ZMP
epha2
Ensembl ID:
ZFIN ID:
Description:
ephrin type-A receptor 2 [Source:RefSeq peptide;Acc:NP_571490]
Human Orthologue:
EPHA2
Human Description:
EPH receptor A2 [Source:HGNC Symbol;Acc:3386]
Mouse Orthologue:
Epha2
Mouse Description:
Eph receptor A2 Gene [Source:MGI Symbol;Acc:MGI:95278]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
hu3575 | Nonsense | Available for shipment | Available now |
sa1266 | Essential Splice Site | Available for shipment | Available now |
sa33949 | Nonsense | Available for shipment | Available now |
sa40777 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44642 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33948 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20802 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
hu3575
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 |
---|---|---|---|---|---|
ENSDART00000025428 | Nonsense | 371 | 984 | 5 | 17 |
ENSDART00000136964 | None | None | 52 | None | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 45825020)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 45885954 |
GRCz11 | 6 | 45887836 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGACGTCACATACAGTGTGGCATGCGAGCGCTGTGAGGGTGGTCTGTG[T/A]ACGCTGTGTGGCGGAAGGGTGCGATTCGAGCCTGCGCAGACGGCCTTGAG
Long Flanking Sequence:
GAATTTAAATTATTGTGTGAACTATCCCTTTAATACAATGTGTAAATGTTATCTGTATTGTTTTAATTCATTAAATGTCTCATCATGTTCAACATTTCTTCGTGTCTACAGCTTGTGAACCGGGTTTCTACAAGAGCACTGATTCCAGCCAGCCTTGTGAAGTGTGTCCAGAAAACACCCAACGTTCGGGACGGGGAGCACTGTTGTGCCCCTGCATGGAGGGTTTCTACCGGGCTCCTACAGACCTAAACTCTGCTCCTTGCTCTTGTAAGTTTAAATCTTCATTCTGAAAAGTTCATTCTGAAACTACTGACCTAATTCTCAAACATTTTACACTGCTCTGCTTCTCTAGCTCTTCCTAGCCCACCCCGAGACCTGGTTTACACTCCTCTCCTGACAGCAGGAAGTTTGCAGCTGCTTTGGCGCCCACCGGCAGACACTGGTGGTCGGAGTGACGTCACATACAGTGTGGCATGCGAGCGCTGTGAGGGTGGTCTGTG[T/A]ACGCTGTGTGGCGGAAGGGTGCGATTCGAGCCTGCGCAGACGGCCTTGAGAGCCCCTGAGGTTGTGGTTAGCGAGCTGGAGCCTCATGTGAACTACACTTTTACAGTCGAGGCCCAAAATGGCGTCTCCCAGTTCAGTCGAAAGAGAGCCATGGCTAGCATCACAACAGTGCTTCACTTCACAGGTTAGATTTTGCATATAAAGCTATTGTAATGCCTAAATCACAGCTAATCACATTTAATTTGATGCTACTTGAAGCTGAGTTTTGTACCAGCGTGGGTAATTGTGGGCGGAGCTAGCTTGTGAGCTTCATTGCTTGTCACGGCTGGAGAAGATTAACAGATTAGTAAGGAGGGGAATTGACAACATGTCATGCCTGCTTAAGACATGGCGTATCAAATTCTGTTCACTTGTAATCTGTTTCGTTGATGGTTTTAGCCAAAATACTGATGACTGCTTGTGCTTCTGTTGTTCAGATGGCCCGAGGGTGCTGTACTTGA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa1266
