ZMP
zgc:153148
Ensembl ID:
ZFIN ID:
Description:
enolase superfamily 1 [Source:RefSeq peptide;Acc:NP_001070210]
Human Orthologue:
ENOSF1
Human Description:
enolase superfamily member 1 [Source:HGNC Symbol;Acc:30365]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31608 | Essential Splice Site | Available for shipment | Available now |
sa21100 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31608
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055956 | Essential Splice Site | 102 | 441 | None | 15 |
ENSDART00000098412 | Essential Splice Site | 102 | 308 | None | 12 |
ENSDART00000135068 | Essential Splice Site | 102 | 205 | None | 8 |
The following transcripts of ENSDARG00000038359 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 58376466)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 56811792 |
GRCz11 | 7 | 57113203 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCCGAGGCTTCTACAGACTCCTGAGCAGCGATGGTCAGATGAGATGGG[T/A]AAGAGAGACACACTGAGTGCAGACCCTTCAGTTCATTAACAGCTAAATGA
Long Flanking Sequence:
CAGTGGAAACAGAATGTAACTGAGCTAAAATTAGAGCTTCAGGCAAAGGCTGTGAATACTGATGTACATTGGATTTTCAGGTTTTTTATTTTTAATAAATTTGCAACAAATTTCAAAAACTCTTTTTTTCCACATTGTTATTATGGGGTATTGTGTGTAGAATTATGAGGCAAAAAATGAATTTAATCCATTTCGGAATAAGGCTGTAACAAAAAATGAGGAAAAAGTGAAGCGTTGTGAATGCTTTCCGCATGCACTGTATGGTATAGAGTTTGGATAGGGACAGAGTTTGGACAGCCAGTCTAAATAGTACAGAATTTGTTGAATCCATGGGAATTCCAAATAAAGCATGAAAACAAATGTATGTGTTTTTCTATTTTTAGTTGTGTGTGCAGTTAAAGCTTTATCCACCCTGGTGGTGGGGAAGACTTTAGAGGAAATAACCAGTGACTTCCGAGGCTTCTACAGACTCCTGAGCAGCGATGGTCAGATGAGATGGG[T/A]AAGAGAGACACACTGAGTGCAGACCCTTCAGTTCATTAACAGCTAAATGAATAGATGAACTCACTTACAGATCGGACCAGAGAAAGGAGTCATTCATCTGGCAACAGCAGCCGTATTGAATGCTGTCTGGGATTTATGGGCAAGAGTAGAGAGAAAGGTGAGCAATAAAACCTTCAGGACAAATTCGTCTGCATGCTGTCTGCTTGCATTCAGTAGGTGATGTAATAATGAATGTAGAATACCATTAAAAGTCAGAATCAATGTGTTTTGCAGCCCTTGTGGAAGCTACTTGTTGACATGGTAAGTGTAAATGATATTTGGTATTTATACGATTATATGTAAGATATAAAAAAAGAAGTTACTGCAGTTAGGCATTATTAGACATTGATTGGTGATTGGACTGCAGTTTTGATAATATGAGGGGCAAAATGTAAAAAAAAAAAAAAAACAATAAATTAATATTTTAAATTATTACATTAAGAAGACTAATAAGGTTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21100
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055956 | Essential Splice Site | 178 | 441 | None | 15 |
ENSDART00000098412 | Essential Splice Site | 178 | 308 | None | 12 |
ENSDART00000135068 | Essential Splice Site | 178 | 205 | None | 8 |
The following transcripts of ENSDARG00000038359 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 58378850)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 56814176 |
GRCz11 | 7 | 57115587 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTTTTTAGATATATTGGTAAAAGGCAAAAAAGATCAGAAAAGTAGAGG[T/C]AAGAACCGTTGTTTAGACATCACTGAAGTCCTTACATGAACTACAGTTCA
Long Flanking Sequence:
AATGCACACCCTCCCTTGCCATAGAAAACACTAGTGATGTCTATGAAGGATGAGAAGCTCTTAGATTAAATCTCAAATATCTTAATTTGTGTTCTGAAGATGAACAAAGGTCACATGAGATTTTAATGACATGAGAGTCAGTCATTAATAACACAACGTTCATTTTTAGGGTGAAATTATTAAAAGTTATAATTAATCTACAAATCATTCATTGAGGTCGAGGTATATTGCGCAGCTCTTAAACACTGAACGTTCATCATTATGTTTATTTTCATATATATTTTAAATCTTCTGCTTAGGATCCTGCAAAGCTGATCAGCTGTATTGATTTCAGATATCTCACTGATGCTCTGACGGAGCAGGAAGCTTTAGGTCAGGATTTTATCAGCTTTGTTAAATATTGAGCTGTTTTATACATTTACATGTAATGCTTTGCCTTTTTATTCTGTCTTCTTTTTAGATATATTGGTAAAAGGCAAAAAAGATCAGAAAAGTAGAGG[T/C]AAGAACCGTTGTTTAGACATCACTGAAGTCCTTACATGAACTACAGTTCAAAGGTTTAGATATGATCATATTGAATTCATATTTCTCATAGAGTTTCCTTTGATCACAGAAGTACTATATATATTCAGTAATAATGCTTAAAATTGTAGGTAAACAGAGTTTTATTATTATTATTATTTAAATCTATATTTTTCTGTTCCTGTAGCATGCATTTAATTGTTCCAAGGTGATGATAAATATTGTACATTGCTAAAATATGTTTATTTATTGCTAAATAATGAATTCTGAGAAAACTCTGAGAAAATCGTGAAAAAAGAAAAACTGTTTCCAGCATTGATAATGACTGATGATGATAAAAAAGATGTTGCATCAAATAAAAGTATGGGAATATGATCTAAAGGATTATGTCTTTGAAGACTGGAATGCTGAGTATGTTTCAGCTTTGTCACCACAGTAATAACTTGAATTAAAAAAAAAAACAAATATGGTTATTTTAAATA
Associated Phenotype:
Not determined