ZMP
akap9
Ensembl ID:
ZFIN ID:
Human Orthologues:
AC104809.3, CEP110, CEP250, CROCC, GOLGA4
Human Descriptions:
centrosomal protein 110kDa [Source:HGNC Symbol;Acc:1858]
centrosomal protein 250kDa [Source:HGNC Symbol;Acc:1859]
ciliary rootlet coiled-coil, rootletin [Source:HGNC Symbol;Acc:21299]
golgin A4 [Source:HGNC Symbol;Acc:4427]
centrosomal protein 250kDa [Source:HGNC Symbol;Acc:1859]
ciliary rootlet coiled-coil, rootletin [Source:HGNC Symbol;Acc:21299]
golgin A4 [Source:HGNC Symbol;Acc:4427]
Mouse Orthologues:
Cep110, Cep250, Crocc, Golga4
Mouse Descriptions:
centrosomal protein 110 Gene [Source:MGI Symbol;Acc:MGI:1889576]
centrosomal protein 250 Gene [Source:MGI Symbol;Acc:MGI:108084]
ciliary rootlet coiled-coil, rootletin Gene [Source:MGI Symbol;Acc:MGI:3529431]
golgi autoantigen, golgin subfamily a, 4 Gene [Source:MGI Symbol;Acc:MGI:1859646]
centrosomal protein 250 Gene [Source:MGI Symbol;Acc:MGI:108084]
ciliary rootlet coiled-coil, rootletin Gene [Source:MGI Symbol;Acc:MGI:3529431]
golgi autoantigen, golgin subfamily a, 4 Gene [Source:MGI Symbol;Acc:MGI:1859646]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25075 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa29112 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43191 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36744 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25075
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 |
---|---|---|---|---|---|
ENSDART00000110495 | Nonsense | 441 | 2229 | 5 | 30 |
Genomic Location (Zv9):
Chromosome 19 (position 539832)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 561319 |
GRCz11 | 19 | 561128 |
KASP Assay ID:
554-7390.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGCAGAAGGTGGAGGAGCTGACGACTGAATGCAATTCTCTGCACCTT[C/T]AATATGAACAACTTCAGGAGGAGACGAGGGATCACGAGGACATGAAGAAG
Long Flanking Sequence:
TGGAGGAACTGACAGCTGAATCAAACGCACTACGCCTGCAATGTGAACAAGTGCAGGTGGAGACGAGAGATCCAGAGGAGATGAAGCTGAAGATGGAGGAACTGACCAATGAATCCAATACACTACAACTTCAAGATGAACAACTGCAGGGAGGGACGAGAGATCATGAGGAGGTGAAGAACATGGAGGAACTGACAACTGAATGCAATTCTCTGCGCCTTCAATGTGAACAACTGCAGGAAGAGACGAGAGATTATAAGGAGATGAAGCAGAGGGTGGAGGAACTGACCAAAGAATCCAATGCACTACGCCTTCAATATGAACAACTGCAGGAGGAGACGAGAAATCATGAGGAGATGAAGAAGAAGATGGAGGAACTGACCAATGATTCCAATGCACTACGCCTTCAATATGAACAACTGCAGGCGGAGACGAGAGATCATGAGGAGATGAAGCAGAAGGTGGAGGAGCTGACGACTGAATGCAATTCTCTGCACCTT[C/T]AATATGAACAACTTCAGGAGGAGACGAGGGATCACGAGGACATGAAGAAGAAGATAGAGGAGCTGACCAATGAATTCAATACTCTACGCCTGCAATATGACCAACTGCAGGAGGAGACCAGAGATCACGAGAAAATGAAGTTGAAGATGGAGGCGGTGACGACTGAATGCAATACGCTACGCTTACGATACGAGCAGTTGCAAGAGGAGACAAGGGATCATGAGGAGATGGGTAAGAAGATGCAGGAGGTGTCCAATGAATCCAATACACTACGCCTTCAATATGAACAACTGCAGGCAGAGATGAAAGATCACGAGGAGATGAAGCAGAAGATGGAAGGCATGACGACAGAGAGAGACTCTCTGCATCTCCAATATGAACGCCTCCATCAGGAGACTCTTCTGGAGCTGCAGGAGGCGCTGCGGGAGAAAACCGCAGCGTCTGTGGTGATGCAGGCTCAGGTGCAGGCGCTGGAGGAGAGCGCAGCCGCCAGGGTCGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29112
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 |
---|---|---|---|---|---|
ENSDART00000110495 | Nonsense | 477 | 2229 | 5 | 30 |
Genomic Location (Zv9):
Chromosome 19 (position 539940)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 561427 |
GRCz11 | 19 | 561236 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGCTGACCAATGAATTCAATACTCTACGCCTGCAATATGACCAACTG[C/T]AGGAGGAGACCAGAGATCACGAGAAAATGAAGTTGAAGATGGAGGCGGTG
Long Flanking Sequence:
ATGAATCCAATACACTACAACTTCAAGATGAACAACTGCAGGGAGGGACGAGAGATCATGAGGAGGTGAAGAACATGGAGGAACTGACAACTGAATGCAATTCTCTGCGCCTTCAATGTGAACAACTGCAGGAAGAGACGAGAGATTATAAGGAGATGAAGCAGAGGGTGGAGGAACTGACCAAAGAATCCAATGCACTACGCCTTCAATATGAACAACTGCAGGAGGAGACGAGAAATCATGAGGAGATGAAGAAGAAGATGGAGGAACTGACCAATGATTCCAATGCACTACGCCTTCAATATGAACAACTGCAGGCGGAGACGAGAGATCATGAGGAGATGAAGCAGAAGGTGGAGGAGCTGACGACTGAATGCAATTCTCTGCACCTTCAATATGAACAACTTCAGGAGGAGACGAGGGATCACGAGGACATGAAGAAGAAGATAGAGGAGCTGACCAATGAATTCAATACTCTACGCCTGCAATATGACCAACTG[C/T]AGGAGGAGACCAGAGATCACGAGAAAATGAAGTTGAAGATGGAGGCGGTGACGACTGAATGCAATACGCTACGCTTACGATACGAGCAGTTGCAAGAGGAGACAAGGGATCATGAGGAGATGGGTAAGAAGATGCAGGAGGTGTCCAATGAATCCAATACACTACGCCTTCAATATGAACAACTGCAGGCAGAGATGAAAGATCACGAGGAGATGAAGCAGAAGATGGAAGGCATGACGACAGAGAGAGACTCTCTGCATCTCCAATATGAACGCCTCCATCAGGAGACTCTTCTGGAGCTGCAGGAGGCGCTGCGGGAGAAAACCGCAGCGTCTGTGGTGATGCAGGCTCAGGTGCAGGCGCTGGAGGAGAGCGCAGCCGCCAGGGTCGACAGTCTGAGCCGGCGGGTAGAGGAGCTGCAGGAGTGTGTGGAGGAGAAGGACCGGGAGCTCCGAGCCTGCAGGATGAGGGTGGAACAAGCTCAAACTGATGCCCACGGA
Associated Phenotype:
Not determined
Mutation Details
This allele has been removed from public view.
