Busch Lab

ZMP

zgc:136925

Ensembl ID:
ENSDARG00000069852
ZFIN ID:
ZDB-GENE-060312-18
Description:
Putative lipoyltransferase 2, mitochondrial [Source:UniProtKB/Swiss-Prot;Acc:Q29R99]
Human Orthologue:
LIPT2
Human Description:
lipoyl(octanoyl) transferase 2 (putative) [Source:HGNC Symbol;Acc:37216]
Mouse Orthologue:
Lipt2
Mouse Description:
lipoyl(octanoyl) transferase 2 (putative) Gene [Source:MGI Symbol;Acc:MGI:1914414]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa32012 Nonsense Available for shipment Available now
sa8968 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa32012
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
ENSDART00000101992 Nonsense 25 224 2 3
Genomic Location (Zv9):
Chromosome 15 (position 4823943)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 4973996
GRCz11 15 4965143
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAAGCGGTTCATCTAGGAAGGATCTCCTACCACAGTGCCTTGAAAATA[C/T]AGCAGCAGCACATACAGCAGCATCTGGATTCATCCAGCAACATCCCAAAC
Long Flanking Sequence:
TCTCAAAAAAAGACATGATAGTGTCATTAGAAACTGAATTGGAAATGACCTTATTTTATAGTCAAGTCGTGAACTGAGGTGGGCCGGTCTGAGGCTTGAAATTCCAGGGCTAAAAAGGAGTCCCACTCCGGCCCTGCTTTGTAATGTTGCAAAATTAAAATAAAGTGGTTAAAAAAATCTTAATCCTAAATGTATTTATAAAAAATATTAAATAATTATCAATATAGAGTAATATGAATCATGATATCATGACAATGATTTTCTTTGCAATATCGCCTGCACTACTTTAAAAGTACTTGATTTTGGTAATCTCACTACATCATCCAGACTGCATCTACCATCCAGCTCTGTACATGTACAACTTTATGCAAATAACAGTCTTTTCCCATGTTCACAGCTGATGCTTTATAACCCCATCTAAAGACACAATGTCGGTCACAAAAGCAGCTGTCAAAGCGGTTCATCTAGGAAGGATCTCCTACCACAGTGCCTTGAAAATA[C/T]AGCAGCAGCACATACAGCAGCATCTGGATTCATCCAGCAACATCCCAAACACGTTATTACTCTGCGAACACGAGCCGGTGTACACCATCGGTCTCAGACAGGCTCCGTACCCACCAGCAGAGGAGCAGAGACTGAAGGCTCTGGGTGCAGATTTCTGCCGCACCAACAGAGGAGGACTCATTACTTTCCACGGGCCGGGACAGCTGGTCTGTTACCCCATCCTCAACCTGGGCTGCTTCAAGAAGAGCGTGAGATGGTACGTGTGTGAACTGGAAAGGACCGTGATCAAGATGTGCGGTAAATTTGGGATTAAAGCCTCAACTTCTCCGGATACTGGAGTCTGGGTGGGAGACAACAAAATCTGCGCAATTGGTAAGTTCTGTTTTGAAATATTTTTATTATGTATATATATGTATATATATATGTATATATATATGTGTATATATATATATATATATGTATATATGTATGTATATGTATATATATGTATATGTATATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8968
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101992 Nonsense 110 224 2 3
Genomic Location (Zv9):
Chromosome 15 (position 4823686)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 4973739
GRCz11 15 4964886
KASP Assay ID:
2260-8099.1 (used for ordering genotyping assays)
KASP Sequence:
GTCTGTTACCCCATYCTCAACCTGGGCTGCTTCAAGAAGAGCGTGAGATG[G/A]TACGTGTGTGAACTGGAAAGRACCGTGATCAAGATGTGCGGTAAATTTGG
Long Flanking Sequence:
ATTTTCTTTGCAATATCGCCTGCACTACTTTAAAAGTACTTGATTTTGGTAATCTCACTACATCATCCAGACTGCATCTACCATCCAGCTCTGTACATGTACAACTTTATGCAAATAACAGTCTTTTCCCATGTTCACAGCTGATGCTTTATAACCCCATCTAAAGACACAATGTCGGTCACAAAAGCAGCTGTCAAAGCGGTTCATCTAGGAAGGATCTCCTACCACAGTGCCTTGAAAATACAGCAGCAGCACATACAGCAGCATCTGGATTCATCCAGCAACATCCCAAACACGTTATTACTCTGCGAACACGAGCCGGTGTACACCATCGGTCTCAGACAGGCTCCGTACCCACCAGCAGAGGAGCAGAGACTGAAGGCTCTGGGTGCAGATTTCTGCCGCACCAACAGAGGAGGACTCATTACTTTCCACGGGCCGGGACAGCTGGTCTGTTACCCCATCCTCAACCTGGGCTGCTTCAAGAAGAGCGTGAGATG[G/A]TACGTGTGTGAACTGGAAAGGACCGTGATCAAGATGTGCGGTAAATTTGGGATTAAAGCCTCAACTTCTCCGGATACTGGAGTCTGGGTGGGAGACAACAAAATCTGCGCAATTGGTAAGTTCTGTTTTGAAATATTTTTATTATGTATATATATGTATATATATATGTATATATATATGTGTATATATATATATATATATGTATATATGTATGTATATGTATATATATGTATATGTATATATATATTAGGGTTGCGCGATGTTGACCACTTTGGCATCTTATGCCTAGTTCAGACTGCGTGATTTTAGCCCCGATTTTGGCTCGCTGACAGGTTTTGAGAAATCGCCGACAAATGCCTGAAATCACAGGCAAATCGCTGCTTGTGCACGTGAGTGACAATCACACAGTATGAACTATCAAAGACGCGATCTGTGAGAATCGCCGATGAGTCGCAGATGCCCGCGAGATATTTGACATGCTAAATATCTAAAGCTGTCGG
Associated Phenotype:
Not determined