ZMP
si:ch73-289a15.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
C3orf63
Human Description:
chromosome 3 open reading frame 63 [Source:HGNC Symbol;Acc:30314]
Mouse Orthologue:
D14Abb1e
Mouse Description:
DNA segment, Chr 14, Abbott 1 expressed Gene [Source:MGI Symbol;Acc:MGI:1921694]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12409 | Nonsense | Available for shipment | Available now |
sa17870 | Nonsense | Available for shipment | Available now |
sa24294 | Essential Splice Site | Available for shipment | Available now |
sa43946 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31086 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32438 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12409
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009092 | Nonsense | 286 | 1827 | 7 | 23 |
ENSDART00000137026 | Nonsense | 67 | 1608 | 4 | 20 |
Genomic Location (Zv9):
Chromosome 23 (position 19771647)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 19556754 |
GRCz11 | 23 | 19483097 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAATGTCCTGTTATTCTAATTGTTGTGTTTCATTMCAGCAATAYTTTTA[T/A]GAATTTGCATATGATGAGCTCAAGTCAAGGCCTAGACATGTGTTGCCATA
Long Flanking Sequence:
TTGGATTACCCTAGGGCTTGTTTTTGTGTCTCACAGAACGTCACCCCAAGTAACTCTTCCATCCTTTTCTATTTTTAGGGGTTTACCTTTCGAAATACTCTGATTTGTTACAAATGAATCCATTTGAAGTAGGTGCTGCAGGAGAGATAATATTATTTAAAGTCATGAAGGTAAGGAGGTATAACAGCTAGAGTTATCAAGCATTAAATGTAATTTATTTTAATTTCAATGCATAGTTTCACAATAGTAAAAACCAATCAACTTTTTTTTTTCTGCAGGGTAAAGTGAAGATAATTGAGAATATTCCTAAAAATACTCTTGAGCCCACCCTTAAATATGACAGCCATGTGTACAAAAATGCCAGCAAAGTGACCTCATTATTATCCTACCGAGCCTTTGAGCACACTCAGGTAAGTGTTTTTTGTAACCTTTTATTTTGTCTTGTTTGCTAAAATGTCCTGTTATTCTAATTGTTGTGTTTCATTCCAGCAATACTTTTA[T/A]GAATTTGCATATGATGAGCTCAAGTCAAGGCCTAGACATGTGTTGCCATACGCGGTTGTGTCTTTTCAATACAAAGGCAAAGAATCGAGCATTGGCACACACAGGTATGAATTAATTTATTGATAATGTACATAGAAATTGTAACAAACATTTTTGGTTTAATCTAAATTTCACTCCTTTTCTCTTGTAGCAGAGTAAACAGCATGTTACATGAGGGACAAAGAGGTATGATTTGTATTTATCACCATAGATCTCTAAAGAGATAATTTAATACAGTGCTGTACACCCTCACAGCTCACTCTTAAGTCTATATTTTCTTATAGGATGCTTTAAAATAATATATTTGTGCATATACATTACATTAGTCTGTACCAAGGACAAAACTGAAACTAATTAAGCAAAAAATCTTGAGATCACAATTCAAAAATTAGTACACCCAAATGATTGTTGAAGGAAAAATAATAAATAAAGAGGACAAATCTAGAGAAACATAAAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17870
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009092 | Nonsense | 436 | 1827 | 11 | 23 |
ENSDART00000137026 | Nonsense | 217 | 1608 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 23 (position 19769885)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 19554992 |