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025428 | Essential Splice Site | 433 | 984 | 6 | 17 |
ENSDART00000136964 | None | None | 52 | None | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 45824545)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 45885479 |
GRCz11 | 6 | 45887361 |
KASP Assay ID:
554-1181.1 (used for ordering genotyping assays)
KASP Sequence:
GTTGATGGTTTTAGCCAAAATACTGATGACTGCTTGTGCTTCTGTTGTTC[A/T]GATGGCCCGAGGGTGCTGTACTTGAGAGTTGAAGATCGGACCACCAGYAG
Long Flanking Sequence:
GCGAGCGCTGTGAGGGTGGTCTGTGTACGCTGTGTGGCGGAAGGGTGCGATTCGAGCCTGCGCAGACGGCCTTGAGAGCCCCTGAGGTTGTGGTTAGCGAGCTGGAGCCTCATGTGAACTACACTTTTACAGTCGAGGCCCAAAATGGCGTCTCCCAGTTCAGTCGAAAGAGAGCCATGGCTAGCATCACAACAGTGCTTCACTTCACAGGTTAGATTTTGCATATAAAGCTATTGTAATGCCTAAATCACAGCTAATCACATTTAATTTGATGCTACTTGAAGCTGAGTTTTGTACCAGCGTGGGTAATTGTGGGCGGAGCTAGCTTGTGAGCTTCATTGCTTGTCACGGCTGGAGAAGATTAACAGATTAGTAAGGAGGGGAATTGACAACATGTCATGCCTGCTTAAGACATGGCGTATCAAATTCTGTTCACTTGTAATCTGTTTCGTTGATGGTTTTAGCCAAAATACTGATGACTGCTTGTGCTTCTGTTGTTC[A/T]GATGGCCCGAGGGTGCTGTACTTGAGAGTTGAAGATCGGACCACCAGTAGTCTGACCTTGTCCTGGGCTGTGGACCATCATGTGCAGAATCAACCCTCCCCTCGCTACGAGCTCATGTACCGCAAGAAGGTGATTAAGCCTCTTTTTTCTCTAACGTTCATTCATTTTCTTTTCGGCTTAGTCCCTTAATTAATCAGGGGTCGCCACAGAGGAATGAACCGCCAACTTATCCAGCATATGTTTTACACAGTGGATGCCCTTCCAGCTGCAACCCATCACTGGGAAACACCCATACACTCTCATTCACACACATTCACTACGGACAATTTCGTTTACCCAATTCACCTATAGTGCACATCTTTAGACTGTGGGGAAACCGGAGCACCTGGAGGAAACCCATGCCAACACGGGGAGAACATGCAAACTCCACACAGAAATGCCAAATAACCCAGCTGAGGCTCGGACCAGCAACCTTTTTGCTTTGAGGCTACAGCGATACC
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa33949
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 |
---|---|---|---|---|---|
ENSDART00000025428 | Nonsense | 586 | 984 | 9 | 17 |
ENSDART00000136964 | None | None | 52 | None | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 45821667)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 45882601 |
GRCz11 | 6 | 45884483 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCTGAATTCCCACGTCAGACGGAGGGTTGATGGAGATTACTTTTCATG[T/A]CCAGGTATGACATGGATTTTGGCATTTGTGTGCATCTGTTTGGTATTTGA
Long Flanking Sequence:
