Busch Lab

ZMP

zgc:66474

Ensembl ID:
ENSDARG00000026453
ZFIN ID:
ZDB-GENE-030131-5711
Description:
hypothetical protein LOC327500 [Source:RefSeq peptide;Acc:NP_956109]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa40022 Nonsense Mutation detected in F1 DNA Not yet available
sa40021 Nonsense Mutation detected in F1 DNA Not yet available
sa26018 Nonsense Mutation detected in F1 DNA Not yet available
sa26017 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa40022
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
ENSDART00000026658 None None 1026 None 8
ENSDART00000115022 Nonsense 418 464 4 4
ENSDART00000126913 None None 1026 None 14

The following transcripts of ENSDARG00000026453 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 3 (position 15260429)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 15506035
GRCz11 3 15655835
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCACCTTAGAATAAAACACCAGCATGCTTACGTGGAAGCAAAAGGTTAC[C/T]GACCGGTCAATATGCGGATCGACACTTTGGACACCGTTCCAATTAAATTA
Long Flanking Sequence:
ATGTAACAAGAACTAATCTTAAAATATAATTAGCTGGAAAACTGTCAAGAAATGTTTACTATGGAGTCATCTCTAGGGTGCCAGACTAGTATTTGTAGTGAGCTAAAGCAAATGTTGGATAATTAAATGTATTAGTTACTATTTATTTAATCCAGATAAGCTCGGTTTTAGGCTTGCTATTACCCATAGCCGTAATAACTAACTGAATGCATACCATTTGTTTTAGAATTCTTTGTAGTTTCTTAATGTAAATGGTGACATTTAAAGCTTATGCGTTTCTTTCTTTTCTCATTGTTTCACAGGTGTCATTTCTACCAAACCGCTGTTTTAGCAAAGTTTGGGACTACTTCATAAAAGATGCGTTTGGAGAAGTCTTCTGTCGTGAATGTTCAGCCAGAGTTAGCCAGGGGTCCAGCAAGGCTGCTAACAAGAACACTTCTAATTTGTGGTCTCACCTTAGAATAAAACACCAGCATGCTTACGTGGAAGCAAAAGGTTAC[C/T]GACCGGTCAATATGCGGATCGACACTTTGGACACCGTTCCAATTAAATTAGAGAAGTTAGAACCTGAAGAATGCATCATACAAAGCGGAAGTCAGATAAATGAGGTCTTGATAACAGAAATACCGTCTAATGAGAACTTGTAAAGAAATGTAGATATGCCAAAGAGAAGTTTGATTTTTCAAAGGTGTATATATGCAGTGTGATTTATAAAGTGGTGGTTTAATAAAATCTCTTTTGAAAAACATTATTATCAGTCTATTGATTCATTACTTTAGGCGTTCTGCCATTTGCTATAGTAATATACAGTGCTGAGAAGTAACAGCTTTATATAATCGCTGTCTTCAAAAATTTTAAATGCTGATTATGTTGATTTGCTTAAGTTTAGTAATATAAATATAAGAATACATTATATACATACACGCACAGTTGGAAACTATTAGCTCTCCTTTAAAAATGTTTATTCTTTTTCAATTTTGTAATAATAATAATAAAACTAATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40021
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
ENSDART00000026658 Nonsense 523 1026 6 8
ENSDART00000115022 None None 464 None 4
ENSDART00000126913 Nonsense 523 1026 6 14

The following transcripts of ENSDARG00000026453 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 3 (position 15253658)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 15499264
GRCz11 3 15649064
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGGTGAAACGGGAAACGATGGAATCACAAAAGGTCTTAACCAAGGCA[C/T]AGGCAATCACTGAAGAGACAAAAGGTGAAACAGAAGCATCAAAGGTCAAC
Long Flanking Sequence:
TTTTCAAATCATGTTTCTTTTTAAGGTCGAACATTTTGTGTTTCTTTTAGCCTCCCAAAGAAGAAGCAATAGAGCGTAAAAGAACAGCAATGCAGAATTCGAAAAGGCCACAGAAAACTTTTTCCTGCCCTGTTTGCAATAAAGTATTTACTCGTGAAGGATGGTTGGAGCCGCACATTCGAAGTCAGCACGGGGCAGTAAACATCAAGAAGCGTAAATATAACAAAGTGCTTGTCAAGGGAAAGAAGCGAAGGTCAATGCGGATTTCAAAGGTTAGTTTTGAGATTTCTTTTTAAATATGTTGATGTTGCAATGTACTTGCCGAGACGATGCCTGTTTTATTTCTGTATAATAACCCACATTCCTTTTTTGTATTGATCGGTAAGCAATCGCGTCAGGTAGCAATTGAAGAATCAAAAAAGGTCACGAGTGAGACACAGCGAGACACCGAGGAGGTGAAACGGGAAACGATGGAATCACAAAAGGTCTTAACCAAGGCA[C/T]AGGCAATCACTGAAGAGACAAAAGGTGAAACAGAAGCATCAAAGGTCAACGCTAAACCATGTCAGTCAAGAAAAAACTCCAGCCCAGTTGTGGTAATGTCCAAACTCAATGCAGATCTTATTAAAAAAGTTACAGATGACGCAAACGGTCCTCATAAAGACACACCAGGATCTGACGGAGGAACGTCAGATATTCAAAATCAGACAAGCTTTACATGCCTATATTGTGGCGAGTCATTTTTTCAGAAACGGAAGTTCAAGCATCACAGAATGAAACACATCGCAGCTAACTTGCAGGTTTTAAGAAAAAGGAAAAGGGAAGCAAGAAGATTGGAAGAAGAGCAAGAAGAAAAGAGATTGAAGGAGGAGAAAGACAAAGTGAGGCTTAACAAGACGTCGACAAGCAATCACAAAACTAATACTACGGTATGTGTCTACCCTAGCCTGAAGAATGATCTGCACAAGTTCTTCACATTTCATAGTTTTATATAATTTTAAGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26018
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
ENSDART00000026658 Nonsense 629 1026 6 8
ENSDART00000115022 None None 464 None 4
ENSDART00000126913 Nonsense 629 1026 6 14

