTTATGTAAACAGGAGAACCCGATTTGATCAGATTCTGCCTGACCATCATCAGTCTGCAAAAATGACTGATTTGTAGAATGTAGACTGGCTTTTAAAAGACCCCCAGATTTCTGTTTTTCAACTTTCTGCCTTTTGTGACCCTGTTTCCTTCCTTATTTGTTCTCC[A/T]GAGAAATACATTCTGCGAGGAGACGAGACGTACGCTGTGCTGCACCGGCTGGCCAGTCAGGGGAAGAAGCTTTTCCTTATTACCAACAGCCCCTTCAGCTTTGTGTGAGTTTTTGTGCTTCATCACATTCAAATGCATTCATAATGTGAAGTAGATTTAAAGGCCTCCTTAAAGTGAAGCTCCCCCCCAATATTCATTAATTCAGAGTATTTGTGTCTGTGTTTTTTCCAGTGATAAAGGCATGAAGTACATGGTCGGAAAAGAGTGGAGGGACTTCTTTGATGTTGTCATTGTTCAAGCAGACAAACCACATTTCTTTAATGACTGCATAAAGTAAGTTTGCCTTAATGTAAATGGAAGATTTTGAAGGATTAAAAAAAAAAAAAGTAGTCTTCAGCATTTATTTAGTCGATCATGCATAAAACAGGTGAAATGCCGTTTATACGCATGCGCCCGTCAGGATTAGCAGGCGAGCCCAGACATGGCATTGAAAATACGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15749
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083108 | Essential Splice Site | 448 | 603 | 11 | 14 |
The following transcripts of ENSDARG00000059646 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 24503125)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 23628943 |
GRCz11 | 8 | 23650182 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGATCCAAGGTTTTTTATTTTGGAGATCATCTCTACAGTGATTTGGCC[G/A]TGAGTCATCTTCATGCTTCTGTCTGCACATTTGTTGSGCATATGCCYGGC
Long Flanking Sequence:
TATCTGAGTGATTTATCCACATTATTCTGCTGTTTCAATTTGGAAAAAGTGGAAAAGAAGGTGACGAGGTCAACCTGAGTCTCAACGGAAAAATCAATGTAACACAGTTCAGTGTTGTCAGGCTTGTACGAACACACTTGGCTGACCAGCACTGAAACTACGTGCACACACTCAAGCTAAAACAGCAAATGAAAACCATCCTAAATTGGGAAAGACTTATGGGAAAGTTCCCTGGCAGAAACCTTAGAGCAAACCCTTCCAACTATACGACACGAGTGTTGACACGTAGCTTCCAGAAAACCCAAGTGAAAAAACCTGCAGGGTGTTGTCATTTTAGCTTAGTTGAGACTTTTACATCAATCACAAAATTAGCAGTTGGCTAACAAAACTGCCTTTGCTTTGCTTCATTTCAGGGAAACCTTGTGGATTTTCTCAAGCTGACAGGATGGCGAGGATCCAAGGTTTTTTATTTTGGAGATCATCTCTACAGTGATTTGGCC[G/A]TGAGTCATCTTCATGCTTCTGTCTGCACATTTGTTGCGCATATGCCTGGCTTTTGTTTTACTGCTTTAAGCTTTAGTGTTTTCAGCAAAAGCTGCAGTGAATATCACTGTGTAGCTTCTATAGTCAAACCCCCTAGTTTTTCATGATTTTCTTTGTGATTGTTTTGACAATGACACAAATCATAAAAATAAAGATTCTTTATTTTGGTCTCTTGTCAAGACAATATCTAAAATGGTAGGGATTAAGCCAAAGGAAGTTTGTATGACTTTTATTTTTATCCACAATCTTACTTTCTCACTCCCTGGAGCATCTGACATCATGTCACAGATAGGACATGGGCTTCCTCTACCTTAATATACCTAAAACACGGATTGCCGTAAAACTCGTTAATGGCAGGGAAACGTTTTCTCTTTTTAATTGCAGGGAAAGAGTTAAATGAAAACATTTATCAATTTGACGCACACCATAATACTGTCTATACATGTAAAGAATAAATAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41196
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083108 | Essential Splice Site | 495 | 603 | 12 | 14 |
The following transcripts of ENSDARG00000059646 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 24504368)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 23630186 |
GRCz11 | 8 | 23651425 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGTCTCACGTGGCTGCAGGCGCTTACTGGGCTGCTAGAGCGCATGCAG[G/A]TGAGCATTAAGACTTCTTCAAAATGCTTCCTGTTGAGCGTTGCTAAATGT
Long Flanking Sequence:
TAATGTAATGATTGTGAGGGCGCAGGTGAGACGTCATTTTTTTTCCCGTGACACTTAAAAACCTCACATGCGCTGTGCATACAACGTTTGTAAGTCATGTAAAACAAATGCAAACTGAAATAAATATAATTTGATTATATGGTTTGGAATTTGATGTTTTATGATGAGATTATTTACATTTTTTTGATTATTTTGTGTTTAATTAAGAATTTTGTGTGATCGTAAAAATTAGCGACTTTTTTAGATTTTGCGTTGGATTCAGCAATTGCAGAATTGCGAAAAAACTAGGGGGTCTGAATAGTCATAAAATGTAATTATGAATTGATTATTGTCTAAACATCCCATTCTGTCATTTTTAGGACCTGATGTTGCGTCATGGCTGGAGAACAGGAGCGATTGTTCCCGAACTGGAGGTGGAGACGAAGGTGGTGAACACAGAGCAGTACGCGCAGAGTCTCACGTGGCTGCAGGCGCTTACTGGGCTGCTAGAGCGCATGCAG[G/A]TGAGCATTAAGACTTCTTCAAAATGCTTCCTGTTGAGCGTTGCTAAATGTTGGCATGAGTCAGGAATTACAGGGGTATTGATGTGAAATTTGCAGTAAAAACTTAAAACATGAATGCAAATAGAAAAAATATATAATAACATTATATTGAAATTATCTGTTACAAACCACAGAGTTATGGGATCAGAAAAATATCAACCTGTAAACATTTTTTATACTTTTTAAGTGAGTGAAAATAAACATGCATTTTGGATGTGACCAAAAGAGTTTGATAGTAATGTAGAGGCTGTTTATAAGAAGACCAGTCAGCGTCTCTGTCTCTTCCCCAAGTGGAGAAGTTTTGATATTAGTACTGTTACAACCGGCTCAAAGTTGCAACATTAGAGAGACAATACGGACCAGGTAAATTGAAAAGAGAAATGATTTATTAACAAAACATATAATTAACAAAAGTATTTAAAGCAATCCAAGTCAGTATAGGTGAAAGTCAGTAGTGAAAAG
Associated Phenotype:
Not determined