ZMP
ccdc149a
Ensembl ID:
ZFIN ID:
Description:
Coiled-coil domain-containing protein 149-A [Source:UniProtKB/Swiss-Prot;Acc:Q5XJA2]
Human Orthologue:
CCDC149
Human Description:
coiled-coil domain containing 149 [Source:HGNC Symbol;Acc:25405]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25378 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa34244 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7109 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25378
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112841 | Essential Splice Site | 269 | 463 | 8 | 12 |
ENSDART00000124031 | Essential Splice Site | 218 | 352 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 73944580)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 71133465 |
GRCz11 | 7 | 71374365 |
KASP Assay ID:
554-7380.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCAAGTCCAGTAGCAGATCTCTCACTGGTGTCCTTTCTCCTAAACAAG[G/A]TGCTCAAAAGAAGTGTACTAACAGGAATTGGTTGAAATGTTGTTATTTAG
Long Flanking Sequence:
GCTAATCAAGGTCTTACTTGGTATACTTTAAACATTCAGGCAGGTGTGTTGAGACAAGTTGGAGCTAAATCCTGAAGGGACACCGGCCCTCCAGGACCGAGATTGGTGACCCCTGTTTTAAAGAGTAGTGTTGGAGATTTAGCTCCTCTTTAATCTTCTCATATTTATGACAAACCTTTGAAGTTCTAAAGCAGCTGTGTCCTTGAAAAACATGTGTTAGTGTCATTAGAAACTGATTTGGAAATGACGTTATTTTAATATAGTCAATCATTAACTGATGGGCCGTTCTAAGGCTTGAAACTTCAGGGCTGAAAAGGAGTCCCACTCCGGCCCTGCCAATATGCCTGGATCTACTTTATCCCTAAGTTATTAAAATGTCATTTGCAATATTCCTGTCATTCTGGATGTCTTCTAGACTGCTCTGGATCGAAGAAAAAACCCTGAAATCGGTGGCAAGTCCAGTAGCAGATCTCTCACTGGTGTCCTTTCTCCTAAACAAG[G/A]TGCTCAAAAGAAGTGTACTAACAGGAATTGGTTGAAATGTTGTTATTTAGTGTATTAAATGAGCAATTTTCTCATACACACACTCTGTTTCTGCTGTCTGCAGTGCATGGCTTTCTGTCAGAGGAGAACGGCTGCAGTTTACCAGCAACACCTCAGTCCATCTCAGACCTGAAGTCTTTAGCCACAGCTTTACTGGAGACCATTCATGAGAAGAACATCATCATTCAGCACCAAAGACAGACCAACAGGTGTGCACGTATTTGTGTTTTAATAGGTCGAGATTGTGATACCAACAGTGCCATTGTGGTCCAGTGGTCAGCACGTTGCATTATGACACTGTCGACCCGAGTTTGATCCTCACCTGAGTAATTTCCATTTTTTGTGTTAAGACATATAATACTGTTTGGGTTACTTATATACGTCATAATATACGTTATTCAATGAGAGTATACGCATGACTTTACGGCTTGCGACCTACTAACTATGGTTTGCTTTATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34244
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 |
---|---|---|---|---|---|
ENSDART00000112841 | Nonsense | 431 | 463 | 12 | 12 |
ENSDART00000124031 | Nonsense | 351 | 352 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 73961220)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 71116825 |
GRCz11 | 7 | 71357725 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCTGTCACCCGTGAGGAGAGCGACCCAAGCGGGACACGCACTAATGGA[C/T]AGGTCAGAGCACTTCAGACAACACACTCATATTCACTGAAAGGGGAAGAG
