ZMP
NDUFA4L2 (1 of 2)
Ensembl ID:
Description:
NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 4-like 2 [Source:HGNC Symbol;Acc:29836]
Human Orthologue:
NDUFA4L2
Human Description:
NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 4-like 2 [Source:HGNC Symbol;Acc:29836]
Mouse Orthologue:
Ndufa4l2
Mouse Description:
NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 4-like 2 Gene [Source:MGI Symbol;Acc:MGI:3039567
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12553 | Nonsense | Available for shipment | Available now |
sa18859 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13088 | Nonsense | Available for shipment | Available now |
sa12542 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12553
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000126870 | Nonsense | 12 | 83 | 1 | 4 |
ENSDART00000126870 | Nonsense | 12 | 83 | 1 | 4 |
ENSDART00000126870 | Nonsense | 12 | 83 | 1 | 4 |
ENSDART00000126870 | Nonsense | 12 | 83 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 59188993)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 59275787 |
GRCz11 | 6 | 59271232 |
KASP Assay ID:
2259-8306.1 (used for ordering genotyping assays)
KASP Sequence:
GTTTCTGAAAGCTGAAGWTGGAGAWCCTCAGAATGAWGCAYCGGCAGGCT[A/T]AAAAACACCCCGGGGTGAGTCCAGATTCATGATCAAAATCAAGGTTATTA
Long Flanking Sequence:
AATACATTTACTGTATGCACACACACACACACACACACACACACACACACACACACGCACACACACACACACACACACACACACACACACACACACATATATACATATACACAAACGCAACATTATAAAAATATTTCTGAATTTTTATTTTTCTAGTTTATTAAATTAAAAGAGACTTTTTCCAGAAACATCTACAATTTCTCAGTGTTTACACTTGCACAAATCATCCTAAATTTTTAAACAATTTTTTTTTCAGCCCAACAAACTAACATGATAACTCAAAGTTTTGTCCTGCAGTCTGAATGCTCTGACTCTCTGCGTGTTGATAGGTCAACAGAAACTGTCAATCACAGACTGACCTGCCCACTCAACACATCTCTGCTGGTTCACTCTCGTTTAGAGTGTTAAAAGTGTGTGTGTGTTCTGAGTGTTTACAGTGTGTGTGTGTTTGTTTCTGAAAGCTGAAGATGGAGATCCTCAGAATGATGCACCGGCAGGCT[A/T]AAAAACACCCCGGGGTGAGTCCAGATTCATGATCAAAATCAAGGTTATTATAGTTTTGCATTTAGTTCAGAATGAGTTTTAGTTCGGTTTAGTTTCATTAATGGTTGTGTCAGTTTTAGTTTAGTTTTTATGCTGTAGACACATTTTTATTTTTAACATTATCTTCATACATTTTTTTACATTAGCAGAAAAATTCAGATACAAACTTTTACAAGTGTATACGTTGTTGTTTTTACAACAATTTTTTTACATCATAAACTGTATATGGGGGAAAGGAAAAAAGAAATTCAGAGGAAATGATAGGGAAAAAATAATAATAAATAAAGAAAATAAGTAACAAAAATAAAAAAATGAAAAGGGCTGTTTCAAATAAAAAAAGTAAAATGTAAAAAAATGTTTTAATTAATTAAGACAATTGGGTTGTTTCTAATTAAATAAAATGTGATAAATAAATAAATAAATAAATAAAATAGGCTTCTTTTTTTAAAATTAAATACCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18859
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000126870 | Nonsense | 12 | 83 | 1 | 4 |