GRCz11 | 23 | 19481335 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTAAACAGGAAAACAGCCWCACGGGACTGCTGCAACGGCTTGAGAGAGAA[A/T]GAATGGTGAGCTAATTCACACCCTGCTTTACGCWTTGATACAATTAATKC
Long Flanking Sequence:
AGCCTTTAAATGTCACTTAAAACTGTATAGAAGTGTCATGAAATATATCTAGTAAATATGATGTACTGTCATTATGGCAAAGATAAAATAAATCAGTTATTAGAAATAAGTTATTAAAACTATTATGTTTAGAAATGTGTTGAAAAAACTGGGCTAATAATTCTGACTTCAACTGTTAATTTCATGGGTTTAAATGTCTTTTTTTTTATTTTTCAGCCCAGACAAGCTTGACATCAATACGGCTATGCATCTGGATCAAGTGAAGCGAAAGATCCCACCTGTTTTGCTGTCGTGGGAAGCGTACAGTGGAGCACGAGAAGGTAGAATGAACCCCAATGATGCTTTTCAGCCCAACACCTGGTTGTTGATATTGATGTGGTAATGTGTTGTGGTATTTTGCAGTGCTGAAGTGTGGGATGCACTGTAGCCTGTATGAGGTCATGGGGAAGAGTAAACAGGAAAACAGCCTCACGGGACTGCTGCAACGGCTTGAGAGAGAA[A/T]GAATGGTGAGCTAATTCACACCCTGCTTTACGCTTTGATACAATTAATGCCTGCAGCTTTACTCTAGCCGAGCTTCACCTCCCACCCTCTCGTCTCCGTGCTGTATCATAATAGAATCTGTGTCAGCGATCTGATATGCACAAGTTAAACTGCCGATGTTTTATTATAGGCATACTATAATTAAACTCTTCACTCTAGGTTTTGGTGAAGCCATTGGTAGACAAAGGATTTCTCTTCCTCCTTTCGTCCTCTCAGTTGTTCACTAGCATGGGTAGGTTTACACACAGCCTTTAAACTCATATGTGGCTGCTGGAATTGCTGTTGGATAACAGAGTCTATTTCTTGTTTCTCTAAAGAGCGACGGGGAAGAAGTGACAGGGTGTTACAGGCGCTTTTTATCTTTCAAGAGCAAAGAAGCATCTCGAAGTTGAGTAAGTGCCTCTAATGTTTTTTTTCTCCCCACACTTACTTTAACTTGTTTTCAATAGCCAAGTTAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24294
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 |
---|---|---|---|---|---|
ENSDART00000009092 | Essential Splice Site | 437 | 1827 | 11 | 23 |
ENSDART00000137026 | Essential Splice Site | 218 | 1608 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 23 (position 19769878)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 19554985 |
GRCz11 | 23 | 19481328 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAAACAGCCTCACGGGACTGCTGCAACGGCTTGAGAGAGAAAGAATGG[T/C]GAGCTAATTCACACCCTGCTTTACGCTTTGATACAATTAATGCCTGCAGC
Long Flanking Sequence:
AAATGTCACTTAAAACTGTATAGAAGTGTCATGAAATATATCTAGTAAATATGATGTACTGTCATTATGGCAAAGATAAAATAAATCAGTTATTAGAAATAAGTTATTAAAACTATTATGTTTAGAAATGTGTTGAAAAAACTGGGCTAATAATTCTGACTTCAACTGTTAATTTCATGGGTTTAAATGTCTTTTTTTTTATTTTTCAGCCCAGACAAGCTTGACATCAATACGGCTATGCATCTGGATCAAGTGAAGCGAAAGATCCCACCTGTTTTGCTGTCGTGGGAAGCGTACAGTGGAGCACGAGAAGGTAGAATGAACCCCAATGATGCTTTTCAGCCCAACACCTGGTTGTTGATATTGATGTGGTAATGTGTTGTGGTATTTTGCAGTGCTGAAGTGTGGGATGCACTGTAGCCTGTATGAGGTCATGGGGAAGAGTAAACAGGAAAACAGCCTCACGGGACTGCTGCAACGGCTTGAGAGAGAAAGAATGG[T/C]GAGCTAATTCACACCCTGCTTTACGCTTTGATACAATTAATGCCTGCAGCTTTACTCTAGCCGAGCTTCACCTCCCACCCTCTCGTCTCCGTGCTGTATCATAATAGAATCTGTGTCAGCGATCTGATATGCACAAGTTAAACTGCCGATGTTTTATTATAGGCATACTATAATTAAACTCTTCACTCTAGGTTTTGGTGAAGCCATTGGTAGACAAAGGATTTCTCTTCCTCCTTTCGTCCTCTCAGTTGTTCACTAGCATGGGTAGGTTTACACACAGCCTTTAAACTCATATGTGGCTGCTGGAATTGCTGTTGGATAACAGAGTCTATTTCTTGTTTCTCTAAAGAGCGACGGGGAAGAAGTGACAGGGTGTTACAGGCGCTTTTTATCTTTCAAGAGCAAAGAAGCATCTCGAAGTTGAGTAAGTGCCTCTAATGTTTTTTTTCTCCCCACACTTACTTTAACTTGTTTTCAATAGCCAAGTTAACAACTGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43946
