Busch Lab

ZMP

ndufa10

Ensembl ID:
ENSDARG00000013333
ZFIN ID:
ZDB-GENE-030131-670
Description:
NADH dehydrogenase [Source:RefSeq peptide;Acc:NP_955872]
Human Orthologue:
NDUFA10
Human Description:
NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 10, 42kDa [Source:HGNC Symbol;Acc:7684]
Mouse Orthologue:
Ndufa10
Mouse Description:
NADH dehydrogenase (ubiquinone) 1 alpha subcomplex 10 Gene [Source:MGI Symbol;Acc:MGI:1914523]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa5540 Nonsense F2 line generated Not yet available
sa38740 Nonsense Mutation detected in F1 DNA Not yet available
sa21484 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa5540
Status:
F2 line generated
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
ENSDART00000010311 Nonsense 187 355 5 10
ENSDART00000141461 Nonsense 187 340 5 10
Genomic Location (Zv9):
Chromosome 9 (position 24778342)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23934128
GRCz11 9 23744997
KASP Assay ID:
554-3521.1 (used for ordering genotyping assays)
KASP Sequence:
TGTTGTTAGAACGTATGYGTTGCTTGTTATTTTGCAGGCGTGAATCACTA[T/A]AATGAGATTAAGGGTATCAGTATTTGTGAGTTTCTTCCCCCTCATCTTGT
Long Flanking Sequence:
TGCTCTCTGGAGAAGTTCTACTTGGAGCCCAAAGCCAGTGATGGAAACTCATACCGCCTGCAGGCTTGGATGTACCTCATGAGGCTTCTGCAGTACTCTGATGCTGTTGAACACCTGCTCACGACAGGTTACCAAAGCACACTTGTATTACATGGAGATGTAGATTGATGTTGCAATTAAGAATGAAGTACTTTTTACTTTATAAACCAAGTTTTGAGAACACTGTTGCTCTTAAGGACACAATCATACTTAGGGGGTTTCTCTTTGATTTTTTTCCCTTCAGGACAGGGAGTTATACTGGAACGATCTCCTTTTAGTGACGTTGTGTTTTTGGAGGCCATGTTCAAAGAAGGATACATCCGCAAGCAGTGTGAGTGATAGTGTGTGAATTTCATAATGTAAAAAGATATGAAAGAGTACTAGAGTCATATTGGATGTACATCAAAGCTGTGTTGTTAGAACGTATGTGTTGCTTGTTATTTTGCAGGCGTGAATCACTA[T/A]AATGAGATTAAGGGTATCAGTATTTGTGAGTTTCTTCCCCCTCATCTTGTCATCTACGTGGACTCACCTGCTGAAGAGGTCCAGAAGAAGCTCAAAGCATCAGGAAAGGTATGTGTGAGGACAGAAACAAACTAAGTTTTGGCCAGAATAAATAGCTGCTTGATTTGTGGTTGTGTAAACTAGACCTTGCTGAGACTTTTGTTTCAGTTTGTTTATGTACTTCTAACTTAAAGATAATATTGAGTAGGGCCGCATCATTTACTTGTAGCAAACTAAAGGTGAGGGGGCAGGGTTAAGAATATTGTGGTTGAGTCATCAAACTGATGTCAACAGAGAAGGTCCACCACTCCAAACGCAGAAGAAATAGTCAGACTTTAATTGTTCCTTCGCTAAGCCACACTCGAAAACTGCCACACACCAATCATGGCTTAACAACCGTAGCTACATGCGGGAGGTCTGTCAAGCTTTGAGCAACGGAAAAAAGCCAAATCGTTGTGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38740
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
ENSDART00000010311 Nonsense 221 355 5 10
ENSDART00000141461 Nonsense 221 340 5 10
Genomic Location (Zv9):
Chromosome 9 (position 24778241)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23934027
GRCz11 9 23744896
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTACGTGGACTCACCTGCTGAAGAGGTCCAGAAGAAGCTCAAAGCAT[C/A]AGGAAAGGTATGTGTGAGGACAGAAACAAACTAAGTTTTGGCCAGAATAA