AGTTTGAATGCTTTCGGGCATGAGAAAGTGTGTAACTTAGATGCATTGGTGATAGGCTGTGTGCGTGTGCGTGTGTGGTGCGTCAGTGTTTGTCAGTATAAGTAAAGTGAACTTCTTTTTTTATTCTCACAGCGGAATCTCGGACACAGAACAGTTCCATGGTTGTCATGGGAGCCATCGCCGGGGGCGGGGTCATGTTGCTGATTGTGGTGGTTATTCTGCTTCTGCACAAAAGGTTAGCGAACGTATCTCTGCTCTCACTTTTTCCAGTCTATTCTCTTCTTTATCTCTATCCAGACCGCAGAGCAGGATTTCCCAACTTGGCCTTCAATGCCTGCCCACACTGTTTACATTCCAGCTTTGATCTACAATCATGCTCATTTAAAGAAACCATCGAGATAGCAGCTTTAATTATCTCGCTAATGTGATGTTGAATGCTCTTTCATCAGGAGGCTGAATTCCCACGTCAGACGGAGGGTTGATGGAGATTACTTTTCATG[T/A]CCAGGTATGACATGGATTTTGGCATTTGTGTGCATCTGTTTGGTATTTGAAATGATCTGATGGTCAGCAATAACTTTGTATGAATCACTGAAGATCATCGTACAGTGGGTGTCGTCTAATCCAAGGTCAAATCTTTTCTTATTTTGAAGAAAAACTCCTTCCGTTGAAGACCTACATCGATCCCCACACATATGAAGACCCCTGTGCGGCCATCCTCAAGTTTGCCAGTGAGATTCATCCTGGTCACATCACCAAGCAGAAAGTCATTGGTGCAGGTCAGTGTTCATATTGTGTTAGCCGTATGGTATATTAATAGTATACATGGACTAATATAAATATCTAAATATTTTAGAATATATTTTATTTTTAAGTATTTTTGGGTTTATTTTAGTTGAAGTAAACATTTTTTTATTCAGTTTGTTATTCATTCATGGTAGAATATTGCGAAATGAATACACCAGATGACCTGAATAGCTTAATGTAGAAAAAAGAAATCTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40777
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 |
---|---|---|---|---|---|
ENSDART00000025428 | Essential Splice Site | 629 | 984 | 10 | 17 |
ENSDART00000136964 | None | None | 52 | None | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 45821391)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 45882325 |
GRCz11 | 6 | 45884207 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGAGATTCATCCTGGTCACATCACCAAGCAGAAAGTCATTGGTGCAG[G/A]TCAGTGTTCATATTGTGTTAGCCGTATGGTATATTAATAGTATACATGGA
Long Flanking Sequence:
CTCTTCTTTATCTCTATCCAGACCGCAGAGCAGGATTTCCCAACTTGGCCTTCAATGCCTGCCCACACTGTTTACATTCCAGCTTTGATCTACAATCATGCTCATTTAAAGAAACCATCGAGATAGCAGCTTTAATTATCTCGCTAATGTGATGTTGAATGCTCTTTCATCAGGAGGCTGAATTCCCACGTCAGACGGAGGGTTGATGGAGATTACTTTTCATGTCCAGGTATGACATGGATTTTGGCATTTGTGTGCATCTGTTTGGTATTTGAAATGATCTGATGGTCAGCAATAACTTTGTATGAATCACTGAAGATCATCGTACAGTGGGTGTCGTCTAATCCAAGGTCAAATCTTTTCTTATTTTGAAGAAAAACTCCTTCCGTTGAAGACCTACATCGATCCCCACACATATGAAGACCCCTGTGCGGCCATCCTCAAGTTTGCCAGTGAGATTCATCCTGGTCACATCACCAAGCAGAAAGTCATTGGTGCAG[G/A]TCAGTGTTCATATTGTGTTAGCCGTATGGTATATTAATAGTATACATGGACTAATATAAATATCTAAATATTTTAGAATATATTTTATTTTTAAGTATTTTTGGGTTTATTTTAGTTGAAGTAAACATTTTTTTATTCAGTTTGTTATTCATTCATGGTAGAATATTGCGAAATGAATACACCAGATGACCTGAATAGCTTAATGTAGAAAAAAGAAATCTTGAATTTAGATAGATTGGGGTAATTTTGTATGAAAATTGGGATGTGAAATAATTGCAAGCAAGAGTAATTACAATAGAGCAAAGAAATAAAGTTAAATAAACATAGATTTATAGTTTTCTAGAGAGTCAAACACTATTCAGACACAGTAAGCGAGTAATGAAATGTAAAAATAACTCTATATAGTCTTAGTTATATTAATATTTCATTAAAAGTATTCTTCAATAAAGTTACAAATGTGCTTTTTTTTTTACCCGAACTCTCTTGAAATGCCTTTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44642
