ZMP
txlng
Ensembl ID:
ZFIN ID:
Description:
gamma-taxilin [Source:RefSeq peptide;Acc:NP_001037776]
Human Orthologues:
CYorf15A, CYorf15B, TXLNG
Human Descriptions:
chromosome Y open reading frame 15A [Source:HGNC Symbol;Acc:18473]
chromosome Y open reading frame 15B [Source:HGNC Symbol;Acc:18577]
taxilin gamma [Source:HGNC Symbol;Acc:18578]
chromosome Y open reading frame 15B [Source:HGNC Symbol;Acc:18577]
taxilin gamma [Source:HGNC Symbol;Acc:18578]
Mouse Orthologues:
Gm8258, Txlng
Mouse Descriptions:
predicted gene 8258 Pseudogene [Source:MGI Symbol;Acc:MGI:3644429]
taxilin gamma Gene [Source:MGI Symbol;Acc:MGI:3590652]
taxilin gamma Gene [Source:MGI Symbol;Acc:MGI:3590652]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41795 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41795
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103449 | Nonsense | 362 | 468 | 9 | 9 |
ENSDART00000104143 | Nonsense | 383 | 489 | 9 | 9 |
ENSDART00000121539 | None | None | 355 | None | 8 |
ENSDART00000124936 | Nonsense | 383 | 489 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 11 (position 12843581)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 12727990 |
GRCz11 | 11 | 12785649 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAATTAGTTTTAAAGTCCCTGTTTTCATTTGTCTTGAAGAAAACAGTG[C/T]GAGACAAAAATTACAAGGCCCTCCAAGGTAAACTGGATCGTCTGGAGAAG
Long Flanking Sequence:
GCTTCAGATAACTCGAAACAGCAACCACAAGTCTCTCCTTCATCTTCAAAAGTCTCCATAGTCATCTTGACTACACAAACACTGCTGTCACCTCAGTGAAAACCCCCGCTTCTGCTTTCATTTGATTGGAGAATTAAAAGTTTATGTGAGGGAGAATTAAAAATATGCGACACTGCACTTTTTCCGCTCATAGTTGACGTTTTTTCAACGGTGGGCTCAACAGCAATAACTCGAAGAGCAGCATGTGGTTAAAATGCTTCCATGCTGTGCAGGTCTCACAATGTGAAAAACGCTCCTGGCCATTAGTAAATTACTCAAAGGCGCCTCTCAACGCAAAAAAATGTGTTCGGTGTGATCGGCTACTTATGATGTCTTTTAAGCTCTAAACACACACAAAAAAGAAAAGAGCTATAAGTATATCAGTGCCTTTACTCAAACCTTTGAATATTTCAGAATTAGTTTTAAAGTCCCTGTTTTCATTTGTCTTGAAGAAAACAGTG[C/T]GAGACAAAAATTACAAGGCCCTCCAAGGTAAACTGGATCGTCTGGAGAAGCTCTGCAGGGCCCTGCAGCGAGAGCGCAACGACCTAAACCAGAAACTCCGAGTACTTCAGGGCCCTGCAAAAGATCCTGAGGAAGAGGGTACTGGACCTCCAGACCCCCAGCCGGAGGAGCTGTCTAACCCAGAGCTGGAAAGAGAGGTGGAGGGAGAGGTGGAGAGAGAAGTAGAGGGAGAGATGGAGGCTTTGGTGCCTGAAACAGAGAAAGTCGGTCTTCAGCCTGACGATTCGAGCAGCACATCATCCACACAACTTATTGACGACTGAGCCTGGCCTTCTGGTGGCCTTTCTTTTTTTGTGGAGGTATATATTTTTGTCTAACAATTATTATCATAAAGTTTGTGAGGAAAAAGCAGGACATTAGTGAAGACGCTAACTGCTCTATACGTTGATAATCCGCTTTGTGGCGAGCACTTTTTACTCCCTATTTTCTATCACATTGTA
Associated Phenotype:
Not determined