Busch Lab

ZMP

zgc:152953

Ensembl ID:
ENSDARG00000068636
ZFIN ID:
ZDB-GENE-061103-607
Description:
hypothetical protein LOC571919 [Source:RefSeq peptide;Acc:NP_001073526]
Human Orthologue:
KIAA0649
Human Description:
KIAA0649 [Source:HGNC Symbol;Acc:29089]
Mouse Orthologue:
Gm347
Mouse Description:
predicted gene 347 Gene [Source:MGI Symbol;Acc:MGI:2685193]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa35144 Nonsense Available for shipment Available now
sa16533 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa35144
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
ENSDART00000099351 Nonsense 69 1004 2 3
Genomic Location (Zv9):
Chromosome 11 (position 38626991)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 7547815
GRCz11 21 7109306
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATTGAGAGCCTTCACAGTACCCAGTCTTCGGGCATGAGTGAAAACGAG[C/T]AGGCTGAAAAGGCTGCTCATTCCAGTCACGAGGCTGGCTACAAGGGTCAG
Long Flanking Sequence:
TTTCTTGTGCGCTCTCAAATAAATGCGGCTGAAGGGCGATTTAGTGTGCATGGATATAAGGGGTATGTCTCCAACATGTATTAAATCAGCACTACTAAGATTACAGAAAAGTTTGCTCAAAAACATTTTGATGCATTTATAACCCGCTGCAAAAGAAAAAACATCACAACTGAAGGAATGTTTTTACAATTACATGTTTTAAATGAAGATTTCTGCTTCTTTCTTTCAGGATGTAAACAAGATCACTGGTGGAGCTTCCCCATGCACCTGCATCCCTTCCATTCTGACTATCTAGAATGTTCCTGAAGACAGTTCCTCCGGCTGTGGCTATTCATTCAGAATGGAGGTCCAGTAAGAGCTGCAGCCTGCCTCTCTATTTCAATGACAGTGCCTCCGACAGCGACCTTGCCTCAGTTAGTGGCACCCCGTTCCCACAGAAGATCCAGATGATAATTGAGAGCCTTCACAGTACCCAGTCTTCGGGCATGAGTGAAAACGAG[C/T]AGGCTGAAAAGGCTGCTCATTCCAGTCACGAGGCTGGCTACAAGGGTCAGATGCGACTCATGGACATGTCGGCGAGAACCCGGCGATCAGGGTCAGACGCTAAGCTGCAGAACAACAGGTCTGATACTGGAGATGATTCAGATAGTGATGACTCTGTGGACAGAGGCATTGAGGAGGCCATACAGGAGTATTTAAAGGAGAAGGTGGACCACAAGCGCAAAGGGGATCCAGTGACAAGTTCACCCCCAGCGCCCAAACTTCAGCGAAGGGAACTAGATGCTCCGAAACAACAGACACATTCCAGCAGTGCTAAGGTGCTGACTGCTAGCAATCATATCCAGAGACTCTCAAGCGGGATGGTGGCCTTAAAAAAGAAAGTCAAAAAGAAGCAGCTGAGCAAAGAAAATCCCTTTAAGAAAGCAGACGCGAGTAAAGTTTCGCCTTTAAAAAGTCTTCCTCCACCCAGAGCTAAAAAAGGATCCTCCTCGTCTTCTGAGATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16533
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
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099351 Nonsense 627 1004 3 3
Genomic Location (Zv9):
Chromosome 11 (position 38624990)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 7549816
GRCz11 21 7111307
KASP Assay ID:
2260-4595.1 (used for ordering genotyping assays)
KASP Sequence:
CTAAAGGCAAATGYGAGGTTCAAAACTTCAAGCCTTCTAAAAGCYTTGCG[C/T]AGACTGACAAGGTGACCGGGAATGGAGGRATTTCCTCAGCCCCAGGTGGA
Long Flanking Sequence:
CTACCACTCCCACTGCGATTTCACATTCAAGTAGTGTGAAAAATAGCAAACTGAAACAGAACTCTCCTCCTCGCAAGGGTGCAGATCATGTAACTAAAGACAACGTTTCCTCTTGTAGTGCATCCAGCCCAAAGGCTGCGATCGGCTCTGAGAGAAACGACAGCAGTGACAAAAGCAGCTCCTTGGACAGTGACGAGGATTTAGATGCAGCAATTAAAGACCTACTCAAGACGAAGAAAAAAGTCAAGAAGAAGGTAAGGGACTTGAAGGCGAGAAAAAGTGACAAACCTTTTGAGGCGTCATCTTTGGATGCCATAAAAAAGCAGAAGCCTTTAACCGAGCAGAAGTGTATCCCACTCAACAGGCTTGTTAAATCTAGCATCTTGAAAGGTGGGAAAGAATCCCTGAACATTCAGGCTAAAAATGACAAGGTGCCTAAAAGCAAACCAGCTAAAGGCAAATGTGAGGTTCAAAACTTCAAGCCTTCTAAAAGCTTTGCG[C/T]AGACTGACAAGGTGACCGGGAATGGAGGGATTTCCTCAGCCCCAGGTGGAGACACACTTTCACCAAGTCTGCATGCAGATGACGACAGTGATGTGGACAGCGATGACAGCATTGAGCGAGAGATCAGGAGATTTCTAGCTGAAAGAGCTAAGGTGTCCGCACCTGTAACCACAAACATTAAAAGTGAGGAGAAGGGCATCAACTCCTCATCTGCAGAGACTGAGGAAAATCCAGATCTTCAAAAGACTCAAACTGAAACTCCAGTATCTGCTGCGACATCAACCTCCGGGAGACTCTGGAAGACTGAACTCACAGGTACGTCCACAAAATCTACAGAAACACCTGCAGAACTCAACAAGGGACCAGTCCTGACACCAGGCAGCTCTTGCATAATGGGATTCAGGAGGACTGAAAGTCAAAAACCTGAGAACTCTGCTCCAAGAGATCCAACGAATGGCAGCTGCCAGACAGGCAAGGACACTCCGACAGGTCATGTCATC
Associated Phenotype:
Not determined