Busch Lab

ZMP

si:dkeyp-93d12.1

Ensembl ID:
ENSDARG00000014039
ZFIN ID:
ZDB-GENE-041014-303
Description:
Tudor domain-containing protein 6 [Source:RefSeq peptide;Acc:NP_001182210]
Human Orthologue:
AC010872.2
Human Description:
Uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:B5MCY1]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa43513 Nonsense Mutation detected in F1 DNA Not yet available
sa7472 Missense Mutation detected in F1 DNA Not yet available
sa7473 Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa43513
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000034184 Nonsense 1081 1882 1 2
ENSDART00000129472 Nonsense 1075 1876 2 2
ENSDART00000134066 Nonsense 1082 1883 3 5
Genomic Location (Zv9):
Chromosome 20 (position 42586285)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 42657444
GRCz11 20 42554554
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGAATCTTCCAGAGGGGGAACATTTGCCGGAAGTCAACAAGTGGCTT[G/T]AGACTGAAATCCTCAACAAGTCTTTCAAGGCCAAGTTTGTGTCAAGCGAC
Long Flanking Sequence:
AGAAAGGTGTTGCAGCAGAAGTACAAGCTCCAGACAAGCATACAATTTCATCGGCTCACCCTTGGTCATTCGTTTACTCCTCTTTCAACATAAGTTGTGGAAGTGAAGAACTGGTGCATGTTACTTATGTCTGTAGCCCTTGGGAAATCTATTTCCAGCTCGATAGAAATACAGAGATCCTTAATAGACTGACAGAGAGAGTTGCAGAGGAAAGTCAGCTCTTCACTTCAATTTCTGACAACTGCAGCAGTAAAGTTTGCTTGGCCAAATATTTCTGTGACGGCAGTTGGTACAGGGCTCTGGTACACCCTGTTCAATCTAATCAGCATGTGAGTGTTGTCTTTGTTGATTATGGCAATAAGGAGATTGCAGAGAAAACAAATGTCATGGCAATTCCGACAACAGCAGTTGACGTATTGCTAACACCAATGCAGGCTCTGAGATGCAGTCTTTTGAATCTTCCAGAGGGGGAACATTTGCCGGAAGTCAACAAGTGGCTT[G/T]AGACTGAAATCCTCAACAAGTCTTTCAAGGCCAAGTTTGTGTCAAGCGACACCAATGGACATTTTGTTTGTGATCTTTATGATGGCAATTTGCATATCAATGAAAAAGTCAAAGAGCTCATGGCTGCTCATGGTGTGGCACAAAGTGACCTAGCTGTCAACAAACTTGAGTTAGATTTCCCCAAAGAAGAAGCGCATGCCAGCTTACCGAACTGTAAACGTAACCACAAAGCAACCAGACGCAGTAAAGCCAAACAAAATGGAAAGCAAACTCCAAGATCCACAAACCATTCCAAGAAGCAACTCAAGGAACCTGTTGAAATGGAAGACCAGAATGCTCCCTGTCCACTTAAAGTAGTGCCATCTCATCAGAGCTTGCCAAAACTTTGTGATCTTCCTGCTGTCACAATGAAACCAGGTTCTAGAGGTGTGGGCTTTGTCTCTCATAGCATTTCTGCTGGAAGATTTTTTATCCAGATGGAAGATGATGAACCGAAATTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7472
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 > C
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000034184 Missense 1321 1882 1 2
ENSDART00000129472 Missense 1315 1876 2 2
ENSDART00000134066 Missense 1322 1883 3 5
Genomic Location (Zv9):
Chromosome 20 (position 42587006)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 42658165
GRCz11 20 42555275
KASP Assay ID:
554-4333.1 (used for ordering genotyping assays)
KASP Sequence:
CATTGATTATGGCAATAYTGCWACTGTCGACAGGAAGAATGTTCACATGC[T/C]AACCAATACGTTTTTGTCTCAGCCCAGATTGAGCATGSCCTGCACACTTG
Long Flanking Sequence:
TAACCACAAAGCAACCAGACGCAGTAAAGCCAAACAAAATGGAAAGCAAACTCCAAGATCCACAAACCATTCCAAGAAGCAACTCAAGGAACCTGTTGAAATGGAAGACCAGAATGCTCCCTGTCCACTTAAAGTAGTGCCATCTCATCAGAGCTTGCCAAAACTTTGTGATCTTCCTGCTGTCACAATGAAACCAGGTTCTAGAGGTGTGGGCTTTGTCTCTCATAGCATTTCTGCTGGAAGATTTTTTATCCAGATGGAAGATGATGAACCGAAATTACTACAGATGATTGAGGAACTAAATGGTACTAACTTCAAGGATAAAAGAAGAAATGTGGAAACCGAAATAAAAGTAGGGGACCTTGTTGCAGCAGAGTATGAAGAAGACTTGGCTTTGTACAGAGCTGTCGTCACCAACGTGTTAAACTCTGACCTACTAGCTGTTGAGTTCATTGATTATGGCAATACTGCAACTGTCGACAGGAAGAATGTTCACATGC[T/C]AACCAATACGTTTTTGTCTCAGCCCAGATTGAGCATGCCCTGCACACTTGCAAAACCGCACCCATTTGAAAATGATGACTCCTTTACGGAGAAAGCAGTTGGTAAACCCTTATTAGTTGAATTCATTCAAAGTCTGGAAGGTTCATGGAAAGTGAACATCGAGTTTGACGACGACCACTTGCAAGGGGACTTGAAGTATGATGCTGATCATAGTAAAGATGTAGATTTGGCAAGTCAAGATAAATTACCAAAAGATTCCCAGACGCAAAGCCAATCTGATCAATACAACCAAAGTATTAAAGAAGTTCAAAGCTTCCAGCAAAAGGAGCAGTTCAGACATCAACTTGCAAACAATCAGACTGTTAGAACCTTCCAGCAAAAGACAACATCAAATACACAAAGCATTTGTGAATTCAGAACCAAACCAACGGAAGTTAGAACCATCCAGCAAAAGACCAAGTCAAACACACAACAACGTAAATGTGAATTGACGTTCGCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7473
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 > C
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000034184 Missense 1624 1882 1 2
ENSDART00000129472 Missense 1618 1876 2 2
ENSDART00000134066 Missense 1625 1883 3 5
Genomic Location (Zv9):
Chromosome 20 (position 42587914)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 42659073
GRCz11 20 42556183
KASP Assay ID:
554-4090.1 (used for ordering genotyping assays)
KASP Sequence:
TGAACTTCGAATATGAAGGATTTGCAGCAGCGGTCACAACCCCATCYGAA[T/C]TTTATATCATTCTAGAGGATCTGCTTTTGATAGCAGAKACAGTCTCATYC
Long Flanking Sequence:
GTGAATTCAGAACCAAACCAACGGAAGTTAGAACCATCCAGCAAAAGACCAAGTCAAACACACAACAACGTAAATGTGAATTGACGTTCGCAACTAAGCAAATAAAGAAAGCAGCCATATATGTACAAACAAGTGTCAAAACAAGGGACATTTGGAGAAGAAAGTACAAGAAACAAAATTTCAAGCCAAAAGTTGTGGTTAACGCAGAACCACAATGTGAGACCAGTATTCCAGTGGCTAAAATTTCAGAAGGACTACAAGAAAATGTCCAACAAGAAAATAAAAACTCTGAGTCACTTGCTTGCGTTGCTCTGCATGATGTGAAAGACAGTGAGCCAGTAAAAATTTATGAGGATTTGTCTGTCGTGACTGATCATCCTCCCTCCCCAAAGACTTCTTTAAGGACCAATTTGGATCCACCACAGACCCTCTTCCAGGCCCCTGTGAAAATGAACTTCGAATATGAAGGATTTGCAGCAGCGGTCACAACCCCATCTGAA[T/C]TTTATATCATTCTAGAGGATCTGCTTTTGATAGCAGATACAGTCTCATCCATTCTTGAGAACCTTCCTGAAGTGTTGGAACCATTACCTGAAGTTCATTTTGTTCCTGGTACGAGCTGTTTGGTGAAATTGGTGGAGAATCAAAAATGGTGCAGGGCAGAGATTGTGCAATGCGATTCAACTTCAGTGCTTATAAACTTGGTTGACTGTGGACTGTATTCTGTTCTGTCTCGGCTAGATGCCTCCCAGCTAAGAAAACTTCCTGAGGAGCTCGGTAGATTGCCTAAAGTCACCTACCATTGTTTACTAAGGGGAGTTAAACCCAATGCTCCAGACTGGTCTGATGATGCCATCCTGTTTTTTCAAAACTCCATGTGTCACAAGAACCTTAAGATACGCTTCAGACAACATGTTTCTGAGACACAATGGGAGGTTGACATTATCACCGGGAGTCAAAATCTTGCAAAGGAGTTAGTAGATTCTGATCATGCAATGTATATT
Associated Phenotype:
Not determined