The following transcripts of ENSDARG00000026453 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 3 (position 15253340)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 15498946
GRCz11 3 15648746
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATGAAACACATCGCAGCTAACTTGCAGGTTTTAAGAAAAAGGAAAAGG[G/T]AAGCAAGAAGATTGGAAGAAGAGCAAGAAGAAAAGAGATTGAAGGAGGAG
Long Flanking Sequence:
TTGCCGAGACGATGCCTGTTTTATTTCTGTATAATAACCCACATTCCTTTTTTGTATTGATCGGTAAGCAATCGCGTCAGGTAGCAATTGAAGAATCAAAAAAGGTCACGAGTGAGACACAGCGAGACACCGAGGAGGTGAAACGGGAAACGATGGAATCACAAAAGGTCTTAACCAAGGCACAGGCAATCACTGAAGAGACAAAAGGTGAAACAGAAGCATCAAAGGTCAACGCTAAACCATGTCAGTCAAGAAAAAACTCCAGCCCAGTTGTGGTAATGTCCAAACTCAATGCAGATCTTATTAAAAAAGTTACAGATGACGCAAACGGTCCTCATAAAGACACACCAGGATCTGACGGAGGAACGTCAGATATTCAAAATCAGACAAGCTTTACATGCCTATATTGTGGCGAGTCATTTTTTCAGAAACGGAAGTTCAAGCATCACAGAATGAAACACATCGCAGCTAACTTGCAGGTTTTAAGAAAAAGGAAAAGG[G/T]AAGCAAGAAGATTGGAAGAAGAGCAAGAAGAAAAGAGATTGAAGGAGGAGAAAGACAAAGTGAGGCTTAACAAGACGTCGACAAGCAATCACAAAACTAATACTACGGTATGTGTCTACCCTAGCCTGAAGAATGATCTGCACAAGTTCTTCACATTTCATAGTTTTATATAATTTTAAGGATAAAGGATTCAAAGAATAAAGAACTGCCTGAGGATGTGGCCATCATAAAGGAATAACCGATTCTAGGACAAACAAGTCCGAGACCAATAGAAAACTAAAAAATAACTAGTGGGAAACTTGTACATAGAAATATAGTAATAGTGAGCACATCAGAATAAGTGCCTTTTGTTTTGATTTTTTAGTGGATAGCAATTAATTTTATTTGTATACTGACTGCAAGGCTAATAATATCTTTCTAAACCTTCAATCATTGGCTTGAGAAGGTGCAATGCAAGCTATTGGGTTTAAATATTTATTTCATACATTATACATAGTTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26017
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000026658 Nonsense 916 1026 8 8
ENSDART00000115022 None None 464 None 4
ENSDART00000126913 Nonsense 916 1026 8 14

The following transcripts of ENSDARG00000026453 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 3 (position 15251887)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 15497493
GRCz11 3 15647293
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGTTAGTCCTGGGAACGTAGAGGTCTCTGTGCTGGCTAGTTCTCAAT[C/A]GAAAGTAAAGCTTGACAACTCTGGGGGCTCAGCGGCCATTCAAGAGTCTG
Long Flanking Sequence:
ACAGTCCGTCGGTGAAGAAAAGGGGAAGGGGGACCCTTCTACAAATCTGAGCAGCCATGAAGCTTATGGAGACACTGCACTGGAAGACAATCCTGGCAGCCTTCTACCTCAGTCACCTATTGAGCAGCCTGCCATCTGCAACAACAGTGATGAACAAAACAAATCTGAGCTTGCCAAGGATCTCATGGGCCACTTCACTTTGCAACCCAGGATTGTTCTGCGACCAATTACAACGGGTTCCAAATATTCCACCTTGAATCCTGGTGATGTAAAATCAGGGCACATTGATCATGAAGAAACCTCATGCTCAGTATTGGTAGATGATACACTAGAAATTGGTAGTACGGATGGAGATAGTGATGTAATGGAGGTGGAAGATACACCAGAGGGCGGCAATCTTTGCACGATACCAGTGGAAAGCACAAGTGATGGCAATCCTGAAATACGTTGCAGTGTTAGTCCTGGGAACGTAGAGGTCTCTGTGCTGGCTAGTTCTCAAT[C/A]GAAAGTAAAGCTTGACAACTCTGGGGGCTCAGCGGCCATTCAAGAGTCTGAGGCAAAAAACTCAGTTGGTCGACAAGAAGAGGACCGAAACCGTAATTTTCCTTGTGTAATTGCTGGTGAAAATGGCCAATCAGAATGTGGTAAAAAGAATTGTGATTGGACGTGTGATTGTGATAGCATTGAGTCAATGAAATTAACTGTAATGCCAGAGGCCAGTAATTTAGATTCTTTGTTCAAGGAAACTAGTTCCGGAGCCATGCAGGATGCTGACTCTGAATTAAGTTGTGTTGTCATCTCGGATGGTGAAGATACCGATGAAATGCCTAGCATTTAAAATGAACAGTTAGAGATGGCCAGCGAACTGCACAAAAATCCTTCCAGCGACTTTCCATCTAAATCGAGAATATCAATTCCACATGTGTTCACACCAAGTCTATCGGCAGTCCCTCAAAACAGTCTGATGTTGAGCTCTTATCTCGTCAAAAGAAGGGTCAGAGCAT
Associated Phenotype:
Not determined