ZMP
suclg2
Ensembl ID:
ZFIN ID:
Description:
Suclg2 protein [Source:UniProtKB/TrEMBL;Acc:Q6PHH4]
Human Orthologue:
SUCLG2
Human Description:
succinate-CoA ligase, GDP-forming, beta subunit [Source:HGNC Symbol;Acc:11450]
Mouse Orthologue:
Suclg2
Mouse Description:
succinate-Coenzyme A ligase, GDP-forming, beta subunit Gene [Source:MGI Symbol;Acc:MGI:1306824]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41804 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa27752 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41804
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087520 | Nonsense | 305 | 354 | 8 | 9 |
ENSDART00000122222 | Nonsense | 305 | 432 | 8 | 11 |
ENSDART00000131079 | Nonsense | 292 | 341 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 11 (position 17234507)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 16715207 |
GRCz11 | 11 | 16849842 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGGCAAAATACGACCTCAAATACATCGGAATGGATGGAAACATCGCCTG[T/A]TTCGGTATGTTTTTAAACTTCCATAAAATTTACAAGATCATTAACAATAC
Long Flanking Sequence:
GCGCGTTGGAGATAAATGACGTCAGTACATAATAACCGGTTATGATTATTACTGAACCGATAATGTATTGTCCGCGTCTGCATCGCGGTGCACCAAAAAAACAATTAATTTTGACACCCCTAATATATATATTTTTAATTTACAATATTTATGTCAGCTATAAAATGTATTATGAGCTTTAAAACAAATCTTTAATATAAAAAGGGACACTTTAAAGCTCCTAAATATAACTTTTTAATTCTAAATTTAATTAATGAACAACTGTACCAAAAATGCTGCAATACGAGCTAAATTTCAAAAGACTGCCCGAGTTAGAACACGTTTCTTCTTTCTCTTTCAACAGTTGTGTGCTTTGATGCTAAAATCAACTTCGACGACAATGCAGAATTCAGACAGAAAGCGGTTTTCTCCATGGACGACACTGCAGAAAGTGACCCCATCGAAACCGAAGCGGCAAAATACGACCTCAAATACATCGGAATGGATGGAAACATCGCCTG[T/A]TTCGGTATGTTTTTAAACTTCCATAAAATTTACAAGATCATTAACAATACACGAGATGAACTTTTTCAAAACATCCTGATTTCAAAGCTCTCAAAAACCTGCTCTGCATCAATCTCATGTCTCAAGAGAGATTTCAAACCTGAGTCTTCTTAGTAGTTTCCGACGCATTTATTTTAGTCTTGAGGACGGGATTTTTGTGAAAGTGTTACCAAATGGGCGCCAATCCAGTCATCATCTCCAGCAGCTTTGAAACAGCTCCATAAGGGACCTGCCTGAACCGATGGGCTCTAATTAGCAGGAATCTTCCGGAAAACGACTCAAGCAAATATGATTGTTAGGCTACACATTTAAGTGGTCCCTCATTATAAATCAGGGCTCTCACAGCAAAGCATTGAGAACAAGACGAGCGCATTGGTGACTCTAACTGACCTTGTCGTGTACACACAAACGCACTCACGCACAATTTACTCGCAGTTAGTTTGCACCTTAAAAGCTTTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27752
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087520 | Nonsense | 322 | 354 | 9 | 9 |
ENSDART00000122222 | Nonsense | 322 | 432 | 9 | 11 |
ENSDART00000131079 | Nonsense | 309 | 341 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 11 (position 17232581)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 16713281 |
GRCz11 | 11 | 16847916 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAGTTAATGGTGCTGGCCTTGCTATGGCAACATGTGACATCATTGACT[T/A]GCATGGCGGGAAGCCGGCAAACTTCTTGGACCTGGGCGGAGGTGTAAAGG
Long Flanking Sequence:
ATACTTTCATTTGTAAATGCAGGGTTCCACACAATTCATTCATGGTGTCCCAACACAAATCATTTAAGTTAACTTAAAACTTTTTACAAATTTATGTGGATTGAAAAAAAAAAAAAAAAGTTGTCCCAATAAAATCTTAAGAAGTGTGTTGATTTTAAATAAGTAGTTTGAACAAGCAAAACAAGAAAAATAATAAATTGAGTGTACTCAAAATCTCTGGTCTACATTTATTTGACCTTACAAGCGAATCATTTTAAAAAGTCACATTATTTCTTCCTGGAAAGATAGATATTCAGTATGAGGGTGAATGTACGGTAGTCAACATTTGAAGTGGATAAAAATATTTTTTCCCAAAATTGTCCAAAGGTGATGATTATCTTCATACTGTCTTATCATACCGTACGACAAGACCGTATTTATTTTAGCTGATGCTGTAATATGATCTGTGTCCACAGTTAATGGTGCTGGCCTTGCTATGGCAACATGTGACATCATTGACT[T/A]GCATGGCGGGAAGCCGGCAAACTTCTTGGACCTGGGCGGAGGTGTAAAGGAGAACCAGGTGTATGCAGCCTTCAAACTTCTCACTGCCGACCCCAAGGTATGAACCAGTCTATAATAGTTCAATCAAAACCCAGCGGTTAAATACCCCAATAAAAGGTTAATATAGAGGTGTTCTGAGAAGATTATAAGAAATAAGAAAAAGTTCAAGCTGCTCTTCTTTAACTTCGTTACAGTTTTTACTTTTCTACTCTTTGAAGTTTCCTTCATCTGAGACTTTGTTGACTCCTTAGGCACCACAAAAGACTGTGGGCTTGCGGCCGAACTCAGTTCTTTTTAACCATCATTACGAGTTTGCACTCTGATCAATATCTTTGCTACAGTCACACTTTTCTGCTCCAGAATTGTAAACACACTGAGACTCACACACACACACACATCTCATAACTCATCTTTTTACCAATTCTTTTCTCCCCCAGACACACACTTGCTGTCCTCCTCAT
Associated Phenotype:
Not determined