Busch Lab

ZMP

sdccag8

Ensembl ID:
ENSDARG00000078947
ZFIN ID:
ZDB-GENE-090313-318
Description:
Novel protein similar to vertebrate serologically defined colon cancer antigen 8 (SDCCAG8) [Source:U
Human Orthologue:
SDCCAG8
Human Description:
serologically defined colon cancer antigen 8 [Source:HGNC Symbol;Acc:10671]
Mouse Orthologue:
Sdccag8
Mouse Description:
serologically defined colon cancer antigen 8 Gene [Source:MGI Symbol;Acc:MGI:1924066]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa38924 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa15391 Nonsense Available for shipment Available now
sa18223 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa38924
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114911 Essential Splice Site 524 701 14 18
ENSDART00000131320 None None 86 None 4
ENSDART00000134398 Essential Splice Site 446 524 14 15
ENSDART00000134888 None None 101 None 6
ENSDART00000137816 None None 197 None 8
ENSDART00000148100 None None 186 None 7
Genomic Location (Zv9):
Chromosome 13 (position 10685010)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 10987339
GRCz11 13 11119814
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTGTTTTCTTGCTCTCTCTCTCTCTCTCTTTCTCTCTCTCACTCTGC[A/T]GGCAGGAGAAGGAGGCATCAGAACGCTGCTGTGGTGAGGACATGGCCGCT
Long Flanking Sequence:
TTGGTCCCGCCCTGACTCGTCAGCGCTACCAAGCCGAAACAATCACAGAGTTTGCACTAAGTGTCGTTGCGACGTGTAGTTACATTTTGTGAGAGGTGTGTGTCAGCGACGCTGACGACCACAGGGTAGGGCTATGCGACAACCTGTAGGCTGCGCCCTAGCATACACGTGCGCTTGACGCAGAAGTATAAATCAGCCTTTATTGCGCCGGGTGTATGACAGGGCCCTCTGACTCTTAACTCATAGCATTATTCTGTTTGTATAAGCATCCTGGTCCAGTCCAGCATAGCAGGTTTTTTAAAAAAAATTCTGACCAATGACAGAGGGGAGTGACCAGGAAACCTGTTTTGAACCTTAAATTTTGCAAGACCATTTGGTGACGCTAGTGGCCCAGAAATCTCTCTCTTTAAGCAGCTCTTCATGTGCATGACTGATCTACATGTGTTTGACTCTCTGTTTTCTTGCTCTCTCTCTCTCTCTCTTTCTCTCTCTCACTCTGC[A/T]GGCAGGAGAAGGAGGCATCAGAACGCTGCTGTGGTGAGGACATGGCCGCTCTGACCTTCCAGGCACAGCGGCGCGAACGTGAGCTGACACAGACGCTCCAGCAAATGGAGGCGCAGCACGAAAAGAGTGGTGGGTGTTCGCCGGTGTACTGCCCCTTTGCCAGAACAAGCGCCTCTCCCGCCCTTCCGCCTGCCTCACCCCCGCATGCTCCGAGCGTGAGCCACACTGTGCGGGACGGCATCAGGAACACCTGTAACCTTTGGCTGGCCGAAGGGAGCAGATGCTCGGCGCTCCAGAGCTTCGGCGCTACGTATTAGTTAGCGTTTAAAAATGGGGGGGAGGCGGGCTAGCGCTGCCCACTGTCTGCTGATTTCAGAGTGCTGCTCTCACATCTGTTGCACCATCTGGATGGGCGAGTTTAGTTTATTTACCTGTGTTTCCAGAAACTTGAGGCATGCTGATTGCCAGAACAAAGCACGGAGAAAACAAAGGGCTTCTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15391
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114911 Nonsense 533 701 14 18
ENSDART00000131320 None None 86 None 4
ENSDART00000134398 Nonsense 455 524 14 15
ENSDART00000134888 None None 101 None 6
ENSDART00000137816 None None 197 None 8
ENSDART00000148100 None None 186 None 7
Genomic Location (Zv9):
Chromosome 13 (position 10685039)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 10987368
GRCz11 13 11119843
KASP Assay ID:
2260-6119.1 (used for ordering genotyping assays)