Allele Name:
sa7869
Status:
Allele not cryopreserved
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:
n/a
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110495 | Nonsense | 670 | 2229 | 5 | 30 |
Genomic Location (Zv9):
Chromosome 19 (position 540519)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 562006 |
GRCz11 | 19 | 561815 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAATCTCAGGGAGAAAGTGGCTGCCGTTTTGGTCAGTCAAGCACAACTG[G/T]AAGCYGTTCAGACGCAAACCAAAGAGCTCCAYGCTGAGGCTATAGTAGGC
Long Flanking Sequence:
GATACGAGCAGTTGCAAGAGGAGACAAGGGATCATGAGGAGATGGGTAAGAAGATGCAGGAGGTGTCCAATGAATCCAATACACTACGCCTTCAATATGAACAACTGCAGGCAGAGATGAAAGATCACGAGGAGATGAAGCAGAAGATGGAAGGCATGACGACAGAGAGAGACTCTCTGCATCTCCAATATGAACGCCTCCATCAGGAGACTCTTCTGGAGCTGCAGGAGGCGCTGCGGGAGAAAACCGCAGCGTCTGTGGTGATGCAGGCTCAGGTGCAGGCGCTGGAGGAGAGCGCAGCCGCCAGGGTCGACAGTCTGAGCCGGCGGGTAGAGGAGCTGCAGGAGTGTGTGGAGGAGAAGGACCGGGAGCTCCGAGCCTGCAGGATGAGGGTGGAACAAGCTCAAACTGATGCCCACGGACTGTACGATAAAGTGGCTCAGCTTGAGGACAATCTCAGGGAGAAAGTGGCTGCCGTTTTGGTCAGTCAAGCACAACTG[G/T]AAGCCGTTCAGACGCAAACCAAAGAGCTCCACGCTGAGGCTATAGTAGGCTCCGGAACACAGCTGCAAGAGGGCATCTGGATGCAGGATGATCTAATGGCACAGGTGGGCCTCAGGGTGCAGAAGAGCCTCAGGATGCAGGAGGATTTCACTGTGCAGGAGGGCCTTGAGGTGCAGGAGGGTCGAACGACGCTGGAGGGCCTCACAGTACAGGAGGGTCTCACAATGCTGCCGGGCCTCACAATGCAGGAGGGCTTCAGGGCGCAGGCTAAAGCCTCTGGAGGGAAGGTGAACTTGCTGACGGAGAAGCTGAAGGAGCTGGAGGAGGGCTTGATTGTCATGCAGAAGGACCAGGAGTTGCAGAAGGAGCTGTTGTGTAGCTCTGAGGAGGAGGTGATGGAGTATGAGAGCAGGTTATCCGTCATGATGGACCTGCTCAGCCAGATGAAAACCAAACCCAGCGCTCTCAGACCACTGCCGTCGTCTCAGGTGAGTCTTTGC
Associated Phenotype:
Not determined
Mutation Details
This allele has been removed from public view.
Allele Name:
sa4774
Status:
Allele not cryopreserved
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:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110495 | Nonsense | 780 | 2229 | 5 | 30 |
Genomic Location (Zv9):
Chromosome 19 (position 540850)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 562337 |
GRCz11 | 19 | 562146 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGGAAGGTGAACTTGCTGACGGAGAAGCTSAAGGAGCTGGAGGAGGGCT[T/A]GATTGTCATGCAGAAGGACCAGGAGTTGCAGAAGGAGCTKTTGTGTAGCT
Long Flanking Sequence:
AGAGGAGCTGCAGGAGTGTGTGGAGGAGAAGGACCGGGAGCTCCGAGCCTGCAGGATGAGGGTGGAACAAGCTCAAACTGATGCCCACGGACTGTACGATAAAGTGGCTCAGCTTGAGGACAATCTCAGGGAGAAAGTGGCTGCCGTTTTGGTCAGTCAAGCACAACTGGAAGCCGTTCAGACGCAAACCAAAGAGCTCCACGCTGAGGCTATAGTAGGCTCCGGAACACAGCTGCAAGAGGGCATCTGGATGCAGGATGATCTAATGGCACAGGTGGGCCTCAGGGTGCAGAAGAGCCTCAGGATGCAGGAGGATTTCACTGTGCAGGAGGGCCTTGAGGTGCAGGAGGGTCGAACGACGCTGGAGGGCCTCACAGTACAGGAGGGTCTCACAATGCTGCCGGGCCTCACAATGCAGGAGGGCTTCAGGGCGCAGGCTAAAGCCTCTGGAGGGAAGGTGAACTTGCTGACGGAGAAGCTGAAGGAGCTGGAGGAGGGCT[T/A]GATTGTCATGCAGAAGGACCAGGAGTTGCAGAAGGAGCTGTTGTGTAGCTCTGAGGAGGAGGTGATGGAGTATGAGAGCAGGTTATCCGTCATGATGGACCTGCTCAGCCAGATGAAAACCAAACCCAGCGCTCTCAGACCACTGCCGTCGTCTCAGGTGAGTCTTTGCTGCCTGGTCGCCATGCACGACTAGTGTGAATGATGTTTAGAGGAGTCTCTGGTGTTAGTGTGAGTCCCTGTGGTGTTTGCATGAGTCTCTGTGGTGTTTGCATGAGTCTCTGTGGTGTTTGCATGAATCTCTGTGGTGTTTGCATGAGTCTCTGTGGTGTTTGCATGAATCTCTGGGGTGTTTGCATGAGTCTCTGTGGTGTTTGCATGAATCTCTGGGGTGTTTGCATGAGTCTCTGGGGTGTTTGCATGAGTCTCTGTGGTGTTTGCATGAATCTCTGTGGTGTTTGCATGAATCTCTGGGGTGTTTGCATGAGTCTCTGTGGTGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43191
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110495 | Essential Splice Site | 949 | 2229 | 9 | 30 |
Genomic Location (Zv9):
Chromosome 19 (position 543685)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 565172 |
GRCz11 | 19 | 564981 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGACAGAGAGATGAGTCTGGCTCTGCTGAAGGATCAGCTAAACCGGG[T/C]GAGTGGATATACACCTATAATCATTATAAAGTACATGCAGATACTCATAT
Long Flanking Sequence:
TGTACTTCCAACTGAAACTGAATATTGAGTAGGGGCGGGGCTTAATTTCAGTAGGTTAATGTACTTCCAACTGAAACTGAATATTGAGTAGGTGCGGGGCTTAATTTCAGTTGGTTAGTGTACTTACAACTGGAACAGAAAAATTGTGTAGAGGCGGGGCTTTCTCTAGCACATCATTCCCTTATAGCAAACTAAAGGTAAGAGAGGGTATTGATATGCAGTTGCTATGGAAACCCTCAGGGTGACATCAGCAGAAGGAGCAAATACAAACGCAGAAGCAAATGCTCAGACTTTCATTGAAGATTACCAAAATAAATACATTCCTTCAGTAAATTAACTTGCGCTGATTAATTATTCAGCTTTTGAATAACAACGTGAGCTAGCAGAATAAACAGTGTAGATTTAGATTTCAGACGGACTTTAAAACTGTGTGTGTGTGTGTGTGTGTGCGCAGGACAGAGAGATGAGTCTGGCTCTGCTGAAGGATCAGCTAAACCGGG[T/C]GAGTGGATATACACCTATAATCATTATAAAGTACATGCAGATACTCATATTGTGGACACTTACAGTAAATAATCATCAGTGTTTAGACTTGTTTTTAAGAGTGTTCAGAGTGTATTTGCAGTGGTGTTCATAACAGACCAGTTCTAGGAGATTTCATTGGTTAATTAGCTTAACAATTCAAACATCATGATGTTAATCTGAACAAATATTGACTATTGTGTGACTGTTTATAGAGCTGTTGTACATCAACACTGTGCAGTAAAGCTCCACTAGTTGACATTAAGCTGAACTAAACTCACTTTTATTCATCTTTACTGATGTGAATTTTTATTTAAAGTCTAATCATGCATTCAAGTCATAATCATAATCTGATTACCAGAGTCAGAATTGTTTTATTAAATGCATTTAATAATTAATAACATTTTTAAGTAATAAAATGAACTCATATTAAAGCAGTATATCTATTAAATCAGCTTTTCTCACTGATTTTAATGCATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36744
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 |
---|---|---|---|---|---|
ENSDART00000110495 | Nonsense | 1513 | 2229 | 17 | 30 |
Genomic Location (Zv9):
Chromosome 19 (position 551126)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 572613 |
GRCz11 | 19 | 572422 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCTGAACTGAACCACACTAAACTAGAGCTGGAGAGCGCTCTGAACACA[C/T]AACACACACACCTGAGGGAGCTTGACACACTCAGGTAACGCACACGCGCG
Long Flanking Sequence:
ACACTCATCACTGCGGTCGTCTGTTCTGGGAGTGATGTTTACTTCTGTTCTCATCAGGAATGCTGAGCTCTGATAGGCTGGAGGAGAGGCTGCTGAGCTCTGATAGGCTGGAGGAGAGGCTGCTGAGCTCTGATAGGCCGGAGGAGAGGCTGTTGAGCTCTGATAGGCTGGAGGAGAGGCTGCTGAGCTCTGATAGGCTGGAGGAGAGGCTGCTGAGCTCTGATAGGCTGGAGGAGAGGCTGCTGAGCTCTGATAGGCCGGAGGAGAGGCTGTTGAGCTCTGATAGGCTGGAGGAGAGGCTGCTGAGCTCTGATAGGCCGGAGGAGAGGCTGCTGAGCTCTGATAGGCCGGAGGAGAGGCTGTTGAGCTCTGATAGGCTGGAGGAGAGGCTGCTGAGCTCTGATAGGCCGGAGGAGAGGCTGCTGAGCTCTGATAGGCTGGAGGAGATGAAGTCTGAACTGAACCACACTAAACTAGAGCTGGAGAGCGCTCTGAACACA[C/T]AACACACACACCTGAGGGAGCTTGACACACTCAGGTAACGCACACGCGCGCAATACAATACTTGCAGACATCTGAACGAGCTCAACACACTCCGATAACAAACACACACACACGTACTTGTGACATACACAAACACACACCTTAAAGAGCTGGTAACATGCACACTTTGGTAACACAGATGCAAAACACACACCTGAGGGAGCTCGACACACTCGGGTAACAGACAATAAAATGCAAAACAACACACACACACACACACTCGGATAGCACACACACACACGACACATACACTACAAACATCTGAATATAGTAACATATTCGGGTAACACAGATGCACAACACACACACACACACACTTATGTGACACACACACCTGACAGAGATTGATACACTCAGGTAATACACATATACTTCTTACAAACACACACACACACACCTAAAAGAGCTGGTAACATGCTCACTCAGGGAACACACGTGCACAACACACACACACGCACTTA
Associated Phenotype:
Not determined
Mutation Details
This allele has been removed from public view.
Allele Name:
sa29113
Status:
Less stringent filtering
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:
n/a
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110495 | Essential Splice Site | 1673 | 2229 | 20 | 30 |
Genomic Location (Zv9):
Chromosome 19 (position 553690)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 575177 |
GRCz11 | 19 | 574986 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCTGGGACGCAGAACACACTCCTGGAGGCCGAAGCCACCTGCAGCCAG[G/A]TGAACAAAGACACGCACACATGGACGGAACCAAACCATTGCATTTTTTCC
Long Flanking Sequence:
AGCAACAGCAACACCTTAACAACATCATAGCAATGTTCTAGCAACCACTTGGAACACCCTGGCAACAGCAACACCTTAACAACAGCATAGCATTGTCTTAACAACATTATAACAATGTACTAGCAACCACTTAGAACACCCTAGCAACACCCTTACAACAGCATAGCAACGTATTACAAATACTCGAGCATTACATATATTGTGTTACTGTCACAGCTCAGTGAATGGGTGTTTACAATGATTGTGTGTTTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACAGGTTCAGTTAGACGCTCAGAGGGCTCGATGCGCAGAGCTCAGCGGCGCTCTAGAGAAGGAGAAACAGCTCAACACACAGCTGATCCAGCGCTTCCAGAGCGGCTCCTCAACACACACACTGCCTTCTGGGACGCAGAACACACTCCTGGAGGCCGAAGCCACCTGCAGCCAG[G/A]TGAACAAAGACACGCACACATGGACGGAACCAAACCATTGCATTTTTTCCTATCAAATGAAAAGTTTATCCTGCTCAGCACACACGGTTCATCCATAGCTAAAGTAGCTGCAGGGAAACAGAGCTGCTGATGCGGCACACATCCACAACTGCATGATGCTTATGAGGATTTCTAAGTTCATGAATAAATCTGATGCTGTGTTTGGGCTCAGGTGGAGGCCGGAGTGGAGTCGGTGGAGTCTCTGCTGCAGACGCTGCAGTCTCAGCTGATGGAGAAGCAGACGCAGGTGGTGCAGATGATGGAGGAGATGGAGAAGCAGCAGCTGGAGGCGCTGCAGCACAGAAGACAGAGCCAGGAGGAGAGATCCGCCCTCGCCCGCACCGCGGCTGAGCACCAGAGCGCCCTGCAGACGGCCCGCGAGAGCCTGAGAGAGATGCAGAGTCAGCTGCAGGCGGAGAGAGAGAACGGCAGGAGGATGGAGACGGAGAGAGAGAAACTGC
Associated Phenotype:
Not determined