ENSDART00000126870 | Nonsense | 12 | 83 | 1 | 4 |
ENSDART00000126870 | Nonsense | 12 | 83 | 1 | 4 |
ENSDART00000126870 | Nonsense | 12 | 83 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 59188993)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 59275787 |
GRCz11 | 6 | 59271232 |
KASP Assay ID:
2259-8306.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTCTGAAAGCTGAAGATGGAGATCCTCAGAATGATGCACCGGCAGGCT[A/T]AAAAACACCCCGGGGTGAGTCCAGATTCATGATCAAAATCAAGGTTATTA
Long Flanking Sequence:
AATACATTTACTGTATGCACACACACACACACACACACACACACACACACACACACGCACACACACACACACACACACACACACACACACACACACATATATACATATACACAAACGCAACATTATAAAAATATTTCTGAATTTTTATTTTTCTAGTTTATTAAATTAAAAGAGACTTTTTCCAGAAACATCTACAATTTCTCAGTGTTTACACTTGCACAAATCATCCTAAATTTTTAAACAATTTTTTTTTCAGCCCAACAAACTAACATGATAACTCAAAGTTTTGTCCTGCAGTCTGAATGCTCTGACTCTCTGCGTGTTGATAGGTCAACAGAAACTGTCAATCACAGACTGACCTGCCCACTCAACACATCTCTGCTGGTTCACTCTCGTTTAGAGTGTTAAAAGTGTGTGTGTGTTCTGAGTGTTTACAGTGTGTGTGTGTTTGTTTCTGAAAGCTGAAGATGGAGATCCTCAGAATGATGCACCGGCAGGCT[A/T]AAAAACACCCCGGGGTGAGTCCAGATTCATGATCAAAATCAAGGTTATTATAGTTTTGCATTTAGTTCAGAATGAGTTTTAGTTCGGTTTAGTTTCATTAATGGTTGTGTCAGTTTTAGTTTAGTTTTTATGCTGTAGACACATTTTTATTTTTAACATTATCTTCATACATTTTTTTACATTAGCAGAAAAATTCAGATACAAACTTTTACAAGTGTATACGTTGTTGTTTTTACAACAATTTTTTTACATCATAAACTGTATATGGGGGAAAGGAAAAAAGAAATTCAGAGGAAATGATAGGGAAAAAATAATAATAAATAAAGAAAATAAGTAACAAAAATAAAAAAATGAAAAGGGCTGTTTCAAATAAAAAAAGTAAAATGTAAAAAAATGTTTTAATTAATTAAGACAATTGGGTTGTTTCTAATTAAATAAAATGTGATAAATAAATAAATAAATAAATAAAATAGGCTTCTTTTTTTAAAATTAAATACCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13088
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000126870 | Nonsense | 12 | 83 | 1 | 4 |
ENSDART00000126870 | Nonsense | 12 | 83 | 1 | 4 |
ENSDART00000126870 | Nonsense | 12 | 83 | 1 | 4 |
ENSDART00000126870 | Nonsense | 12 | 83 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 59188993)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 59275787 |
GRCz11 | 6 | 59271232 |
KASP Assay ID:
2259-8306.1 (used for ordering genotyping assays)
KASP Sequence:
GTTTCTGAAAGCTGAAGWTGGAGAWCCTCAGAATGAWGCAYCGGCAGGCT[A/T]AAAAACACCCCGGGGTGAGTCCAGATTCATGATCAAAATCAAGGTTATTA
Long Flanking Sequence:
AATACATTTACTGTATGCACACACACACACACACACACACACACACACACACACACGCACACACACACACACACACACACACACACACACACACACATATATACATATACACAAACGCAACATTATAAAAATATTTCTGAATTTTTATTTTTCTAGTTTATTAAATTAAAAGAGACTTTTTCCAGAAACATCTACAATTTCTCAGTGTTTACACTTGCACAAATCATCCTAAATTTTTAAACAATTTTTTTTTCAGCCCAACAAACTAACATGATAACTCAAAGTTTTGTCCTGCAGTCTGAATGCTCTGACTCTCTGCGTGTTGATAGGTCAACAGAAACTGTCAATCACAGACTGACCTGCCCACTCAACACATCTCTGCTGGTTCACTCTCGTTTAGAGTGTTAAAAGTGTGTGTGTGTTCTGAGTGTTTACAGTGTGTGTGTGTTTGTTTCTGAAAGCTGAAGATGGAGATCCTCAGAATGATGCACCGGCAGGCT[A/T]AAAAACACCCCGGGGTGAGTCCAGATTCATGATCAAAATCAAGGTTATTATAGTTTTGCATTTAGTTCAGAATGAGTTTTAGTTCGGTTTAGTTTCATTAATGGTTGTGTCAGTTTTAGTTTAGTTTTTATGCTGTAGACACATTTTTATTTTTAACATTATCTTCATACATTTTTTTACATTAGCAGAAAAATTCAGATACAAACTTTTACAAGTGTATACGTTGTTGTTTTTACAACAATTTTTTTACATCATAAACTGTATATGGGGGAAAGGAAAAAAGAAATTCAGAGGAAATGATAGGGAAAAAATAATAATAAATAAAGAAAATAAGTAACAAAAATAAAAAAATGAAAAGGGCTGTTTCAAATAAAAAAAGTAAAATGTAAAAAAATGTTTTAATTAATTAAGACAATTGGGTTGTTTCTAATTAAATAAAATGTGATAAATAAATAAATAAATAAATAAAATAGGCTTCTTTTTTTAAAATTAAATACCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12542
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000126870 | Nonsense | 12 | 83 | 1 | 4 |
ENSDART00000126870 | Nonsense | 12 | 83 | 1 | 4 |
ENSDART00000126870 | Nonsense | 12 | 83 | 1 | 4 |
ENSDART00000126870 | Nonsense | 12 | 83 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 59188993)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 59275787 |
GRCz11 | 6 | 59271232 |
KASP Assay ID:
2259-8306.1 (used for ordering genotyping assays)
KASP Sequence:
GTTTCTGAAAGCTGAAGWTGGAGAWCCTCAGAATGAWGCAYCGGCAGGCT[A/T]AAAAACACCCCGGGGTGAGTCCAGATTCATGATCAAAATCAAGGTTATTA
Long Flanking Sequence:
AATACATTTACTGTATGCACACACACACACACACACACACACACACACACACACACGCACACACACACACACACACACACACACACACACACACACATATATACATATACACAAACGCAACATTATAAAAATATTTCTGAATTTTTATTTTTCTAGTTTATTAAATTAAAAGAGACTTTTTCCAGAAACATCTACAATTTCTCAGTGTTTACACTTGCACAAATCATCCTAAATTTTTAAACAATTTTTTTTTCAGCCCAACAAACTAACATGATAACTCAAAGTTTTGTCCTGCAGTCTGAATGCTCTGACTCTCTGCGTGTTGATAGGTCAACAGAAACTGTCAATCACAGACTGACCTGCCCACTCAACACATCTCTGCTGGTTCACTCTCGTTTAGAGTGTTAAAAGTGTGTGTGTGTTCTGAGTGTTTACAGTGTGTGTGTGTTTGTTTCTGAAAGCTGAAGATGGAGATCCTCAGAATGATGCACCGGCAGGCT[A/T]AAAAACACCCCGGGGTGAGTCCAGATTCATGATCAAAATCAAGGTTATTATAGTTTTGCATTTAGTTCAGAATGAGTTTTAGTTCGGTTTAGTTTCATTAATGGTTGTGTCAGTTTTAGTTTAGTTTTTATGCTGTAGACACATTTTTATTTTTAACATTATCTTCATACATTTTTTTACATTAGCAGAAAAATTCAGATACAAACTTTTACAAGTGTATACGTTGTTGTTTTTACAACAATTTTTTTACATCATAAACTGTATATGGGGGAAAGGAAAAAAGAAATTCAGAGGAAATGATAGGGAAAAAATAATAATAAATAAAGAAAATAAGTAACAAAAATAAAAAAATGAAAAGGGCTGTTTCAAATAAAAAAAGTAAAATGTAAAAAAATGTTTTAATTAATTAAGACAATTGGGTTGTTTCTAATTAAATAAAATGTGATAAATAAATAAATAAATAAATAAAATAGGCTTCTTTTTTTAAAATTAAATACCAT
Associated Phenotype:
Not determined