ZMP
cept1
Ensembl ID:
ZFIN ID:
Description:
choline/ethanolaminephosphotransferase 1 [Source:RefSeq peptide;Acc:NP_001103187]
Human Orthologue:
CEPT1
Human Description:
choline/ethanolamine phosphotransferase 1 [Source:HGNC Symbol;Acc:24289]
Mouse Orthologue:
Cept1
Mouse Description:
choline/ethanolaminephosphotransferase 1 Gene [Source:MGI Symbol;Acc:MGI:2139793]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13460 | Nonsense | Available for shipment | Available now |
sa15095 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13460
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035514 | Nonsense | 117 | 415 | 4 | 10 |
ENSDART00000081593 | Nonsense | 117 | 415 | 2 | 8 |
ENSDART00000137522 | None | None | 180 | None | 5 |
Genomic Location (Zv9):
Chromosome 22 (position 857281)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 860193 |
GRCz11 | 22 | 877091 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTGAAYTTATGATAAATTAATGTAATTGAGTGTTTTAGGCTCCRCTGTG[G/A]GCGTAWCTCCTGTGYGCGGTGGGTTTGTTTGTCTATCAGTCGCTGGAYGC
Long Flanking Sequence:
TTGATCTGGTTTGGGATTCTACAGTTGCTATGGTAACACAACAACTATAGTAATTGATCTGTTGTGGTGATTCTACAGTTGCTATAGTAACACAACTACTATAGTAATTGATCTGTTGTGGTGATTCTACAGTTGCTATAGTAACACAACTACTATAGTAATTGATCTGTTGTGGTGATTCTACAGTTGCTATGGTAACAACTTCTATAGTAATTGATCTGTTGTGGTGATTCTACAGTTGCTATGGTAACAACTATAGTAATTAATCTGTTGTGGTCATTCTACAGTTGCTGTGGTAACACAACAACAATAGTAATGTAAACAAATGAGCCAATGCTGTCGTTTTCTACAGCTATTAGGTATATTATACTACAATACACCATCGTTTACTGTAGTAAAAACTAAAGTATACTACAGTATTTATCAGTTTACTATAATTAATACAGCCGCACTGAACTTATGATAAATTAATGTAATTGAGTGTTTTAGGCTCCGCTGTG[G/A]GCGTATCTCCTGTGCGCGGTGGGTTTGTTTGTCTATCAGTCGCTGGACGCCATTGATGGGAAACAGGCCAGACGCACTAACAGCAGTTCACCACTGGGGGAGCTGTTTGACCACGGCTGTGATTCACTCTCGACAGGTGAACAGCACACATTTTCTATACGAATCATAGGAAACGATATATCGCTTGAGCATTGATATCGCAATGTGTGTATCCGCAATAGTCAATAATATTATTGACTACTACTGTCGGTAATAGTAATAATATTGAATTGTACGTTAATGCTAAATATTTTGTTTTTGAATGTTAAACGTATTAATACACAGTTTTGTTAAATTTTTACATGCAAAATAACTATTAAATTAGTAACTATTAAATCTATTTTTAGGCAAAGTAGAATATTTCAGTGTGTACATTGGTTCAGAGTAGACAAAGGACATTTTTTCGCATGCAATTTCACCAAATTATCCACAGATGAAATAGTATTTTTGATAAGAAACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15095
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035514 | Nonsense | 201 | 415 | 5 | 10 |
ENSDART00000081593 | Nonsense | 201 | 415 | 3 | 8 |
ENSDART00000137522 | Nonsense | 33 | 180 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 22 (position 856599)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 859511 |
GRCz11 | 22 | 876409 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCTGTTTCGCCGGCATGTTTATGTTTTATTGYGCACACTGGCAGACCTA[C/A]GTCTCCGGTACGCTGCGCTTCGGCATGTGAGTATAAAAAAYGAAYACART
Long Flanking Sequence:
CGCTTGAGCATTGATATCGCAATGTGTGTATCCGCAATAGTCAATAATATTATTGACTACTACTGTCGGTAATAGTAATAATATTGAATTGTACGTTAATGCTAAATATTTTGTTTTTGAATGTTAAACGTATTAATACACAGTTTTGTTAAATTTTTACATGCAAAATAACTATTAAATTAGTAACTATTAAATCTATTTTTAGGCAAAGTAGAATATTTCAGTGTGTACATTGGTTCAGAGTAGACAAAGGACATTTTTTCGCATGCAATTTCACCAAATTATCCACAGATGAAATAGTATTTTTGATAAGAAACTACACAACTGTTCATTTGTTAGCTGCTGTATACATCTTTCAGCTCCTTGTTTAACGTGTGTTTCTCAGTGTTCGTGGTTTTGGGCACCAGTATAGCGGTTCAGCTGGGCACTCACCCTGACTGGATGTTCTTCTGCTGTTTCGCCGGCATGTTTATGTTTTATTGCGCACACTGGCAGACCTA[C/A]GTCTCCGGTACGCTGCGCTTCGGCATGTGAGTATAAAAAACGAACACAATTGATTATATAAGTGGATTATTTTGTCGGTAAGGTGTGGTCACATTTAAAGTTCAATAGTCTTCTGCAGAGATTTAAGGGTTGATGTTGGACAATGGATGCATATTCGACAAATTTATAGAAATGAGAAATTAAATTGTGTAATTGTGACATATTTCCCTTAAGAGTTACACAATAGGTAATCGCATTGCTTATGCGCATTGTGCTGTGGTCACACCAGACGCAGAACGCGCGGATAAATCGCTCTACTCGCGCATAAATAGCCGCGTGAACATGTGAGTTTACTCGCTTCATTCGCGCGTGAAATCCGCTTCATTCGCGTGTCAAATTCACTTCAGAACAGAGTCTCGCATGATGGGCTGGGCTTCTGTCTGCCCGGTGACTGTAGCTTCGTTGCTAAAAGGATTTTATGAGCTCTTTTTAATGCTCAATTCGCCCCGCACCATTTGAGC
Associated Phenotype:
Not determined