Busch Lab

ZMP

zgc:123008

Ensembl ID:
ENSDARG00000058562
ZFIN ID:
ZDB-GENE-051113-232
Description:
hypothetical protein LOC641418 [Source:RefSeq peptide;Acc:NP_001032484]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa24080 Nonsense Available for shipment Available now
sa29722 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa24080
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
ENSDART00000081446 Nonsense 17 646 2 3
ENSDART00000129401 None None 646 None 2
ENSDART00000138343 Nonsense 17 242 2 3
Genomic Location (Zv9):
Chromosome 22 (position 10004359)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 9864527
GRCz11 22 9894209
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATGAGTGATTCAGGAGTCTGCACAATAAAACAGGAAGATGCTGAAGAA[C/T]AAATAGGTTGGTGATTATTCTTGATTCTGTCTTTTACCAAAACTAGCAGC
Long Flanking Sequence:
TTATCTTTGCTGATTTGCCAAATCAGTATGTAAAATATCTGTAAAACTGTCAAATATACATTCATTTGGTAAGTGTTCTTTTTTTTTTTTGCCATCCTTGCATTCACTATCACTCAGATGAAATAAGTAGCTTTTAAATTTATGGTTTTTATTAATTTTCTGTCTCTAAATTGACTTTATTAAAAGAGCAATATACTGTGCTTCTGTGTTGCTGTGTAACCACTGTATCAACAGTCTTGGTGCTGGAGCGCATGACATTGGGCACTTTTTCTGCAGAGAGCTGTCTTTTATTATCATTTAATTTGTAAATTATACAAGCAATTACTATAAAGTTGATAACAGTTTTATGTTTTATTTTGGCAGTTCTTTAACTGTGAAGCTTCACCAGTAAATGCTGAAACATTCCCATCAACCAAGAAGTGAAGCAAAGTTTGTGAGAGAACAGTGAGAACATGAGTGATTCAGGAGTCTGCACAATAAAACAGGAAGATGCTGAAGAA[C/T]AAATAGGTTGGTGATTATTCTTGATTCTGTCTTTTACCAAAACTAGCAGCAACTCATTAGCTAAAGTTTTTATTTACAACAAAGATTTCCCACAAAATCCAACAATTTAAATGAACATGTGGAAATGTTCATATTTGCAAATATTATTTCAGGAAATTATTTTATTTGTTGTACTGTATGTGCTAACATTTCCTTTTTGTAAAAATAATGAGTTTGAGTTGTTCAAAAATGGTGGGGTCAGTGGCGTGGCGGACGGGCCCTCAGGAAAGGGAAGTGATCCCTGCAGTGCTACGCCACTGGGTGGGGTCAAATGAAAAGATAACTAGAGTAGAATGATTATAAGGATGTTGTTTTGTGACATCTAATTTTTTTTGTCTTTAATATTTCTAACTTTTTGAAGCCTGTTTTTCTTTTGCTTTCATTTTAGACTTGTTAAATGAGAACAAGGAGATTGAAGATCTGATTAAAAGGGGAGAGAAACATCACATCAAAACAGAAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29722
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000081446 Nonsense 151 646 3 3
ENSDART00000129401 Nonsense 151 646 2 2
ENSDART00000138343 Nonsense 151 242 3 3
Genomic Location (Zv9):
Chromosome 22 (position 10003534)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 9863702
GRCz11 22 9893384
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCGGAGAGAAGCCCTTCATGTGTGATCTATGTGGGAGGAGTTTTCTTTA[T/A]GCAAATACATTAAAAAAACACCGAAATTTACACAGCGCTGTGAAGAATCA
Long Flanking Sequence:
AGAGTAGAATGATTATAAGGATGTTGTTTTGTGACATCTAATTTTTTTTGTCTTTAATATTTCTAACTTTTTGAAGCCTGTTTTTCTTTTGCTTTCATTTTAGACTTGTTAAATGAGAACAAGGAGATTGAAGATCTGATTAAAAGGGGAGAGAAACATCACATCAAAACAGAAGAAAACCTTTACAGTATCTCAACGATAAGAAAAGACAATCCATGTTTCACATGCCTTCAGTGTAAAAACACTTTCTCATGCGAGGAAAGTCTAAATCTTCACATGAAGATTCATAGAGAGGTGAAGCCACACACCTCTGATCAATGTGATGAGATTTTCACCGTAAAAGTTACAAATAACGTAAATGTCCACGCTGAGGAAACGGTGTACAATTGTGATCAGTGTGACAGGACTTTCACAGATAAGAGAAATTTAGCCGCACACATGAAATTTCACAGCGGAGAGAAGCCCTTCATGTGTGATCTATGTGGGAGGAGTTTTCTTTA[T/A]GCAAATACATTAAAAAAACACCGAAATTTACACAGCGCTGTGAAGAATCACGTCTGCTCCAAGTGTGGCAAGAGCTTTTTCACATTCAGTCAATTAAAAATCCACCACACAGCTCACGCTACAGAAAAACCTTTCAAATGTTCACACTGTGGCAAGGCGTTCAAATCATTACAGTGTCAACGAATACATGAGATGATCCACAGCGGAGAAAAGCCACACAAGTGCGATCAGTGCGAGAAGACTTTCAGACAGAGGAAAAGTTTAAACATCCACATCAGAATCCACACTGGAGAGAAGCCGTACACGTGCGATCATTGTGGGAGGAGTTTCAGCAGAAAGGAAACCCTTAACAGTCACTTGAAAACCCACTCTGGGAATATGCTGTACACTTGTGCTGAGTGTGGGGAAGGTTTCAACAATACAGGAGATTTTACAGCACACATGAAAACTCACTTTGGAGAGAACCCTTTCTTATGTGATCAATGTGGGAAGGGTTTTCC
Associated Phenotype:
Not determined