Long Flanking Sequence:
TGCTGTTGAACACCTGCTCACGACAGGTTACCAAAGCACACTTGTATTACATGGAGATGTAGATTGATGTTGCAATTAAGAATGAAGTACTTTTTACTTTATAAACCAAGTTTTGAGAACACTGTTGCTCTTAAGGACACAATCATACTTAGGGGGTTTCTCTTTGATTTTTTTCCCTTCAGGACAGGGAGTTATACTGGAACGATCTCCTTTTAGTGACGTTGTGTTTTTGGAGGCCATGTTCAAAGAAGGATACATCCGCAAGCAGTGTGAGTGATAGTGTGTGAATTTCATAATGTAAAAAGATATGAAAGAGTACTAGAGTCATATTGGATGTACATCAAAGCTGTGTTGTTAGAACGTATGTGTTGCTTGTTATTTTGCAGGCGTGAATCACTATAATGAGATTAAGGGTATCAGTATTTGTGAGTTTCTTCCCCCTCATCTTGTCATCTACGTGGACTCACCTGCTGAAGAGGTCCAGAAGAAGCTCAAAGCAT[C/A]AGGAAAGGTATGTGTGAGGACAGAAACAAACTAAGTTTTGGCCAGAATAAATAGCTGCTTGATTTGTGGTTGTGTAAACTAGACCTTGCTGAGACTTTTGTTTCAGTTTGTTTATGTACTTCTAACTTAAAGATAATATTGAGTAGGGCCGCATCATTTACTTGTAGCAAACTAAAGGTGAGGGGGCAGGGTTAAGAATATTGTGGTTGAGTCATCAAACTGATGTCAACAGAGAAGGTCCACCACTCCAAACGCAGAAGAAATAGTCAGACTTTAATTGTTCCTTCGCTAAGCCACACTCGAAAACTGCCACACACCAATCATGGCTTAACAACCGTAGCTACATGCGGGAGGTCTGTCAAGCTTTGAGCAACGGAAAAAAGCCAAATCGTTGTGCATATAGATGGTGCAAATATGATACCCGGCATCCTTAAAGTTTGGACGGGGTGGTGAATTTTTTTTTTCCTTTCCAAAATCTAAAACCAAATGGGAGAAATGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21484
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000010311 Essential Splice Site 268 355 7 10
ENSDART00000141461 Essential Splice Site 268 340 7 10
Genomic Location (Zv9):
Chromosome 9 (position 24776085)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 23931871
GRCz11 9 23742740
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCAGAGGTTCTTACATATGGTGCAGTTGAAGCCCAGGACGTTGAGAAG[G/A]TAATGATCCAGTCTGTGTATTTAGCACCTGAGGCAGGCAAATGTGACTTA
Long Flanking Sequence:
TATTATATATGAATAAGGGCTTTTGTACATCGTTTAATTATTTACAAAATAACTTACACAAAACATTAACCGAAGCAGCTTATGATTTTTTTTCTTTTCAATGCTCTAACTTTGTTAGTAAATACCTAATTGCCTAAATACTAGATATACAAGATTTTATGAATTTAGTAACTGGTGTTTATAAAAGTATGACAGTGAAATAATCCTTATCTCCTTCTACAGCCATACCTACAGAATGTTCCTTTGAGCTACCTGAAGAGCATTGAGACTGCATACAAGAAGACCTTCCTTCCTAAAATCAGGTCAGTACCAAAGCAACCAGGTTCATGTTGGAAATGTTACTAATATAAAAATGCTTAAATATTTATAAAAAGCAGTTGTTTATTAAAATAATTAAAATATATCAATCAGTTTTCATTGATGGTGTGGTAAATTTCATTTTCAGTGAAGAAGCAGAGGTTCTTACATATGGTGCAGTTGAAGCCCAGGACGTTGAGAAG[G/A]TAATGATCCAGTCTGTGTATTTAGCACCTGAGGCAGGCAAATGTGACTTATTTCTCTATTCTGCTTTTGCAGGTTGTTGAGGATATTGAATGCCTCAAGTTTCAGAAGGGCCCTTGGGTGAATCAGAATGATGTCTCTTTCCATCATATGCGAATGTTGTGAGTATTGTTTTTGTGTGCCTTTTTTCATTCCATTGTTTTTTACAGAGATTGGACATCTGTTTTGAGAGATCTATTTTTTTTTATACCTTTTTCCCTCATTTATTAGGGTGGAAGACAAGCAGAGGGTAACCAGCCTGACCAGCTTTCCCAGCTTTATCCCAGAAATCACAATTGGTGCTCATGAGTTAGATTCCACCTATTATGCTTTCAAATCGGTATGTGAATGCTGAAACTGTGCTAAATGTAGTGATTCATATGTGTTTAAAATCAAATTTTAGCCCTGTCCTACCATGCCTTTCAAGCGTGAACTGTTTTAGAAAAAGTTGTTCTTGTTTATTT
Associated Phenotype:
Not determined