Long Flanking Sequence:
ACCAGTAACCATTGACTTCCATTGTAGGAAAAATGGTTCCTCAATGGTTACAGGTTTCCAACATTCTTCAAAATATCTTCTTTTGGTGTTTAACAGATAAAATAAACTCAAGTGAAGGGAGAGTATTTGTCATATTTTCAGAATTGTGGGTGAAATATCCCTTTAACACTTGAGGTGATCTCTGACTGAATCAATCAACCAAGCAGACTTGAGTAAACCGTTAACCGAGCTCCACTACTGTGGTAGATTACACACGAGCCTCGCGGGATGCGATCATGGCATCAAAACAATGAGCATTAATCTTCTTTGTCCCCTTGATTGGCTCAGATGACAGGACAGGAAGAGGAGGGCCGTCGCTGTGGGAACGGGACACAGCTGGCGATGACAGCTTCCCGAACATGTGGCGCGGTTCCCGGCCCGGTCCAGATGGAGGCGCAGAGGAGGAGGACACACCTGTCACCCGTGAGGAGAGCGACCCAAGCGGGACACGCACTAATGGA[C/T]AGGTCAGAGCACTTCAGACAACACACTCATATTCACTGAAAGGGGAAGAGAAGCTGATTTGTGACTTGTGTGATGTTGATCCTGGACCATCAAGATTATAAATTCACTATTGTTGATCCTGGACCATCAAGATTATAAATTCACTAATGTTGATCCTGGACCATCAAGATTATAAATTCACTATTGTTGATCCTGGACCATCAAGATTATAAATTCACTAATGTTGATCCTGGACCATCAAGATTATAAATTCACTATTGTTGATCCTGGACCATCAAGATTATAAATTCACTAATGTTGATCCTGGACCATCAAGATTATAAATTCACTATTGTTGATCCTGGACCATCAAGATTATAAATTCACTATTGTTGATCCTGGACCATCAAGATTATAAATTCACTATTGTTGATCCTGGACCATCAAGATTATAAATTCACTATTGTTGATCCTGGACCATCAAGATTATAAATTCACTAATGTTGATCCTGGACCATCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7109
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112841 | Nonsense | 441 | 463 | 12 | 12 |
ENSDART00000124031 | None | None | 352 | None | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 73961252)
KASP Assay ID:
554-5226.1 (used for ordering genotyping assays)
KASP Sequence:
GGGACACGCACTAATGGACAGGTCAGAGCACTTCAGACNAACACACTCATA[T/G]TCACTGAAAGGGGAAGAGAAGCTGATTTGTGACTTGTGTGATGTTGATCC
Long Flanking Sequence:
ATGGTTCCTCAATGGTTACAGGTTTCCAACATTCTTCAAAATATCTTCTTTTGGTGTTTAACAGATAAAATAAACTCAAGTGAAGGGAGAGTATTTGTCATATTTTCAGAATTGTGGGTGAAATATCCCTTTAACACTTGAGGTGATCTCTGACTGAATCAATCAACCAAGCAGACTTGAGTAAACCGTTAACCGAGCTCCACTACTGTGGTAGATTACACACGAGCCTCGCGGGATGCGATCATGGCATCAAAACAATGAGCATTAATCTTCTTTGTCCCCTTGATTGGCTCAGATGACAGGACAGGAAGAGGAGGGCCGTCGCTGTGGGAACGGGACACAGCTGGCGATGACAGCTTCCCGAACATGTGGCGCGGTTCCCGGCCCGGTCCAGATGGAGGCGCAGAGGAGGAGGACACACCTGTCACCCGTGAGGAGAGCGACCCAAGCGGGACACGCACTAATGGACAGGTCAGAGCACTTCAGACAACACACTCATA[T/G]TCACTGAAAGGGGAAGAGAAGCTGATTTGTGACTTGTGTGATGTTGATCCTGGACCATCAAGATTATAAATTCACTATTGTTGATCCTGGACCATCAAGATTATAAATTCACTAATGTTGATCCTGGACCATCAAGATTATAAATTCACTATTGTTGATCCTGGACCATCAAGATTATAAATTCACTAATGTTGATCCTGGACCATCAAGATTATAAATTCACTATTGTTGATCCTGGACCATCAAGATTATAAATTCACTAATGTTGATCCTGGACCATCAAGATTATAAATTCACTATTGTTGATCCTGGACCATCAAGATTATAAATTCACTATTGTTGATCCTGGACCATCAAGATTATAAATTCACTATTGTTGATCCTGGACCATCAAGATTATAAATTCACTATTGTTGATCCTGGACCATCAAGATTATAAATTCACTAATGTTGATCCTGGACCATCAAGATTAATTATAAATTCACCATTGTTGATCCTG
Associated Phenotype:
Not determined