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 |
---|---|---|---|---|---|
ENSDART00000009092 | Nonsense | 486 | 1827 | 13 | 23 |
ENSDART00000137026 | Nonsense | 267 | 1608 | 10 | 20 |
ENSDART00000009092 | Nonsense | 486 | 1827 | 13 | 23 |
ENSDART00000137026 | Nonsense | 267 | 1608 | 10 | 20 |
Genomic Location (Zv9):
Chromosome 23 (position 19769456)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 19554563 |
GRCz11 | 23 | 19480906 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGTTACAGGCGCTTTTTATCTTTCAAGAGCAAAGAAGCATCTCGAAGT[T/A]GAGTAAGTGCCTCTAATGTTTTTTTTCTCCCCACACTTACTTTAACTTGT
Long Flanking Sequence:
TGTATGAGGTCATGGGGAAGAGTAAACAGGAAAACAGCCTCACGGGACTGCTGCAACGGCTTGAGAGAGAAAGAATGGTGAGCTAATTCACACCCTGCTTTACGCTTTGATACAATTAATGCCTGCAGCTTTACTCTAGCCGAGCTTCACCTCCCACCCTCTCGTCTCCGTGCTGTATCATAATAGAATCTGTGTCAGCGATCTGATATGCACAAGTTAAACTGCCGATGTTTTATTATAGGCATACTATAATTAAACTCTTCACTCTAGGTTTTGGTGAAGCCATTGGTAGACAAAGGATTTCTCTTCCTCCTTTCGTCCTCTCAGTTGTTCACTAGCATGGGTAGGTTTACACACAGCCTTTAAACTCATATGTGGCTGCTGGAATTGCTGTTGGATAACAGAGTCTATTTCTTGTTTCTCTAAAGAGCGACGGGGAAGAAGTGACAGGGTGTTACAGGCGCTTTTTATCTTTCAAGAGCAAAGAAGCATCTCGAAGT[T/A]GAGTAAGTGCCTCTAATGTTTTTTTTCTCCCCACACTTACTTTAACTTGTTTTCAATAGCCAAGTTAACAACTGATTTGTATCTTACTTTTAAGTTTCCAAAAACTCCGGAGTGGAGGAGGACCCTCTTGTTCCATTGGAGCCGAAAGACGCAGTCATCCATCAGCTTGACACTTTTGTACCTGCCCTGCATCATTGCTTCTATAAACTACGTGCCAATCCCCCCAAAGAACTTGCAGCAGGGGTGAAACGGCAGGCACTGGACTACCTCAGTCAGAAGGAGCAAGGTGCTTTACGGCCTTTTCACATCGCAGAGTACCGGCACACTTTGGATGACCGGACCAGCCAACACCTTGCACCTCGACCTAAGAATATAGATGTGGTGCTGAAATCATACGTGTACAGTCCGGGGCACTTCCAGCTCCCAGTGGAGGTACTACAGCAAGGCCTAATGGACAGCCAACAAGCAGAAGCATCTCCCCCTGCGGGTGCAGAAGAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31086
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 |
---|---|---|---|---|---|
ENSDART00000009092 | Nonsense | 486 | 1827 | 13 | 23 |
ENSDART00000137026 | Nonsense | 267 | 1608 | 10 | 20 |
ENSDART00000009092 | Nonsense | 486 | 1827 | 13 | 23 |
ENSDART00000137026 | Nonsense | 267 | 1608 | 10 | 20 |
Genomic Location (Zv9):
Chromosome 23 (position 19769456)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 19554563 |
GRCz11 | 23 | 19480906 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGTTACAGGCGCTTTTTATCTTTCAAGAGCAAAGAAGCATCTCGAAGT[T/A]GAGTAAGTGCCTCTAATGTTTTTTTTCTCCCCACACTTACTTTAACTTGT
Long Flanking Sequence:
TGTATGAGGTCATGGGGAAGAGTAAACAGGAAAACAGCCTCACGGGACTGCTGCAACGGCTTGAGAGAGAAAGAATGGTGAGCTAATTCACACCCTGCTTTACGCTTTGATACAATTAATGCCTGCAGCTTTACTCTAGCCGAGCTTCACCTCCCACCCTCTCGTCTCCGTGCTGTATCATAATAGAATCTGTGTCAGCGATCTGATATGCACAAGTTAAACTGCCGATGTTTTATTATAGGCATACTATAATTAAACTCTTCACTCTAGGTTTTGGTGAAGCCATTGGTAGACAAAGGATTTCTCTTCCTCCTTTCGTCCTCTCAGTTGTTCACTAGCATGGGTAGGTTTACACACAGCCTTTAAACTCATATGTGGCTGCTGGAATTGCTGTTGGATAACAGAGTCTATTTCTTGTTTCTCTAAAGAGCGACGGGGAAGAAGTGACAGGGTGTTACAGGCGCTTTTTATCTTTCAAGAGCAAAGAAGCATCTCGAAGT[T/A]GAGTAAGTGCCTCTAATGTTTTTTTTCTCCCCACACTTACTTTAACTTGTTTTCAATAGCCAAGTTAACAACTGATTTGTATCTTACTTTTAAGTTTCCAAAAACTCCGGAGTGGAGGAGGACCCTCTTGTTCCATTGGAGCCGAAAGACGCAGTCATCCATCAGCTTGACACTTTTGTACCTGCCCTGCATCATTGCTTCTATAAACTACGTGCCAATCCCCCCAAAGAACTTGCAGCAGGGGTGAAACGGCAGGCACTGGACTACCTCAGTCAGAAGGAGCAAGGTGCTTTACGGCCTTTTCACATCGCAGAGTACCGGCACACTTTGGATGACCGGACCAGCCAACACCTTGCACCTCGACCTAAGAATATAGATGTGGTGCTGAAATCATACGTGTACAGTCCGGGGCACTTCCAGCTCCCAGTGGAGGTACTACAGCAAGGCCTAATGGACAGCCAACAAGCAGAAGCATCTCCCCCTGCGGGTGCAGAAGAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32438
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009092 | Nonsense | 911 | 1827 | 17 | 23 |
ENSDART00000137026 | Nonsense | 692 | 1608 | 14 | 20 |
Genomic Location (Zv9):
Chromosome 23 (position 19767175)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 19552282 |
GRCz11 | 23 | 19478625 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTGATGGAGGCACAGCATATAATCTACAACTCACAGCCTCCTTTGCCA[C/T]GAAATGAGGACCTGACCATACGATCCAGTCCCGCATTCTCACCTTTTGTC
Long Flanking Sequence:
ACAGTGTTTATTTTAAATAGAAGCCTTTTCTATTATTACAAATATCTAATATCTATTTTGTCAACGTTGGTCAAATTAATTAGACCAGTAGTGCCCAAACTCTTGGAGGGCCAATGTCTTGCAGAGTTTAGCTTCAACTTGCTTCAATACACCTGCCAGGATGCTCTTAATATGCTTGTTAGATCTTGATTAGTTGGTTCAGGTGTGTCTAATTTTGGTTTGAGCTAAACTCTGCAGAACATCGGCCTTCTAGCACCTGAATTAGACCTTGCCAAATCTTTGCTAAGTTCTTTGAACTTACTTTGACAAATAAAAATATGCTTTTTTTTTTTTTAGATGGTGTTGTTGAACCTTGTCTGAGCGAATCAGAGAAGCCAGTACAATGCCTGGGGAAAGTAGTGGACACTATTCTTGACCGTGAATTTCAGAACCTGTGCACAGGGATCCATAAATTGATGGAGGCACAGCATATAATCTACAACTCACAGCCTCCTTTGCCA[C/T]GAAATGAGGACCTGACCATACGATCCAGTCCCGCATTCTCACCTTTTGTCTCCAAATATGTTACTCCGCTGCCTGTGCAGGGCTACGTTAAAACTCTCTGTGAAAAGATGAACCATCTGATTCATTCTCCTAGTGTGTCTTTAGAACATGTGGCCATCGCAACACCACCTGCTGTTGTCCCAGTGCCTGCCCCCTTACCACCTGCTCCACCTCCTTTTGCCATTCCGGCTCCTGCCCAGCCCAAACTGCCCTCACCTCCTGCTCAACCTCGCACTAAAACATTATCTCCAGTGCCTAAGTCTAAGGCTTCATCAAGCAAGCCACAAACTACAGTTAAGCAACCTTCTTCAGGCAAACATCGCCTAGGTACTGTCAAAGAGGTCCACCTGTTTCAACCTGAAAAATCAGCTGATCCCAAGGGTACAGATATTGTAGAAACTTCTGTCTCAGAGTTATCCGCAGAATCTTCTCTGGCAGGAACATCAAGCACTGTTATTGGG
Associated Phenotype:
Not determined