KASP Sequence:
TCTTTCTCTCTCTCACTCTGCAGGCAGGAGAAGGAGGCATCAGARCGCTG[C/A]TGTGGYGAGGACATGGCCGCTCTGACCTTCCAGGCACAGCGGCGCGAAMG
Long Flanking Sequence:
CAAGCCGAAACAATCACAGAGTTTGCACTAAGTGTCGTTGCGACGTGTAGTTACATTTTGTGAGAGGTGTGTGTCAGCGACGCTGACGACCACAGGGTAGGGCTATGCGACAACCTGTAGGCTGCGCCCTAGCATACACGTGCGCTTGACGCAGAAGTATAAATCAGCCTTTATTGCGCCGGGTGTATGACAGGGCCCTCTGACTCTTAACTCATAGCATTATTCTGTTTGTATAAGCATCCTGGTCCAGTCCAGCATAGCAGGTTTTTTAAAAAAAATTCTGACCAATGACAGAGGGGAGTGACCAGGAAACCTGTTTTGAACCTTAAATTTTGCAAGACCATTTGGTGACGCTAGTGGCCCAGAAATCTCTCTCTTTAAGCAGCTCTTCATGTGCATGACTGATCTACATGTGTTTGACTCTCTGTTTTCTTGCTCTCTCTCTCTCTCTCTTTCTCTCTCTCACTCTGCAGGCAGGAGAAGGAGGCATCAGAACGCTG[C/A]TGTGGTGAGGACATGGCCGCTCTGACCTTCCAGGCACAGCGGCGCGAACGTGAGCTGACACAGACGCTCCAGCAAATGGAGGCGCAGCACGAAAAGAGTGGTGGGTGTTCGCCGGTGTACTGCCCCTTTGCCAGAACAAGCGCCTCTCCCGCCCTTCCGCCTGCCTCACCCCCGCATGCTCCGAGCGTGAGCCACACTGTGCGGGACGGCATCAGGAACACCTGTAACCTTTGGCTGGCCGAAGGGAGCAGATGCTCGGCGCTCCAGAGCTTCGGCGCTACGTATTAGTTAGCGTTTAAAAATGGGGGGGAGGCGGGCTAGCGCTGCCCACTGTCTGCTGATTTCAGAGTGCTGCTCTCACATCTGTTGCACCATCTGGATGGGCGAGTTTAGTTTATTTACCTGTGTTTCCAGAAACTTGAGGCATGCTGATTGCCAGAACAAAGCACGGAGAAAACAAAGGGCTTCTTTCTGGCGCGGCTGCACGGCACACATGTTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18223
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114911 Essential Splice Site 603 701 None 18
ENSDART00000131320 None None 86 None 4
ENSDART00000134398 None 525 524 None 15
ENSDART00000134888 None None 101 None 6
ENSDART00000137816 None None 197 None 8
ENSDART00000148100 None None 186 None 7
Genomic Location (Zv9):
Chromosome 13 (position 10689005)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 10991334
GRCz11 13 11123809
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATGTCACACACTCGGGGCAAAGCTGGAGGAACTGGCTCAGAGCAGCAGG[T/C]ATGTTGCACTTTCATTTAAGMTCACGTATACCAYTAWAACAAGGTTGAAG
Long Flanking Sequence:
TTCAATGTCATTTTTTCAAACAAGTTATTTTGTGAGAGTAGTCATGTCAGGTGTTCTTCCACTAATATCCCAGATGCACTTTTGTGTCATCTCAAATCATTCTGAAAGTCAGGTTTCACACAGACCTGTGGAGTTCATGTTTCTTAAGGTAAAGTAGAAAACGCATAAATAATAGGCCTTACATAAATTTAAAATCCATATTATGATTAAATAAATGACATAAAAATAACCCCATTTTCTGGTTTCTGAGTTTGACACATGACCTTGAACCCTTTTAGGGCTAAGAAGAGCATCAATGTTTTGTGTTGCTGTACCTGTGTTATATAAAGCATGTATTTCAGCACATCTGTGTTTGCTGTGTTAATGAGTCAATACTTGATCTGTTCACAGTCAGAGAAACAGATGCTCTGCTGAGTGCTCAGAACAGCCTGATCAGGAAACTGAAGGAGGAATGTCACACACTCGGGGCAAAGCTGGAGGAACTGGCTCAGAGCAGCAGG[T/C]ATGTTGCACTTTCATTTAAGATCACGTATACCACTATAACAAGGTTGAAGAATGGAGGAGGTGGGAATTGACAAATGATGAATGCAAGATTTAATTGTCAAGCAAATATATAACACAATGAAAGTTGCCCCCCAGCCTTTTGTAGAACTTTAATGTGGCACACAGGTTTCTGCTTACTTTGCTTTCTACCCTACACCTCTCAAAACATCTTTATTTAAATTCAGTACAAAGTCAAATGCAATGCAAAACCCACATTTGTGGTCACACAAGACTTTTTATTCCATTGACTTTTATTCATACTTATACGAACGAATGCATCAGACCAGAAATGAAGGTCTATGCGCAGATATTTTACTGTGTAGCAAAGCTGAAGTTTAGTGAATACTGACCTGTGAATTTGTGTCACGTAATTTTGTGAGACTCAGTGGAACATCAAAACATGAGCACTCAGTCCAGAAATGTAAAACATAAATCAAACAATTGTTTATTGTGGTAATGAC
Associated Phenotype:
Not determined