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 |
---|---|---|---|---|---|
ENSDART00000025428 | Nonsense | 659 | 984 | 11 | 17 |
ENSDART00000136964 | None | None | 52 | None | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 45819213)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 45880147 |
GRCz11 | 6 | 45882029 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGGGCCGCAGTGAGGTCGCAGTAGCCATAAAGACACTGAAGCCAGGCTA[T/A]ACGGAAAAGCAGAGGCAAGACTTCCTCAGCGAGGCCAGCATCATGGGCCA
Long Flanking Sequence:
ATTATTAAGCCCTCTATATATTTTTCTCCCAATTTGTATAACGATGAGAGGAATTTTTAACATATATCTAAGCATAATAGTTTTAATAAATAATTTCTTATCCTATCTTTGTCATGATGACAGTAGATAACATTTCAAGATAGTAATAGTAGTATTCAGCTTGTAGTGGCGTTTAAAGGCTTGACTAGGTTAATTAGGTTAATTTGGCAAGTTAGGTTAAATTAAACAACCTAAAATTGTTTTAAAATATAAAAACTGCTTTTATTCTAGCTAAAATAAAACAAATAAGACTTTTTCCAATAGAAAAGATATTTTAGGTATTACTGTGATTTTTTTTTCTGTGTACAATTTTACCGGACTTCATTTTATTAGTTAAGATCAATAATTTTAAGAACCCATAATTGTCCAACAGGCGAGTTTGGGGAGGTGTTTCGTGGCTCTCTGAAGATGCCGGGCCGCAGTGAGGTCGCAGTAGCCATAAAGACACTGAAGCCAGGCTA[T/A]ACGGAAAAGCAGAGGCAAGACTTCCTCAGCGAGGCCAGCATCATGGGCCAGTTTTCCCACAAGAACATTATCCGTCTGGAAGGTGTCGTCACCAAATGTAAGTAATGTAATGTAATCAGATTATAAATGCATGCTTCTGGCAACTCTACATAGCAGTGCATGTTTTAACAGGATGTTCTCCTTCATTTCAGTCAAAGATGCCATGATTATCACCGAGTACATGGAGAATGGAGCTCTGGACCAGTATTTAAGGGTGTGTTTTGGTCTATGAATAAACAAATCTGAATAATCTGAAATGTATTAGAATCACTGATGATTTTATTTGTGCTTAACAGGATCACGATGGGGATTTTTCCTCATACCAGCTTGTGGGGATGTTGAACGGCATTGCAGCAGGAATGAAGTATCTCTCAGACATGAACTACGTCCATCGGGACCTCGCAGCTCGCAATGTGCTGGTCAACAGCAACTTGGAGTGTAAAGTGTCCGATTTCGGCTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33948
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 |
---|---|---|---|---|---|
ENSDART00000025428 | Essential Splice Site | 832 | 984 | 14 | 17 |
ENSDART00000136964 | None | None | 52 | None | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 45816071)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 45877005 |
GRCz11 | 6 | 45878887 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGATGTCATTTGGAGAAAGACCCTACTGGGACATGAGCAACCAAGAGG[T/C]ATGGAGTGTTACTTATGTTTTTTTGATCGATGGCTATACATCAAAATGGG
Long Flanking Sequence:
AGGTCACTGGTTCGAGTCCCGGCTGAGTCAGTTGGCATTTCAGTGTGGAGTTTACATGTTCATGTGGGTTTTCTCCAGGTTCTCCGGTTTCCCCCTCAGTTTAAAGACATGAGCTATAGGTGAATTGAGTAAAATATATTGGCCGTATAGTATGTGTGTGAATAAGTGTGTATTAATGTTTCCCAGCTGGAAGGGCAACCGCTGTGTAAAAGCGGATACTGGATAAGTTGGTGGTTCATTCCGCTGTGACGACCCCTGATGAGAAAAGGAACTAAGCCAAAAGAAAATGAATGAATGAATTGTATACAAAAGTCTGACATTGTATGTTGTTTGTTTTATTTGTTTTTAGGGCGGAAAGATTCCTATTCGCTGGACTGCACCAGAGGCAATAGCTTACAGGAAGTTCACTTCTGCTAGTGATGTGTGGAGCTTCGGCATAGTCATGTGGGAAGTGATGTCATTTGGAGAAAGACCCTACTGGGACATGAGCAACCAAGAGG[T/C]ATGGAGTGTTACTTATGTTTTTTTGATCGATGGCTATACATCAAAATGGGTGATGATGAAAAACATGAATTAAGTAAAAGACATTTCTAGGAAACAAAAAGTGAAAGGGTTCGTTTACCTCAAAATGTTGTCATTCTGAACTCATAAGTTTTTAGTTGGTCCTCTGGGGCCAGATTCTCCAGCAGTACGTAAGTTTAAACGTAGCCTAGTTGTGACTTAAAGGGACACTAAGTTAAAACATTACTAAAATTTATTTGTGTTGCACCACTGAACGTAGTTTAAATGTGACGCTATGTTACAACTAAATATTTACAGCAGCCTCCCCCATGTATAACGGTAGAAAAGAGACGACAGCGATTATAATGAAGAATGATCTTCCTCTACTCGCAACCTTATTTTCCTCCCAAATCTCGATGTATTTTTTTCAGTTTATGAAATGTGTTTAATTTTTTTTCAAGGAGTGTTTTGCGTTATTCATATTCATCAATTAAAACAAGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20802
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 |
---|---|---|---|---|---|
ENSDART00000025428 | Nonsense | 970 | 984 | 17 | 17 |
ENSDART00000136964 | None | None | 52 | None | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 45812399)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 45873333 |
GRCz11 | 6 | 45875215 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTGGAGTTCGGCTGGCAGGTCATCAGAAGAGAATAGCATACAGCATTT[T/A]GGGCCTGCAAGACCCAGTGGGGGCCTTGGATTTGTTTGCAATGTGATAAT
Long Flanking Sequence:
AAAACATCAGCATGCAAAATAAGACAAAAGATCATGGAAATCCCATTTGCCCAAGTCATTTTTAACAAATGATCCACTTGTGATTTATACTTCAAAACAGCGCAGAATAGTGCATGAAATACAAACTGGGATGCAGCAATGTTCACTAAAACCTGGTTTATTTTCATCACAGTGTCTCCATTCGTCTACCCAGCACTAGTGGTTGTGATGGCGCCCCCTTCAGGTCAGTGGACGAATGGCTGGAATCCATCAAAATGGCCCAGTACAGAGAAACCTTCGCCCTCGCTGGCATTAAATCTTTCGACCAGGTGCTGCGCTTGAAAATTGAGTAAGTATCCTCTGCATTCAAAAACCAAACACAAATGTAACCAAATGTGTATTACCAAAAATTCCATATGCCATCATATAACGTTTTTCTATCAACTTCTTTTTCTAAAGGGACATCGGGAATATTGGAGTTCGGCTGGCAGGTCATCAGAAGAGAATAGCATACAGCATTT[T/A]GGGCCTGCAAGACCCAGTGGGGGCCTTGGATTTGTTTGCAATGTGATAATACGGTCGACTGAAGCAACACTGTTTTGAATGGATTTTAAAAAAAACTGACTAAAGACTAGAATGCCCTTTTTCAATCAAACGGACTCCCTCTGGGAATATGAACACTTTACTGTTAGTTTGTTTATGCATTTTATAGTCTATTTTTCCACATGTCAGATGGACCCTTATGCTCTTTGCCATGTTTTAAACATAAGCCATATTAAGCACACGTATGATGGTAAGCTTTGAAATGCTATAACTACTGTCTCAGGTCTGATGATTAGGGTACTATCAAGTCTACGGTAGTAACCTTGGATATTACTGTGGTGCCCTTATAGTGAACAAAGCTGCCCGAATATGAGGGGTTGAAGTCTGATTAAACTTTGTACAATTGTAATTGTAAAAATGTTTGTAGTAAACATGATTTTTTTTTTTTTGTCAAATTGTTGACCTGCATCCTTTTCTGTCAA
Associated Phenotype:
Not determined